KR910018408A - Cyclodextrin Coated Solid Substrates and Methods for Making the Same - Google Patents

Cyclodextrin Coated Solid Substrates and Methods for Making the Same Download PDF

Info

Publication number
KR910018408A
KR910018408A KR1019900005225A KR900005225A KR910018408A KR 910018408 A KR910018408 A KR 910018408A KR 1019900005225 A KR1019900005225 A KR 1019900005225A KR 900005225 A KR900005225 A KR 900005225A KR 910018408 A KR910018408 A KR 910018408A
Authority
KR
South Korea
Prior art keywords
diisocyanate
cyclodextrin
polyisocyanate
substrate
solid substrate
Prior art date
Application number
KR1019900005225A
Other languages
Korean (ko)
Other versions
KR930001315B1 (en
Inventor
피. 로어바크 로날드
Original Assignee
원본미기재
유오피
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.)
Filing date
Publication date
Application filed by 원본미기재, 유오피 filed Critical 원본미기재
Priority to KR1019900005225A priority Critical patent/KR930001315B1/en
Publication of KR910018408A publication Critical patent/KR910018408A/en
Application granted granted Critical
Publication of KR930001315B1 publication Critical patent/KR930001315B1/en

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08BPOLYSACCHARIDES; DERIVATIVES THEREOF
    • C08B30/00Preparation of starch, degraded or non-chemically modified starch, amylose, or amylopectin
    • C08B30/06Drying; Forming

Abstract

내용 없음No content

Description

시클로 덱스트린 피복된 고체 기질 및 그의 제조방법Cyclodextrin Coated Solid Substrates and Methods for Making the Same

본 내용은 요부공개 건이므로 전문내용을 수록하지 않았음Since this is an open matter, no full text was included.

Claims (9)

폴리이소시아네이트 교차 결합된 시크리로덱스트린 수지로 피복된 고체 기질에 있어서, 세라믹, 유리, 플래스틱, 금속, 직물및 섬유질 제품으로 구성된 그룹에서 선택되고 가공된 폴리이소시아네이트 교차 결합된 시클로덱스트린 수지제품을 기본으로 0.1내지 10중량퍼센트인 피복층을 갖는 고체 기질을 포함하는데, 상기 수지는 시클로덱스트린과 폴리이소시아네이트의 반응 생성물로서, 반응생성물의 수용해도가 약 200ppm 이하이고 적어도 하나의 쌍극자 비양자성 용매에서의 용해도가 적어도 1.0중량 퍼센트가 되도록하는 몰비로 반응하는 것을 특징으로 하는 피복된 고체기질.For solid substrates coated with polyisocyanate crosslinked cyclodextrin resins, 0.1 based on polyisocyanate crosslinked cyclodextrin resin products selected and processed from the group consisting of ceramic, glass, plastic, metal, textile and fibrous products And a solid substrate having a coating layer of from about 10% by weight, wherein the resin is a reaction product of cyclodextrin and polyisocyanate, having a water solubility of the reaction product of about 200 ppm or less and a solubility in at least one dipole aprotic solvent at least 1.0. A coated solid substrate, characterized in that it reacts at a molar ratio such that it is by weight percent. 제1항에 있어서, 상기 시클로 덱스트린은 베타-시클로덱스트린, 또는 알파- 시클로덱스트린, 또는 감마-시클로 덱스트린인 것을 특징으로 하는 피복된 고체 기질.The coated solid substrate of claim 1, wherein the cyclodextrin is beta-cyclodextrin, or alpha-cyclodextrin, or gamma-cyclodextrin. 제1항에 있어서, 상기 기질은 알루미나, 티타니아, 실리카, 마그네시아, 보리아 토리아, 지르코니아, 및 이들의 결합물로 구성된 그룹에서 선택되는 것을 특징으로 하는 피복된 고체 기질.The coated solid substrate of claim 1, wherein the substrate is selected from the group consisting of alumina, titania, silica, magnesia, boria, zirconia, and combinations thereof. 제1항에 있어서 상기 폴리이소시아네이트는 톨루엔 디이소시아네이트, p-및 m-페니렌 디이소시아네트, 테트라메틸렌 디이소시아네이트, 1,6-헥사메틸렌 디이소시아네이트, 1,4-시클로 헥실렌 디이소시아네이트, 4,4′-메틸렌 디시클로헥실 디이소시아네이트, 4,4′-메틸렌 디페닐 디이소시아네이트, 3,3′-디메틸-4,4′-디페닐메탄 디이소시아네이트, 1,5-테트라히드라메틸렌 디이소시아네이트, 디아니소딘 디이소시아네이트, 비톨리렌 디이 소시아네이트, 나프탈렌-1,4-디이소시아네이트, 비스(2-메틸-3-이소시아나토페닐) 메탄, 비스(3-메틸-4-이소시아나토페닐) 메탄, 4,4′-디페닐프로판 디이소시아네이트, 및 메틸렌-다리 폴리페닐 폴리이소시아네이트로 구성된 그룹에서 선택되는 디이소시아네이트 인것을 특징으로하는 피복된 고체기질.The method of claim 1 wherein the polyisocyanate is toluene diisocyanate, p- and m-phenylene diisocyanate, tetramethylene diisocyanate, 1,6-hexamethylene diisocyanate, 1,4-cyclohexylene diisocyanate, 4, 4'-methylene dicyclohexyl diisocyanate, 4,4'-methylene diphenyl diisocyanate, 3,3'-dimethyl-4,4'-diphenylmethane diisocyanate, 1,5-tetrahydramethylene diisocyanate, di Anisodine diisocyanate, bitorylene diisocyanate, naphthalene-1,4-diisocyanate, bis (2-methyl-3-isocyanatophenyl) methane, bis (3-methyl-4-isocyanatophenyl) methane, A coated solid substrate, characterized in that the diisocyanate is selected from the group consisting of 4,4′-diphenylpropane diisocyanate, and methylene-bridged polyphenyl polyisocyanate. 고체 기질을 폴리이소시아네이트 교차 결합된 시클로덱스트린 수지로 피복하는 방법에 있어서, 쌍극자 비양자성 용매내의 폴리이소시아네이트 교차 결합된 시클로덱스트린 수지 용액을 습한기질이 되도록 상기 기질과 접촉시키는 단계;폴리이소시아네이트 교차 결합된 시클로덱스트린 수지로 피복된 기질을 제공하기 위하여 상기습한 기질로부터 용매를 제거하는 단계, 상기 피복된 단계를 포함하는데, 상기 수지는 시클로덱스트린과 폴리이소시아네이트의 반응생성물로서, 반응생성물의 수용해도가 약 200ppm이하이고 적어도 하나의 쌍극자 비양자성 용매에서의 용해도가 적어도 0.1중량 퍼센트가 되도록하는 몰비로 반응하는 것을 특징으로 하는 고체 기질의 피복방법.A method of coating a solid substrate with a polyisocyanate crosslinked cyclodextrin resin, the method comprising: contacting a solution of polyisocyanate crosslinked cyclodextrin resin in a dipole aprotic solvent with the substrate to make a wet substrate; polyisocyanate crosslinked cyclo Removing the solvent from the wet substrate to provide a substrate coated with dextrin resin, the coating step, wherein the resin is a reaction product of cyclodextrin and polyisocyanate, the water solubility of the reaction product being less than about 200 ppm And reacting at a molar ratio such that the solubility in at least one dipole aprotic solvent is at least 0.1 weight percent. 제5항에 있어서, 상기 시클로 덱스트린은 베타-시클로덱스트린, 또는 알파-시클로 덱스트린, 또는 감마-시클로덱스티린인것을 특징으로 하는 고체기질의 피복 방법.6. The method of claim 5, wherein the cyclodextrin is beta-cyclodextrin, or alpha-cyclodextrin, or gamma-cyclodextrin. 제5항 또는 6항에 있어서, 상기 기질은 유리, 플래스틱, 금속, 직물, 섬유질제품,알루미나, 티타니아, 실리카, 마그네시아, 보리아, 토리아, 지르코니아, 및 이들이 결합물로 구성된 그룹으로부터 선택되는 것을 특징으로 하는 고체기질의 피복 방법.The method of claim 5 or 6, wherein the substrate is selected from the group consisting of glass, plastics, metals, textiles, fibrous products, alumina, titania, silica, magnesia, boria, toria, zirconia, and combinations thereof. Solid substrate coating method. 제5항에 있어서, 상기 폴리이소시아네이트는 톨루엔 디이소시아네이트, p-및 m-페닐렌 디이소시아네트, 테트라메틸렌 디이소시아네이트, 1,6-헥사메틸렌 디이소시아네이트, 1,4-시클로 헥실렌 디이소시아네이트, 4,4′-메틸렌 디시클로헥실 디이소시아네이트, 4,4′-메틸렌 디페닐 디이소시아네이트, 3,3′-디메틸-4,4′-디페닐메탄 디이소시아네이트, 1,5-테트라히드라메틸렌 디이소시아네이트, 디아니소딘 디이소시아네이트, 비톨리렌 디이소시아네이트, 나프탈렌-1,4-디이소시아네이트, 비스(2-메틸-3-이소시아나토페닐)메탄, 비스(3-메틸-4-이소시아나토페닐)메탄, 4,4′-디페닐프로판 디이소시아네이트, 및 메틸렌- 다리 폴리페닐 폴리이소시아네이트로 구성된 그룹에서 선택되는 디이소시아네이트 인것을 특징으로하는 고체 기질의 피복방법.6. The polyisocyanate of claim 5, wherein the polyisocyanate is toluene diisocyanate, p- and m-phenylene diisocyanate, tetramethylene diisocyanate, 1,6-hexamethylene diisocyanate, 1,4-cyclohexylene diisocyanate, 4 , 4'-methylene dicyclohexyl diisocyanate, 4,4'-methylene diphenyl diisocyanate, 3,3'-dimethyl-4,4'-diphenylmethane diisocyanate, 1,5-tetrahydramethylene diisocyanate, Dianisodine diisocyanate, bitolylene diisocyanate, naphthalene-1,4-diisocyanate, bis (2-methyl-3-isocyanatophenyl) methane, bis (3-methyl-4-isocyanatophenyl) methane, A 4,4'-diphenylpropane diisocyanate, and a diisocyanate selected from the group consisting of methylene- bridged polyphenyl polyisocyanate. 제5항에 있어서, 상기 쌍극자 비양자성 용매는 피리딘, 디메틸포름아미드, 디메틸 설폭사이드, n-메틸피롤리돈, 헥사메틸포스포라미드, 및 디메틸 아세트 아미드로 구성된 그룹으로 부터 선택되는 것을 특징으로 하는 고체 기질의 피복방법.6. The method of claim 5, wherein the dipole aprotic solvent is selected from the group consisting of pyridine, dimethylformamide, dimethyl sulfoxide, n-methylpyrrolidone, hexamethylphosphoramide, and dimethyl acetamide. Method of coating solid substrate. ※ 참고사항 : 최초출원 내용에 의하여 공개하는 것임.※ Note: The disclosure is based on the initial application.
KR1019900005225A 1990-04-16 1990-04-16 Cyclodextrin-coated solid-substrate KR930001315B1 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
KR1019900005225A KR930001315B1 (en) 1990-04-16 1990-04-16 Cyclodextrin-coated solid-substrate

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
KR1019900005225A KR930001315B1 (en) 1990-04-16 1990-04-16 Cyclodextrin-coated solid-substrate

Publications (2)

Publication Number Publication Date
KR910018408A true KR910018408A (en) 1991-11-30
KR930001315B1 KR930001315B1 (en) 1993-02-25

Family

ID=19298035

Family Applications (1)

Application Number Title Priority Date Filing Date
KR1019900005225A KR930001315B1 (en) 1990-04-16 1990-04-16 Cyclodextrin-coated solid-substrate

Country Status (1)

Country Link
KR (1) KR930001315B1 (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101365715B1 (en) * 2011-09-07 2014-02-25 순천향대학교 산학협력단 Antifoul agent and antifouling paint composition comprising cyclodextrin complex
CN115386320A (en) * 2022-09-26 2022-11-25 北京聚创恒诚科技发展有限公司 Isocyanate-coated aldehyde-free adhesive and application thereof

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR100785913B1 (en) * 2006-11-29 2007-12-17 한국과학기술연구원 Polymerized beta-cyclodextrin powder and its preparation method

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101365715B1 (en) * 2011-09-07 2014-02-25 순천향대학교 산학협력단 Antifoul agent and antifouling paint composition comprising cyclodextrin complex
CN115386320A (en) * 2022-09-26 2022-11-25 北京聚创恒诚科技发展有限公司 Isocyanate-coated aldehyde-free adhesive and application thereof
CN115386320B (en) * 2022-09-26 2023-11-24 北京聚创恒诚科技发展有限公司 Isocyanate-coated formaldehyde-free adhesive and application thereof

Also Published As

Publication number Publication date
KR930001315B1 (en) 1993-02-25

Similar Documents

Publication Publication Date Title
DE69812336T2 (en) RESINS FOR CAN AND TAPE COATINGS
DE69623647T2 (en) POLYURETHANE MADE OF POLYSILOXANE-POLYOL MACROMER
CA2049622A1 (en) Deactivatable electronic article surveillance tags, tag webs and method of making tag webs
PT1037935E (en) PROCESS FOR THE MANUFACTURE AND USE OF STRATEGIC OR POST-STORAGE AND LATENT-REACTION POSSES CONSTITUTED BY SOLID POLYISOCYANATES DISABLED ON THE SURFACE AND BY DISPERSION POLYMERS WITH FUNCTIONAL GROUPS
KR880007364A (en) Antifouling fabric
CN101107292B (en) Method for producing polyimide film
FI935221A (en) Staerkelsebaserat material
EP0281923B1 (en) Polyimide film
CN106957427A (en) Poly- (acid imide acid amides) copolymer, the product comprising it, its preparation method and the electronic device including the product
KR910018408A (en) Cyclodextrin Coated Solid Substrates and Methods for Making the Same
CA2300384A1 (en) Coated, long fiber reinforcing composite structure and process of preparation thereof
NO954549L (en) Surface treatment articles and methods for making the same
Kaplan Plasma processes for wide fabric, film and non-wovens
ATE127653T1 (en) CARRIER FOR COPPER FILMS OF FLEXIBLE CIRCUIT BOARDS.
KR920017807A (en) Laminated film
US4985509A (en) Heat curable resin composition
BR8506428A (en) ANTISTATIC ITEM AND PROCESS FOR ITS PRODUCTION
EP0496334A1 (en) A flexible base laminated with metal on both the surfaces and a process for producing same
JP2889976B2 (en) Polyimide film and method for producing the same
JPH04207094A (en) Flexible printed-circuit board and its manufacture
FR2636986B1 (en) PROCESS FOR PRODUCING A BIREACTIVE THERMAL-STICKING TEXTILE PRODUCT AND RESULTING PRODUCT
JPS6266932A (en) Resin film and manufacture thereof
KR100867528B1 (en) Monomer for synthesizing polyimide, and polyimide precursor and flexible metal clad laminate including the same
KR19990081495A (en) Manufacturing method of polyester release film excellent in release property
WO2002044291A2 (en) Polyimide-containing coating composition and film formed from the same

Legal Events

Date Code Title Description
A201 Request for examination
G160 Decision to publish patent application
E701 Decision to grant or registration of patent right
NORF Unpaid initial registration fee