TW201710464A - 撥水撥油劑組成物及撥水撥油性纖維製品之製造方法 - Google Patents

撥水撥油劑組成物及撥水撥油性纖維製品之製造方法 Download PDF

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Publication number: TW201710464A
Authority: TW; Taiwan
Prior art keywords: group; repellent; water; oil; monomer
Prior art date: 2015-05-07

Application number

TW105114140A

Other languages

English (en)

Chinese (zh)

Inventor

Gou Yoshino

Makoto Nishikawa

Min-Si JUNG

Hye-Won Bae

Ji-Hyuk IM

Original Assignee

Nicca Chemical Co

Nicca Korea Co Ltd

Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)

2015-05-07

Filing date

2016-05-06

Publication date

2017-03-16

2016-05-06 Application filed by Nicca Chemical Co, Nicca Korea Co Ltd filed Critical Nicca Chemical Co

2017-03-16 Publication of TW201710464A publication Critical patent/TW201710464A/zh

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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/18—Materials not provided for elsewhere for application to surfaces to minimize adherence of ice, mist or water thereto; Thawing or antifreeze materials for application to surfaces
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08F—MACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
- C08F220/00—Copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and only one being terminated by only one carboxyl radical or a salt, anhydride ester, amide, imide or nitrile thereof
- C08F220/02—Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
- C08F220/10—Esters
- C08F220/22—Esters containing halogen
- D—TEXTILES; PAPER
- D06—TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
- D06M—TREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/21—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/244—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of halogenated hydrocarbons
- D06M15/256—Macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds of halogenated hydrocarbons containing fluorine

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Organic Chemistry (AREA)
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Medicinal Chemistry (AREA)
Polymers & Plastics (AREA)
Health & Medical Sciences (AREA)
Combustion & Propulsion (AREA)
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Textile Engineering (AREA)
Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)
Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Materials Applied To Surfaces To Minimize Adherence Of Mist Or Water (AREA)

TW105114140A 2015-05-07 2016-05-06 撥水撥油劑組成物及撥水撥油性纖維製品之製造方法 TW201710464A (zh)

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JP7009675B1 (ja)	2020-06-03	2022-01-25	明成化学工業株式会社	撥水剤組成物、キット、撥水性繊維製品及びその製造方法
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CN102898583A (zh) *	2011-07-27	2013-01-30	苏州大学	一种双氟烷基酯聚合物型织物整理剂及其制备方法
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- 2016-05-02 JP JP2017516620A patent/JPWO2016178429A1/ja active Pending
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CN107532069A (zh)	2018-01-02
JPWO2016178429A1 (ja)	2018-02-22
KR20180004750A (ko)	2018-01-12
KR102652086B1 (ko)	2024-04-01
WO2016178429A1 (fr)	2016-11-10

Publication	Publication Date	Title
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