焦化废水处理工程调试运行研究

针对焦化废水处理调试运行存在的问题,以实际运行中的焦化废水处理工程为例,介绍了其调试运行过程.指出焦化废水调试及稳定运行的控制要点,并提出调试运行过程中可能出现的问题及解决措施,为同类废水的调试和运行提供参考.     

Effects of metal cations on sorption-desorption of p-nitrophenol onto wheat ash

The mutual e ects of metal cations (Cu2+, Pb2+, Zn2+, and Cd2+) and p-nitrophenol (NP) on their adsorption desorption behavior onto wheat ash were studied. Results suggested that Cu2+, Pb2+, and Zn2+ diminished the adsorption and increased the desorption of NP remarkably, while Cd2+ had no such e ect. In contrast, NP diminished the adsorption of Cu2+, Pb2+, and Zn2+ onto ash, however, this suppression e ect depended on the initial concentrations of metal cations. NP had no e ect on Cd2+ adsorption on ash. Fourier transform infrared (FT-IR) and X-ray absorption spectroscopic (XAS) studies suggested the following mechanisms responsible for the metal suppression e ect on NP adsorption: (1) large hydrated Cu2+, Pb2+, and Zn2+ shells occupied the surface of ash and prevent nonspecific adsorption of NP onto ash surface; (2) Cu2+, Pb2+, and Zn2+ may block the micropores of ash, resulting in decreased adsorption of NP; (3) complexation of Cu2+, Pb2+, and Zn2+ was likely via carboxyl, hydroxylic and phenolic groups of wheat ash and these same groups may also react with NP during adsorption. As a “soft acid”, Cd2+ is less e cient in the complexation of oxygencontaining acid groups than Cu2+, Pb2+, and Zn2+. Thus, Cd2+ had no e ect on the adsorption of NP on wheat ash.     

吹扫捕集-气相色谱法测定水中的乙醛和丙烯醛

建立了吹扫捕集-气相色谱法测定水样中乙醛和丙烯醛的方法,并对吹扫捕集测试条件进行优化,考察了吹扫温度和吹扫时间对吹扫捕集效率和方法检出限的影响。在50℃下,吹扫时间为20 min时,该方法乙醛和丙烯醛的检出限分别为0.001 2 mg/L、0.000 6 mg/L,相对标准偏差分别为3.5%～6.9%、2.9%～5.8%,加标回收率分别为91.6%～108%、92.0%～105%。与GB3838-2002推荐使用的分析方法相比较,该方法具有操作简便、灵敏度高、重复性好、基本上不消耗有机溶剂等特点,可满足地表水和废水中乙醛和丙烯醛的测定要求。     

有机质对土壤气相抽提去除四氯化碳效率的影响

某重要岩溶地下水源地因附近农药厂排放含四氯化碳污水而受到严重污染,实验采用土柱通风试验模拟土壤气相抽提(SVE),研究环境温度为20℃,通风速率为40mL/min,土壤含水率10%,而土壤有机质含量分别为3.02%和0.13%条件下的两种供试土壤中四氯化碳污染物的去除过程.结果表明,土柱通风能有效去除土壤中的四氯化碳污...     

紫外辐射对小分子有机酸化学凝聚性作用途径探讨

通过烧杯实验系统考察了紫外辐射对脂肪羧酸类和酚酸类小分子有机酸的化学凝聚性的作用途径.结果表明,溶液pH对柠檬酸、草酸、酒石酸和丁二酸等脂肪羧酸类有机物的混凝性能影响较小.紫外辐射处理后,脂肪羧酸类小分子有机物的混凝去除率均高于未经紫外辐射处理的水样.进一步研究表明,紫外辐射过程中发生了光化学反应,使得脂肪羧酸的表面负电性降低,进而提高了其化学凝聚性.与脂肪类小分子有机酸不同,苯酚、水杨酸和苯甲酸的化学凝聚性较差,且受紫外辐射过程的影响小.单宁酸的混凝性能较好,pH=6时的去除率最高可达90%以上,这可能与其分子中脂肪酸碳链结构的存在以及单宁酸分子较大,易与PACl的水解产物发生吸附电中和反应有关.     

电絮凝去除废水中多种重金属影响因素研究

目的以铁作为电极,研究电絮凝法处理含多种重金属废水的影响因素及效果。方法通过控制pH、停留时间、电流密度、电导率、废水初始浓度等因素至不同水平,考察处理效果、能耗及极板消耗的变化。结果随着停留时间、pH值及电流密度的升高,处理效果越好,但升高至一定程度后,处理效果提升并不明显;电导率对处理效果影响并不显著,但过低的电导率会增加能耗;废水初始浓度越高,要达到处理目标所需的能耗及极板消耗均越高。结论当pH为8.5~9.0、进水电导率为1500~2000μs/cm、停留时间为3~4 min、废水初始质量浓度20 mg/L、电流密度为13.2~19.8 A/m2时,处理效果最理想,对总铜、总镍、总铅、总锌、总镉及总铬的去除率达到99%以上,且能耗与极板消耗均为最低,电絮凝法更适合于重金属废水的深度处理。     

城镇污泥蚯蚓堆肥硝化进程及其影响因素

硝化是城镇污泥蚯蚓堆肥稳定化的最后一个阶段,研究硝化进程及其影响因素对减少蚯蚓堆肥过程中的NH_4~+积累、氮素损失和加快蚯蚓堆肥稳定化过程具有重要意义.文章考察了蚯蚓生物量、环境温度以及好氧条件对蚯蚓堆肥NH_4~+、NO_3~-变化的影响.结果发现,蚯蚓生物量对NH_4~+、NO_3~-含量变化影响较大,并存在显著的跃变特点,即当蚯蚓生物量超过一定数量时,会显著加快氨化和硝化速率.环境温度显著影响堆肥氨化作用,影响大小顺序为25℃20℃15℃;环境温度仅对蚯蚓堆肥硝化速率产生影响,但不改变堆肥的硝化进程.蚯蚓堆肥好氧条件对硝化影响大于对氨化的影响,好氧条件优劣不但影响硝化进程还影响硝化速率,氧环境条件好的蚯蚓堆肥硝化进程启动早,硝化速率高.     

南京某城市污水二级处理系统中酞酸酯类的分布及去除特征

以南京某城市污水厂污水和污泥中的酞酸酯类（PAEs）为研究对象，分别采用固相萃取-气相色谱-质谱联用（SPE—Gc．Ms）和超声提取．气相色谱．质谱联用（USE—GC—Ms）检测其中的优先控制污染物邻苯二甲酸二甲酯（DMP）、邻苯二甲酸二乙酯（DEP）、邻苯二甲酸二丁酯（DBP）和邻苯二甲酸单（2-乙基己基）酯（MEHP），研究其在厌氧／好氧（A／O）污泥处理过程中的分布特征及降解规律。研究结果表明，各类PAEs在该污水厂的污水和污泥中均有检出，二级处理出水中4种酞酸酯类物质的浓度在0．151—2．419μg／L。污水中4种酞酸酯的分布规律为MEHP〉DBP〉DMP〉DEP，污泥中4种酞酸酯的分布规律为MEHP〉DBP〉DEP〉DMP。该污水厂二级处理工艺对4种PAEs的去除效果较明显，去除效率DBP〉DEP〉DMP〉MEHP．     

南京某城市污水二级处理系统中酞酸酯类的分布及去除特征简

以南京某城市污水厂污水和污泥中的酞酸酯类（PAEs）为研究对象，分别采用固相萃取-气相色谱-质谱联用（SPE-GC-MS）和超声提取-气相色谱-质谱联用（USE-GC-MS）检测其中的优先控制污染物邻苯二甲酸二甲酯（DMP）、邻苯二甲酸二乙酯（DEP）、邻苯二甲酸二丁酯（DBP）和邻苯二甲酸单（2-乙基己基）酯（MEHP），研究其在厌氧/好氧（A/O）污泥处理过程中的分布特征及降解规律。研究结果表明，各类PAEs在该污水厂的污水和污泥中均有检出，二级处理出水中4种酞酸酯类物质的浓度在0.151~2.419 μg/L。污水中4种酞酸酯的分布规律为MEHP>DBP>DMP>DEP，污泥中4种酞酸酯的分布规律为MEHP>DBP>DEP>DMP。该污水厂二级处理工艺对4种PAEs的去除效果较明显，去除效率DBP>DEP>DMP>MEHP。     

Joint Impact of Scaling and Hysteresis on NAPL Flow Simulation

The hysteresis of capillary pressure versus saturation (P–S) relation is an important constitutive relation in multiphase flow, since the P–S relation is widely used to predict P–S relations in the simulation of the non-aqueous phase liquids (NAPLs). This work examined the performance of the scaling rule on predicting the P–S relationship and then studied the joint impact of the scaling and hysteresis on the multiphase NAPL flow simulation. Various experimental P–S values of distinct fluid pairs were compared with the scaled P–S curves using the scaling rule. The comparison indicated that the prediction of P–S is more accurate when the water–air P–S curve is used to scale other P–S curves. The joint impact of the scaling and hysteresis on the NAPLs flow simulation was then investigated by numerical simulation studies. The NAPL simulator was used to simulate the outcome of several scenarios based on a system with water–NAPL–air in a hypothetical sand tank. For both gasoline and trichloroethylene, the difference of the injected NAPL volume between no hysteretic and hysteretic simulations over a given time period was the smallest when the water–air P–S curve was used to scale other P–S curves. Simulation results of this study are valuable references for predicting the distribution of NAPLs.