WO2000056812A1 - Stabilization of polymers after exposure to oxidation - Google Patents
Stabilization of polymers after exposure to oxidation Download PDFInfo
- Publication number
- WO2000056812A1 WO2000056812A1 PCT/GB2000/000247 GB0000247W WO0056812A1 WO 2000056812 A1 WO2000056812 A1 WO 2000056812A1 GB 0000247 W GB0000247 W GB 0000247W WO 0056812 A1 WO0056812 A1 WO 0056812A1
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- WO
- WIPO (PCT)
- Prior art keywords
- stabilizer
- polymer according
- roco
- independently selected
- groups
- Prior art date
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- 229920000642 polymer Polymers 0.000 title claims abstract description 63
- 230000003647 oxidation Effects 0.000 title claims abstract description 9
- 238000007254 oxidation reaction Methods 0.000 title claims abstract description 9
- 230000006641 stabilisation Effects 0.000 title description 2
- 238000011105 stabilization Methods 0.000 title description 2
- 239000003381 stabilizer Substances 0.000 claims abstract description 78
- -1 polyethylene Polymers 0.000 claims abstract description 29
- 125000003118 aryl group Chemical group 0.000 claims abstract description 24
- 229910052757 nitrogen Inorganic materials 0.000 claims abstract description 24
- 229910052718 tin Inorganic materials 0.000 claims abstract description 24
- 229920000915 polyvinyl chloride Polymers 0.000 claims abstract description 23
- 239000004800 polyvinyl chloride Substances 0.000 claims abstract description 23
- 229910052796 boron Inorganic materials 0.000 claims abstract description 16
- 229910052710 silicon Inorganic materials 0.000 claims abstract description 16
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 15
- 229910052698 phosphorus Inorganic materials 0.000 claims abstract description 15
- 239000004698 Polyethylene Substances 0.000 claims abstract description 14
- 239000004743 Polypropylene Substances 0.000 claims abstract description 14
- 229910052760 oxygen Inorganic materials 0.000 claims abstract description 14
- 229920000573 polyethylene Polymers 0.000 claims abstract description 14
- 229910052717 sulfur Inorganic materials 0.000 claims abstract description 14
- 229920000515 polycarbonate Polymers 0.000 claims abstract description 13
- 239000004417 polycarbonate Substances 0.000 claims abstract description 13
- 229910052739 hydrogen Inorganic materials 0.000 claims abstract description 12
- 239000001257 hydrogen Substances 0.000 claims abstract description 12
- 125000000217 alkyl group Chemical group 0.000 claims abstract description 11
- 229920001155 polypropylene Polymers 0.000 claims abstract description 11
- 229920000728 polyester Polymers 0.000 claims abstract description 10
- 229920000570 polyether Polymers 0.000 claims abstract description 10
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N Boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 claims abstract description 8
- 239000004952 Polyamide Substances 0.000 claims abstract description 8
- 239000004642 Polyimide Substances 0.000 claims abstract description 8
- 239000004721 Polyphenylene oxide Substances 0.000 claims abstract description 8
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 claims abstract description 8
- 125000002877 alkyl aryl group Chemical group 0.000 claims abstract description 8
- 125000003710 aryl alkyl group Chemical group 0.000 claims abstract description 8
- 150000002431 hydrogen Chemical class 0.000 claims abstract description 8
- 229920002647 polyamide Polymers 0.000 claims abstract description 8
- 229920001721 polyimide Polymers 0.000 claims abstract description 8
- 229920001328 Polyvinylidene chloride Polymers 0.000 claims abstract description 7
- 229910052736 halogen Inorganic materials 0.000 claims abstract description 7
- 150000002367 halogens Chemical class 0.000 claims abstract description 7
- 229920002689 polyvinyl acetate Polymers 0.000 claims abstract description 7
- 239000011118 polyvinyl acetate Substances 0.000 claims abstract description 7
- 239000005033 polyvinylidene chloride Substances 0.000 claims abstract description 7
- 238000000034 method Methods 0.000 claims abstract description 5
- 125000002947 alkylene group Chemical group 0.000 claims description 18
- 230000005855 radiation Effects 0.000 claims description 10
- 229920002635 polyurethane Polymers 0.000 claims description 9
- 239000004814 polyurethane Substances 0.000 claims description 9
- 125000000732 arylene group Chemical group 0.000 claims description 6
- 125000001797 benzyl group Chemical group [H]C1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])* 0.000 claims description 6
- UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 claims description 4
- 238000002156 mixing Methods 0.000 claims description 4
- ORTVZLZNOYNASJ-UPHRSURJSA-N (z)-but-2-ene-1,4-diol Chemical group OC\C=C/CO ORTVZLZNOYNASJ-UPHRSURJSA-N 0.000 claims description 3
- 230000001590 oxidative effect Effects 0.000 claims description 3
- 229920000379 polypropylene carbonate Polymers 0.000 claims description 3
- VEXZGXHMUGYJMC-UHFFFAOYSA-M Chloride anion Chemical compound [Cl-] VEXZGXHMUGYJMC-UHFFFAOYSA-M 0.000 claims description 2
- BAKUAUDFCNFLBX-UHFFFAOYSA-N 4,7-dihydro-1,3-dioxepine Chemical group C1OCC=CCO1 BAKUAUDFCNFLBX-UHFFFAOYSA-N 0.000 claims 2
- CGLJRLXTVXHOLX-PLNGDYQASA-N (z)-4-phenylmethoxybut-2-en-1-ol Chemical group OC\C=C/COCC1=CC=CC=C1 CGLJRLXTVXHOLX-PLNGDYQASA-N 0.000 claims 1
- SHOJWWNYFPQUHH-FPLPWBNLSA-N [(z)-4-phenylmethoxybut-2-enoxy]methylbenzene Chemical group C=1C=CC=CC=1COC\C=C/COCC1=CC=CC=C1 SHOJWWNYFPQUHH-FPLPWBNLSA-N 0.000 claims 1
- 101000941879 Homo sapiens Leucine-rich repeat serine/threonine-protein kinase 2 Proteins 0.000 abstract 2
- 102100032693 Leucine-rich repeat serine/threonine-protein kinase 2 Human genes 0.000 abstract 2
- 0 CC1C(CBr)CCC(C)(CCCC=CCC*)CNC1 Chemical compound CC1C(CBr)CCC(C)(CCCC=CCC*)CNC1 0.000 description 16
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 6
- OKKJLVBELUTLKV-UHFFFAOYSA-N Methanol Chemical compound OC OKKJLVBELUTLKV-UHFFFAOYSA-N 0.000 description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 4
- ZMXDDKWLCZADIW-UHFFFAOYSA-N N,N-Dimethylformamide Chemical compound CN(C)C=O ZMXDDKWLCZADIW-UHFFFAOYSA-N 0.000 description 3
- 150000001875 compounds Chemical class 0.000 description 3
- 150000002148 esters Chemical class 0.000 description 3
- 239000002904 solvent Substances 0.000 description 3
- DLFVBJFMPXGRIB-UHFFFAOYSA-N Acetamide Chemical compound CC(N)=O DLFVBJFMPXGRIB-UHFFFAOYSA-N 0.000 description 2
- KFZMGEQAYNKOFK-UHFFFAOYSA-N Isopropanol Chemical compound CC(C)O KFZMGEQAYNKOFK-UHFFFAOYSA-N 0.000 description 2
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- 238000006243 chemical reaction Methods 0.000 description 2
- 238000013329 compounding Methods 0.000 description 2
- 238000002845 discoloration Methods 0.000 description 2
- 239000012760 heat stabilizer Substances 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 2
- OYPRJOBELJOOCE-UHFFFAOYSA-N Calcium Chemical compound [Ca] OYPRJOBELJOOCE-UHFFFAOYSA-N 0.000 description 1
- UGFAIRIUMAVXCW-UHFFFAOYSA-N Carbon monoxide Chemical compound [O+]#[C-] UGFAIRIUMAVXCW-UHFFFAOYSA-N 0.000 description 1
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 1
- IAZDPXIOMUYVGZ-UHFFFAOYSA-N Dimethylsulphoxide Chemical compound CS(C)=O IAZDPXIOMUYVGZ-UHFFFAOYSA-N 0.000 description 1
- SECXISVLQFMRJM-UHFFFAOYSA-N N-Methylpyrrolidone Chemical compound CN1CCCC1=O SECXISVLQFMRJM-UHFFFAOYSA-N 0.000 description 1
- 235000021355 Stearic acid Nutrition 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- GTDPSWPPOUPBNX-UHFFFAOYSA-N ac1mqpva Chemical compound CC12C(=O)OC(=O)C1(C)C1(C)C2(C)C(=O)OC1=O GTDPSWPPOUPBNX-UHFFFAOYSA-N 0.000 description 1
- 150000001299 aldehydes Chemical class 0.000 description 1
- 150000001350 alkyl halides Chemical class 0.000 description 1
- 239000003963 antioxidant agent Substances 0.000 description 1
- QVGXLLKOCUKJST-UHFFFAOYSA-N atomic oxygen Chemical group [O] QVGXLLKOCUKJST-UHFFFAOYSA-N 0.000 description 1
- BJQHLKABXJIVAM-UHFFFAOYSA-N bis(2-ethylhexyl) phthalate Chemical compound CCCCC(CC)COC(=O)C1=CC=CC=C1C(=O)OCC(CC)CCCC BJQHLKABXJIVAM-UHFFFAOYSA-N 0.000 description 1
- 229910052791 calcium Inorganic materials 0.000 description 1
- 239000011575 calcium Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 125000004122 cyclic group Chemical group 0.000 description 1
- 238000006731 degradation reaction Methods 0.000 description 1
- 150000005690 diesters Chemical class 0.000 description 1
- 235000014113 dietary fatty acids Nutrition 0.000 description 1
- SBZXBUIDTXKZTM-UHFFFAOYSA-N diglyme Chemical compound COCCOCCOC SBZXBUIDTXKZTM-UHFFFAOYSA-N 0.000 description 1
- 229960001760 dimethyl sulfoxide Drugs 0.000 description 1
- 150000002009 diols Chemical class 0.000 description 1
- 238000007580 dry-mixing Methods 0.000 description 1
- 238000001035 drying Methods 0.000 description 1
- 150000002170 ethers Chemical class 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000194 fatty acid Substances 0.000 description 1
- 229930195729 fatty acid Natural products 0.000 description 1
- 150000004665 fatty acids Chemical class 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 150000004820 halides Chemical class 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 239000000314 lubricant Substances 0.000 description 1
- 238000005259 measurement Methods 0.000 description 1
- 238000013508 migration Methods 0.000 description 1
- 230000005012 migration Effects 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 239000000178 monomer Substances 0.000 description 1
- QIQXTHQIDYTFRH-UHFFFAOYSA-N octadecanoic acid Chemical compound CCCCCCCCCCCCCCCCCC(O)=O QIQXTHQIDYTFRH-UHFFFAOYSA-N 0.000 description 1
- OQCDKBAXFALNLD-UHFFFAOYSA-N octadecanoic acid Natural products CCCCCCCC(C)CCCCCCCCC(O)=O OQCDKBAXFALNLD-UHFFFAOYSA-N 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000001301 oxygen Substances 0.000 description 1
- 238000004806 packaging method and process Methods 0.000 description 1
- 229920002492 poly(sulfone) Polymers 0.000 description 1
- 229920001470 polyketone Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001296 polysiloxane Polymers 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 239000002516 radical scavenger Substances 0.000 description 1
- 239000000376 reactant Substances 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000002002 slurry Substances 0.000 description 1
- 239000007787 solid Substances 0.000 description 1
- 235000012424 soybean oil Nutrition 0.000 description 1
- 239000003549 soybean oil Substances 0.000 description 1
- 239000008117 stearic acid Substances 0.000 description 1
- 230000001954 sterilising effect Effects 0.000 description 1
- 238000004659 sterilization and disinfection Methods 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000009827 uniform distribution Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 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
- C08K5/0008—Organic ingredients according to more than one of the "one dot" groups of C08K5/01 - C08K5/59
- C08K5/005—Stabilisers against oxidation, heat, light, ozone
Definitions
- THIS INVENTION relates to the use of stabilizers to reduce the discoloration of certain polymers after they have been exposed to oxidation.
- a number of different polymers including polyvinyl chloride (PNC), polycarbonates, polyurethane, polyethylene, and polypropylene, are used to make various medical devices and as packaging for food. Sterilization can be accomplished by exposing the devices or packages to gamma radiation. However, the gamma radiation can degrade or yellow the polymer, making it unsuitable or less acceptable for certain applications. Polymers such as polyethylene, polypropylene, and PVC can also degrade and yellow after heating.
- a polymer which comprises polyvinyl chloride, polyvinylidene chloride, polycarbonate, polyurethane, polyethylene, polypropylene, polyamide, polyimide, polyether, polyester, or polyvinyl acetate containing about 0.005 to about 10 plir of a stabilizer having the general formula:
- each Y is independently selected from O, S, and N, each R is independently selected
- aralkyl from C 7 to C 2 is independently selected from R, OR, RCO, ROCO,
- ROCO 2 P(R) 2 , P(OR) 2 , PR(OR), N(R) 2 , (R) 2 NCO, (R) 2 NCO 2 , SR , and halogen , where
- each R 2 is independently selected from R, RCO, ROCO, P(OR) 2l Sn(R) q (OR) ⁇ , SnR ⁇ OCOR) ⁇ , Si(R) q (OR) ⁇ ,
- R 3 is independently selected from R, RCO, ROCO, ROCO 2 , OR, SR, N(R) 2 , OP(R) 2 ,
- n 0 when A is P or B and is 1 when A is Sn, Si, or C, n is 0 when
- Y is O or S and is 1 when Y is N
- p is 0 to 4, depending on the number of available sites
- q is 0 to 3 for the tin stabilizers and 0 tp 2 for the boron stabilizers.
- the stabilizers of this invention have the general fomula:
- each Y is independently selected from O, S, and N, each R is independently selected
- each R is independently selected from R, OR, RCO, ROCO,
- ROCO 2 P(R) 2 , P(OR) 2 , PR(OR), N(R) 2 , (R) 2 NCO, (R) 2 NCO 2 , SR, and halogen, where
- each R 2 is independently selected from R, RCO, ROCO, P(OR) 2 , Sn(R) q (OR) ⁇ , SnR ⁇ OCOR) ⁇ , Si(R) q (OR) ⁇ ,
- R 3 is independently selected from R, RCO, ROCO, ROCO 2 , OR, SR, N(R) 2 , OP(R) 2 , and OP(OR) 2 , m is 0 when A is P or B and is 1 when A is Sn, Si, or C, n is 0 when
- Y is O or S and is 1 when Y is N
- p is 0 to 4, depending on the number of available sites
- q is 0 to 3 for the tin stabilizers and 0 to 2 for the boron stabilizers.
- A is C
- Y is O
- R is benzyl
- R is H
- R 2 is R
- R 3 is R_ R 4 is alkylene from C, to C 8 , (aryl)alkylene from C 7 to C 8 , or -CO- (aryl)alkylene-CO- from C 7 to C 8
- q is O because those compounds work well and are readily available.
- Stabilizers where each R, is hydrogen are especially preferred as they are more effective.
- stabilizers having a cyclic structure examples include:
- stabilizers having the above structure include 4,7-dihydro-l,3- dioxepins, ethers and esters of butene-l,4-diol, and phthalans. These stabilizers can be prepared by condensing an allylic diol, or an aromatic analog of an allylic diol, with an aldehyde, ketone, acid, acid halide, ester, alkyl halide, or alcohol or by other reactions known to those skilled in the art, to form derivatives.
- Preferred stabilizers include cis-2-butene-l,4-diol, cis-4- benzyloxy-2-buten-l-ol, and cis-l,4-dibenzyloxy-2-butene.
- the stabilizer may be a phthalan.
- r can be 1 to 1000, but is preferably 1 to 5. Examples of
- polymers having formula A include poly(2-butenylene adipate), poly(2-butenylene- terephthalate, and poly[oxy(2-butenylene)j. in formulas B and C , the preferred
- backbones are polyesters, polyethers, and polyketones, and the preferred pendant groups are 4,7-dihydro-l ,3-dioxe ⁇ in, phthalan, and 2-butene- 1 ,4-diol. Examples of
- Such compounds include the condensate of poly(ethylene-co-carbo ⁇ monoxide) with 2-butene-1 ,4-diol.
- the polymeric stabilizers are expected to be more effective as
- the polymeric esters can be prepared by reacting the diol (see the first formulas where Y is oxygen and R ⁇ is hydrogen) with a diester, diacid, diacid chloride, or dianhydride.
- the stabilizers of this invention are effective against oxidation of PVC, polycarbonates, polyurethane, polypropylene, polyethylene, polyvinylidene chloride, polyamides, polyimides, polyethers, polyesters, polysiloxanes, polyurethanes, polysulfones, and polysulfides.
- the preferred polymers are PVC, polycarbonates, polypropylene, and polyethylene because those polymers are more frequently used in medical applications where they are subjected to gamma radiation; particularly preferred is PVC.
- the invention also relates to a polymer that has been subjected to oxidizing heat or radiation.
- the polymer can be stabilized by the addition of about 0.005 to about 10 phr (parts by weight per 100 parts by weight of the polymer) of the stabilizer to the polymer. Less stabilizer is less effective and more stabilizer offers little additional benefit.
- the preferred amount of stabilizer is about 0.2 to about 6 phr.
- the stabilizer can be added to a polymer in a variety of ways, such as mixing the reactants at the beginning or during polymerization.
- the stabilizer is preferably added after at least 70 wt% of the monomer has polymerized.
- the stabilizer can be added as a solid or with a solvent as a slurry or a solution.
- Common organic solvents such as N-methylpyrrolidone, diglyme, acetamide, acetone, methanol, ethanol, isopropanol, dimethysulfoxide, and dimethylformamide can be used; water can also be used.
- Water miscible solvents such as acetone, tetrahydrofuran, and methanol, are preferred for PVC. It is preferable to add the stabilizer in a solvent as that achieves a more uniform distribution of the stabilizer in the polymer. The stabilizer can also be added during the drying or compounding of the polymer.
- Various methods can be used to add the stabilizer in a solvent as that achieves a more uniform distribution of the stabilizer in the polymer.
- the stabilizer can also be added during the drying or compounding of the polymer.
- the stabilizers function as antioxidants to inhibit various forms of oxidation.
- the invention also provides polyvinyl chloride, polyurethane, polyethylene, polypropylene, or polycarbonate containing about 0.2 to about 6 phr of a stabilizer having the general formula:
- R 2 is R
- R 3 is R
- R 4 is alkylene from C, to C 8 , (aryl)alkylene from C 7 to C ⁇ , or
- This polymer may have been subjected to gamma radiation.
- the invention additionally provides a method of preventing a polymer which comprises polyvinyl chloride, polyvinylidene chloride, polycarbonate, polyethylene, polypropylene, polyamide, polyimide, polyether, polyester, or polyvinyl acetate from discoloring after exposure to oxiddation comprising mixing into said polymer about 0.005 to about 10 phr of a stabilizer having the general formula:
- each Y is independently selected from O, S, and N, each R is independently selected
- each R is independently selected from R, OR, RCO, ROCO,
- ROCO 2 P(R) 2l P(OR) 2 , PR(OR), N(R) 2 , (R) 2 NCO, (R) 2 NCO 2 , SR, and halogen, where
- each R 2 is independently
- R 3 is independently selected from R, RCO, ROCO, ROCO 2 , OR, SR, N(R) 2 , OP(R) 2 ,
- n 0 when A is P or B and is 1 when A is Sn, Si, or C, n is 0 when
- Y is O or,S and is 1 when Y is N, p is 0 to 4, depending on the number of available
- q is 0 to 3 for the tin stabilizers and 0 to 2 for the boron stabilizers.
- the resulting PVC sheet was cut and pressed into a 4"x3"xl/4" (10x8x0.6 cm) plaque at 165.5°C (330°F).
- the plaque was divided into two smaller pieces. One was saved for comparison and one was subjected to ⁇ radiation at a dose of 50 kGy.
- the irradiated piece was again divided into two pieces and one of these pieces was oven aged at 50°C for 48 hours. All of the samples were measured for yellowness index with a Macbeth 2020 Plus Color Eye Spectrometer, as described by the Hunter equations (see "The Measurement of Appearance” by Richard S. Hunter, John Wiley & Sons, New York, 1975). The following table gives the stabilizers used and the results.
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- 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)
- Macromolecular Compounds Obtained By Forming Nitrogen-Containing Linkages In General (AREA)
- Polymers With Sulfur, Phosphorus Or Metals In The Main Chain (AREA)
- Materials For Medical Uses (AREA)
- Dental Preparations (AREA)
Abstract
Disclosed is polyvinyl chloride, polyvinylidene chloride, polycarbonate, polyethylene, polypropylene, polyamide, polyimide, polyether, polyester, or polyvinyl acetate containing about 0.005 to about 10 phr of a stabilizer having general formula (I), (II) or (III): where A is C, P, Sn, Si, or B, X is =C=C=, -C C-, (a), (b), (c), (d) each Y is idependently selected from O, S, and N, each R is idependently selected from hydrogen, alkyl from C1 to C24, aryl from C6 to C24, alkaryl from C7 to C24 and aralkyl from C7 to C24, each R1 is independently selected from R, OR, RCO, ROCO, ROCO2, P(R)2, P(OR)2, PR(OR), N(R)2, (R)2NCO, (R)2 NCO2, SR, and halogen, where two R1 groups can be bridged together to form a ring, each R2 is independently selected from R, RCO, ROCO, P(OR)2, Sn(R)q(OR)3-q, SnRq(OCOR)3-q, Si(R)q(OR)3-q, and BRq(OR)2-q, where two R2 groups can be bridged together to form a ring, each R3 is independently selected from R, RCO, ROCO, ROCO2, OR, SR, N(R)2, OP(R)2, and OP(OR)2, m is 0 when A is P or B and is 1 when A is Sn, Si, or C, n is 0 when Y is O or S and is 1 when Y is N, p is 0 to 4, depending on the number of available sites, and q is 0 to 3 for the tin stabilizers and 0 to 2 for the boron stabilizers. Also disclosed is a method of preventing these polymers from discoloring after exposure to oxidation.
Description
"STABILIZATION OF POLYMERS AFTER EXPOSURE TO OXIDATION"
THIS INVENTION relates to the use of stabilizers to reduce the discoloration of certain polymers after they have been exposed to oxidation.
A number of different polymers, including polyvinyl chloride (PNC), polycarbonates, polyurethane, polyethylene, and polypropylene, are used to make various medical devices and as packaging for food. Sterilization can be accomplished by exposing the devices or packages to gamma radiation. However, the gamma radiation can degrade or yellow the polymer, making it unsuitable or less acceptable for certain applications. Polymers such as polyethylene, polypropylene, and PVC can also degrade and yellow after heating.
According to one aspect of this invention there is provided a polymer which comprises polyvinyl chloride, polyvinylidene chloride, polycarbonate, polyurethane, polyethylene, polypropylene, polyamide, polyimide, polyether, polyester, or polyvinyl acetate containing about 0.005 to about 10 plir of a stabilizer having the general formula:
where A is C, P, Sn, Si, or B, X is =C=C=, -C≡C-
each Y is independently selected from O, S, and N, each R is independently selected
from hydrogen, alkyl from C, to C24, aryl from C6 to C24, alkaryl from C7 to C24, and
aralkyl from C7 to C2,,.each R, is independently selected from R, OR, RCO, ROCO,
ROCO2, P(R)2, P(OR)2, PR(OR), N(R)2, (R)2NCO, (R)2NCO2, SR, and halogen, where
two R, groups can be bridged together to form a ring, each R2 is independently selected from R, RCO, ROCO, P(OR)2l Sn(R)q(OR)^, SnR^OCOR)^, Si(R)q(OR)^,
and BRq(OR)2-q, where two R2 groups can be bridged together to form a ring, each
R3 is independently selected from R, RCO, ROCO, ROCO2, OR, SR, N(R)2, OP(R)2,
and OP(OR)2, m is 0 when A is P or B and is 1 when A is Sn, Si, or C, n is 0 when
Y is O or S and is 1 when Y is N, p is 0 to 4, depending on the number of available sites, and q is 0 to 3 for the tin stabilizers and 0 tp 2 for the boron stabilizers.
When a particular type of stabilizer is added to certain polymers the polymers degrade and yellow substantially less after exposure to oxidation. Some of the stabilizers of this invention are novel compounds while others are commercially available. Some of these stabilizers are polymeric and resist leaching or migration from the polymer, thereby further extending the life of the polymer.
The stabilizers of this invention have the general fomula:
where A fs C, P, Sn, Si, or B, X is =C=C= -C≡C-,
each Y is independently selected from O, S, and N, each R is independently selected
from hydrogen, alkyl from C, to C24, aryl from C6 to C24, alkaryl from C7 to C24, and aralkyl from C7 to C24, each R, is independently selected from R, OR, RCO, ROCO,
ROCO2, P(R)2, P(OR)2, PR(OR), N(R)2, (R)2NCO, (R)2NCO2, SR, and halogen, where
two Rt groups can be bridged together to form a ring, each R2 is independently
selected from R, RCO, ROCO, P(OR)2, Sn(R)q(OR)^, SnR^OCOR)^, Si(R)q(OR)^,
and
where two R2 groups can be bridged together to form a ring, each
R3 is independently selected from R, RCO, ROCO, ROCO2, OR, SR, N(R)2, OP(R)2, and OP(OR)2, m is 0 when A is P or B and is 1 when A is Sn, Si, or C, n is 0 when
Y is O or S and is 1 when Y is N, p is 0 to 4, depending on the number of available sites, and q is 0 to 3 for the tin stabilizers and 0 to 2 for the boron stabilizers.
Groups that can bridge two R, or two R2 groups together to form a ring include R4, -HC=CH- -CH2O- -CH2NH- -HC=N-, and -CH2S, where R4 is alkylene from C, to
C24l arylene from C6 to C24, (aryl)alkylene from C7 to C24, (alkyl)arylene from C7 to C24l alkanediyl from C, to C24l (aryl)alkanediyl from C7 to C24, -CO-(alkyiene)-CO-
fram C, to C24l -CO-arylene-CO- from C6 to C24, -CO-(aryl)alkylene-CO- from C7 to
C24,-CO-(alkyl)arylene-CO)-fromC7toC24, Si(R)2, SiR(OR), Si(OR)2, P(OR), B(OR), Sn(R)2l SnR(OR), or SnR(O-CO-R).
Preferably, A is C, X is -HC=HC-, Y is O, R is benzyl, R, is H, R2 is R, R3 is R_ R4 is alkylene from C, to C8, (aryl)alkylene from C7 to C8, or -CO- (aryl)alkylene-CO- from C7 to C8, and q is O because those compounds work well and are readily available. Stabilizers where each R, is hydrogen are especially preferred as they are more effective. When X is =C=C= the stabilizers can be either cis or trans, but the cis stabilizers are preferred because they are less expensive.
The following are examples of some of the stabilizers included within the scope of the above formulas (if Y is N, there is an additional R3 group on Y):
R,
Examples of stabilizers having a cyclic structure include:
A B c
In the above. formulas, r can be 1 to 1000, but is preferably 1 to 5. Examples of
polymers having formula A include poly(2-butenylene adipate), poly(2-butenylene- terephthalate, and poly[oxy(2-butenylene)j. in formulas B and C, the preferred
backbones are polyesters, polyethers, and polyketones, and the preferred pendant groups are 4,7-dihydro-l ,3-dioxeρin, phthalan, and 2-butene- 1 ,4-diol. Examples of
such compounds include the condensate of poly(ethylene-co-carboπ monoxide) with 2-butene-1 ,4-diol. The polymeric stabilizers are expected to be more effective as
they have less tendency to migrate or leach out of the stabilized polymer.
Preparation of these polymers can be achieved by reactions known to those skilled
in the art. For example, the polymeric esters can be prepared by reacting the diol (see the first formulas where Y is oxygen and R\ is hydrogen) with a diester, diacid, diacid chloride, or dianhydride.
The stabilizers of this invention are effective against oxidation of PVC, polycarbonates, polyurethane, polypropylene, polyethylene, polyvinylidene chloride, polyamides, polyimides, polyethers, polyesters, polysiloxanes, polyurethanes, polysulfones, and polysulfides. The preferred polymers are PVC, polycarbonates, polypropylene, and polyethylene because those polymers are more frequently used in medical applications where they are subjected to gamma radiation; particularly preferred is PVC. Thus the invention also relates to a polymer that has been subjected to oxidizing heat or radiation.
The polymer can be stabilized by the addition of about 0.005 to about 10 phr (parts by weight per 100 parts by weight of the polymer) of the stabilizer to the polymer. Less stabilizer is less effective and more stabilizer offers little additional benefit. The preferred amount of stabilizer is about 0.2 to about 6 phr. The stabilizer can be added to a polymer in a variety of ways, such as mixing the reactants at the beginning or during polymerization. The stabilizer is preferably added after at least 70 wt% of the monomer has polymerized. The stabilizer can be added as a solid or with a solvent as a slurry or a solution. Common organic solvents such as N-methylpyrrolidone, diglyme, acetamide, acetone, methanol, ethanol, isopropanol, dimethysulfoxide, and dimethylformamide can be used; water can also be used. Water miscible solvents, such as acetone, tetrahydrofuran, and methanol, are preferred for PVC. It is preferable to add the stabilizer in a solvent as that achieves a more uniform distribution of the stabilizer in the polymer. The stabilizer can also be added during the drying or compounding of the polymer. Various methods can
be used for compounding, including milling, dry mixing, and extrusion. The stabilizers function as antioxidants to inhibit various forms of oxidation.
The invention also provides polyvinyl chloride, polyurethane, polyethylene, polypropylene, or polycarbonate containing about 0.2 to about 6 phr of a stabilizer having the general formula:
where R2 is R, R3 is R, R4 is alkylene from C, to C8, (aryl)alkylene from C7 to Cβ, or
-CO-(aryl)alkylene-CO- from C7 to C8 , R is benzyl, and r is 1 to 5.
This polymer may have been subjected to gamma radiation.
The invention additionally provides a method of preventing a polymer which comprises polyvinyl chloride, polyvinylidene chloride, polycarbonate, polyethylene, polypropylene, polyamide, polyimide, polyether, polyester, or polyvinyl acetate from discoloring after exposure to oxiddation comprising mixing into said polymer about 0.005 to about 10 phr of a stabilizer having the general formula:
where A is C, P, Sn, Si, or B, X is =C=C=, -C≡C-,
each Y is independently selected from O, S, and N, each R is independently selected
from hydrogen, alkyl from C, to C24, aryl from C6 to C24, alkaryl from C7 to C24l and
aralkyl from C7 to C24, each R, is independently selected from R, OR, RCO, ROCO,
ROCO2, P(R)2l P(OR)2, PR(OR), N(R)2, (R)2NCO, (R)2NCO2, SR, and halogen, where
two R, groups can be bridged together to form a ring, each R2 is independently
selected from R, RCO, ROCO, P(OR)2, Sn(R)q(OR)^, SnR^OCOR)^. Si(R)q(OR)^,
and BR^OR)^, where two R2 groups can be bridged together to form a ring, each
R3 is independently selected from R, RCO, ROCO, ROCO2, OR, SR, N(R)2, OP(R)2,
and OP(OR)2, m is 0 when A is P or B and is 1 when A is Sn, Si, or C, n is 0 when
Y is O or,S and is 1 when Y is N, p is 0 to 4, depending on the number of available
sites, and q is 0 to 3 for the tin stabilizers and 0 to 2 for the boron stabilizers.
The following examples further illustrate this inventioi
EXAMPLES 1 to 13
To a mixture of 150.00 g PVC (sold by Occidental Chemical Corporation as "Oxy 240"), 0.30 g stearic acid (used as a lubricant), 0.23 g of a zinc and calcium mixed salts of mixed fatty acids (used as a heat stabilizer, sold by Witco as "Mark 152 S"), 97.50g dioctyl phthalate (used as a heat stabilizer and to increase flexibility). 15.00 g epoxidized soy bean oil (used as an HC1 scavenger to reduce degradation; sold by Witco as "Drapex 6.8"), was added a stabilizer. The mixture was thoroughly blended and hot milled at 149°C (300°F) for 5 minutes. The resulting PVC sheet was cut and pressed into a 4"x3"xl/4" (10x8x0.6 cm) plaque at 165.5°C (330°F). The plaque was divided into two smaller pieces. One was saved for comparison and one was subjected to γ radiation at a dose of 50 kGy. The irradiated piece was again divided into two pieces and one of these pieces was oven aged at 50°C for 48 hours. All of the samples were measured for yellowness index with a Macbeth 2020 Plus Color Eye Spectrometer, as described by the Hunter equations (see "The Measurement of Appearance" by Richard S. Hunter, John Wiley & Sons, New York, 1975). The following table gives the stabilizers used and the results.
As can be observed from the above table, after γ rad.at.on the po.ymers that
contained a stabilizer had sign.f.cant.y less discoloration than the contro. samples
Claims
1. A polymer which comprises polyvinyl chloride, polyvinylidene chloride, polycarbonate, polyurethane, polyethylene, polypropylene, polyamide, polyimide, polyether, polyester, or polyvinyl acetate containing about 0.005 to about 10 phr of a stabilizer having the general formula:
where A is C, P, Sn, Si,- or B, X is =C=C=. -C≡C-,
each Y is independently selected from O, S, and N, each R is independently selected
from hydrogen, alkyl from C, to C24, aryl from C6 to C24, alkaryl from C7 to C24, and
aralkyl from C7 to C24, each R, is independently selected from R, OR, RCO, ROCO,
ROCO2, P(R)2l P(OR)2, PR(OR), N(R)2, (R)2NCO, (R)2NCO2, SR, and halogen, where
two R, groups can be bridged together to form a ring, each R2 is independently
selected from R, RCO, ROCO, P(OR)2, Sn(R)q(OR)^, SnR^OCOR)^,, Si(R)q(OR)^,
and BR^OR^, where two R2 groups can be bridged together to form a ring, each
R3 is independently selected from R, RCO, ROCO, ROCO2. OR, SR, N(R)2, OP(R)2,
and OP(OR)2, m is 0 when A is P or B and is 1 when A is Sn, Si, or C, n is 0 when Y is O or S and is 1 when Y is N, p is 0 to 4, depending on the number of available sites, and q is 0 to 3 for the tin stabilizers and 0 to 2 for the boron stabilizers.
2. A polymer according to Claim 1 wherein said polymer is polyvinyl chloride.
3. A polymer according to Claim 1 wherein said stabilizer has the general formula
R,
4. A polymer according to Claim 1 wherein said stabilizer has the general formula:
R3
5. A polymer according to Claim 1 wherein said stabilizer is cis-2-butene-l ,4-
diol.
6. A polymer according to Claim 1 wherein said stabilizer is cis-4-benzyioxy-2-buten-1 -of.
7. A polymer according to Claim 1 wherein said stabilizer is cis-1 ,4-dibenzyloxy-2-butene.
8. A polymer according to Claim 1 wherein said stabilizer is a 4,7-dihydro-1 ,3- dioxepin.
9. A polymer according to Claim 1 wherein said stabilizer is a phthalan
10. A polymer according to Claim 1 wherein said stabilizer has the structure
C2_,, (alkyl)arylene from C7 to C2<, alkanediyl from C, to C2 , (aryl)alkanediyl from C7
to C24, -CO-(alkylene)-CO- from C, to C24, -CO-arylene-CO- from C6 to C24, -CO-
(aryl)alkylene-CO- from C7 to C2<. -CO-(aikyl)arylene-CO)- from C7 to C2„, Si(R)2l
SiR(OR). Si(OR)2 , P(OR). B(OR). Sn(R)2, SnR(OR), or SnR(O-CO-R), and r is 1 to
1000.
11. A polymer according to Claim 10 wherein said stabilizer has pendant 4,7-dihydro-l,3-dioxepin groups.
12. A polymer according to Claim 10 wherein said stabilizer has pendant phthalan groups.
13. A polymer according to Claim 10 wherein said stabilizer has pendant 2- butene-1, 4-diol groups.
14. A polymer according to Claim 10 wherein said stabilizer is a polyether having pendant 2-butene-l, 4-diol groups.
15. A polymer according to Claim 10 wherein said stabilizer is a polyester having pendant 2-butene-l, 4-diol groups.
16. A polymer according to Claim 1 wherein A is C, X is -HC=CH-, Y is O, R is
benzyl, R, is H, R2 is R, R3 is R, R„ is alkylene from C, to Cβ, (aryl)alkylene from C6
to Cβ, or -CO-(aryl)alkylene-CO- from C6 to Cfl , or q is 0.
17. A polymer according to any one of the preceding Claims that has been subj ected to oxidizing heat or radiation .
18. Polyvinyl chloride, polyurethane, polyethylene, polypropylene, or polycarbonate containing about 0.2 to about 6 phr of a stabilizer having the general
formula:
where R2 is R, R3 is R, R4 is alkylene from C, to C8l (aryl)alkylene from C7 to C8, or -CO-(aryl)alkylene-CO- from C7 to Cβ , R is benzyl, and r is 1 to 5.
19. Polyvinyl chloride according to Claim 18 that has been subjected to gamma radiation.
20. A method of preventing a polymer which comprises polyvinyl chloride, polyvinylidene chloride, polycarbonate, polyethylene, polypropylene, polyamide, polyimide, polyether, polyester, or polyvinyl acetate from discoloring after exposure to oxidation comprising mixing into said polymer about 0.005 to about 10 phr of a stabilizer having the general formula:
each Y is independently selected from O, S, and N, each R is independently selected
from hydrogen, alkyl from C, to C24, aryl from'fc6 to C24( alkaryl from C7 to C24l and
aralkyl from C7 to C24, each R, is independently selected from R, OR, RCO, ROCO,
ROCO2, P(R)2, P(OR)2, PR(OR), N(R)2, (R)2NCO, (R)2NCO2, SR, and halogen, where
two R groups can be bridged together to form a ring, each R2 is independently
selected from R, RCO, ROCO, P(OR)2, Sn(R)q(OR)^. SnR^OCOR);^, Si(R)q(OR)^,
and BRq(OR)2_q, where two R2 groups can be bridged together to form a ring, each
R3 is independently selected from R, RCO, ROCO, ROCO2, OR, SR, N(R)2, OP(R)2,
and OP(OR)2, m is 0 when A is P or B and is 1 when A is Sn, Si, or C, n is 0 when
Y is O or.-S and is 1 when Y is -N, p is 0 to 4, depending on the number of available
sites, and q is 0 to 3 for the tin stabilizers and 0 to 2 for the boron stabilizers.
AMENDED CLAIMS
[received by the International Bureau on 18 July 2000 (18.07.00); original claims 1, 5-20 replaced by new claims 1, 5-16; remaining claims unchanged (8 pages)]
1. A polymer which comprises polyvinyl chloride, poly inylidene chloride polycarbonate, polyurethane, polyethylene, polypropylene, polyamide, polyimide,
polyether, polyester, or polyvinyl acetate containing about 0.005 to about 10 phr of a stabilizer having the general formula:
where A is C. P. Sn, Si,- or B, X is -R1C=CRι-l -C≡C-,
each Y is independently selected from O, S, and N, each R is independently selected
from hydrogen, alkyl from C, to C24, aryl from C6 to C24, alkaryl from C7 to C24, and
aralkyl from C7 to C24, each R, is independently selected from R, OR, RCO, ROCO,
ROCO2, P(R)2, P(OR)2, PR(OR), N(R)2, (R)2NCO, (R)2NCO2, SR, and halogen, where
O 00/56812
25
two R, groups can be bridged together to form a ring, each R2 is independently
selected from R, RCO, ROCO, P(OR)2l Sn(R)q(OR)^, SnR^OCOR)^, Si(R)q(OR)3 ),
and BR^OR^. where two R2 groups can be bridged together to form a ring, each
R3 is independently selected from R, RCO, ROCO, ROCO2, OR. SR, N(R)2, OP(R)2,
and OP(OR)2, m is 0 when A is P or B and is 1 when A is Sn, Si, or C, n is 0 when
Y is O or S and is 1 when Y is N, p is 0 to 4, depending on the number of available
sites, and q is 0 to 3 for the tin stabilizers and 0 to 2 for the boron stabilizers, with the provisos that; in general formula (I), when X= -HC=CH-, Y=O and R2=H, then at least one of the Ri groups is not H; and, in general formula (II), when X= -R1C=CR , Y=0 and A=C, then at least one of the R3 groups on A is not hydrogen.
2. A polymer according to Claim 1 wherein said polymer is polyvinyl chloride.
3. A polymer according to Claim 1 wherein said stabilizer has the general formula
R .
28
- A polymer according to Claim 1 wherein said stabilizer is
cis-4-benzyloxy-2-buten-1 -ol.
6- A polymer according to Claim 1 wherein said stabilizer is
cis-1 ,4-dibeπzyloxy-2-butene.
- A polymer according to Claim 1 wherein said stabilizer is a 4,7-dihydro-1 ,3- dioxepin.
8- A polymer according to Claim 1 wherein said stabilizer is a phthalan
9. A polymer according to Claim 1 wherein said stabilizer has the structure
where R< is alkylene from C, to C24, arylene from CG to C2<, (aryl)alkylene from C7 to
C2_t, (alkyl)arylene from C7 to C2<. alkanediyl from C, to C2/. (aryl)alkanediyl from C7
to C24, -CO-(alkylene)-CO- from C, to C24, -CO-arylene-CO- from C6 to C24, -CO-
(aryl)alkyiene-CO- from C7 to C2<. -CO-(alkyl)arylene-CO)- from C7 to C2 , Si(R)2.
SiR(OR), Si(OR)2. P(OR), B(OR). Sn(R)2, SnR(OR), or SnR(O-CO-R). and r is 1 to
1000.
10. A polymer according to Claim 9 wherein said stabilizer has pendant 4,7- dihydro-l,3-dioxepin groups.
11. A polymer according to Claim 9 wherein said stabilizer has pendant phthalan groups.
12. polymer according to Claim 1 wherein A is C, X is -HC=CH-, Y is O, R is
benzyl, R, is H, R2 is R, R3 is R, R< is alkylene from C, to Cβ. (aryl)alkylene from C6
to Cβ, or -CO-(aryl)alkylene-CO- from C6 to C8 , or q is 0.
13. A polymer according to any one of the preceding Claims that has been subj ected to oxidizing heat or radiation .
14w Polyvinyl chloride, polyurethane, polyethylene, polypropylene, or
polycarbonate containing about 0.2 to about 6 phr of a stabilizer having the general
formula:
where R2 is R, R3 is R, RΛ is alkylene from C, to C6, (aryl)alkylene from C7 to C„. or
-CO-(aryl)alkylene-CO- from C7 to C6 , R is benzyl, and r is 1 to 5.
15. , Polyvinyl chloride according to Claim 14 that has been subjected to gamma
radiation.
16. A method of preventing a polymer which comprises polyvinyl chloride,
polyvinylidene chloride, polycarbonate, polyethylene, polypropylene, polyamide, polyimide, polyether, polyester, or polyvinyl acetate from discoloring after exposure
to oxidation comprising mixing into said polymer about 0.005 to about 1 0 phr of a
stabilizer having the general formula:
where A is C, P, Sn, Si. or B, X is -R^CR , -C≡C-
each Y is independently selected from O, S, and N, each R is independently selected
from hydrogen, alkyl from C, to C2„, aryl from'C6 to C24, alkaryl from C7 to C24, and
aralkyl from Cτ to C2<, each R, is independently selected from R, OR, RCO, ROCO,
ROCO2, P(R)2. P(OR)2, PR(OR). N(R)2. (R)2NCO, (R)2NCO2, SR, and halogen, where two R, groups can be bridged together to form a ring, each R2 is independently
selected from R. RCO. ROCO. P(OR)2. Sn(R)q(OR)^. SnRq(OCOR)^,, Si(R)q(OR)^,, and BRt_(OR)2_q. where two R2 groups can be bridged together to form a ring, each
R3 is independently selected from R, RCO, ROCO, ROCO2, OR. SR, N(R)2, OP(R)2,
and OP(OR)2, m is 0 when A is P or B and is 1 when A is Sn, Si, or C, n is 0 when
Y is O or-S and is 1 when Y is -N, p is 0 to 4, depending on the number of available
sites, and q is 0 to 3 for the tin stabilizers and 0 to 2 for the boron stabilizers, with the provisos that; in general formula (I), when X= -HC=CH-, Y=O and R =H, then at least one of the Ri groups is not H; and, in general formula (II), when X- -RιC=CRr, Y=O and A=C, then at least one of the R3 groups on A is not hydrogen.
Priority Applications (5)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| AU21199/00A AU2119900A (en) | 1999-03-19 | 2000-01-28 | Stabilization of polymers after exposure to oxidation |
| AT00901243T ATE291056T1 (en) | 1999-03-19 | 2000-01-28 | STABILIZATION OF POLYMERS AFTER EXPOSURE TO OXIDATION |
| DE60018724T DE60018724T2 (en) | 1999-03-19 | 2000-01-28 | STABILIZATION OF POLYMERS AFTER SUSPENSION OF OXIDATION |
| HU0200404A HU229127B1 (en) | 1999-03-19 | 2000-01-28 | Stabilization of polymers after exposure to oxidation |
| EP00901243A EP1169380B1 (en) | 1999-03-19 | 2000-01-28 | Stabilization of polymers after exposure to oxidation |
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US27284399A | 1999-03-19 | 1999-03-19 | |
| US09/272,843 | 1999-03-19 |
Publications (1)
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|---|---|
| WO2000056812A1 true WO2000056812A1 (en) | 2000-09-28 |
Family
ID=23041548
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| PCT/GB2000/000247 WO2000056812A1 (en) | 1999-03-19 | 2000-01-28 | Stabilization of polymers after exposure to oxidation |
Country Status (10)
| Country | Link |
|---|---|
| US (1) | US7019055B2 (en) |
| EP (1) | EP1169380B1 (en) |
| AT (1) | ATE291056T1 (en) |
| AU (1) | AU2119900A (en) |
| DE (1) | DE60018724T2 (en) |
| DK (1) | DK1169380T3 (en) |
| ES (1) | ES2240056T3 (en) |
| HU (1) | HU229127B1 (en) |
| PT (1) | PT1169380E (en) |
| WO (1) | WO2000056812A1 (en) |
Cited By (4)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002017973A2 (en) * | 2000-09-01 | 2002-03-07 | Occidental Chemical Corporation | Preparing sterile articles from certain polymers |
| US7405304B2 (en) | 2002-01-10 | 2008-07-29 | The Penn State Research Foundation | Methods for the preparation of alkyl diaryl borinates and complexed diarylboronic acids |
| US9198898B2 (en) | 2013-06-24 | 2015-12-01 | Tigercat Pharma, Inc. | Use of NK-1 receptor antagonists in pruritus |
| US9486439B2 (en) | 2013-06-24 | 2016-11-08 | Menlo Therapeutics Inc. | Use of NK-1 receptor antagonist serlopitant in pruritus |
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CA2373279A1 (en) * | 1999-05-25 | 2000-12-14 | The Penn State Research Foundation | Dna methyltransferase inhibitors |
| US20050227933A1 (en) * | 2001-11-29 | 2005-10-13 | Benkovic Stephen J | Treatment of bacterial induced diseases using DNA methyl transferase inhibitors |
| CN103013076B (en) * | 2012-11-25 | 2016-03-30 | 安徽六方重联机械股份有限公司 | A kind of preparation method of the packaging plastic substrate film containing modified Nano attapulgite |
| CN109232952A (en) * | 2018-08-07 | 2019-01-18 | 广东元星工业新材料有限公司 | A kind of polyurethane product surface treatment method |
| US20220080086A1 (en) * | 2020-09-14 | 2022-03-17 | Carefusion 303, Inc. | Alkaline resistant halogenated plastic for medical devices |
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| DE3621958A1 (en) * | 1985-07-15 | 1987-01-15 | Grace W R & Co | VINYLIDE CHLORIDE COMPOSITION AND FILM MADE THEREOF |
| EP0584679A1 (en) * | 1992-08-14 | 1994-03-02 | Mitsubishi Chemical Corporation | Compatible polyphenylene ether/polyamide composition. |
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| DE2625167C3 (en) * | 1976-06-04 | 1980-01-31 | Hoechst Ag, 6000 Frankfurt | Process for improving the properties of powdered polyvinyl chloride |
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-
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- 2000-01-28 ES ES00901243T patent/ES2240056T3/en not_active Expired - Lifetime
- 2000-01-28 AT AT00901243T patent/ATE291056T1/en active
- 2000-01-28 HU HU0200404A patent/HU229127B1/en unknown
- 2000-01-28 DE DE60018724T patent/DE60018724T2/en not_active Expired - Lifetime
- 2000-01-28 AU AU21199/00A patent/AU2119900A/en not_active Abandoned
- 2000-01-28 DK DK00901243T patent/DK1169380T3/en active
- 2000-01-28 WO PCT/GB2000/000247 patent/WO2000056812A1/en active IP Right Grant
- 2000-01-28 PT PT00901243T patent/PT1169380E/en unknown
- 2000-01-28 EP EP00901243A patent/EP1169380B1/en not_active Expired - Lifetime
-
2001
- 2001-01-17 US US09/761,625 patent/US7019055B2/en not_active Expired - Lifetime
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| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE3621958A1 (en) * | 1985-07-15 | 1987-01-15 | Grace W R & Co | VINYLIDE CHLORIDE COMPOSITION AND FILM MADE THEREOF |
| EP0584679A1 (en) * | 1992-08-14 | 1994-03-02 | Mitsubishi Chemical Corporation | Compatible polyphenylene ether/polyamide composition. |
Cited By (16)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO2002017973A2 (en) * | 2000-09-01 | 2002-03-07 | Occidental Chemical Corporation | Preparing sterile articles from certain polymers |
| WO2002017973A3 (en) * | 2000-09-01 | 2002-06-13 | Occidental Chem Co | Preparing sterile articles from certain polymers |
| US7405304B2 (en) | 2002-01-10 | 2008-07-29 | The Penn State Research Foundation | Methods for the preparation of alkyl diaryl borinates and complexed diarylboronic acids |
| US9198898B2 (en) | 2013-06-24 | 2015-12-01 | Tigercat Pharma, Inc. | Use of NK-1 receptor antagonists in pruritus |
| US9381188B2 (en) | 2013-06-24 | 2016-07-05 | Tigercat Pharma, Inc. | Use of NK-1 receptor antagonists in pruritus |
| US9474741B2 (en) | 2013-06-24 | 2016-10-25 | Menlo Therapeutics Inc. | Use of NK-1 receptor antagonists in pruritus |
| US9486439B2 (en) | 2013-06-24 | 2016-11-08 | Menlo Therapeutics Inc. | Use of NK-1 receptor antagonist serlopitant in pruritus |
| US9737507B2 (en) | 2013-06-24 | 2017-08-22 | Menlo Therapeutics Inc. | Use of NK-1 receptor antagonist serlopitant in pruritus |
| US9737508B2 (en) | 2013-06-24 | 2017-08-22 | Menlo Therapeutics Inc. | Use of NK-1 receptor antagonists in pruritus |
| US9968588B2 (en) | 2013-06-24 | 2018-05-15 | Menlo Therapeutics Inc. | Use of NK-1 receptor antagonists in pruritus |
| US9974769B2 (en) | 2013-06-24 | 2018-05-22 | Menlo Therapeutics Inc. | Use of NK-1 receptor antagonist serlopitant in pruritus |
| US10278953B2 (en) | 2013-06-24 | 2019-05-07 | Menlo Therapeutics Inc. | Use of NK-1 receptor antagonist serlopitant in pruritus |
| US10278952B2 (en) | 2013-06-24 | 2019-05-07 | Menlo Therapeutics Inc. | Use of NK-1 receptor antagonists in pruritus |
| US10617671B2 (en) | 2013-06-24 | 2020-04-14 | Menlo Therapeutics Inc. | Use of NK-1 receptor antagonist serlopitant in pruritus |
| US10702499B2 (en) | 2013-06-24 | 2020-07-07 | Menlo Therapeutics Inc. | Use of NK-1 receptor antagonists in pruritus |
| US11026920B2 (en) | 2013-06-24 | 2021-06-08 | Vyne Therapeutics Inc. | Use of NK-1 receptor antagonist serlopitant in pruritus |
Also Published As
| Publication number | Publication date |
|---|---|
| EP1169380A1 (en) | 2002-01-09 |
| ES2240056T3 (en) | 2005-10-16 |
| DE60018724D1 (en) | 2005-04-21 |
| ATE291056T1 (en) | 2005-04-15 |
| DE60018724T2 (en) | 2006-06-14 |
| HUP0200404A3 (en) | 2003-08-28 |
| EP1169380B1 (en) | 2005-03-16 |
| US20010007884A1 (en) | 2001-07-12 |
| PT1169380E (en) | 2005-06-30 |
| AU2119900A (en) | 2000-10-09 |
| HU229127B1 (en) | 2013-08-28 |
| DK1169380T3 (en) | 2005-07-04 |
| HUP0200404A2 (en) | 2002-06-29 |
| US7019055B2 (en) | 2006-03-28 |
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