Synthesis and biodegradation of poly(γ-butyrolactone-co-l-lactide)

Biodegradable polyesters were synthesized by ring-opening copolymerization of -butyrolactone (BL) and its derivatives withl-lactide (LLA). Although tetraphenyl tin was the main catalyst used, other organometallic catalysts were used as well.¹H and¹³C NMR spectra showed that poly(BL-co-LLA)s were statistical and that their number-average molecular weights were as high as 7×10⁴. The maximum BL content obtained from copolymerization BL/LLA was around 17%. TheT _m andT _g values of the copolymers showed a gradual depression with an increase in BL content. NoT _m was obtained for the copolymers containing more than 13 mol% BL. The biodegradability of the copolyesters was evaluated by enzymatic hydrolysis and nonenzymatic hydrolysis tests. The enzymatic hydrolysis was carried out at 37°C for 24 h using lipases fromRhizopus arrhizus andR. delemar. Hydrolyses by both lipases showed that an increase in BL content of the copolymer resulted in enhanced biodegradability. Nonenzymatic accelerated hydrolysis of copolymers at 70°C was found to increase proportionally to their exposure time. The hydrolysis rate of these copolymers was considerably faster than that of PLLA. The higher hydrolyzability was recorded for the BL-rich copolymers. The copolymerization of -methyl--butyrolactone (MBL) or -ethyl--butyrolactone (EBL) with LLA resulted in relatively LA-rich copolymers.     

Enzymatic degradation of poly([R,S] β-hydroxybutyrate)

The synthetic analogue of a bacterially produced polyester, poly(-hydroxybutyrate) (PHB) was synthesized from racemic -butyrolactone using anin situ trimethyl aluminum-water catalyst. The polymer was fractionated into samples differing in molecular weight and isotactic diad content. The latter was closely related to degree of crystallinity. The biodegradation of these fractions were examined by monitoring mass loss over time in the presence of anAlcaligenes faecalis T1 extracellular bacterial poly(-hydroxybutyrate) depolymerase. The fraction with high isotactic diad tacticity content showed little or no degradation over a 50 hour incubation period, whereas the fraction of intermediate isotactic diad content degraded in a continuous steady fashion at a rate that was less than that for bacterial PHB. The low isotactic diad fraction underwent a rapid initial degradation, followed by no further mass loss. The presence of stereoblocks in the polymer structure of the various fractions was an influence on the degree of susceptibility towards degradation and is related to sample crystallinity.     

瓷砖釉面TiO2薄层对甲基橙的光催化降解

采用溶胶-凝胶法，在瓷砖釉面上制备了良好光催化活性TiO2薄层材料，研究结果表明瓷砖釉面TiO2薄层材料对甲基橙的光催化反应遵循一级动力学规律，光催化降解率与液层厚度符合指数关系。在太阳光照射下，釉面瓷砖TiO2薄层材料能对甲基橙有效地降解。     

采用消声障板控制通风管路送、回风口声辐射的研究

根据扁矩形消声通道二维消声理论替代一维理论导出的消声系数Φ（α），研究了障板消声结构的Φ（α）计算机程序和消声量与障板几何尺寸的关系     

ClO2处理含铁,锰及细菌饮用水的应用研究

为了除去水中高含量的铁，锰及细菌，采用ＣｌＯ２氧化Ｆｅ＾２＋，Ｍｎ＾２＋和灭菌的方法。研究结果表明，处理后水平铁，锰都末检出，细菌指标符合国家饮用水标准。此法具有工艺简单，操作方便，反应速度快，去除率极高，不产生致癌物质ＴＨＭ、且能很好地除水中的异味及色度等优点。此法适用于各种生活给水系统。     

太阳能光催化降解法去除水中罗丹明染料的研究

在太阳光的紫外线辐射下，应用载有ＴｉＯ２薄层的平板式光催化反应器，进行了光催化降解法去除水中罗丹明染料的试验，结果表明，当紫外线辐射强度平均为３３Ｗ／ｍ＾２，反应时间为１８ｍｉｎ时，水中罗丹明染料浓度由１０ｍｇ／Ｌ降至０．０１ｍｇ／Ｌ，在室国家排放标准，探讨了太阳能光催化反应系统的改进方向及工业化应用的有关问题。     

二氧化硫排放总量控制若干问题的思考

根据国家《“十一五”规划纲要》对削减二氧化硫排放总量的要求，在对电力行业脱硫现状及前景的具体阐述中指出实现这个目标的可能性，并从多方面对二氧化硫总量控制的关键问题进行了详尽的论述与分析。     

TiO2光催化氧化的研究进展

概述了TiO2光催化氧化降解水中污染物的原理及TiO2光催化剂的制备，提出了增强其活性的途径。TiO2光催化氧化可应用于印染、农药、造纸等工业废水及饮用水处理中，研制高效的负栽型纳米TiO2光催化剂、解决太阳能利用问题、开发多功能光催化反应器是今后TiO2光催化氧化的发展趋势。     

淮河流域旱涝易发区农田的陆气相互作用——CO2通量、能量交换和水汽输送的季节变化特征

利用淮河流域旱涝易发区的安徽省寿县农田下垫面陆气相互作用观测试验资料,重点分析观测期内CO2通量、能量交换和水汽输送的季节变化,并讨论了与此有关的辐射分量通量、下垫面反射率、波恩比、能量闭合守恒、土壤温度和土壤湿度的季节变化.结果表明CO2通量、能量分配受地表农作物长势影响明显,其中,水稻灌浆、成熟期,被稻田吸收的CO2通量最大可超过2 mg·m-2·s-1,潜热通量达到正的极大值.稻田光合作用最旺盛时期吸收的CO2通量和释放的潜热通量均大于小麦田光合作用最旺盛时期的对应量.较大土壤热通量对应于较低的土壤水含量.试验观测期的下垫面平均反射率为0.14.作物生长期,稻田表面潜热是下垫面吸收能量的主要消费者,小麦田表面潜热和感热相当.能量闭合率ε的变化范围为0.4～1.     

南昌市环境空气质量分析和控制

利用多年的环境监测数据,分析南昌市环境空气中主要污染物尘类、二氧化硫和氮氧化物产生的原因,并提出有效控制上述污染物的具体措施。