LU83688A1 - Perfectionnement a la sterilisation d'objets en polymeres halogeno-vinyliques par des rayonnements ionisants - Google Patents
Perfectionnement a la sterilisation d'objets en polymeres halogeno-vinyliques par des rayonnements ionisants Download PDFInfo
- Publication number
- LU83688A1 LU83688A1 LU83688A LU83688A LU83688A1 LU 83688 A1 LU83688 A1 LU 83688A1 LU 83688 A LU83688 A LU 83688A LU 83688 A LU83688 A LU 83688A LU 83688 A1 LU83688 A1 LU 83688A1
- Authority
- LU
- Luxembourg
- Prior art keywords
- mercapto
- ester
- mercaptan
- polymer
- mercaptan ester
- Prior art date
Links
- 230000005865 ionizing radiation Effects 0.000 title claims description 12
- 230000001954 sterilising effect Effects 0.000 title abstract description 9
- 230000006872 improvement Effects 0.000 title description 4
- 229920002554 vinyl polymer Polymers 0.000 title description 4
- 238000000034 method Methods 0.000 claims abstract description 18
- 229920000642 polymer Polymers 0.000 claims abstract description 18
- 150000002148 esters Chemical class 0.000 claims abstract description 8
- 239000012760 heat stabilizer Substances 0.000 claims abstract description 7
- 125000004432 carbon atom Chemical group C* 0.000 claims abstract description 5
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 4
- 150000002367 halogens Chemical class 0.000 claims abstract description 4
- -1 mercaptan ester Chemical class 0.000 claims description 24
- 239000004800 polyvinyl chloride Substances 0.000 claims description 14
- 229920000915 polyvinyl chloride Polymers 0.000 claims description 13
- 150000001875 compounds Chemical class 0.000 claims description 11
- CWERGRDVMFNCDR-UHFFFAOYSA-M thioglycolate(1-) Chemical compound [O-]C(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-M 0.000 claims description 9
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 claims description 8
- 125000003976 glyceryl group Chemical group [H]C([*])([H])C(O[H])([H])C(O[H])([H])[H] 0.000 claims description 7
- 229920003023 plastic Polymers 0.000 claims description 4
- 239000004033 plastic Substances 0.000 claims description 4
- 125000004429 atom Chemical group 0.000 claims description 3
- 229910052799 carbon Inorganic materials 0.000 claims description 3
- 229920005862 polyol Polymers 0.000 claims description 3
- 150000003077 polyols Chemical class 0.000 claims description 3
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-L Malonate Chemical group [O-]C(=O)CC([O-])=O OFOBLEOULBTSOW-UHFFFAOYSA-L 0.000 claims description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 claims description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-L adipate(2-) Chemical compound [O-]C(=O)CCCCC([O-])=O WNLRTRBMVRJNCN-UHFFFAOYSA-L 0.000 claims description 2
- JFCQEDHGNNZCLN-UHFFFAOYSA-N glutaric acid Chemical compound OC(=O)CCCC(O)=O JFCQEDHGNNZCLN-UHFFFAOYSA-N 0.000 claims description 2
- TYFQFVWCELRYAO-UHFFFAOYSA-L suberate(2-) Chemical compound [O-]C(=O)CCCCCCC([O-])=O TYFQFVWCELRYAO-UHFFFAOYSA-L 0.000 claims description 2
- 125000001424 substituent group Chemical group 0.000 claims description 2
- KDYFGRWQOYBRFD-UHFFFAOYSA-L succinate(2-) Chemical compound [O-]C(=O)CCC([O-])=O KDYFGRWQOYBRFD-UHFFFAOYSA-L 0.000 claims description 2
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 claims 3
- OKTJSMMVPCPJKN-UHFFFAOYSA-N Carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims 2
- 150000005690 diesters Chemical group 0.000 claims 2
- 125000000217 alkyl group Chemical group 0.000 claims 1
- 150000004662 dithiols Chemical group 0.000 claims 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 claims 1
- BJEPYKJPYRNKOW-UHFFFAOYSA-L malate(2-) Chemical compound [O-]C(=O)C(O)CC([O-])=O BJEPYKJPYRNKOW-UHFFFAOYSA-L 0.000 claims 1
- 125000005358 mercaptoalkyl group Chemical group 0.000 claims 1
- 229940116351 sebacate Drugs 0.000 claims 1
- CXMXRPHRNRROMY-UHFFFAOYSA-L sebacate(2-) Chemical compound [O-]C(=O)CCCCCCCCC([O-])=O CXMXRPHRNRROMY-UHFFFAOYSA-L 0.000 claims 1
- 150000003573 thiols Chemical class 0.000 claims 1
- LSDPWZHWYPCBBB-UHFFFAOYSA-N Methanethiol Chemical group SC LSDPWZHWYPCBBB-UHFFFAOYSA-N 0.000 abstract description 21
- 238000004659 sterilization and disinfection Methods 0.000 abstract description 7
- 230000008569 process Effects 0.000 abstract description 3
- 239000002861 polymer material Substances 0.000 abstract 1
- 229920005989 resin Polymers 0.000 description 15
- 239000011347 resin Substances 0.000 description 15
- 239000000203 mixture Substances 0.000 description 13
- 239000003381 stabilizer Substances 0.000 description 10
- 239000000654 additive Substances 0.000 description 6
- 239000004014 plasticizer Substances 0.000 description 6
- 230000004075 alteration Effects 0.000 description 4
- 238000004040 coloring Methods 0.000 description 4
- 229920001577 copolymer Polymers 0.000 description 4
- NUKZAGXMHTUAFE-UHFFFAOYSA-N methyl hexanoate Chemical compound CCCCCC(=O)OC NUKZAGXMHTUAFE-UHFFFAOYSA-N 0.000 description 4
- 230000005855 radiation Effects 0.000 description 4
- CWERGRDVMFNCDR-UHFFFAOYSA-N thioglycolic acid Chemical compound OC(=O)CS CWERGRDVMFNCDR-UHFFFAOYSA-N 0.000 description 4
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 3
- 239000002253 acid Substances 0.000 description 3
- 230000009471 action Effects 0.000 description 3
- 230000000996 additive effect Effects 0.000 description 3
- 229910052787 antimony Inorganic materials 0.000 description 3
- 125000003178 carboxy group Chemical group [H]OC(*)=O 0.000 description 3
- 125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 description 3
- 239000000463 material Substances 0.000 description 3
- 238000012360 testing method Methods 0.000 description 3
- VBICKXHEKHSIBG-UHFFFAOYSA-N 1-monostearoylglycerol Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCC(O)CO VBICKXHEKHSIBG-UHFFFAOYSA-N 0.000 description 2
- FPRWILGFWFTOHA-UHFFFAOYSA-N 2-sulfanylethyl octadecanoate Chemical compound CCCCCCCCCCCCCCCCCC(=O)OCCS FPRWILGFWFTOHA-UHFFFAOYSA-N 0.000 description 2
- GUTLYIVDDKVIGB-OUBTZVSYSA-N Cobalt-60 Chemical compound [60Co] GUTLYIVDDKVIGB-OUBTZVSYSA-N 0.000 description 2
- XBDQKXXYIPTUBI-UHFFFAOYSA-M Propionate Chemical compound CCC([O-])=O XBDQKXXYIPTUBI-UHFFFAOYSA-M 0.000 description 2
- BZHJMEDXRYGGRV-UHFFFAOYSA-N Vinyl chloride Chemical compound ClC=C BZHJMEDXRYGGRV-UHFFFAOYSA-N 0.000 description 2
- 239000002671 adjuvant Substances 0.000 description 2
- 230000000703 anti-shock Effects 0.000 description 2
- WATWJIUSRGPENY-UHFFFAOYSA-N antimony atom Chemical compound [Sb] WATWJIUSRGPENY-UHFFFAOYSA-N 0.000 description 2
- 239000003795 chemical substances by application Substances 0.000 description 2
- 239000003623 enhancer Substances 0.000 description 2
- 125000002573 ethenylidene group Chemical group [*]=C=C([H])[H] 0.000 description 2
- SFANDLQUSKLLPM-UHFFFAOYSA-N ethyl 2-sulfanyloctadecanoate Chemical compound CCCCCCCCCCCCCCCCC(S)C(=O)OCC SFANDLQUSKLLPM-UHFFFAOYSA-N 0.000 description 2
- 238000010348 incorporation Methods 0.000 description 2
- 239000004615 ingredient Substances 0.000 description 2
- 238000004898 kneading Methods 0.000 description 2
- 239000000314 lubricant Substances 0.000 description 2
- 238000004806 packaging method and process Methods 0.000 description 2
- 238000012545 processing Methods 0.000 description 2
- 230000006641 stabilisation Effects 0.000 description 2
- 238000011105 stabilization Methods 0.000 description 2
- 239000003017 thermal stabilizer Substances 0.000 description 2
- ZBBLRPRYYSJUCZ-GRHBHMESSA-L (z)-but-2-enedioate;dibutyltin(2+) Chemical compound [O-]C(=O)\C=C/C([O-])=O.CCCC[Sn+2]CCCC ZBBLRPRYYSJUCZ-GRHBHMESSA-L 0.000 description 1
- BQCIDUSAKPWEOX-UHFFFAOYSA-N 1,1-Difluoroethene Chemical group FC(F)=C BQCIDUSAKPWEOX-UHFFFAOYSA-N 0.000 description 1
- ISGHUYCZFWLBRU-UHFFFAOYSA-N 2-[2-(2-sulfanylacetyl)oxyethoxy]ethyl 2-sulfanylacetate Chemical compound SCC(=O)OCCOCCOC(=O)CS ISGHUYCZFWLBRU-UHFFFAOYSA-N 0.000 description 1
- SPOKRKBHYLSEPJ-UHFFFAOYSA-N 6-methyl-1-(6-methylheptylsulfanyl)heptane Chemical compound CC(C)CCCCCSCCCCCC(C)C SPOKRKBHYLSEPJ-UHFFFAOYSA-N 0.000 description 1
- NIXOWILDQLNWCW-UHFFFAOYSA-M Acrylate Chemical compound [O-]C(=O)C=C NIXOWILDQLNWCW-UHFFFAOYSA-M 0.000 description 1
- JFRNKHRLBMGFQY-UHFFFAOYSA-N C(CC(=O)OO)C(=O)OCCS Chemical compound C(CC(=O)OO)C(=O)OCCS JFRNKHRLBMGFQY-UHFFFAOYSA-N 0.000 description 1
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 description 1
- 239000004709 Chlorinated polyethylene Substances 0.000 description 1
- RWSOTUBLDIXVET-UHFFFAOYSA-N Dihydrogen sulfide Chemical class S RWSOTUBLDIXVET-UHFFFAOYSA-N 0.000 description 1
- 229920009204 Methacrylate-butadiene-styrene Polymers 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 229920001328 Polyvinylidene chloride Polymers 0.000 description 1
- 239000007983 Tris buffer Substances 0.000 description 1
- XTXRWKRVRITETP-UHFFFAOYSA-N Vinyl acetate Chemical compound CC(=O)OC=C XTXRWKRVRITETP-UHFFFAOYSA-N 0.000 description 1
- ODUIXUGXPFKQLG-QWRGUYRKSA-N [2-(4-chloro-2-fluoroanilino)-5-methyl-1,3-thiazol-4-yl]-[(2s,3s)-2,3-dimethylpiperidin-1-yl]methanone Chemical compound C[C@H]1[C@@H](C)CCCN1C(=O)C1=C(C)SC(NC=2C(=CC(Cl)=CC=2)F)=N1 ODUIXUGXPFKQLG-QWRGUYRKSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 150000001336 alkenes Chemical class 0.000 description 1
- RLKBOGLIOLFMEK-NSCUHMNNSA-N amino (e)-but-2-enoate Chemical compound C\C=C\C(=O)ON RLKBOGLIOLFMEK-NSCUHMNNSA-N 0.000 description 1
- 230000000181 anti-adherent effect Effects 0.000 description 1
- 238000013459 approach Methods 0.000 description 1
- 230000008901 benefit Effects 0.000 description 1
- SDBQMGGFXXVCCV-UHFFFAOYSA-N bis(2-sulfanylethyl) hexanedioate Chemical compound SCCOC(=O)CCCCC(=O)OCCS SDBQMGGFXXVCCV-UHFFFAOYSA-N 0.000 description 1
- YHHOOFOGVNOPMN-UHFFFAOYSA-N bis(3-sulfanylpropyl) propanedioate Chemical compound SCCCOC(=O)CC(=O)OCCCS YHHOOFOGVNOPMN-UHFFFAOYSA-N 0.000 description 1
- GZVYQBFTVZVHAI-UHFFFAOYSA-K bis[[2-(6-methylheptylsulfanyl)acetyl]oxy]stibanyl 2-(6-methylheptylsulfanyl)acetate Chemical compound CC(C)CCCCCSCC(=O)O[Sb](OC(=O)CSCCCCCC(C)C)OC(=O)CSCCCCCC(C)C GZVYQBFTVZVHAI-UHFFFAOYSA-K 0.000 description 1
- LKAVYBZHOYOUSX-UHFFFAOYSA-N buta-1,3-diene;2-methylprop-2-enoic acid;styrene Chemical compound C=CC=C.CC(=C)C(O)=O.C=CC1=CC=CC=C1 LKAVYBZHOYOUSX-UHFFFAOYSA-N 0.000 description 1
- 239000001273 butane Substances 0.000 description 1
- ADKBGLXGTKOWIU-UHFFFAOYSA-N butanediperoxoic acid Chemical compound OOC(=O)CCC(=O)OO ADKBGLXGTKOWIU-UHFFFAOYSA-N 0.000 description 1
- SHZIWNPUGXLXDT-UHFFFAOYSA-N caproic acid ethyl ester Natural products CCCCCC(=O)OCC SHZIWNPUGXLXDT-UHFFFAOYSA-N 0.000 description 1
- UUAGAQFQZIEFAH-UHFFFAOYSA-N chlorotrifluoroethylene Chemical group FC(F)=C(F)Cl UUAGAQFQZIEFAH-UHFFFAOYSA-N 0.000 description 1
- 239000003086 colorant Substances 0.000 description 1
- 238000011109 contamination Methods 0.000 description 1
- 239000013256 coordination polymer Substances 0.000 description 1
- 239000002537 cosmetic Substances 0.000 description 1
- 230000002939 deleterious effect Effects 0.000 description 1
- 230000006866 deterioration Effects 0.000 description 1
- POULHZVOKOAJMA-UHFFFAOYSA-M dodecanoate Chemical compound CCCCCCCCCCCC([O-])=O POULHZVOKOAJMA-UHFFFAOYSA-M 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 230000032050 esterification Effects 0.000 description 1
- 238000005886 esterification reaction Methods 0.000 description 1
- FCFWXRWOVCYEEM-UHFFFAOYSA-N ethane-1,2-diol;2-sulfanylacetic acid Chemical compound OCCO.OC(=O)CS FCFWXRWOVCYEEM-UHFFFAOYSA-N 0.000 description 1
- 230000002349 favourable effect Effects 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 229940075507 glyceryl monostearate Drugs 0.000 description 1
- DOGJSOZYUGJVKS-UHFFFAOYSA-N glyceryl monothioglycolate Chemical compound OCC(O)COC(=O)CS DOGJSOZYUGJVKS-UHFFFAOYSA-N 0.000 description 1
- 125000005843 halogen group Chemical group 0.000 description 1
- 231100000206 health hazard Toxicity 0.000 description 1
- FUZZWVXGSFPDMH-UHFFFAOYSA-M hexanoate Chemical compound CCCCCC([O-])=O FUZZWVXGSFPDMH-UHFFFAOYSA-M 0.000 description 1
- 239000008240 homogeneous mixture Substances 0.000 description 1
- 238000002347 injection Methods 0.000 description 1
- 239000007924 injection Substances 0.000 description 1
- 125000001905 inorganic group Chemical group 0.000 description 1
- 229940070765 laurate Drugs 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 244000005700 microbiome Species 0.000 description 1
- 239000001788 mono and diglycerides of fatty acids Substances 0.000 description 1
- 150000002763 monocarboxylic acids Chemical class 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- IJDNQMDRQITEOD-UHFFFAOYSA-N n-butane Chemical compound CCCC IJDNQMDRQITEOD-UHFFFAOYSA-N 0.000 description 1
- OFBQJSOFQDEBGM-UHFFFAOYSA-N n-pentane Natural products CCCCC OFBQJSOFQDEBGM-UHFFFAOYSA-N 0.000 description 1
- DLPRONUCBAPMMX-UHFFFAOYSA-N o-ethyl 2-hydroxypropanethioate Chemical compound CCOC(=S)C(C)O DLPRONUCBAPMMX-UHFFFAOYSA-N 0.000 description 1
- WWZKQHOCKIZLMA-UHFFFAOYSA-M octanoate Chemical compound CCCCCCCC([O-])=O WWZKQHOCKIZLMA-UHFFFAOYSA-M 0.000 description 1
- 125000002347 octyl 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])[H] 0.000 description 1
- 125000002524 organometallic group Chemical group 0.000 description 1
- 239000000825 pharmaceutical preparation Substances 0.000 description 1
- 229940127557 pharmaceutical product Drugs 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-K phosphate Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 1
- 239000010452 phosphate Substances 0.000 description 1
- 125000005498 phthalate group Chemical group 0.000 description 1
- 239000000049 pigment Substances 0.000 description 1
- 229920002620 polyvinyl fluoride Polymers 0.000 description 1
- 239000005033 polyvinylidene chloride Substances 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 239000012744 reinforcing agent Substances 0.000 description 1
- 229920001897 terpolymer Polymers 0.000 description 1
- 150000007970 thio esters Chemical class 0.000 description 1
- 125000004149 thio group Chemical group *S* 0.000 description 1
- 125000003396 thiol group Chemical group [H]S* 0.000 description 1
- 101150051314 tin-10 gene Proteins 0.000 description 1
- 235000012431 wafers Nutrition 0.000 description 1
- DGVVWUTYPXICAM-UHFFFAOYSA-N β‐Mercaptoethanol Chemical compound OCCS DGVVWUTYPXICAM-UHFFFAOYSA-N 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
- C08K5/36—Sulfur-, selenium-, or tellurium-containing compounds
- C08K5/37—Thiols
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L2/00—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor
- A61L2/02—Methods or apparatus for disinfecting or sterilising materials or objects other than foodstuffs or contact lenses; Accessories therefor using physical phenomena
- A61L2/08—Radiation
Landscapes
- Health & Medical Sciences (AREA)
- Chemical & Material Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Organic Chemistry (AREA)
- General Health & Medical Sciences (AREA)
- Public Health (AREA)
- Veterinary Medicine (AREA)
- Life Sciences & Earth Sciences (AREA)
- Epidemiology (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Animal Behavior & Ethology (AREA)
- Apparatus For Disinfection Or Sterilisation (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
- Wrappers (AREA)
- Transition And Organic Metals Composition Catalysts For Addition Polymerization (AREA)
- Food Preservation Except Freezing, Refrigeration, And Drying (AREA)
- Treatments Of Macromolecular Shaped Articles (AREA)
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| FR8021662A FR2491871A1 (fr) | 1980-10-10 | 1980-10-10 | Perfectionnement a la sterilisation d'objets en polymeres halogeno-vinyliques par des rayonnements ionisants, et resines pour sa realisation |
| FR8021662 | 1980-10-10 |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| LU83688A1 true LU83688A1 (fr) | 1982-05-07 |
Family
ID=9246734
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| LU83688A LU83688A1 (fr) | 1980-10-10 | 1981-10-09 | Perfectionnement a la sterilisation d'objets en polymeres halogeno-vinyliques par des rayonnements ionisants |
Country Status (14)
| Country | Link |
|---|---|
| US (1) | US4616046A (es) |
| EP (1) | EP0050070B1 (es) |
| JP (1) | JPS5796657A (es) |
| AT (1) | ATE5943T1 (es) |
| AU (1) | AU546339B2 (es) |
| BE (1) | BE890672A (es) |
| BR (1) | BR8106556A (es) |
| CA (1) | CA1181884A (es) |
| DE (1) | DE3162044D1 (es) |
| DK (1) | DK449781A (es) |
| ES (1) | ES506668A0 (es) |
| FR (1) | FR2491871A1 (es) |
| IT (1) | IT1144922B (es) |
| LU (1) | LU83688A1 (es) |
Families Citing this family (21)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US4427631A (en) * | 1982-05-27 | 1984-01-24 | Euroceltique, S.A. | Povidone irradiation |
| DE3247736A1 (de) * | 1982-12-23 | 1984-07-05 | Henkel KGaA, 4000 Düsseldorf | Stabilisierte polyvinylchlorid-formmassen |
| JPS6035037A (ja) * | 1983-04-29 | 1985-02-22 | テーハー・ゴールトシュミット・アクツィエンゲゼルシャフト | ハロゲン化樹脂用熱安定剤 |
| JPS59221243A (ja) * | 1983-05-24 | 1984-12-12 | オザキ軽化学株式会社 | 無菌包装用袋 |
| FR2550213B1 (fr) * | 1983-08-02 | 1986-12-26 | Elf Aquitaine | Procede de stabilisation thermique de polymeres halogeno-vinyliques et resines ainsi stabilisees |
| US4939185A (en) * | 1984-02-10 | 1990-07-03 | General Electric Company | Enhancing color stability to sterilizing radiation of polymer compositions |
| US4996245A (en) * | 1984-02-10 | 1991-02-26 | General Electric Company | Enhancing color stability to sterilizing radiation of polymer compositions |
| FR2617175B1 (fr) * | 1987-06-26 | 1989-10-27 | Kornbaum Simon | Procede de stabilisation des resines halogeno-vinyliques lors de leur transformation |
| JPH02189352A (ja) * | 1989-01-18 | 1990-07-25 | Nitto Kasei Co Ltd | 耐γ線性ハロゲン含有樹脂組成物 |
| US6348517B1 (en) * | 2000-09-01 | 2002-02-19 | Oxy Services, Inc. | Preparing sterile articles from polymers containing a stabilizer based on a poly(oxyalkylene) |
| US6762231B2 (en) * | 2000-12-15 | 2004-07-13 | The College Of William And Mary | Organic thiol metal-free stabilizers and plasticizers for halogen-containing polymers |
| US6667357B2 (en) | 2000-12-15 | 2003-12-23 | The College Of William And Mary | Organic thiol metal-free stabilizers and plasticizers for halogen-containing polymers |
| US7312266B2 (en) * | 2000-12-15 | 2007-12-25 | The College Of William And Mary | Organic thiol metal-free stabilizers and plasticizers for halogen-containing polymers |
| US6927247B2 (en) * | 2000-12-15 | 2005-08-09 | The College Of William And Mary | Organic thiol metal-free stabilizers and plasticizers for halogen-containing polymers |
| KR20030084932A (ko) * | 2001-02-16 | 2003-11-01 | 크롬프톤 비닐 아디티베스 게엠베하 | 할로겐 함유 중합체를 안정화시키기 위한 질소 함유시너지스트를 가지는 염소산염 함유 안정화제 시스템 |
| DE10118179A1 (de) * | 2001-04-11 | 2002-10-24 | Baerlocher Gmbh | Stabilisatorkombination für halogenhaltige Polymere und deren Verwendung |
| EP1589902A1 (en) * | 2003-01-27 | 2005-11-02 | Medtronic Vascular Connaught | Improved packaging for stent delivery systems |
| US7695674B2 (en) * | 2003-09-29 | 2010-04-13 | Medtronic Vascular, Inc. | Method of sterilizing balloon with ionizing radiation |
| JP2006342343A (ja) * | 2005-05-11 | 2006-12-21 | Showa Denko Kk | エラストマー組成物 |
| CN104710334B (zh) * | 2013-12-13 | 2017-01-25 | 湖北南星化工总厂 | 一种用于稳定pvc的金属硫醇盐化合物及制备方法 |
| CN106458876B (zh) * | 2014-06-09 | 2018-06-05 | 可奥熙搜路司有限公司 | 新的硫醇化合物和包含其的聚合性组合物 |
Family Cites Families (12)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| GB771857A (en) * | 1954-08-26 | 1957-04-03 | Metal & Thermit Corp | Composition |
| GB827393A (en) * | 1955-11-07 | 1960-02-03 | Metal & Thermit Corp | Stabilized vinyl chloride polymers |
| NL121580C (es) * | 1961-01-26 | |||
| US3537967A (en) * | 1966-07-29 | 1970-11-03 | Dart Ind Inc | Radiation sterilized,thiodipropionic acid ester stabilized,propylene polymers |
| US4036719A (en) * | 1973-10-11 | 1977-07-19 | Raychem Corporation | Irradiatable polymer composition with improved oxidation resistance |
| JPS5169587A (en) * | 1974-12-13 | 1976-06-16 | Tetsukosha Kk | Jugotaichuno zanzonenkabinirutanryotaijokyohoho |
| US3928285A (en) * | 1975-01-16 | 1975-12-23 | Cincinnati Milacron Inc | Synergistic organotin borate stabilizer composition and resins containing same |
| US4180447A (en) * | 1977-01-10 | 1979-12-25 | Lonza Ltd. | Process for the production of hard plastic foams using a polyvinylchloride base |
| FR2434835A1 (fr) * | 1978-08-29 | 1980-03-28 | Elf Aquitaine | Perfectionnement a la stabilisation de resines halogeno-vinyliques |
| DE2964543D1 (en) * | 1978-08-29 | 1983-02-24 | Elf Aquitaine | Improvement in the stabilisation of halogenated vinyl resins |
| US4336168A (en) * | 1980-04-28 | 1982-06-22 | Tenneco Chemicals, Inc. | Stable liquid antimony stabilizer compositions and vinyl halide resins containing same |
| FR2491936A1 (fr) * | 1980-10-13 | 1982-04-16 | Ato Chimie | Procede pour rendre des polymeres resistants aux radiations ionisantes, et compositions obtenues |
-
1980
- 1980-10-10 FR FR8021662A patent/FR2491871A1/fr active Granted
-
1981
- 1981-09-30 DE DE8181401511T patent/DE3162044D1/de not_active Expired
- 1981-09-30 EP EP81401511A patent/EP0050070B1/fr not_active Expired
- 1981-09-30 AT AT81401511T patent/ATE5943T1/de not_active IP Right Cessation
- 1981-10-08 CA CA000387578A patent/CA1181884A/fr not_active Expired
- 1981-10-08 IT IT24394/81A patent/IT1144922B/it active
- 1981-10-08 BE BE0/206197A patent/BE890672A/fr not_active IP Right Cessation
- 1981-10-08 AU AU76147/81A patent/AU546339B2/en not_active Ceased
- 1981-10-08 ES ES506668A patent/ES506668A0/es active Granted
- 1981-10-09 JP JP56160357A patent/JPS5796657A/ja active Granted
- 1981-10-09 BR BR8106556A patent/BR8106556A/pt not_active IP Right Cessation
- 1981-10-09 LU LU83688A patent/LU83688A1/fr unknown
- 1981-10-09 DK DK449781A patent/DK449781A/da not_active Application Discontinuation
-
1984
- 1984-05-07 US US06/607,510 patent/US4616046A/en not_active Expired - Fee Related
Also Published As
| Publication number | Publication date |
|---|---|
| FR2491871B1 (es) | 1984-10-19 |
| BR8106556A (pt) | 1982-06-29 |
| DK449781A (da) | 1982-04-11 |
| JPS5796657A (en) | 1982-06-16 |
| AU546339B2 (en) | 1985-08-29 |
| US4616046A (en) | 1986-10-07 |
| ATE5943T1 (de) | 1984-02-15 |
| EP0050070B1 (fr) | 1984-01-25 |
| AU7614781A (en) | 1982-04-22 |
| BE890672A (fr) | 1982-04-08 |
| CA1181884A (fr) | 1985-01-29 |
| JPH0212578B2 (es) | 1990-03-22 |
| ES8306982A1 (es) | 1983-07-01 |
| EP0050070A3 (en) | 1982-05-05 |
| EP0050070A2 (fr) | 1982-04-21 |
| FR2491871A1 (fr) | 1982-04-16 |
| IT8124394A0 (it) | 1981-10-08 |
| ES506668A0 (es) | 1983-07-01 |
| DE3162044D1 (en) | 1984-03-01 |
| IT1144922B (it) | 1986-10-29 |
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