Professional Documents
Culture Documents
Data Guides
Over the years, a series of data guides and technical notes have been published as a service to our customers and friends. We have updated these documents and included additional information about our services.
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The mission of Safety Management Services is to safeguard people, processes, and the environment. Our mission is accomplished by assisting our clients in maintaining the safety of their operations through the systematic identification of safety related deficiencies, and the development and implementation of solutions.
Caution--No Warranties Safety Management S e ~ c e sInc. , disclaims any warranties with respect to the information herein, whether expressed or implied, including, without limitation, any implied warranty of merchantabilityor fitness for a particular purpose and/or any other warranty as to the accuracy, safety or suitability of the information or the results obtained by the application of the information, whether used alone or in combination with other information, product or service. User assumes all risk, responsibility and liability whatsoever for any and all injuries (including death), losses or damages to persons or property arising from the use of the information. User must determine the accuracy, safety and suitability of the information and the results to be obtained from the application of the information for their own business. Safety Management Services, Inc. neither assumes nor authorizes any person to assume any liability in connection with the use of the information.
July 1999
1 Section &Technical
Notes
Capabilities Overview OSHA and EPA Regulation Compliance Process Hazards Analysis Phases Process Hazards Analysis Techniques Hazardous Materials Testina Services Facilrty Siting for Reactive Chemicals & Explosives Explosive Venting Suppressive Shielding Technology (SST) Electrostatics in Materials Handlina Omrations Streaming Currents Aqueous Solutions of Flammable Materials Flash Points of Aqueous Solution
1-1 1-2 1-3 1-4 1-5 1-8 1-9 1-10 1-11 1-12 1-15 1-17 1-19 2-2 24 2-8 2-12 2-14 2-16 2-17 2-19 2-20 2-21 2-22 2-23 2-24 2-25 2-26 2-27 2-28 2-29 2-30 2-31 2-32 2-33 2-34 2-35 2-36 2-37 2-38 2-39 2-40 2-41 2-42 2-43 2-44 2-45 246 2-47 2-48
Flash Points of Chemical Compounds Autoignition Temperatures of Organic Chemicals Limits of Flammabilitv of Individual Gases and Vaoors in Air at Atmos~heric Pressure flame Velociti Calculation of Stoichiometric Compositions Flammability Data Guides--Introduction Acetal, CH3CH(OGH5)(1,1-Dietho~yethane)~ Acetaldehyde, CH3CH0 Acetic Acid, CH3COOH Acetic Anhydride, (CH3C0)70 Acetone, CH3CHOCH3 (Propanone) Acetonitrile, CH3CN(Methyl Cyanide) Acrolein, CH2:CHCH0 (Acrylaldehyde) Acrylonitrile, CH,:CHCN (Propenenitrile, Vinyl Cyanide) Allyl Alcohol, CH2:CHCH70H(2-Propen-1-01) Allyl Chloride, CH2:CHCH7CI(3-Chloropropene) n-Amyl Alcohol, CH3CH3CH2CH2CH20H (1-Pentanol) seeAmyl Alcohol CH3CH2CH2CH(OH)CH3 Aniline, C6H5NH2 (Aminobenzene, Phenylamine) Benzene, C6H6 Biphenyl, C6H5C6H5 1.3-Butadiene, CH2:CHCH:CH2 (Vinyiethylene) 1 -Butanol, CH3(CH2)9CH20H (Butyl Alcohol) 2-Butanol, CH3CH2CHOHCH2 (seeButyl Alcohol) 2-Butanone, CH3COCH2CH3 (Methyl Ethyl Ketone) Butyl Acetate, CH3COOC4H9 (Butylthanoate) Butyl Acrylate, CH2:CHCOOC4H9 BUMBenzene, C6H5C4H9 seeButyi Benzene, C6H5C(CH3)C2H5 fert-BUMBenzene, C6H5C(CH3)3 Butyl Bromide, CH3(CH7)2CH7Br ~Buty Chloride, l CH3CH7CH2CH2CI (1-Chlorobutane) n-Butyl Forrnate, CH3CH2CH2CHCOOH (Butyl Methanoate) Butylene Oxide, (CH3)2COCH7 Butraldehyde, CH3(CH2)2CH0 Camphor, CIo~r60
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CONTENTS (Cont)
Carbon Disulfide, CS2 Chlorobenzene, C6ti&I (Monochlorobenzene) Cumene, C6H5.C3H7 (Isopropylbenzene) Cyclohexane, C6H12 (Hexamethylene) Cyclohexanone, CsHloO pcyrnene, CH3C6H4CH(CH3)2 (Isopmpyttoluene) Decane, CH3 (CH7)&H3 Dibutyl Ether, (C4H9)90 Dichlorobenzene, C 6 H I C h 1,2-Dichloroethylene, CICH:CHCI Diethylamine, (C,H&NH Diethylene Glycol Methyl Ether, CH30CpH40C7H40H Diethylene Glycol Monoethyl Ether, CH,0HCH70CH7CH70C2H5 Diethyl Ether, C2H50&H5(Ethyl Ether) Dimethylamine, (CH3)2NH 2,2-Dimethylbutane, (CH3)3CCH2CH3 (Neohexane) 1,4-Dioxane, 0CH2CH20CH,CH2 (Diethylene Dioxide) Ethanol, GH50H (Ethyl Alcohol) Ethyl Acetate, CH3COOC2H5 Ethyl Benzene, C6HSC2H5 (Phenylethane) Ethylene Chlorohydrin, CICH7CH70H (2-Chloroethanol) Ethyl Propionate, CH3CH7COOCH2CH3 Heptane, CH3(CH2)5CH3 Hexane, CH3(CH2)4CH3 lsoamyl Acetate, CH3COOCH,CH,CH(CH3)2 (Banana Oil) Methanol, CH30H(MethylAlcohol) Methyl Butyl Ketone, CH3CO(CH,)3CH3 (2-Hexanone) 2-Methyl-1-Propanol, (CH3)2CHCH70H (Isobutyl Alcohol) 2-Methyl-2-Propanol, (CH3)3COH (tert-Butyl Alcohol) Methyl Propionate, CH3CH2COOCH3 Naphthalene, CloH8 (Tar Camphor) Pentane, CH3(CH7)3CH3 1-Propanol, CH3CH2CH20H (n-Propyl Alcohol) 2-Propanol, CH3CHOHCH3 (Isopropyl Alcohol, Isopropanol) Styrene Monomer, C6H5CHCH2 Toluene, C6H5CH3 (Methyl Benzene) Vinyl Acetate, CH3COOCH:CH2 Vinyl Chloride, CH2:CHCI (Chloroethylene) 2-49 2-50 2-51 2-52 2-53 2-54 2-55 2-56 2-57 2-58 2-59 2-60 2-61 2-62 2-63 2-64 2-65 2-66 2-67 2-68 2-69 2-70 2-71 2-72 2-73 2-74 2-75 2-76 2-77 2-78 2-79 2-80 2-81 2-82 2-83 2-84 2-85 2-86
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Section I
Technical Notes
TECHNOTES
CAPABILITIES OVERVIEW SAFETY MANAGEMENT SERVICES (SMS) Safety Management Services, Inc. (SMS) provides regulatory compliance, process hazards analysis, material testing, training, and documentation control services specifically tailored to customer requirements and needs. REGULATORY COMPLIANCE OSHA regulations, 'Process Safety Management" (29 CFR 1910.1 19) and EPA 'Risk Management Programsw (40 CFR Part 68), encourage the same systematic approach to pmess safety management that we have used since 1958. Disciplines and tools are in place to help others compty with these stringent regulations through a coordinated, cost-effective team approach. Our techniques can be applied to any process in any industry, and can be tailored to complement the client's capabilities. PROCESS HAZARDS ANALYSIS With more than 35 years of application, our process hazards analysis approach has become an industry standard. Our methodology, which complies with the latest OSHA and EPA requirements, is based on formalized engineering and risk analysis techniques. Our personnel are highly trained in hazards analysis techniques and have extensive experience analyzing a wide variety of energetic, hazardous, and reactive materials and processes. Process Hazards Analysis services include: Process hazards review and assessment W hat-if and Checklist Analysis Failure Modes and Effects Analysis (FMEA) Hazard and OperabilRy Study (HAZOP) Fault Tree Analysis (FTA) In-process energy modeling Riskkost tradeoff Accidenthncident investigation Dispersion modeling and explosion siting Explosive venting and pressure relief criteria Reliabilrty/availability/maintainability analysis TESTING SERVICES A broad range of material testing services are available that can be applied independently or in conjunction with our Process Hazards Analysis services. Lab-scale, bench-scale and full-scale capabilrty is available. Testing services include: Material sensitivity Thermal response Dust and vapor explosibility DOT and DoD classification Chemical and physical analysis Electrical properties Specialized and on-site testing Sensitivity test equipment and training
TECHNOTES
MECHANICAL INTEGRITY SERVICES OSHA Process Safety Management and EPA Risk Management regulations require a Mechanical lntegrity Program. SMS services include:
Identificationfprioritization of applicable equipment. Maintenance/administrativeprocedures Employee training Inspection and Testing Plans and Procedures Equipment Deficiency and Quality Assurance Plans Mechanical Integrity Program implementation
working conditions where cumulative trauma disorders (CTDs), repetitive strain injuries (RSls), acute soft tissue injuries, or other ergonomic concerns are present. SMS personnel are experienced in workplace design, manual material handling, human factors, office ergonomics, and developing corporate ergonomic programs. INDUSTRIAL HYGIENE Industrial hygiene augments SMS risk management capabilities. These capabilities include air contaminant and physical agents monitoring and control, facility safety and health inspections, employee training, and heatth and safety programs development. These activities are done under the direction of a Certified Industrial Hygienist. TRAINING Customized training courses are available to train employees and management in regulation compliance, process hazards analysis techniques, hazardous material properties, and mechanical integnty compliance.
ERGONOMIC ANALYSIS Ergonomic analyses allow for the identification, prioritization, and mitigation of ergonomic hazards in the workplace. SMS has developed and applied systematic ergonomic analysis methodology to a variety of operations. This methodology facilitates clear identificationand communication of ergonomic issues. SMS provides practical solutions to ergonomic hazards encountered in a myriad of
TECHNOTES
OSHA AND EPA REGULATION COMPLIANCE OSHA PROCESS SAFETY MGT REG The OSHA 29 CFR 1910.119 Process Safety management (PSM) regulation requires the management of hazards associated with handling and processing highly hazardous chemicals and establishment of a comprehensive management program that integrates technologies, procedures, and management practices. The elements of the PSM regulation are shown as an arch, with the elements of Process Safety Information and Process Hazards Analysis as keystone elements and management commitment and documentation controVaccess as the structure base. We can provide in-plant consulting and assistance to the management/employeeteam for all of these elements. For example, process hazards analysis, sensitivity testing, mechanical integrity program development, and employee training services are routinely provided.
EPA RISK MGT PROGRAMS REG
Safety Review
Protection of Employees
in~estigathl
Compliance Audits
Trade
Secrets
DocumentationContrd/Acc~ss
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Management Commitment
1-3429
The EPA Risk Management Programs (RMP) regulation requires measures to protect the public and the environment. As shown in the arch, it contains the same elements as the OSHA regulation with additional elements for the risk assessment and the consequences of releasing hazardous chemicals outside the boundaries of the handling or manufacturing facility. Process Safety worst-case Release Information, Risk Assessment, and Process Hazards Analysis elements off-sie make up the keystone, supporting all the e q other elements. Safety Management Services can provide help with the key elements, program management assistance, and all of the regulation elements. Expertise is available to assist with the important issues such as consequences of an accident to the public and environment including plume dispersion, release probabilities, and off-site issues.
DocumentationConWlAcc8ss
Management Commitment
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TECHNOTES
PROCESS HAZARDS ANALYSIS PHASES PROCESS HAZARDS ANALYSIS (PHA) The h i g n Hazards Analysis (DHA) phase addresses the concept, design and early construction stages of the process. The flowcharts, equipment drawings, and discussions with engineers may be the only items that can be evaluated during this phase. At this point, however, it is easy and cost effective to correct design problems discovered by the DHA. Safety guidelines can be recommendedthat will help direct the process design toward a safe and perhaps more economical configuration. The Operational Hazards Analysis (OHA) can begin as equipment is put in place during construction, start-up, and early production phases. An OHA can be done when equipment is in place, procedures are available, and the operator interface with equipment is observed. The DHA and OHA may overlap at times if part of the process is still under construction but another part is ready to go into operation. The total Process Hazards Analysis (PHA) consists of both the DHA and the OHA phases. Of course, if the process is an existing process the PHA can be performed in one phase using all the process safety information.
PHA is a systematic approach to i d e m potential hazards and to recommend actions to eliminate (or minimize) process hazards. OSHA Process Safety 0.1 19 Management (PSM) regulation 29 CFR 191 requires that an 'appropriatewformal analysis technique is used and lists some specific methodologies. The complexity of the hazards analysis technique or combination of techniques used should reflect the complexity of the process. The phases of a project will also determine the most suitable method. The common types of hazards analysis methods are discussed in later sections along with their advantages and disadvantages. SMS uses the method or combination of methods that is best suited for the specific process type and complexity.
PHA PHASES The PHA phases correspond to the phases in a process, as shown in the diagram. A typical process development will go through many phases from concept to design, construction, start-up, production, and then changes as improvements need to be made.
PHA Phases
ProcessPheses
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PROCESS HAZARDS ANALYSIS TECHNIQUES HAZARDS ANALYSIS SELECTION TECHNIQUES Selection of the proper PHA methodology for a process should be made on the basis of whid technique lends itself to the type and complexity of the process being analyzed. To be able to make a wise choice, the advantages, disadvantages, and differences of the various techniques must be known. SMS has a thorough knowledge of these PHA techniques and has expertise in applying them to a wide spectrum of processes and operations. Our personnel are available to cost-effectively help our clients meet the OSHA Process Safety Management (PSM) and EPA Risk Management Plan (RMP) requirements using any of the following hazards analysis methods or combinations of methods. CHECKLIST ANALYSIS Checklist Analysis is appropriate for simple processes where failure scenarios and consequences ate straight forward. It consists of listing critical items or procedural steps to be done before the process is performed. It usually can be completed within days (sometimes hours), and can be easily understood by non-safety-orientedpersonnel. The effectiveness of this method is limited by the experience of the personnel making the checklist. These personnel must have an intimate understandingof the process, equipment, and controls. This type of analysis is easy to complete and can be done at any stage in the life of a project once the appropriate checklist is compiled. WHAT-IF TECHNIQUE The what-if technique is a relatively unstructured approach that takes advantages of team brainstorming. The team leader assembles information on the process and invites individuals with the appropriate backgrounds in safety, processing, engineering, maintenance, etc. to be part of the What-if team. A scribe is designated to record the resutts of the session. The team steps through the process and members verbalize their safety concerns by posing "What-if" questions such as, "What if the reaction vessel overheats?" Discussion resutting from each question is pursued and the consequences, hazards, safeguards, and recommendations or other comments recorded. Follow-up assignments may be made. Advantages of the what-if method are that it is easy to organize and conduct and it promotes interaction of people with different backgrounds to bring out and develop safety issues. Usually, it is used with relatively simple processes and can be very cost-effective if conducted appropriately. However, some safety issues may be overlooked and may require a more structures, systematic hazards analysis method. WHAT-IFtCHECKLIST TECHNIQUE The W hat-#/Checklist methodology combines both the W hat-if and the Checklist techniques. A W hat-if brainstorming approach is conducted but a Checklist appropriate for the process to be analyzed is used to help generate the questions. This helps make the analysis more complete. The combination is still limited since it is relatively unstructured and is not the systematic approach needed for more complex processes. HAZARD AND OPERABILITY STUDY (HAZOP) The HAZOP is a structured technique in which a team with varied backgrounds performs a systematic study of a process to determine how deviations from the design intent can occur in equipment, actions, or materials, and to establish if the consequences of these deviations can resutt in a hazard. Recommendations for changes in design, procedures, etc., are made to improve the safety of the system. A wellprepared and disciplined leader prepares the information, documents, and procedures for the team to review and prepares sheets with guide words to drive the brainstorming process, and to document findings and recommendations. The process is broken down into components and the appropriate guide words and possible deviations considered for each section. The HAZOP is particularty useful for continuous processes such as chemical or petroleum processes that have interconnectedequipment. tf done properly the analysis will be very complete and the issues and recommendations will be well documented. The HAZOP analysis process can be time consuming and expensive and may not be appropriate for simple processes. Complex and/or interactive systems may require the use of additional hazards analysis methodologies for more detailed assessment.
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techniques such as the FMEA or HAZOP to help identdy potential safety issues in a client's process. We have found that by using deductive logic followed by inductive bgic that a high level of certainty can be achieved regarding identificationof failure scenarios and combinations of scenarios. In addition, we use a systematic engineering approach to prudently apply quantitative risk analysis. SYSTEMATIC ENGINEERING APPROACH The Systematic Engineering Approach to Process Hazards Analysis is outlined in the diagram and includes the following steps: Assess the process and provide level setting guidelines such as prioritizing hazardous operations and equipment so that the scope of the analysis is bounded and taken to the appropriate depth. Identify failure scenarios. Select a methodology or combination of methodologies that reflects the complexity of the process. Both deductive and inductive forms of logic can be used. Evaluate potential hazards using qualitative risk assessment such as hazard categories (MIL-STD882C) where appropriate or using quantitative risk assessment such as a probabilistic technique for more critical scenarios. Energy in a process and reactive process materials can be evaluated and compared using engineering testing and analysis techniques to help make decisions about the process. For example, the data obtained from sensitivity testing such as impact, friction, electrostatic discharge, thermal property testing, etc. can be used for comparison against the calculated or measured energy, pressure, temperature etc., in the process. From this comparison, a safety factor or probability of initiation can be obtained. Combined with component failure rates, human error probabilities and other process event probabilities, a probability of a major event can be determined. Quantitative analysis data can also be used in a risklcost trade-off analysis to compare the cost of safety with the potential cost of an accident to help management make decisions related to safety programs.
TECHNOTES
Process Hazards Analysis
A Systematic Engineering Approach
ASSESS PROCESS
s
CRITERIA
TECHNOTES
HAZARDOUS MATERIALS TESTING SERVICES Safety Management Services, Inc. has extensive testing capabilities for characterization of hazardous materials. These services can be used independently or in conjunction with our process hazards analysis services. Over f i standard tests are available to characterize materials under conditions that simulate typical process conditions. Testing capabilities include both standard and custom testing tailored specifically to the client's needs. Recommendations based on statistical evaluation of the material test data are made to help the client minimize the process risks. Prices and additional information are available on request for the following tests and additional customized tests.
NOL Card Gap Explosive Cap Testing (No. 8 Cap) Ignitionand Unconfined Bum Thin Layer Propagation
Internal Ignition Bureau of Mines Gap Deflagration to Detonation Low-Level Shock Low-Energy Mechanical Shock Bonfire Critical Diameter Wedge and Standard Critical Height Transparent Pipe Bullet lmpact Shotgun Pressuremime Modified UN Screening Bum-rate Test Closed Bomb Closed Pipe Detonation Stack Single Package Free Fall lmpingement Heat of Combustion Heat of Reaction Mass Bum Rate Solid lmpingement Liquid lmpingement Thin Layer Burning Surveillance Detonation Velocity Insensitive Munitions Cook-off Slow Cook-off Fast Cook-off, Jet Fuel Fast Cook-off, Propane Shaped Charge Jet Shaped Charge Spall Sympathetic Detonation
Large Scale Tests TNT Equivalency Large Scale Critical Height Large Scale Critical Diameter Experimental Machining Separation Ring Coupon Skid Tests
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FAClLrrV SITING FOR REACTIVE CHEMICALS AND WPLOSIVES SITING EVALUATIONS including catastrophic releases of EPA regulated substances that may cause emissions, fire, or explosions that could endanger the public or the environment near your plant sites. We use vaporlplurne dispersion modeling to evaluate worstcase off-site consequences. SMS can provide your company with the documentation to meet the EPA Risk Management Plan (RMP) or provide the hazard assessment recommendations to meet the RMP requirements. INFORMATION NEEDED FOR SITING EVALUATIONS The OSHA 29 CFR 1910.1 19 'Process Safety Managemenr regulation requires that the Process Hazards Analysis include facility siting if siting is identified as a process hazard and is likely to lead to catastrophic consequences in the workplace. The following is typical of the information gathered for facility or process siting evaluations: ldentifiition of any Do0 regulations and local, state, and national codes with which the facilrty must comply. TNT Equivalence for explosives or the reactivtty of chemicals at the facilityloperation. Quantity of material available to react under worst-case conditions for the operation under consideration. Known history of any incidents that would confirm or refute the reactive characteristics of the materials in question. Layout of the general facilrty including location, buildings nearby, distances to property lines, public roads, and other plant site operations. The EPA 40 CFR Part 68, 'Risk Management Plan" regulation requires the following additional information to complete the Off-site Consequence Analysis: The chemical names of regulated substances Physical state of toxic substances Scenario (explosion, fire, toxic releaselspill) Quantrty released in pounds Distance to potential off-site targets Process systems to mitigate releases
TECHNOTES
EXPLOSIVE VENTING
Hazardous materials can react very rapidly. When explosive solids or liquids, flammable dusts, or flammable chemical vapors are present in an industrial process, the potential for explosion hazards exists. It is always essential to have design features in the system that will minimize the possibilityof having an explosion such as controlling the fuel concentration below the lower flammable limit or limiting potential ignition sources. An appropriate hazards analysis of the process will determine potential failure modes and recommend ways to minimize risk. Explosiveventing is often the most practical solution to minimize the effects if an explosive event inadvertently does occur. The concept of explosion venting is quite simple. When a deflagration begins in confined equipment, hot gases are formed and pressures rapidly rise to a point where the equipment is ruptured and badly damaged. Explosive venting can reduce the damage to facilities and injury to personnel caused by these rapid reactions. If appropriate vents have been installed, the vent will open at a low pressure and allow the hot gases to escape so that destructive pressures are never reached. Proper design and sizing of vents depend on the rate of reaction of these hazardous materials and the configuration and environment to which they are subjected. Some materials detonate and produce extremely damaging overpressure shock waves that travel out from the center of the explosion. Other materials deflagrate or bum very rapidly but produce less damaging overpressure waves. Items to consider in vent design are maximum pressure and maximum pressure rate; design parameters such as volumes, shapes, and interconnections; and process variables such as particle size and concentration. With such data and modeling techniques, the proper vent sizes, vent placement, and number of vents to be used can be determined.
If a material can detonate in its environment, then it should be treated as a detonating material and evaluated with the TNT Equivalency Model for explosives. If a material can only deflagrate in the worst case environment, then it should be treated as a deflagrating material and evaluated with the TNT Equivalency Model for explosives using the appropriate lower TNT equivalency.
If a material is a flammable chemical vapor, it may detonate, or deflagrate in the worst case environment. It may have to be evaluated W-WI the TNT Equivalency Model for explosives or with the Muttienergy Model that is more typical for some chemical plant reactions.
The U. S. Military has characterized the damaging effects of explosives with the TNT Equivalency Model as used in manuals such as TM5-1300, "Structures to Resist the Effects of Accidental Explosions," November 1990. A manual published by the Center For Chemical Process Safety of AlChE can provide assistance in defining the potential effects from hazardous chemical reactions. The manual's title is 'Guidelines for Evaluating the Characteristics of Vapor Cloud Explosions, Flash Fires and BLEVEs," 1994. The National Fire Prevention Association's recommendations are in NFPA 68 Guide for Venting Deflagrations 1994 version, and NFPA 69 Explosive Prevention System - 1992 version, and NFPA 495 Explosive Material Code - 1992.
SMS can help model and/or test your hazardous materials and assist you in developing the appropriate explosive venting configuration and help you with other precautions to protect your employees, facilities, and equipment from potentially harmful and damaging explosive events.
TECHNOTES
SUPPRESSIVE SHIELDING TECHNOLOGY ( S T ) WHAT IS SST? SST APPLICATIONS
SST devices prevent blast pressure, fragments, and flame generated by an explosion from damaging equipment, buildings, and injuring people outside the exclusion zone. SST can be designed as a barrier wall or container and is constructed of perforated metal sheets, spaced layers of metal angles or Ibeams, and screening. A barrier wall or container can be any size, ranging from a table tool box to a room-sized enclosure.
Each SST device is designed using specialized technology, owned by SMS, for a specific type of hazard and anticipated explosive quantity. SST devices are designed and assembled to overcome each anticipated hazard. Components necessary to defeat each of these hazards are assembled in a composite matrix structure. SEVEN APPROVED VSS GROUP DESIGNS
SST scale model and prototype devices have been extensively tested. The US Department of Defense (DoD) Explosive Safety Board has approved seven SST group design structures that protect against fragments and blast effects generated by 0.4 kg to 1136 kg of explosives with a TNT equivalency of 1.O.
Public Safety Airport luggage handling and security zones Post offices and corporate mail rooms Embassy buildings Local police bomb squads
Explosive manufacturing Explosive/energeticmanufacturing buildings In-process storage containers and cabinets Inter-line propagation barriers Operator shielding Magazine and material storage units Transportation Explosives and pyrotechnics shipping Experimentaland material storage units Military Uses Explosive ordnance disposal Mine clearing operations Chemical munitions remediation Noise Suppression Explosivestesting Explosives disposal
TECHNOTES
ELECTROSTATICSIN MATERIALS HANDLING OPERATIONS INTRODUCTION citing a specific example where conditions were 'just righr for causing inadvertent ignition.
One of the more exasperating problems in industrial operations today is the control of electrostatic charges to prevent inadvertent ignition of flammable vapors or dusts. In instances where the process equipment is all metal and the process materials are reasonably conductive, proper attention to grounding and bonding practices can eliminate or control buildup of electrostatic charges. However, in instances where plastic or glass is used in process equipment and/or the process materials are nonconductors, the engineering manager must assure himself that electrostatic charges cannot accumulate in his process in such a manner as to occasion an unwarranted risk.
In order for electrostatic energies to cause inadvertent ignition, three mechanisms must occur. charge generation, charge accumulation, and discharge. Charge generation occurs any time two dissimilar materials in contact separate. The charge can be accumulated onto one or both of the materials, depending upon the details of the process. Consider the simple pouring or chuting of a granular material. If a nonconducting material slides down a surface (of a conductor or a nonconductor) and falls into a pile, a charge can be accumulated on the pile. The amount of the total charge on the pile will, of course, depend on the amount of the material and the charge densrty. Experiments show that the amount of charge per mass of material (or in some instances, per volume of material) is constant for a given set of process conditions (e.g., throughputs, angles, materials of construction, humiddy, etc.). Table Ishows typical values for some process materials. Table I Charge Densities for Selected Process Materials As Determined in Controlled Chuting Experiments
Process Material Plastic flake Benzidine yellow Gilsonite TNT Charge Densities, C k g 7.1 loe7 9.4 x lo4 2.6 x 1 O& 2.1 x lo-'
THE INCIDENT
An incident occurred several years ago in an everyday dumping operation where a 'dusty" powder was being emptied from a drum into a piece of fixed process equipment. The fixed equipment was metallic and well grounded, as is usually the case in equipment of this kind. After the operator had dumped the material and was withdrawing the drum, a dust explosion occurred. (See Figure 1.) In this case, the dust cloud was essentially unconfined, and the operator received only superficial bums. Nevertheless, an accident investigation was promptly initiated, and it was determined that the fueVair mixture of the dust cloud had been ignited by an electrostatic spark as the operator moved the drum across the lip of process equipment. Figure 1 Dumping Operation
THE INVESTIGATION
It was established that the operator was dumping 40 pounds of the process material from a drum 16 inches in diameter and 20 inches high. The operation carried out at this plant location for several years. There has been no previous indication that a potential hazard
This is an easily demonstrated mechanism for accumulating an electrostatic charge, but in materials handling operations it can be of little or no consequence, depending on operating conditions. Perhaps the best way of providing an insight into the problem is by
TECHNOTES
existed. However, a recent process change had been introduced: all-metal drums had been replaced with plastic drums having metal chimes around the upper periphery. (See Figure 2.)
Figure 2 Drums Charge Accumulation
During the dumping operation, a total charge of 3.6 x lo9 coulombs was generated and stored on the interior surface of the drum. If a charge is uniformly distributed, the surface charge density, a, can be easily calculated: Height of drum, h = 0.508 m (20 in.) Diameter of drum, d = 0.406 m (16 in.) The surface area, S, of the drum is then given by: S = &+adh 4 i.e., S = 0.777 m2 The surface charge density is given by:
All-Metal Drum
Plastic Drum With Metal Chime If one considers the interior of the drum as a Gaussian surface over which a sheet of charge is distributed, the electric field, E, adjacent to the surface is given by:
The investigation quickly established the presence of the fuellair mixture in the dust cloud-a situation that was invariably created when the material was dumped. In situ measurements showed that a dust cloud concentration of 0.25 kg/m3was typical. When this value is compared with the minimum concentration for a dust explosion in the Hartmann apparatus of 0.06 kg/m3, it is shown that this operation created an explosible dust cloud. The investigation was then directed toward identrfyng the source of ignition. In this case, the mechanisms for electrostatic charge generation, charge accumulation, and discharge were obvious. Charge generation can occur when the process material slides over the plastic drum. Charge accumulation can occur on the surface of the plastic drum and can be transferred to the chime. And finally, discharge can occur when the metal chime is moved across the lip of the fixed process equipment. THE MECHANISMS
However, in the experiments with the field test meter, it was found that the charge was not uniformly distributed. On the side of the drum opposite the place where the process material slid down, the field was essentially zero. In the area where the sliding took place, the field test meter indicated its maximum value of 5,000 Vlcmi.e., twice the calculated value. Electrostatic charges, if left undisturbed, will eventually relax. A quantitative measure of this ability to relax is the relaxation time, 7, which is the time required for the charge to reach U e of its original value. From the relaxation quation,' where E = permittivity and y = conductivity is mhoslm The permittivity of the process material was determined to be 4.1 in its as-received or in-process condition. Its mhoslm; conductivity was determined to be 2.5 x therefore, the relaxationtime of the process material is given by:
Charge Generation
A drum of process material was taken to the laboratory and a mass of 18.1 kg (40 Ib) of process material was dumped into a Farada ca e. It was found that a charge, Q, of 3.6 x 101 coulombs was generated and remained on the process material; thus, the charge density was 2 x lo-' coulombs/kg. Since this was the charge on the material, an equal and opposite charge remained on the drum. A field test meter showed that the surface of the plastic became charged during the pouring operations. These experiments indicated that a charge was generated by the sliding of the material over the plastic, and that charge accumulation occurred when the process material was dumped from the drum.
i.e., T = 24 minutes
TECHNOTES
i.e., J = 0.020 joule or J=20mJ This is the same order of energies that have been shown to ignite dust clouds. ckhoff2 reports that Australian wheat dust can be ignited with spark energies as low as 20 mJ, and that fine aluminum powder can be readily ignited with spark energies on the order of 1 mJ. It should be pointed out that the probability of ignition at these energies is less than one; nevertheless, such a probability is unacceptable. In the accident investigation, a probabilistic determination was made, but a discussion of that methodology is beyond the scope of this Tech-Note.
SUMMARY
This calculation demonstrates that the process material was capable of retaining the charge for a period that is long compared with the time of the operation. Similarly, it can be shown that the charge will be retained on the plastic drum. The rate at which the charge can dissipate from the drum is dependent on a number of conditions, primarily those having to do with surface conductivity, surface cleanliness, moisture, etc. For the process conditions at the time of the incident, the relaxation time was found to be on the order of tens of minutes to hours. Since these relaxation times are long compared with the times of the operation, the right conditions for charge generation and accumulation existed for the process conditions.
Discharge
The capacitance, C, of the metal chime on the drum was determined to be 7.1 x lo-" farads. It is necessary to make this measurement in the process environment since the presence of other objects can have a significant effect on the capacitance of such a freestanding conductor. The charge on the interior surface of the drum was induced on the metal chime of the drum, and discharge occurred from the chime to the fixed process equipment as the operator withdrew the drum by sliding it over the edge of the fixed equipment. A.reasonable estimate of the energy in the discharge can be calculated from considerations of the geometry of the chime and the quantity of the induced charge. If all of the charge is induced onto the metal chime, it can be shown that the surface charge denstty will exceed maximum value of 2.6 x c1m2, at which point corona discharge will occur. The surface area of the chime, s, can be approximated from the equation for a torus. s =47t?~r where R = major radius and r = minor radius The 'minor diameter" of the chime was 1.6 cm. Then s = 4 2 (0.203) (0.008) i.e., s = 0.0641 m2 The surface charge density @ given by:
The example given was chosen in an effort to provide the reader with some insight into the mechanisms of electrostatics, and an understanding of how the various factors must come into play for an unacceptable operation to result. This example was intended to point up the fact that an engineering manager must exercise caution in the introduction of plastic components into process equipment. This is particularly so in cases where the process materials have low conductivities, or where they have a propensity for generating and accumulating electrostatic charges. Engineering managers who suspect they may have a similar situation in their process are invited to call us for a telephone consulation. REFERENCES
1. F. G. Eichel, 'Electrostatics," Chemical Engineering, March 13, 1967, pp. 153-67. 2. R. K. Eckhoff, Towards Absolute Minimum Ignition Energies for Dust Clouds?", Combustion and Flame, 24, pp. 5344,1975.
Therefore, a nonincendiary corona discharge will occur from the free-standing chime until a surface charge density of approximately 2.6 x 1oe5 c1m2 is reached, at which time a charge of 1.7 x lo6 coulombs will remain on the chime having a capacitance of 7.1 x 10-l1farads. Therefore, the energy on the chime that will be discharged when sparking occurs between the chime and the grounded equipment will be given b y
1. ElectrostaticHazards, Their Evaluation and Control, Heinze Haase, Verlag Chemie, Weinheim, New York, 1977. 2. Static Electtifitcation, lnstitute of Physics and Physical Society, Conference Series No. 4, London, England, 1967. 3. Static Electrifkation, The lnstitute of Physics, Conference Series No. 11, London, England, 1971. 4. Static Electrification, The Institute of Physics, Conference Series No. 27, London, England, 1975. 5. Electrostatics and Its Applications, A. D. Moore, ed., John Wiley & Sons, New York, New York, 1973.
TECHNOTES
STREAMING CURRENTS BY T. H. Pratt INTRODUCTION One of the more vexing problems in industrial safety today is the ignition of flammable liquids by electrostatic discharges. Handbooks on the subject are replete with procedures and precautions having to do with electmstatics-inerting, grounding of equipment, using proper containers, etc. Nevertheless, serious incidents continue to occur in places where electrostatic discharges were thought to be unusual or unlikely.
One such mechanism, often overlooked, is that of streaming currents that occur when liquids having the proper electrical qualities flow through process equipment. In cases where the liquids are also flammable, there are conditions where the liquids can bootstrap themselves to self-ignition. The potential for such ignition can be identified (and subsequently eliminated) by a careful examination of a process when one has a working knowledge of the mechanisms involved. Perhaps the best way of providing insight into the problem is by citing an example. An actual boot strapping scenario was reconstructed in an accident investigation that took place several years ago.
During the investigation of the accident it was concluded that the operator had opened the valve, withdrawn his hands, and was simply looking at the bucket when ignition occurred. In the consideration of the ignition source, electrostatics were considered to be the most probable; however, discharge from the operator was ruled out since he was not near the bucket. ' I was just standing there looking at it when it caught fire," he said. Also ruled out as a source was the possibility of a charge having been generated on the bucket prior to the operation. The mechanism of a streaming current was then considered. THE MECHANISMS The conductivity of the sample of toluene taken from the process was measured in the laboratory at 2.9 x 10 mhosicm. The literature value for the viscosity of toluene is 5.9 cps, and its dielectric constant is given as 2.4. Knowing from the process that a pressure drop of 35 psi occurs in the last two feet of pipe (i.e., from the filter to the end of the pipe) and knowing the capacitance of the bucket as being of the order of 20 pf, and remembering that ignition occurred approximately 10 seconds after the valve was opened, a mechanism of the charge being generated by the flowing of the toluene and subsequent discharge from the bucket can be made quantitative as follows: Charge Generation
If it is postulated that the charge was generated by the flowing of the toluene through the pipe, the question arises as to whether or not sufficient energy could be generated to result in a discharge that could ignite toluene.
THE INCIDENT A fire started when an operator was drawing a bucket of toluene from a tank that was an integral part of process equipment. He had placed a metal bucket with a wire bail and a plastic handle under a globe valve that was two feet downstream from an in-line filter. He had opened the valve to draw the toluene. In a few seconds, the toluene ignited. The operator left the scene and quickly retumed with a small fire extinguisher, which proved to be inadequate. He then left the scene again and retumed with a larger extinguisher, but by this time the bucket was overflowing and the fire was out of control.
First, streaming current ( I , ) is calculated from the streaming current equation of Reference 1.
TECHNOTES
In this situation the vottage can be determined from the energy relation of Reference 1. where A = area of the pipe in cm2r(3.14) (2.5412/4] E = dielectric constant for toluene (2.4) = absolute dielectric constant in sedohm cm (8.85 x 10-14) 6 = zeta potential in volts (0.1) AP = pressure drop in dynes/cm2(35 x 6.89 x lo4) L = pipe length in cm (2 x 12 x 2.54) p = viscos' of toluene in poise or dyne seckm (0.059) . = 7.2 x 1O4 ampere i.e., I
If this current flows for 10 seconds and is stored on the bucket, which has a capacitance of approximately20 pf , the energy (J) is given by
This compares with the requirement of 30,000 volts to discharge between 2 cm electrodes at a separation of 1.8 cm, as given in Reference 3. Thus, ample potential was present to support the bootstrap scenario. (A further discussion of the discharge path as examined in the accident investigation is beyond the scope of this Tech-Note.) SUMMARY We hope this example has given the reader some insight as to where and how streaming currents can lead to fires and what to look for in a process to determine if precautions are in order. One must look for the right combination of all the parameters in the foregoing equations, but one should be especially concerned with flammable liquids of low conductivity in processes having high flow rates and large pressure drops.
REFERENCES
F. G. Eichel, 'Electrostatics," Chem. Eng., March 13, 1967, pp. 153-167. H. F. Calcote, C. A. Gregory, Jr., C. M. Bamett, and Ruth B. Gilmer, 'Spark Ignition," Ind. and Eng. Chem. 44,2656 (1952). H. Pender and K. Mcllwain, ElectnkalEngineers Handbook, John Wiley 8 Sons, Inc. (1950). N. Gibson and F. C. Lloyd, 'Electrification of Toluene Flowing in Large Diameter Metal Pipes," J. Phys. D : Appl. Phys. 3, p. 562 (1970). Static Electrification, Institute of Physics and Physical Society, Conference Series No. 4, London, England (1967). Static EEleMmtion, The lnstitute of Physics, Conference Series No. 11, London, England (1971). Static Electrification, The lnstitute of Physics, Conference Series No. 27, London, England (1975). Electrostatics and Its Applications, A. 0. Moore, Editor, John Wiley & Sons, New York, New York (1973).
where Q = charge in coulombs C = capacitance in farads (20 x 10-12) t = time in seconds (10) i.e., J = 0.013 joule This is, by order of magnitude, more energy than that required for ignition of compounds of this type, as discussed in Reference 2.
Charge Storage
The charge that has been generated by the streaming current initially resides in the toluene. In this instance, the charge is quickly transferred to the exterior of the bucket, as shown by a calculation of the relaxation time ($) of the charge from the body of the toluene, from the relaxation equation of Reference 1.
In other instances, toluene may have conductivities of <10-14,in which case a space charge would remain on the body of the toluene for much longer periods. In such a case a different mechanism prevails, but a hazardous situation would still exist.
Discharge
Discharge could take place to any convenient ground (around the plastic handle) if the voltage is high enough.
TECHNOTES
AQUEOUS SOLUTIONS OF FLAMMABLE MATERIALS
By Thomas H. Pratt INTRODUCTION The publication of Data Guides(') has prompted a number of requests and/or inquiries that translate to something like "what about aqueous solutions of flammable materials?" The answer is simply that one treats the vapor space above the liquid in essentially the same manner, except that one plots the vapor-phase concentration of flammable material as a function of liquid-phase concentration at a constant temperature and pressure, rather than as a function of temperature for a concentration of 10O0/0. A discussion of such determinations is the subject of this Tech-Note. In the case of flammable liquids that are watersoluble, the addition of water can cause the vapors above the liquid (under equilibrium or near-equilibrium conditions) to go from a nonflammable state to a flammable state. This occurs upon dilution of the liquid and consequent dilution of the flammable in the vapor phase, causing the vapor concentration to go from a point above the UFL to a point below the UFL. Thus, there are certain conditions under which a process can go from a nonhazardousstate to a hazardousstate by the addition of water. Since this is contrary to the concept of putting out fires with water, it sometimes comes as a surprise to chemical operators. Therefore, project engineers should realize the importance of a process analysis where water-soluble flammables are present. THE GRAPH During a process analysis, it is necessary to determine what specific process conditions must exist for aqueous solutions of flammable solvents to form flammable vapors in closed-process equipment. Such a determination is quite straightforward when vapor-phase activities for aqueous solutions and flammabilitydata for the materials are available from the literature. Acetone has been selected as an example to demonstrate how the determinations are made. The in-processconditions that have been selected are equilibrium conditions at one atmosphere and 25C (77F). The first task is to construct a graph depicting the vapor-phase concentrationof the flammable material as a function of its liquid-phase concentration. The vaporphase concentrationis typically expressed as the partial pressure of the flammable materialand the liquid-phase concentration is typically expressed as a percent (weight percent, volume percent, etc., whichever is apFIGURE 1. VAPOR DATA FOR ACETONEIWATER AT 25C (77F)
140
120
I"
100
B
W K W K
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30
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propriate). For example, partial pressures in mm Hg and weight percent in liquid phase have been chosen. Thus, the Nterature for acetone'.2 yielded the vapor concentration curve of Fiaure 1.
TECHNOTES
the UFL and the vapors become flammable (Figure 1). As dilution continues beyond this point, conditions for combustion become more favorable, until Ca is reached at a liquid-phase concentration of acetone of approximately 8%. It is at this point that the most favorable conditions for combustion exist since the amount of acetone in the vapor phase is balanced with the amount of atmospheric oxygen. Upon further dilution of the liquid, the amount of vapor-phase acetone is decreased, and the LFL is reached at a liquid-phase concentration of acetone of appmximately 4%. These numbers should be used advisedly, since there are significant temperature effects. However, it was determined in a flash point apparatus at 27C that the vapors above an acetonehater solution would not flash at a liquid-phase concentration of 7%, but exhibited a flash at 8%; that is, solutions of acetone in water at concentrations of 8% and greater are flammable liquids at 27C and above.
REFERENCES
The vapor space above pure acetone in a closed container, at one atmosphere and 25"C, is nonflammable because the vapors are fuel-rich, or above the UFL. However, if acetone is diluted with water, the amount of acetone in the vapor phase will be reduced. When the concentration of acetone in the liquid phase reaches approximately 26%, the concentration of acetone in the vapor phase reaches
Beare, McVicor, and Ferguson, J. Phys. Chem., 34, p. 1310 (1930). Taylor, J. Phys. Chem, 4, p. 355 (1900).
M. G. Zabetakis, 'Flammability Characteristics of Combustible Gases and Vapors," Bureau of Mines Bulletin 627 (1965).
TECHNOTES
FLASH POINTS OF AQUEOUS SOLUTIONS
L. R. ALBAUGH and T. H. PRA'TT INTRODUCTION Aqueous solutions of flammable liquids are sometimes misunderstood by chemical operators-and by engineers-in that they are sometimes considered to be nonflammableand thus nonhazardous, when indeed the vapors above the liquid are within the flammable limits. Such misunderstandings come about because of the concept of putting out fires with water. Some people find it incredible that 8% solutions of flammable materials in water will constitute explosion hazards for ordinary process conditions. The Flammability Data Guided1)discuss the flammability characteristics of a vapor space above pure materials as a function of temperature. Tech-Note Number 2(l)discussed the flammability characteristics
CONCENTRATKWI OF ETHYL ALCOHOL IN LIQUID PHASE, wt %
of vapor spaces above aqueous solutions as a function of concentration at a fixed temperature. It is the purpose of this Tech-Note to discuss the flash points of aqueous solutions as a function of concentration. THE GRAPHS Ethyl alcohol (ethanol) has been selected for the example in this Tech-Note. An examination of the Flammability Data Guide for Ethanol (Bulletin HE-117) shows that the approximate temperature range where flammable vapors exist over pure liquid ethanol (at equilibrium in dry air at one atmosphere) is 12.8 to 420~ This . showithat the vapor spaces in closed containers of 100%ethyl alcohol are flammableat ambient conditions (25C and one atmosphere). If the liquidphase ethyl alcohol is diluted with water, there results
CONCENTRATIONOF WATER, vol K
i m a a m r n m s o 4 o ~ 0 2 o i o o
Fiw, 1. Vapor Data tor Ethyl AkohoWatw Mixtures at 2SC 0 and One Atmospbm Total P m w r e
TECHNOTES
a concomitant dilution of ethyl alcohol in the vapor phase. By the use of activity coefficients, a plot of liquid-phase concentration vs vapor-phase concentration (or partial pressure) can be constructed for a process condition of 25C and one atmosphere. (See Figure 1.) This graph shows that the stoichiometric point, Ca, occurs very close to the azeotrope, and that the lower flammable limit, LFL, is reached when the liquid-phase concentration is 44 vol % ethyl alcohol (or 38 wt %). This is the same kind of graph that was discussed in Tech-Note Number 2 for acetone, and is useful for process analyses at ambient conditions. However, at process conditions other than 2SC, this particular kind of graph is of limited utilrty. If an aqueous solution of ethyl alcohol at a concentration somewhat below 44 vol % is warmed to a temperature above 25C. the concentration of ethyl alcohol in the vapor phase will increase to such an extent that the lower flammable limit will be exceeded. For example, the vapors above a 30% ethyl alcohol solution can be ignited at temperatures of 29C and above; that is, the flash point for 30% ethyl alcohol solutions is 29C. An experimentally determined curve (Reference 1) for the flash point of ethyl alcohol solutions as a function of liquid-phase concentration is shown in Figure 2. The flash point can be considered as the temperature at which the lower flammable limit, LFL, is exceeded. Note that for a flash point of 25"C, the liquid-phase concentration of ethyl alcohol is 44 vol %, which corresponds to the LFL point in Figure 1. There is also a curve for the upper flammable limit on Figure 2, but it has not been experimentally determined. From the Flammability Data Guide for Ethanol, however, it can be determined that the UFL is exceeded at 42C. This establishes a point at 100% ethyl alcohol in Figure 2. Activity coefficients were used to estimate the upper limit of flammability for other concentrations; the region of flammabilrty is shown as the shaded portion of Figure 2. Since the most approximate of methods for the upper limit was used, the validity of the graph should be checked by actual experiment wherever reliable data are needed. THE INTERPRETATION The curve drawn in Figure 2 is the flash point as a function of concentration, and the ordinate has been so labeled. Scales are given for the flash point in both Celsius and Fahrenheit degrees. The shaded region of Figure 2, which represents the region of flammability, was added simply for completeness. The curve is the closed-cup flash point; other curves for open-cup flash point and fire point have also been determined, and lie above the closed-cup flash point curve in the region of flammability. The ethyl alcohol data find some application when applied to commercially available distilled spirits-e.g., vodka. When one performs the parlor trick of dropping a lighted match in a just-emptied bottle, the vapors are observed to bum. When 80-proof vodka (40 vol %) is used, a lazy, nonpersistent flame, if any, is observed. When 100-proof vodka is used, a rather satisfymg 'whoosh" comes from the bottle. When 1%proof "grain neutral spiritsw is used, an alarming whistle of hot gases issues from the neck of the bottle. (See Figure 1.) Additionally, in the making of flaming desserts, one does not use a wine that typically has a concentration of 12% as the source of the flame. Neither does one attempt to make an ice cream flamM with a brandyor even grain neutral spiritssince the vapors will be below the lower flammable limit at the temperature of the ice cream. (See Figure 2.) REFERENCE 1. H. Stem, "Inflammability of Liquid Mixtures with Inflammable and Nonflammable Components," Proceedings of the 1st International Symposium, The Hague/Delft, The Netherlands, May 28-30, 1974; Loss Prevention and Safeiy Pmmotion in the Prvcess Industries, p. 293.
Management
Section I1
Data Guides
DATA GUIDE
Saturated hydrocarbons Ethane Propane Methane n-Pentane lsobutane lsopentane n-Heptane Triptane lsooctane 2,2-Dimethylpropane 2,2-Dimethylbutane Unsaturated hydrocarbons Acetylene Vinylacetylene Ethylene Methylacetylene 1,3-Butadiene Propylene 1-Heptyne 2-Pentene Diisobutylene Substituted alkyls Methanol lsopropyl mercaptan lsopropyl alcohol Allyl chloride n-Propyl chloride Triethylamine n-Butyl chloride Isopropyl chloride lsopropylamine Ethylamine Aldehydes Acrolein Propionaldehyde Acetaldehyde
Minimum I nition ~nerg~!.) 10 J O U ~ ~ S Ketones 2.85 Methyl ethyl ketone 3.05 Acetone
(a) H.F. Calcote, C. A. Gregory, Jr., C. M. Barnett, and Ruth 8. Gilmer, %park Ignition, Effect of Molecular Structure.' Ind. Eng. Chem. 44,
2659,1952.
DATA GUIDE
Minimum Ignition Energy, Joules
0.00015 0.0009
Vapour
Carbon disulphide Dioxane Ethyl ether Benzene Ethyl acetate
0.00045
0.0005
0.0005 0.00075
0.0005 0.00065 0.0006 0.0006 0.0011
Butyl acetate
Methyl alcohol Ethyl alcohol Butyl alcohol Acetone Heptane
@)
F. J. Lewellyn. 'Incendiary Action o f Electric Sparks in Relation to Their Physical Properties," Chemistry Department, The University of Edgbaston, Birmingham 15, England.
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synonym Hexalin; hexahydrophend Ketahexamethylene Hedin acetate Aminocyclohexane Pentarnethylene 4-lsopmpyl-1-methylbenzene Decalin Decyl hydf'ide Di-n-amylamine
Nnn
Diiropanohmine Diisoprqylamine D i i i y l benzene Diketene Dimethoxy ethyl -late Dimethoxymethane Dimethoxy tetragiyd Dimethylaniline Dimethylbutane-2.2 Dimettrylbutane-2.3 Dimethykhloracetal Dimethylcycbhexane-p Dimethyldichlorosilane Dimethyl-o,o diilomvinyl-22 phosphate Dimethyl dioxane Dimethylethondarnine Dimethyl ether Dimethvl formarnide ~ i m e t h h 2 . 4 DimethylpMhalate-o Dimethylsebacate Dimethyld a t e Dinitroaniline-2.4 Dinitrobenzene-1.2 Dinitrochlorobenzene Dioctyl m a t e MPA
Synonym
Diamyl naphthalene phenol-2.4 Dt-tert-amylphenoxyethand D h M phthalate-n sulfide ~iama Dianiidine Dibenzyl ether Dibutoxy ethyl pMhalate Dibulomethane Dibutylaminen Dibutylarninoehml Dibutyl ether-n omlaten phosphite phthalate-n
Hexahydroxyld DDS DDVP Methyl ether; methoxym#hm DMF D i i r o p y l methane DMP Methyl sebacate Methyl sutfate 2,4-Dinitrophenylamine eDinitrobenzd DinitrocMorobenmi Di-2-ethylhexylphthalate; DOP See Diethylenedioxide Limonene; cinene See Biphenyl Phenylaniline; DPA Phenyl ether; diphenyl odde Benzylbenzene See Diphenyl ether
Vinylidene chloride
-DEA
1-3-Diiloro-2.4-heradiene Dichbroisopmpylether
1,l -Dichlom, 1nitroethane 1.1-Dichlom. 1&mrooane 3chloropentanes (&xed) kydohexylamine Mydopmtadiene 3iethandamine Diethylamine 3iethylaminoethand Bethylaniline Diethylbenzene-1.3 Mylbenzene-1.4 3i-2-ethylbutyl pMhalate M y l carbonate M y l Whenyl urea %ethylenegtycd %ethyleneoxide Diethin ether Diethyl glycol phthalate Diethyl hexylamine 3i-2sthylhexyladipate 3i-2-ethylhexyl adipate Diettryl ketone Diethyl malonate %ethyloxalate %ethylphthalate-o %ethylphthalate-p 3iethyl sulfate Yiwromonochbmethane Yiwromonochloromethane 3iglycd chlorohydrin %glycoldiacetate Y i y c d dilevulinate 3ihydropyran 31sobutylketone 3iisobutyl phthalate
D i n e glycol Divinyl ether Dodecane-n Ephichlarohydrin Ethane Ethylacetanilide Ethyl ecetate Ethvl acetoacetate ~ t ha h Ethyl aniline-n Eth$ benzene Ethyl benzoyl acetate Ethyl borate butad ~thyr 2-Ethyl buM acetate 2-~thh bu&l alcohol 2-EU1yl butyl carbonate 2-Ethylkrtyraldehyde Ethyl butyrete-n 2-Ethymyric acid Ethyl carbonate Ethyl m d e Ethyl chlorocaMate Ethyl chloroformate Ethvl crotonate ~ t h cydohewne a Ethyl diethanolamine ~thylene Ethylenecarbanate Ethylene chlomhydrin Ethylenediamine Ethylene dichloride
Ethylene glycol Ethylene glycol diacetate Ethyleneirnine
Ethyl c a h a t e N,N'Gethykarbanilide Diiydroxydkthyl ether 1,bDixane 2.2-Diiinodiethylamine See Diethvlarninoethanol Ether; eth$ ether Diethoxyethylphthalate DiocMamine Dioctyl adipate; DOA D i phthalate; DOP Wentanone Ethyl malonate; malonic ester Ethyl ethanedioate Ethyl-o-phthalate Ethyl-pphthalate Ethyl sulfate See Chlorodiftwroethane See Chlorodifluoromethane Diethyleneglycol diacetate aycd dilevulinate ~iethylene
Diethyl acetaldehyde Ethyl butanoate Diethyl acetic acid See ~iethyl carbonate Chlomethane Ethyl chloroformate See Ethyl chlorocarbonate
Ethene Gylcd carttonate 2Chloroethanol 1.2-Ethanediamine 12-Dichloroethane; ethylene chloride Glycol Glycol diacetate Dimethyleneimine
DATA GUIDE
Name Ethylene oxide Ethylethanolamine-1 Ethyl ether Ethyl fonnate Ethyl hexaldehyde 2-Ethylhewnedid-1.3 2-Ethylhexanoic acid Ethyl h e x a d E m lactate
Ethyl morphdine Ethyl nitrate Ethvl nitrite ~th;t oxalate Ethyl ohend ethandamine ~ t h phtha~w 4 ethyi m t e Ethyl pmpionate 2-Ethyl-3pmpyIacrdein Ethyl n-proWf ether Ethyl silicate Ethyl ptduene sulfonamide Fonnal Formic acid Furan Furfural Furfuryl alcohol Furfurylamine Glvcerol ~l~cer triacetate yl Glycor diacetate Synonym 1.2-Epoxyethane Ethyhrmnoettaand See Diethyi ether Ethyl methanoate Ethylheglycd Odoic acid 2-Ethyl hexyl alcohol Ethyl 2hydroxy propanoate
cup
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See Ethylene glycol diacetate Ethylene glycol difonnate
Nafne 2-Methyl butadiine-1.3 ~-~eth 1-butand + %Methyl butene-l Methyl rrbutyl ketone-/ Methvl butvrate Methyl caftmlate Methyl cydohexane Methyl cydohexand Methyl cydohexanone Methyl cydonexyl acetate Methyldiethanolamine Methyl ether Methyl ethyl ether Methyl ethyl ketone 2-Methyi-5-ethyl @dine Methyl formate Methyl glycol acetate Methyl hexyl ketone Methyl 3-hydroxVbutyrate Methyl isoamyl ketone Methyl isobutyl ketone Methyl lactate Methyl mecaptan Methyl methacrylate Methyl monochloroacetate Methyl morphdine 1-Methylnaphthalene Methylpentadiene 2-Methyl pentane
2-Methyl propene Methyl propionate ~ e t h pro& 3 carbind Methyl mpropyl ketone Methyl pyrrole-n Methyl pyrrdiine-n Methyl sakcylate Methyl sterate Methyl trichlorosihne Methyl vinyl ketone Monochloroethylene Monoethylamine Monomethylamine Morphdine Naphthalene Naphthd, P Naphthylamine. a Nitroaniliiep Niibobenzene Nib.obiphend-0 Niirobenr8ne-p N i i Nitranethane Nitronaphthalene, a 1-Nitropropane 2-Nitmpmpane Nitrotoluene-p rnN-tduidine Nonane-n Octane-n 1-0ctand-n 2Uctand-n Octyl acetate octyl aldehyde glycd
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57
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See Dimethyl ether Methoxyetbne 2-8utanone; MEK Aldehydine; MEP Methyl methanoate Pmwlene glycd acetate 2atanone
Methanethid
~~
Isohexane; dimethylpropyl methane See Isobutylene Methyl propanoate See Pentad-2 2-Pentanone Oil of wintergreen
Hexyl alcohol-n Hexyl alcohol-pseudo ~ex&ne glycol Hexyl ether-n Hydraane Hydrocyanic acid Hydroquinone Hydroxyethyl morpfiolene h m y l alcohd Lsabutane Lsobutyl acetate Lsobutylamine lsobutytbenzene lsobutylene lsobutyl heptyl ketone lsobutyraldehyde lsooctane Lsophorone isoprene Isopropenylacetate Isopwyl alcohd Isopropylamine lsoprupylbenzene m r o dether LauM alcohol Maleic anhydride 2-Mercaptoethand Mesityl oxide Metaldehyde Methacrdein Methoxy ethyl phthalate Methoxytriglycd acetate Methyl acetate Methy( acetoacetate Methyl acrylate Methylal Methvl alcohol Methylaminemono Methylamyl acetate Methylamyi alcohol
See Vinyl chloride See Ethylamine See Methylamine 1.4-Owadne Moth Rakes white tar p-Hydroxy naphthalene
para-Nitraniline Nitrobenml; oil of mirbane
Methylnitrobenzene
pOctyl alcohol-n
Capryl aicohd
9~ ohcaad
4-Methyl-3-penterte-2-one
1 Dirnethoxymethane, formal
Methand; carbind; wood alcohol Amifmetham See Hexyl acetate Methyl lsotmyl cafthlol Heptanorre-2
Paraform 2.4,f5-Trimethyl-l.3,5-t1ioxane Amyl hydride 2-Methyl butane See Acetyhcetone Amyl alcohdsec-n; methyl p r o d carbinol Amyl alcohdsec-n; d i i y l caltlid ptert-Amy(phenol Phenanthrin pEthoxyaniline Carbdic acid; hydroxybenzene Acetyl p h e d Diaminobenzene
DATA GUIDE
Tiiq
Cloud 185 188
Synocrym
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Name
Tduene Tduidine-o Tdumep Tduol
Synonym
Methylbenzene Methylaniline pMethylaniline See Tduene
*
363
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a-Methyl pyridine Pineclea Pdyvmyl alcohol (mixture) Prooandamine-iso Propionic acid Propionic anhydride Propionyl chb-ride P W acetaten P r o p y l acetateis0 Prod alcohol-n Propyla~iso Pmpylaminen Propybnzene-n ProoVlbenzene-iso
Propanoic anhydride
504
365 20 385 240 250 65 1
43
35
113 149 235 30 < 68 15 20 -108
80 78
Propylenecabnate Pmpylene chlorohydrin Prowlendmine Pmpylene oxide Pmpyl ether-is0 Proovl fomte-n propionate-n Pyridine f'vmcatechd Resorcind
1ChbPpfopad 19-Diamimpmpane Dichlowropane-1.2 12-Dihydroxypropane 1.2-Epowypropane ~~lsO9rop0xy~ro~a~ Pmpyl methanoate lsopropyl methanoate
74 165 35 1 200
34 140 70
I F 212
75
Xylene-p Xylidene
Reproduced by permission from NFPA No. 325M-1977 (Flammable Liquids, Gases and Volatile Solids), Copyright 1977, National Fire ProtectionAssociation, Boston, MA
retradecyl alcohol
Tetraethylene glycol Tetraethylenepentarnine Tetrahydrofuran Tetrahydrofurfuryl alcohol Tetrahydronaphthalene Pentamethyleneoxide
1 4
DATA GUIDE
AUTOIGNITION TEMPERATURES OF ORGANIC CHEMICALS
L o m s t Reportal AIT If 0thThan G k u or UnspecIfkd Ref 17 24 20 14 20 20
14
Lowest R.ported AIT i n Glass Ref 1. I Straight-Win Paraffins Methane Ethane Propane Butane Pentane Hexane Heplane Octane Nonane Decane Dodecane (dthexyl) Tetradecane Hexadecane (cetane) Octadecane Nonadecane Emsane 1.2 S l n g k B r a n c h d Paraffins 2-Methylpropane(tsobutane) 2-Melhylbutane (Isopenlane) 2-Memylpentane(tsohenane) 3-Methylpenlane 2-Melhylhexane 3-Methylhexane 2-Methylheptane 2-Methyloctane (tsononane) 3-Melhyloctane 4-Methyloctane 2-Methylnonane 2-Methyldecane 2-Methyluodecane 2-Ethyloctane 3-Ethyloctane 4-Ethyloctane
1.3 TweBranch.4 Paraffins
2 3 14 5 6 6
6 6 6 5
2 5
20
8 8 8
3 3
6 6
20
20 20
5 19 19 19 19
I9
20 20 20 20 8 12 8 20 20
2.2-D~methylpropane (neopentane) 2.2-D~melhylbulane (neohexane) 2.3-Dtmethylbulane 2.3-Dtmelhylpentane 2.3-Dtmethylhexane 3.3-Dtmethylheplane 2.3-Dmethyloctane 4.5-Dmethyloctane 2-Methyl-3-ethylpenlane 2-Methyl-4-ethylhe~~ane 3.3-D~ethylpentane 4-lsopropylheptane
19
6 6
20
19 19 19
20 12 20 20 8 20 20 20
(aWm)
1.3-D1met~ruene
(m-xwne)
1.4-ChmWbenzene @.r*ne) 1-2.3-Tnmthylbenzene 1-2.4-Tnmthylbenrene 1.3.5-Tr~rnefhytberuene
~ ~ ) 1-Methyl-2athylbemene
6 6 6 2 19 19 2 19
20 20 8
22
20 13 20 20 20
1-Methyl-3-ethylbruene 1-MelhylJamylbemene 13-hmylbenzene 1,3-[)lethylbenzene 1-4-Chethylbenzene 1-Melhyi-3,5-d1ethylbruene 1-MethylJ-tsopropylbenzene (P-CFern) D~ts~~benzene Styrene (wnylbenzene) (anmmne) a-Melhyl$(yr@ne
Excerpted by special permission from an article by Carlos J. Hilado and S. W. Clark of Union Carbide Corporation. Charleston. W. Va.. Chemical Engmeenng, September 4, 1972. by McGraw-Hill, Inc.. New York, N. Y: 10020.
-L L o m t Repormd A l l i n Glass
Ref 3.2 TwbRing Aromatics BWeW 2-Methylbiphenyl 2-Ethylbphenyl 2-Propylkphenyl 2-lsopropylkphenyl 2-Bulylblphenyl Dlphenylmethane 1.1-DIphenylethane. symmetrical
unsymmetrical
1.4.5.6-D~endomethylema-
u k d
Rei hydronaphthalene trans. trans. C I S 1 59-Cydodecatrlene 5.1 Straight-Chain Alcohds Methanol (methyl alcohol) Ethanol (ethyl aicohol) 1-Propano4 (propyl atohol) 2-Propanol (lsopropyl atohol) 1-8utanol (butyl alcohol) 2-Butan04 ten-Butanol 1-Penlano4 (amyl alcohol) 2-Pentanol 3-Pentand Decanol (decyl alcohol) 1-Dodecanol (lauryl alcohol) 5.2 Br8nch.d-Chain Alcohds 2-Methyl-1-pfOpanO( 2-Methyl-2-propano( 2-Methyl-1 -butanol 3-Methyl-1 -butanol (fuse1 011) 1-8utoxyethoxy-2-propanol 5.3 Cyclic Alcohols Cyclohexanol (Hexalm) w-Methylcycbhexanol p-Methylcyclohexanol 5.4 Aromatic Alcohds Phenol Benryl alcohol tr-Cresol (aesylc acld) m-Cresol p-Cred 5.5 Dihydroxy Alcohols Tetramethyleneglycol Ethylene glycol Dlethylene glycol Trtethylene glycol Propylene glycol Oclylene glycol 1.3-Butanedld 2.3-Butanedl01 1.5-Pentanedd 2-Ethyl-1.3-hexanedlol Thmd~glycol Buroxytrglycol p-Dthydroxybenzene fhydroqutnone) 5.6 Trihydroxy AIcoko(s Glycerol (glycerin) 5.7 Unuturated Alcohols Allyl akohd 20 20 20 20 20 17 20 20 20 20 20 20 20 20 21 20 20 20 8 20 20 20 20
2 19 19 19 19 2 19 19 19 2 2 19 19 19
1,I -Dlphenylpropane 1.1-Dlphenylbutane Naphthalene 1-Methylnaphthalene 1-Ethylnaphthalene Tetrahydronaphthakne (tetralln) Decahydronaphthalene (decahn) trans-Decahydronaphthalene Dlmethyl decaltn 3.3 ThreeRing Aromatics Anthracene 4.1 SinglaRing Cycloparaffins Cyclopropane Ethylcyclobutane Cyclopentane Methylcyclopentane Ethylcyclopentane Propylcyclopentane Butylcyclopentane Hexylcycbpentane Cyckhexane Methylcyclohexane Ethykyclohexane Propylcyclohexane lsopropylcyclohexane Butylcyclohexane lSObutylcyclohexane sec-Butylcyclohexane ten-Bulylcyclohexane Arnylcyclohexane Octylcyclohexane 1.2-D~methylcyclohexane 1.3-DImethylcyclohexane 1.4-D~melhylcyclohexane 1.2.4-Tr~methylcyclohexane 1.3.5-Tr~methylcyclohexane Dlethylcyclohexane Dmopopylcyclohexane
1-Methyl-4-~sopropylcyclohexane
2
3 2 6 6 2 15 15 15 5
6 6
15 15 15 15 15 15 15 15 15 15 15 15 15 15 15 15 15 15 15 15 15 15 15 15 15 15 15 15 15
20 20 20
Hexarnelhylcyclohexane Cyclodecane 4.2 Two-Ring Cycloparaftins Dlcyclopentyl Cyclohexylcyclopentane D~cyclohexyl Dlcyclohexylmethane 1.1-Dcyclohexylethane 1.2-Dqclohexylethane Hydrlndane Decahydronaphthalene (Decalln) Methyldecalln D~methyldecalln &cycb(2.2.1)heplane Plnane 4.3 T h r n R i n g Cycloprraffins 1-Cyclohexyldecaltn 1.2-Cyclopentanodecal~n Perhydroacenaphthene Perhydrofluorens 1.2.3.4-WcWntanocyclohexane Perhydroanthracene Perhydrophenanthrene Pemydrophenalene endo-Tetrahydrodtcyclopenta&elm Adamanran, 1.3-DwneMyladsmantane 1-Ethyladamantans
4.4 Four-Rlng and Fi-Ring 1.4.5.8-DIendomethylene-
6.1 Saturated Acids Form~c actd Acetlc acld Propionlc acld Butyrlc actd lsobutync acld P e n t a m acld (valerlc actd) Isopentaotc actd H e x a m acd (caproc actd) 2-Methylpentam acld 2-Ethylhexanolc acld Mtpc acd IsooctanO(Cacd
20
20 20 20
2-Ethybutyncacid
15 15 15 15 15 15 15 15 15 15 15 15 Stenc acid
20 20
7.1 Format. stom Methyl formate Ethyl tOnnate P r Wm a t e sopr rod fonate Buryl tormate lsobutyl formate
17 20 20 20 21 20 17 20 20 20 17
20
decahn 1.4.5.8-Dtrnethylene2.3-tnmethylenedecahydronaphthakne
15 15 15 15
7.2 h o t a t e Estm Methyl r e t e Ethyl acetate Prom acetate lsopropyl acetate Buryl acetate Isobutyl acetate Amyl acetate Isounyl acetate (banana 011) Vlnyl r e l a t e Methyl vlnyI8wtate Benzyi acetate CyciohexyI -late
7.4 Butyr8te and Higher b t u s Ethyl krtyrate Butyl slecrr:cs Ethyl lactate Butyl lactate
7.5 UM8turated Eatws Methyl acry(ate Ethyl acfyiate lsoknyl auylate 2-Ethghexyl acrylate Isodecyl acrylate Glycldyl acrylate
7.6 Arocrutk Esters Ethyl beruoate Benryl benzoate Methyl salqiate (011 of wntergreen) 7.7 Mestem Dmethyl phthalste Dibutyl phthalate Dlethyl maleate
7.8 T r h . 1 . r ~ Glycery( tnacetate (lnacetln)
0.1 Alip4uUc Oxid..
12.1 A m i m Methylamme D~methylamlne Ethylamme Dlethylamlne Propylamlne Dlpopylamlne lsopropylamne D n s ~ n Butylam~ne totT-&nvlarn~ne Allyiamlne Cydohexylarmne
Ethylene oxlde (oxwane) Propylene oxlde Bulyma oxlde Dlethyiene ox& (tetrahydrobran) Dlethylene dloxuie (pdoxane) Mesltyl ox* 8.2 Aromatic Oxid.. Styrene oxlde D~phenyl ox*
9.1 Saturated Ethers
Dlmethyl ether Diethyl ether Dipropyl ether Dils4propyI ether Dibutyl ether Dtamyl ether Dlhexyl ether Dtoclyl ether D~decyl ether Methyl ethyl ether 1.2-D~ethoxyethane
9.2 Unntur8t.d ethers
Dwnyl ether Vmyl methyl ether Vmyl ~sopropyl ether Vlnyl butyl ether
9.4 Arommtic Ethers
13.1 C.llosohm Glycol Ethers Methyl celkmolve (2*metho*yethanol) Ethyl Cellosob (2-etethanol) Butyl CellosOIve (2-butoxyethanol) Wxyl ~ U o s d v e (2-hexoxy ethanol)
DATA GUIDE
C. W. Sortman, H. A. Beatty, and S. D. Heron, Spontaneous lgnition of Hydrocarbons, Zones of Nonignition, Ind. Eng. Chem., 33, No. 3, Mar 1941, pp. 357-360. (Ethyl Gasoline Corp., 1941.) G. W. Jones, H. Seaman, and R. E. Kennedy, Explosive Properties of Dioxan-Air Mixtures, Ind. Eng. Chem., 25, No. 11, Nov. 1933, pp. 1283-1286. (Bureau of Mines, 1933.) A . L. Fumo, A . C. Imhof, and J. M. Kuchta, Effect of Pressure and Oxidant Concentration on Autoignition Temperatures of Selected Combustibles in Various Oxygen and Nitrogen . Chem. Eng. Data, Tetroxide Atmospheres, J 13, No. 2, Apr 1968, pp. 243-249. (Bureau of Mines, 1968.) M. Kuras, S. Hala, and S. landa, Erdoel Kohle, Erdgas, Petmhem., 24, No. 7, July 1971, pp. 467-471. (Czechoslovakia, 1971). N. J. Thompson, Autoignition Temperatures of Flammable Liquids, Ind. Eng. Chem., 21, No. 2, Feb 1929, pp. 134-1 39. (Factory Mutual, 1929.) Associated Factory Mutual Fire Insurance Companies, Properties Flammable Liquids, Gases, and Solids, Ind. Eng. Chem., 32, No. 6, June 1940, pp. 880-884. (Factory Mutual, 1940.) Factory Mutual Engineering Corp., "Handbook of Industrial Loss Prevention," 2nd ed., McGraw-Hill, New York (1967). (Factory Mutual, 1967.) J. L. Jackson, Spontaneous lgnition Temperatures, Ind. Eng. Chem., 43, No. 12, Dec 1951, pp. 2869-2870. (National Advisory Committee for Aeronautics, 1951.) National Fire Protection Assn., "Fire Protection Guide on Hazardous Materials," 3rd ed., Boston, Mass., 1969. (National Fire Protection Assn., 1969.) Union Carbide Corp., Tables of Physical Properties, Laboratory Manual, Vol. 40, Tables of Flammable Limits and Fire Protection Data," May 30, 1966. (Union Carbide Corp., 1966.) Union Carbide Corp., unpublished data from Fire Research Laboratory. (Union Carbide Corp., 1972.) Union Carbide Corp. data, 1961. H. F. Coward, et al., U.S. Bureau of Mines, Bulletin 30 (1926).
M. G. Zabetakis, et al., Minimum Spontaneous lgnition Temperatures of Combustibles in Air, lnd. Eng. Chem., 46, No. 10, Oct. 1954, pp. 2173-2178. (Bureau of Mines, 1954.) G. S. Scott, G. W. Jones, and F. E. Scott, Determinationof lgnition Temperatures of Combustible Liquids and Gases, Anal. Chem., 20, No. 3, Mar 1948, pp. 238-241. (Bureau of Mines, 1933.) J. L. Jackson, Spontaneous lgnition Temperatures, Ind. Eng. Chem., 43, No. 12, Dec 1951, pp. 2869-2870. N. P. Setchkin, Self-IgnitionTemperatures of Combustible Liquids, J. Res. Nat. Bur. Std., 53, No. 1, July 1954, pp. 49-66. (National Bureau of Standards, 1954.) W. A. Affens, et. al., Effect of Chemical Structure . on Spontaneous lgnition of Hydrocarbons, J Chem. Eng. Data, 6, No. 4, Oct 1961, pp. 613619. (US. Naval Research Laboratory, 1961.) C. E. Frank and A. U. Blackham, Spontaneous lgnition of Organic Compounds, Ind. Eng. Chem., 44, No. 4, Apr 1952, pp. 862-867. (University of Cincinnati, 1952.)
DATA GUIDE
LIMITS OF FLAMMABILITY OF INDIVIDUAL GASES AND VAPORS IN AIR AT ATMOSPHERIC PRESSURE
Combustible Lmits of Flammability (Volume Percent) Combustible
of FlamLim~ts mability (Volume Percent) of FlamL~m~ts mabllity (Volume Percent)
Acetic anhydr- ------Acetanillde - - - - - - - - - - - Acetone - - - - - - - - - - - - - - Acetone cyanohydrin - - Acetophenone - - - - - - - - Acetylacetone- - - - - - - - - Acetyl chbnde --------Acetylene - - - - - - - - - - - - Acrolein - - - - - - - - - - - - - - Aaybnitnle - - - - - - - - - - - Adipic acld -----------Allylamine - - - - - - - - - - - - Alyl brwnlde----------Allyl chlonde ----------o-Aminodiphen yl - - - - - - -
n-Amyl acetate - - - - - - - - n-Amy1alcohol - - - - - - - - tert-Amyi alcohol - - - - --n-Amyl chlonde - - - - - - - tert-Amyl chloride -- - - - -n-Amyl ether - - - - - - - - - - Amyl nitrite --- - -------n-Amyl nitrate - - .. - - - - - - n-Amyl proponate - - - - - Amylene - - - - - - - - - - - - - Aniline - - - - - - - - - - - - - - - Anthracene - - - - - - - - - - - Benzene - - - - - - - - - - - - - Benzyl benzoate - - - - - - Bqcbhexyl - - - - - - - - - - Biphenyl - - - - - - - - - - - - - 2-B~phenylamine --- ---Bromobenzene- , - -- - - , n-&rtane - - -- - - - - -, - -- 1,3-&nanedlol - - - - - - - - Butene-1 --------- - ---Butem-2 - - - - - - - - - - - - - n-8utyl acetate --------n-Butyl alcahol----,---sec-Butyl alcohol - - - - - - tert-ButyI alcohol -----,tert-Butyl mine -------n-Wybmmw , -- -, -sec-&Rylbenzene-----Benzyl chloride
Ammonia - - - - - - - - - - - - - -
--------
&Radiene (1.3)
-----,--
tert-Butyl benzene , , , , , n-8utyl bromide -----,-Butyl Cellosdve ---,---n-tkrtyl &bride ---,---, n-Butyl knnate-- , , --- , n-Butyl stearale - --, - -, &Itync acid ,,,-----,,-- a
,
-- - --,
DATA GUIDE
Combustible
Combustible
Combustible
"t=WC. lZt= 53" C . 13t=WG. "t = 130C. 15t = 720 C . 16t=11PC. 17t = 125" C. "'t = 200" C . lgt = 78" C. 201 = 122C.
DATA GUIDE
FLAME VELOCITIES
Compounds 2-Butyne Experimental Flame Velocity, cm/sec 51.5
3 3 . 8
40.1 39.0 37.9
38.5
38.5 38.6
40.7
Compounds Propane Butane Pentane Heptane Ethylene Acetylene Propyne 1-Heptyne Cyclopropane Cyclohexane
' Volume %
Ethylene Propene 1-Butene 1-Pentene 1-Hexene 2-Methylpropene 2-Methyl-1-butene 3-Methyl-1-butene 2-Ethyl-1-butene 2-Methyl-1-pentene 4-Methyl-1-pentene 1.2-Butadiene 1,3-Butadiene cis l,3-Pentadiene transl,3-Pentadiene 1,2-Pentadiene 2,sPentadiene 1,4-Pentadiene 1,5-Hexadiene 2-Methyl-1, 3-butadiene 2,3-Dimethyl-1,Sbutadiene Propyne 1-Butyne 1-Pentyne 1-Hexyne
4.6 3.4 2.8 2.0 7.4 10.7 5.4 2.2 4.8 2.5
55.3
43.6
Compounds Ethylene oxide Propylene oxide Acrolein Methanol Diethyl ether Propionaldehyde Acetone Isopropyl alcohol Ethyl acetate
Te.
Flame_Velocity, crn/sec
a. Volume percent of hydrocarbon in air. b. Calculated equilibrium flame temperature = air fuel at stoichiometric mixture c. = q u b l e n t air fuel of experimental mixture
DATA GUIDE
Laminar flames in premixed gaseous mixtures are considered to have unique characteristics that depend only on the initial condition of the gas-pressure, temperature, and compositiin. Two properties of such flames are laminar burning velocity and flame temperature. The data contained herein are for premixed laminar flames in air at ambient temperatures and pressures for mixtures in the region of their stoichiornetric point.
It is in this region where the flame velocities are at a maximum in laminar flames. In practical situations, however, it must be remembered that turbulence has a profound effect in increasing the overall velocity of a flame front.
REFERENCES: Dorothy M. Simon, 'Flame Propagation, Active Particle Diffusion Theory," Industrial and Engineering Chemistry, 43, No. 12, 1951; National Advisory Committee for Aeronautics, Lewis Flight Propulsion Laboratory, Cleveland, Ohio. 2. H. F. Calcote, et al., Paper presented at the 116th Meeting of the American Chemical Society, Atlantic Clty, New Jersey; Experiment Inc., Richmond, Virginia.
S@tu
DATA GUIDE
m -k -2A )&-nM2+(-!!!$-) 4
H2D+kHF. Thus. Cs =
lo0
4.773 is the reciprocal of 0.2095, the molar concentratton of oxygen in dry air. The following table lists the values of C,, for a range of
m-k-2~
'N = n
combustible.
m-k-2A
;where n, m, A, and k are the number of carbon, hydrogen, oxygen, and halogen atoms, respectively, in the
For example, the stoichiometric mixture composibon of acetyl chbnde (C2H,0CI) in air may be found by noting that
The entry for N=2.0 in the precedingtable is 9.48 volume percent, which is the value of C , , for this combustible in air. REFERENCE: M. G. Zabetakis, "Flamrnabibty Characteristics of Combustible Gases and Vapors," U.S. Department of the Interior, Bureau of Mines. Bulletin 627. 1965.
DATA GUIDE
pressurelternperaturedata at one atmosphere in dry air over the region of flammability. Melting points and autoignition temperatures are also included. Theoretically, the line for saturated vapor-air mixtures should meet the lower flammable limit line at the flashpoint; i-e., the three lines should intersect at a point as is the case for Ethanol. That is, the flash point is the temperature at which the equilibrium vapors reach the lower flammable limit. Because of differences in experimental techniques, there are anomalies among data. In some cases, dotted lines have been added to the Flammabilrty Data Guides to remind the user of these anomalies. There are cases where the reported flash point is outside of the range of flammability as determined by the reported flammability limits and vapor pressure data. GLOSSARY Limits of flammability-Homogeneous, combustible vapor-air mixtures can propagate combustion waves only within a limited range of compositions. Compositions in this range are said to be within the limits of flammability. Lower flammability limit-The composition of a vapor-air mixture that contains the minimum amount of vapor in air to form a combustible mixture expressed as a volume percent of vapor in air in the Data Guides.
- Isaturated
Upper flammable limit-The composition of a vaporair mixture that contains the maximum amount of vapor in air to form a combustible mixture expressed as a volume percent of vapor in air in the Data Guides. Flash point-The minimum temperature at which a liquid gives off vapor within a test vessel in sufficient concentration to form an ignitable mixture with air near the surface of the liquid. A standard method of test for flash point is the Tag closed cup, ASTM D 56-70. When available, the value for this method is used in the Data Guides.
AIT Tu Temperature Figure 1 . Flammability limits of a cornbustiMe vapor as a function of temperature in air at a constant initial pressure.
Temperature range-The approximate temperature range where flammable vapors exist over a liquid at equilibrium conditions in dry air at a pressure of one atmosphere has been estimated as being between the
DATA GUIDE
flashpoint and the temperature where the fuel concentration is at the upper flammable limit; i.e., the intersection of the upper flammable limit line and the vapor pressure curve. In those cases where the intersection of the lower flammable limit line intersects the vapor pressure curve at a temperature significantly below the flash point, a vertical dashed line has been drawn and is used as the estimate of the lower boundary of the temperature range.
Autoignition Temperature (A-The minimum temperature at which a material begins to self-heat at a high enough rate to result in combustior+ reported in the Data Guides as the temperature in air at one atmosphere.
NOMOGRAPHS FOR EXPLOSION REUEF VENTING The Data Guides of Nomographs for Explosion Relief Venting were published to provide workers in the field of explosion relief venting with the basic nomographs in a form convenient to use. The nomographs presented in this series of Data Guides should be used in conjunction with the cited references where the precautions and extrapolations are discussed. They should not be used alone. These nomographs are based on the cubic scaling law, which may be expressed as follows:
Cdtoichiometric composition of combustible vapor in air - expressed as a volume percent. T d q u i l i b r i u m temperature at which Ca exists over liquid in dry air at one atmosphere. TL-Equilibrium temperature at which the lower flammable limit composition exists over liquid in dry air at one atmosphere (theoretical flash point). TrEquilibrium temperature at which the upper flammable limit composition exists over liquid in dry air at one atmosphere. MP-Metting point (freezing point). BP--Boiling point. REFERENCES M. G. Zabetakis, 'Flammability Characteristics of Combustible Gases and Vapors," U.S. Department of the Interior, Bureau of Mines, 1965. H. F. Coward, G. W. Jones, 'Limits of Flammability of Gases and Vapors," U.S. Department of the Interior, Bureau of Mines, 1952. C. J. Hilado, S. W. Clark, 'Autoignition Temperatures of Organic Compounds," ChemicalEngineering, September 4, 1972, pp. 75-80.
Dust C l l u ~ ST-1 ST-2
ST3
(s)
max
VIR= constant
is the minimum rate of pressure rise resulting from the deflagration of a fuel with air in an endosed vessel (bar sec-') is the volume of the vessel (m? and V The constant is referred to as for dusts and for gases (bar m lsec-I). Three classifications of dusts for two ignition energies have been selected as reference points, as follows:
Weak Ignition (-10 J)
100 101-200
2 1 W )
A nomograph is presented for each combination. Three gases have been selected as reference points in the nomographs: methane, KG = 55 bar m sec-'; = 140 bare m lsec"; and hydrogen, coke gas, = 550 bar m sec"; (weak ignition, no turbulence). A nomograph is presented for each gas. In the ten nomographs presented, PSM is the static pressure at which a vent is designed to open, and PRn, is the highest pressure that will occur in the vented vessel (bar, gauge). REFERENCES W . Bartknecht, Gplosives, Course Prevention Pmtectron, Springer-Verlag, New York, 1981. NationalFire Codes, NFPA-68- 1979, National Fire Protection Association, Boston, 1979.
Servrces, Inc.
DATA
AIT 446'F
I E
w3
W
V)
ea
E a
cn
I ! + a
P
0
V)
s!
s z
a a
0 0
All
23O0C,
TEMPERATURE, 'C
Sewrces, Inc.
-ACETALDEHYDE, CH,CHO
TEMPERATURE,
OF
DATA GUIDE
AIT 365" F
I E
0 ,
E a
W
u -
2
V)
5 I u
(3
i f
z c l
z
V)
g
0
0
u u
AlT 185OC
T E M P E R A T U R E , OC
SllfCtv
I
Management
~crvrcesI , ~C.
DATA GUIDE
ACETIC ACID, CH,COOH
TEMPERATURE,
OF
AIT 961F
I"
a 3 cn cn W a n
E E w -
: a
J
a n
z 0
z
W
(3
: cn
a
a
0
AIT 516OC
DATA GUIDE
ACETIC ANHYDRIDE, (CH,CO),O
TEMPERATURE,
OF
AIT 734F
0 ,
E E
w3
V) V)
a
W
u n
J
a a a
0
Z
I -
Q:
z n
g
V)
a
K
0
0
AIT
39O0C*
DATA GUIDE
ACETONE, CH3CHOCH3 (Propanone)
TEMPERATURE, O F
AIT 1 F L
.we
I
E E w-
0 ,
a 3 cn cn
2
z
W
I + a
(3
z n
8 cn
0
0
a a
AIT 56O0C
TEMPERATURE. " C
Management
s m r c z , Ik.
DATA GUIDE
AIT
TEMPERATURE. "C
DATA GUIDE
ACROLEIN, CH2:CHCH0 (Acrylaldehyde)
TEMPERATURE, "F
AIT UNSTABLE
UNSTABLE
TEMPERATURE, 'C
$5
a
CONCENTRATION,VOLUME %
I U
yltn+ar,coo
2:
A
nA 8 8 t5 8 8 8 8 8
I ILI I I 11
I I I I 1111-
rU
tn-mcos
8888g
ScwY
-
Management
se?-vztes,Inc.
TEMPERATURE, 'F
0 20 40 60
80
100
DATA GUIDE
AIT 713'F
I E
w3
V) V)
0 ,
E a
a n
A
+ K
a n
0
z
W
(3
g
V)
TEMPERATURE, ' C
DATA GUIDE
ALLY L CHLORIDE, CH2:CHCH2CI (3CHLOROPROPENE)
TEMPERATURE. " F
AIT 485C
_ I I )
TEMPERATURE. " C
Management
Srrwccs, In c.
DATA GUIDE
ALCOHOL, CH&H2CH2CH2CH20H(1-Pentanol)
TEMPERATURE, "F
0 200 220 240 260 280 300
BP. 280F
7 1
AIT
0)
I E E
FLAMMABLE LIMIT 10% (76 mm)
K
W
w0
( I )
3
K
a +
a a a
0
i
10 9
8
z 0
z
W
:
0
0
0
6 5
BP, 138C
AIT 300C
C TEMPERATURE, '
S4c9
Management -
DATA GUIDE
AIT
650oF
AIT
343oc
TEMPERATURE. " C
smvzces, Inc.
DATA
TEMPERATURE, 'C
DATA GUIDE
BENZENE, C6H6
TEMPERATURE. " F
AIT 1 076OF
I"
E E w-
V)
a
a
I -
[ r
$
0
0
z
W
z
V)
?
a
0
0
AIT
-40
-30
-20
-10
10
20 30 40 TEMPERATURE. " C
50
60
70
80
90
100
S4@Y
Management -
DATA GUIDE
BIPHENYL, C6H5C6H5
TEMPERATURE. " F
AIT 1004oF
AIT 540OC
TEMPERATURE.
"C
DATA GUIDE
(Vinyiethylene)
AIT 788'F
S.fc~
Management
DATA GUIDE
TEMPERATURE. " F
0 20 40
60
80
100
120
140
160
180
200
220 240
AIT 678' F
I E E w3
V)
0 ,
[ I
V)
a
n
J
I -
5 n
8
z
a
[ I
8 cn
W
AIT
-20
-10
10
20
30
40
50
60
70
80
9O
100
110
120
TEMPERATURE. "C
Sewzces, Inc.
DATA GUIDE
2=BUTANOL, CH3CH2CHOHCH3(sec-ButylAlcohol)
TEMPERATURE. " F
AIT 777O F
AIT
L
414OC
DATA
2=BUTANONE, CH3COCH,CH3 (Methyl Ethyl Ketone)
TEMPERATURE, " F
AIT
960' F
AIT 515.SC
-40
-30
-20
-10
10
20 30 40 50 TEMPERATURE. "C
60
70
80
90
100
DATA GUIDE
I00
!OO
UPPER
LOO 30 30
ro
i0
i0
t0 30
20
10
9
8 7
6
5
4
1 TEMPERATURE.
AIT
425oC
"C
ATA GUIDE
BUTYL ACRYLATE, CH2:CHCOOC4H9
TEMPERATURE. " F
AIT
5 5 9oF
w a
3
cn I E E
V)
a
k
n
. J
a
0 .
C3
f
z
W
B v ,
a
I I
AIT
292OC
TEMPERATURE OC
Sewrccs, Inc.
DATA GUIDE
BUTYL BENZENE, C6H5C4H9
TEMPERATURE ' F
300 300 700 500 500 too 300
200
LOO 30 30 70
i0
i0
10 30
20
LO 3
5
7
a
3
TEMPERATURE.
OC
DATA GUIDE
sec - BUTYL BENZENE, C,H& (CH&H~
TEMPERATURE
"F
1,000 900
AIT 418OC
TEMPERATURE
"C
DATA GUIDE
tert-BUTYL BENZENE, C,H,C(CH,),
TEMPERATURE " F
AIT
AIT 450OC
TEMPERATURE. "C
DATA GUIDE
n=BUTYL CHLORIDE, CHgCH2CH2CH2CI (1Chlorobutane)
1,000 BOO
BOO 700
A IT 464 'F
200
100
u l I E E
wCT)
D O BO 70 60 50 40 30 20
a 3 cn
W K 0
J
5
I -
a n
C3
z
W
g cn
a
0
0
10 9 8 7 6
5
4 3
AIT
240 ' C
. 1 1 1 )
-50
-40
-30
-20
-10
10
20
30
40
50
60
70
80
TEMPERATURE, ' C
S m r c e s , Inc.
DATA GUIDE
A IT 612'F
I E
CI)
u i -
a
CI)
2
a
9 I a a
(3
z a
a
2 OC
0
AIT
TEMPERATURE, 'C
DATA GUIDE
BUTYLENE OXIDE, (CH& COCH2
TEMPERATURE " F
AIT
439oc
_ I I )
TEMPERATURE. " C
CONCENTRATION VOLUME %
Safe9
Management
DATA GUIDE
CAMPHOR, CmHI6O
TEMPERATURE. " F
AIT 871oF
1 1 1 1 )
TEMPERATURE. " C
DATA GUIDE
CARBON DISULFIDE, CS,
TEMPERATURE,
OF
AIT
100"C
AIT
TEMPERATURE.
OC
DATA GUIDE
CHLOROBENZENE, CsH5CI(Monochlorobenzene)
TEMPERATURE, "F
AIT 1,099'F
I
0 ,
0 :
3
Cr)
2 a
I-
5
u a a
8
z_
: cn
a
Oz
W
0
0
20 - 1 0
10
20
30
40
50
60
70
80
90
100
110
120
130
140
TEMPERATURE, 'C
s * ? Y MmgS-a,
IRC.
DATA GUIDE
AIT 795.2' F
cn I
E E
w-
2 cn
W
a
J
k K
a
a
z n
? c n
W
z
d
0
0
AIT 424" C
TEMPERATURE.
OC
S@9
Ma~gtm~tf
S ,
Inr.
DATA GUIDE
CYCLOHEXANE, C6tiI2 (Hexamethylene)
TEMPERATURE,
OF
1
000
I"
MIXTURES
E E
uc
3
V) V)
FLAMMABLE LlMl
a a
F a n
CT
(3
z 0
z
u
2 m
W
FLAMMABLE LIM
BP, 80.7OC
AIT 246' C
-50
-40
TEMPERATURE,
OC
DATA GUIDE
CYCLOHEXANONE, C,H,,O
TEMPERATURE. O
F
AIT 788OF
AIT 420OC
TEMPERATURE. "C
DATA GUIDE
pCYMENE, CH3C,H,CH(CH3), (Isopropyltoluene)
TEMPERATURE, 'F
AIT
436 "C
TEMPERATURE, 'C
S4c9
M~MFS-CCS,
IC.
DATA GUIDE
AIT 410F
TEMPERATURE. "C
DATA GUIDE
DIBUTYL ETHER, (C~H&O
TEMPERATURE, " F
AIT 194OC
TEMPERATURE. O C
DATA GUIDE
DICHLOROBENZENE ,C6H4C12
TEMPERATURE. " F
AIT 648OC
TEMPERATURE, " C
~ e r v u e s Inc. ,
DATA GUIDE
AIT
TEMPERATURE. O C
DATA GUIDE
DIETHYLAMINE, (C2H&NH
TEMPERATURE, 'F
AIT
594 'F
AIT
312 ' C
DATA GUIDE
TEMPERATURE. " f
AIT
L
465oF
TEMPERATURE.
O C
AIT
204OC
TEMPERATURE. " C
DATA GUIDE
DIETHYL ETHER, C2H,0C2H, (Ethyl Ether)
-100
-80
-60
-40
-20
TEMPERATURE, " F 0 20 40
60
80
100
120
140
AIT 356" F
-80
-70
-60
-50
-40
-30
-20
-10
10
20
30
40
50
60
TEMPERATURE. " C
S4.9
>
M-g-
mces,
Inc.
DATA GUIDE
DIMETHYLAMINE, (CH& NH
TEMPERATURE. " F
AIT 752oF
. 1 1 1 )
x
80 70
( J ,
14.4% (109.4mm)
E E
w ' a
3
V)
V)
a
Q. A
C
i t (3 z 0
2
V)
z
Q
W
0
0
AIT 400oC
T EMPERATURE. ' C
DATA GUIDE
2,2 - DIMETHYLBUTANE, ( c H ~CCH2 ) ~ CH3 ( ~eohexane)
TEMPERATURE. " F
AIT
761oF
Smces,
Inc.
DATA GUIDE
I I
- 40 - 20
20
40
60
80
100
120
140
160
180
200
220
240
AIT 356'F
20
30
40
50
60
70
80
90
100
110
TEMPERATURE, 'C
DATA GUIDE
ETHANOL, C,H,OH (Ethyl Alcohol)
TEMPERATURE, OF
AIT
685' F
I"
a
V) V)
E E w 3
a a
J
F a a n
I 0 z
2
W
V)
0
0
a a
All 363'C
TEMPERATURE. OC
DATA GUIDE
ETHYL ACETATE, CH3COOC,H,
TEMPERATURE, " F
AIT
774" F L
AIT
DATA GUIDE
ETHYL BENZENE, C,H,C,H, (Phenylethane)
TEMPERATURE, OF
AIT
809.7O F
AIT
432" C
Management
S mrrcs, Inc.
DATA GUIDE
AIT
425 ' C
DATA GUIDE
-
AIT
-30
-20
-10
10
20
30
40
50
60
70
80
90
100
TEMPERATURE, 'C
S m c e s , Inc.
*
DATA GUIDE
HEPTANE, CH3(CH&CH3
TEMPERATURE. " F
AIT
433"F
_ I I )
AIT
TEMPERATURE. "C
DATA GUIDE
HEXANE, CH3(CH2)&H3
TEMPERATURE, " F
AIT
L
433"F
I E E
3
V)
0 ,
uu
cn
W
[ r
5
I -
i ?
(3
0
V)
2
W
z
u
CT
0
0
AIT
L
223"C
TEMPERATURE, "C
DATA GUIDE
ISOAMYL ACETATE, CH3COOCH&H2CH(CH3)2 (Banana Oil)
TEMPERATURE, 'F
40 60 80 100 120 140 160 180 200 220 240 260
280
300
See
MatlclgGrnMtt
S m s t c s , Inr.
DATA GUIDE
AIT 725" F
I
E E
9,
ua
3
V)
c n
W
a n
A
C
2
0
n
W
z
V)
:
0
a u
0
I
I
AIT 385" C
TEMPERATURE. "C
~erersces,inc.
ATA GUIDE
600
500 400 300 200
AIT
7 9 5 ' F
100 90 80 70 60
50
I E E w-
Q,
40 30 20
cn cn W a
2 a
a a
0 , J
10 9
8
8 cn
0
0
z E z
W
(3
7 6 5 4 3
AIT
423' C
TEMPERATURE, ' C
DATA GUIDE
(Isobutyl Alcohol)
TEMPERATURE. " F
AIT
0 ,
I E E
w u
3
V)
n
I -
z 0
z
(3
B m
W
a a
0 0
AIT 426.7" C
TEMPERATURE.
"C
DATA GUIDE
2=METHYL=2=PROPANOL, (CH&COH (tert-Butyl Alcohol)
TEMPERATURE. " F
AIT
I
E
E
w ' a
3
V) V)
a
C1 I [r
2
C3
z 0
z
W
cn
B
0
[ I
AIT 478" C
TEMPERATURE. "C
DATA GUIDE
METHYL PROPIONATE, CH3CH2COOCHa
10
20
30
TEMPERATURE, 'C
CONCENTRATION, VOLUME %
DATA GUIDE
PENTANE, CH3(CH&CH3
TEMPERATURE. " F
AIT 496" F
AIT
L
258' C
SIlf.9
DATA GUIDE
AIT 810" F
_ _ I )
I"
u
W
E E u-
3
V)
V)
u a
a F
u
2 0 z 0
z
u
u
0
0
W
V)
AIT 432" C
TEMPERATURE. "C
DATA GUIDE
2=PROPANOL,CH,CHOHCH, (Isopropyl Alcohol, Isopropanol)
TEMPERATURE. " F
900
B O O 700 600 500 400 300
L
AIT 750' F
200
100 90 80 70 60 50 10 30
w CT
3
V)
V)
I E E
0 ,
n
J
[ I :
5 k u
2 0
:
V)
z
W
z 0
CT
0
10 9 B
7
5
4
w
1
AIT 399"C
TEMPERATURE. "C
DATA GUIDE
TOLUENE, C,H,CH, (Methyl Benzene)
TEMPERATURE. " F
AIT 1.026O F
AIT
Management
Smxcs, k .
DATA GUIDE
I
E E wV)
Q,
a:
3
cn W
a
1
0=
2 a
(3
2 z n
z
V)
2
W
a a:
0
AIT 427O C
10
20
30
OC
40
50
60
70
80
90
TEMPERATURE,
M-g-
Strenccs, Inc.
DATA GUIDE
AIT 882'F
. 1 1 1 )
AIT 472'C
TEMPERATURE, 'C
DATA GUIDE
XYLENE, C,H,(CH,), (Dimethyl Benzene)
T E M P E R A T U R E . OF
984" F
I"
3
V) V)
E E w-
+
a a
( r
z n
m
W
C3
2
0
0
z
a a
AIT
o b
464" C m 528"C
P
529" C
T E M P E R A T U R E . OC