CN111806001A - 一种耐浸焊高柔韧cem-1覆铜板的制备方法 - Google Patents
一种耐浸焊高柔韧cem-1覆铜板的制备方法 Download PDFInfo
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- CN111806001A CN111806001A CN202010652634.0A CN202010652634A CN111806001A CN 111806001 A CN111806001 A CN 111806001A CN 202010652634 A CN202010652634 A CN 202010652634A CN 111806001 A CN111806001 A CN 111806001A
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- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 claims description 20
- 229910052698 phosphorus Inorganic materials 0.000 claims description 20
- 239000011574 phosphorus Substances 0.000 claims description 20
- 239000003063 flame retardant Substances 0.000 claims description 19
- 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 claims description 18
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- 229910052757 nitrogen Inorganic materials 0.000 claims description 8
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- DWSWCPPGLRSPIT-UHFFFAOYSA-N benzo[c][2,1]benzoxaphosphinin-6-ium 6-oxide Chemical compound C1=CC=C2[P+](=O)OC3=CC=CC=C3C2=C1 DWSWCPPGLRSPIT-UHFFFAOYSA-N 0.000 claims description 5
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- PTFIPECGHSYQNR-UHFFFAOYSA-N cardanol Natural products CCCCCCCCCCCCCCCC1=CC=CC(O)=C1 PTFIPECGHSYQNR-UHFFFAOYSA-N 0.000 claims description 2
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- FPAFDBFIGPHWGO-UHFFFAOYSA-N dioxosilane;oxomagnesium;hydrate Chemical compound O.[Mg]=O.[Mg]=O.[Mg]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O.O=[Si]=O FPAFDBFIGPHWGO-UHFFFAOYSA-N 0.000 claims description 2
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- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 claims description 2
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- TXCDCPKCNAJMEE-UHFFFAOYSA-N dibenzofuran Chemical compound C1=CC=C2C3=CC=CC=C3OC2=C1 TXCDCPKCNAJMEE-UHFFFAOYSA-N 0.000 description 2
- 230000007613 environmental effect Effects 0.000 description 2
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- 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
本发明公开了一种耐浸焊高柔韧CEM‑1覆铜板的制备方法,包括表料半固化片胶液的制备、里料一浸树脂胶液制备、里料二浸树脂胶液制备、制备半固化片和热压成型等步骤。本发明的有益效果是:本发明制得的覆铜板板材的耐热性能够达到288℃、20s以上浮焊不分层、不起泡,耐热性有明显提高;阻燃达到FV0级;柔韧性明显改善,具有优良的冲孔加工性,适用于无铅回流焊制程,可提高加工效率和焊接可靠性。
Description
技术领域
本发明涉及覆铜板领域,尤其涉及一种耐浸焊高柔韧CEM-1覆铜板的制备方法。
背景技术
覆铜板广泛用于制造各类家用电器、电子信息产品及工业电子产品所用的印制电路板,作为印制电路板的基板材料,起着承载装联电子元器件、形成导电线路图形及在层间和线路间绝缘的三大功能,是一种重要的电子基础材料。
覆铜板的阻燃性是电子产品重要的安全性能之一。卤素类阻燃材料(含Cl、Br)以其经济性与可靠性,在印制电路基材产业中已应用多年,然而,随着全球性环境保护呼声的日益高涨,卤素类阻燃材料的环境负荷及对人体健康的影响正密切受到关注,已有许多国家的组织和机构相继在含卤产品的燃烧产物中检测出二噁英、二苯并呋喃等致癌物质。含卤产品在燃烧过程中发烟量很大,会释放出剧毒物质卤化氢,严重威胁人体健康。因此研发和应用无卤型阻燃材料,生产环保型印制电路基材,已成为近年来覆铜板技术发展的新趋势。
目前无卤化覆铜板是利用氮磷协同阻燃,并添加无机填料,达到阻燃 FV0级。但是在CEM-1板材中,里料增强材料为木浆纸,其本身易燃,要想达到FV0级需要大量的氮磷阻燃剂,这样势必会影响板材的其他性能,导致其耐热性、柔韧性普遍较差。
发明内容
针对上述问题,本发明提供一种耐浸焊高柔韧CEM-1覆铜板的制备方法,包括以下步骤:
1)表料半固化片胶液的制备:将45-60重量份含磷环氧树脂、1-5增韧环氧、1-5重量份低分子环氧、3-7重量份潜伏性固化剂、20-35重量份表料填料和20-30重量份溶剂混合,搅拌均匀;
2)里料一浸树脂胶液制备:将5-10重量份含磷阻燃剂、1-10重量份低分子热固性树脂和80-90重量份溶剂混合、搅拌均匀;
3)里料二浸树脂胶液制备:将20-35重量份低分子含磷环氧、5-15重量份低分子普通环氧、10-20重量份含氮酚醛、1-5重量份改性酚醛、10-20 重量份阻燃填料、1-10重量份里料填料、20-30重量份溶剂混合,搅拌均匀;
4)将电子级玻纤布浸渍在步骤1)制得的胶液中,在130-190℃条件下烘干,控制含胶量为40-50%,流动度为6-14%,得表料半固化片;
5)将湿强木浆纸浸渍在步骤2)制得的胶液中,在130-150℃条件下烘干,控制含胶量为10-20%的一浸料片,再将一浸料片浸渍在步骤3)制得的胶液中,在160-180℃条件下烘干,控制含胶量为58-62%,得里料半固化片;
6)取2-6张步骤5)制得的里料半固化片叠加在一起,在两侧均铺覆一张步骤4)所得的表料半固化片,再在每张表料半固化片的外侧铺覆有一张铜箔,在160-180℃条件下热压90-150min,即得CEM-1覆铜板。
步骤1)中,所述含磷环氧树脂为DOPO型环氧树脂、NQ改性DOPO 性环氧树脂或HQ改性DOPO型环氧树脂的一种或多种的组合;所述低分子环氧为E-51和/或F-51;所述潜伏性固化剂为DICY和/或DDS;所述表料填料为氢氧化铝、氢氧化镁、磷酸三苯酯或氮磷阻燃剂中的一种或多种的组合。
步骤2)中,所述含磷阻燃剂的磷含量为20-26%;所述低分子热固性树脂为三聚氰胺树脂和/或酚醛树脂。
步骤3)中,所述低分子普通环氧为DOPO型环氧树脂,环氧当量为 200-300g/eq;所述含氮酚醛的氮含量为12-16%,羟基当量为120-130;所述改性酚醛为腰果酚改性酚醛和/或桐油改性酚醛;所述阻燃填料为含磷、氮的热固性反应物,没有反应活性,磷含量10-15%,氮含量20-30%,粒径2-5um;所述里料填料为氢氧化铝、氢氧化镁、硅微粉或滑石粉中的一种或多种的组合。
本发明每一步骤所用溶剂均独立地选自甲醇、丙酮、丁酮、丙二醇甲醚、 DMF或甲苯中的一种或多种的组合。
在本发明中,含胶量是指浸胶用树脂乳液纯固体占浸胶料片重量的百分比;流动度是指浸胶用树脂乳液在70±5kg/cm2的压力、160±2℃下流出的重量占浸胶用树脂乳液总重量的百分比。
本发明的有益效果是:本发明制得的覆铜板板材的耐热性能够达到 288℃、20s以上浮焊不分层、不起泡,耐热性有明显提高;阻燃达到FV0 级;柔韧性明显改善,具有优良的冲孔加工性,适用于无铅回流焊制程,可提高加工效率和焊接可靠性。
具体实施方式
以下结合实例对本发明进行描述,所举实例只用于解释本发明,并非用于限定本发明的范围。
实施例1
一种耐浸焊高柔韧CEM-1覆铜板的制备方法,包括如下步骤:
(1)表料半固化片胶液的制备:将47份含磷环氧树脂、3增韧环氧、5 低分子环氧、3.5份潜伏性固化剂、25份填料、16.5份溶剂混合,搅拌均匀;
(2)里料一浸树脂胶液制备:将8含磷阻燃剂、7低分子热固性树脂、85份溶剂混合、搅拌均匀;
(3)里料二浸树脂胶液制备:将30份低分子含磷环氧、5份低分子普通环氧、15份含氮酚醛、3份改性酚醛、15份阻燃填料、5份普通填料、27 份溶剂混合,搅拌均匀;
(4)将电子级玻纤布浸渍在步骤(1)制得的胶液中,在130-190℃条件下烘干,控制含胶量为45±5%,流动度为10±4%,制得表料半固化片;
(5)将湿强木浆纸浸渍在步骤(2)制得的胶液中,在130-150℃条件下烘干,控制含胶量为10-20%的一浸料片,然后再将其浸渍在步骤(3)制得的胶液中,在160-180℃条件下烘干,控制含胶量为60±2%的里料半固化片;
(6)取4张步骤(5)制得的里料半固化片叠加在一起,在双面覆有一张步骤(4)所得的表料半固化片,最后在表料半固化片上覆有一张铜箔,在160-180℃条件下热压90-150min,制得无卤CEM-1覆铜板。
实施例2
一种耐浸焊高柔韧CEM-1覆铜板的制备方法,包括如下步骤:
(1)表料半固化片胶液的制备:将55份含磷环氧树脂、2增韧环氧、3 低分子环氧、4份潜伏性固化剂、20份填料、16份溶剂混合,搅拌均匀;
(2)里料一浸树脂胶液制备:将10含磷阻燃剂、5低分子热固性树脂、 85份溶剂混合、搅拌均匀;
(3)里料二浸树脂胶液制备:将25份低分子含磷环氧、10份低分子普通环氧、20份含氮酚醛、5份改性酚醛、10份阻燃填料、5份普通填料、25 份溶剂混合,搅拌均匀;
(4)将电子级玻纤布浸渍在步骤(1)制得的胶液中,在130-190℃条件下烘干,控制含胶量为45±5%,流动度为10±4%,制得表料半固化片;
(5)将湿强木浆纸浸渍在步骤(2)制得的胶液中,在130-150℃条件下烘干,控制含胶量为10-20%的一浸料片,然后再将其浸渍在步骤(3)制得的胶液中,在160-180℃条件下烘干,控制含胶量为60±2%的里料半固化片;
(6)取6张步骤(5)制得的里料半固化片叠加在一起,在双面覆有一张步骤(4)所得的表料半固化片,最后在表料半固化片上覆有一张铜箔,在160-180℃条件下热压90-150min,制得无卤CEM-1覆铜板。
将实施例1和2所得CEM-1覆铜板以及现有CEM-1覆铜板进行相关指标检测,如表1所示。
表1.指标检测
指标名称 | 单位 | 实施例1 | 实施例2 | 现有CEM-1 |
剥离强度 | N/mm | 1.53 | 1.50 | 1.37 |
耐浸焊/288℃ | s | 24 | 26 | 10 |
阻燃 | s | 27 | 28 | 26 |
弯曲强度(纵向) | MPa | 360 | 380 | 420 |
弯曲强度(横向) | MPa | 320 | 330 | 350 |
以上所述仅为本发明的较佳实施例,并不用以限制本发明,凡在本发明的精神和原则之内,所作的任何修改、等同替换、改进等,均应包含在本发明的保护范围之内。
Claims (5)
1.一种耐浸焊高柔韧CEM-1覆铜板的制备方法,其特征在于,包括如下步骤:
1)表料半固化片胶液的制备:将45-60重量份含磷环氧树脂、1-5增韧环氧、1-5重量份低分子环氧、3-7重量份潜伏性固化剂、20-35重量份表料填料和20-30重量份溶剂混合,搅拌均匀;
2)里料一浸树脂胶液制备:将5-10重量份含磷阻燃剂、1-10重量份低分子热固性树脂和80-90重量份溶剂混合、搅拌均匀;
3)里料二浸树脂胶液制备:将20-35重量份低分子含磷环氧、5-15重量份低分子普通环氧、10-20重量份含氮酚醛、1-5重量份改性酚醛、10-20重量份阻燃填料、1-10重量份里料填料、20-30重量份溶剂混合,搅拌均匀;
4)将电子级玻纤布浸渍在步骤1)制得的胶液中,在130-190℃条件下烘干,控制含胶量为40-50%,流动度为6-14%,得表料半固化片;
5)将湿强木浆纸浸渍在步骤2)制得的胶液中,在130-150℃条件下烘干,控制含胶量为10-20%的一浸料片,再将一浸料片浸渍在步骤3)制得的胶液中,在160-180℃条件下烘干,控制含胶量为58-62%,得里料半固化片;
6)取2-6张步骤5)制得的里料半固化片叠加在一起,在两侧均铺覆一张步骤4)所得的表料半固化片,再在每张表料半固化片的外侧铺覆有一张铜箔,在160-180℃条件下热压90-150min,即得CEM-1覆铜板。
2.根据权利要求1所述的方法,其特征在于,步骤1)中,所述含磷环氧树脂为DOPO型环氧树脂、NQ改性DOPO性环氧树脂或HQ改性DOPO型环氧树脂的一种或多种的组合;所述低分子环氧为E-51和/或F-51;所述潜伏性固化剂为DICY和/或DDS;所述表料填料为氢氧化铝、氢氧化镁、磷酸三苯酯或氮磷阻燃剂中的一种或多种的组合。
3.根据权利要求1所述的方法,其特征在于,步骤2)中,所述含磷阻燃剂的磷含量为20-26%;所述低分子热固性树脂为三聚氰胺树脂和/或酚醛树脂。
4.根据权利要求1所述的方法,其特征在于,步骤3)中,所述低分子普通环氧为DOPO型环氧树脂,环氧当量为200-300g/eq;所述含氮酚醛的氮含量为12-16%,羟基当量为120-130;所述改性酚醛为腰果酚改性酚醛和/或桐油改性酚醛;所述阻燃填料为含磷、氮的热固性反应物,没有反应活性,磷含量10-15%,氮含量20-30%,粒径2-5um;所述里料填料为氢氧化铝、氢氧化镁、硅微粉或滑石粉中的一种或多种的组合。
5.根据权利要求1-4任一项所述的方法,其特征在于,步骤1)、2)和3)中,溶剂独立地选自甲醇、丙酮、丁酮、丙二醇甲醚、DMF或甲苯中的一种或多种的组合。
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