CN105369631A - 一种合成革用无黄变高光油皮及其制备方法 - Google Patents

一种合成革用无黄变高光油皮及其制备方法 Download PDF

Info

Publication number
CN105369631A
CN105369631A CN201510990351.6A CN201510990351A CN105369631A CN 105369631 A CN105369631 A CN 105369631A CN 201510990351 A CN201510990351 A CN 201510990351A CN 105369631 A CN105369631 A CN 105369631A
Authority
CN
China
Prior art keywords
synthetic leather
gloss oil
leather
xanthochromia
molecular weight
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.)
Pending
Application number
CN201510990351.6A
Other languages
English (en)
Inventor
陈勇刚
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.)
Jiangsu Baoze Polymer Materials Co Ltd
Original Assignee
Jiangsu Baoze Polymer Materials 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 Jiangsu Baoze Polymer Materials Co Ltd filed Critical Jiangsu Baoze Polymer Materials Co Ltd
Priority to CN201510990351.6A priority Critical patent/CN105369631A/zh
Publication of CN105369631A publication Critical patent/CN105369631A/zh
Priority to PCT/CN2016/106294 priority patent/WO2017107709A1/zh
Pending legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/564Polyureas, polyurethanes or other polymers having ureide or urethane links; Precondensation products forming them
    • D06M15/572Reaction products of isocyanates with polyesters or polyesteramides
    • 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
    • C08G18/08Processes
    • C08G18/10Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
    • C08G18/12Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step using two or more compounds having active hydrogen in the first polymerisation step
    • 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
    • C08G18/30Low-molecular-weight compounds
    • C08G18/32Polyhydroxy compounds; Polyamines; Hydroxyamines
    • 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
    • C08G18/4236Polycondensates having carboxylic or carbonic ester groups in the main chain containing only aliphatic groups
    • C08G18/4238Polycondensates having carboxylic or carbonic ester groups in the main chain containing only aliphatic groups derived from dicarboxylic acids and dialcohols
    • 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
    • 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
    • C08G18/6633Compounds of group C08G18/42
    • C08G18/6637Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38
    • C08G18/664Compounds of group C08G18/42 with compounds of group C08G18/32 or polyamines of C08G18/38 with compounds of group C08G18/3203
    • 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
    • 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

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Treatment And Processing Of Natural Fur Or Leather (AREA)
  • Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)

Abstract

本发明提供一种合成革用无黄变高光油皮,其用于合成革的后段工艺,包含以下组分:1000分子量BG-AA二元醇、BDO、IPDI、DMF、反应型二甲基硅油和IPDA。本发明还提供一种合成革用无黄变高光油皮的制备方法。本发明的合成革用无黄变高光油皮的各组分相互协调、共同作用,该合成革用无黄变高光油皮具有高光泽,手感滑爽,膜厚感强,有水晶透感的特点,且由于是脂肪族树脂,不会黄变,物性好。本发明的合成革用无黄变高光油皮是后段处理的一种新型材料,能够用于现有的合成革生产线,工艺简单,无需改变生产设备,不会增加生产成本。本发明的合成革用无黄变高光油皮的流平性好,抗热回粘出色,且比普通高光光油更透。

Description

一种合成革用无黄变高光油皮及其制备方法
技术领域
本发明涉及合成革用表面处理剂领域,具体涉及一种合成革用无黄变高光油皮。本发明还涉及一种合成革用无黄变高光油皮的制备方法。
背景技术
合成革目前在各种领域都可替代真皮。合成革物理性好、耐曲折、柔软、抗拉伸强度大,且也有一定的透气性。合成革表面需用一些处理剂改善其表面色泽、光泽、手感。
合成革表面处理剂可以根据产品的类别进行表面涂饰,其可以改善合成革的亮度、色泽以及手感。然而,随着消费者对皮革表面的色泽和手感要求越来越高,不但要增加合成革的触感,还要保证合成革表面的亮度及色泽度等。而现有的表面处理剂已经不能满足消费者对合成革的亮度及手感日益增加的要求,因此急需一种既能提高合成革触感,又能提高合成革的手感,亮度、光泽等综合效果的处理剂。
发明内容
为了解决上述问题及缺陷,本发明的目的在于提供一种合成革用无黄变高光油皮。本发明还提供一种合成革用无黄变高光油皮的制备方法。
本发明的合成革用无黄变高光油皮通过以下技术方案实现:
一种合成革用无黄变高光油皮,其用于合成革的后段工艺,包含以下组分:1000分子量BG-AA二元醇、BDO、IPDI、DMF、反应型二甲基硅油和IPDA。
进一步地,所述1000分子量BG-AA二元醇与BDO的重量比为1∶0.06-0.5,所述1000分子量BG-AA二元醇与IPDI的重量比为1∶0.6-2,所述1000分子量BG-AA二元醇与DMF的重量比为1∶3.5-6.5,所述1000分子量BG-AA二元醇与反应型二甲基硅油的重量比为1∶0.03-0.1,所述1000分子量BG-AA二元醇与IPDA的重量比为1∶0.2-0.5。
本发明还提供一种合成革用无黄变高光油皮的制备方法,包含以下步骤:
(1)按重量配比称取各组分物质:将1000分子量BG-AA二元醇、BDO、IPDI、DMF、和反应型二甲基硅油混合,加热搅拌进行反应;
(2)当步骤(1)所得的混合物的异氰酸酯(-NCO)的百分含量小于0.3%时,加入DMF降温至室温;
(3)在步骤(2)所得的混合物中滴加IPDA,搅拌均匀,即得所述合成革用无黄变高光油皮。
进一步地,所述1000分子量BG-AA二元醇与BDO的重量比为1∶0.06-0.5。
进一步地,所述1000分子量BG-AA二元醇与IPDI的重量比为1∶0.6-2。
进一步地,所述1000分子量BG-AA二元醇与DMF的重量比为1∶3.5-6.5。
进一步地,所述1000分子量BG-AA二元醇与反应型二甲基硅油的重量比为1∶0.03-0.1。
进一步地,所述1000分子量BG-AA二元醇与IPDA的重量比为1∶0.2-0.5
进一步地,步骤(1)的反应温度为60℃-80℃。
进一步地,步骤(1)的反应时间为3-5小时。
由于采用以上技术方案,本发明与现有技术相比具有如下有益技术效果:
(1)本发明的合成革用无黄变高光油皮的各组分相互协调、共同作用,该合成革用无黄变高光油皮具有高光泽,手感滑爽,膜厚感强,有水晶透感的特点,且由于是脂肪族树脂,不会黄变,物性好;
(2)本发明的合成革用无黄变高光油皮是后段处理的一种新型材料,能够用于现有的合成革生产线,工艺简单,无需改变生产设备,不会增加生产成本;
(3)由于本发明的合成革用无黄变高光油皮具有无黄变的特点,因此其处理一版,烘干后涂膜量相当于普通光油皮处理的2-3版;
(4)本发明的合成革用无黄变高光油皮的流平性好,抗热回粘出色,且比普通高光光油更透。
具体实施方式
为了使本发明的目的、技术方案及优点更加清楚明白,下面结合实施例,对本发明进行进一步详细说明。应当理解,此处所描述的具体实施例仅用以解释本发明,并不用于限定本发明。
实施例1
合成革用无黄变高光油皮由以下配比的组分组成:1000分子量BG-AA二元醇(聚己二酸丁二醇酯)10重量份、BDO(1,4-丁二醇)1重量份、IPDI(异佛尔酮二异氰酸酯)10重量份、DMF(N,N-二甲基甲酰胺)55重量份、反应型二甲基硅油0.5重量份和IPDA(异佛尔酮二胺)3重量份。
以上合成革用无黄变高光油皮的制备方法为:
(1)将10重量份的1000分子量BG-AA二元醇、1重量份的BDO、10重量份的IPDI、55重量份的DMF、0.5重量份的反应型二甲基硅油混合,在80℃下搅拌反应3小时;
(2)当步骤(1)所得的混合物的-NCO的百分含量小于0.3%时,加入55重量份的DMF降温至室温;
(3)在步骤(2)所得的混合物中滴加3重量份的IPDA,搅拌至少30分钟至混合物混合均匀,即得所述合成革用无黄变高光油皮。所得到的合成革用无黄变高光油皮的性能指标见表1。上述制备过程中所采用的搅拌等方法均为本领域内惯用的方法。
实施例2
合成革用无黄变高光油皮由以下配比的组分组成:1000分子量BG-AA二元醇12重量份、BDO(1,4-丁二醇)2重量份、IPDI(异佛尔酮二异氰酸酯)14重量份、DMF(N,N-二甲基甲酰胺)58重量份、反应型二甲基硅油0.7重量份和IPDA(异佛尔酮二胺)4重量份。
以上合成革用无黄变高光油皮的制备方法为:
(1)将12重量份的1000分子量BG-AA二元醇、2重量份的BDO、14重量份的IPDI、58重量份的DMF、0.7重量份的反应型二甲基硅油混合,在70℃下搅拌反应4小时;
(2)当步骤(1)所得的混合物的-NCO的百分含量小于0.3%时,加入58重量份的DMF降温至室温;
(3)在步骤(2)所得的混合物中滴加4重量份的IPDA,搅拌至少30分钟至混合物混合均匀,即得所述合成革用无黄变高光油皮。所得到的合成革用无黄变高光油皮的性能指标见表1。上述制备过程中所采用的搅拌等方法均为本领域内惯用的方法。
实施例3
合成革用无黄变高光油皮由以下配比的组分组成:1000分子量BG-AA二元醇14重量份、BDO(1,4-丁二醇)4重量份、IPDI(异佛尔酮二异氰酸酯)16重量份、DMF(N,N-二甲基甲酰胺)62重量份、反应型二甲基硅油0.8重量份和IPDA(异佛尔酮二胺)4重量份。
以上合成革用无黄变高光油皮的制备方法为:
(1)将14重量份的1000分子量BG-AA二元醇、4重量份的BDO、16重量份的IPDI、62重量份的DMF、0.8重量份的反应型二甲基硅油混合,在60℃下搅拌反应3小时;
(2)当步骤(1)所得的混合物的-NCO的百分含量小于0.3%时,加入62重量份的DMF降温至室温;
(3)在步骤(2)所得的混合物中滴加4重量份的IPDA,搅拌至少30分钟至混合物混合均匀,即得所述合成革用无黄变高光油皮。所得到的合成革用无黄变高光油皮的性能指标见表1。上述制备过程中所采用的搅拌等方法均为本领域内惯用的方法。
实施例4
合成革用无黄变高光油皮由以下配比的组分组成:1000分子量BG-AA二元醇15重量份、BDO(1,4-丁二醇)5重量份、IPDI(异佛尔酮二异氰酸酯)20重量份、DMF(N,N-二甲基甲酰胺)65重量份、反应型二甲基硅油1重量份和IPDA(异佛尔酮二胺)5重量份。
以上合成革用无黄变高光油皮的制备方法为:
(1)将15重量份的1000分子量BG-AA二元醇、5重量份的BDO、20重量份的IPDI、65重量份的DMF、1重量份的反应型二甲基硅油混合,在60℃下搅拌反应3小时;
(2)当步骤(1)所得的混合物的-NCO的百分含量小于0.3%时,加入65重量份的DMF降温至室温;
(3)在步骤(2)所得的混合物中滴加5重量份的IPDA,搅拌至少30分钟至混合物混合均匀,即得所述合成革用无黄变高光油皮。所得到的合成革用无黄变高光油皮的性能指标见表1。上述制备过程中所采用的搅拌等方法均为本领域内惯用的方法。
表1
以上所述仅为本发明的较佳实施例,并非用来限定本发明的实施范围;如果不脱离本发明的精神和范围,对本发明进行修改或者等同替换,均应涵盖在本发明权利要求的保护范围当中。

Claims (10)

1.一种合成革用无黄变高光油皮,其用于合成革的后段工艺,其特征在于,包含以下组分:1000分子量BG-AA二元醇、BDO、IPDI、DMF、反应型二甲基硅油和IPDA。
2.根据权利要求1所述的合成革用无黄变高光油皮,其特征在于,所述1000分子量BG-AA二元醇与BDO的重量比为1∶0.06-0.5,所述1000分子量BG-AA二元醇与IPDI的重量比为1∶0.6-2,所述1000分子量BG-AA二元醇与DMF的重量比为1∶3.5-6.5,所述1000分子量BG-AA二元醇与反应型二甲基硅油的重量比为1∶0.03-0.1,所述1000分子量BG-AA二元醇与IPDA的重量比为1∶0.2-0.5。
3.一种合成革用无黄变高光油皮的制备方法,其特征在于,包含以下步骤:
(1)按重量配比称取各组分物质:将1000分子量BG-AA二元醇、BDO、IPDI、DMF、和反应型二甲基硅油混合,加热搅拌进行反应;
(2)当步骤(1)所得的混合物的-NCO的百分含量小于0.3%时,加入DMF降温至室温;
(3)在步骤(2)所得的混合物中滴加IPDA,搅拌均匀,即得所述合成革用无黄变高光油皮。
4.根据权利要求3所述的合成革用无黄变高光油皮,其特征在于,所述1000分子量BG-AA二元醇与BDO的重量比为1∶0.06-0.5。
5.根据权利要求3所述的合成革用无黄变高光油皮,其特征在于,所述1000分子量BG-AA二元醇与IPDI的重量比为1∶0.6-2。
6.根据权利要求3所述的合成革用无黄变高光油皮,其特征在于,所述1000分子量BG-AA二元醇与DMF的重量比为1∶3.5-6.5。
7.根据权利要求3所述的合成革用无黄变高光油皮,其特征在于,所述1000分子量BG-AA二元醇与反应型二甲基硅油的重量比为1∶0.03-0.1。
8.根据权利要求3所述的合成革用无黄变高光油皮,其特征在于,所述1000分子量BG-AA二元醇与IPDA的重量比为1∶0.2-0.5。
9.根据权利要求3所述的合成革用无黄变高光油皮,其特征在于,步骤(1)的反应温度为60℃-80℃。
10.根据权利要求3所述的合成革用无黄变高光油皮,其特征在于,步骤(1)的反应时间为3-5小时。
CN201510990351.6A 2015-12-25 2015-12-25 一种合成革用无黄变高光油皮及其制备方法 Pending CN105369631A (zh)

Priority Applications (2)

Application Number Priority Date Filing Date Title
CN201510990351.6A CN105369631A (zh) 2015-12-25 2015-12-25 一种合成革用无黄变高光油皮及其制备方法
PCT/CN2016/106294 WO2017107709A1 (zh) 2015-12-25 2016-11-17 一种合成革用无黄变高光油皮及其制备方法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201510990351.6A CN105369631A (zh) 2015-12-25 2015-12-25 一种合成革用无黄变高光油皮及其制备方法

Publications (1)

Publication Number Publication Date
CN105369631A true CN105369631A (zh) 2016-03-02

Family

ID=55372225

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201510990351.6A Pending CN105369631A (zh) 2015-12-25 2015-12-25 一种合成革用无黄变高光油皮及其制备方法

Country Status (2)

Country Link
CN (1) CN105369631A (zh)
WO (1) WO2017107709A1 (zh)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2017107709A1 (zh) * 2015-12-25 2017-06-29 江苏宝泽高分子材料股份有限公司 一种合成革用无黄变高光油皮及其制备方法

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101831048A (zh) * 2010-05-05 2010-09-15 嘉兴市罗星化工有限公司 高光聚氨酯类树脂和用途
CN102060973A (zh) * 2010-12-21 2011-05-18 浙江华峰合成树脂有限公司 一种合成革用耐寒型高耐磨耗聚氨酯树脂
CN103755910A (zh) * 2013-12-27 2014-04-30 浙江华峰合成树脂有限公司 耐寒耐酒精不黄变革用聚氨酯树脂及其制法
CN104313888A (zh) * 2014-11-14 2015-01-28 江苏宝泽高分子材料股份有限公司 一种合成革用耐黄变油皮树脂及其制备方法
CN104672740A (zh) * 2015-03-04 2015-06-03 建德市顺发化工助剂有限公司 光亮油皮合成革专用的聚氨酯树脂及其制备方法

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN100402574C (zh) * 2006-05-23 2008-07-16 山东圣光化工集团有限公司 聚硅氧烷-聚醚共聚物改性水性聚氨酯的制造方法
KR20100099701A (ko) * 2007-12-25 2010-09-13 닛카카가쿠가부시키가이샤 인공 피혁용 수계 우레탄 수지 조성물, 인공 피혁의 제조 방법, 및 인공 피혁
CN102898613B (zh) * 2012-11-09 2014-07-16 陕西邦希化工有限公司 水溶性有机硅改性聚氨酯树脂的制备方法
CN103319682B (zh) * 2013-07-11 2015-08-26 清远市美乐仕油墨有限公司 一种皮革用低光泽水性聚氨酯分散体及其制备方法和应用
CN105369631A (zh) * 2015-12-25 2016-03-02 江苏宝泽高分子材料股份有限公司 一种合成革用无黄变高光油皮及其制备方法

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101831048A (zh) * 2010-05-05 2010-09-15 嘉兴市罗星化工有限公司 高光聚氨酯类树脂和用途
CN102060973A (zh) * 2010-12-21 2011-05-18 浙江华峰合成树脂有限公司 一种合成革用耐寒型高耐磨耗聚氨酯树脂
CN103755910A (zh) * 2013-12-27 2014-04-30 浙江华峰合成树脂有限公司 耐寒耐酒精不黄变革用聚氨酯树脂及其制法
CN104313888A (zh) * 2014-11-14 2015-01-28 江苏宝泽高分子材料股份有限公司 一种合成革用耐黄变油皮树脂及其制备方法
CN104672740A (zh) * 2015-03-04 2015-06-03 建德市顺发化工助剂有限公司 光亮油皮合成革专用的聚氨酯树脂及其制备方法

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2017107709A1 (zh) * 2015-12-25 2017-06-29 江苏宝泽高分子材料股份有限公司 一种合成革用无黄变高光油皮及其制备方法

Also Published As

Publication number Publication date
WO2017107709A1 (zh) 2017-06-29

Similar Documents

Publication Publication Date Title
CN106609033B (zh) 一种热塑性聚氨酯组合物及其制备方法
CN104163909B (zh) 一种耐水解沙发革用聚氨酯树脂及其制备方法
CN103724583B (zh) 合成革耐高温特黑特雾处理剂用脂肪族聚氨酯树脂及其制备方法
CN106432667B (zh) 自消光柔感水性聚氨酯皮革涂饰剂及制备方法
CN101974141A (zh) 水性聚丙烯酸酯改性聚氨酯分散体的制备方法
CN105505280A (zh) Tpu热熔胶及其制备方法
CN105482054A (zh) 一种改性聚氨酯树脂及其制备方法
CN111944111B (zh) 一种水性自消光聚氨酯分散体和制备方法及其组合物
CN110183611A (zh) 一种水性聚氨酯自消光树脂及其制备方法、印花胶浆
CN104672740A (zh) 光亮油皮合成革专用的聚氨酯树脂及其制备方法
CN108192490B (zh) 一种水性复合树脂组合物、水性塑胶漆及其制备方法
CN103205898A (zh) 肤感聚氨酯皮革表面处理剂及其制备方法
CN102701999A (zh) 阳离子水性聚氨酯皮革涂饰剂及其制备方法
CN102733198B (zh) 水性聚氨酯光油及制备方法
CN109322169A (zh) 一种水性雾面、耐刮、柔软合成革
CN104893537A (zh) 一种具有高拉伸力涂层薄膜的水性聚氨酯涂料的生产工艺
CN113999367A (zh) 一种耐污uv固化水性聚氨酯丙烯酸酯分散体及其制备方法
CN106397678A (zh) 一种丙烯酸改性的水性聚氨酯及其制备方法和用途
CN105482439A (zh) 一种硅油改性聚氨酯手感剂及其制备方法与应用
CN104358131A (zh) 一种合成革用高温细羊巴树脂及其制备方法
CN105369631A (zh) 一种合成革用无黄变高光油皮及其制备方法
CN104047178B (zh) 一种合成革用绒感处理剂及其制备方法
CN112280450A (zh) 一种pvc人造革水性改色处理剂及其制备方法
CN111705522A (zh) 一种泼水型聚氯乙烯人造革及其制备方法
CN110922563A (zh) 一种泳衣印花用水性聚氨酯胶浆乳液及制备方法

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication

Application publication date: 20160302

RJ01 Rejection of invention patent application after publication