应用质子变化滴定测量法监测氨氧化的化学计量关系

开发了一套监测批式废水生物处理系统质子变化的自动滴定测量装置.装置由批式反应器、数据自动采集与保存系统和药品自动投加系统组成.通过实际测量活性污泥氨氧化反应中氢离子产生量与氨消耗量的化学计量比值,考察自动滴定测量装置的测试精度.在1L的反应器中改变氨氮浓度(以N计)分别为1.67、3.33、8.33、16.66和30.00mg/L下实测比值与其理论值十分接近,相对误差在2.09%～6.34%之间;保持氨氮浓度16.66mg/L,在1、2、3和4L的反应器中实测比值相对误差在2.09%～-18.57%之间,随反应器体积增大而明显增大.反应器系统中的碳酸氢盐和氨盐缓冲体系,特别是在较大容积反应器中的滴定动态效应是导致测试误差的重要原因.研究成果为滴定测量方法在废水生物处理过程中监测质子变化提供了一种重要方法.     

江苏句容水库农业流域水塘和河流N_2O排放速率的研究

在句容水库农业流域的水塘和河流中,用密闭箱法于2007年8、11月和2008年2、5月采集水体表面排放的N2O气样,研究水塘和河流N2O排放速率的季节变化及其影响因素.结果显示,水塘N2O的排放速率范围在-0.42～16.76μg.m-.2h-1之间,河流N2O排放速率在0.29～8.41μg.m-.2h-1之间.由于...     

基于环境一号卫星多光谱影像数据的三湖一库富营养化状态评价

环境一号卫星是我国2008年自主发射的环境与灾害监测小卫星,其2d的时间分辨率使其成为环境变化监测的重要数据源.根据实测的太湖、巢湖、滇池和三峡水库的水面光谱信息以及水质参数,构建基于环境一号卫星多光谱数据的富营养化评价模型,对太湖、巢湖、滇池和三峡水库2009年水体营养状况进行了评价分析.研究结果表明:利用环境一号卫...     

谱系聚类法在小区域粮食安全预测中的应用——以昆山市为例

粮食安全对国民经济的可持续发展起着不可替代的基础性作用,小区域由于受政策因素的影响较大,粮食安全相关指标的变化呈一定阶段性,长时间序列的数学规律并不突出,不利于规划工作的展开。论文基于昆山市的研究,提出谱系聚类与数学模型相结合的基本思路,在此基础上推出了聚类结果有效性的量化判定标准并对聚类法运用准则做了深入的探讨。实际数据分析结果表明:昆山的粮食安全相关的社会经济指标变化确实呈明显阶段性;与利用全部时间序列数据建立的模型相比,运用谱系聚类的模型拟合和预测效果都有明显优势;至2015年,昆山市粮食自给率将下降至6%,最小人均耕地面积降低至0.022 hm²。通过进一步的分析、对比及讨论,文章认为,谱系聚类法运用于小区域粮食安全预测,方法可操作性强,结论科学性显著。     

团粒喷播在废弃采石场生态恢复方面的应用

废弃采石场严重影响城市周边的生态景观,极易导致生态环境的继续恶化。以文登某一采石场破损山体的绿化工程为例,运用团粒喷播生态修复技术对废弃矿山进行生态性治理,并探讨其生态恢复方法,以期为今后废弃矿山的残损山体植被恢复和生态环境重建提供参考。     

基于我国规范与PIARC标准的公路隧道需风量分析

以某长大高速公路隧道为例,结合我国隧道通风设计规范JTJ026.1-1999与PIARC2007标准(世界道路协会),针对不同行车速度,不同车辆更新情况、不同排放标准组合形式以及是否考虑NOx等情况,对各个不同工况的需风量分别进行计算,并从需风量计算方法、机动车排放量和污染物设计浓度三个方面对隧道需风量差异进行分析。研究结果表明:我国设计规范与PIARC2007存在较大差距,为了适应当前及今后我国交通量及机动车排放特点的发展趋势,我国现行规范应在机动车排放量、污染物设计浓度限值等方面做出必要改进以达到合理确定隧道需风量的目的。     

半干法脱硫配套布袋除尘器的特殊要求

由于半干法脱硫工艺对布袋除尘器的特殊要求,使得其配套的布袋除尘器构造不同于以往常规的布袋除尘器.从布袋除尘器的过滤风速、滤料选择、沉降室设置、布风均匀性、灰斗特性、旁路系统的要求做详细的说明.     

印钞废水处理工艺的改进实验

印钞废水属高浓度难降解有机废水,对环境污染严重。鉴于现有处理工艺出水普遍不达标的情况,通过对比实验确定了改进方案:超滤浓缩液离心出水在进入接触氧化池前,增加新的处理单元(Fenton氧化-混凝)。Fenton氧化最佳条件:FeSO4.7H2O投加量14 g/L,H2O2的投加量34 mL/L,初始pH值6.0,氧化反应时间1.5h,温度18.8℃;混凝过程最佳条件:PAC投加量4 g/L,PAM(5‰)投加量10 mg/L,pH值7。新增单元对废水中COD去除率接近80%,可生化性提高1.6倍,色度降低36%。     

Potential particulate pollution derived from UV-induced degradation of odorous dimethyl sulfide

UV-induced degradation of odorous dimethyl sulfide (DMS) was carried out in a static White cell chamber with UV irradiation. The combination of in situ Fourier transform infrared (FT-IR) spectrometer, gas chromatograph-mass spectrometer (GC-MS), wide-range particle spectrometer (WPS) technique, filter sampling and ion chromatographic (IC) analysis was used to monitor the gaseous and potential particulate products. During 240 min of UV irradiation, the degradation e ciency of DMS attained 20.9%, and partially oxidized sulfur-containing gaseous products, such as sulfur dioxide (SO2), carbonyl sulfide (OCS), dimethyl sulfoxide (DMSO), dimethyl sulfone (DMSO2) and dimethyl disulfide (DMDS) were identified by in situ FT-IR and GC-MS analysis, respectively. Accompanying with the oxidation of DMS, suspended particles were directly detected to be formed by WPS techniques. These particles were measured mainly in the size range of accumulation mode, and increased their count median diameter throughout the whole removal process. IC analysis of the filter samples revealed that methanesulfonic acid (MSA), sulfuric acid (H2SO4) and other unidentified chemicals accounted for the major non-refractory compositions of these particles. Based on products analysis and possible intermediates formed, the degradation pathways of DMS were proposed as the combination of the O(1D)- and the OH- initiated oxidation mechanisms. A plausible formation mechanism of the suspended particles was also analyzed. It is concluded that UV-induced degradation of odorous DMS is potentially a source of particulate pollutants in the atmosphere.     

Modeling assessment for ammonium nitrogen recovery from wastewater by chemical precipitation

Chemical precipitation to form magnesium ammonium phosphate (MAP) is an effective technology for recovering ammonium nitrogen (NH4 +-N). In the present research, we investigated the thermodynamic modeling of the PHREEQC program for NH4 +-N recovery to evaluate the effect of reaction factors on MAP precipitation. The case study of NH4 +-N recovery from coking wastewater was conducted to provide a comparison. Response surface methodology (RSM) was applied to assist in understanding the relative significance of reaction factors and the interactive effects of solution conditions. Thermodynamic modeling indicated that the saturation index (SI) of MAP followed a polynomial function of pH. The SI of MAP increased logarithmically with the Mg2+/NH4 + molar ratio (Mg/N) and the initial NH4 +-N concentration (CN), respectively, while it decreased with an increase in Ca2+/NH4 + and CO3 2??/NH4 + molar ratios (Ca/N and CO3 2??/N), respectively. The trends for NH4 +-N removal at different pH and Mg/N levels were similar to the thermodynamic modeling predictions. The RSM analysis indicated that the factors including pH, Mg/N, CN, Ca/N, (Mg/N) (CO3 2??/N), (pH)2, (Mg/N)2, and (CN)2 were significant. Response surface plots were useful for understanding the interaction effects on NH4 +-N recovery.