CN111409333A - 一种防毒阻燃氯醚橡胶防护胶布及制备方法 - Google Patents
一种防毒阻燃氯醚橡胶防护胶布及制备方法 Download PDFInfo
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- CN111409333A CN111409333A CN202010237274.8A CN202010237274A CN111409333A CN 111409333 A CN111409333 A CN 111409333A CN 202010237274 A CN202010237274 A CN 202010237274A CN 111409333 A CN111409333 A CN 111409333A
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- epichlorohydrin rubber
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- 229920005558 epichlorohydrin rubber Polymers 0.000 title claims abstract description 53
- 239000003063 flame retardant Substances 0.000 title claims abstract description 28
- 239000002390 adhesive tape Substances 0.000 title claims abstract description 27
- 230000001681 protective effect Effects 0.000 title claims abstract description 27
- RNFJDJUURJAICM-UHFFFAOYSA-N 2,2,4,4,6,6-hexaphenoxy-1,3,5-triaza-2$l^{5},4$l^{5},6$l^{5}-triphosphacyclohexa-1,3,5-triene Chemical compound N=1P(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP(OC=2C=CC=CC=2)(OC=2C=CC=CC=2)=NP=1(OC=1C=CC=CC=1)OC1=CC=CC=C1 RNFJDJUURJAICM-UHFFFAOYSA-N 0.000 title claims abstract description 21
- 238000002360 preparation method Methods 0.000 title claims description 10
- 239000002574 poison Substances 0.000 title claims description 8
- 239000000203 mixture Substances 0.000 claims abstract description 32
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- 239000003795 chemical substances by application Substances 0.000 claims abstract description 22
- 239000000463 material Substances 0.000 claims abstract description 20
- TWNQGVIAIRXVLR-UHFFFAOYSA-N oxo(oxoalumanyloxy)alumane Chemical compound O=[Al]O[Al]=O TWNQGVIAIRXVLR-UHFFFAOYSA-N 0.000 claims abstract description 16
- 239000006229 carbon black Substances 0.000 claims abstract description 15
- 239000004677 Nylon Substances 0.000 claims abstract description 11
- CPLXHLVBOLITMK-UHFFFAOYSA-N magnesium oxide Inorganic materials [Mg]=O CPLXHLVBOLITMK-UHFFFAOYSA-N 0.000 claims abstract description 11
- 239000000395 magnesium oxide Substances 0.000 claims abstract description 11
- AXZKOIWUVFPNLO-UHFFFAOYSA-N magnesium;oxygen(2-) Chemical compound [O-2].[Mg+2] AXZKOIWUVFPNLO-UHFFFAOYSA-N 0.000 claims abstract description 11
- 229920001778 nylon Polymers 0.000 claims abstract description 11
- XOOUIPVCVHRTMJ-UHFFFAOYSA-L zinc stearate Chemical compound [Zn+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O XOOUIPVCVHRTMJ-UHFFFAOYSA-L 0.000 claims abstract description 11
- 238000001125 extrusion Methods 0.000 claims abstract description 8
- 239000002994 raw material Substances 0.000 claims abstract description 8
- 238000002156 mixing Methods 0.000 claims description 26
- XMFOQHDPRMAJNU-UHFFFAOYSA-N lead(ii,iv) oxide Chemical compound O1[Pb]O[Pb]11O[Pb]O1 XMFOQHDPRMAJNU-UHFFFAOYSA-N 0.000 claims description 12
- 238000000034 method Methods 0.000 claims description 12
- 229920001971 elastomer Polymers 0.000 claims description 9
- 238000001914 filtration Methods 0.000 claims description 6
- 229940035105 lead tetroxide Drugs 0.000 claims description 6
- 238000001816 cooling Methods 0.000 claims description 3
- 238000007599 discharging Methods 0.000 claims description 3
- 238000005485 electric heating Methods 0.000 claims description 3
- 238000005096 rolling process Methods 0.000 claims description 3
- 238000010074 rubber mixing Methods 0.000 claims description 3
- 238000004073 vulcanization Methods 0.000 claims description 3
- 231100000614 poison Toxicity 0.000 claims description 2
- 230000002265 prevention Effects 0.000 claims description 2
- 230000007123 defense Effects 0.000 abstract description 2
- 230000001147 anti-toxic effect Effects 0.000 description 8
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- WEVYAHXRMPXWCK-UHFFFAOYSA-N Acetonitrile Chemical compound CC#N WEVYAHXRMPXWCK-UHFFFAOYSA-N 0.000 description 3
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- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 2
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- ADCOVFLJGNWWNZ-UHFFFAOYSA-N antimony trioxide Chemical compound O=[Sb]O[Sb]=O ADCOVFLJGNWWNZ-UHFFFAOYSA-N 0.000 description 2
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- WHHGLZMJPXIBIX-UHFFFAOYSA-N decabromodiphenyl ether Chemical compound BrC1=C(Br)C(Br)=C(Br)C(Br)=C1OC1=C(Br)C(Br)=C(Br)C(Br)=C1Br WHHGLZMJPXIBIX-UHFFFAOYSA-N 0.000 description 1
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- 231100000167 toxic agent Toxicity 0.000 description 1
- 239000003440 toxic substance Substances 0.000 description 1
- DXZMANYCMVCPIM-UHFFFAOYSA-L zinc;diethylphosphinate Chemical compound [Zn+2].CCP([O-])(=O)CC.CCP([O-])(=O)CC DXZMANYCMVCPIM-UHFFFAOYSA-L 0.000 description 1
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Abstract
本发明公开了一种防毒阻燃氯醚橡胶防护胶布,以尼龙为骨架材料覆盖有氯醚橡胶组合物,所述氯醚橡胶组合物包括如下重量份原料:氯醚橡胶100份,四氧化三铅3~8份,NA‑22 0.5~2份,硬脂酸锌0.5~1.5份,氧化镁1.5~3份,防老剂NBC 1.1~2份,防老剂MB 0.1~1份,快压出炭黑15~30份,陶土20~30份,三氧化二铝10~50份。本发明将氯醚橡胶应用于防护胶布的制备方法,与国内外现有技术相比,本发明胶布可在不使用卤化阻燃剂的情况下,同时兼顾防毒、阻燃及耐低温的性能要求。
Description
技术领域
本发明涉及防护材料技术领域,具体为一种防毒阻燃氯醚橡胶防护胶布及制备方法。
背景技术
目前防护服、防毒靴套等产品的防护材料主要采用氯化丁基橡胶、丁基橡胶或氯丁橡胶制备,其具有良好的气密型,可以满足对大部分毒剂、酸碱、乙腈、丙酮等工业化学品的防护,但主要有以下几方面的缺陷:(1)、丁基橡胶和氯化丁基橡胶不具备阻燃性能,需要添加三氧化二锑、十溴二苯醚、氯化石蜡等阻燃剂,随着环保的不断提高,卤化阻燃剂不能满足环保要求,而三氧化二铝等无卤阻燃剂阻燃效果差,使用量大,降低了胶料的含胶率,降低了胶布的防毒性能,因此不能同时满足阻燃和防毒性能的需求;(2)、氯丁橡胶阻燃效果好,但是耐低温性能差,低温时易发僵发硬,不能满足防护服、防毒靴套在冬季环境下使用。因此现有胶布材料不能在满足环保要求下同时兼顾防毒、阻燃、耐低温性能的要求。
发明内容
本发明目的是提供一种防毒阻燃胶布,可在不使用卤化阻燃剂的情况下,同时兼顾防毒、阻燃及耐低温的性能要求。
本发明是采用如下技术方案实现的:
一种防毒阻燃氯醚橡胶防护胶布,以尼龙为骨架材料覆盖有氯醚橡胶组合物,所述氯醚橡胶组合物包括如下重量份原料:氯醚橡胶100份,四氧化三铅3~8份,NA-22 0.5~2份,硬脂酸锌0.5~1.5份,氧化镁1.5~3份,防老剂NBC 1.1~2份,防老剂MB 0.1~1份,快压出炭黑15~30份,陶土20~30份,三氧化二铝10~50份。
氯醚橡胶是主链由C-O和C-C组成,其侧链含氯原子的饱和橡胶,主链呈醚型结构,由于有氧原子存在,分子易于旋转,主链柔顺,无双键存在,侧链含有极性基团或不饱和键。这种结构特征决定聚醚橡胶具有耐臭氧、耐天候、耐化学品、耐寒等优点,但是其存在加工性和物理强度不好的问题。因此通过添加陶土、三氧化二铝、快压出炭黑对橡胶进行补强填充后,可改善氯醚橡胶的加工性能和物理强度,用于防护胶布的制备。
上述防毒阻燃氯醚橡胶防护胶布的制备方法主要包括混炼Ⅰ—过滤—混炼Ⅱ—压延—硫化五个过程,具体如下:
(1)、混炼Ⅰ过程
混炼胶料采用XK-160mm 开放式炼胶机,滚筒速比为1:1.25,混炼时前辊辊温为50~60℃,后辊辊温为60~70℃;混炼工艺如下:
1.1、辊距调至0.8mm,加入氯醚橡胶,令其包前辊;
1.2、加入硬脂酸锌、氧化镁进行混炼,2~3分钟;
1.3、加入防老剂MB、防老剂NBC进行混炼,1~2分钟;
1.4、加入一半快压出炭黑、陶土、三氧化二铝混炼均匀,10~15分钟;
1.5、辊距调至1.2mm,加入剩下一半快压出炭黑、陶土、三氧化二铝,混炼均匀,10~15分钟,每边割刀四次,混炼均匀;
1.6、最后辊距调至所需厚度,出片,冷却。
(2)、过滤过程
将胶料在100℃下,采用120目筛网在挤出机上进行过滤。
(3)、混炼Ⅱ过程
3.1、辊距调至1.5mm,加入四氧化三铅、NA-22,2~3分钟;
3.2、辊距调至0.5mm,前后薄通五次。
(4)、压延
将热炼后氯醚橡胶放在压延机上,以尼龙为骨架材料,制的厚度为0.35mm厚度的防护胶布。
(5)、硫化
采用硫化罐电加热间接硫化的方式,130℃硫化90分钟即可。
采用上述方法制地的防护胶布性能如下:
本发明将氯醚橡胶应用于防护胶布的制备方法,与国内外现有技术相比,本发明胶布可在不使用卤化阻燃剂的情况下,同时兼顾防毒、阻燃及耐低温的性能要求。
具体实施方式
下面对本发明的具体实施例进行详细说明。
实施例1
一种防毒阻燃氯醚橡胶防护胶布,以尼龙为骨架材料覆盖有氯醚橡胶组合物,所述氯醚橡胶组合物包括如下重量份原料:氯醚橡胶 100份,四氧化三铅 5份,NA-22 1.5份,硬脂酸锌 1份,氧化镁 1.5份,防老剂NBC 1份,防老剂MB 0.1份,快压出炭黑 15份,陶土 20份,三氧化二铝 10份。
上述防毒阻燃氯醚橡胶防护胶布的制备方法,包括如下步骤:
(1)、混炼Ⅰ过程
混炼胶料采用XK-160mm 开放式炼胶机,滚筒速比为1:1.25,混炼时前辊辊温为50~60℃,后辊辊温为60~70℃;混炼工艺如下:
1.1、辊距调至0.8mm,加入氯醚橡胶,令其包前辊;
1.2、加入硬脂酸锌、氧化镁进行混炼,2~3分钟;
1.3、加入防老剂MB、防老剂NBC进行混炼,1~2分钟;
1.4、加入一半快压出炭黑、陶土、三氧化二铝混炼均匀,10~15分钟;
1.5、辊距调至1.2mm,加入剩下一半快压出炭黑、陶土、三氧化二铝,混炼均匀,10~15分钟,每边割刀四次,混炼均匀;
1.6、最后辊距调至所需厚度,出片,冷却;
(2)、过滤过程
将胶料在100℃下,采用120目筛网在挤出机上进行过滤;
(3)、混炼Ⅱ过程
3.1、辊距调至1.5mm,加入四氧化三铅、NA-22,2~3分钟;
3.2、辊距调至0.5mm,前后薄通五次;
(4)、压延
将热炼后氯醚橡胶放在压延机上,以尼龙为骨架材料,制的厚度为0.35mm厚度的防护胶布;
(5)、硫化
采用硫化罐电加热间接硫化的方式,130℃硫化90分钟即可。
实施例2
一种防毒阻燃氯醚橡胶防护胶布,以尼龙为骨架材料覆盖有氯醚橡胶组合物,所述氯醚橡胶组合物包括如下重量份原料:氯醚橡胶 500份,四氧化三铅 23份,NA-22 8份,硬脂酸锌 5份,氧化镁 10份,防老剂NBC 6份,防老剂MB 0.5份,快压出炭黑 80份,陶土 100份,三氧化二铝 50份。
上述防毒阻燃氯醚橡胶防护胶布的制备方法同实施例1。
实施例3
一种防毒阻燃氯醚橡胶防护胶布,以尼龙为骨架材料覆盖有氯醚橡胶组合物,所述氯醚橡胶组合物包括如下重量份原料:氯醚橡胶 400份,四氧化三铅 20份,NA-22 8份,硬脂酸锌 5份,氧化镁 8份,防老剂NBC 6份,防老剂MB 0.4份,快压出炭黑 80份,陶土 100份,三氧化二铝 70份。
上述防毒阻燃氯醚橡胶防护胶布的制备方法同实施例1。
实施例4
一种防毒阻燃氯醚橡胶防护胶布,以尼龙为骨架材料覆盖有氯醚橡胶组合物,所述氯醚橡胶组合物包括如下重量份原料:氯醚橡胶 500份,四氧化三铅 22份,NA-22 10份,硬脂酸锌 5份,氧化镁 10份,防老剂NBC 6份,防老剂MB 1份,快压出炭黑 100份,陶土 100份,三氧化二铝 60份。
上述防毒阻燃氯醚橡胶防护胶布的制备方法同实施例1。
实施例5
一种防毒阻燃氯醚橡胶防护胶布,以尼龙为骨架材料覆盖有氯醚橡胶组合物,所述氯醚橡胶组合物包括如下重量份原料:氯醚橡胶 1000份,四氧化三铅 50份,NA-22 20份,硬脂酸锌 10份,氧化镁 15份,防老剂NBC 12份,防老剂MB 1份,快压出炭黑 150份,陶土 200份,三氧化二铝 100份。
上述防毒阻燃氯醚橡胶防护胶布的制备方法同实施例1。
实施例6
对上述1-5实施例进行性能测试,结果如下:
以上实施例仅用于说明本发明的技术方案而非限制,尽管参照较佳实例对本发明进行了详细描述,本领域技术人员应当理解,可以借鉴本发明的技术方案进行修改或等同替换,而不脱离本发明的范围,都应被视为包括在本发明的权利要求范围之内。
Claims (2)
1.一种防毒阻燃氯醚橡胶防护胶布,其特征在于:以尼龙为骨架材料覆盖有氯醚橡胶组合物,所述氯醚橡胶组合物包括如下重量份原料:氯醚橡胶100份,四氧化三铅3~8份,NA-22 0.5~2份,硬脂酸锌0.5~1.5份,氧化镁1.5~3份,防老剂NBC 1.1~2份,防老剂MB 0.1~1份,快压出炭黑15~30份,陶土20~30份,三氧化二铝10~50份。
2.一种防毒阻燃氯醚橡胶防护胶布的制备方法,其特征在于:包括如下步骤:
(1)、混炼Ⅰ过程
混炼胶料采用XK-160mm 开放式炼胶机,滚筒速比为1:1.25,混炼时前辊辊温为50~60℃,后辊辊温为60~70℃;混炼工艺如下:
1.1、辊距调至0.8mm,加入氯醚橡胶,令其包前辊;
1.2、加入硬脂酸锌、氧化镁进行混炼,2~3分钟;
1.3、加入防老剂MB、防老剂NBC进行混炼,1~2分钟;
1.4、加入一半快压出炭黑、陶土、三氧化二铝混炼均匀,10~15分钟;
1.5、辊距调至1.2mm,加入剩下一半快压出炭黑、陶土、三氧化二铝,混炼均匀,10~15分钟,每边割刀四次,混炼均匀;
1.6、最后辊距调至所需厚度,出片,冷却;
(2)、过滤过程
将胶料在100℃下,采用120目筛网在挤出机上进行过滤;
(3)、混炼Ⅱ过程
3.1、辊距调至1.5mm,加入四氧化三铅、NA-22,2~3分钟;
3.2、辊距调至0.5mm,前后薄通五次;
(4)、压延
将热炼后氯醚橡胶放在压延机上,以尼龙为骨架材料,制的厚度为0.35mm厚度的防护胶布;
(5)、硫化
采用硫化罐电加热间接硫化的方式,130℃硫化90分钟即可。
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