摘要
利用双(β-二酮单亚胺)钛催化乙烯和5-碘甲基降冰片烯(IMNB)的配位共聚,高效合成了高分子量、窄分子量分布和组分可控的烯烃共聚物.将该含有碘甲基侧基的共聚物与N-甲基咪唑进行亲核取代反应,然后再与有机金属盐进行离子交换,制备了一系列带有甲磺酸根(CH3SO3^-)、三氟甲磺酸根(CF3SO3^-)或双(三氟甲磺酰)亚胺负离子(Tf2N^-)的聚乙烯离聚体.研究表明,离子基团的引入会破坏聚合物的结晶,熔融温度和结晶度均随着离子含量的增加而降低.但离聚体的玻璃化转变温度却高于乙烯/IMNB共聚物,表明离子基团之间的强相互作用抑制了链段运动.与共聚物前体相比,聚乙烯离聚体表现出更高的热稳定性、更好的亲水性和更高的抗拉强度.当离子含量相同时,聚乙烯离聚体的抗拉强度顺序为:CH3SO3^->CF3SO3^->Tf2N^-,而断裂伸长率呈现相反的趋势.
The novel ethylene/5-iodomethyl norbornene(IMNB)copolymers with high molecular weight,narrow molecular weight distribution and different incorporation of comonomer were firstly synthesized by using titanium catalysts bearing twoβ-ketiminato chelate ligands,then iodine atoms distributed randomly along the copolymer chains were subsequently converted into ionic groups via nucleophilic substitution reac⁃tion with N-methylimidazole,followed by exchanging the I−counteranions with CH3SO3^−,CF3SO3^−,or Tf2N^−.Thus,a series of imidazolium-based polyethylene ionomers bearing different counteranions were readily obtained.As observed,the introduction of ionic groups destroyed the crystallization of copolymers,contributing to the decrease of melting temperature and crystallinity.Such effect became more significant with increasing the ion content.Ionomers had higher glass transition temperature(Tg)than that of ethylene/IMNB copolymer,suggesting the interaction between ionic groups restricted the mobility of surrounding segments.Compared with copolymer,polyethylene ionomers exhibited better thermal stability,hydrophilic property and tensile strength.With the same ion content,the stress-at-break values of the ionomers followed the order:CH3SO3^−>CF3SO3^−>Tf2N^−,whereas the strain-at-break values in the opposite order.
作者
张俊
王彬
潘莉
马哲
李悦生
ZHANG Jun;WANG Bin;PAN Li;MA Zhe;LI Yuesheng(School of Materials Science and Engineering,Tianjin University,Tianjin 300350,China)
出处
《高等学校化学学报》
SCIE
EI
CAS
CSCD
北大核心
2020年第9期2070-2077,共8页
Chemical Journal of Chinese Universities
基金
国家自然科学基金(批准号:21690071)资助.
关键词
聚烯烃
离聚体
热稳定性
亲水性
拉伸强度
Polyolefin
Ionomer
Thermal stability
Hydrophilic property
Tensile strength