CN117659534A - 用于a类阻燃聚乙烯电缆料的制备方法 - Google Patents
用于a类阻燃聚乙烯电缆料的制备方法 Download PDFInfo
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- 239000003063 flame retardant Substances 0.000 title claims abstract description 48
- 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 47
- 239000000463 material Substances 0.000 title claims abstract description 36
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- 238000002360 preparation method Methods 0.000 title claims description 12
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- 230000003078 antioxidant effect Effects 0.000 claims abstract description 17
- YUWBVKYVJWNVLE-UHFFFAOYSA-N [N].[P] Chemical compound [N].[P] YUWBVKYVJWNVLE-UHFFFAOYSA-N 0.000 claims abstract description 13
- 229920000092 linear low density polyethylene Polymers 0.000 claims abstract description 12
- 239000004707 linear low-density polyethylene Substances 0.000 claims abstract description 12
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- 229920002873 Polyethylenimine Polymers 0.000 claims abstract description 5
- WNROFYMDJYEPJX-UHFFFAOYSA-K aluminium hydroxide Chemical compound [OH-].[OH-].[OH-].[Al+3] WNROFYMDJYEPJX-UHFFFAOYSA-K 0.000 claims abstract description 5
- PBOSTUDLECTMNL-UHFFFAOYSA-N lauryl acrylate Chemical compound CCCCCCCCCCCCOC(=O)C=C PBOSTUDLECTMNL-UHFFFAOYSA-N 0.000 claims abstract description 5
- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 claims abstract description 5
- 239000000347 magnesium hydroxide Substances 0.000 claims abstract description 5
- 229910001862 magnesium hydroxide Inorganic materials 0.000 claims abstract description 5
- DQXBYHZEEUGOBF-UHFFFAOYSA-N but-3-enoic acid;ethene Chemical compound C=C.OC(=O)CC=C DQXBYHZEEUGOBF-UHFFFAOYSA-N 0.000 claims abstract description 4
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- HBGGXOJOCNVPFY-UHFFFAOYSA-N diisononyl phthalate Chemical compound CC(C)CCCCCCOC(=O)C1=CC=CC=C1C(=O)OCCCCCCC(C)C HBGGXOJOCNVPFY-UHFFFAOYSA-N 0.000 claims abstract description 4
- 239000005038 ethylene vinyl acetate Substances 0.000 claims abstract description 4
- FPYJFEHAWHCUMM-UHFFFAOYSA-N maleic anhydride Chemical compound O=C1OC(=O)C=C1 FPYJFEHAWHCUMM-UHFFFAOYSA-N 0.000 claims abstract description 4
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- XFZRQAZGUOTJCS-UHFFFAOYSA-N phosphoric acid;1,3,5-triazine-2,4,6-triamine Chemical compound OP(O)(O)=O.NC1=NC(N)=NC(N)=N1 XFZRQAZGUOTJCS-UHFFFAOYSA-N 0.000 claims description 6
- CJZGTCYPCWQAJB-UHFFFAOYSA-L calcium stearate Chemical group [Ca+2].CCCCCCCCCCCCCCCCCC([O-])=O.CCCCCCCCCCCCCCCCCC([O-])=O CJZGTCYPCWQAJB-UHFFFAOYSA-L 0.000 claims description 5
- 239000008116 calcium stearate Substances 0.000 claims description 5
- 235000013539 calcium stearate Nutrition 0.000 claims description 5
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- 239000004114 Ammonium polyphosphate Substances 0.000 claims description 4
- BGYHLZZASRKEJE-UHFFFAOYSA-N [3-[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxy]-2,2-bis[3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoyloxymethyl]propyl] 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CC(C)(C)C1=C(O)C(C(C)(C)C)=CC(CCC(=O)OCC(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)(COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)COC(=O)CCC=2C=C(C(O)=C(C=2)C(C)(C)C)C(C)(C)C)=C1 BGYHLZZASRKEJE-UHFFFAOYSA-N 0.000 claims description 4
- 235000019826 ammonium polyphosphate Nutrition 0.000 claims description 4
- 229920001276 ammonium polyphosphate Polymers 0.000 claims description 4
- CZQYVJUCYIRDFR-UHFFFAOYSA-N phosphono dihydrogen phosphate;1,3,5-triazine-2,4,6-triamine Chemical compound NC1=NC(N)=NC(N)=N1.NC1=NC(N)=NC(N)=N1.OP(O)(=O)OP(O)(O)=O CZQYVJUCYIRDFR-UHFFFAOYSA-N 0.000 claims description 4
- 229920000388 Polyphosphate Polymers 0.000 claims description 3
- SSDSCDGVMJFTEQ-UHFFFAOYSA-N octadecyl 3-(3,5-ditert-butyl-4-hydroxyphenyl)propanoate Chemical compound CCCCCCCCCCCCCCCCCCOC(=O)CCC1=CC(C(C)(C)C)=C(O)C(C(C)(C)C)=C1 SSDSCDGVMJFTEQ-UHFFFAOYSA-N 0.000 claims description 3
- 239000001205 polyphosphate Substances 0.000 claims description 3
- 235000011176 polyphosphates Nutrition 0.000 claims description 3
- TVOKLFHQSPUILS-UHFFFAOYSA-N N1=C(N)N=C(N)N=C1N.P(=O)(O)(O)OCC(C)(CO)C Chemical compound N1=C(N)N=C(N)N=C1N.P(=O)(O)(O)OCC(C)(CO)C TVOKLFHQSPUILS-UHFFFAOYSA-N 0.000 claims description 2
- JKIJEFPNVSHHEI-UHFFFAOYSA-N Phenol, 2,4-bis(1,1-dimethylethyl)-, phosphite (3:1) Chemical compound CC(C)(C)C1=CC(C(C)(C)C)=CC=C1OP(OC=1C(=CC(=CC=1)C(C)(C)C)C(C)(C)C)OC1=CC=C(C(C)(C)C)C=C1C(C)(C)C JKIJEFPNVSHHEI-UHFFFAOYSA-N 0.000 claims description 2
- 238000005336 cracking Methods 0.000 abstract description 13
- 230000006353 environmental stress Effects 0.000 abstract description 10
- 230000000052 comparative effect Effects 0.000 description 6
- LYCAIKOWRPUZTN-UHFFFAOYSA-N Ethylene glycol Chemical compound OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 2
- 239000000779 smoke Substances 0.000 description 2
- 231100000331 toxic Toxicity 0.000 description 2
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- WZCQRUWWHSTZEM-UHFFFAOYSA-N 1,3-phenylenediamine Chemical compound NC1=CC=CC(N)=C1 WZCQRUWWHSTZEM-UHFFFAOYSA-N 0.000 description 1
- NBIIXXVUZAFLBC-UHFFFAOYSA-L Phosphate ion(2-) Chemical compound OP([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-L 0.000 description 1
- 238000004891 communication Methods 0.000 description 1
- 230000007547 defect Effects 0.000 description 1
- 238000011161 development Methods 0.000 description 1
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- 230000007613 environmental effect Effects 0.000 description 1
- 238000011156 evaluation Methods 0.000 description 1
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- 229910052736 halogen Inorganic materials 0.000 description 1
- 150000002367 halogens Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 239000012796 inorganic flame retardant Substances 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- 231100000956 nontoxicity Toxicity 0.000 description 1
- 229920000098 polyolefin Polymers 0.000 description 1
- 230000002035 prolonged effect Effects 0.000 description 1
- 229920001169 thermoplastic Polymers 0.000 description 1
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Abstract
本发明公开了一种A类阻燃聚乙烯电缆料,由以下重量份的组分组成:熔体流动速率为3~8g/10min高密度聚乙烯树脂100份、线性低密度聚乙烯树脂35~55份、马来酸酐接枝乙烯醋酸乙烯酯5~15份、炭黑3~5份、氢氧化铝50~60份、氢氧化镁10~30份、磷氮阻燃剂2~8份、金属皂类润滑剂3~6份、抗氧剂0.5~2份、邻苯二甲酸二异壬酯1~5份、丙烯酸月桂酯2~5份、超支化聚乙烯亚胺1~3份。本发明A类阻燃聚乙烯电缆料在保证阻燃性能的同时,延长了阻燃聚乙烯耐环境应力开裂时间,超过了260小时,使得燃聚乙烯电缆料形成电缆护套后,具有更好的耐环境应力开裂性性能。
Description
技术领域
本发明涉及电缆材料技术领域,尤其涉及一种用于A类阻燃聚乙烯电缆料的制备方法。
背景技术
聚乙烯护套材料是一种常用的质轻、无毒环保、具有优异电绝缘性能的热塑性塑料,广泛的应用于电线电缆领域。由于以前的电线电缆多为PVC制品,PVC制品有毒有害,不环保,燃烧后会释放出大量的有毒有害气体,造成的危害极大。低烟无卤聚烯烃电缆为了满足低烟和无卤两个要求,而大量加入无机阻燃剂,致使材料的开裂性能大幅度下降而不能满足要求。因此,需要开发阻燃聚乙烯电缆料,保证材料具有良好的阻燃性同时,同时使得该材料具有优异耐开裂性能。
发明内容
本发明目的在于提供一种用于A类阻燃聚乙烯电缆料的制备方法,该制备方法获得的A类阻燃聚乙烯电缆料在保证阻燃性能的同时,延长了阻燃聚乙烯耐环境应力开裂时间,超过了260小时,使得燃聚乙烯电缆料形成电缆护套后,具有更好的耐环境应力开裂性能。
为达到上述目的,本发明采用的技术方案是:一种用于A类阻燃聚乙烯电缆料的制备方法,包括如下步骤:
步骤一、将熔体流动速率为3~8g/10min高密度聚乙烯树脂100份、线性低密度聚乙烯树脂35 ~55份、马来酸酐接枝乙烯醋酸乙烯酯5~15份、炭黑3~5份、氢氧化铝50~60份、氢氧化镁10~30份、磷氮阻燃剂2~8份、金属皂类润滑剂3~6份加入密炼机中,然后开始混炼,混炼至料温为120℃~150℃获得第一混合料;
步骤二、在第一混合料中添加抗氧剂0.5~2份、邻苯二甲酸二异壬酯1~5份、丙烯酸月桂酯2~5份、超支化聚乙烯亚胺1~3份,在密炼机中混炼,混炼温度为100~110℃,得到第二混合料;
步骤三、将第二混合料送入双螺杆挤出机中,在160~170℃下挤出造粒,获得所述聚乙烯电缆料。
上述技术方案中进一步改进的技术方案如下:
1、上述方案中,所述金属皂类润滑剂为硬脂酸钙或硬脂酸锌。
2、上述方案中,所述抗氧剂为抗氧剂1010、抗氧剂1076、抗氧剂168、抗氧剂626、抗氧剂300P中的一种。
3、上述方案中,所述磷氮阻燃剂为三聚氰胺、聚磷酸三聚氰胺、焦磷酸二三聚氰胺、正磷酸三聚氰胺、聚磷酸铵、磷酸酯三聚氰胺盐、二新戊二醇间苯二胺双磷酸酯和新戊二醇磷酸酯三聚氰胺盐中的至少一种。
4、上述方案中,所述线性低密度聚乙烯树脂的熔体流动速率为0.05~2 g/10min。
5、上述方案中,所述步骤一中混炼时间为30~60分钟,所述步骤二中混炼时间为10~15分钟。
由于上述技术方案的运用,本发明与现有技术相比具有下列优点:
本发明用于A类阻燃聚乙烯电缆料的制备方法,其基于氢氧化铝50~60份、氢氧化镁 10~30份、磷氮阻燃剂 2~8份添加了丙烯酸月桂酯2~5份、超支化聚乙烯亚胺1~3份,在保证阻燃性能的同时,克服了由于添加三种类型阻燃剂导致开裂性能变差的缺陷,延长了阻燃聚乙烯耐环境应力开裂时间,超过了260小时,使得获得的燃聚乙烯电缆料形成电缆护套后,具有更好的耐环境应力开裂性能。
具体实施方式
在本发明的描述中,需要说明的是,术语“中心”、“上”、“下”、“左”、“右”、“竖直”、“水平”、“内”、“外”等指示的方位或位置关系为基于技术方案所示的方位或位置关系,仅是为了便于描述本发明和简化描述,而不是指示或暗示所指的装置或元件必须具有特定的方位、以特定的方位构造和操作,因此不能理解为对本发明的限制;术语“第一”、“第二”、“第三”仅用于描述目的,而不能理解为指示或暗示相对重要性;此外,除非另有明确的规定和限定,术语“安装”、“相连”、“连接”应做广义理解,例如,可以是固定连接,也可以是可拆卸连接,或一体地连接;可以是机械连接,也可以是电连接;可以是直接相连,也可以通过中间媒介间接相连,可以是两个元件内部的连通。对于本领域的普通技术人员而言,可以具体情况理解上述术语在本发明中的具体含义。
下面结合实施例对本发明作进一步描述:
实施例1~4:一种用于A类阻燃聚乙烯电缆料的制备方法,所述A类阻燃聚乙烯电缆料由以下重量份的组分组成,如表1所述:
表1
;
包括如下步骤:
步骤一、将熔体流动速率为3~8g/10min高密度聚乙烯树脂100份、线性低密度聚乙烯树脂35 ~55份、马来酸酐接枝乙烯醋酸乙烯酯5~15份、炭黑3~5份、氢氧化铝50~60份、氢氧化镁10~30份、磷氮阻燃剂2~8份、金属皂类润滑剂3~6份加入密炼机中,然后开始混炼,混炼至料温为120℃~150℃获得第一混合料;
步骤二、在第一混合料中添加抗氧剂0.5~2份、邻苯二甲酸二异壬酯1~5份、丙烯酸月桂酯2~5份、超支化聚乙烯亚胺1~3份,在密炼机中混炼,混炼温度为100~110℃,得到第二混合料;
步骤三、将第二混合料送入双螺杆挤出机中,在160~170℃下挤出造粒,获得所述聚乙烯电缆料。
实施例1中金属皂类润滑剂为硬脂酸钙,抗氧剂为抗氧剂1010,磷氮阻燃剂为焦磷酸二三聚氰胺、聚磷酸铵按照1:2的重量份形成的混合物,上述线性低密度聚乙烯树脂的熔体流动速率为2 g/10min,高密度聚乙烯树脂的熔体流动速率为4g/10min。
实施例2中金属皂类润滑剂为硬脂酸锌,抗氧剂为抗氧剂626,磷氮阻燃剂为聚磷酸三聚氰胺,上述线性低密度聚乙烯树脂的熔体流动速率为1 g/10min,高密度聚乙烯树脂的熔体流动速率为5g/10min。
实施例3中金属皂类润滑剂为硬脂酸锌,抗氧剂为抗氧剂300P,所述磷氮阻燃剂为正磷酸三聚氰胺,上述线性低密度聚乙烯树脂的熔体流动速率为2 g/10min,高密度聚乙烯树脂的熔体流动速率为4g/10min。
实施例4中金属皂类润滑剂为硬脂酸钙,抗氧剂为抗氧剂1076,所述磷氮阻燃剂为三聚氰胺,上述线性低密度聚乙烯树脂的熔体流动速率为1 g/10min,高密度聚乙烯树脂的熔体流动速率为5g/10min。
对比例1~3:一种用于阻燃聚乙烯电缆料的制备方法,所述阻燃聚乙烯电缆料由以下重量份的组分组成,如表2所述:
表2
;
对比例制备方法的步骤同实施例制备方法的步骤。
对比例1和对比例2中金属皂类润滑剂为硬脂酸钙,抗氧剂为抗氧剂1010,磷氮阻燃剂为焦磷酸二三聚氰胺、聚磷酸铵按照1:2的重量份形成的混合物,上述线性低密度聚乙烯树脂的熔体流动速率为2 g/10min,高密度聚乙烯树脂的熔体流动速率为4g/10min。
对比例3中金属皂类润滑剂为硬脂酸锌,抗氧剂为抗氧剂300P,所述磷氮阻燃剂为正磷酸三聚氰胺,上述线性低密度聚乙烯树脂的熔体流动速率为2 g/10min,高密度聚乙烯树脂的熔体流动速率为4g/10min。
上述实施例1~4制得的A类阻燃聚乙烯电缆料,性能如表3所示:
表3
上述对比例1~3制得的A类阻燃聚乙烯电缆料,性能如表4所示:
表4
如表3和表4的评价结果所示,实施例1~4制得的A类阻燃聚乙烯电缆料,耐环境应力开裂时间,均超过了260 h;对比例1~3制得的A类阻燃聚乙烯电缆料,耐环境应力开裂时间最长时间为218h。因此,本发明实施例制备方法获得的A类阻燃聚乙烯电缆料, 在保证阻燃性能的同时,延长了阻燃聚乙烯耐环境应力开裂时间,超过了260小时,使得燃聚乙烯电缆料形成电缆护套后,具有更好的耐环境应力开裂性能。
上述实施例只为说明本发明的技术构思及特点,其目的在于让熟悉此项技术的人士能够了解本发明的内容并据以实施,并不能以此限制本发明的保护范围。凡根据本发明精神实质所作的等效变化或修饰,都应涵盖在本发明的保护范围之内。
Claims (6)
1.一种用于A类阻燃聚乙烯电缆料的制备方法,其特征在于:包括如下步骤:
步骤一、将熔体流动速率为3~8g/10min高密度聚乙烯树脂100份、线性低密度聚乙烯树脂35 ~55份、马来酸酐接枝乙烯醋酸乙烯酯5~15份、炭黑3~5份、氢氧化铝50~60份、氢氧化镁10~30份、磷氮阻燃剂2~8份、金属皂类润滑剂3~6份加入密炼机中,然后开始混炼,混炼至料温为120℃~150℃获得第一混合料;
步骤二、在第一混合料中添加抗氧剂0.5~2份、邻苯二甲酸二异壬酯1~5份、丙烯酸月桂酯2~5份、超支化聚乙烯亚胺1~3份,在密炼机中混炼,混炼温度为100~110℃,得到第二混合料;
步骤三、将第二混合料送入双螺杆挤出机中,在160~170℃下挤出造粒,获得所述聚乙烯电缆料。
2.根据权利要求1所述的用于A类阻燃聚乙烯电缆料的制备方法,其特征在于:所述金属皂类润滑剂为硬脂酸钙或硬脂酸锌。
3.根据权利要求1所述的用于A类阻燃聚乙烯电缆料的制备方法,其特征在于:所述抗氧剂为抗氧剂1010、抗氧剂1076、抗氧剂168、抗氧剂626、抗氧剂300P中的一种。
4.根据权利要求1所述的用于A类阻燃聚乙烯电缆料的制备方法,其特征在于:所述磷氮阻燃剂为三聚氰胺、聚磷酸三聚氰胺、焦磷酸二三聚氰胺、正磷酸三聚氰胺、聚磷酸铵、磷酸酯三聚氰胺盐、二新戊二醇间苯二胺双磷酸酯和新戊二醇磷酸酯三聚氰胺盐中的至少一种。
5.根据权利要求1所述的用于A类阻燃聚乙烯电缆料的制备方法,其特征在于:所述线性低密度聚乙烯树脂的熔体流动速率为0.05~2 g/10min。
6.根据权利要求1所述的A类阻燃聚乙烯电缆料的制备方法,其特征在于:所述步骤一中混炼时间为30~60分钟,所述步骤二中混炼时间为10~15分钟。
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