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Browse by: INVENTOR PATENT HOLDER PATENT NUMBER DATE
 
 
Inventor:
Moczygemba; George A.
Address:
Bartlesville, OK
No. of patents:
47
Patents:




Patent Number Title Of Patent Date Issued
RE30460 Coupling of alkali metal-terminated polymers December 23, 1980
Alkali metal-terminated polymers of one or more alkadienes and of one or more vinyl-substituted aromatic monomers are effectively coupled by an anhydride of a monocarboxylic acid having 2 to 8 carbon atoms per molecule.
6835778 Conjugated diene/monovinylarene block copolymers blends December 28, 2004
This invention relates to polymer blends, which comprise at least one tapered conjugated diene-monovinylarene block copolymer and at least one styrenic polymer. The polymer blends possess good optical and mechanical properties.
6444755 Conjugated diene/monovinylarene block copolymers blends September 3, 2002
A block copolymer comprising at least three consecutive conjugated diene/monovinylarene tapered blocks is provided. Other aspects of this invention include a polymerization process for preparing the block copolymer and polymer blends comprising the block copolymer. The block copolyme
6420486 Conjugated diene/monovinylarene block copolymers, methods for preparing same, and polymer blends July 16, 2002
A block copolymer comprising at least three consecutive conjugated diene/monovinylarene tapered blocks is provided. Other aspects of this invention include a polymerization process for preparing the block copolymer and polymer blends comprising the block copolymer. The block copolyme
6265485 Tapered block copolymers of monovinylarenes and conjugated dienes July 24, 2001
A method for preparing tapered block copolymers which are particularly useful for blend components in blends with polymers of styrene. In the first embodiment of this invention the copolymers are prepared in a polymerization process by sequentially charging: (1) an initiator and mono
6265484 Tapered block copolymers of monovinylarenes and conjugated dienes July 24, 2001
A method for preparing tapered block copolymers which are particularly useful for blend components in blends with polymers of styrene. In the first embodiment of this invention the copolymers are prepared in a polymerization process by sequentially charging: (1) an initiator and mono
6232415 Process to produce a monovinylaromatic/ monoolefin polymer and said monovinylaromatic/monoolefin May 15, 2001
A process to produce a monovinylaromatic/monoolefin polymer is provided. Said monovinylaromatic/monoolefin polymer is provided.
6232414 Process to make a monovinylaromatic polymer and said monovinylaromatic polymer May 15, 2001
A process to produce a monovinylaromatic polymer is provided. Said monovinylaromatic polymer is provided.
6127487 Process to produce coupled block copolymers and said copolymers October 3, 2000
This invention provides a process to produce coupled block copolymers and said coupled block copolymers.
6096828 Conjugated diene/monovinylarene block copolymers, methods for preparing same, and polymer blends August 1, 2000
A block copolymer comprising at least three consecutive conjugated diene/monovinylarene tapered blocks is provided. Other aspects of this invention include a polymerization process for preparing the block copolymer and polymer blends comprising the block copolymer. The block copolyme
6093285 Purification of 1,3-butadiene July 25, 2000
A system and process for purifying a 1,3-butadiene feedstock containing 1,3-butadiene and various impurities by first introducing the 1,3-butadiene feedstock stream to a separation column to produce an intermediate product stream containing 1,3-butadiene and residual impurities and t
6066708 Copolymer production, product thereof and diluent removal therefrom May 23, 2000
This invention provides a process to produce a composition that comprises diluent and copolymer and also provides the composition. The process of this invention comprises: (a) producing a composition that comprises diluent and copolymer; and (b) removing a portion of said diluent from
5910546 Tapered block copolymers of monivinylarenes and conjugated dienes June 8, 1999
A method for preparing tapered block copolymers which are particularly useful for blend components in blends with polymers of styrene. In the first embodiment of this invention the copolymers are prepared in a polymerization process by sequentially charging: (1) an initiator and mono
5705569 Block copolymers of monovinylarenes and conjugated dienes and preparation thereof January 6, 1998
A method for preparing resinous polymodal monovinylarene-conjugated diene block copolymers and polymers produced thereby are provided. The method comprises sequentially contacting under polymerization conditions:(a) a monovinylarene monomer and initiator;(b) initiator and a monovinylarene mo
5587425 Blends of copolymers of monovinylarenes and conjugated dienes containing two interior tapered bl December 24, 1996
A method for preparing blends of a copolymer in a polymerization process by sequentially charging: (1) an initiator and monovinylaromatic monomer in the presence of a randomizer; (2) an initiator and monovinylaromatic monomer; (3) a mixture of monovinylaromatic and conjugated diene monom
5545690 Tapered block copolymers of monovinylarenes and conjugated dienes August 13, 1996
A method for preparing tapered block copolymers which are particularly useful for blend components in blends with polymers of styrene. In the first embodiment of this invention the copolymers are prepared in a polymerization process by sequentially charging: (1) an initiator and mono
5438103 Block copolymers of monovinylaromatic and conjugated diene monomers August 1, 1995
A method for preparing block copolymers from which can be made transparent blue articles comprising sequentially charging under polymerization conditions at least one monovinylaromatic monomer and at least one conjugated diene monomer, wherein at least the first monomer charge is a m
5436298 Block copolymers of monovinylarenes and conjugated dienes and preparation thereof July 25, 1995
A method for preparing resinous polymodal monovinylarene-conjugated diene block copolymers and polymers produced thereby are provided. The method comprises sequentially contacting under polymerization conditions:(a) a monovinylarene monomer and initiator;(b) initiator and a monovinylarene mo
5422389 Method for stabilizing monovinylarene/conjugated diene copolymers and a method for preparing a s June 6, 1995
A process for stabilizing polymers is provided comprising:(1) contacting at least one hindered phenolic compound and an organic phosphite to form a stabilizing mixture,wherein said contacting is at a temperature sufficient to at least partially dissolve said hindered phenolic compound,wherei
5399628 Block copolymers of monovinylarenes and conjugated dienes containing two interior tapered blocks March 21, 1995
A method for preparing tapered block copolymers in a polymerization process by sequentially charging: (1) an initiator and monovinylaromatic monomer in the presence of a randomizer; (2) an initiator and monovinylaromatic monomer; (3) a mixture of monovinylaromatic and conjugated diene mo
5393838 Conjugated diene/monovinylarene block copolymers with multiple tapered blocks February 28, 1995
A method for preparing polymodal tapered block copolymers in a polymerization process by sequentially charging: (a) an initiator and monovinylaromatic monomers in the presence of a randomizer; (b) an initiator and monovinylaromatic monomers; (c) a mixture of monovinylaromatic and con
5384349 Conjugated diene/monovinylarene copolymers and preparation thereof January 24, 1995
A block copolymer comprising about 5 weight percent to about 95 weight percent monovinylarene monomer, about 95 to about 5 weight percent butadiene, and an effective amount of a thermal stabilizing agent selected from the group consisting of ascorbic acid, citric acid, disodium citrate,
5319033 Tapered block monovinyl aromatic/conjugated diene copolymer June 7, 1994
A method for preparing tapered block copolymers in a polymerization process by charging an initiator and monomers sequentially with one or more charges of first one of the monomers, then with a mixture of the two monomers, and then with one or more charges of the second monomer alter
5290875 Conjugated diene/monovinylarene block copolymers with multiple tapered blocks March 1, 1994
A method for preparing polymodal tapered block copolymers in a polymerization process by sequentially charging: (a) an initiator and monovinylaromatic monomers in the presence of a randomizer; (b) an initiator and monovinylaromatic monomers; (c) a mixture of monovinylaromatic and con
5270396 Sequential coupling in formation of resinous block copolymers December 14, 1993
A method for preparing resinous copolymers by sequential charge copolymerization of at least two charges, at least one being a conjugated diene and at least one being a monovinylarene; followed by a charge of a polyfunctional coupling agent; and the final charge being an essentially
5256736 Tapered block copolymers of conjugated dienes and monovinylarenes October 26, 1993
A method for preparing tapered block copolymers in a polymerization process by sequentially charging: (1) an initiator and monovinylaromatic monomers in the presence of a randomizer; (2) an initiator and a mixture of monovinylaromatic and conjugated diene monomers; (3) an initiator and a
5227419 Tapered block styrene/butadiene copolymers July 13, 1993
A method for preparing tapered block copolymers in a polymerization process by charging an initiator and monomers sequentially with one or more charges of first one of the monomers, then with a mixture of the two monomers, and then with one or more charges of the first monomer to pro
5220178 Apparatus and process for detecting the presence of defects on a moving sheet of material June 15, 1993
A defect detection system for the optical inspection of defects in transparent and translucent sheets of materials. The system utilizes the differing optical properties of different defects to distinguish between such defects as fisheye defects, speck defects and scratches.
5130377 Tapered block styrene/butadiene copolymers July 14, 1992
A method for preparing tapered block copolymers in a polymerization process by charging an initiator and monomers sequentially with one or more charges of first one of the monomers, then with a mixture of the two monomers, and then with one or more charges of the second monomer alter
4405754 Haze-free, clear, impact-resistant resinous polymers September 20, 1983
Haze-free, clear, impact-resistant resinous copolymers are produced by coupling polymer-lithium with a mixture of coupling agents wherein one is a lactone such as butyrolactone and the other is a halo-silane such as phenyltrichlorosilane. The combination of coupling agents reduces haze,
4403074 Clear haze-free impact-resistant resinous polymers September 6, 1983
Clear, haze-free, colorless, impact-resistant resinous copolymers are produced by terminating the coupled polymer-lithium with water and linear saturated aliphatic dicarboxylic acids selected from C.sub.2, C.sub.3, and C.sub.5 to C.sub.16 acids.
4232137 Cooling an alpha-methylstyrene polymerization mass November 4, 1980
An alpha-methylstyrene polymerization reaction mass is cooled by including therein a component which is readily vaporizable under the conditions of polymerization thereby to remove undesirable or excess heat, thus controlling the reaction temperature to a desired value. In one embodiment
4223116 Conjugated diene polymerization process and catalyst September 16, 1980
At least one conjugated diene is polymerized in the presence of a catalyzing amount of a catalyst consisting essentially of at least one Lewis acid and at least one cyclopolyolefin nickel complex.
4174360 Coupling of alkali metal-terminated polymers November 13, 1979
Alkali metal-terminated polymers of one or more alkadienes and of one or more vinyl-substituted aromatic monomers are effectively coupled by an anhydride of a monocarboxylic acid having 2 to 8 carbon atoms per molecule.
4168286 Tetrablock polymers and their hydrogenated analogs September 18, 1979
Tetrablock polymers having the configuration B--A.sub.1 --C--A.sub.2 and C--A.sub.1 --B--A.sub.2 and their hydrogenated counterparts are disclosed, wherein B is a low vinyl poly 1,3-butadiene block, A.sub.1 and A.sub.2 can be the same or different polymerized blocks of a monovinylarene m
4163765 Polymeric compositions August 7, 1979
Linear and branched teleblock copolymers having the configuration (A--B--C).sub.n Z and their hydrogenated derivatives are disclosed, wherein n is an integer from 2 to 4, Z is the residue of either a polyfunctional coupling agent or a polyfunctional initiator or is a covalent chemica
4158654 Carboxylic acid in alkali metal carboxylate rubber solution June 19, 1979
A mixture of a carboxylic acid and an alkali metal carboxylate-containing rubber in a vinyl monomer is provided. The resulting composition has a relatively low viscosity and is particularly adapted for preparing a thermosettable composition suitable for preparing reinforced plastic a
4152370 Preparation, composition, and use of block polymers May 1, 1979
Linear block copolymers having the formula A-B/A'-C and C-B/A'-A are prepared, wherein terminal block A is a poly(monovinylarene) block, terminal block C is a block of low vinyl poly(1,3-butadiene), having less than about 30 mole percent vinyl pendant groups, and the center block B/A'
4134928 Tetrablock polydienes January 16, 1979
Hydrogenated tetrablock polydienes such as polybutadiene-polyisoprene-polybutadiene-polyisoprene exhibit improved elongation as compared to both of the very similar hydrogenated triblock polydienes polybutadiene-polyisoprene-polybutadiene and polyisoprene-polybutadiene-polyisoprene.
4113930 Hydrogenated 1,3-cyclohexadiene/1,3-butadiene copolymers September 12, 1978
Hydrogenated 1,3-cyclohexadiene/1,3-butadiene copolymers having unexpectedly high green tensile strength are disclosed. The method for producing such hydrogenated copolymers is also disclosed.
4076914 Treatment of coupled polymers prior to hydrogenation February 28, 1978
An organopolyhalide-coupled conjugated diene polymer is treated with an organometal compound after the coupling step and prior to hydrogenation. The treated polymer is hydrogenated to result in hydrogenated polymers exhibiting low residual unsaturation.
4057601 Block copolymers of alkadienes and monovinyl arenes November 8, 1977
A copolymer having the formula A--B--C is disclosed, which becomes a thermoplastic elastomer after essentially all the olefinic unsaturation therein has been removed by hydrogenation. A is a low vinyl poly-1,3-butadiene block, C is a poly(monovinyl arene) block, and B is either a blo
4055713 Iodine molecular weight regulators in suspension polymerization systems October 25, 1977
Iodine or organic iodides are effective in suspension polymerization systems as molecular weight regulators or modifiers. These modifiers are especially suited for the suspension ABS processes.
4049753 Coupling of alkali metal-terminated polymers September 20, 1977
Alkali metal-terminated polymers of one or more alkadienes and of one or more vinyl-substituted aromatic monomers are effectively coupled by an anhydride of a monocarboxylic acid having 2 to 8 carbon atoms per molecule.
4035570 Method and catalyst for the production of high trans-polyalkadiene July 12, 1977
Polyalkadienes with high percentage of trans configurations are produced by employing a catalyst system obtained by admixing (A) at least one hydride having the general formula MZR.sub.a H.sub.(4-a) wherein M is lithium, sodium, potassium, rubidium or cesium, Z is aluminum or boron, R is
3983187 Iodine molecular weight regulators in suspension polymerization systems September 28, 1976
Iodine or organic iodides are effective in suspension polymerization systems as molecular weight regulators or modifiers. These modifiers are especially suited for the suspension ABS processes.
3962195 Terpolymers of a furan, a maleic anhydride and one of a conjugated diene and a vinyl aromatic co June 8, 1976
A furan, a maleic anhydride and at least one unsaturated compound selected from a conjugated diene, e.g., butadiene and a vinyl aromatic, e.g., styrene are reacted in presence of a free-radical initiator, e.g., an organic peroxide or azo compound for example di-t-butyl peroxide or 2,


 
 
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