CN109233024A - 一种轻量sbr发泡海绵 - Google Patents

一种轻量sbr发泡海绵 Download PDF

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CN109233024A
CN109233024A CN201810769577.7A CN201810769577A CN109233024A CN 109233024 A CN109233024 A CN 109233024A CN 201810769577 A CN201810769577 A CN 201810769577A CN 109233024 A CN109233024 A CN 109233024A
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范沈杰
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HUZHOU DAOCHANGXIANG ASSET MANAGEMENT Co Ltd
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Abstract

本发明公开了一种轻量SBR发泡海绵的制备方法,其步骤如下:(1)配备原料:按照重量份数,取SBR 100份,玉米淀粉接枝丙烯酰胺3‑8份,炭黑2份,氧化锌1‑1.5份,云母粉20‑40份,环烷油4‑6份,苯二磺酰肼/AC复合发泡剂2份,促进剂DZ 3份;硫化剂1份;(2)制备:置于密炼机中,依次加入步骤(1)的原料,在95下混炼15min;然后将混炼胶置于开炼机中,控制辊温为45℃,薄通6次,打三角包3次,下片;硫化发泡。本发明在从工艺到配方都进行优化,从而何获得轻量化的均匀微发泡,而且减震性能好,寿命长。

Description

一种轻量SBR发泡海绵
技术领域
本发明涉及一种轻量SBR发泡海绵,属于改性发泡塑料制备技术领域。
背景技术
汽车材料轻量化是实现整车轻量化的有效途径。微发泡技术是汽车轻量化的最有效途径之一,将其引入汽车材料的制备技术中,在保证材料基本性能的前提下,显著减轻制件重量,有利于实现汽车轻量化。其中,具有轻量化特征的聚丙烯微发泡材料替代未发泡材料,在性能满足的情况下,零部件减重10%以上。已在部分汽车部件,如仪表板、座椅、后备箱盖板等部件得到应用,市场前景广阔。
SBR 高发泡海绵是一种新型弹性体材料。1998 年美国Li G Q 等以粉碎后的SBR为原料, 添加玻璃微球、纳米粘土和碾碎的玻璃纤维来增强, 研制具有夹层结构的复合泡沫材料, 该复合泡沫材料能吸收相当高的冲击能。美国固特异橡胶公司公开了一种具有复合开孔结构的发泡材料, 该发泡材料采用羧基化SBR 制备, 具有优异的耐压力和耐磨性能。孔令香等研究了促进剂( 噻唑类、次磺酰胺类和秋兰姆类) 在SBR 发泡硫化过程中对发泡剂OT 分解速度的影响。
本发明旨在发明一种轻量SBR 发泡海绵,其具有新型的轻量化,减震好,寿命长的特点。本发明在从工艺到配方都进行优化,从而何获得轻量化的均匀微发泡,而且减震性能好,寿命长。
发明内容
本发明的目的是提供一种轻量SBR 发泡海绵,其具有新型的轻量化,减震好,寿命长的特点。本发明在从工艺到配方都进行优化,从而何获得轻量化的均匀微发泡,而且减震性能好,寿命长。
玉米是最常见的农产品之一,其中含有大量淀粉,容易获得,价格便宜,且所形成的产物能够完全被生物降解。国内关于接枝淀粉的研究比较多,以玉米淀粉和丙烯酰胺作为原料,以硫酸铵为引发剂,通过水溶液聚合法成功合成了淀粉接枝丙烯酰胺絮凝剂。本发明人发现,在SBR 发泡海绵体系中,加入适量的玉米淀粉接枝丙烯酰胺可以预料不到的提高发泡的均匀度,降低密度,提升减震性能。
本发明是这样实现的:
一种轻量SBR 发泡海绵的制备方法,其步骤如下:
(1)配备原料:
按照重量份数,取SBR 100份,玉米淀粉接枝丙烯酰胺3-8份,炭黑2份,氧化锌1-1.5份,云母粉20-40份,环烷油4-6份, 苯二磺酰肼/ AC 复合发泡剂 2份, 促进剂DZ 3份;硫化剂1份;
(2)制备:
置于密炼机中, 依次加入步骤(1)的原料,在95 下混炼15 min; 然后将混炼胶置于开炼机中, 控制辊温为45℃ , 薄通6 次, 打三角包3 次, 下片;
硫化发泡:硫化条件为120-125℃,35-40 min, 然后置于另一台平板硫化机中, 进行二段硫化发泡, 硫化条件为170℃,10min, 然后置于第三台平板硫化机中, 进行三段硫化发泡, 硫化条件为140℃,20min, 再经自然冷却定型, 制成SBR 海绵。
本发明不仅仅在配方上进行优化,而且进行三段发泡工艺。
本发明的优点:
本发明一种轻量SBR发泡海绵,其具有新型的轻量化,减震好,寿命长的特点。本发明在从工艺到配方都进行优化,从而何获得轻量化的均匀微发泡,而且减震性能好,寿命长。
具体实施方式
下面详细描述本发明的实施例,所述实施例仅用于解释本发明,而不能理解为对本发明的限制。
本发明所用的玉米淀粉接枝丙烯酰胺接枝率为60-70%。
实施例1
一种轻量SBR发泡海绵的制备方法,其步骤如下:
(1)配备原料:
按照重量份数,取SBR 100份,玉米淀粉接枝丙烯酰胺3份,炭黑2份,氧化锌1份, 云母粉20份,环烷油4份, 苯二磺酰肼/ AC 复合发泡剂 2份, 促进剂DZ 3份;硫化剂1份;
(2)制备:
置于密炼机中, 依次加入步骤(1)的原料,在95 下混炼15 min; 然后将混炼胶置于开炼机中, 控制辊温为45℃ , 薄通6 次, 打三角包3 次, 下片( 试样厚度为2 mm);
硫化发泡:硫化条件为120℃,35min, 然后置于另一台平板硫化机中, 进行二段硫化发泡, 硫化条件为170℃,10min, 然后置于第三台平板硫化机中, 进行三段硫化发泡, 硫化条件为140℃,20min, 再经自然冷却定型, 制成SBR 海绵片形试样。
该配方SBR 高发泡海绵的物理性能为:拉断伸长率209% , 密度为0.120Mg *m- 3, 回弹值78. 8% , 具有密度低、柔软度好、弹性高和减震性能好等特点。
实施例2:
一种轻量SBR 发泡海绵的制备方法,其步骤如下:
(1)配备原料:
按照重量份数,取SBR 100份,玉米淀粉接枝丙烯酰胺8份,炭黑2份,氧化锌1.5份, 云母粉40份,环烷油6份, 苯二磺酰肼/ AC 复合发泡剂 2份, 促进剂DZ 3份;硫化剂1份;
(2)制备:
置于密炼机中, 依次加入步骤(1)的原料,在95 下混炼15 min; 然后将混炼胶置于开炼机中, 控制辊温为45℃ , 薄通6 次, 打三角包3 次, 下片( 试样厚度为2 mm);
硫化发泡:硫化条件为125℃, 40 min, 然后置于另一台平板硫化机中, 进行二段硫化发泡, 硫化条件为170℃,10min, 然后置于第三台平板硫化机中, 进行三段硫化发泡,硫化条件为140℃,20min, 再经自然冷却定型, 制成SBR 海绵片形试样。
该配方SBR 高发泡海绵的物理性能为:拉断伸长率219% , 密度为0.115Mg *m- 3, 回弹值78. 9% , 具有密度低、柔软度好、弹性高和减震性能好等特点。
实施例3
一种轻量SBR 发泡海绵的制备方法,其步骤如下:
(1)配备原料:
按照重量份数,取SBR 100份,玉米淀粉接枝丙烯酰胺5份,炭黑2份,氧化锌1.5份, 云母粉30份,环烷油5份, 苯二磺酰肼/ AC 复合发泡剂 2份, 促进剂DZ 3份;硫化剂1份;
(2)制备:
置于密炼机中, 依次加入步骤(1)的原料,在95 下混炼15 min; 然后将混炼胶置于开炼机中, 控制辊温为45℃ , 薄通6 次, 打三角包3 次, 下片( 试样厚度为2 mm);
硫化发泡:硫化条件为122℃,38min, 然后置于另一台平板硫化机中, 进行二段硫化发泡, 硫化条件为170℃,10min, 然后置于第三台平板硫化机中, 进行三段硫化发泡, 硫化条件为140℃,20min, 再经自然冷却定型, 制成SBR 海绵片形试样。
该配方SBR 高发泡海绵的物理性能为:拉断伸长率229% , 密度为0.112Mg *m- 3, 回弹值78. 8% , 具有密度低、柔软度好、弹性高和减震性能好等特点。
实施例4
一种轻量SBR 发泡海绵的制备方法,其步骤如下:
(1)配备原料:
按照重量份数,取SBR 100份,玉米淀粉接枝丙烯酰胺7份,炭黑2份,氧化锌1.5份, 云母粉32份,环烷油5份, 苯二磺酰肼/ AC 复合发泡剂 2份, 促进剂DZ 3份;硫化剂1份;
(2)制备:
置于密炼机中, 依次加入步骤(1)的原料,在95 下混炼15 min; 然后将混炼胶置于开炼机中, 控制辊温为45℃ , 薄通6 次, 打三角包3 次, 下片( 试样厚度为2 mm);
硫化发泡:硫化条件为123℃,39 min, 然后置于另一台平板硫化机中, 进行二段硫化发泡, 硫化条件为170℃,10min, 然后置于第三台平板硫化机中, 进行三段硫化发泡, 硫化条件为140℃,20min, 再经自然冷却定型, 制成SBR 海绵片形试样。
该配方SBR 高发泡海绵的物理性能为:拉断伸长率218% , 密度为0.116Mg *m- 3, 回弹值79.2% , 具有密度低、柔软度好、弹性高和减震性能好等特点。
实施例5
一种轻量SBR 发泡海绵的制备方法,其步骤如下:
(1)配备原料:
按照重量份数,取SBR 100份,玉米淀粉接枝丙烯酰胺7份,炭黑2份,氧化锌1.5份, 云母粉29份,环烷油6份, 苯二磺酰肼/ AC 复合发泡剂 2份, 促进剂DZ 3份;硫化剂1份;
(2)制备:
置于密炼机中, 依次加入步骤(1)的原料,在95 下混炼15 min; 然后将混炼胶置于开炼机中, 控制辊温为45℃ , 薄通6 次, 打三角包3 次, 下片( 试样厚度为2 mm);
硫化发泡:硫化条件为123℃,35min, 然后置于另一台平板硫化机中, 进行二段硫化发泡, 硫化条件为170℃,10min, 然后置于第三台平板硫化机中, 进行三段硫化发泡, 硫化条件为140℃,20min, 再经自然冷却定型, 制成SBR 海绵片形试样。
该配方SBR 高发泡海绵的物理性能为:拉断伸长率218% , 密度为0.118Mg *m- 3, 回弹值79.1% , 具有密度低、柔软度好、弹性高和减震性能好等特点。
实施例6(对比例)
(1)配备原料:
按照重量份数,取SBR 100份,炭黑2份,氧化锌1.5份, 云母粉30份,环烷油5份, 苯二磺酰肼/ AC 复合发泡剂 2份, 促进剂DZ 3份;硫化剂1份;
(2)制备:
置于密炼机中, 依次加入步骤(1)的原料,在95 下混炼15 min; 然后将混炼胶置于开炼机中, 控制辊温为45℃ , 薄通6 次, 打三角包3 次, 下片( 试样厚度为2 mm);
硫化发泡:硫化条件为122℃,38min, 然后置于另一台平板硫化机中, 进行二段硫化发泡, 硫化条件为170℃,10min, 再经自然冷却定型, 制成SBR 海绵片形试样。
该配方SBR 高发泡海绵的物理性能为:拉断伸长率159% , 密度为0.327Mg *m- 3, 回弹值78. 6%。
可见,三段发泡工艺和玉米淀粉接枝丙烯酰胺的加入都非常重要,可以降低密度,提升强度。
在本说明书的描述中,参考术语“一个实施例”、“一些实施例”、“示例”、“具体示例”、或“一些示例”等的描述意指结合该实施例或示例描述的具体特征、结构、材料或者特点包含于本发明的至少一个实施例或示例中。在本说明书中,对上述术语的示意性表述不一定指的是相同的实施例或示例。而且,描述的具体特征、结构、材料或者特点可以在任何的一个或多个实施例或示例中以合适的方式结合。
尽管已经示出和描述了本发明的实施例,本领域的普通技术人员可以理解:在不脱离本发明的原理和宗旨的情况下可以对这些实施例进行多种变化、修改、替换和变型,本发明的范围由权利要求及其等同物限定。

Claims (3)

1.一种轻量SBR发泡海绵的制备方法,其步骤如下:
(1)配备原料:
按照重量份数,取SBR 100份,玉米淀粉接枝丙烯酰胺3-8份,炭黑2份, 氧化锌1-1.5份, 云母粉20-40份,环烷油4-6份, 苯二磺酰肼/ AC 复合发泡剂 2份, 促进剂DZ 3份;硫化剂1份;
(2)制备:
置于密炼机中, 依次加入步骤(1)的原料,在95 下混炼15 min; 然后将混炼胶置于开炼机中, 控制辊温为45℃ , 薄通6 次, 打三角包3 次, 下片;
硫化发泡。
2.权利要求1所述的方法,其特征在于∶
硫化发泡: 硫化条件为120-125℃,35-40 min, 然后置于另一台平板硫化机中, 进行二段硫化发泡, 硫化条件为170℃,10min, 然后置于第三台平板硫化机中, 进行三段硫化发泡, 硫化条件为140℃,20min, 再经自然冷却定型, 制成SBR海绵。
3.权利要求1-2所述的方法制备得到的轻量SBR发泡海绵。
CN201810769577.7A 2018-07-13 2018-07-13 一种轻量sbr发泡海绵 Pending CN109233024A (zh)

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Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5244861A (en) * 1975-10-07 1977-04-08 Hirono Kagaku Kogyo Kk Process for preparing crosslinked products of liquid diene rubbers hav ing terminal hydroxyl groups and improved physical properties
CN1800249A (zh) * 2005-01-05 2006-07-12 项爱民 可生物降解的淀粉基发泡组合物及其包含它的发泡制品
CN103627136A (zh) * 2012-08-21 2014-03-12 山东固安特新材料科技股份有限公司 煤矿充填密闭用高分子发泡材料
CN105713262A (zh) * 2016-04-14 2016-06-29 陕西科技大学 一种低收缩率丁苯橡胶发泡鞋底材料的制备工艺
CN106217734A (zh) * 2016-07-18 2016-12-14 柳州弘蓝科技有限公司 一种制备保温隔音墙体砌块的方法

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5244861A (en) * 1975-10-07 1977-04-08 Hirono Kagaku Kogyo Kk Process for preparing crosslinked products of liquid diene rubbers hav ing terminal hydroxyl groups and improved physical properties
CN1800249A (zh) * 2005-01-05 2006-07-12 项爱民 可生物降解的淀粉基发泡组合物及其包含它的发泡制品
CN103627136A (zh) * 2012-08-21 2014-03-12 山东固安特新材料科技股份有限公司 煤矿充填密闭用高分子发泡材料
CN105713262A (zh) * 2016-04-14 2016-06-29 陕西科技大学 一种低收缩率丁苯橡胶发泡鞋底材料的制备工艺
CN106217734A (zh) * 2016-07-18 2016-12-14 柳州弘蓝科技有限公司 一种制备保温隔音墙体砌块的方法

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