CN106243969A - 一种涂料及其制备方法 - Google Patents

一种涂料及其制备方法 Download PDF

Info

Publication number
CN106243969A
CN106243969A CN201610631042.4A CN201610631042A CN106243969A CN 106243969 A CN106243969 A CN 106243969A CN 201610631042 A CN201610631042 A CN 201610631042A CN 106243969 A CN106243969 A CN 106243969A
Authority
CN
China
Prior art keywords
coating
pfpe
trimer
auxiliary agent
isocyanate
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.)
Granted
Application number
CN201610631042.4A
Other languages
English (en)
Other versions
CN106243969B (zh
Inventor
徐涛
张恒英
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sinochem Environmental Protection Chemicals Taicang Co Ltd
Original Assignee
Sinochem Environmental Protection Chemicals Taicang 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.)
Filing date
Publication date
Application filed by Sinochem Environmental Protection Chemicals Taicang Co Ltd filed Critical Sinochem Environmental Protection Chemicals Taicang Co Ltd
Priority to CN201610631042.4A priority Critical patent/CN106243969B/zh
Publication of CN106243969A publication Critical patent/CN106243969A/zh
Application granted granted Critical
Publication of CN106243969B publication Critical patent/CN106243969B/zh
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D175/00Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
    • C09D175/04Polyurethanes
    • C09D175/06Polyurethanes from polyesters
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/42Polycondensates having carboxylic or carbonic ester groups in the main chain
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/42Polycondensates having carboxylic or carbonic ester groups in the main chain
    • C08G18/4244Polycondensates having carboxylic or carbonic ester groups in the main chain containing oxygen in the form of ether groups
    • C08G18/4247Polycondensates having carboxylic or carbonic ester groups in the main chain containing oxygen in the form of ether groups derived from polyols containing at least one ether group and polycarboxylic acids
    • C08G18/425Polycondensates having carboxylic or carbonic ester groups in the main chain containing oxygen in the form of ether groups derived from polyols containing at least one ether group and polycarboxylic acids the polyols containing one or two ether groups
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/48Polyethers
    • C08G18/4854Polyethers containing oxyalkylene groups having four carbon atoms in the alkylene group
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/40High-molecular-weight compounds
    • C08G18/48Polyethers
    • C08G18/50Polyethers having heteroatoms other than oxygen
    • C08G18/5003Polyethers having heteroatoms other than oxygen having halogens
    • C08G18/5015Polyethers having heteroatoms other than oxygen having halogens having fluorine atoms
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/65Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
    • C08G18/66Compounds of groups C08G18/42, C08G18/48, or C08G18/52
    • C08G18/6603Compounds of groups C08G18/42, C08G18/48, or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38
    • C08G18/6614Compounds of groups C08G18/42, C08G18/48, or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3225 or C08G18/3271 and/or polyamines of C08G18/38
    • C08G18/6622Compounds of groups C08G18/42, C08G18/48, or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3225 or C08G18/3271 and/or polyamines of C08G18/38 with compounds of group C08G18/3271
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/28Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
    • C08G18/65Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
    • C08G18/66Compounds of groups C08G18/42, C08G18/48, or C08G18/52
    • C08G18/6666Compounds of group C08G18/48 or C08G18/52
    • C08G18/667Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38
    • C08G18/6681Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/32 or C08G18/3271 and/or polyamines of C08G18/38
    • C08G18/6688Compounds of group C08G18/48 or C08G18/52 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/32 or C08G18/3271 and/or polyamines of C08G18/38 with compounds of group C08G18/3271
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/74Polyisocyanates or polyisothiocyanates cyclic
    • C08G18/75Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic
    • C08G18/751Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring
    • C08G18/752Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group
    • C08G18/753Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group
    • C08G18/755Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing only one cycloaliphatic ring containing at least one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group containing one isocyanate or isothiocyanate group linked to the cycloaliphatic ring by means of an aliphatic group having a primary carbon atom next to the isocyanate or isothiocyanate group and at least one isocyanate or isothiocyanate group linked to a secondary carbon atom of the cycloaliphatic ring, e.g. isophorone diisocyanate
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G18/00Polymeric products of isocyanates or isothiocyanates
    • C08G18/06Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
    • C08G18/70Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
    • C08G18/72Polyisocyanates or polyisothiocyanates
    • C08G18/77Polyisocyanates or polyisothiocyanates having heteroatoms in addition to the isocyanate or isothiocyanate nitrogen and oxygen or sulfur
    • C08G18/78Nitrogen
    • C08G18/79Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates
    • C08G18/791Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups
    • C08G18/792Nitrogen characterised by the polyisocyanates used, these having groups formed by oligomerisation of isocyanates or isothiocyanates containing isocyanurate groups formed by oligomerisation of aliphatic and/or cycloaliphatic isocyanates or isothiocyanates
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING 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
    • C09D5/00Coating compositions, e.g. paints, varnishes or lacquers, characterised by their physical nature or the effects produced; Filling pastes
    • C09D5/16Antifouling paints; Underwater paints
    • C09D5/1606Antifouling paints; Underwater paints characterised by the anti-fouling agent
    • C09D5/1637Macromolecular compounds

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Materials Engineering (AREA)
  • Wood Science & Technology (AREA)
  • Application Of Or Painting With Fluid Materials (AREA)
  • Paints Or Removers (AREA)
  • Polyurethanes Or Polyureas (AREA)

Abstract

本发明涉及一种涂料及其制备方法,按重量百分含量计,所述涂料的原料配方包括:聚酯多元醇15~25%;异氰酸酯5~10%;全氟聚醚基助剂0.1~5%;催化剂0.01~0.1%;溶剂65~75%。本发明的涂料添加了全氟聚醚基助剂,该全氟聚醚基助剂以全氟聚醚羧酸或全氟聚醚酯化合物为原料,通过嫁接聚氨酯链段、末端引入了反应活性基团醇羟基,提高全氟聚醚基助剂与聚氨酯、醇酸或环氧等涂料的相容性和反应活性,提高涂料的抗污性,避免漆膜雾影的出现。

Description

一种涂料及其制备方法
技术领域
本发明属于涂料领域,具体涉及一种涂料及其制备方法。
背景技术
提高现有涂料漆膜表面的防污、防粘和防涂鸦性能,一直是涂料研究的热点和难点,尤其是应用于计算机、通信和消费电子等表面的3C涂料,以及显示器和触控屏等光学膜表面的增硬涂料,还有用于防治城市牛皮癣的防涂鸦涂料等低表面能涂料。从技术角度讲,实现材料表面的疏水疏油功能,主要有两种途径,一是在材料表面添加低表面能物质,主要是有机氟和有机硅;二是在材料表面构建粗糙结构。毫无疑问地是,研究在现有涂料配方中添加一种高效的抗污助剂,而不改变原有涂料的其它性能,是一种快捷、高效而且实用的方法。
专利CN200580014573.9公布一种具有抗污效果的全氟聚醚改性丙烯酸酯,然而该化合物不含有醇羟基CH2-OH,与聚氨酯、醇酸树脂或环氧树脂等涂料固化体系的反应活性和相溶性差。从一方面讲,全氟聚醚(PFPE)与涂料中其它碳氢组份相溶性差,成膜过程中会上浮于漆膜的表面,降低漆膜的表面能,最终实防油、防水和防尘等功能;从另一方面来看,对PFPE进行化学嫁接可以增加其与涂料配方体系的相溶性或反应性,否则将导致涂料的防水、防油和防污性能变差,而且漆膜表面会出现雾影,影响外观和透明度。
全氟聚醚可以由六氟环氧丙烷HFPO经阴离子聚合而制备,具体原理和方法可以参考专利CN200910231435.6,该工艺的初始产物为全氟聚醚基酰氟,再简单水解或酯化可以制备出全氟聚醚羧酸及酯化物。若要获得全氟聚醚基亚甲基醇(PFPE-CH2-OH)通常需要高度易燃、易爆的氢气、硼氢化钠和四氢铝锂等还原剂,具体原理和工艺可以参考US7388114,全氟聚醚基酰氟的结构如下式所示:
其中:n为自然数
专利CN201310084408.7公布了一种全氟聚醚基的二元醇及其嵌段共聚物,然而该路线所采用的全氟聚醚原料是全氟聚醚基亚甲基醇,如下式所示:
因此,直接以全氟聚醚羧酸及酯化物为原料开发下游产品,具有极为重要的安全价值。现有技术中,还没有以全氟聚醚羧酸及酯化物为原料开发的下游产品,更没有此类下游产品用于涂料中。
发明内容
本发明所要解决的技术问题是克服现有技术的不足,提供一种涂料及其制备方法。
为解决以上技术问题,本发明采用如下技术方案:
一种涂料,按重量百分含量计,所述涂料的原料配方包括:
所述全氟聚醚基助剂的结构式如式Ⅰ所示,
其中,n为自然数且2≤n≤30;
X为或-HN-R2,R1、R2分别为含有聚氨酯结构的取代基,且X的末端含有醇羟基。
进一步地,所述X的数均分子量为500~10000。
进一步地,所述R1、R2独立地选自-R3-O-CO-NH-R4-NH-CO-O-R5-OH,其中,R3a、e为小于等于10的正整数;-CO-NH-R4-NH-CO-为含有至 少二个NCO基的异氰酸酯类化合物单元,-O-R5-OH为多元醇单元。
更进一步地,所述异氰酸酯类化合物为异氰酸酯单体、异氰酸酯二聚体、异氰酸酯三聚体中的一种或多种的组合。
更进一步优选地,所述异氰酸酯类化合物为异佛尔酮二异氰酸酯及其三聚体,甲苯二异氰酸酯及其二聚体、三聚体,六亚甲基二异氰酸酯及其二聚体、三聚体,二环己基甲烷二异氰酸酯中的一种或多种的组合。
更进一步地,所述多元醇为聚醚多元醇、聚酯多元醇中的一种或多种的组合。
更进一步优选地,所述多元醇为聚四氢呋喃醚二醇、聚氧化丙烯二醇、聚氧化乙烯二醇、聚氧化丙烯-氧化乙烯二醇、聚三亚甲基醚二醇、聚己二酸乙二醇酯二醇、聚己二酸二甘醇酯二醇、聚碳酸酯二醇、聚己丙酯多元醇中的一种或多种的组合。
更进一步地,所述R3为-CH2CH2-或-CH2CH2-O-CH2CH2-。
本发明中,所述全氟聚醚基助剂中所述全氟聚醚基的质量含量为5~50%。
根据本发明,所述全氟聚醚基助剂为如下结构式表示的化合物中的一种:
其中,b、c、d为正整数。
所述全氟聚醚基助剂的制备方法,所述制备方法包括以下步骤:
(1)全氟聚醚羧酸或全氟聚醚酯化合物与含有醇羟基的有机胺化合物进行酰胺化反应,制得产物1;
(2)在催化剂作用下,使得步骤(1)得到的产物1与含有至少二个NCO基的异氰酸酯类化合物进行反应,制得产物2;
(3)在催化剂作用下,使得步骤(2)得到的产物2与多元醇进行反应,制得所述全氟聚醚基助剂。
根据本发明的进一步实施方式,所述制备方法包括以下步骤:
(1)全氟聚醚羧酸或全氟聚醚酯化合物与含有醇羟基的有机胺化合物在80℃~200℃温度下反应3~5小时,制得产物1,其中,全氟聚醚化合物中羰基和有机胺化合物中醇羟基的官能团摩尔比为1:1;
(2)在催化剂作用下,使得产物1与含有至少二个NCO基的异氰酸酯类化合物在80℃~120℃温度下反应3~5小时,制得产物2,其中,异氰酸酯类化合物中NCO和产物1中羟基的官能团摩尔比为3:1~2:1;
(3)在催化剂作用下,使得产物2与多元醇在80℃~120℃温度下反应3~5小时,制得所述全氟聚醚基防涂鸦助剂,其中,多元醇中OH和产物2中NCO的官能团摩尔比为3:1~2:1;
所述催化剂为有机锡催化剂。优选地,所述催化剂为二月桂酸二丁基锡。
根据本发明的又进一步实施方式,所述制备方法为在氮气保护下,全氟聚醚羧酸或全氟聚醚酯化合物与含有醇羟基的有机胺化合物在80℃~200℃温度下反应3~5小时,然后加入含有至少二个NCO基的异氰酸酯化合物和催化剂,在80℃~120℃温度下反应3~5小时,再加入多元醇,在80℃~120℃温度下反应3~5小时,反应完成后得到所述全氟聚醚基助剂。
所述催化剂的投料质量占总原料量的0.1~1%。
所述全氟聚醚酯化合物是指全氟聚醚甲酯或全氟聚醚乙酯或二者的混合。
所述含有醇羟基的有机胺化合物为含有醇羟基的伯胺化合物和/或含有醇羟基的仲胺化合物。具体为乙醇胺、丙醇胺、丁醇胺、二乙醇胺、二甘醇胺中的一种或多种。
所述含有至少二个NCO基的异氰酸酯类化合物包括异氰酸酯单体、异氰酸酯二聚体、异氰酸酯三聚体。例如异佛尔酮二异氰酸酯及其三聚体,甲苯二异氰酸酯及其二聚体、三聚体,六亚甲基二异氰酸酯及其二聚体、三聚体,二环己基甲烷二异氰酸酯中的一种或多种的组合。
所述多元醇为聚醚多元醇、聚酯多元醇中的一种或多种。例如聚四氢呋喃醚二醇、聚氧化丙烯二醇、聚氧化乙烯二醇、聚氧化丙烯-氧化乙烯二醇、聚三亚甲基醚二醇、聚己二酸乙二醇酯二醇、聚己二酸二甘醇酯二醇、聚碳酸酯二醇、聚己丙酯多元醇中的一种或多种的组合。
本发明中,所述涂料的原料配方中,所述聚酯多元醇为羟值为50~300mgKOH/g的聚酯多元醇。可以选取拜耳科思创公司的1100、800、华峰公司的PE-1280S等聚酯多元醇。
本发明中,所述涂料的原料配方中,所述异氰酸酯为六亚甲基二异氰酸酯及其二聚体、三聚体,异佛尔酮二异氰酸酯及其三聚体,二环己基甲烷二异氰酸酯中的一种或多种的组合。
本发明中,所述涂料的原料配方中,所述催化剂为二月桂酸二丁基锡。
本发明中,所述溶剂可为制备涂料的常用溶剂,如乙酸丁酯。
本发明中,全部所述的原料均可通过商购和/或采取已知的手段来制备得到,没有加以特别说明时,均满足标准化工产品要求。
本发明采取又一技术方案:一种上述涂料的制备方法,所述制备方法为:按配方,先将聚酯多元醇、异氰酸酯、全氟聚醚基助剂、催化剂、溶剂混合,搅拌反应,反应完成后即得所述涂料。
由于上述技术方案的实施,本发明与现有技术相比具有如下优点:
本发明的涂料通过在涂料配方中添加特定全氟聚醚基助剂,该助剂以全氟聚醚羧酸或全 氟聚醚酯化合物为原料,避免使用制备工艺中存在较大安全隐患的全氟聚醚基亚甲基醇为原料,且在全氟聚醚分子链末端嫁接聚氨酯链段、末端引入了反应活性基团醇羟基,克服了现有技术中全氟聚醚基抗污树脂与涂料配方的相溶性和反应性差等缺点,提高涂料抗污性,避免漆膜雾影的出现。
附图说明
图1为实施例1的PFPE-1的核磁H1NMR分析谱图。
具体实施方式
下面结合具体实施例对本发明做进一步详细的说明,但本发明并不限于以下实施例。
实施例1
本实施例提供一种全氟聚醚基助剂1#试样(PFPE-1),其制备方法如下:
在氮气保护下,将30.6g乙醇胺和500g全氟聚醚甲酯加入不锈钢反应釜,缓慢升温至120℃,保温反应4小时,然后在0.5kPa的真空度下脱除低沸物;将上述所得产品物料冷却至80℃,缓慢加入111.2g异佛尔酮二异氰酸酯(IPDI)和2g二月桂酸二丁基锡(DBTL),在80℃条件下保温反应4小时;再缓慢加入500g聚四氢呋喃醚二醇(简称PTHF,分子量是1000g/mol),在100℃条件下反应4小时,制备出产物PFPE-1。
对产物PFPE-1化合物进行核磁H1NMR分析,PFPE-1的H1NMR分析结果如图1所示,由图1可知:在1.1~1.2ppm、1.5ppm、3.4ppm、3.0和3.5ppm、4.0和4.4ppm出现位移峰,其中,1.1~1.2ppm处的化学位移峰归属于IPDI分子环上的取代甲基CH3;1.5ppm处的化学位移峰归属于聚四氢呋喃醚二醇链节中的中间的两个亚甲基CH2;3.4ppm处的化学位移峰归属于聚四氢呋喃醚二醇链节中的靠近氧原子的两个亚甲基CH2;3.0和3.5ppm处杂乱的化学位移峰归属于与酰胺基直接相连的次甲基CH和亚甲基CH2;4.0和4.4ppm处的化学位移峰归属于与胺基甲酸酯键中氧原子直接相连的亚甲基CH2
实施例2
本实施例提供一种全氟聚醚基助剂2#试样(PFPE-2)。
按照实施例1所示的步骤和工艺,将IPDI的质量更换为222.4g,乙醇胺更换为52.5g二乙醇胺,PTHF的质量更换为1000g,其余条件和质量均与实施例1相同,制备全氟聚醚基助剂2#试样(PFPE-2)。
实施例3
本实施例提供一种全氟聚醚基助剂3#试样(PFPE-3)。
按照实施例1所示的步骤和工艺,将IPDI的质量更换为222.4g,乙醇胺更换为52.5g二乙醇胺,PTHF更换为2000g聚己二酸二甘醇酯二醇(简称PDA,分子量是2000g/mol),其余条件和质量均与实施例1相同,制备全氟聚醚基助剂3#试样(PFPE-3)。
对比例1
本对比例提供一种全氟聚醚基助剂4#试样(PFPE-4)。
按照实施例1所示的步骤和工艺,将PTHF更换为58.0g丙烯酸羟乙酯(简称HEA),其余条件和质量均与实施例1相同,制备全氟聚醚基助剂4#试样(PFPE-4)。
对比例2
本对比例提供一种全氟聚醚基助剂5#试样(PFPE-5)。
按照实施例1所示的步骤和工艺,将PTHF更换为45.2g丙烯酰氯,不使用IPDI原料,其余条件和质量均与实施例1相同,全氟聚醚基助剂5#试样(PFPE-5)。
涂料的制备
按照表1所示的配方(各组分添加量以重量份计)进行复配聚氨酯涂料(PU漆),再将涂料喷涂于铝基涂料测试板上,并置于80℃烘箱内烘烤1小时。表中,N3300代表德国拜耳生产的脂肪族聚异氰酸酯(HDI三聚体),PE-1280S代表华峰公司生产的聚酯多元醇(羟基为80mg KOH/g,分子量为1300g/mol)。
涂料漆膜性能测试
漆膜外观
在天然光线下进行目测,观察漆膜的透明度和均一度,以及是否有雾化现象,并按照如下标准进行分级标示:
1级:表示漆膜完全透明,漆膜平整均一,无任何雾化,表面没有针孔或桔皮;
2级:表示漆膜透明,漆膜平整均一,无雾化,表面局部有针孔或桔皮;
3级:表示漆膜透明,漆膜平整,局部有雾化,表面没有无针孔或桔皮;
4级:表示漆膜透明,雾化较严重,表面没有无针孔或桔皮。
漆膜防涂鸦测试方法:采用得力油性黑色记号笔(红色、蓝色和黑色)在漆膜表面涂鸦并在室温下干燥4小时后,用干纸巾擦试漆膜表面的污渍,观察漆膜表面是否留有污渍。按照如下标准进行分级标示:
1级:表示可以容易擦去污渍,并且漆膜内部无任何残留;
2级:表示可以擦去污渍,但是比较费力,并且漆膜内部无任何残留;
3级:表示不能擦去污渍。
表1为涂料的配方和性能测试结果
通过涂料1~5与空白试样涂料6相对比,可以看出在涂料配方中引入PFPE可以显著提升防涂鸦性能,并且避免了桔皮和针孔问题的发生;涂料4和涂料5分别采用了与PU漆体系相溶性较差抗污助剂PFPE-4和PFPE-5,虽然所获得的漆膜表面无针孔和桔皮,但是涂层透明度较差且有雾化现象;涂料7加入了少量的抗污助剂PFPE-4,并没有影响PU漆的外观,然而由于加入量过少,所得涂料的耐污性能并没有得到提升;通过对比涂料1~3可以看出,PFPE含量的增加有利于防污性能的提升,便是PFPE含量过大会导致漆膜外观透明度下降,涂料2获得了最佳的透明度和防涂鸦性能。
以上对本发明做了详尽的描述,其目的在于让熟悉此领域技术的人士能够了解本发明的内容并加以实施,并不能以此限制本发明的保护范围,且本发明不限于上述的实施例,凡根据本发明的精神实质所作的等效变化或修饰,都应涵盖在本发明的保护范围之内。

Claims (10)

1.一种涂料,其特征在于:按重量百分含量计,所述涂料的原料配方包括:
所述全氟聚醚基助剂的结构式如式Ⅰ所示,
其中,n为自然数且2≤n≤30;
X为或-HN-R2,R1、R2分别为含有聚氨酯结构的取代基,且X的末端含有醇羟基。
2.根据权利要求1所述的涂料,其特征在于:所述R1、R2独立地选自-R3-O-CO-NH-R4-NH-CO-O-R5-OH,其中,R3a、e为小于等于10的正整数;-CO-NH-R4-NH-CO-为含有至少二个NCO基的异氰酸酯类化合物单元;-O-R5-OH为多元醇单元。
3.根据权利要求2所述的涂料,其特征在于:所述R3为-CH2CH2-或-CH2CH2-O-CH2CH2-。
4.根据权利要求2所述的涂料,其特征在于:所述异氰酸酯类化合物为异氰酸酯单体、异氰酸酯二聚体、异氰酸酯三聚体中的一种或多种的组合。
5.根据权利要求4所述的涂料,其特征在于:所述异氰酸酯类化合物为异佛尔酮二异氰酸酯及其二聚体、三聚体,甲苯二异氰酸酯及其二聚体、三聚体,六亚甲基二异氰酸酯及其二聚体、三聚体,二环己基甲烷二异氰酸酯中的一种或多种的组合。
6.根据权利要求2所述的涂料,其特征在于:所述多元醇为聚醚多元醇、聚酯多元醇中的一种或多种的组合。
7.根据权利要求6所述的涂料,其特征在于:所述多元醇为聚四氢呋喃醚二醇、聚氧化丙烯二醇、聚氧化乙烯二醇、聚氧化丙烯-氧化乙烯二醇、聚三亚甲基醚二醇、聚己二酸乙二醇酯二醇、聚己二酸二甘醇酯二醇、聚碳酸酯二醇、聚己丙酯多元醇中的一种或多种的组合。
8.根据权利要求1所述的涂料,其特征在于:所述全氟聚醚基助剂为如下结构式表示的化合物中的一种:
其中,b、c、d为正整数。
9.根据权利要求1所述的涂料,其特征在于:所述聚酯多元醇为羟值为50~300mgKOH/g的聚酯多元醇。
10.根据权利要求1所述的涂料,其特征在于:所述异氰酸酯为六亚甲基二异氰酸酯及其二聚体、三聚体,异佛尔酮二异氰酸酯及其三聚体,二环己基甲烷二异氰酸酯中的一种或多种。
CN201610631042.4A 2016-08-04 2016-08-04 一种涂料及其制备方法 Active CN106243969B (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610631042.4A CN106243969B (zh) 2016-08-04 2016-08-04 一种涂料及其制备方法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610631042.4A CN106243969B (zh) 2016-08-04 2016-08-04 一种涂料及其制备方法

Publications (2)

Publication Number Publication Date
CN106243969A true CN106243969A (zh) 2016-12-21
CN106243969B CN106243969B (zh) 2018-06-01

Family

ID=58077679

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610631042.4A Active CN106243969B (zh) 2016-08-04 2016-08-04 一种涂料及其制备方法

Country Status (1)

Country Link
CN (1) CN106243969B (zh)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108329820A (zh) * 2018-01-03 2018-07-27 中车青岛四方机车车辆股份有限公司 一种聚氨酯涂料
CN112574390A (zh) * 2021-03-01 2021-03-30 太仓中化环保化工有限公司 一种具有抗指纹功能的高耐磨uv树脂及其制备方法
CN113474424A (zh) * 2019-02-01 2021-10-01 普莱克斯S.T.技术有限公司 用于保护金属部件的耐侵蚀和耐腐蚀的包覆型涂层系统

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1950427A (zh) * 2004-05-07 2007-04-18 3M创新有限公司 含有丙烯酰基的全氟聚醚
CN101143840A (zh) * 2007-09-14 2008-03-19 海洋化工研究院 含全氟烷基链段的多异氰酸酯的制备及应用
CN101528807A (zh) * 2004-07-01 2009-09-09 3M创新有限公司 硬涂料组合物及其方法
CN102686642A (zh) * 2009-09-16 2012-09-19 3M创新有限公司 氟化涂料和用其制作的底片
CN103328528A (zh) * 2010-12-10 2013-09-25 Ppg俄亥俄工业股份有限公司 显示理想外观和防指纹特性的色漆加清漆涂料系统及相关方法
JP2016065233A (ja) * 2014-09-19 2016-04-28 荒川化学工業株式会社 缶内面塗料用樹脂組成物

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1950427A (zh) * 2004-05-07 2007-04-18 3M创新有限公司 含有丙烯酰基的全氟聚醚
CN101528807A (zh) * 2004-07-01 2009-09-09 3M创新有限公司 硬涂料组合物及其方法
CN101143840A (zh) * 2007-09-14 2008-03-19 海洋化工研究院 含全氟烷基链段的多异氰酸酯的制备及应用
CN102686642A (zh) * 2009-09-16 2012-09-19 3M创新有限公司 氟化涂料和用其制作的底片
CN103328528A (zh) * 2010-12-10 2013-09-25 Ppg俄亥俄工业股份有限公司 显示理想外观和防指纹特性的色漆加清漆涂料系统及相关方法
JP2016065233A (ja) * 2014-09-19 2016-04-28 荒川化学工業株式会社 缶内面塗料用樹脂組成物

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108329820A (zh) * 2018-01-03 2018-07-27 中车青岛四方机车车辆股份有限公司 一种聚氨酯涂料
CN113474424A (zh) * 2019-02-01 2021-10-01 普莱克斯S.T.技术有限公司 用于保护金属部件的耐侵蚀和耐腐蚀的包覆型涂层系统
CN112574390A (zh) * 2021-03-01 2021-03-30 太仓中化环保化工有限公司 一种具有抗指纹功能的高耐磨uv树脂及其制备方法
CN112574390B (zh) * 2021-03-01 2021-06-29 太仓中化环保化工有限公司 一种具有抗指纹功能的高耐磨uv树脂及其制备方法

Also Published As

Publication number Publication date
CN106243969B (zh) 2018-06-01

Similar Documents

Publication Publication Date Title
CN106220839B (zh) 一种全氟聚醚基防涂鸦助剂及其制备方法
CN104559617B (zh) 一种涂覆型水性双组分氟碳涂料及其制备和应用
CN109824555B (zh) 一种氨基磺酸及其制备方法与应用
CN100460435C (zh) (封端)多异氰酸酯组合物及使用该组合物的涂料组合物
Pathak et al. Non-isocyanate polyurethane (NIPU) from tris-2-hydroxy ethyl isocyanurate modified fatty acid for coating applications
DK2668240T3 (en) Moisturizing and dispersing agent, method of preparation and use
CN112574390B (zh) 一种具有抗指纹功能的高耐磨uv树脂及其制备方法
CN103890027B (zh) 氟化水-油排斥剂
CN101775144B (zh) 氟硅树脂及其制备方法和防污涂料
CN109897176B (zh) 一种全氟聚醚硅氧烷化合物及其合成方法和应用
CN106243969A (zh) 一种涂料及其制备方法
CN102757533B (zh) 一种水性聚氨酯乳液及其制备方法和一种双组份水性银粉涂料组合物
CN107531871A (zh) 含氟化合物、光固化性组合物、涂布液、硬质涂层形成用组合物以及物品
CN105482604A (zh) 一种水性防涂鸦涂料及其制备方法
CN102212307A (zh) 双组份聚氨酯防水涂料及其制备方法
CN110358440A (zh) 一种零voc水性聚氨酯丙烯酸酯木器漆及其制备方法
CN106380569A (zh) 一种水性聚氨酯防眩光涂层材料及其制备方法
CN108624105A (zh) 一种水溶性防污防涂鸦助剂的制备方法
CN104558580A (zh) 含氟超支化聚酯马来酸酯及其制备、用途和涂料组合物
CN105440238A (zh) 适合作为分散剂或防沉降剂的加合化合物
CN109180904A (zh) 一种桐油基阳离子型水性聚氨酯乳液及其制备方法和应用
CN105085890B (zh) 一种亲水性超支化的封闭型异氰酸酯及其制备方法和其在涂料中的应用
CN109504266A (zh) 一种基于生物基聚合物改性的快干无溶剂聚氨酯漆及其制备方法
CN103044649A (zh) 一种含氟阳离子水性聚氨酯及其制备方法
CN109096847B (zh) 一种水性高延长性防爆涂料的组成物

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant