生物质固体成型燃料NO_x排放规律研究现状

介绍了生物质固体成型燃料NOx排放危害、监控标准和生成类型;阐述了国内外生物质固体成型燃料NOx排放规律的研究现状;分析了温度、过量空气系数、分层多次配风、废气再循环等因素对NOx排放规律的影响;指出了我国在生物质固体成型燃料NOx排放规律研究中的不足,提出了下一步研究方向。     

中国生物质燃烧排放SO2、NOx量的估算

根据各地区生物质燃料消耗状况和SO2、NOx排放因子，估算了20世纪90年代中国生物质能源利用过程中的SO2、NOx排放量，并给出了分省区，分生物质燃料类型的排放清单，研究表明，中国生物质燃料消耗及其排放的SO2，NOx量分别从1991年的38.1万t和54.9万下降为1999年的33.2万t和45.3万t，在地区，燃料类型上分布不平衡；SO2和NOx排放量均较大的包括山东，江苏、河北，内蒙古，湖北等，其中，内蒙古SO2排放量最大而山东省NOx排放量最 ；秸杆是SO2和NOx排放的最主要来源，薪柴次之；牲畜粪便对SO2贡献率接近30%，而对NOx贡献率仅3%-4%。     

辽宁省1980-2003年氮氧化物排放清单初步研究

根据能源消费历史状况和氮氧化物(NOx)排放因子,分别对辽宁省20多年(1980-2003年)来的NOx排放总量以及不同燃料类型和行业的NOx排放量进行了估算.结果表明:尽管个别年份存在一些波动,但NOx排放总量总体上仍呈增长的趋势,年均增长率为4.30%.2003年辽宁省NOx排放总量达108×104 t.NOx排放总量增长趋势与能源消费总量的增长趋势基本吻合,煤炭消耗是大气中NOx排放的主要来源,占总量的65%以上,最大排放量为2003年的10.17×104 t.绝大部分NOx排放来自能源加工转换、工业和交通运输业,三者约占总量的90%,其中电力行业占28.10%～40.85%,预计在未来一段时间内电力行业仍将是辽宁省NOx排放的主要来源;交通运输部门NOx排放所占比例逐年上升,尤其在2000年后的增长趋势更为明显.      

上海市区道路地面氮氧化物污染现场调查

为了解城市道路地面NOx污染的状况和特征，对上海典型道路路边NOx污染进行现场实测。结果表明：在交通繁忙的路段，路边NOx污染严重。调查发现：路边NOx的浓度与交通状况有关，车流量越大，车辆阻塞时间越长，NOx的浓度越高；不同类型车辆对路边NOx的贡献不同，大型车和中型车的贡献要比小型车、摩托车和助动车大得多；路边空气污染和影响因素与传统空气监测数据有较大差别。     

杭州市区机动车污染物排放特征及分担率

选取杭州市区绕城高速、快速路、主干道和民用支路4种典型道路进行工况测试,建立了2010年机动车CO、HC、NOx和PM10排放清单,获得了分车型、燃料类型、排放标准以及道路类型的机动车污染物排放分担率.结果表明,杭州市机动车的污染物排放分担率差别显著,乘用车、出租车和公交车是CO和HC排放的主要来源,重型货车和公交车是NOx和PM10排放的主要来源,且乘用车的NOx排放分担率也较大;柴油车的NOx和PM10的排放分担率远大于其保有量的贡献率,是其排放的主要来源,汽油车是CO和HC排放的主要来源;占保有量30%的国0和国I车辆,对CO、HC、NOx和PM10排放分担率分别为67%、69%、58%和82%;主干道是机动车CO、HC和NOx排放的主要来源,其排放分担率分别为66%、65%和64%,民用支路是PM10排放的主要来源,分担率为55%.     

中国生物质燃烧大气污染物排放清单

根据2000-2007年各省市生物质燃烧消耗量和排放因子,估算了中国大陆生物质燃烧所导致的NOx、SO2、CO、CO2、CH4、NMHC、PM、BC排放量,并给出了分省区、分生物质类型的排放清单.研究表明,2007年中国生物质燃烧排放的NOx、SO2、CO、CO2、CH4、NMHC、PM和BC排放量分别为109万t,1...     

哈尔滨市道路机动车尾气排放清单及特征分析研究

通过对哈尔滨市道路机动车信息的调研,完成了2016年哈尔滨市道路机动车尾气排放清单的建立,同时分析了研究区域内机动车尾气的排放特征。结果表明,2016年哈尔滨市道路机动车尾气CO、NOx、HC、PM2.5、PM10排放总量分别约为76 569.55、10 763.78、35 014.53、1 106.04、1 228.39吨。其中,小型载客汽车是CO、HC的主要贡献源,而载货汽车是NOx、PM2.5、PM10的主要贡献源;就燃料类型而言,汽油是CO、HC的主要贡献源,而NOx、PM2.5及PM10的主要贡献源是柴油。     

水泥工业NOX减排目标及实现途径简

目前我国水泥工业的氮氧化物（NOx）的排放量已占到了我国NOx排放总量的10％。NOx能直接损害人类的肺部导致呼吸系统疾病,NOx污染物的排放会引起光化学烟雾和酸雨等环境污染问题。作为NOx的排放大户,水泥工业的NOx减排已日趋受到关注与重视。笔者就结合我国现行的相关法律政策阐述了水泥工业NOx的减排目标。并从低氮燃烧技术和烟气脱硝技术两个方面分析了水泥工业NOx减排的可行途径。     

中国机动车污染物排放因子及其修正方法研究

中国机动车污染物排放已成为影响空气质量的重要源。机动车污染的研究中,排放因子的确定是关键。根据机动车使用状况,车用燃料硫含量和行驶状况,运用MOBILE6．2的方法和原理确定了中国各类型机动车HC、CO、NOx的综合排放因子。小型汽油客车国0阶段CO、HC、NOx的综合排放因子分别为34．29g／km、3．45g／km和0．856g／km;国Ⅰ阶段CO、HC、NOx的综合排放因子分别为2．80g／km、0．25g/km和0．40g／km;国Ⅱ阶段CO、HC、NOx的综合排放因子分别为1．39g／km、0．16g／km和0．09g／km。     

运用CMEM模型计算北京市机动车排放因子

采用由美国加州大学Riverside分校开发的综合模式排放模型(CMEM)分析和研究北京市机动车污染物的排放特征,以9辆代表北京市典型技术类型的轻型机动车为实验车辆,收集了运行CMEM模型所需要的数据和参数.通过CMEM模型Access 2.02版本计算,得到了在不同交通行驶状况下北京市4类典型轻型机动车的CO2,CO,HC,NOx单车排放因子及各车型综合排放因子.通过与同一车辆的在路实测排放因子比较发现,用CMEM模型计算的CO,HC和NOx与实测排放因子及排放特征有较好的一致性,因此适用于计算北京市机动车CO,HC和NOx排放因子.      

Distribution and ecological effect of mercury in Laogang landfill, Shanghai, China

Laogang landfill near Shanghai is the largest landfill in China, and receives about 10000 t of daily garbage per day, Samples of topsoil and plants were analyzed to evaluate mercury pollution from the landfill. For topsoil samples, there were significant correlations among total mercury （HgT）, combinative mercury （Hgc） and gaseous mercury （HgG）, and content of total organic carbon （TOC）, but, no significantly relationship was found between Hg content and filling time. Hg content changes in vertical profiles with time showed that the average Hgv of profiles 1992, 1996, and 2000 was similar, but their average HgG was quite different. HgT was significantly correlated with Hgc in profile 1992 and 2000, and Hgv was significantly correlated with Hg6 in profile 1996. HgG/Hgv ratio in profile samples decreased in the order of （HgG,/HgT）1992〉（HgG/HgT）1996〉〉（HgG/HgT）2000. A simple outline of Hg release in landfill could be drawn： with increasing of filling time, degradation undergoes different biodegradation, accordingly, gaseous mercury goes through small, more, and small proportion to total mercury. Distribution of Hg in plants was inhomogeneous, following the order of leaf〉root〉stem. The highest value of leaf may be associated with higher atmospheric Hg from landfill. Ligneous plants （e.g. Phyllostachys glanca, Prunus salicina and Ligustrum lucidum） are capable of enriching more Hg than herbaceous plants.     

EDTA-enhanced phytoremediation of lead contaminated soil by Bidens maximowicziana

Phytoremediation is a potential cleanup technology for the removal of heavy metals from contaminated soils.Bidens maximowicziana is a new Pb hyperaccumulator,which not only has remarkable tolerance to Pb but also extraordinary accumulation capacity for Pb.The maximum Pb concentration was 1509.3 mg/kg in roots and 2164.7 mg/kg in overground tissues.The Pb distribution order in the B. maximowicziana was:leaf>stem>root.The effect of amendments on phytoremediation was also studied.The mobility of soil Pb and the Pb concentrations in plants were both increased by EDTA application.Compared with CK(control check),EDTA application promoted translocation of Pb to overground parts of the plant.The Pb concentrations in overground parts of plants was increased from 24.23-680.56 mg/kg to 29.07-1905.57 mg/kg.This research demonstrated that B.maximowicziana appeared to be suitable for phytoremediation of Pb contaminated soil,especially,combination with EDTA.     

Decomposition of alachlor by ozonation and its mechanism

Decomposition and corresponding mechanism of alachlor, an endocrine disruptor in water by ozonation were investigated. Results showed that alachlor could not be completely mineralized by ozone alone. Many intermediates and final products were formed during the process, including aromatic compounds, aliphatic carboxylic acids, and inorganic ions. In evoluting these products, some of them with weak polarity were qualitatively identified by GC-MS. The information of inorganic ions suggested that the dechlorination was the first and the fastest step in the ozonation of alachlor.     

Enzymatic oxidation of aqueous pentachlorophenol

The influence of the nonionic surfactant Tween 80 on pentachlorophenol （PCP） oxidation catalyzed by horseradish peroxidase was studied. The surfactant was tested at concentrations below and above its critical micelle concentration （CMC）. Enhancement of PCP removal was observed at sub-CMCs. The presence of Tween 80 in the reaction mixture reduced enzyme inactivation which occurred through a combination of free radical attack and sorption by precipitated products. A simple first-order model was able to simulate time profiles for enzyme inactivation in the presence or absence of Tween 80. At supra-CMCs, the surfactant caused noticeable reductions in PCP removal, presumably through micelle partitioning of PCP which precluded the hydrophobic PCP molecule from interacting with the enzyme.     

基于综合水质标识指数和对应分析法的校园河道水质评价

以三峡大学的校园河道求索溪为研究对象,利用综合水质标识指数法确定求索溪水质类别,分析其水质时空变化规律,并利用对应分析法得出求索溪中不同监测点的主要污染因子.研究结果表明:求索溪整体的综合水质标识指数为7.423,整体水质为劣V类(地表水环境质量标准GB 3838-2002)且黑臭.从时间变化来看,求索溪4月份的水质最差,5月份次之,4、5月份所有监测点的水质都劣于V类且黑臭;8月份水质最好,水质为Ⅳ类;从空间分布来看,8个监测点综合水质标识指数均超过6.0,水质为劣V类,其中6号监测点的水质相对最好,监测点3号的水质相对最差;对应分析法得出求索溪的整体水体污染程度受总氮因子的影响最大,其次为总磷.该研究拟为求索溪及类似校园河道的水环境治理研究提供基础依据和参考.     

Effects of chitosan on growth of an aquatic plant (Hydrilla verticillata) in polluted waters with different chemical oxygen demands

Effects of chitosan on a submersed plant, Hydrilla verticillata, were investigated. Results indicated that H. venicillata could prevent ultrastructure phytotoxicities and oxidativereaction from polluted water with high chemical oxygen demand (COD). Superoxide dismutase (SOD) activity and malondialdehyde (MDA) contents in H. verticillata treated with 0.1% chitosan in wastewater increased with high COD (980 mg/L) and decreased with low COD (63 mg/L), respectively. Ultrastructural analysis showed that the stroma and grana of chloroplast basically remained normal. However, plant cells from the control experiment (untreated with chitosan) were vacuolated and the cell interval increased. The relict of protoplast moved to the center, with cells tending to disjoint. Our findings indicate that wastewater with high COD concentration can cause a substantial damage to submersed plant, nevertheless, chitosan probably could alleviate the membrane lipid peroxidization and ultrastructure phytotoxicities, and protect plant cells from stress of high COD concentration polluted water.     

Removal of cadmium using MnO2 loaded D301 resin

MnO2 loaded weak basic anion exchange resin D301 （Anion exchange resin, macroreticular weak basic styrene） as adsorbent has been prepared and applied to the removal of cadmium. The adsorption characteristics have been investigated with respect to effect of pH, equilibrium isotherms, removal kinetic data, and interference of the coexisting ions. The results indicated that the Cd^2＋ could be efficiently removed using MnO2 loaded D301 resin in the pH range of 3-8 from aqueous solutions with the co-existence of high concentration of alkali and alkaline-earth metals ions. The saturate adsorption capacity of the Cd^2＋ was 77.88 mg/g. The adsorption process followed the pseudo first-order kinetics. The equilibrium data obtained in this study accorded excellently with the Langmuir adsorption isotherm.     

Effect of coagulation pretreatment on the fouling of ultrafiltration membrane

The purpose of this study is to understand the effect and mechanism of preventing membrane fouling, by coagulation pretreatment, in terms of fractional component and molecular weight of natural organic matter （NOM）. A relatively higher molecular weight （MW） of hydrophobic compounds was responsible for a rapid decline in the ultrafiltration flux. Coagulation could effectively remove the hydrophobic organics, resulting in the increase of flux. It was found that a lower MW of neutral hydrophilic compounds, which could remove inadequately by coagulation, was responsible for the slow declining flux. The fluxes in the filtration of coagulated water and supernatant water were compared and the results showed that a lower MW of neutral hydrophilic compounds remained in the supernatant water after coagulation could be rejected by a membrane, resulting in fouling. It was also found that the coagulated flocs could absorb neutral hydrophilic compounds effectively. Therefore, with the coagulated flocs formed on the membrane surface, the flux decline could be improved.     

Penetration analysis of elements and bioleaching treatment of spent refractory for recycling

Acidithiobacillus ferrooxidans ATCC23270 and Acidithiobacillus thiooxidans TM-32 were used for bioleaching of spent refractories of aluminium and copper melting furnaces for their recycling.Firstly,penetration of elements into aluminium melting furnace refractory was investigated and it was found that up to 7 cm from surface was contaminated.Comparison on leaching efficiency by the strains ATCC23270 and TM-32 found that the strain ATCC23270 could treat larger amount of the refractories than the strain TM-32 could do.In the experiment of bioleaching of spent refractory aluminium melting furnace by the strain ATCC23270,high leaching efficiency were obtained on Al,Si,and Ca,and extremely low leaching performance was,however,shown on the rest of elements i.e.,Na,Mn,and Zn.Under the strain TM-32 use,relatively high leaching performance was recognized on Al,Si,Ca,Na,Mn,and Zn.In the experiment of bioleaching for spent refractory copper melting furnace,almost the same leaching trends were shown on Cu,Zn,Al,and Si under the strains ACTT23270 and TM-32 uses.     

Simultaneous removal of ammonium and phosphate by zeolite synthesized from coal fly ash as influenced by acid treatment

Zeolite synthesized from fly ash （ZFA） without modification is not efficient for the purification of NH4＋ and phosphate at low concentrations that occur in real effluents, despite the high potential removal capacity. To develop an effective technique to enhance the removal efficiency of ammonium and phosphate at low concentrations, ZFA was modified with acid treatment and the simultaneous removal of ammonium and phosphate in a wide range of concentration was investigated. It was seen that when compared with untreated ZFA, only the treatment by 0.01 mol/L of H2SO4 significantly improved the removal efficiency of ammonium at low initial concentrations. The behavior was well explained by the pH effect. Treatment by more concentrated H2SO4 led to the deterioration of the ZFA structure and a decrease in the cation exchange capacity. Treatment by 0.01 mol/L H2SO4 improved the removal efficiency of phosphate by ZFA at all initial P concentrations, while the treatment by concentrated H2SO4 （≥0.9 mol/L） resulted in a limited maximum phosphate immobilization capacity （PIC）. It was concluded that through a previous mild acid treatment （e.g. 0.01 mol/L of H2SO4）, ZFA can be used in the simultaneous removal of NH4＋ and P at low concentrations simulating real effluent.