KR930021700A - 초 미립 솔비톨 아세탈 및 크실리톨 아세탈을 함유하는 폴리올레핀 조성물 - Google Patents
초 미립 솔비톨 아세탈 및 크실리톨 아세탈을 함유하는 폴리올레핀 조성물 Download PDFInfo
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- KR930021700A KR930021700A KR1019930007530A KR930007530A KR930021700A KR 930021700 A KR930021700 A KR 930021700A KR 1019930007530 A KR1019930007530 A KR 1019930007530A KR 930007530 A KR930007530 A KR 930007530A KR 930021700 A KR930021700 A KR 930021700A
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- microns
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- purifying agent
- purifier
- carbon atoms
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- 239000000203 mixture Substances 0.000 title claims 10
- 229920000098 polyolefin Polymers 0.000 title claims 2
- DHKHKXVYLBGOIT-UHFFFAOYSA-N acetaldehyde Diethyl Acetal Natural products CCOC(C)OCC DHKHKXVYLBGOIT-UHFFFAOYSA-N 0.000 title 2
- -1 sorbitol acetal Chemical class 0.000 title 2
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 title 1
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 title 1
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 title 1
- 239000000600 sorbitol Substances 0.000 title 1
- 239000000811 xylitol Substances 0.000 title 1
- 229960002675 xylitol Drugs 0.000 title 1
- 235000010447 xylitol Nutrition 0.000 title 1
- 125000000217 alkyl group Chemical group 0.000 claims abstract 20
- 238000000034 method Methods 0.000 claims abstract 14
- 239000012629 purifying agent Substances 0.000 claims abstract 13
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract 10
- 239000002245 particle Substances 0.000 claims abstract 9
- 229920005989 resin Polymers 0.000 claims abstract 8
- 239000011347 resin Substances 0.000 claims abstract 8
- 229920005672 polyolefin resin Polymers 0.000 claims abstract 6
- 125000006700 (C1-C6) alkylthio group Chemical group 0.000 claims abstract 3
- 125000003545 alkoxy group Chemical group 0.000 claims abstract 3
- 125000005332 alkyl sulfoxy group Chemical group 0.000 claims abstract 3
- 229910052736 halogen Inorganic materials 0.000 claims abstract 3
- 150000002367 halogens Chemical class 0.000 claims abstract 3
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract 3
- 238000002156 mixing Methods 0.000 claims abstract 3
- WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 claims 7
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 claims 7
- GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 claims 7
- 229910052794 bromium Inorganic materials 0.000 claims 7
- 229910052801 chlorine Inorganic materials 0.000 claims 7
- 239000000460 chlorine Substances 0.000 claims 7
- 150000003568 thioethers Chemical class 0.000 claims 7
- 150000001875 compounds Chemical class 0.000 claims 5
- 238000002844 melting Methods 0.000 claims 4
- 230000008018 melting Effects 0.000 claims 4
- 239000000843 powder Substances 0.000 claims 4
- 239000012459 cleaning agent Substances 0.000 claims 2
- 238000010438 heat treatment Methods 0.000 claims 2
- 238000004090 dissolution Methods 0.000 claims 1
- FMZUHGYZWYNSOA-VVBFYGJXSA-N (1r)-1-[(4r,4ar,8as)-2,6-diphenyl-4,4a,8,8a-tetrahydro-[1,3]dioxino[5,4-d][1,3]dioxin-4-yl]ethane-1,2-diol Chemical compound C([C@@H]1OC(O[C@@H]([C@@H]1O1)[C@H](O)CO)C=2C=CC=CC=2)OC1C1=CC=CC=C1 FMZUHGYZWYNSOA-VVBFYGJXSA-N 0.000 description 2
- 229940087101 dibenzylidene sorbitol Drugs 0.000 description 2
- OHWBOQAWKNFLRG-UEQSERJNSA-N (3s,4s,5s,6r)-1,8-bis(4-ethylphenyl)octa-1,7-diene-2,3,4,5,6,7-hexol Chemical compound C1=CC(CC)=CC=C1C=C(O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=CC1=CC=C(CC)C=C1 OHWBOQAWKNFLRG-UEQSERJNSA-N 0.000 description 1
- CTPBWPYKMGMLGS-CIAFKFPVSA-N (3s,4s,5s,6r)-1,8-bis(4-methylphenyl)octa-1,7-diene-2,3,4,5,6,7-hexol Chemical compound C1=CC(C)=CC=C1C=C(O)[C@@H](O)[C@@H](O)[C@H](O)[C@@H](O)C(O)=CC1=CC=C(C)C=C1 CTPBWPYKMGMLGS-CIAFKFPVSA-N 0.000 description 1
- 238000000879 optical micrograph Methods 0.000 description 1
Classifications
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- 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
- C08K5/156—Heterocyclic compounds having oxygen in the ring having two oxygen atoms in the ring
- C08K5/1575—Six-membered rings
-
- 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
-
- 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
- C08K2201/00—Specific properties of additives
- C08K2201/002—Physical properties
- C08K2201/005—Additives being defined by their particle size in general
-
- 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
- C08L23/10—Homopolymers or copolymers of propene
- C08L23/12—Polypropene
-
- 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
- C08L23/16—Ethene-propene or ethene-propene-diene copolymers
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- 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)
- Heterocyclic Carbon Compounds Containing A Hetero Ring Having Oxygen Or Sulfur (AREA)
- Processes Of Treating Macromolecular Substances (AREA)
Abstract
Description
Claims (28)
- 폴리올레핀수지 100중량부 및 하기 일반식의 화합물로부터 선택된 정화제 0.01 내지 100중량부를 혼합하고 :
-
- (상기식에서, p는 0또는 1이고, m 및 n은 각각 0 내지 3이며 R은 각각 C1-8알킬, C1-4알콕시, 히드록시, 할로겐, C1-6알킬티오, C1-6알킬설폭시 및 불포화 고리의 인접한 탄소원자와 카르보사이클 고리를 형성하는 4 또는 5멤버드 알킬그룹으로 부터 선택되며 상기 정화제가 분말형태라면 d97은 30마이크론이하 및 평균입자 크기가 15마이크론 이하이다.)
- 상기 수지의 용해온도이상에서 적어도 170℃까지 상기 혼합물을 가열하며, 상기 정화제가 수지내 용해될 때까지 상기 수지가 용융상태인 동안 상기 혼합물을 배합시키는 단계로 구성되는 것을 특징으로 하는 정화제를 반-결정 폴리올레핀수지에 배합시키는 방법.
- 제1항에 있어서, 혼합물이 폴리올레핀수지 100중량부당 상기 정화제 0.1 내지 15중량부로 구성되는 것을 특징으로 하는 방법.
- 제2항에 있어서, 상기 정화제가 d9720마이크론 이하이고 평균입자 크기가 10마이크론 이하인 것을 특징으로 하는 방법.
- 제3항에 있어서, p는 1이고 R은 C1-4알킬, 염소, 브롬, 티오에테르 및 불포화 고리의 인접한 탄소원자로 카르보사이클 고리를 형성하는 4멤버드 알킬그룹으로부터 선택되는 것을 특징으로 하는 방법.
- 제2항에 있어서, 상기 정화제가 10마이크로 이하의 d97및 6마이크로 하여 평균입자 크기를 가지는 것을 특징으로 하는 방법.
- 제5항에 있어서, p가 1이고 R은 C1-4알킬, 염소, 브롬, 티오에테르 및 불포화 고리의 인접한 탄소원자로 카르보사이클 고리를 형성하는 4멤버드 알킬그룹으로부터 선택되는 것을 특징으로 하는 방법.
- 제6항에 있어서, 상기 혼합물이 적어도 180℃의 온도까지 가열되는 것을 특징으로 하는 방법.
- 제1항에 있어서, 상기 혼합물이 상기 폴리올리펜 수지 100중량부당 정화제 0.1 내지 3중량부로 구성되는 것을 특징으로 하는 방법.
- 제8항에 있어서, 상기 정화제가 20마이크론 이하의 d97및 10마이크론 이하의 평균입자 크기를 가지는 것을 특징으로 하는 방법.
- 제9항에 있어서, p가 1이고, R이 C1-4알킬, 염소, 브롬, 티오에테르 및 불포화고리의 인접한 탄소원자와 카르보사이클 고리를 형성하는 4멤버드 알킬그룹으로 부터 선택되는 것을 특징으로 하는 방법.
- 상기 폴리올레핀 100중량부 및 다음 일반식의 화합물로 부터 선택되는 정화제 0.01 내지 100중량부를 혼합하고;
-
- (상기식에서, p는 0또는 1이고, m 및 n은 각각 0 내지 3이며 R은 각각 C1-4알킬, 염소, 브롬, 티오에테르 및 불포화고리의 인접한 탄소원자와 카르보사이클고리를 형성하는 4멤버드 알킬그룹으로 부터 각각 선택되며 또한 정화제가 분말형태라면 d97은 20마이크론 이하이고 평균입자 크기는 10마이크론이하이다); 상기 혼합물을 상기 수지의 융점이상에서 적어도 170℃ 및 상기 정화제의 융점이하의 온도에서 상기 혼합물을 가열시키며, 상기 정화제가 상기 수지내 용해될 때까지 수지가 용융상태인 동안 상기 혼합물을 배합하는 단계로 구성되는 것을 특징으로 하는 정화제를 반-결정 폴리올레핀 수지에 배합시키는 방법.
- 제11항에 있어서, p는 1이고 R이 C1-4알킬, 염소, 브롬, 티오에테르 및 불포화고리의 인접한 탄소원자와 카르보사이클고리를 형성하는 4멤버드 알킬그룹으로 부터 선택되는 것을 특징으로 하는 방법.
- 제12항에 있어서, 상기 혼합물을 180℃ 내지 230℃의 온도로 가열시키는 것을 특징으로 하는 방법.
- 다음 일반식의 화합물로 구성되고 d97은 30마이크론 이하이고, 평균입자크기가 15마이크론 이하인 것을 특징으로 하는 분말로 만들어진 정화제.
-
- (상기식에서, p는 0또는 1이고, m 및 n은 각각 0 내지 3이며 R은 각각 C1-8알킬, C1-4알콕시, 히드록시, 할로겐, C1-6알킬티오, C1-6알킬설폭시 및 불포화 고리의 인접한 탄소원자와 카르보사이클 고리를 형성하는 4 또는 5멤버드 알킬그룹이다.)
- 제14항에 있어서, 상기 정화제가 20마이크론 이하의 d97및 10마이크론 이하의 평균입자 크기를 가지는 것을 특징으로 하는 분말로 만들어진 정화제.
- 제15항에 있어서, p가 1이고 R이 C1-4알킬, 염소, 브롬, 티오에테르 및 불포화 고리의 인접한 탄소원자와 카르보사이클 고리를 형성하는 4멤버드 알킬그룹으로 부터 선택되는 것을 특징으로 하는 분말로 만들어진 정화제.
- 제14항에 있어서, 상기 정화제가 10마이크론이하의 d97및 6마이크론 이하의 평균입자 크기를 가지는 것을 특징으로 하는 분말로 만들어진 정화제.
- 제17항에 있어서, p가 1이고 R이 C1-4알킬, 염소, 브롬, 티오에테르 및 불포화 고리의 인접한 탄소원자와 카르보사이클 고리를 형성하는 4멤버드 알킬그룹으로 부터 선택되는 것을 특징으로 하는 분말로 만들어진 정화제.
- 제16항에 있어서, 상기 정화제가 250℃이상이 융점을 가지는 것을 특징으로 하는 분말로 만들어진 정화제.
- 제14항에 있어서, 상기 정화제가 250℃이상의 융점을 가지는 것을 특징으로 하는 분말로 만들어진 정화제.
- ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1019980035446A KR0183364B1 (en) | 1992-05-01 | 1998-08-27 | Polyolefin composition containing ultrafine sorbitol and xylitol acetals |
Applications Claiming Priority (4)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP877,405 | 1992-05-01 | ||
US07/877,405 US5198484A (en) | 1992-05-01 | 1992-05-01 | Polyolefin composition containing ultrafine sorbitol and xylitol acetals |
US877,405 | 1992-05-01 | ||
JP92-257743 | 1992-09-28 |
Publications (2)
Publication Number | Publication Date |
---|---|
KR930021700A true KR930021700A (ko) | 1993-11-22 |
KR0183059B1 KR0183059B1 (ko) | 1999-05-15 |
Family
ID=25369901
Family Applications (2)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019930007530A KR0183059B1 (ko) | 1992-05-01 | 1993-04-30 | 초미립 솔비톨 아세탈 및 크실리톨 아세탈로 이루어진 정화제 |
KR1019980035446A KR0183364B1 (en) | 1992-05-01 | 1998-08-27 | Polyolefin composition containing ultrafine sorbitol and xylitol acetals |
Family Applications After (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
KR1019980035446A KR0183364B1 (en) | 1992-05-01 | 1998-08-27 | Polyolefin composition containing ultrafine sorbitol and xylitol acetals |
Country Status (13)
Country | Link |
---|---|
US (2) | US5198484A (ko) |
EP (1) | EP0569198B1 (ko) |
JP (1) | JP2610772B2 (ko) |
KR (2) | KR0183059B1 (ko) |
CN (1) | CN1044127C (ko) |
AU (1) | AU658995B2 (ko) |
BR (1) | BR9301707A (ko) |
CA (1) | CA2094697C (ko) |
DE (1) | DE69322542T2 (ko) |
FI (1) | FI115917B (ko) |
MX (1) | MX9302529A (ko) |
MY (1) | MY108763A (ko) |
RU (2) | RU2203898C2 (ko) |
Families Citing this family (48)
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US6458873B1 (en) | 1995-05-03 | 2002-10-01 | Phillips Petroleum Company | Polyolefin compositions |
US5961914A (en) * | 1996-05-03 | 1999-10-05 | Milliken & Company | Method of thermoforming polyolefin resin |
CN1117120C (zh) | 1997-01-17 | 2003-08-06 | 新日本理化株式会社 | 在聚烯烃树脂中重结晶二缩醛的方法 |
CA2199551C (en) * | 1997-03-10 | 2006-10-03 | Henry F. Hay | Polyolefin drums |
CA2199556C (en) * | 1997-03-10 | 2006-10-03 | James Arthur Auger | Polyolefin pipe |
MY120763A (en) * | 1997-09-19 | 2005-11-30 | Hitachi Chemical Co Ltd | Photosensitive film, process for laminating photosensitive resin layer, photosensitive resin layer-laminated substrate and process for curing photosensitive resin layer |
EP0969036B1 (en) * | 1997-11-06 | 2003-09-10 | New Japan Chemical Co.,Ltd. | Method of molding gel of oriented polyolefin resin composition and molded object obtained by the method |
US5973043A (en) * | 1997-11-26 | 1999-10-26 | Milliken & Company | Carbamoyl substituted acetals and compositions containing the same |
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US6586007B2 (en) * | 2001-02-16 | 2003-07-01 | Milliken & Company | Polyolefin additive composition comprising 3,4-dimethyl dibenzylidene sorbitol and rho-methyl dibenzylidene |
US7351478B2 (en) | 2001-03-16 | 2008-04-01 | Fina Technology, Inc. | Heat-seal films and method of manufacture |
US6913829B2 (en) * | 2002-12-20 | 2005-07-05 | Nyacol Nano Technologies, Inc. | Polymer nucleating agents |
CN1816587A (zh) * | 2003-02-26 | 2006-08-09 | 欧姆里顿科技有限公司 | 聚合物胶凝方法和高模数产品 |
US7135234B2 (en) * | 2003-06-12 | 2006-11-14 | Nova Chemicals (International) S.A. | Multilayer coextrusions |
ES2587353T3 (es) * | 2004-07-09 | 2016-10-24 | Basf Se | Proceso de preparación de una composición pulverulenta de acetal de alditol |
JP4322757B2 (ja) * | 2004-09-06 | 2009-09-02 | 富士フイルム株式会社 | パターン形成材料及びパターン形成方法 |
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EP3467022B1 (en) * | 2016-06-07 | 2021-08-04 | Sumitomo Chemical Company, Limited | Propylene-based resin composition and injection-molded object thereof |
US11634427B2 (en) | 2016-07-29 | 2023-04-25 | New Japan Chemical Co., Ltd. | Crystal nucleating agent for polyolefin resin, method for producing crystal nucleating agent for polyolefin resin, and method for improving fluidity of crystal nucleating agent for polyolefin resin |
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JPS5630449A (en) * | 1979-08-21 | 1981-03-27 | Mitsui Toatsu Chem Inc | Polypropylene composition |
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JPS59129239A (ja) * | 1983-01-14 | 1984-07-25 | New Japan Chem Co Ltd | 結晶性ポリオレフイン系樹脂組成物 |
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US5049605A (en) * | 1989-09-20 | 1991-09-17 | Milliken Research Corporation | Bis(3,4-dialkylbenzylidene) sorbitol acetals and compositions containing same |
-
1992
- 1992-05-01 US US07/877,405 patent/US5198484A/en not_active Expired - Lifetime
-
1993
- 1993-01-21 US US08/007,260 patent/US5310950A/en not_active Expired - Lifetime
- 1993-04-22 CA CA002094697A patent/CA2094697C/en not_active Expired - Lifetime
- 1993-04-23 AU AU37093/93A patent/AU658995B2/en not_active Expired
- 1993-04-29 DE DE69322542T patent/DE69322542T2/de not_active Expired - Lifetime
- 1993-04-29 EP EP93303395A patent/EP0569198B1/en not_active Expired - Lifetime
- 1993-04-29 MX MX9302529A patent/MX9302529A/es unknown
- 1993-04-29 MY MYPI93000802A patent/MY108763A/en unknown
- 1993-04-30 CN CN93105006A patent/CN1044127C/zh not_active Expired - Lifetime
- 1993-04-30 KR KR1019930007530A patent/KR0183059B1/ko not_active IP Right Cessation
- 1993-04-30 RU RU98119891/04A patent/RU2203898C2/ru active
- 1993-04-30 RU RU93005145A patent/RU2128198C1/ru active
- 1993-04-30 FI FI931977A patent/FI115917B/fi active IP Right Grant
- 1993-04-30 BR BR9301707A patent/BR9301707A/pt not_active IP Right Cessation
- 1993-05-06 JP JP5130001A patent/JP2610772B2/ja not_active Expired - Lifetime
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1998
- 1998-08-27 KR KR1019980035446A patent/KR0183364B1/ko not_active IP Right Cessation
Also Published As
Publication number | Publication date |
---|---|
CN1079974A (zh) | 1993-12-29 |
AU658995B2 (en) | 1995-05-04 |
RU2128198C1 (ru) | 1999-03-27 |
CA2094697A1 (en) | 1993-11-02 |
US5310950A (en) | 1994-05-10 |
DE69322542T2 (de) | 1999-05-06 |
KR0183059B1 (ko) | 1999-05-15 |
AU3709393A (en) | 1993-11-04 |
MY108763A (en) | 1996-11-30 |
DE69322542D1 (de) | 1999-01-28 |
JP2610772B2 (ja) | 1997-05-14 |
KR0183364B1 (en) | 1999-05-15 |
JPH06145431A (ja) | 1994-05-24 |
EP0569198A1 (en) | 1993-11-10 |
EP0569198B1 (en) | 1998-12-16 |
FI931977A0 (fi) | 1993-04-30 |
RU2203898C2 (ru) | 2003-05-10 |
US5198484A (en) | 1993-03-30 |
FI115917B (fi) | 2005-08-15 |
CN1044127C (zh) | 1999-07-14 |
FI931977A (fi) | 1993-11-02 |
CA2094697C (en) | 2002-08-27 |
BR9301707A (pt) | 1993-11-03 |
MX9302529A (es) | 1993-11-01 |
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