ZA200106156B - Vinylcyclohexane-based polymer/copolymer mixture and stabilizer system. - Google Patents

Vinylcyclohexane-based polymer/copolymer mixture and stabilizer system. Download PDF

Info

Publication number: ZA200106156B
Authority: ZA; South Africa
Prior art keywords: alkyl; formula; mixture according; independently; vinylcyclohexane
Prior art date: 1999-02-19

Application number

ZA200106156A

Other languages

English (en)

Inventor

Volker Wege

Konstadinos Douzinas

Friedrich Bruder

Original Assignee

Bayer Ag Teijin Ltd

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.)

1999-02-19

Filing date

2001-07-26

Publication date

2002-07-26

2001-07-26 Application filed by Bayer Ag Teijin Ltd filed Critical Bayer Ag Teijin Ltd

2002-07-26 Publication of ZA200106156B publication Critical patent/ZA200106156B/en

Links

229920000642 polymer Polymers 0.000 title claims description 52
239000003381 stabilizer Substances 0.000 title claims description 29
239000000203 mixture Substances 0.000 title claims description 28
LDLDYFCCDKENPD-UHFFFAOYSA-N ethenylcyclohexane Chemical compound C=CC1CCCCC1 LDLDYFCCDKENPD-UHFFFAOYSA-N 0.000 title claims description 20
229920001577 copolymer Polymers 0.000 title claims description 9
229910052739 hydrogen Inorganic materials 0.000 claims description 20
239000001257 hydrogen Substances 0.000 claims description 20
150000001875 compounds Chemical class 0.000 claims description 17
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 14
230000003287 optical effect Effects 0.000 claims description 14
ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 12
150000002596 lactones Chemical class 0.000 claims description 11
238000004519 manufacturing process Methods 0.000 claims description 9
238000000034 method Methods 0.000 claims description 7
OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims description 7
-1 phosphite compound Chemical class 0.000 claims description 6
238000002360 preparation method Methods 0.000 claims description 6
150000002431 hydrogen Chemical class 0.000 claims description 5
MYRTYDVEIRVNKP-UHFFFAOYSA-N 1,2-Divinylbenzene Chemical compound C=CC1=CC=CC=C1C=C MYRTYDVEIRVNKP-UHFFFAOYSA-N 0.000 claims description 4
239000000654 additive Substances 0.000 claims description 4
239000000969 carrier Substances 0.000 claims description 4
125000000391 vinyl group Chemical group [H]C([*])=C([H])[H] 0.000 claims description 4
229910052799 carbon Inorganic materials 0.000 claims description 3
125000004432 carbon atom Chemical group C* 0.000 claims description 3
239000003795 chemical substances by application Substances 0.000 claims description 3
NVZWEEGUWXZOKI-UHFFFAOYSA-N 1-ethenyl-2-methylbenzene Chemical compound CC1=CC=CC=C1C=C NVZWEEGUWXZOKI-UHFFFAOYSA-N 0.000 claims description 2
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 claims description 2
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 claims description 2
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 claims description 2
QYKIQEUNHZKYBP-UHFFFAOYSA-N Vinyl ether Chemical class C=COC=C QYKIQEUNHZKYBP-UHFFFAOYSA-N 0.000 claims description 2
150000008360 acrylonitriles Chemical class 0.000 claims description 2
150000001336 alkenes Chemical class 0.000 claims description 2
125000002947 alkylene group Chemical group 0.000 claims description 2
239000002216 antistatic agent Substances 0.000 claims description 2
239000000975 dye Substances 0.000 claims description 2
229930195733 hydrocarbon Natural products 0.000 claims description 2
150000002430 hydrocarbons Chemical class 0.000 claims description 2
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims description 2
239000000178 monomer Substances 0.000 claims description 2
239000002667 nucleating agent Substances 0.000 claims description 2
239000000049 pigment Substances 0.000 claims description 2
150000003440 styrenes Chemical class 0.000 claims description 2
229920001567 vinyl ester resin Polymers 0.000 claims description 2
125000000217 alkyl group Chemical group 0.000 claims 2
NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 claims 1
239000006057 Non-nutritive feed additive Substances 0.000 claims 1
125000005907 alkyl ester group Chemical group 0.000 claims 1
239000003054 catalyst Substances 0.000 description 12
238000005984 hydrogenation reaction Methods 0.000 description 9
239000004793 Polystyrene Substances 0.000 description 8
229920002223 polystyrene Polymers 0.000 description 8
238000006243 chemical reaction Methods 0.000 description 7
238000001125 extrusion Methods 0.000 description 6
PXHVJJICTQNCMI-UHFFFAOYSA-N Nickel Chemical compound [Ni] PXHVJJICTQNCMI-UHFFFAOYSA-N 0.000 description 5
238000001746 injection moulding Methods 0.000 description 5
239000011148 porous material Substances 0.000 description 5
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 4
125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 4
239000000463 material Substances 0.000 description 4
239000002904 solvent Substances 0.000 description 4
XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 3
229920001400 block copolymer Polymers 0.000 description 3
238000013500 data storage Methods 0.000 description 3
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 3
XRBCRPZXSCBRTK-UHFFFAOYSA-N phosphonous acid Chemical compound OPO XRBCRPZXSCBRTK-UHFFFAOYSA-N 0.000 description 3
239000004417 polycarbonate Substances 0.000 description 3
239000000243 solution Substances 0.000 description 3
238000003860 storage Methods 0.000 description 3
239000000126 substance Substances 0.000 description 3
IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 2
KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 description 2
BEIOEBMXPVYLRY-UHFFFAOYSA-N [4-[4-bis(2,4-ditert-butylphenoxy)phosphanylphenyl]phenyl]-bis(2,4-ditert-butylphenoxy)phosphane Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(C=1C=CC(=CC=1)C=1C=CC(=CC=1)P(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C BEIOEBMXPVYLRY-UHFFFAOYSA-N 0.000 description 2
238000013329 compounding Methods 0.000 description 2
MGNZXYYWBUKAII-UHFFFAOYSA-N cyclohexa-1,3-diene Chemical compound C1CC=CC=C1 MGNZXYYWBUKAII-UHFFFAOYSA-N 0.000 description 2
HGCIXCUEYOPUTN-UHFFFAOYSA-N cyclohexene Chemical compound C1CCC=CC1 HGCIXCUEYOPUTN-UHFFFAOYSA-N 0.000 description 2
ZSWFCLXCOIISFI-UHFFFAOYSA-N cyclopentadiene Chemical compound C1C=CC=C1 ZSWFCLXCOIISFI-UHFFFAOYSA-N 0.000 description 2
229920001519 homopolymer Polymers 0.000 description 2
125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
229910052698 phosphorus Inorganic materials 0.000 description 2
239000011574 phosphorus Substances 0.000 description 2
229920000515 polycarbonate Polymers 0.000 description 2
239000007787 solid Substances 0.000 description 2
HECLRDQVFMWTQS-RGOKHQFPSA-N 1755-01-7 Chemical class C1[C@H]2[C@@H]3CC=C[C@@H]3[C@@H]1C=C2 HECLRDQVFMWTQS-RGOKHQFPSA-N 0.000 description 1
238000005160 1H NMR spectroscopy Methods 0.000 description 1
ACZGCWSMSTYWDQ-UHFFFAOYSA-N 3h-1-benzofuran-2-one Chemical class C1=CC=C2OC(=O)CC2=C1 ACZGCWSMSTYWDQ-UHFFFAOYSA-N 0.000 description 1
CYHYIIFODCKQNP-UHFFFAOYSA-N 5,7-ditert-butyl-3-(3,4-dimethylphenyl)-3h-1-benzofuran-2-one Chemical group C1=C(C)C(C)=CC=C1C1C(C=C(C=C2C(C)(C)C)C(C)(C)C)=C2OC1=O CYHYIIFODCKQNP-UHFFFAOYSA-N 0.000 description 1
NLHHRLWOUZZQLW-UHFFFAOYSA-N Acrylonitrile Chemical compound C=CC#N NLHHRLWOUZZQLW-UHFFFAOYSA-N 0.000 description 1
229910052684 Cerium Inorganic materials 0.000 description 1
VQTUBCCKSQIDNK-UHFFFAOYSA-N Isobutene Chemical group CC(C)=C VQTUBCCKSQIDNK-UHFFFAOYSA-N 0.000 description 1
BZLVMXJERCGZMT-UHFFFAOYSA-N Methyl tert-butyl ether Chemical compound COC(C)(C)C BZLVMXJERCGZMT-UHFFFAOYSA-N 0.000 description 1
GYCMBHHDWRMZGG-UHFFFAOYSA-N Methylacrylonitrile Chemical compound CC(=C)C#N GYCMBHHDWRMZGG-UHFFFAOYSA-N 0.000 description 1
238000005481 NMR spectroscopy Methods 0.000 description 1
OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 1
239000007868 Raney catalyst Substances 0.000 description 1
229910000564 Raney nickel Inorganic materials 0.000 description 1
IYABWNGZIDDRAK-UHFFFAOYSA-N allene Chemical group C=C=C IYABWNGZIDDRAK-UHFFFAOYSA-N 0.000 description 1
238000000149 argon plasma sintering Methods 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
230000001427 coherent effect Effects 0.000 description 1
238000006731 degradation reaction Methods 0.000 description 1
230000006866 deterioration Effects 0.000 description 1
230000000694 effects Effects 0.000 description 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 1
230000008020 evaporation Effects 0.000 description 1
238000001704 evaporation Methods 0.000 description 1
230000003203 everyday effect Effects 0.000 description 1
239000007789 gas Substances 0.000 description 1
229920000578 graft copolymer Polymers 0.000 description 1
239000008187 granular material Substances 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
238000007654 immersion Methods 0.000 description 1
239000011261 inert gas Substances 0.000 description 1
238000002347 injection Methods 0.000 description 1
239000007924 injection Substances 0.000 description 1
230000002452 interceptive effect Effects 0.000 description 1
239000007788 liquid Substances 0.000 description 1
239000000314 lubricant Substances 0.000 description 1
239000011159 matrix material Substances 0.000 description 1
229910052751 metal Inorganic materials 0.000 description 1
239000002184 metal Substances 0.000 description 1
YFKIWUQBRSMPMZ-UHFFFAOYSA-N methane;nickel Chemical compound C.[Ni] YFKIWUQBRSMPMZ-UHFFFAOYSA-N 0.000 description 1
238000002156 mixing Methods 0.000 description 1
229910052757 nitrogen Inorganic materials 0.000 description 1
229910000510 noble metal Inorganic materials 0.000 description 1
125000003518 norbornenyl group Chemical class C12(C=CC(CC1)C2)* 0.000 description 1
229910052763 palladium Inorganic materials 0.000 description 1
150000002989 phenols Chemical class 0.000 description 1
229910052697 platinum Inorganic materials 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
239000004926 polymethyl methacrylate Substances 0.000 description 1
230000001681 protective effect Effects 0.000 description 1
230000005855 radiation Effects 0.000 description 1
150000003254 radicals Chemical class 0.000 description 1
229920005604 random copolymer Polymers 0.000 description 1
229910052703 rhodium Inorganic materials 0.000 description 1
229910052707 ruthenium Inorganic materials 0.000 description 1
229930000044 secondary metabolite Natural products 0.000 description 1
238000004611 spectroscopical analysis Methods 0.000 description 1
239000007858 starting material Substances 0.000 description 1
238000003756 stirring Methods 0.000 description 1
125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
238000000870 ultraviolet spectroscopy Methods 0.000 description 1

Classifications

- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/13—Phenols; Phenolates
- C08K5/134—Phenols containing ester groups
- C08K5/1345—Carboxylic esters of phenolcarboxylic acids
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/15—Heterocyclic compounds having oxygen in the ring
- C08K5/151—Heterocyclic compounds having oxygen in the ring having one oxygen atom in the ring
- C08K5/1535—Five-membered rings
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K5/00—Use of organic ingredients
- C08K5/49—Phosphorus-containing compounds
- C08K5/51—Phosphorus bound to oxygen
- C08K5/52—Phosphorus bound to oxygen only
- C08K5/524—Esters of phosphorous acids, e.g. of H3PO3
- C08K5/526—Esters of phosphorous acids, e.g. of H3PO3 with hydroxyaryl compounds
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/18—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms
- C08L23/20—Homopolymers or copolymers of hydrocarbons having four or more carbon atoms having four to nine carbon atoms
- G—PHYSICS
- G11—INFORMATION STORAGE
- G11B—INFORMATION STORAGE BASED ON RELATIVE MOVEMENT BETWEEN RECORD CARRIER AND TRANSDUCER
- G11B7/00—Recording or reproducing by optical means, e.g. recording using a thermal beam of optical radiation by modifying optical properties or the physical structure, reproducing using an optical beam at lower power by sensing optical properties; Record carriers therefor
- G11B7/24—Record carriers characterised by shape, structure or physical properties, or by the selection of the material
- G11B7/241—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material
- G11B7/252—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers
- G11B7/253—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of substrates
- G11B7/2533—Record carriers characterised by shape, structure or physical properties, or by the selection of the material characterised by the selection of the material of layers other than recording layers of substrates comprising resins

Landscapes

Chemical & Material Sciences (AREA)
Health & Medical Sciences (AREA)
Chemical Kinetics & Catalysis (AREA)
Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Organic Chemistry (AREA)
Compositions Of Macromolecular Compounds (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Optical Record Carriers And Manufacture Thereof (AREA)

ZA200106156A 1999-02-19 2001-07-26 Vinylcyclohexane-based polymer/copolymer mixture and stabilizer system. ZA200106156B (en)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE19906983A DE19906983A1 (de)	1999-02-19	1999-02-19	Mischung aus Vinylcyclohexan basierenden Polymer/Copolymer und Stabilisatorsystem

Publications (1)

Publication Number	Publication Date
ZA200106156B true ZA200106156B (en)	2002-07-26

Family

ID=7898028

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ZA200106156A ZA200106156B (en)	1999-02-19	2001-07-26	Vinylcyclohexane-based polymer/copolymer mixture and stabilizer system.

Country Status (14)

Country	Link
US (1)	US6803397B1 (de)
EP (1)	EP1157065A1 (de)
JP (1)	JP2002537430A (de)
KR (1)	KR20010102253A (de)
CN (1)	CN1183189C (de)
AU (1)	AU762336B2 (de)
BR (1)	BR0008291A (de)
CA (1)	CA2362824A1 (de)
DE (1)	DE19906983A1 (de)
HK (1)	HK1045164B (de)
RU (1)	RU2246507C2 (de)
TW (1)	TW500750B (de)
WO (1)	WO2000049078A1 (de)
ZA (1)	ZA200106156B (de)

Family Cites Families (7)

* Cited by examiner, † Cited by third party
Publication number	Priority date	Publication date	Assignee	Title
JPS61138648A (ja)	1984-12-10	1986-06-26	Mitsui Petrochem Ind Ltd	光学デイスク
JPH0794496B2 (ja)	1987-11-18	1995-10-11	日本合成ゴム株式会社	光学材料
JP2586575B2 (ja) *	1988-05-23	1997-03-05	三菱化学株式会社	光ディスク基板
US4911966A (en)	1988-12-02	1990-03-27	Mitsubishi Monsanto Chemical Company	Optical disk substrate
JP3393655B2 (ja)	1992-02-27	2003-04-07	パイオニア株式会社	光ディスクプレーヤ
WO1999003915A1 (en) *	1997-07-14	1999-01-28	Dover Chemical Corporation	Lactone/phosphite blends
WO1999041307A1 (en) *	1998-02-17	1999-08-19	The Dow Chemical Company	Hydrogenated aromatic polymer compositions containing stabilizers

1999
- 1999-02-19 DE DE19906983A patent/DE19906983A1/de not_active Withdrawn
2000
- 2000-02-09 CN CNB008040117A patent/CN1183189C/zh not_active Expired - Fee Related
- 2000-02-09 BR BR0008291-0A patent/BR0008291A/pt not_active Application Discontinuation
- 2000-02-09 HK HK02106732.8A patent/HK1045164B/zh not_active IP Right Cessation
- 2000-02-09 AU AU29086/00A patent/AU762336B2/en not_active Ceased
- 2000-02-09 WO PCT/EP2000/001026 patent/WO2000049078A1/de not_active Ceased
- 2000-02-09 CA CA002362824A patent/CA2362824A1/en not_active Abandoned
- 2000-02-09 KR KR1020017010522A patent/KR20010102253A/ko not_active Ceased
- 2000-02-09 US US09/913,747 patent/US6803397B1/en not_active Expired - Fee Related
- 2000-02-09 JP JP2000599813A patent/JP2002537430A/ja active Pending
- 2000-02-09 EP EP00907527A patent/EP1157065A1/de not_active Withdrawn
- 2000-02-09 RU RU2001125724/04A patent/RU2246507C2/ru not_active IP Right Cessation
- 2000-02-18 TW TW089102768A patent/TW500750B/zh not_active IP Right Cessation
2001
- 2001-07-26 ZA ZA200106156A patent/ZA200106156B/en unknown

Also Published As

Publication number	Publication date
AU762336B2 (en)	2003-06-26
DE19906983A1 (de)	2000-08-31
HK1045164A1 (en)	2002-11-15
CN1344288A (zh)	2002-04-10
EP1157065A1 (de)	2001-11-28
CA2362824A1 (en)	2000-08-24
TW500750B (en)	2002-09-01
JP2002537430A (ja)	2002-11-05
US6803397B1 (en)	2004-10-12
CN1183189C (zh)	2005-01-05
KR20010102253A (ko)	2001-11-15
HK1045164B (zh)	2005-08-19
AU2908600A (en)	2000-09-04
WO2000049078A1 (de)	2000-08-24
BR0008291A (pt)	2001-11-06
RU2246507C2 (ru)	2005-02-20

Publication	Publication Date	Title
JP3857234B2 (ja)	2006-12-13	改良された水素化スチレン−共役ジエン−スチレンブロック共重合体およびその製造方法
US6365694B1 (en)	2002-04-02	Amorphous vinyl cyclohexane polymers
US6803397B1 (en)	2004-10-12	Vinylcyclohexane—based polymer/copolymer mixture and stabilizer system
JP2000006181A (ja)	2000-01-11	水添α−オレフィン−ジシクロペンタジエン系共重合体の成形方法およびそれから得られる成形物
US6649723B1 (en)	2003-11-18	Vinylcyclohexane-based polymers
JPH06211937A (ja)	1994-08-02	少なくとも１種のシクロオレフィン共重合体からなる記録媒体用基材、およびその製造法
JP2002201213A (ja)	2002-07-19	水素化スチレン系共重合体および光学材料
CA2373712A1 (en)	2000-11-23	Substrates for optical storage media
CA2362829A1 (en)	2000-08-24	Polymers based on vinylcyclohexane
EP1441007A1 (de)	2004-07-28	Hydrierte styrolpolymere enthaltende harzzusammensetzung und optische elemente
JP2003508284A (ja)	2003-03-04	水素添加ブロック共重合体からの光媒体ディスクの製造方法
JP2003535418A (ja)	2003-11-25	高データ密度光媒体ディスク
JP2002069257A (ja)	2002-03-08	水素化スチレン系重合体組成物
JP2002114919A (ja)	2002-04-16	シクロアルカン構造を有する重合体シートおよびその製造方法