CN1382171A - 嵌段共聚物及其制备方法和用途 - Google Patents
嵌段共聚物及其制备方法和用途 Download PDFInfo
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- CN1382171A CN1382171A CN00814826A CN00814826A CN1382171A CN 1382171 A CN1382171 A CN 1382171A CN 00814826 A CN00814826 A CN 00814826A CN 00814826 A CN00814826 A CN 00814826A CN 1382171 A CN1382171 A CN 1382171A
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- Prior art keywords
- methyl
- weight
- ester
- segmented copolymer
- hydrogen
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- 229920001400 block copolymer Polymers 0.000 title abstract 3
- 238000004519 manufacturing process Methods 0.000 title description 2
- -1 ester compounds Chemical class 0.000 claims abstract description 87
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 62
- 239000000203 mixture Substances 0.000 claims abstract description 52
- 239000001257 hydrogen Substances 0.000 claims abstract description 47
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 47
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 45
- 229920001577 copolymer Polymers 0.000 claims abstract description 34
- 239000000178 monomer Substances 0.000 claims abstract description 34
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims abstract description 27
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims abstract description 25
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 claims abstract description 15
- 229910052799 carbon Inorganic materials 0.000 claims description 53
- 239000003921 oil Substances 0.000 claims description 38
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- 239000000654 additive Substances 0.000 claims description 17
- 238000000034 method Methods 0.000 claims description 15
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- 239000003999 initiator Substances 0.000 claims description 12
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- 101710141544 Allatotropin-related peptide Proteins 0.000 description 5
- 239000004215 Carbon black (E152) Substances 0.000 description 5
- 125000003342 alkenyl group Chemical group 0.000 description 5
- 238000010560 atom transfer radical polymerization reaction Methods 0.000 description 5
- 238000009826 distribution Methods 0.000 description 5
- 125000000623 heterocyclic group Chemical group 0.000 description 5
- 125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 description 5
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- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 4
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- SNRUBQQJIBEYMU-UHFFFAOYSA-N Dodecane Natural products CCCCCCCCCCCC SNRUBQQJIBEYMU-UHFFFAOYSA-N 0.000 description 3
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- 150000001298 alcohols Chemical class 0.000 description 3
- 125000000304 alkynyl group Chemical group 0.000 description 3
- 238000004458 analytical method Methods 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 229910052794 bromium Inorganic materials 0.000 description 3
- 230000000052 comparative effect Effects 0.000 description 3
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- 238000004821 distillation Methods 0.000 description 3
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- 125000003055 glycidyl group Chemical group C(C1CO1)* 0.000 description 3
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- GWVDBZWVFGFBCN-UHFFFAOYSA-N tetratriacontane Chemical compound CCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCCC GWVDBZWVFGFBCN-UHFFFAOYSA-N 0.000 description 3
- JSPLKZUTYZBBKA-UHFFFAOYSA-N trioxidane Chemical compound OOO JSPLKZUTYZBBKA-UHFFFAOYSA-N 0.000 description 3
- UWNADWZGEHDQAB-UHFFFAOYSA-N 2,5-dimethylhexane Chemical group CC(C)CCC(C)C UWNADWZGEHDQAB-UHFFFAOYSA-N 0.000 description 2
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- 125000004493 2-methylbut-1-yl group Chemical group CC(C*)CC 0.000 description 2
- 125000003903 2-propenyl group Chemical group [H]C([*])([H])C([H])=C([H])[H] 0.000 description 2
- YYROPELSRYBVMQ-UHFFFAOYSA-N 4-toluenesulfonyl chloride Chemical compound CC1=CC=C(S(Cl)(=O)=O)C=C1 YYROPELSRYBVMQ-UHFFFAOYSA-N 0.000 description 2
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- OIPMQULDKWSNGX-UHFFFAOYSA-N bis[[ethoxy(oxo)phosphaniumyl]oxy]alumanyloxy-ethoxy-oxophosphanium Chemical compound [Al+3].CCO[P+]([O-])=O.CCO[P+]([O-])=O.CCO[P+]([O-])=O OIPMQULDKWSNGX-UHFFFAOYSA-N 0.000 description 2
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- AABBHSMFGKYLKE-UHFFFAOYSA-N propan-2-yl but-2-enoate Chemical class CC=CC(=O)OC(C)C AABBHSMFGKYLKE-UHFFFAOYSA-N 0.000 description 1
- ZHDCHCTZRODSEN-UHFFFAOYSA-N propyl but-2-enoate Chemical compound CCCOC(=O)C=CC ZHDCHCTZRODSEN-UHFFFAOYSA-N 0.000 description 1
- RYYCFQTWLMFJIG-UHFFFAOYSA-N propylcyanamide Chemical compound CCCNC#N RYYCFQTWLMFJIG-UHFFFAOYSA-N 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- UMJSCPRVCHMLSP-UHFFFAOYSA-N pyridine Natural products COC1=CC=CN=C1 UMJSCPRVCHMLSP-UHFFFAOYSA-N 0.000 description 1
- 150000003233 pyrroles Chemical class 0.000 description 1
- 238000007342 radical addition reaction Methods 0.000 description 1
- 238000010526 radical polymerization reaction Methods 0.000 description 1
- 238000007348 radical reaction Methods 0.000 description 1
- 239000002994 raw material Substances 0.000 description 1
- 238000007670 refining Methods 0.000 description 1
- 229910052702 rhenium Inorganic materials 0.000 description 1
- 229910052703 rhodium Inorganic materials 0.000 description 1
- DCKVNWZUADLDEH-UHFFFAOYSA-N sec-butyl acetate Chemical compound CCC(C)OC(C)=O DCKVNWZUADLDEH-UHFFFAOYSA-N 0.000 description 1
- 238000000926 separation method Methods 0.000 description 1
- 239000003079 shale oil Substances 0.000 description 1
- 239000010703 silicon Substances 0.000 description 1
- 229920002545 silicone oil Polymers 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 125000004079 stearyl group Chemical group [H]C([*])([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])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- 230000035882 stress Effects 0.000 description 1
- 150000003440 styrenes Chemical class 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 239000000725 suspension Substances 0.000 description 1
- 239000003765 sweetening agent Substances 0.000 description 1
- 230000002194 synthesizing effect Effects 0.000 description 1
- QHSPZGZEUDEIQM-UHFFFAOYSA-N tert-butyl but-2-enoate Chemical compound CC=CC(=O)OC(C)(C)C QHSPZGZEUDEIQM-UHFFFAOYSA-N 0.000 description 1
- VZGDMQKNWNREIO-UHFFFAOYSA-N tetrachloromethane Chemical compound ClC(Cl)(Cl)Cl VZGDMQKNWNREIO-UHFFFAOYSA-N 0.000 description 1
- NCYNWQDLQJUTIY-UHFFFAOYSA-N tetradecyl but-2-enoate Chemical compound CCCCCCCCCCCCCCOC(=O)C=CC NCYNWQDLQJUTIY-UHFFFAOYSA-N 0.000 description 1
- 230000008646 thermal stress Effects 0.000 description 1
- 229930192474 thiophene Natural products 0.000 description 1
- 125000003944 tolyl group Chemical group 0.000 description 1
- 230000007704 transition Effects 0.000 description 1
- 125000002889 tridecyl group Chemical group [H]C([*])([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])[H] 0.000 description 1
- ITMCEJHCFYSIIV-UHFFFAOYSA-N triflic acid Chemical class OS(=O)(=O)C(F)(F)F ITMCEJHCFYSIIV-UHFFFAOYSA-N 0.000 description 1
- 239000010723 turbine oil Substances 0.000 description 1
- 125000002948 undecyl group Chemical group [H]C([*])([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
- 239000010913 used oil Substances 0.000 description 1
- 238000005292 vacuum distillation Methods 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
- 229920001567 vinyl ester resin Polymers 0.000 description 1
- 125000005023 xylyl group Chemical group 0.000 description 1
- 229910052725 zinc Inorganic materials 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
- C08F293/00—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule
-
- 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
- C08F293/00—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule
- C08F293/005—Macromolecular compounds obtained by polymerisation on to a macromolecule having groups capable of inducing the formation of new polymer chains bound exclusively at one or both ends of the starting macromolecule using free radical "living" or "controlled" polymerisation, e.g. using a complexing agent
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L53/00—Compositions of block copolymers containing at least one sequence of a polymer obtained by reactions only involving carbon-to-carbon unsaturated bonds; Compositions of derivatives of such polymers
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L1/00—Liquid carbonaceous fuels
- C10L1/10—Liquid carbonaceous fuels containing additives
- C10L1/14—Organic compounds
- C10L1/18—Organic compounds containing oxygen
- C10L1/192—Macromolecular compounds
- C10L1/195—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds
- C10L1/196—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derived from monomers containing a carbon-to-carbon unsaturated bond and a carboxyl group or salts, anhydrides or esters thereof homo- or copolymers of compounds having one or more unsaturated aliphatic radicals each having one carbon bond to carbon double bond, and at least one being terminated by a carboxyl radical or of salts, anhydrides or esters thereof
- C10L1/1963—Macromolecular compounds obtained by reactions involving only carbon-to-carbon unsaturated bonds derived from monomers containing a carbon-to-carbon unsaturated bond and a carboxyl group or salts, anhydrides or esters thereof homo- or copolymers of compounds having one or more unsaturated aliphatic radicals each having one carbon bond to carbon double bond, and at least one being terminated by a carboxyl radical or of salts, anhydrides or esters thereof mono-carboxylic
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L10/00—Use of additives to fuels or fires for particular purposes
- C10L10/14—Use of additives to fuels or fires for particular purposes for improving low temperature properties
-
- C—CHEMISTRY; METALLURGY
- C10—PETROLEUM, GAS OR COKE INDUSTRIES; TECHNICAL GASES CONTAINING CARBON MONOXIDE; FUELS; LUBRICANTS; PEAT
- C10L—FUELS NOT OTHERWISE PROVIDED FOR; NATURAL GAS; SYNTHETIC NATURAL GAS OBTAINED BY PROCESSES NOT COVERED BY SUBCLASSES C10G, C10K; LIQUEFIED PETROLEUM GAS; ADDING MATERIALS TO FUELS OR FIRES TO REDUCE SMOKE OR UNDESIRABLE DEPOSITS OR TO FACILITATE SOOT REMOVAL; FIRELIGHTERS
- C10L10/00—Use of additives to fuels or fires for particular purposes
- C10L10/14—Use of additives to fuels or fires for particular purposes for improving low temperature properties
- C10L10/16—Pour-point depressants
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E50/00—Technologies for the production of fuel of non-fossil origin
- Y02E50/10—Biofuels, e.g. bio-diesel
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Oil, Petroleum & Natural Gas (AREA)
- Health & Medical Sciences (AREA)
- Engineering & Computer Science (AREA)
- Polymers & Plastics (AREA)
- Medicinal Chemistry (AREA)
- Combustion & Propulsion (AREA)
- Emergency Medicine (AREA)
- General Chemical & Material Sciences (AREA)
- Graft Or Block Polymers (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Lubricants (AREA)
- Liquid Carbonaceous Fuels (AREA)
Abstract
Description
实施例1 | 实施例2 | 对比例 | |
PDI | 4.18 | 1.41 | 2.11;2.02 |
混合物的聚合物含量(%重量) | 0.036 | 0.03 | 0.018+0.018=0.036 |
倾点 | -27 | -24 | -24 |
MRV | |||
粘度(Pa·sec) | 22.5 | 19.2 | 12.1 |
屈服应力(Pa) | 0 | 0 | 175 |
扫描Brookfield | |||
在-20℃下的粘度(mPa·sec) | 11400 | 8400 | 32900 |
在3000mPa·sec下的温度(℃) | -24.2 | -26.9 | -19.4 |
胶凝指数和温度℃ | 7.8在-19℃ | 6.9在-28℃ | 32.3在-18℃ |
Claims (17)
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US45074499A | 1999-11-30 | 1999-11-30 | |
US09/450,744 | 1999-11-30 |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1382171A true CN1382171A (zh) | 2002-11-27 |
CN100475871C CN100475871C (zh) | 2009-04-08 |
Family
ID=23789326
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CNB008148260A Expired - Fee Related CN100475871C (zh) | 1999-11-30 | 2000-11-18 | 嵌段共聚物及其制备方法和用途 |
Country Status (10)
Country | Link |
---|---|
EP (1) | EP1235870B1 (zh) |
JP (1) | JP5259901B2 (zh) |
KR (1) | KR100640679B1 (zh) |
CN (1) | CN100475871C (zh) |
AU (1) | AU1703301A (zh) |
BR (1) | BR0015825B1 (zh) |
CA (1) | CA2392727C (zh) |
DE (1) | DE10015533A1 (zh) |
MX (1) | MXPA02005366A (zh) |
WO (1) | WO2001040339A1 (zh) |
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1984981B (zh) * | 2004-07-16 | 2010-11-17 | 可乐丽股份有限公司 | 含有丙烯酸系聚合物的润滑油添加剂及润滑油组合物 |
US8288327B2 (en) | 2003-03-31 | 2012-10-16 | Evonik Rohmax Additives Gmbh | Lubricating oil composition with good frictional properties |
Families Citing this family (14)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP4778688B2 (ja) * | 2003-05-30 | 2011-09-21 | 三洋化成工業株式会社 | 流動点降下剤 |
US7691797B2 (en) * | 2003-11-26 | 2010-04-06 | Arkema Inc. | Controlled radical acrylic copolymer thickeners |
US7906468B2 (en) | 2005-02-23 | 2011-03-15 | Arkema Inc. | Acrylic block copolymer low temperature flow modifiers in lubricating oils |
DE102005015931A1 (de) * | 2005-04-06 | 2006-10-12 | Rohmax Additives Gmbh | Polyalkyl(meth) acrylat-Copolymere mit hervorragenden Eigenschaften |
DE102005041528A1 (de) | 2005-08-31 | 2007-03-01 | Rohmax Additives Gmbh | Öllösliche Polymere |
US7632788B2 (en) | 2005-12-12 | 2009-12-15 | Afton Chemical Corporation | Nanosphere additives and lubricant formulations containing the nanosphere additives |
DE102006016588A1 (de) * | 2006-04-06 | 2007-10-18 | Rohmax Additives Gmbh | Kraftstoffzusammensetzungen umfassend nachwachsende Rohstoffe |
US7867958B2 (en) * | 2006-04-28 | 2011-01-11 | Afton Chemical Corporation | Diblock monopolymers as lubricant additives and lubricant formulations containing same |
US8236069B2 (en) | 2007-06-11 | 2012-08-07 | Arkema Inc. | Acrylic polymer low temperature flow modifiers in bio-derived fuels |
DE102007036856A1 (de) | 2007-08-06 | 2009-02-26 | Evonik Rohmax Additives Gmbh | Verwendung von Estergruppen-umfassenden Polymeren als Antifatigue-Additive |
WO2009077396A1 (en) * | 2007-12-18 | 2009-06-25 | Basf Se | Biodiesel cold flow improver |
FR2930263A1 (fr) * | 2008-04-18 | 2009-10-23 | Arkema France | Additif pour biocarburant et son procede de preparation a partir d'une matiere premiere renouvelable |
DE102009001446A1 (de) | 2009-03-10 | 2010-09-23 | Evonik Rohmax Additives Gmbh | Verwendung von Kammpolymeren als Antifatigue-Additive |
US8975346B2 (en) | 2012-05-18 | 2015-03-10 | Sabic Global Technologies B.V. | Polycarbonate copolymers via controlled radical polymerization |
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DE3207291A1 (de) * | 1982-03-01 | 1983-09-08 | Röhm GmbH, 6100 Darmstadt | Konzentrierte emulsionen von olefincopolymerisaten |
DE3613247C2 (de) * | 1986-04-19 | 1995-04-27 | Roehm Gmbh | Konzentrierte Emulsionen aus Ethylen-Vinylacetat-Copolymeren, Verfahren zu deren Herstellung und deren Verwendung als Stockpunktverbesserer |
US4940761A (en) * | 1986-05-29 | 1990-07-10 | E. I. Du Pont De Nemours And Company | Group transfer polymerization of glycidyl (meth)acrylate copolymers to form oxirane group-terminated block copolymers |
US5098959A (en) * | 1988-03-23 | 1992-03-24 | The Dow Chemical Company | Block polymers of methacrylates |
DE4139962A1 (de) * | 1991-12-04 | 1993-06-09 | Basf Ag, 6700 Ludwigshafen, De | Blockcopolymere aus acrylat- und methacrylateinheiten |
US5219945A (en) * | 1992-02-20 | 1993-06-15 | E. I. Du Pont De Nemours And Company | ABC triblock methacrylate polymers |
US5310807A (en) * | 1992-12-30 | 1994-05-10 | E. I. Du Pont De Nemours And Company | Star polymers made from macromonomers made by cobalt chain transfer process |
US5807937A (en) * | 1995-11-15 | 1998-09-15 | Carnegie Mellon University | Processes based on atom (or group) transfer radical polymerization and novel (co) polymers having useful structures and properties |
US5789487A (en) * | 1996-07-10 | 1998-08-04 | Carnegie-Mellon University | Preparation of novel homo- and copolymers using atom transfer radical polymerization |
US6140431A (en) * | 1997-02-27 | 2000-10-31 | Rohm And Haas Company | Process for preparing continuously variable-composition copolymers |
US5834408A (en) * | 1997-10-24 | 1998-11-10 | Ethyl Corporation | Pour point depressants via anionic polymerization of (meth)acrylic monomers |
US6409778B1 (en) * | 1997-11-21 | 2002-06-25 | Rohmax Additives Gmbh | Additive for biodiesel and biofuel oils |
US6084718A (en) * | 1998-03-23 | 2000-07-04 | Trw Inc. | Method and apparatus for high energy propagation back focus control |
CA2265345A1 (en) * | 1998-03-25 | 1999-09-25 | The Lubrizol Corporation | Vinyl aromatic-(vinyl aromatic-co-acrylic) block copolymers prepared by stabilized free radical polymerization |
AR035311A1 (es) * | 1999-01-27 | 2004-05-12 | Wyeth Corp | Derivados de acido hidroxamico que contienen alquinilo, como inhibidores de las metalloproteinasas de matriz y de la tace, composicion farmaceutica y el uso de los mismos para la manufactura de un medicamento |
US6391996B1 (en) * | 1999-11-30 | 2002-05-21 | Rohmax Additives Gmbh | Copolymers obtainable by the ATRP method and a method for their preparation and their use |
-
2000
- 2000-03-30 DE DE10015533A patent/DE10015533A1/de not_active Withdrawn
- 2000-11-18 CA CA002392727A patent/CA2392727C/en not_active Expired - Fee Related
- 2000-11-18 EP EP00993230.2A patent/EP1235870B1/de not_active Expired - Lifetime
- 2000-11-18 MX MXPA02005366A patent/MXPA02005366A/es active IP Right Grant
- 2000-11-18 BR BRPI0015825-9A patent/BR0015825B1/pt not_active IP Right Cessation
- 2000-11-18 KR KR1020027006954A patent/KR100640679B1/ko not_active IP Right Cessation
- 2000-11-18 AU AU17033/01A patent/AU1703301A/en not_active Abandoned
- 2000-11-18 WO PCT/EP2000/011502 patent/WO2001040339A1/de active Application Filing
- 2000-11-18 CN CNB008148260A patent/CN100475871C/zh not_active Expired - Fee Related
- 2000-11-18 JP JP2001541091A patent/JP5259901B2/ja not_active Expired - Lifetime
Cited By (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US8288327B2 (en) | 2003-03-31 | 2012-10-16 | Evonik Rohmax Additives Gmbh | Lubricating oil composition with good frictional properties |
CN103254974B (zh) * | 2003-03-31 | 2015-11-11 | 赢创罗曼克斯添加剂有限公司 | 具有优良摩擦性能的润滑油组合物 |
CN1984981B (zh) * | 2004-07-16 | 2010-11-17 | 可乐丽股份有限公司 | 含有丙烯酸系聚合物的润滑油添加剂及润滑油组合物 |
Also Published As
Publication number | Publication date |
---|---|
CA2392727A1 (en) | 2001-06-07 |
WO2001040339A1 (de) | 2001-06-07 |
AU1703301A (en) | 2001-06-12 |
DE10015533A1 (de) | 2001-06-28 |
KR20020068361A (ko) | 2002-08-27 |
JP2003516430A (ja) | 2003-05-13 |
BR0015825B1 (pt) | 2011-06-14 |
JP5259901B2 (ja) | 2013-08-07 |
CA2392727C (en) | 2010-03-09 |
MXPA02005366A (es) | 2002-11-29 |
CN100475871C (zh) | 2009-04-08 |
KR100640679B1 (ko) | 2006-11-02 |
EP1235870A1 (de) | 2002-09-04 |
EP1235870B1 (de) | 2017-05-24 |
BR0015825A (pt) | 2002-10-22 |
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