US2157049A - Process of treating cast polymeric resin sheets - Google Patents
Process of treating cast polymeric resin sheets Download PDFInfo
- Publication number
- US2157049A US2157049A US137024A US13702437A US2157049A US 2157049 A US2157049 A US 2157049A US 137024 A US137024 A US 137024A US 13702437 A US13702437 A US 13702437A US 2157049 A US2157049 A US 2157049A
- Authority
- US
- United States
- Prior art keywords
- sheet
- mold
- heating
- sheets
- strains
- 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
Links
- 238000000034 method Methods 0.000 title description 13
- 230000008569 process Effects 0.000 title description 12
- 239000002952 polymeric resin Substances 0.000 title description 3
- 229920003002 synthetic resin Polymers 0.000 title description 3
- 238000010438 heat treatment Methods 0.000 description 26
- 239000000463 material Substances 0.000 description 7
- 239000000113 methacrylic resin Substances 0.000 description 7
- 238000011282 treatment Methods 0.000 description 6
- 230000015572 biosynthetic process Effects 0.000 description 5
- 239000012530 fluid Substances 0.000 description 5
- 230000006872 improvement Effects 0.000 description 5
- 229920000642 polymer Polymers 0.000 description 5
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 4
- 125000005395 methacrylic acid group Chemical group 0.000 description 4
- 239000011347 resin Substances 0.000 description 4
- 229920005989 resin Polymers 0.000 description 4
- 239000002904 solvent Substances 0.000 description 4
- 238000012546 transfer Methods 0.000 description 4
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- NIXOWILDQLNWCW-UHFFFAOYSA-N acrylic acid group Chemical group C(C=C)(=O)O NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 3
- 230000009471 action Effects 0.000 description 3
- 239000007788 liquid Substances 0.000 description 3
- 238000006116 polymerization reaction Methods 0.000 description 3
- 125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 description 3
- 229920002554 vinyl polymer Polymers 0.000 description 3
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 3
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 2
- 230000008602 contraction Effects 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 239000003350 kerosene Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical compound CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-M Methacrylate Chemical compound CC(=C)C([O-])=O CERQOIWHTDAKMF-UHFFFAOYSA-M 0.000 description 1
- -1 acrylic ester Chemical class 0.000 description 1
- YNQLUTRBYVCPMQ-UHFFFAOYSA-N alpha-methyl toluene Natural products CCC1=CC=CC=C1 YNQLUTRBYVCPMQ-UHFFFAOYSA-N 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- 238000005266 casting Methods 0.000 description 1
- 238000007598 dipping method Methods 0.000 description 1
- 239000000428 dust Substances 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 125000004494 ethyl ester group Chemical group 0.000 description 1
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 239000002245 particle Substances 0.000 description 1
- PNJWIWWMYCMZRO-UHFFFAOYSA-N pent‐4‐en‐2‐one Natural products CC(=O)CC=C PNJWIWWMYCMZRO-UHFFFAOYSA-N 0.000 description 1
- 229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 239000004926 polymethyl methacrylate Substances 0.000 description 1
- 230000000284 resting effect Effects 0.000 description 1
- 238000007789 sealing Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 230000008719 thickening Effects 0.000 description 1
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C71/00—After-treatment of articles without altering their shape; Apparatus therefor
- B29C71/02—Thermal after-treatment
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C71/00—After-treatment of articles without altering their shape; Apparatus therefor
- B29C71/02—Thermal after-treatment
- B29C2071/022—Annealing
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2033/00—Use of polymers of unsaturated acids or derivatives thereof as moulding material
- B29K2033/04—Polymers of esters
- B29K2033/12—Polymers of methacrylic acid esters, e.g. PMMA, i.e. polymethylmethacrylate
Definitions
- This invention relates to a process of treating cast vinyl and methacrylic resins to avoid the formation of the minute surface cracks that frequently appear when cast objects of these resins 5 are placed in service. It consists in a heat treatment that removes the strains that cause these cracks.
- This process while it provides a means for keeping the mold well filled during polymerization sets up surface strains in those surfaces that contact the rigid side walls. During storage or service the non-uniform release of these strains causes the formation of a myriad of minute cracks, giving the surface an undesirable crazed no appearance.
- the object of this invention is to prevent the formation of these surface cracks.
- sheets can be tested for a. crazing" tendency by subjecting them to the action of solvents or solvent vapors such as acetone, ethyl acetate, and benzene. This is conveniently done by dipping the piece to be tested in the solvent for about ten seconds and then fanning it dry. If the piece being tested contains the surface strains that cause crazing, the action of solvent accelerates the formation of the minute cracks and shows immediately whether the sheet is subject to crazing.
- a test of this kind applied to a test strip cut from a larger sheet either before or after the herein described heat treatment will show whether the sheet needs to be treated and, in the case of treated sheets, whether the treat ment has been suillcient to produce the desired results.
- any gas or liquid having no chemical action on the polymeric material may be used.
- Liquids have the advantage of more rapid heat transfer but make necessary more cumbersome apparatus. For this reason a gaseous heating fluid is preferred except for relatively thick slabs in which the rate of heat transfer is a more important consideration.
- Air and kerosene are the preferred heating fluids because of their cheapness and inertness to the polymers.
- Water is preferable to kerosene for those polymers on which it has no effect, as for instance, the methacrylic esters.
- heating in water causes the formation of a whitish translucency that increases with the percentage of acrylic ester in the polymer. On such interpolymers water should not be used.
- the invention is applicable to cast objects made from those vinyl and methacrylic compounds that form hard polymers, also to interpolymers of these materials and other polymerizable resin forming materials such as the acrylic derivatives.
- methacrylic resin as herein used is intended to include interpolymers in which the methacrylate is the major polymerizable component.
- the invention has been described with particular reference to the treatment of cast sheets for it is in them that the undesirable crazing is most apparent.
- the principle is also applicable to objects of other shapes when such objects have been cast in molds having one or more rigid surfaces. Since the strains that cause the crazing" are apparently the result of the force due to the polymer adhering to the mold surface acting in opposition to the force of contraction, the invention can be applied to all cast objects made under conditions in which these opposing forces exist.
- Thick- Heating Heating ness time tempera- 532?? (inches) (minutes) ture G.) g
- the improvement which consists in heating the sheet after it is removed from the mold and while it retains the shape imparted to it in the mold to a temperature of from 80 to 120 C. torelease the surface strains, said heating being carried out before the appearance of the minute cracks and under conditions that do not destroy the sheet.
Landscapes
- Physics & Mathematics (AREA)
- Thermal Sciences (AREA)
- Casting Or Compression Moulding Of Plastics Or The Like (AREA)
Description
Patented May 2, 1939 UNITED STATES PROCESS OF TREATING CAST POLYMERIC RESIN SHEETS Willard F.- Bartoe, Hulmcville, Pa., asaignor to Riihm & Haas Company, Philadelphia, Pa.
No Drawing.
Application April 15, 1937,
Serial No. 137.024
Claims.
This invention relates to a process of treating cast vinyl and methacrylic resins to avoid the formation of the minute surface cracks that frequently appear when cast objects of these resins 5 are placed in service. It consists in a heat treatment that removes the strains that cause these cracks.
The vinyl and methacrylic resins during polymerization undergo a substantial increase in denlO sity amounting in some instances to approximately 25%. This causes a corresponding decrease in volume. For this reason cast objects can be made from these materials only with dimculty. In the present-day methods of casting them in the form of sheets and slabs, the contraction in volume is compensated for by making the edges of the mold of'a flexible or plastic material so that the two side walls can approach each other during the polymerization. Such a process is dis- :Ai closed and claimed in the copending application of Otto Rohm and Walter Bauer, Serial No. 52,782 filed December 4, 1935 now Patent 2,154,- 639. This process while it provides a means for keeping the mold well filled during polymerization sets up surface strains in those surfaces that contact the rigid side walls. During storage or service the non-uniform release of these strains causes the formation of a myriad of minute cracks, giving the surface an undesirable crazed no appearance.
The object of this invention is to prevent the formation of these surface cracks.
It has been found that if the sheets after they are removed from the mold are given a short heat treatment at a temperature of from 80 to 120 C., the surface does not become crazed even after extended weathering. During this heating the sheet contracts in the direction of the plane of its surfaces and undergoes a slight thickening that is equivalent thereto. It has been determined that an approximately 2% shrinkage is the maximum that the herein described process will cause and that a heat treatment that causes any shrinkage above about 1% will give the desired release in surface strains. The time of heating necessary to produce this result will vary, depending upon the temperature, the thickness of the sheet and the rate of heat transfer from heating fluid to sheet. This latter will depend upon the nature of the heating fluid; liquids, as is well known, giving more rapid heat transfer than gases. On thin sheets of poly methyl methacrylate heated to a temperature in the neighborhood of 120 C. a five or ten minute treatment will produce a non-crazing sheet, but such treatment is not recommended because temperatures as high as this produce an undesirable softening of the sheet and make the surfaces tacky to particles of dust and dirt. A temperature of from 90 to 100 C. is preferred. In sheets of M; to V inch in thickness a thirty I minute treatment within this temperature range gives the desired result. A two hour heating at 80 C. also gives good results on sheets of this thickness. A measurement of the amount of shrinkage affords a means of determining if a particular sheet has been given a sumcient heating, a shrinkage of approximately 1% or more indicating that all strains have been removed.
It has also been found that sheets can be tested for a. crazing" tendency by subjecting them to the action of solvents or solvent vapors such as acetone, ethyl acetate, and benzene. This is conveniently done by dipping the piece to be tested in the solvent for about ten seconds and then fanning it dry. If the piece being tested contains the surface strains that cause crazing, the action of solvent accelerates the formation of the minute cracks and shows immediately whether the sheet is subject to crazing. A test of this kind applied to a test strip cut from a larger sheet either before or after the herein described heat treatment will show whether the sheet needs to be treated and, in the case of treated sheets, whether the treat ment has been suillcient to produce the desired results.
As heating fluid any gas or liquid having no chemical action on the polymeric material may be used. Liquids have the advantage of more rapid heat transfer but make necessary more cumbersome apparatus. For this reason a gaseous heating fluid is preferred except for relatively thick slabs in which the rate of heat transfer is a more important consideration. Air and kerosene are the preferred heating fluids because of their cheapness and inertness to the polymers. Water is preferable to kerosene for those polymers on which it has no effect, as for instance, the methacrylic esters. On those interpolymers that contain acrylic esters, such as ethyl acrylate, heating in water causes the formation of a whitish translucency that increases with the percentage of acrylic ester in the polymer. On such interpolymers water should not be used.
The invention is applicable to cast objects made from those vinyl and methacrylic compounds that form hard polymers, also to interpolymers of these materials and other polymerizable resin forming materials such as the acrylic derivatives.
It is particularly suitable to cast objects made from the lower alkyl methacrylic esters such as the methyl and ethyl, either when polymerized alone or in admixture with each other or with an ester of acrylic acid especially the lower methyl and ethyl esters.' The term "methacrylic resin" as herein used is intended to include interpolymers in which the methacrylate is the major polymerizable component.
The invention has been described with particular reference to the treatment of cast sheets for it is in them that the undesirable crazing is most apparent. The principle is also applicable to objects of other shapes when such objects have been cast in molds having one or more rigid surfaces. Since the strains that cause the crazing" are apparently the result of the force due to the polymer adhering to the mold surface acting in opposition to the force of contraction, the invention can be applied to all cast objects made under conditions in which these opposing forces exist.
To illustrate the invention and its mode of application the following table is given showing the effect of the process on sheets of polymeric methyl methacrylate of varying thickness. The sheets used were made by polymerizing methyl methacrylate in cells made of interposing spacing elements of plastic material between two sheets of glass and sealing the edges by means of paper in accordance with the disclosure of the above mentioned Rohm and Bauer application. In each instance the, treatment given produced a product that showed no tendency to craze even after long exposure to the weather.
Thick- Heating Heating ness time tempera- 532?? (inches) (minutes) ture G.) g
9. O9 30 80 0. 95 0. O9 60 80 1. l0 0. 09 5 90 l. 25 0. 09 1O 90 1. 65 0 09 2O 9O 1. 0s 09 30 9O 1. 0. 09 30 100 1. 0. 10 1D 90 1. 55 0. 10 20 90 1:75 0- 10 30 90 1. 80 0. 1O 60 90 1. 9O
Plus 30 Plus 60 2. 00
0. 23 10 90 1. 3O 0. 23 20 90 1. 50 O. 23 3O 90 1. 60 0. 23 30 100 1. 65 0. 53 30 90 1. 10 O. 53 60 9O 1. 50 0. 53 100 1. 55
Large sheets when treated in this manner, frequently show a tendency to warp. This can be overcome by. heating to a somewhat higher temperature so as to soften the sheet slightly more and allowing it to cool while resting on a soft flat surface.
It is intended that the following claims shall I claim:
1. In the process of forming a sheet of polymeric resin wherein a material containing a single CHa=C group is polymerized in a mold under conditions which produce surface strains that tend to form minute cracks on the surface of the sheet, the improvement which consists in subjecting the sheet after it is removed from the mold and while it retains the shape imparted to it in the mold to a heat treatment sufficient to release the surface strains but insufficient to destroy its sheet form, said heat treatment being carried out before the appearance of the minute cracks.
2. In the process of forming a sheet of polymeric methacrylic resin wherein the methacrylic resin is polymerized in a mold under conditions which produce surface strains that tend to form minute cracks on the surface of the sheet, the improvement which consists in subjecting the sheet after it is removed from the mold and while it retains the shape imparted to it in the mold to a heat treament suificient to release the surface strains but insufficient to destroy its sheet form, said heat treatment being carried out before the appearance of the minute cracks.
3. In the process of forming a sheet of polymeric methacrylic resin wherein the methacrylic resin is polymerized in a mold under conditions which produce surface strains that tend to form minute cracks on the surface of the sheet, the improvement which consists in heating the sheet after it is removed from the mold and while it re-' tains the shape imparted to it in the mold to a temperature of from 80 to C. to release the surface strains, said heating being carried out before the appearance of the minute cracks and under conditions that do not destroy the sheet.
4. In the process of forming a sheet of polymeric methyl methacrylate wherein the methyl methacrylate is polymerized in a mold under conditions which produce surface strains that tend to form minute cracks on the surace of the sheet,
the improvement which consists in heating the sheet after it is removed from the mold and while it retains the shape imparted to it in the mold to a temperature of from 80 to 120 C. torelease the surface strains, said heating being carried out before the appearance of the minute cracks and under conditions that do not destroy the sheet.
5. In the process of forming cast objects of polymeric methacrylic resin wherein the methacrylic resin is polymerized in a mold under conditions which produce surface strains that tend to form minute cracks on the surface of the object, the improvement which consists in subjecting the cast object after it is removed from the mold and while it retains the shape imparted to it in the mold, to a heat treatment sufficient to release the surface strains but insufficient to destroy the form imparted to it by the mold, said heat treatment being carried out before the appearance of the minute cracks.
WILLARD F. BARTOE.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US137024A US2157049A (en) | 1937-04-15 | 1937-04-15 | Process of treating cast polymeric resin sheets |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US137024A US2157049A (en) | 1937-04-15 | 1937-04-15 | Process of treating cast polymeric resin sheets |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2157049A true US2157049A (en) | 1939-05-02 |
Family
ID=22475477
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US137024A Expired - Lifetime US2157049A (en) | 1937-04-15 | 1937-04-15 | Process of treating cast polymeric resin sheets |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2157049A (en) |
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2418936A (en) * | 1944-02-23 | 1947-04-15 | Remington Arms Co Inc | Target manufacture |
| US2420565A (en) * | 1943-02-20 | 1947-05-13 | Carbide & Carbon Chem Corp | Synthetic textile articles |
| US2468165A (en) * | 1943-10-22 | 1949-04-26 | Bakelite Corp | Resin covered wire or cable and method of making |
| US2473708A (en) * | 1943-06-30 | 1949-06-21 | Monsanto Chemicals | Polymerized vinyl aromatic materials |
| US2767434A (en) * | 1952-08-07 | 1956-10-23 | American Cyanamid Co | Pearlescent plastic materials |
| US2947036A (en) * | 1957-01-17 | 1960-08-02 | Gen Aniline & Film Corp | Treatment of polymeric alpha-chloroacrylic acid esters |
| US3155756A (en) * | 1960-03-08 | 1964-11-03 | Bayer Ag | Molding of stress-free polycarbonate articles |
| US3415925A (en) * | 1967-08-01 | 1968-12-10 | Grace W R & Co | Process for preparing permeable polyethylene film |
| US4247506A (en) * | 1978-05-19 | 1981-01-27 | The B. F. Goodrich Company | Processing extruded elastomers |
| WO1993008558A1 (en) * | 1991-10-24 | 1993-04-29 | Stephen Weinreich | Color display apparatus |
-
1937
- 1937-04-15 US US137024A patent/US2157049A/en not_active Expired - Lifetime
Cited By (10)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2420565A (en) * | 1943-02-20 | 1947-05-13 | Carbide & Carbon Chem Corp | Synthetic textile articles |
| US2473708A (en) * | 1943-06-30 | 1949-06-21 | Monsanto Chemicals | Polymerized vinyl aromatic materials |
| US2468165A (en) * | 1943-10-22 | 1949-04-26 | Bakelite Corp | Resin covered wire or cable and method of making |
| US2418936A (en) * | 1944-02-23 | 1947-04-15 | Remington Arms Co Inc | Target manufacture |
| US2767434A (en) * | 1952-08-07 | 1956-10-23 | American Cyanamid Co | Pearlescent plastic materials |
| US2947036A (en) * | 1957-01-17 | 1960-08-02 | Gen Aniline & Film Corp | Treatment of polymeric alpha-chloroacrylic acid esters |
| US3155756A (en) * | 1960-03-08 | 1964-11-03 | Bayer Ag | Molding of stress-free polycarbonate articles |
| US3415925A (en) * | 1967-08-01 | 1968-12-10 | Grace W R & Co | Process for preparing permeable polyethylene film |
| US4247506A (en) * | 1978-05-19 | 1981-01-27 | The B. F. Goodrich Company | Processing extruded elastomers |
| WO1993008558A1 (en) * | 1991-10-24 | 1993-04-29 | Stephen Weinreich | Color display apparatus |
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