US2391092A - Polystyrene sheet material - Google Patents
Polystyrene sheet material Download PDFInfo
- 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
- Authority
- US
- United States
- Prior art keywords
- polystyrene
- solvent
- solution
- sheet material
- volume
- 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.)
- Expired - Lifetime
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- 239000004793 Polystyrene Substances 0.000 title description 43
- 229920002223 polystyrene Polymers 0.000 title description 43
- 239000000463 material Substances 0.000 title description 18
- 239000002904 solvent Substances 0.000 description 38
- 150000004945 aromatic hydrocarbons Chemical class 0.000 description 10
- 238000005266 casting Methods 0.000 description 8
- 239000010408 film Substances 0.000 description 8
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 7
- CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 7
- 239000008096 xylene Substances 0.000 description 7
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 6
- WVDDGKGOMKODPV-UHFFFAOYSA-N Benzyl alcohol Chemical compound OCC1=CC=CC=C1 WVDDGKGOMKODPV-UHFFFAOYSA-N 0.000 description 6
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 6
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 6
- KBPLFHHGFOOTCA-UHFFFAOYSA-N 1-Octanol Chemical compound CCCCCCCCO KBPLFHHGFOOTCA-UHFFFAOYSA-N 0.000 description 5
- 150000001298 alcohols Chemical class 0.000 description 5
- 239000000203 mixture Substances 0.000 description 5
- 239000011521 glass Substances 0.000 description 4
- ZSIAUFGUXNUGDI-UHFFFAOYSA-N hexan-1-ol Chemical compound CCCCCCO ZSIAUFGUXNUGDI-UHFFFAOYSA-N 0.000 description 4
- 239000002184 metal Substances 0.000 description 4
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 3
- 150000001338 aliphatic hydrocarbons Chemical class 0.000 description 3
- 239000011888 foil Substances 0.000 description 3
- 235000011187 glycerol Nutrition 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000002360 preparation method Methods 0.000 description 3
- YIWUKEYIRIRTPP-UHFFFAOYSA-N 2-ethylhexan-1-ol Chemical compound CCCCC(CC)CO YIWUKEYIRIRTPP-UHFFFAOYSA-N 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- HEDRZPFGACZZDS-UHFFFAOYSA-N Chloroform Chemical compound ClC(Cl)Cl HEDRZPFGACZZDS-UHFFFAOYSA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- 125000001931 aliphatic group Chemical group 0.000 description 2
- -1 aromatic alcohols Chemical class 0.000 description 2
- 235000019445 benzyl alcohol Nutrition 0.000 description 2
- 125000004432 carbon atom Chemical group C* 0.000 description 2
- 229930195733 hydrocarbon Natural products 0.000 description 2
- 150000002430 hydrocarbons Chemical class 0.000 description 2
- 238000000034 method Methods 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- RFFLAFLAYFXFSW-UHFFFAOYSA-N 1,2-dichlorobenzene Chemical compound ClC1=CC=CC=C1Cl RFFLAFLAYFXFSW-UHFFFAOYSA-N 0.000 description 1
- 229920013683 Celanese Polymers 0.000 description 1
- 238000005219 brazing Methods 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 150000008280 chlorinated hydrocarbons Chemical class 0.000 description 1
- MVPPADPHJFYWMZ-UHFFFAOYSA-N chlorobenzene Chemical compound ClC1=CC=CC=C1 MVPPADPHJFYWMZ-UHFFFAOYSA-N 0.000 description 1
- HPXRVTGHNJAIIH-UHFFFAOYSA-N cyclohexanol Chemical compound OC1CCCCC1 HPXRVTGHNJAIIH-UHFFFAOYSA-N 0.000 description 1
- XCIXKGXIYUWCLL-UHFFFAOYSA-N cyclopentanol Chemical compound OC1CCCC1 XCIXKGXIYUWCLL-UHFFFAOYSA-N 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 239000000975 dye Substances 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 230000001151 other effect Effects 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 239000004014 plasticizer Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000005846 sugar alcohols Polymers 0.000 description 1
- 210000004243 sweat Anatomy 0.000 description 1
- 239000010409 thin film Substances 0.000 description 1
- ZIBGPFATKBEMQZ-UHFFFAOYSA-N triethylene glycol Chemical compound OCCOCCOCCO ZIBGPFATKBEMQZ-UHFFFAOYSA-N 0.000 description 1
- KJIOQYGWTQBHNH-UHFFFAOYSA-N undecanol Chemical compound CCCCCCCCCCCO KJIOQYGWTQBHNH-UHFFFAOYSA-N 0.000 description 1
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
- C08J3/00—Processes of treating or compounding macromolecular substances
- C08J3/02—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques
- C08J3/09—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids
- C08J3/091—Making 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
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions 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
-
- 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
- C08J2325/02—Homopolymers or copolymers of hydrocarbons
- C08J2325/04—Homopolymers or copolymers of styrene
- C08J2325/06—Polystyrene
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.
Landscapes
- 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
Priority Applications (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| 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 |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US446377A US2391092A (en) | 1942-06-09 | 1942-06-09 | Polystyrene sheet material |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2391092A true US2391092A (en) | 1945-12-18 |
Family
ID=23772360
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US446377A Expired - Lifetime US2391092A (en) | 1942-06-09 | 1942-06-09 | Polystyrene sheet material |
Country Status (2)
| Country | Link |
|---|---|
| US (1) | US2391092A (en) |
| GB (1) | GB567985A (en) |
Cited By (7)
| 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 |
-
1942
- 1942-06-09 US US446377A patent/US2391092A/en not_active Expired - Lifetime
-
1943
- 1943-04-30 GB GB6887/43A patent/GB567985A/en not_active Expired
Cited By (7)
| 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 |
Also Published As
| Publication number | Publication date |
|---|---|
| GB567985A (en) | 1945-03-13 |
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