中国东部主要河流河水腐殖酸的起源、含量及地域分异规律

测定了中国东部地区主要河流河水、悬浮物和沉积物中腐殖酸含量,研究了该地区河水腐殖酸含量的地域分异规律,并探讨了河水腐殖酸的可能来源。结果表明,所研究河流河水腐殖酸含量在0.9—14.4mg/L范围内,中值为4.16mg/L,并有北高南低的一般趋势。黑龙江上游及松花江北部支流的河水腐殖酸含量在8.5mg/L以上,滦河以北其它地区在3.9—6.4mg/L范围内,黄河以南区域则在0.9—3.3mg/L之间,所研究地区河水中的腐殖酸为混合起源的,它既来自河流悬浮物和沉积物中腐殖酸的释放,又来自流域表土中腐殖酸的淋溶。     

硫酸羟胺的自加速分解温度和稳定性研究

通过快速筛选热分析试验对硫酸羟胺热危险性进行定性分析,对其热分解过程进行初步研究,获得温度、压力变化规律;再运用C80微量热仪对硫酸羟胺进行深入分析,得到硫酸羟胺的化学反应动力学参数,根据Semenov模型计算其自加速分解温度（SADT）。试验结果表明：由RSD初步筛选试验得到硫酸羟胺在164．2℃时即发生分解放热;用C80法得到硫酸羟胺的起始热分解温度为137．1℃,并计算了该物质在3种典型包装下的自加速分解温度。由SADT得到储存、运输过程中硫酸羟胺的控制温度,从而为减少硫酸羟胺事故的发生提供必要的参考数据。     

基于排队论的城市垃圾箱最佳间距研究

针对城市垃圾箱最佳间距的研究不够精细的现状,本文通过建立排队论模型得到了可供不同城市参考的城市垃圾箱最佳间距参数表。通过对部分城市街道的垃圾箱摆放间距情况进行实地调查,运用层次分析法将影响垃圾箱间距分布的多重因素转化为单因素;建立了基于指数分布的教学模型,利用排队论分析单因素状态下的垃圾箱间距分布,得到了求解城市垃圾箱最佳间距的一般方法。     

有机氯农药污染土壤的Fenton氧化修复研究

研究了Fenton氧化对某实际有机氯农药污染场地土壤的修复效果。结果显示:Fenton氧化能够快速有效地降解污染土壤中的六氯和DDTs。当Fe2+浓度为80 mmol/L,Fe2+与H2O2的摩尔浓度比为1∶5,水土比10∶1时,反应6 h,土壤中六氯和总DDT的去除率分别为:96.7%和78.2%。每方土的修复成本估算为951元。     

SBR在高校中水回用领域的工程应用研究

采用SBR工艺对高校校园废水进行了处理,运行结果表明:废水中COD含量从200～360mg/L降至60mg/L以下,BOD5含量从70～110mg/L降至20mg/L以下,氨氮含量从60～80mg/L降至10mg/L以下,SS含量从75～160mg/L降至50mg/L以下,达到了北京市DB11307—2005《水污染物排放标准》的二级排放标准。     

巢湖流域水资源可持续性评价方法研究

水资源可持续性评价模型(WRSEM,Water Resource Sustainability Evaluation Model)能够定量地评价流域水资源的可持续性,是流域水资源管理的一个有效工具。本文为了科学地衡量巢湖流域水资源开发、利用和管理的可持续性,构建了巢湖流域水资源可持续性评价模型和评价指标体系。巢湖流域水资源可持续性评价指标体系由4个一级指标(经济效率、社会公平、环境保护和保障能力)和20个二级指标构成。最后根据相对权重综合计算得到流域水资源可持续性指数。评价结果表明了巢湖流域水资源可持续性的程度,同时研究结果为巢湖流域水资源管理及其相关政策制定提供了科学依据。     

Experimental study on filtration and continuous regeneration of a particulate filter system for heavy-duty diesel engines

This study investigated the filtration and continuous regeneration of a particulate filter system on an engine test bench, consisting of a diesel oxidation catalyst（DOC） and a catalyzed diesel particulate filter（CDPF）. Both the DOC and the CDPF led to a high conversion of NO to NO2 for continuous regeneration. The filtration efficiency on solid particle number（SPN） was close to100%. The post-CDPF particles were mainly in accumulation mode. The downstream SPN was sensitively influenced by the variation of the soot loading. This phenomenon provides a method for determining the balance point temperature by measuring the trend of SPN concentration.     

Fenton/微波深度处理增塑剂废水

探讨微波功率、活性炭投加量、pH及反应时间等因素对微波处理效果的影响;考察废水pH、Fe2+和H2O2比例、Fe2+离子浓度及处理时间等因素对Fenton处理效果的影响。分别选择最优条件进行Fenton/微波联合处理邻苯二甲酸酯废水实验,COD去除率达98.7%,出水满足国家综合排放标准中一级标准。     

Removal of Cd2+ from water by Friedel’s salt (FS: 3CaO.Al2O3·CaCl2·10H2O): Sorption characteristics and mechanisms

The development of low-cost and efficient new mineral adsorbents has been a hot topic in recent years. In this study, Friedel’s salt (FS:3CaO·A12O3 ·CaCl2 ·10H2O), a hexagonal layered inorganic absorbent, was synthesized to remove Cd2+ from water. The adsorption process was simulated by Langmuir and Freundlich models. The adsorption mechanism was further analyzed with TEM, XRD, FT-IR analysis and monitoring of metal cations released and solution pH variation. The results indicated the adsorbent FS had an outstanding ability for Cd(Ⅱ) adsorption. The maximum adsorption capacity of the FS for Cd(Ⅱ) removal can reach up to 671.14 mg/g. The nearly equal numbers of Cd2+ adsorbed and Ca2+ released demonstrated that ion-exchange (both surface and inner) of the FS for Cd(Ⅱ) played an important role during the adsorption process. Furthermore, the surface of the FS after adsorption was microscopically disintegrated while the inner lamellar structure was almost unchanged. The behavior of Cd(Ⅱ) adsorption by FS was significantly affected by surface reactions. The mechanisms of Cd2+ adsorption by the FS mainly included surface complexation and surface precipitation. In the present study, the adsorption process was fitted better by the Langmuir isotherm model (R2 = 0.9999) than the Freundlich isotherm model (R2 = 0.8122). Finally, due to the high capacity for ion-exchange on the FS surface, FS is a promising layered inorganic adsorbent for the removal of Cd(Ⅱ) from water.     

On the determination of nitrous oxide emission factor during biomass burning

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