影响侧沟式膜泥法一体化OCO工艺脱氮效率的因素研究

采用侧沟式膜泥法一体化OCO工艺处理模拟生活污水，考察了DO、HRT和C/N 3种影响因素对模拟生活污水脱氮的效果。研究结果表明：在好氧区DO为2 mg/L左右、HRT=12 h、C/N为7.5左右时，具有较理想的脱氮效果，TN去除率达到了80%；试验还表明本工艺具有较强的抗冲击负荷能力。     

摇动床生物膜反应器处理生活污水

介绍了一种新型的生物膜反应器——摇动床反应器,并采用模拟生活污水进行了小试试验研究。试验结果表明,在HRT=6h,DO=3～4mg/L,T=20～25℃,pH=7～8,C/N=20的条件下,该工艺可以达到最佳运行状况,有机负荷为0.64～3.00kgCOD/(m3.d)下,COD去除率平均达到85%,出水TN≤10mg/L,达到国家一级排放标准。     

侧沟式一体化OCO工艺中DO和C/N对同步硝化反硝化的影响

以自配模拟生活污水为处理对象,研究了不同DO和C/N对侧沟式一体化OCO反应器同步硝化反硝化和COD降解效果的影响。实验结果表明,维持进水COD均值约为300 mg/L,TN约为40 mg/L,MLSS约为2 600 mg/L,进水流量为20 L/h时,COD去除率随着DO的增大逐步提高,当好氧区DO均值约为2.0 mg/L时,同步硝化反硝化效果最好,TN去除率达到了80%以上;维持好氧区DO均值约为2.0 mg/L,MLSS约为2 600 mg/L,进水流量为20 L/h时,不同C/N对COD去除率影响不大,当进水C/N约为8时,同时硝化反硝化效果最好,TN去除率均值达到了82%。     

管式反应器处理生活污水的效能

研发了一种基于射流曝气的管式反应设备,考察了负荷和DO对反应器处理效能的影响。实验结果表明,在温度为15℃、DO 6.0 mg/L、有机负荷为1.0 kg COD/(m3.d)、氮负荷为0.30 kg TN/(m3.d)、HRT为8 h的条件下,管式反应器可使生活污水的COD、NH4+-N及TN分别从335 mg/L、105 mg/L及110 mg/L降至43 mg/L、14 mg/L及18 mg/L,去除率分别为87%、86%和83%。DO对反应器脱氮效能影响显著,DO为6 mg/L时,能构建出同步硝化反硝化系统,NH4+-N和TN的去除率分别为96.6%和86.7%。     

低温条件下生态槽深度处理农村生活污水的日变化特性

针对农村生活污水处理设施出水水质偏高污染环境的现状,构建了以水生植物为主体的生态槽深度处理农村生活污水,研究了低温条件下生态槽深度处理生活污水过程中DO、pH、COD、NH4+-N、TP等指标的日变化特性。结果表明,生活污水COD为37.67～60.23 mg/L、NH4+-N为13.66～16.76 mg/L、TP为1.32～1.78 mg/L、水温为9～11℃,HRT为5 d时,生态槽出水COD、NH4+-N和TP平均为21.07 mg/L、0.99 mg/L和0.19 mg/L,均可达《地表水环境质量标准》(GB3838-2002)之Ⅳ类水标准。各级生态槽内DO浓度夜间低于昼间。夜间植物对NH4+-N和TP具有较强的吸收作用,平均去除率分别达94.83%和89.87%;而TN去除效果稍差,平均去除率为59.9%。     

一种基于脱氮和除磷分开的强化污染物去除组合工艺中试研究

针对北京等严重缺水地区提高污水综合排放标准,用于地表水和地下水补充水的需求,以强化COD、N和P去除为目的,研发了N和P不同单元处理的缺氧立体循环氧化沟单元/好氧立体循环氧化沟单元/除磷过滤器单元组合工艺,通过中试实验研究了该工艺的去除效果,并优化了该工艺水力停留时间(HRT)和溶解氧(DO)参数。结果表明,当缺氧和好氧立体循环氧化沟单元的HRT和DO分别为12 h、DO 0.5 mg/L和6 h、2.0 mg/L,除磷过滤器滤速6~8 m/h时,该工艺的平均出水浓度COD 25 mg/L,TN 11 mg/L,NH_4~+-N 1.2 mg/L,TP 0.15 mg/L,平均去除率分别为88%、57%、94%和96%。其中缺氧立体循环氧化沟单元COD、NH_4~+-N和TN平均去除率为70%、80%和57%,好氧立体循环氧化沟单元进一步去除COD和NH_4~+-N(去除率为18%和14%);经缺氧、好氧氧化沟处理去除50%左右的TP,除磷单元吸附作用去除46%的TP。经过该组合工艺处理,COD、N和P都能达到北京市2013年出台的地方污水排放新标准一级B排放要求。     

加压溶气生化气浮法处理生活污水的脱氮试验研究

将加压溶气气浮技术与加压曝气生物氧化技术相结合,开发了加压溶气生化气浮(PA-DAF)法,用于处理生活污水。结果表明,DO和C/N对反应器的脱氮效果有显著影响。DO质量浓度提高到3.5mg/L后,氨氮去除率提高到将近99%。当DO质量浓度为2.5mg/L时,TN去除率达到最大值77.50%。高C/N条件下系统会抑制硝化能力。该反应器能很好地创造缺氧微环境,出现了同步硝化反硝化现象,并对其形成机制进行了分析。     

流量分配比对改良型多级A/O工艺去除污染物的影响

改良型多级A/O工艺处理低碳源(C/N4.0)生活污水。在HRT为8 h、污泥回流比为60%、SRT为10 d的条件下,考察了流量分配比对系统去除有机物、TN、TP及硝化/反硝化能力的影响。结果表明:不同流量分配比(5∶3∶1∶1、1∶0∶0∶0、1∶1∶1∶1)对系统去除有机物及硝化能力的影响不大,出水COD、NH+4-N分别低于23.7、2.23 mg/L,但对系统脱氮除磷及反硝化能力的影响较大。流量分配比为5∶3∶1∶1时,系统能够有效利用进水碳源进行反硝化,且反硝化效果最好,出水TN、TP浓度分别为14.15和0.99 mg/L,去除率分别为79.6%和79.5%。总体而言,改良型多级A/O工艺对低碳源生活污水中污染物有很好的去除效果,这可为实际生活污水的处理提供理论依据。     

湿地植物作为低C?N比生活污水反硝化碳源的研究

以风车草、香根草、再力花、芦荻、美人蕉5种湿地植物作为低C/N比生活污水的反硝化碳源材料。静态碳源释放实验中,5种湿地植物释碳能力为风车草再力花芦荻香根草美人蕉,风车草COD释放量最高,可达(129.2±6.2)mg/(g·L),其TN、TP的释放量相对较低。静态反硝化脱氮实验中,风车草和再力花脱氮效果最好,反硝化出水中硝态氮质量浓度均降低至3mg/L左右,硝态氮去除率均达88%左右,出水COD均在100mg/L左右,COD去除率均达到84%左右。在低C/N比生活污水反硝化脱氮中试实验中,以风车草为反硝化碳源,出水中TN、COD去除率可分别达到73%、75%左右,说明风车草是一种良好的低C/N比生活污水深度处理的反硝化碳源材料。     

A/O工艺N_2O的产生与释放的影响因素

采用A/O工艺,在连续运行条件下,以DO、SRT和硝化液回流比(R)为影响因素,对A/O生物脱氮工艺处理模拟城市生活污水过程中N2O的释放进行了研究。实验结果表明,SRT对A/O工艺N2O释放的影响最大,其次是DO,R的影响最小。N2O转化率随着SRT的升高而降低,当SRT从10 d升高到20 d时,总N2O平均转化率从0.319%下降到0.002%。总N2O转化率随着好氧池DO的升高先降低后有所升高,当DO分别为0.6 mg O2/L、1.2 mg O2/L、2.5 mg O2/L时,反应器的总N2O平均转化率分别为0.306%、0.007%和0.013%。R对N2O释放的影响差异不明显,总N2O平均转化率在300%时最低,为0.007%。N2O释放量最低的工艺运行条件组合是SRT为20 d、DO为1.2 mg O2/L、R为300%。     

次氯酸钠发生器的研制

介绍了电解法生产次氯酸钠的原理 ,并在原有生产工艺的基础上进行了重新设计和对设备的重新选择、改造 ,得出了各个工艺参数的最佳值 ,生产出高品质的次氯酸钠     

Estimation of uncertainty of sampling for analysis of pesticide residues

Abstract

A computer model was used to take random samples from primary sample populations obtained from field trials to simulate the uncertainty of sampling for residue analysis of plant commodities and soil. The results indicate about 40%, 30% and 20% relative uncertainty when random samples of size 5, 10 and 25 are taken respectively, from a single lot. Therefore the sample size should be the same for establishing and enforcing legal limits.     

不同泥源对厌氧氨氧化反应器启动的影响

采用2套上流式生物膜反应器,分别接种少量厌氧氨氧化污泥和大量硝化污泥,考察其对厌氧氨氧化反应器启动的影响。污泥接种入反应器后,测得接种厌氧氨氧化污泥的反应器(R1)内MLSS为0.22 g/L,另一个反应器(R2)MLSS为2.7 g/L。与直接接种厌氧氨氧化污泥相比,R1经过72 d的运行才显现出厌氧氨氧化特性。经过114 d的培养,前者氮去除速率由0.23 kg/(m3.d)提升到5.29 kg/(m3.d),总氮去除率大于89%;R2的氮去除速率由0.01 kg/(m3.d)提升到1.1 kg/(m3.d),总氮去除率大于84.6%。说明普通污泥启动需要一个较长的筛选过程,直接接种少量的厌氧氨氧化污泥比接种普通的污泥能够更快启动厌氧氨氧化反应器。     

Evaluation of the presence of drugs of abuse in tap waters

A total of seventy samples of drinking water were tested for non-controlled and illicit drugs. Of these, 43 were from Spanish cities, 15 from seven other European countries, three from Japan and nine from seven different Latin American countries. The most frequently detected compounds were caffeine, nicotine, cotinine, cocaine and its metabolite benzoylecgonine, methadone and its metabolite EDDP. The mean concentrations of non-controlled drugs were: for caffeine 50 and 19 ng L⁻¹, in Spanish and worldwide drinking water respectively and for nicotine 13 and 19 ng L⁻¹. Illicit drugs were sparsely present and usually at ultratrace level (<1 ng L⁻¹). For example, cocaine has mean values of 0.4 (Spain) and 0.3 ng L⁻¹ (worldwide), whereas for benzoylecgonine, these mean values were 0.4 and 1.8 ng L⁻¹, respectively. Higher concentrations of benzoylecgonine were found in Latin American samples (up to 15 ng L⁻¹). No opiates were identified in any sample but the presence of methadone and EDDP was frequently detected. Total mean values for EDDP were 0.4 ng L⁻¹ (Spain) and 0.3 ng L⁻¹ (worldwide). Very few samples tested positive for amphetamines, in line with the reactivity of chlorine with these compounds. No cannabinoids, LSD, ketamine, fentanyl and PCP were detected.     

An application of the theory of kinematics of mixing to the study of tropospheric dispersion

The most common technique used for numerical simulations of tracer mixing is that of the numerical solution of the advection–diffusion equation with the unresolved fluxes parameterized using the similarity theory. Despite correct predictions of the overall directions of transport, models based on a numerical solution of the advection–diffusion equation lack sufficient accuracy to correctly reproduce the coupling of mixing with small scale processes which are sensitive to the microstructure of the tracer distribution. The objective of this paper is to revisit the basic formalism employed in numerical models used to investigate atmospheric tracers. The main mathematical method proposed here is the theory of kinematics of mixing which could be applied effectively for simulations of atmospheric transport processes. At the beginning of the paper, we introduce simple mathematical transformations in order to demonstrate how complex topological structures are created by mixing processes. These idealistic flow systems are essential to explain transport properties of much more complex three-dimensional geophysical flows. An example of the application of the kinematics of mixing to the analysis of tracer transport on a planetary scale is presented in the following sections. The complex filamentary structures simulated in the numerical experiment are evaluated using some commonly applied statistical measures in order to compare the results with the data published in the literature. The results of the experiment are also analysed with the help of simple conceptual models of fluid filaments. The microstructure of the tracer distribution introduced in the paper is essential to increase our understanding of atmospheric transport and to develop more realistic parameterizations of small-scale mixing. The presented results could also be used to improve calculations of the coupling between microphysical processes and tracer mixing.     

Mechanisms of biodegradation of dibenzoate plasticizers

Biodegradation mechanisms were elucidated for three dibenzoate plasticizers: diethylene glycol dibenzoate (D(EG)DB), dipropylene glycol dibenzoate (D(PG)DB), both of which are commercially available, and 1,6-hexanediol dibenzoate, a potential green plasticizer. Degradation studies were done using Rhodococcus rhodochrous in the presence of pure alkanes as a co-substrate. As expected, the first degradation step for all of these systems was the hydrolysis of one ester bond with the release of benzoic acid and a monoester. Subsequent biodegradation of the monobenzoates of diethylene glycol (D(EG)MB) and dipropylene glycol (D(PG)MB) was very slow, leading to significant accumulation of these monoesters. In contrast, 1,6-hexanediol monobenzoate was quickly degraded and characterization of the metabolites indicated that the biodegradation proceeded by way of the oxidation of the alcohol group to generate 6-(benzoyloxy) hexanoic acid followed by β-oxidation steps. This pathway was blocked for D(EG)MB and D(PG)MB by the presence of an ether function.The use of a pure hydrocarbon as a co-substrate resulted in the formation of another class of metabolites; namely the esters of the alcohols formed by the oxidation of the alkanes and the benzoic acid released by hydrolysis of the original diesters. These metabolites were biodegraded without the accumulation of any intermediates.     

造纸废水混凝处理中SFT助凝替代性研究

中小造纸厂废水处理常用PAC作混凝剂 ,PAM作助凝剂。由于PAM成本很高 ,影响了处理设备的投运率。用超细滑石粉 (SFT)替代PAM助凝 ,与混凝剂PAC配合 ,其混凝处理效果基本相当 ,但是处理成本降低 0 .10元 /m3 。由于SFT属环境无害材料 ,不会给排泥带来二次污染     

混凝试验搅拌器的研制

影响混凝效果的因素众多,混凝沉淀烧杯试验是进行水的混合、絮凝、沉淀工艺研究、设计和生产指导的最有效方法之一,阐述了智能型混凝试验搅拌器的设计原理和技术性能.     

产油微藻培养与回收的关键技术研究进展

寻找廉价而高效的替代原料是实现生物柴油产业化的关键所在.微藻以含油量高、生长周期短、环境适应能力强、生物产量高等优点,有望成为一种极具潜力的生物柴油生产原料.然而,目前尚存在微藻培养低效成本高和微藻回收效率低两大难题.综述了微藻培养与回收过程中的关键技术,并对存在的两大难题及其改进技术进行了详细的探讨.最后,总结并展望了微藻培养、回收技术未来的发展趋势.     

生物质快速热裂解主要参数对生物油产率的影响

以松木木屑为原料,在自制的小型流化床上,开展了生物质热裂解温度、生物质粒径和进料速率对生物油产率的影响实验研究.结果表明,在热裂解温度分别为450、475、500、525和550℃条件下,当热裂解温度为500℃时,生物油产率最高,平均产率达到53.33%（质量百分比）.反应温度越高,炭产量越低,不可冷凝气体产量越高,气体发热值越高;粒径＜1 mm的生物质其粒径对生物油产率影响不大;生物质进料速率增加时,生物油产率增加.本研究为生物能的利用提供了新的途径.