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UCRL-51319^/fitr./)

PROPERTIES OF CHEMICAL EXPLOSIVES

AND EXPLOSIVE SIMULANTS

Compiled and edited by Brigitta M. Dobratz

December 15, 1972

Prepared for U.S. Atomic Energy Commission under contract No. W-7405-Eng-48

LANA/RENCE

LIVERMORE

LABORATORY

University of Califomia/Livermore

i | I Q T I

T H ; C - • ,_ ,• ,:^ji

Mlh

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DISCLAIMER

This report was prepared as an account of work sponsored by an

agency of the United States Government. Neither the United States

Government nor any agency Thereof, nor any of their employees,

makes any warranty, express or implied, or assumes any legal

liability or responsibility for the accuracy, completeness, or

usefulness of any information, apparatus, product, or process

disclosed, or represents that its use would not infringe privately

owned rights. Reference herein to any specific commercial product,

process, or service by trade name, trademark, manufacturer, or

otherwise does not necessarily constitute or imply its endorsement,

recommendation, or favoring by the United States Government or any

agency thereof. The views and opinions of authors expressed herein

do not necessarily state or reflect those of the United States

Government or any agency thereof.

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DISCLAIMER

Portions of this document may be illegible in

electronic image products. Images are produced

from the best available original document.

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LAWRENCE UVERMORE LAB0RA1ORY

Chtari«ya/CMR>rnit/lA«mnr«C»M»«(/]M550

UCRL-51319^ Bui-,/

PROPERTIES OF CHEMICAL EXPLOSIVES

ANO EXPLOSIVE SIMULANTS

Compiled and edited by Brigitta M. Dobratz MS. date: December 15, 1972 (Supersedes UCRL-6759, Vol. 1,

and UCRL-14592)

N O T I C E

-This report was prepared as an account of work sponsored by the United States Government. Neither the United States nor the United States Atomic Energy Commission, nor any of their employees, nor any of their contractors, subcontractors, or their employees, maizes any warranty, express or implied, or assumes any legal liability or responsibility for the accuracy, com-pleteness or usefulness of any information, apparatus, product or process disclosed, or represents that its use would not infringe privately owned rights.

DISTRIBUTION OF THIS DOCUMENT IS UNLIMITED

NOTICE

mtelns information ^ u u ^ M B H s r y nature ^ S i m ^ ^ ^ j u r e d p r i n u ^ ^ M i ^ ^ e r n a l use at the o r i g i n a t i n ^ l ^ k M ^ ^ ^ n s s u b j e c t to r e -vision or c o r r e c t ^ | M i m ^ ^ | H ^ ^ o e 8 not repz%-sent a tinalra^f^^ is p a s B ^

confidenc|Mirshould not be abstracted or" d i s a J ^ P ^ i t h o u t the approval of the originating

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Contents

Foreword vii Conversion F a c t o r s viii Glossary ix I. High Explosives 1-1 1. Introduction 1-1 2. Manufacture 2-1 Specifications 2-1 3. Names and Formulations 3-1

4. Physical P r o p e r t i e s 4-1 Physical State and Density 4-2

Molecular Weight and Atomic Composition 4-4 Melting Point, Boiling Point, and Vapor P r e s s u r e . . . 4-6

Crystallographic and Optical P r o p e r t i e s 4-9

References 4-10 5. Chemical P r o p e r t i e s 5-1 Heat of Formation 5-1 Heat of Detonation 5-2 Conapatibility 5-4 Solubility 5-7 References 5-8 6. T h e r m a l P r o p e r t i e s 6-1 T h e r m a l Conductivity 6-1 T h e r m a l Expansion 6-4 Specific Heat 6-6 T h e r m a l Stability 6-8 Thermal Stability of L a r g e r Explosive Charges . . . 6-51

References 6-52 7. Mechanical P r o p e r t i e s 7-1 Static Mechanical P r o p e r t i e s 7-4 Initial Modulus 7-5 Creep 7-6 S t r e s s - S t r a i n Relationships 7-8 F a i l u r e Envelope 7-9 Friction 7-10 Complex Shear . . . , ' 7-14 Dynamic Mechanical P r o p e r t i e s 7-15 Compressive S t r e s s - S t r a i n and Tensile Strength . . . 7 - 1 5

Hugoniot Data 7-17 Sound Velocity 7-21

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References 7-23 8. P e r f o r m a n c e 8-1 Detonation Velocity 8-1 Estimation . 8-2 Equations 8-5 Chapman-Jouguet Detonation P r e s s u r e 8-6

Cylinder Test Measurements of Explosive Energy . . . . 8 - 8

Equation of State 8-10 Detonation Energy 8-12

References 8-14 9. Sensitivity and Initiation 9-1

Drop Weight Test 9-1

Susan Test 9-3 Comp B-3 9-5 Cyclotol 75/25 9-6 LX-02-1 9-7 LX-04-1 9-8 LX-07-2 9-9 LX-09-0 9-10 LX-10-0 9-11 LX-11-0 9-12 LX-14-0 9-13 Octol 75/25 9-14 PBX-9010 9-15 PBX-9011 9-16 PBX-9205 9-17 PBX-9404-03 9-18 PBX-9501 9-19 TNT 9-20 XTX-8003 9-21 Skid T e s t 9-22 Gap Test 9-26 Shock Initiation 9-29 Critical Energy 9-29 Initial Shock P r e s s u r e 9-30 References 9-32 10. E l e c t r i c a l P r o p e r t i e s 10-1 Dielectric Constant 10-1 References 10-3 11. Toxicity 11-1 References 11-2 - i v - 7/74

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II. Mock Explosives 12-1 12. Introduction 12-1 13. Names and Formulations 13-1

14. Physical P r o p e r t i e s 14-1 References 14-1 15. Thermal P r o p e r t i e s 15-1

Thermal Conductivity and Specific Heat 15-1

T h e r m a l Expansion 15-4 References 15-4 16. Mechanical P r o p e r t i e s 16-1 Static Mechamical P r o p e r t i e s 16-2 Initial Modulus 16-2 Tension Creep 16-3 F a i l u r e Envelope 16-4 Friction 16-5 Dynamic Mechanical P r o p e r t i e s 16-6 Compressive S t r e s s - S t r a i n 16-6 Hugoniot Data 16-7 References . . . 16-8

III. Code Designations 17-1 LLL Code Designations 17-1

Formulations in Production (LX Code) 17- 1

R e s e a r c h Explosives (RX Code) 17-3

LASL Code Designations 17-7 IV. Data Sheets: Collected P r o p e r t i e s of Explosives and

Energetic Materials 18-1

V. Bibliography 19-1 Chemical Analysis 19-1

General Reference Works 19-3

Health and Safety 19-7 Initiation and Sensitivity 19-9

Mechanical and Physical P r o p e r t i e s 19-13

P e r f o r m a n c e 19-15 Radiation Effects 19-21 T h e r m a l P r o p e r t i e s 19-23

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d

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Foreword

This handbook p r e s e n t s information axid data for high explosives of i n t e r e s t to p r o g r a m s of Lawrence L i v e r m o r e L a b o r a t o r y . The loose-leaf format i s designed to p e r m i t easy revision and updating as new information and data become available. Thus, additions and c o r r e c t i o n s a r e welcomed by the compiler.

High Explosives (HE) a r e divided into two c l a s s e s : initial detonating or p r i m a r y explosives and noninitiating or secondary HEs. The p r i m a r y HEs, such as azides and fulminates, a r e extremely sensitive to ignition by heat, shock, and e l e c t r i c a l d i s c h a r g e ; ignition goes to high-order detonation even for m i l l i g r a m quantities. Their use is

therefore limited to squibs and stairting m a t e r i a l s for low-energy detonators. Since p r i m a r y explosives have little application h e r e , their p r o p e r t i e s have been specifically excluded from this compilation. Hereafter, secondary explosives a r e designated as

H E s . Since many of the secondary high explosives (which a r e formulated and manu-factured within the AEC complex) a r e m i x t u r e s , the p r o p e r t i e s of the additives and binders used have been included.

The data a r e the most up-to-date and a c c u r a t e available to the knowledge of the compiler. Some data, however, can r e p r e s e n t only a range, an approximation, or comparative values; this is especially t r u e of explosive m i x t u r e s . Such c a s e s a r e noted in the text as they occur. The s o u r c e s of information include textbooks, journal a r t i c l e s , technical r e p o r t s , memoranda, l e t t e r s , and p e r s o n a l communications. Var-ious s c h e m e s considered in the past to annotate the tables with the apposite r e f e r e n c e s proved too c u m b e r s o m e . However, an attempt is naade in this revision and will be continued in subsequent revisions to provide p r e c i s e r e f e r e n c e s to the information and data p r e s e n t e d . Data not specifically referenced w e r e obtained from UCRL-14592 ; further information and additional r e f e r e n c e s can be obtained from the co m p i l e r. References a r e listed at the end of each section.

The compilation consists of sections on high explosives and mock explosives, code designations, data sheets on individual m a t e r i a l s , and a bibliography. A l i s t of abbreviations p r e c e d e s the section on high explosives. The data a r e given in the units (metric or English) in which they were reported originally. All values and units, however, a r e converted to the International System of Units (S.I.)^; throughout this handbook the SI values a r e given in p a r e n t h e s e s following the values in English or m e t r i c units. The imits a r e given in the table below and on other tables and figures where used.

Reference to a company o r product name in this compilation does not imply approval o r recommendation of the product by the University of California o r the U. S. Atomic Energy Commission to the exclusion of o t h e r s that may be suitable.

P r o p e r t i e s of Chenaical Explosives, Lawrence L i v e r m o r e Laboratory, Rept. UCKL-145S2 (1965).

' M e t r i c P r a c t i c e Guide. American Society for Testing and M a t e r i a l s , Philadelphia, E 380-70 (1970).

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CONVERSION FACTORS

Units and factors for conversion to SI s y s t e m .

Angle C-J p r e s s u r e Creep compliance Density Detonation velocity Heat of ^ detonation Heat of . formation Initial modulus Length P r e s s u r e Sliding velocity Specific heat^ T e m p e r a t u r e T h e r m a l conductivity^* T h e r m a l expansion Vapor p r e s s u r e Weight Symbol P C J P D ^ d e t AH, ^ 0 P V

s

T k CTE v.p. U. S^British 1/psi (= in.2/lbf) p s i m i l p s i in. /min fl/sec BTU/lb-°F o p BTU/hr-ft-°F in./in.-°F l b Unit system c g s d e g b a r ^ c m ^ mm/^tsec c a l / g c a l / g k c a l / m o l o A a t m b a r cal/g-°C °C SKm/k/s)^ r a d P a m2/N Mg/m^ km/s J/kg J/kg kJ/mol Pa m m P a P a P a m/s m/s J/kg-K K K W/m-K ca]/cm-sec-°C W/m-K cnVcm-°C m/m-K n^m-K mm Hg, T o r r Pa kg Multiplication factor 1.745329 X 10-2 10^ 1.450377 X 10-4 1 1 4.184 X 10^ 4.184 X 10^ 4.184 6.894757 X 10^ 10-10 2.54 X 10"^ 6.894757 X 10^ 1.01 X 105 1.00 X 10^ 4.233 X 10-4 3.048 X 10-1 4.184 X 10^ [ ( T p - 32)/1.8] +273.15 T^ + 273.15 1.729577 4.184 X 102 1.8 1 1.333 X 102 4.535924 X l O " ! In this column, the abbreviations used a r e those of the International System of Units (SI)2; in this system, degrees Kelvin = K .

Thermochemical BTU or c a l o r i e .

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Glossary

AFNOL

A W R E

b.p.

BDNPA

BDNPF

BEAF

B K W

BTF

% C

P

CAB

CEF

CJ

CTE

D

DATB

dec.

DFTNB

DINOL

DIPAM

DMFA

DMSO

DNPA

DNPN

DOP

E

EDNP

EGDN

f

f.p.

FEFO

G

^50

HE

H M X

HNAB

HNS

HVD

polymerization product of p r i m a r i l y DINOL and 4,4-dinitropimeloyl chloride

Atomic Weapons R e s e a r c h Establishment, U.K. boiling point

bis(2,2-dinitropropyl) acetal bis(2,2-dinitropropyl) formal

1,2-ethanediol bisdifluoronitroacetate

Brinkley-Kistiakowski-Wilson (equation of state) benzotrifuroxan

calculated bulk sonic velocity calculated longitudinal velocity specific heat

cellulose acetate butyrate t r i s - ^ - c h l o r o e t h y l phosphate Chapman-Jouguet coefficient of t h e r m a l expansion detonation velocity l,3-diamino-2,4,6-trinitrobenzene decomposition difluorotrinitrobenzene 2 , 2 , 8 , 8 - t e t r a n i t r o - 4 , 6 - d i o x a - l , 9 - n o n a n e diol 2,2',4,4',6,6'-diaminohexanitrobiphenyl, d i p i c r a m i d e dimethylformamide dim'ethylsulfoxide 2,2-dinitropropyl acrylate 4,4-dinitropentanonitrile dioctylphthalate, di-(2-ethylhexyl)-phthalate energy ethyl 4, 4-dinitropentanoate ethylene glycol dinitrate ultrasonic modulus coefficient of friction freezing point

bis(2-fluoro-2, 2-dinitroethyl) formal complex s h e a r modulus

drop weight sensitivity high explosive

1, 3, 5, 7 - t e t r a n i t r o - 1 , 3, 5, 7 - t e t r a z a c y c l o o c t a n e 2, 2', 4, 4', 6, 6'-hexanitroazobenzene

2, 2', 4, 4', 6, 6 ' - hexanitrostilbene high velocity detonation

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J W L K k L A S L L L L L V D m . p . MEK MIBK MW N n N C NG N M N O L NONA NQ P C J P B X P E N T E K P E T N P R R RDX R T V S . I . S T P T T g T A C O T T A T B T E F T e t r y l T H F T M D T N M T N T V V v . p . W L F J o n e s - W i l k i n s - L e e ( e q u a t i o n of s t a t e ) d e g r e e s K e l v i n t h e r m a l c o n d u c t i v i t y L o s A l a m o s S c i e n t i f i c L a b o r a t o r y L a w r e n c e L i v e r m o r e L a b o r a t o r y low v e l o c i t y d e t o n a t i o n m e l t i n g p o i n t m ethyl ethylk e t o n e m e t h y l i s o b u t y l k e t o n e m o l e c u l a r w e i g h t n e w t o n ( p o u n d - f o r c e ) r e f r a c t i v e i n d e x n i t r o c e l l u l o s e n i t r o g l y c e r i n e n i t r o m e t h a n e N a v a l O r d n a n c e L a b o r a t o r y n o n a n i t r o t e r p h e n y l n i t r o g u a n i d i n e C h a p m a n - J o u g u e t p r e s s u r e p l a s t i c - b o n d e d e x p l o s i v e p e n t a e r y t h r i t o l p e n t a e r y t h r i t o l t e t r a n i t r a t e P o i s s o n ' s r a t i o m o l e c u l a r r e f r a c t i o n 1, 3, 5 - t r i n i t r o - l , 3, 5 - t r i a z a c y c l o h e x a n e r o o m - t e m p e r a t u r e v u l c a n i z i n g S y s t e m e I n t e r n a t i o n a l e ( I n t e r n a t i o n a l S y s t e m of U n i t s ) s t a n d a r d t e m p e r a t u r e and p r e s s u r e t e m p e r a t u r e g l a s s t r a n s i t i o n t e m p e r a t u r e t e t r a n i t r o - 1 , 2, 5, 6 - t e t r a z a d i b e n z o c y c l o o c t a t e t r e n e 1, 3, 5 - t r i a m i n o - 2 , 4, 6 - t r i n i t r o b e n z e n e t r i s - ^ - c h l o r o e t h y l p h o s p h a t e 2, 4 , 6 - t r i n i t r o p h e n y l m e t h y l n i t r a m i n e t e t r a h y d r o f u r a n t h e o r e t i c a l m a x i m u m d e n s i t y t e t r a n i t r o m e t h a n e 2, 4, 6 - t r i n i t r o t o l u e n e v o l u m e v e l o c i t y v a p o r p r e s s u r e W i l l i a m s - L a n d e l - F e r r y (shift e q u a t i o n ) X

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a linear coefficient of expsinsion P cubical coefficient of expansion

AH , , heat of detonation AH- heat of formation

r adiabatic coefficient of expansion

a linear CTE

i3 cubical CTE

e dielectric constant

V sliding velocity

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PROPERTIES OF CHEMICAL EXPLOSIVES

AND EXPLOSIVE SIMULANTS

I. High Explosives

1. INTRODUCTION

High explosives a r e metastable compounds or m i x t u r e s that can r e a c t rapidly to give gaseous products at high t e m p e r a t u r e and p r e s s u r e . The attendant expansion of these products is the mechanism by which explosives do useful work. As with p r i m a r y explosives, reaction can be initiated by shock and heat. High explosives, however, differ from p r i m a r y explosives in t h r e e ways:

1. Small unconfined charges, even though ignited, will not usually detonate high-order.

2. E l e c t r o s t a t i c ignition is v e r y difficult (except in explosive dust clouds). 3. Ignition of any s o r t r e q u i r e s considerably l a r g e r shocks.

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2. MANUFACTURE

P u r e explosives a r e usually synthesized by s u l f u r i c / n i t r i c a c i d nitration of o r -ganic compounds. The product is separated from the mixed acids by filtration, then worked free of impurities and dried.

TNT is one of the few pure explosives that can be fabricated directly by melting and casting into a desired shape. Most other m a t e r i a l s must be diluted either with TNT (thereby castable) or with plastic (thereby p r e s s a b l e ) before they can be fabri-cated into useful shapes.

The p r o c e d u r e used for fabricating castable, TNT-containing formulations is as follows: TNT is melted and the desired solid ingredients a r e added with s t i r r i n g . The melt is p r e c r y s t a l l i z e d into a s l u r r y , and vacuum is applied just before pouring into a mold. Cracking and variations in density and composition a r e minimized by careful control of the cooling r a t e .

Plastic-bonded explosives (PBX) a r e p r e s s e d from "molding" powders, which may be produced in s e v e r a l ways. A typical p r e p a r a t i o n is by the s l u r r y technique: powdered explosive and water a r e agitated in a container equipped with cover, con-denser, and s t i r r e r . A lacquer composed of the plastic (together with a p l a s t i c i z e r , if required) dissolved in a suitable solvent is added to the s l u r r y . The solvent is r e -moved by distillation, causing the plastic phase to p r e c i p i t a t e out onto the explosive a s a coating. The plastic-explosive a g g l o m e r a t e s into " b e a d s " as the s t i r r i n g and r e m o v a l of solvent a r e continued. Finally, w a t e r is removed from the beads by filter-ing and dryfilter-ing, leavfilter-ing the moldfilter-ing powder. Good moldfilter-ing powders have a high bulk density and a r e free-flowing and d u s t l e s s .

PBX molding powder can be p r e s s e d into usable shapes by two methods: com-p r e s s i o n molding with steel dies, or hydrostatic or isostatic com-p r e s s i n g . In the l a t t e r method the explosive is placed in rubber s a c k s and subjected to fluid p r e s s u r e . With either method, consolidation of the molding powder to reasonable densities (97% of theoretical) is obtained at p r e s s u r e s between 12,000 and 20,000 p s i (83 and 138 MPa) and molding t e m p e r a t u r e s between 25 and 120°C ( 298 and 313 K). An important and n e c e s s a r y feature of molding is the use of vacuum. The molding powder is normally evacuated to a p r e s s u r e of l e s s than 1000 lu Hg (133 Pa) before p r e s s i n g .

Both p r e s s e d and cast explosives a r e usually machined to final shape. Many intricate forms have been cut successfully. As a r u l e , the machining of explosives is s i m i l a r to the machining of a conventional plastic, except that water is used as a cuttingtool coolant. New explosives a r e machined by r e m o t e control until their b e -havior under machining has been carefully evaluated.

Specifications

Manufacture and testing a r e controlled by specifications for production explosives. A list of pertinent specifications is given in Table 2 - 1 .

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Table 2. 1. Specifications for manufacture and testing. Specification number Title Explosives BDNPA/BDNPF Comp B Comp-B-3 F E F O HMX HNAB LX-04 LX-07 LX-09 LX-10 LX-13 Octol PBX-9007 PBX-9011 PBX-9205 PBX-9404 PBX-9407 PBX-9501 PETN KDX Tetryl TNT XTX-8003

WS-1141 U capons Specification for Mixture of

Bis(2,2-dinitropropyl)acetal-Bis(2,2-dinitro-propyl) formal.

MIL-C-401 Military Specification for Composition B. MIL-C-45113 Military Specification for Composition B - 3 . RM-253202 I I I Material Specification for I iquid Explosive

Bis(2,2-dinitro-2-fluoro-ethyl) formal (FEFO). MlL-H-45444 Military Specification for HMX.

SS274590 Sandia Spec itication for Synthesis of HNAB (Hexa-nitroazobenzene).

RM-252353 I I I Material Specification for I X-04 Molding Powder. RM-253379 I 1 I Material Specification for I X-07 Molding Powder. RiVl-253200 1 1 I Material Specification for I X-09 Molding Powder. RM-253511 I I I Material Specification for I X-10 Molding Powder. RM-253520 I I I General Spec ific ation for I X-13. (CRD)

Mil -0-45445 Military Specification for Octol.

PA-PD-711 Pi( atinny Arsenal Pure base Description for Powder, Molding Compound Explosive (PBX). (PBX-9007). 13Y-101030 I ASI Material Specification for PBX-9011 Molding

Powder.

13Y-103317 I AS! Material Specification for PBX-9205 Manufac-tured by the Slurry Method.

13^-103159 I ASI Material Specification for PBX-9404 Molding Powder.

RM-252336 I I I Vlaterial Specification for P B \ - 9 4 0 4 Molding Powder.

13Y-109098 I ASI Material Specification for PBX-9407 Molding Powder.

13\-109643 I ASI Material Specification for PBX-9501 Molding Powder.

Mil -P-387 Military Specification for Pentaerythritol T e t r a n i t r a t e (PFTN).

Mil -R-398 Military Specification for RDX.

JAN-T-339 Joint Army-Navy Specification for Tetryl (Trinitrophenylinethjlnitramine).

Mil - 1 - 2 4 8 Military Specification for I N T

13Y-104481 I ASI Material Specification for XTX-8003 Extrudable Explosive. Binders Estane F l u o r o -e l a s t o m -e r pDNPA Polystyrene Sylgard

13Y-101031 I ASI Material Specification for Estane 5740 X - 2 . RM252988 LI L Material Specification for Uncured F l u o r o

-e l a s t o m -e r Bind-er

RM-253201 I I L Material Specification for 2,2-DinitropropyI-acrylate Polymer (pDNPA) Plastic Binder

MIL-P-55026 Military Specification for Polystyrene, Unmodified (For Use as a Binder in Explosives).

13Y-104480 I ASI Material Specification for Dow Corning Resin 93-022 (Aerospace Grade Sylgard 182).

Explosive P a r t s and Testing RM-253391

RM-252356

I I L Specification for Mechanical P r o p e r t i e s Testing of Plastic-Bonded High Explosive P a r t s .

LI L General Specifications for Plastic-Bonded High Explosives.

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3. NAMES AND FORMULATIONS

This section consists of Tables 3-1 through 3-4, which list the n a m e s and formu-lations of various explosives and energetic compounds.

Table 3 - 1 . P u r e explosive compounds.

M a t e r i a l ' C h e m i c a l n a m e O t h e r d e s i g n a t i o n s C o l o r B T F D A T B DIPAM DNPA EDNP FEFO HMX HNAB HNS NC (12% N)"^ NC (13,35% N, minll^ NG NM NQ P E T N RDX T A C O T T A T B ' T e t r y l •TNM "TNT B e n z o t r i s [ l , 2, 5] o x a d i a z o l e -[ 4 , 4 , 7 ] - t r i o x i d e 1, 3 D i a m i n o 2 , 4, 6 t r i n i t r o -b e n z e n e 3 , 3 D i a m i n o 2 , 2 ' , 4 , 4 ' , 6, 6 ' -h e x a n i t r o b i p -h e n y l 2 , 2 - D i n i t r o p r o p y l a c r y l a t e E t h y l - 4 , 4 - d i n i t r o p e n t a n o a t e B i s ( 2 f l u o r o 2 , 2 d i n i t r o e t h y l ) -f o r m a l 1, 3, 5, 7 T e t r a n i t r o 1 , 3, 5, 7 -t e -t r a a z a c y c l o o c -t a n e 2, 2 ' , 4 , 4 ' , 6, 6 ' H e x a n i t r o a z o -b e n z e n e 2, 2 ' , 4, 4 ' , 6, 6 ' - H e x a n i t r o s t i l b e n e P a r t i a l l y n i t r a t e d c e l l u l o s e P a r t i a l l y n i t r a t e d c e l l u l o s e 1, 2, 3 - P r o p a n e t r i o l t r i n i t r a t e N i t r o m e t h a n e N i t r o g u a n i d i n e P e n t a e r y t h r i t o l t e t r a n i t r a t e 1, 3, 5 T r i n i t r o l , 3 , 5 t r i a z a c y c l o h e x a n e , h e x a h y d r o -1, 3 , 5 - t r i n i t r o - s - t r i a z i n e T e t r a n i t r o l , 2 , 5 , 6 t e t r a a z a d i -b e n z o c y c l o o c t a t e t r e n e 1, 3, 5 T r i a m i n o 2 , 4 , 6 t r i n i t r o -b e n z e n e 2, 4 , 6 T r i n i t r o p h e n y l m e t h y l -n i t r a m i -n e T e t r a n i t r o m e t h a n e 2 , 4 , 6 - T r i n i t r o t o l u e n e B e n z o t r i f u r o x a n , h e x a n i t r o s o b e n z e n e H e x a n i t r o d i p h e n y l -a m i n e h e x i t e , d i p i c r y l a m i n e C y c l e t e t r a m e t h y l e n e t e t r a n i t r a m i n e , o c t o g e n N i t r o c e l l u l o s e ( l a c q u e r g r a d e ) , c e l l u l o s e t r i n i t r a t e , p i r o k s i l i n N i t r o c e l l u l o s e , g u n c o t t o n T r o t y l , T, tol Buff Yellow O f f - w h i t e Yellow Straw W h i t e O r a n g e Yellow White White N i t r o g l y c e r i n A m i n o m e t h a n e a m i d i n e P e n t h r i t e , T E N C y c l o t r i m e t h y l e n e t r i n i t r a m i n e . h e x o g e n c y c l o n i t e , Gh T e t r a n i t r o d i b e n z o 1, 3a, 4, 6 a -t e -t r a a z a p e n -t a l e n e C l e a r C l e a r White W h i t e White R e d -o r a n g e B r i g h t yellow Yellow C l e a r Buff to b r o w n P r o p e r t i e s of m a t e r i a l s m a r k e d with a s t e r i s k s a r e s u m m a r i z e d in d a t a s h e e t s (Section IV). N i t r o c e l l u l o s e i s not, s t r i c t l y s p e a k i n g , a s i n g l e c h e m i c a l c o m p o u n d . D i f f e r e n t g r a d e s a r e c o m m e r c i a l l y a v a i l a b l e , t h e g r a d e d e n o t i n g t h e d e g r e e of n i t r a t i o n . F o r t h i s h a n d b o o k we c i t e , w h e r e p o s s i b l e , d a t a c h a r a c t e r i s t i c of l a c q u e r - g r a d e n i t r o c e l l u l o s e (12.0% N) and g u n c o t t o n (13.3 5% N, m i n ) . L a c q u e r - g r a d e n i t r o c e l l u l o s e i s not an e x p l o s i v e but an e n e r g y - c o n t r i b u t i n g p l a s t i c b i n d e r in P B X - 9 4 0 4 . 7/74 3 - 1

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Table 3-2. Cast explosives: n a m e s and formulations. E x p l o s i v e B a r a t o l B o r a c i t o l * C o m p B , G r a d e A^ C o m p B - 3 ^Cyclotol'^ H-6 *Octol * P e n t o l i t e d T r i t o n a l TNT 24 40 36 40 25 30 25 50 80 F o r m u l a t i o n (wt%) RDX 63 60 75 45 O t h e r i n g r e d i B a ( N 0 3 ) 2 B o r i c acid W a x W a x Al C a C l g HMX P E T N Al Lents 76 60 1 5 20 0.5 75 50 20 P r o p e r t i e s of m a t e r i a l s marked with a s t e r i s k s a r e s u m -m a r i z e d in data sheets (Section IV).

The weight percent values given in the table a r e nominal and subject to some variation.

^Comp B, Grade A is formulated as a 60/40 RDX/TNT mixture, but high-quality castings usually a r e higher in RDX content due to the removal of a T N T - r i c h section at the top of the casting.

T h e r e a r e several cyclotols and pentolites. The most common cyclotol is RDX/TNT 7 5 / 2 5 . The most common pentolite is P E T N / T N T 50/50.

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Table 3 - 3 . Plastic-bonded e x p l o s i v e s : Names and formulations. E x p l o s i v e ^ * L X - 0 4 - l * L X - 0 7 - 2 * L X - 0 9 - 0 L X - 0 9 - 1 * L X - 1 0 - 0 L X - 1 0 - 1 * L X - l l - 0 * L X - 1 4 - 0 * P B X - 9 0 0 7 - P B X - 9 0 1 0 'i't-BX-gOll * P B X - 9 2 0 5 * P B X - 9 4 0 4 - P B X - 9 4 0 7 * P B X - 9 501 O t h e r d e s i g n a t i o n s P B H V - 8 5 / j R X - 0 4 - B A R X - 0 9 - C B R X - 0 4 - D E R X - 0 4 - P I P B X - 9 0 0 7 X - 0 0 0 8 P B X 9 4 0 4 -15 T y p e B -03 F o r m u l a t i o n I n g r e d i e n t HMX V i t o n A HMX V i t o n A HMX p D N P A F E F O HMX p D N P A F E F O HMX V i t o n A HMX V i t o n A HMX V i t o n A HMX E s t a n e 5 7 0 2 - F l RDX P o l y s t y r e n e D i ( 2 e t h y l h e x y l ) -p h t h a l a t e R o s i n RDX K e l - F HMX E s t a n e 5 7 4 0 - X 2 RDX P q l y s t y r e n e D i ( 2 e t h y l h e x y l ) -p h t h a l a t e HMX NC (12.0% N) T r i s ( i 3 c h l o r o e t h y l ) -p h o s -p h a t e R D X E x o n 4 6 1 HMX E s t a n e BDNPA B D N P F wt% 85 15 90 10 93 4.6 2.4 93.3 4.4 2.3 95 5 9 4 . 5 4 . 5 80 20 95.5 4 . 5 90 9.1 0.5 0.4 90 10 90 92 6 2 94 3 3 94 6 95 2.5 1.25 1.25 C o l o r Yellow O r a n g e P u r p l e P u r p l e B l u e - g r e e n s p o t s on w h i t e B l u e - g r e e n s p o t s on white W h i t e V i o l e t s p o t s on white W h i t e o r m o t t l e d g r a y ° W h i t e Off-white W h i t e W h i t e o r b l u e W h i t e o r black*^ W h i t e P r o p e r t i e s of m a t e r i a l s marked with (Section IV).

Depending on graphite content.

a s t e r i s k s a r e s u m m a r i z e d in data sheets

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T a b l e 3 - 4 . M i s c e l l a n e o u s e x p l o s i v e s : N a m e s and f o r m t i l a t i o n s . F o r m u l a t i o n E x p l o s i v e ^ O t h e r d e s i g n a t i o n s I n g r e d i e n t RDX D i ( 2 e t h y l h e x y l ) -s e b a c a t e P o l y i s o b u t y l e n e M o t o r oil P E T N B i n d e r P E T N B i n d e r N i t r o m e t h a n e T e t r a n i t r o m e t h a n e 1 - N i t r o p r o p a n e P E T N B u t y l r u b b e r A c e t y l t r i b u t y l c i t r a t e C a b - O - S i l P E T N S i l i c o n e r u b b e r C a b - O - S i l P E T N S i l i c o n e r u b b e r N i t r o m e t h a n e M e t h a n o l E t h y l e n e d i a m i n e P E T N S i l i c o n e r u b b e r wt% 91 5.3 2.1 1.6 85 15 63 37 51.7 33.2 15.1 73,5 17.6 6.9 2.0 63.7 34.3 2.0 80 20 72.2 23.4 4.4 80 20 C o l o r W h i t e Red Red C l e a r Buff B l u e G r e e n C l e a r W h i t e C o m p C - 4 E L - 5 0 6 A E L - 5 0 6 C * L X - 0 1 * L X - 0 2 - l * L X - 0 8 L X - 1 3 M E N - I I * X T X - 8 0 0 3 N T N E L - 5 0 6 L - 3 R X - O l - A C E x t e x P r o p e r t i e s ( S e c t i o n IV). of m a t e r i a l s m a r k e d w i t h a s t e r i s k s a r e s u m m a r i z e d in d a t a s h e e t s

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Table 3 - 5 . Additives and b i n d e r s .

Material" Chemical name Other designation Color BDNPA/BDNPF Cab-O-Sil M-5 DOP Estane 5702-Fl Exon 461 Kel-F 800 Kel-F 3700 Polystyrene Sylgard 182 TEF Viton A Bis(2,2-dinitropropyl) acetal/

bis(2,2-dinitroprDpyl) formal 50/50 w/o Di(2-ethylhexyl)-phthalate

Trifluorochloroethylene/ vinylidine chloride copolymer Poly (trifluorochloroethylene) Poly (trifluorochloroethylene) Tris-|8-chloroethylphosphate Hexafluoropropylene/ vinylidine fluoride 1:2 dioctylphthalate polyurethane solution system Silicone resin Straw White Clear Light amber White Off-white Off-white Clear Light straw Clear White Properties of these materials are summarized in data sheets (Section IV).

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4. PHYSICAL PROPERTIES

This section contains information relating to selected physical constants and p r o p e r t i e s of HEs of i n t e r e s t . These p r o p e r t i e s a r e physical state and density

(Table 4-1); moleciilar weight MW and atomic composition (Table 4-2); melting point m. p . , boiling point b . p . , and vapor p r e s s u r e v . p . (Table 43 and Fig. 41); c r y s t a l -lographic ajid optical p r o p e r t i e s (Table 4-4).

Many p r o p e r t i e s a r e density-dependent. F o r calculations for m i x t u r e s , some useful auxiliary relationships between composition and density a r e a s follows:

y mi y (v^Pi)

p (TMD) = - ^ - ^•^—

I (-i/Pi) I V,

V. = W ipjp.) v^ 100 m . / p . ^ V. ^ (mi/Pi) ' W. = 100 ViPi 100 m.

' I^Vi^ S-i

Void V. = 1 - ( P Q / T M D ) ,

where TMD is theoretical maximum density, m is m a s s , v is volume, W is weight percent, V is volume percent, p is theoretical density, subscript i designates the component, and p„ is the actual density of the m i x t u r e .

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P h y s i c a l S t a t e and D e n s i t y T a b l e 4 - 1 . P h y s i c a l S t a t e s and d e n s i t i e s . M a t e r i a l T M D ^ , P P h y s i c a l s t a t e (g/cm^ (Mg/m^)) N o m i n a l d e n s i t y , p (g/cm^ (Mg/m^)) A F N O L B a r a t o l B D N P A / B D N P F ^ B o r a c i t o l B T F C a b - O - S i l ^ C o m p B , G r a d e A C o m p B - 3 C o m p C - 4 C y c l o t o l 7 5/25 D A T B DIPAM^ DNPA D O P E D N P E L - 5 0 6 A E L - 5 0 6 C E s t a n e ^ E x o n 4 6 1 ^ F E F O H - 6 HMX H N A B - I ^ HNAB-11^ HNAB-III^ H N S ^ ' ^ K e l - F 8 0 0 ^ ° K e l - F 3 7 0 0 ^ ° L X - 0 1 L X - 0 2 L X - 0 4 L X - 0 7 L X - 0 8 L X - 0 9 L X - 1 0 - 0 L i q u i d Solid L i q u i d Solid Solid Solid Solid Solid P u t t y l i k e solid Solid Solid Solid Solid L i q u i d L i q u i d Solid Solid R u b b e r y s o l i d Solid L i q u i d Solid Solid Solid Solid Solid Solid Solid Solid L i q u i d P u t t y l i k e s o l i d Solid Solid P u t t y l i k e s o l i d Solid Solid 1.48 2 . 6 3 1 . 3 8 3 - 1 . 3 9 7 ^b 1.901 2.3 1.74 1.75 1.77 1.837 1.79 1.47 0-.9861 1.28 1.607 1.900 1.795 c a l c . 1.799 o b s . 1.744 c a l c . 1.750 o b s . 1.718 o b s . 1.74 1.23 1.44 1.889 1.892 1.439 1.867 1.896 1.48 2 . 6 0 - 2 . 6 1 1 . 5 3 - 1 . 5 4 1.87 2.2 1.71 1.72 1.59 1 . 7 5 - 1 . 7 6 1.79 1.48 1.48 1.18 1.70 1.74 ( c a s t ) 1.89 1 2 1 1 1 1 .72 .02 .85 .43-1 .860->1.42 1 1 .837- .858-..44 •1,870 •1.870 •1.845 -1.868

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Table 4 - 1 . (continued) T M D ^ p Material Physical state (g/cm^ (Mg/m^))

Nominal density, p (g/cm^ (Mg/m^)) LX-10-1 LX-11 LX-13 LX-14 MEN-II NC (12.0% N) NC (13.3 5% N, min) NG N M NQ Octol PBX-9007 PBX-9010 PBX-9011 PBX-9205 PBX-9404 PBX-9407 PBX-9501^ Pentolite 50/50 PETN 12 Polystyrene RDX^^ Sylgard 182^^ TACOT TATB TEF Tetryl TNM Solid Solid Putty curable to rubbery solid Solid Liquid Solid Solid Liquid Liquid Solid Solid Solid Solid Solid Solid Solid Solid Solid Solid Solid Solid Solid Liquid Solid Solid Liquid Solid Liquid TNT Solid 15 Viton A' XTX-8003 Putty curable to rubbery solid 1.895 1.558 1.849 (286 K) 1.654 Rubbery solid 1,556 1.870 1.87-1.876 =1.53 1.834 1 . U i 1 1.59 1.13 at 20°C (293 K) 1.72 1.83 1.697 1.822 1.795 1.72 1.865 1.81 1.855 1.71 1.77 1.12 1.806 1.05 1.85 1.938 1.425 1.73 1.6.'S0 at 13°C 1.58 1.58 1.55 1.80-1.82 1.66 1.789 1.770 1.68 1.831-1.844 1.60-1.62^ 1.843 1.67 1.76 1.05 1.61 1.88 1,71 Cast: 1.5-1.6 P r e s s e d : 1.63-1.64 1.815 =^1.53 Theoretical maximum density.

A TMD value based on boric acid and TNT is 1.52; during the vacuum casting at over 80°C (3 53 K), however, some of the boric acid b r e a k s down to B2O2

of increasing the TMD by an unpredictable amount.

Nominal density in detonator and booster applications.

This has the effect

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M o l e c u l a r W e i g h t and A t o m i c C o m p o s i t i o n T a b l e 4 - 2 . M o l e c u l a r w e i g h t s and a t o m i c c o m p o s i t i o n s . F o r m a t e r i a l s t h a t a r e p u r e c h e m i c a l c o m p o u n d s , m o l e c u l a r w e i g h t s and m o l e c u l a r f o r m u l a s a r e g i v e n : f o r t h o s e t h a t a r e m i x t u r e s , an a r b i t r a r y m o l e c u l a r w e i g h t of 100 i s a s s i g n e d , and a n e m p i r i c a l f o r m u l a c o r r e s p o n d i n g to t h i s w e i g h t i s g i v e n . F o r such m i x t u r e s , the w e i g h t p e r c e n t a g e of an e l e m e n t i s g i v e n by t h e p r o d u c t of t h e a t o m i c w e i g h t and i t s s u b s c r i p t in t h e e m p i r i c a l f o r m u l a . E x p l o s i v e B a r a t o l B D N P A / B D N P F B o r a c i t o l B T F C a b - O - S i l C o m p B , G r a d e A^ C o m p B-S*^ C o m p C-4 C y c l o t o l 7 5 / 2 5 D A T B D I P A M DNPA D O P E D N P E L - 5 0 6 A E L - 5 0 6 C E s t a n e 5 7 0 2 F - 1 F E F O E x o n 461 H - 6 HMX HNAB HNS K e l - F 3700 L X - 0 1 - 0 L X - 0 2 - 1 L X - 0 4 - 1 L X - 0 7 - 2 L X - 0 8 - 0 L X - 0 9 - 0 L X - 0 9 - 1 MW 100 100 100 2 5 2 . 1 60.09 100 100 100 100 2 4 3 . 1 4 54.1 2 0 4 . 1 390.57 220.2 100 100 100 3 2 0 . 1 (213.43)^^ 100 296.2 4 5 2 . 2 1 4 5 0 . 3 (116.48)^^ 100 100 100 100 100 100 100

c

0.74 1.23 6 2.03 2 . 0 5 1.82 1.78 6 12 6 24 7 2.41 3.25 5.137 5 4 1.890 4 12 14 2 1.52 2.77 1.55 1.48 1.93 1.43 1.425 E l H 0.53 3.79 0 2.64 2.51 3.54 2.58 5 6 8 38 12 4.29 5.94 7,500 6 2 2.590 8 4 6 3.73 4.86 2.58 2.62 4.39 2.74 2.735 e m e n t a l N 0.90 0.53 6 2.18 2 . 1 5 2.46 2.36 5 8 2 2 1.08 0.87 0.187 4 1.612 8 8 6 1.69 0.93 2.30 2.43 0.81 2.59 2.592 c o m p o s i t i o n O 2.38 3.97 6 2,67 2.67 2.51 2.69 6 12 6 4 6 3.27 2.68 1.7 58 10 2.009 8 12 12 3.39 2.99 2.30 2.43 2 . 9 5 2.72 2.721 O t h e r B a 0.29 B 0.97 F 2 CI 3 F 3 Ca 0.0045 CI 0.0090 Al 0 . 7 4 1 CI 1 F 3 Si 0.03 F 0.52 F 0.35 Si 0.50 F 0.02 F 0,0144

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Table 4 - 2 . (continued) E x p l o s i v e L X - 1 0 - 0 L X - 1 0 - 1 L X - 1 1 - 0 L X - 1 3 S e e X T X - 8 0 0 3 L X - 1 4 M E N - I I NC (12.0% N) NC (13.35% N, m i n ) NG NM NQ Octol P B X - 9 0 0 7 P B X - 9 0 1 0 P B X - 9 0 1 1 P B X - 9 2 0 5 P B X - 9 4 0 4 P B X - 9 4 0 7 P B X - 9 5 0 1 P e n t o l i t e 5 0 / 5 0 P E T N P o l y s t y r e n e RDX S y l g a r d 182 T A C O T T A T B T E F T e t r y l TNM T N T Viton A X T X - 8 0 0 3 MW 100 100 100 100 100 262.6 274.1 227.1 61.0 104.1 100 100 100 100 100 100 100 100 100 316.2 (104.15)^ 222,1 ( 74.16)„ 388,2 258.2 2 8 5 , 5 287.0 196.0 227.1 (187.08)j^ 100 C 1.42 1.410 1.61 1.521 2.06 6 6 3 1 1 1,78 1.97 1.39 1.73 1.83 1.40 1.41 1.47 2.33 5 8 3 2 12 6 6 7 1 7 5 1.80 E l H 2.66 2,663 2,53 2.917 7,06 7 7 5 3 4 2.58 3.22 2.43 3.18 3.14 2 . 7 5 2.66 2,86 2,37 8 8 6 6 4 6 12 5 0 5 3,5 3.64 e m e n t a l N 2.57 2.579 2.16 2.587 1.33 2.25 2.5 3 1 4 2.36 2.43 2.43 2.45 2.49 2.57 2,54 2.60 1.29 4 6 8 6 5 4 3 1.01 c o m p o s i t i o n O 2.57 2.579 2.16 2.658 3,10 9.5 10 9 2 2 2.69 2.44 2.43 2.61 2.51 2.69 2,54 2,69 3,22 12 6 1 8 6 4 8 8 6 3.31 O t h e r F 0.17 F 0.156 F 0.70 CI 0.09 F 0.26 CI 0.03 P 0 , 0 1 CI 0,07 F 0.09 Si 1 CI 3 P 1 F 6.5 Si 0.27 Based on nominal composition of 63% RDX, 36% TNT, and 1% wax. The wax was a s s u m e d to have the composition CH2,

Based on nominal composition of BDX/TNT 60/40.

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Table 4 - 3 . Melting points m^p., boiling points b. p,, and vapor p r e s s u r e s v, p. b p . M a t e r i a l A F N O L B a r a t o l B D N P A / B D N P F B o r a c i t o l B T F C o m p B , G r a d e A C o m p B - 3 C o m p C - 4 C y c l o t o l 7 5 / 2 5 D A T B D I P A M D N P A D O P E D N P Ref. 16 4 18 (°C) 1 0 5 - 1 1 0 7 9 - 8 0 7 9 - 8 0 1 9 8 - 2 0 0 - 8 0 7 9 - 8 0 --7 9 - 8 0 286 304 --- 6 (K) ( 3 7 8 - 3 8 3 ) ( 3 5 2 - 3 5 3 ) ( 3 5 2 - 3 5 3 ) ( 4 7 1 - 4 7 3 ) (~3 53) ( 3 5 2 - 3 5 3 ) b ( 3 5 2 - 3 5 3 ) (559) (377) (268) F e f 2 17 18 C O ( - 1 5 0 a t (0 01 m m 2 2 2 - 2 3 0 83 a t 0 OD m m (K) --(423 a t 1 33 P a ) --( 4 ' ) 5 - 5 0 3 ) (356 a t 6 7 P a ) E L - 5 0 6 A E L - 5 0 6 C F E F O Ref ( m m Hg) 0 1 a t 100°C 1 1 . 3 - 1 2 9 ( 2 8 4 - 2 8 6 ) 1 2 0 - 1 2 4 a t 0 3 m m (3'iJ-3<)7 a t 40 P a ) 0 1 a t 100»C 0 1 a t 100°C <0 06 a t 150°C 1 2 a t 200-'C 2 14 X 10 at 2 J ° C (13 33 a t 373 h ) (13 33 a t 3 7 3 K) (13 33 at 373 K) (<8 0 a t 423 K) (159 9 a t 473 K) (2 85 X 10 a t 298 K) HMX H N A B L X L X -L X L X L X L X L X L X L X L X 0 1 - 0 02 04 07 08 - 0 9 -10 -11 -13 -14 M E N 11 NC (12 0% NC (13.3570 S e e X T N) N, m i n ) 20 9 19 19 2 8 5 - 2 8 7 2 1 0 - 2 1 6 3 1 6 1. 313 11 318 ( 5 5 8 - a 6 0 ) ( 4 8 8 - 4 8 9 ) (589) (586) (591) (219) (>523) (•>523) D e c > 2 5 0 D e c > 2 5 0 1 2 9 - 1 3 5 ( 4 0 2 - 4 0 8 ) w i t h d e c o m p o s i t i o n D e c > 2 8 0 ^ 5 5 3 ) D e c > 2 5 0 {>523) D e c '•250 (>523) D e c > 2 7 0 (>543) D e c 1 3 5 (408) D e c 135 (408) ^10 m m - 9 3 X 1 0 a t 100°C 1 X 1 0 " ^ a t 100°C ^10 n i m II 1 X 10"-^ a t lOO-C 29 0 a t 25°C 'T7KT (4 X 1 0 " ' ' a t 373 K) (1 33 X lO" a t 373 K) 9347 ' ' TTKT (1 33 X 1 0 " ' ' a t 373 k ) (3866 a t 298 K)

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;

Table 4 - 3 . (continued)

m . p . b.p. V P

Material Ref. (°C) (K) Ref. (°C) (K) Ref. (mm Hg) (Pa)

See XTX-8003 LX-09 LX-10 LX-11 LX-13 LX-14 MEN II NC (12.0% N) NC (13.35% N, min) NG NM N(3 Octal PBX-9007 PBX-9010 PBX-9011 PBX-9205 PBX-9404 PBX-9407 PBX-9501 Pentolite 50/50 PETN Dec.>280 Dec.>250 Dee.>250 Dec.>270 Dec. 135 Dec. 135 13.2 - 2 9 246-247 with decom 79-80 Dec.>200 Dec.>200 Dec.^250 Dec.>200 Dec.>250 Dec.>200 Dec.>240 7 6 139-142 0 5 5 3 ) (>523) (^523) (^543) (408) (408) (286) (244) (519-520) ;position (352-353) (--473) (-473) (-'523) 0 4 7 3 ) ( 523) (-•473) (-513) (349) (412-415) P o l y s t y r e n e R D X TACOT TATB T E F T e t r y l T N M T N T 12 13 24 2 5 2 6 2 4 0 2 0 5 Dec >3B0 Dec.>325 2 0 3 130 14 2 80.9 (513) (478) (-653) ( 598) (476) (403) (287) (3 54) 101-101.5 (374-375) 8 i3 125.7 ( o 9 ' ) ) 0.0015 at 20°C 37 at 25°C 0.1 at 100°C (0.2 at 293 K) (49J3 at 298 K) (13.33 at 373 K) 0.1 at 100 t 8 X 10"^ at 100°C (13 33 at J 7 i h) ( 1 1 X 1 0 at 373 K) , . ^^ 6352 10 mm r (K) 3850 '"^10 ' cm ' " " ' 1 (K) from 111-130 C (384-403 K) 13 at 25°C 0 106 at 100°C (1733 at 298 K) (14 13 at 373 K) 3850 '^lO r m 1 (K) from 200-350 C (473-623 K) X T X - 8 0 0 3 1 mm Hg = 1.33323 X 10^ Pa No fixed melting point.

'^Two types of HNS a r e in production: HNS-I, <10 /j p a r t i c l e s i z e , and HNS-I], 100-300 ji p a r t i c l e size D e c : d e c o m p o s e s .

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> — ^ — — Extrapolation (3.4) (3.2) (3,0) (2.8) (2,6) (2,4) (2.2) (2,0) Temperature — 1000/T°K J L J L 30 49 71 97 127 161 203 Temperature — ° C

Fig, 4 - 1 , Vapor p r e s s u r e of F E F O , ^ ^ PETN,^^ RDX,^^ DATB-I,^^ /3-HMX,^^ TATB,^^ HNS.29 Conversion factor: 1 T o r r = 1.333 X 10^ P a .

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Crystallographic and Optical Properties

Table 4-4. Crystallographic and optical properties.'

Material BDNPA/BDNPF^ BTF29.30 Cab-O-Sil^ DATB^® DOP^^ HNAB^ HNs" K e l - F 800^° N Q 2 1 P E T N 3 6 - 4 0 12 Polystyrene j , O x " . 4 0 , 4 1 , 4 2 Sylgard 182^'* TATB'*^"^'* Tetryl'*^ TNT46-50 ^Refractive indexes 10 A = 1 nm. Polymorph I II (a) I (3) HI (y) IV (6) I II I (ff) (p = 1.778) II (|3) (p = 1.716) I II and molecular Unit cell dimension (A (10"1 nm)) a = 9.92 b = 19.52 c = 6.52 a = 7.30 b = 5.20 c = 11.63 a = 15.14 b = 23.89 c = 5.91 a = 6.54 b = 11.05 c = 8.70 a = 10.95 b = 7.93 c - 14.61 a - 7.66 b = c - 32.49 a = 10.15 b = 8.26 c - 10.06 a - 10.63 b - 21.87 c - 7.59 a = 20.93 b - 5.57 c - 14.67 a - 17.58 b - 24.84 c - 3.58 a 9.38 b = 9.38 c = 6.71 a = 13.22 b - 13.49 c = 6.83 a - 21.90 b = 21.90 c - 6.63 a = 13.18 b = 11.57 c = 10.71 Unstable a = 9.01 b - 9.03 c - 6.81 a = 14.13 b = 7.37 c = 10.61 a = 14.99 b = 40.00 c = 6.10 refractions a r e at Crystal s t r u c t u r e Orthorhomic Amorphous Orthorhombic Monoclinic Monoclinic Hexagonal Orthorhombic Orthorhombic Tetragonal Orthorhombic Rhombohedral Orthorhombic T n c l i n i c Monoclinic Space group Pna2j P c 2 Fdd2 P2j/c P c , P 2 / c , P2/n P6i22, P6522 P 2 , / c P2j/a Fdd2 P42j/c Pcnb Pbca P T P2^/c Refractive index n 1.462-1.464 at 25°C (298 K) 1.46 1.485 at 25°C (298 K) a - 1.561-1.565 (3 = 1.562-1.566 T = 1.72-1.74 a - 1.589 3 = 1.594 y = 1.73 a = 1.537 (3 = 1.585 T - 1.666 1.46 n = 16 a = 1.526 /3 = 1.694 7 = 1.81 u = 1.558 in Na e = 1.551 light 1.59-1.60 n = 8 ^ a = 1.578 I at 20°C /3 = 1.597 ["(283 K) 7 = I.6O2J 1.430 at 25°C (298 K) a = 1.45 3 = 2.3 7 = 3.1 a = 1.546 0 = 1.632 7 =1.74 c a l c . n = 16 a = 1.543 |3 = 1.674 7 = 1.717

5893 A and 25°C (589.3 nm and 298 K).unless otherwise

Molecular refraction H 58 calc. 55.7 obs. 58 calc. 56.1 obs. 58 calc. 55.4 obs. 58 calc. 55.9 obs. 25.2 calc. 22.2 obs. 43.7 calc. 41.4 obs. 44.3 calc. 49.6 obs. stated; 7/74 4 - 9

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References

1. H. Hornig, Lawrence L i v e r m o r e Laboratory, personal communication (1972). 2. M. Finger, P r o p e r t i e s of Bis(2,2-dinitropropyl)acetal and Bis(2,2,-dinitropropyl)

formal, Eutectic Mixture, Lawrence L i v e r m o r e Laboratory, Rep.t. UCID-16088 (1972).

3. Cabot Corporation, Boston, Mass., Cab-O-Sil, Rept. Cgen-7 (no date). 4. E. E. Kilmer, J. Spacecr. Rockets 5, 1216-1219 (1968).

5. B. F . Goodrich Company, Cleveland, Ohio, Estane Polyurethane M a t e r i a l s , Service Bulletin 64-14; Estane Polyurethane Solution Systems, Service Bulletin TSR 64-18 (1964).

6. F i r e s t o n e P l a s t i c s Company, Pottstown, P e n n . , Exon, Sales Service Bulletin No. 20 (1956).

7. E. J. Graeber, Sandia L a b o r a t o r i e s , Albuquerque, N. Mex., personal communica-tion (1972).

8. A. C. Schwartz, Application of Hexanitrostilbene (HNS) in Explosive Components, Sandia L a b o r a t o r i e s , Albuquerque, N. Mex., Rept. SC-RR-710673 (1972).

9. K. G. Shipp, J . Org. Chem. 2£, 2620-2623 (1964).

10. Minnesota Mining and Manufacturing Company, St. Paul, Minn., K e l - F E l a s t o m e r — P r o p e r t i e s and Applications (no date).

11. J. R. Humphrey, L X - 1 0 - 1 : A High-Energy Plastic-Bonded Explosive, Lawrence L i v e r m o r e Laboratory, Rept. UCRL-51629 (1974).

12. J . Brandrup and E. H. Immergut, Eds., P o l y m e r Handbook, Interscience, N. Y. (1966).

13. C. S, Choi and E. P r i n c e , Acta C r y s t . B28, 2857-2862 (1972).

14. Dow Corning, Hemlock, Mich., Information about Electronic Materials, Bulletin 07-123 (1964).

15. S. Dixon, D. R. Rexford, and J. S. Rugg, Ind. Eng. Chem. 49^, 1687-1690 (1957). 16. J . R. Holden, Acta Cryst.. 22, 545-550 (1966).

17. Food Machinery Corporation, Ohio Apex Division, Nitro, W. Va., P l a s t i c i z e r s , Data Sheet (1955).

18. M. Finger, Lawrence L i v e r m o r e L a b o r a t o r y , personal communication (1972). 19. K. G. Shipp, U . S . Naval Ordnance Laboratory, White Oak, Md., personal

communication (1965).

20. G. P . Sharnin, B . J. Buzykin, and K. Kh. Shakurova, J. Org. Chem. (USSR) Q,, 1039-1041 (1970).

21. W. C. McCrone, Anal. Chem. 23^, 205-206 (1951).

22. T. M. Benziger, X-0242: A High-Energy Plastic-Bonded Explosive, Los Alamos Scientific Laboratory, N. Mex., Rept. LA-4872-MS (1972).

23. F . T. C r i m m i n s , The Vapor P r e s s u r e of P e n t a e r y t h r i t o l t e t r a n i t r a t e (PETN) in the T e m p e r a t u r e Range of 50 to 98 D e g r e e s Centigrade, Lawrence L i v e r m o r e

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24. E. I. Dupont de Nemours and Company, Technical Information on Military Specialties--TACOT (manufacturer's data sheet), E. I. DuPont de Nemours and Company, Inc., Wilmington, Del. (no date).

25. L. C. Smith, Los Alamos Scientific L a b o r a t o r y , N. Mex., personal communica-tion (1962).

26. Celanese Corporation, Chemical Division, New York, N. Y., Celluflex CEF, Products Bulletin N-46-2 (1955).

27. F . T. C r i m m i n s , Lawrence L i v e r m o r e L a b o r a t o r y , personal communication (1969).

28. J, M. Rosen and C. Dickenson, J . Chem. Eng, Data 14, 120-124 (1969).

29. H. H. Cady, A. C. Larson, and D, T. C r o m e r , Acta Cryst. 20, 336-341 (1966), 30. E. N. Maslen, Acta Cryst. B24, 1170-1172 (1968).

3 1 . H. H. Cady, A. C. Larson, and D. T. C r o m e r , Acta Cryst, 16, 617-623 (1963). 32. W. C. McCrone, Anal. Chem. 22, 1225-1226 (1950).

3 3 . A, Filhol, Contribution to the Study of the Hexogen Molecule in the Crystalline and the F r e e State, Thesis.Universite de Bordeaux, F r a n c e (1971). (In F r e n c h ) . 34. C. S, Choi and H, P. Boutin, Acta C r y s t . B26, 1235-2340 (1970).

35. W. Selig, Explosivestoffe 17, 201-202 (1969). 36. J. E. Knoggs, Mineral, Mag, 20, 346-352 (1925),

37. A. D. Booth and F . J. Llewellyn, J . Chem. Soc. (London) 1947, 837-846 (1947). 38. J . T r o t t e r , Acta Cryst. 16^, 698-699 (1963).

39. H. H. Cady, Los Alamos Scientific L a b o r a t o r y , N. Mex., personal communica-tion (1972).

40. A. T. Bloomquist, Microscopic Examination of High Explosives and B o o s t e r s , Office of Scientific Research and Development, Rept. NDRC-B-3014 (AD-29944) (1957).

4 1 . W. C. McCrone, Anal, Chem. 22, 954-955 (1950).

42. P, M. H a r r i s , P . Reed, and R. E . Gluyas, S t r u c t u r e s of T r i n i t r o Aromatic C ry s ta ls and Related Substances, U . S . Dept, of Commerce, Rept. 156-104 (1959).

4 3 . H, H. Cady, Microscope 14, 27 (1963).

44. H. H. Cady and A, C, Larson, Acta C r y s t , 1£, 485-496 (1965). 45. H. H. Cady, Acta C r y s t . 23^, 601-609 (1967),

46. W, C, McCrone, Anal. Chem. 21^, 1583-1584 (1949).

47. F , G, J, May, B. W. Thorpe, and W. Connick, J . C r y s t . Growth 5, 312 (1969). 48. W. Connick, F . G. J. May, and B . W, Thorpe, A u s t r , J. Chem, 22, 2685-2688

(1969).

49. D. G. Grabar, F . C. Rauch, and A. J . Fanelli, J . P h y s, Chem. 73, 3514-3516 (1969).

50. L. A, Burkhardt and J . H, Bryden, Acta C r y s t , 7_, 135-136 (1954).

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5. CHEMICAL PROPERTIES

This section gives information on heat of formation AH heat of detonation AH , compatibility, and solubility.

Heat of F o r m a t i o n

Heat of formation AH^, r e f e r s to the enthalpy of the r e a c t i o n a C, V + ^ H„, . + ^ N„- ^ + 4 0 „ , ^ + • • • - * C H. N O , (s) 2 2(g) 2 2(g) 2 2(g) a 13 c d

at 1 atm (101 kPa) and 298°C (571 K). The sign convention is such that the AH„ is neg-ative when the above reaction is exothermic. Tables 5-1 and 5-2 give heats of formation of various explosive m a t e r i a l s and of additives and b i n d e r s , r e s p e c t i v e l y .

Table 5 - 1 . Heats of formation, AH„, of explosives.

E x p l o s i v e B a r a t o l B o r a c i t o l B T F C o m p B , G r a d e A° C o m p B - 3 ° C o m p C - 4 ° C y c l o t o l 7 5 / 2 5 D A T B D I P A M D K P A E D N P E L - 5 0 6 A E L - 5 0 6 C F E F O H M X H N A B HNS L X - 0 1 - 0 I X - 0 2 - l d L X - 0 4 - 1 L X - 0 7 - 2 L X - 0 8 d L X - 0 9 - 0 L X - 0 9 - 1 L X - 1 0 - 0 L X - 1 1 - 0 L X - 1 3 L X - 1 4 M E M - 1 1 N C (12.0% N) NC ( 1 3 . 3 5 % N, n u n ) NG NM NQ O c t o l P B X - 9 0 0 7 a r B X - 9 0 1 0 ° P H X - t O l l " ^ P B X - 9 2 0 5 ' ^ P B X - 9 4 0 4 - 3 ^ P B X - 9 4 0 7 ' ^ P B X - 9 5 0 1 ' ' P e n t o l i t e 5 0 / 50 P E I N RDX T A C O T T A T B T e t r y l T M l T N T X T X - 8 0 0 3 ( k c a l / m o U ^ - 7 0 . 8 - 2 5 7 . 5 + 1 4 4 . 5 +1.0 + 0 . 8 4 + 3 . 3 3 +3.01 - 2 9 . 2 3 - 2 0 . 1 - 1 1 0 - 1 4 0 - 1 7 7 . 5 + 1 7 . 9 3 + 5 7 . 8 + 1 3 . 8 8 - 2 7 . 5 - 4 9 . 1 - 2 1 . 5 - 1 2 . 3 - 4 4 +1.82 +2.004 - 3 . 1 4 - 3 0 . 7 3 S e e X T X - 8 0 0 3 n . 5 0 - 7 4 3 - 2 1 6 - 2 0 0 - 9 0 . 8 - 2 7 0 - 2 3 . 6 +2.37 +7.13 - 7 . 8 7 - 4 . 0 5 + 5.81 +0.08 + 1 1 . 6 +2 3 - 2 4 . 3 - 1 2 8 . 7 +14.71 + 128 - 3 6 . 8 5 +4.67 + 1 3 . 0 - 1 5 - 4 4 . 4 ( k J / m o l ) ' ' ( - 2 9 5 ) ( - 1 , 0 7 6 ) (+606) ( + 5.78) ( + 5 . 2 8 ) ( + 1 3 . 9 ) ( + 1 3 . 8 ) ( - 1 2 2 ) (-84 1) ( - 4 6 0 ) ( - 5 8 5 . 8 ) ( - 1 6 7 ) ( - 1 7 8 ) ( - 7 4 2 8) ( + 7 5 . 0 2 ) ( + 2 4 1 . 8 ) (+58.1) ( - 1 1 5 . 2 ) ( - 2 0 5 . 3 ) ( - 9 0 . 1 ) ( - 5 1 . 7 ) ( - 1 8 5 . 9 ) ( • 7 . 6 1 ) (+8 38) ( - 1 3 . 1 ) ( - 1 2 8 . 6 ) (t-6.28) ( - 3 1 0 7) ( - " 0 4 ) ( - 8 3 7 ) ( - 3 8 0 ) ( - 1 1 3 ) ( - 9 8 . 7 ) ( t l l . U ) ( * 2 9 . 8 ) ( - J 2 . U ) (-17 0) ( + 2 4 . 3 0 ) (•0 3 3 1 ) ( + 4 8 . 4 ) ( + 9 j ) ( 9 9 , 4 ) ( - 3 9 3 ) ( • 6 1 . 5 3 ) ( + 5 i 6 ) ( - 1 3 4 . 2 ) ( 4 1 9 . 1 ) ( • 5 4 . 4 ) ( 6 4 . 4 ) ( - 1 8 5 . 9 ) ( c a l / g ) - 7 0 8 - 2 , 5 7 5 +573 +10.0 +8.4 +33.3 + 3 0 . 1 - 1 2 0 - 4 4 3 - 5 3 9 - 6 3 5 - 5 5 4 . 4 +61 +128 +30 83 - 2 7 5 - 4 9 1 - 2 1 5 - 1 2 3 - 4 4 4 +18.2 + 2 0 . 0 4 - 3 1 4 - 3 0 7 . 3 +15.0 - 7 4 3 823 730 - 4 0 0 - 4 4 2 - 2 2 7 +2 5,7 +71.3 - 7 8 . 7 - 4 0 . 5 +58.1 +0.8 + 116 •22 8 - 2 4 3 - 4 0 7 +66 • 3 3 0 - 1 4 3 +16 J • 66 - 7 8 - 4 4 4 (kJ/kg)"" ( - 2 , 9 5 2 ) ( - 1 0 , 7 5 5 ) ( + 2 , 3 9 9 ) ( + 5 7 . 8 ) ( + 5 2 . 8 ) (+139) (+138) ( - 5 0 3 ) ( - 1 8 5 ) ( - 2 , 2 5 5 ) ( - 2 , 6 6 0 ) ( - 1 , 6 6 9 ) ( - 1 , 7 7 5 ) ( - 2 , 3 2 0 ) (+253) ( + 5 3 5 ) ( + 1 2 9 ) ( - 1 , 1 5 2 ) ( - 2 , 0 5 3 ) ( - 9 0 1 ) ( - 5 1 7 ) ( - 1 , 8 5 9 ) ( + 7 6 . 1 ) ( + 8 3 . 8 ) ( - 1 3 1 ) ( - 1 , 2 8 6 ) ( • 6 2 8) ( - 3 , 1 0 7 ) ( - 3 , 4 4 1 ) ( - 3 , 0 5 2 ) ( - 1 , 6 7 3 ) ( - 1 , 8 5 3 ) ( - 9 4 9 ) (+119) (+298) ( - 3 2 9 ) ( - 1 7 0 ) (+243) ( + 3 . 3 1 ) (+484) ( + 9 5 . 4 ) ( - 9 9 3 7) ( - 1 , 7 0 2 ) (+277 1) ( + 1 , 3 8 0 ) ( - 5 9 7 2) (+66 6) (+277) ( - 2 8 4 ) ( - 1 , 8 5 9 ) F o r m i x t u r e s , t h e m o l e c u l a r w e i g h t i s a r b i t r a r i l y t a k p n a s 100 g ( s e e T a b l e 4 - 2 ) . "^One k c a l / m o l 4 . 1 8 4 k J m o l . ''^One c a l ' g 4 . 1 8 4 K J / k g . I h e s t a n d a r d e n t h a l p i e s of t o r m a t i o n of t h e n o n e x p l o s i v e c o m p o n e n t s oi t h e m i x t u r e s w e r e e s t i m a t e d f r o m bond e n e r g i e s . 7/74 5-1

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Table 5-2. Heats of formation, AH of additives and b i n d e r s . M a t e r i a l B D N P A / B D N P F ^ C a b - O - S i l DOP*^ E s t a n e 5702 F - 1 K e l - F 3700*^ P o l y s t y r e n e S y l g a r d 182*^ T E F V i t o n A k c a l / m o l - 4 6 . 3 8 -215194 - 2 6 8 . 2 - 9 5 - 1 6 1 .+18.9 - 2 4 . 9 - 3 0 0 - 3 3 2 . 7 ( k J / m o l ) ( - 1 9 4 . 1 ) ( - 9 0 3 , 5 ) ( - 1 , 1 2 2 ) (-397) (-674) (+79.1) ( - 1 0 4 . 1 8 ) ( - 1 , 2 5 5 ) ( - 1 , 3 9 2 ) k c a l / g - 0 . 4 6 4 - 3 . 5 9 7 - 0 . 6 8 7 - 0 . 9 5 - 1 . 3 8 2 +0.181 - 1 . 4 0 - 1 . 0 5 1 - 1 . 7 7 8 (kJ/kg) ( - 1 , 9 4 1 ) ( - 1 5 . 0 5 1 ) ( - 2 , 8 7 4 ) ( - 3 , 9 7 5 ) ( - 5 , 7 8 3 ) (+7 57) ( - 5 , 8 5 8 ) ( - 4 , 3 9 7 ) ( - 7 , 4 3 9 ) Calculation. E s t i m a t e . Heat of Detonation

Heat of detonation ^ H , . r e f e r s to the change in enthalpy for the h i g h - o r d e r detonation of the explosive. Initial and final s t a t e s a r e taken at 25°C (298 K) and 1 atm (101 kPa) p r e s s u r e . The experimental values listed in Table 53 w e r e d e t e r -mined in a detonation c a l o r i m e t e r ; they a r e found to vsiry with density, size, and confinement of the charge a s well as with c a l o r i m e t e r geometry. Therefore, applica-tion of these vailues of detonaapplica-tion energy to other situaapplica-tions r e p r e s e n t s only EUI approx-imation.

The maximum heat of detonation is a calculated value for the enthalpy of the r e a c t i o n

Explosive -• Most Stable P r o d u c t s .

The o r d e r chosen for the most stable products is HgO, COg, C, y and Ng for CHNO explosives. If the explosive contains F a n d / o r CI, then HF suid/or HCl p r e c e d e s HgO in the o r d e r . The values r e p r e s e n t the upper limit of the chemical energy obtain-able from an explosive.

In p r a c t i c e , the effective energy developed by a detonating high explosive is always s m a l l e r than the assumed thermodynamic m a x i m u m energy. The r e a s o n is that the actual shifting equilibrium along the adiabat until freeze-out o c c u r s is not the one assumed h e r e . Also, the actual entropy is higher than for 25°C (298 K) and 1 atm (101 kPa) p r e s s u r e . Such codes as RUBY, BKW, suid TIGER a r e believed to give m o r e r e a l i s t i c e s t i m a t e s of the t r u e composition during expansion.

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Table 5.3. Heats of detonation. A H fc-xper i m c n t a t AH E x p e r i m e n t a l c o n d i t i o n s 1 1 , 0 , , " 2 " ( g ) E x p l o s i v e ( k c a l / g ) ( M J A g ) ( k t a l g) (MJ kg)"" ( k i a l g ) ( V J k g ) " * ( k c a o g ) (MJ kg)*^ (°C(K)) (m ( m m ) ) (Mg/m'^) B a r a t o l B o r a c i t o l B T F ' - l , d C o m p B , G r a d e A C o m p B - s ' - ' ^ C o m p C-4 C y c l o t o l 7 5 / 2 5 DATB^ D I P A M DNPA E D N P E1-506A E L - 5 0 6 C F E F O ^ HMX^ HNAB HNS I X - 0 1 0 L X - 0 2 1^ I X-04 1 LX 07 2 I X oa"^ ' LX 09 0 L X - 0 9 - 1 LX 10 0 L X - n - 0 i,X 13 I X 14 MEN I, NC (12 0% N) NC (13 35% N, m i n ) NG W I ^ NQ Octol P B X 9007 P B X - 9 0 1 0 P B X - 9 0 1 1 P B X - 9 2 0 5 P B X - 9 4 0 4 ' P B X - 9 4 0 7 P B X 9a01 P e n t o l i t e DO OO'* P E T N * RDX^ T A C O T ' T A T B T e t r y l ' TNM'^ ' 2 I N T 0 74 0 40 1 69 1 54 1 54 1 59 1 57 1 26 1 3o 1 06 1 23 1 62 1 41 1 45 1 62 1 47 1 42 1 72 1 42 1 42 1 4 J 1 J8 1 60 1 60 1 5 D 1 38 See X T X 1 58 1 38 1 16 1 16 1 aJ 1 62 1 06 1 57 1 06 1 47 1 oJ 1 46 1 o6 1 60 1 3 ) 1 Dl 1 65 1 62 1 41 I 20 1 51 0 55 1 41 1 88 (3 10) (1 67) (7 07) (6 44) (6 44) (6 65) (6 57) (5 27) (5 65) (4 44) (5 15) (6 78) (5 90) (6 07) (6 78) (6 lo) (a 94) (7 20) (5 94) (o 94) (5 231 (8 D (6 6 )) (6 6)) (6 4 J) (5 77) -800 > (6 jli (1 7 ) (4 8 D ) (4 8o) (6 6 J ) (6 ~!ll (4 44) (6 o7) (6 j31 (6 la) (6 40) (6 11) (5 ^i) (6 6J) (6 60) (6 40) (6 0) (6 78) (a JO) (a 02) (6 32) (2 JO) (5 90) (7 8)) 0 72 0 20 1 69 1 40 1 40 1 40 1 44 1 15 1 27 0 8a 0 J4 1 38 1 12 1 3' 1 48 1 42 1 36 1 a2 1 16 1 11 1 37 1 77 1 46 1 46 1 42 1 28 1 43 1 Oa 1 02 1 02 1 48 1 36 0 88 1 43 1 3 1 36 1 i6 I 41 1 42 1 46 1 44 1 40 I al 1 48 1 35 1 08 1 45 0 55 1 2 ) 1 6 ) 3 01) 0 84) 7 07) a 86) 5 86) 5 86) 6 03) 4 8 1 ) a 3 1 ) 3 57) 3 9 3 ) 5 77) A 69) 8 2 ) 6 19) 5 94) 0 6 ) ) 6 36) 4 8 5 ) a 4 )) a 7 3 ) 7 41) 6 11) 6 11) a 94) a 36) 5 95) 4 3 1) 4 27) 4 27) 6 1 I a 6 )) i 5 8 ) a 81 a 8 2 ) a 6 ) 5 6 ) ) a 9 0 ) 5 J4) 6 11) 6 03) a 86) 6 32) 6 1 )) 5 64) 4 52) 6 07) 2 30) 5 40) 7 07) 1 4 1 (5 90) 1 4 1 (5 90) 2 D ( 2 9 8 ) 1/2 (12 7) 1 8 6 1 20 (5 02) I 12 (4 69) 2 5 ( 2 ) 8 ) 1/3 (8 47) 1 69 0 98 (4 10) 0 91 (3 81) 2 5 ( 2 ) 8 ) 1/3 (8 47) 1 8 0 1 28 1 48 1 23 1 49 1 51 0 98 1 09 1 16 (5 3 6 ) (6 1 J) (4 7 7 ) (4 3 6 ) (4 8 J ) 1 21 (5 06 25(298) 1/2 (12 7) 1 37 (5 73) 25(298) 1/2 (12 7) 1 25 (5 li) 24(297) 1/3 (8 47) 1 06 (4 44) 2a(298) 1 2 (12 7) ! 02 1 Oa (o 36) 2o(298) 1/3 (8 47) (5 15) (6 231 (6 il) (4 10) 1 16 1 37 1 42 0 96 (4 85) (a 73) (5 94) (4 02) 21(294) 25(298) 23(296) 23(296) 1 1/2 1/3 1/3 (25 4) (12 7) (8 47) (8 47) (4 27) 25(298 (4 39) 25(298 1 (25 4) 1/2 (12 7) 1/2 (12 7) 1 61 1 89 1 16 (4 8b) 25(298) 1/2 (12 7) 1 1 65 1 73 1 78 1 74 1 54 1 55 O n e c a l g 4 184 k l kg B a C O s 1 1 t h e f i r s t p r o d u i t c a l t u l a t e d " ^ B Q ^ S I S t h e f i r s t p r o d u c t c a l c u l a t e d Contain'^ l i t t l e o r no h y d r o g e n , t h e r e f o r e ^^lO., IS he f i r s t p r o d u c t c a l c u l a t e d f A v e r y ' m a l l p e r c e n t a g e of CH^ i m p u r i t y

n ) w a t e r i s f o r m e d , and v a l u e s for H j O , ^ ) and B g O , ^ a r e i d e n t i c a l

r a i s e s t h e s e v a l u e s m a r k e d l y

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Compatibility

Many m a t e r i a l s have been tested for compatibility with various HEs; those listed or mentioned in this section a r e the most comnaonly used at the L L L facility for explosive testing. In Tables 5-4 and 5-5, which l i s t adhesives and fillers, those m a t e r i a l s rated "A" have been evaluated extensively; those rated " B " have been screened for g r o s s incompatibility only. If t h e s e m a t e r i a l s a r e used a s they a r e sup-plied, that i s , in the prepackaged c a t a l y s t / r e s i n system, they a r e satisfactory for use as indicated. It is understood that the adhesives will be used in minimum amounts, mixed according to s u p p l i e r ' s instructions, and used only for limited t i m e s , that is, from two to t h r e e months during environmental testing.

The r e s u l t s of our compatibility t e s t s a r e valid only for the specific batch/lot of HE and adhesive tested. F o r different HEs and l a t e r lots of adhesive, even from the same s u p p l i e r s , the reactivity and compatibility t e s t s must be repeated. The supplier may change or " i m p r o v e " the m a t e r i a l without notice; this could r e n d e r the m a t e r i a l incompatible.

The compilation is not to be r e g a r d e d a s complete; many other m a t e r i a l s have been evaluated but a r e not commonly used and therefore not included h e r e . Table 5-6 l i s t s adhesive tapes found to be compatible with various HEs; any other tapes should be tested before u s e .

Table 5-4, Adhesives: Chemical reactivity 3Lnd compatibility with v a r i o u s high explo-s i v e explo-s .

A, compatible; OK for l o n g - t e r m s t o r a g e .

B, compatible; OK for s h o r t - t e r m storage (less than 30 days). Blank, compatibility has not been

checked.

1, bond s t r e n g t h equal to that of explosive.

2, bond strength l e s s than that of explosive. 3, no bond strength. Adhesive Adiprene L-lOO Adiprene L-167 Adiprene LD-213 Aerobond 2017 Eastman 910 Epoxies'' Laminae 4116 3-M #465 3-M #466 3-M #Y9146 / / / / / / / / / ^ / ' ^ / ^ / y * / ^ / / / / / / / / / / / c i / ' v , / 0 / 0 / 0 / / / " w / / i ? / < w / / / / / / o / o / ^ / . . 5 ^ / > / /

i i s h? u^ s M s h ^ ^ L^ h ih

A - l A - l A - l A-2 3 A - l A - l A - l A-2 3 A - l A - l A - l A - l A - l A - l A-2 A - l = A-2 A-2 A-2 A - l A - l A - l A - l A-2 A-l'^ A - l A - l A - l __a A - 2 A - l A - l A - l A - l A - 2 A - l A - l A - l A - l A - 2 A-l'^ A - 2 A - 2 A - 2 A - 2 A - 2 A - 2 A - l A - l A - 2 A - l A - l A - 2 A - l A - l A - l A - l A - 2 A - l = A - 2 A - 2 A - 2 A - l A - l A - l A - l = A - l A - l A - l A - 2 3 /

Do not use Aerobond 2017 with LX-09. The cure of the adhesive is inhibited by the explosive. BIPAX-2902, EPY-150, and Hysol epoxy patch kit a r e epoxies certified for bonding strain gauges to LX-04, LX-07, LX-09, LX-10. and PBX-9404.

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Table 5-5. F i l l e r s and coatings: Chemical reactivity and compatibility. A, # B compatible; OK for l o n g - t e r m storage. compatible; OK for s h o r t - t e r m storage (less than 30 davs). Blank, compatibility has not been

checked.

bond s t r e n g t h equal to that of explosive.

2, bond s t r e n g t h l e s s than that of explosive. 3, no bond strength. / > / '^J / C O /

i h r r

F i l l e r or coating / ^ / ^ / ^ j ^ DC 93-109^*'^ DC 93-119^^ DC 93-120*^ DC 93-122^''^ DuPont 4817 conductive silver FDA 2 Red FDA 3 Green GE RTV 632^'^ Silastic Q 93-009*^ Silastic Q 93-029*^ Silastic RTV 140*^ Silastic RTV 732^ Silastic RTV 891^^ A-3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 2 A - 2 A - 2 / • A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 2 A - 2 A - 2 / . / ^ A - 3 A - 3 A - 3 A - 3 B - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 2 A - 2 A - 2

A

/ -v

A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 2 A - 2 A - 2

L'

A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 2 A - 2 A - 2

1

B - 3 A - 3 A - 3

iilil

A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 3 A - 2 A - 2 A - 2

Nonflowing RTV silicone rubber used mostly for potting s p a c e r s , detonators, and detonator cables.

Do not attempt to use Nuocure 12, Nuocure 28, or Thermolite 12 catalysts with Silastic Q 93-109 or Q 93-029 when the m a t e r i a l will be in contact with LX-09 or other formulations containing F E F O or DNPA.

These s y s t e m s contain a platinum catalyst. Do not mix them in a container which has been used to mix the m o r e conventional RTV silicones, e . g . . Silastic Q 93-009 and Q 93-029. The catalyst in these and s i m i l a r RTV s y s t e m s poisons the platinum catalyst and thus inhibits the c u r e .

RTV: r o o m - t e m p e r a t u r e vulcanizing.

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T a b l e 5 - 6 . A d h e s i v e t a p e s found to be c o m p a t i b l e w i t h v a r i o u s high e x p l o s i v e s . Any t a p e not l i s t e d s h o u l d be t e s t e d b e f o r e u s e . M a n u f a c t u r e r T r a d e n a m e N u m b e r C o l o r 3M 3M 3M 3M 3M 3M 3M 3M 3M 3M 3M 3M 3M 3M 3M 3M 3M B e h r - M a n n i n g H a m p t o n M a n u f a c t u r i n g C o m p a n y M y s t i k T a p e , I n c . O k o n i t e Compajiy P e r m a c e l P e r m a c e l P e r m a c e l S a u n d e r s E n g i n e e r i n g C o r p o r a t i o n T e c h n i c a l T a p e C o r p o r a t i o n T e c h n i c a l T a p e C o r p o r a t i o n S c o t c h B r a n d E l e c t r i c a l T a p e S c o t c h B r a n d M y l a r S c o t c h B r a n d E l e c t r i c a l S c o t c h B r a n d M a s k i n g S c o t c h B r a n d P h o t o T a p e S c o t c h B r a n d Double Sided M a s k i n g S c o t c h B r a n d T a p e S c o t c h B r a n d D o u b l e Sided M a s k i n g S c o t c h B r a n d D o u b l e Sided M a s k i n g S c o t c h B r a n d P l a s t i c S c o t c h B r a n d P l a s t i c S c o t c h B r a n d P l a s t i c S c o t c h B r a n d C e l l o p h a n e T a p e S c o t c h B r a n d C e l l o p h a n e T a p e S c o t c h B r a n d M a g i c M e n d i n g S c o t c h F i l a m e n t T a p e S c o t c h B r a n d D o u b l e Sided M a s k i n g B e a r T a p e B l u e C r o s s T a p e M y s t i c T a p e High V o l t a g e R u b b e r T a p e P e r m a c e l P e r m a c e l P e r m a c e l C e l l o p h a n e T a p e T e f l o n T a p e T u c k T a p e T u c k T a p e #33 #56 #57 #232 #235 #400 #420 B l a c k Yellow Yellow T a n B l a c k T a n L e a d #465 T a n #466 #471 #471 #471 #600 #850 #810 #880 #Y9146 # 4 / 1 #5803 #29 #32 #S15 #S16 #S18 T a n Yellow R e d W h i t e C l e a r C l e a r C l e a r P e a r l T a n T a n Yellow B l a c k B r o w n B l a c k R e d C l e a r B l u e / b r o w n Yellow B l a c k

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- 0

Table 5-7. Qualitative solubilities of pure explosives. Solubilities a r e expressed as follows, in t e r m s of weight of lubstance dissolved at room t e m p e r a t u r e per 100 ml of solvent: i - insoluble (less than 0.1 g).

sl = slightly soluble (0.1 to 5 g), s = soluble (over 5 g).

Solvent BTF DATB DIPAM DNPA EDNP FEFO HMX HNAB° HNS' NC NG NM NQ PETN RDX T A C O T " TATB Tetryl TNM TNT

Acetone Benzene Carbon disulfide Carbon tetrachloride Chloroform DMFA DMSO Ethanol Ethyl acetate Ethyl ether Nitric acid Sulfuric acid Pyridine Water sl sl sl sl sl s s sl sl s -_ s sl 1 1 1 s s s sl S S 1 s — sl sl sl sl sl ,10 sl sl sl sl s l S 1 sl OI I - J

Table 5-8, Qualitative solubilities of additives and b i n d e r s . Solubilities a r e expressed as follows, in t e r m s of weight of substance dissolved at room t e m p e r a t u r e per 100 ml of solvent: i = insoluble (less than 0.1 g), sl = slightly soluble (0.1 to 5 g), s = soluble (over 5 g).

Solvent BDNPA/

B D N P F l l Cab-O-Sil

D O P 12 Estane

5 7 0 2 - F l l 3 Exon K e l - F ^ ^ Polystyrene^^ Sylgard TEF^^ Viton A 4 6 l l 4 182 Acetone Benzene Dichloroethane DMFA DMSO Gasoline Glycerine MEK MIBK THF Toluene Water Xylene

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References

D. L. Ornellas, Lawrence L i v e r m o r e Laboratory, personal communication (1974).

D. L. Ornellas, J . Phys. Chem. 72, 2390-2394 (1968).

H. W. Sexton, A r m a m e n t Research and Development Establishment, F o r t Halstead, United Kingdom, personal communication (1956),

D. L. Ornellas, J . C. Carpenter, and S. R. Gunn, Rev. Sci. Inst. 37^. 907-912 (1966).

A. Ya. A pin and Yu. A. Lebedev, Dokl. Akad. Nauk USSR 114, 819-821 (1957). D. O'Keefe, Sandia L a b o r a t o r i e s , Albuquerque, N. Mex., personal communica-tion (1972).

K. G. Shipp, J. Org. Chem. 29, 2620-2623 (1964).

T, Urbanski, Chemistry and Technology of Explosives (McMillan, New York, 1964-1967), vols, 1-3,

W. Selig, Some Analytical Methods for Explosives and Explosive Simulants, Lawrence L i v e r m o r e Laboratory, Rept. UCRL-7873 P t s . 1-4 (1964-1973). V. D. Gupta and B. L. Deopura, Mol. P h y s . 1_9, 589-592 (1970).

M. Finger, P r o p e r t i e s of Bis(2,2dinitropropyl)acetal and B i s ( 2 , 2

-dinitropropyDformal, Eutectic Mixture, Lawrence L i v e r m o r e Laboratory, Rept. UCID-16088 (1972).

Food Machinery and Chemical Corporation, Ohio-Apex Division, Nitro, W. V., P l a s t i c i z e r s (no date),

B. F . Goodrich Company, Cleveland, Ohio, Estane Polyurethane Solution Systems, Service Bulletin, TSR 64-18 (1964).

F i r e s t o n e P l a s t i c s Company, Pottstown, Pa., Exon, Sales Service Bulletin No. 20 (1956).

Minnesota Mining and Manufacturing Company, St. Paul, Minn., K e l - F E l a s t o m e r — P r o p e r t i e s and Applications, Service Bulletin (no date).

J . Brandrup and E. H. Immergut, Eds., P o l y m e r Handbook ( I n t e r s c i e n c e , N.Y., 1966),

Celanese Chemical Corporation, New York, N.Y., Celluflex CEF, P r o d u c t Bulletin N-46-2 (1955),

References

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