离子化有机污染物在沉积物和水相间的平衡分配计算

本文从热力学平衡原理出发,推导出离子化有机污染物在沉积物／水相间分配系数的理论计算模型,并以苯酚,邻氯酚,２,４－二氯酚、五氯酚和苯胺的吸附实验数据为例,计算了它们在中性分子和带电荷的离子形态下的分配系数Ｋｄ和Ｋｄｉ。以及总体分配系数Ｋｄｏ研究结果表明,离子化有机污染物在沉积物和分配行为不仅与该化学物的ｐＫａ和存在形态有关。而且还取决于环境介质的ｐＨ。     

固定化微生物法去除模拟渗滤液中氨氮的研究

采用固定化微生物曝气生物滤池（I-BAF）技术成功处理了模拟垃圾渗滤液,探讨了pH和溶解氧（DO）对系统脱氮性能的影响。结果表明,固定化微生物曝气生物滤池反应系统启动迅速,运行稳定,可以有效去除模拟垃圾渗滤液中的有机物和氨氮,其去除率分别达到97.1%和99.9%。在pH为7.5～8.5之间,DO 4.0 mg/L左右的条件下对模拟垃圾渗滤液中氮的去除最为有利,同步硝化反硝化效率以及总氮去除率均达到最高,分别为96.2%和94.3%。这主要是由于I-BAF系统中大孔载体提供了厌氧-兼氧-好氧的微环境,使硝化和反硝化反应在同一个反应器内发生,共同作用实现模拟垃圾渗滤液中总氮的去除。     

Photo-dissociation of dimethylamine by KrBr excilamp

A study of dimethylamine photo-dissociation in the gas phase has been conducted using UV radiation delivered from a KrBr^* excilamp, driven by a sinusoidal electronic control gear with maximum emission at wavelength of 207 nm. The electrical input power and radiant power of the lamp were measured to determine their effects on the degradation. The influence of flow velocity and initial concentration of dimethylamine were also examined. In order to evaluate the photo-dissociation process comprehensively, several parameters were investigated, including removal efficiency, energy yield, carbon balance and CO₂ selectivity. It is shown that the removal efficiency increases with enhanced input power and decreased gas flow rate. A high removal efficiency of 68% is achieved for lamp power 102 W and flow velocity 15 m³ h⁻¹. The optimum dimethylamine initial concentration is around 3520 mg m⁻³, for which the energy yield reaches up to 442 g kW h⁻¹ when the input power is 65 W. In addition, two chain compounds (1,3-bis-dimethylamino-2-propanol; 3-penten-2-one, 4-amino) and three ring organic matters (1-azetidinecarboxaldehyde, 2,2,4,4-tetramethyl; N-m-tolyl-succinamic acid; p-acetoacetanisidide), were identified by GC–MS as secondary products, in order to demonstrate the pathways of the dimethylamine degradation.     

Different reaction mechanisms of diphenylether and 4-bromodiphenylether with nitrous acid in the 355 nm laser flash photolysis of mixed aqueous solution

The microscopic reaction mechanisms of diphenylether (DPE) and 4-bromodiphenylether (4-BrDPE) with nitrous acid (HNO(2)) in the absence of O(2) have been explored by the 355nm laser flash photolysis. It was proposed that OH radical, from the photolysis of HNO(2), added to DPE forms the C(12)H(10)O-OH adduct while added to 4-BrDPE forms the 4-BrDPE-OH and 4-BrOH-DPE adducts. The first-order decay rate constants of the C(12)H(10)O-OH adduct, 4-BrDPE-OH adduct and 4-BrOH-DPE adduct were measured to be (1.86+/-0.14)x10(5)s(-1), (2.19+/-0.04)x10(5)s(-1) and (1.56+/-0.03)x10(5)s(-1), respectively. The final photolysis products of DPE and HNO(2) identified by GC/MS analysis were phenol, o-hydroxydiphenylether, p-hydroxydiphenylether and p-nitrodiphenylether, while the final photolysis product of 4-BrDPE and HNO(2) identified by LC/MS analysis was mainly the dimer.     

Ce掺杂纳米TiO2光催化剂的制备及降解甲醛的研究

介绍了溶胶-凝胶法制备Ce离子掺杂纳米TiO2的工艺流程.采用X射线衍射(XRD)、紫外可见分光光度法(UV-Vis)等方法表征了Ce掺杂TiO2的相组成、紫外可见漫反射率与掺杂量的关系.结果表明,掺杂的TiO2在520℃、650℃焙烧2 h呈锐钛矿结构,在520℃焙烧2 h的TiO2的晶粒尺寸大约为20 nm,而掺杂Ce后其晶粒尺寸均减小,大约为12nm.UV-Vis吸光度分析表明,掺Ce后吸收带边明显发生红移,但随着Ce掺杂浓度的增大,其对可见光的吸收影响不大.光催化降解反应表明,未掺杂Ce的TiO2反应2 h后对甲醛的没有降解作用,而Ce掺杂TiO2反应2 h后甲醛降解率达15%.     

Pt-CuMnCeOx/堇青石微波催化燃烧VOCs性能

微波催化燃烧是一项新的VOCs处理技术,提升VOCs处理效率的关键在于开发催化活性更高、性能更稳定的催化剂。将贵金属Pt与铜锰铈金属氧化物复合制备了Pt-CuMnCeO_x/堇青石催化剂,SEM、BET和XRD表征基础上测试催化剂对双组分VOCs-甲苯和乙酸乙酯的催化活性与稳定性。研究表明,Pt的复合提高了催化剂表面活性颗粒的分散性,增大了催化剂的比表面积和孔体积,升高了铜锰价态而提高了催化剂的低温催化活性。微波功率40 W时,Pt-CuMnCeO_x/堇青石催化剂的甲苯和乙酸乙酯的降解效率高出CuMnCeO_x/堇青石16%和11%;微波功率70 W时,Pt-CuMnCeO_x/堇青石催化剂可完全去除甲苯和乙酸乙酯,总VOCs去除率达97%左右且活性保持稳定。本研究结果可为微波催化燃烧VOCs技术提供参考。     

氧化硫硫杆菌JJU-1生物淋滤去除污泥中的重金属

将前期分离得到的嗜酸性氧化硫硫杆菌JJU-1（Thiobacillus thiooxidans JJU-1）接种于污水处理厂污泥中,进行为期7 d的生物淋滤实验,对淋滤过程中的pH值、氧化还原电位（ORP）和重金属去除率进行检测。研究结果表明：氧化硫硫杆菌JJU-1不同接种量处理浸出液的pH下降幅度不同,当接种量为15%时,浸出液pH下降最快,其ORP达到最大值（444 mV）,Cu、Cd和Pb的去除率分别高达79.2%、96.6%和93.4%。添加能源物质S可以明显降低淋滤液的pH,当能源物质S投入量增加到12 g·L-1时,淋滤7 d后,浸出液的pH下降至1以下,浸出液的ORP在S添加量为16 g·L-1时达到最大值（477 mV）,20 g·L-1 S粉添加量条件下,Cr、Cu和Pb的去除率最大,分别为98.8%、74.3%和85.8%;然而,添加能源物质S对Cd的浸出无明显影响。以上研究结果表明,氧化硫硫杆菌JJU-1在去除污泥中重金属方面有着广阔的前景。     

氧化物催化剂对非热等离子体催化降解甲苯的影响

考察了在干燥气氛下不同氧化物催化剂对非热等离子体催化降解甲苯的影响。从甲苯降解率、碳平衡、CO2选择性和O3去除4个方面,对比了氧化物催化剂的介电性能、表面供氧能力和比表面积与多孔结构对反应产生影响的强弱。结果表明,催化剂的介电性能有利于甲苯降解率、碳平衡和O3产量的提高,但对CO2选择性和O3去除的影响极小;一定能量密度下,催化剂比表面积与多孔结构对CO2选择性和O3去除所产生的影响要强于介电性能;催化剂表面供氧能力可明显促进反应的进行,其对反应所产生的影响要强于比表面积与多孔结构。     

Acute and chronic toxicity of organophosphate monocrotophos to Daphnia magna

The acute and chronic toxicity of monocrotophos (MCP), the binary joint toxicity of MCP and bifenthrin (BF), and sodium dodecyl benzene sulfonate (SDBS) to Daphnia magna (D. magna) was evaluated. The 24 h-median effective concentration (24 h-EC₅₀) and 48 h-median lethal concentration (48 h-LC₅₀) of MCP towards D. magna were 161 and 388 μ g/L, respectively. In addition, the lowest-observed effective concentration (LOEC) and non-observed effective concentration (NOEC) of MCP to D. magna were 10 and 5 μ g/L, respectively. Furthermore, the chronic value (ChV) of MCP against D. magna was 7 μ g/L and the acute chronic ratio (ACR) was 55. The number of offspring per female and the intrinsic rate of natural increase (r) were identified as the parameters that were most sensitive to MCP. In addition, toxic unit (TU) analysis was employed to evaluate the joint toxicities. The calculated TU_mix values of binary equitoxic mixtures of MCP + BF and MCP + SDBS were 1.47 and 1.63, respectively, which suggests that both equitoxic mixtures exert a limited antagonistic effect. The results of this study revealed that the toxic threshold of MCP towards D. magna is higher than its reported highest residue (4 μ g/L) in the ordinary aquatic environment, and that concurrent exposure to BF or SDBS may exert a slight antagonistic effect.