JP2002543261A - 熱可塑性成形材料及びポリマー添加物 - Google Patents
熱可塑性成形材料及びポリマー添加物Info
- Publication number
- JP2002543261A JP2002543261A JP2000615686A JP2000615686A JP2002543261A JP 2002543261 A JP2002543261 A JP 2002543261A JP 2000615686 A JP2000615686 A JP 2000615686A JP 2000615686 A JP2000615686 A JP 2000615686A JP 2002543261 A JP2002543261 A JP 2002543261A
- Authority
- JP
- Japan
- Prior art keywords
- antioxidant
- hydroxy groups
- thermoplastic molding
- hydroxyl compound
- aliphatic
- 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- Withdrawn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
- 229920000642 polymer Polymers 0.000 title claims abstract description 50
- 239000000654 additive Substances 0.000 title claims abstract description 47
- 238000009757 thermoplastic moulding Methods 0.000 title claims abstract description 31
- 239000012778 molding material Substances 0.000 title claims abstract description 26
- -1 polyethylene terephthalate Polymers 0.000 claims abstract description 98
- IKHGUXGNUITLKF-UHFFFAOYSA-N Acetaldehyde Chemical compound CC=O IKHGUXGNUITLKF-UHFFFAOYSA-N 0.000 claims abstract description 76
- 125000002887 hydroxy group Chemical group [H]O* 0.000 claims abstract description 56
- 229920000139 polyethylene terephthalate Polymers 0.000 claims abstract description 52
- 239000005020 polyethylene terephthalate Substances 0.000 claims abstract description 51
- 239000000203 mixture Substances 0.000 claims abstract description 45
- 238000000034 method Methods 0.000 claims abstract description 35
- 230000000996 additive effect Effects 0.000 claims abstract description 31
- 150000001875 compounds Chemical class 0.000 claims abstract description 25
- 229920001634 Copolyester Polymers 0.000 claims abstract description 19
- 239000007788 liquid Substances 0.000 claims abstract description 16
- 238000012545 processing Methods 0.000 claims abstract description 13
- FBPFZTCFMRRESA-KVTDHHQDSA-N D-Mannitol Chemical compound OC[C@@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-KVTDHHQDSA-N 0.000 claims abstract description 12
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical compound CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims abstract description 10
- TXBCBTDQIULDIA-UHFFFAOYSA-N 2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)CO TXBCBTDQIULDIA-UHFFFAOYSA-N 0.000 claims abstract description 9
- HEBKCHPVOIAQTA-UHFFFAOYSA-N meso ribitol Natural products OCC(O)C(O)C(O)CO HEBKCHPVOIAQTA-UHFFFAOYSA-N 0.000 claims abstract description 9
- PTJWCLYPVFJWMP-UHFFFAOYSA-N 2-[[3-hydroxy-2-[[3-hydroxy-2,2-bis(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propoxy]methyl]-2-(hydroxymethyl)propane-1,3-diol Chemical compound OCC(CO)(CO)COCC(CO)(CO)COCC(CO)(CO)CO PTJWCLYPVFJWMP-UHFFFAOYSA-N 0.000 claims abstract description 7
- FBPFZTCFMRRESA-FSIIMWSLSA-N D-Glucitol Natural products OC[C@H](O)[C@H](O)[C@@H](O)[C@H](O)CO FBPFZTCFMRRESA-FSIIMWSLSA-N 0.000 claims abstract description 6
- FBPFZTCFMRRESA-JGWLITMVSA-N D-glucitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)[C@H](O)CO FBPFZTCFMRRESA-JGWLITMVSA-N 0.000 claims abstract description 6
- TVXBFESIOXBWNM-UHFFFAOYSA-N Xylitol Natural products OCCC(O)C(O)C(O)CCO TVXBFESIOXBWNM-UHFFFAOYSA-N 0.000 claims abstract description 6
- 235000010355 mannitol Nutrition 0.000 claims abstract description 6
- 229960002920 sorbitol Drugs 0.000 claims abstract description 6
- 239000000811 xylitol Substances 0.000 claims abstract description 6
- HEBKCHPVOIAQTA-SCDXWVJYSA-N xylitol Chemical compound OC[C@H](O)[C@@H](O)[C@H](O)CO HEBKCHPVOIAQTA-SCDXWVJYSA-N 0.000 claims abstract description 6
- 235000010447 xylitol Nutrition 0.000 claims abstract description 6
- 229960002675 xylitol Drugs 0.000 claims abstract description 6
- 229920001169 thermoplastic Polymers 0.000 claims abstract description 5
- 239000004416 thermosoftening plastic Substances 0.000 claims abstract description 5
- 238000010128 melt processing Methods 0.000 claims abstract description 3
- 239000003963 antioxidant agent Substances 0.000 claims description 58
- 235000006708 antioxidants Nutrition 0.000 claims description 58
- 230000003078 antioxidant effect Effects 0.000 claims description 43
- 238000001746 injection moulding Methods 0.000 claims description 12
- 229910052799 carbon Inorganic materials 0.000 claims description 11
- GVJHHUAWPYXKBD-IEOSBIPESA-N α-tocopherol Chemical compound OC1=C(C)C(C)=C2O[C@@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-IEOSBIPESA-N 0.000 claims description 10
- GVJHHUAWPYXKBD-UHFFFAOYSA-N (±)-α-Tocopherol Chemical compound OC1=C(C)C(C)=C2OC(CCCC(C)CCCC(C)CCCC(C)C)(C)CCC2=C1C GVJHHUAWPYXKBD-UHFFFAOYSA-N 0.000 claims description 9
- 125000004432 carbon atom Chemical group C* 0.000 claims description 9
- 238000004519 manufacturing process Methods 0.000 claims description 9
- 229960000984 tocofersolan Drugs 0.000 claims description 9
- 239000002530 phenolic antioxidant Substances 0.000 claims description 8
- 229940087168 alpha tocopherol Drugs 0.000 claims description 7
- 239000001257 hydrogen Substances 0.000 claims description 7
- 229910052739 hydrogen Inorganic materials 0.000 claims description 7
- 125000004435 hydrogen atom Chemical group [H]* 0.000 claims description 7
- 230000009467 reduction Effects 0.000 claims description 7
- 239000002076 α-tocopherol Substances 0.000 claims description 7
- 235000004835 α-tocopherol Nutrition 0.000 claims description 7
- 238000000465 moulding Methods 0.000 claims description 6
- 235000001815 DL-alpha-tocopherol Nutrition 0.000 claims description 5
- 239000011627 DL-alpha-tocopherol Substances 0.000 claims description 5
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 claims description 4
- 238000000071 blow moulding Methods 0.000 claims description 4
- 239000003086 colorant Substances 0.000 claims description 4
- 239000003921 oil Substances 0.000 claims description 4
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical compound OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 claims 6
- 229920000728 polyester Polymers 0.000 description 18
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical group OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 15
- 239000004952 Polyamide Substances 0.000 description 12
- 229920002647 polyamide Polymers 0.000 description 12
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 description 8
- 239000000049 pigment Substances 0.000 description 7
- MTHSVFCYNBDYFN-UHFFFAOYSA-N diethylene glycol Chemical compound OCCOCCO MTHSVFCYNBDYFN-UHFFFAOYSA-N 0.000 description 6
- 235000013305 food Nutrition 0.000 description 6
- 239000007789 gas Substances 0.000 description 6
- 239000000463 material Substances 0.000 description 6
- AOBORMOPSGHCAX-DGHZZKTQSA-N tocofersolan Chemical compound OCCOC(=O)CCC(=O)OC1=C(C)C(C)=C2O[C@](CCC[C@H](C)CCC[C@H](C)CCCC(C)C)(C)CCC2=C1C AOBORMOPSGHCAX-DGHZZKTQSA-N 0.000 description 6
- 235000013361 beverage Nutrition 0.000 description 5
- 239000000047 product Substances 0.000 description 5
- UYEMGAFJOZZIFP-UHFFFAOYSA-N 3,5-dihydroxybenzoic acid Chemical compound OC(=O)C1=CC(O)=CC(O)=C1 UYEMGAFJOZZIFP-UHFFFAOYSA-N 0.000 description 4
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 4
- ABLZXFCXXLZCGV-UHFFFAOYSA-N Phosphorous acid Chemical compound OP(O)=O ABLZXFCXXLZCGV-UHFFFAOYSA-N 0.000 description 4
- 230000004888 barrier function Effects 0.000 description 4
- WERYXYBDKMZEQL-UHFFFAOYSA-N butane-1,4-diol Chemical compound OCCCCO WERYXYBDKMZEQL-UHFFFAOYSA-N 0.000 description 4
- DMBHHRLKUKUOEG-UHFFFAOYSA-N diphenylamine Chemical compound C=1C=CC=CC=1NC1=CC=CC=C1 DMBHHRLKUKUOEG-UHFFFAOYSA-N 0.000 description 4
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 description 4
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 4
- 239000000126 substance Substances 0.000 description 4
- UNXHWFMMPAWVPI-UHFFFAOYSA-N Erythritol Natural products OCC(O)C(O)CO UNXHWFMMPAWVPI-UHFFFAOYSA-N 0.000 description 3
- WSFSSNUMVMOOMR-UHFFFAOYSA-N Formaldehyde Chemical compound O=C WSFSSNUMVMOOMR-UHFFFAOYSA-N 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 230000002411 adverse Effects 0.000 description 3
- 150000001299 aldehydes Chemical class 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 150000001721 carbon Chemical group 0.000 description 3
- 235000014171 carbonated beverage Nutrition 0.000 description 3
- 238000012937 correction Methods 0.000 description 3
- 238000004042 decolorization Methods 0.000 description 3
- 239000000796 flavoring agent Substances 0.000 description 3
- 235000019634 flavors Nutrition 0.000 description 3
- 229930195733 hydrocarbon Natural products 0.000 description 3
- 150000002430 hydrocarbons Chemical class 0.000 description 3
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 3
- 238000002347 injection Methods 0.000 description 3
- 239000007924 injection Substances 0.000 description 3
- 150000002596 lactones Chemical class 0.000 description 3
- 238000004806 packaging method and process Methods 0.000 description 3
- WXZMFSXDPGVJKK-UHFFFAOYSA-N pentaerythritol Chemical compound OCC(CO)(CO)CO WXZMFSXDPGVJKK-UHFFFAOYSA-N 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- SVTBMSDMJJWYQN-UHFFFAOYSA-N 2-methylpentane-2,4-diol Chemical compound CC(O)CC(C)(C)O SVTBMSDMJJWYQN-UHFFFAOYSA-N 0.000 description 2
- ALYNCZNDIQEVRV-PZFLKRBQSA-N 4-amino-3,5-ditritiobenzoic acid Chemical compound [3H]c1cc(cc([3H])c1N)C(O)=O ALYNCZNDIQEVRV-PZFLKRBQSA-N 0.000 description 2
- FJKROLUGYXJWQN-UHFFFAOYSA-N 4-hydroxybenzoic acid Chemical compound OC(=O)C1=CC=C(O)C=C1 FJKROLUGYXJWQN-UHFFFAOYSA-N 0.000 description 2
- QNVNLUSHGRBCLO-UHFFFAOYSA-N 5-hydroxybenzene-1,3-dicarboxylic acid Chemical compound OC(=O)C1=CC(O)=CC(C(O)=O)=C1 QNVNLUSHGRBCLO-UHFFFAOYSA-N 0.000 description 2
- 239000004953 Aliphatic polyamide Substances 0.000 description 2
- 239000004215 Carbon black (E152) Substances 0.000 description 2
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- UNXHWFMMPAWVPI-QWWZWVQMSA-N D-Threitol Natural products OC[C@@H](O)[C@H](O)CO UNXHWFMMPAWVPI-QWWZWVQMSA-N 0.000 description 2
- SRBFZHDQGSBBOR-IOVATXLUSA-N D-xylopyranose Chemical compound O[C@@H]1COC(O)[C@H](O)[C@H]1O SRBFZHDQGSBBOR-IOVATXLUSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 2
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 2
- NBIIXXVUZAFLBC-UHFFFAOYSA-N Phosphoric acid Chemical compound OP(O)(O)=O NBIIXXVUZAFLBC-UHFFFAOYSA-N 0.000 description 2
- LGRFSURHDFAFJT-UHFFFAOYSA-N Phthalic anhydride Natural products C1=CC=C2C(=O)OC(=O)C2=C1 LGRFSURHDFAFJT-UHFFFAOYSA-N 0.000 description 2
- DNIAPMSPPWPWGF-UHFFFAOYSA-N Propylene glycol Chemical compound CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 description 2
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 description 2
- 150000001298 alcohols Chemical class 0.000 description 2
- 229920003231 aliphatic polyamide Polymers 0.000 description 2
- 229920005628 alkoxylated polyol Polymers 0.000 description 2
- 150000001412 amines Chemical class 0.000 description 2
- PYMYPHUHKUWMLA-UHFFFAOYSA-N arabinose Natural products OCC(O)C(O)C(O)C=O PYMYPHUHKUWMLA-UHFFFAOYSA-N 0.000 description 2
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical compound [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 2
- SRBFZHDQGSBBOR-UHFFFAOYSA-N beta-D-Pyranose-Lyxose Natural products OC1COC(O)C(O)C1O SRBFZHDQGSBBOR-UHFFFAOYSA-N 0.000 description 2
- 125000002619 bicyclic group Chemical group 0.000 description 2
- JHIWVOJDXOSYLW-UHFFFAOYSA-N butyl 2,2-difluorocyclopropane-1-carboxylate Chemical compound CCCCOC(=O)C1CC1(F)F JHIWVOJDXOSYLW-UHFFFAOYSA-N 0.000 description 2
- 239000000969 carrier Substances 0.000 description 2
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- 150000002009 diols Chemical class 0.000 description 2
- HNPSIPDUKPIQMN-UHFFFAOYSA-N dioxosilane;oxo(oxoalumanyloxy)alumane Chemical compound O=[Si]=O.O=[Al]O[Al]=O HNPSIPDUKPIQMN-UHFFFAOYSA-N 0.000 description 2
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- XRVCFZPJAHWYTB-UHFFFAOYSA-N prenderol Chemical compound CCC(CC)(CO)CO XRVCFZPJAHWYTB-UHFFFAOYSA-N 0.000 description 1
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- HFHDHCJBZVLPGP-UHFFFAOYSA-N schardinger α-dextrin Chemical compound O1C(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC(C(O)C2O)C(CO)OC2OC(C(C2O)O)C(CO)OC2OC2C(O)C(O)C1OC2CO HFHDHCJBZVLPGP-UHFFFAOYSA-N 0.000 description 1
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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
- C08K5/04—Oxygen-containing compounds
- C08K5/05—Alcohols; Metal alcoholates
- C08K5/053—Polyhydroxylic alcohols
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Blow-Moulding Or Thermoforming Of Plastics Or The Like (AREA)
- Injection Moulding Of Plastics Or The Like (AREA)
- Other Resins Obtained By Reactions Not Involving Carbon-To-Carbon Unsaturated Bonds (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Containers Having Bodies Formed In One Piece (AREA)
- Manufacture Of Macromolecular Shaped Articles (AREA)
- Moulds For Moulding Plastics Or The Like (AREA)
Applications Claiming Priority (3)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| GB9909956.6 | 1999-04-29 | ||
| GBGB9909956.6A GB9909956D0 (en) | 1999-04-29 | 1999-04-29 | Thermoplastic moulding compositions and polymer additives |
| PCT/GB2000/001646 WO2000066659A1 (en) | 1999-04-29 | 2000-04-28 | Thermoplastic moulding compositions and polymer additives |
Related Child Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011093817A Division JP5496943B2 (ja) | 1999-04-29 | 2011-04-20 | 熱可塑性成形材料及びポリマー添加物 |
Publications (2)
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| JP2002543261A true JP2002543261A (ja) | 2002-12-17 |
| JP2002543261A5 JP2002543261A5 (https=) | 2011-01-20 |
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| JP2011093817A Expired - Fee Related JP5496943B2 (ja) | 1999-04-29 | 2011-04-20 | 熱可塑性成形材料及びポリマー添加物 |
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| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP2011093817A Expired - Fee Related JP5496943B2 (ja) | 1999-04-29 | 2011-04-20 | 熱可塑性成形材料及びポリマー添加物 |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US6936204B2 (https=) |
| EP (1) | EP1173508B1 (https=) |
| JP (2) | JP2002543261A (https=) |
| AT (1) | ATE272091T1 (https=) |
| AU (1) | AU4587200A (https=) |
| DE (2) | DE1173508T1 (https=) |
| ES (1) | ES2225131T3 (https=) |
| GB (1) | GB9909956D0 (https=) |
| PL (1) | PL204374B1 (https=) |
| WO (1) | WO2000066659A1 (https=) |
Cited By (6)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004523637A (ja) * | 2001-03-28 | 2004-08-05 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | 安定化されたポリエステルの調製方法 |
| JP2006528995A (ja) * | 2003-05-27 | 2006-12-28 | ザ・コカ−コーラ・カンパニー | 熔融加工されたポリエステルのアセトアルデヒド含量を減少させる方法 |
| JP2008509299A (ja) * | 2004-08-12 | 2008-03-27 | シル＋ザイラッヒャー・アクチエンゲゼルシャフト | 薬剤濃縮物に対するキャリア液およびその使用 |
| JP2012111921A (ja) * | 2010-11-29 | 2012-06-14 | Wintech Polymer Ltd | ポリブチレンテレフタレート系樹脂組成物の製造方法及び成形用ポリブチレンテレフタレート系樹脂組成物 |
| JP2012520364A (ja) * | 2009-03-13 | 2012-09-06 | ビーエーエスエフ ソシエタス・ヨーロピア | ポリエステルとポリアミドの安定化ブレンド |
| JP2022518704A (ja) * | 2019-01-17 | 2022-03-16 | フラウンホーファー－ゲゼルシャフト ツゥア フェアデルング デア アンゲヴァンドテン フォァシュング エー．ファウ． | 縮合ポリマーの制御された分解促進のための添加剤組成物の使用 |
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|---|---|---|---|---|
| GB9909956D0 (en) | 1999-04-29 | 1999-06-30 | Univ Aston | Thermoplastic moulding compositions and polymer additives |
| US6274212B1 (en) * | 2000-02-22 | 2001-08-14 | The Coca-Cola Company | Method to decrease the acetaldehyde content of melt-processed polyesters |
| US7759449B2 (en) | 2000-12-15 | 2010-07-20 | Wellman, Inc. | Methods for introducing additives into polyethylene terephthalate |
| US6599596B2 (en) | 2000-12-15 | 2003-07-29 | Wellman, Inc. | Methods of post-polymerization injection in continuous polyethylene terephthalate production |
| US6569991B2 (en) | 2000-12-15 | 2003-05-27 | Wellman, Inc. | Methods of post-polymerization extruder injection in polyethylene terephthalate production |
| EP1341836B1 (en) * | 2000-12-15 | 2005-03-02 | Wellman, Inc. | Methods of post-polymerization injection in condensation polymer production |
| WO2002051616A2 (en) * | 2000-12-15 | 2002-07-04 | Wellman, Inc. | Methods of post-polymerisation extruder injection in condensation polymer production |
| US6590069B2 (en) | 2000-12-15 | 2003-07-08 | Wellman, Inc. | Methods of post-polymerization extruder injection in condensation polymer production |
| EP1355986B1 (en) * | 2000-12-29 | 2007-01-24 | Ciba SC Holding AG | Polyester compositions of low residual aldehyde content |
| US6908650B2 (en) | 2001-03-02 | 2005-06-21 | Ciba Specialty Chemicals Corporation | Polyester and polyamide compositions of low residual aldehyde content |
| US20030039783A1 (en) | 2001-03-30 | 2003-02-27 | Stafford Steven Lee | Polyesters and polyester containers having a reduced coefficient of friction and improved clarity |
| US6632874B2 (en) | 2001-05-01 | 2003-10-14 | The Coca-Cola Company | Method to decrease aldehyde content in polyolefin products |
| EP1421141B1 (en) * | 2001-08-13 | 2005-03-09 | Ciba SC Holding AG | Polyester compositions of low residual aldehyde content |
| US20050176859A1 (en) * | 2001-10-09 | 2005-08-11 | Michael Tinkl | Polyester and polyamide compositions of low residual aldehyde content |
| EP1347005A1 (en) * | 2002-03-23 | 2003-09-24 | Zimmer AG | Polytrimethylene terephtalate resins with improved properties |
| US6709746B2 (en) | 2002-06-05 | 2004-03-23 | Arteva North America S.á.r.l. | Reducing concentration of organic materials with substituted cyclodextrin compound in polyester packaging materials |
| US7041350B1 (en) | 2002-08-30 | 2006-05-09 | The Coca-Cola Company | Polyester composition and articles with reduced acetaldehyde content and method using hydrogenation catalyst |
| WO2005040261A1 (en) * | 2003-10-15 | 2005-05-06 | Polyone Corporation | Use of tocopherol to scavenge acetaldehyde in polyethylene terephthalate containers |
| US7825176B2 (en) * | 2005-08-31 | 2010-11-02 | Sabic Innovative Plastics Ip B.V. | High flow polyester composition |
| GB0520004D0 (en) * | 2005-10-01 | 2005-11-09 | Colormatrix Europe Ltd | Thermoplastic polymer additive compositions |
| GB0526260D0 (en) * | 2005-12-23 | 2006-02-01 | Colormatrix Europe Ltd | Polymeric materials |
| GB0902941D0 (en) * | 2009-02-20 | 2009-04-08 | Colormatrix Holdings Inc | Polyesters |
| WO2010103030A2 (en) | 2009-03-13 | 2010-09-16 | Basf Se | Stabilized blends of polyester and polyamide |
| US9428292B2 (en) | 2013-03-13 | 2016-08-30 | Silgan White Cap LLC | Fluid injection system and method for supporting container walls |
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- 2000-04-28 DE DE1173508T patent/DE1173508T1/de active Pending
- 2000-04-28 ES ES00927469T patent/ES2225131T3/es not_active Expired - Lifetime
- 2000-04-28 AT AT00927469T patent/ATE272091T1/de not_active IP Right Cessation
- 2000-04-28 JP JP2000615686A patent/JP2002543261A/ja not_active Withdrawn
- 2000-04-28 DE DE60012497T patent/DE60012497T2/de not_active Expired - Lifetime
- 2000-04-28 EP EP00927469A patent/EP1173508B1/en not_active Expired - Lifetime
- 2000-04-28 PL PL351141A patent/PL204374B1/pl unknown
- 2000-04-28 AU AU45872/00A patent/AU4587200A/en not_active Abandoned
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Cited By (9)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JP2004523637A (ja) * | 2001-03-28 | 2004-08-05 | チバ スペシャルティ ケミカルズ ホールディング インコーポレーテッド | 安定化されたポリエステルの調製方法 |
| JP2006528995A (ja) * | 2003-05-27 | 2006-12-28 | ザ・コカ−コーラ・カンパニー | 熔融加工されたポリエステルのアセトアルデヒド含量を減少させる方法 |
| JP4825675B2 (ja) * | 2003-05-27 | 2011-11-30 | ザ・コカ−コーラ・カンパニー | 熔融加工されたポリエステルのアセトアルデヒド含量を減少させる方法 |
| JP2008509299A (ja) * | 2004-08-12 | 2008-03-27 | シル＋ザイラッヒャー・アクチエンゲゼルシャフト | 薬剤濃縮物に対するキャリア液およびその使用 |
| JP2012520364A (ja) * | 2009-03-13 | 2012-09-06 | ビーエーエスエフ ソシエタス・ヨーロピア | ポリエステルとポリアミドの安定化ブレンド |
| JP2012111921A (ja) * | 2010-11-29 | 2012-06-14 | Wintech Polymer Ltd | ポリブチレンテレフタレート系樹脂組成物の製造方法及び成形用ポリブチレンテレフタレート系樹脂組成物 |
| JP2022518704A (ja) * | 2019-01-17 | 2022-03-16 | フラウンホーファー－ゲゼルシャフト ツゥア フェアデルング デア アンゲヴァンドテン フォァシュング エー．ファウ． | 縮合ポリマーの制御された分解促進のための添加剤組成物の使用 |
| JP7397086B2 (ja) | 2019-01-17 | 2023-12-12 | フラウンホーファー－ゲゼルシャフト ツゥア フェアデルング デア アンゲヴァンドテン フォァシュング エー．ファウ． | 縮合ポリマーの制御された分解促進のための添加剤組成物の使用 |
| US12428556B2 (en) | 2019-01-17 | 2025-09-30 | Fraunhofer-Gesellschaft zur Förderung der angewandten Forschung e.V. | Use of an additive composition for the controlled accelerated decomposition of condensation polymers |
Also Published As
| Publication number | Publication date |
|---|---|
| DE60012497D1 (en) | 2004-09-02 |
| JP2011208145A (ja) | 2011-10-20 |
| EP1173508A1 (en) | 2002-01-23 |
| DE1173508T1 (de) | 2002-07-04 |
| AU4587200A (en) | 2000-11-17 |
| WO2000066659A1 (en) | 2000-11-09 |
| ATE272091T1 (de) | 2004-08-15 |
| JP5496943B2 (ja) | 2014-05-21 |
| GB9909956D0 (en) | 1999-06-30 |
| EP1173508B1 (en) | 2004-07-28 |
| US20030004244A1 (en) | 2003-01-02 |
| ES2225131T3 (es) | 2005-03-16 |
| US6936204B2 (en) | 2005-08-30 |
| PL204374B1 (pl) | 2010-01-29 |
| PL351141A1 (en) | 2003-03-24 |
| DE60012497T2 (de) | 2004-12-02 |
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