CN109575503A - 一种微发泡阻燃abs镭雕材料及其制备方法 - Google Patents

一种微发泡阻燃abs镭雕材料及其制备方法 Download PDF

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CN109575503A
CN109575503A CN201811456281.6A CN201811456281A CN109575503A CN 109575503 A CN109575503 A CN 109575503A CN 201811456281 A CN201811456281 A CN 201811456281A CN 109575503 A CN109575503 A CN 109575503A
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laser engraving
fretting map
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胡勤
皮正亮
葛嘉宝
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Guangdong Vlin Plastics Engineering Ltd By Share Ltd
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Abstract

本发明公开了一种微发泡阻燃ABS镭雕材料及其制备方法,其技术方案要点是包括以下重量组分:ABS树脂65%~75%,分散剂0~0.5%,复配增韧剂5%~15%,环保溴系阻燃剂12%~16%,复配阻燃协效剂2.5%~3.5%,抗滴落剂0~0.5%,微发泡剂0~2%,镭雕粉0~0.6%,抗氧剂0.3%~0.6%,润滑剂0.3%~1.5%。本发明的一种微发泡阻燃ABS镭雕材料其制备方法,产品具有较低的密度、优异的阻燃性、优异的韧性、优异的镭雕性、650℃灼热丝不起火、优异的尺寸稳定性,并且加工工艺简单,可用于轻量化的阻燃产品、表面镭雕刻字或图形产品等领域,且制备工艺简单。

Description

一种微发泡阻燃ABS镭雕材料及其制备方法
【技术领域】
本发明属于高分子材料技术领域,具体涉及一种微发泡阻燃ABS镭雕材料及其制备方法。
【背景技术】
市场上通用阻燃ABS材料的比重较大,很难满足阻燃产品的轻量化需求。丙烯腈-丁二烯-苯乙烯共聚物(简称ABS)具有很好的韧性、良好的耐化学药品性、高的光泽度、优异的尺寸稳定性、良好的加工流动性、优异的着色性、优异的电镀性等,但其耐候性差。市场常用的低密度阻燃材料主要是阻燃PP材料,市场上低密度阻燃ABS材料很少,但其韧性较差,尺寸稳定性低,在耐高温、表面光泽方面没有优势,且不能满足对韧性或尺寸精度要求高的产品的需求,难以作为镭雕基材进行加工。
【发明内容】
本发明的一种微发泡阻燃ABS镭雕材料,具有较低的密度、优异的阻燃性、优异的韧性、优异的镭雕性、650℃灼热丝不起火、优异的尺寸稳定性,并且加工工艺简单,可用于轻量化的阻燃产品、表面镭雕刻字或图形产品等领域。
本发明还提供一种微发泡阻燃ABS镭雕材料的制备方法。
本发明技术方案如下:
一种微发泡阻燃ABS镭雕材料,包括以下重量组分:
优选的,所述的ABS树脂(丙烯腈-丁二烯-苯乙烯共聚物树脂)为宁波甬兴,HI-121H,熔融指数23g/10min。
优选的,所述的分散剂为白矿油、硅油或聚乙烯蜡粉中一种或两种混合。优选分散剂为德国瓦克,AK-1000,粘度(25℃,CS)1000±50‰。
优选的,所述的复配增韧剂为乙烯-醋酸乙烯共聚物、氯化聚乙烯以重量百分比2:3~5:8复配制得。优选为泰国石化,SV1055;潍坊亚星,CPE-2135,氯含量35±1%,熔融指数40g/10min,氯化聚乙烯具有优异的耐臭氧性、耐候性,色稳定性、耐化学药品性、耐油性和难燃性等特性,耐屈挠性和耐磨耗性等机械性能也很好。其单真独配合寸的用途有耐化学药品胶辊、电线、模型制品及其他工业制品等。
优先的,所述的环保溴系阻燃剂为四溴双酚A、溴代三嗪中一种。四溴双酚A优选为山东天一,Z-58,溴含量58%,熔点180℃;溴代三嗪优选山东旭锐,SR-103,溴含量67%,熔点230℃。
优先的,所述的复配阻燃协效剂为三氧化二锑、硅系化合物按重量百分比为7:3~5:5复配。优选复配阻燃协效剂为湖南闪星,三氧化二锑,有效物质含量99.5%;广州青晏,SF-200。
优先的,所述的抗滴落剂为聚四氟乙烯,所述的微发泡剂为白色粉末微发泡剂。优选抗滴落剂为森赛逖康,SN3300B7,有效物质含量99.9%,优选微发泡剂为安徽汇利,W3835,发泡温度150~180℃,发气量150~160mL/g。
优先的,所述的镭雕粉为白雕黑镭雕粉或黑雕白镭雕粉中一种。
优先黑雕白镭雕粉为佛山和琦润,HZ-889A;白雕黑镭雕粉为佛山和琦润,HZ-890。
优先的,所述的抗氧剂为四[β-(3,5-二叔丁基-4-羟基苯基)丙酸]季戊四醇酯(1010)或β-(3,5-二叔丁基-4-羟基苯基)丙酸正十八碳醇酯(1076)与三(2,4-二叔丁基苯基)亚磷酸酯(168)按重量百分比为1:2复配,所述的润滑剂为硬脂酸、硬脂酸钙、乙撑双硬脂酸酯、特殊改性乙撑双硬脂酸酯和季戊四醇硬脂酸酯中一种或两种,优选为可赛成功,EBS,熔点140℃左右。
一种微发泡阻燃ABS镭雕材料的制备方法,包括以下步骤:
1)、先将称好的丙烯腈-丁二烯-苯乙烯共聚物树脂、分散剂加入到高速混合机中,混合1~2min,再将称好的复配增韧剂、抗滴落剂、微发泡剂、镭雕粉、抗氧剂和润滑剂加到上述混合均匀的物料中,混合1~2min,然后将称好的环保溴系阻燃剂、复配阻燃协效剂加到上述混合均匀物料中,混合1~2min;
2)、最后将混合均匀的物料加到双螺杆挤出机中,所述的双螺杆挤出机的加工温度为170~200℃,螺杆转速为350~450rpm/min,喂料螺杆转速12~20rpm/min,经双螺杆挤出机熔融挤出后并经水冷、风干、切粒和包装。
本发明相对于现有技术,有以下优点:
本发明的一种微发泡阻燃ABS镭雕材料,采用中等韧性ABS树脂作为ABS基材,四溴双酚A或溴代三嗪作为阻燃剂,三氧化二锑与硅系化合物复配比例为2:1~1:1,乙烯-醋酸乙烯共聚物与氯化聚乙烯复配作为增韧剂,ABS专用镭雕助剂,ABS专用微发泡剂,再加其它助剂,所制备的微发泡阻燃ABS镭雕材料,具有很低的密度、优异的阻燃性、优异的韧性、优异的镭雕性、优异的加工流动性、高光泽、优异的尺寸稳定性、较低的成本、650℃灼热丝不起火、优异的着色性等特点,产品具有较低的密度、优异的阻燃性、优异的韧性、优异的镭雕性、优异的加工流动性、较低的成本等,并且通过650℃灼热丝30秒全程不起火测试;
本发明的一种微发泡阻燃ABS镭雕材料的制备方法,工艺简便,反应温和,适合大批量连续生产。
【具体实施方式】
下面对本发明技术作具体说明:
结合具体实施例1~4说明本发明的具体技术方案:
实施例1:
将称量好的丙烯腈-丁二烯-苯乙烯共聚物树脂(HI-121H)、分散剂加到高速混合机中,混合1~2min,再将称好的乙烯-醋酸乙烯共聚物、抗氧剂(1010/168=1:2)和润滑剂加到上述混合均匀的物料中,混合1~2min,然后将称好的氯化聚乙烯、四溴双酚A(Z-58)和三氧化二锑加到上述混合均匀的物料中,混合1~2min,最后将混合均匀的物料加到双螺杆挤出机料斗中熔融挤出,双螺杆挤出机各段温度为:1区温度80℃、2区温度190℃、3区温度185℃、4区温度175℃、5区温度170℃、6区温度180℃、7区温度170℃、8区温度180℃、9区温度185℃、模头温度195℃。双螺杆挤出机转速400rpm/min,喂料螺杆转速16rpm/min。对比例1所生产的产品记作A1或A2。
实施例2:
将称量好的丙烯腈-丁二烯-苯乙烯共聚物树脂(HI-121H)、分散剂加到高速混合机中,混合1~2min,再将称好的乙烯-醋酸乙烯共聚物、抗氧剂(1076/168=1:2)和润滑剂加到上述混合均匀的物料中,混合1~2min,然后将称好的氯化聚乙烯(CPE-2135)、溴代三嗪(SR-103)和三氧化二锑加到上述混合均匀的物料中,混合1~2min,最后将混合均匀的物料加到双螺杆挤出机料斗中熔融挤出,双螺杆挤出机各段温度为:1区温度80℃、2区温度190℃、3区温度185℃、4区温度175℃、5区温度170℃、6区温度180℃、7区温度170℃、8区温度180℃、9区温度185℃、模头温度195℃。双螺杆挤出机转速400rpm/min,喂料螺杆转速16rpm/min。对比例2所生产的产品记作A3或A4。
对比例1:
先按表1将称好的丙烯腈-丁二烯-苯乙烯共聚物树脂(HI-121H)、分散剂加到高速混合机中,混合1~2min,再将称好的乙烯-醋酸乙烯共聚物、抗滴落剂、抗氧剂(1010/168=1:2)和润滑剂(EBS)加到上述混合均匀的物料中,混合1~2min,然后将称好的氯化聚乙烯(CPE-2135)、四溴双酚A(Z-58)、三氧化二锑、硅系化合物(SF-200)和微发泡剂(W3835)加到上述混合均匀的物料中,混合1~2min,最后将混合均匀的物料加到双螺杆挤出机料斗中熔融挤出,双螺杆挤出机各段温度为:1区温度80℃、2区温度190℃、3区温度185℃、4区温度175℃、5区温度170℃、6区温度180℃、7区温度170℃、8区温度180℃、9区温度185℃、模头温度195℃。双螺杆挤出机转速400rpm/min,喂料螺杆转速16rpm/min。对比例1所生产的产品记作B1-2。
对比例2:
按设计称量好的丙烯腈-丁二烯-苯乙烯共聚物树脂(HI-121H)、分散剂加到高速混合机中,混合1~2min,再将称好的乙烯-醋酸乙烯共聚物(SV1055)、抗滴落剂、黑雕白镭雕粉/白雕黑镭雕粉、抗氧剂(1076/168=1:2)和润滑剂(EBS)加到上述混合均匀的物料中,混合1~2min,然后将称好的氯化聚乙烯(CPE-2135)、溴代三嗪(SR-103)、三氧化二锑、硅系化合物(SF-200)和微发泡剂(W3835)加到上述混合均匀的物料中,混合1~2min,最后将混合均匀的物料加到双螺杆挤出机料斗中熔融挤出,双螺杆挤出机各段温度为:1区温度80℃、2区温度190℃、3区温度185℃、4区温度175℃、5区温度170℃、6区温度180℃、7区温度170℃、8区温度180℃、9区温度185℃、模头温度195℃。双螺杆挤出机转速400rpm/min,喂料螺杆转速16rpm/min。对比例2所生产的产品记作B3-4。
表1:实施例1~4各组分含量
表2:对比例1~4各组分含量
将实施例1~4所生产的产品进行性能测试,测试结果如下
表3:产品A1~A4的性能测试结果
表4:产品B1~B4的性能测试结果
由上表可知,加四溴双酚A的阻燃ABS材料的缺口冲击强度、热变形温度比加溴代三嗪的差,但其加工流动性要比加溴代三嗪的好很多,加硅系阻燃协效剂、微发泡剂的阻燃ABS材料的密度比没加的明显小很多,能满足轻量化阻燃产品的需求,加镭雕助剂的阻燃ABS材料的镭雕性能比没加镭雕粉的好很多,能满足表面镭雕刻字或图形的阻燃产品的需求。
本发明优选中等韧性ABS树脂作为ABS基材,四溴双酚A或溴代三嗪作为阻燃剂,三氧化二锑与硅系化合物复配比例为2:1~1:1,乙烯-醋酸乙烯共聚物与氯化聚乙烯复配作为增韧剂,ABS专用镭雕助剂,ABS专用微发泡剂,再加其它助剂,所制备的微发泡阻燃ABS镭雕材料具有很低的密度、优异的阻燃性、优异的韧性、优异的镭雕性、优异的加工流动性、高光泽、优异的尺寸稳定性、较低的成本、650℃灼热丝不起火、优异的着色性等,并且加工工艺简单,可用于轻量化的阻燃产品、表面镭雕刻字或图形产品等领域。

Claims (10)

1.一种微发泡阻燃ABS镭雕材料,其特征在于包括以下重量组分:
2.根据权利要求1所述的一种微发泡阻燃ABS镭雕材料,其特征在于:所述的丙烯腈-丁二烯-苯乙烯共聚物树脂的熔融指数20~50g/10min。
3.根据权利要求1所述的一种微发泡阻燃ABS镭雕材料,其特征在于:所述的分散剂为白矿油、硅油或聚乙烯蜡粉中一种或两种混合。
4.根据权利要求1所述的一种微发泡阻燃ABS镭雕材料,其特征在于:所述的复配增韧剂为乙烯-醋酸乙烯共聚物、氯化聚乙烯以重量百分比2:3~5:8复配制得。
5.根据权利要求1所述的一种微发泡阻燃ABS镭雕材料,其特征在于:所述的环保溴系阻燃剂为四溴双酚A、溴代三嗪中一种。
6.根据权利要求1所述的一种微发泡阻燃ABS镭雕材料,其特征在于:所述的复配阻燃协效剂为三氧化二锑、硅系化合物按重量百分比为7:3~5:5复配。
7.根据权利要求1所述的一种微发泡阻燃ABS镭雕材料,其特征在于:所述的抗滴落剂为聚四氟乙烯,所述的微发泡剂为白色粉末微发泡剂。
8.根据权利要求1所述的一种微发泡阻燃ABS镭雕材料,其特征在于:所述的镭雕粉为白雕黑镭雕粉或黑雕白镭雕粉中一种。
9.根据权利要求1所述的一种微发泡阻燃ABS镭雕材料,其特征在于:所述的抗氧剂为四[β-(3,5-二叔丁基-4-羟基苯基)丙酸]季戊四醇酯(1010)或β-(3,5-二叔丁基-4-羟基苯基)丙酸正十八碳醇酯(1076)与三(2,4-二叔丁基苯基)亚磷酸酯(168)按重量百分比为1:2复配,所述的润滑剂为硬脂酸、硬脂酸钙、乙撑双硬脂酸酯、特殊改性乙撑双硬脂酸酯和季戊四醇硬脂酸酯中一种或两种。
10.一种微发泡阻燃ABS镭雕材料的制备方法,其特征在于包括以下步骤:
1)、先将称好的丙烯腈-丁二烯-苯乙烯共聚物树脂、分散剂加入到高速混合机中,混合1~2min,再将称好的复配增韧剂、抗滴落剂、微发泡剂、镭雕粉、抗氧剂和润滑剂加到上述混合均匀的物料中,混合1~2min,然后将称好的环保溴系阻燃剂、复配阻燃协效剂加到上述混合均匀物料中,混合1~2min;
2)、最后将混合均匀的物料加到双螺杆挤出机中,所述的双螺杆挤出机的加工温度为170~200℃,螺杆转速为350~450rpm/min,喂料螺杆转速12~20rpm/min,经双螺杆挤出机熔融挤出后并经水冷、风干、切粒和包装。
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Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110483891A (zh) * 2019-08-23 2019-11-22 江苏金发科技新材料有限公司 一种塑胶表面凹纹理的制备方法
CN110498947A (zh) * 2019-08-23 2019-11-26 上海金发科技发展有限公司 一种增加塑胶产品表面摩擦力的方法
CN110527238A (zh) * 2019-08-23 2019-12-03 上海金发科技发展有限公司 一种具有气泡效果皮纹的制备方法
CN115260697A (zh) * 2022-08-24 2022-11-01 江南大学 一种低密度abs珠粒泡沫及其制备方法和应用

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5576377A (en) * 1994-03-30 1996-11-19 Bayer Ag Polymer moulding materials for producing a partial color change by laser energy, particularly for the production of colored markings
JPH0920855A (ja) * 1995-07-07 1997-01-21 Teijin Ltd Abs樹脂組成物からなる黒発色レーザマーキング性を有するキーボード
EP0827980A2 (en) * 1996-09-10 1998-03-11 Daicel Chemical Industries, Ltd. A resin composition for a white marking
CN101333325A (zh) * 2007-06-29 2008-12-31 美泰塑胶股份有限公司 Abs镭雕材料及其加工方法
CN103030920A (zh) * 2012-12-27 2013-04-10 易业电子(深圳)有限公司 用于激光雕刻的树脂组合物及其制备方法

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5576377A (en) * 1994-03-30 1996-11-19 Bayer Ag Polymer moulding materials for producing a partial color change by laser energy, particularly for the production of colored markings
JPH0920855A (ja) * 1995-07-07 1997-01-21 Teijin Ltd Abs樹脂組成物からなる黒発色レーザマーキング性を有するキーボード
EP0827980A2 (en) * 1996-09-10 1998-03-11 Daicel Chemical Industries, Ltd. A resin composition for a white marking
CN101333325A (zh) * 2007-06-29 2008-12-31 美泰塑胶股份有限公司 Abs镭雕材料及其加工方法
CN103030920A (zh) * 2012-12-27 2013-04-10 易业电子(深圳)有限公司 用于激光雕刻的树脂组合物及其制备方法

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110483891A (zh) * 2019-08-23 2019-11-22 江苏金发科技新材料有限公司 一种塑胶表面凹纹理的制备方法
CN110498947A (zh) * 2019-08-23 2019-11-26 上海金发科技发展有限公司 一种增加塑胶产品表面摩擦力的方法
CN110527238A (zh) * 2019-08-23 2019-12-03 上海金发科技发展有限公司 一种具有气泡效果皮纹的制备方法
CN115260697A (zh) * 2022-08-24 2022-11-01 江南大学 一种低密度abs珠粒泡沫及其制备方法和应用

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