CN112574463A - 一种发泡母料、其制备方法及应用 - Google Patents
一种发泡母料、其制备方法及应用 Download PDFInfo
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Abstract
本发明公开了一种发泡母料、其制备方法及应用。发泡母料包括液体载体、发泡剂及助剂;所述的发泡母料的制备方法为:将原料加入容器中,以500r/min‑3000r/min的转速研磨分散均匀;所述发泡母料应用于注塑、挤出发泡塑料。本发明所述发泡母料,发泡剂溶于液体载体中或以微米级的尺度均匀分散于液体载体中,生产效率高且工艺安全简单,不会造成污染;避免了挤出工艺,防止发泡剂分解,生产安全;发泡液体母料使用时均匀附着在塑料颗粒表面,在树脂中具有极佳的分散性,有力保证了发泡剂与颜料的均匀分散。
Description
技术领域
本发明属于发泡技术领域,具体涉及一种发泡母料、其制备方法及应用。
背景技术
在塑料加工领域,为减轻塑料的重量,增强材料的隔热性能、隔音性能以及防震性能,或者实现材料的某种外观设计,通常在塑料中添加发泡剂,经过发泡工艺,使材料内部形成许多细小泡孔,应用十分广泛。
目前使用化学发泡剂的发泡塑料在生产中主要有两种形式:一种直接使用发泡剂,易造成粉尘飞扬,存在安全隐患和危害环境。一种是使用发泡母粒。发泡母粒是将超量发泡剂、与分散剂、发泡助剂和树脂载体等混合,经过塑炼拉片切粒或挤出造粒而成,发泡母粒使发泡塑料的生产更为环保简单。然而发泡母粒的加工和使用过程仍旧存在问题。一是发泡母粒需要将树脂载体、发泡剂、分散剂、发泡助剂等混合在一起,经高速捏合、塑炼拉片切粒或挤出机塑炼切粒而成,工序繁琐、能耗高,且混料过程会造成粉尘污染。二是发泡剂高温易分解的特性也限制了发泡母粒的塑炼或挤出工艺,如果加工工艺控制不当造成发泡剂分解,极易造成产品废弃甚至生产安全问题。三是在发泡塑料生产时,发泡母粒以一定比例加入到基体树脂粒料或粉料中,物料之间的混合不均匀会造成发泡剂分散不均,易造成发泡塑料泡孔不均匀等问题。
发明内容
为了克服现有技术中的缺陷,本发明提供了一种发泡母料。
本发明还提供一种发泡母料的制备方法。
本发明还提供一种发泡母料的应用。
本发明通过以下技术方案来实现上述目的,一种发泡母料,包括液体载体、发泡剂及助剂。
上述的发泡母料,以液体载体和发泡剂为原料,发泡剂溶于液体载体中或以微米级的尺度均匀分散于液体载体中,生产效率高且工艺安全简单,不会造成污染;避免了挤出工艺,防止发泡剂分解,生产安全;发泡液体母料使用时均匀附着在塑料颗粒表面,在树脂中具有极佳的分散性,有力保证了发泡剂与颜料的均匀分散。
一实施例中,所述的发泡母料包括如下重量份的组分:液体载体20-60份、发泡剂10-80份及助剂适量。
一实施例中,所述液体载体为液体低聚物、增塑剂、植物油和/或矿物油。
一实施例中,所述液体低聚物包括丙烯酸酯类液体聚合物及丙烯酰胺类液体聚合物。
一实施例中,所述助剂包括发泡助剂与分散助剂。
一实施例中,所述助剂还包括抗氧剂及稳定剂。
一实施例中,所述发泡剂为碳酸氢钠、碳酸锌、偶氮二甲酰胺、偶氮二异丁腈、偶氮二羧酸钡盐、偶氮胺基苯、偶氮二甲酸二异丙酯、偶氮二甲酸二乙酯、二亚硝基五亚甲基四胺、苯磺酰肼、对甲苯磺酰肼、对甲苯磺酰氨基脲、1,3-苯二磺酰肼、4,4’-氧化双苯磺酰肼、3,3’-二磺酰肼二苯砜、4,4’-氧代双(苯磺酰氨基脲)、三肼基三嗪、5-苯基四唑、硝基胍、二乙酰肼、肼撑酰胺中的一种或几种的混合物。
本发明还提供一种所述的发泡母料的制备方法,包括如下步骤:将原料加入容器中,以500r/min-3000r/min的转速研磨分散均匀。
本发明还提供一种发泡母料在注塑、挤出发泡塑料的应用。
一实施例中,所述发泡母料与发泡材料的质量比为0.5-6:100。
具体实施方式
为使本发明的上述目的、特征和优点能够更加明显易懂,下面将对本发明的具体实施方式做详细的说明。在下面的描述中阐述了很多具体细节以便于充分理解本发明。但是本发明能够以很多不同于在此描述的其它方式来实施,本领域技术人员可以在不违背本发明内涵的情况下做类似改进,因此本发明不受下面公开的具体实施例的限制。
本发明所述的发泡母料,包括液体载体、发泡剂及助剂。该发泡母料,以液体载体和发泡剂为原料,发泡剂溶于液体载体中或以微米级的尺度均匀分散于液体载体中,生产效率高且工艺安全简单,不会造成污染;避免了挤出工艺,防止发泡剂分解,生产安全;发泡液体母料使用时均匀附着在塑料颗粒表面,在树脂中具有极佳的分散性,有力保证了发泡剂与颜料的均匀分散。
一实施例中,发泡母料包括如下重量份的组分:液体载体20-60份、发泡剂10-80份及助剂适量。
例如,液体载体20份、25份、30份、35份、40份、50份、55份及60份;发泡剂10份、20份、25份、30份、40份、50份、55份、65份及80份。质量份数可以在范围内任意组合。
其中,液体载体为液体低聚物、增塑剂、植物油和/或矿物油。发泡剂可以分散在这些液体载体中,形成良好的发泡母料。
优选地,上述的液体低聚物包括丙烯酸酯类液体聚合物及丙烯酰胺类液体聚合物。
例如,液体载体为偏苯三酸三辛酯(TOTM)、邻苯二甲酸二丁酯(DBP)、邻苯二甲酸二辛酯(DOP)、对苯二甲酸二辛酯(DOTP)、癸二酸二丁酯(DBS)、癸二酸二(2-乙基己酯)(DOS)、己二酸二(2-乙基己酯)(DOA)、环己烷1,2-二甲酸二异壬基酯、磷酸三甲苯酯(TCP)、磷酸三辛酯(TOP)、工业级或食品级白油、环氧化油、环氧化脂肪酸酯、及环氧四氢邻苯二甲酸二(2-乙基己)酯、四聚蓖麻油酸酯及六聚蓖麻油酸酯中的一种或几种的组合。发泡剂均可以分散于上述的液体载体中,从而制备成液体发泡母料。
发泡剂可选自碳酸氢钠、碳酸锌、偶氮二甲酰胺、偶氮二异丁腈、偶氮二羧酸钡盐、偶氮胺基苯、偶氮二甲酸二异丙酯、偶氮二甲酸二乙酯、二亚硝基五亚甲基四胺、苯磺酰肼、对甲苯磺酰肼、对甲苯磺酰氨基脲、1,3-苯二磺酰肼、4,4’-氧化双苯磺酰肼、3,3’-二磺酰肼二苯砜、4,4’-氧代双(苯磺酰氨基脲)、三肼基三嗪、5-苯基四唑、硝基胍、二乙酰肼及肼撑酰胺中的一种或几种的混合物。
助剂包括发泡助剂与分散助剂。发泡助剂可以协助进行发泡,而分散助剂和协助发泡剂分散在液体载体中。其中,发泡助剂0.5-30份、分散助剂0.1-10份。
其中,发泡助剂包括发泡促进剂、成核剂、填充剂、交联剂等。
具体地,发泡助剂例如是:碳酸钙、硬脂酸钙、氧化钙、二氧化硅、二氧化钛、滑石粉、碳黑、醋酸锌、硬脂酸锌、氧化锌、云母及过氧化二异丙苯中的一种或几种的混合物。
其中,分散助剂为润湿分散剂或粘度调节剂。
具体地,分散助剂包括毕克BYK-108、BYK-111、BYK-160、BYK-185、BYK-9076、BYK-9077、BYK-2100、BYK-2105、ANTI-TERRA-U100、路博润8000、20000、27000、24000、32500、36000、47000超分散剂、赢创迪高685、740W、气相二氧化硅、膨润土、聚乙二醇及聚异丁烯的一种或几种的混合物。
一实施例中,上述的助剂还包括其他助剂,如抗氧剂、稳定剂等。其他助剂为0.1-10份。
具体地,抗氧剂包括抗氧剂168、抗氧剂1010、抗氧剂1076、抗氧剂245中的一种或几种的混合物,稳定剂包括三碱式硫酸铅、二碱式亚磷酸铅及二碱式硬脂酸铅中的一种或几种的混合物。
本发明还提供一种上述的发泡母料的制备方法,包括如下步骤:将原料加入容器中,以500r/min-3000r/min的转速研磨分散均匀。
在研磨过程中,会产生热量,可以用冷却水在研磨容器外进行冷却,以控制原料的温度不会过高,例如控制温度不高于60℃。当然,也可以采用其他方法进行冷却,保证原料的温度不会过高。
研磨分散时间可以是20min-60min。
本发明还提供一种发泡母料在注塑、挤出发泡塑料的应用。
具体地,该发泡母料可用于以下发泡材料的制备:聚乙烯(PE)、聚丙烯(PP)、聚氯乙烯(PVC)、乙烯-乙酸乙烯酯共聚物(EVA)、热塑性橡胶(TPR)、聚苯乙烯(PS)、丙烯睛-丁二烯-苯乙烯共聚物(ABS)及聚碳酸酯(PC)的发泡加工。
一实施例中,发泡母料与发泡材料的质量比为0.5-6:100。采用该质量比例,可以较好地实现发泡效果,而用量又不会过多而造成浪费。
以下将通过几个实施例来进一步说明本发明的实施方式。
实施例一
本实施例所述的发泡母料包括:对苯二甲酸二辛酯40份、偶氮二甲酰胺50份、BYK-111 1份、氧化锌10份、硬脂酸锌3份、抗氧剂168 0.5份、气相二氧化硅0.5份,将上述原料加入到高速研磨机中,研磨过程采用冷却水循环冷却,使液体温度不高于60℃,研磨转速1200r/min,研磨时间20min。研磨完成后得到的发泡母料,可用于挤出低发泡PP,添加比例为3%。
实施例二
本实施例所述的发泡母料包括:对苯二甲酸二辛酯40份、偶氮二甲酰胺50份、路博润20000 0.5份、过氧化二异丙苯4份、滑石粉10份、抗氧剂168 0.5份,将上述原料加入到高速研磨机中,研磨过程采用冷却水循环冷却,使液体温度不高于60℃,研磨转速1500r/min,研磨时间20min。研磨完成后得到的发泡母料,可用于挤出低发泡PE,添加比例为2%。
实施例三
本实施例所述的发泡母料包括:磷酸三甲苯酯35份、碳酸氢钠65份、路博润200000.5份、聚异丁烯PB2000 2份、抗氧剂1010 0.5份,将上述原料加入到高速研磨机中,研磨过程采用冷却水循环冷却,使液体温度不高于60℃,研磨转速1500r/min,研磨时间20min。研磨完成后得到的发泡液体母料,可用于挤出发泡PE,添加比例为4%。
实施例四
本实施例所述的发泡母料包括:白油68#45份、偶氮二羧酸钡盐55份、BYK-111 1份、氧化锌5份、硬脂酸锌1份、碳酸钙5份、抗氧剂1010 0.5份,将上述原料加入到高速研磨机中,研磨过程采用冷却水循环冷却,使液体温度不高于60℃,研磨转速1500r/min,研磨时间20min。研磨完成后得到的发泡母料,可用于注塑发泡ABS,添加比例为2%。
实施例五
本实施例所述的发泡母料包括:环己烷1,2-二甲酸二异壬基酯40份、偶氮二甲酰胺40份、路博润20000 0.5份、过氧化二异丙苯2份、氧化锌15份、钛白粉1份,将上述原料加入到高速研磨机中,研磨过程采用冷却水循环冷却,使液体温度不高于60℃,研磨转速1500r/min,研磨时间20min。研磨完成后得到的发泡母料,可用于挤出发泡PE,添加比例为4%。
实施例六
本实施例所述的发泡母料包括:丙烯酸酯类液体聚合物40份、偶氮二甲酰胺40份、BYK-9076 1份、氧化锌5份、硬脂酸锌1份、碳酸钙5份、抗氧剂168 0.5份,将上述原料加入到高速研磨机中,研磨过程采用冷却水循环冷却,使液体温度不高于60℃,研磨转速1500r/min,研磨时间20min。研磨完成后得到的发泡母料,可用于注塑ABS发泡,添加比例为3%。
实施例七
本实施例所述的发泡母料包括:丙烯酸酯类液体聚合物60份、偶氮二羧酸钡盐35份、德固赛迪高685 1份、氧化锌5份、硬脂酸锌1份、抗氧剂10100.5份,将上述原料加入到高速研磨机中,研磨过程采用冷却水循环冷却,使液体温度不高于60℃,研磨转速1500r/min,研磨时间20min。研磨完成后得到的发泡母料,可用于注塑PC发泡,添加比例为2%。
实施例八
本实施例所述的发泡母料包括:丙烯酸酯类液体聚合物30份、邻苯二甲酸二辛酯10份、偶氮二甲酰胺20份、三碱式硫酸铅25份、二碱式亚磷酸铅1份、二碱式硬脂酸铅2份、碳酸钙10份,将上述原料加入到高速研磨机中,研磨过程采用冷却水循环冷却,使液体温度不高于60℃,研磨转速2000r/min,研磨时间30min。研磨完成后得到的发泡母料,可用于挤出PVC发泡,添加比例为3%。
实施例九
本实施例所述的发泡母料包括:对苯二甲酸二辛酯40份、磷酸三辛酯20份、偶氮二甲酰胺50份、偶氮二异丁腈30份、BYK-111 1份、氧化锌10份、硬脂酸锌3份、抗氧剂168 0.5份、气相二氧化硅0.5份,将上述原料加入到高速研磨机中,研磨过程采用冷却水循环冷却,使液体温度不高于60℃,研磨转速1200r/min,研磨时间60min。研磨完成后得到的发泡母料,可用于挤出低发泡PP,添加比例为6%。
实施例十
本实施例所述的发泡母料包括:磷酸三辛酯20份、偶氮二甲酰胺10份、氧化锌10份、抗氧剂168 0.5份、气相二氧化硅0.5份,将上述原料加入到高速研磨机中,研磨过程采用冷却水循环冷却,使液体温度不高于60℃,研磨转速1200r/min,研磨时间15min。研磨完成后得到的发泡母料,可用于挤出低发泡PP,添加比例为0.5%。
对比例一
称取100份PP、35份偶氮二甲酰胺、10份氧化锌、3份硬脂酸锌、0.5份抗氧剂168,混合混匀,使用Z型捏合机,温度120℃,时间60min,再经过二辊塑炼薄通,温度120℃,辊隙0.5mm,薄通3次,充分塑化,然后在二辊车上拉片,冷却冲切,再将拉片切粒得到发泡母粒。再加入PP中进行挤出发泡,得到低发泡PP。
对比例二
以重量份数计,称取100份LDPE、40份偶氮二甲酰胺、4份过氧化二异丙苯、10份滑石粉、0.5份抗氧剂168,混合混匀,使用Z型捏合机,温度120℃,时间60min;再经过二辊塑炼薄通,温度120℃,辊隙0.5mm,薄通3次,充分塑化,然后在二辊车上拉片,冷却冲切,再将拉片切粒得到发泡母粒。再加入LDPE中进行挤出发泡,得到低发泡PE。
将上述实施例一至实施例十以及对比例一至对比例二制备得到的发泡塑料样板进行外观比较分析,发现,实施例一至实施例八制备得到的发泡塑料样板的泡孔均分散良好、大小均匀,而对比例一至对比例二制备得到的发泡塑料样板的发泡情况相近,泡孔均匀度不高,工序较繁琐。
以上所述实施例仅表达了本发明的几种实施方式,其描述较为具体和详细,但并不能因此而理解为对发明专利范围的限制。应当指出的是,对于本领域的普通技术人员来说,在不脱离本发明构思的前提下,还可以做出若干变形和改进,这些都属于本发明的保护范围。因此,本发明专利的保护范围应以所附权利要求为准。
Claims (10)
1.一种发泡母料,包括液体载体、发泡剂及助剂。
2.根据权利要求1所述的发泡母料,其特征在于,所述的发泡母料包括如下重量份的组分:液体载体20-60份、发泡剂10-80份及助剂适量。
3.根据权利要求1所述的发泡母料,其特征在于:所述液体载体为液体低聚物、增塑剂、植物油和/或矿物油。
4.根据权利要求3所述的发泡母料,其特征在于:所述液体低聚物包括丙烯酸酯类液体聚合物及丙烯酰胺类液体聚合物。
5.根据权利要求1所述的发泡母料,其特征在于:所述助剂包括发泡助剂与分散助剂。
6.根据权利要求5所述的发泡母料,其特征在于:所述助剂还包括抗氧剂及稳定剂。
7.根据权利要求1-6任一项所述的发泡母料,其特征在于:所述发泡剂为碳酸氢钠、碳酸锌、偶氮二甲酰胺、偶氮二异丁腈、偶氮二羧酸钡盐、偶氮胺基苯、偶氮二甲酸二异丙酯、偶氮二甲酸二乙酯、二亚硝基五亚甲基四胺、苯磺酰肼、对甲苯磺酰肼、对甲苯磺酰氨基脲、1,3-苯二磺酰肼、4,4’-氧化双苯磺酰肼、3,3’-二磺酰肼二苯砜、4,4’-氧代双(苯磺酰氨基脲)、三肼基三嗪、5-苯基四唑、硝基胍、二乙酰肼、肼撑酰胺中的一种或几种的混合物。
8.一种如权利要求1-7任一项所述的发泡母料的制备方法,其特征在于,包括如下步骤:将原料加入容器中,以500r/min-3000r/min的转速研磨分散均匀。
9.一种如权利要求1-7任一项所述的发泡母料在注塑、挤出发泡塑料的应用。
10.根据权利要求9所述的发泡母料的应用,其特征在于:所述发泡母料与发泡材料的质量比为0.5-6:100。
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CN115141406A (zh) * | 2021-12-13 | 2022-10-04 | 江苏索普化工股份有限公司 | 一种低粉尘化学发泡剂及其制备方法 |
Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102666689A (zh) * | 2009-10-16 | 2012-09-12 | 嘉洛斯控股有限公司 | 液体制剂 |
CN104341688A (zh) * | 2013-07-25 | 2015-02-11 | 上海英科实业有限公司 | 一种用于聚苯乙烯微孔发泡材料的发泡母粒及其制备方法 |
CN105175896A (zh) * | 2015-10-12 | 2015-12-23 | 福建师范大学泉港石化研究院 | 一种无机矿物粉体填充发泡母料及其制备方法 |
CN106883490A (zh) * | 2017-03-21 | 2017-06-23 | 合肥华凌股份有限公司 | 微发泡母粒及其制备方法以及冰箱发泡板 |
CN107001678A (zh) * | 2014-12-08 | 2017-08-01 | 嘉洛斯控股有限公司 | 热塑性聚合物 |
-
2020
- 2020-11-09 CN CN202011239982.1A patent/CN112574463A/zh active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102666689A (zh) * | 2009-10-16 | 2012-09-12 | 嘉洛斯控股有限公司 | 液体制剂 |
CN104341688A (zh) * | 2013-07-25 | 2015-02-11 | 上海英科实业有限公司 | 一种用于聚苯乙烯微孔发泡材料的发泡母粒及其制备方法 |
CN107001678A (zh) * | 2014-12-08 | 2017-08-01 | 嘉洛斯控股有限公司 | 热塑性聚合物 |
CN105175896A (zh) * | 2015-10-12 | 2015-12-23 | 福建师范大学泉港石化研究院 | 一种无机矿物粉体填充发泡母料及其制备方法 |
CN106883490A (zh) * | 2017-03-21 | 2017-06-23 | 合肥华凌股份有限公司 | 微发泡母粒及其制备方法以及冰箱发泡板 |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN115141406A (zh) * | 2021-12-13 | 2022-10-04 | 江苏索普化工股份有限公司 | 一种低粉尘化学发泡剂及其制备方法 |
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