CN106366236A - Pvc发泡人造革用发泡调节剂的制备方法 - Google Patents

Pvc发泡人造革用发泡调节剂的制备方法 Download PDF

Info

Publication number
CN106366236A
CN106366236A CN201610760288.1A CN201610760288A CN106366236A CN 106366236 A CN106366236 A CN 106366236A CN 201610760288 A CN201610760288 A CN 201610760288A CN 106366236 A CN106366236 A CN 106366236A
Authority
CN
China
Prior art keywords
preparation
control agent
pvc foam
foaming control
emulsion
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
CN201610760288.1A
Other languages
English (en)
Other versions
CN106366236B (zh
Inventor
张效全
徐铎
窦锦鑫
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.)
Shandong Donglin New Materials Co Ltd
Original Assignee
Shandong Donglin New 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 Shandong Donglin New Materials Co Ltd filed Critical Shandong Donglin New Materials Co Ltd
Priority to CN201610760288.1A priority Critical patent/CN106366236B/zh
Publication of CN106366236A publication Critical patent/CN106366236A/zh
Application granted granted Critical
Publication of CN106366236B publication Critical patent/CN106366236B/zh
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00Copolymers 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
    • C08F220/02Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10Esters
    • C08F220/12Esters of monohydric alcohols or phenols
    • C08F220/16Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
    • C08F220/18Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2/00Processes of polymerisation
    • C08F2/12Polymerisation in non-solvents
    • C08F2/16Aqueous medium
    • C08F2/22Emulsion polymerisation
    • C08F2/24Emulsion polymerisation with the aid of emulsifying agents
    • C08F2/26Emulsion polymerisation with the aid of emulsifying agents anionic
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2/00Processes of polymerisation
    • C08F2/12Polymerisation in non-solvents
    • C08F2/16Aqueous medium
    • C08F2/22Emulsion polymerisation
    • C08F2/24Emulsion polymerisation with the aid of emulsifying agents
    • C08F2/30Emulsion polymerisation with the aid of emulsifying agents non-ionic
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00Copolymers 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
    • C08F220/02Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10Esters
    • C08F220/26Esters containing oxygen in addition to the carboxy oxygen
    • C08F220/28Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L27/00Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
    • C08L27/02Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
    • C08L27/04Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
    • C08L27/06Homopolymers or copolymers of vinyl chloride
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00Copolymers 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
    • C08F220/02Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10Esters
    • C08F220/12Esters of monohydric alcohols or phenols
    • C08F220/16Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
    • C08F220/18Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
    • C08F220/1803C3-(meth)acrylate, e.g. (iso)propyl (meth)acrylate
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00Copolymers 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
    • C08F220/02Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10Esters
    • C08F220/12Esters of monohydric alcohols or phenols
    • C08F220/16Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms
    • C08F220/18Esters of monohydric alcohols or phenols of phenols or of alcohols containing two or more carbon atoms with acrylic or methacrylic acids
    • C08F220/1804C4-(meth)acrylate, e.g. butyl (meth)acrylate, isobutyl (meth)acrylate or tert-butyl (meth)acrylate
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F220/00Copolymers 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
    • C08F220/02Monocarboxylic acids having less than ten carbon atoms; Derivatives thereof
    • C08F220/10Esters
    • C08F220/26Esters containing oxygen in addition to the carboxy oxygen
    • C08F220/28Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety
    • C08F220/281Esters containing oxygen in addition to the carboxy oxygen containing no aromatic rings in the alcohol moiety and containing only one oxygen, e.g. furfuryl (meth)acrylate or 2-methoxyethyl (meth)acrylate

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
  • Synthetic Leather, Interior Materials Or Flexible Sheet Materials (AREA)

Abstract

本发明公开了一种PVC发泡人造革用发泡调节剂的制备方法,包括以下步骤:⑴、采用多段乳液,在去离子水、乳化剂、引发剂、分子量调节剂的存在下进行共聚,温度为70℃‑95℃;⑵、向步骤⑴共聚后的乳液中加入外层单体,70℃‑95℃之间在进行聚合,凝聚、干燥,得PVC发泡人造革用发泡调节剂。本发明操作简单,制备出的超低分子量的丙烯酸酯共聚物,它能和含有增塑剂的PVC基体互溶,在基本不降低PVC基体流动性的情况下,增加PVC基体的熔体强度,能够促进PVC发泡皮革的发泡均匀度。

Description

PVC发泡人造革用发泡调节剂的制备方法
技术领域
本发明涉及人造革技术领域,尤其是一种PVC发泡人造革用发泡调节剂的制备方法。
背景技术
目前由于PVC发泡人造革在烘箱中熔融塑化阶段存在着人造革发泡大小不均匀,出现发泡大小不均一、并泡和泡孔破裂现象,造成人造革柔韧性变差,手感较差,拉伸强度降低等现象。造成皮革整体性能下降。
发明内容
本发明针对现有技术的不足,提出一种PVC发泡人造革用发泡调节剂的制备方法,操作简便,产品基本不降低PVC基体流动性的情况下,增加PVC基体的熔体强度。
为了实现上述发明目的,本发明提供以下技术方案:一种PVC发泡人造革用发泡调节剂的制备方法,包括以下步骤:
⑴、采用多段乳液,在去离子水、乳化剂、引发剂、分子量调节剂的存在下进行共聚,温度为70℃-95℃;
⑵、向步骤⑴共聚后的乳液中加入外层单体,70℃-95℃之间在进行聚合,凝聚、干燥,得PVC发泡人造革用发泡调节剂。
进一步地,步骤⑴中,两段乳液按重量百分比70-80:20-30进行共聚。
进一步地,一段乳液由如下重量百分比的单体构成:0-20%丙烯酸酯、10-20%甲基丙烯酸甲酯和60-80%甲基丙烯酸酯;另一段乳液由如下重量百分比的单体构成:80-100%甲基丙烯酸甲酯和0-20%丙烯酸丁酯。
进一步地,两段乳液的总单体重量: 去离子水为0.1~1.0 :1。
进一步地,步骤⑴中,乳化剂为烷基硫酸盐、烷基磷酸盐、烷基苯磺酸盐、聚氧乙烯烷基醚、聚氧乙烯烷基脂肪酸酯中一种或多种;总用量为多段乳液总重量的0.2-5%。
进一步地,步骤⑴中,乳化剂为阴离子乳化剂或阴离子乳化剂和非离子乳化剂的复配物,用量为多段乳液总重量的0.5%-3.0%。
进一步地,步骤⑴中,引发剂为过硫酸盐、有机过氧化物、偶氮类化合物中的一种,或与亚硫酸盐、亚硫酸氢盐、硫代硫酸盐中的一种构成氧化还原引发剂体系;用量为多段乳液总重量的0.1-2%。
进一步地,步骤⑴中,分子量调节剂为C4-C20的烷基硫醇,用量为多段乳液总重量的0.1-3%。
进一步地,具体操作过程为:
a、向搅拌的去离子水中,加入乳化剂、丙烯酸酯、甲基丙烯酸甲酯、甲基丙烯酸酯、分子量调节剂,通入氮气,升温至75℃,再加入引发剂,在75~95℃聚合;
b、在75℃下,向步骤⑴聚合物中加入甲基丙烯酸甲酯和丙烯酸丁酯的混合物,10分钟后加入引发剂,在75~95℃聚合;在85℃以上保温1~2小时,降温至40℃,过滤得产品乳液。
一种如上所述PVC发泡人造革用发泡调节剂的制备方法制得的产品,其特性粘度为0.1-3.0,优选为0.1-2.0,更优选为0.1-1.0,最优选为0.2-0.5。
与现有技术相比,本发明具有以下优点:操作简单,制备出的超低分子量的丙烯酸酯共聚物,它能和含有增塑剂的PVC基体互溶,在基本不降低PVC基体流动性的情况下,增加PVC基体的熔体强度,能够促进PVC发泡皮革的发泡均匀度。
具体实施方式
下面结合实施例对本发明进行详细描述,本部分的描述仅是示范性和解释性,不应对本发明的保护范围有任何的限制作用。
一种PVC发泡人造革用发泡调节剂的制备方法,包括如下步骤:
A:按照拟定配方加入去离子水、开启搅拌,然后分别向反应釜中加入乳化剂,聚合用的混合单体、分子量调节剂,通入氮气,并向反应釜夹套通蒸汽升温、稳定在75℃后加入配方量的引发剂进行反应。控制温度在75~95℃聚合;此步可以分为一步或多步聚合。
B.上述反应完后,温度稳定在75℃左右,在向反应釜中加入二次混合单体或一种单体,10分钟后加入配方量的引发剂,进行聚合反应。控制温度在75~95℃聚合,反应完毕后,升温至85℃ 以上保温1-2小时。降温至40℃,过滤得丙烯酸共聚物乳液,聚合转化率为99.5%以上,特性粘度在0.1-3.0,备用;
C.喷雾、干燥:步骤B制备的丙烯酸酯共聚乳液经喷雾干燥,即可得到白色粉末状聚合物。或将乳液进行凝聚,然后离心,干燥即可得到白色粉末状聚合物。
D.质量检验,合格后,包装、入库。
表1实施例1-7原料重量份 及产品性能指标
以上所述仅是本发明的优选实施方式,应当指出,对于本技术领域的普通技术人员来说,在不脱离本发明原理的前提下,还可以做出若干改进和润饰,这些改进和润饰也应视为本发明的保护范围。

Claims (10)

1.一种PVC发泡人造革用发泡调节剂的制备方法,其特征在于:包括以下步骤:
⑴、采用多段乳液,在去离子水、乳化剂、引发剂、分子量调节剂的存在下进行共聚,温度为70℃-95℃;
⑵、向步骤⑴共聚后的乳液中加入外层单体,70℃-95℃之间在进行聚合,凝聚、干燥,得PVC发泡人造革用发泡调节剂。
2.如权利要求1所述PVC发泡人造革用发泡调节剂的制备方法,其特征在于:步骤⑴中,两段乳液按重量百分比70-80:20-30进行共聚。
3.如权利要求2所述PVC发泡人造革用发泡调节剂的制备方法,其特征在于:一段乳液由如下重量百分比的单体构成:0-20%丙烯酸酯、10-20%甲基丙烯酸甲酯和60-80%甲基丙烯酸酯;另一段乳液由如下重量百分比的单体构成:80-100%甲基丙烯酸甲酯和0-20%丙烯酸丁酯。
4.如权利要求2所述PVC发泡人造革用发泡调节剂的制备方法,其特征在于:两段乳液的总单体重量: 去离子水为0.1~1.0 :1。
5.如权利要求1所述PVC发泡人造革用发泡调节剂的制备方法,其特征在于:步骤⑴中,乳化剂为烷基硫酸盐、烷基磷酸盐、烷基苯磺酸盐、聚氧乙烯烷基醚、聚氧乙烯烷基脂肪酸酯中一种或多种;总用量为多段乳液总重量的0.2-5%。
6.如权利要求1所述PVC发泡人造革用发泡调节剂的制备方法,其特征在于:步骤⑴中,乳化剂为阴离子乳化剂或阴离子乳化剂和非离子乳化剂的复配物,用量为多段乳液总重量的0.5%-3.0%。
7.如权利要求1所述PVC发泡人造革用发泡调节剂的制备方法,其特征在于:步骤⑴中,引发剂为过硫酸盐、有机过氧化物、偶氮类化合物中的一种,或与亚硫酸盐、亚硫酸氢盐、硫代硫酸盐中的一种构成氧化还原引发剂体系;用量为多段乳液总重量的0.1-2%。
8.如权利要求1所述PVC发泡人造革用发泡调节剂的制备方法,其特征在于:步骤⑴中,分子量调节剂为C4-C20的烷基硫醇,用量为多段乳液总重量的0.1-3%。
9.如权利要求1所述PVC发泡人造革用发泡调节剂的制备方法,其特征在于:具体操作过程为:
a、向搅拌的去离子水中,加入乳化剂、丙烯酸酯、甲基丙烯酸甲酯、甲基丙烯酸酯、分子量调节剂,通入氮气,升温至75℃,再加入引发剂,在75~95℃聚合;
b、在75℃下,向步骤⑴聚合物中加入甲基丙烯酸甲酯和丙烯酸丁酯的混合物,10分钟后加入引发剂,在75~95℃聚合;在85℃以上保温1~2小时,降温至40℃,过滤得产品乳液。
10.一种如权利要求1所述PVC发泡人造革用发泡调节剂的制备方法制得的产品,其特征在于:其特性粘度为0.1-3.0,优选为0.1-2.0,更优选为0.1-1.0,最优选为0.2-0.5。
CN201610760288.1A 2016-08-30 2016-08-30 Pvc发泡人造革用发泡调节剂的制备方法 Active CN106366236B (zh)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610760288.1A CN106366236B (zh) 2016-08-30 2016-08-30 Pvc发泡人造革用发泡调节剂的制备方法

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610760288.1A CN106366236B (zh) 2016-08-30 2016-08-30 Pvc发泡人造革用发泡调节剂的制备方法

Publications (2)

Publication Number Publication Date
CN106366236A true CN106366236A (zh) 2017-02-01
CN106366236B CN106366236B (zh) 2019-06-21

Family

ID=57901312

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610760288.1A Active CN106366236B (zh) 2016-08-30 2016-08-30 Pvc发泡人造革用发泡调节剂的制备方法

Country Status (1)

Country Link
CN (1) CN106366236B (zh)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN117757129A (zh) * 2024-02-21 2024-03-26 山东三润助剂科技股份有限公司 一种pvc发泡调节剂及其制备方法

Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4800214A (en) * 1986-10-21 1989-01-24 Lonseal Corporation Open cell body made of hard vinyl chloride resin
US6391976B1 (en) * 1998-02-24 2002-05-21 Mitsubishi Rayon Co., Ltd. Processing aid for foam molding use and vinyl chloride resin composition containing the same
CN102443096A (zh) * 2010-10-15 2012-05-09 河北精信化工集团有限公司 一种可控制分子量的聚氯乙烯发泡助剂及制备方法
CN102746444A (zh) * 2012-08-02 2012-10-24 田岳南 丙烯酸酯类共聚物及使用该共聚物的聚氯乙烯树脂组合物
CN102504088B (zh) * 2011-11-29 2013-11-27 山东瑞丰高分子材料股份有限公司 丙烯酸酯类加工助剂以及制备方法和应用
CN103980413A (zh) * 2014-06-04 2014-08-13 随州市晶辉高分子材料有限公司 一种发泡pvc木塑复合材料用发泡调节剂的制备方法

Patent Citations (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4800214A (en) * 1986-10-21 1989-01-24 Lonseal Corporation Open cell body made of hard vinyl chloride resin
US6391976B1 (en) * 1998-02-24 2002-05-21 Mitsubishi Rayon Co., Ltd. Processing aid for foam molding use and vinyl chloride resin composition containing the same
CN102443096A (zh) * 2010-10-15 2012-05-09 河北精信化工集团有限公司 一种可控制分子量的聚氯乙烯发泡助剂及制备方法
CN102504088B (zh) * 2011-11-29 2013-11-27 山东瑞丰高分子材料股份有限公司 丙烯酸酯类加工助剂以及制备方法和应用
CN102746444A (zh) * 2012-08-02 2012-10-24 田岳南 丙烯酸酯类共聚物及使用该共聚物的聚氯乙烯树脂组合物
CN103980413A (zh) * 2014-06-04 2014-08-13 随州市晶辉高分子材料有限公司 一种发泡pvc木塑复合材料用发泡调节剂的制备方法

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
李克友 等: "丙烯酸酯共聚物的合成", 《四川联合大学学报(工程科学版)》 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN117757129A (zh) * 2024-02-21 2024-03-26 山东三润助剂科技股份有限公司 一种pvc发泡调节剂及其制备方法

Also Published As

Publication number Publication date
CN106366236B (zh) 2019-06-21

Similar Documents

Publication Publication Date Title
CN105237675B (zh) 一种具有核壳双交联结构的聚丙烯酸木器乳液及其制备方法
CN100577697C (zh) 制备(甲基)丙烯酸酯浆料的方法
CN104628961B (zh) 一种丙烯酸酯类聚合物接枝共聚脂肪酸乙烯酯制备聚羧酸减水剂的方法
CN109054570B (zh) 一种环保型高强度弹性涂料及其制备方法
CN105254817B (zh) 核壳结构丙烯酸酯类发泡调节剂的制备方法
CN107130463B (zh) 一种用于纸张增强的互穿网络聚合物及其制备方法
CN105461866B (zh) 一种降粘型聚羧酸减水剂及其制备方法
CN105037648A (zh) 一种保坍减水型聚羧酸减水剂及其低温快速制备方法
CN101735541A (zh) 一种保温材料用环保型乳液及其制备方法
CN107840919A (zh) 一种核壳型叔醋丙乳液及其制备方法与应用
CN110372817A (zh) 一种纳米金属氧化物改性热膨胀微球的制备方法
CN109575311A (zh) 一种乙酸乙烯酯-乙烯共聚乳液的制备方法
CN105820780A (zh) 一种基于预乳化技术的木材用淀粉胶粘剂及其制备方法
CN103130962B (zh) 氯化聚乙烯橡胶、丙烯酸丁酯、丙烯腈、n‑苯基马来酰亚胺接枝共聚物及其制备方法
CN104497230A (zh) 酯醚共聚型聚羧酸减水剂、其制备方法及用途
CN103450399B (zh) 一种乳液聚合法制备丁腈橡胶方法
CN105949409A (zh) 一种含壳聚糖的聚羧酸系混凝土减水剂及其制备方法
CN106366236A (zh) Pvc发泡人造革用发泡调节剂的制备方法
CN104761673A (zh) 一种卡波姆及其制备方法
CN105037631B (zh) 核壳型有机硅改性聚丙烯酸酯的硬挺剂及其制备方法
CN103665238B (zh) 一种宽分子量分布氟橡胶的合成方法
CN106366234A (zh) 丙烯酸酯共聚物及其制备方法和用途
Gao et al. Preparation and properties of two-component and double-crosslinking waterborne polyurethane-acrylic dispersions
CN104327210A (zh) 一种高粘度发泡型改性剂丙烯酸acr树脂的制备
CN106366227A (zh) Pvc管件专用加工改性剂的制备方法

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
GR01 Patent grant
GR01 Patent grant
PE01 Entry into force of the registration of the contract for pledge of patent right
PE01 Entry into force of the registration of the contract for pledge of patent right

Denomination of invention: Preparation method of foaming regulator for PVC foamed artificial leather

Effective date of registration: 20230515

Granted publication date: 20190621

Pledgee: Postal Savings Bank of China Limited by Share Ltd. Weifang branch

Pledgor: SHANDONG DONGLIN NEW MATERIALS Co.,Ltd.

Registration number: Y2023980040635

PC01 Cancellation of the registration of the contract for pledge of patent right
PC01 Cancellation of the registration of the contract for pledge of patent right

Granted publication date: 20190621

Pledgee: Postal Savings Bank of China Limited by Share Ltd. Weifang branch

Pledgor: SHANDONG DONGLIN NEW MATERIALS Co.,Ltd.

Registration number: Y2023980040635