DE10064752A1 - Geruchlose Polyethylenhomo- und copolymere mit guten mechanischen Eigenschaften - Google Patents
Geruchlose Polyethylenhomo- und copolymere mit guten mechanischen EigenschaftenInfo
- Publication number
- DE10064752A1 DE10064752A1 DE10064752A DE10064752A DE10064752A1 DE 10064752 A1 DE10064752 A1 DE 10064752A1 DE 10064752 A DE10064752 A DE 10064752A DE 10064752 A DE10064752 A DE 10064752A DE 10064752 A1 DE10064752 A1 DE 10064752A1
- Authority
- DE
- Germany
- Prior art keywords
- copolymers
- ethylene
- chen
- injection molded
- molded products
- 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.)
- Withdrawn
Links
- 229920001577 copolymer Polymers 0.000 title claims abstract description 12
- -1 polyethylene Polymers 0.000 title claims description 13
- 229920000573 polyethylene Polymers 0.000 title description 8
- 239000004698 Polyethylene Substances 0.000 title description 6
- 230000009965 odorless effect Effects 0.000 title description 6
- VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 35
- 239000005977 Ethylene Substances 0.000 claims abstract description 32
- 238000000034 method Methods 0.000 claims abstract description 18
- 229920001519 homopolymer Polymers 0.000 claims abstract description 17
- 239000003999 initiator Substances 0.000 claims abstract description 12
- 238000004519 manufacturing process Methods 0.000 claims abstract description 9
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 claims abstract description 7
- 239000001301 oxygen Substances 0.000 claims abstract description 7
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 7
- 235000013305 food Nutrition 0.000 claims abstract description 6
- 239000002537 cosmetic Substances 0.000 claims abstract description 5
- 239000003814 drug Substances 0.000 claims abstract description 3
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical group CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 claims description 27
- 238000006116 polymerization reaction Methods 0.000 claims description 8
- 238000004806 packaging method and process Methods 0.000 claims description 7
- 238000002347 injection Methods 0.000 claims description 5
- 239000007924 injection Substances 0.000 claims description 5
- 125000000753 cycloalkyl group Chemical group 0.000 claims description 3
- 239000000155 melt Substances 0.000 claims description 3
- 125000004169 (C1-C6) alkyl group Chemical group 0.000 abstract 1
- RXKJFZQQPQGTFL-UHFFFAOYSA-N dihydroxyacetone Chemical compound OCC(=O)CO RXKJFZQQPQGTFL-UHFFFAOYSA-N 0.000 abstract 1
- 238000006243 chemical reaction Methods 0.000 description 10
- 229920000642 polymer Polymers 0.000 description 10
- NBBJYMSMWIIQGU-UHFFFAOYSA-N Propionic aldehyde Chemical compound CCC=O NBBJYMSMWIIQGU-UHFFFAOYSA-N 0.000 description 8
- 239000000178 monomer Substances 0.000 description 7
- 238000012360 testing method Methods 0.000 description 7
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 6
- QQONPFPTGQHPMA-UHFFFAOYSA-N Propene Chemical compound CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 6
- 229920003023 plastic Polymers 0.000 description 5
- 239000004033 plastic Substances 0.000 description 5
- OTMSDBZUPAUEDD-UHFFFAOYSA-N Ethane Chemical compound CC OTMSDBZUPAUEDD-UHFFFAOYSA-N 0.000 description 4
- BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical compound COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 4
- ZTQSAGDEMFDKMZ-UHFFFAOYSA-N butyric aldehyde Natural products CCCC=O ZTQSAGDEMFDKMZ-UHFFFAOYSA-N 0.000 description 4
- 239000000047 product Substances 0.000 description 4
- 230000000052 comparative effect Effects 0.000 description 3
- 229920001684 low density polyethylene Polymers 0.000 description 3
- 239000004702 low-density polyethylene Substances 0.000 description 3
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 3
- 230000003287 optical effect Effects 0.000 description 3
- 238000012545 processing Methods 0.000 description 3
- 239000001294 propane Substances 0.000 description 3
- 150000003254 radicals Chemical class 0.000 description 3
- 239000011541 reaction mixture Substances 0.000 description 3
- VXNZUUAINFGPBY-UHFFFAOYSA-N 1-Butene Chemical compound CCC=C VXNZUUAINFGPBY-UHFFFAOYSA-N 0.000 description 2
- AFFLGGQVNFXPEV-UHFFFAOYSA-N 1-decene Chemical compound CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 2
- LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 2
- KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 2
- NIXOWILDQLNWCW-UHFFFAOYSA-N 2-Propenoic acid Natural products OC(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-N 0.000 description 2
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
- SOGAXMICEFXMKE-UHFFFAOYSA-N Butylmethacrylate Chemical compound CCCCOC(=O)C(C)=C SOGAXMICEFXMKE-UHFFFAOYSA-N 0.000 description 2
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 2
- VZCYOOQTPOCHFL-OWOJBTEDSA-N Fumaric acid Chemical compound OC(=O)\C=C\C(O)=O VZCYOOQTPOCHFL-OWOJBTEDSA-N 0.000 description 2
- NTIZESTWPVYFNL-UHFFFAOYSA-N Methyl isobutyl ketone Chemical compound CC(C)CC(C)=O NTIZESTWPVYFNL-UHFFFAOYSA-N 0.000 description 2
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
- FUSUHKVFWTUUBE-UHFFFAOYSA-N buten-2-one Chemical compound CC(=O)C=C FUSUHKVFWTUUBE-UHFFFAOYSA-N 0.000 description 2
- 229910002091 carbon monoxide Inorganic materials 0.000 description 2
- 238000007334 copolymerization reaction Methods 0.000 description 2
- 125000000582 cycloheptyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 description 2
- 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 2
- 125000001511 cyclopentyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 2
- 238000009826 distribution Methods 0.000 description 2
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
- 239000011888 foil Substances 0.000 description 2
- 239000007789 gas Substances 0.000 description 2
- 125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 2
- 125000001972 isopentyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 150000002576 ketones Chemical class 0.000 description 2
- 239000000463 material Substances 0.000 description 2
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- 125000004108 n-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 125000004123 n-propyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
- 150000001451 organic peroxides Chemical class 0.000 description 2
- XNLICIUVMPYHGG-UHFFFAOYSA-N pentan-2-one Chemical compound CCCC(C)=O XNLICIUVMPYHGG-UHFFFAOYSA-N 0.000 description 2
- YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
- 239000000843 powder Substances 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- 125000002914 sec-butyl group Chemical group [H]C([H])([H])C([H])([H])C([H])(*)C([H])([H])[H] 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 125000000999 tert-butyl group Chemical group [H]C([H])([H])C(*)(C([H])([H])[H])C([H])([H])[H] 0.000 description 2
- VZCYOOQTPOCHFL-UHFFFAOYSA-N trans-butenedioic acid Natural products OC(=O)C=CC(O)=O VZCYOOQTPOCHFL-UHFFFAOYSA-N 0.000 description 2
- 239000013638 trimer Substances 0.000 description 2
- SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-UHFFFAOYSA-N 0.000 description 1
- JAHNSTQSQJOJLO-UHFFFAOYSA-N 2-(3-fluorophenyl)-1h-imidazole Chemical compound FC1=CC=CC(C=2NC=CN=2)=C1 JAHNSTQSQJOJLO-UHFFFAOYSA-N 0.000 description 1
- GOXQRTZXKQZDDN-UHFFFAOYSA-N 2-Ethylhexyl acrylate Chemical compound CCCCC(CC)COC(=O)C=C GOXQRTZXKQZDDN-UHFFFAOYSA-N 0.000 description 1
- 125000003542 3-methylbutan-2-yl group Chemical group [H]C([H])([H])C([H])(*)C([H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 240000004385 Centaurea cyanus Species 0.000 description 1
- CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical compound CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
- UIHCLUNTQKBZGK-UHFFFAOYSA-N Methyl isobutyl ketone Natural products CCC(C)C(C)=O UIHCLUNTQKBZGK-UHFFFAOYSA-N 0.000 description 1
- OFOBLEOULBTSOW-UHFFFAOYSA-N Propanedioic acid Natural products OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical compound [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 description 1
- 229910052782 aluminium Inorganic materials 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 230000004888 barrier function Effects 0.000 description 1
- CQEYYJKEWSMYFG-UHFFFAOYSA-N butyl acrylate Chemical compound CCCCOC(=O)C=C CQEYYJKEWSMYFG-UHFFFAOYSA-N 0.000 description 1
- 239000006227 byproduct Substances 0.000 description 1
- 150000001728 carbonyl compounds Chemical class 0.000 description 1
- 125000002915 carbonyl group Chemical group [*:2]C([*:1])=O 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 150000001875 compounds Chemical class 0.000 description 1
- 235000009508 confectionery Nutrition 0.000 description 1
- 239000002826 coolant Substances 0.000 description 1
- 238000001816 cooling Methods 0.000 description 1
- LDHQCZJRKDOVOX-NSCUHMNNSA-N crotonic acid Chemical compound C\C=C\C(O)=O LDHQCZJRKDOVOX-NSCUHMNNSA-N 0.000 description 1
- 125000001995 cyclobutyl group Chemical group [H]C1([H])C([H])([H])C([H])(*)C1([H])[H] 0.000 description 1
- 125000006547 cyclononyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000000640 cyclooctyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C([H])([H])C1([H])[H] 0.000 description 1
- 125000001559 cyclopropyl group Chemical group [H]C1([H])C([H])([H])C1([H])* 0.000 description 1
- 238000000354 decomposition reaction Methods 0.000 description 1
- 230000001419 dependent effect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
- 239000000539 dimer Substances 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 235000015203 fruit juice Nutrition 0.000 description 1
- 239000001530 fumaric acid Substances 0.000 description 1
- 125000000524 functional group Chemical group 0.000 description 1
- 238000004817 gas chromatography Methods 0.000 description 1
- 229930195733 hydrocarbon Natural products 0.000 description 1
- 150000002430 hydrocarbons Chemical class 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
- 239000012535 impurity Substances 0.000 description 1
- 238000001746 injection moulding Methods 0.000 description 1
- 125000004491 isohexyl group Chemical group C(CCC(C)C)* 0.000 description 1
- VZCYOOQTPOCHFL-UPHRSURJSA-N maleic acid Chemical compound OC(=O)\C=C/C(O)=O VZCYOOQTPOCHFL-UPHRSURJSA-N 0.000 description 1
- 239000011976 maleic acid Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- DCUFMVPCXCSVNP-UHFFFAOYSA-N methacrylic anhydride Chemical compound CC(=C)C(=O)OC(=O)C(C)=C DCUFMVPCXCSVNP-UHFFFAOYSA-N 0.000 description 1
- LVHBHZANLOWSRM-UHFFFAOYSA-N methylenebutanedioic acid Natural products OC(=O)CC(=C)C(O)=O LVHBHZANLOWSRM-UHFFFAOYSA-N 0.000 description 1
- TVMXDCGIABBOFY-UHFFFAOYSA-N n-Octanol Natural products CCCCCCCC TVMXDCGIABBOFY-UHFFFAOYSA-N 0.000 description 1
- 125000001280 n-hexyl group Chemical group C(CCCCC)* 0.000 description 1
- 125000000740 n-pentyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
- 125000001971 neopentyl group Chemical group [H]C([*])([H])C(C([H])([H])[H])(C([H])([H])[H])C([H])([H])[H] 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 230000008520 organization Effects 0.000 description 1
- 239000012785 packaging film Substances 0.000 description 1
- 229920006280 packaging film Polymers 0.000 description 1
- 239000003505 polymerization initiator Substances 0.000 description 1
- 230000000379 polymerizing effect Effects 0.000 description 1
- 235000013606 potato chips Nutrition 0.000 description 1
- 108090000623 proteins and genes Proteins 0.000 description 1
- 150000003384 small molecules Chemical class 0.000 description 1
- 235000014347 soups Nutrition 0.000 description 1
- 239000007858 starting material Substances 0.000 description 1
- 230000009967 tasteless effect Effects 0.000 description 1
- SJMYWORNLPSJQO-UHFFFAOYSA-N tert-butyl 2-methylprop-2-enoate Chemical compound CC(=C)C(=O)OC(C)(C)C SJMYWORNLPSJQO-UHFFFAOYSA-N 0.000 description 1
- ISXSCDLOGDJUNJ-UHFFFAOYSA-N tert-butyl prop-2-enoate Chemical compound CC(C)(C)OC(=O)C=C ISXSCDLOGDJUNJ-UHFFFAOYSA-N 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- LDHQCZJRKDOVOX-UHFFFAOYSA-N trans-crotonic acid Natural products CC=CC(O)=O LDHQCZJRKDOVOX-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 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
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F10/00—Homopolymers and copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F10/02—Ethene
-
- 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
- C08F210/00—Copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F210/02—Ethene
-
- 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
- C08F110/00—Homopolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond
- C08F110/02—Ethene
-
- 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
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
- Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
-
- 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
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/13—Hollow or container type article [e.g., tube, vase, etc.]
- Y10T428/1352—Polymer or resin containing [i.e., natural or synthetic]
- Y10T428/139—Open-ended, self-supporting conduit, cylinder, or tube-type article
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Injection Moulding Of Plastics Or The Like (AREA)
- Polymerisation Methods In General (AREA)
- Polymerization Catalysts (AREA)
- Coloring Foods And Improving Nutritive Qualities (AREA)
Priority Applications (11)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10064752A DE10064752A1 (de) | 2000-12-22 | 2000-12-22 | Geruchlose Polyethylenhomo- und copolymere mit guten mechanischen Eigenschaften |
| CNB018211364A CN1210316C (zh) | 2000-12-22 | 2001-12-12 | 具有优良力学性能的无味的乙烯均聚物与共聚物 |
| AT01272001T ATE546470T1 (de) | 2000-12-22 | 2001-12-12 | Verwendung von geruchlosen ethylenhomopolymeren |
| RU2003122783/04A RU2003122783A (ru) | 2000-12-22 | 2001-12-12 | Не обладающие запахом гомо- и сополимеры этилена с хорошими механическими свойствами |
| KR10-2003-7008325A KR20030065559A (ko) | 2000-12-22 | 2001-12-12 | 양호한 기계적 성질을 갖는 무취의 에틸렌 단일중합체 및공중합체 |
| CA002431886A CA2431886A1 (en) | 2000-12-22 | 2001-12-12 | Nonodorous ethylene homopolymers and copolymers having good mechanical properties |
| JP2002552975A JP4104126B2 (ja) | 2000-12-22 | 2001-12-12 | 良好な機械的特性を有する無臭のエチレンホモポリマー及びコポリマー |
| EP01272001A EP1351999B1 (de) | 2000-12-22 | 2001-12-12 | Verwendung von geruchlosen Ethylenhomopolymeren |
| PCT/EP2001/014570 WO2002051885A2 (de) | 2000-12-22 | 2001-12-12 | Geruchlose ethylenhomo- und copolymere mit guten mechanischen eigenschaften |
| US10/450,774 US7709584B2 (en) | 2000-12-22 | 2001-12-12 | Nonodorous ethylene homopolymers and copolymers having good mechanical properties |
| BR0116375-2A BR0116375A (pt) | 2000-12-22 | 2001-12-12 | Processo de preparação de homopolìmeros de etileno, homopolìmero de etileno, utilização do mesmo, e, produto moldado por injeção |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE10064752A DE10064752A1 (de) | 2000-12-22 | 2000-12-22 | Geruchlose Polyethylenhomo- und copolymere mit guten mechanischen Eigenschaften |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE10064752A1 true DE10064752A1 (de) | 2002-07-04 |
Family
ID=7668793
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE10064752A Withdrawn DE10064752A1 (de) | 2000-12-22 | 2000-12-22 | Geruchlose Polyethylenhomo- und copolymere mit guten mechanischen Eigenschaften |
Country Status (11)
| Country | Link |
|---|---|
| US (1) | US7709584B2 (enExample) |
| EP (1) | EP1351999B1 (enExample) |
| JP (1) | JP4104126B2 (enExample) |
| KR (1) | KR20030065559A (enExample) |
| CN (1) | CN1210316C (enExample) |
| AT (1) | ATE546470T1 (enExample) |
| BR (1) | BR0116375A (enExample) |
| CA (1) | CA2431886A1 (enExample) |
| DE (1) | DE10064752A1 (enExample) |
| RU (1) | RU2003122783A (enExample) |
| WO (1) | WO2002051885A2 (enExample) |
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002100907A1 (de) * | 2001-06-11 | 2002-12-19 | Basell Polyolefine Gmbh | Verfahren zur herstellung von ethylenhomo- und -copolymeren durch radikalische hochdruckpolymerisation |
| US6815571B1 (en) | 2001-01-23 | 2004-11-09 | Basf Aktiengesellschaft | Method for producing ethylene polymers in a high-pressure process |
Families Citing this family (18)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE10064752A1 (de) | 2000-12-22 | 2002-07-04 | Basell Polyolefine Gmbh | Geruchlose Polyethylenhomo- und copolymere mit guten mechanischen Eigenschaften |
| WO2002051360A2 (de) * | 2000-12-22 | 2002-07-04 | Basf Aktiengesellschaft | Kosmetische präparate und anwendungen, enthaltend polyethylenwachse mit verbesserten organoleptischen eigenschaften |
| BRPI0914059A2 (pt) | 2008-10-07 | 2015-11-03 | Dow Global Technologies Llc | polímero a base de etileno e processo para preparar um polímero a base de etileno |
| US20110196105A1 (en) * | 2010-02-08 | 2011-08-11 | Dow Global Technologies Inc. | Novel high pressure, low density polyethylene resins produced through the use of highly active chain transfer agents |
| US8637607B2 (en) | 2010-07-28 | 2014-01-28 | Equistar Chemicals, Lp | Polyethylene blends and films |
| JP6449651B2 (ja) | 2011-12-21 | 2019-01-09 | ダウ グローバル テクノロジーズ エルエルシー | 共重合体組成物およびその製造方法 |
| JP2017538817A (ja) | 2014-12-01 | 2017-12-28 | ダウ グローバル テクノロジーズ エルエルシー | ポリマー組成物、収縮フィルム、及びそれらの作製方法 |
| MX2017006889A (es) | 2014-12-01 | 2017-09-01 | Dow Global Technologies Llc | Películas de contracción, y métodos para su fabricación. |
| WO2017058493A1 (en) | 2015-09-29 | 2017-04-06 | Dow Global Technologies Llc | Shrink films, and methods of making thereof |
| BR112018069347B1 (pt) | 2016-03-31 | 2022-11-29 | Dow Global Technologies Llc | Método para aumentar a resistibilidade de fusão ou baixa viscosidade de cisalhamento de uma resina de polietileno |
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| WO2019067320A1 (en) | 2017-09-22 | 2019-04-04 | Dow Global Technologies Llc | REFERMABLE PACKAGE COMPRISING A REFERMABLE FILM AND METHOD OF MANUFACTURING THE SAME |
| US11193009B2 (en) | 2017-09-27 | 2021-12-07 | Dow Global Technologies Llc | Modified polyethylene compositions and method for making the same |
| EP4247637A1 (en) | 2020-11-20 | 2023-09-27 | Dow Global Technologies LLC | Multilayer structures and articles with coating layers |
| WO2025072154A1 (en) | 2023-09-29 | 2025-04-03 | Dow Global Technologies Llc | Processes for polymerizing ethylene |
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| US2870130A (en) * | 1956-01-04 | 1959-01-20 | Union Carbide Corp | Ethylene polymers |
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| US3092614A (en) * | 1962-02-15 | 1963-06-04 | Union Carbide Corp | Ethylene polymerization process |
| BE636721A (enExample) * | 1962-08-29 | |||
| US3917577A (en) * | 1968-09-20 | 1975-11-04 | Basf Ag | Continuous production of ethylene homopolymers |
| DE1908964C3 (de) * | 1969-02-22 | 1980-04-30 | Basf Ag, 6700 Ludwigshafen | Verfahren zum kontinuierlichen Herstellen von Äthylenhomopolymerisaten |
| US4175169A (en) * | 1971-03-19 | 1979-11-20 | Exxon Research & Engineering Co. | Production of polyethylene |
| US4000357A (en) * | 1974-08-29 | 1976-12-28 | Union Carbide Corporation | Polymerization of ethylene with oxygen and organic initiators |
| DE2557653A1 (de) * | 1975-12-20 | 1977-06-30 | Basf Ag | Verfahren zur herstellung von aethylenpolymerisaten in einem zweizonen-rohrreaktor bei druecken oberhalb 500 bar |
| US4135044A (en) * | 1977-08-08 | 1979-01-16 | Exxon Research & Engineering Co. | Process for achieving high conversions in the production of polyethylene |
| RO75587A2 (ro) | 1979-04-18 | 1981-06-22 | Combinatul Petrochimic,Ro | Procedeu de obtinere a polietilenei de joasa densitate |
| DE3308926A1 (de) | 1983-03-12 | 1984-09-13 | Basf Ag, 6700 Ludwigshafen | Verfahren zur herstellung von ethylenpolymerisaten bei druecken oberhalb von 500 bar in einem einzonen-rohrreaktor |
| DE4010271A1 (de) * | 1990-03-30 | 1991-10-02 | Basf Ag | Verfahren zur herstellung von ethylenpolymerisaten bei druecken oberhalb von 500 bar in einem rohrreaktor mit einspritzfinger |
| DE4219983A1 (de) * | 1992-06-19 | 1993-12-23 | Basf Ag | Verfahren zur Herstellung von Copolymerisaten des Ethylens mit Acrylsäureestern oder Acrylsäure |
| DE19741097A1 (de) * | 1997-09-18 | 1999-03-25 | Basf Ag | Verfahren zur Copolymerisation von Ethylen mit Vinylcarboxylaten |
| ATE275590T1 (de) | 1998-01-12 | 2004-09-15 | Dow Global Technologies Inc | Äthylenpolymere mittlerer dichte, verfahren zur herstellung dieser polymere und verwendung von carbonyl-haltigen kettenübertragungsmitteln in diesem verfahren |
| DE10021886A1 (de) * | 2000-05-05 | 2001-11-15 | Basell Polyolefine Gmbh | Verfahren zum Herstellen von Phillips-Katalysatoren für die Polymerisation von Olefinen mit verbesserten Produktivitäten im Paricle-Form-Verfahren |
| DE10060372A1 (de) | 2000-12-05 | 2002-06-06 | Basell Polyolefine Gmbh | Vorrichtung zur Initiatoreinspeisung an Reaktoren |
| DE10064752A1 (de) | 2000-12-22 | 2002-07-04 | Basell Polyolefine Gmbh | Geruchlose Polyethylenhomo- und copolymere mit guten mechanischen Eigenschaften |
| DE10102937A1 (de) * | 2001-01-23 | 2002-07-25 | Basf Ag | Verfahren zur Herstellung von Ethylenpolymerisaten im Hochdruckverfahren |
-
2000
- 2000-12-22 DE DE10064752A patent/DE10064752A1/de not_active Withdrawn
-
2001
- 2001-12-12 BR BR0116375-2A patent/BR0116375A/pt not_active Application Discontinuation
- 2001-12-12 KR KR10-2003-7008325A patent/KR20030065559A/ko not_active Withdrawn
- 2001-12-12 EP EP01272001A patent/EP1351999B1/de not_active Expired - Lifetime
- 2001-12-12 WO PCT/EP2001/014570 patent/WO2002051885A2/de not_active Ceased
- 2001-12-12 RU RU2003122783/04A patent/RU2003122783A/ru not_active Application Discontinuation
- 2001-12-12 AT AT01272001T patent/ATE546470T1/de active
- 2001-12-12 CA CA002431886A patent/CA2431886A1/en not_active Abandoned
- 2001-12-12 JP JP2002552975A patent/JP4104126B2/ja not_active Expired - Fee Related
- 2001-12-12 US US10/450,774 patent/US7709584B2/en not_active Expired - Fee Related
- 2001-12-12 CN CNB018211364A patent/CN1210316C/zh not_active Expired - Fee Related
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US6815571B1 (en) | 2001-01-23 | 2004-11-09 | Basf Aktiengesellschaft | Method for producing ethylene polymers in a high-pressure process |
| US6949611B2 (en) | 2001-01-23 | 2005-09-27 | Basell Polyolefine Gmbh | Preparation of ethylene polymers by the high-pressure method |
| WO2002100907A1 (de) * | 2001-06-11 | 2002-12-19 | Basell Polyolefine Gmbh | Verfahren zur herstellung von ethylenhomo- und -copolymeren durch radikalische hochdruckpolymerisation |
| US6894126B2 (en) | 2001-06-11 | 2005-05-17 | Basell Polyolefine Gmbh | Method for producing ethylene homopolymers and copolymers by means of radical high pressure polymerization |
Also Published As
| Publication number | Publication date |
|---|---|
| JP2004535476A (ja) | 2004-11-25 |
| CA2431886A1 (en) | 2002-07-04 |
| CN1210316C (zh) | 2005-07-13 |
| WO2002051885A2 (de) | 2002-07-04 |
| RU2003122783A (ru) | 2004-12-27 |
| BR0116375A (pt) | 2004-06-15 |
| JP4104126B2 (ja) | 2008-06-18 |
| EP1351999B1 (de) | 2012-02-22 |
| WO2002051885A3 (de) | 2003-01-30 |
| ATE546470T1 (de) | 2012-03-15 |
| CN1483046A (zh) | 2004-03-17 |
| US20040054097A1 (en) | 2004-03-18 |
| KR20030065559A (ko) | 2003-08-06 |
| US7709584B2 (en) | 2010-05-04 |
| EP1351999A2 (de) | 2003-10-15 |
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Legal Events
| Date | Code | Title | Description |
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| 8127 | New person/name/address of the applicant |
Owner name: BASELL POLYOLEFINE GMBH, 50389 WESSELING, DE |
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| 8141 | Disposal/no request for examination |