模拟环境传热性能试验室的研制

试验室由室外、室内构成,外室由空气处理机组模拟户外气候环境,内室配置温度、湿度、风速、热流计等传感器,测量由模拟空气调节器发出的热量,以对流和辐射的方式通过被测件传递到室外的能力。适用欧标、美标和国标试验要求。试验室用于测试各种部件和整体构件的环境传热性能,以减少空调能耗,提高节能水平。     

基于热红外遥感数据和光谱混合分解模型的城市不透水面估算

不透水面的迅速增长是城市化的显著特征之一,针对大范围的城市监测,运用遥感技术迅速提取城市不透水面是当前国内外研究的热点。论文选用Landsat 7的ETM+影像,基于光谱混合分解模型,结合热红外遥感数据反演生成的地表温度,研究杭州市的不透水面分布信息的提取。通过高、低反照率、植被及土壤4类光谱端元的线性组合来表征不同城市土地类型,并利用地表温度和土壤分量分别剔除高、低反照率分量中的"噪声",综合修正后的高反照率分量和低反照率分量估算杭州市不透水面分布。结果显示,研究区中均方根误差的平均值为0.003 6,不透水面分布结果与同期Google earth上的高分辨率影像和SPOT 4影像的解译结果对比分析,绝大多数样本的估算值与解译值之差落在±0.15区间内,精度令人满意。研究表明,热红外遥感数据和光谱混合分解模型相结合,可以实现对不透水面进行快速、精确的估算。     

汞污染土壤热解吸处理过程中不同形态汞的温度效应

选择贵州省具有代表性的汞污染土壤样品进行热解吸修复的试验研究,同时采用连续化学浸提法对土壤样品中5种形态的汞分别进行提取,探究了不同形态汞在热解吸修复过程中的浓度变化和转化规律. 结果表明,土壤样品中各形态汞所占比例为w(王水溶汞)(占76.52%)>w(酸溶汞)(占22.40%)>w(硝酸溶汞)(占0.87%)>w(水溶性汞)(占0.14%)>w(碱溶汞)(占0.06%). w(王水溶汞)与w(Σ汞)(各形态汞总量)的相关系数可达0.978 1. 升温过程中,w(酸溶汞)和w(王水溶汞)明显降低,而其余形态汞含量则呈先升后降的趋势. 采用热解吸技术可以有效处理汞污染土壤,在370 ℃条件下能够将土壤中w(Σ汞)降至1 mg/kg以下,处理率可达95.73%,处理后土壤中的汞以残渣态汞为主,环境风险较小.      

火电厂炉内喷钙法烟气脱硫改造实践

采用石灰石-石膏湿法脱硫工艺对1×350 MW燃煤电厂原有炉内喷钙尾部增湿脱硫工艺进行改造,改造后运行表明:脱硫效率!95%,确保在常用煤种情况下二氧化硫排放浓度≤100 mg/m3,同时年运行费用相对改造前直接降低数百万元,实现了环境效益和经济效益的双赢。     

有机物污染土壤热脱附技术研究与应用

介绍了热脱附技术原理、特点和适用范围,对传统热脱附技术滚筒式热脱附和流化床式热脱附、微波热脱附、远红外线热脱附等新兴热脱附技术的发展现状进行了总结和评价,还探讨了热脱附技术存在的问题和发展方向。     

煤氧化阻化过程中的热特性研究

化学阻燃剂通过化学作用破坏或降低煤分子中活化能较低易被氧化的活性基团,使煤自燃链式反应中断难以达到自燃。为研究煤氧化阻化过程中的热特性变化,通过煤的热重实验,从微观角度研究了次磷酸盐在煤自燃氧化过程中对其表面官能团的影响,分析了阻化剂添加前后的热特性曲线和特征温度,研究了不同升温速率及不同粒径下阻化煤样的热特性变化规律。结果显示:随升温速率的增大和煤样粒径的减小,热特性曲线及特征温度均出现向后推移,特征温度出现不同程度的升高。     

基于详细化学动力学的甲烷热着火影响因素分析

利用化学动力学软件CHEMKIN4.1,在不同初始温度、浓度、湿度和压强下,对甲烷热着火进行了详细化学动力学 模拟。通过对主要组分摩尔浓度分析和温度敏感性分析,得到了甲烷热着火过程的主要基元反应和引发热着火发生的主 要原因。通过对甲烷热着火的延迟时间、热着火发生后主要生成物摩尔浓度和反应后的温度的对比分析,揭示了初始浓 度、湿度和压强对甲烷热着火的影响规律。本研究可以为甲烷为主的气体如瓦斯、天然气等可燃气体的燃烧和爆炸提供 理论支撑,从而有效利用这些可燃气体,降低灾害的发生。     

Degradation of carbon tetrachloride in thermally activated persulfate system in the presence of formic acid

The thermally activated persulfate (PS) degradation of carbon tetrachloride (CT) in the presence of formic acid (FA) was investigated. The results indicated that CT degradation followed a zero order kinetic model, and CO ₂ ^– · was responsible for the degradation of CT confirmed by radical scavenger tests. CT degradation rate increased with increasing PS or FA dosage, and the initial CT had no effect on CT degradation rate. However, the initial solution pH had effect on the degradation of CT, and the best CT degradation occurred at initial pH 6. Cl^– had a negative effect on CT degradation, and high concentration of Cl^– displayed much strong inhibition. Ten mmol·L^–1HCO ₃ ^– promoted CT degradation, while 100 mmol·L^–1NO ₃ ^– inhibited the degradation of CT, but SO ₄ ^2– promoted CT degradation in the presence of FA. The measured Cl–concentration released into solution along with CT degradation was 75.8% of the total theoretical dechlorination yield, but no chlorinated intermediates were detected. The split of C-Cl was proposed as the possible reaction pathways in CT degradation. In conclusion, this study strongly demonstrated that the thermally activated PS system in the presence of FA is a promising technique in in situ chemical oxidation (ISCO) remediation for CT contaminated site.     

Benzene removal by nano magnetic particles under continuous condition from aqueous solutions

Benzene removal evaluated using Fe304 nano continuous condition. A 44 initial benzene concentration, from aqueous solutions was magnetic particles （NM） in factorial design including NM dose, contact time and pH was investigated in 16 experiments （Taguchi OA design）. The results indicated that all factors were significant and the optimum condition was： pH 8, NM dose of 2000 mg.L-1, benzene concentrations of 100 mg.L-1 and contact time of 14min. The maximum benzene uptake and distribution ratio in the optimum situation were 49.4mg.g-1 and 38.4L.g-1, respectively. The nano particles were shown to capture 98.7% of the benzene in optimum batch condition and 94.5% in continuous condition. The isotherm data proved that the Bmnauer-Emmett-Teller model fit more closely and produced an isotherm constant （b） less than one, indicating favorable adsorption. Regeneration studies verified that the benzene adsorbed by the NM could be easily desorbed by temperature, and thereby, NM can be employed repeatedly in water and wastewater management.     

Variation in humic and fulvic acids during thermal sludge treatment assessed by size fractionation,elementary analysis,and spectroscopic methods

Thermal pretreatment can be applied to sludge anaerobic digestion or dewatering. To analyze the variation in humic substances during thermal sludge treatment, sludge humic and fulvic acids were extracted before and after 30-min thermal treatment at 180℃, and then their contents, molecular weight distributions, elementary compositions, and spectral characteristics were compared. The results showed that the total contents of humic and fulvic acids in the sludge almost remained constant during thermal treatment, but 35% ofhumic and fulvic acids were dissolved from the sludge solids. Moreover, both humic and fulvic acids were partly decomposed and 32% of humic acids were converted to fulvic acids. The median value of the molecular weights of humic acids decreased from 81 to 41 kDa and that of fulvic acids decreased from 15 to 2 kDa. Besides the reduction in molecular size, the chemical structures of humic and fulvic acids also exhibited a slight change, i.e. some oxygen functional groups disappeared and aromatic structures increased after thermal sludge treatment.