绿色制造评价系统与评价方法的研究及应用

 绿色制造是实现可持续发展的必然选择.绿色制造评价是保证工业产品制造“绿色程度”的关键技术.本文论述了绿色制造及其评价系统和评价方法,并通过实例验证了该评价系统的可行性和实用性.     

中国对流层二氧化硫光化学氧化过程的数值研究

利用一个三维非静力区域大气化学输送模式与中尺度气象模式MM5相连接构成一个数值模拟系统，模拟了中国地区对流层臭氧与其前体物的分布以及二氧化硫转化为硫酸盐的过程，模式扬地面源排放、大气输送和扩散、干沉积、气相化学反应和云雨过程。结果表明：日间，O3浓度主要由NOx和NMHC的源排放和光化学反应过程支配，大气辐射是光化学反应强弱的决定因子，其强度可使SO2、O3和SO4^2-的生成浓度呈现不同的日变化和季节变化，结果表明高浓度的O3对二氧化硫转化为硫酸盐的化学过程有很大的促进作用，然而，这种作用受NMHC浓度的影响很大，较高浓度的NMHC使O3浓度上升，但同时增加了对OH等自由基的消耗，使SO2的转化率降低。     

用改进的高密度污泥法处理高炉废水

改进的高密度污泥法是一种处理含有大量锌和氰化物的高炉废水的方法。该方法是将铁加入高炉废水中以分解锌——氰化物络合物,用高密度污泥法使锌呈氢氧化锌,氰化物呈亚铁氰化物沉淀析出。试验室结果表明,对于含锌达70mg/L,含氰化物达30mg/L的高炉废水,加入可溶性铁可使可溶锌浓度降低到0.3mg/L以下,总氰化物浓度降低到2.0mg/L以下。浓缩池浓浆的污泥密度可达到10～25%(含固体),从而使处理费用降至最少。     

ICP—AES法直接测定电镀废水中金属元素

ICP—AES方法能同时测定多种元素,且具有灵敏度高、稳定性好、线性范围宽、干扰少等优点。因此,已被广泛应用于多种样品的测定。对于工业污水的测定,只需对水样作简单处理(或不处理),即可同时直接测定多种元素。我们利用国产仪器,以ICP—AES技术直接测定了电镀废水中Cr、Cd、Pb、Zn、Cu和Ni 6种元素。实验结果表明,精密度和准确度较好,基本满足电镀废水测定的要求。实验部分一、仪器与试剂(一)仪器与参数1.ICP—D型高频等离子体发生器频率:31+4MHz,最大输出功率:3.5kw,阳极电流:0.85A,阳极电压:3800V,栅极     

等速电泳法测定水中Cl^—,NO2^—,I^—含量

等速电泳是利用电化学进行分离和分析的新技术。1985年.J.Vacik报道了井水和废水中 Cl~-、NO_3~-、SO_4~(2-)的测定。J.C.Reijenga报道了重水中金属离子的测定。本文对前导电介质、尾随电介质、仪器参数等方面作了探     

利用碱厂碱泥生产内墙涂料的研究

在以苛化法制烧碱的制碱企业，每年要产生大量的碱泥。文中从碱泥性质入手，介绍了利用碱泥生产内墙涂料的有关碱泥预处理、化学配方及涂料性能等几个方面的内容。利用碱泥生产内墙涂料具有成本低、工艺简单、性能好等优点，为碱泥的处理、利用开辟了新途径     

Removal of high concentrated ammonia nitrogen from landfill leachate by landfilled waste layer

The landfill of municipal solid waste(MSW) could be regarded as denitrification reactor and involved in ammonia nitrogen biological removal process. In this research, the process was applied to municipal solid waste collected in Shanghai, China, which was characterized by high food waste content. The NH4^ removal efficiency in the system of SBR nitrifying reactor followed by fresh and matured landfilled waste layer in series was studied. In the nitrifying reactor, above 90% of NH4^ in leachate was oxidized to NO2^- and NO3^- . Then high concentrated NO2^- and NO3^- were removed in the way of denitrification process in fresh landfilled waste layer. At the same time, degradation of fresh landfilled waste was accelerated. Up to the day 120, 136.5 gC/(kg dry waste) and 17.9 gN/(kg dry waste) were converted from waste layer. It accounted for 50.15 % and 86.89 % of the total carbon and nitrogen content of preliminary fresh waste, which was 4.42 times and 5.17 times higher than that of reference column respectively. After filtering through matured landfilled waste, BOD5 concentration in leachate dropped to below 100 mg/L, which would not affect following nitrification adversely. Because the matured landfilled waste acted as a well methanogenic reactor, 23% of carbon produced accumulatively from fresh landfilled waste degradation was converted into CH4.