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作 者:王睿[1] 朱志国[1] 戈欢 马萌[1] 王锐[1]
机构地区:[1]北京服装学院材料科学与工程学院,北京100029
出 处:《塑料》2016年第3期68-72,共5页Plastics
摘 要:文章以左旋丙交酯(L—LA)为单体,以辛酸亚锡和月桂醇分别作为催化剂和引发剂,在二甲苯中开环聚合得到3种不同分子量的左旋聚乳酸(PLLA),然后以其作为大分子引发剂,在基本同样的条件下,继续引发右旋丙交酯(D—LA)开环聚合,期望获得PLLA和PDLA的立构嵌段共聚物(sb—PLA)。采用核磁共振谱、X射线衍射、红外光谱和凝胶渗透色谱等对产物的结构进行了表征。结果表明:产物为单一立构嵌段聚乳酸。结合差示扫描量热仪(DSC)、热失重(TGA)和偏光显微镜(POM)对产物热性能和结晶性能进行了研究。与PLLA相比,sb-PLA的冷结晶温度(Tcc)下降25oC,但熔点(Tm)却高出50~60cc,这主要归因于PLLA—b—PDLA分子链中形成了更高紧密堆积的立构复合晶体,立体复合聚乳酸的结晶能力要明显强于PLLA或者PDLA。Poly(L-lactide) (PLLA) with varied molecular weights were synthesized by using ring-opening polymerization (ROP) of L-lactide (L-LA) , in which lauryl alcohol and Sn(Oct) 2 as initiator and catalyst, respectively. Subsequently, the PLLA were used as macroinitiator to initiate the ROP of D-lactide(D-LA). The stereoblock PLA (sb-PLA) were expected to form through sequent ROP of L-LA and D-LA. A series of characterization methods, namely nuclear magnetic resonance spectroscopy (NMR), X-ray diffraction (XRD), IR spectrum and gel permeation chromatography (GPC) were applied to investigate the structure and properties of the products. Completely stereoblock-PLA (sb-PLA) were verified. Results from differential scanning calorimetry(DSC) indicated that the melting temperature ( Tm ) of sb-PLA was above 200 ~C , much higher than that of pure PLLA. In addition, the cooling crystallization temperature( Tcc ) of sb-PLA decreased by 25 ~C compared with the PLLA. It was largely attributed to the closely packed stereocomplex crystals, which possess higher crystallization rate than homo crystals of PLLA or PDLA.
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