发酵液作为EBPR碳源的动力学模拟

发酵液是一种优质的碳源,能够提高生物除磷系统(EBPR)的除磷效果.采用基于碳源代谢的修正ASM2模型,能够较好地模拟发酵液作为EBPR碳源的动力学变化规律.发酵液作为EBPR唯一碳源时,系统中的异养菌不仅不对聚磷菌(PAO)的生长构成竞争关系,反而促进PAO的生长.发酵液作为实际污水的补充碳源时,优化了污水中的碳源组成,创造了有利于聚磷菌生长的环境,使EBPR中聚磷菌达到微生物总量的40%以上,比实际污水作为碳源的EBPR中的PAO含量提高了3.3倍.     

基于废陶瓷的多孔陶瓷研制及其对Ni2+的吸附性能

通过SEM、XRD、FT-IR表征及多孔陶瓷对废水中镍的去除能力,确定多孔陶瓷的制备条件:原料中田菁粉掺杂质量分数为4%,焙烧温度为800℃.SEM和孔结构表征说明,焙烧使多孔陶瓷形貌、结构发生变化;随着焙烧温度的升高,多孔陶瓷的比表面积和孔容呈现降低的趋势,而孔径呈现增大的趋势;EDS分析能表明,原废瓷粉和多孔陶瓷的主要元素组成均为Si、Al、O.SEM、XRD和FT-IR分析表明,多孔陶瓷吸附前后结构稳定.吸附Ni2+的系列实验表明,多孔陶瓷用量为10 g·L-1,吸附时间为60 min,进水pH值为6.32,进水Ni2+浓度在100 mg.L-1以内.在此条件下废水的Ni2+去除率可达89.7%,多孔陶瓷对废水中镍有较好的去除效果.以制备的多孔陶瓷处理含镍废水,考察多孔陶瓷对废水中Ni2+的吸附动力学和吸附等温线,结果表明,多孔陶瓷对Ni2+的吸附过程符合准二阶动力学模型(R2=0.999 9),Qe为9.09 mg·g-1;吸附过程可用Freundlich方程和Langmuir方程来描述,温度由20℃升高至40℃,最大吸附量Qm由14.49 mg·g-1上升至15.38 mg·g-1.     

Investigation of acetylated kapok fibers on the sorption of oil in water

Kapok fibers have been acetylated for oil spill cleanup in the aqueous environment. The structures of raw and acetylated kapok fiber were characterized using Fourier transform infrared (FT-IR) spectroscopy and scanning electron microscopy (SEM). Without severe damage to the lumen structures, the kapok fibers were successfully acetylated and the resulting fibers exhibited a better oil sorption capacity than raw fibers for diesel and soybean oil. Compared with high viscosity soybean oil, low viscosity diesel shows a better affinity to the surface of acetylated fibers. Sorption kinetics is fitted well by the pseudo second-order model, and the equilibrium data can be described by the Freundlich isotherm model. The results implied that acetylated kapok fiber can be used as the substitute for non-biodegradable oil sorption materials.     

Pb(II) removal from water using Fe-coated bamboo charcoal with the assistance of microwaves

Bamboo charcoal(BC) was used as starting material to prepare iron-modified bamboo charcoal(Fe-MBC) by its impregnation in FeCl 3 and HNO 3 solutions simultaneously,followed by microwave heating.The material can be used as an adsorbent for Pb(Ⅱ) contaminants removal in water.The composites were prepared with Fe molar concentration of 0.5,1.0 and 2.0 mol/L and characterized by means of N 2 adsorption-desorption isotherms,X-ray diffraction spectroscopy(XRD),scanning electron microscopy coupled with energy dispersive X-ray spectrometry(SEM-EDS),Fourier transform infrared(FT-IR) and point of zero charge(pH pzc) measurements.Nitrogen adsorption analyses showed that the BET specific surface area and total pore volume increased with iron impregnation.The adsorbent with Fe molar concentration of 2 mol/L(2Fe-MBC) exhibited the highest surface area and produced the best pore structure.The Pb(Ⅱ) adsorption process of 2Fe-MBC and BC were evaluated in batch experiments and 2Fe-MBC showed an excellent adsorption capability for removal Pb(Ⅱ).The adsorption of Pb(Ⅱ) strongly depended on solution pH,with maximum values at pH 5.0.The ionic strength had a significant effect on the adsorption at pH < 6.0.The adsorption isotherms followed the Langmuir isotherm model well,and the maximum adsorption capacity for Pb(Ⅱ) was 200.38 mg/g for 2Fe-MBC.The adsorption processes were well fitted by a pseudo second-order kinetic model.Thermodynamic parameters showed that the adsorption of Pb(Ⅱ) onto Fe-MBC was feasible,spontaneous,and exothermic under the studied conditions,and the ion exchange mechanism played an significant role.These results have important implications for the design of low-cost and effective adsorbents in the removal of Pb(Ⅱ) from wastewater.     

Photocatalytic degradation of carbofuran in TiO2 aqueous solution：Kinetics using design of experiments and mechanism by HPLC/MS/MS

The photocatalytic degradation kinetics of carbofuran was optimized by central composite design based on response surface methodology for the first time. Three variables, TiO2 concentration, initial pH value and the concentration of carbofuran, were selected to determine the dependence of degradation efficiencies on independent variables. Response surface methodology modeling results indicated that the degradation efficiency of carbofuran was highly affected by the initial pH value and the concentration of carbofuran. Then nine degradation intermediates were detected by HPLC/MS/MS. The Frontier Electron Densities of carbofuran were calculated to predict the active sites on carbofuran attacked by hydroxyl radicals and photoholes. Point charges were used to elucidate the chemisorption pattern on TiO2 catalysts during the photocatalytic process. By combining the experimental results and calculation data, the photocatalytic degradation pathways of carbofuran were proposed, including the addition of hydroxyl radicals and the cleavage of the carbamate side chain.     

吸附法油气回收系统在成品油库中的应用

介绍了活性炭吸附法油气回收系统在成品油库汽油装车过程中的应用情况。结合油库油气回收改造的实际情况,重点介绍了了吸附法油气回收装置的工艺流程、油库油气回收系统的组成、监控系统主要功能、环保检测的相关事项,并分析了油气回收系统的经济效益,结合实际经验对油库油气回收改造提出了建议。     

酸性水汽提及硫磺回收工艺的研究及应用研究

文章主要通过对酸性水气体及硫磺回收工艺特点的介绍与比选,着重分析“无在线炉硫磺回收及尾气处理工艺”（SSR）,其中硫回收为一段高温转化,二级催化转化的克劳斯工艺,尾气处理为加氢还原一吸收工艺,并介绍原辅材料成分及处理效率。该工艺能够有效解决石化企业的酸性气及酸水排放问题,具有良好的社会、环境效益显著。     

乡镇垃圾综合利用途径分析研究

社会主义新农村建设推动了乡镇经济的发展,但乡镇的环境问题并没有随之解决,而固体废弃物的综合利用成为解决当前乡镇环境问题的有效手段之一。乡镇垃圾现状分析表明,其组分以有机易腐成分为主．不适用于城市垃圾的处理方式。乡镇垃圾经合理分类,其综合利用的主要途径有三条,包括可回收垃圾一回收一循环再利用,有机垃圾制肥-肥料-回田,餐厨垃圾、人畜粪便、秸秆等有机垃圾厌氧发酵-沼气-热能或电能。该途径可最终实现乡镇垃圾的资源化和能源化。     

含油污泥三相离心分离处理技术研究

针对原油生产过程中产生的大量含油污泥,油泥成分复杂、严重污染周边环境且造成资源浪费的情况,采用三相离心分离工艺对含油污泥进行处理。通过室内试验研究,确定了含油污泥处理的最佳条件。添加分离剂能够改善油泥分离性能,提高油泥温度能够改善油泥流动效果,摸索出油泥离心分离的最佳时间和离心速率,并对分离后的三相物质进行物性检测。该工艺处理含油污泥可以有效的回收原油,处理后固相减量75%,实现含油污泥减量化、资源化处理的目的。     

低C/N条件下MUCT工艺数学模型的参数校正与验证

基于ASM2d模型建立了稳定运行的MUCT工艺营养物质去除过程的动力学反应模型,比较各种COD、TN、NH 4＋-N、TP的实测值和模拟值,以确定系统在低C/N条件下运行时的动力学和化学计量学参数.模拟结果表明,稳态模型中的动力学参数qPHA、KA、KPP、YPO3-4、μAUT和ηNO-3分别取值2.90 g.（g.d）-1、3.85 g.m-3、1.35 g.（g.d）-1、0.35、1.6和0.8.其他的动力学和化学计量学参数可采用IWA给出的默认值.