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A variety of novel polymeric materials ranging from elastomers to tough, rigid plastics have been prepared by the cationic copolymerization of regular soybean oil, low-saturation soybean oil, or conjugated low-saturation soybean oil with various alkene commonomers. Using appropriate compositions and reaction conditions, 70–100% of the soybean oil is covalently incorporated into the cross-linked polymer networks, contributing significantly to cross-linking during copolymerization. The resulting thermosets exhibit thermophysical and mechanical properties that are competitive with those of their petroleum-based counterparts. In addition, good damping and shape memory properties have been obtained by controlling the degree of cross-linking and the rigidity of the polymer backbone. New materials with similar characteristics have also been produced from other biological oils, including tung, and fish oils using the same technique. The new, more valuable properties of these bioplastics suggest numerous promising applications of these novel polymeric materials. 相似文献
13.
Seung-Hwan?LeeEmail author Tsutomu?Ohkita 《Journal of Polymers and the Environment》2004,12(4):203-210
Ring-opening polymerization of cyclic esters (-caprolactone, -valerolactone, and l-lactide) onto liquefied biomass (LB) was conducted to obtain the polyester-type polyol and to regulate the characteristics of LB. IR and 1H-NMR spectra of the obtained polyol showed that the polymerization was successfully conducted in the presence of acid catalyst, which is used in liquefaction. The molecular weight (Mw), hydroxyl value, and viscosity were controllable by changing the reaction conditions. Polyester-type polyurethane foams with a wide range of properties were prepared from the obtained polyol with the appropriate combinations of foaming agents. 相似文献
14.
Mihail Ionescu Zoran S. Petrović Xianmei Wan 《Journal of Polymers and the Environment》2007,15(4):237-243
Soybean polyols prepared by ring opening reactions of epoxidized soybean oil with hydrogen active compounds (water, alcohols,
organic or inorganic acids, thiols, hydrogen etc.) have a low reactivity in the reaction with isocyanates because the hydroxyl
groups are secondary. This paper presents a simple and convenient method to increase the reactivity of soybean polyols with
secondary hydroxyl groups by ethoxylation reactions with the preservation of triglyceride ester bonds. The method uses mild
reaction conditions: low alkoxylation temperature of 35–45 °C, low pressure of 0.1–0.2 MPa (15–30 p.s.i.) and a superacid
as catalyst (HBF4). The new soybean polyols have a higher reactivity toward isocyanates in polyurethane formation due to the high percentage
of primary hydroxyl groups. The primary hydroxyl content was determined by the second order kinetics of polyol reaction with
phenyl isocyanate. 相似文献
15.
Biodegradation of Polycaprolactone Powders Proposed as Reference Test Materials for International Standard of Biodegradation Evaluation Method 总被引:1,自引:0,他引:1
Masahiro Funabashi Fumi Ninomiya Masao Kunioka 《Journal of Polymers and the Environment》2007,15(1):7-17
Polycaprolactone (PCL) powders were prepared from PCL pellets using a rotation mechanical mixer. PCL powders were separated
by sieves with 60 and 120 meshes into four classes; 0–125 μm, 125–250 μm, 0–250 μm and 250–500 μm. Biodegradation tests of
PCL powders and cellulose powders in an aqueous solution at 25°C were performed using the coulometer according to ISO 14851.
Biodegradation tests of PCL powders and cellulose powders in controlled compost at 58°C were performed by the Mitsui Chemical
Analysis and Consulting Service, Inc. according to ISO 14855-1 and by using the Microbial Oxidative Degradation Analyzer (MODA)
instrument according to ISO/DIS 14855-2. PCL powders were faster biodegraded than cellulose powders. The reproducibility of
biodegradation of PCL powders is excellent. Differences in the biodegradation of PCL powders with different class were not
observed by the ISO 14851 and ISO/DIS 14855-2. An enzymatic degradation test of PCL powders with different class was studied
using an enzyme of Amano Lipase PS. PCL with smaller particle size was faster degraded by the enzyme. PCL powders with regulated sizes from 125 μm to 250 μm
are proposed as a reference material for the biodegradation test. 相似文献
16.
目的 系统研究前驱体聚合反应时间对PI膜及其碳化、石墨化后薄膜结构和性能的影响规律。方法 通过调整聚合合成聚酰胺酸(PAA)溶液过程中的反应时间,制备石墨膜前驱体聚酰亚胺(PI)原膜,将不同工艺条件下制得的PI膜进行碳化、石墨化处理,得到高导热率石墨膜。利用扫描电镜、红外光谱、拉曼光谱仪和LFA激光闪射仪对制备的PI膜、碳化膜及石墨膜的微观结构和热导率进行检测。结果 随聚合反应时间的延长,PI膜酰亚胺化程度和石墨膜的石墨化程度及导热性能先增高、后降低。反应时间为3 h时,制得的石墨膜结构致密,石墨片层取向性好,导热性能最好,热导率可达765.2 W/(m.K)。结论 PI膜前驱体聚合反应时间显著影响PI膜酰亚胺化的程度和有序度,进而影响石墨膜的定向性和导热性能。 相似文献
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19.
用丙酮作溶剂将三油酸甘油酯分散到醋酸纤维(CA)基体中,采用悬浮聚合的方法制备出了一种兼具亲水性,又能高倍富集持久性有机污染物的球形复合吸附剂。通过对分散剂的种类及其用量、悬浮介质的种类及其用量的研究,获得了球形复合吸附剂的最佳合成路线与工艺.球形吸附剂粒径为1~2mm。通过荧光分析和电镜扫描分析,表明三油酸甘油酯已被包埋到醋酸纤维基体中,并得到了均匀分散。采用七氯、狄氏剂、异狄氏剂、灭蚁灵为代表性的持久性有机污染物(POPs)。动力学吸附实验表明,当初始浓度为1μg/L时,在快速吸附阶段,溶液中80%的氯、狄氏剂、异狄氏剂可得到有效去除,但并没有达到吸附平衡。快速吸附完后,还在持续地进行慢速吸附。而对于灭蚁灵,吸附速度远远低于其他几种POPs。实验证明了吸附速度不仅与辛醇/水系数有关,而且还与有机污染物的分子结构有关。 相似文献
20.
富营养化水体中微囊藻毒素(MCs)去除技术研究进展 总被引:2,自引:1,他引:1
当前,随着工业的发展水体富营养化程度日益严重。引起富营养化的主要藻类一蓝藻,能够释放对人体及鱼类具有多器官毒性、遗传性和致癌性的毒素——微囊藻毒素(MCs)。MCs治理技术种类繁多,传统的物理法如:混凝沉淀、膜过滤、活性炭吸附、气浮以及直接过滤只能对简单的处理细胞内的MCs;化学氧化法、光催化氧化法以及高级氧化法虽然能有效处理水体中的MCs.但有成本高、易二次污染和操作复杂等缺点,难以满足日益严格的环保要求;生物酶法除了具有生物降解法所具有的廉价、无二次污染、降解彻底和易操作等特点外,还被刺用来监控水体中MCs,它将成为今后重点研究的技术领域. 相似文献