I. CHEM. E. SYMPOSIUM SERIES No. 49

Similar documents
COMBUSTION OF FUEL 12:57:42

Inertization Effects on the Explosion Parameters of Different Mix Ratios of Ethanol and Toluene Experimental Studies

Thermochemistry/Calorimetry. Determination of the enthalpy of combustion with a calorimetric bomb LEC 02. What you need:

FIRE RESEARCH STATION

THE USE OF DEWAR CALORIMETRY IN THE ASSESSMENT OF CHEMICAL REACTION HAZARDS

He measures the steady temperature of the water before adding the lithium iodide.

The student s results are shown in the table below. Time / minutes Time / minutes

Explosion Properties of Highly Concentrated Ozone Gas. 1 Iwatani International Corporation, Katsube, Moriyama, Shiga , Japan

QUENCHING DISTANCES OF STOICHIOMETRIC ETHYLENE-AIR MIXTURE WITH CO 2 ADDITION. Introduction. Experimental

11B, 11E Temperature and heat are related but not identical.

(ii) Compare the movement and arrangement of the molecules in solid nitrogen to those in nitrogen gas.

Stoichiometry Rockets

IFE Level 3 Diploma in Fire Science and Fire Safety (VRQ)

ALE 26. Energy Changes ( E) and Enthalpy Changes ( H) in Chemical Reactions

APPENDIX A: LAMINAR AND TURBULENT FLAME PROPAGATION IN HYDROGEN AIR STEAM MIXTURES*

EXPERIMENT 6 Empirical Formula of a Compound

I. CHEM. E. SYMPOSIUM SERIES NO. 68

Vapour pressure of water at high temperature

F322: Chains, Energy and Resources Enthalpy Changes

3.2.1 Energetics. Enthalpy Change. 263 minutes. 259 marks. Page 1 of 41

Fundamentals of Static Electricity

Deflagration Parameters of Stoichiometric Propane-air Mixture During the Initial Stage of Gaseous Explosions in Closed Vessels

CHEMISTRY HIGHER LEVEL

Atmospheric Analysis Gases. Sampling and analysis of gaseous compounds

Statistical Analysis of Electrostatic Spark Ignition

Catalytic bead sensors are used primarily to detect

SAFETY TRAINING LEAFLET 08 ACETYLENE, CALCIUM CARBIDE, LIME SLUDGE AND PURIFYING MATERIALS

5 Energy from chemicals

Hydrogen addition to the Andrussow process for HCN synthesis

Name AP Chemistry / / Chapter 5 Collected AP Exam Free Response Questions Answers

Planet Earth. Topic. Unit 1. Introducing chemistry. Unit 2. The atmosphere. Unit 3. The ocean. Unit 4. Rocks and minerals

exothermic reaction and that ΔH c will therefore be a negative value. Heat change, q = mcδt q = m(h 2

Minimum Ignition Energy (MIE)

IFE Level 3 Diploma in Fire Science and Fire Safety

Specimen Paper. Double Award. AQA Level 1/2 Certificate in Science: Double Award Specimen Paper TOTAL. Chemistry Paper 1F. Time allowed 60 minutes

Globally Harmonized System of Classification and Labelling of Chemicals (GHS) Classification criteria for substances and mixtures Physical hazards

Define the term enthalpy change of formation of a compound

Burgoyne Consultants Ltd., Burgoyne House, Chantry Drive, Ilkley, West Yorkshire, U.K.

1. Enthalpy changes of reaction can be determined indirectly from average bond enthalpies and standard enthalpy changes.

1.4 Enthalpy. What is chemical energy?

glossary 6 of. boxes with and units. question. the syllabus. to see if. nature. Day. Teacher. Pre readings. Topic. Mr Stocker.

Evaluation and Prevention of Electrostatic Hazards in Chemical Plants

CHEMISTRY HIGHER LEVEL

Energy Changes in Chemical Reactions

Thermochemistry Chapter 8

Coimisiún na Scrúduithe Stáit State Examinations Commission

Based on the work you have completed in S1 to S3, complete Prior Learning 3.1.

Ignition. Jerry Seitzman. Temperature (K) School of Aerospace Engineering Review. stable/steady self-sustained propagation of premixed flames

DEPOSITION OF THIN TiO 2 FILMS BY DC MAGNETRON SPUTTERING METHOD

Flammability Limits, Ignition Energy and Flame Speeds in H 2 CH 4 NH 3 N 2 O O 2 N 2 Mixtures

PROPULSION LAB MANUAL

Understanding catalytic LEL combustible gas sensor performance

The names and formulae of three hydrocarbons in the same homologous series are:... (1) Which homologous series contains ethane, propane and butane?

Q1. (a) Explain the meaning of the terms mean bond enthalpy and standard enthalpy of formation. Mean bond enthalpy

Unit 08 Review: The KMT and Gas Laws

Questions, Myths and Misconceptions about Using Photoionization Detectors

Name (Print) Section # or TA name. 1. You may use a calculator and one 8 by 11-1/2 handwritten crib sheet during this

Chemistry CH1HP. (Jun15CH1HP01) General Certificate of Secondary Education Higher Tier June Unit Chemistry C1. Unit Chemistry C1 TOTAL

Thermodynamics. Joule-Thomson effect Ideal and Real Gases. What you need: Complete Equipment Set, Manual on CD-ROM included

Safety Engineering. -Static Electricity and Charge Accumulation-

MARIYA INTERNATIONAL SCHOOL. Work sheet III. Term I. Level 8 Chemistry [MCQ] Name: CHEMICAL REACTIONS & SULFUR

D DAVID PUBLISHING. Thermodynamic Equilibrium for Mixtures of Combustible Gases and Air. 1. Introduction

Experiment 5 Reactions of Hydrocarbons

KENYA NATIONAL EXAMINATION COUNCIL REVISION MOCK EXAMS 2016 TOP NATIONAL SCHOOLS NAIROBI SCHOOL CHEMISTRY PAPER 2 TIME: 2 HOURS

Globally Harmonized System of Classification and Labelling of Chemicals (GHS)

PhysicsAndMathsTutor.com 1

Chemistry Entrance Material for Grade 10 to

Understanding KMT using Gas Properties and States of Matter

Introduction to Chemical Engineering Thermodynamics. Chapter 4. KFUPM Housam Binous CHE 303

Ideal Gases. 247 minutes. 205 marks. theonlinephysicstutor.com. facebook.com/theonlinephysicstutor. Name: Class: Date: Time: Marks: Comments:

UNIVERSITY OF CAMBRIDGE INTERNATIONAL EXAMINATIONS General Certifi cate of Education Advanced Level

Ignition of n-hexane-air Mixtures by Moving Hot Spheres

Freezing point depression (Item No.: P )

4.1. Physics Module Form 4 Chapter 4 - Heat GCKL UNDERSTANDING THERMAL EQUILIBRIUM. What is thermal equilibrium?

All gases display distinctive properties compared with liquid or solid. Among them, five properties are the most important and listed below:

The Effect of Initial Pressure on Explosions of Hydrogen- Enriched Methane/Air Mixtures

Stewards Pooi Kei College Integrated Science Secondary One Teaching Schedule in Textbook Chapter 1 Introducing Science Book 1A, 1B

Natural Gas Measurement Using Temperature-Dependent Thermal Conductivity

Chemistry 1011 TOPIC TEXT REFERENCE. Electrochemistry. Masterton and Hurley Chapter 18. Chemistry 1011 Slot 5 1

EXPLOSION DEVELOPMENT IN A SPHERICAL VESSEL

I. CHEM. E. SYMPOSIUM SERIES No. 49

The Effect of Mixture Fraction on Edge Flame Propagation Speed

g of CO 2 gas is at a temperature of 45 o C and a pressure of 125 kpa. What is the volume of the container? 11 L

10. 2 P R O B L E M S L I Q U I D S A N D G A S E S

for free past papers visit: Index Number 233/1 Candidate s Signature CHEMISTRY Nov hours

Experimental Study of Minimum Ignition Energy of Lean H 2 -N 2 O Mixtures. Abstract

CFD study of gas mixing efficiency and comparisons with experimental data

Organic Chemistry. Alkanes are hydrocarbons in which the carbon atoms are joined by single covalent bonds.

HEAT- I Part - A C D A B. Te m p. Heat input

4.1. Physics Module Form 4 Chapter 4 - Heat GCKL UNDERSTANDING THERMAL EQUILIBRIUM. What is thermal equilibrium?

12. Heat of melting and evaporation of water

Which row correctly describes the type of reaction and the energy of the reactants and products? energy of the reactants and products

CHAPTER-11 NCERT SOLUTIONS

5072 CHEMISTRY (NEW PAPERS WITH SPA) TOPIC 3: FORMULAE, STOICHIOMETRY AND THE MOLE CONCEPT

CHEM 254 EXPERIMENT 2 Critical point determination for SF 6

Ch 6 Gases 6 GASES. Property of gases. pressure = force/area

Same theme covered in Combined but extra content Extra parts atomic symbols (first 20, Group 1 and Group 7)

Partial molar volumes (Item No.: P )

LECTURE 4 Variation of enthalpy with temperature

MAHESH TUTORIALS I.C.S.E.

Transcription:

FLAMMABILITY AND EXPLOSIBILITY OF AMMONIA G.F.P.Harris, P.E.MacDermott Research Dept. ICI Organics Division, Blackley, Manchester The flammability limits of oxygen/nitrogen/ammonia mixtures have been determined at ambient temperature, 300 o C and 400 o C. The explosibility characteristics of ammonia/air mixtures have also been measured. Investigation of the flammability characteristics of ammonia/water vapour/ air mixtures has shown that no aqueous solution of ammonia gives rise to flammable vapours when its temperature exceeds 49 o C. It was also shown that solutions containing less than 5 mol. % ammonia in water do not produce flammable vapours at any temperatures. INTRODUCTION It is well known that vapours of hydrocarbons, hydroxylic compounds and even some chlorinated solvents can form flammable mixtures when mixed with air. The combustible nature of ammonia is much less well known, however, though explosions have occurred both with anhydrous ammonia/air mixtures and with the vapours from aqueous solutions of ammonia mixed with air. Since ammonia is widely used in the gaseous form and also as an aqueous solution for the amination of organic compounds, reliable data is required on the flammability of both the anhydrous and aqueous material. Some literature data exists on both systems. Coward and Jones (l) have reviewed the literature on the flammability of ammonia. White (2), Burgoyne and Neal (3), Frank and Doering (4) and Berl and Bausch (5) all obtained experimental data on the flammability of anhydrous ammonia/air mixtures under atmospheric and elevated pressures. There is inadequate information, however, on ammonia with oxygen deficient atmospheres and on flammability limits at high temperatures. Even less literature data exist on the flammability of aqueous ammonia. Some German workers (6) carried out a limited amount of experimental work on this topic, but did not show how their results could be applied to practical situations. The most comprehensive work on the flammability of both anhydrous and aqueous ammonia was carried out by DeCoursey et al (7). These workers carried out a more systematic examination of the flammability of ammonia. They did not, however, obtain any data at high temperatures or for oxygen deficient atmospheres. They also used a flat flame burner technique for their work rather than the more conventional open ended ignition tube. The experimental work reported in the present paper was, therefore, carried out to provide more comprehensive data on the flammability of aqueous solutions of ammonia. Further information on the combustion properties of anhydrous ammonia at high temperatures and with oxygen deficient atmosphereswas also obtained. A limited amount of work was also carried out on the ignition energy and explosibility of ammonia/air mixtures. PART I:- FLAMMABILITY AND EXPLOSIBILITY OF ANHYDROUS AMMONIA 1. EXPERIMENTAL The apparatus used for the flammability measurements is shown in Fig (1). This is essentially a 50 mms. internal diameter pyrex glass tube connected in series with a glass solenoid operated circulating pump and a glass sampling vessel. For measurements at ambient temperatures the system was evacuated to a pressure of less than 29

I. CHEM.-E. SYMPOSIUM SERIES No. 49 2 torr. and ammonia admitted to the required pressure. The solenoid pump was started and the desired premixed supporting atmosphere of oxygen and nitrogen let in until atmospheric pressure was reached. After 20 minutes circulation the pump was switched off and the sampling vessel removed for analysis. The ground glass plate at the base of the tube was removed and a 1.5 Joule inductance spark passed between the electrodes. The mixture under test was considered to be flammable if a flame travelled away from the electrodes for the full length of the tube. A similar procedure was adopted for measurements at elevated temperatures except that the ammonia/ oxygen/nitrogen mixtures were prepared in a heated 6 litre stainless steel bomb at above atmospheric pressure. The heated mixture was then analysed and admitted to the evacuated ignition tube. The ignition tube was surrounded by an electrically wound jacket and any passage of flame along the tube on sparking as observed through slits in the jacket. A few experiments were carried out on the explosibility of ammonia mixtures. In this work the desired mixtures were prepared in the 6 litre bomb, ignited by a hot resistance wire at the centre of the bomb and the maximum explosion pressure and rates of pressure rise measured by a capacitance transducer sited in the vessel wall. Check experiments were carried out in both the stainless steel bomb and the 50 mm. diameter glass tube to see if ammonia was lost by oxidation before the mixture could be ignited. In both cases a maximum of 4% of the ammonia was lost at the highest temperature used (400 o C) and the longest residence time in the apparatus. 2. RESULTS 2.1 Flammability Limit Measurements Flammability limit measurements were carried out at three temperatures - ambient, 500 C and 400 C with supporting atmospheres containing from 21% oxygen (air) down to 11.0% oxygen. All these experiments were carried out under atmospheric pressure. The results of this work are shown in Fig. (2), where vol. % ammonia in the mixture is plotted against vol. % oxygen in the supporting atmosphere. The data in Fig. (2) show that ammonia behaves in a similar manner to hydrocarbon vapours and the flammability limits widen as temperature increases. Thus the limits for ammonia in air increase from 16.6-27.2% ammonia in the mixture at ambient temperatures to 13.1-34.3% at 300 o C and 11.2-37.1% at 400 o C. Compilations of data such as Coward and Jones (1) and Zabetakis (8) give lower limits for ammonia and air at ambient temperatures between 15.O and 17-1 vol % and upper limits between 26.4 and 28.0 vol %. None of these measurements were carried out with an open ended tube (i.e. at constant pressure), which is the preferred method. The influence of temperature on the flammability limit has been measured by White (2) and more recently by Rolingson (9). Their results show the same increase in the flammable range with temperature increase as found in the present work. All these higher temperature flammability limit data are plotted in Fig. (3) together with the more recent literature data of De Coursey et al (7) obtained at ambient temperature using a flat flame burner technique. The value of the lower flammability limit at ambient temperature found in the present work agrees well with the flat flame burner determinations (7) and with other literature data. Agreement is not as good for the upper limit. This limit is always practically more difficult to measure than the lower limit and both limits are influenced to some extent by the strength of the ignition source. In the experience of the authors powerful ignition sources e.g. gun cotton tend to give an unrealistic widening of the limits, particularly if they are measured in a closed vessel. One further parameter shown in Fig.(2) is of importance for application to chemical plant design. This is the minimum oxygen concentration in the supporting atmosphere, below which no ammonia containing mixture will burn. Examination of Fig. (2) shows that this decreases from 17 vol. % oxygen at ambient temperature to 12.8% at 300 o C and 11.0% at 400 o C. These minimum oxygen concentrations are plotted against temperature in Fig. (4) together with similar data obtained under elevated pressure by Buckley and Husa (10). As can be seen all the data lie on a good straight line enabling extrapolation to temperatures of 500-600 C (where experimental work is difficult to be carried out with reasonable accuracy). 2.2 Explosibility Measurements The measurements of the explosibility of ammonia were carried out in a 6 litre stainless steel bomb with ammonia containing mixtures initially under atmospheric pressure. Explosion pressures were measured at the three temperatures - ambient, 300 C and 4OO o C used in the flammability limit work, but the only supporting atmosphere investigated was air. 30

The results showed the same characteristics as measurements made with hydrocarbon/air mixtures. Both the maximum explosion pressure and rates of pressure rise gave a maximum value for an ammonia/air mixture with a composition close to the stoichiometric. Tabie (1) shows the maximum values of these 3 parameters together with the maximum explosion pressure and rates of pressure rise for the most explosive mixture of a typical hydrocarbon (pentane) in the same 6 litre bomb. TABLE (1):- Explosibility of Ammonia (most explosive ammonia/air mixture) m Temperature Max. Explosion ( o c) Press (bars) Ambient 5.93 300 3.45 400 2.76 Av. Rate Press Rise (bars/sec.) 9.65 28.95 40.67 Max. Rate Press Rise (bars/sec.) 17.92 66.17 84.78 3.0 mol % Pentane in air Ambient 8.13 189.5 448.0 These results show that explosion pressure decreases with increase in temperature as would be expected for explosions in a vessel with a constant volume. This temperature effect has already been seen in the work of Crouch et al (11). The maximum explosion pressure for ammonia is also appreciably less than for a typical hydrocarbon - pentane. The rates of pressure rise both increase with increase in temperature and, in line with the reduced maximum explosion pressure, the rates of pressure rise are considerably less than those for pentane at ambient temperature. This rexplosibility data indicated that when ammonia/air mixtures are ignited they burn much more slowly than hydrocarbon/air mixtures. It was of interest to see whether ammonia containing mixtures were also less easy to ignite than hydrocarbon mixtures. 2.3 Ease of Ignition of Ammonia Measurement of ignition energy presents considerable practical difficulties - nature of spark (capacitance or inductance), geometry of electrodes, electrode gap etc. The limited amount of literature on this subject Buckley and Husa (10) and Magison (12) show considerable discrepancies in the measured values of ammonia ignition energies, probably because of the practical difficulties listed above. A few measurements were, however, carried out using first an inductive spark and then a capacitance spark. The results obtained with these two sparks for the most explosive ammonia/air mixture are given in Table (2) together with the literature data. 31

I. CHEM.E. SYMPOSIUM SERIES No. 49 TABLE (2):- Minimum Ignition Energies of Ammonia Source of Data Explosive Mixture Type of Igniting Circuit Voltage (Volts) Current (amps) Inductance (Henrys) Minimum Ignition Energy (mj) This Work Magison Magison Buckley and Husa Magison Magison Ammonia/Air Pentane/Air Pentane/Air Capacitive Capacitive 350 10,000 24 24 Variable 24 24 0.11-1.13 0.25-0.16 0.045 15 0.095 1.1-0.095 1.1 <90 170 60 40 680 1.2 1.0 Examination of Table (2) shows that the data obtained with inductance sparks agrees reasonably well with that of Magison, but the measured ignition energy was higher with the capacitance spark. The ignition energies given by Magison and those obtained in the present work are considerably lower than the data of Buckley and. Husa. The most important conclusion from the data in Table (2) is that mixtures of ammonia and air are appreciably more difficult to ignite than those of a typical hydrocarbon, pentane, and air (40-170 mj vs 1.0-1.2 mj). 3. CONCLUSIONS The flammability data for anhydrous ammonia/oxygen/nitrogen mixtures obtained in the present work provides adequate information for plant design purposes for a range of supporting atmospheres and temperatures up to HOO C. Agreement with other published data is good, at least for the lower flammability limit. Some doubt still exists about the upper flammability limit, but the data presented are from experiments in an open tube using a realistic source of ignition (high energy spark), where flames were seen to travel an appreciable distance from the source of ignition. Explosibility measurements show that ammonia/air mixtures are significantly less explosive than a typical hydrocarbon, pentane, mixed with air. A few measurements on ease of ignition showed that the most explosive mixture of ammonia and air was much more difficult to ignite than the corresponding pentane/air mixture. PART (2):- FLAMMABILITY OF AQUEOUS AMMONIA 1. EXPERIMENTAL The flammability limits of ammonia/air/water vapour mixtures were determined in the apparatus used for the work on anhydrous ammonia (see Fig. (1)). The equipment was again evacuated to less than 2 torr. and the required amounts of ammonia and water vapour admitted in turn. Air was then admitted until the pressure reached atmospheric and the ammonia, water vapour and air mixed by means of the solenoid pump. In each experiment a sample of the mixture under test was taken and analysed for ammonia and water vapour content. A 1.5 Joule inductance spark was again used to ignite the mixture and the ground glass plate at the base of the ignition tube was removed before ignition. All the experiments on ammonia/water vapour/air mixtures were carried out at one temperature, 80 C, to prevent condensation of water vapour inside the equipment. For this purpose all the equipment, solenoid pump and sample tube included was enclosed in an oven. 2. RESULTS The results of these experiments are shown in Fig.(5), where vol. % oxygen in the mixture under test is plotted against vol. % ammonia in the same mixture. For comparison purposes the flammability limits of anhydrous ammonia/air at the same temperature, 80 C, are plotted on the graph. 32

Examination of this figure shows that a minimum oxygen content of 14.5% in the total gases (at 80 C) is required to support combustion where water vapour is present, but mixtures containing as little as 13.0 vol. % oxygen in the total gases will burn for anhydrous ammonia/air mixtures. Thus water vapour is a more efficient quenching agent than nitrogen, as would be expected from its higher molar heat capacity. Comparison of the results of this work with the limited amount of literature data (6), (7) is difficult because of the different experimental conditions employed by the various sets of workers. The data of Schliephake (6) is taken from some old German work, which was carried out in a closed vessel at 44 o C, while DeCoursey et al (7) made their measurements at 65 C using a flat flame burner technique at various linear velocities. To give an approximate comparison the minimum water level (vol %) in the total gases to completely suppress combustion was calculated for each set of data. These figures are shown in Table (3)«TABLE (3):- Minimum Water Content to Suppress Combustion (vol %) Present Work Open Tube 80 C De Coursey et al Flat Flame Burner 65 C Schliephake et al Closed Vessel 44 o C 11.0 10.8 7.2 Considering the wide variation in experimental techniques these results are reasonably consistent with the expected decrease in the amount of water required to suppress flame as mixture temperature decreases. 3. APPLICATION OF RESULTS TO PLANT DESIGN Much the most important aspect of this work on the flammability of aqueous ammonia is the way in which it can be applied to problems of plant design. If an aqueous solution of ammonia of known strength is being handled it is possible to calculate the composition of the vapour phase above the solution from vapour/liquid equilibrium data. Suitable data for aqueous ammonia is given in Perry (13). Using this data the vol. % oxygen and ammonia in the gas phase above aqueous ammonia solutions with strengths of 5-25% were calculated for a series of temperatures. The results of these calculations are shown along with the flammability limit measurements made at 80 C in Fig. (6). Examination of this figure shows that the vapour phase above solutions containing 5% or less ammonia (by vol.) are non-flammable up to 80 C (temperature at which limits determined). More concentrated solutions of ammonia give flammable vapours when the solution is between certain temperatures. A few solution temperatures are shown in Fig. (6) to illustrate this point. Fig. (/) shows the above data plotted in a different way. Here the vapour phase composition, at a given solution temperature, for all the aqueous ammonia solutions are shown to lie on straight lines. Again the flammability limits (80 C) are plotted on the graph. From this figure it can be seen that the vapour phase above any ammonia solution will be nonflammable if the temperature of the solution is above 49 o C. 4. CONCLUSIONS The experimental data on the flammability of aqueous ammonia/air vapour mixtures can readily be applied to the hazards of handling aqueous solutions of ammonia. Two important points emerge from this work (a) the vapour above solutions containing 5% or less ammonia are non flammable at any solution temperature (b) no aqueous solution of ammonia will give flammable vapour when its temperature is above 49 o C. These conclusions apply only to solutions of ammonia in open vessels, but similar calculations based on vapour/liquid equilibrium data can be made for ammonia solutions in sealed vessels. 33

REFERENCES 1. Coward and Jones, 1952, U.S. Bureau of Mines Bulletin, 505 2. White, 1922, J.Chem Soc,121, 1688 3. Burgoyne and Neal, 1955, Fuel 5, 52 4. Frank and Doering, 1931, Z.Angew. Chem. 44, 273. 5. Berl and Bausch, 1929, Z.Phys. Chem. A145, 347 6. Schliephake et al, 1930, Z. Angew. Chem 43, 302 7. DeCoursey et al, 1962, Can. J. Chem. Eng. 40, 203 8. Zabetakis, 1965, U.S. Bureau of Mines Bulletin 627 9. Rolingson, 1960, J. Chem. Eng. Data 5, 349 10. Buckley and Husa, 1962, Chem. Eng. Prog. 58, 81 11. Crouch et al, 1952, Eastman Kodak Co., Rept. of Manufacturing Division 12. Magison, 1966, Electrical Instruments in Hazardous Locations Plenum Press, New York 15. Perry, Chem. Engineers Hand Book, 4th Edit., 3

FIG. 1 V ERTICAL TUBE FOR ROOM TEMPERATURE WORK FIG. 2 FLAMMABLE LIMITS AMMONIA - AIR -NITROGEN MIXTURES : AMMONIA VS OXYGEN CONTENT OF SUPPORTING ATMOSPHERE 35

I. CHEM.-E. SYMPOSIUM SERIES No. 49 FIG. 3 FLAMMABILITY OF AMMONIA - AIR MIXTURES FIG.4 OXYGEN CONTENT OF SUPPORTING ATMOSPHERE AT ELEVATED TEMPERATURES TO SUPPORT COMBUSTION AT VARIOUS TEMPERATURES FIG. 5 FLAMMABILITY LIMITS OF AMMONIA SYSTEMS AT 80 C AND ATMOSPHERIC PRESSURE 36

FIG. 6 FLAMMABILITY OF AMMONIA - WATER VAPOUR - AIR SHOWING VAPOUR COMPOSITION ABOVE AQUEOUS AMMONIA SOLUTIONS AT VARIOUS TEMPS. FIG. 7 FLAMMABILITY OF AMMONIA - WATER VAPOUR - AIR WITH ISOTHERMS SHOWING COMPOSITION OF VAPOUR OVER AQUEOUS AMMONIA SOLUTIONS 37