反机场跑道润滑技术研究

反机场跑道润滑是一种新概念非致命性武器技术.本文以硬脂酸、甲基硅油及其他添加剂在常压下合成了一种新型硅油脂,并将其与几种常用润滑剂进行润滑摩擦系数的实验对比.通过摩擦学实验得到了0～72 h内其摩擦系数的变化曲线,并从分子结构角度对实验结果进行理论分析.结果表明,在对混凝土-橡胶轮胎摩擦副的润滑中,自制硅油脂可以使其摩擦系数保持在制动困难状态(μ≤0.35),并且可以维持较长时间(t≥72 h).综合各因素,它在机场跑道润滑过程中具有明显的优势,具有军事应用前景.     

利用酵母菌处理高浓度味精废水的连续小试

利用批量实验对从高浓度味精废水中筛选出的一组酵母菌混合菌群进行了脱氢酶活性(DHA)测试.结果表明用该菌群对COD、硫酸根和氨氮均接近20000mg/L的味精离交尾液进行处理时,其DHA值在前36h高于对离交尾液稀释液的处理,说明高浓度氨氮和硫酸盐对酵母菌活性的影响不显著.利用接种了该酵母菌群的生物接触氧化反应器对味精废水进行的连续小试处理结果表明,COD容积负荷2.0～14.3kg/(m³·d)时,COD去除率稳定在80%以上;适当地补充磷源有利于维持稳定的处理效果对出水pH值和C     

Bacterial degradation of a new polyester,polyethylene glycol-phthalate polyester

Microorganisms which can assimilate a new polyester synthesized from polyethylene glycol (PEG) as a dihydroxyl compound and phthalic acid as a dicarboxyl compound were isolated from soils by enrichment culture techniques. Two cultures, K and N, were obtained: Culture K grew on PEG 4000 polyester and culture N assimilated PEG 6000 polyester. Each culture included two bacteria indispensable for the degradation of polyesters: bacteria K1 and K2 for PEG 4000 polyester-utilizing culture K and bacteria N1 and N2 for PEG 6000 polyester-utilizing culture N. Bacteria K2 and N2 were responsible for the hydrolysis of ester bonds in a polyester and both were identified as the same species,Comamonas acidovorans. Bacteria K1 and N6 could assimilate PEG as a sole carbon and energy source. Both are Gram-negative, non-spore-forming rods and resembled each other on their colony characteristics, although strain K1 could not grow on PEG 6000.C. acidovorans N2 (K2) grew on dialkyl phthalates (C₂–C₄) and phthalate and tributyrin, but not on PEG, diphthalic PEG, and PEG phthalate polyesters. Their culture supernatant and washed cells hydrolyzed PEG (400–20,000) phthalate and sebacate polyesters.C. acidovorans had higher esterase activity toward PEG phthalate, isophthalate, and terephthalate polyesters than known esterase and lipases. The esterase seemed to be an extracellular one and attached to the cell surface.     

Graft Copolymers, for Erodible Resins, from α-Hydroxyacids Oligomers Macromonomers and Acrylic Monomers

Environmental concerns result in a progressive withdrawal of antifouling paints containing organotin derivatives. The nature of the binders is critical with regard to the erosion of the protecting film through factors such as bond cleavage, dissolution, and diffusion of the degradation products. The versatility of acrylic polymers, due to the possibility of varying their chemical structure had conducted, in the first stage, to combine different types of repeating units in the macromolecular backbone. Formulation and evaluation, in natural sites, of these binders, with a well-defined hydrophobic/hydrophilic balance and with hydrolyzable pendant groups, have shown the possibility to prepare new organotin free resins which can be formulated and which are erodible in seawater over a long period (more than 2 years). A further step has been engaged with the development of graft copolymers containing biocompatible and hydrolyzable oligomers of -hydroxyacids. Their preparation requires the synthesis of -methacryloyloxyoligo--hydroxyacid macromonomers. Copolymers prepared from a mixture of the macromonomer and of an alkyl ester of acrylic acid were formulated with a biocide and deposited on a plate. Their ability to release cuprous oxide, as a model molecule, has been checked and quantified by the inductively coupled plasma analytical method. The uptake of water in the paint, which is enhanced by the hydrolysis of -hydroxyacid oligomers, as determined by the enzymatic measurement of liberated L-lactic acid, conducts to the polymer erosion and to a protecting bioactive surface.     

水解酸化-UASB-SBR组合法处理印染废水

根据印染废水的特性，提出了水解酸化－UASB－SBR组合法处理的处理方法。该不的实际应用表明，废水CDO用2500－4500mg/L降至80－150mg/L,BOD5，可由600－1000mg/L降至30-40mg/L，色度可由100－600倍降至50－60倍，该法具有以废治废，投资少，运用费用低，操作简单的特点。     

Hydrolyzable poly(ethylene terephthalate)

Due to the enormous annual increase in the volume of municipal solid waste, society's attention is focused on how to manage the solid waste problem. Plastic materials not only contribute a great deal to the litter problem but also create serious danger to the ecology. Every year, countless birds, sea turtles, and other marine mammals die from eating or getting entangled in plastic litter. Synthesizing degradable polymers can have a great impact on solving the problem of plastic litter. We have modified the structure of poly(ethylene terephthalate) to make it degradable in typical environmental conditions in presence of water. The change of physical properties of modified poly(ethylene terephthalate), resulting from hydrolysis, has been monitored and compared with those of pure poly(ethylene terephthalate).     

Degradation of Commercial Biodegradable Packages under Real Composting and Ambient Exposure Conditions

The use of long-lasting polymers as packaging materials for short lived applications is not entirely justified. Plastic packaging materials are often soiled due to foodstuffs and other biological substances, making physical recycling of these materials impractical and normally unwanted. Hence, there is an increasing demand for biodegradable packaging materials which could be easily renewable. Use of biopolymer based packaging materials allows consideration of eliminating issues such as landfilling, sorting and reprocessing through taking advantage of their unique functionality, that is compostability. Composting allows disposal of biodegradable packages and is not as energy intensive compared to sorting and reprocessing for recycling, although it requires more energy than landfilling. The aim of this work was to study the degradation of three commercially available biodegradable packages made of poly (ld-lactide) (PLA) under real compost conditions and under ambient exposure by visual inspection, gel permeation chromatography, differential scanning calorimetry, and thermal gravimetric analysis. A novel technique to study the degradability of these packages and to track the degradation rate under real compost conditions was used. The packages were subjected to composting for 30 days, and the degradation of the physical properties was measured at 1, 2, 4, 6, 9, 15 and 30 days. PLA packages made of 96% l-lactide exhibited lower degradation than PLA packages made of 94% l-lactide, mainly due to their highly ordered structure, therefore, higher crystallinity. The degradation rate changed as the initial crystallinity and the l-lactide content of the packages varied. Temperature, relative humidity, and pH of the compost pile played an important role in the total degradation of the packages. A first order degradation of the molecular weight as a function of time was observed for the three packages.     

外加酶强化剩余污泥水解的研究

采用向污泥中外加酶强化污泥水解的处理方式,考察了单一酶和复合酶的加入对城市污水厂剩余污泥的破解及减量化的影响,并探讨了酶水解过程动力学.结果表明,外加酶可以促进污泥中悬浮固体的溶解和大分子有机物的降解.当酶最佳投加量(以TS中加入酶量计)为60 mg/g时,淀粉酶比蛋白酶的水解效果好,SCOD/TCOD由16.3%上升到22.3%,VSS去除率由39.8%提高到54.24%.同时,复合酶的水解效果较单一酶的效果好,当水解温度为50℃,蛋白酶和淀粉酶的比例为1∶3时,水解效果最佳,VSS去除率达68.43%,还原糖、NH+4-N浓度分别由37.29和47.60 mg/L增加至177.8和143.43 mg/L.酶水解过程的前4 h,蛋白酶和淀粉酶活力均呈上升趋势,符合一级反应动力学,水解4 h左右达最大值,分别为2.57 U/mL和4.64U/mL,之后酶活力逐渐下降.     

垃圾焚烧飞灰熔融过程烟气中重金属的迁移分布规律

采用重庆同兴垃圾焚烧(MSWI)发电厂飞灰,开展了高温熔融及铁浴熔融重金属分布迁移规律实验研究.采用布袋式除尘法收集捕捉熔融过程烟气中的烟尘,并对烟尘中的重金属组分、含量、形态和结构进行测试分析,研究了高温熔融分离过程各金属元素在烟气中的迁移分布规律.结果表明,迁移到烟气中的主要元素为Zn、Pb、Cl、K、Na,并以ZnS、ZnO、PbCl2、KCl、NaCl形态存在于熔融飞灰上;Rb、Cd、Sn、Sb等低沸点易挥发金属元素在熔融烟气中以硅酸盐、磷酸盐形态存在;Hg主要以氯氧化物、硫氯化物形态存在.铁浴熔融可有效抑制Ti、Mn、Fe、Se的挥发,提高Cd、Sn、Sb的挥发速率,有利于提高Rb在熔融飞灰上的分配率,但对Zn、Rb、Pb的挥发没有影响.     

碱辅助条件下的污泥微波热水解特性研究

向污泥中加入NaOH进行微波热水解实验.结果表明,每1 g污泥悬浮固体(SS)添加NaOH 0.1 g时,污泥中的挥发性悬浮固体(VSS)快速水解,170℃的VSS溶解率达到60%以上,热水解后污泥的有机物含量(VSS/SS)降低至25%.80、120、150和170℃热水解5 min的污泥液相COD浓度分别为9.8、12.8、15.1和14.5 g/L,相应SCOD/TCOD为24.0%、31.3%、36.9%和35.6%.随温度的升高和时间的延长热水解污泥pH越低,最低值10.5.在每1 g SS添加0~0.2g NaOH的范围内,当添加量0.05 g时,VSS和SS的溶解率增加幅度降低.分别对NaOH添加量0.05 g热水解5 min和添加量0.1 g热水解1 min的污泥进行BMP厌氧消化实验.结果表明,添加量为0.05 g时热水解污泥的厌氧消化性能提高,经150℃处理污泥的产气量最大,比未处理污泥高28.5%,而在添加量为0.1 g时,污泥的厌氧消化性能受到抑制,产气量低于未处理污泥.