采用体积信息熵表征颗粒污泥系统稳定性及其稳定机制

SBR反应器中培养自养硝化颗粒污泥,在絮体转化为颗粒过程中,颗粒的体积信息熵从2.05(27 d,初见颗粒)降低为1.85(95 d),熵值降低的主要动力来自于松散的絮体在较快沉速选择压条件下被淘洗出系统.当絮体被淘洗出系统即完成颗粒化过程,在129 d时测得系统中颗粒沉速分布的中位数为6.27 m.h-1,因此颗粒体积熵值的变化不再受沉速选择压(6m.h-1)的控制.颗粒的粒径、沉速及体积熵值分布均呈现周期性变化,其中信息熵的均值为2.16,最小值为1.79,最大值为2.63.在这种周期性变化过程中,系统总是表现为粒径均值先增大后减小.熵值的波动的驱动力来自于颗粒的破碎与破碎体的成长,体积分布信息熵的大小可以很好地表征系统的稳定性及其稳定机制.     

基于响应曲面法的遗煤自燃分析与研究*

为研究高瓦斯易自燃煤层不同供风量、高抽巷抽采流量、低抽巷抽采流量3因素对采空区自燃“三带”分布影响规律,选取阳煤五矿8406工作面为研究对象,在数值模拟研究基础上,采用Design Expert软件进行Box Behnken试验设计,构建采空区氧化升温带宽度在3因素、3水平条件下的二次回归响应曲面模型,并对不同条件下采空区氧化升温带宽度进行预测与分析。结果表明:二次回归方程P值为0.001 6,预测模型显著,模型的失拟项为0.606 3,不显著,回归方程具有统计学意义;当供风量为1 500~2 000 m3/min,低抽流量为450~650 m3/min,高抽流量为100~200 m3/min时,对氧化升温带宽度一次项重要度排序为C（高抽巷抽采流量）>A（供风量）>B（低抽巷抽采流量）,二次项重要度排序为AC（供风量和高抽巷抽采流量）>AB（供风量和低抽巷抽采流量）>BC（低抽巷抽采流量和高抽巷抽采流量）,且AB,AC,BC之间均无交互作用。     

对氯气校正法测定高氯废水化学需氧量的方法研究

氯气校正法(HJ/T70-2001)是测定高氯废水化学需氧量的国标方法,为了减少样品测定过程带来的环境污染,研究在不改变HJ/T70-2001氧化体系及测试条件的情况下,将取样体积由20 mL减半为10 mL,试剂的使用量相应减半,对方法的检出限、相对误差、相对标准偏差等指标进行验证。结果表明,该方法的检出限符合要求,准确度较高,精密度较好,可用于高氯废水化学需氧量的测定。     

地表水环境遥感监测关键技术与系统

介绍了地表水环境遥感监测的关键技术与系统及其典型应用,其代表性机理模型和应用示范成果主要来自于中国科学院遥感与数字地球研究所的高光谱遥感团队在最近几年中取得的一些研究进展,主要包括建立了基于改进双峰法的水体分布自动化遥感提取方法,实现了简单、高效和高精度的水体提取;提出了大型湖泊长时序水量估算方法,并以青藏高原湖区为例,重建了典型湖泊面积、水位和水量序列;发展了基于“软分类”的典型内陆水体叶绿素a浓度反演方法,构建了基于生物光学模型的高度浑浊水体悬浮物浓度遥感反演半解析方法,提高了反演方法的区域和季节适用性;构建了基于水色指数的大范围湖库营养状态和透明度遥感监测方法,实现了全球大型湖库营养状态遥感监测,以及全国大型湖库透明度遥感监测;在此基础上,开发了地表水环境遥感监测系统,提高了水环境遥感监测效率,促进了卫星遥感在水环境监测中的高精度业务化应用。     

关于植物中氟化物测定结果的计算

针对植物中氟化物测定时由于绘制校准曲线的标准溶液体积与分析样品的定容体积不一样而引出的结果计算时的某些问题,提出了正确的计算方法和建议。     

Identification of Odor Causing Compounds in a Commercial Dairy Farm

The odorous air emissions from confined animal feeding operations (CAFOs), such as swine, poultry and dairy farms, are increasingly raising community complaints. Odorous emissions can result in health damages, psychological discomforts and adverse aesthetic effects in the community. However, these emissions are not well characterized up to now due to the lack of legislation, the limitations in sampling and instrumentation techniques, and the complexity of the emissions themselves. This study is aimed at the development of a high volume sampler and sorbent assembly to identify the odor causing compounds from a diary CAFO. The sorbent was custom designed to target the potential compounds that may exist in a dairy farm and was validated in laboratory with a synthetic odor from the swine manure. The actual samples at the diary farm were collected in spring and summer of 2005. The sorbents were solvent extracted and individual odor compounds were identified using GC–MS (gas chromatography–mass spectroscopy). The data obtained indicated that high volume sampling can shorten the sampling time from days to within 4 h. Both volatile organic compounds (VOCs) and volatile fatty acids (VFAs) have been identified from the dairy farm, such as phenol, methylphenol, 4-ethyl phenol, indole, methyl indole, benzyl alcohol, hexanoic acid, valeric acid and iso-valeric acid, together with some nitrogen containing compounds that have not been reported before.     

DPX快速萃取程序升温大体积进样GC/MS法测定水中19种多溴联苯化合物

建立DPX快速吸附萃取、程序升温(PTV)大体积进样与气相色谱/质谱(GC/MS)联用,SIM模式同时测定水中19种多溴联苯(PBBs)单体的方法。该方法在PBBs质量浓度1~50μg/L范围内线性良好,19种PBBs单体检出限为0.147~0.230μg/L,相对标准偏差为6.61%~10.5%,加标回收率为61.5%~82.6%。     

生物滴滤塔处理模拟甲硫醚废气

在常温条件下,采用生物滴滤塔处理模拟甲硫醚废气,考察了气体空床停留时间(EBRT)、容积负荷、喷淋密度及营养液pH对生物滴滤塔性能的影响。实验结果表明:当EBRT为90 s、进气甲硫醚质量浓度为150 mg/m~3、喷淋密度为0.65 m~3/(m~2·h),营养液pH为6.8时,甲硫醚去除率为90%;容积负荷高于15 g/(m~3·h)时,对生物滴滤塔的性能产生抑制作用;EBRT为90 s及60 s时,最佳喷淋密度分别为0.56~0.65 m~3/(m~2·h)及0.65~0.75 m~3/(m~2·h);降解甲硫醚的微生物对pH的变化较敏感,最适营养液pH为6~7。     

成都市餐厨垃圾产量分析预测及监管体系建设研究

整理汇总了成都市中心城区及郊县餐厨垃圾产生和收运现状,对其产量作出预测;在此基础上提出适合成都市自身情况的餐厨垃圾监管体系构建设想。     

Chromium speciation in river sediment pore water contaminated by tannery effluent

Cr(VI) is far more soluble and toxic than Cr(III). Sediment pore water was investigated in a river adjacent to the property of a large former tannery, into which Cr-contaminated effluent was discharged over a 55-year period, and where extremely high Cr concentrations have been found in the sediments. Dialysis cells, or peepers, were used to generate depth profiles of Cr concentration in sediment pore water. Samples were analyzed for total Cr using inductively coupled plasma-mass spectrometry (ICP-MS) and for Cr species using high performance liquid chromatography (HPLC)-ICP-MS. The results show an absence of Cr(VI) in all samples. Furthermore, incomplete recovery of Cr(VI) added to the samples collected at the locations with highest sediment Cr concentrations indicate strong reducing conditions at those locations, which are not conducive to the presence of Cr(VI).