燃煤钙基固砷剂的影响因素研究

利用电石渣、CaCO3、CaCO3·Ca(OH)3和Ca(OH)2作为燃煤钙基固砷剂,通过正交试验研究了固砷剂种类、固砷剂用量、燃烧温度及煤粒径对固砷效果的影响.结果表明,燃烧温度是影响燃煤固砷的最显著因素,最佳为1 050℃;钙基固砷剂中CaCO3和电石渣的固砷效果最好,其次是CaCO3·Ca(OH) 2,Ca(OH) 2的固砷效果最差;钙基固砷剂用量按Ca、S摩尔比计量为2.0、煤粒径为160～200目时,钙基固砷剂具有较好的固砷效果,而且具有固砷固硫的双重作用.     

印染污泥与煤在循环流化床上混烧实验

印染污泥热值较低,直接燃烧较为困难,需要添加辅助燃料进行混燃.通过对印染污泥与煤在循环流化床中混烧实验研究,发现印染污泥着火特性较差,启动时需将炉温提升至800℃以上,加入的污泥才能进行燃烧;污泥与煤在循环流化床中可以实现充分燃烧,温度在800～900℃之间均匀稳定,燃烧效率超过95%;混烧工况下烟气SO2含量高,在炉...     

复合固硫剂对型煤固硫的影响研究

固硫型煤作为煤燃烧中脱硫的一种重要方法,在燃煤SO2的减排方面起着重要的作用。为了考察固硫剂和固硫添加剂对型煤固硫及其对型煤燃烧释放SO2的规律的影响,对利用氧化镁和氧化钙为固硫剂,以煤矸石和粉煤灰为固硫添加剂进行了研究,同时通过XRD和SEM表征,进一步探讨了固硫剂及添加剂的固硫作用和机理。研究结果表明：(1)CaO...     

广西城镇污泥掺烧利用组分特性的分析

对广西城镇污水处理厂污泥进行元素分析、组分分析、工业分析和热重分析,探讨污泥掺烧应用特性,为广西的污泥资源化利用提供数据。结果表明,污泥的元素组成与煤差别较大,如污泥中的氮元素含量为4.627%,高于煤的1.628%;污泥焚烧灰含有高达15%的Si O2;污泥的挥发分为34.6377%比煤的25.089%略高;污泥的焚烧可分为3个阶段,分别为水分析出阶段(室温~160℃)、挥发分析出燃烧阶段(160~500℃)、固定碳及剩余可燃物燃烧阶段(510~950℃),升温速率升高,挥发分析出阶段提前了约50℃,粒径对析出温度影响不大,但粒径小更利于干污泥燃烧。因此,广西污泥是一种低热值,燃烧剧烈的燃料,可以用于掺烧,焚烧灰分具有较高的建材价值。     

含化学沉淀物废水污泥的土壤降解

本文比较四种污泥在土壤中的降解,其中三种是脱磷污泥含有Ca(OH)_2、FeCl_3、Al_2(SO_4)_3。所有污泥降解速率很快,降解时释放的CO_2速率<25mg/g,接近于没有处理过的土壤15天的释放量,而较高速率时相当于50天的释放量。每种污泥中都含有生石灰,故每一种添加污泥都使土壤的pH值增加。使pH值升高最多的Ca污泥比Fe、Al、污泥增加和释放的CO_2量大。Ca污泥释放52％的污泥碳,未处理的含铝污泥释放20％,而Fe污泥释放量是5％,土壤加入CaCO_3,增加了Al污泥的降解,但就释放污泥碳的百分率而言,这些污泥之间没有明显的不同。这些污泥的降解作用与pH的关系要比除磷时流出物的化学处理的关系更密切。     

百色市右江区大气PM10中水溶性无机离子的化学特征与来源

2010年10月至2011年9月采集百色市右江区大气PM10样品,分析PM10及其水溶性无机离子的化学特征与来源。结果表明:(1)百色市右江区大气PM10为13.89～319.44μg/m3,年均117.48μg/m3,年均值超过《环境空气质量标准》(GB 3095-2012)二级标准(100μg/m3)。百色市右江区大气可吸入颗粒物的污染主要出现在春冬季节。(2)水溶性无机离子浓度年均值依次为SO24->NO3->Cl->NH4+>K+>Na+>Mg2+>F-,SO24-、NO3-和Cl-浓度最高,分别占水溶性无机离子的57.7%、14.9%和14.5%。(3)百色市右江区大气PM10呈较强的酸性,高浓度的SO42-可能是导致百色市右江区大气PM10呈较强酸性的主要原因。(4)PM10的季节变化受气温和风速的影响极显著;气象因素对SO42-、NO3-、F-的影响不显著。(5)主因子分析表明,PM10中水溶性无机离子可能来自3个方面,Cl-和NO3-主要来自于当地低烟卤煤燃烧排放的烟气;Mg2+、K+和Na+主要来自于自然源;F-、SO24-和NH4+主要来自于混合源。     

市政污泥与不同烟煤混合燃烧特性

使用非等温热重法,研究了淮北烟煤和神华烟煤在6种不同市政污泥掺混比条件下对混合燃烧特性的影响,并对混合燃烧过程的动力学特性进行了分析。实验结果表明:污泥与煤的混合燃烧特性从总体上表现为污泥与煤共同作用的结果,最优的污泥掺混比受到煤种的影响。在不同煤中污泥掺烧比少于20%对煤的活性影响较小。活化性能较差的淮北烟煤在污泥掺混比为30%时,在不同的温度区间分别表现出污泥与煤的反应特征。活化性能较好的神华烟煤在污泥掺混比为40%时表现这一趋势。     

鼓泡反应器中液相络合催化同时脱硫脱硝的研究

在鼓泡反应器中考察了[Co(en)3]2+同时吸收去除SO2和NO的影响因素,实验结果表明,pH值和脱硫剂种类是影响乙二胺合钴同时脱除NO和SO2的最重要影响因素,烟气中的氧促进乙二胺合钴吸收NO和SO2,烟气中的SO2,CO2和NO2对乙二胺合钴吸收NO具有抑制作用。在实验条件温度为20℃,pH为13.0,[Co(en)3]2+浓度为0.025 mol/L,加入1 g NH3.H2O的脱硝率更好,连续吸收60 min,脱硝率均保持在93.5%,加入NaOH和NH3.H2O的脱硫效果最好。乙二胺合钴络合同时脱除NO和SO2完全可以在一个装置中完成。     

生活污泥与煤混烧及热解特性

采用热重分析法,对生活污泥与煤以1∶1质量比混合的试样进行燃烧及热解实验研究,重点分析了升温速率对其热解及燃烧特性的影响,为煤泥混烧及热解技术的工业化应用提供理论支持。结果表明:煤泥混合样燃烧失重分为4个阶段,混燃过程中污泥与煤共同影响着混合试样的燃烧特性,随着升温速率从15℃·min~(-1)增加到50℃·min~(-1),其可燃性指数C增幅达60%和综合燃烧特性指数S提高了4倍多,燃烧性能得到明显提高;煤泥混合样的热解失重分为2个阶段,各阶段热解的挥发份最大析出速率(dw/dt)_(max)及挥发分析出特性指数D均随升温速率的升高而大幅增大,且试样总的挥发综合释放指数D从0.081 7×10~(-8)K~(-3)·min~(-2)增大到5.868×10~(-8)K~(-3)·min~(-2),可见升温速率越高,煤泥混合物的热解性能越好。     

铝污泥吸附六价铬的特征和机理

铝污泥是给水处理过程中不可避免的副产物,为了解其资源化利用作为吸附剂对Cr(Ⅵ)的吸附行为和吸附特征,本研究通过静态实验研究了铝污泥的水解特征、Cr(Ⅵ)在铝污泥上的吸附机理和影响因素。结果表明,(1)铝污泥表面的主要官能团为羟基、SO24-和Cl-;(2)铝污泥与Cr(Ⅵ)的吸附过程中,液相中Cr(Ⅵ)的浓度随吸附时间延长而降低(由20 mg/L降为15.42 mg/L),同时,液相中pH由6.01升高为7.06、SO24-由8.79 mg/L升高为11.40 mg/L、Cl-由10.54 mg/L升高为11.88 mg/L,这一结果表明,HCrO4-与铝污泥表面的羟基、SO24-、Cl-等官能团交换,其吸附机理为配体交换;(3)pH是影响Cr(Ⅵ)在铝污泥上的吸附量的主要因素,当pH由4.0升高至10.0时,吸附容量由7.63 mg/g下降为0.70 mg/g。实验表明,铝污泥作为一种新型的Cr(Ⅵ)吸附剂具有较高吸附能力和应用前景,并为优化吸附工艺提供了技术支撑。     

Field and laboratory studies of the fate and enantiomeric enrichment of venlafaxine and O-desmethylvenlafaxine under aerobic and anaerobic conditions

The stereoselectivity of R,S-venlafaxine and its metabolites R,S-O-desmethylvenlafaxine, N-desmethylvenlafaxine, O,N-didesmethylvenlafaxine, N,N-didesmethylvenlafaxine and tridesmethylvenlafaxine was studied in three processes: (i) anaerobic and aerobic laboratory scale tests; (ii) six wastewater treatment plants (WWTPs) operating under different conditions; and (iii) a variety of wastewater treatments including conventional activated sludge, natural attenuation along a receiving river stream and storage in operational and seasonal reservoirs. In the laboratory and field studies, the degradation of the venlafaxine yielded O-desmethylvenalfaxine as the dominant metabolite under aerobic and anaerobic conditions. Venlafaxine was almost exclusively converted to O-desmethylvenlafaxine under anaerobic conditions, but only a fraction of the drug was transformed to O-desmethylvenlafaxine under aerobic conditions. Degradation of venlafaxine involved only small stereoisomeric selectivity. In contrast, the degradation of O-desmethylvenlafaxine yielded remarkable S to R enrichment under aerobic conditions but none under anaerobic conditions. Determination of venlafaxine and its metabolites in the WWTPs agreed well with the stereoselectivity observed in the laboratory studies. Our results suggest that the levels of the drug and its metabolites and the stereoisomeric enrichment of the metabolite and its parent drug can be used for source tracking and for discrimination between domestic and nondomestic wastewater pollution. This was indeed demonstrated in the investigations carried out at the Jerusalem WWTP.     

骆马湖富营养化和生态状况调查与评价

为了了解骆马湖水质状况，在2005年对骆马湖富营养化状态和生态特性进行了调查，并结合“十五”期间的监测资料进行了分析。2005年骆马湖水体中总氮和总磷的平均值超《地表水环境质量标准》（GB3838-2002）中Ⅲ类，超标情况分别为0．78倍和0．54倍，达到湖库特定项目Ⅳ类水标准，骆马湖处于轻度富营养化状态。对骆马湖生态特征分析表明，由于该湖泊的形态以及“藻型浊水状态”和“泥沙型浊水状态”交替出现，遏制了湖水从高营养盐含量向全面富营养化状态演变，保障了底栖动物的良好生长环境，从而形成了骆马湖独特的环境生态平衡。     

剩余污泥浓缩脱水投药量优化和模型建立

应用高分子阳离子絮凝剂（CPF-100）和聚丙烯酰胺（PAM）对污水厂剩余污泥进行浓缩脱水实验,研究表明：CPF-100的浓缩脱水效果优于PAM;当CPF-00投加量为1．16‰时,污泥沉降性能改善程度为37．51％;且在CPF-100投加量逐渐增大的初始阶段,污泥沉降性能改善程度随投加量的增加而增大,但CPF-100投加量也不宜过大,当CPF-100投加量超过1．16‰后,反而会使浓缩脱水效果变差。同时,建立了污泥沉降性能改善程度与絮凝剂CPF-100投加量、沉降时间之间的数学模型,其能较好地反映污水厂剩余污泥的浓缩脱水效果。     

Copper-catalyzed chlorination and condensation of acetylene and dichloroacetylene

The chlorination and condensation of acetylene at low temperatures is demonstrated using copper chlorides as chlorinated agents coated to model borosilicate surfaces. Experiments with and without both a chlorine source and borosilicate surfaces indicate the absence of gas-phase and gas-surface reactions. Chlorination and condensation occur only in the presence of the copper catalyst. C₂ through C₈ organic products were observed in the effluent; PCDD/F were only observed from extraction of the borosilicate surfaces. A global reaction model is proposed that is consistent with the observed product distributions. Similar experiments with dichloroacetylene indicate greater reactivity in the absence of the copper catalyst. Reaction is observed in the gas-phase and in the presence of borosilicate surfaces at low temperatures. The formation of hexachlorobenzene is only observed in the presence of a copper catalyst. PCDD/F were only observed from extraction of the borosilicate surfaces. A global reaction model is proposed for the formation of hexachlorobenzene from dichloroacetylene.     

Aerobic and anaerobic degradation of profluralin and trifluralin

Abstract

The degradation of profluralin [N‐(cyclopropylmethyl)‐α,α,α‐trifluoro‐2,6‐dinitro‐N‐propyl‐]p‐toluidine] and trifluralin (α,α,α‐trifluoro‐2,6‐dinitro‐N,N‐dipropyl‐p‐toluidine) was studied under aerobic and anaerobic soil conditions. Three soils (Goldsboro loamy sand, Cecil loamy sand, Drummer clay loam) were each treated with 1 ppmw herbicide; anaerobic conditions were maintained by flooding. Soil samples were extracted monthly and subjected to TLC analysis. No degradation was detected in sterile controls. Aerobic degradation of both herbicides was greatest in the Cecil loamy sand soil over the entire incubation period. Degradation of profluralin in Cecil soil under aerobic conditions was 86 percent after 4 months with three products detected; 83 percent of the trifluralin was degraded with two products detected. Anaerobic degradation accounted for 72 percent of the profluralin and 78 percent of the trifluralin after 4 months. Degradation of both herbicides increased with incubation time for the first 3 months and decreased slightly thereafter. Generally there was more extensive degradation (percent and in number of products formed) of profluralin than trifluralin under the conditions tested. More degradation products were detected for both herbicides under aerobic conditions than under anaerobic conditions.     

Quantification of carbamazepine and atrazine and screening of suspect organic contaminants in surface and drinking waters

A new approach for the identification of suspect trace organic contaminants in drinking and surface waters is presented. Samples were initially analyzed using a target determination method for two contamination tracers, carbamazepine (CBZ) and atrazine (ATZ). This method used offline solid-phase extraction and online solid-phase extraction techniques coupled to liquid chromatography-triple quadrupole mass spectrometry to accelerate the sample preparation process and improve method performance. CBZ and ATZ were found respectively in 31% and 56% of the samples, and concentrations were usually <20 ng L⁻¹. These samples were re-analyzed with a similar method on a quadrupole time-of-flight mass spectrometer to identify suspect contaminants by means of exact mass measurements and isotope patterns. A database of 264 common organic contaminants was built and used in conjunction with a Molecular Feature algorithm to identify the presence of these substances in drinking and surface water collected from different sources at various locations across Canada. Several organic contaminants were identified in the samples, but only the presence of caffeine, desethylatrazine, simazine and venlafaxine could be verified by comparison to pure standards. The presence of desethylatrazine was also confirmed by MS/MS experiments. These results suggest that target analysis for tracers of organic contamination may be a helpful tool to prioritize samples which should be further screened for suspect contaminants. This study also shows that the combination of separation techniques (offline and online SPE, LC) contribute to advance the applicability of high-resolution mass spectrometry for the identification of trace organic contaminants by accelerating the preparation step, reducing complexity and increasing analyte concentrations for optimal detection.     

Persistence and dissipation kinetics of trifloxystrobin and tebuconazole in onion and soil

The persistence and dissipation kinetics of trifloxystrobin and tebuconazole on onion were studied after application of their combination formulation at a standard and double dose of 75 + 150 and 150 + 300 g a.i. ha^?1. The fungicides were extracted with acetone, cleaned-up using activated charcoal (trifloxystrobin) and neutral alumina (tebuconazole). Analysis was carried out by gas chromatograph (GC) and confirmed by gas chromatograph mass spectrometry (GC-MS). The recovery was above 80% and limit of quantification (LOQ) 0.05 mg kg^?1 for both fungicides. Initial residue deposits of trifloxystrobin were 0.68 and 1.01 mg kg^?1 and tebuconazole 0.673 and 1.95 mg kg^?1 from standard and double dose treatments, respectively. Dissipation of the fungicides followed first-order kinetics and the half life of degradation was 6–6.6 days. Matured onion bulb (and field soil) harvested after 30 days was free from fungicide residues. These findings suggest recommended safe pre-harvest interval (PHI) of 14 and 25 days for spring onion consumption after treatment of Nativo 75 WG at the standard and double doses, respectively. Matured onion bulbs at harvest were free from fungicide residues.     

Sources and distribution of polychlorinated-dibenzo-p-dioxins and -dibenzofurans in soil and sediment from the Yellow Sea region of China and Korea

Polychlorinated-dibenzo-p-dioxins and -dibenzofurans (PCDD/Fs) were measured in soils and sediments from the Yellow Sea region. Korean soils and sediments mostly contained detectable PCDD/Fs and showed a widespread distribution among locations. Soil and sedimentary PCDD/Fs from China were comparable to or less than those in Korea. The patterns of relative concentrations of individual congeners in soils were different between the two countries, but similar in sediments. Sources of PCDD/Fs in China and Korea were found to be independent of each other and their distributions reflected matrix-dependent accumulation. Spatial distribution indicated some point sources in Korea while Chinese sources were more widespread and diffuse. PCDD/Fs measured in the coastal areas of the Yellow Sea were comparable to or less than those previously reported in for eastern Asia. However, ∑TEQs in soils and sediments were near to or, in some cases exceeded environmental quality guidelines.     

Effects of compositional heterogeneity and nanoporosity of raw and treated biomass-generated soot on adsorption and absorption of organic contaminants

A biomass-generated soot was sequentially treated by HCl-HF solution, organic solvent, and oxidative acid to remove ash, extractable native organic matter (EOM), and amorphous carbon. The compositional heterogeneity and nano-structure of the untreated and treated soot samples were characterized by elemental analysis, thermal gravimetric analysis, BET-N₂ surface area, and electron microscopic analysis. Sorption properties of polar and nonpolar organic pollutants onto the soot samples were compared, and individual contributions of adsorption and absorption were quantified. The sorption isotherms for raw sample were practically linear, while were nonlinear for the pretreated-soot. The removal of EOM enhanced adsorption and reduced absorption, indicating that EOM served as a partitioning phase and simultaneously masked the adsorptive sites. By drastic-oxidation, the outer amorphous carbon and the inner disordered core of the soot particles were completely removed, and a fullerene-like nanoporous structure (aromatic shell) was created, which promoted additional π-π interaction between phenanthrene and the soot.     

Sorption and Desorption Behavior of Chloroanilines and Chlorophenols on Montmorillonite and Kaolinite

The bioavailability of pollutants, pesticides and/or their degradation products in soil depends on the strength of their sorption by the different soil components, particularly by the clay minerals. This study reports the sorption-desorption behavior of the environmentally hazardous industrial pollutants and certain pesticides degradation products, 3-chloroaniline, 3,4-dichloroaniline, 2,4,6-trichloroaniline, 4-chlorophenol, 2,4-dichlorophenol and 2,4,6-trichlorophenol on the reference clays kaolinite KGa-1 and Na-montmorillonite SWy-l. In batch studies, 2.0 g of clay were equilibrated with 100.0 mL solutions of each chemical at concentrations ranging from 10.0 to 200.0 mg/L. The uptake of the compounds was deduced from the results of HPLC-UV-Vis analysis. The lipophilic species were best retained by both clay materials. The most lipophilic chemical used in the study, 2,4,6-trichloroaniline, was also the most strongly retained, with sorption of up to 8 mg/g. In desorption experiments, which also relied on HPLC-UV-Vis technique, 2,4,6-trichloroaniline was the least desorbed from montmorillonite. However, on kaolinite all of the compounds under study were irreversibly retained. The experimental data have been modelled according to the Langmuir and Freundlich isotherms. A hypothesis is proposed concerning the sorption mechanism and potential applications of the findings in remediation strategies have been suggested.