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％.     

海峡西岸经济区大气污染物排放清单的初步估算

以2009年为基准年,结合污染源普查数据、统计年鉴及工业活动、居民生活等多个方面对海峡西岸经济区包括SO2、NOx、PM2.5、VOCs和NH3在内的大气污染物的排放量进行了估算,建立了海西区大气污染物排放清单.结果发现,上述5类污染物基准年的排放量分别为40.67×104、55.84×104、50.57×104、152.26×104和26.18×104t.其中,SO2、NOx及PM2.5的排放主要来自电厂,占排放总量的比例分别为25.58%、34.89%和38.75%;VOCs和NH3的主要排放源分别来自植被排放和养殖业,其贡献量分别为49.12%和47.07%.采用GIS对排放清单进行网格化处理,得出SO2、NOx及PM2.5的高排放强度区域与固定源的空间分布较为一致.此外,结合国家和地方"十二五"发展规划,采用情景分析方法估算了2015年海西区大气污染物的排放清单.与基准年相比,SO2、NOx和NH3的排放量呈下降趋势,PM2.5和VOCs的排放量呈大幅度增加.基准年排放清单的不确定性分析显示,VOCs排放估算的不确定度最大,为225%.     

天津市大气污染源排放清单的建立

通过调研天津市工、农业生产和居民生活的统计资料,研究分析文献报道的各种污染源排放因子,计算出天津市各行业、各区县NOx、SO2、NMVOC、CO、NH3、PM10、PM2.5等污染物的排放量,发展了天津市2003年排放源清单.结果显示,天津市2003年各类污染物质的排放量NOx为1.77×105t,SO2为2.59 ×105t,NMVOC为2.24×105t,CO为1.33×106t,NH3为7.40×104t,PM10为2.52×105t,PM2.5为1.10×105t.从排放源的行业分布来看,燃煤源、汽车移动源、秸秆燃烧源是天津市大气污染物的重要排放源,燃煤源对各污染物的贡献分别为NOx46%,SO284%,NMVOC 1%,CO 58%,PM1018%,PM2.5 24%.火电、水泥、钢铁、炼焦、原油加工等行业依然是重要的工业污染排放源,火电对SO2的贡献为13%,钢铁对SO2的贡献为24%,对CO的贡献为30%.2003年天津市区对NO,、S02、NMVOC、CO等污染物的贡献均高于其它区县,对PM10、PM2.5的贡献也很高;塘沽区对NOx、SO2、NMVOC、CO等污染物的贡献很大,蓟县、武清区、宝坻区对NH3、PM10、PM2.5的贡献很大.     

海峡西岸地区人为源大气污染物排放特征研究

采用以"自下而上"为主的方法建立了2007年海峡西岸地区的人为源大气污染物排放清单.计算结果显示,海西地区人为源SO2、NOx、CO、PM10、PM2.5、VOCs和NH3排放总量分别为69.5×104、96.1×104、413.1×104、93.9×104、40.6×104、85.0×104和28.5×104t.电厂和工业燃烧设施分别占SO2排放的48%和39%,以及NOx排放的51%和25%.水泥、砖瓦等制造过程贡献了约51%的PM10排放和36%的PM2.5排放.秸秆燃烧、加油站和涂料等VOCs面源分别占到其排放总量的27%、15%和4%.NH3的主要排放源为畜禽养殖和氮肥施用等农业部门,占到总排放量的89%.海西地区的单位面积大气污染物排放量仅相当于长三角地区的25%左右,略高于全国平均水平.该地区人为源和天然源VOCs排放比重分别占56%和44%,人为源VOCs排放比重低于全国大部分地区.海西大气污染高排放地区主要集中在沿海一带,以泉州、潮汕、福州和温州等地区为主,建议"十二五"发展过程中,重点关注上述高排放地区,限制重点排放源的发展,开发低耗能、低污染的发展模式.     

长江三角洲地区人为源大气污染物排放特征研究

在收集整理长江三角洲地区（简称＂长三角＂）各城市人为大气污染源资料的基础上,采用以＂自下而上＂为主的方法建立了2007年长三角地区人为源大气污染物排放清单.清单结果显示,2007年长三角地区的SO2、NOx、CO、PM10、PM2.5、VOCs和NH3等大气污染物排放总量分别达到2391.8、2292.9、6697.1...     

珠江三角洲大气排放源清单与时空分配模型建立

收集整理2012年珠江三角洲地区(简称“珠江三角洲”)各种大气人为源及天然源基础活动数据,以排放因子法“自下而上”为主计算多污染物排放量,并建立本地化污染物空间分配方案及基于行业排污特征的时间分配谱,构建了具备时空分布属性的区域性网格化大气源排放清单.清单结果显示,2012年珠江三角洲SO2、NOx、CO、PM10、PM2.5、VOCs和NH3排放总量分别为55.2万t、102.9万t、349.2万t、95.2万t、38.5万t、153.9万t和17.7万t. 固定燃烧源是珠江三角洲SO2和NOx的最大排放贡献源,其中电厂和锅炉分别贡献了35.0%和41.8%的SO2排放,以及28.2%和16.2%的NOx排放;VOCs的最大贡献源是过程源,其中家具制造、石油精炼、油气码头排放量总和占比为52.4%;扬尘源是颗粒物的主要来源之一,对PM2.5的排放贡献达42.3%;NH3的主要排放源为畜禽养殖和化肥施用源,两者排放量占比分别为50.7%和26.8%.珠江三角洲大气污染物空间与时间分布结果显示,高排放污染源主要集中于“东莞-广州-佛山”一带,呈半环带状结构分布;白天时段(9:00~20:00)的排放强度明显高于夜晚时段(21:00~次日8:00);夏秋季节(4~10月)的排放强度略高于冬春季节(11月~次年3月).     

长沙市人为源大气污染物排放清单及特征研究

根据收集的长沙市人为源活动水平数据,建立了该地区2014年1 km×1 km人为源大气污染物排放清单.结果显示,2014年长沙市SO_2、NO_x、CO、PM_(10)、PM_(2.5)、BC、OC、VOCs和NH_3排放总量分别为53.5×10~3、78.3×10~3、284.6×10~3、102.3×10~3、42.1×10~3、4.0×10~3、7.2×10~3、64.2×10~3、27.1×10~3t.化石燃料固定燃烧源为最大的SO_2排放贡献源,道路移动源是主要的NO_x贡献源,CO排放主要来自化石燃料固定燃烧源和道路移动源,长沙市VOCs的最大贡献源是溶剂使用源,PM_(10)、PM_(2.5)最主要的排放源是扬尘源,BC最大的排放贡献源为化石燃料固定燃烧源,生物质燃烧源是最大的OC贡献源,NH_3排放主要来源于畜禽养殖和农业施肥.空间分布结果显示,长沙市NH_3的排放在宁乡县、望城区、长沙县、浏阳市分布较多,主要呈现片状分布.其他污染物排放高值区则主要分布在中心城区、工业区及道路分布区域.     

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%.     

沈阳市人为源大气污染物排放清单研究

为全面评估沈阳市大气污染物排放状况，文章收集和整理了相关活动水平信息和排放因子数据并采用排放因子法建立了2016年沈阳市人为源大气污染物排放清单。结果显示：2016年沈阳市人为源CO、NO_x、SO₂、NH₃、VOCs、PM2.5、PM10、BC和OC的排放总量分别为38.64×10⁴、10.63×10⁴、3.17×10⁴、5.28×10⁴、14.03×10⁴、5.54×10⁴、10.59×10⁴、0.57×10⁴和1.82×10⁴ t。按照排放源分类，CO、NO_x和BC主要来自移动源，SO₂主要来自化石燃料固定燃烧源，NH₃主要来自农业源，VOCs主要来自工艺过程源，PM_2.5和PM₁₀主要来自扬尘源，OC主要来自其他...     

广东省人为源BC、OC排放清单建立与校验

根据收集的人为源活动水平数据和最新的排放因子,采用"自下而上"和"自上而下"相结合的排放因子法建立了广东省2012年人为源BC、OC排放清单.结果显示,2012年广东省人为源BC、OC排放量分别为53.5×103、78.8×103t.BC排放主要来自道路移动源和生物质燃烧源,贡献率分别为30.1%和29.4%,生物质燃烧源和餐饮源是主要的OC排放贡献源,贡献率分别为48.5%和16.9%.建立的BC、OC排放源清单仍然具有较大的不确定性,分别为-66%~154%和-63%~126%.其中,道路移动源和生物质燃烧源是主要的不确定贡献源,餐饮源和扬尘源次之,不确定性主要来自由质量分数间接得到的BC和OC排放因子.最后,采用清单结果横向比较法和基于环境监测浓度结果对比法2种方法对本研究的结果进行了校验,结果表明,本研究清单结果基本合理.建议统一不同排放源成分谱的建立方法,加强排放源颗粒物测试,并重视清单结果校验的研究以降低不确定性,从而改进BC、OC排放源清单.     

Toxic effects of acetochlor, methamidophos and their combination on nifH gene in soil

Toxic effects of two agrochemicals on nifH gene in agricultural black soil were investigated using denaturing gradient gel electrophoresis （DGGE） and sequencing approaches in a microcosm experiment. Changes of soil nifH gene diversity and composition were examined following the application of acetochlor, methamidophos and their combination. Acetochlor reduced the nifH gene diversity （both in gene richness and diversity index values） and caused changes in the nifH gene composition. The effects of acetochlor on nifH gene were strengthened as the concentration of acetochlor increased. Cluster analysis of DGGE banding patterns showed that nifH gene composition which had been affected by low concentration of acetochlor （50 mg/kg） recovered firstly. Methamidophos reduced nifH gene richness that except at 4 weeks. The medium concentration of methamidophos （150 mg/kg） caused the most apparent changes in nifH gene diversity at the first week while the high concentration of methamidophos （250 mg/kg） produced prominent effects on nifH gene diversity in the following weeks. Cluster analysis showed that minimal changes of nifH gene composition were found at 1 week and maximal changes at 4 weeks. Toxic effects of acetochlor and methamidophos combination on nifH gene were also apparent. Different nifH genes （bands） responded differently to the impact of agrochemicals： four individual bands were eliminated by the application of the agrochemicals, five bands became predominant by the stimulation of the agrochemicals, and four bands showed strong resistance to the influence of the agrochemicals. Fifteen prominent bands were partially sequenced, yielding 15 different nifH sequences, which were used for phylogenetic reconstructions. All sequences were affiliated with the alpha- and beta-proteobacteria, showing higher similarity to eight different diazotrophic genera.     

Arsenic uptake by arbuscular mycorrhizal maize （Zea mays L.） grown in an arsenic-contaminated soil with added phosphorus

The effects of arbuscular mycorrhizal (AM) fungus (Glomus mosseae) and phosphorus (P) addition (100 mg/kg soil) on arsenic (As) uptake by maize plants (Zea mays L.) from an As-contaminated soil were examined in a glasshouse experiment.Non-mycorrhizal and zero-P addition controls were included.Plant biomass and concentrations and uptake of As,P,and other nutrients,AM colonization,root lengths,and hyphal length densities were determined.The results indicated that addition of P significantly inhibited root colonization and development of extraradical mycelium.Root length and dry weight both increased markedly with mycorrhizal colonization under the zero-P treatments,but shoot and root biomass of AM plants was depressed by P application.AM fungal inoculation decreased shoot As concentrations when no P was added,and shoot and root As concentrations of AM plants increased 2.6 and 1.4 times with P addition,respectively.Shoot and root uptake of P,Mn,Cu,and Zn increased,but shoot Fe uptake decreased by 44.6%,with inoculation, when P was added.P addition reduced shoot P,Fe,Mn,Cu,and Zn uptake of AM plants,but increased root Fe and Mn uptake of the nonmycorrhizal ones.AM colonization therefore appeared to enhance plant tolerance to As in low P soil,and have some potential for the phytostabilization of As-contaminated soil,however,P application may introduce additional environmental risk by increasing soil As mobility.     

Potential of plant polyphenol oxidases in the decolorization and removal of textile and non-textile dyes

In this study an effort has been made to use plant polyphenol oxidases; potato （Solanum tuberosum） and brinjal （Solanum melongena）, for the treatment of various important dyes used in textile and other industries. The ammonium sulphate fractionated enzyme preparations were used to treat a number of dyes under various experimental conditions. Majority of the treated dyes were maximally decolorized at pH 3.0. Some of the dyes were quickly decolorized whereas others were marginally decolorized. The initial first hour was sufficient for the maximum decolorization of dyes. The rate of decolorization was quite slow on long treatment of dyes. Enhancement in the dye decolorization was noticed on increasing the concentration of enzymes. The complex mixtures of dyes were treated with both preparations of polyphenol oxidases in the buffers of varying pH values. Potato polyphenol oxidase was significantly more effective in decolorizing the dyes to higher extent as compared to the enzyme obtained from brinjal polyphenol oxidase. Decolorization of dyes and their mixtures, followed by the formation of an insoluble precipitate, which could be easily removed simply by centrifugation.     

Removal of heavy metals from sewage sludge by low costing chemical method and recycling in agriculture

ＲｅｍｏｖａｌｏｆｈｅａｖｙｍｅｔａｌｓｆｒｏｍｓｅｗａｇｅｓｌｕｄｇｅｂｙｌｏｗｃｏｓｔｉｎｇｃｈｅｍｉｃａｌｍｅｔｈｏｄａｎｄｒｅｃｙｃｌｉｎｇｉｎａｇｒｉｃｕｌｔｕｒｅＷｕＱｉｔａｎｇ，ＮｙｉｒａｎｄｅｇｅＰａｓｃａｓｉｅ，ＭｏＣｅｈｕｉＦ...     

Single and joint effects of pesticides and mercury on soil urease

The influence of two pesticides including chlorimuron-ethyl and furadan and mercury （Hg） on urease activity in 4 soils （meadow burozem and phaeozem） was investigated. The soils were exposed to various concentrations of the two pesticides and Hg individually and simultaneously. Results showed that there was a close relationship between urease activity and organic matter content in soil. Chlorimuron-ethyl and furadan could both activate urease in the 4 soils. The maximum increment of urease activity by chlorimuronethyl was up to 14%-18%. There was almost an equal increase （up to 13%-21%） in the urease activity by furadan. On the contrary, Hg markedly inhibited soil urease activity. A logarithmic equation was used to describe the relationship （P〈0.05） between the concentration of Hg and the activity of soil urease in the 4 tested soils. Semi-effect dose （ED50） values by the stress of Hg based on the inhibition of soil urease in the 4 soils were 88, 5.5, 24 and 20 mg/kg, respectively, according to the calculation of the corresponding equations. The interactive effect of chlorimuron-ethyl or furadan with metal Hg on soil urease was mainly synergic at the highest tested concentrations.     

Isolation and preliminary characterization of a 3-chlorobenzoate degrading bacteria

A study was conducted to compare the diversity of 2-, 3-, and 4-chlorobenzoate degraders in two pristine soils and one contaminated sewage sludge. These samples contained strikingly different populations of mono-chlorobenzoate degraders. Although fewer cultures were isolated in the uncontaminated soils than contaminated one, the ability of microbial populations to mineralize chlorobenzoate was widespread. The 3- and 4-chlorobenzoate degraders were more diverse than the 2-chlorobenzoate degraders. One of the strains isolated from the sewage sludge was obtained. Based on its phenotype, chemotaxonomic properties and 16S rRNA gene, the organism S-7 was classified as Rhodococcus erythropolis. The strain can grow at temperature from 4 to 37℃. It can utilize several （halo）aromatic compounds. Moreover, strain S-7 can grow and use 3-chlorobenzoate as sole carbon source in a temperatures range of 10-30℃ with stoichiometric release of chloride ions. The psychrotolerant ability was significant for bioremediation in low temperature regions. Catechol and chlorocatechol 1,2-dioxygenase activities were present in cell free extracts of the strain, but no （chloro）catechol 2,3- dioxygenase activities was detected. Spectral conversion assays with extracts from R. erythropolis S-7 showed accumulation of a compound with a similar UV spectrum as chloro-cis,cis-muconate from 3-chlorobenzoate. On the basis of these results, we proposed that S-7 degraded 3-chlorobenzoate through the modified ortho-cleave pathway.     

Organochlorine pesticides in soils under different land usage in the Taihu Lake region, China

A field study was conducted in the Taihu Lake region, China in 2004 to reveal the organochlorine pesticide concentrations in soils after the ban of these substances in the year 1983. Thirteen organochlorine pesticides (OCPs) were analyzed in soils from paddy field, tree land and fallow land. Total organochlorine pesticide residues were higher in agricultural soils than in uncultivated fallow land soils. Among all the pesticides, ΣDDX (DDD, DDE and DDT) had the highest concentration for all the soil samples, ranging from 3.10 ng/g to 166.55 ng/g with a mean value of 57.04 ng/g and followed by ΣHCH, ranging from 0.73 ng/g to 60.97 ng/g with a mean value of 24.06 ng/g. Dieldrin, endrin, HCB and α-endosulfan were also found in soils with less than 15 ng/g. Ratios of p,p'-(DDD DDE)/DDT in soils under three land usages were: paddy field ＞ tree land ＞ fallow land, indicating that land usage inlfuenced the degradation of DDT in soils. Ratios of p,p'-(DDD DDE)/DDT ＞1, showing aged residues of DDTs in soils of the Taihu Lake region. The results were discussed with data from a former study that showed very low actual concentrations of HCH and DDT in soils in the Taihu Lake region, but according to the chemical half-lives and their concentrations in soils in 1980s, the concentration of DDT in soils seemed to be underestimated. In any case our data show that the ban on the use of HCH and DDT resulted in a tremendous reduction of these pesticide residues in soils, but there are still high amounts of pesticide residues in soils, which need more remediation processes.     

Sorption of 1-naphthol by plant cuticular fractions

The contribution of aliphatic-rich plant biopolymer to sorption of hydrophobic organic compounds is significantly important because of their preservation and accumulation in the soil environment,but sorption mechanism is still not fully understood.In this study, sorption of 1-naphthol by plant cuticular fractions was examined to better understand the contributions of respective fraction.Toward this end,cuticular materials were isolated from the fruits of tomato by chemical method.The tomato cuticle sheet consisted of waxes (6.5 wt%),cuticular monomer (69.5 wt%),and polysaccharide (24.0 wt%).Isotherms of l-naphthol to the cuticular fractions were nonlinear (N value (0.82-0.90)) at the whole tested concentration ranges.The KodKow ratios for bulk cuticle (TC1),dewaxed cuticle (TC2),cutin (TC4),and desugared cuticle (TC5) were larger than unity,suggested that tomato bulk cuticle and cutin are much powerful solption medium.Sorption capability of cutin (TC4) was 2.4 times higher than the nonsaponifiable fraction (TC3).The 1-naphthol interactions with tomato cuticular materials were governed by both hydrophobic-type interactions and polar (H-bonding) interactions. Removal of the wax and polysaccharide materials from the bulk tomato cuticle caused a significant increase in the sorption ability of the cuticular material.There was a linear negative trend between K_(oc) values and the amount of polysaccharides or fraction's polarities ((N O)/C);while a linear positive relationship between K_(oc) values and the content of cutin monomer (linear R~2=0.993) was observed for present in the cuticular fractions.Predominant sorbent of the hydrophobic organic compounds (HOCs) in the plant cuticular fraction was the cutin monomer,contributing to 91.7% of the total sorption of tomato bulk cuticle.     

Alterations of organ histopathology and metallolhionein mRNA expression in silver barb, Puntius gonionotus during subchronic cadmium exposure

Common silver barb,Puntius gonionotus,exposed to the nominal concentration of 0.06 mg/L Cd for 60 d,were assessed for histopathological alterations(gills,liver and kidney),metal accumulation,and metallothionein(MT)mRNA expression.Fish exhibited pathological symptoms such as hypertrophy and hyperplasia of primary and secondary gill lamellae,vacuolization in hepatocytes,and prominent tubular and glomerular damage in the kidney.In addition,kidney accumulated the highest content of cadmium,more than gills and liver.Expression of MT mRNA was increased in both liver and kidney of treated fish.Hepatic MT levels remained high after fish were removed to Cd-free water.In contrast,MT expression in kidney was peaked after 28 d of treatment and drastically dropped when fish were removed to Cd-free water.The high concentrations of Cd in hepatic tissues indicated an accumulation site or permanent damage on this tissue.     

Seed selections for crystallization of calcium phosphate for phosphorus recovery

Seed induces and promotes the crystallization of calcium phosphate, and acts as carrier of the recovered phosphorus （P）. In order to select suitable seed for P recovery from wastewater, three seeds including Apatite （AP）, Juraperle （JP） and phosphate-modified Juraperle （M-JP） were tested and compared. Batch and fixed-bed column experiments of seeded crystallization of calcium phosphate were undertaken by using synthetic wastewater with 10 mg/L P phosphate. It shows that AP has bad enduring property in the crystallization process, while JP has better performance for multiple uses, and M-JP is a hopeful seed for P recovery by crystallization of calcium phosphate.