2007年中国大陆地区生物质燃烧排放污染物清单

采用排放因子法计算了中国2007年间CH4、SO2、NOx、NH3、EC、OC、NMVOC、CO、CO2、TSP、PM10、PM2.5的排放总量,建立了生物质燃烧污染物排放清单,计算了各污染物总排放量的空间分布及不同生物质燃烧类型对各污染物总排放量的贡献率,重点完善了各省市生物质燃烧排放不同粒径颗粒物清单.结果显示,2007年我国大陆生物质燃烧排放CH4、SO2、NOx、NH3、OC、EC、NMVOC、CO、CO2、TSP、PM10、PM2.5排放总量分别分为3332.7, 335.3, 951.3, 7754.9, 783.7, 267.7, 6049.6, 76579.6, 743743.7, 7677.8, 6668.9, 4043.7kt.四川、安徽、广西、山东、河南、江苏等地区生物质燃烧各污染物排放量较高,北京、天津、海南、宁夏、青海和西藏等省区各污染物排放量较少.不同地区排放污染物的主要生物质类型存在较大的差异,单位面积排放强度和人均排放量区域间差异显著.人类活动是生物质燃烧排放污染物的主要影响因素,秸秆和薪柴燃烧是污染物排放量最大的2种生物质,其对各种污染物的贡献率为93.8%~98.7%.     

贵州省生物质燃烧源大气污染物排放清单

为准确掌握贵州省生物质燃烧源大气污染物的排放状况,基于收集资料和实地调查结合的方式获取活动水平,引用文献和本地实测数据结合的方式选取排放系数,采用排放系数法结合GIS技术,建立了贵州省2019年3 km×3 km生物质燃烧源9种大气污染物排放清单.结果表明：(1)全省生物质燃烧源CO、 NO_x、 SO₂、 NH₃、 VOCs、 PM_2.5、 PM₁₀、 BC和OC的排放量分别为：293 505.53、 14 781.19、 4 146.11、 8 501.07、 45 025.70、 39 463.58、 41 879.31、 6 832.33和15 134.74 t.户用生物质炉具CO、 SO₂、 NH₃和BC的排放量贡献率最大,秸秆露天焚烧NO_x、 VOCs、 PM_2.5、 PM₁₀和OC的排放量贡献率最大.(2)各市(州)生物质燃烧源排放的大气污染物分布不均衡,主...     

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...     

西宁市生物质燃烧源大气污染物排放清单

本研究根据调查的西宁市生物质燃烧源活动水平数据,采用排放因子方法,建立了 2018年西宁市生物质燃烧源9种大气污染物的排放清单,并分析了清单的时空分布特征和不确定性.结果表明,西宁市2018年生物质燃烧源CO、NOx、SO2、NH3、VOCs、PM2.5、PM10、BC 和OC 的排放量分别为 11 718.34、604.41、167.80、209.72、1 617.97、2 054.04、2 135.04、281.07和 1 224.78 t.秸秆露天焚烧 CO、NOx、VOCs、PM2.5、PM10、BC 和OC 的排放对生物质燃烧源的排放贡献率最高;其中,秸秆露天焚烧NOx、VOCs和CO的贡献率分别为72.35％、63.94％和53.18％.户用生物质炉NH3和SO2的排放对生物质燃烧源的贡献率最大,分别为41.49％和42.05％.生物质燃烧源大气污染物排放地区分布不均衡,主要集中于大通县和湟中区.生物质燃烧源9项污染物的排放量在1、2、3、10、11和12月较大,占比在5％～33％.蒙特卡罗模拟结果表明,在95％置信区间下,不确定度最高的是森林和草原火灾的PM2.5排放,不确定度为-26.71％～29.78％.     

京津冀地区散煤燃烧大气污染物排放清单

为研究京津冀地区民用散煤燃烧大气污染物的排放情况，结合散煤燃烧活动水平与燃用特征，根据排放因子法自下而上建立了2018年京津冀地区民用散煤燃烧污染物排放清单，研究了污染物排放的时空分布特征并使用蒙特卡罗方法对排放清单进行了不确定性分析.结果表明：2018年京津冀地区民用散煤燃烧量共计3799.22万t，PM_2.5、CO、SO₂、NO_x的排放量分别为9.27，341.31，5.17，5.44万t.污染物排放集中在11月份~次年3月份，大多数地区呈现出相同的日排放趋势.8：00、11：00、18：00、21：00左右出现污染物排放峰值，小时排放系数平均值分别为11%，6%，7%，13%.PM_2.5排放高值区主要集中在北部、东部及部分南部地区，CO主要集中在北京和天津地区，SO₂和NO_x主要集中在天津和承德地区.     

南方林区2000~2016年林火释放污染物动态变化研究

以南方林区为研究区域,基于林业统计年鉴和MODIS卫星火点数据,结合相关文献中不同林型各类污染物的排放因子数据,估算2000~2016年间研究区域各省森林生物质燃烧及污染物排放总量,并分析其时空变化情况.结果表明,南方林区森林火灾总体呈先升后降的趋势,林火空间分布较为分散.2000~2016年南方林区森林生物质燃烧总量4.79×10⁴kt.其中,温带常绿针叶林、温带常绿阔叶林、温带落叶阔叶林、热带常绿阔叶林和灌木的燃烧比例分别为65.24%,17.45%,1.55%,1.10%和14.66%.CO、CO₂、NO_x、CH₄、VOCs和PM_2.5等主要污染物的排放总量均值依次为3.73×10³,5.87×10⁴,48.05,347.27,358.54和365.06kt.此外,各类污染物的时空分布差异性明显：福建、广东、广西全省,海南西部,以及江西和湖南南部是各类污染物网格排放高值区;江西和湖北各类污染物的排放呈显著下降,福建NO_x、VOCs和PM_2.5,以及广东CH₄和VOCs下降趋势显著,其余省份各类污染物排放下降但不显著.林火释放污染物占工业粉尘比例呈波动性上升,表明该地区森林火灾对大气环境的影响程度逐渐增加.     

中美贸易间隐含的大气污染物排放估算

随着中国能源消耗和国际贸易的快速增长,中国国际贸易尤其是中美贸易对气候变化的影响受到了广泛关注,但国际贸易对于大气污染的影响却鲜见系统研究. 基于环境投入产出法和结构分解分析法,采用基于技术的、自下而上的大气污染物排放清单,探讨了中美贸易隐含的大气污染物排放问题. 结果表明:由于中国对美国出口贸易顺差较大且商品污染物排放强度较高,造成了中国对美国的出口贸易隐含着较大的污染物排放逆差. 2007年中国对美国出口贸易隐含的SO₂、NO_x和PM_2.5的排放逆差分别为174.26×104、131.15×104和46.88×104t. 有行业针对性的污染物减排措施可以降低中美贸易隐含的污染物排放量;1997—2007年污染物燃烧排放因子和非燃烧直接排放强度的下降就可使出口贸易隐含的SO₂和PM_2.5排放量降低96.41%和226.26%. 占出口份额最高的机械类制造品的SO₂、NO_x和PM_2.5排放强度分别为72.63、58.38和20.74t/108元,低于所有出口商品的污染物排放强度的平均值, 中国应加强这种高附加值、低污染物排放的商品出口.      

我国人为源CO排放量的估算研究

根据中国人为源(包括固定燃烧源、工业过程源、移动源和生物质燃烧源)的活动水平数据和相应的排放因子,对中国2000-2012年的CO排放量进行了估算。研究表明:2000-2012年,中国人为源CO排放总量呈现持续增长的趋势,年均增长率为3.53%,其中工业过程源是其主要排放源,2012年其排放量占总排放量的42%左右;固定燃烧源、工业过程源、移动源和生物质燃烧源排放的主要来源分别为工业部门、钢铁行业、道路移动源和室内秸秆燃烧;CO排放量在地区间的分布极不平衡,2012年排放量最高的5个省份依次是河北、山东、江苏、河南和辽宁;排放强度较大的地区主要集中在环渤海经济圈和长三角地区,其中又以上海、天津2个直辖市的排放强度最大。     

生物质锅炉与燃煤锅炉颗粒物排放特征比较

选择2台设计结构不同的生物质锅炉(BB1、BB2),针对木质和秸秆2种生物质燃料开展烟尘、PM₁₀和PM_2.5排放特征的研究,并与燃煤锅炉进行比较. 结果表明:2台生物质锅炉的大气污染物排放质量浓度都未达到北京市DB 11/139—2007《锅炉大气污染物排放标准》的要求;2台生物质锅炉颗粒物的排放因子存在差别,燃烧木质成型燃料时,BB1和BB2生物质锅炉除尘器后的烟尘排放因子分别为207.10和465.51mg/kg,PM₁₀排放因子分别为75.18和149.61mg/kg, PM_2.5排放因子分别为58.48和106.86mg/kg;燃烧秸秆成型燃料时,BB1和BB2生物质锅炉除尘器后的烟尘排放因子分别为142.86和1200.86mg/kg,PM₁₀排放因子分别为63.63和102.01mg/kg,PM_2.5的排放因子分别为50.90和76.51mg/kg. 与热功率相近的燃煤锅炉比较,2台生物质锅炉除尘器前的PM₁₀平均排放因子低30.41%,PM_2.5平均排放因子却高36.84%,即PM_2.5在生物质锅炉烟尘中所占比例更高. 尽管利用可再生能源的生物质锅炉具有很好的发展前景,但目前该类锅炉仍存在污染物排放不达标的现象,因此,需要提高热能利用效率和除尘效率,以减少污染.      

焚烧麦杆对稻田CH4 和N2O 排放的影响

采用3 种麦杆处理方式(不还田、均匀混施和原位焚烧)进行田间试验,观测稻田CH₄ 和N₂O 的排放情况,以探讨原位焚烧麦杆对稻田CH₄ 和N₂O 排放的影响.结果表明,与不还田处理相比,原位焚烧显著增加稻田CH₄ 排放量,同时显著减少稻田N₂O 排放量;与均匀混施处理相比,原位焚烧显著减少稻田CH₄ 排放量,二者的N₂O 排放量无明显差异.     

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.