活性污泥系统优化设计对不确定性参数的灵敏度研究

在活性污泥系统优化设计模型参数不确定性分析的基础上,考察了进水负荷、生物动力学参数、曝气设备性能参数和二沉池浓缩常数变化对优化设计的影响。灵敏度分析结果表明,对优化设计影响较大的参数为：进水水量水质、与氧转移效率相关的校正参数以及二沉池的浓缩常数等。研究结果对于低灵敏度系统的设计,提高优化设计结果的工程实用性具有重要的意义。     

ASM1中化学计量系数与动力学参数的测定

为了应用活性污泥1号模型模拟印染废水为主的污水集中处理厂,针对该厂实际废水,选取关键的化学计量系数YH和动力学参数bH及H进行测定.详细叙述了YH、bH和H的测定原理及具体操作过程.YH、bH和H的实测结果分别为0.65、0.50、3.23,这些值不同于ASM1中20 ℃下城市污水的推荐值0.67、0.62、6.0.     

两种A~2/O工艺的活性污泥2D模型动力学参数灵敏度分析

使用GPS-X软件对传统A~2/O工艺和氧化沟型A~2/O工艺的污染物(COD、硝酸盐氮、氨氮和溶解性正磷酸盐)去除效果进行模拟,选用活性污泥2D模型(ASM2D)对厌氧池、缺氧池和好氧池中20个重要动力学参数进行了灵敏度分析。结果发现,在两种A~2/O工艺中,动力学参数对出水COD和硝酸盐氮浓度的灵敏度影响较小,对出水氨氮和溶解性正磷酸盐浓度的灵敏度影响很大。与聚磷菌相关的动力学参数灵敏度最高,与异养菌相关的动力学参数灵敏度最低。参数向上浮动与向下浮动对同一水质指标的影响程度不同,饱和/抑制系数类参数的灵敏度一般低于其他参数。     

鸭绿江下游水质模型研究

本文采用含有藻类光合、呼吸作用的DO—BOD耦合模型,模拟鸭绿江下游河流段的水质状态;采用二维曲线正交坐标系统模拟河口段的BOD、COD、DO、NH_4~-—N、NO_2~-—N、NO_3~-—N和酚的状态。对于河流模型中的各个参数作了比较详尽的研究,探讨了估计参数初始值和综合估值的多种方法;对于河口模型,重点研究了二维曲线正交坐标系统的离散化处理和多水质组分的耦合计算问题。河流模型和河口模型都已经过实际监测数据的验证。这两个模型对于含藻类的河流与二维河口的水质模拟具有推广意义。     

粉末活性污泥处理含铀废水的特性

以生活污水处理厂剩余活性污泥为原料,制备粉末活性污泥(PAS)作为生物吸附剂,考察p H值,PAS投加量,U(Ⅵ)初始浓度和吸附时间对PAS吸附U(Ⅵ)的影响,探讨了PAS吸附U(Ⅵ)的作用机理。实验结果表明,在U(Ⅵ)初始浓度为10 mg/L时,其最佳吸附p H值为3,去除率97.77%,吸附平衡时间120 min;吸附过程较好地拟合了准二级动力学模型(R2≈1)和Freundlich等温模型(R2≈1);X射线能谱和离子交换实验分析表明,离子交换为其主要吸附方式,参与交换的主要离子为Ca2+;红外光谱分析表明,PAS吸附U(Ⅵ)后自身结构未发生改变。以0.1 mol/L的HCl溶液作为解吸液,初次解吸率达92.83%,循环利用3次仍具有较好的吸附效果。     

呼吸计量法对甲醇和葡萄糖为基质的ASM1参数测定

污水水质和污泥特性不同,活性污泥1号模型(ASM 1)参数的测定结果也不相同。研究以甲醇和葡萄糖为基质,对分别经过甲醇和葡萄糖驯化的活性污泥,通过呼吸计量法测定高食微比、中食微比和零食微比下的氧利用速率(OUR)随时间变化的曲线。确定了异养菌产率系数(YH)、异养菌最大比增长速率(μ^H)和衰减系数(bH),并根据YH、μ^H和bH的测定结果和对中食微比下OUR曲线的数值拟合确定了异养菌半饱和常数(ks)、最大比水解速率(kh)和慢速可生物降解底物水解的半饱和常数(KX)。研究结果表明,在20℃下,采用甲醇和葡萄糖为基质测得的YH、bH、μ^H、ks、KX和kh分别为0.53、0.48、5.75、0.9、0.03、3.0和0.87、1.03、2.27、4.45、0.01、7.0。YH、bH、μ^H和ks的值与ASM1中城市污水的推荐值0.67、0.62、6.0、20.0不同,反映了不同基质对参数测定结果的影响。对于慢速可生物降解有机物(Xs)含量低的水质来说,KX和kh对生化反应过程影响不大,可采用ASM1模型的推荐值。     

活性污泥处理系统的计算机模拟

介绍了以活性污泥1号模型(ASMI)和固体通量沉淀模型为基础．结合反应器原理．用VB6．0计算机语言建立城市污水活性污泥模拟器的方法,探讨了生物反应器和二沉池的模拟工艺流程、各组分的物料平衡关系和欧拉法数值积分的步长选取等问题。模拟器的校准结果表明,该模拟器建立的思路和方法是可靠的．可以用于城市污水生物处理系统的模拟和预测。     

采用序半连续反应器进行硝化和反硝化工艺的数学模拟

研究了生物废水处理应用于序半连续式反应器(SFBR)工艺中的微生物生长、硝化和反硝化动力学。基于活性污泥1号模型(ASMNo. 1)中的原理和结论,导出了在有氧阶段和缺氧阶段微生物生长速率、铵、硝酸盐、易生物降解基质等的反应速率及它们的物料平衡方程。在实验的基础上,对模型中的各参数采用了合适的方法进行参数估值,即:龙格库塔法解常微分方程组和黄金分割法搜索最小误差,该模型的最小误差ε≈4 799;得出了应用于本工艺中数学模型中的各动力学参数和化学计量系数,如KS 39. 997,KNO 0 .397,KNH 1 997,KOA 0 .404,KOH 0. 297, μA 0 .0026,μH 0. 207,YA 0 .24,YH. 0 6。     

曝气条件对浸没式膜生物反应器内流场的影响

为深入研究流场动力学特性对浸没式膜生物反应器系统内膜面污染的控制,应用fluent软件对浸没式膜生物反应器内气液两相流动进行了三维数值模拟研究。采用标准k-ε湍流模型和欧拉多相流模型,考察了改变曝气条件对膜面气液速度场及气含率分布的影响。模拟结果表明,在相同曝气强度下,1 mm曝气孔径下膜面气液两相的速度增加较孔径2mm、3 mm的快;曝气孔径为1 mm时,膜面的液相速度随着曝气强度的增加逐渐增大;曝气孔径为1 mm时,曝气量为5.5m3/h所形成的漩涡区较大,膜面气含率值较高且分布较均匀,气液两相接触面积较大,膜面冲刷效果较好;模拟观察到反应器底部靠近壁面局部气含率较低,不利于活性污泥中微生物的生长,需要进一步优化曝气和反应器结构。     

采用序半连续反应器进行硝化和反硝化工艺的数学模拟

研究了生物废水处理应用于序半连续式反应器(SFBR)工艺中的微生物生长、硝化和反硝化动力学。基于活性污泥1号模型(ASM No．1)中的原理和结论，导出了在有氧阶段和缺氧阶段微生物生长速率、铵、硝酸盐、易生物降解基质等的反应速率及它们的物料平衡方程。在实验的基础上，对模型中的各参数采用了合适的方法进行参数估值，即：龙格-库塔法解常微分方程组和黄金分割法搜索最小误差，该模型的最小误差ε≈4．799；得出了应用于本工艺中数学模型中的各动力学参数和化学计量系数，如Ks39．997，KNO0．397，KNH1．997，KOA0．404，KOH0．297，μA0．0026，μH0．207，YA0．24，YH0．6。     

Genetic polymorphisms in CYP1A1 and GSTM1 predispose humans to PCBs/PCDFs-induced skin lesions

INTRODUCTION: Polychlorinated biphenyls (PCBs) and dibenzofurans (PCDFs) are ubiquitous persistent pollutants in humans. Whether people with different genotypes are with different susceptibility to these chemicals are unknown. In a group of people highly exposed to PCBs/PCDFs, we tested the hypothesis that genotypic polymorphisms affected susceptibility for development of skin manifestations. METHODS: In 1979, approximately 2000 people in central Taiwan ingested cooking oil contaminated with PCBs/PCDFs. Skin disorder such as chloracne, abnormal nail, hyperkeratosis and skin allergy were found in PCBs/PCDFs exposed group. We recruited exposed and community background exposure subjects for blood testing and telephone-interview. Single nucleotide polymorphisms, AhR Arg554Lys, CYP1A1 Ile462Val, CYP1A1 T6235C, and GSTM1/T1 deletion, were determined. Occurrence of skin manifestations was compared among people with different genotypes while stratified by PCB exposure levels by logistic regression. RESULTS: Data on exposure, medical history, and genotypes were obtained from 393 exposed and 181 background exposure groups. Skin manifestations including chloracne, allergy, abnormal nail, and hyperkeratosis were more prevalent in exposed people in a dose-related manner. Among highly exposed individuals, combined CYP1A1-MspI mutant genotype and GSTM1-null genotype were associated with increased risk of chloracne (odds ratio 2.8, 95% confidence interval 1.1-7.6). Among intermediately exposed individuals, GSTM1 null genotype was associated with skin allergy. AhR Arg554Lys genotype and GSTT1 null genotype were not related to susceptibility to skin manifestations in PCB/PCDF-exposed population. CONCLUSION: CYP1A1 and GSTM1 genotypic polymorphisms might be related to the susceptibility to PCB/PCDF-induced skin manifestations.     

废旧锂电池正极材料LiNi1/3Co1/3Mn1/3O2中钴的回收

随着新能源汽车工业的快速发展,废旧三元动力锂电池的量在不断地增加。三元动力锂电池中含有丰富的Co、Mn、Li和Ni资源,回收三元动力锂电池是防止环境污染和回收贵重金属的理想选择。利用抗坏血酸(C6H8O6)的酸性和还原性对废旧三元锂电池正极材料进行浸出,KMnO_4的强氧化性回收浸出液中的Co制备β-CoC_2O_4·2H_2O,采用浓度为1.3 mol·L~(-1)的C_6H_8O_6,在60℃的条件下对正极材料浸出20 min,向浸出夜中加入1 mol·L-1的H_2SO_4反应20 min后加入KMnO_4继续反应1 h,制得β-CoC_2O_4·2H_2O。实验结果表明,Co的回收率达91%,Li的浸出率可达96.4%,Mn和Ni完全浸出,可实现简单环保地浸出有价金属并回收Co。     

Heterogeneous reactions of ozone with pyrene, 1-hydroxypyrene and 1-nitropyrene adsorbed on particles

This work deals with the kinetic study of the reactions of ozone with pyrene, 1-hydroxypyrene and 1-nitropyrene, adsorbed on model particles. Experiments were performed at room temperature and atmospheric pressure, using a quasi-static flow reactor in the absence of light. Compounds were extracted from particles using pressurized fluid extraction (PFE) and concentration measurements were performed using gas chromatography/mass spectrometry (GC/MS). The pseudo-first order rate constants were obtained from the fit of the experimental decay of particulate polycyclic compound concentrations versus reaction time. Experiments were performed at three different O₃ concentrations from which second order rate constants were calculated. The following rate constant values were obtained at 293 K: k(O₃ + Pyrene) = (3.2 ± 0.7) × 10^?16 cm³ molecule^?1 s^?1; k(O₃ + 1OHP) = (7.7 ± 1.4) ×10 ^?16 cm³ molecule^?1 s^?1; and k(O₃ + 1NP) = (2.2 ± 0.5) × 10^?17 cm³ molecule^?1 s^?1, for pyrene, 1-hydroxypyrene and 1-nitropyrene adsorbed on silica particles. The variation in the rate constants demonstrates the strong influence of the substituent (OH or NO₂) on the heterogeneous reactivity of pyrene. The pyrene particulate concentration was also varied in order to check how this parameter may influence the experiments. Finally, oxidation products were investigated for all reactions and some were detected and identified for the first time for ozone heterogeneous reaction with pyrene adsorbed on particles.     

Recommended Standard Method for Continuing Dust Fall Survey (APM-1, Revision 1)

The suggested standard method of dust fall collection, as set forth in the following sections, is presented in an effort to promote a uniform approach to measurement of rate of dust fall     

Biosynthesis of (S)-1-(1-naphthyl) ethanol by microbial ketoreductase

Environmental Science and Pollution Research - (S)-1-(1-naphthyl) ethanol (SNE) is a chiral drug intermediate for the production of mevinic acid analog, a potent cholesterol agent. It acts as an...     

Effects of dietary habits and CYP1A1 polymorphisms on blood dioxin concentrations in Japanese men

The major source of dioxin impurities in Japan in the past was agrochemical formulations; more recently, it has been exhaust from waste incinerators. To examine the environmental and genetic factors that influence blood dioxin concentration, we investigated the relationship among dioxin concentrations, dietary habits and cytochorome P450 1A1 (CYP1A1) polymorphisms (MspI type and Ile-Val type) in Japanese fishermen and farmers, including also a group of office workers as controls. The mean dioxin concentrations in the fishermen, the farmers and the controls were 161369, 79079 and 100500 pg/g fat, respectively. The elevated dioxin concentration with polychlorinated dibenzo-p-dioxins, polychlorinated dibenzofurans and coplanar-PCBs found in the fishermen may be due to the frequent consumption of fish; no such relationship was found both in the farmers and the controls. We found that the concentrations of congeners found as impurities in certain chemicals such as those previously used in agriculture showed no significant differences among the three groups; we consider it unlikely that the farmers would be directly exposed to dioxins from such chemicals. Thus, it is probable that the primary route of dioxin exposure in the Japanese population is through the food chain via fish consumption, regardless of occupation. No meaningful relationship between blood dioxin concentration and CYP1A1 polymorphisms was found in this study, although there was a significant difference between the concentration of total non-ortho-PCBs in genotypes A and B. Further studies on more subjects, including those of genotype C, are needed to confirm the relationship between blood dioxin concentrations and MspI polymorphisms.     

微生物絮凝剂EBU-1的化学性质分析

对一株产碱假单胞菌(Pseudomonas alcaligenes)产生的微生物絮凝剂EBU1的化学性质进行初步研究,结果显示，EBU-1具有良好的热稳定性；呈色反应为多糖的颜色反应，没有蛋白质的颜色反应；紫外和红外扫描确定EBU-1含多糖及少量核酸，含量分别为82.3%和8.6%；电负性实验表明，EBU-1是阴离子型微生物絮凝剂。     

Atmospheric chemistry of 1-methyl-2-pyrrolidinone

Rate constants for the atmospheric reactions of 1-methyl-2-pyrrolidinone with OH radicals, NO₃ radicals and O₃ have been measured at 296±2 K and atmospheric pressure of air, and the products of the OH radical and NO₃ radical reactions investigated. Using relative rate techniques, rate constants for the gas-phase reactions of OH and NO₃ radicals with 1-methyl-2-pyrrolidinone of (2.15±0.36)×10^-11 cm³ molecule^-1 s^-1 and (1.26±0.40)×10^-13 cm³ molecule^-1 s^-1, respectively, were measured, where the indicated errors include the estimated overall uncertainties in the rate constants for the reference compounds. An upper limit to the rate constant for the O₃ reaction of <1×10^-19 cm³ molecule^-1 s^-1 was also determined. These kinetic data lead to a calculated tropospheric lifetime of 1-methyl-2-pyrrolidinone of a few hours, with both the daytime OH radical reaction and the nighttime NO₃ radical reaction being important loss processes. Products of the OH radical and NO₃ radical reactions were analyzed by gas chromatography with flame ionization detection and combined gas chromatography–mass spectrometry. N-methylsuccinimide and (tentatively) 1-formyl-2-pyrrolidinone were identified as products of both of these reactions. The measured formation yields of N-methylsuccinimide and 1-formyl-2-pyrrolidinone were 44±12% and 41±12%, respectively, from the OH radical reaction and 59±16% and ∼4%, respectively, from the NO₃ radical reaction. Reaction mechanisms consistent with formation of these products are presented.     

The ozone formation potential of 1-bromo-propane

1-Bromo-propane (1-BP) is a replacement for high-end chlorofluorocarbon (HCFC) solvents. Its reaction rate constant with the OH radical is, on a weight basis, significantly less than that of ethane. However, the overall smog formation chemistry of 1-BP appears to be very unusual compared with typical volatile organic compounds (VOCs) and relatively complex because of the presence of bromine. In smog chamber experiments, 1-BP initially shows a faster ozone build-up than what would be expected from ethane, but the secondary products containing bromine tend to destroy ozone such that 1-BP can have a net overall negative reactivity. Alternative sets of reactions are offered to explain this unusual behavior. Follow-up studies are suggested to resolve the chemistry. Using one set of bromine-related reactions in a photochemical grid model shows that 1-BP would be less reactive toward peak ozone formation than ethane with a trend toward even lower ozone impacts in the future.