SU694078A3 - Способ получени привитых сополимеров - Google Patents

Способ получени привитых сополимеров

Info

Publication number: SU694078A3
Authority: SU; USSR - Soviet Union
Prior art keywords: polystyrene; solution; mol; polymerization; hours
Prior art date: 1972-04-14

Application number

SU731907451A

Other languages

English (en)

Russian (ru)

Inventor

Милкович Ральф

Т.Чанг Матонг

О.Шульц Геральд

Original Assignee

Спс Интернэшнл Инк. (Фирма)

Priority date (The priority date 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 date listed.)

1972-04-14

Filing date

1973-04-13

Publication date

1979-10-25

1972-04-14 Priority claimed from US00244205A external-priority patent/US3832423A/en

1973-04-13 Application filed by Спс Интернэшнл Инк. (Фирма) filed Critical Спс Интернэшнл Инк. (Фирма)

1979-10-25 Application granted granted Critical

1979-10-25 Publication of SU694078A3 publication Critical patent/SU694078A3/ru

Links

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IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 54
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238000006116 polymerization reaction Methods 0.000 claims description 33
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238000007334 copolymerization reaction Methods 0.000 claims description 23
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HRPVXLWXLXDGHG-UHFFFAOYSA-N Acrylamide Chemical compound NC(=O)C=C HRPVXLWXLXDGHG-UHFFFAOYSA-N 0.000 description 1
239000004342 Benzoyl peroxide Substances 0.000 description 1
OMPJBNCRMGITSC-UHFFFAOYSA-N Benzoylperoxide Chemical compound C=1C=CC=CC=1C(=O)OOC(=O)C1=CC=CC=C1 OMPJBNCRMGITSC-UHFFFAOYSA-N 0.000 description 1
229920002799 BoPET Polymers 0.000 description 1
241000283690 Bos taurus Species 0.000 description 1
244000024671 Brassica kaber Species 0.000 description 1
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 1
QTNHGXAVLCFCAW-UHFFFAOYSA-N Cl(=O)(=O)[V](Cl(=O)=O)Cl(=O)=O Chemical compound Cl(=O)(=O)[V](Cl(=O)=O)Cl(=O)=O QTNHGXAVLCFCAW-UHFFFAOYSA-N 0.000 description 1
SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 1
238000004566 IR spectroscopy Methods 0.000 description 1
102000003812 Interleukin-15 Human genes 0.000 description 1
108090000172 Interleukin-15 Proteins 0.000 description 1
WHXSMMKQMYFTQS-UHFFFAOYSA-N Lithium Chemical compound [Li] WHXSMMKQMYFTQS-UHFFFAOYSA-N 0.000 description 1
LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical compound SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 description 1
239000005041 Mylar™ Substances 0.000 description 1
229920003171 Poly (ethylene oxide) Polymers 0.000 description 1
239000005062 Polybutadiene Substances 0.000 description 1
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VMHLLURERBWHNL-UHFFFAOYSA-M Sodium acetate Chemical compound [Na+].CC([O-])=O VMHLLURERBWHNL-UHFFFAOYSA-M 0.000 description 1
WSRGYQPQNAUVAJ-UHFFFAOYSA-N [V].Cl=O Chemical compound [V].Cl=O WSRGYQPQNAUVAJ-UHFFFAOYSA-N 0.000 description 1
238000010521 absorption reaction Methods 0.000 description 1
CWRYPZZKDGJXCA-UHFFFAOYSA-N acenaphthalene Natural products C1=CC(CC2)=C3C2=CC=CC3=C1 CWRYPZZKDGJXCA-UHFFFAOYSA-N 0.000 description 1
230000002411 adverse Effects 0.000 description 1
150000007933 aliphatic carboxylic acids Chemical class 0.000 description 1
125000005907 alkyl ester group Chemical group 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium peroxydisulfate Substances [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 1
VAZSKTXWXKYQJF-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)OOS([O-])=O VAZSKTXWXKYQJF-UHFFFAOYSA-N 0.000 description 1
229910001870 ammonium persulfate Inorganic materials 0.000 description 1
238000013459 approach Methods 0.000 description 1
150000004945 aromatic hydrocarbons Chemical class 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
230000008901 benefit Effects 0.000 description 1
WIRUZQNBHNAMAB-UHFFFAOYSA-N benzene;cyclohexane Chemical compound C1CCCCC1.C1=CC=CC=C1 WIRUZQNBHNAMAB-UHFFFAOYSA-N 0.000 description 1
235000019400 benzoyl peroxide Nutrition 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
OOCMUZJPDXYRFD-UHFFFAOYSA-L calcium;2-dodecylbenzenesulfonate Chemical compound [Ca+2].CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O.CCCCCCCCCCCCC1=CC=CC=C1S([O-])(=O)=O OOCMUZJPDXYRFD-UHFFFAOYSA-L 0.000 description 1
229910052799 carbon Inorganic materials 0.000 description 1
230000003197 catalytic effect Effects 0.000 description 1
238000006555 catalytic reaction Methods 0.000 description 1
238000005119 centrifugation Methods 0.000 description 1
239000012986 chain transfer agent Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
239000000460 chlorine Substances 0.000 description 1
229910052801 chlorine Inorganic materials 0.000 description 1
FOCAUTSVDIKZOP-UHFFFAOYSA-M chloroacetate Chemical compound [O-]C(=O)CCl FOCAUTSVDIKZOP-UHFFFAOYSA-M 0.000 description 1
229940089960 chloroacetate Drugs 0.000 description 1
HRYZWHHZPQKTII-UHFFFAOYSA-N chloroethane Chemical compound CCCl HRYZWHHZPQKTII-UHFFFAOYSA-N 0.000 description 1
238000004587 chromatography analysis Methods 0.000 description 1
230000015271 coagulation Effects 0.000 description 1
238000005345 coagulation Methods 0.000 description 1
238000012718 coordination polymerization Methods 0.000 description 1
230000010485 coping Effects 0.000 description 1
229920006037 cross link polymer Polymers 0.000 description 1
230000006378 damage Effects 0.000 description 1
239000008367 deionised water Substances 0.000 description 1
229910021641 deionized water Inorganic materials 0.000 description 1
230000001419 dependent effect Effects 0.000 description 1
125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
230000000694 effects Effects 0.000 description 1
239000000806 elastomer Substances 0.000 description 1
239000003480 eluent Substances 0.000 description 1
238000004945 emulsification Methods 0.000 description 1
LPUZTLKYAOOFDX-QXMHVHEDSA-N ethenyl (z)-octadec-9-enoate Chemical compound CCCCCCCC\C=C/CCCCCCCC(=O)OC=C LPUZTLKYAOOFDX-QXMHVHEDSA-N 0.000 description 1
AFSIMBWBBOJPJG-UHFFFAOYSA-N ethenyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OC=C AFSIMBWBBOJPJG-UHFFFAOYSA-N 0.000 description 1
125000005670 ethenylalkyl group Chemical group 0.000 description 1
125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 1
229960003750 ethyl chloride Drugs 0.000 description 1
IPWNYSIHONRXRY-UHFFFAOYSA-N ethyl prop-2-enoate 2-methylidenehexanoic acid Chemical compound CCOC(=O)C=C.CCCCC(=C)C(O)=O IPWNYSIHONRXRY-UHFFFAOYSA-N 0.000 description 1
MJEMIOXXNCZZFK-UHFFFAOYSA-N ethylone Chemical compound CCNC(C)C(=O)C1=CC=C2OCOC2=C1 MJEMIOXXNCZZFK-UHFFFAOYSA-N 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
230000007717 exclusion Effects 0.000 description 1
238000002474 experimental method Methods 0.000 description 1
239000000284 extract Substances 0.000 description 1
238000000605 extraction Methods 0.000 description 1
239000004744 fabric Substances 0.000 description 1
238000001914 filtration Methods 0.000 description 1
239000006260 foam Substances 0.000 description 1
239000011953 free-radical catalyst Substances 0.000 description 1
230000008014 freezing Effects 0.000 description 1
238000007710 freezing Methods 0.000 description 1
235000011087 fumaric acid Nutrition 0.000 description 1
150000002238 fumaric acids Chemical class 0.000 description 1
230000009477 glass transition Effects 0.000 description 1
125000001475 halogen functional group Chemical group 0.000 description 1
IXCSERBJSXMMFS-UHFFFAOYSA-N hcl hcl Chemical compound Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
239000012456 homogeneous solution Substances 0.000 description 1
239000001257 hydrogen Substances 0.000 description 1
229910052739 hydrogen Inorganic materials 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
229910000037 hydrogen sulfide Inorganic materials 0.000 description 1
230000002209 hydrophobic effect Effects 0.000 description 1
239000005457 ice water Substances 0.000 description 1
239000012535 impurity Substances 0.000 description 1
238000002329 infrared spectrum Methods 0.000 description 1
230000003993 interaction Effects 0.000 description 1
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 description 1
JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
150000002605 large molecules Chemical class 0.000 description 1
125000000400 lauroyl group Chemical group O=C([*])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
150000002689 maleic acids Chemical class 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
230000007246 mechanism Effects 0.000 description 1
238000002844 melting Methods 0.000 description 1
230000008018 melting Effects 0.000 description 1
125000005641 methacryl group Chemical group 0.000 description 1
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
229940088644 n,n-dimethylacrylamide Drugs 0.000 description 1
YLGYACDQVQQZSW-UHFFFAOYSA-N n,n-dimethylprop-2-enamide Chemical compound CN(C)C(=O)C=C YLGYACDQVQQZSW-UHFFFAOYSA-N 0.000 description 1
150000004767 nitrides Chemical class 0.000 description 1
239000012074 organic phase Substances 0.000 description 1
150000002924 oxiranes Chemical class 0.000 description 1
238000005192 partition Methods 0.000 description 1
YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 1
229920001618 poly(2-methyl styrene) Polymers 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
229920001495 poly(sodium acrylate) polymer Polymers 0.000 description 1
229920002857 polybutadiene Polymers 0.000 description 1
229920000728 polyester Polymers 0.000 description 1
229920000120 polyethyl acrylate Polymers 0.000 description 1
239000002861 polymer material Substances 0.000 description 1
239000012985 polymerization agent Substances 0.000 description 1
239000004926 polymethyl methacrylate Substances 0.000 description 1
229920000036 polyvinylpyrrolidone Polymers 0.000 description 1
239000001267 polyvinylpyrrolidone Substances 0.000 description 1
235000013855 polyvinylpyrrolidone Nutrition 0.000 description 1
239000000843 powder Substances 0.000 description 1
230000001376 precipitating effect Effects 0.000 description 1
HJWLCRVIBGQPNF-UHFFFAOYSA-N prop-2-enylbenzene Chemical compound C=CCC1=CC=CC=C1 HJWLCRVIBGQPNF-UHFFFAOYSA-N 0.000 description 1
108090000623 proteins and genes Proteins 0.000 description 1
238000000746 purification Methods 0.000 description 1
239000007870 radical polymerization initiator Substances 0.000 description 1
239000011541 reaction mixture Substances 0.000 description 1
230000009467 reduction Effects 0.000 description 1
238000010992 reflux Methods 0.000 description 1
239000005266 side chain polymer Substances 0.000 description 1
239000010802 sludge Substances 0.000 description 1
239000001632 sodium acetate Substances 0.000 description 1
235000017281 sodium acetate Nutrition 0.000 description 1
CHQMHPLRPQMAMX-UHFFFAOYSA-L sodium persulfate Substances [Na+].[Na+].[O-]S(=O)(=O)OOS([O-])(=O)=O CHQMHPLRPQMAMX-UHFFFAOYSA-L 0.000 description 1
NNMHYFLPFNGQFZ-UHFFFAOYSA-M sodium polyacrylate Chemical compound [Na+].[O-]C(=O)C=C NNMHYFLPFNGQFZ-UHFFFAOYSA-M 0.000 description 1
239000012265 solid product Substances 0.000 description 1
238000004611 spectroscopical analysis Methods 0.000 description 1
238000001228 spectrum Methods 0.000 description 1
229910001220 stainless steel Inorganic materials 0.000 description 1
239000010935 stainless steel Substances 0.000 description 1
235000013547 stew Nutrition 0.000 description 1
BDHFUVZGWQCTTF-UHFFFAOYSA-M sulfonate Chemical compound [O-]S(=O)=O BDHFUVZGWQCTTF-UHFFFAOYSA-M 0.000 description 1
238000003786 synthesis reaction Methods 0.000 description 1
BFKJFAAPBSQJPD-UHFFFAOYSA-N tetrafluoroethene Chemical group FC(F)=C(F)F BFKJFAAPBSQJPD-UHFFFAOYSA-N 0.000 description 1
238000010257 thawing Methods 0.000 description 1
XJDNKRIXUMDJCW-UHFFFAOYSA-J titanium tetrachloride Chemical compound Cl[Ti](Cl)(Cl)Cl XJDNKRIXUMDJCW-UHFFFAOYSA-J 0.000 description 1
238000012549 training Methods 0.000 description 1
FAQYAMRNWDIXMY-UHFFFAOYSA-N trichloroborane Chemical compound ClB(Cl)Cl FAQYAMRNWDIXMY-UHFFFAOYSA-N 0.000 description 1
IAHBIMWHYUOIOH-UHFFFAOYSA-N vanadium hydrochloride Chemical compound Cl.[V] IAHBIMWHYUOIOH-UHFFFAOYSA-N 0.000 description 1
PXXNTAGJWPJAGM-UHFFFAOYSA-N vertaline Natural products C1C2C=3C=C(OC)C(OC)=CC=3OC(C=C3)=CC=C3CCC(=O)OC1CC1N2CCCC1 PXXNTAGJWPJAGM-UHFFFAOYSA-N 0.000 description 1
KOZCZZVUFDCZGG-UHFFFAOYSA-N vinyl benzoate Chemical compound C=COC(=O)C1=CC=CC=C1 KOZCZZVUFDCZGG-UHFFFAOYSA-N 0.000 description 1
229920001567 vinyl ester resin Polymers 0.000 description 1
238000004073 vulcanization Methods 0.000 description 1
238000005406 washing Methods 0.000 description 1
239000004711 α-olefin Substances 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08C—TREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
- C08C19/00—Chemical modification of rubber
- C08C19/30—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule
- C08C19/42—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with metals or metal-containing groups
- C08C19/44—Addition of a reagent which reacts with a hetero atom or a group containing hetero atoms of the macromolecule reacting with metals or metal-containing groups of polymers containing metal atoms exclusively at one or both ends of the skeleton
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F290/00—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups
- C08F290/02—Macromolecular compounds obtained by polymerising monomers on to polymers modified by introduction of aliphatic unsaturated end or side groups on to polymers modified by introduction of unsaturated end groups
- C08F290/04—Polymers provided for in subclasses C08C or C08F
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G85/00—General processes for preparing compounds provided for in this subclass

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)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Graft Or Block Polymers (AREA)

SU731907451A 1972-04-14 1973-04-13 Способ получени привитых сополимеров SU694078A3 (ru)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
US00244205A US3832423A (en)	1971-02-22	1972-04-14	Chemically joined, phase separated graft copolymers having hydrocarbon polymeric backbones

Publications (1)

Publication Number	Publication Date
SU694078A3 true SU694078A3 (ru)	1979-10-25

Family

ID=22921801

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
SU731907451A SU694078A3 (ru)	1972-04-14	1973-04-13	Способ получени привитых сополимеров
SU752119508A SU671734A3 (ru)	1972-04-14	1975-04-03	Способ получени реакционноспособных полимеров

Family Applications After (1)

Application Number	Title	Priority Date	Filing Date
SU752119508A SU671734A3 (ru)	1972-04-14	1975-04-03	Способ получени реакционноспособных полимеров

Country Status (5)

Country	Link
AT (1)	AT339592B (de)
BE (1)	BE798165A (de)
CS (1)	CS194160B2 (de)
SU (2)	SU694078A3 (de)
ZA (1)	ZA732134B (de)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE4342605A1 (de) *	1993-12-14	1995-06-22	Buna Gmbh	Funktionalisierte Olefinhomo- und -copolymere
US11780953B2 (en)	2018-01-30	2023-10-10	Johnson & Johnson Vision Care, Inc.	Ophthalmic devices containing localized grafted networks and processes for their preparation and use
US11820850B2 (en)	2016-08-05	2023-11-21	Johnson & Johnson Vision Care, Inc.	Polymer compositions containing grafted polymeric networks and processes for their preparation and use
US11834547B2 (en)	2018-01-30	2023-12-05	Johnson & Johnson Vision Care, Inc.	Ophthalmic devices derived from grafted polymeric networks and processes for their preparation and use

1973
- 1973-03-28 ZA ZA732134A patent/ZA732134B/xx unknown
- 1973-04-13 SU SU731907451A patent/SU694078A3/ru active
- 1973-04-13 BE BE2052684A patent/BE798165A/xx not_active IP Right Cessation
- 1973-04-13 AT AT329473A patent/AT339592B/de not_active IP Right Cessation
- 1973-04-14 CS CS732680A patent/CS194160B2/cs unknown
1975
- 1975-04-03 SU SU752119508A patent/SU671734A3/ru active

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
DE4342605A1 (de) *	1993-12-14	1995-06-22	Buna Gmbh	Funktionalisierte Olefinhomo- und -copolymere
US11820850B2 (en)	2016-08-05	2023-11-21	Johnson & Johnson Vision Care, Inc.	Polymer compositions containing grafted polymeric networks and processes for their preparation and use
US12331146B2 (en)	2016-08-05	2025-06-17	Johnson & Johnson Vision Care, Inc.	Polymer compositions containing grafted polymeric networks and processes for their preparation and use
US11780953B2 (en)	2018-01-30	2023-10-10	Johnson & Johnson Vision Care, Inc.	Ophthalmic devices containing localized grafted networks and processes for their preparation and use
US11834547B2 (en)	2018-01-30	2023-12-05	Johnson & Johnson Vision Care, Inc.	Ophthalmic devices derived from grafted polymeric networks and processes for their preparation and use
US12391789B2 (en)	2018-01-30	2025-08-19	Johnson & Johnson Vision Care, Inc.	Ophthalmic devices containing localized grafted networks and processes for their preparation and use

Also Published As

Publication number	Publication date
CS194160B2 (en)	1979-11-30
AT339592B (de)	1977-10-25
ZA732134B (en)	1974-02-27
BE798165A (fr)	1973-07-31
SU671734A3 (ru)	1979-06-30
ATA329473A (de)	1977-02-15

Publication	Publication Date	Title
US4085168A (en)	1978-04-18	Chemically joined, phase separated self-cured hydrophilic thermoplastic graft copolymers and their preparation
US3928255A (en)	1975-12-23	Chemically joined, phase separated self-cured hydrophilic thermoplastic graft copolymers and their preparation
US3786116A (en)	1974-01-15	Chemically joined,phase separated thermoplastic graft copolymers
US3842059A (en)	1974-10-15	Acrylate and methacrylate terminated polystyrene macromolecular monomers having a substantially uniform molecular weight distribution
US3842146A (en)	1974-10-15	Polymerizable diblock macromolecular monomers having a substantially uniform molecular weight distribution and their preparation
US3989768A (en)	1976-11-02	Chemically joined phase separated thermoplastic graft copolymers
US3862077A (en)	1975-01-21	Stable latexes of a chemically joined, phase separated thermoplastic graft copolymer and method for preparing the same
US4816520A (en)	1989-03-28	Terminally functionalized polymers and preparation thereof
US3879494A (en)	1975-04-22	Polyblends of chemically joined, phase separated thermoplastic graft copolymers
US4029720A (en)	1977-06-14	Block or graft copolymers of polyalkylene oxides and vinylaromatic or diene polymers
US3862098A (en)	1975-01-21	Alpha-olefin terminated polystyrene macromolecular monomers having a substantially uniform molecular weight distribution
US4104330A (en)	1978-08-01	Synthesis and copolymerization of tapered block macromer monomers
US3862102A (en)	1975-01-21	Alpha-olefin terminated polydiene macromolecular monomers having a substantially uniform molecular weight distribution
US3842058A (en)	1974-10-15	Vinyl ether terminated polystyrene macromolecular monomers having a substantially uniform molecular weight distribution
CA1037636A (en)	1978-08-29	Polymers and processes therefor
US3842057A (en)	1974-10-15	Vinyl ester terminated macromolecular monomers having a substantially uniform molecular weight distribution and process for preparing same
EP0189174B1 (de)	1990-04-25	Polymere von substituierten 1,3-Butadienverbindungen und Verfahren zu deren Herstellung
SU694078A3 (ru)	1979-10-25	Способ получени привитых сополимеров
US3862101A (en)	1975-01-21	Acrylate and methacrylate terminated polydiene macromolecular monomers having a substantially uniform molecular weight distribution
JP2002500696A (ja)	2002-01-08	ゴム製品用エラストマー物質
Price et al.	1990	Polymerization and copolymerization using high intensity ultrasound
US3842050A (en)	1974-10-15	Maleic acid half ester terminated polystyrene macromolecular monomers having a substantially uniform molecular weight distribution
Abdel-Razik	1990	Homogeneous graft copolymerization of acrylamide onto ethylcellulose
DK160151B (da)	1991-02-04	Copolymer med liniaer hovedkaede og lineaere polymere sidekaeder anvendelig til fremstilling af film samt fremgangsmaade til fremstilling deraf
US4029718A (en)	1977-06-14	Pivalolactone random graft copolymers