Degradation of nitrobenzene in wastewater by γ-ray irradiation

The degradation of nitrobenzene(NB) by γ-ray irradiation was studied. The influences of dose rate and initial NB concentration were investigated in details. At a dose rate of 55 Gy/min, the degradation kinetics was pseudo-first-order at NB concentrations from 0.2 mmol/L to 4.0 mmol/L. At an initial NB concentration of 0.8 mmol/L, the degradation of NB at various dose rates also followed pseudo-first-order kinetics. Dissolved oxygen was found to have a positive effect on NB degradation. The degradation products were identified as nitrophenol, nitrosobenzene, and hydroquinone, and so on. Based on the product analysis, possible degradation pathways of nitrobenzene were proposed.     

Microwave-assisted regeneration of hypercrosslinked polymeric adsorbent saturated with nitrophenols

Thermal regeneration ofhypercrosslinked polymeric adsorbent （HPA） was performed at 67℃. Experiments were carried out using a multimode microwave oven operating at 2450 MHz and a thermostatic water bath so as to compare the effect of the different heating mechanisms on the regeneration efficiency of the HPA saturated with nitrophenols. The temperature rise action of the heterogeneous regeneration system under microwave irradiation was described. Additionally, a complete structure and chemical characterization of the regenerated HPA was also carried out in order to study the influence of the subsequent regeneration cycles on the structure and the adsorption capacities of the adsorbents. Structure characterization of the regenerated HPA was accomplished by means of the analysis of FTIR spectra.     

影响平板式太阳能热水器热效率诸因素的研究

本文根据辐射传热和对流传热理论,利用Ｍａｔｌａｂ 程序结合太阳能热水器本身的尺寸以及与其有关的水和空气的物理弹性详细分析了影响平板式太阳能热水器热效率的因素包括太阳能热水器表面的太阳光辐射的吸收率αｓ 和辐射系数ε,太阳能热水器的水进口温度Ｔｃ,ｉｎ和流量ｍｃ 太阳辐射能力Ｇｓ,,环境大气温度Ｔｅ,大气辐射系数εｓｋｙ 以及太阳能热水器内部的总传热系数Ｕ。分析结果表明较高的太阳照射能力、环境温度和总传热系数有利于提高集热效率,而增加水量和水进口温度、热水器辐射系数和大气辐射系数则有相反的效果。     

垃圾渗沥液中有机污染物的超声去除

采用超声辐照技术去除垃圾渗沥液中的有机污染物。研究了输入电功率、初始浓度、初始pH、曝气对垃圾渗沥液中COD的超声去除效果影响,探讨了垃圾渗沥液中有机物的超声去除主要是通过羟自由基的氧化反应,高温热解反应虽然存在,但贡献相对很小。超声去除垃圾渗沥液中COD的动力学模式不能简单用动力学原理来解释,一方面由于超声降解有机物的机理和垃圾渗沥液中有机物的种类都很复杂,另一方面由于基于K2Cr2O7法测定出的COD指标不能完全表征超声去除垃圾渗沥液中有机污染物的程度。     

环境辐射有关问题的讨论

本文论述了与环境辐射有关的问题。根据其剂量当量和危险水平,讨论了公众剂量限值的实践性     

兰州市大气TSP中28种元素的测定与变化规律的研究

报导了兰州市一年内大气中TSP内的28种元素含量的监测结果,污染程度和变化规律.为兰州市进一步加强环境管理和治理,不断改善环境质量提供科学依据.     

微波辐照法再生载硫活性炭的研究

用活性炭对低浓度SO2气体进行物理吸附，饱和后用微波辐照解吸。结果显示，载硫活性炭在微波场中升温很快，210s能达到温度最大值；吸附在活性炭上的S02气体在570s以后基本解吸完全；解吸产物SO2气体的体积分数最高可达25％以上；微波功率和载气量对再生后活性炭的质量损耗影响较大，在微波功率为300w和载气量为0．06m^3／h条件下，活性炭的质量损耗约为6．21％。     

Decomposition of aqueous chlorinated contaminants by UV irradiation with H2O2

In the present study, the decomposition rates of carbon tetrachloride (CCl₄) and 2,4-dichlorophenol (2,4-DCP) in water by the ultraviolet (UV) light irradiation alone and H₂O₂/UV were experimentally investigated. The detailed experimental studies have been conducted for examining treatment capacities of the two different ultraviolet light sources (low and medium pressure Hg arc) in H₂O₂/UV processes. The low or medium UV lamp alone resulted in a 60%–90% decomposition of 2,4-DCP while a slight addition of H₂O₂ resulted in a drastic enhancement of the 2,4-DCP decomposition rate. The decomposition rate of 2,4-DCP with the medium pressure UV lamp alone was about 3–6 times greater than the low pressure UV lamp alone. In the direct photolysis of aqueous CCl₄, the medium pressure UV lamp had advantage over the low pressure UV lamp because the molar extinction coefficient of CCl₄ at shorter wavelength (210–220 nm) is about 20 to 50 times higher than that at 254 nm. However, adding H₂O₂ to the medium pressure UV lamp system rendered a negative oxidation rate because H₂O₂ acted as a UV absorber being competitive with CCl₄ due to negligible reaction between CCl₄ and OH radicals. The results from the present study indicated significant influence of the photochemical properties of the target contaminants on the photochemical treatment characteristics for designing cost-effective UV-based degradation of toxic contaminants.     

Kinetics of microwave-enhanced oxidation of phenol by hydrogen peroxide

Aqueous solutions of phenol were oxidized by hydrogen peroxide assisted by microwave (MW) irradiation. A simple kinetic model for the overall degradation of phenol in the presence of excess H₂O₂ is proposed in which the degradation rate of phenol is expressed as a linear function of the concentrations of phenol and H₂O₂. A detailed parametric study showed that the degradation rate of phenol increased with increasing [H₂O₂] until saturation was observed. Phenol degradation followed apparent zero-order kinetics under MW radiation or H₂O₂ oxidation. However, after 90 min of irradiation, the observed kinetics shifted to pseudo first order. The overall reaction rates were significantly enhanced in the combined MW/H₂O₂ system, mainly because microwave could accelerate H₂O₂ to generate hydroxyl radical (^·OH) and other reactive oxygen intermediates. The observed synergetic effects of the MW/H₂O₂ process resulted in an increased in the net reaction rate by a factor of 5.75. When hydrogen peroxide is present in a large stoichiometric excess, the time required to achieve complete mineralization is reduced significantly.     

类脂/醋酸纤维素复合吸附材料的制备与性能

采用相转化法将类脂包埋到醋酸纤维素(CA)中,制备出了具有对水中低剂量亲脂性有机污染物高效吸附去除的平板膜.以扫描电子显微镜观察了复合材料的结构形貌和表面特征.利用机械搅拌方式和超声方式对类脂进行分散的实验表明,超声对类脂的均匀分散具有强化作用.同时考察了铸膜温度(室温、0℃)对类脂分散的效果,表明低温有助于形成小的脂滴.另外,通过复合膜的红外谱图证实,类脂和CA属于物理混合,不会改变类脂的分子结构,从而不会影响类脂对亲脂性有机污染物的吸附性能.通过荧光分析法分析复合膜在正己烷溶剂中的稳定情况,表明类脂已被完好地包埋到膜中,因而在去除有机污染物的过程中不会从复合膜中渗出.