US2966474A - Method of preparing stable polyolefin dispersion - Google Patents
Method of preparing stable polyolefin dispersion Download PDFInfo
- Publication number
- US2966474A US2966474A US70037557A US2966474A US 2966474 A US2966474 A US 2966474A US 70037557 A US70037557 A US 70037557A US 2966474 A US2966474 A US 2966474A
- Authority
- US
- United States
- Prior art keywords
- polyolefine
- molecular weight
- solution
- high molecular
- polyethylene
- 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
Images
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
- C08J3/11—Making solutions, dispersions, lattices or gels by other methods than by solution, emulsion or suspension polymerisation techniques in organic liquids from solid 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
- C08J2323/00—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers
- C08J2323/02—Characterised by the use of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Derivatives of such polymers not modified by chemical after treatment
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T137/00—Fluid handling
- Y10T137/8593—Systems
Definitions
- the invention relates to the production of filamentary aliphatic polyolefines, and in particular, to an improved method of preparing a high molecular weight polyolefine spinning solution to be employed in the extrusion or spinning of fine filaments. fibers or the like.
- the filaments obtained'by spinning these solutions especially solutions of polyethylene having a molecular weight of at least 70,000, exhibit an excellent tensile strength and are generally superior by comparison to filaments of low molecular weight polyolefines which have been prepared by the so-called high pressure process and spun from the melt or from a solution.
- high molecular weight polyolefine is employed herein to define a polyolefine having a molecular weight of about 70,000 or higher and which is pre- Polyethylene prepared by the low pressure process is particularly characterized by a virtually unbranched carbon chain.
- low molecular weight polyolefine is employed herein to define a polyolefine which has a molecular weight of about 5,000 to 60,000 and which is prepared by a high pressure process.
- the high molecular weight polyolefine is spun from the oil solvent spinning solution at a constant elevated temperature, e.'g., ISO-250 C., and subsequently precipitated and stretched several times its original length.
- a constant elevated temperature e.'g., ISO-250 C.
- no particular difficulty is encountered in preparing the spinning solution since it is possible to work with relatively small quantities.
- a substantial quan- 'tity' of a polyolefine powder be uniformly dispersed in the petroleum oil solvent and stored in a tank or other suitable vessel from which the small portion required for spinning is immediately available after a simple heating.
- the spinning solution it is advisable to store the spinning solution at about room temperature or slightly below, preferably at about C. to 25 C., even though the polyolefine does not .dissolve at this low temperature and must be uniformly dispersed as a finely divided powder in the hydrocarbon oil.
- the improved method of preparing a stable dispersion which can be heated to form a spinning solution requires that first a low concentration solution be obtained by dissolving in the petroleum oil solvent a small quantity of about 0.01% by weight, and preferably about 0.5% by weight, up to not more than 2% by weight of a finely powdered polyethylene.
- a true solution can be obtained at elevated temperatures above the melting point of the polyethylene, preferably at temperatures of about ning filaments after again heating.
- this low .concentration of polyethylene does not provide the most desired propertiesin a polyethylene filament.
- a high molecular weight polyethylene powder is then added to the at most 2% solution of either a low or high molecular weight polyethyleneso as to obtain the preferred properties of a polyethylene having 'a mo- It is essential, however, that the total content of polyethylene in the oil solvent be not more than 18% by weight, preferably be tween about 12and 16% by weight. Where a low molecular weight polyethylene. is employed in the 0.01-2% it-is preferable to add about 10 to 16% by weight of the finely divided polyethylene powder to an initial 0.5-2% solution.
- the polyolefine-solvent dispersions containing at most 18%. of the polyolefine which are prepared by the method of the invention can be produced in relatively large quantities for storage and thereby provide a composition which can be readily heated to obtain a spinning solution with an accurately adjusted and constant concentration.
- Genin a om erc pp at on of e proce s- Suitable petroleum oil solvents within the scope of the invention are those which are obtained as the intermediate to heavy distillates in the fractionation of petroleum and which have intermediate boiling points, e.g., between 150 C. and 380 C. or higher, preferably above 150 C. up to about 300 C.
- solvents consist essentially of parafiin and naphthene hydrocarbons as mixtures which are commonly known under such commercial or familiar names as mineral oil, gas oil, parafiin oil, spindle oil, white oil, and the like.
- paraifin and naphthene refer to saturated aliphatic and oycloaliphatic hydrocarbons.
- the solvent employed herein must be in the liquid phase during storage of the polyolefine dispersion as well as at the spinning temperatures.
- the saturated hydrocarbon oils should also have a somewhat viscous consistency and are preferably 'as colorless as possible. The selection of suitable solvents having these various properties can be easily accomplished by one who is familiar with the usual requirements of a spinning process.
- a low or high molecular weight polyolefine can he used in the initial dispersion of not more than 2% concentration, the polymers having molecular weights of over 70,000 are preferred.
- the nozzle openings or spinning orifices have a diameter of 200p. each.
- the threads or filaments of the heated solution emerge from the spinning head, and after traversing a 10 cm. long air space, are then conducted through a C. warm precipitation bath of propanol. The filaments then pass into a washing bath of petroleum ether,
- Example I ture is employed for the preparation of a more concentrated dispersion. For this, 14% by weight of polyethylene powder of a molecular weight of 125,000 is stirred into the cooled solution. The dispersion prepared in this manner has a. tendency todePO it polyethylene particles only after about 24 hours of standing.
- the dispersion is converted to a heated spinning solution and spun in the apparatus shown'in the accompanying drawing.
- the dispersion is first stored in the dispersion tank 1, cooled to about 20 C., and placed under a pressure of about 3 atmospheres of a substantially inert gas (e.g., nitrogen or compressed air).
- a substantially inert gas e.g., nitrogen or compressed air.
- the gas inlet is indicated at 2.
- the dispersion tank contains a stirrer or other suitable mixing device 3, which is securely connected with the dissolving and mixing worm 4 and,
- the upper part of the double worm and the dispersion tank are surrounded by a cooling mantle or jacket 5.
- the lower part of the double worm is surrounded by a heating jacket 6, which is heated to about l80-220 C., preferably about 200 C.
- the dispersed polyethylene powder is converted into a clear viscous solution.
- This solution first enters through the pumping block 7 into the spinning pump '8 and is then conveyed to the spinning head 9.
- the pumping and spinning head are likewise heated in a conventional manner, preferably'to' about 200 C.
- the spinning solution produced inthe hot portion of the double worm (14.5% solution) is spun through a the bath having a length of 4 meters. Thereafter, in a 4 meter hot water bath maintained at C., the filaments are stretched to double their original length. The filaments are then again washed in a petroleum ether washing tube. Finally, in a hot glycerine bath at about 124 C., the filaments are again stretched to 4 times their length (a total stretching, therefore, of eight times the original spun length).
- the resulting filaments have a strength of Rkm at 6% elongation and an individual titer of approximately 1.4 denier.
- Example II Polyethylene of a molecular weight of 50,000 (produced by the high-pressure process) is dissolved at 150 C. in a gas oil having a boiling point of 225230 C. to produce a 1% solution of polyethylene. The dissolving requires about 5 minutes. After cooling the 1% solution, approximately 13% by weight of a finely powdered polyethylene of a molecular weight of 150,000 is uniformly dispersed in the initial solution by stirring. The resulting 14% dispersion of polyethylene shows no ap' preciable particle deposition, even after standing for 24 hours.
- the further treatment of this 14% dispersion including storage followed by heating to obtain a hot spinning solution and the subsequent spinning of filaments is accomplished with the same apparatus and in the same manner as that described in Example I.
- the filaments are conducted through a 4 meter washing bath containing petroleum ether and pass immediately into a glycerine bath heated to 124 C. where they are stretched to 8 times their original length.
- the resulting filaments have a strength of 84 Rkm at 14% elongation and an indi vidual titer of approximately 2.3 denier.
- An improved method of preparing a stable dispersion of a high molecular weight polyolefine capable of being heated to form a spinning solution which comprises: dissolving at a temperature above about C. in a hot liquid petroleum oil selected from the group consisting of paraffin and naphthene hydrocarbons from 0.01 to not more than 2 percent by weight of a low to high molecular weight polyolefine of the group consisting of poly -ethylene, -proplyene, -butylene and -pentene; cooling the resulting solution to from about 0 C.
- An improved method of preparing a stable dispersion of a high molecular weight polyethylene capable of being heated to form a spinning solution which comprises: dissolving at a temperature above about 140 C. in a hot liquid petroleum oil selected from the group consisting of paraffin and naphthene hydrocarbons from about 0.5 to not more than 2 percent by weight of a low to high molecular weight polyethylene; cooling the resultthe total content of polyethylene has a high molecular ing solution to from about 10 C. to 25 C.; and uniweight of at least 70,000.
Landscapes
- Chemical & Material Sciences (AREA)
- Dispersion Chemistry (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Artificial Filaments (AREA)
Description
Dec. 27, 1960 w. JURGELEIT METHOD OF PREPARING STABLE POLYOLEFIN DISPERSION Filed Dec. 3, 1957 INVENTOR.
9 WOLFGANG duRe-ELErr BY hwy .pared by the low pressure process.
METHOD OF PREPARING STABLE POLYOLEFIN DISPERSION Wolfgang .Jurgeleit, Davenport, Iowa, assiguor to Vereinigte Glanzstoif Fabriken AG., Wuppertal- Elberfeld, Germany Filed Dec. 3, 1957, Ser. No. 700,375
Claims priority, application Germany Dec. 8, 1956 '7 Claims. (Cl. 260-3345) The invention relates to the production of filamentary aliphatic polyolefines, and in particular, to an improved method of preparing a high molecular weight polyolefine spinning solution to be employed in the extrusion or spinning of fine filaments. fibers or the like.
The production of high molecular weight polyolefine filaments is more fully described in my copending application, Serial No. 664,289, filed June 7, 1957, the disclosure of which is incorporated herein by reference as fully as if it had been set forth in its entirety. In this copending application there is described a process whereby a high molecular Weight polyolefine prepared by the so-called low pressure polymerization of an olefine having from 2 to 5 carbon atoms, i.e., ethylene, propylene, butylene and pentene, is dissolved in a hot liquid petroleum oil consisting essentially of parafiin and/or-naphthene hydrocarbons so as to obtain an at most 18% solution of the polyolefine, and the solution is :then extruded or spun into fine filaments. The filaments obtained'by spinning these solutions, especially solutions of polyethylene having a molecular weight of at least 70,000, exhibit an excellent tensile strength and are generally superior by comparison to filaments of low molecular weight polyolefines which have been prepared by the so-called high pressure process and spun from the melt or from a solution.
The expression high molecular weight polyolefine is employed herein to define a polyolefine having a molecular weight of about 70,000 or higher and which is pre- Polyethylene prepared by the low pressure process is particularly characterized by a virtually unbranched carbon chain.
The expression low molecular weight polyolefine is employed herein to define a polyolefine which has a molecular weight of about 5,000 to 60,000 and which is prepared by a high pressure process.
In the copending application referred to above, the high molecular weight polyolefine is spun from the oil solvent spinning solution at a constant elevated temperature, e.'g., ISO-250 C., and subsequently precipitated and stretched several times its original length. On a laboratory basis, no particular difficulty is encountered in preparing the spinning solution since it is possible to work with relatively small quantities. However, when a -continuous spinning process is to be executed on a relatively large scale, it is necessary that a substantial quan- 'tity' of a polyolefine powder be uniformly dispersed in the petroleum oil solvent and stored in a tank or other suitable vessel from which the small portion required for spinning is immediately available after a simple heating. It is advisable to store the spinning solution at about room temperature or slightly below, preferably at about C. to 25 C., even though the polyolefine does not .dissolve at this low temperature and must be uniformly dispersed as a finely divided powder in the hydrocarbon oil.
It was found, however, that when spinning overa relatively long period of time, e.g., up to 24 hours and longer,
United States PatentO vlecular weight of at least 70,000.
that the supply of the polyolefine in dispersed form is unstable and produces a rapid deposition of the polyolefine powder even during constant stirring. This phenomenon of deposition is extremely disadvantageous because it is impossible under these conditions to maintain a constant concentration of the polyolefine in the subsequent heated spinning solution. Even the paraffin oils which are known to have the best solvent effect upon polyethylene, for example, do not alleviate this condition which occurs in the dispersion form of the spinning composition.
in accordance with the invention, it has now been discovered that this problem of deposition from the'polyolefine-solvent dispersion can be avoided for all practical purposes by following the procedure hereinafter set forth. This novel procedure is described with reference to polyethylene but is equally applicable to polypropylene, polybutylene, and polypentene so that the description and examples are intended to be illustrative only and not exclusive.
The improved method of preparing a stable dispersion which can be heated to form a spinning solution requires that first a low concentration solution be obtained by dissolving in the petroleum oil solvent a small quantity of about 0.01% by weight, and preferably about 0.5% by weight, up to not more than 2% by weight of a finely powdered polyethylene. A true solution can be obtained at elevated temperatures above the melting point of the polyethylene, preferably at temperatures of about ning filaments after again heating. However, this low .concentration of polyethylene does not provide the most desired propertiesin a polyethylene filament.
Surprisingly, it was found that additional-amounts of a finely powdered polyethylene can be added to the initial solution and uniformly dispersed therein by .sufficient stirring or mixing without showing any pronounced tendency toward a deposition of polymer particles. Ac-
cordingly, a high molecular weight polyethylene powder is then added to the at most 2% solution of either a low or high molecular weight polyethyleneso as to obtain the preferred properties of a polyethylene having 'a mo- It is essential, however, that the total content of polyethylene in the oil solvent be not more than 18% by weight, preferably be tween about 12and 16% by weight. Where a low molecular weight polyethylene. is employed in the 0.01-2% it-is preferable to add about 10 to 16% by weight of the finely divided polyethylene powder to an initial 0.5-2% solution.
The polyolefine-solvent dispersions containing at most 18%. of the polyolefine which are prepared by the method of the invention can be produced in relatively large quantities for storage and thereby provide a composition which can be readily heated to obtain a spinning solution with an accurately adjusted and constant concentration. Genin a om erc pp at on of e proce s- Suitable petroleum oil solvents within the scope of the invention are those which are obtained as the intermediate to heavy distillates in the fractionation of petroleum and which have intermediate boiling points, e.g., between 150 C. and 380 C. or higher, preferably above 150 C. up to about 300 C. These solvents consist essentially of parafiin and naphthene hydrocarbons as mixtures which are commonly known under such commercial or familiar names as mineral oil, gas oil, parafiin oil, spindle oil, white oil, and the like. The terms paraifin and naphthene refer to saturated aliphatic and oycloaliphatic hydrocarbons.
Of course, the solvent employed herein must be in the liquid phase during storage of the polyolefine dispersion as well as at the spinning temperatures. The saturated hydrocarbon oils should also have a somewhat viscous consistency and are preferably 'as colorless as possible. The selection of suitable solvents having these various properties can be easily accomplished by one who is familiar with the usual requirements of a spinning process.
While either a low or high molecular weight polyolefine can he used in the initial dispersion of not more than 2% concentration, the polymers having molecular weights of over 70,000 are preferred. Likewise, even with the low molecular weight polymers, those having 30-hole spinning head 9 at a rate of 14.4 cmfi/min. with the pressure exerted by the spinning pump 8. The nozzle openings or spinning orifices have a diameter of 200p. each. The threads or filaments of the heated solution emerge from the spinning head, and after traversing a 10 cm. long air space, are then conducted through a C. warm precipitation bath of propanol. The filaments then pass into a washing bath of petroleum ether,
a molecular weight of, for example 25,000to 50,000 ,3
are preferred over those of 5,000 to 25,000.-
The following examples further illustrate the present invention with reference to the accompanying-drawing which indicates suitable apparatus especially adapted for preparing the spinning solution and the subsequently spinning of filaments therefrom. The abbreviation Rkm which appears in the following examples stands for Reisskilometer, one unit Rkm being equal to 9 grams per denier.
Example I ture, is employed for the preparation of a more concentrated dispersion. For this, 14% by weight of polyethylene powder of a molecular weight of 125,000 is stirred into the cooled solution. The dispersion prepared in this manner has a. tendency todePO it polyethylene particles only after about 24 hours of standing.
The dispersion is converted to a heated spinning solution and spun in the apparatus shown'in the accompanying drawing. The dispersion is first stored in the dispersion tank 1, cooled to about 20 C., and placed under a pressure of about 3 atmospheres of a substantially inert gas (e.g., nitrogen or compressed air). The gas inlet is indicated at 2. The dispersion tank contains a stirrer or other suitable mixing device 3, which is securely connected with the dissolving and mixing worm 4 and,
turns at the same rate as the worm. Parallel to the worm 4 there is a second worm 10, so that by an intensive kneading or mixing with the double worm, an especially uniform and rapid dissolving effect can be achieved. The upper part of the double worm and the dispersion tank are surrounded by a cooling mantle or jacket 5. The lower part of the double worm is surrounded by a heating jacket 6, which is heated to about l80-220 C., preferably about 200 C. As soon as the polyethylene-gas oil dispersion is conveyed from the dispersion tank downward into and through the hot region of the double worm, the dispersed polyethylene powder is converted into a clear viscous solution. This solution first enters through the pumping block 7 into the spinning pump '8 and is then conveyed to the spinning head 9. The pumping and spinning head are likewise heated in a conventional manner, preferably'to' about 200 C. i
The spinning solution produced inthe hot portion of the double worm (14.5% solution) is spun through a the bath having a length of 4 meters. Thereafter, in a 4 meter hot water bath maintained at C., the filaments are stretched to double their original length. The filaments are then again washed in a petroleum ether washing tube. Finally, in a hot glycerine bath at about 124 C., the filaments are again stretched to 4 times their length (a total stretching, therefore, of eight times the original spun length).
The resulting filaments have a strength of Rkm at 6% elongation and an individual titer of approximately 1.4 denier.
Example II Polyethylene of a molecular weight of 50,000 (produced by the high-pressure process) is dissolved at 150 C. in a gas oil having a boiling point of 225230 C. to produce a 1% solution of polyethylene. The dissolving requires about 5 minutes. After cooling the 1% solution, approximately 13% by weight of a finely powdered polyethylene of a molecular weight of 150,000 is uniformly dispersed in the initial solution by stirring. The resulting 14% dispersion of polyethylene shows no ap' preciable particle deposition, even after standing for 24 hours.
The further treatment of this 14% dispersion including storage followed by heating to obtain a hot spinning solution and the subsequent spinning of filaments is accomplished with the same apparatus and in the same manner as that described in Example I. The filaments are conducted through a 4 meter washing bath containing petroleum ether and pass immediately into a glycerine bath heated to 124 C. where they are stretched to 8 times their original length. The resulting filaments have a strength of 84 Rkm at 14% elongation and an indi vidual titer of approximately 2.3 denier.
The invention is hereby claimed as follows:
1. An improved method of preparing a stable dispersion of a high molecular weight polyolefine capable of being heated to form a spinning solution which comprises: dissolving at a temperature above about C. in a hot liquid petroleum oil selected from the group consisting of paraffin and naphthene hydrocarbons from 0.01 to not more than 2 percent by weight of a low to high molecular weight polyolefine of the group consisting of poly -ethylene, -proplyene, -butylene and -pentene; cooling the resulting solution to from about 0 C. to 40 C; and uniformly dispersing in said cooled solution a finely powdered high molecular weight polyolefine of said group, the total content of polyolefine in said oil being not more than 18 percent by weight of which at least a predominant proportion has a high molecular weight of at least about 70,000.
2. An improved method as defined in claim 1 wherein the polyolefine is polyethylene.
3. An improved method as defined in claim 1 wherein the polyolefine is polypropylene.
4. An improved method as defined in claim 1 wherein the polyolefine is polybutylene.
5. An improved method as defined in claim 1 wherein the polyolefine is polypentene.
6. An improved method of preparing a stable dispersion of a high molecular weight polyethylene capable of being heated to form a spinning solution which comprises: dissolving at a temperature above about 140 C. in a hot liquid petroleum oil selected from the group consisting of paraffin and naphthene hydrocarbons from about 0.5 to not more than 2 percent by weight of a low to high molecular weight polyethylene; cooling the resultthe total content of polyethylene has a high molecular ing solution to from about 10 C. to 25 C.; and uniweight of at least 70,000.
formly dispersing in said cooled solution about 10 to 16 percent by weight of a finely powdered polyethylene References Cited in the file of this patent having a high molecular weight of at least 70,000, the 5 total content of polyethylene in said oil being not more UNITED STATES PATENTS than 18 percent by weight. 2,210,771 Myles et a1 Aug. 6, 1940 7. An improved method as defined in claim 6 wherein 2,773,053 Field et al Dec. 4, 1956
Claims (1)
1. AN IMPROVED METHOD OF PREPARING A STABLE DISPERSION OF A HIGH MOLECULAR WEIGHT POLYOLEFINE CAPABLE OF BEING HEATED TO FORM A SPINNING SOLUTION WHICH COMPRISES: DISSOLVING AT A TEMPERATURE ABOVE ABOUT 140*C. IN A HOT LIQUID PETROLEUM OIL SELECTED FROM THE GROUP CONSISTING OF PARAFFIN AND NAPHTHENE HYDROCARBONS FROM 0.01 TO NOT MORE THAN 2 PERCENT BY WEIGHT OF A LOW TO HIGH MOLECULAR WEIGHT POLYOLEFINE OF THE GROUP CONSISTING OF POLY -ETHYLENE, -PROPYLENE, -BUTYLENE AND -PENTENE, COOLING THE RESULTING SOLUTION TO FROM ABOUT 0*C. TO 40*C., AND UNIFORMLY DISPERSING IN SAID COOLED SOLUTION A FINELY POWDERED HIGH MOLECULAR WEIGHT POLYOLEFINE OF SAID GROUP, THE TOTAL CONTENT OF POLYOLEFINE IN SAID OIL BEING NOT MORE THAN 18 PERCENT BY WEIGHT OF WHICH AT LEAST A PREDOMINANT PROPORTION HAS A HIGH MOLECULAR WEIGHT OF AT LEAST ABOUT 70,000.
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DE2966474X | 1956-12-08 |
Publications (1)
Publication Number | Publication Date |
---|---|
US2966474A true US2966474A (en) | 1960-12-27 |
Family
ID=8034063
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US70037557 Expired - Lifetime US2966474A (en) | 1956-12-08 | 1957-12-03 | Method of preparing stable polyolefin dispersion |
Country Status (1)
Country | Link |
---|---|
US (1) | US2966474A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3095388A (en) * | 1957-05-27 | 1963-06-25 | Ici Ltd | Dispersion polymerisation of an acrylate in the presence of a rubber and a non-polar organic solvent and product obtained |
US3118857A (en) * | 1961-03-09 | 1964-01-21 | Phillips Petroleum Co | Solid polyolefin containing an aryl substituted polyolefin and having improved clarity |
US3257340A (en) * | 1960-05-04 | 1966-06-21 | Ici Ltd | Dispersion polymerisation of monomer in presence of alkyl mercaptan |
US4156672A (en) * | 1978-03-27 | 1979-05-29 | The Continental Group, Inc. | Method for preparing dispersions of propylene polymers |
EP0015151A1 (en) * | 1979-02-27 | 1980-09-03 | General Technology Applications,Inc | Process for dissolving thermoplastic polymers in compatible liquids and the application thereof to reducing friction of hydrocarbons flowing through a conduit |
US4440916A (en) * | 1980-10-20 | 1984-04-03 | General Technology Applications, Inc. | Process for solid state free radical reactions |
US4452928A (en) * | 1982-11-08 | 1984-06-05 | El Paso Polyolefins Company | Additive-containing polyolefin beads and process for their preparation |
Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2210771A (en) * | 1938-02-11 | 1940-08-06 | Ici Ltd | Manufacture of shaped articles from polymeric materials |
US2773053A (en) * | 1953-07-22 | 1956-12-04 | Standard Oil Co | Ethylene polymerization with catalyst of group va metal oxide and alkaline earth hydride |
-
1957
- 1957-12-03 US US70037557 patent/US2966474A/en not_active Expired - Lifetime
Patent Citations (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US2210771A (en) * | 1938-02-11 | 1940-08-06 | Ici Ltd | Manufacture of shaped articles from polymeric materials |
US2773053A (en) * | 1953-07-22 | 1956-12-04 | Standard Oil Co | Ethylene polymerization with catalyst of group va metal oxide and alkaline earth hydride |
Cited By (8)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3095388A (en) * | 1957-05-27 | 1963-06-25 | Ici Ltd | Dispersion polymerisation of an acrylate in the presence of a rubber and a non-polar organic solvent and product obtained |
US3257340A (en) * | 1960-05-04 | 1966-06-21 | Ici Ltd | Dispersion polymerisation of monomer in presence of alkyl mercaptan |
US3257341A (en) * | 1960-05-04 | 1966-06-21 | Ici Ltd | Dispersion polymerization of monomer in presence of mercaptan added during polymerization |
US3118857A (en) * | 1961-03-09 | 1964-01-21 | Phillips Petroleum Co | Solid polyolefin containing an aryl substituted polyolefin and having improved clarity |
US4156672A (en) * | 1978-03-27 | 1979-05-29 | The Continental Group, Inc. | Method for preparing dispersions of propylene polymers |
EP0015151A1 (en) * | 1979-02-27 | 1980-09-03 | General Technology Applications,Inc | Process for dissolving thermoplastic polymers in compatible liquids and the application thereof to reducing friction of hydrocarbons flowing through a conduit |
US4440916A (en) * | 1980-10-20 | 1984-04-03 | General Technology Applications, Inc. | Process for solid state free radical reactions |
US4452928A (en) * | 1982-11-08 | 1984-06-05 | El Paso Polyolefins Company | Additive-containing polyolefin beads and process for their preparation |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
US5032338A (en) | Method to prepare high strength ultrahigh molecular weight polyolefin articles by dissolving particles and shaping the solution | |
US3048465A (en) | Polyolefin wet spinning process | |
US2420565A (en) | Synthetic textile articles | |
DE3280442T2 (en) | Process for the production of polymer fibers with high tensile strength and high modulus. | |
EP0080274A2 (en) | Process of melt spinning of a blend of a fibre-forming polymer and an immiscible polymer and melt spun fibres produced by such process | |
US3017238A (en) | Method for solvent spinning polyolefins | |
GB2051667A (en) | Preparing polyethylene filaments | |
JPS602406B2 (en) | A method for producing yarn or fiber made of thermoplastic synthetic polymer and having a large number of coexisting independent discontinuous cavities. | |
US3471426A (en) | Polyamide containing dispersed polyolefin and fatty dispersing agent | |
US2966474A (en) | Method of preparing stable polyolefin dispersion | |
IL26206A (en) | Polymer filaments and films of low density | |
US2611929A (en) | Method of producing shaped articles from artificial or synthetic fiberor film-forming materials | |
US5252394A (en) | Molecular orientation articles molded from high-molecular weight polyethylene and processes for preparing same | |
JP3143886B2 (en) | Method for producing colored high-strength polyethylene fiber | |
EP0139141B1 (en) | Production of stretched polymeric material having high strength and high modulus | |
JPH0246053B2 (en) | CHOKOBUNSHIRYOHORIECHIRENYOEKINOSEIZOHOHO | |
DE69715867T2 (en) | ULTRA-ORIENTED CRYSTALLINE FILAMENTS AND METHOD OF ESTABLISHING THEIR | |
JPH05503552A (en) | Halogenated carbon for flash spinning of polyethylene plexifilament | |
EP0212133B1 (en) | Method to prepare high strength ultrahigh molecular weight polyolefin articles by dissolving particles and shaping the solution | |
JPS58208343A (en) | Homogeneous solution based on polyvinyl chloride and manufacture | |
KR910005543B1 (en) | Antistatic cospun polyester-polyamide yarns | |
US3600493A (en) | Method for drawing fibers comprised of cellulose acetate-polymer blends | |
US3415921A (en) | Process for spinning fibers of poly(4-methyl-1-pentene) | |
US2978292A (en) | Manufacture of rayon | |
DE1494553A1 (en) | Process for the production of fibers from polymers or copolymers of acrylonitrile by the dry spinning process |