CN109517149A - 一种耐水解干混粉末涂料用聚酯树脂的配方及其制备方法 - Google Patents
一种耐水解干混粉末涂料用聚酯树脂的配方及其制备方法 Download PDFInfo
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- CN109517149A CN109517149A CN201811406453.9A CN201811406453A CN109517149A CN 109517149 A CN109517149 A CN 109517149A CN 201811406453 A CN201811406453 A CN 201811406453A CN 109517149 A CN109517149 A CN 109517149A
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- polyester resin
- hydrolysis
- formula
- acid value
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- 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.)
- Pending
Links
- 229920001225 polyester resin Polymers 0.000 title claims abstract description 64
- 239000004645 polyester resin Substances 0.000 title claims abstract description 64
- 230000007062 hydrolysis Effects 0.000 title claims abstract description 57
- 238000006460 hydrolysis reaction Methods 0.000 title claims abstract description 57
- 239000011248 coating agent Substances 0.000 title claims abstract description 35
- 238000000576 coating method Methods 0.000 title claims abstract description 35
- 239000011812 mixed powder Substances 0.000 title claims abstract description 29
- 238000002360 preparation method Methods 0.000 title claims description 10
- 238000009472 formulation Methods 0.000 title description 2
- KKEYFWRCBNTPAC-UHFFFAOYSA-N Terephthalic acid Chemical compound OC(=O)C1=CC=C(C(O)=O)C=C1 KKEYFWRCBNTPAC-UHFFFAOYSA-N 0.000 claims abstract description 111
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 38
- 239000003054 catalyst Substances 0.000 claims abstract description 35
- 230000032050 esterification Effects 0.000 claims abstract description 34
- 238000005886 esterification reaction Methods 0.000 claims abstract description 34
- 239000003963 antioxidant agent Substances 0.000 claims abstract description 33
- SLCVBVWXLSEKPL-UHFFFAOYSA-N neopentyl glycol Chemical class OCC(C)(C)CO SLCVBVWXLSEKPL-UHFFFAOYSA-N 0.000 claims abstract description 30
- 239000003153 chemical reaction reagent Substances 0.000 claims abstract description 23
- DSKYSDCYIODJPC-UHFFFAOYSA-N 2-butyl-2-ethylpropane-1,3-diol Chemical compound CCCCC(CC)(CO)CO DSKYSDCYIODJPC-UHFFFAOYSA-N 0.000 claims abstract description 22
- 239000002253 acid Substances 0.000 claims description 59
- WNLRTRBMVRJNCN-UHFFFAOYSA-N adipic acid Chemical compound OC(=O)CCCCC(O)=O WNLRTRBMVRJNCN-UHFFFAOYSA-N 0.000 claims description 44
- 235000011037 adipic acid Nutrition 0.000 claims description 25
- 239000001361 adipic acid Substances 0.000 claims description 22
- QQVIHTHCMHWDBS-UHFFFAOYSA-N isophthalic acid Chemical compound OC(=O)C1=CC=CC(C(O)=O)=C1 QQVIHTHCMHWDBS-UHFFFAOYSA-N 0.000 claims description 19
- 230000003078 antioxidant effect Effects 0.000 claims description 17
- ZJCCRDAZUWHFQH-UHFFFAOYSA-N Trimethylolpropane Chemical class CCC(CO)(CO)CO ZJCCRDAZUWHFQH-UHFFFAOYSA-N 0.000 claims description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 12
- XDTMQSROBMDMFD-UHFFFAOYSA-N Cyclohexane Chemical compound C1CCCCC1 XDTMQSROBMDMFD-UHFFFAOYSA-N 0.000 claims description 12
- 239000000376 reactant Substances 0.000 claims description 12
- 239000000463 material Substances 0.000 claims description 9
- DNIAPMSPPWPWGF-UHFFFAOYSA-N monopropylene glycol Natural products CC(O)CO DNIAPMSPPWPWGF-UHFFFAOYSA-N 0.000 claims description 8
- 238000006243 chemical reaction Methods 0.000 claims description 7
- SRPWOOOHEPICQU-UHFFFAOYSA-N trimellitic anhydride Chemical compound OC(=O)C1=CC=C2C(=O)OC(=O)C2=C1 SRPWOOOHEPICQU-UHFFFAOYSA-N 0.000 claims description 7
- -1 2- ethyl -2- butyl Chemical group 0.000 claims description 6
- 230000015572 biosynthetic process Effects 0.000 claims description 6
- 238000012423 maintenance Methods 0.000 claims description 6
- 229910052757 nitrogen Inorganic materials 0.000 claims description 6
- 238000003786 synthesis reaction Methods 0.000 claims description 6
- 238000010792 warming Methods 0.000 claims description 6
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 claims description 5
- OQBLGYCUQGDOOR-UHFFFAOYSA-L 1,3,2$l^{2}-dioxastannolane-4,5-dione Chemical group O=C1O[Sn]OC1=O OQBLGYCUQGDOOR-UHFFFAOYSA-L 0.000 claims description 4
- 150000003242 quaternary ammonium salts Chemical group 0.000 claims description 4
- 150000001279 adipic acids Chemical class 0.000 claims description 3
- 238000007599 discharging Methods 0.000 claims description 3
- 238000007711 solidification Methods 0.000 claims description 3
- 230000008023 solidification Effects 0.000 claims description 3
- BXGYYDRIMBPOMN-UHFFFAOYSA-N 2-(hydroxymethoxy)ethoxymethanol Chemical compound OCOCCOCO BXGYYDRIMBPOMN-UHFFFAOYSA-N 0.000 claims description 2
- BGJPCIFNQHHMFU-UHFFFAOYSA-N 2-butylpentane-1,3-diol Chemical compound CCCCC(CO)C(O)CC BGJPCIFNQHHMFU-UHFFFAOYSA-N 0.000 claims description 2
- 150000008064 anhydrides Chemical class 0.000 claims description 2
- ZSDJVGXBJDDOCD-UHFFFAOYSA-N benzene dioctyl benzene-1,2-dicarboxylate Chemical compound C(C=1C(C(=O)OCCCCCCCC)=CC=CC1)(=O)OCCCCCCCC.C1=CC=CC=C1 ZSDJVGXBJDDOCD-UHFFFAOYSA-N 0.000 claims 1
- 238000010438 heat treatment Methods 0.000 claims 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 abstract description 11
- 239000003973 paint Substances 0.000 abstract description 9
- 238000009835 boiling Methods 0.000 abstract description 6
- 230000007547 defect Effects 0.000 abstract description 6
- 239000007888 film coating Substances 0.000 abstract description 6
- 238000009501 film coating Methods 0.000 abstract description 6
- 238000005336 cracking Methods 0.000 abstract description 5
- 238000000034 method Methods 0.000 abstract description 2
- 239000000843 powder Substances 0.000 description 5
- UHOVQNZJYSORNB-UHFFFAOYSA-N Benzene Chemical compound C1=CC=CC=C1 UHOVQNZJYSORNB-UHFFFAOYSA-N 0.000 description 3
- 230000003301 hydrolyzing effect Effects 0.000 description 3
- 229920000728 polyester Polymers 0.000 description 3
- MQIUGAXCHLFZKX-UHFFFAOYSA-N Di-n-octyl phthalate Natural products CCCCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCCC MQIUGAXCHLFZKX-UHFFFAOYSA-N 0.000 description 2
- ISWSIDIOOBJBQZ-UHFFFAOYSA-N Phenol Chemical compound OC1=CC=CC=C1 ISWSIDIOOBJBQZ-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 230000006978 adaptation Effects 0.000 description 2
- 230000008901 benefit Effects 0.000 description 2
- 230000000052 comparative effect Effects 0.000 description 2
- OLLMEZGFCPWTGD-UHFFFAOYSA-N hexane;methanol Chemical compound OC.OC.CCCCCC OLLMEZGFCPWTGD-UHFFFAOYSA-N 0.000 description 2
- BDAGIHXWWSANSR-UHFFFAOYSA-N methanoic acid Natural products OC=O BDAGIHXWWSANSR-UHFFFAOYSA-N 0.000 description 2
- 239000000178 monomer Substances 0.000 description 2
- OJMIONKXNSYLSR-UHFFFAOYSA-N phosphorous acid Chemical class OP(O)O OJMIONKXNSYLSR-UHFFFAOYSA-N 0.000 description 2
- XNGIFLGASWRNHJ-UHFFFAOYSA-N phthalic acid Chemical compound OC(=O)C1=CC=CC=C1C(O)=O XNGIFLGASWRNHJ-UHFFFAOYSA-N 0.000 description 2
- YPFDHNVEDLHUCE-UHFFFAOYSA-N propane-1,3-diol Chemical compound OCCCO YPFDHNVEDLHUCE-UHFFFAOYSA-N 0.000 description 2
- OSWFIVFLDKOXQC-UHFFFAOYSA-N 4-(3-methoxyphenyl)aniline Chemical compound COC1=CC=CC(C=2C=CC(N)=CC=2)=C1 OSWFIVFLDKOXQC-UHFFFAOYSA-N 0.000 description 1
- UWKWMTBKFCNDDH-UHFFFAOYSA-N N(=NC=NN)CCCCCCN=NC=NN Chemical compound N(=NC=NN)CCCCCCN=NC=NN UWKWMTBKFCNDDH-UHFFFAOYSA-N 0.000 description 1
- 150000008065 acid anhydrides Chemical class 0.000 description 1
- 150000001335 aliphatic alkanes Chemical class 0.000 description 1
- 239000012752 auxiliary agent Substances 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- 230000007812 deficiency Effects 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 235000019253 formic acid Nutrition 0.000 description 1
- 125000004836 hexamethylene group Chemical group [H]C([H])([*:2])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[*:1] 0.000 description 1
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 1
- 125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 229920005989 resin Polymers 0.000 description 1
- 239000011347 resin Substances 0.000 description 1
- 238000006467 substitution reaction Methods 0.000 description 1
- 230000009466 transformation Effects 0.000 description 1
- 238000005406 washing Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/16—Dicarboxylic acids and dihydroxy compounds
- C08G63/18—Dicarboxylic acids and dihydroxy compounds the acids or hydroxy compounds containing carbocyclic rings
- C08G63/199—Acids or hydroxy compounds containing cycloaliphatic rings
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/02—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds
- C08G63/12—Polyesters derived from hydroxycarboxylic acids or from polycarboxylic acids and polyhydroxy compounds derived from polycarboxylic acids and polyhydroxy compounds
- C08G63/16—Dicarboxylic acids and dihydroxy compounds
- C08G63/20—Polyesters having been prepared in the presence of compounds having one reactive group or more than two reactive groups
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G63/00—Macromolecular compounds obtained by reactions forming a carboxylic ester link in the main chain of the macromolecule
- C08G63/78—Preparation processes
- C08G63/82—Preparation processes characterised by the catalyst used
- C08G63/85—Germanium, tin, lead, arsenic, antimony, bismuth, titanium, zirconium, hafnium, vanadium, niobium, tantalum, or compounds thereof
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D167/00—Coating compositions based on polyesters obtained by reactions forming a carboxylic ester link in the main chain; Coating compositions based on derivatives of such polymers
- C09D167/02—Polyesters derived from dicarboxylic acids and dihydroxy compounds
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
- C09D5/00—Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
- C09D5/03—Powdery paints
Landscapes
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Health & Medical Sciences (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Materials Engineering (AREA)
- Wood Science & Technology (AREA)
- Paints Or Removers (AREA)
- Polyesters Or Polycarbonates (AREA)
Abstract
Description
起泡 | 开裂 | 剥落 | 掉粉 | 明显失光 | |
实施例1 | 无 | 无 | 无 | 无 | 无 |
实施例2 | 无 | 无 | 无 | 无 | 无 |
实施例3 | 无 | 无 | 无 | 无 | 无 |
对比实施例 | 无 | 无 | 无 | 无 | 失光 |
Claims (10)
Priority Applications (1)
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CN201811406453.9A CN109517149A (zh) | 2018-11-23 | 2018-11-23 | 一种耐水解干混粉末涂料用聚酯树脂的配方及其制备方法 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
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CN201811406453.9A CN109517149A (zh) | 2018-11-23 | 2018-11-23 | 一种耐水解干混粉末涂料用聚酯树脂的配方及其制备方法 |
Publications (1)
Publication Number | Publication Date |
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CN109517149A true CN109517149A (zh) | 2019-03-26 |
Family
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Family Applications (1)
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CN201811406453.9A Pending CN109517149A (zh) | 2018-11-23 | 2018-11-23 | 一种耐水解干混粉末涂料用聚酯树脂的配方及其制备方法 |
Country Status (1)
Country | Link |
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CN (1) | CN109517149A (zh) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110563934A (zh) * | 2019-09-09 | 2019-12-13 | 安徽神剑新材料股份有限公司 | 一种耐手印型聚酯树脂及其制备方法 |
CN111019492A (zh) * | 2019-12-27 | 2020-04-17 | 上海邦中高分子材料股份有限公司 | 一种耐水煮性粉末涂料及其制备方法 |
CN111440295A (zh) * | 2020-03-25 | 2020-07-24 | 广东工业大学 | 一种耐水煮、高流平粉末涂料用聚酯树脂及其制备方法和应用 |
CN112062941A (zh) * | 2020-09-16 | 2020-12-11 | 浙江中法新材料有限公司 | 一种6040型聚酯树脂及其制备方法 |
WO2021022389A1 (zh) | 2019-08-02 | 2021-02-11 | 擎天材料科技有限公司 | 一种聚酯树脂组合物、粉末涂料及工件 |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20090007819A1 (en) * | 2007-07-05 | 2009-01-08 | Ppg Industries Ohio, Inc. | Aqueous dispersion comprising a branched triol having trimellitic anhydride and associated method |
CN105601892A (zh) * | 2015-11-17 | 2016-05-25 | 广东伊诗德新材料科技有限公司 | 一种低挥发分含量粉末涂料用聚酯树脂及其制备方法 |
CN106543420A (zh) * | 2016-10-24 | 2017-03-29 | 广州擎天材料科技有限公司 | 一种耐水煮色牢度高的tgic型粉末涂料用聚酯树脂及其制备方法 |
-
2018
- 2018-11-23 CN CN201811406453.9A patent/CN109517149A/zh active Pending
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20090007819A1 (en) * | 2007-07-05 | 2009-01-08 | Ppg Industries Ohio, Inc. | Aqueous dispersion comprising a branched triol having trimellitic anhydride and associated method |
CN105601892A (zh) * | 2015-11-17 | 2016-05-25 | 广东伊诗德新材料科技有限公司 | 一种低挥发分含量粉末涂料用聚酯树脂及其制备方法 |
CN106543420A (zh) * | 2016-10-24 | 2017-03-29 | 广州擎天材料科技有限公司 | 一种耐水煮色牢度高的tgic型粉末涂料用聚酯树脂及其制备方法 |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
WO2021022389A1 (zh) | 2019-08-02 | 2021-02-11 | 擎天材料科技有限公司 | 一种聚酯树脂组合物、粉末涂料及工件 |
CN110563934A (zh) * | 2019-09-09 | 2019-12-13 | 安徽神剑新材料股份有限公司 | 一种耐手印型聚酯树脂及其制备方法 |
CN111019492A (zh) * | 2019-12-27 | 2020-04-17 | 上海邦中高分子材料股份有限公司 | 一种耐水煮性粉末涂料及其制备方法 |
CN111440295A (zh) * | 2020-03-25 | 2020-07-24 | 广东工业大学 | 一种耐水煮、高流平粉末涂料用聚酯树脂及其制备方法和应用 |
CN112062941A (zh) * | 2020-09-16 | 2020-12-11 | 浙江中法新材料有限公司 | 一种6040型聚酯树脂及其制备方法 |
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Address after: 313300 Xiaoshu Industrial Park, Lingang Economic Zone, Meixi Town, Anji County, Huzhou City, Zhejiang Province Applicant after: New Sino French polymer materials Limited by Share Ltd. Address before: 313300 Xiaoshu Industrial Park, Lingang Economic Zone, Meixi Town, Anji County, Hangzhou City, Zhejiang Province Applicant before: New Sino French polymer materials Limited by Share Ltd. |
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