CN105670185A - 一种耐热pvc - Google Patents

一种耐热pvc Download PDF

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CN105670185A
CN105670185A CN201610243134.5A CN201610243134A CN105670185A CN 105670185 A CN105670185 A CN 105670185A CN 201610243134 A CN201610243134 A CN 201610243134A CN 105670185 A CN105670185 A CN 105670185A
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赖树兴
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Abstract

本发明涉及塑料领域,特别涉及一种耐热PVC。一种耐热PVC,由如下重量份数的组分组成:聚氯乙烯40~60份,增塑剂5~20份,填充剂10~25份;阻燃剂0.5~1.2份;抗氧剂0.01~1份,三羟甲基丙烷三甲基丙烯酸酯1~2份,热稳定剂1~5份。与现有技术相比,本发明的新型耐热PVC不但具有良好的热稳定性,而且也具有良好的机械性能,在市场中具有较大的竞争力。

Description

一种耐热 PVC
技术领域
本发明涉及塑料领域,特别涉及一种耐热PVC。
背景技术
PVC材料经常用于我们的生活中,如PVC管,PVC地板,PVC墙纸等等。现有市场对PVC的需求量正在逐年增加,未来社会对PVC仍将继续增大。随着社会城市化、科技化、人性化的发展,PVC行业的高速发展,PVC材料越来越贴近人们的生活,随之而来的是PVC材料使用量的增加,和PVC产品大多不抗老化、易受光氧化和韧性低,热稳定性差、阻燃性差,不耐酸碱腐蚀等问题的彰显。
发明内容
本发明所要解决的技术问题是提供一种耐热PVC。
一种耐热PVC,由如下重量份数的组分组成:
聚氯乙烯40~60份,增塑剂5~20份,填充剂10~25份;阻燃剂0.5~1.2份;抗氧剂0.01~1份,三羟甲基丙烷三甲基丙烯酸酯1~2份,热稳定剂1~5份,其中,所述的热稳定剂化学式为(C12H12N2S)(C5H6O4)Zn,其中,C5H6O4为戊二酸,C12H12N2S为二(吡啶-4-基甲基)硫烷。
进一步的,所述热稳定剂为三斜晶系,P-1空间群,晶胞参数为a=12.853(2) Å,b=9.719(3) Å,c=12.315(9) Å,α=83.58(3) º,β=75.03(5) º,γ=78.71(2) º,V=1538.36 (8) Å3
进一步的,所述增塑剂为邻苯二甲酸二辛酯、二(2—乙基丁酸)三缩乙二醇酯、磷酸三甲苯酯、邻苯二甲酸二异丁酯、邻苯二甲酸二异癸酯中的至少一种。
进一步的,所述填充剂为碳酸钙、滑石粉、高岭土中的至少一种。
进一步的,所述阻燃剂三氧化二锑。
其中,抗氧剂选自本发明常用的抗氧剂均可实现本发明,如抗氧剂1010、抗氧剂168等。
本发明采用三羟甲基丙烷三甲基丙烯酸酯作为加工助剂,能够有效解决本发明采用的新型热稳定剂的分散性问题,使其在PVC产品中分散更好,有利于本发明产品性能的进一步提高。
本发明具有如下有益效果:
与现有技术相比,本发明的新型耐热PVC不但具有良好的热稳定性,而且也具有良好的机械性能,在市场中具有较大的竞争力。
附图说明
图1为热稳定剂以金属中心Zn的配位环境图。
具体实施方式
下面结合实施例对本发明进行详细的说明,实施例仅是本发明的优选实施方式,不是对本发明的限定。
本发明的PVC的制备方法为本技术领域的常用技术,在本发明中不再详细描述。
本发明所述的热稳定剂均按照如下制备方法制备:将0.1mmol二(吡啶-4-基甲基)硫烷、0.1mmol戊二酸和0.1mmol硝酸锌溶于10mL二甲基甲酰胺和5mL乙醇的混合溶剂当中,在室温下搅拌溶解后形成混合液A,然后将所述混合液A在55℃下反应回流36小时得到混合液B,随后将混合液B转移到聚四氟乙烯高压反应釜中,将其放在170℃烘箱中反应36小时,之后以5℃/小时降至室温过滤得到所述热稳定剂。
其中,二(吡啶-4-基甲基)硫烷英文为:bis(pyridin-4-ylmethyl)sulfane。
然后将上述热稳定剂进行结构表征。
该热稳定剂的X射线衍射数据是在Bruker Smart Apex CCD面探衍射仪上,用MoKα辐射(λ = 0.71073 Å),以ω扫描方式收集并进行Lp因子校正,吸收校正使用SADABS程序。用直接法解结构,然后用差值傅立叶法求出全部非氢原子坐标,并用理论加氢法得到氢原子位置(C−H 1.083 Å),用最小二乘法对结构进行修正。计算工作在PC机上用SHELXTL程序包完成。该热稳定剂结构见图1。
经测试解析可知,该热稳定剂化学式为(C12H12N2S)(C5H6O4)Zn,其中,C5H6O4为戊二酸,C12H12N2S为二(吡啶-4-基甲基)硫烷,所述热稳定剂为三斜晶系,P-1空间群,晶胞参数为a=12.853(2) Å,b=9.719(3) Å,c=12.315(9) Å,α=83.58(3) º,β=75.03(5) º,γ=78.71(2) º,V=1538.36 (8) Å3,Z=4。
从晶体结构来看,该热稳定剂属于三斜晶系,P-1空间群,该不对称单元中含有一个Zn原子、一个二(吡啶-4-基甲基)硫烷和一个其中戊二酸,Zn原子采取6配位八面体的模式与4个O原子配位和2个N原子配位,其中4个O原子采取螯合配位的模式,而2个N原子采取单齿配位的模式,如图1所示;二(吡啶-4-基甲基)硫烷用两头的吡啶基上的N原子,而戊二酸用两头氧原子,采用2头连接的方式,将Zn原子延伸连接成一种特殊的三维结构,而这种特殊的三维结构有利于HCl的吸收,使得这种热稳定剂具有良好的性能。
以下实施例和对比例如无特殊说明,均采用上述合成方法制备的热稳定剂。
实施例 1
一种耐热PVC,由如下重量份数的组分组成:
聚氯乙烯55份,邻苯二甲酸二辛酯12.5份,碳酸钙10份;高岭土5份;三氧化二锑1份;抗氧剂1010 0.05份,三羟甲基丙烷三甲基丙烯酸酯1.5份,热稳定剂3份。
实施例 2
一种耐热PVC,由如下重量份数的组分组成:
聚氯乙烯41份,二(2—乙基丁酸)三缩乙二醇酯18份,滑石粉25份;三氧化二锑0.6份;抗氧剂168 0.3份,三羟甲基丙烷三甲基丙烯酸酯1份,热稳定剂1.2份。
实施例 3
一种耐热PVC,由如下重量份数的组分组成:
聚氯乙烯57份,磷酸三甲苯酯8.5份,碳酸钙10.5份;三氧化二锑0.6份;抗氧剂168 0.8份,三羟甲基丙烷三甲基丙烯酸酯1.8份,热稳定剂4份。
对比例 1
一种耐热PVC,由如下重量份数的组分组成:
聚氯乙烯55份,邻苯二甲酸二辛酯12.5份,碳酸钙10份;高岭土5份;三氧化二锑1份;抗氧剂1010 0.05份,三羟甲基丙烷三甲基丙烯酸酯1.5份,硬脂酸锌3份。
对比例 2
一种耐热PVC,由如下重量份数的组分组成:
聚氯乙烯55份,邻苯二甲酸二辛酯12.5份,碳酸钙10份;高岭土5份;三氧化二锑1份;抗氧剂1010 0.05份,甲基丙烯酸甲酯1.5份,热稳定剂3份。
然后将上述所得的实施例和对比例测试性能。
按照GB/T 2917.1-2002规定的刚果红法,在 200℃进行热稳定性测试。如表1 所示。
表1刚果红法测试表
由表1数据可以看出,添加了本发明热稳定剂的PVC材料由于其能够有效吸附游离的HCl,因此具有很好的热稳定效果,其效果远远强于现有使用常用PVC热稳定剂的PVC材料。
按照GB/T 15595-2008规定的白度法进行测试。
然后将上述所得的PVC材料表2为测试性能表。
表2白度法测试表
由表2数据可以看出,本发明实施例1~3的24、48、72 和 120h 时的样品白度均高于对比例的样品白度。随着时间的延长,对比例的样品白度减小的比较明显,在120h时,对比专利的样品白度为60.1%和79.5%,而采用本发明PVC白度高于85%以上,这说明本发明的热稳定剂也一样具有良好的耐候性。
按照GB/T 1040.1-2006和HG/T 3841-2006性能进行测试, 测试结果如表3 所示。
表3性能测试表
由表3数据可以看出,本发明实施例1~3的PVC具有良好的拉伸强度和冲击强度,和对比例的数据相比可以看出本发明的PVC通过添加新型的热稳定剂,在一定程度上也可以提高PVC的机械性能。
以上所述实施例仅表达了本发明的实施方式,其描述较为具体和详细,但并不能因此而理解为对本发明专利范围的限制,但凡采用等同替换或等效变换的形式所获得的技术方案,均应落在本发明的保护范围之内。

Claims (5)

1.一种耐热PVC,其特征在于由如下重量份数的组分组成:
聚氯乙烯40~60份,增塑剂5~20份,填充剂10~25份;阻燃剂0.5~1.2份;抗氧剂0.01~1份,三羟甲基丙烷三甲基丙烯酸酯1~2份,热稳定剂1~5份,其中,所述的热稳定剂化学式为(C12H12N2S)(C5H6O4)Zn,其中,C5H6O4为戊二酸,C12H12N2S为二(吡啶-4-基甲基)硫烷。
2.根据权利要求1所述一种耐热PVC,其特征在于,所述热稳定剂为三斜晶系,P-1空间群,晶胞参数为a=12.853(2) Å,b=9.719(3) Å,c=12.315(9) Å,α=83.58(3) º,β=75.03(5) º,γ=78.71(2) º,V=1538.36 (8) Å3
3.根据权利要求1所述一种耐热PVC,其特征在于,所述增塑剂为邻苯二甲酸二辛酯、二(2—乙基丁酸)三缩乙二醇酯、磷酸三甲苯酯、邻苯二甲酸二异丁酯、邻苯二甲酸二异癸酯中的至少一种。
4.根据权利要求1所述一种耐热PVC,其特征在于,所述填充剂为碳酸钙、滑石粉、高岭土中的至少一种。
5.根据权利要求1所述一种耐热PVC,其特征在于,所述阻燃剂三氧化二锑。
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Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1765961A (zh) * 2004-10-27 2006-05-03 罗门哈斯公司 用于含卤素的乙烯基聚合物的热稳定剂组合物
CN101092492A (zh) * 2007-06-26 2007-12-26 杭州新新塑料助剂科研有限公司 一种复配型热稳定剂
CN105237911A (zh) * 2015-11-01 2016-01-13 吕小方 一种热稳定剂

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1765961A (zh) * 2004-10-27 2006-05-03 罗门哈斯公司 用于含卤素的乙烯基聚合物的热稳定剂组合物
CN101092492A (zh) * 2007-06-26 2007-12-26 杭州新新塑料助剂科研有限公司 一种复配型热稳定剂
CN105237911A (zh) * 2015-11-01 2016-01-13 吕小方 一种热稳定剂

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