WO2017107710A1 - 一种合成革用水性高光光油及其制备方法 - Google Patents
一种合成革用水性高光光油及其制备方法 Download PDFInfo
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Definitions
- the invention relates to the field of surface treatment agents for synthetic leather, in particular to an aqueous high gloss varnish for synthetic leather.
- the invention also relates to a preparation method of an aqueous high gloss varnish for synthetic leather.
- Synthetic leather is currently a replacement for leather in a variety of fields. Synthetic leather has good physical properties, resistance to tortuosity, softness, high tensile strength, and also has a certain gas permeability. The surface of the synthetic leather needs some treatment agent to improve the surface color, luster and hand feeling.
- the synthetic leather surface treatment agent can be surface-coated according to the type of the product, which can improve the brightness, color and feel of the synthetic leather.
- the synthetic leather surface treatment agent can be surface-coated according to the type of the product, which can improve the brightness, color and feel of the synthetic leather.
- it is necessary not only to increase the touch of the synthetic leather, but also to ensure the brightness and color of the surface of the synthetic leather.
- the existing surface treatment agents can not meet the increasing demands of consumers for the brightness and feel of synthetic leather. Therefore, there is an urgent need for a comprehensive effect of improving the touch of synthetic leather and improving the feel, brightness and gloss of synthetic leather. Treatment agent.
- an object of the present invention is to provide an aqueous high gloss varnish for synthetic leather.
- the invention also provides a preparation method of water-based high gloss varnish for synthetic leather.
- the invention relates to a synthetic high-gloss glazing oil for use in the latter stage of synthetic leather, comprising the following components: 1000 molecular weight BG-AA glycol, DMPA, BDO, reactive dimethicone, IPDI, acetone, three Ethylamine, ethylenediamine, water, aqueous defoamer, leveling agent and thickener.
- the weight ratio of the 1000 molecular weight BG-AA glycol to DMPA is 1:1000-0.15
- the weight ratio of the 1000 molecular weight BG-AA glycol to BDO is 1:0.025-0.1
- the weight ratio of the 1000 molecular weight BG-AA glycol to the reactive dimethicone is 1 0.005-0.02
- the weight ratio of the 1000 molecular weight BG-AA glycol to IPDI is 1:0.5-1
- the weight ratio of the 1000 molecular weight BG-AA glycol to acetone is 1:0.1-0.3.
- the weight ratio of 1000 molecular weight BG-AA diol to triethylamine is 1:0.025-0.1, and the weight ratio of the 1000 molecular weight BG-AA diol to ethylenediamine is 1:0.05-0.15, the 1000 The weight ratio of the molecular weight BG-AA glycol to water is 1:2.5-4, and the weight ratio of the 1000 molecular weight BG-AA glycol to the aqueous antifoaming agent is 1:0.005-0.02, and the 1000 molecular weight BG-
- the weight ratio of the AA glycol to the leveling agent is 1:0.025-0.1, and the weight ratio of the 1000 molecular weight BG-AA glycol to the thickener is 1:0.075-0.2.
- the invention also provides a preparation method of the synthetic high-gloss glazing oil, comprising the following steps:
- the weight ratio of the 1000 molecular weight BG-AA glycol to DMPA is 1:0.05-0.15
- the weight ratio of the 1000 molecular weight BG-AA glycol to BDO is 1:0.025-0.1.
- the weight ratio of the 1000 molecular weight BG-AA diol to the reactive dimethyl silicone oil is 1:0.005-0.02, and the weight ratio of the 1000 molecular weight BG-AA glycol to IPDI is 1:0.5- 1.
- the weight ratio of the 1000 molecular weight BG-AA glycol to acetone is 1:0.1-0.3
- the weight ratio of the 1000 molecular weight BG-AA glycol to triethylamine is 1:0.025-0.1.
- the weight ratio of the 1000 molecular weight BG-AA glycol to ethylenediamine is 1:0.05-0.15, and the weight ratio of the 1000 molecular weight BG-AA glycol to water is 1:2.5-4.
- the weight ratio of the 1000 molecular weight BG-AA glycol to the aqueous antifoaming agent is 1:0.005-0.02, and the weight ratio of the 1000 molecular weight BG-AA glycol to the leveling agent is 1:0.025- 0.1, the weight ratio of the 1000 molecular weight BG-AA glycol to the thickener is 1:0.075-0.2.
- reaction temperature of the step (2) is from 60 ° C to 80 ° C, and the reaction time is from 4 to 6 hours.
- reaction temperature of the step (3) is from 30 ° C to 40 ° C, and the reaction time is from 30 to 50 minutes.
- the present invention has the following beneficial technical effects as compared with the prior art:
- the aqueous high gloss varnish of the present invention is a novel polyurethane system in which water is used as a dispersion medium instead of an organic solvent. Since water-based polyurethane uses water as a dispersion medium, the process does not require an organic solvent, so that it is environmentally friendly and has no health to the operator. Harmful, and water-based polyurethane has low odor, is not easy to burn, and the process is safe and reliable. Waterborne polyurethane uses water as solvent, has no pollution, is safe and reliable, has excellent mechanical properties, good compatibility and easy modification.
- the aqueous system of water-based polyurethane can be blended or copolymerized with other aqueous emulsions or copolymerized, which can reduce the cost or obtain a polyurethane emulsion with more diversified properties, thus bringing synthetic leather products with different styles and properties.
- aqueous polyurethane emulsion with more diversified properties, thus bringing synthetic leather products with different styles and properties.
- the finished product made by using the water-based high-gloss varnish of the invention has full hand feeling, soft texture, comfort, non-combustible, non-toxic, non-pollution and the like.
- the oxygen permeability, moisture permeability, low temperature resistance, dryness and wetness resistance, and aging resistance of the finished leather were compared with the synthetic leather after solvent-based polyurethane coating.
- the water-based polyurethane replaces the traditional solvent-based polyurethane to complete the finishing of the synthetic leather.
- the leather has better permeability, moisture permeability, low-temperature resistance, dry-wet resistance and the like. The whole process has no solvent emission and is environmentally friendly. ;
- the synthetic high-gloss glazing oil of the invention is a novel material for the latter stage treatment, and can be used in the existing synthetic leather production line, and the process is simple, no need to change the production equipment, and the production cost is not increased.
- Synthetic leather water-based high gloss varnish consists of the following components: 1000 molecular weight BG-AA glycol (polybutylene adipate) 150 parts by weight, DMPA (2,2-dimethylolpropionic acid) 10 parts by weight, 5 parts by weight of BDO (1,4-butanediol), 1 part by weight of reactive dimethyl silicone oil, 100 parts by weight of IPDI (isophorone diisocyanate), 20 parts by weight of acetone, and triethylamine 5 parts by weight, 10 parts by weight of ethylenediamine, 500 parts by weight of water, 1 part by weight of an aqueous antifoaming agent, 5 parts by weight of a leveling agent, and 15 parts by weight of a thickener.
- the preparation method of the above synthetic leather water-based high gloss varnish is:
- Synthetic leather water-based high gloss varnish consists of the following components: 1000 parts by weight of BG-AA glycol, 160 parts by weight of DMPA, 7 parts by weight of BDO, 1.5 parts by weight of reactive dimethyl silicone oil, IPDI 120 The parts by weight, 30 parts by weight of acetone, 8 parts by weight of triethylamine, 14 parts by weight of ethylenediamine, 550 parts by weight of water, 1.5 parts by weight of an aqueous antifoaming agent, 7 parts by weight of a leveling agent, and 18 parts by weight of a thickener.
- the preparation method of the above synthetic leather water-based high gloss varnish is:
- Synthetic leather water-based high gloss varnish consists of the following components: 1000 parts by weight of BG-AA glycol, 180 parts by weight of DMPA, 12 parts by weight of BDO, 2 parts by weight of reactive dimethicone, IPDI 140 Parts by weight, 35 parts by weight of acetone, 12 parts by weight of triethylamine, 18 parts by weight of ethylenediamine, 600 parts by weight of water, 2 parts by weight of an aqueous antifoaming agent, 12 parts by weight of a leveling agent, and 22 parts by weight of a thickener.
- the preparation method of the above synthetic leather water-based high gloss varnish is:
- Synthetic leather water-based high gloss varnish consists of the following components: 1000 molecular weight BG-AA glycol 200 parts by weight, DMPA 20 parts by weight, BDO 15 parts by weight, reactive dimethicone 3 parts by weight, IPDI 150 The parts by weight, 40 parts by weight of acetone, 15 parts by weight of triethylamine, 20 parts by weight of ethylenediamine, 600 parts by weight of water, 3 parts by weight of an aqueous antifoaming agent, 15 parts by weight of a leveling agent, and 25 parts by weight of a thickener.
- the preparation method of the above synthetic leather water-based high gloss varnish is:
- Example 1 Example 2 Example 3 Example 4 pH value 7.0 7.2 7.5 8.0 Exterior Light blue translucent liquid Light blue semi-liquid Light blue semi-liquid Light blue semi-liquid Viscosity (cps/25°C) 800 1000 1200 1500 stability No precipitation, no discoloration No precipitation, no discoloration No precipitation, no discoloration No precipitation, no discoloration Solvent system water water water water Solid content (%) 39 39.5 40 41
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Abstract
本发明提供一种合成革用水性高光光油,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、DMPA、BDO、反应型二甲基硅油、IPDI、丙酮、三乙胺、乙二胺、水、水性消泡剂、流平剂和增稠剂。本发明还提供一种合成革用水性高光光油的制备方法。本发明的水性高光光油的各组分相互协调、共同作用,处理后手感独特,用高光、高透,色泽清晰,综合效果佳,同时配出的喷涂稀释溶液有很好的储存稳定性,颜料不容易沉降。本发明的合成革用水性高光光油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。
Description
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水性高光光油。本发明还涉及一种合成革用水性高光光油的制备方法。
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水性高光光油。本发明还提供一种合成革用水性高光光油的制备方法。
本发明的合成革用水性高光光油通过以下技术方案实现:
一种合成革用水性高光光油,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、DMPA、BDO、反应型二甲基硅油、IPDI、丙酮、三乙胺、乙二胺、水、水性消泡剂、流平剂和增稠剂。
进一步地,所述1000分子量BG-AA二元醇与DMPA的重量比为
1∶0.05-0.15,所述1000分子量BG-AA二元醇与BDO的重量比为1∶0.025-0.1,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∶0.005-0.02,所述1000分子量BG-AA二元醇与IPDI的重量比为1∶0.5-1,所述1000分子量BG-AA二元醇与丙酮的重量比为1∶0.1-0.3,所述1000分子量BG-AA二元醇与三乙胺的重量比为1∶0.025-0.1,所述1000分子量BG-AA二元醇与乙二胺的重量比为1∶0.05-0.15,所述1000分子量BG-AA二元醇与水的重量比为1∶2.5-4,所述1000分子量BG-AA二元醇与水性消泡剂的重量比为1∶0.005-0.02,所述1000分子量BG-AA二元醇与流平剂的重量比为1∶0.025-0.1,所述1000分子量BG-AA二元醇与增稠剂的重量比为1∶0.075-0.2。
本发明还提供一种合成革用水性高光光油的制备方法,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、DMPA、BDO、反应型二甲基硅油混合,加热熔化;
(2)在步骤(1)所得的混合物中加入IPDI进行反应;
(3)当步骤(2)所得的混合物的-NCO的百分含量小于0.3%时,加入丙酮降温,然后在所得的混合物中加入三乙胺进行反应;
(4)将步骤(3)所得的混合物在高速分散下投入到水中,然后滴加乙二胺;
(5)在步骤(4)所得的混合物中加入水性消泡剂,流平剂和增稠剂,搅拌均匀,即得所述合成革用水性高光光油。
进一步地,所述1000分子量BG-AA二元醇与DMPA的重量比为1∶0.05-0.15,所述1000分子量BG-AA二元醇与BDO的重量比为1∶0.025-0.1。
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∶0.005-0.02,所述1000分子量BG-AA二元醇与IPDI的重量比为1∶0.5-1。
进一步地,所述1000分子量BG-AA二元醇与丙酮的重量比为1∶0.1-0.3,所述1000分子量BG-AA二元醇与三乙胺的重量比为1∶0.025-0.1。
进一步地,所述1000分子量BG-AA二元醇与乙二胺的重量比为1∶0.05-0.15,所述1000分子量BG-AA二元醇与水的重量比为1∶2.5-4。
进一步地,所述1000分子量BG-AA二元醇与水性消泡剂的重量比为1∶0.005-0.02,所述1000分子量BG-AA二元醇与流平剂的重量比为1∶0.025-0.1,所述1000分子量BG-AA二元醇与增稠剂的重量比为1∶0.075-0.2。
进一步地,步骤(2)的反应温度为60℃-80℃,反应时间为4-6小时。
进一步地,步骤(3)的反应温度为30℃-40℃,反应时间为30-50分钟。
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)本发明的水性高光光油是以水代替有机溶剂作为分散介质的新型聚氨酯体系,由于水性聚氨酯以水作分散介质,加工过程无需有机溶剂,因此对环境无污染,对操作人员无健康危害,并且水性聚氨酯气味小、不易燃烧,加工过程安全可靠。水性聚氨酯以水为溶剂,无污染、安全可靠、机械性能优良、相容性好、易于改性等优点;
(2)本发明的水性高光光油的各组分相互协调、共同作用,处理后手感独特,用高光、高透,色泽清晰,综合效果佳,同时配出的喷涂稀释溶液有很好的储存稳定性,颜料不容易沉降;
(3)水性聚氨酯体系中基本不残留有毒的异氰酸酯(-NCO)基团,由于水性聚氨酯无有毒有机溶剂,因此产品中无有毒溶剂残留,产品安全、环保,无出口限制;
(4)水性聚氨酯产品的透湿透汽性要远远好于同类的溶剂型聚氨酯产品,因为水性聚氨酯的亲水性强,因此和水的结合能力强,所以其产品
具有很好的透湿透汽性;
(5)水作连续相,使得水性聚氨酯体系粘度与聚氨酯树脂分子量无关,且比固含量相同的溶剂型聚氨酯溶液粘度低,加工方便,易操作;
(6)水性聚氨酯的水性体系可以与其它水性乳液共混或共聚共混或共聚,可降低成本或得到性能更为多样化的聚氨酯乳液,因此能带来风格和性能各异的合成革产品,满足各类消费者的需求;并且,由于近年来溶剂价格高涨和环保部门对有机溶剂使用和废物排放的严格限制,使水性聚氨酯取代溶剂型聚氨酯成为一个重要发展方向;
(7)使用本发明的水性高光光油制成的成品手感丰满,质地柔软,舒适,具有不燃、无毒、无污染等优点。将成革的透氧气性、透湿性、低温耐曲折性、耐干湿擦性、耐老化性等,与溶剂型聚氨酯涂饰后的合成革进行了对比研究。采用水性聚氨酯替代传统的溶剂型聚氨酯完成合成革的后整理,成革的透气性、透湿性、低温耐曲折性、耐干湿擦等性能均优于前者,整个工艺过程没有溶剂排放,环境友好;
(8)该产品还可根据需求进行二次研发,具有良好的市场应用价值;
(9)本发明的合成革用水性高光光油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。
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
合成革用水性高光光油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)150重量份、DMPA(2,2-二羟甲基丙酸)10重量份、BDO(1,4-丁二醇)5重量份、反应型二甲基硅油1重量份、IPDI(异佛尔酮二异氰酸酯)100重量份、丙酮20重量份、三乙胺5重量份、
乙二胺10重量份、水500重量份、水性消泡剂1重量份、流平剂5重量份和增稠剂15重量份。
以上合成革用水性高光光油的制备方法为:
(1)将150重量份的1000分子量BG-AA二元醇、10重量份的DMPA、5重量份的BDO、1重量份的反应型二甲基硅油混合,加热熔化;
(2)在步骤(1)所得的混合物中加入100重量份的IPDI在60℃反应6小时;
(3)当步骤(2)所得的混合物的-NCO的百分含量小于0.3%时,加入20重量份的丙酮降温至30℃,然后在所得的混合物中加入5重量份的三乙胺反应50分钟;
(4)将步骤(3)所得的混合物在高速分散下投入到500重量份的水中,然后滴加10重量份的乙二胺;
(5)在步骤(4)所得的混合物中加入1重量份的水性消泡剂,5重量份的流平剂和15重量份的增稠剂,搅拌至少30分钟至混合物混合均匀,即得所述合成革用水性高光光油。所得到的合成革用水性高光光油的性能指标见表1。上述制备过程中所采用的熔化、加热、搅拌、高速分散等方法均为本领域内惯用的方法。
实施例2
合成革用水性高光光油由以下配比的组分组成:1000分子量BG-AA二元醇160重量份、DMPA 14重量份、BDO 7重量份、反应型二甲基硅油1.5重量份、IPDI 120重量份、丙酮30重量份、三乙胺8重量份、乙二胺14重量份、水550重量份、水性消泡剂1.5重量份、流平剂7重量份和增稠剂18重量份。
以上合成革用水性高光光油的制备方法为:
(1)将160重量份的1000分子量BG-AA二元醇、14重量份的DMPA、7重量份的BDO、1.5重量份的反应型二甲基硅油混合,加热熔化;
(2)在步骤(1)所得的混合物中加入120重量份的IPDI在70℃反
应5小时;
(3)当步骤(2)所得的混合物的-NCO的百分含量小于0.3%时,加入30重量份的丙酮降温至35℃,然后在所得的混合物中加入8重量份的三乙胺反应40分钟;
(4)将步骤(3)所得的混合物在高速分散下投入到550重量份的水中,然后滴加14重量份的乙二胺;
(5)在步骤(4)所得的混合物中加入1.5重量份的水性消泡剂,7重量份的流平剂和18重量份的增稠剂,搅拌至少30分钟至混合物混合均匀,即得所述合成革用水性高光光油。所得到的合成革用水性高光光油的性能指标见表1。上述制备过程中所采用的熔化、加热、搅拌、高速分散等方法均为本领域内惯用的方法。
实施例3
合成革用水性高光光油由以下配比的组分组成:1000分子量BG-AA二元醇180重量份、DMPA 18重量份、BDO 12重量份、反应型二甲基硅油2重量份、IPDI 140重量份、丙酮35重量份、三乙胺12重量份、乙二胺18重量份、水600重量份、水性消泡剂2重量份、流平剂12重量份和增稠剂22重量份。
以上合成革用水性高光光油的制备方法为:
(1)将180重量份的1000分子量BG-AA二元醇、18重量份的DMPA、12重量份的BDO、2重量份的反应型二甲基硅油混合,加热熔化;
(2)在步骤(1)所得的混合物中加入140重量份的IPDI在70℃反应5小时;
(3)当步骤(2)所得的混合物的-NCO的百分含量小于0.3%时,加入35重量份的丙酮降温至40℃,然后在所得的混合物中加入12重量份的三乙胺反应30分钟;
(4)将步骤(3)所得的混合物在高速分散下投入到600重量份的水中,然后滴加18重量份的乙二胺;
(5)在步骤(4)所得的混合物中加入2重量份的水性消泡剂,12重量份的流平剂和22重量份的增稠剂,搅拌至少30分钟至混合物混合均匀,即得所述合成革用水性高光光油。所得到的合成革用水性高光光油的性能指标见表1。上述制备过程中所采用的熔化、加热、搅拌、高速分散等方法均为本领域内惯用的方法。
实施例4
合成革用水性高光光油由以下配比的组分组成:1000分子量BG-AA二元醇200重量份、DMPA 20重量份、BDO 15重量份、反应型二甲基硅油3重量份、IPDI 150重量份、丙酮40重量份、三乙胺15重量份、乙二胺20重量份、水600重量份、水性消泡剂3重量份、流平剂15重量份和增稠剂25重量份。
以上合成革用水性高光光油的制备方法为:
(1)将200重量份的1000分子量BG-AA二元醇、20重量份的DMPA、15重量份的BDO、3重量份的反应型二甲基硅油混合,加热熔化;
(2)在步骤(1)所得的混合物中加入150重量份的IPDI在80℃反应4小时;
(3)当步骤(2)所得的混合物的-NCO的百分含量小于0.3%时,加入40重量份的丙酮降温至40℃,然后在所得的混合物中加入15重量份的三乙胺反应30分钟;
(4)将步骤(3)所得的混合物在高速分散下投入到600重量份的水中,然后滴加20重量份的乙二胺;
(5)在步骤(4)所得的混合物中加入3重量份的水性消泡剂,15重量份的流平剂和25重量份的增稠剂,搅拌至少30分钟至混合物混合均匀,即得所述合成革用水性高光光油。所得到的合成革用水性高光光油的性能指标见表1。上述制备过程中所采用的熔化、加热、搅拌、高速分散等方法均为本领域内惯用的方法。
表1
实施例1 | 实施例2 | 实施例3 | 实施例4 | |
pH值 | 7.0 | 7.2 | 7.5 | 8.0 |
外观 | 浅蓝色半透明液体 | 浅蓝色半明液体 | 浅蓝色半明液体 | 浅蓝色半明液体 |
粘度(cps/25℃) | 800 | 1000 | 1200 | 1500 |
稳定性 | 无沉淀、不变色 | 无沉淀、不变色 | 无沉淀、不变色 | 无沉淀、不变色 |
溶剂体系 | 水 | 水 | 水 | 水 |
固含量(%) | 39 | 39.5 | 40 | 41 |
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)
- 一种合成革用水性高光光油,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、DMPA、BDO、反应型二甲基硅油、IPDI、丙酮、三乙胺、乙二胺、水、水性消泡剂、流平剂和增稠剂。
- 根据权利要求1所述的合成革用水性高光光油,其特征在于,所述1000分子量BG-AA二元醇与DMPA的重量比为1∶0.05-0.15,所述1000分子量BG-AA二元醇与BDO的重量比为1∶0.025-0.1,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∶0.005-0.02,所述1000分子量BG-AA二元醇与IPDI的重量比为1∶0.5-1,所述1000分子量BG-AA二元醇与丙酮的重量比为1∶0.1-0.3,所述1000分子量BG-AA二元醇与三乙胺的重量比为1∶0.025-0.1,所述1000分子量BG-AA二元醇与乙二胺的重量比为1∶0.05-0.15,所述1000分子量BG-AA二元醇与水的重量比为1∶2.5-4,所述1000分子量BG-AA二元醇与水性消泡剂的重量比为1∶0.005-0.02,所述1000分子量BG-AA二元醇与流平剂的重量比为1∶0.025-0.1,所述1000分子量BG-AA二元醇与增稠剂的重量比为1∶0.075-0.2。
- 一种合成革用水性高光光油的制备方法,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、DMPA、BDO、反应型二甲基硅油混合,加热熔化;(2)在步骤(1)所得的混合物中加入IPDI进行反应;(3)当步骤(2)所得的混合物的-NCO的百分含量小于0.3%时,加入丙酮降温,然后在所得的混合物中加入三乙胺进行反应;(4)将步骤(3)所得的混合物在高速分散下投入到水中,然后滴加乙二胺;(5)在步骤(4)所得的混合物中加入水性消泡剂,流平剂和增稠剂, 搅拌均匀,即得所述合成革用水性高光光油。
- 根据权利要求3所述的合成革用水性高光光油,其特征在于,所述1000分子量BG-AA二元醇与DMPA的重量比为1∶0.05-0.15,所述1000分子量BG-AA二元醇与BDO的重量比为1∶0.025-0.1。
- 根据权利要求3所述的合成革用水性高光光油,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∶0.005-0.02,所述1000分子量BG-AA二元醇与IPDI的重量比为1∶0.5-1。
- 根据权利要求3所述的合成革用水性高光光油,其特征在于,所述1000分子量BG-AA二元醇与丙酮的重量比为1∶0.1-0.3,所述1000分子量BG-AA二元醇与三乙胺的重量比为1∶0.025-0.1。
- 根据权利要求3所述的合成革用水性高光光油,其特征在于,所述1000分子量BG-AA二元醇与乙二胺的重量比为1∶0.05-0.15,所述1000分子量BG-AA二元醇与水的重量比为1∶2.5-4。
- 根据权利要求3所述的合成革用水性高光光油,其特征在于,所述1000分子量BG-AA二元醇与水性消泡剂的重量比为1∶0.005-0.02,所述1000分子量BG-AA二元醇与流平剂的重量比为1∶0.025-0.1,所述1000分子量BG-AA二元醇与增稠剂的重量比为1∶0.075-0.2。
- 根据权利要求3所述的合成革用水性高光光油,其特征在于,步骤(2)的反应温度为60℃-80℃,反应时间为4-6小时。
- 根据权利要求3所述的合成革用水性高光光油,其特征在于,步骤(3)的反应温度为30℃-40℃,反应时间为30-50分钟。
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