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US2391092A - Polystyrene sheet material - Google Patents

Polystyrene sheet material Download PDF

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Publication number
US2391092A
US2391092A US446377A US44637742A US2391092A US 2391092 A US2391092 A US 2391092A US 446377 A US446377 A US 446377A US 44637742 A US44637742 A US 44637742A US 2391092 A US2391092 A US 2391092A
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United States
Prior art keywords
polystyrene
solvent
solution
sheet material
volume
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Expired - Lifetime
Application number
US446377A
Inventor
Horback William
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Celanese Corp
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Celanese Corp
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Priority to US446377A priority Critical patent/US2391092A/en
Priority to GB6887/43A priority patent/GB567985A/en
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Publication of US2391092A publication Critical patent/US2391092A/en
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    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/02Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
    • C08J3/09Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids
    • C08J3/091Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids characterised by the chemical constitution of the organic liquid
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00Compositions 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 a halogen; Compositions of derivatives of such polymers
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
    • C08J2325/00Characterised 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
    • C08J2325/02Homopolymers or copolymers of hydrocarbons
    • C08J2325/04Homopolymers or copolymers of styrene
    • C08J2325/06Polystyrene

Definitions

  • This invention relates to the preparation of fllms'or foils, and relates more particularly to the preparation of thin film or foil having a basis of polystyrene.
  • Polystyrene film or foil hereinafter referred to as sheet material, is usually prepared by casting a solution of polystyrene in a hydrocarbon solvent such as benzene, toluene, xylene, or mixtures thereof on to a glass or metal surface and stripping the resultant sheet material from the casting surface.
  • a hydrocarbon solvent such as benzene, toluene, xylene, or mixtures thereof
  • polystyrene sheet material prepared in this manner does not easily strip from the casting surface; tearing and crazing difficulties being often encountered. It is, accordingly, an important'object of this invention to provide a process for the production of polystyrene sheet material which will be free from the foregoing and other disadvantages and which will be especially simple and inexpensive in operation.
  • Another object of this invention is the provision of an improved solution for use in the preparation of polystyrene sheet material which may be stripped from the casting surface without difiiculty and without harmfully affecting the product.
  • the polystyrene may be employed in accordance with my invention.
  • the alcohols which I have found to give the optimum results are aliphatic monohydric alcohols containing at least five carbon atoms such as my] alcohol, hexanol, octyl alcohol, undecanol and their isomers, polyhydric alcohols such as ethylene glycol, triethylene glycol and glycerlne, and aromatic alcohols such as cyclopentanol, cyclohexanol and benzyl alcohol.
  • non-solvent alcohol may be employed in my process in amounts ranging from-about 0.5% to 25% or more, based on the volume of the aromatic hydrocarbon or .de-.-
  • aromatic hydrocarbons such as benzene, toluene, xylene or mixtures thereof may be employed as solvents for the polymay also be employedas solvents, such as ethylene dichloride, chloroform and nuclear chlorinated hydrocarbons such as monochlorbenzene, dichlorbenzene or mixtures thereof.
  • the sheet forming-solution may contain dyes
  • pigments plasticizers or other effect or modifying agents.
  • I prepare the sheet forming solution by dissolving the polystyrene in a solvent medium containing from 75 to 99 parts of the aromatic hydrocarbon and from 25 to 1% of the non-solvent alcohol, the ratio of polystyrene to solvent medium being from 1:14)
  • the solution of polystyrene in the solvent medium is then cast upon a suitable casting surface, the solvent removed by subjecting the sheet material, while on the casting surface, preferably to elevated temperatures, and then stripping the sheet material from the casting surface.
  • Example I A solution is prepared by dissolving 20 parts by-weight of polystyrene in 80 parts by weight of a solvent medium containing 97% by volume of xylene and 3% by volume of octyl alcohol (2- ethyl hexanol) This solution is cast on a metal plate and on a glass plate and the solvent caused to evaporate. Uniform, clear films of polystyrene are'obtained, which films easily strip from the plates without tearing or crazingJ'
  • a solution is prepared by dissolving 20 parts by weight of polystyrene in parts by weight of a' solvent medium containing by volume of xylene and 5% by volume of glycerine. This solution is cast on a metal plate and on a glass plate and the solvent caused to evaporate. Uniform,
  • Example III solvent medium consisting essentially of a sub- A solution is prepared by dissolving 20 pa ts by weight of polystyrene in 80 parts by weight of a solvent medium containing 90% by volume of xylene and 10% by volume of benzyl alcohol. This solution is-cast on a metal'plate and on a glass plate and the solvent caused to evaporate. Uniform films of polystyrene are obtained, which films easily strip from the plates without tearing or crazing.”
  • the films cast on the plates were 0.001" in thickness and were seasoned for two hours at 140 0., although the drying or removal of solvent may be carried out at room temperature.
  • polystyrene material comprising polystyrene dissolved in a solvent medium consisting essentially of a substance, selected from the group consisting of aromatic hydrocarbons, chlorinated aliphatic and aromatic hydrocarbons, and mixtures thereof, as solvent for the polystyrene, and from 1 to 5%, based on the volume of the solvent, of an alcohol which is a non-solvent for the polystyrene, said ing at least 5 carbon atoms, liquid polyhydrio alcohols and liquid aromatic alcohols.
  • solvent medium consisting essentially of a substance, selected from the group consisting of aromatic hydrocarbons, chlorinated aliphatic and aromatic hydrocarbons, and mixtures thereof, as solvent for the polystyrene, and from 1 to 5%, based on the volume of the solvent, of an alcohol which is a non-solvent for the polystyrene, said ing at least 5 carbon atoms, liquid polyhydrio alcohols and liquid aromatic alcohols.
  • alcohol being selected from the group consisting of liquid aliphatic monohydric alcohols contain- 2.
  • Solution for use in preparing polystyrene material comprising polystyrene dissolved in a stance, selected from the group consisting of aromatic hydrocarbons, chlorinated aliphatic and aromatic hydrocarbons, and mixtures thereof, as
  • solvent for the polystyrene and from 1 to 5%, based on the volume of the solvent, of hexanol.
  • Solution for use in preparing polystyrene material comprising polystyrene dissolved in a solvent medium consisting essentially of an aromatic hydrocarbon, as solvent for the polystyrene, and from 1 to 5%. based on the volume oi the solvent, of octyl alcohol.
  • Solution for use in preparing polystyrene material comprising polystyrene dissolved in a solvent medium consisting essentially of xylene, as solvent for the polystyrene, and from 1 to 5%, based on-the volume of the solvent, of octyl alcohol.
  • Solution for use in preparing polystyrene material comprising polystyrene 'dissolved in a solvent medium consisting essentially 'ofxylene, as solvent for the polystyrene, and from 1 to 5%, based on the volume of the solvent, of glycerine.
  • Solution for use in preparing polystyrene material comprising polystyrene dissolved in a solvent medium consisting of 97% .by volume of l xylene and 3% by volume. of octyl alcohol.

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  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Dispersion Chemistry (AREA)
  • Manufacture Of Macromolecular Shaped Articles (AREA)

Description

Patented Dec. 18, 1945 UNITED STATES PATENT OFFICE POLYSTYRENE SHEET MATERIAL William Horback, Newark, N. 1., asslgnor to Celanese Corporation of' America, a corporation of Delaware No Drawing. Application June 9, 1942,
v Serial No. 446,377
8 Claims. (o1. zoo-s2) This invention relates to the preparation of fllms'or foils, and relates more particularly to the preparation of thin film or foil having a basis of polystyrene.
Polystyrene film or foil, hereinafter referred to as sheet material, is usually prepared by casting a solution of polystyrene in a hydrocarbon solvent such as benzene, toluene, xylene, or mixtures thereof on to a glass or metal surface and stripping the resultant sheet material from the casting surface. However, polystyrene sheet material prepared in this manner does not easily strip from the casting surface; tearing and crazing difficulties being often encountered. It is, accordingly, an important'object of this invention to provide a process for the production of polystyrene sheet material which will be free from the foregoing and other disadvantages and which will be especially simple and inexpensive in operation.
Another object of this invention is the provision of an improved solution for use in the preparation of polystyrene sheet material which may be stripped from the casting surface without difiiculty and without harmfully affecting the product.
Y styrene in preparing the sheet forming solution, halogenated aliphatic or aromatic hydrocarbons Other objects of this invention will appear from the following detailed description and will be pointed out more particularly in the claims;
I have found that highly satisfactory, clear, flexible and easily stripping sheet material having a basis of polystyrene may be prepared by cast-- ing on to a surface a solution of polystyrene in a suitable solvent such as an aromatic hydrocarbon to which has been added a relatively small proportion of an alochol which is substantially a non-.-
. substantially so, for the polystyrene may beemployed in accordance with my invention. How-'- ever, the alcohols which I have found to give the optimum results are aliphatic monohydric alcohols containing at least five carbon atoms such as my] alcohol, hexanol, octyl alcohol, undecanol and their isomers, polyhydric alcohols such as ethylene glycol, triethylene glycol and glycerlne, and aromatic alcohols such as cyclopentanol, cyclohexanol and benzyl alcohol.
All of these alcohols are compatible with the polystyrene, but where too great an amount of 4 the alcohol is employed it has a tendency to sweat out, or exude, from the sheet material, causing some blushing. While the non-solvent alcohol may be employed in my process in amounts ranging from-about 0.5% to 25% or more, based on the volume of the aromatic hydrocarbon or .de-.-
rivative thereof used as solvent for the polystyrene, with good results, I prefer to add from 1 to 5% of alcohol tothe solvent.
While, as stated above, aromatic hydrocarbons such as benzene, toluene, xylene or mixtures thereof may be employed as solvents for the polymay also be employedas solvents, such as ethylene dichloride, chloroform and nuclear chlorinated hydrocarbons such as monochlorbenzene, dichlorbenzene or mixtures thereof.
The sheet forming-solution may contain dyes,
pigments, plasticizers or other effect or modifying agents.
In accordance with my invention, I prepare the sheet forming solution by dissolving the polystyrene in a solvent medium containing from 75 to 99 parts of the aromatic hydrocarbon and from 25 to 1% of the non-solvent alcohol, the ratio of polystyrene to solvent medium being from 1:14)
The solution of polystyrene in the solvent medium is then cast upon a suitable casting surface, the solvent removed by subjecting the sheet material, while on the casting surface, preferably to elevated temperatures, and then stripping the sheet material from the casting surface.
In order further to illustrate my invention, the following examples are given, it being understood, however, that the examples are not to'oe construed as limiting the scope of the invention.
Example I A solution is prepared by dissolving 20 parts by-weight of polystyrene in 80 parts by weight of a solvent medium containing 97% by volume of xylene and 3% by volume of octyl alcohol (2- ethyl hexanol) This solution is cast on a metal plate and on a glass plate and the solvent caused to evaporate. Uniform, clear films of polystyrene are'obtained, which films easily strip from the plates without tearing or crazingJ' Example II A solution is prepared by dissolving 20 parts by weight of polystyrene in parts by weight of a' solvent medium containing by volume of xylene and 5% by volume of glycerine. This solution is cast on a metal plate and on a glass plate and the solvent caused to evaporate. Uniform,
clear films of polystyrene are obtained, which films easily strip from the plate without tearing or brazing! I a Example III solvent medium consisting essentially of a sub- A solution is prepared by dissolving 20 pa ts by weight of polystyrene in 80 parts by weight of a solvent medium containing 90% by volume of xylene and 10% by volume of benzyl alcohol. This solution is-cast on a metal'plate and on a glass plate and the solvent caused to evaporate. Uniform films of polystyrene are obtained, which films easily strip from the plates without tearing or crazing."
In all the above examples the films cast on the plates were 0.001" in thickness and were seasoned for two hours at 140 0., although the drying or removal of solvent may be carried out at room temperature.
It is to be understood that theforegoing detailed description is merely given by way of illustration and that many variations may be made therein without departing from the spirit of my invention.
Having described my invention, what I desire to secure by Letters Patent is:
1. Solution for use in preparing. polystyrene material, comprising polystyrene dissolved in a solvent medium consisting essentially of a substance, selected from the group consisting of aromatic hydrocarbons, chlorinated aliphatic and aromatic hydrocarbons, and mixtures thereof, as solvent for the polystyrene, and from 1 to 5%, based on the volume of the solvent, of an alcohol which is a non-solvent for the polystyrene, said ing at least 5 carbon atoms, liquid polyhydrio alcohols and liquid aromatic alcohols.
. material, comprising polystyrene dissolved in a.
, alcohol being selected from the group consisting of liquid aliphatic monohydric alcohols contain- 2. Solution for use in preparing polystyrene material, comprising polystyrene dissolved in a stance, selected from the group consisting of aromatic hydrocarbons, chlorinated aliphatic and aromatic hydrocarbons, and mixtures thereof, as
solvent for the polystyrene and from 1 to 5%, based on the volume of the solvent, of hexanol.
3. Solution for use in preparing polystyrene material, comprising polystyrene dissolved in a solvent medium consisting essentially of an aromatic hydrocarbon, as solvent for the polystyrene, and from 1 to 5%. based on the volume oi the solvent, of octyl alcohol.
4. Solution for use in preparing P lystyrene solventmedium consisting essentially of an aro= 'matic hydrocarbon, as solvent for the polystyrene, I
and from 1 to 5%, based on the volume of the solvent, of glycerine.
5. Solution for use in preparing polystyrene material, comprising polystyrene dissolved in a solvent medium consisting essentially of xylene, as solvent for the polystyrene, and from 1 to 5%, based on-the volume of the solvent, of octyl alcohol. I
6. Solution for use in preparing polystyrene material, comprising polystyrene 'dissolved in a solvent medium consisting essentially 'ofxylene, as solvent for the polystyrene, and from 1 to 5%, based on the volume of the solvent, of glycerine. 7. Solution for use in preparing polystyrene material, comprising polystyrene dissolved in a solvent medium consisting of 97% .by volume of l xylene and 3% by volume. of octyl alcohol.
0.. Solution for use. in preparing polystyrene
US446377A 1942-06-09 1942-06-09 Polystyrene sheet material Expired - Lifetime US2391092A (en)

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US446377A US2391092A (en) 1942-06-09 1942-06-09 Polystyrene sheet material
GB6887/43A GB567985A (en) 1942-06-09 1943-04-30 Improvements relating to sheet materials having a basis of polystyrene

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Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2423927A (en) * 1942-05-22 1947-07-15 Standard Oil Co Constant viscosity hydraulic fluid compositions
US2438446A (en) * 1945-05-25 1948-03-23 Standard Oil Dev Co Lubricant and hydraulic fluid composition
US2492420A (en) * 1945-07-12 1949-12-27 American Viscose Corp Plasticized copolymers of vinyl chlorides
US2510908A (en) * 1947-03-03 1950-06-06 Dow Chemical Co Adhesive for polystyrene
US2915482A (en) * 1957-04-05 1959-12-01 Dow Chemical Co Depigmenting polymeric compositions with amine settling aids
US2971876A (en) * 1956-12-04 1961-02-14 Bell Telephone Labor Inc Adhesive composition
US3070554A (en) * 1958-07-15 1962-12-25 Dow Chemical Co Depigmenting alkenyl aromatic polymer compositions with certain saline settling aids

Cited By (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2423927A (en) * 1942-05-22 1947-07-15 Standard Oil Co Constant viscosity hydraulic fluid compositions
US2438446A (en) * 1945-05-25 1948-03-23 Standard Oil Dev Co Lubricant and hydraulic fluid composition
US2492420A (en) * 1945-07-12 1949-12-27 American Viscose Corp Plasticized copolymers of vinyl chlorides
US2510908A (en) * 1947-03-03 1950-06-06 Dow Chemical Co Adhesive for polystyrene
US2971876A (en) * 1956-12-04 1961-02-14 Bell Telephone Labor Inc Adhesive composition
US2915482A (en) * 1957-04-05 1959-12-01 Dow Chemical Co Depigmenting polymeric compositions with amine settling aids
US3070554A (en) * 1958-07-15 1962-12-25 Dow Chemical Co Depigmenting alkenyl aromatic polymer compositions with certain saline settling aids

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Publication number Publication date
GB567985A (en) 1945-03-13

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