采用紫外光谱、XPS研究了羧甲基纤维素型高分子表面活性剂在硅胶/水界面上的吸附形态,结果表明随着高分子表面活性剂溶液浓度增大,分子在硅胶表面的吸附由单层逐渐变为多层,生成半胶束结构。

采用紫外光谱、相图、动态激光光散射、同位素示踪、光学显微镜、电导率等研究了羧甲基纤维素系列高分子表面活性剂与甲苯-水-异丙醇体系微乳液的形成过程, 发现微乳液粒子大小均一, 形态一致, 其尺寸比低分子表面活性剂所形成的微乳液粒子大得多。 醇分子插入到油水界面, 改变了两相界面结构, 促使微乳液的生成。电导率测定表明所形成的微乳液区均为水包油结构, 即使在富含甲苯区域, 亦不会有油包水的反相胶束形成。

采用动态激光光散射及环境扫描电镜研究了羧甲基纤维素系列高分子表面活性剂与大庆原油形成超低界面张力的机理。 结果表明, CMC系列高分子表面活性剂具有与低分子量表面活性剂相比拟的表/界面活性, 其水溶液的表面张力可达2835mN/m, 界面张力达到10-110mN/m。 碱的加入可显著降低高分子表面活性剂与原油的界面张力, 在适当条件下界面张力达到超低值(10-3mN/m), 可望作为三次采油的驱油剂。等效烷烃模型研究表明, 用碱与原油酸性组分的作用来解释碱能使界面张力下降至超低值的传统观点是不完善的, 加入碱能使高分子表面活性剂胶束解缔, 胶束数量增多, 胶束粒径减小, 单分子自由链增加, 有利于高分子表面活性剂向界面迁移和排布, 这是高分子表面活性剂和碱复配体系与原油界面张力下降至超低值的主要原因。

The morphological structure and mechanical properties of isotactic polypropylene (PP)/zinc-neutralized sulfonated ethylene propylene diene monomer rubber (Zn-SEPDM)/CaCO3 blends were studied. PP/Zn-SEPDM/CaCO3 blends were prepared through two different sequences. A: Blending PP with Zn-SEPDM, then adding CaCO3; B: Blending Zn-SEPDM with CaCO3, then adding PP. The blending sequence has substantial influence on the mechanical properties. SEM micrographs and X-ray photoelectron spectrometry indicate that the CaCO3 filler is encapsulated by Zn-SEPDM in those blends prepared through sequence B, which caused an extra increase of impact strength.

Flow performance of metallocene linear lowdensity polyethylene (mLLDPE) containing small amounts of polyethylene glycol (PEG) diatomite and diatomite/PEG binary processing aids respectively was investigated. The mLLDPE melt viscosity is increased by the addition of diatomite, but is decreased by addition of PEG or the diatomite/PEG binary processing aids. It was also found that the viscosity reduction of mLLDPE with the addition of diatomite/PEG binary processing aid was significantly greater than that obtained with the addition of only PEG. The flow curves of mLLDPE containing diatomite/PEG binary processing aid show extremely lower value and stronger dependence on shear rate than the others. It is suggested that the rheological improvement of mLLDPE with diatomite/PEG binary processing aids resulted not entirely from the wall slip promoted by PEG; the intrinsic structure may have changed under the application of shear flow.