用铁泥制氧化铁红

研究了以染化厂废料铁泥和工业废硫酸为原料,采用高温干法制取氧化铁红的工艺,简要介绍了该法生产氧化铁红的反应机理,探讨了氧化剂,氧化时间,氧化温度等对产品质量的影响,确定了适宜工艺条件,提出了工业生产流程和尾气治理方案。     

Enhanced photocatalytic activities of silicon nanowires/graphene oxide nanocomposite: Effect of etching parameters

Homogeneous and vertically aligned silicon nanowires (SiNWs) were successfully fabricated using silver assisted chemical etching technique. The prepared samples were characterized using scanning electron microscopy, transmission electron microscopy and atomic force microscopy. Photocatalytic degradation properties of graphene oxide (GO) modified SiNWs have been investigated. We found that the SiNWs morphology depends on etching time and etchant composition. The SiNWs length could be tuned from 1 to 42 µm, respectively when varying the etching time from 5 to 30 min. The etchant concentration was found to accelerate the etching process; doubling the concentrations increases the length of the SiNWs by a factor of two for fixed etching time. Changes in bundle morphology were also studied as function of etching parameters. The SiNWs diameter was found to be independent of etching time or etchant composition while the size of the SiNWs bundle increases with increasing etching time and etchant concentration. The addition of GO was found to improve significantly the photocatalytic activity of SiNWs. A strong correlation between etching parameters and photocatalysis efficiency has been observed, mainly for SiNWs prepared at optimum etching time and etchant concentrations of 10 min and 4:1:8. A degradation of 92% was obtained which further improved to 96% by addition of hydrogen peroxide. Only degradation efficiency of 16% and 31% has been observed for bare Si and GO/bare Si samples respectively. The obtained results demonstrate that the developed SiNWs/GO composite exhibits excellent photocatalytic performance and could be used as potential platform for the degradation of organic pollutants.     

太湖水-气界面温室气体N2O日通量变化特征

阐述了最重要的温室效应气体N2O的来源,湖泊中N2O产生机理,监测了太湖水-气界面四季N2O日通量,并分析了N2O日通量变化特征,发现太湖大部分时间是N2O的源,少部分时间是N2O的汇.春、夏、秋、冬四季的平均N2O日通量分别是0.018 mg/(m2·h)、0.065 mg/(m2·h)、0.003 mg/(m2·h)和-0.002 mg/(m2·h).夏季较高,而春、秋、冬季较低.     

工作场所有害物质氮氧化物测定的质量保证

工作场所空气中产生的有毒物质氮氧化物的测定是用吸收液采集空气样品后送达实验室检测，是采样与显色同时进行，方法的关键是采样前吸收液的配制与采样后样品的运输、保存及其测定。要得到准确、可靠的监测数据，一定要从样品的采集、保存，实验室分析等各个环节加以控制。     

Relationships of nitrous oxide fluxes with water quality parameters in free water surface constructed wetlands

The effects of chemical oxygen demand (COD) concentration in the influent on nitrous oxide (N₂O) emissions, together with the relationships between N₂O and water quality parameters in free water surface constructed wetlands, were investigated with laboratoryscale systems. N₂O emission and purification performance of wastewater were very strongly dependent on COD concentration in the influent, and the total N₂O emission in the system with middle COD influent concentration was the least. The relationships between N₂O and the chemical and physical water quality variables were studied by using principal component scores in multiple linear regression analysis to predict N₂O flux. The multiple linear regression model against principal components indicated that different water parameters affected N₂O flux with different COD concentrations in the influent, but nitrate nitrogen affected N₂O flux in all systems.     

利用水泥窑灰生产钾肥

水泥窑灰含有一定量的钾,是生产钾肥的良好原料。通过试验确定了用水泥窑灰与工业硝酸生产钾肥的配比及其它工艺参数,为水泥窑灰的综合利用提供了一项新方法。     

Evaluation of the First Phase of Sulfur Dioxide and Nitrogen Oxides Provisions of the 1990 Clean Air Act: A Plant-Based Approach

Electric power generating plants that use coal were among the key targets of Title IV of the 1990 Clean Air Act. Under the first phase of the act, 110 coal-fired electric power plants were required to reduce their sulfur dioxide emissions by 1995 and nitrogen oxide emissions by 1996. Phase 2 of the act requires even greater reduction of sulfur dioxide emissions by 2000 and nitrogen oxide emissions by 2008. This study examines whether the 107 targeted plants (three plants went off-line) have achieved the desired sulfur dioxide and nitrogen oxide emission levels. The analysis of sulfur dioxide is based on data from 1990, 1995, and 1999. The findings show that although sulfur oxide increased by 3% from 1995 to 1999, it decreased by 45% over the 1990–1999 period at the firm level for the targeted firms. The findings also indicate that the overall reduction in sulfur dioxide was achieved by utilizing low sulfur coal and by purchasing emission allowances. So far as nitrogen oxides are concerned, there has been a reduction of 14% over the 1990–1999 period, of which 7% was achieved during the 1995–1999 period. An evaluation of emissions at the plant level indicates that several plants do not meet the emissions level for sulfur dioxide or nitrogen oxides. These results provide a mixed scorecard for reduction in emissions both for sulfur dioxide and nitrogen oxides. Even though there is reduction in the emissions on an overall basis at the firm level, several plants that have not been able to reduce emissions deserve special attention to meet the goals of the act in reducing emissions.     

Winter and Spring Thaw Measurements of N2O,NO and NOx Fluxes using a Micrometeorological Method

The impact of nitrogen fertilizers on gaseous emissions duringwinter and spring-thaw is not well understood and was the objective of this research. Using a micrometeorological method,N₂O, NO and NO_x fluxes from ryegrass were measured from November 1997 to March 1998. Three different mineralfertilizers were applied in November: urea (U), slow-release urea(SRU) and ammonium nitrate (AN). N₂O emissions during the winter were small, increasing significantly in March. Total losses of N₂O-N were significantly higher from SRU and U plots, with winter N₂O emissions accounting for 50% of annual losses. Nitric oxide fluxes from all plots weresmall during the measurement period (<0.9 ng N m^-2 s^-1). The NO fluxes from U and AN fertilized plots were significantly higher than from SRU and control plots. NO₂ fluxes were always negative (–6 ng N m^-2 s^-1)indicating deposition, but decreased to –2 ng N m^-2s^-1 when snow was present on the soil surface. Our resultsindicate that the form of inorganic N applied has an effect on NO+ N₂O emissions but not on NO₂ fluxes.Sponsored by CAPES – Brasília, Brazil     

Spatially Disaggregated Inventories of Soil NO and N2O Emissions for Great Britain

Estimates of soil N₂O and NOemissions at regional and country scales arehighly uncertain, because the most widely usedmethodologies are based on few data, they do notinclude all sources and do not account forspatial and seasonal variability. To improveunderstanding of the spatial distribution of soilNO and N₂O emissions we have developedsimple multi-linear regression models based onpublished field studies from temperate climates.The models were applied to create spatialinventories at the 5 km² scale of soil NOand N₂O emissions for Great Britain. The N₂O regression model described soilN₂O emissions as a function of soil N input,soil water content, soil temperature and land useand provided an annual N₂O emission of 128 kt N₂O-N yr^-1. Emission rates largerthan 12 kg N₂O-N ha^-1 yr^-1 werecalculated for the high rainfall grassland areasin the west of Great Britain.Soil NO emissions were calculated using tworegression models, which described NO emissionsas a function of soil N input with and without afunction for the water filled pore space. Thetotal annual emissions from both methods, 66 and7 kt NO-N yr^-1, respectively, span the rangeof previous estimates for Great Britain.     

溶剂萃取法对苯甲酸废水预处理的研究

甲苯液相空气氧化法生产苯甲酸废水的成分复杂,属生物难降解体系,COD_Cr值高达20000～100000mg/L.本研究分别采用磷酸三丁酯、三烷基胺、三烷基氧膦为络合剂,正辛醇为助溶剂,煤油为稀释剂,通过萃取-反萃的方式,对苯甲酸废水进行处理.结果表明,多级错流萃取能有效地回收溶质苯甲酸,将原废水的COD_Cr值降低至1/6,使之满足其它末端处理的要求,而且反萃工艺简单易行,可生产苯甲酸盐,溶剂可重复使用.