文蛤对环境中TN、TP的影响及其指示微生物活性指标的确定

为确定文蛤活动对海水及沉积物中TN、TP的影响并筛选指示文蛤活动对环境中总氮、TP影响的微生物活性指标,本研究进行了围塘埋栖文蛤的现场实验以及室内模拟实验。于2009年8月在双台子河口盘山海域的滩涂高潮线附近设置了投放文蛤的实验池塘和未投放文蛤的对照池塘。于2010年8月、10月、12月及2011年5月分别采集了实验池塘和对照池塘的海水及表层沉积物,并对其进行了主要微生物活性指标(微生物生物量碳、微生物基础呼吸、海水及沉积物中细菌总数、硝化细菌和反硝化细菌数量)以及TN、TP的测定,从而确定文蛤活动对海水及沉积物中TN、TP的影响。通过相关性分析,确定能指示文蛤活动对TN、TP影响的微生物活性指标。同时进行室内模拟实验测定上述指标。通过对现场和室内模拟实验结果的综合分析发现,投放文蛤之后,海水中的TN、TP含量下降,海水及沉积物中的细菌总数下降,说明文蛤的投放对海水富营养化起到缓解的作用。此外通过相关性分析发现海水中细菌总数、沉积物中细菌总数及微生物生物量碳这3个微生物指标与海水及沉积物中TN、TP之间均具有显著相关性,可用于反应文蛤扰动对环境中TN、TP的影响。     

治霾背景下浅层地温能产业规模化发展研究

为了实现治霾目标,国家大力推广可再生能源应用,《关于促进地热能开发利用的指导意见》(国能新能[2013]48号),明确提出将积极推广浅层地温能,扩大其在城镇建筑用能中的比例。我国浅层地温能产业发展面临一系列障碍,为了克服市场调节失灵问题,借助事物发展动力原则,结合全寿命周期理论,依托层次分析法,推导能源发展的核心影响因素,据此提出了浅层地温能产业规模化发展的关键路径,构建了浅层地温能开发利用的长效管理体系。     

水溶性吸收剂对甲苯废气的吸收性能

液体吸收法应用于处理工业有机废气涉及到2个关键因素,即吸收剂的选择与吸收液的再生处理. 选择8种水溶性吸收剂——2种氟碳表面活性剂(FSO100和FSN100)、2种非离子表面活性剂〔TW80(吐温80)和SP20(斯盘20)〕、2种阴离子表面活性剂〔脂肪醇聚氧乙烯醚硫酸钠(AES)和脂肪醇聚氧乙烯醚羧酸钠(AEC)〕及2种类表面活性剂〔β-CD(β-环糊精)和SA(乙酸钠), 对模拟甲苯废气进行了动力学吸收试验,研究吸收性能和加热蒸馏法对甲苯回收与吸收剂溶液再生的可行性. 结果表明:吸收剂类型是影响甲苯吸收能力的最主要因素. 2种氟碳表面活性剂吸收液的甲苯吸收能力最强,其次是SP20与AES,而其他4种吸收剂溶液对甲苯的吸收能力很弱. 上述3类吸收剂对甲苯的初始去除率分别为80%～90%、75%左右与60%～70%,甲苯饱和吸收浓度(以w计)分别为0.58～3.45、0.38～1.44与0.14～1.01 mg/g. 除TW80吸收液热稳定性差、不宜采用加热蒸馏方法再生外, 其他吸收剂溶液经5次重复使用,甲苯回收率可达70%～85%,并能保持其原有吸收性能. 甲苯分配系数计算结果表明,FSO100和FSN100分别为0.41、0.62, SP20和AES分别为0.76、0.95, 其他4种吸收剂溶液在1.12～3.54之间;甲苯分配系数与饱和吸收浓度呈负相关、与体积传质系数呈正相关. 因此,2种氟碳表面活性剂吸收液对甲苯的吸收能力强,加热蒸馏法回收甲苯与再生吸收液具有经济性,用于处理甲苯废气具有广泛的应用前景.      

Removal of organic matter and disinfection by-products precursors in a hybrid process combining ozonation with ceramic membrane ultrafiltration

The performance of an integrated process including coagulation, ozonation, ceramic ultrafiltration (UF) and biologic activated carbon (BAC) filtration was investigated for the removal of organic matter and disinfection by-products (DBPs) precursors from micro-polluted surface water. A pilot scale plant with the capacity of 120 m³ per day was set up and operated for the treatment of drinking water. Ceramic membranes were used with the filtration area of 50 m² and a pore size of 60 nm. Dissolved organic matter was divided into five fractions including hydrophobic acid (HoA), base (HoB) and neutral (HoN), weakly hydrophobic acid (WHoA) and hydrophilic matter (HiM) by DAX-8 and XAD-4 resins. The experiment results showed that the removal of organic matter was significantly improved with ozonation in advance. In sum, the integrated process removed 73% of dissolved organic carbon (DOC), 87% of UV₂₅₄, 77% of trihalomethane (THMs) precursors, 76% of haloacetic acid (HAAs) precursors, 83%of trichloracetic aldehyde (CH) precursor, 77% of dichloroacetonitrile (DCAN) precursor, 51% of trichloroacetonitrile (TCAN) precursor, 96% of 1,1,1-trichloroacetone (TCP) precursor and 63% of trichloronitromethane (TCNM) precursor. Hydrophobic organic matter was converted into hydrophilic organic matter during ozonation/UF, while the organic matter with molecular weight of 1000–3000 Da was remarkably decreased and converted into lower molecular weight organic matter ranged from 200–500 Da. DOC had a close linear relationship with the formation potential of DBPs.     

Effects of water quality on the coagulation performances of humic acids irradiated with UV light

The presence of humic acid in drinking water treatment has received significant attention in recent years because of its adverse effects on the removal of many pollutants in coagulation. In this paper, the effects of water quality including pH, turbidity, alkalinity, and hardness on the removal of humic acid were investigated in a UV light hybridized coagulation process. Our results suggested that UV light radiation could effectively improve the removal rate of humic acid in coagulation under both neutral and basic conditions, and the variations of the selected water quality parameters had little adverse effect on the function of UV light. After UV light radiation, the removal rate of the nitro-humic acid (NHA) increased from 20% to 60% in coagulation, and increased further to 75% and 85% for the raw waters with 10.0 NTU kaolin and 100 mg·L^-1 hardness, respectively. In addition to NHA, the removal rates of the humic acid extracted from peat coal (PHA) and the humic acid provided by Japan metals and chemicals company (JHA) in coagulation were also improved, both in the range of 80%–90% after undergoing UV light radiation. By changing the radiation location from prior to coagulation to the flocculation process, similar experimental results were obtained. The formation of positive charged sites after UV light radiation was considered to be the primary factor that led to an enhanced removal of the humic acid in coagulation.     

张集矿综采工作面瓦斯治理措施及效果分析

张集矿属于煤与瓦斯突出矿井,针对目前所开采的17266工作面地质构造条件复杂、瓦斯涌出量大、处于突出危险区等瓦斯治理难题,采取"风排瓦斯、高抽巷穿层钻孔抽采、运输巷、回风巷顺层钻孔抽采和上隅角埋管抽采"等瓦斯综合治理措施,用分源预测法得出工作面绝对瓦斯涌出量为30.3 m3/min。结果表明,工作面的主要瓦斯涌出来源为本煤层瓦斯涌出。工作面风排瓦斯量11.0 m3/min,工作面瓦斯抽采率达63.0%以上。     

节能耐磨型电梯导靴靴衬应用研究

很多电梯使用的导靴靴衬存在容易磨损的问题,从而导致电梯运行中的抖动和不平稳现象,影响乘坐的舒适性。常用的靴衬材料摩擦系数偏大,造成电梯运行过程中摩擦力偏大,能耗增加。因此对这类电梯的导轨与导靴间的摩擦行为进行研究,将新型复合材料应用于电梯靴衬,实现减摩以降低能耗,提升靴衬的耐磨性,延长使用寿命,降低成本,具有较大的实际意义和应用价值。     

蒸汽相变促进可溶PM2.5凝结增长的数值分析

为利用蒸汽相变原理促进氨法脱硫系统排放细颗粒物(PM2.5)的脱除,建立多分散颗粒的凝结增长动力学模型,利用数值模拟方法研究了可溶硫酸铵颗粒的凝结增长规律,并将典型粒径可溶与不可溶颗粒的凝结增长过程进行对比分析.结果表明:不同粒径硫酸铵颗粒的增长速率相近,等温系统的凝结增长效果优于绝热系统;对于同一初始粒径分布下的可溶和不可溶颗粒,微米尺度可溶颗粒的增长速率始终大于不可溶颗粒,亚微米尺度可溶颗粒的增长速率先大于而后小于不可溶颗粒,使得二者的增长曲线存在一个交叉点;蒸汽饱和度增大能显著促进硫酸铵颗粒的增长;等温系统中温度对硫酸铵颗粒的增长影响显著,绝热系统中温度的影响较弱.     

巢湖重污染汇流湾区沉积物重金属污染特征及风险评价

对巢湖重污染汇流湾区沉积物中主要重金属分布和累积特征及生态风险进行了分析评价.结果表明:受底泥分布影响,湾区沉积物重金属主要累积于距岸边约700m以上的低洼区,且表层沉积物(0~2cm)重金属含量大致随泥深增加而增大.基于地积累指数法和潜在生态风险指数法的评价结果表明,除Hg(Eri=325.5)和Cd(Eri=240.28)外,大多数重金属处于低风险状态,各金属元素污染顺序为Hg>Cd>Zn>Pb>Cu>As>Cr>Ni.其中,富集倍数最高的Hg和Cd具有同源性,污染等级均为3级.垂向分析表明,受Hg和Cd的影响,0~14cm沉积物已达严重生态风险程度(RI>525),14~34cm沉积物中Hg具有中度生态风险.建议亟须从流域角度对该汇流湾区重金属特别是Hg和Cd进行控制.     

吸附存储-间歇放电法氧化甲苯的反应过程研究

以SBA-15为催化剂,对比连续降解法和吸附存储-间歇放电法净化低浓度甲苯的活性,结果表明吸附存储-间歇放电法下甲苯去除率、碳平衡和CO2选择性更高.运用GC-MS分析了2种降解方式催化剂表面中间产物随时间的变化,苯甲醛进一步氧化分解进而打开苯环,是等离子体催化降解甲苯的控制步骤.对比SBA-15、Mn/SBA-15、Ag/SBA-15、AgMn/SBA-15 4种催化剂在吸附存储-间歇放电法下降解甲苯的活性.结果显示Ag和Mn的引入加速了对2-庚烯醇的氧化催化,AgMn/SBA-15表现出最好的碳平衡、CO2选择性.