- 1、原创力文档(book118)网站文档一经付费(服务费),不意味着购买了该文档的版权,仅供个人/单位学习、研究之用,不得用于商业用途,未经授权,严禁复制、发行、汇编、翻译或者网络传播等,侵权必究。。
- 2、本站所有内容均由合作方或网友上传,本站不对文档的完整性、权威性及其观点立场正确性做任何保证或承诺!文档内容仅供研究参考,付费前请自行鉴别。如您付费,意味着您自己接受本站规则且自行承担风险,本站不退款、不进行额外附加服务;查看《如何避免下载的几个坑》。如果您已付费下载过本站文档,您可以点击 这里二次下载。
- 3、如文档侵犯商业秘密、侵犯著作权、侵犯人身权等,请点击“版权申诉”(推荐),也可以打举报电话:400-050-0827(电话支持时间:9:00-18:30)。
- 4、该文档为VIP文档,如果想要下载,成为VIP会员后,下载免费。
- 5、成为VIP后,下载本文档将扣除1次下载权益。下载后,不支持退款、换文档。如有疑问请联系我们。
- 6、成为VIP后,您将拥有八大权益,权益包括:VIP文档下载权益、阅读免打扰、文档格式转换、高级专利检索、专属身份标志、高级客服、多端互通、版权登记。
- 7、VIP文档为合作方或网友上传,每下载1次, 网站将根据用户上传文档的质量评分、类型等,对文档贡献者给予高额补贴、流量扶持。如果你也想贡献VIP文档。上传文档
查看更多
聚二甲基硅烷高温高压合成聚碳硅烷工艺研究-复合材料学报
39
Synthesis of Polycarbosilane from Polydimethylsilane at
High Temperature and High Pressure
, , , ,
(
, 410073)
HENG Xiang-zhen, SONG Yong-cai, XIE Zheng-fang, XIAO Jia-yu, Wang Ying-de
(State Key Lab of Novel eramic Fibers omposites,
Institute of Aerospace and Materials Engineering,
National University of Defense T echnology, hangsha 410073, hina)
: ( PDM S) , (P S) ,
Si- H ,
, , , ,
460 46 , 450 67 , 200220 ,
PDMS h h P S
5%10 % ( ) , Si- H 0.9, , Si
: ; ;
: T Q343: A: 1001-4381 (2004) 08-0039-05
Abstract : The polycarbosilane (P S) , the precursor of Si fiber, was synthesized at high tempera-
ture and high pressure by thermal decomposition of polydimethylsilane (PDMS) . The influence of
synthesis conditions on final pressure at room temperature, Si- H bond content, P S yield, soften-
ing point, the molecular weight and distributions, and spinnability were investigated. The results
show that the molecular weight and softening point of P S increase while the reaction temperature
increase T he spinnability of P S decreases gradually with temperature. Suitable reaction time for
the synthesis of P S from PDMS in autoclave should be 46h at 460 , or 67h at 450 . The as-
synthesized P S, in which the high molecular weight content was about 5% 10% ( mass fraction)
200 220 , - 0.9, ,
with softening point about to Si H bond content more than and good spinnability
was the suitable precursor for the preparat
原创力文档


文档评论(0)