TiO2与Cu2O光催化降解对硝基苯酚比较研究

分别采用自制的纳米TiO2和Cu2O研究对硝基苯酚的光催化降解.结果表明,模拟阳光条件下,100mg·l-1对硝基苯酚水溶液的氧化亚铜催化反应半衰期为20.0min,而二氧化钛不具备可见光催化能力;在SGY-1多功能光化学反应器中,TiO2催化降解对硝基苯酚的半衰期是48.1min.产物分析表明,n-型半导体二氧化钛的光催化反应存在两种降解历程,生成二羟基硝基苯或脱除硝基.而p-型半导体氧化亚铜催化的光降解反应未检出脱硝基产物,仅检出1,2-二羟基-4-硝基苯.     

Development of new monthly global and diffuse solar irradiation estimation methodologies and comparisons

In assessing and deciding the prediction schemes of solar irradiation countrywide, better the accuracy means better the management of energy transition toward renewables. Consequently, the present study is on the development of new models to make the most accurate possible estimations of the global and diffuse solar irradiation based on ground measurements. Such analysis produces the most accurate estimations for the input of solar energy systems. This is utmost significant for deciding the investments on solar energy systems and their design periods. Turkey is a high-potent country whose solar energy market has been growing rapidly. She doesn’t have adequate reliable measurement network and there is no estimation methodology developed for each and every point within its territory. Moreover, installing such a measurement system network doesn’t seem to be economically feasible and technically possible, inter alia. Accordingly, this study defines a methodology to make the most accurate estimations of monthly mean daily solar irradiation on horizontal surface and its diffuse and beam components. For the global and diffuse estimations, new methodologies in linear and quadratic forms are developed, compared, and discussed. The comparison is applied by using mean bias error and root mean square error statistical comparison methods. The measured data values used for modeling and comparisons are provided from the State Meteorological Service of Turkey responsible authority for solar irradiation measurements. The results revealed that the methodologies explained in this study give very high accurate values of total solar irradiation on a horizontal surface and its diffuse component.     

Are policy incentives for solar power effective? Evidence from residential installations in the Northeast

State incentives for solar power have grown significantly in the past several years. This paper examines the effectiveness of policy incentives to increase residential solar photovoltaic (PV) capacity. We use county-level panel data and control for demographic characteristics, solar resources, and pro-environmental preferences. Results show that among financial incentives, rebates have the most impact with an additional $1 per watt rebate increasing annual PV capacity additions by close to 50%. Factors that affect financial returns to solar PV such as electricity price and solar insolation are also found to be significant. Results also point to a significant positive relationship between hybrid vehicle sales and residential PV capacity growth, indicating the importance of pro-environmental preferences as a predictor of solar PV demand. Back of the envelope calculations suggest that the cost of carbon mitigation through rebates is around $184 per ton of CO₂.     

总量控制约束下区域用水结构调控策略及动态模拟

在既定水资源供给下,通过调控区域用水结构,提高用水效率与效益,使经济社会发展与用水总量限制的水资源约束相适应,是目前区域经济社会发展面临与亟待解答的关键科学问题。选择若干指标定量描述用水系统与社会经济系统耦合关系的基础上,以国民经济部门划分和用水主体划分相结合的方式,细化第一、二、三产业、生活和生态用水指标,建立了江苏省用水结构与产业结构、用水需求与经济社会发展指标互动反馈的模拟调控的系统动力学模型。在对当前发展模式下的江苏省用水总量发展趋势模拟预测分析基础上,选择对系统影响显著的参数作为调控变量,设计了5种对比情景,动态模拟水资源供求变化和用水结构变化情况,提出了江苏省用水总量控制下用水结构调控方案和对策,为区域落实最严格水资源管理制度提供决策依据。     

太湖竺山湾沉积物碳氮磷分布特征与污染评价

为了揭示太湖竺山湾沉积物中碳、氮和磷的分布特征,本研究在太湖竺山湾设置3个断面(湖湾内,A断面;湖湾中部,B断面;开敞湖区,C断面) 10个采样点,采集沉积物柱状样,每2 cm间隔分层测定沉积物中总氮(TN)、总磷(TP)和总有机碳(TOC)含量,以揭示其水平分布和垂向分布特征.结果表明,在空间上竺山湾表层沉积物呈现开敞湖区向湖湾富集的特征,湖湾内部碳、氮和磷含量显著高于开敞湖区(P 0. 01),其中湖湾内(A断面)表层沉积物TN、TP和TOC含量分别为1. 53、1. 55和11. 31 mg·g~(-1),而靠近开敞湖区(C断面)表层沉积物TN、TP和TOC含量仅为0. 75、0. 57和6. 70 mg·g~(-1).垂向分布特征表现为表层富集,3个断面TN、TP和TOC含量随着底泥深度的增加均呈现出下降趋势,表层沉积物TN、TP和TOC含量分别是底层的2～3、2～5和2～3倍.整体而言,竺山湾沉积物TP含量均值为0. 93 mg·g~(-1),属于重度污染,而TN平均含量为1. 11 mg·g~(-1),属于轻度污染;有机氮指数和综合污染指数显示,竺山湾北部地区污染水平为重度污染区,有机污染相对较强,TP的污染指数(STP)处于1. 03～3. 87之间,属于重度污染.     

长江流域总氮排放量预测

水环境污染是长江流域突出的环境问题之一,预测污染物排放特征可为流域水污染防治提供科学基础.本研究综合采用灰色理论预测模型、Conversion of land use and its effects at small region extent(CLUE-S)模型以及 Integrated valuation of ecosystem services and tradeoffs(InVEST)模型,预测2025年长江流域非点源以及点源总氮排放趋势.结果表明:①非点源总氮排放呈减少趋势,2015～2025年区域非点源总氮排放量减少23.96％,中下游农业区总氮排放骤减,而上游局部地区呈增加趋势;②点源总氮排放总体呈现增加趋势,2015～2025年区域点源总氮排放量增加1.79％,主要是由于城镇废水排放的增加以及中下游沿江城市群生活污水排放显著增加,而中下游丘陵地区点源总氮排放呈现减少趋势;③长江流域总氮排放量呈现减少趋势,2015～2025年减少2.67％,但仍有37.64％区域呈现总氮排放增加的趋势.长江流域未来应加强对上游面源污染治理以及中下游工业、城镇废水排放的管控.采用多模型结合的手段可以精细揭示了长江流域总氮排放空间格局及未来趋势,可为明确流域总氮排放控制目标提供科学基础,也可为实现高效的水环境治理提供科学依据.     

不同水分梯度下UV-B辐射对2个稻田土壤碳氮转化的影响

UV-B辐射对土壤碳氮转化的影响与土壤物理化学性质有关,为明确土壤水分状态对UV-B辐射的影响,以有机质含量不同的两个水稻土(有机质含量低的记为L,高的记为H)为研究材料,在室内研究了含水量为25%(W1)、50%(W2)和100%(W3)时,UV-B辐射对土壤总有机碳(TOC)、可溶性有机碳(DOC)、铵态氮(NH_4~+-N)、硝态氮(NO_3~--N)以及累积净矿化氮量的影响.结果表明:120 h后,与避光(对照,CK)相比,UV-B辐射显著降低了土壤TOC的含量(P0.05);UV-B辐射下,水分从低到高,L土壤的TOC分别降低了9.9%、4.5%和6.3%,H土壤降低了10.9%、5.6%和6.3%.但与对照相比,UV-B辐射却促使土壤DOC增加;且在UV-B辐射下水分为100%的处理中,土壤DOC含量高于25%和50%的处理,120 h时,L土壤的DOC分别增加了21.5%(W1)、9.4(W2)和26.3%(W3),H土壤分别降低了26.7%(W1)、14.2%(W2)和33.8%(W3).与对照相比,UV-B辐射使NH_4~+-N含量有所下降;且在UV-B辐射中,NH_4~+-N含量的变化幅度在不同水分条件下的整体表现为W1W2W3.较对照处理,UV-B辐射促进NO_3~--N的累积,NO_3~--N变化幅度在不同水分条件下的表现为:W1W3W2.24 h后与对照相比,UV-B辐射对土壤累积净矿化氮量有显著影响(P0.05),且UV-B辐射下累积净矿化氮量在不同水分之间差异显著(P0.05).这表明光降解在土壤有机质的稳定中扮演着重要角色,UV-B辐射会加速土壤有机碳的损失,影响土壤矿质态氮的转化,且水分不同,UV-B辐射对土壤碳氮转化的影响存在一定差异.     

浙江省畜禽养殖污染减排对策研究

浙江省畜禽养殖总体数量大、规模小、布局分散,严重影响浙江省水环境质量和农村生态环境质量。本报告以浙江省水环境质量状况、畜禽养殖业调查资料、现状实测数据为研究依据,通过剖析污染结构特征和空间特征,得出浙江省畜禽养殖污染的特点、存在问题及污染物总量减排存在的主要困难。根据各类污染产生机理和排污特征,参考点源污染物排放总量控制的传统思路,探索畜禽养殖污染减排的途径与管理政策集成,推广来端治理与源头控制相结会的生态减排理念．     

质量控制图在辐射测量仪器工作稳定性中的作用研究

在低放射性环境样品进行测量时,要求测量仪器具有较好的稳定性。仪器在工作一段时间后,要了解所作的测量数据是否具有统计重复性,仪器指标发生的变化是否在统计基础上,仪器工作是否正常,绘制仪器质量控制图是一种有效方法。通过绘制质量控制图表的方法,可随时了解仪器的稳定性和仪器的技术指标,直观地展示出测量过程是否处于统计控制中。以确保仪器的测量精度。     

Photochemical degradation of nonylphenol in aqueous solution：The impact of pH and hydroxyl radical promoters

The degradation of nonylphenol (NP) in aqueous solution with UV, H₂O₂/UV, and Fenton/photo-Fenton processes was studied. The efficacy of direct and hydrogen peroxide photolysis proved to be dependent on the pH value. The addition of H₂O₂ to UV treatment improved NP degradation. The application of UV photolysis and the H₂O₂/UV system at pH 7 resulted in low pseudo first-order rate constants at 10^-4 sec^-1. In the experiments at elevated pH values the pseudo-first order rate constants increased to 10^-3 sec^-1. The efficacy of the Fenton process was lower in comparison with UV and hydrogen peroxide photolysis. The addition of UV irradiation to the H₂O₂/Fe²⁺ system substantially improved NP degradation efficacy. In terms of performance, the photo-Fenton process was similar to the H₂O₂/UV process. The most favourable process for complete nonylphenol degradation considering both operational cost and treatment efficacy was H₂O₂/UV at pH 11 and 250 mol/L H₂O₂.