污水厂污泥一体化竖式强化渗滤浓缩自然干化与消化研究

针对目前国内污泥处理处置存在的问题,为实现污泥浓缩消化一体化,开发了污泥一体化强化渗滤浓缩自然干化与消化新工艺反应器,并进行了城市水厂污泥处理试验.结果表明,在有机负荷为0.8 kg VSS/(m3·d)、平均水力停留时间为8.3 d、污泥停留时间为120 d的条件下,污泥有机物去除率可达到44.4%,排泥含水率达到79.1%,污泥消化与浓缩过程起到了相互促进的作用.渗滤液须抽回至污水处理厂处理.     

山梨酸废水在ABR中的基质降解行为

稳态条件下,采用厌氧折流板反应器(anaerobic baffled reactor,ABR)处理山梨酸废水并进行基质降解动力学研究.实验表明,在污泥负荷为0.54～1.63 kg COD/(kg VSS·d)的范围内,COD去除率随着负荷的增加从85%降到55%.各隔室出水COD沿程递减,前3个隔室承担了去除COD的重要作用,但随着污泥负荷的增加,后部承担的COD去除率比例增大.基于各串联隔室完全混合的假定,推导ABR中山梨酸废水的基质降解动力学方程,并通过实验确定相关动力学参数及相应的动力学方程.实测值与预测值基本吻合.     

改性粉煤灰在酸雾治理方面的研究

为去除化工生产等过程中产生的酸雾废气,首先用水作用法、微波法和传统湿法对粉煤灰进行改性试验,结果显示:传统湿法中的碱法效果最佳,改性后粉煤灰的BET比表面积是改性前的8.23倍.再用改性后的粉煤灰与廉价易得的天然矿物沸石和熟石灰作为活性组分,制得一种新型的复合吸附剂.常温常压下,动态吸附盐酸雾,实验结果表明:由改性粉煤灰制作的吸附剂G对盐酸雾的吸附性能比未经改性的吸附剂W有所提高,在文中所述条件下,饱和吸附量由改性前的331.4 mg/g提高到改性后的445.2 mg/g.     

错流式生物滴滤床净化甲苯废气

采用焦化厂污泥为菌源驯化甲苯降解菌,接种错流式生物滴滤床,净化含甲苯废气。研究了生物滴滤床的挂膜启动和长期运行情况,填料和营养液对滴滤床去除能力的影响,并对长期运行的压降进行了观察分析。反应器挂膜启动需要6 d时间,稳定运行的平均去除效率为95％,单位体积最大去除负荷为251 g/(m³·h)。结果表明,采用错流式生物滴滤床可以有效去除甲苯废气;以比表面积大的生物陶粒作为填料以及定期适量更换营养液,均有助于提高生物滴滤床的去除能力;错流式生物滴滤床具有压降小、气液分布均匀的特点。     

强化混凝处理城市纳污河污水运行过程中搅拌能量的影响

介绍了采用混凝技术大规模处理运河污水时所遇到的问题,并通过混凝试验分析了问题的原因。提出并初步探讨了混凝搅拌能量及其计算方式,利用混凝搅拌能量参数分析混凝反应效果的差异,说明在实际生产中混凝反应过程需要有足够的能量。     

沙尘天气强度特征指数研究——以北京地区为例

利用1970—2000年北京及其周边地区以及影响北京沙尘天气的上风向共14个基准气象站的沙尘天气与相关气象因子资料,分析了沙尘天气与各因子之间的相关性。研究发现,风速、相对湿度与沙尘天气的相关关系最显著;同时,对能见度与沙尘浓度观测值的分析得出,二者存在非线性关系。在上述分析的基础上,用能见度、风速、相对湿度构建了沙尘强度特征指数,该指数与这3个因子均呈非线性关系,指数值越大表示沙尘天气强度越大,反之,指数值越小表示沙尘天气强度越小。经验说明,沙尘强度特征指数与相应沙尘浓度观测值有着较一致的变化趋势,该指数从气象和环境两个方面反映了沙尘天气的强度特征。     

受侧向土体位移斜桩的特性

通过三维有限单元法分析了斜桩受侧向土体位移的特性。变动柱和土体参数进行敏感性分析,得出桩的柔度、侧向土体位移的大小、桩顶约束条件、土体位移形状和土体移动层厚度等对斜桩的影响。刚性桩的挠度小于柔性桩,但弯矩和剪力大于柔性桩。斜桩非线性弹簧的土抗力—位移关系(p-y曲线)表现为双曲线特征,可基于直桩的Winkler地基反力法对斜桩进行简化计算分析,但应对直桩的极限土抗力值进行修正,以期更好的反映斜桩的特性。     

基于信息扩散理论的地震风险评估

利用基于信息扩散理论的风险评估方法 ,对地震灾害进行了风险分析。该方法简单易行 ,分析结果意义清楚 ,对防灾抗灾具有一定的指导作用。     

Modeling in-situ uranium(VI) bioreduction by sulfate-reducing bacteria

We present a travel-time based reactive transport model to simulate an in-situ bioremediation experiment for demonstrating enhanced bioreduction of uranium(VI). The model considers aquatic equilibrium chemistry of uranium and other groundwater constituents, uranium sorption and precipitation, and the microbial reduction of nitrate, sulfate and U(VI). Kinetic sorption/desorption of U(VI) is characterized by mass transfer between stagnant micro-pores and mobile flow zones. The model describes the succession of terminal electron accepting processes and the growth and decay of sulfate-reducing bacteria, concurrent with the enzymatic reduction of aqueous U(VI) species. The effective U(VI) reduction rate and sorption site distributions are determined by fitting the model simulation to an in-situ experiment at Oak Ridge, TN. Results show that (1) the presence of nitrate inhibits U(VI) reduction at the site; (2) the fitted effective rate of in-situ U(VI) reduction is much smaller than the values reported for laboratory experiments; (3) U(VI) sorption/desorption, which affects U(VI) bioavailability at the site, is strongly controlled by kinetics; (4) both pH and bicarbonate concentration significantly influence the sorption/desorption of U(VI), which therefore cannot be characterized by empirical isotherms; and (5) calcium-uranyl-carbonate complexes significantly influence the model performance of U(VI) reduction.     

Aerobic degradation of bisphenol A by Achromobacter xylosoxidans strain B-16 isolated from compost leachate of municipal solid waste

A novel bacterium designated strain B-16 was isolated from the compost leachate of the municipal solid waste (MSW) in a laboratory reactor. This strain was identified as a gram-negative bacterium, Achromobacter xylosoxidans that could grow on bisphenol A (BPA, a representative endocrine disruptor) as a sole carbon source under aerobic condition. BPA-degrading characteristics of strain B-16 were investigated in liquid cultures. The results show that BPA degradation was influenced by several factors (e.g. inoculum size, substrate concentration, temperature and pH, etc). The half-lives, optimum temperature and pH were found to be 0.58-3.1d, 35 degrees C and 7.0, respectively. BPA-degrading activity and cell growth were inhibited at high substrate concentration. Metabolic intermediates detected during the degradation process were identified as p-hydroxybenzaldehyde, p-hydroxybenzoic acid and p-hydroquinone, respectively. Metabolic pathway of BPA degradation was proposed in this study.