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0509922
TOWOLDMONOQ35189
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TOWOLDMONOQ35190
AROCLOR COMPOUNDS
ARE...
Fire-Retardant Inert Chemical Resistant Heat Stable "Adjustable" Properties
Adhesive Nonvolatile Thermoplastic Nonoxidizing Low Cost
FOR...
Plasticizing Impregnating Bulking Reducing Volatility Tackifying
Insulating Coating Inert Matrixes Dedusting Film Forming
The aroclor* compounds--produced by Monsanto -Chemical Company--are the only low-cost, inert, in
tercompatible liquids and solids that can be inter mixed to provide plasticizing, fire-retardant, insulat ing, lubricating liquids, with tailored viscosities from the consistency of light mineral oil to that of the most viscous syrup (or solid resin) and with the capacity to perform such a variety of functions in so many industries.
aroclor is registered in the U. S. Patent Office as
the trademark for Monsanto Ghemtcat^Company's
chlorinated aromatic hydrocarbons and their deriva
tives, including chlorinated biphenyl. When^yer in
this bulletin, for the convenience of the reader,
aroclor is used as a plural noun, the term refers, to
Monsanto's aroclor brand of chlorinated polyphenyl
compounds'.
''
The information contained 5n this bulletin it to our bett knowl
edge, true end accurate, but all recommendation* or suggestiont
ere made without guarantee, tince the condition* of ute ere
beyond our control. The Monsanto G^ermeet Company disclaim*
any liability incurred in connection with the use of theie data or
suggestions.
.
Furthermore, nothing contained herein shall be construed as a recommendation to use any product in conflict with existing patents covering any material or its use.
CONTENTS
INTRODUCTION ....................................................................................................................................... 1 DESCRIPTION ........................................................................................................................................... 2 COMPATIBILITY....................................................................................................................................... 3 AROCLOR^IN SYNTHETIC RESINS .............................................................................................. 4
Polyvinyl Chloride ...................................................................................................................... 4 Polyvinyl Acetate ....................................................................................................................... 11 Epoxies.......................................................................................................................................... 13 Polyesters...................................................................................................................................... 16 Polyethylene ................................................................................................................................ 17 Polystyrene .................................................................................................................................. 18 Polyurethanes ............................................................................................................................. 18 Phenolics ...................................................................................................................................... 19 AROCLOR^ IN RUBBERS ................................................................................................................... 20 Chlorinated Rubber and Polypropylene .............................................................................. 20 Styrene-Butadiene Copolymers ............................................................................................... 22 Synthetic and Natural Rubbers............................................................................................. 23 AROCLOR^IN CELLULOSIC RESINS ........................................................................................... 27 Ethyl Cellulose ............................................................................................................................ 27 Nitrocellulose ............................................................................................................................. 28 Cellulose Acetate-Butyrate ..................................................................................................... 31 AROCLOR\ IN PALNT, VARNISH, WAX, AND ASPHALT .................................................. 32 Paint and Varnish ..................................................................................................................... 32 Wax ............................................................................................................................................... 34
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TOWOLDMONOQ35192
Asphalt......................................................................................................................................... 35 Allyl Starch .............................................................................................................................. 35
AROCLOR^ IN MISCELLANEOUS APPLICATIONS ............................................................... 36
Dust Prevention and Dust Catching..................................................................................... 36
Vapor Suppression (Longer-lasting Insecticides) ............................................................. 36
Moisture Proofing...................................................................................................................... 36
Pigment Dispersion .......................................................
37
Sealing and Impregnation ....................................................................................................... 37
PROPERTIES OF THE AROCLOR COMPOUNDS .................................................................. 39 Solubility ............................................................ .V..................................................................... 40 Monsanto Specifications and GeneralPhysical Properties (Chart)......................... 41,42 Density ....................................................................................................................................... 43 Specific Volume ..........................................................................................................................43 Volatility ..................................................................................................................................... 44 Vapor Pressure ............................................................................................................................45 Viscosity .......................................................................................................................................46 Stability .........................................................................................................................................46 Nonflammability..........................................................................................................................47 Nondrying and Thermoplastic Properties ........................................................................ 47 Electrical Properties ............................................................................................................... 47 How to Emulsify aroclors .................................................................................................... 48
DERMATOLOGY AND TOXICOLOGY ............................................................................................49
SAFE HANDLING .................................................................................................................................. 50
SHIPPING ................................................................................................................................................. 50
0*09926
TOWOLDMONOQ35193
6___________
'L INTRODUCTION
/ The unique aroclor plasticizers are among the most versatile chemically-produced materials known to industry. One outstanding characteristic--inertness--makes aroclor^ useful in many ways for many different applications. The major benefits offered by the arocloi^ include:
Chemical Resistance Fire Retardance Compatibility with most resins Nonoxidation Adhesivity Low Cost
*
In this bulletin are described- some of their many important plasticizing and related applica tions, including numerous suggested starting formulations. Examination of their physical properties, also given in considerable detail, may suggest scores of new uses that could not be performed by any other known material.
Additional information about the aroclor compounds is available from vour nearest Monsanto
district sales office in the following technical bulletins:
-
n . The aroclor Compounds (general, including mechanical, electrical,
.' : .
heat-transfer, and other non-plasticizer applications)
' ,, ' J ' PL-307 ............ Monsanto Plasticizers in Synthetic-Resin Adhesives
j' (, j j
PL-311 ..............aroclor Plasticizers for Chlorinated Rubber
*v v j t
PL-321 ..............aroclor 1221, 1232, 1242 for Polyvinyl Acetate-Emulsion Adhesives
' /,v ; , "PL-327 ............. Monsanto Plasticizers in Protective Coatings \ / ` ^ PL-331 ..............Monsanto Modifiers for Polysulfides
^ ' CS-14 .............. aroclor Plasticizers in Epoxy Resins
1
0509927
TOWOLDMONOQ35194
Monsanto's aroclor plasticizers comprise a series of chlorinated biphenyls and chlorinated polyphenyls. They vary from mobile, oily liquids to white crystals and hard, transparent resins.
Twelve of the aroclor compounds, each of which represents a series, are discussed in this bul
letin. An understanding of the system for designation of each aroclor should prove useful in
the evaluation of the property gradations among them: the last two digits indicate the
approximate weight percentage of chlorine in the product, and the first two digits indicate
the type of material, as follows:
*
12 -- chlorinated biphenyls 25 -- blend of chlorinated biphenyls and chlorinated triphenyls (60:40) 44 -- blend of chlorinated biphenyls and chlorinated triphenyls (75:25) 54 -- chlorinated triphenyls
For nearly every aroclor mentioned, a darker, less-pure grade exists* with about the same physical and chemical characteristics, but with a lower price.
aroclor compounds are nonoxidizing, inert, permanently thermoplastic, of low volatility, non corrosive to metals, and low cost, aroclor compounds are not hydrolyzed by water and resist alkalies, acids, and corrosive chemicals. The viscous, more-highly-chlorinated liquids and resins do not support combustion, and they impart fire retardance to other materials.
The crystalline aroclor compounds are relatively insoluble, but the liquid and resinous com pounds are soluble in most of the common organic solvents, thinners, and oils. All aroclor compounds are insoluble in water and glycerine, aroclor 5460 is insoluble in lower-molecularweight alcohols: aroclor 4465 is only partly soluble in the lower alcohols.
aroclor compounds plasticize a great many resins without softening them unduly. The aroclor compounds are unsurpassed for the plasticizing of protective coatings, particularly for use in chemical plants and other facilities that require a tough, chemically resistant surface, aroclor plasticizers can also be used to flexibilize sealing compounds, adhesives, lacquers, inks, var nishes, free films, fabric coatings, and pigment dispersions. They are also used as components or extenders in elastomers and waxes. The properties of many end products can be improved -- vet at reduced overall cost-- by the use of an aroclor as either a primary or a secondary plasticizer.
The properties imparted by aroclor compounds (and their usefulness in particular applica tions) vary in regular gradient over the series. Selection of the right aroclor for a particular use can generally be made by comparison of the properties, by blending" two or more, and by adjusting the percentages used in the particular mixture in which the aroclor compounds are formulated.
Monsanto's Plasticizer Council can provide specific formulation guidance that many help you improve your product or lower your processing cost. Processors are invited to ask the nearest Monsanto office for help on special problems.
2 0509928
TOWOLDMONOQ35195
0
m COMPATIBILITY
The aroclor plasticizers are compatible with most common plastics materials; they are com patible to the.extent of practical use with the following;
Asphalt
Benzyl Cellulose
Carnauba Wax
Cellulose Acetate-Butyrate
Chlorinated Rubber
Coumarone-Indene Resins
Damar Resin
Ester Gum
Ethyl Cellulose
Epoxy Resins
Nitrocellulose
'
Paraffin
Phenolic Resins
Polyethylene Polyester Resins Polystyrene Resins Polyisobutylene Polysulfides Polyurethanes Polyvinyl Acetate Polyvinyl Butyral Polyvinyl Chloride Polyvinylidene Chloride Rosin Rubber Stvrene-Butadiene Copolymers
aroclor compounds are not compatible with phenolic resins in the final stage of condensation or with cellulose acetate.
aroclor compounds generally impart progressively increasing properties in the direction of the arrows in the following diagram:
Liquid aroclor^
Soft, Resinous AROCLOR^
Hard, Resinous AROCLOR^
Hardness
Flame Flexibility Retardance Volatility Density
Viscosity
Usually the desired balance between flexibility and hardness can be obtained either by selec tion of an aroclor with the appropriate physical characteristics or by use of a blend of two or more aroclor compounds.
In evaluation of formulations that contain aroclor plasticizers, the compounder should thor oughly test an experimental product for compatibility, heat and light stability, and other properties, according to normal industry practices.
3
0509929
TOWOLDMONOQ35196
6 ___________________ _
L AROCLOR PLASTICIZERS IN SYNTHETIC RESINS
a
Low-cost aroclor plasticizers are valuable for a variety of applications, aroclor plasticizers improve chemical resistance, flame retardance, and oxidation resistance. Depending upon the use, the various aroclor compounds offer a number of benefits to the user. In almost all formulations, the use of an aroclor plasticizer reduces the over-all cost per pound.
IN POLYVINYL CHLORIDE
The aroclor compounds are valuable in polyvinyl chloride and copolymers as secondary plasticizers or as plasticizer extenders. The aroclor plasticizers impart flame retardance and chemical resistance. Selection of the proper aroclor enables compounders to impart such special properties to their formulations as:
Resistance to migration to nitrocellulose lacquers (aroclor 1260 and 1262).
Fine, uniform cell structure in vinyl foam (aroclor 1262 and 1268). Adhesion in vinyl coatings (aroclor 1260 and 5460).
Viscosity stability in plastisols (aroclor 1248 and 1254).
The control specimen burns rapidly; the one containing Aroclor does not even ignite. 4
0509930
TOWOLDMONOQ35197
Compatibility
aroclor compounds (except aroclor 126$) are compatible to about 25 per cent of the total plasticizer content in polyvinyl chloride and usually somewhat greater in copolymer resins. At these levels, no exudation occurs in the loop-compatibility test, one of the most severe used by the industry.
Performance
As an illustration of the performance of aroclor plasticizers, Table I shows evaluation of the five most commonly used in polyvinyl chloride.
TABLE I -- PERFORMANCE EVALUATION OF FIVE AROCLOR PLASTICIZERS IN POLYVINYL CHLORIDE
Hard Concen- * ness
trafion (Shore ROCLOR (parts) "A")
1248 1254 1260 4465 5442
15 87 15 88 15 89 17.5 89 17.5 87
Vola-* tility (Plasti cizer lost, %)
Kerosene c Extraction (Plasticizer lost. %)
Low-Temp Flexibility
(Clash & Berg) (T,,'C)
19 23 --26 14 24 --24 11 32 --22
6 19 --19 6 16 --20
Tensile Strength
(Psi)
Modulus M
2330 2310 2200
--
1320 1360 1330 --
Elonga tion (%}
342 334 315
--
Ingredients a) Opalon* 660 PVC resin
Dioctyl Phthalate Calcium Carbonate Stabilizer AROCLOR
b) 24 hours at 87C over activated carbon
c) 96 hours at 25C
Parts by Weight
100 45 40
3 indicated
Heat and Light Stability
aroclor compounds impart good heat stability but somewhat reduce the light stability of vinyl formulations, but no more so than do many other secondary plasticizers commonly used in the industry. Light stability of the system may be improved by incorporation of a small amount of light-screening agent, such as 0.1 per cent Timtvin P.**
Owlen: Monaanto Chemical Company trademark. Reciitcred in U. S. Patent Office. Trademark of Geijy Chemical Co.
5
0^> O'*
TOWOLDMONOQ35198
Chemical Resistance
For imparting resistivity to chemical attack, the aroclor compounds are unsurpassed. Inde pendent evaluations of the chemical resistance of vinyl chloride-vinyl acetate copolymer paint, modified by eight types of materials (atkyd resin, phenolic-chinawood oil varnish, ester gumlinseed oil varnish, aroclor 1254, dioctyl phthalate, tricresyl phosphate, polymeric plasticizer, and acrylic polymer), showed that aroclor 1254 has the "best all-around chemical resistance, failing badly only in the gasoline test/'
Paints were sprayed onto solvent-cleaned, unprimed, cold-rolled-steel panels, which were then immersed in seven types of solutions until failure. The. data in Table II, excerpted from the November 1955 issue of OJficial Digest of the Federation of Paint and Varnish Production Clubs, compare the chemical resistance imparted by aroclor 1254 and by dioctyl phthalate.
TABLE II --COMPARATIVE CHEMICAL RESISTANCE OF PLASTICIZERS IN VINYL CHLORIDE. VINYL ACETATE COPOLYMER PAINT
Plasticizers
Time to Failure in Corrosive Media
Dioctyl Phtha* AROCLOR
lata 1254 i%) (%)
10% Sodium Hydrox-
ide (day*)
10% Hydro* chloric
Acid (hours)
Gasoline (days)
s% Sodium Hypochlorite (days)
10% Acetic Acid (hours)
Linseed Oil
Fatty Acids (days)
i% Tide at I60"F (days)
10 ___
120* 92
0.4
4
--
10
120* 168"
5
13
84 60
21
168" 90" 22
25 --
60 24
0.4
4
84 27
25
_ 25 120* 120 0.4 14.5 120 90" 22
40 ___ -- 50
60 24
0.4
4
120* 96 0.4 11
48 22 100 60
25 22
a) End of test
In other corrosion-resistance tests of polyvinyl chloride plastisols, containing 70 parts plasti cizer per 100 parts resin a formulation that contained 1 part aroclor 1254 to 3 parts dioctyl phthalate was much more resistant to 15 per cent nitric acid at either 23 or 50C for six months than a compound plasticized with dioctyl phthalate alone.
The plastisol modified with both aroclor 1254 and dioctyl phthalate was also more resistant to 25 per cent chromic oxide at 50C for four weeks and was equivalent at 23C for six months in comparison with the dioctyl phthalate-modified vinyl plastisol.
Migration Resisfanca
The use of aroclor 1262 as a coplasticizer with dioctyl phthalate greatly enhances the re sistance of plasticizer migration to nitrocellulose lacquers and films. Table III compares this property for four formulations.
6
0309932
TOWOLDMONOQ35199
TABLE 111 -- PLASTICIZER MIGRATION TO NITROCELLULOSE LACQUERS AND FILMS
Plasticizer *
Dioctyl Phthalate Polymeric Plasticizer AKOCLOK 1262 Hardness, Shore "A"
Time (weeks) Room Temperature
i 2 3
4
S
10
so0 c 1
2
3
4
5
10
AROCLOR and DOP (parts) 66 -- 20 72
No Change No Change No Change
No Change
No Change
No Change
No Change
No Change
No Change
No Change
No Change No Change
General Motors Lacquer Test (158F; 72 hr.; yi-psi load)
Indentation, Very Slight Softening
a) Formulation Ingredients Opalon 660 PVC Resin
v Epoxy Soybean Oil Barium-Cadmium Laurate Calcium Carbonate Plasticizer
Control (OOP) (parts)
71 --
--
72
AROCLOR, DOP, and
Polymeric (parts)
36 33 20 72
Polymeric and DOP
(parts)
38 35
--
73
No Change No Change No Change
No Change
No Change
No Change
No Change No Change Very Slight Marking Very Slight Marking Very Slight Marking Very Slight Marking
Slight Marking
Slight Marking
Slight Marking
Moderate Marking Moderate Marking Moderate Marking
Moderate Marking Severe Marking Very Slight Softening Slight Softening Slight Softening Slight Softening
Extreme Softening
Lifting
Slight Marking Slight Marking Slight Marking
Slight Marking
Slight Marking
Slight Marking
Very Slight Softening Very Slight Softening Slight Softening Slight Softening Slight Softening Moderate Softening
Extreme Softening
Parts by Weight 100 3 3 25
as indicated
7
TOWOLDMON0035200
Plastisols
The use of an aroclor as a coplasticizer with dioctyl phthalate in polyvinyl chloride plastisols or organosols contributes greatly to the viscosity stability of these materials, especially at elevated temperatures. This benefit is especially important whenever shelf stability is required. Although the initial viscosity of the pastisol or organosol is increased by the use of an aroclor in the formulation, the viscosity reduction upon temperature elevation (before the fusion temperature is reached) is much greater than when most other plasticizers are used.
A comparison of the viscosity stability of plastisol formulations with and without aroclor is given in Table IV.
25*C Initial 1 Day x Week 2 Weeks 4 Weeks
40*C Initial 1 Day 1 Week 2 Weeks 4 Weeks
50'C
Initial 1 Day 1 Week 2 Weeks 4 Weeks
TABLE IV --VISCOSITY STABILITY OF PLASTISOLS
Dioctyl Phthalate (80 PHR) Viscosity * (poises)
AROCLOR 1254(20 PHR) Dioctyl Phthalate (60 PHR)
Viscosity * (poises)
AROCLOR 5460 (20 PHR) Dioctyl Phthalate (60 PHR)
Viscosity4 (poises]
36 65 97 116 132
49 63 78 75 148
92 154 161 178 252
37 48 84 98 215 . 108 305 110 426 209
68 136 139 164 274
66 94 gel 660
980 gel
100 470 900 gel
c) Brookfield LYF viscometer, Xo. 4 spindle, 12 rpm
8 050993*
TOWOLDMONOQ35201
Dipping Plastisols. The chemical resistance of aroclor compounds is used to good advantage in chrome-plating-bath coatings and in glove coatings, as illustrated by the following formula tion for a clear glove-dipping plastisol:
Ingredient*
Opalon 440 PVC resin
aroclor 12S4 Diisodecyl Phthalate Santicizer* 160 HB-40* Secondary Plasticizer Liquid Barium-Cadmium Stabilizer Liquid Chelator-Stabilizer Santoed* 54 Silica Aerogel
Parts by Weight
100 20 SO 25 20 2 0.5 3
Sealers. The adhesion-imparting characteristics of aroclor compounds, their oxidation stabili ty, and their chemical resistance are utilized in the manufacture of automotive sealers, such as the following suggested starting formulations:
ingredient*
Opalon 440 PVC resin ''Vinylite** VMCH resin
aroclor 1260 Diisodecyl Phthalate Santicizer 160 Calcium Carbonate Epoxy Soybean Oil Dibasic Lead Phosphite
Parts by Weight
96 4
50 100
28 125
5 3
Fabrk'Coating Vinyl Dispersions. The use of aroclor plasticizers in organosol or plastisol formulations enables the manufacture of fire-retardant free films and coated fabrics with a high degree of hardness, yet flexibility. The following typical starting formulation for a vinyl organosol to be used for free film or coated fabric illustrates this effect:
Ingredient*
Opalon 440 PVC resin Dioctyl Phthalate aroclor 1254 Liquid Barium-Cadmium Stabilizer Epoxy Soybean Oil \ Thinner Xylene
Parts by Weight
100 33 10 2.5 3 20-35 15-25
HB 40. Saniiciw'. end Sentocel: Mowinto Qxmiul Compeny Trademark*. Retiittrtd in U. S. P*ot Office. **Trdcmrk of Union Carbide PUetici Co.
0509935
TOWOLDMON0035202
'.J <T\
Rigid Plastisoh. The viscosity characteristics of the arociok plasticizers are utilized in the following formulation for rigid, rotationally-cast objects. The formulation is very viscous when first made up, but when heat is applied, the viscosity decreases so that a smoothlyflowing plastisol is obtained. The finished object has a Shore "IV* hardness of 63.
Ingredients
Opalon 440 PVC resin
Geon* 202 PVC resin s' AROCLOR 1254
Santicizer 141 Epoxy Octyl Tallate Liquid Barium-Cadmium Stabilizer Liquid Zinc Stabilizer Polyethylene Glycol 400 Monolaurate
Parts by Weight
55
45 35 10
5 2* 0.5 1
Vinyl Foam
aroclor 1262 and 1268 impart fine, uniform cell structure and flame resistance to chemicallyblown vinyl foam, as exemplified by the following formulations:
Ingredients
Opalon 440 PVC resin AROCLOR 1262 AROCLOR 1268 Dioctyl Phthalate Diisodecyl Phthalate Di-(-Octyl, n-Decyl) Adipate Santicizer 214 Santicizer 409 Butyl Oleat? Liquid Barium-Cadmium Stabilizer Epoxy Resin Neutral Calcium Petronate Calcium Oxide Sodium Lauryl Sulfate Nitrosan** Chemical blowing agent
Parts by Weight
100 --
20 40 --
-- --
50 5 2
-- 3.6
-- -- 10
.
100 20 --
-- 50 10 15 -- --
3 2 3.6 1 1.6 10
100 -- 10 -- 30 30 -- --
-- 3 2 3.6 1 1.6 5
Flame-Retardant Floor Tile
The nonflammability of the aroclor compounds suggests their use in the manufacture of flame-retardant vinyl-asbestos floor tile for military applications. In Table V is presented an evaluation of three aroclor plasticizers in typical vinyl-asbestos-tile formulations. Substitution of antimony oxide for part of the limestone is suggested for still greater fire retardance.
*Trdcmrk of B. F. Coodricb Ckrmiot Co. Td*mrli of E. I. du Pom d< Nemour* V Co.. Inc.
10 0509936
TOWOLDMONOQ35203
TABLE V --EVALUATION OF AROCLOR IN FLAME-RETARDANT, VINYL-ASBESTOS FLOOR TILE
Souticiser 160 aroclor 1254 aroclor 1260 AROCLOR 5460 Me Burney Inden tation Hardness Banbury Time (to reach 280F, sec.) Time to band on roll mill (sec.)
Plasticity
Tack
Surface
Controla (parts)
37 -- -- --
7.8
AROCLOR 1254 AROCLOR 1260 AROCLOR 5460
(parts)
(parts)
(parts)
30 15 -- -- 9.6
.
36 -- 17 -- 10.4
40 20 11.2
99 96 102 ns
IS 10
10
5
Excellent Excellent Excellent
Excellent ' Excellent ' Fair
Excellent Excellent Excellent
Excellent Excellent Excellent
a) Formulation
Ingredients
Opalon 506 PVC Resin Santicizer 160 AROCLOR Asbestos Limestone Titanium Dioxide Stabilizer
Parts by Weight
100 As Indicated As Indicated
160 290
15 5
IN POLYVINYL ACETATE
aroclor compounds are excellent plasticizers for polyvinyl acetate-emulsion adhesives and hotmelt adhesives. The excellent tack and strong bonding power they impart and their low cost contribute greatly to the profitability of these adhesives.
Emulsion Adhesives -
The liquid aroclorV--such as aroclor 1221, 1232, and 1242 -- blend readily by simple stir ring with polyvinyl acetate emulsion at up to 11 parts per 100 parts of emulsion. They greatly improve the quick-tack and fiber-tear properties of the adhesive. The performance of aroclor plasticizers in polyvinyl acetate-emulsion adhesives is compared with that imparted by dibutyl
11
TOWOLDMONOQ35204
phthalate in Table VI. The following is suggested as a typical starting formulation for a lowcost, quick-tack adhesive:
Ingredients
Celva* S-5S PVAc Emulsion aroclor 1232
Parts by Weight
100 11
TABLE VI --PERFORMANCE OF PLASTICIZERS IN POLYVINYL ACETATE-EMULSION ADHESIVES
Hardness (Shore "A")
Low-Temperature Flexibility (Clash St Berg, T,, C)
Volatility (24 hr., 86C over activated charcoal) (Plasticizer lost, %)
Kerosene Extraction (24 hr., 2SC) (Plasticizer lost, %)
Dibutyl Phthalate (II PHR)
69
AROCLOR 1221
(11 PHR)
66
AROCLOR 1232
(11 PHR)
86
AROCLOR 1242
(11 PHR)
97
-- 10.2
-5.9
4.0
5.3
4.0 4.8 4.3 4.0
4.1 4.5 3.8 4.2
Formulation Viscosity (cp.)
Initial * 1 Day 3 Days 4 Days 5 Days 7 Days
10 Days
2420 2460 -- 2520 -- -- --
2240
2200
2200 2180 2260
2160
2060
2040 2020 2060
--
--
______ -- --
a) Initial viscosity of unplasticized emulsion: 1500 centipoises
When the slight odor of aroclor is objectionable in an adhesive for certain applications, it can be easily masked, at negligible cost, by the addition of six grams of either Odormasque** 1004 (camphor) or Odormasque 1066 (fruit) per drum of adhesive.
Rniw Gorp- Trademark. Reniatercd in U. S. Patent Office. Trademark of Polnk V Schwart, Inc.
12 0509938
TOWOLDMONOQ35205
Hot-Melt Adhesives
aroclor compounds are widely used as plasticizers in polyvinyl acetate hot-melt adhesives for
bookbinding and other applications. Four suggested started formulations for evaluation are
as follows:
.,
Ingredimt
Part* by Weight
Application Temperature 165* - I75*C
LowMelting
AlkatiDispersable
Polyvinyl Acetate Opolon 505 PVC resin Modified Rosin Coumarone-Indene Resin (soft) AROCLOR 1254 AROCLOR 1260 Dibutyl Phthalate Santicizer 160 (or dibutyl phthalate) Clay Fluxing Resin (Filtros* Resin \VW) Acrawax C** Sodium Benzoate Viscosity (centipoises)
955
-- -- -- 50-75 -- 50-75 -- -- -- --
100-
-- -- -- 55 -- -- 30 25 _ 75 .--
a) Gclva V-7 (Shawihigan Resins Corp.)
50 b 38(
---- 25 -- -- 28.3 12 27 ---- 13 7
--
---- ---- --1 -- 0.76 2000 (120C) 3500 (175C) Non-blocking Non-blocking
b) Gelva C-3 V-10 (Shawinigan Resins Corp.)
c) Gelva C-5 V-16 (Shawinigan Resins Corp.)
IN EPOXY RESINS
The aroclor compounds probably have greater compatibility with epoxy resins than any other available, nonreactive, plasticizer-modifiers. The excellent chemical resistance, oxidation resis tance, and adhesive qualities imparted by the aroclor compounds reinforce these important beneficial properties of epoxies and thereby help the compounder reduce his formulation costs materially without significant adverse affect on performance.
The lower-molecular-weight, liquid aroclor compounds (such as 1221 and 1232) have maxi mum plasticizing efficiency and impart the most flexibilizing to epoxy compounds. The more viscous, resinous aroclor compounds have progressively less effect on epoxy flexibility: the high-molecular-weight, solid aroclor compounds (1268, 2565, 4465, 5460, etc.), in fact, tend to reinforce the compound.
The effects of aroclor 1221 and 1248 on the properties and performance of an epoxy resin are indicated by the data in Table VII.
Filtre*: Filtered Rotin Product* Co. Trademark. Reentered in U. S. Patent Office. ''Trademark of Clyco Chemical*.
n 0509939
TOWOLDMONOQ35206
TABLE VII-- EFFECT OF AROCLOR 1221 AND 1248 ON PROPERTIES OF EPOXY RESINS
Formulation **
AROCLOR AROCLOR
1221
1248
Viscosity b Before After Curing Curing Agent Agent
Physical Property f
Physical Properties
After Heat Aging
liod Clarity Hardness Hardness Weight
Impact (Light Shore "D** Shore "D" Resis Reflect- (10 sec.) (10 sec.) tance d|(%l
Loss (%)
-
-
12,800 7900
0.2
5.0
76
86 0.012
(30 rpm)
25
--
1650
1200
--
3.0 . 8
81 2.118
--
25
7700
4500
0.6
5.0
40
88 0.682
Ingredients
Parts by Weight
a) Liquid Epoxy Resin Tetraethylenepentamine AROCLOR 1221 or 1248 Cure: 30 minutes at 100C
100 8
As Indicated
b) Brookfield LVF #4 spindle; 60 rpm unless otherwise specified
c) '2A hours at 86C in activated charcoal
Development of flame-retardant epoxy resins is of wide-spread interest. Aliphatic amine-cured epoxy-resin formulations are made selj extinguishing by the use of 20 parts of liquid aroclor per hundred parts of resin. The incorporation of antimony oxide at 5 PHR, with 15 parts of aroclor per hundred parts of resin, yields nonburning formulations (TABLE VIII).
The use of liquid aroclor^ in aliphatic amine-cured epoxies also improves flexural strength and compressive-yield strength, has little effect on tensile strength, and slightly lowers heatdistortion temperature and compressive ultimate strength.
The use of solid aroclor compounds in phthalic anhydride-cured epoxy systems also reduces flammability and, in combination with antimony oxide, produces nonburning formulations. The solid aroclor compounds also greatly improve such important properties as compressive strength, flexural strength, compressive-yield strength, and tensile strength, although they slightly lower the heat-distortion temperature (TABLE IX).
Extension of epoxy-resin adhesives with aroclor compounds greatly reduces the formulation cost, with minimum effect on the bonding characteristic of the adhesive or surface coating.
14 0509940
TOWOLDMONOQ35207
TABLE VIII --EFFECT OF AROCLOR 1242 AND 1240 ON FLAMMABILITY AND PHYSICAL PROPERTIES OF EPOXY RESINS
Formulation *
AROCLOR AROCLOR Antimony
Hardness
1242
1260
Oxide (Rockwell "M'
Flammability
(ASTM 635-56T)
inches
Rate
HeatDistortion Temp. (-C)
Flexural Strength
(p)
Tensile Strength
(ps!)
Compres sive Yield Strength
Compres sive
Strength
ei
(PHR)
(PHR)
(PHR)
burned (in/min.)
(Psi) tP5')
_ ___ --
104 4
0.8Z
117.5
20,100
11,400
15.700
43,000
20 _ --
___ 20 --
15 --
5
-- 15
5
108
2.125
b
103
1.125
b
107 0
c
106 0
c
79.5 87 81 92
21,800 23,800 22,200 22,100
10,700 13,000 12,800 9,800
17,900 17,250 16.700 i 6,950
32,500 32,900 32,400 38,150
Ingredients
P*** *>Y Weight
) Liquid Epoxy Resin
100
Diethylenetriamine aroclor 1242 or 1260
1^ as indicated
Antimony oxide
35 indicated
cure: 16 hours at room temperature, plus 2 hours at 100'C
.
) Self extinguishing
c) Nonburning
TABLE IX -- EFFECT OF SOLID AROCLORS
ON FLAMMABILITY AND PHYSICAL PROPERTIES OF EPOXY RESINS
AROCLOR 1268 (PHR)
Formulation * AROCLOR
5460 (PHR)
Antimony Oxide (PHR)
_ ___ --
20 -- --
-- 20 --
15 --
5
-- 15
5
Hardness
Flammability
(Rockwell "M") (in./min.)
113 0.6 112 0.38 113 0.38 112 b 111 b
HeatDistortion
Temp. (*C)
143 128 135.5 134 135
Flexural Strength
(Psil
16,900 25,900 26,300 20,000 19,000
Tensile Strength
fpsi)
11,000 13,500 11,500 11,100 10,200
Compres sive Yield Strength
(P*'l
Compressive Strength
M
20,900 22,300 21,000 20,500 21,200
23,400 36,500 41.700 30.700 40.700
Ingredients a) Liquid Epoxy Resin
Phthalic Anhydride DMP-30* catalyst aroclor 1268 or 5460 Antimony Oxide Cure: 20 hours at 150C b) Nonburning
Parts by Weight 100 75 0.1
as indicated as indicated
*Tiad<in*rk o( Rohm V Hiu Co.
TV ft60?0
TOWOLDMONOQ35208
In epoxy-resin protective surface coatings, the use of aroclor 1254, 1260, or 1262 economi cally imparls excellent chemical resistance, particularly to acids and alkalies. When resistance to solvents is desired, however, aroclor^should not be used, since they are true plasticizers and do not combine chemically with the epoxy resin. Frequently, about 10 to 15 per cent aroclor 1260 or 1262 is added to increase the flexibility of the epoxy composition, with mini mum effect on the corrosion resistance and adhesion of the film.
IN POLYESTER RESINS
The highly chlorinated, less-volatile aroclor compounds such as aroclor 1260, 4465, and 5460, are very effective and economical fire retardants for polyester resins, and they do not significantly affect the physical properties oi the resin.
The aroclor compounds are effectively used in combination with equal amounts of antimony oxide, since the two materials are synergistic: aroclor imparts self-extinguishing properties to the resin, and antimony oxide reduces afterglow.
Table X indicates the degree of flame resistance imparted to a general-purpose polyester resin (with a 35-pcr cent styrene content) by various equal concentrations of antimony oxide and one of these three aroclor compounds.
TABLE X--FIRE RETARDANCE IMPARTED TO POLYESTER RESINS BY AROCLOftS^AND ANTIMONY OXIDE
Antimony Oxide and AROCLOR
1260
4465
5460
2.5% --
--
flammable
5% 7.5% semiflammable semiflammable
flammable
self extinguishing
60 seconds
self extinguishing
5 seconds
"
10%
self extinguishing
30 seconds
self extinguishing
S seconds
self extinguishing
5 seconds
15%
self extinguishing
immediate
self extinguishing
immediate
self extinguishing
immediate
:) Formulation
Ingredients
Polyester Resin (general purpose) Styrene Methyl Ethyl Ketone Peroxide
(60% in dibutyl phthalate) Cobalt Xaphthenate (1% solution) aroclor and Antimony Oxide
Weight Per Cent
62 35
2 1 as indicated
16
0509942
TOWOLDMONOQ35209
Inclusion of an aroclor increases the flexural strength of the naturally brittle polyester and makes addition of a more-expensive plasticizing polyester unnecessary, At a concentration of 10 per cent (enough for fire retardencv), none of the aroclor compounds reduced the flexu ral strength of the cure resin significantly (Table XI), and their effect was comparable to that of a plasticizing polyester. At 20-per cent addition, they improved the impact strength, where as the plasticizing polyester reduced it. The solid aroclor compounds are preferred for fireresistant surface coatings.
TABLE XI--EFFECT OF AROCLOR\ON STRENGTH OF FIBER-GLASS-REINFORCED POLYESTER RESINS
Plasticizer
Flexural Strength (%) IP*')
Flexural Modulus
M
None Plasticizing Polyester aroclor 1260 AROCLOR 4465 AROCLOR 5460
0
10 20
10 20
10 20
10 20
47,210
43,310 39,930
45,600 33,880
40,740 33,390
37,400 35,890
2,190,000
2,000,000 1,560,000
2,090,000 1,690,000
2,190,000 1,290,000
1,700,000 1,550,000
Impact Strength (ft.-lb./in.)
1.73
1.64 1.24
1.33 2.04
1.41 2.48
1.85 3.06
IN POLYETHYLENE
,
The need to make polyethylene and other polyolefins flame retardant is well recognized. The well-known flame retardancy of the aroclor compounds suggests their evaluation for poly olefin applications such as molded products, coatings, and hot-melt adhesives.
Preliminary evaluation of aroclor 5460 (20 per cent) and antimony oxide (10 per cent) showed good results in imparting flame retardancy to low-density, noncrystalline polyethylene. Com pared to the use of chlorinated aliphatic hydrocarbons, the use of aroclor greatly improved the heat stability and had considerably less effect on tensile strength, yield, and elongation of the formulation.
17 0&09943
TOWOLDMONOQ35210
IN POLYSTYRENE
The aroclor compounds are good plasticizers for polystyrene. The lower * molecular - weight aroclor compounds have greater solvating power than the higher-molecular-weight aroclor compounds. The gelling rate of various plasticizers in polystyrene resin is shown in Table XII; each plasticizer was added to the polystyrene resin at a concentration of 2 parts plasti cizer per part of resin, and the time required for the material to gel was noted.
TABLE XII -- GELLING RATE OF PLASTICIZERS IN POLYSTYRENE
Plasticizer (200 PHR)
Time to Gel (min.)
aroclor 1221 Diethyl Phthalate Dimethvl Phthalate
immediate 0.6 0.75
aroclor 1242 Santicizir 141 Sanlicizcr 160 Saitlicizcr B-16 HB`40
3 6 18 30
IN POLYURETHANES
aroclor compounds are useful as plasticizers and flame retardants in polyurethane rubbers, foams, adhesives, and coatings. The following formulation illustrates the use of aroclor 1254 in a polyurethane flocking adhesive:
Part A Part B
Ingredients
Multranil** I-'LD Urethane Resin Mondur** C Isocyanate aroclor 1254
Multranil FLD Mondur C
Parts by Weight
100 5
20
100 5-10
Part A is applied to the fabric by knife coating and allowed to dry thoroughly. The fabric is then coated with Part B, and the material is flocked immediately.
.......................................................
...... Qffm
**Muliranil and MonJu>. Mobay Ch.mical Company tiad.mjrli. Rci'iiuroJ in U. S. Pai.ni Ollici.
IE 0509944
TOWOLDMONOQ35211
Protective urethane coatings are unusually well suited for application to concrete and metal. aroclor 1254 is incorporated to improve adhesion and sealing. The first of the following formulations is the preferred prime coat for concrete storage tanks for gasoline and fuel oils. The second formulation is the base coat for a concrete wood-kiln coating, which remained in perfect condition after two-and-one-half-years' continuous exposure to heat, moisture, and wood distillates. The other two formulations, for primer and intermediate light-metal coating, contain aroclor 1254 for better adhesion to metal.
Ingredients
Mondur C Multron* R-4 Polyester Resin Multron ,R-10 aroclor 1254 Polyvinyl Acetate Polyvinyl Butyral Methyl Glycol Acetate Butyl Acetate Ethyl Acetate Toluene Pigment (colored) Zinc Chromate Titanium Dioxide (rutile) Talc (micronized)
UnsealedConcrete Prime Coat
[parts)
HighTemperature
Concrete Primer [parts)
19.0 12.0 ---- 10.0 12.0 5.0 2.9 0.2 -- -- 0.4 8.7 9.0 8.7 5.4 8.7 4.0 8.7 6.9 12.5 -
-- ..
-- >5 0 12.5 13.9
Light-Metal Coating
Primer
Intermediate
(par+s)
(parts)
21.0 2.6 10.5 2.7 0.3
25.1 72 7.2 1.8 0.3
8.0 8.0 15.1 6.7 7.9
13.2
7.5 7.5 14.2 21.0 --
5.5
IN PHENOLIC RESINS
Considerable interest has been shown in the use of aroclor compounds to make phenolic lam inating resins flame retardant. The higher-molecular-weight aroclor compounds (1262 and 5460) are usually evaluated for this purpose.
aroclor 1268 and 2565 are useful in the manufacture of brake linings.
*Mu1<tok; Ttidemitk o( Moby Chemical Company. Rtittuted in U. S. Patent Oifit*.
19
05099*5
TOWOLDMONOQ35212
IN CHLORINATED RUBBER AND CHLORINATED POLYPROPYLENE
Protective coatings based on chlorinated rubber generally contain aroclor compounds to en hance their chemical resistance (to water, alkali, and acid), corrosion resistance, and electrical insulating properties and to impart flame retardance. When properly pigmented, they are un usually weather resistant, aroclor compounds strengthen the adhesive grip of chlorinated-rub ber lacquers, varnishes, and paints to structural materials and improve the flexibility and life of the coating. Typical applications include protective and decorative coatings for swimming pools, stucco homes, steel structures, tank cars, and both wood and metal maritime equipment. Their out standing chemical resistance qualifies these coatings for use in manufacturing plants where chemical attack is prevalent, aroclor 1254 and 1260 are used in chlorinated-rubber coatings as flexibilizing plasticizers, commonly in combination with aroclor 5460, which serves as a resin fortifier. A variety of suggested starting formulations based on chlorinated rubber is given in the following table.
> 20
TOWOLDMONOQ35213
Ingredients
Paints for Alkaline Surfaces
Concrete
Fed. Spec.
Swimming
TT-P-91
Pool
(parts)
(parts)
Maximum Acid end Alkali Resistance (parts)
Parlott* (20 cp.) Chlorinated Rubber
aroclor 1254
aroclor 1260 AROCLOR 5460
Long-oil, oxidizing, alkyd resin
Medium-oil, drying, alkyd resin
Carbon Black
Iron Oxide
Titanium Dioxide
Zinc Oxide
Asbestine** 3X (magnesium.silicate)
Bentone*** 34 gelling agent
Epichlorohydrin
*
Stabilizer
Solvcsso**** 150
Solvesso 100
Turpentine
Xylene
Hi-Flash Naphtha
IS 10 -- 6 -- -- 0.5 -- 16 2 -- -- -- -- 42.75 --
4.75 __ __
10.2 5.1
5.1
___
11.4
11.7 1.3 0.1 -- 9.1
45.7
___
18 8 6
-
18 --
-- -- 0.09 0.9
45 0e
__
White Marine
Paint (parts)
20 6
6
__
25
-- -- -- --
-
23 20
aroclor compounds are also incorporated in chlorinated-rubber formulations used for heat-seal ing adhesives, electrical coatings, paper and textile coatings, and printing inks. The following starting formulation is for an acid- and flame-resistant adhesive:
Ingredients
Chlorinated Rubber (125-cp. type) aroclor 1254 aroclor 5460 Toluene
Parts by Weight
20 6 6
68
Chlorinated polypropylene, a new film-forming resin, produces clear, colorless films, appears equal to chlorinated natural rubber in chemical resistance, and is noticeably more heat and
Trademark of Hercules Powder Company Trademark of International Talc Co. Trademark of National Lead Company Trademark of Standard Oil Company (N. J.)
21
0&099S7
TOWOLDMONOQ35214
(
light stable. AROCLO^are very compatible with the resin and are recommended in the following starting formulations:
Ingredients
Chlorinated Polypropylene AROCLOR S460 AROCLOR 1254 Dioctyl Sebacate Epoxy stabilizer Solids, wt. per cent in toluene
Composition (wt. %)
50.0 15.0 24.0
4.3 1.7 50.0
55.0 b 15.0 24.0
4.3 1.7 50.0
Film Properties
300F heat stability 1 hour 2 hours 3 hours 5 hours
18 hours
v. si. yellow v. si. yellow si. yellow mod. yellow ` black
v. si. yellow si. yellow mod. yellow
-- --
Fada-Ometer* stability
24 hours
si. yellow
v. si. yellow
48 hours 96 hours
si. yellow mod. yellow
si. yellow si. yellow
144 hours
mod. yellow
brown
Two-week chemical resistance water 10% hydrochloric acid 1% sodium hydroxide
excellent excellent excellent
excellent excellent excellent
c) Parlott P (10-cp, 20% in toluene) --Hercules Powder Co. b) Parlon P (20-cp, 20% in toluene) --Hercules Powder Co.
c) Lacquers were sprayed on "bonderized" steel panels. Films were 2.5-io 3.0-mils thick after 72-hours' air drying.
IN STYRENE-BUTADIENE COPOLYMERS
aroclor compounds are very often incorporated in coatings based on styrene-butadiene co polymers to impart resistance to acids, alkalies, moisture, and corrosive chemicals. These coat ings are suited for use on masonry, wood, and metal for such applications as concrete floors; architectural finishes; metal primers and finishes on maritime equipment, structures, and tank cars; baking primers; corrosion-resistant industrial films; and oil- and grease-resistant coatings.
Trademark of Atlas Electric Devices Co.
22
OiO^**8
TOWOLDMONOQ35215
The following suggested formulations for typical applications of styrene butadiene - copolymer coatings offer excellent performance:
Ingredient
Clear Vehicle K%)
Wall Sealer (lb./100 gal.]
Aluminum Enamel M.%)
Styrene-Butadiene AROCLOR 1254 AROCLOR 1260 AROCLOR 5460
16.608.39 -- 9.11
123.2 b 41.4 --
41.4
7.40c 6.00 -- 13.40
Raw Tung Oil Hydrogenated Methyl Abietate Troykyd* ABC Lecithin Soya Lechithin
Petroleum Naphtha Hi-Flash Naphtha Mineral Spirits #10 Toluene Xylene
1.655 -- -- 0.545 --
6--2.70
-- ------ :
--
____ -- -- ____
5.9
246.4 -- 185.3 -- --------
____
--------
__
--
__
--
33.60 ____
22.40
Lithopone Titanium Dioxide Aluminum Stearate Aluminum Paste Zinc Oxide Barium Sulfate
-- -- -- -- -- -------
Asbestine 3X (magnesium silicate)____
Calcium Carbonate, ground
____
Diatomaceous Earth
____
Mica
--
'339.3 59.2 5.9 --
-- -------
75.0 ____ ____ --
____ ____ ____
8.55 ____
--
__
____ ____
8.00
a) Marbon "9200" MV (Marbon Chemical Div., Borg-Warner Corp.) b) Pliolite S-5A (Goodyear Tire and Rubber Company) c) Marbon "9200" LV (Marbon Chemical Div., Borg-Warner Corp.) d) Flaked Piccoflex 120 (Pennsylvania Industrial Chemical Corp.) e) Pliolite S-SB (Goodyear Tire and Rubber Company) /) or AROCLOR 1248
Paint (lb.)
147 d --
31 --
__
8
__3
--
__
395 -- --
--
____
--179
____ 60 90
____
236 76 30
Traffic Paint (parti)
250' 1201 -- 130
____ --__
--
__
--
__
--
340 340 --
____ -- -- ____ -- --
____ ____ ____ --
IN SYNTHETIC AND NATURAL RUBBERS
The liquid aroclor compounds -- 1221, 1232, 1242, and 1248--have a strong plasticizing action on both natural and synthetic rubbers. Solid aroclor^-- 1254 and 1260 -- impart per manent tackiness and adhesion to the rubber composition.
*Tndemark of Troy Chemical Co.
23 OS099<i9
TOWOLDMONOQ35216
Neoprene
Compositions containing up to 40 parts of aroclor 5460, 2565, 4465, or 1268 in 100 parts of neoprene rubber are extremely fire retardant. About 1.5 parts of aroclor 1268 per hundred parts of neoprene imparts excellent working qualities at 225 to 325 F for injection mold ings. Neoprene modified with aroclor compounds has proved extremely useful as a wire and cable coating.
aroclor 5460 imparts plasticization and adhesion to decorative and protective coatings that have been commercially used on rubber products for many years. Suggested starting formula tions for a clear, dull coating and for three pigmented coatings are as follows:
Ingredients
AROCLOR 5460 Neoprene GRN-10 Chlorinated rubber (21 cps.) High-styrene resin Isobutyl methacrylate Toluene
Paris by Weight
base for
clear, dull
pigmented
coating
coatings
3.70 3.50 1.30 1.00 . 0.40 90.10
16.00 8.00
4.38 1.75 69.87
Ingredients
Paste:
Base Chromium Oxide Zinc Oxide #3 Titanium Dioxide Aluminum Hydrate Toluene
Ready-to-Use Coating:
Base Paste
green coating
20.0 6.4 3.6
----
10.0
60.0 40.0
white (high gloss)
--43.0
10.5 15.0 -- 31.5
70.0 30.0
white (luster modifier)*
--29.0 --
-- 25.0 52.0
*
To modify the luster of the white, high-gloss coating, the selected amount of the modifier com position is incorporated into the high-gloss paste to achieve the desired degree of flatness.
Polybutene
aroclor plasticizers and Indopot polybutenes are blended in various proportions to make permanently tacky coatings for fabric or paper. Insecticides, for example, can be blended into such coatings to make insect traps or barriers on tree trunks for foliage or fruit protection. Such coatings can also be used for tape and sign backing.
24
0309930
TOWOLDMONOQ35217
Excellent sealing and caulking compounds are made with blends of aroclor compounds and polybutenes with inorganic fillers, such as:
Ingredient
Whiting Talc Lithopone Asbestos
Per Cent
50 30 10 10
By various combinations of selected aroclor compounds and polybutenes, a wide range of hardness, viscosity, flow, and bonding characteristics can be produced in durable sealing and caulking compounds.
Specialty mastics, too, are obtained by selective blends of aroclor plasticizers with polybutenes. They have excellent adhesivity for such uses as: automobile-body sealants.
Paper-transparentizing liquids (for making tracing paper, window envelopes, and special pack aging) can be formulated with aroclor 546D and polybutenes. A typical economical formuiation is as follows:
Ingredient
AROCLOR 5460 Polybutene (Indopol* H-300) Toluene
Per Cent
30 25 45
Butadiene-Acrylonitrife Rubber The aroclor compounds -- particularly aroclor 5460 -- are useful as softeners for Buna X rubber.
Silicone Rubber aroclor is a very effective flame retardant for silicone rubbers.
Crepe Rubber (Natural) aroclor 1262 is used as a low-cost plasticizer for crepe rubber in paint compositions. In con centrations of from 5 to 50 per cent of the weight of the rubber, the aroclor increases the film's alkali resistance, gloss, and adhesivity to steel.
#Trdfmrk of Amoco Chcmicrli Corporation
25
0509951
TOWOLDMONOQ35218
POLYSULFIDE RUBBER
aroclor compounds are widely used to flcxibilize, improve the bonding strength, increase the chemical resistance, and reduce the cost of Thiokol* polysulfide liquid rubbers. Among the many uses of polysulfide formulations are joint-sealant compounds used in construction, sol vent-resistant gaskets, adhesives for concrete, potting and encapsulation, protective coatings, and binders.
Although the aroclor compounds are highly compatible with polysulfide rubbers --up to 100 PHR -- the concentration to be used depends on the handling and performance proper ties required in the finished compounds. Suggested concentrations of aroclor range from about 15 PHR for sealant compounds to about 40 PHR for casting formulations.
Liquid aroclor compounds (such as aroclor 1248) are used to reduce the viscosity and per mit the use of higher filler concentration, whereas the solid aroclor compounds (such as aroclor 5460) are useful where low volatility is desired.
The following suggested starting formulations illustrate the use of aroclor 1252 in a jointsealant compound and of aroclor 1248 in a polysulfide casting formulation:
Ingredient
**
Thiokol LP-32 polysulfide Thiokol LP-2 polysulfide aroclor 1232 aroclor 1248 Calcium Carbonate Calcined Clay Titanium Dioxide Phenolic Resin Stearic Acid Zinc Sulfide Sulfur C-5 Paste4
Sealant
(parti)
100
--
5-15
--
20 20 10
5 1
--
0.1 15
Casting Compound
(parts)
___
100
--
20-40
___ -- -- ___ --
40 0.1 15
Property
Cast sheets, after cure of 7 days at room temperature:
Tensile strength, psi Elongation, per cent Hardness, Shore "A"
150 - 200 500-700 30-40
150-200 300 - 400
25-35
a) lead peroxide, 50%; dibutyl phthalate, 45%, stearic acid, 5%: passed three times through a tight paint mill.
"Trademark of Thiokol Chemical Corp.
26
OiO^2
TOWOLDMONOQ35219
6
\AROCLOR IN CELLULOS 1C RESINS
IN ETHYL CELLULOSE
Ethyl cellulose formulations plasticized with aroclor compounds are used as protective lac* quers, adhesives, and strippable coatings. The solids, such as aroclor 5460, are widely used with ethyl cellulose or cellulose acetate-butyrate resins in hot-melt applications for the protec tion of tools and metal parts.
The aroclor plasticizers are highly compatible with ethyl cellulose: the liquid aroclor compounds impart flexibility: the solids, hardness. For example, 75 parts of AROCLOR 1242 with 100 parts of ethyl cellulose produces a very flexible, slightly tacky material, aroclor 5460 at the same concentration yields a very hard, somewhat brittle composition. Hard films that contain aroclor 4465 are not brittle at ordinary temperatures.
For high-gloss coatings with exceptional weathering qualities to be applied to rigid surfaces, compositions containing equal parts by weight of aroclor 5460 and ethyl cellulose are sug gested. When a more-flexible coating is required, a softer aroclor should replace either all or part of the aroclor 5460.
The following five typical formulations indicate the versatility of various aroclor plasticizers in compounding for widely different types of applications. They are intended as guides to the use of aroclor compounds with ethyl cellulose.
Ingredients
Lacquer (parts)
White AlkaliResistant Lacquer (parts)
Liquid Adhesive
(parts)
Strippable Coating
(parts)
Hot-Melt Adhesive
(parts)
Ethyl Cellulose
50 25 50 49 24
aroclor 1254
--- 16 -- 49 --
aroclor 1260
50 -- -- _ --
AROCLOR 5460
-- 76 40 --
7
Dow 276, V-9
----
8----
Octylphenol
-- 1 2 1--
Stearic Acid
-- ----
1--
Rutile Titanium Oxide
--
50
--
--
--
Epoxy Resin
-- 1 ------
Santonox* Antioxidant
--
--
--
--
1
_Mineral Oil
----_
57
Castor Oil
--*
--
--
__
5
Epoxidized Soya Oil -- -- -- _
3
Paraffin'Wax (m.p. 135 F) -- -- -- --
3
The first four of these formulations may be dissolved in suitable solvents, such as mixtures o about four parts of toluene to one part of butanol, to obtain the desired viscosity.
*SanioMk: Mtin*nu> Chemical Company Trademark. RtKiitcrcd in U. S. Patent Office.
27
O^1
TOWOLDMONOQ35220
IN NITROCELLULOSE
In nitrocellulose lacquers, the aroclor compounds can function either as plasticizers to modify the properties of the film or as resin extenders to add film-forming body. They are highly com patible with nitrocellulose and with other resins and plasticizers commonly used in lacquer formulations. They impart weather resistance, luster, adhesion, and flame retardance. Their ex cellent electrical characteristics and their ability to retard the passage of moisture and gases through nitrocellulose films make the aroclor compounds especially valuable in coatings for electric-insulating materials.
The following trilinear diagrams (Figure 1), show the limits of practical compatibility of aroclor 1254, 1260, and 1262 when used in nitrocellulose lacquers in combination with some other resins or plasticizers. The less viscous aroclor compounds (1242 and 124S) are more compatible than those shown; the more resinous aroclor compounds (1268, 2565, 4465, 5442, and 5460) are less compatible.
In these trilinear diagrams, compositions represented by any point in an unshaded area pro
duce homogenous nitrocellulose-lacquer films. On the other hand, compositions represented
by points in the shaded areas produce impractical (segregated, brittle, or soft) films. J-er
detailtTTtufiiMiii'llun
and-iH^~f^the>e- diagramsj-please-refer tcwiieWoitewiag.
a4desr
ESTER GUM RESIN, percent pig. |--Limits of Practical Compatibility of AROCLOR^ in Nitrocellulose Lacquers
28 0509V5*
TOWOLDMONOQ35221
Fig. I (Continued)
AROCLOR 1260 or 1262. per cent 29
0509955
TOWOLDMONOQ35222
fig. 1 (Continued)
AROCIOR 1260 or 1262. per cent
The following formulations arc given to illustrate modifications that can be obtained by varia tions in composition. They all have excellent durability, but the first two are much harder and less flexible that the third. The first two also have excellent sanding and polishing qualities, but No. 3 is too soft for sanding. The cable lacquer (no. 4) has extremely high flexibility, as required for high-tension automobile cables.
Ingredient Nitrocellulose (% sec.) (wet) Nitrocellulose (Vz sec.) (dry) Nitrocellulose (15-20 sec.) AROCLOR 1242 AROCLOR 1260 AROCLOR 5460 Dibutyl Phthalate Tricresyl Phosphate Damar Resin Ester Gum
No.l (parts)
-- 100
-- -- 20-39 -- 20- 0 80
No. 2 (parts)
-- 100 --' -- 20 -- 20 -- 80
No. 3 (parts)
-- 100 -- -- 80-70 -- -- 39-70 --
No. 4 Cable Lacquer (parts)
-- -- 100 80
-- -- -- 120
--
No. 5 Chrome Lacquer (parts)
100
--
-- -- -- 47
32.5
--
30
0&099!>6
TOWOLDMONOQ35223
IN CELLULOSE ACETATE-BUTYRATE
The high-chlorine-content aroclor plasticizers are highly compatible with cellulose acetate-bu tyrate and arc widely used in the manufacture of low-cost, flame-resistant lacquers. Typical uses for these products include paper coatings, lacquers for plastics, strippable coatings for paint booths, and hot-melt adhesives. Typical starling formulations, illustrative of these uses, are suggested as follows:
Ingredients
Praappeer Lacquers Low-Cost Curl
Flame- Resistant Resistant
M- %) M- %!
Clear Wood Filler ("* Vo)
Plastics 4 Lacquer
K V.)
Paint-Booth Hot-Melt Strippable Adhesive Coating
K V.) K V.)
Half-Second Cellulose Acetate-Butyrate
20 20 7 6 20 35
AROCLOR 1260
-- 20 --
1.5 --
--
AROCLOR 1262
IS -- -- -- -- --
AROCLOR 5460
-- 15 --
9 30
Dioctyl Phthalate
-- ------
9 15
Epoxy Soybean oil
-- "-- -- --
9.5 --
Acrylic Resin
----
2.5
Dow 276.V9
-- '--
...
1.5
Socony Vacuum 200
-- ------
2.5 ...
Newport V-40 pine resin -- -- -- -- -- 19.8!
Acetone
-- 10 -- -- 10 --
Methyl Ethyl Ketone
-- _ -- 10
--
Methyl Isobutyl Ketone -- -- --
5
--
Isobutyl Acetate
5 10 22 --
5--
Ethanol
12
10 --
33.5 10
--
Butanol
----
S ------
Isobutanol
-- -- -- 25 -- --
Toluene
48 30
6 15 25 --
Santonox Antioxidant
----------
0.1
Syn Fleur #6 odorant
----------
o.o:
Asbestine X (magnesium silicate) -- -- 45 -- -- --
a) Coatings for cellophane, cellulose acetate, and cellulose acetate-butyrate.
31
TOWOLDMONOQ35224
c
AROCLOR IN PAINT, VARNISH, WAX, ASPHALT
IN PAINT AND VARNISH
aroclor compounds are soluble in paint and varnish oils and solvents and are compatible with most film-forming coating resins. The* aroclor compounds improve adhesion to the substrate and impart to the film properties that correspond to the particular character of the aroclor used: the hard, resinous aroclors tend to give increased hardness; the viscous aroclor ` flexibility.
aroclor 4465 and 5460 produce paints that are very quick drying and yet have excellent dura bility. The amount of aroclor used may be from 30 to 50 per cent of the weight of the oils.
aroclor 1260 is best for short-oil varnishes that are required to be flexible. The aroclor com pounds impart water and alkali resistance and also enhance the value of the other resins used in the varnish. A suggested starting formulation is two parts of oil, one part of aroclor 1260, and one part of other resin. These proportions can be varied as required. The aroclor may be considered to play the same role in the varnish formulation as oil, except that it does not oxidize and lose its flexibility on exposure.
The aroclor compounds do not react chemically with oils, hence there is no advantage in beat ing together in making a varnish. They are best added as a "chill back" or as a cold cut in the thinning operation. The only reason to heat the aroclor compounds is to fluidize them so they can be more readily mixed with the oils. Alkyd, phenolic, or ester gum resins, with a harder aroclor such as 5460, may be used in making varnish formulations. To illustrate the use of aroclor compounds in alkyd resins the following suggested starting formulation is shown.
Ingredients
Parts by Weight
Alkyd (60% Nonvolatile) Kettle Bodied Linseed Oil (Gardner-Holdt Vise. Z-2) Raw Linseed Oil aroclor 5460 Titanium Dioxide (Rutile) Titanium Dioxide (Anatase) Magnesium Silicate Mineral Spirits Drier-Absorption Agent Phenyl Mercury Naphthenate (10% Mercury) Cobalt Naphthenate (6% cobalt) Lead Naphthenate (24% lead) Anti-Skinning Agent (Volatile type)
81 20 35 34 34 67 100 38 1.3 2.7 1.5 3.2 0.67
32
05099*8
TOWOLDMONOQ35225
The following suggested starting formulation for a fire-retardant enamel illustrates use of the flame retardancy of an aroclor in alkyds:
Ingredients
38% Phthalic Anhydride-Soya Alkyd aroclor 5460 Solution
(aroclor 5460, 53; Hi-Flash Naphtha, 22) Whiting Colloidal Grinding and Dispersing Agent Antimony Oxide Titanium Dioxide (Rutile)
Grind above ingredients, and thin with: 38% Phthalic Anhydride-Soya Alkyd Xylene Cobalt Kaphthenate (6% cobalt) Manganese Naphthenate (6% manganese) Lead Naphthenate (24% lead)
Parts by Weight
63 75
84 2.7
42 33
96 38
1 1 2.3
aroclor compounds are excellent grinding and dispersion media for pigments used in paints and varnishes, aroclor 1254 is used to disperse aluminum powder in a paste form that can be incorporated easily into paints and varnishes. The aroclor imparts excellent leafing quali ties, brightness, or luster and does not tarnish the aluminum pigment on aging. Moreover, the composition does not support combustion.
aroclor compounds are important ingredients of heat-resistant aluminum paints and enamels that contain silicone resins. For example, the following suggested formuation for a heat-resist ant coating can withstand a maximum temperature of 800 F and continuous-service temp erature of 400 F. The heat-resistant enamel can withstand temperatures of 900 to 1000 F in such applications as jet-engine components, exhaust manifolds, and incinerators. The heat-resistant paint has excellent resistance to a programmed heat test, including 8 hours at 1200 F, and to salt-water spray after programmed heating to 500, 600, and 900 F.
33
05099&9
TOWOLDMONOQ35226
-'Dow Coming 805 Resin (50% Nonvolatile)
G E Silicone Resin SR-82 (60% in xylene)
G E Silicone Resin SR-J12 (50% in xylene)
Styrene-Butadiene (50% in xylene) (Pliolite S-5B)
aroclor 4465 (90% nonvolatile) 60% aroclor Solution
(aroclor 4465, 36 wt. %) (aroclor 1262, 24 wt. %) (Solvesso 100, 24 wt. %)
(Xylene, 16 wt. %) aroclor 5460 (60% in xylene) aroclor 1254 Aluminum Paste (74% nonvolatile) Cobalt Octoate (6% cobalt) Xylene Mineral Spirits
o) Meets Spec. TT-P-0028
Heat-Resistant Coating
(lb./100 gal.)
220
Heat-Resistant Enamel
(lb./100 gal.)
--
-- 174.2
-- 313.3
-- ----
332 '----- 435.6
~-- ---- 384 250.0 -- 4.4 114 --
----
Heat-Resistant Paint4
(lb./100 gal.)
93.6
207.9
93.6 47.8 240.0 140.8 113.1
IN WAXES
The aroclor compounds, especially 5460, are compatible with various natural waxes, and are blended with waxes for many uses, including "lost-wax" casting, impregnating compounds, and inexpensive sealers. Waxes formulated with aroclor compounds are nontacky and stable.
Much of the highest-quality precision-casting wax used in the "lost-wax'* process is formulated
with aroclor compounds, most frequently 5460, 4465, and 1254. Waxes containing aroclor
compounds are widely used in making dental castings, costume jewelry, and precision-cast air
craft parts.
------------- - ------ -- --
"
Usually from one-fourth to one-half the composition consists of aroclor 5460, which con tributes these desirable properties to the formulation: hardness without brittleness, shrinkage resistance, sharp definition, sharp melting point, fire resistance, low volatility, and volatiliza tion without carbonization during final curing.
Excellent impregnating compounds to prevent sticking of furniture drawers, double-hung win dows, etc. are made from selected aroclor compounds, such as 5460, and various waxes. Com binations of resinous aroclor compounds with waxes make excellent and inexpensive sealers for masonry, wood, fiberboard, and paper.
aroclor compounds impart moisture and gas resistance, adhesion, alkali and chemical resist ance, flame resistance, lubricity, and insulation to impregnants for cloth, paper, wood, and
34
0509960
TOWOLDMONOQ35227
asbestos. They are combined with such materials as waxes, asphalt, tars, sulfur, aluminum stearate, and inorganic pigments so as to provide exactly the physical characteristics required for the specific purpose, aroclor 1254, 4465, and 5460 are suggested as most applicable.
Wood is decidedly toughened, hardened, and made more moisture-resistant when impregnated by the vacuum-pressure method with the following mixture:
Ingredients
aroclor 4465 Microcrystalline Wax Sulfur
Per Cent
70 20 10
The coating is very resistant to acids and alkalies but can be attacked by aliphatic, aromatic, or chlorinated hydrocarbons. The paintable surface is not appreciably discolored. Various de grees of hardness and adhesion are obtained by variations in the proportions of the ingred ients.
Blends of aroclor 1268 and 1242 have the unusual capability to extend carnauba wax satis factorily and at an attractive saving in cost:
Ingredients
Parts by Weight
aroclor 1268 AROCLOR 1242 Carnauba Wax Ceresin Wax Paraffin Wax Characteristics Color
Texture
10 5 5 20 60
Pale Yellow, White Smooth,
hard, non-tacky
Softening point, C Melting point, C
60 78
19.6 4.9 6.8 19.6 49.0
Pale Yellow
Smooth, hard,
non-tacky
77 79
30 35 35 5 55
10 30 50 20 20 10 35 10 --
Pale Yellow
Pale Cream
Cream
Smooth, hard,
slightly brittle
78 78
Slight surface crystallinity
79 86
Smooth; carnauba-
ringed surface
80.5 88
IN ASPHALT
Self-extinguishing asphalt formulations for caulking, roof coatings, and sound-deadening coat ings are obtained by incorporation of at least 30 per cent aroclor 5460 or other solid, resin ous aroclor.
IN ALLYL STARCH
Substitution of the hydroxy hydrogen atoms of the starch molecule by ally! groups produces ally! starch, which upon polymerization forms stable, cross-linked molecules. A minimum of 20-weight-per cent plasticizer is required to make the film flexible. The aroclor compounds are highly compatible and very efficient plasticizers for allyl starch.
35 OSG^bk
TOWOLDMONOQ35228
ffk MISCELLANEOUS APPLICATIONS OF AROCLOR
With their wide range of physical properties, their inertness, lubricity, and low vapor pressures -- aroclor compounds are valuable ingredients in an incredible variety of formulated products. They are compatible with many solvents and oils and most resins. They are virtually nonvolatile and permanently thermoplastic; they do not react with other chemicals in the formulation. Finally, their low cost makes their use for special purposes eminently practical and economical.
DUST PREVENTION AND DUST CATCHING aroclor 1254 is a low-cost dedusting agent that "holds down" the dusting of a variety of chemical materials. Since aroclor 1254 resists both oxidation and combustion, it can even be used to control the dusting of highly reactive compounds. As a typical example, a few tenths of a per cent controls the dusting of calcium hypochlorite.
Since aroclor compounds are non-drying and tacky, they make excellent coatings to capture dust, lint, and other fine, airborne particles. Glass fiber, metal mesh, and other materials used to filter air and gas streams are coated with aroclor 1260 and 5460.
VAPOR SUPPRESSION (FOR LONGER INSECTICIDE KILL-LIFE) The effective kill-life of expensive chlorinated insecticides is extended as much as ten-fold by the incorporation of equal parts of aroclor 5460, which acts both as a vapor suppressant and as a sticking agent. Hard surfaces (painted or metallic) sprayed with lindane or benzene hexachloride fortified with aroclor 5460 remain toxic to flies, ants, roaches, and silverfish for as long as three months, compared with one week for unfortified sprays.
The aroclor retards the rapid evaporation of the volatile insecticides without adding odor or objectionable residue. Formulation into an insecticide is simple: a solution of the aroclor in a suitable solvent is merely added and mixed into the other ingredients.
aroclor 5460 is also recommended for noncrop insect formulations containing chlordane, aldrin, and dieldrin. The other resinous aroclor compounds (1254, 1260, 1262, 4465, and 5442), also nonvolatile and sticky or tacky, likewise merit evaluation as insecticide extenders.
MOISTURE PROOFING In moisture-proof coatings for wood, paper, concrete, or brick, the aroclor compounds are best combined with waxes, especially paraffin or Carnauba; oils such as mineral oil or drying oils; or synthetic resins, including modified alkvds, phenolics, chlorinated rubber, polystyrene, styrene-butadiene copolymers, ethyl cellulose, cellulose acetobutyrate, benzyl cellulose, or vinyl resins. The material to be used with the aroclor should be selected according to the end-use requirements of the specific application. Some very simple compositions contain only aroclor and paraffin. One very efficient moisture proofing compound, consisting of 96 weight per cent aroclor 5460 and 4 per cent paraffin (melting point 54C), has an ASTM softening point of about 82C. A similar compound, based on aroclor 4465, has a softening point of about 58C.
3*
0t>099b^
TOWOLDMONOQ35229
Softening point and viscosity when melted are further decreased by the use of mixtures of aroclor compounds. For example, a composition containing 40 per cent aroclor 1260, 56 per cent aroclor 5460, and 4 per cent paraffin, is very soft at room temperature. A higher concen* tration of paraffin also produces softer compounds.
An excellent melt coating for paper and cloth, made according to the following suggested for mulation, may be applied by knife or roller at 350F, requires no solvent, and provides an extremely flexible coating.
Ingredients
Half-second Cellulose Acetate-Butyrate Dioctyl Phthalate AROCLOR 1260 Santonox antioxidant
Per Cent
50 9.9 40 0.1
PIGMENT DISPERSION
aroclor 4465 is a useful resin in rotogravure and other printing inks. It is an important in gredient in the following mimeograph ink suitable for use on bond paper:
Ingredients
aroclor 4465 Lubricating Oil (SUV 1200@100F) Paraffin Oil (SUV 76 @100F) Carbon Black Oil-Soluble Dye
Per Cent
40 35 20
4 1
aroclor 4465 is also used in the preparation of imitation gold leaf. Bronze powder is spread upon a hot coating of aroclor on one side of a sheet of paper. When the paper treated with aroclor and bronze powder is placed on the object to be imprinted and a hot die is pressed against it, the aroclor softens, sticks the bronze to the object, and coats the powder to pre vent tarnishing.
aroclor 1254 and 4465 serve as pigment vehicles for decoration of glass and ceramics. When the decorated object is fired, the aroclor volatilizes without carbonization and thus avoids discoloration, aroclor compounds are also valuable as grinding and dispersing mediums for pigments used in plastics.
SEALING AND IMPREGNATION
The liquid aroclor compounds, 1221 and 1254, because of their low vapor pressures and fire resistance, are excellent sealants. These nonevaporating fluids have good flow at slightly ele vated temperatures and are chemically stable at elevated temperatures. These liquid aroclor compounds therefore are excellent fluid seals wherever the use of oil would create a fire hazard. In the trough of annealing furnaces, for example, aroclor compounds are dependable, fire-safe roof sealants.
37 0^04463
TOWOLDMONOQ35230
Because of their nonflammability, high resistivity and dielectric strength, and low power factor, the liquid and resinous aroclor compounds are extremely valuable impregnants for many electrical applications. One important use of aroclor 1260. 4465, and 5460 is in wire and cable coatings and as impregnants for braided cotton-asbestos insulation. Their high purity and excellent electrical resistance make aroclor 1254, 5460, and 1268 excellent dielectric seal ants: to close the pores of carbon resistors, and to seal electrical bushings and terminals.
aroclor compounds are essential components of coatings for flameproofing cotton drill for outer garments and for rendering olive-drab canvas fire-retardant, water-repellent, and rotproof for tents, tarpaulins, etc., according to the following formulations:
Flameproofing Formula for Cotton Drill
Ingredients
Urea-formaldehyde resin monomer Catalyst for resin Water
Oil-modified alkyd resin AROCLOR 1254 aroclor 5460 Stoddard solvent
Antimony oxide, 300 mesh or finer
Parts by Weight
9.62 0.40 22.26
3.89 12.00 14.40 25.15
12.28
Dissolve the solids in the indicated solvents, add the aqueous solution (A) to the hydrocarbon solution (B) with stirring, and then disperse the antimony oxide in the emulsion.
Fire-Retardant, Water-Repellent, Rot-Proof Canvas Coating
Ingredients
Modified phenol-formaldehyde resin aroclor 1254 aroclor 5460 Antimony Oxide Tricresyl Phosphate Aluminum Stearate
Copper Xaphthenate(8% copper) Mica, ground Limestone, ground Iron Oxide, yellow Chrome Orange V M & P Naphtha
Per Cent
4 16
4 8 1.5 0.5
8 3 6 7 2 40
obo<mA
TOWOLDMONOQ35231
PROPERTIES OF THE AROCLOR COMPOUNDS
^ MOBILE LIQUIDS
4 VISCOUS LIQUIDS
SOFT RESINS
BRITTLE RESINS
* {"
I
Numerous applications for the aroclor compounds have been suggested and described in the preceding sections of this bulletin. Their success depends on the general inertness of the com pounds and on the range and gradation of their physical properties, including physical state, density, viscosity, melting and boiling points, volatility, and solubility. These and other proper ties, as well as handling and shipping information, are presented in detail in the remainder of the bulletin.
39
0509965
TOWOLDMON0035232
SOLUBILITY
The aroclor liquids and resins are readily soluble in most common organic solvents and dry* mg oils. Although all aroclors are insoluble in water, the hard, crystalline materials are gen erally less soluble than the liquids and softer resins. Solubilities of some aroclor plasticizers are shown in Table XIII.
TABLE XIII --SOLUBILITIES OF AROCLOR PLASTICIZERS IN VARIOUS SOLVENTS
SoUrf
Add Acetk Add Okie Add BentofcAdd
Aldehyde 40% Fomaldehyd* FurfunI
Amine Aniline Pyridine
Chloro derivatlvce Any! chloride*--mixed Carbon Tetrachloride Chloroform Dkhlorcthylene Ethylene Dichloride
Mooocblorebcmcne Orthodicblorobeueoe Tctrachlonthana Tricblotethene Trichloretbylene Drying 00
Tung Oil Uneeed Oil Eater Amyl Acetete Butyl Aceute Cellotolve Acetate ''/ Cottoeated Oil * Dlbutyl Phtbalate Diethyl Phthalaie Ethyl Acetete Ethyl Lactate Ethyleoe Glycol Diacetate Methyl Aceute Tricraeyl Pboephate Ethff: Ethyl Ether Ether Alcohol >CttbU! ^ Celloeolve Dkibylene Glycol p^'.Dihydrosy Ethyl Ether Hydrocarhoo Benaene
Gaaollnt Reroeeae Mineral Splriu Paraffin Pina Oil Toluene Turpentine Xylene Hydroiy derivatives Amyl Alcohol Butyl Alcohol Ethyl Alcohol (4-A) Glycerin* Methyl Akahol Phenol--90% Ketone: Acetone MbceUaneoui Carbon Disulfide Nilrobeawne Water
AROCLOR 1241
2S`C
Hot
AROCLOR 1241
2E*C
Hot
S ----
s S ---- 104) ",c __ 100 e __
I vs
s 132.S
VS
s 440 **c
I VS
__ --
1 VS
__ __
ssss s s ss ss ss ---- ----
ss s s ssss -- __ __ __
ssss ssss ss s s
ssss s s $ $
ss s s ssss ssss ssss ssss ss5s ss $s ssss ss ss ssss ss ss ssss
214 "-C
s -- 16.9 *C
307 ***c
s --
19 **c
vs s --
ss
vs s --
ss
vs vs vs vs
Ul"-c
s vs vs V$
VS vs
vs
vs
s
%
vs
vs
vs
s s
23J ***9
1
42.S "*c 194
S
s s MO"*0
I
M.S***
s s
ss ss
1I
vs vs vs vs 20***c vs vs vs
vs
_ __ __
I -- -- _
--_
1
vs vs vs vs s vs vs vs
vs
__ __ __
I __ __ __
__ __
I
AROCLOR 12S4
25*C
Hot
AROCLOR 4461
Cold
Hot
AROCLOR 0460 2I*C
S s SS s
$s
vs
--------
-- -- --
I vs vs
ss H4*c 42S***C
vs
vs vs
vs
vs vs
--
__ --
s s s -- s s _ s s s
s s
s s s s s s s s s s s s
s -- ,*~c
s
-- s s -- s s
$ s
s s $ s s $ s s s s s s
2S9--C s --
10 --c
vs vs vs vs vs vs vs vs vs vs
vs vs
vs vs vs s s
vs vs
ss
ss
$ ss
vs vs vs vs vs vs vs vs vs vs
vs vs
vs vs vs vs vs vs vs vs vs s s _
__
-- __
-- 1S6 -- -- -- -- -- -- __ __
__
--
__ __ __ _ __ __ __ __ __ __ __ __
__ __ _ __
vs vs vs vs __ s vs vs
vs
$
s
10"* 1
IS~
ss s
% %
I
VS vs vs vs s s vs vs
vs
s s
2S"*C 1
22-2***C
s s
s
$ I
vs vs vs vs so s vs vs
vs
ss ss
ss s s
vs vs
vs vs vs vs s s vs vs
vs
s s
--. I __
s s
vs
__
I
143
___
_ __ __
142 _
m
__ __ __
___
260
__
I--Insoluble SS--Slightly Solu k S--Solubk VS--Vcry Soluble, Figure* show grant of abocum per 100 miUititen of *olvent at 2$*Cunlea* otherwise indicated.
Oi
TOWOLDMONOQ35233
TABLE XIV-- MONSANTO SPECIFICATIONS* AND GENERAL PHYSICAL
I
PROPERTY Appearance Color, maximum
AROCLOR 1221
6
Colorless, clear, mobile oil
100 APHA
AROCLOR 1232
6
Practically colorless mobile oil
100 APHA
AROCLOR 1242
6
Practically colorless, clear, mobile oil
100 APHA
AROCLOR 1248
-6
Colorless to light yellowgreen, clear, mobile oil
100 APHA
AROCLOR 1254
0
Light-yellow viscous oil
100 APHA
Chlorine, per cent
20.5-21.5
Acidify, mg KOH/g, maximum
0.014
Moisture, ppm, maximum
Ava. Coefficient of Expansion, cc/cc/C 0.00071 (13**40*0
Specific Gravity
1.182-1.192 (25*/15.5*C)
Density, pounds per gallon, 25C
9.85
Distillation Range, C, corrected (ASTM D-20, modified)
Evaporation Loss, %, 100C, 6 hours (ASTM D-6, mod.) 163C, 5 hours
275-320 1.0-1.5
Rash Point (Cleveland Open Cup), C 141-150 F 286-302
Rre Point (Cleveland Open Cup), >
C 176 oF 349
Pour Point (ASTM E-97),
C 1 (crystals) F 34 (crystals)
Softening Point (ASTM E-28),
C F
Refractive Index, n
1.617-1.618
Viscosity, Seconds Saybolt Universal
(ASTM D-88)
100F (37.8C)
130F (54.4C)
210F (98.9C)
38-41 35-37 30-31
31.5-32.5 0.014
0.00073 (25**100C) 1.270-1.280 (23*/l 5.5*C) 10.55 290-325
1.0-1.5
152-154 305-310 238 460 -35.5 --32
1.620-1.622
44-51 39-41 31-32
42 0.010 50 0.00068 (25*'65C) 1.381-1.392 (25*/15.5*C) 11.50 325-366
0-0.4 3.0-3.6 176-180 348-356
NONE**
-- 19 2
1.627-1.629
82-92 49-56 34-35
48 0.010 50 0.00070 (25*-65'C) 1.405-1.415 (65V15.5*C) 12.04 340-375
0-0.3 3.0-4.0 193-196 379-384
NONE
--7 19.4
1.630-1.631
185-240 73-80 36-37
54 0.010 50 0.00066 (25,'65"C) 1.495-1.505 (65*/l5.5*C) 12.82 365-390
0-0.2 1.1-U
NONE
NONE 10 50
1.639-1.641
1800-2500 260-340 44-48
*Dau in red indicate Monsanto Chemical Company specifications. NONE indicates no flash or fire up to boiling point.
41
0509967
TOWOLDMONOQ35234
PROPERTIES OF REPRESENTATIVE AROCLOR PLASTICIZERS AND RESINS
c
?
AROCLOR 1260
Ught-yellow, clear,soft, sticky resin
150 APHA
60 0.014 50 0.00067 (20*-100*C) 1.555-1.566 (90713.5*0 13.50 . 385-420
0-0.1 0.5-0.8
NONE
NONE 31 88
1.647-1.649
AROCLOR 1262
AROCLOR 5442
<>
Light-yellow soft, sticky clear resin (viscous liquid)
Yellow, clear, sticky resin
150 APHA
2 NPA (molten)
61.5-62.5 0.014
42 0.05
0.00064 (25*'65C) 1.572-1.583 (W7!5.5*C) 13.72 390-425
0-0.1 0.S-0.6 NONE
NONE 35-38 99
1.6501-1.6517
0.00123 (25*-99*C)
1.470 (25725`C)
12.24
215-300 (4 mm. Hg)
0.01 0.2
247 477
350 662
46 115
46-52 115-126
AROCLOR 4465
O
Light-yellow, clear, brittle resin
2 NPA (molten) 65 0.05
0.00061 (25*-65"C) 1.670 C5V25'C) " 13.91 230-320 (4 mm. Hg) 0-0.02 0.2-0.3
NONE
NONE
60-66 140-151
1.664-1.667
AROCLOR 2565
0
Black, opaque, brittle resin
65 1.4
0.00066 (25*-65C) 1.734 (25725*0 14.44
0.2-0.3 NONE
NONE
66-72 149-162
AROCLOR 5460
Clear, yellowto-amber, brittle resin
2 NPA (molten)
58.5-60.6
0.05
.
0.00179 (25M24"C) 1.670 (25725*C) 13.91 280-335 (5 mm. Hg)
0.03
NONE
NONE
98-105.5 208-222
1.660-1.665
AROCLOR 1268
o
White to off-white powder
1.5 NPA (molten) 68 0.05
0.00067 (20MOO*C) 1.804-1.811 (25725*C) 15.09 435-450
0-0 06 0.1-0.2
NONE
NONE
150-170 (hold 302-338 point)
3200-4500 72-78
600-850 (160*F; 7I*C>
86-100
300-400
90-150 (266*F; 130*0
i
TOWOLDMONOQ35235
DENSITY
All the aroclor compounds are heavier than water, a valuable property for many applications. Densities are shown in Figure Z.
Absolute Density, g ./cc.
Fig. 2. DENSITIES OF AROCLOft^AT VARIOUS TEMPERATURES
SPECIFIC VOLUME
The specific volume of aroclor 1248 at different temperatures is as follows:
Temperature (F)
0 100 200 300 400' 500 600
AROCLOR 1248 Specific Volume (ml/g)
0.674 0.699 0.726 0.755 0.790 0.828 0.870
43
0509969
TOWOLDMONOQ35236
VOLATILITY The low vaporization loss of aroclor compounds is indicated in Table XV.
TABLE XV--VAPORIZATION RATES OF AROCLOR COMPOUNDS
Plasticizer (Surface area: 12.28 sq. cm.)
AROCLOR 1221 aroclor 1232 AROCLOR 1242 AROCLOR 1248 Clorafin*-42~S Bioctyl phthalate Dutrex** 25 AROCLOR 1254 Dutrex 20 AROCLOR 1262 AROCLOR 1260 AROCLOR 4465 AROCLOR 5442 AROCLOR 5460 Tricresyl phosphate
-
Wt. Lots (9)
0.5125 0.2572 0.0995 0.0448 0.0745 0.0686 0.0256 0.0156 0.0047 0.0059 0.0026 0.0064 0.0059 0.0052 0.0010
Exposure at I003C
(hr.)
24 24 24 24 48 48 24 24 24 24 24 72 72 72 24
Vaporization Rate
(g/sq. cm./hr.)
0.00174 O.OOOS74 0.000338 0.000152 0.000126 0.000117 0.000087 0.000053 0.000016 0.000013 0.000009 0.000007 0.000004 0.000004 0.000003
U is concluded that the vaporization rates of aroclor plasticizers -- especially the most wide ly used 1254 and 1260 -- compare most favorably with the similar constants of other plasti cizers selected specifically for these tests because of their low vaporization rates.
'Trademark of Hcrcuki Powder Co. "Trademark of She)) Oil Co.
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VAPOR PRESSURE
The vapor pressures of several aroclor compounds are indicated in Figure 3 over the temp*
erature range 150 to 300C.
. y x 10s T, K
c
The estimated vapor pressures of several aroclor plasticizers at 100F shown in the follow ing table were determined by extrapolation from the values shown in Figure 3.
Approximate Vapor Pressure of AROCLOR&x Estimated at 100 F (37.8 CJ
AROCLOR 1232................... ..............0.005 mm. Hg AROCLOR 1242................... ..............0.001 mm. Hg AROCLOR 1248..................................0.00037 mm. Hg AROCLOR 1254................... ..............0.00006 mm. Hg
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VISCOSITY The viscosities of the aroclor plasticizers vary according to whether the base material is a bi phenyl or a polyphenyl and on the degree of chlorination. In general the low-chlorinated bi phenyls have the lowest viscosities (Figure -4).
Temperature, F Fig. 4--VISCOSITY RANGES OF SOME AROCLOR*! STABILITY Toward Alkalies The aroclor plasticizers are remarkably resistant to the action of either hydrolyzing agents or high temperature. They are not affected by boiling with sodium hydroxide solution. Toward Acids No hydrogen chloride was evolved when aroclor 1254 was stirred with an equal volume of 10 per cent sulfuric acid for 150 hours. Even after prolonged treatment (255 hours) with con centrated sulfuric acid only a slight trace (too small for quantitative measurement) of hydrogen chloride was evolved. Toward Heat Because of their stability to heat, the aroclor compounds are useful heat-transfer media. aroclor 1254 and particularly the less viscous aroclor 1248 are recommended for this pur pose, because they may be heated up to 315C (600F) in a closed system for long periods without appreciable decomposition, and because they are non-flammable. .
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Toward Light
The aroclor plasticizers have good light stability in heavily pigmented compounds and fair light stability in clear formulations. The materials become discolored, but their physical prop* erlies are not degraded. For critical applications, incorporation of a small amount of a light screening agent greatly improves light stability at reasonable cost. The following data show that as little as 0.01 per cent Tittuvin P in aroclor 1254 nearly doubles the service life in the 50*to-100-hour range and that 0.1 per cent Tinuvin P results in a 10-fold improvement.
Tinuvin P Concentration 1%)
0 0.01 0.05 0.1
Fade-Ometer Exposure (hours)
0 50 100 150 500 Color (Gardner Units)
0 5' 10 11
14
0 1 5 7 14
0 0 3 4 11
00 1 2 6
Toward Oxidation
When aroclor compounds are heated to 140 C with oxygen in a bomb at 250 psi, no evidence of oxidation occurs, as judged by absence of sludge formation or increased acidity. Also, no increase in acidity occurred after 4 hours heating with air at 260C and 210 psi.
NONFLAMMABILITY
The viscous aroclor liquids and the resins do not support combustion when heated alone, even at their boiling points - above 350C. Most of the aroclor compounds flux readily with resinous and pitch-like materials to give products with decreased fire hazard, aroclor products incorporated in plastic products and rubber foams retard the rate of burning.
NON-DRYING PROPERTIES AND THERMOPLASTICITY
The aroclor compounds are non-drying. When exposed to the air, even in thin films, no noticable oxidation or hardening takes place. Despite this property, aroclor plasticizers do not retard the drying rate of lacquer films. Quick-drying varnishes and paints may be made with aroclor resins without affect on drying characteristics.
The aroclor plasticizers are permanently thermoplastic. They apparently undergo no conden sation or hardening upon repeated melting and cooling. Clear aroclor resins are available with softening points up to 105CC. The opaque crystalline solids are available with melting points up to about 160C.
ELECTRICAL PROPERTIES
The electrical properties of aroclor compounds are extremely interesting: high resistivity and dielectric strength and low power factor, as listed in Table XVI. The dielectric constants of the various aroclor compounds range from 3.3 to 4.9 at 100 C and 1000 cycles.
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TABLE XVI--ELECTRICAL PROPERTIES OF AROCLOR^
AROCLOR
Dielectric
Constant
(ASTM D-150-47T)
1000 cycles
25C
I00C
1232 1242 1248 1254 1260
5.7 5.8 5.6 S.O 4.3
4.6 4.9 4.6 4.3 3.7
1268 5442 5454 5460 4465
2.5 3.0 2.7 2.5 2.7
4.9 4.2 3.7 3.3
Volume Resistivity (ASTM D-257-46) 500 Volts D.C.,
I00C (ohm-cm.)
Dielectric Strength (ASTM D-149-44)
(KV)
Power Factor (ASTM D-I50-47T) 1000 cycles, I003C
(%)
Above 500 x 10n Above 500 x 10" Above 500 x 10 Above 500 x 10*
Above 35 Above 35 Above 35 AbQve 35
Below 0.1 Below 0.1 Below 0.1 Below 0.1
Above 500 x 10s
HOW TO EMULSIFY AROCLORj
Emulsions of aroclor plasticizers can be made simply in several ways: the method can be selected to suit the particular aroclor and the type of formulation in which it will be used.
Emulsifiable Concentrated Stock Solutions of AroclorV^
Stock solutions made according to the following formulation are readily emulsified with water. The amount of toluene may be increased as needed to dissolve the more resinous aroclor compounds.
Ingredient
Parts by Weight
aroclor
Toluene Isopropanol Sterox* CD Santomerse*
(nonionicemulsifier) #3(anionicwelting agent)
79 16.70 3.55 1.00 0.75
Emulsifying Liquid Aroclors
Ingredient
Portion 1 AROCLOR 1254 Oleic Acid
Parts by Weight
100 4
Portion 2
Water
--
Ammonium Hydroxide (28^)
Lustrex* X-810 Polystyrene
100 2 2
Santomcnc ,nd Luif'cx: Monunto Chemical Company Ttadvmarka. Rcpiicrcd in U. S. Patent O/fict.
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Mix the polystyrene and ammonium hydroxide in warmed water with vigorous agitation. Mix the aroclor 1254 and oleic acid, heat to 45 C, and agitate vigorously. Maintain the 45 C temperature and agitation, and slowly add in the aqueous portion (Portion 2). Continue agitation for one-half hour until phase inversion is complete.
Emulsifying Viscous Aroclors
Ingredient
Portion 1 aroclor 1254 Stearic Acid
Portion 2 Water Triethanolamine
Parts by Weight
64 4
32
1
Heat the aroclor to a workable viscosity (ISO0 F or higher) and stir in the stearic acid thoroughly. Heat the water almost to boiling (207 F) and stir in the triethanolamine thorough ly. Pour the AROCLOR-stearic acid portion into the water-triethanolamine portion with vigorous agitation. Process the combined portions either with a high-speed emulsifying stirrer or through a colloid mill.
___________________________________________________ _
It DERMATOLOGY AND TOXICOLOGY
At ordinary temperatures the aroclor chlorinated polvphenyls have not presented industrial
I toxicological problems. The hazard of potential toxic exposure varies with their volatility: the lower-chlorinated ones, being more volatile, present more of a potential problem from the stand point of both inhalation and skin contact. When aroclor compounds are used at elevated temperatures, engineering controls must be applied, either by the use of closed systems or by effective local-exhaust ventilation together with genera! workroom exhaust.'
Inhalation tests on animals indicate that the maximum safe concentration of vapor is in the range of from 0.5 to 1.0 milligram of the lower-chlorinated aroclor compounds per cubic meter of air. The threshold limits (maximum allowable concentration for an 8-hour working day) set by the American Conference of Government Hygienists are 1.0 milligram of the lowerchlorinated aroclor compounds per cubic meter of air and 0.5 milligram of the more-highlychlorinated compounds, such as aroclor 1254, per cubic meter of air.
Schwartz patch tests on 200 volunteers showed that neither aroclor 1254 alone when applied to gauze nor a polyvinyl chloride film containing 11.5-weight-per cent aroclor 1254 was a pri mary irritant or a sensitizer. Canvas coated with an oil-modified alkyd resin (17-weight-per cent of the paint-film solids and 7-weight-per cent of the painted fabric was aroclor 5460) likewise did not produce primary skin irritancy or sensitization according to the same Schwartz technique.
Continuous or repeated skin contact with the aroclor compounds must be avoided because of the possible occurance of a condition called chloracne. Although reports of this condition caused by aroclor compounds are rare, it can be produced by excessive skin contact.
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i, SAFE HANDLING
Vapor of the liquid aroclor compounds at room temperature should not be breathed in a con fined space, and no vapor of any aroclor compound evolved at elevated temperatures should be allowed to be dispersed into the general workroom.
Continuous or repeated skin contact with the aroclor compounds must be avoided by the use of gloves and protective garments. If any aroclor is spilled on the skin, the skin should be washed in the usual maimer with a soap solution.
A bum caused by contact with a hot aroclor should be treated like any ordinary bum. aroclor adhering to the burned area need not be removed immediately, unless treatment of the burn demands it, in which case either soap and water or repeated washings with a vegetable oil are recommended.
______
L SHIPPING
Freight Classification aroclor 1221,1243, 1242,1248, 1254,1260,1262
Rail Classification aroclor 1268, 2565, 4465, 5442, 5460
Truck Classification aroclor 1268, 2565 aroclor 4465, 5442, 5460
Shipping Regulations Standard Containers
AROCLOR 1221
aroclor 1232
AROCLOR 1242, 1248, 1254,1260, 1262
AROCLOR 1268
aroclor 2565, 4465
AROCLOR 5442
--
aroclor 5460 (flaked)
WFWt LSI SM.11/0i 1M-S/S2
Synthetic Resin, Liquid, N01BX
Synthetic Resin, Other Than Liquid, XOIBX
Synthetic Resin, Powder, N'OI Synthetic Resin, Lumps or Solid Mass, KOI None
Tank car, 520-lb. steel drum, 50-lb. can
Tank car, 550-lb. steel drum, 50-lb. can
Tank car, 600-lb. steel drum, 50-lb. can
200-lb. fiber drum, 50-lb. can 500-lb. steel drum, 50-lb. can 450-lb. steel drum, 50-lb. can 100-lb. bag
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