重庆村镇住宅热湿环境现状及评价

通过对重庆地区村镇住宅的实地调研和村镇典型住宅温湿度连续监测,获得了重庆地区村镇住宅的主要围护结构形式以及典型房屋2010年1～9月的室内热湿环境状况，并利用重庆地区自然通风适应性热舒适性评价模型进行了分析。结果表明：现有墙体热工性能最好的是180红砖内外水泥砂浆抹灰外贴瓷砖形式，测试房屋冬季室内最低温度为83℃，最高相对湿度为962%，夏季室内最高温度为344℃，最高相对湿度为99%。监测数据中相对湿度大于70%的时数占总测试时数的93%。住宅围护结构的冷热抵御能力和湿舒适湿卫生条件都很差。采暖季节室内达到舒适只有2 d，空调季节有58 d，村镇地区围护结构冬季保温要求比夏季隔热显得更为突出     

环丁砜-哌嗪溶液吸收烟道气中二氧化碳

采用搅拌实验装置,研究环丁砜溶液及不同配比的环丁砜-PZ复合溶液对烟道气中二氧化碳的吸收和解吸性能,揭示了吸收容量与酸碱度、时间之间的内在联系,并对CO2初始逸出温度、试液再生温度、试液再生率、再生pH下降率进行了细致记录分析。实验结果表明,环丁砜-PZ复合溶液配比为0.4∶0.6时:吸收效果最佳,吸收量约为0.126 mol;再生温度最高,为105℃;再生率最高,为90.34%。同时与相同配比的MEA、DEA相比具有较大再生优势。实验结果还表明,环丁砜-PZ复合体系之间存在负交互作用。     

旋转填料床/柠檬酸盐法吸收-解吸SO2

提出采用旋转填料床结合柠檬酸盐法脱除烟气中SO2的方法,考察了旋转填料床转子转速、液气比、初始柠檬酸根浓度和初始pH值等因素对脱硫效率的影响。结果表明,采用超重力法超重机转子转速为1 000 r/min、液气比为7L/m3、初始柠檬酸根浓度为1.5 mol/L、吸收液的初始pH值为5.0,脱硫效率稳定在99%左右。研究了水蒸气汽提法解吸SO2时初始柠檬酸根浓度、初始pH值、SO2浓度、富液流量和水蒸气流量对解吸效率的影响,得出了影响SO2解吸率的基本规律,并进行了分析。通过实验证明该方法在技术上是可行的,具有良好的应用前景。     

热解吸对土壤中POPs农药的去除及土壤理化性质的影响

为探索土壤热解吸修复技术对POPs污染土壤的修复效果及修复后土壤可耕作性,选择北京某农药厂旧址的POPs农药污染土壤,研究了不同温度下热解吸处理后土壤中滴滴涕(DDTs)和六六六(HCHs)各组分的去除率以及土壤理化性质的变化。结果表明,热解吸修复技术可有效去除土壤中POPs农药,其中,p,p’-DDE与α-HCH组分去除率受热解吸温度的影响比其他组分更为明显。∑HCH与∑DDT在310℃、340℃时分别达到97%、99%的去除率,且此时土壤中的污染物含量低于我国《展览会用地土壤环境质量评价标准》,此后去除率受温度的影响不明显。热解吸温度对修复后土壤的理化性质有一定的影响,不同温度影响的程度各不相同,其中,有机质含量与全氮含量分别由0.78%、0.0352%降至0.14%、0.0107%;pH波动幅度较小,由7.80变至8.25;阳离子交换量变化存在波动,但呈整体下降趋势,由7.87 mg/kg降至5.00mg/kg;土壤中速效磷显著增加,由7.59 mg/kg升至21.8 mg/kg。而在最优温度条件下,土壤理化性质受热解吸温度的影响较小。由此可以说明,热解吸技术可以用于POPs污染土壤的修复,选择适当的热解吸温度对土壤的可耕作性影响有限,因而是一种潜在的绿色修复技术。     

Sorption and Desorption Behavior of Chloroanilines and Chlorophenols on Montmorillonite and Kaolinite

The bioavailability of pollutants, pesticides and/or their degradation products in soil depends on the strength of their sorption by the different soil components, particularly by the clay minerals. This study reports the sorption-desorption behavior of the environmentally hazardous industrial pollutants and certain pesticides degradation products, 3-chloroaniline, 3,4-dichloroaniline, 2,4,6-trichloroaniline, 4-chlorophenol, 2,4-dichlorophenol and 2,4,6-trichlorophenol on the reference clays kaolinite KGa-1 and Na-montmorillonite SWy-l. In batch studies, 2.0 g of clay were equilibrated with 100.0 mL solutions of each chemical at concentrations ranging from 10.0 to 200.0 mg/L. The uptake of the compounds was deduced from the results of HPLC-UV-Vis analysis. The lipophilic species were best retained by both clay materials. The most lipophilic chemical used in the study, 2,4,6-trichloroaniline, was also the most strongly retained, with sorption of up to 8 mg/g. In desorption experiments, which also relied on HPLC-UV-Vis technique, 2,4,6-trichloroaniline was the least desorbed from montmorillonite. However, on kaolinite all of the compounds under study were irreversibly retained. The experimental data have been modelled according to the Langmuir and Freundlich isotherms. A hypothesis is proposed concerning the sorption mechanism and potential applications of the findings in remediation strategies have been suggested.     

Sorption and desorption kinetics of diuron,fluometuron, prometryn and pyrithiobac sodium in soils

Abstract

The sorption and desorption characteristics of four herbicides (diuron, fluometuron, prometryn and pyrithiobac‐sodium) in three different cotton growing soils of Australia was investigated. Kinetics and equilibrium sorption and desorption isotherms were determined using the batch equilibrium technique. Sorption was rapid (> 80% in 2 h) and sorption equilibrium was achieved within a short period of time (ca 4 h) for all herbicides. Sorption isotherms of the four herbicides were described by Freundlich equation with an r² value > 0.98. The herbicide sorption as measured by the distribution coefficient (K_d) values ranged from 3.24 to 5.71 L/kg for diuron, 0.44 to 1.13 L/kg for fluometuron, 1.78 to 6.04 L/kg for prometryn and 0.22 to 0.59 L/kg for pyrithiobac‐sodium. Sorption of herbicides was higher in the Moree soil than in Narrabri and Wee Waa soils. When the K_d values were normalised to organic carbon content of the soils (K_oC), it suggested that the affinity of the herbicides to the organic carbon increased in the order: pyrithiobac‐sodium < fluometuron < prometryn < diuron. The desorption isotherms were also adequately described by the Freundlich equation. For desorption, all herbicides exhibited hysteresis and the hysteresis was stronger for highly sorbed herbicides (diuron and prometryn) than the weakly sorbed herbicides (fluometuron and pyrithiobac‐sodium). Hysteresis was also quantified as the percentage of sorbed herbicides which is not released during the desorption step ω = [n_ad / n_de ‐1] x 100). Soil type and initial concentration had significant effect on ω. The effect of sorption and desorption properties of these four herbicides on the off‐site transport to contaminate surface and groundwater are also discussed in this paper.     

A new direct thermal desorption-GC/MS method: Organic speciation of ambient particulate matter collected in Golden, BC

Particulate matter having an aerodynamic diameter less than 2.5 μm (PM2.5) is thought to be implicated in a number of medical conditions, including cancer, rheumatoid arthritis, heart attack, and aging. However, very little chemical speciation data is available for the organic fraction of ambient aerosols. A new direct thermal desorption-gas chromatography/mass spectrometry (TD-GC/MS) method was developed for the analysis of the organic fraction of PM2.5. Samples were collected in Golden, British Columbia, over a 15-month period. n-Alkanes constituted 33–98% by mass of the organic compounds identified. PAHs accounted for 1–65% and biomarkers (hopanes and steranes) 1–8% of the organic mass. Annual mean concentrations were: n-alkanes (0.07–1.55 ng m⁻³), 16 PAHs (0.02–1.83 ng m⁻³), and biomarkers (0.02–0.18 ng m⁻³). Daily levels of these organics were 4.89–74.38 ng m⁻³, 0.27–100.24 ng m⁻³, 0.14–4.39 ng m⁻³, respectively. Ratios of organic carbon to elemental carbon (OC/EC) and trends over time were similar to those observed for PM2.5. There was no clear seasonal variation in the distribution of petroleum biomarkers, but elevated levels of other organic species were observed during the winter. Strong correlations between PAHs and EC, and between petroleum biomarkers and EC, suggest a common emission source – most likely motor vehicles and space heating.     

热水解超声组合预处理对污泥厌氧消化产气潜力的影响研究

针对城市污泥厌氧消化由于融胞困难所导致的消解速率低、产气量低等问题,采用热水解与超声组合的方法对污泥进行预处理,考察经预处理后污泥融胞效率的变化及对厌氧消化产气潜力的影响.结果显示,热水解与超声波组合工艺对污泥的破胞作用明显,在30 min热水解与0.53 W/mL超声声能密度组合工艺反应60 min条件下,相对于处理前污泥,预处理后污泥溶解性COD(SCOD)溶出率可提高41.6％,蛋白质增加值达282.7 mg/L,污泥厌氧消化的产气潜力显著增加；30 min热水解分别与0.53、0.33 W/mL超声声能密度组合工艺对污泥破胞效率的差异不大；随着超声时间的延长,在组合预处理工艺前20 min内SCOD的溶出速率较慢,20260 min时溶出速率逐渐提高.试验结果可为城市污泥厌氧消化预处理工艺的选择提供一定的理论依据.     

漓江上游植被覆盖度时空变化对地表热场影响

自20世纪80年代以来，桂林漓江由于上游森林遭受破坏出现水生态环境快速恶化的趋势。地表热场的时空变化直接影响森林蒸散及水文效应。因此，对漓江上游1989~2006年5景TM/ETM+卫星图像，利用归一化植被指数反演植被覆盖度，利用单窗算法反演地表温度，提出归一化温度使不同时相地表热场具有可比性，分析植被覆盖度时空变化对地表热场的影响。结果表明，在空间上，地表温度随植被覆盖度的增加而降低，在植被覆盖度很高或很低时，这种影响相对变弱；在时间上，漓江上游1989~2000年植被中、高度覆盖面积从96.1%逐年下降到65.9%，导致归一化地表温度数值较高的像元比例相应增加；2000~2006年植被中、高度覆盖面积逐渐恢复上升到90.8%，但仍略低于1989年，使得归一化地表温度数值较高的像元比例相应减少。植被覆盖可以有效地降低漓江上游地表温度     

城市污水污泥微波热水解特性研究

在80～170 ℃进行1～30 min的城市污水污泥微波热水解,微波频率2 450 MHz,最大输出功率1 kW,考察挥发性悬浮固体(VSS)和悬浮固体(SS)溶解率,污泥上清液COD和TOC浓度、污泥粒径、形态变化和碳氢氮含量等污泥热水解特征,分析污泥离心脱水性能的改善和减量化效果.结果表明,微波加热使污泥有机物水解反应快速发生,水解过程受温度影响显著.热水解5 min时,150℃和170℃的VSS溶解率为15.8%和29.4%;10 min时COD溶解率达到19.07%和25.75%,COD和TOC浓度在170℃分别为9 860.0 mg/L和2 949.70 mg/L.超过5～10 min,VSS和COD水解率增加缓慢.通过扫描电镜(SEM)观察到污泥热水解后菌体细胞破裂.与碳和氢相比,污泥中氮的水解率更高,170℃微波热水解5 min氮的水解率达到67%.150℃和170℃热水解10 min离心脱水污泥含水率降低到73.1%和65.5%,脱水性能改善,相应减量化率为33.9%和51.7%.