铜与铜包铝接地线缆短路熔断特性理论计算与试验

为研究用于高压电力系统的临时接地装置抗突然短路能力及短路火灾限制措施,通过铜导体Onderdonk公式的推广算法,得到铜包铝接地线缆熔断电流的理论计算方法,以6 300 kVA大容量变压器为电流源模拟实际工作中挂接地线时可能出现的短路熔断情况,对常用的铜材料接地线缆及轻质铜包铝材料接地线缆在10 kA以上短时大电流下的熔断过程进行了试验。结果表明:绝热过程下接地线缆熔断电流的理论计算结果偏严格,通过计算公式选取接地线缆截面积具有一定的安全裕度;理论等效截面下铜包铝线缆相比铜线缆更不容易发生熔断,12. 9 kA、16. 3 kA、21. 7 kA短路电流下60 mm^2铜层体积比为10%的铜包铝裸导线熔断时间比35 mm^2铜线分别增加32. 0%、30. 1%、24. 3%;外加阻燃护层可以增加铜线缆的熔断时间而对铜包铝线缆熔断时间的影响不明显,但外加护层可以显著减少铜包铝线缆迸溅熔珠的数量,降低熔珠的引燃能力,从而对短路火灾进行有效抑制。     

Bestimmung und Bewertung der Emissionen von PCDD/PCDF,PAK und kurzkettigen Aldehyden in den Brandgasen von Kerzen

Exhaust fumes of paraffin, beeswax and stearin candles without any further paint or decorative element were analysed for the toxicological important substance classes of PCDD/PCDF, PAH and short chain aldehydes. The candle waxes and wicks were investigated for chlorinated dioxins, furans and some known precursors. Toxicological risk assessment shows that emissions of the investigated candles are much lower than all administrative limitation values — even under “worst case conditions”. Thus, they do not produce a toxicological risk for human health.     

基于Meta分析的土壤呼吸对凋落物输入的响应

凋落物输入是影响土壤呼吸的一个重要因素,然而从国内外目前研究结果来看,土壤呼吸响应凋落物输入的影响因素尚不清楚。利用国内外已发表的30篇研究论文共1393对有效数据,通过Meta分析,从凋落物管理措施、气候、植被、地形、土壤理化性质等因素揭示凋落物输入对土壤呼吸的影响程度。研究发现:与清除凋落物处理相比较而言,(1)凋落物输入后显著增加了土壤呼吸,且土壤呼吸的增加程度呈现出倍增凋落物处理是自然凋落物处理的1.33倍;(2)不同气候条件下的土壤呼吸增加程度呈现出强降雨(>1000 mm)是微弱降雨(<1000 mm)的1.34倍,以及高温气候(>20℃)是低温气候(<20℃)的1.7倍;(3)土壤呼吸的增加程度在不同植被带下呈现出针叶林带(34.1%)>阔叶林带(28%)>混交林带(22%)>草地(17.3%)的趋势;(4)不同海拔梯度条件下土壤呼吸的增加程度呈现出高海拔(59.6%)>中海拔(34.2%)>低海拔(26.7%)的趋势;(5)不同土壤理化性质条件下的土壤呼吸增量呈现出低容重(77.5%)分别是中容重(26.9%)和高容重(18.0%)的2.9倍和4.3倍,同时中性土壤(79.6%)的呼吸增量远远大于酸性(28.2%)和碱性(24.1%)土壤的呼吸增量,以及高土壤碳氮比(81.2%)的土壤呼吸增量远远大于低土壤碳氮比(19.4%)和中土壤碳氮比(29.6%)的土壤呼吸增量。由此可见,凋落物输入后会导致土壤呼吸的显著增加,但是不同气候、不同植被、不同地形、不同土壤理化性质等条件下其土壤呼吸增加的幅度不同。     

农药杀螟硫磷酶促降解的研究

从长期受农药杀螟硫磷污染的土壤中分离到一株高效降解菌株,研究了其最适产酶条件:培养温度为30℃,培养液起始pH为7.0,培养时间为30 h.从该降解菌中提取的粗酶液在pH 7.5和30℃时显示最大的降解活性,其米氏常数Km为2.92×10-4mol/L,最大降解速率为2 422.79 nmolm in-1mg-1.图7参15     

可持续发展观的化学发展目标:生态化学

通过阐述化学发展与自然和人的关系,认为追求人与自然的和谐是整个世界的自然观的最高目标。从生态学角度研究了化学发展史,认为化学发展过程可分为原始生态化学时期、非生态化学时期和生态化学时期,提出了生态化学的新概念,认为生态化学针对传统化学的资源利用率低、环境污染严重的缺陷,提出了废物的减量化、无害化和资源化,并使原料利用率最大化;生态化学是站在对环境友好的高度,使环境资源的化学变换体系成为一种更有效的运行模式,对环境系统有更小的破坏作用,进而对改善环境质量做出贡献。因此,生态化学融被动处理污染的环境化学及主动出击的绿色化学为一体,是更加关注生态的先进理论。     

TiO2光催化剂的超临界CO2萃取法制备及其降解甲基橙的活性

用超临界二氧化碳萃取TiO2醇凝胶制备纳米二氧化钛粉体，对萃取工艺条件进行了讨论，并用XRD，FT-IR，BET和DRS对上述粉体进行表征．以光催化降解甲基橙为模型反应，结果表明，与超临界二氧化碳干燥所得的粒子比较，该工艺干燥的TiO2粉体粒径小，比表面积大，光催化活性较高。     

Photo-assisted fenton oxidation of refractory organics in UASB-pretreated leachate

Nearly 91% of organic pollutants in Hong Kong leachate could be effectively removed by the UASB(upflow anaerobic sludge blanket)process followed by the fenton coagulation.The COD(chemical oxygen demand)of leachate was lowered from an average of 5620 mg/L to 1910 mg/L after the UASB treatment at 37℃,and was further lowered to 513 mg/L after fenton coagulation.The remaining refractory residues could be further removed by plotochemical oxidation with the addition of H2O2.The BOD/COD ratio was greatly increased from 0.062 to 0.142,indicating the biodegradability of organic residues was improved.The photochemical oxidation for the fenton-coagulation supernatant was most effective at pH3-4,with the addition of 800 mg/L of H2O2,and UV radiation time of 30 minutes.The final effluent contained only 148 mg/L of COD,21 mg/L of BOD(biochemical oxygen demand)and 56 mg/L of TOC (total organic carbon).     

SDBS及腐殖酸对涕灭威及其氧化产物水解的影响

 研究了腐殖酸(胡敏酸,HA和富里酸,FA)和表面活性剂十二烷基苯磺酸钠(SDBS)对氨基甲酸酯农药涕灭威及其氧化产物涕灭威亚砜和涕灭威砜的水解作用的影响.结果表明,SDBS可以促进涕灭威及其氧化产物的水解,随着SDBS的浓度由0增加为1200mg/L,涕灭威,涕灭威亚砜和涕灭威砜的水解速率常数K值分别增加了约8倍,7倍和6倍.腐殖酸可抑制涕灭威及其氧化产物的水解.在pH值为12的水溶液中,当FA的浓度由0增大到1000mg/L时,涕灭威,涕灭威亚砜和涕灭威砜的水解速率常数K值分别下降了83%,50%,68%;随着HA的浓度由0增大到1000mg/L时,涕灭威,涕灭威亚砜和涕灭威砜的水解速率常数K值分别下降了45%,56%,22%.研究结果对受农药污染土壤的修复有一定的指导意义.     

Use of spent mushroom compost to bioremediate PAH-contaminated samples

Spent mushroom compost (SMC) is a bulky waste byproduct of mushroom industry and produced abundantly. The SMC of Pleurotus pulmonarius immobilized laccase (0.88 mmoles min(-1) g(-1)) and manganese peroxidase (0.58 mmoles min(-1) g(-1)) of which the optimal temperatures were 45 and 75 degrees C, respectively. In laboratory test, complete degradative removal of individual naphthalene, phenanthrene, benzo[a]pyrene and benzo[g,h,i]perylene (200 mg PAH kg(-1) sandy-loam soil) by 5% SMC was obtained in two days under continuous shaking at 80 degrees C. The SMC-treated PAH samples had significantly reduced or removed their toxicities as revealed by the Microtox bioassay. These results were confirmed by gas chromatography-mass spectrometry analysis on the breakdown products. A phthalic derivative which is reported as a degradative product of PAHs by ozonation or ligninolysis was also detected in the SMC-treated samples. The results demonstrate the potential in employing SMC in ex situ bioremediation.     

Observations of 2,4,6-trichlorophenol degradation by ozone

The aqueous reactivity of 2,4,6-trichlorophenol (TCP) with ozone has been studied at laboratory-scale using a simple gas bubble/liquid contacting system. Degradation rate constants were measured directly and found to be 7.6 and 77.2 M(-1)s(-1) at pH 2 and 7.5, respectively. At pH 7.5, 10 min of ozonation ( identical with 15 mM ozone consumption) achieved a 90% degradation of TCP, which corresponded to the release of approximately 2 mol Cl(-) per mol TCP. The presence of hydrogen peroxide in solution did not significantly increase the TCP degradation but increased the overall dechlorination to 2.7 mol Cl(-) per mol TCP. The presence of humic acid (HA) in solution was found to enhance the degradation rate of TCP at low relative HA concentrations (<0.6 g/g HA:TCP), but to reduce the rate at higher HA concentrations.