Lipase‐catalyzed synthesis of aliphatic poly(β‐thioether ester) with various methylene group contents: thermal properties,crystallization and degradation

A series of novel aliphatic poly(β‐thioether ester)s with various methylene group contents were prepared by direct lipase‐catalyzed polycondensation of the monomer with an acid‐labile β‐thiopropionate group. The polycondensation reaction using immobilized lipase B from Candida antarctica was carried out in diphenyl ether at 90 °C. Poly(β‐thioether ester)s with high molecular weights of 20 500–57 000 Da and narrow polydispersities in the range 1.40–1.48 were obtained. Thermogravimetric analysis, differential scanning calorimetry and wide‐angle X‐ray diffraction were used to investigate the thermal properties and crystal structures of these polyesters. All the poly(β‐thioether ester)s were semicrystalline polymers and thermally stable up to at least 200 °C. In vitro degradation studies showed that they can rapidly degrade under acidic conditions by the hydrolysis of the β‐thiopropionate groups, suggesting their potential as acid‐degradable polymeric materials. © 2019 Society of Chemical Industry     

交联透明质酸的降解及其释药性能

用己二酸二酰肼（ADH）对透明质酸（HA）进行化学修饰，制备交联透明质酸（HA-ADH）薄膜。粘度法测试表明HA-ADH是一种可降解的生物材料，并且与HA相比，HA．ADH的降解速率减慢。在此基础上，研究了以疏水性的替硝唑（TDZ）和亲水性的头孢唑啉钠（CEZ）为模拟药物的HA-ADH药物载体薄膜的释药性能。紫外-可见（UV-Vis）吸收光谱检测表明，HA-ADH是一种疏水性药物TDZ的优良缓释制荆，这是由于TDZ的疏水性和HA-ADH薄膜的缓慢溶胀和降解性能的结合而得到的，药物的释放主要受扩散机制控制。     

绿色包装材料——生物降解塑料

对绿色包装材料-生物降解塑料的降解机理、特点，国内外研究现状和进展及存在的问题和发展前景进行了介绍。     

生物降解塑料的研究现状及问题

生物降解塑料这一领域的研究和发展正成为人们普遍关注的焦点。生物降解塑料根据其降解机理和破坏形式，可分为完全生物降解塑料和生物崩坏性(致劣性)塑料两种。这种新型塑料涉及化工、高分子、生物学等多门学科，属于一项高新技术。尽管各国投入了较大的人力、物力，但至今还未普遍达到实用阶段，在研究开发、市场、应用等方面还存在许多问题。     

Analyzing the Reliability of Degradable Networks

The reachability of a strongly connected network may be destroyed after link damage,Since many networds have directed links with the potential for reversal,the reachability may be restored by reversing the direction of links.In this paper,the reliability of a network that allows reversal of links in discussed.     

二氧化碳基聚合物的研发现状及发展建议

首先介绍当前我国二氧化碳基聚合物的主要研发现状,然后对二氧化碳基材料的优良性能进行简要概述,并分析了其生物质路线的可行性。最后对我国二氧化碳基聚合物的产业化进程提出了几点建议,即加大研发投入和政府支持力度,组建优秀的产业化科研队伍。     

Surface modification of henequen (Agave fourcroydes) fibers by ultraviolet curing with 2‐hydroxyethylacrylate and ethylacrylate: Effect of additives on degradable properties

Henequen fibers were grafted with a double impregnating monomer 2‐hydroxyethylacrylate (HEA) and ethylacrylate (EA) to improve the physicomechanical properties. The fibers soaked in different concentration (1–10%) of monomer + MeOH solution along with photoinitiator Irgacure 907 [2%] were cured under ultraviolet (UV) lamp at different UV radiation intensities (2–14 passes). Concentration of monomer at different radiation intensities was optimized with extent of mechanical properties such as polymer loading, tensile strength, and elongation at break. Enhanced tensile strength (268%) and elongation at break (110%) were achieved by the polymer treated fibers than untreated virgin fibers. We observed that, henequen fibers treated by 3% EA showed better physico‐mechanical properties than those treated by 5% HEA. The tensile properties of henequen fibers treated by 3% EA can be enhanced by adding aloxysilane; 3‐(trimethoxysilyl) propylmethacrylate additives with bulk monomer EA (3%). The degradability of the treated and untreated fibers due to accelerated weathering were also studied and it has been found that surface modified henequen fibers produced more resistivity towards different weathering conditions than untreated fibers. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 102: 4000–4006, 2006     

淀粉-聚乙烯醇可生物降解塑料研究进展

本文详细综述了近年来国内外淀粉基聚乙烯醇塑料的研究进展。     

可降解植物纤维餐具成型工艺的研究

考察了含水率、成型压力、下模温度、上模温度、定型时间、保温时间对餐具使用性能的影响。通过正交试验,选择餐具的最佳成型工艺条件为：含水率为7％,压力为1500kN,下模温度270℃,上模温度290℃,定型时间6S,保温时间20S。     

Poly(silyl ester)s: A new route of synthesis via the condensation of Di‐tert‐butyl ester of dicarboxylic acid with dichlorosilane

Poly(silyl ester)s were synthesized by a new route via the condensation of di‐tert‐butyl ester of dicarboxylic acid with dichlorosilane by the elimination of tert‐butyl chloride as a driving force. Three new poly(silyl ester)s with molecular weights typically ranging from 2000 to 5000 amu were produced by the condensation of di‐tert‐butyl adipate with 1,5‐dichloro‐1,1,5,5‐tetramethyl‐3,3‐diphenyl trisiloxane and di‐tert‐butyl fumarate with 1,5‐dichloro‐1,1,5,5‐tetramethyl‐3,3‐diphenyl trisiloxane or 1,3‐dichlorotetramethyl disiloxane. Each polymer was characterized with infrared, ¹H‐NMR, and ¹³C‐NMR spectroscopy, gel permeation chromatography, differential scanning calorimetry, and thermogravimetric analysis. This new approach showed several advantages. First, it did not require a catalyst or solvent. Second, the tert‐butyl chloride byproduct was volatile and was easily eliminated. Third, there was no reaction between the growing poly(silyl ester)s and the condensation byproduct, tert‐butyl chloride. Fourth, the monomers could be readily purified. Finally, the polymerization could be performed at relatively low temperatures and in a short time. © 2006 Wiley Periodicals, Inc. J Appl Polym Sci 100: 1378–1384, 2006