CA2619762A1 - Melanges de cyclo-olefines et procede de collage par solvants de polyolefines - Google Patents

Melanges de cyclo-olefines et procede de collage par solvants de polyolefines Download PDF

Info

Publication number: CA2619762A1
Authority: CA; Canada
Prior art keywords: component; composition; rigid; good; topas
Prior art date: 1999-09-09
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.): Abandoned

Application number

CA002619762A

Other languages

English (en)

Inventor

Yuan-Pang S. Ding

Chuan Qin

Lecon Woo

Michael T.K. Ling

Sherwin Shang

Tahua Yang

Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)

Baxter International Inc

Original Assignee

Individual

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.)

1999-09-09

Filing date

2000-09-08

Publication date

2001-03-15

1999-09-09 Priority claimed from US09/393,052 external-priority patent/US6632318B1/en

1999-09-09 Priority claimed from US09/393,051 external-priority patent/US6297322B1/en

1999-09-09 Priority claimed from US09/392,912 external-priority patent/US6255396B1/en

1999-09-09 Priority claimed from US09/392,913 external-priority patent/US6613187B1/en

2000-09-08 Application filed by Individual filed Critical Individual

2000-09-08 Priority claimed from CA002383117A external-priority patent/CA2383117C/fr

2001-03-15 Publication of CA2619762A1 publication Critical patent/CA2619762A1/fr

Status Abandoned legal-status Critical Current

Links

239000000203 mixture Substances 0.000 title claims abstract description 105
239000002904 solvent Substances 0.000 title description 48
229920000098 polyolefin Polymers 0.000 title description 21
238000000034 method Methods 0.000 title description 20
229920000642 polymer Polymers 0.000 claims abstract description 55
229920000089 Cyclic olefin copolymer Polymers 0.000 claims abstract description 38
VGGSQFUCUMXWEO-UHFFFAOYSA-N Ethene Chemical compound C=C VGGSQFUCUMXWEO-UHFFFAOYSA-N 0.000 claims abstract description 31
239000005977 Ethylene Substances 0.000 claims abstract description 31
239000000178 monomer Substances 0.000 claims abstract description 29
JFNLZVQOOSMTJK-KNVOCYPGSA-N norbornene Chemical compound C1[C@@H]2CC[C@H]1C=C2 JFNLZVQOOSMTJK-KNVOCYPGSA-N 0.000 claims abstract description 14
-1 cyclic olefin Chemical class 0.000 claims description 80
229920001577 copolymer Polymers 0.000 claims description 27
229930195733 hydrocarbon Natural products 0.000 claims description 26
JRZJOMJEPLMPRA-UHFFFAOYSA-N olefin Natural products CCCCCCCC=C JRZJOMJEPLMPRA-UHFFFAOYSA-N 0.000 claims description 22
239000004215 Carbon black (E152) Substances 0.000 claims description 18
230000009477 glass transition Effects 0.000 claims description 14
229920001519 homopolymer Polymers 0.000 claims description 14
239000012968 metallocene catalyst Substances 0.000 claims description 8
229920001038 ethylene copolymer Polymers 0.000 claims description 7
WKBPZYKAUNRMKP-UHFFFAOYSA-N 1-[2-(2,4-dichlorophenyl)pentyl]1,2,4-triazole Chemical compound C=1C=C(Cl)C=C(Cl)C=1C(CCC)CN1C=NC=N1 WKBPZYKAUNRMKP-UHFFFAOYSA-N 0.000 description 69
239000004568 cement Substances 0.000 description 28
PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 26
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239000011347 resin Substances 0.000 description 25
239000000463 material Substances 0.000 description 23
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LIKMAJRDDDTEIG-UHFFFAOYSA-N 1-hexene Chemical compound CCCCC=C LIKMAJRDDDTEIG-UHFFFAOYSA-N 0.000 description 17
150000001338 aliphatic hydrocarbons Chemical class 0.000 description 16
150000004945 aromatic hydrocarbons Chemical class 0.000 description 16
CXWXQJXEFPUFDZ-UHFFFAOYSA-N tetralin Chemical compound C1=CC=C2CCCCC2=C1 CXWXQJXEFPUFDZ-UHFFFAOYSA-N 0.000 description 15
239000004800 polyvinyl chloride Substances 0.000 description 14
229920000915 polyvinyl chloride Polymers 0.000 description 14
KWKAKUADMBZCLK-UHFFFAOYSA-N 1-octene Chemical compound CCCCCCC=C KWKAKUADMBZCLK-UHFFFAOYSA-N 0.000 description 12
ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 12
IMNFDUFMRHMDMM-UHFFFAOYSA-N N-Heptane Chemical compound CCCCCCC IMNFDUFMRHMDMM-UHFFFAOYSA-N 0.000 description 12
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XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 description 11
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NNBZCPXTIHJBJL-UHFFFAOYSA-N decalin Chemical compound C1CCCC2CCCCC21 NNBZCPXTIHJBJL-UHFFFAOYSA-N 0.000 description 10
239000004743 Polypropylene Substances 0.000 description 9
239000012530 fluid Substances 0.000 description 9
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JHIVVAPYMSGYDF-UHFFFAOYSA-N cyclohexanone Chemical compound O=C1CCCCC1 JHIVVAPYMSGYDF-UHFFFAOYSA-N 0.000 description 8
YMWUJEATGCHHMB-UHFFFAOYSA-N dichloromethane Natural products ClCCl YMWUJEATGCHHMB-UHFFFAOYSA-N 0.000 description 8
238000002347 injection Methods 0.000 description 8
239000007924 injection Substances 0.000 description 8
229940127554 medical product Drugs 0.000 description 8
229920002959 polymer blend Polymers 0.000 description 8
238000002834 transmittance Methods 0.000 description 7
QTBSBXVTEAMEQO-UHFFFAOYSA-N Acetic acid Chemical compound CC(O)=O QTBSBXVTEAMEQO-UHFFFAOYSA-N 0.000 description 6
IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 6
ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 6
WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 6
125000000217 alkyl group Chemical group 0.000 description 6
150000001735 carboxylic acids Chemical class 0.000 description 6
RWGFKTVRMDUZSP-UHFFFAOYSA-N cumene Chemical compound CC(C)C1=CC=CC=C1 RWGFKTVRMDUZSP-UHFFFAOYSA-N 0.000 description 6
IIEWJVIFRVWJOD-UHFFFAOYSA-N ethylcyclohexane Chemical compound CCC1CCCCC1 IIEWJVIFRVWJOD-UHFFFAOYSA-N 0.000 description 6
DEDZSLCZHWTGOR-UHFFFAOYSA-N propylcyclohexane Chemical compound CCCC1CCCCC1 DEDZSLCZHWTGOR-UHFFFAOYSA-N 0.000 description 6
239000000126 substance Substances 0.000 description 6
238000012360 testing method Methods 0.000 description 6
OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical group [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 description 5
229920000339 Marlex Polymers 0.000 description 5
CTQNGGLPUBDAKN-UHFFFAOYSA-N O-Xylene Chemical compound CC1=CC=CC=C1C CTQNGGLPUBDAKN-UHFFFAOYSA-N 0.000 description 5
150000001336 alkenes Chemical class 0.000 description 5
GGBJHURWWWLEQH-UHFFFAOYSA-N butylcyclohexane Chemical compound CCCCC1CCCCC1 GGBJHURWWWLEQH-UHFFFAOYSA-N 0.000 description 5
150000001925 cycloalkenes Chemical class 0.000 description 5
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 5
239000008096 xylene Substances 0.000 description 5
FERIUCNNQQJTOY-UHFFFAOYSA-N Butyric acid Chemical compound CCCC(O)=O FERIUCNNQQJTOY-UHFFFAOYSA-N 0.000 description 4
230000000712 assembly Effects 0.000 description 4
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229910052799 carbon Inorganic materials 0.000 description 4
ZGEGCLOFRBLKSE-UHFFFAOYSA-N methylene hexane Natural products CCCCCC=C ZGEGCLOFRBLKSE-UHFFFAOYSA-N 0.000 description 4
239000000243 solution Substances 0.000 description 4
VEXZGXHMUGYJMC-UHFFFAOYSA-N Hydrochloric acid Chemical compound Cl VEXZGXHMUGYJMC-UHFFFAOYSA-N 0.000 description 3
KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 3
229920002633 Kraton (polymer) Polymers 0.000 description 3
XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical class CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 3
239000000654 additive Substances 0.000 description 3
SFFFIHNOEGSAIH-UHFFFAOYSA-N bicyclo[2.2.1]hept-2-ene;ethene Chemical group C=C.C1C2CCC1C=C2 SFFFIHNOEGSAIH-UHFFFAOYSA-N 0.000 description 3
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150000001875 compounds Chemical class 0.000 description 3
239000003814 drug Substances 0.000 description 3
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238000009472 formulation Methods 0.000 description 3
238000001746 injection moulding Methods 0.000 description 3
238000005304 joining Methods 0.000 description 3
VLKZOEOYAKHREP-UHFFFAOYSA-N n-Hexane Chemical class CCCCCC VLKZOEOYAKHREP-UHFFFAOYSA-N 0.000 description 3
AFFLGGQVNFXPEV-UHFFFAOYSA-N n-decene Natural products CCCCCCCCC=C AFFLGGQVNFXPEV-UHFFFAOYSA-N 0.000 description 3
230000037361 pathway Effects 0.000 description 3
239000004014 plasticizer Substances 0.000 description 3
229920001200 poly(ethylene-vinyl acetate) Polymers 0.000 description 3
229920000306 polymethylpentene Polymers 0.000 description 3
239000011116 polymethylpentene Substances 0.000 description 3
239000000047 product Substances 0.000 description 3
XTVMZZBLCLWBPM-UHFFFAOYSA-N tert-butylcyclohexane Chemical compound CC(C)(C)C1CCCCC1 XTVMZZBLCLWBPM-UHFFFAOYSA-N 0.000 description 3
YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 3
238000012546 transfer Methods 0.000 description 3
SMZOUWXMTYCWNB-UHFFFAOYSA-N 2-(2-methoxy-5-methylphenyl)ethanamine Chemical compound COC1=CC=C(C)C=C1CCN SMZOUWXMTYCWNB-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
CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
229920002943 EPDM rubber Polymers 0.000 description 2
JIGUQPWFLRLWPJ-UHFFFAOYSA-N Ethyl acrylate Chemical class CCOC(=O)C=C JIGUQPWFLRLWPJ-UHFFFAOYSA-N 0.000 description 2
229920000181 Ethylene propylene rubber Polymers 0.000 description 2
VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical class COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 2
150000001253 acrylic acids Chemical class 0.000 description 2
239000000956 alloy Substances 0.000 description 2
229910045601 alloy Inorganic materials 0.000 description 2
150000008064 anhydrides Chemical class 0.000 description 2
229940040591 biotech drug Drugs 0.000 description 2
239000008280 blood Substances 0.000 description 2
210000004369 blood Anatomy 0.000 description 2
125000000484 butyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 2
238000007906 compression Methods 0.000 description 2
230000006835 compression Effects 0.000 description 2
125000004122 cyclic group Chemical group 0.000 description 2
DMEGYFMYUHOHGS-UHFFFAOYSA-N cycloheptane Chemical compound C1CCCCCC1 DMEGYFMYUHOHGS-UHFFFAOYSA-N 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
229940079593 drug Drugs 0.000 description 2
BLCTWBJQROOONQ-UHFFFAOYSA-N ethenyl prop-2-enoate Chemical class C=COC(=O)C=C BLCTWBJQROOONQ-UHFFFAOYSA-N 0.000 description 2
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 2
239000005038 ethylene vinyl acetate Substances 0.000 description 2
238000001125 extrusion Methods 0.000 description 2
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150000002430 hydrocarbons Chemical group 0.000 description 2
229920000554 ionomer Polymers 0.000 description 2
239000008155 medical solution Substances 0.000 description 2
UAEPNZWRGJTJPN-UHFFFAOYSA-N methylcyclohexane Chemical compound CC1CCCCC1 UAEPNZWRGJTJPN-UHFFFAOYSA-N 0.000 description 2
YWAKXRMUMFPDSH-UHFFFAOYSA-N pentene Chemical compound CCCC=C YWAKXRMUMFPDSH-UHFFFAOYSA-N 0.000 description 2
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229920002742 polystyrene-block-poly(ethylene/propylene) -block-polystyrene Polymers 0.000 description 2
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WROUWQQRXUBECT-UHFFFAOYSA-N 2-ethylacrylic acid Chemical class CCC(=C)C(O)=O WROUWQQRXUBECT-UHFFFAOYSA-N 0.000 description 1
229920001634 Copolyester Polymers 0.000 description 1
HTTJABKRGRZYRN-UHFFFAOYSA-N Heparin Chemical compound OC1C(NC(=O)C)C(O)OC(COS(O)(=O)=O)C1OC1C(OS(O)(=O)=O)C(O)C(OC2C(C(OS(O)(=O)=O)C(OC3C(C(O)C(O)C(O3)C(O)=O)OS(O)(=O)=O)C(CO)O2)NS(O)(=O)=O)C(C(O)=O)O1 HTTJABKRGRZYRN-UHFFFAOYSA-N 0.000 description 1
CERQOIWHTDAKMF-UHFFFAOYSA-N Methacrylic acid Chemical class CC(=C)C(O)=O CERQOIWHTDAKMF-UHFFFAOYSA-N 0.000 description 1
BAPJBEWLBFYGME-UHFFFAOYSA-N Methyl acrylate Chemical class COC(=O)C=C BAPJBEWLBFYGME-UHFFFAOYSA-N 0.000 description 1
NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
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239000002253 acid Substances 0.000 description 1
150000007513 acids Chemical class 0.000 description 1
150000001252 acrylic acid derivatives Chemical class 0.000 description 1
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150000008360 acrylonitriles Chemical class 0.000 description 1
238000004026 adhesive bonding Methods 0.000 description 1
125000005250 alkyl acrylate group Chemical group 0.000 description 1
125000005336 allyloxy group Chemical group 0.000 description 1
150000001408 amides Chemical class 0.000 description 1
150000001412 amines Chemical class 0.000 description 1
101150059062 apln gene Proteins 0.000 description 1
125000003710 aryl alkyl group Chemical group 0.000 description 1
125000003118 aryl group Chemical group 0.000 description 1
230000009286 beneficial effect Effects 0.000 description 1
230000015572 biosynthetic process Effects 0.000 description 1
239000006227 byproduct Substances 0.000 description 1
239000001569 carbon dioxide Substances 0.000 description 1
229910002092 carbon dioxide Inorganic materials 0.000 description 1
150000001732 carboxylic acid derivatives Chemical class 0.000 description 1
239000003054 catalyst Substances 0.000 description 1
239000003795 chemical substances by application Substances 0.000 description 1
238000004891 communication Methods 0.000 description 1
238000000748 compression moulding Methods 0.000 description 1
238000011109 contamination Methods 0.000 description 1
239000011258 core-shell material Substances 0.000 description 1
238000005260 corrosion Methods 0.000 description 1
230000007797 corrosion Effects 0.000 description 1
150000004292 cyclic ethers Chemical class 0.000 description 1
125000000753 cycloalkyl group Chemical group 0.000 description 1
ZXIJMRYMVAMXQP-UHFFFAOYSA-N cycloheptene Chemical compound C1CCC=CCC1 ZXIJMRYMVAMXQP-UHFFFAOYSA-N 0.000 description 1
URYYVOIYTNXXBN-UPHRSURJSA-N cyclooctene Chemical compound C1CCC\C=C/CC1 URYYVOIYTNXXBN-UPHRSURJSA-N 0.000 description 1
239000004913 cyclooctene Substances 0.000 description 1
150000001941 cyclopentenes Chemical class 0.000 description 1
LPIQUOYDBNQMRZ-UHFFFAOYSA-N cyclopentenylidene Natural products C1CC=CC1 LPIQUOYDBNQMRZ-UHFFFAOYSA-N 0.000 description 1
239000008380 degradant Substances 0.000 description 1
238000000502 dialysis Methods 0.000 description 1
238000012377 drug delivery Methods 0.000 description 1
239000013583 drug formulation Substances 0.000 description 1
230000000694 effects Effects 0.000 description 1
150000002118 epoxides Chemical class 0.000 description 1
UYMKPFRHYYNDTL-UHFFFAOYSA-N ethenamine Chemical class NC=C UYMKPFRHYYNDTL-UHFFFAOYSA-N 0.000 description 1
RTZKZFJDLAIYFH-UHFFFAOYSA-N ether Substances CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 1
230000002349 favourable effect Effects 0.000 description 1
125000000524 functional group Chemical group 0.000 description 1
150000005826 halohydrocarbons Chemical class 0.000 description 1
229960002897 heparin Drugs 0.000 description 1
229920000669 heparin Polymers 0.000 description 1
125000004051 hexyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 1
125000004435 hydrogen atom Chemical group [H]* 0.000 description 1
IXCSERBJSXMMFS-UHFFFAOYSA-N hydrogen chloride Substances Cl.Cl IXCSERBJSXMMFS-UHFFFAOYSA-N 0.000 description 1
229910000041 hydrogen chloride Inorganic materials 0.000 description 1
150000003949 imides Chemical class 0.000 description 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 description 1
150000002576 ketones Chemical class 0.000 description 1
238000003475 lamination Methods 0.000 description 1
239000007788 liquid Substances 0.000 description 1
FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 description 1
239000012567 medical material Substances 0.000 description 1
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125000005395 methacrylic acid group Chemical class 0.000 description 1
GYNNXHKOJHMOHS-UHFFFAOYSA-N methyl-cycloheptane Natural products CC1CCCCCC1 GYNNXHKOJHMOHS-UHFFFAOYSA-N 0.000 description 1
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238000012986 modification Methods 0.000 description 1
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125000002950 monocyclic group Chemical group 0.000 description 1
QJGQUHMNIGDVPM-UHFFFAOYSA-N nitrogen group Chemical group [N] QJGQUHMNIGDVPM-UHFFFAOYSA-N 0.000 description 1
239000002245 particle Substances 0.000 description 1
UCUUFSAXZMGPGH-UHFFFAOYSA-N penta-1,4-dien-3-one Chemical class C=CC(=O)C=C UCUUFSAXZMGPGH-UHFFFAOYSA-N 0.000 description 1
RGSFGYAAUTVSQA-UHFFFAOYSA-N pentamethylene Natural products C1CCCC1 RGSFGYAAUTVSQA-UHFFFAOYSA-N 0.000 description 1
229920003023 plastic Polymers 0.000 description 1
239000004033 plastic Substances 0.000 description 1
229920006112 polar polymer Polymers 0.000 description 1
229920003229 poly(methyl methacrylate) Polymers 0.000 description 1
229920001083 polybutene Polymers 0.000 description 1
239000004417 polycarbonate Substances 0.000 description 1
229920000515 polycarbonate Polymers 0.000 description 1
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230000000379 polymerizing effect Effects 0.000 description 1
238000002360 preparation method Methods 0.000 description 1
230000008569 process Effects 0.000 description 1
125000001436 propyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
QQONPFPTGQHPMA-UHFFFAOYSA-N propylene Natural products CC=C QQONPFPTGQHPMA-UHFFFAOYSA-N 0.000 description 1
125000004805 propylene group Chemical group [H]C([H])([H])C([H])([*:1])C([H])([H])[*:2] 0.000 description 1
229920005604 random copolymer Polymers 0.000 description 1
230000011514 reflex Effects 0.000 description 1
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125000001424 substituent group Chemical group 0.000 description 1
229910052717 sulfur Inorganic materials 0.000 description 1
239000011593 sulfur Substances 0.000 description 1
230000003746 surface roughness Effects 0.000 description 1
229920003002 synthetic resin Polymers 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
238000010998 test method Methods 0.000 description 1
229940124597 therapeutic agent Drugs 0.000 description 1
230000001225 therapeutic effect Effects 0.000 description 1
230000002792 vascular Effects 0.000 description 1
229920001567 vinyl ester resin Polymers 0.000 description 1
238000011179 visual inspection Methods 0.000 description 1
XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1

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Materials For Medical Uses (AREA)
Compositions Of Macromolecular Compounds (AREA)

CA002619762A 1999-09-09 2000-09-08 Melanges de cyclo-olefines et procede de collage par solvants de polyolefines Abandoned CA2619762A1 (fr)

Applications Claiming Priority (9)

Application Number	Priority Date	Filing Date	Title
US09/392,913		1999-09-09
US09/393,051		1999-09-09
US09/393,052 US6632318B1 (en)	1999-09-09	1999-09-09	Method for solvent bonding polyolefins
US09/392,912		1999-09-09
US09/393,052		1999-09-09
US09/393,051 US6297322B1 (en)	1999-09-09	1999-09-09	Cycloolefin blends and method for solvent bonding polyolefins
US09/392,912 US6255396B1 (en)	1999-09-09	1999-09-09	Cycloolefin blends and method for solvent bonding polyolefins
US09/392,913 US6613187B1 (en)	1999-09-09	1999-09-09	Solvent bonding method for polyolefin materials
CA002383117A CA2383117C (fr)	1999-09-09	2000-09-08	Melanges de cyclo-olefines et procede de collage par solvants de polyolefines

Related Parent Applications (1)

Application Number	Title	Priority Date	Filing Date
CA002383117A Division CA2383117C (fr)	1999-09-09	2000-09-08	Melanges de cyclo-olefines et procede de collage par solvants de polyolefines

Publications (1)

Publication Number	Publication Date
CA2619762A1 true CA2619762A1 (fr)	2001-03-15

Family

ID=39315348

Family Applications (2)

Application Number	Title	Priority Date	Filing Date
CA002620651A Abandoned CA2620651A1 (fr)	1999-09-09	2000-09-08	Melanges de cyclo-olefines et procede de collage par solvants de polyolefines
CA002619762A Abandoned CA2619762A1 (fr)	1999-09-09	2000-09-08	Melanges de cyclo-olefines et procede de collage par solvants de polyolefines

Family Applications Before (1)

Application Number	Title	Priority Date	Filing Date
CA002620651A Abandoned CA2620651A1 (fr)	1999-09-09	2000-09-08	Melanges de cyclo-olefines et procede de collage par solvants de polyolefines

Country Status (1)

Country	Link
CA (2)	CA2620651A1 (fr)

2000
- 2000-09-08 CA CA002620651A patent/CA2620651A1/fr not_active Abandoned
- 2000-09-08 CA CA002619762A patent/CA2619762A1/fr not_active Abandoned

Also Published As

Publication number	Publication date
CA2620651A1 (fr)	2001-03-15

Legal Events

Date	Code	Title	Description
2008-02-22	EEER	Examination request
2010-09-08	FZDE	Dead

Publication	Publication Date	Title
US6255396B1 (en)	2001-07-03	Cycloolefin blends and method for solvent bonding polyolefins
US6297322B1 (en)	2001-10-02	Cycloolefin blends and method for solvent bonding polyolefins
EP1216274B1 (fr)	2005-03-16	Melanges de cyclo-olefines et procede de collage par solvants de polyolefines
US6590033B2 (en)	2003-07-08	Cycloolefin blends and method for solvent bonding polyolefins
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US6613187B1 (en)	2003-09-02	Solvent bonding method for polyolefin materials
US6632318B1 (en)	2003-10-14	Method for solvent bonding polyolefins
CA2619762A1 (fr)	2001-03-15	Melanges de cyclo-olefines et procede de collage par solvants de polyolefines
AU2002307552A1 (en)	2002-11-05	Cycloolefin polymer lends with diene polymer
US6036676A (en)	2000-03-14	Surface modified polymeric material formulation
JPH0938196A (ja)	1997-02-10	医療用器具