非定态SO2制酸工艺在铅精矿烧结烟气治理中的应用

介绍了非定态SO2制酸工艺的特点、流程及其在铅精矿烧结烟气治理中的应用效果。该工艺具有良好的社会效益、环境效益和较好的经济效益，具有较高的推广应用价值。     

Human exposure and health risk of alpha-, beta-, gamma- and delta-hexachlorocyclohexane (HCHs) in Tianjin, China

The dynamic exposures to HCHs of individuals born between the years 1913 and 1993 in Tianjin have been simulated by connecting a fugacity model (IV) with a multimedia exposure model. Ingestion is the most important pathway for human beings to take up HCHs, and concentrations in the human body correlate with body weight changes. Accumulations of HCHs were derived assuming that the degradation in human body behaved linearly. The health risk of exposure to HCHs was measured using cancer risk and loss of life expectancy (LLE), and LLE was modified from its original definition to incorporate a dynamic calculation that takes variances in exposure into account. Monte-Carlo simulations were run to analyze the uncertainties of the model.     

建筑陶瓷行业SO2污染物评价及总量控制实用方法

采用高斯点源模型对建陶生产造成的SO2地面浓度增量进行计算.利用比例下降模型计算建陶业的SO2允许排放总量,并根据企业的设备生产能力进行了总量分配,在方法上具有较强的可操作性,计算结果表明,可有效降低所在地区的SO2地面浓度.     

DO和pH值在短程硝化中的作用

在SBR反应器中对DO和pH值在短程硝化和半亚硝化过程中的作用进行试验研究,结果表明,控制低DO和适宜的pH值在短程硝化过程中起着重要的作用.本试验条件下,当DO为0.5～1.0 mg/L、pH值为7.5～8.0时,在SBR反应器中很容易实现短程硝化;当DO＞0.3 mg/L时,DO越低,出水NO2--N积累率越高;当pH值＞6.8时,不会影响系统NO2--N积累的稳定性.另外,研究结果还表明,通过控制DO和pH值可以实现半亚硝化.本试验条件下,当进水氨氮浓度为120 mg/L时,控制DO为0.3～0.4 mg/L可实现出水半亚硝化;当进水氨氮浓度为200 mg/L时,控制DO为0.5～0.6 mg/L或pH值为6.8也可以实现出水半亚硝化.     

以pH和ORP作为脉冲SBR工艺的实时控制参数

为了实现脉冲SBR深度脱氮的实时控制，以某污水处理厂市政污水为处理对象，考察了脉冲SBR在深度脱氮过程中pH及ORP的变化规律。试验结果表明，pH及ORP的变化规律与脉冲SBR有机物去除、硝化与反硝化过程存在较好的相关关系。可以根据pH和ORP变化曲线上的特征点对脉冲SBR进行实时控制。并考察了污水C／N（COD／NH4^＋-N）对pH及ORP的变化规律的影响。在硝化过程中，C／N对pH及ORP曲线变化点的出现没有影响；在反硝化过程中，应结合pH值“硝酸盐峰”和ORP“硝酸盐膝”来判断低C／N污水反硝化的终点。在该试验中，出水TN低于2mg／L，TN去除率可达到96％以上。     

秸秆成型燃料锅炉污染物排放规律试验研究

根据锅炉烟尘测试方法(GB 5468-91)及锅炉大气污染物排放标准(GB 13271-2001),在不同风门的工况下,分别对设计的双层炉排秸秆成型燃料锅炉污染物排放规律进行试验.试验表明,在较好工况下,双层炉排锅炉排烟中CO等中间产物及烟尘含量低于单层炉排锅炉,其排烟中CO、NOx、SO2和烟尘浓度等指标远远低于燃煤锅炉,符合国家关于工业锅炉大气污染物排放标准要求,有较好环保效益.     

Coupled production and transport of selenium vapor in unsaturated soil: evaluation by experiments and numerical simulation

Volatilization of selenium (Se) from soil to the atmosphere involves several sequential chemical reactions that form volatile Se species, followed by transport of the gaseous Se through the soil. This paper describes a numerical model that simulates the chemical and physical processes governing the production and transport of Se vapor in unsaturated soil. The model couples the four Se species involved in the production of Se vapor through chemical reactions, and allows each to migrate through the soil by advection, liquid or vapor diffusion depending on its affinity for the dissolved or vapor phase. The coupled transformations and transport of the four Se species, i.e., selenate, selenite, elemental and organic Se, and Se vapor, were calculated based on the Crank-Nicolson finite difference method. The model was used to analyze fluxes of Se vapor measured from a soil amended with inorganic Se in the form of selenate and covered with unamended clean soil of various thicknesses. Evolution of Se vapor from the soil was very fast, with measurable amounts of Se detected within 24 h. The peak of Se volatilization, detected at the 6th day, reached 3.31 Se microgram/day for the uncovered soil, but was reduced to near the detection limit (0.05 microgram/day) in the presence of a 8- or 16-cm clean soil cover. With two reaction rate coefficients fitted to the data, the model described Se volatilization very well. The estimated rate coefficient of Se methylation was unexpectedly high, with a value of 0.167/day. The net volatilization of Se, however, was severely inhibited by the fast demethylation, i.e., the reverse reaction which converted volatile Se species back into nonvolatile forms. As a result, Se vapor only penetrated a few centimeters in the soil. The demethylation rate coefficient, assessed by independent transport experiments using dimethyl selenide, was estimated as 186.8/day, corresponding to a half-life of only 5.3 min for Se vapor. Results of this study indicated that rapid demethylation of Se vapor during its diffusive transport through a soil is probably an important limiting factor in the volatilization of Se under natural conditions.     

排污收费对企业污染控制技术创新激励作用的研究

运用模型方法研究了排污收费和行政手段对企业污染控制技术创新的激励作用,为环境管理政策应用提供了理论依据。结果表明,无论对创新企业还是模拟企业,在“技术创新－创新扩散－最优啮合反应”的技术创新过程中,排污收费更能刺激企业的污染控制技术创新行为。     

酸雨对污染环境中重金属化学行为的影响

综述了酸雨对污染环境中重金属化学行为的影响。在酸雨作用下 ,不同环境介质中重金属活性明显增强 ,化学形态转化明显 ,迁移能力和生态危害能力亦明显加强。探讨了控制酸雨发生、重金属污染环境修复技术以及开展复合污染环境化学风险评价的必要性     

Investigation on mechanism of phosphate removal on carbonized sludge adsorbent

For the removal of phosphate (PO₄^3 -) from water, an adsorbent was prepared via carbonization of sewage sludge from a wastewater treatment plant: carbonized sludge adsorbent (CSA). The mechanism of phosphate removal was determined after studying the structure and chemical properties of the CSA and its influence on phosphate removal. The results demonstrate that phosphate adsorption by the CSA can be fitted with the pseudo second-order kinetics and Langmuir isotherm models, indicating that the adsorption is single molecular layer adsorption dominated by chemical reaction. The active sites binding phosphate on the surface are composed of mineral particles containing Si/Ca/Al/Fe. The mineral containing Ca, calcite, is the main factor responsible for phosphate removal. The phosphate removal mechanism is a complex process including crystallization via the interaction between Ca^2 + and PO₄^3 -; formation of precipitates of Ca^2 +, Al^3 +, and PO₄^3 -; and adsorption of PO₄^3 - on some recalcitrant oxides composed of Si/Al/Fe.