GB2138819A - Expandable polymeric vinyl aromatic particles - Google Patents
Expandable polymeric vinyl aromatic particles Download PDFInfo
- Publication number
- GB2138819A GB2138819A GB08324647A GB8324647A GB2138819A GB 2138819 A GB2138819 A GB 2138819A GB 08324647 A GB08324647 A GB 08324647A GB 8324647 A GB8324647 A GB 8324647A GB 2138819 A GB2138819 A GB 2138819A
- Authority
- GB
- United Kingdom
- Prior art keywords
- weight
- particles
- blowing agent
- polymeric styrene
- bis
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/16—Making expandable particles
- C08J9/18—Making expandable particles by impregnating polymer particles with the blowing agent
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/02—Halogenated hydrocarbons
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/06—Ethers; Acetals; Ketals; Ortho-esters
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2325/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an aromatic carbocyclic ring; Derivatives of such polymers
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Manufacture Of Porous Articles, And Recovery And Treatment Of Waste Products (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Abstract
An expandable polymeric vinyl aromatic, e.g. poly styrene, particle is provided which contains a blowing agent, 0.1-0.5% bis (allyl ether) of tetrabromobisphenol A and 0.5-2.5% of dibromoethyldibromocyclohexane. The additives can be incorporated during impregnation with the blowing agent or by blending with the expandable particles after impregnation. Molded foamed articles can be produced exhibiting reduced flammability characteristics.
Description
SPECIFICATION
Foamable polymeric styrene particles
This invention relates to foamable polymeric styrene particles, such as foamable polystyrene particles. More particularly, this invention relatesto such foamable particles having increased utility in the manufacture of foamed articles in that such foamed articles exhibit reduced flammability characteristics.
Foamable polymeric styrene particles and the articles produced from such particles are well known in the art. Such articles include insulated building panels, decorative display objects, novelties, cushioning materials, flotation devices, hot or cold beverage containers, portable ice or cooling chests or boxes, etc. The principal utilitarian characteristics of such foamed articles are their light weight and good heat insulation qualities.
The foamable polymeric particles are generally prepared by impregnating the particles with from 1 % to 20% by weight of a suitable expanding or blowing agent such as pentane. In producing the foamed articles, the impregnated particles, or beads, are first subjected to a preexpansion step wherein the beads are heated with steam in an unconfined space to produce a prepuff having a relatively low density. The prepuffed beads are then placed into the desired confined mold and final expansion accomplished with the further introduction of steam, followed by cooling and removal of the molded article.
A prerequisite for the use of foamed articles in certain applications is that such foamed articles must exhibit reduced flammability. This would be particularly true of foamed articles or panels employed in building construction. While the prior art discloses a number of additives that can be employed to reduce the flammability characteristics of foamed articles, there remains much room for further improvement.
It has now been found that finished foamed articles having reduced flammability characteristics are obtained from expandable polymeric styrene particles having incorporated therein a blowing agent, a minor amount of bis (allyl ether) of tetrabromobisphenol A and a minor amount of dibromoethyldibromocyclohexane. It has been-found that in reducing the flammability characteristics of the finished foamed articles, the combination of the two stated additives exhibit a synergistic effect; the reduction in flammability characteristics using the combination of the two additives being greater than the theoretical expected additive effects of the two.
Into a kettle equipped with an agitator was charged 100 parts by weight of water, 2 parts by weight of tricalcium phosphate, .05 parts by weight of sodium dodecylkbenzene sulfonate, 100 parts by weight of polystyrene beads having a bead diameter of about 1 mm. and 8.0 parts by weight of n-pentane. In the examples which follow, the flammability reducing additives of this invention were also charged at this point in the amounts indicated.
The kettle was heated to a temperature of 215"-230"F (102 -110 C) and maintained within this temperature range for 7-10 hours with agitation. The kettle was then cooled to room temperature, the contents acidified with nitric acid, the beads separated from the aqueous medium, washed with water and air dried at room temperature.
For pre-expansion, the beads were placed in a kettle equipped with agitators and means for passing steam through the beads. Prepuffs were formed by passing steam at 5 psig (34 kPa) through the beads for approximately 2 minutes. The prepuff particles had a diameter of approximately 3/16 inch (5 mm.).
To test the qualities and characteristics of the finished molded foamed article, a test mold 6" x 12" x 6" (15 cm. x 30 cm. x 1 5 cm.) was employed. The mold was jacketed to permit steam injection into the contents of the mold. The mold was partially filled with prepuffs, closed and steam passed through the mold at 220 F (104"C) for approximately 10-20 seconds. The molded article was then allowed to cool until capable of removal from the mold.
Samples of molded foamed articles were prepared using the above procedure, with and without the incorporation of the flammability reducing additives of this invention. The following examples illustrate the comparative results obtained.
Examples
To measure the flammability characteristics of finished molded foam articles, using a hot wire a test strip was cut from the molded block prepared as described above. The test strip measured 9" x 4/" x 1/2" (23 cm. x 10 cm. X 1.3 cm.). The test strip was suspended vertically, with its longest dimension in the vertical position. A gas flame approximately 1 /2" (1.3 cm.) long was directed against the test strip approximately 1" (2.5 cm.) above its base. The gas flame was directed against the test strip until the material ignited, and the gas flame then removed.
The vertical (heighth) and horizontal (width) of the burn area were measured and the combination of these two measurements used to establish a burn rating in accordance with
Table 1; rating 1 being excellent and rating 4 failing.
Table 1
Rating Vertical Burn Horizontal Burn 1 from 0 to 10 cm. from 3 to 4 cm.
2 from 10 to 16 cm. from 4 to 6 cm.
3 from 16 to 20 cm. from 6 to 8 cm.
4 greater than 20 cm. greater than 8 cm.
The bis (allyl ether) of terabromobisphenol A employed was an off-white crystalline solid having a molecular weight of 623.9, bromine content of 51.2% by weight and a melting point of 110-1 20'C. The dibromoethyldibromocyclohexane employed was a white crystalline powder having a molecular weight of 428, bromine content of 74% by weight and a melting point of 65-80"C.
Table 2 sets forth the flammability characteristics of molded foamed polystyrene articles containing the flammability reducing additives of this invention compared with molded foamed polystyrene articles containing no additives. In each case the content of the additive is:
Table 2
Example Additive Test Burn Rating 1 None 4 2 0.2% bis(allyl ether) of
tetrabromobisphenol A 4 3 1.0% dibromoethyldibromo
cyclohexane 4 4 0.2% bis(allyl ether) of
tetrabromobisphenol A
and 1.5-2 1.0% dibromoethyldibromo
cyclohexane 5 0.5% bis (allyl ether) of
tetrabromobisphenol A
and 2.1
0.6% dibromoethyldibromo
cyclohexane
Comparing the results of Examples 2 and 3 with the results of Examples 4 and 5, clearly illustrates the synergistic effect of the flammability reducing additives of this invention.
The improved flammability characteristics of expandable polymeric styrene particles discussed herein are realized by incorporating only minor amounts of bis (allyl ether) of terabromobisphenol A and dibromoethyldibromocyclohexane into the polymeric styrene particles. Expandable polymeric styrene particles containing from 0. 1% to 0.5% of bis (allyl ether) of tetrabromobisphenol A and from 0.5% to 2.5% of dibromoethyldibromocyclohexane both by weight of polymeric styrene, are particularly useful. In accordance with the preferred embodiment of this invention, the additives are preferably incorporated into the polymeric styrene particles during the incorporation of the blowing agent. However, advantageous results are also accomplished by external blending of the additives with expandable polymeric styrene particles after first incorporating the blowing agent.This can be carried out by tumbling dried expandable polymeric styrene particles with the desired quantity of the additives.
The invention has been described herein with particular regard to expandable polystyrene particles having incorporated therein a minor amount of the additives of this invention. In its applicability, the invention is not limited to polystyrene as other vinyl aromatic polymers can be employed. These include polymers derived from such vinyl aromatic monomers as vinyl toluene, isopropylstyrene, alpha-methyl-styrene, chlorostyrene, tert.-butylstyrene as well as to copolymers of vinyl aromatic monomers and butadiene, alkyl acrylates, acrylonitrile, etc. As used in the specification and claims the expression "polymeric styrene particles" is meant to include particles of all such polymers and copolymers.
The invention has been described herein using pentane as the blowing agent. The invention is not limited to the use of pentane as other blowing agents can be employed. Suitable blowing agents include butane, isopentane, cyclopentane, hexane, heptane, cyclohexane and the lower boiling halogenated hydrocarbons. Mixtures of the various mentioned blowing agents can also be employed. Expandable polymeric styrene particles usually contain from 1 to 20% by weight of the blowing agent. Impregnation with the blowing agent to produce expandable polymeric styrene particles can be carried out over a wide temperature range, namely, at temperatures ranging from about 140 (60'C) to about 302"F (150"C).
Claims (9)
1. An expandable polymeric styrene particle having incorporated therein a blowing agent, from 0.1% to 0.5% by weight of bis (allyl ether) of tetrabromobisphenol A and from 0.5% to 2.5% by weight of dibromoethyldibromocyclohexane, all percentages being based upon the weight of the polymeric styrene.
2. A particle according to Claim 1, wherein the polymeric styrene is polystyrene.
3. A particle according to Claim 1 or 2, wherein the blowing agent is pentane.
4. Expandable polymeric styrene particles substantially as hereinbefore described with reference to Example 4 or 5.
5. A process for producing expandable polymeric styrene particles which process comprises:
(a) impregnating the polymeric styrene particles with a blowing agent, and
(b) either impregnating the polymeric styrene particles, during impregnation thereon with the blowing agent, with from 0. 1 O/o to 0.5% by weight of bis (allyl ether) of tetrabromobisphenol A and from 0.5% to 2.5% by weight of dibromoethyldibromocyclohexane, or blending from 0. 1% to 0.5% by weight of bis (allyl ether) of tetrabromobisphenol A and from 0.5% to 2.5% by weight of dibromoethyldibromocyclohexane, with the polymeric styrene particles after impregnation with the blowing agent, all said percentages being based upon the weight of the polymeric styrene.
6. A process according to Claim 5, wherein the polymeric styreme is polystyrene.
7. A process according to Claim 5 or 6, wherein the blowing agent is pentane.
8. A process according to Claim 5 substantially as hereinbefore described with reference to
Example 4 or 5.
9. Expanded polystyrene particles whenever produced by the process of any one of Claims 5 to 8.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US06/483,407 US4417003A (en) | 1982-09-24 | 1983-04-08 | Foamable polymeric styrene particles |
Publications (3)
Publication Number | Publication Date |
---|---|
GB8324647D0 GB8324647D0 (en) | 1983-10-19 |
GB2138819A true GB2138819A (en) | 1984-10-31 |
GB2138819B GB2138819B (en) | 1985-10-02 |
Family
ID=23919941
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
GB08324647A Expired GB2138819B (en) | 1983-04-08 | 1983-09-14 | Expandable polymeric vinyl aromatic particles |
Country Status (7)
Country | Link |
---|---|
JP (1) | JPS59189136A (en) |
BE (1) | BE897627A (en) |
CS (1) | CS240977B2 (en) |
DE (1) | DE3333022A1 (en) |
FR (1) | FR2543962A1 (en) |
GB (1) | GB2138819B (en) |
IT (1) | IT1167234B (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPH0791407B2 (en) * | 1990-10-19 | 1995-10-04 | 積水化成品工業株式会社 | Method for producing flame-retardant expandable resin particles |
Family Cites Families (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE1794347B2 (en) * | 1964-11-20 | 1975-05-07 | Chemische Fabrik Kalk Gmbh, 5000 Koeln | Process for the production of flame-retardant and self-extinguishing molded parts from styrene-containing molding compounds |
DE2950098A1 (en) * | 1979-12-13 | 1981-07-09 | Basf Ag, 6700 Ludwigshafen | FLAME-RETARDED STYRENE POLYMERISATE |
US4388418A (en) * | 1982-09-24 | 1983-06-14 | Cosden Technology, Inc. | Foamable polymeric styrene particles |
-
1983
- 1983-08-31 BE BE211426A patent/BE897627A/en not_active IP Right Cessation
- 1983-09-13 DE DE19833333022 patent/DE3333022A1/en not_active Withdrawn
- 1983-09-14 GB GB08324647A patent/GB2138819B/en not_active Expired
- 1983-09-19 FR FR8314829A patent/FR2543962A1/en active Pending
- 1983-09-28 JP JP58178365A patent/JPS59189136A/en active Pending
- 1983-09-29 CS CS837109A patent/CS240977B2/en unknown
- 1983-09-30 IT IT8323088A patent/IT1167234B/en active
Also Published As
Publication number | Publication date |
---|---|
GB8324647D0 (en) | 1983-10-19 |
CS240977B2 (en) | 1986-03-13 |
FR2543962A1 (en) | 1984-10-12 |
IT8323088A0 (en) | 1983-09-30 |
BE897627A (en) | 1984-02-29 |
DE3333022A1 (en) | 1984-10-18 |
GB2138819B (en) | 1985-10-02 |
IT1167234B (en) | 1987-05-13 |
JPS59189136A (en) | 1984-10-26 |
IT8323088A1 (en) | 1985-03-30 |
CS710983A2 (en) | 1985-06-13 |
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Legal Events
Date | Code | Title | Description |
---|---|---|---|
PE20 | Patent expired after termination of 20 years |