Professional Documents
Culture Documents
Process Knowledge
Process Knowledge
Process Knowledge
5.1. Overview
5.7. T. Introduction
The design, operation, and maintenance of a process facility requires a consider-
able amount of process knowledge. This information, which encompasses process
chemicals, technology and equipment, is the foundation for understanding the
potential hazards of a process and for supporting a comprehensive process safety
management (PSM) program. Documentation of process knowledge, therefore,
can be detailed and extensive. Process knowledge which is incomplete or incorrect
increases the potential for an incident.
Many aspects of process knowledge are discussed elsewhere, especially in
other CCPS Guidelines books, thus the description here is brief. Emphasis in this
chapter is placed on how to assemble, manage, and maintain, throughout the life
of a facility, the process knowledge essential to a facility's safe operation.
Process knowledge is also used in preparing the documentation for procure-
ment, fabrication, installation, and testing of equipment that will comprise the
hardware of the facility. This aspect is discussed in more detail in Chapter 8- Process
Equipment Integrity.
5.2.7. Objectives
The objective of process knowledge documentation is to record relevant process
information so that it is possible to retrieve, use, and update information required
to support PSM efforts. Some specific objectives are to provide:
definition of original design;
justification of design decisions and changes;
information for training;
basis for continued operation; and
information for other PSM elements;
Each of these objectives is discussed herein.
Use of a standard format such as that given above should help all those who
use MSDSs to find the required information quickly. Missing information can be
a serious problem, and those individuals responsible for MSDS preparation should
ensure that pertinent information is not omitted. If a section of the MSDS is not
applicable for a particular substance (e.g., substance is not flammable and,
therefore, Section 5 does not apply) that section should be so marked.
Purchased raw materials should be accompanied by a MSDS issued by the
material supplier. The information on manufacturer or vendor supplied MSDSs
should be checked for adequacy prior to use. Occasionally, an MSDS is not
provided by a material supplier and, despite prompting, is not produced. Should
an MSDS be unavailable from a supplier for any raw material, it is necessary for
the organization to prepare or obtain an MSDS from an alternate source, prior
to receipt of the material.
MSDSs should be prepared for all facility products. Preparation of MSDSs
should also be considered for process intermediates, by-products and waste
streams. When MSDSs are prepared for the first time, sufficient time should be
allocated to complete the appropriate test work. Standard test procedures should
be used and referenced in the documentation.
An example of an MSDS is included as Table 5-1, which illustrates the style
and type of information contained. This MSDS is provided for illustration
purposes only and should not be used as an actual source of information.
TABLE 5-1
Material Safety Data Sheet
This MSDS is presented for illustration purposes only and should not be used as an actual
source of information.
CHLORINE
Material Identification
CAS Number: 7782-50-5
Formula: Cb
CAS Name: CHLORINE
Trade Names and Synonyms
Cl2
Company Identification
Manufacturer/distributor
ABC CHEMICAL COMPANY
ANYWHERE, USA
Phone Numbers
Product Information : 1 -800-555-5555
Transport Emergency : CHEMTREC: 1 -800-424-9300
Medical Emergency: 1-800-555-5555
COMPOSITION/INFORMATION ON INGREDIENTS
Components
Material CAS Number %
*CHLORINE 7782-50-5 100
* Regulated as a Toxic Chemical under Section 313 of Title III of the Superfund
Amendments and Reauthorization Act of 1986 and 40 CFR part 372.
HAZARDS IDENTIFICATION
FIRSTAIDMEASURES
First Aid
Contact with moisture in air or tissue may produce hydrochlorous and hy-
drochloric acids.
INHALATION
If inhaled, remove patient to an uncontaminated atmosphere. Call a physi-
cian. Check for breathing and pulse. If not breathing, give artificial respira-
tion. If breathing is difficult, give oxygen as soon as possible (6 liters per
minute). Check for other injuries. Keep the patient warm and at rest.
SKIN CONTACT
Immediately, within seconds of contact or suspected contact, shower with
large quantities of water and completely remove all personal protective
equipment, clothing, and shoes while in the shower. Flush the skin thor-
oughly with water for at least 5 minutes. Call for medical help while flush-
ing the skin. Keep the affected area cool. Avoid freezing affected area.
Wash clothing before reuse.
EYE CONTACT
Immediately flush eyes with large quantities of water while holding the eye-
lids apart. Continue flushing for 5 minutes. Do not try to neutralize the
acid. Call a physician immediately. Transfer promptly to a medical facility.
Apply cool packs on the eyes while transporting patient. Avoid freezing af-
fected area.
INCESTION
Do not induce vomiting. Give large quantities of water. Call a physician immediately
and transfer promptly to a medical facility. Never give anything by mouth to an un-
conscious person.
page 2 of 6
FIRE FIGHTING MEASURES
Flammable Properties
Will not burn in air. Strong Oxidizer.
Fire and Explosion Hazards:: Contact with combustible materials may
cause fire. Dangerous when heated; emits highly toxic fumes. Follow appro-
priate National Fire Protection Association (NFPA) codes.
Extinguishing Media
As appropriate for combustibles in area.
Fire Fighting Instructions
Wear self-contained breathing apparatus. Wear full protective equipment.
Shut off source of fuel, if possible and without risk.
Keep personnel removed and upwind of fire. Do not apply water directly to
leak. Cool tank/container with water spray. Run-off from fire control may
cause pollution.
Safeguards (Personnel)
NOTE: Review FIRE FIGHTING MEASURES and HANDLING (PERSONNEL) sec-
tions before proceeding with clean-up. Use appropriate PERSONAL PROTEC-
TIVE EQUIPMENT during clean-up.
Evacuate personnel, thoroughly ventilate area, use self-contained breathing
apparatus. Keep upwind of leak—evacuate until gas has dispersed.
Initial Containment
Dissipate vapor with water spray. Prevent material from entering sewers, wa-
terways, or low areas.
Accidental Release Measures
Specially trained personnel should stop the leak if possible, dike spill, and
neutralize any water that may be used with caustic. Comply with Federal,
State, and local regulations on reporting releases. The CERCLA Reportable
Quantity for a spill, leak, or release is 10 lbs.
Handling (Personnel)
Do not breathe gas. Do not get in eyes, on skin, or on clothing. Wash thor-
oughly after handling.
Storage
Store in a cool place away from heat, sparks, and flame. Keep containers
tightly closed.
page 3 of 6
EXPOSURE CONTROLS/PERSONAL PROTECTION
Engineering Controls
Use sufficient ventilation to keep employee exposure below recommended
exposure limits.
Personal Protective Equipment
Have available and wear as appropriate for exposure conditions: chemical
splash goggles; safety glasses, (side shields preferred); full-length face shield;
gloves, pants, jacket, apron, and footwear or acid suit made of butyl,
"Chemfab", "Chloropel", "Neoprene", nitrile, "Saranex" coated "Tyvek",
urethane, or "Viton" and NIOSH/MSHA approved respiratory protection.
Exposure Limits CHLORINE
PEL (OSHA): 1 ppm, 3 mg/m3, Ceiling
TLV (ACGIH) : 0.5 ppm, 1.5 mg/m3, 8 Hr. TWA
STEL 1 ppm, 2.9 mg/m3 TWA
Physical Data
Boiling Point: -34.60C (-30.30F) @ 760 mm Hg
Vapor Pressure: 4,800 mm/Hg @ 2O0C (680F)
Vapor Density: 2.5 (Air = 1)
Melting Point: -1010C (-15O0F)
Evaporation Rate: (Butyl Acetate = 1) Greater than 1
Solubility, Water: 0.57 wt% @ 3O0C (860F)
Odor: Acrid
Odor Threshold: 0.2-0.4 ppm
Form: Gas at STP/Liquid
Color: Gas: Greenish yellow;
Liquid: Amber
Specific Gravity : 1.56 @ -350C (-310F) Liquid
STABILITYAND REACTIVITY
Chemical Stability
Dry chlorine is stable in steel containers at room temperature.
Decomposition
Hydrochloric and hypochlorous acids are formed with water or steam.
Polymerization
Polymerization will not occur.
page 4 of 6
Other Hazards
Incompatibility: Incompatible with alkalies, reducing agents, and organic materi-
als. Reacts explosively or forms explosive compounds with acetylene, turpen-
tine, fuel gas, hydrogen, ether, ammonia gas, and finely divided metals. Reacts
vigorously with titanium, zinc, and tin. Reaction with aluminum may result in
generation of flammable hydrogen gas. May also form explosive mixtures with
combustible organic vapors and cause runaway reactions with certain polymers
if contacted in confined areas. Combines with carbon monoxide and sulfur di-
oxide to form toxic and corrosive phosgene and sulfuryl chloride.
TOXICOLOGICAL INFORMATION
Animal Data
Inhalation 1-hour LCso: 293 ppm in rats
The compound is corrosive to eyes and skin. Toxic effects described in ani-
mals from short exposures by inhalation include upper and lower respira-
tory, kidney, liver, and lung effects. Long-term inhalation exposures caused
eye irritation and nonspecific effects such as weight loss. By ingestion, the
effects included irritation and corrosion of mucosal surfaces; kidney, liver,
and lung effects; and nonspecific effects such as decreased weight gain. No sig-
nificant adverse effects were observed from long-term dietary administration.
Animal testing indicates that the compound does not have carcinogenic or
reproductive effects. Tests for embryotoxic activity in animal species have
been inconclusive, with positive results in some studies and negative results
in others. Tests in bacterial cell cultures demonstrate mutagenic activity.
ECOLOGICAL INFORMATION
DISPOSAL CONSIDERATIONS
TRANSPORTATION INFORMATION
page 5 of 6
REGULATORY INFORMATION
OTHER INFORMATION
NFPA, NPCA-HMIS
NFPA Rating
Health: 3
Flammability: O
Reactivity: O
Oxidizer
NPCA-HMIS Rating
Health: 3
Flammability: O
Reactivity: 1
Personal Protection rating to be supplied by user depending on use conditions.
Additional Information
NSf LIMITS: NSF Maximum Drinking Water Use Concentration: 30 mg/L as
chlorine.
The data in this Material Safety Data Sheet relate only to the specific material
designated herein and does not relate to use in combination with any other
material or in any process.
Responsibility for MSDS: ABC CHEMICALS COMPANY
Address: ANYWHERE, USA
Telephone: 555-555-5555
page 6 of 6
Companies handling large numbers of different substances may amass a data
base for MSDSs. While MSDSs can be obtained from inhouse development or
from suppliers of purchased material, there are also a few sets of published MSDSs
commercially available. These publications seldom include all chemicals used at a
particular site, but they may be useful to organizations handling the more common
materials. Among these are MSDSs published by:
Genium Publishing Corporation
One Genium Plaza
Schenectady, NY 12304-4690
(518) 377-8855
containing nearly 1000 titles.
MSDS Software sources include:
MSDS-CCOHS
Canadian Center for Occupational Health and Safety (over 70,000 tides);
CHEMTOX
Resource Consultants; and
TAPP
Europa Scientific Software Corp., Hollis, NH.
In addition, other physical or chemical characteristics of materials, beyond
those typically found in a MSDS (e.g., specific resistance or dust explosibility),
may need to be determined and documented.
Product Gas
Direct
Contact
Cooling
Steam
Waste Water Pump/ Stripping
Tank
Condenser Heat
Primary Exchanger Compressor
Liquifier
Liquid Product
Accumulation Product to Customer
Tank Railroad
Tank Cars
35 100
PSlG PSIQ Evaporator Steam
Storage Storage
Tank Tank
FIGURE 5-1. Example of Block Flow Diagram.
PRESSURE TO TO
CONTROL VALVE SCRUBBER SCRUBBER
CL2
STORAGE FEED
TANK TANK
(90 TONS) (1 TON)
PURdF
PURGL ^
REACTOR
(50 psig)
FIGURE 5-2. Example of Simplified Process Flow Diagram
Safe Upper and Lower Limits for such Parameters as Temperatures, Pressures,
Flows or Compositions—Safe operating limits should be considered from several
points of view. Each equipment item has a certain upper and lower design
temperature and pressure. The equipment documentation should define such
limits for safe operation of equipment. Processes have safe operating limits as well,
above or below which undesirable or potentially hazardous by-products may
form, or run-away reactions may take place. These limits include temperatures,
pressures, flows, and concentrations.
TABLE 5-2
Example of Process Chemistry Documentation3
Component Abbreviation Formula
Product Dimethyl Carbonate DMC CO(OCH3)2
Raw Materials Methanol CH3OH
Carbon monoxide CO
Intermediates Methyl Nitrite CH3ONO
Nitric Oxide NO
By-products Dimethyl oxalate DMO (COOCHs)2
Major Methyl formate HCOOCH3
Minor Methyl acetate CH3COOCH3
Methylal CH2(OCHs)2
Carbon dioxide CO2
Nitric acid HNO3
Purge Gas Contents: Nitrogen, carbon monoxide, carbon dioxide, nitric oxide, methanol,
methyl nitrite and methyl formate
Wastewater contents: DMC, DMO, methanol
Reactions:
CO + 2CHaONO -> CO(OCHs)2 + 2NO - 45.8 kcal/gmole (at STP)
4NO + O2 + 4CH3OH -» 4CH3ONO + 2 H2O - 59.8 kcal/gmole
Overall Reaction:
2CO + O2 + 4CH3OH -> 2CO(OCHs)2 -H 2H2O - 15 1.4 kcal/gmole
By-product, DMO Formation:
4CO + O2 + 4CH3OH -> 2(COOCH3)2 + 2H2O - 168.6 kcal/gmole
a
Data presented in this table are simulated and are shown only for purpose of illustration of form
content.
TABLE 5-3
Example of Hazard Information Dataa
Component /Acetone 7,3 Butadiene Tin Metal Powder
0
Phase @ 2O C Liquid Vapor Solid Powder
Boiling Point @ atm pressure,0C 56 -4.4 2507
Melting Point/FP°C -94 -108.9 231.9
Flash Point, 0C -1 7, Closed Cup <0, Open Cup NA
0
Autoignition Temperature, C 465 Not found cloud 630,
dust layer 430
LFL, vol % 2.9 2 N/A
oz/ft3 N/A N/A 0.19
UFL, vol % 12.8 11.5 NA
TLV-TWA, ppm 750 10 N/A
mg/m3 N/A N/A 2
Resistivity, ohm-cm NA NA N/A
Stability Stable Without inhibitor Oxidizes in the
hazardous presence of
polymerization moisture
occurs
Remarks: NA means not available N/A means not applicable
a
Data presented in this table are simulated and are shown only for purpose of illustration of form
content.
NOTES: PROCESS PLANT AREA MATERIAL AUTQlGNtTlON T RATING
1 LOCAlION
WORK THISDESI
DRAWING WITH
GN BASIS': THE FOLLOWING HAZARDOUS (CLASSIFIED) TANK FARM METHANOL 878T Tl
0.) DESIGN BASIS NO 11A-LlQUID HANDLING AREA. TANK FARM AND ANALYZER BLDG. I REACTION OFK GAS 1075T Tl
YARD AREAS.
ANALYZER BLDG. Il REACTION OFF GAS 1075T Tl
b.) DESIGN BASIS NO 11B-REACTOR STRUCTURES,
ANALYZER BLDG. Ill METHANOL 878TF Tl
c.) DESIGN BASIS NO. 11C-DlSTlLLATlON & EXTRACTION AREAS. WASIE
2. FOR DETAILED AREA CLASSIFICATION OF THE REACTOR STRUCTURES. STORAGEORGANICS
AREA CRESOL 1038T Tl
DISTILLATION AREA 1. DISTILLATION AREA 2 AND EXTRACTION RAILCAR METHANOL 878" F Tl
BLDG. SEE THE FOLLOWING DRAWINGS: UNLOADING AREA
REACTOR "RlT STRUCTURE TANK TRUCK METHANOI 878T TI
!CCPS-7-GROUND FLOOR UNLOADING AREA
CCPS-B PLAN O EL. 112'-O" & EL. 124'-O" TANK
CCPS-9-PLAN O EL. 139'-1" & EL. 149'-6" LOADINTRUCK
G AREA TOLUENE 896*F Tl
AREA CLASSIFICATION
REACTOR "R33" STRUCTURE A ADJACENT AREAS METHANOL i£C£tJD
ICCPS-3-GROUNO FLOOR
JCCPS-4-SECOND FLOOR TANK AREA STORAGE METHANOL 878T T1
CLASS I. DIV. 1. GROUP B
ICCPS-5-3RD & 4TH FLOORS REACTOR R11.R33.R44 METHANOL 878T Tl
fCCPS-27-DlSTlLLATlON VENT SCRUBBER AREA & R55 STRUCTURES CLASS I. DIV. 2. GROUP B
REACTOR 'R44' STRUCTURE 8B»ILDJ8T(LUA1ION METHANOL 878T T1 CLASS I. DIV. 1. GROUP D
ICCPS-IO-GROUND FLOOR AREA
CCPS-11-2ND FLOOR CLASS I. DIV. 2. GROUP D
CCPS-12-3RD & 4TH FLOORS DISTILLATION 2 METHANOL 878T Tl
AREA NON-HAZ ARDOUS
REACTOR "R55" STRUCTURE EQUIPMENT VENT
ICCPS-13-GROUND FLOOR EXTRACTION METHANOL 878T Tl
ICCPS-14-PLAN O EL. 112'-O" BUILDING TO ATMOSPHERE
ICCPS-15-3RD FLOOR
JCCPS-16-4TH & 5TH FLORS 5. LABORATORY SHALL BE CLASSIFIED PER NFPA 45 AND THE
DISTILLATION AREA 1 GUIDELINES OUTLINE IN DESIGN BASIS UA PARA. 1.6.13.
ICCPS-17-PLAN O GRADE (EL. 100'-0") PROCESS SAFETY MANAGEMENT PROGRAM
ifCCPS-18-PLAN O EL. 115'-O" & 140'-O"
!COPS-19-PLAN O GRADE (EL 100'-0")
DISTILLATION AREA 2
|CCPS-20-PLAN
ICCPS-21-PLAN OO GRADE
GRADE & UPPER PLATF. LEVELS
HAZARDOUS (CLASSIFIED)
EXTRACTION AREA LOCATIONS - SAMPLE DRAWING
ICCPS-22-CROUNO FLOOR PLOT PLAN (NOTES & LEGEND)
|CCPS-23-2NO LEVEL Si ROOF REVISED NOTES 2 F4IE4D . PlPERACKS.
ADDED PUMPS CHEMICAL PROCESS PLANT
3. FOR HAZARDOUS (CLASSIFIED) LOCATION DETAILS SEE P-154A/S.
EXTENDED CLASSI
DlV. 2 CLASSIFICATION
DWG |CCPS-2 & !COPS-6. RECOGNIZABLE
BACKGROUND PER CLIENT S.REVIEW
BOUNDARI E REVISEDTO
4. THE ELECTRICAL INSTALLATION IN THE FOLLOWING AREAS SHALL BE MEETI
ISSUEDNG FOR
08SE93.
FIELD SURVEY.
SUITABLE FOR THE MATERIAL WITH THE LOWEST IGNITION ABC CHEMICAL COMPANY
TEMPERATURE. CLASS I TEMPERATURE MARKINGS SHALL NOT ISSUED FOR CLIENT APPROVAL
EXCEED THE AUTOIGNlTlON TEMPERATURE OF THE SPECIFIC MATERIAL
LISTED. DESCRIPTION
FIGURE 5-4 Typical Hazard Classification Drawings (Sheet 1 of 4)
RAILCAR UHLQADING ARCA
SEE
EXTENTDWC. fCCPS-1 FOR
OF CUSSlFIED
AREAS. FOR CUSSlFICATION
DETAILS ASSOCIATED
RAILCAR WITH
UNLOADING SEE
DETAIL A. DWC. jfCCPS-2
TRACK
TRACK
EXTRACTION AREA
PR(XESS STRUCTURE
(NOT OPERATIONAL)
TRACK
EXTRACTION AREA
REACTOR "RU"
STRUCTURE
NOTES:
1. WORK THIS DRAWING WITH LlQUlO HANOLING AREA. TANK FARM AND AREA CLASSIFICATION KEY PLAN
YARD
LOCATIAREAS
ON OWC.OESlfCCPS-2.
CN BASIS NO. IIA ANO HAZARDOUS (CLASSIFIED)
2. THE ELECTRICAL INSTALLATION FOR THE RAILCAR UNLOADING AREA CLASS I. DIV 1. GROUP B
SHALL NOT EXCEED THE AUTO IGNITION TEMPERATURE OF METHANOL CLASS I. DIV 2. GROUP B
47(TC (878TF) OR A T RATING OF Tl.
3 HEIGHT OF DIVISION 2 CLASSIFICATION FOR THE METHANOL UNLOADING CLASS I. DIV. 1. CROUP D
SPOTS EXTENDS FROM GRADE EL. i9-j'~4" TO BOHOM OF CARSPOT ROOF
APPROX. EL. 220--(T. CLASS I. DM 2. GROUP D
4 FOR DETAILED AREA CLASSIFICATION OF TANK FARM SEE DWG. fCCPS-26. NON-HAZARDOUS
5. HEIGHT OF DIVISION 2 CLASSFlCATlON FOR PIPERACK EXTENDS
FROM GRADE (EL. 100'-(T) TO TOP OF PlPERACK STEtL. TOEOUPMENT VENT
ATMOSPHERE
FIGURE 5-4 Typical Hazard Classification Drawings (Sheet 3 of 4)
CARSPOT ROOF 10'-O' RADIUS AROUND
EL. 220'-O" VENT/RELIEF DEVICES
5'-O" RADIUS AROUND
VENT/RELIEF DEVICES
GRADE GRADf
3'-OT RADIUS 3'-O" RADIUS 10'-O" RADIUS BEtOW GRADE 10'-O" RADIUS
(SEE NOTE l\ (SEE NOTE 14 DETAtL 'T BELOW GRADE LOCATION SUCH
THIS DHAIL) THIS DETAIL) LOCATION SUCH AS A SUMP OR
AS A SUMP OR TRENCH
VENT TO .
ATMOSPHERE LEAKAGECLASSIFICATIOLOCATED
SOURCE N OF AREA AROUNDATAGRADE
OUlDOORS. TRENCH LEAKAGE CLASSI
SOURCEFICATILOCATED
ON OF OUTDOORS.
AREA AROUNDABOVE
A GRADE
Relief System Design and Design Basis—Relief devices are installed to ensure
that a process system, or any of its components, is not subject to pressures
exceeding the maximum allowable pressure for the system.
Overpressure is the result of an imbalance or disruption of the normal flows
of material and energy, causing one or both of them to build up in some part of
the system. Therefore, the system should be carefully analyzed for the possibility
of overpressure. Possible causes of overpressure should be considered, and the
design of the relieving device should be based on the potentially worst situation.
Refer to the AIChE-DIERS book Emergency Relief System Design Using DIERS
Technology for design aid where potential runaway reactions have been identified.
Comprehensive documentation of the design and design basis should be
developed and maintained for each relief system. This documentation should
include the following:
• chemicals or materials in the system;
• results of any thermal stability test data to identify runaway reaction
potential;
• nature of the materials which may be relieved;
• causes and effects of deviations from normal process conditions;
• design basis for relief case selected;
• specifications of the relief device selected; and
• requirements for safe disposal of the relieved material.
Table 5-4 illustrates a typical design basis for a relief system.
Design Codes and Standards—Chemical process plants, storage and handling
areas should be designed in accordance with relevant codes and standards. These
should be identified and listed as part of the design records. The listing should
indicate the edition used and/or the year of issue. At the design stage, a decision
is often made concerning which series of standards will be followed. This decision
should be recorded, since it is important that this basic information be known
when modifications are made or equipment is replaced. A more extensive discus-
sion on this subject is found in Chapter 16, Standards, Codes, and Regulations.
5.5. Auditing
The PSM program should establish the requirements for auditing Process Knowl-
edge. Audits should seek to determine whether a documented program, such as
described in Sections 5.3.1 and 5.4, exists and whether it is being administered as
described. The records described in Section 5.3.2 should be audited, not for
technical adequacy but, rather, to determine if they are being compiled and
managed as required by the program. Such audits may reveal potential improve-
ments to be made in the program itself.
Any deficiencies identified during the audit must be documented and
promptly resolved. See Chapter 14 and the CCPS book Guidelines for Auditing
Process Safety Management Systems for more guidance on auditing.
5.6. Examples
5.7. References
AIChE-DIPPR, Physical Property Data, various publications available from Design Insti-
tute for Physical Properties, 345 E. 47th Street, N.Y., N.Y. 10017
AIChE-CCPS, Guidelines for Auditing Process Safety Management Systems,, 1993
AIChE-CCPS, Guidelines for Hazard Evaluation Procedures, Second Edition with Worked
Examples, 1992
AIChE-DIERS, Emergency Relief System Design using DIERS Technology, 1992
The American Chemical Society, The Advances in Chemistry Series, 1959
American National Standards Institute, Standard for the Preparation of Material Safety Data
Sheets ANSI Z400.1, 1993
American National Standards Institute/Instrument Society of America, Area Classification
in Hazardous (Classified) Dust Locations, ANSI/ISA S12.10, New York, NY
American Petroleum Institute, Classification of Locations for Electrical Installations in Petro-
leum Refineries, RP 50OA, Washington, D.C.
Bichowsky, F.R. and Rossini, F.D., The Thermochemistry of Chemical Substances, Reinhold,
1951
Bretherick, L., Handbook of 'Reactive Chemical Hazards, Butterworths, London (UK)
Carson, P. A., andMumford, C. J., Th eSafe Handling of Chemicals in Industry, 2 Volumes,
Longmans/Wiley, 1988
Gallant, R. W., Physical Properties of Hydrocarbons Volumes 1 &2, Gulf Publishing Company,
Houston, 1968
Gmehling, J., Onken, U. and ArIt, W. Vapor-Liquid Equilibrium, Data Collection, Volumes
!through V
Lewis, R. J., Hazardous Chemicals—Desk Reference, Van Nostrand Reinhold, 1993
National Academy of Sciences, International Critical Tables of Numerical Data, Physics,
Chemistry and Technology, Volumes I through VIII, 1929
National Fire Protection Association, Classification of Class I (Classified) Hazardous Loca-
tions for Electrical Installations in Chemical Process Areas, NFPA 497A, Quincy, MA
National Fire Protection Association, Classification of Class II Hazardous (Classified)
Locations in Electrical Chemical Process Areas, NFPA 49 7B, Quincy, MA
National Institute of Occupational Safety and Health, Guide to Chemical Hazards, 1990
National Institute of Occupational Safety and Health, Register of Toxic Effects of Chemical
Substances
Perry's Chemical Engineers Handbook^ McGraw Hill, New York, NY
Occupational Safety and Health Administration, Hazard Communication, 29 CFR 1910.
1200(g), Washington, D.C.
Reid, R.C., Prausnitz, J.M. and Poling, B.E., The Prop erties of Gases and Liquids, McGraw
Hill, New York, NY, 1987
Sax, N. Irving, Dangerous Properties of Industrial Materials, Van Nostrand Reinhold
Simulation Sciences Library, SimSci Data Bank
Appendix 5A. Example of Process Knowledge File Index