生物膜—活性污泥工艺对甲鱼养殖废水的处理效果研究

对甲鱼养殖产生的温室废水和外塘废水的污染情况进行分析,发现温室废水COD、TP、TN、氨氮浓度较高,污染程度明显高于外塘废水,将温室废水和外塘废水混合后集中于囤水池中,采用生物膜—活性污泥(HYBAS)工艺对甲鱼养殖废水进行处理。结果表明,HYBAS工艺对COD、TP处理效果较好,平均去除率分别为63.76%、59.32%;受冬季低温影响,HYBAS工艺运行前期对TN、氨氮去除效果较差,而运行后期去除效果良好,后期TN、氨氮平均去除率分别为42.84%、85.71%,处理出水总体满足《地表水环境质量标准》(GB 3838—2002)中Ⅳ类标准和《浙江省水产养殖池塘生态化建设与改造规范》养殖废水排放标准。HYBAS工艺建设运行费用低、抗冲击负荷能力强、处理效果良好,是一种简单易行的甲鱼养殖废水处理工艺。     

利用微藻同步实现CO2生物固定与养殖废水脱氮除磷

文章欲通过对小球藻Chlorella sp.的优化培养提高微藻的固碳率以及对养殖废水中氮、磷的去除率。探讨了光强、初始氮浓度(ITNC)、CO2通气比、通气间隔时间和连续培养时间等因素对Chlorella sp.固定CO2和净化污水的能力的影响。结果表明,在光强240μmol/(m·s)、初始氮浓度128 mg/L、通气比0.3 m3/(m3·min)、通气通断间隔15 s/60 s条件下培养10 d,微藻达到最高固碳率564.67 mg/(L·d),与此同时,氮、磷去除率和生物质浓度分别达到66.72%、55.95%和3.50 g/L。     

间歇曝气序批式活性污泥法处理农村废水及其效果的模拟预测

采用两种不同运行模式的间歇曝气序批式活性污泥反应器(IASBR)处理农村废水,反应器连续稳定运行235d,考察了5个工况下,缺氧/好氧循环次数、进水碳氮比(C/N,质量比)、水力停留时间(HRT)等对总有机碳(TOC)、氨氮、TN、TP去除效果的影响。在进水C/N低时,缺氧/好氧循环次数为4的1~#IASBR的脱氮效率及稳定性明显比缺氧/好氧循环次数为2的2~#IASBR高,而脱碳和除磷效果无显著差异。氨氮去除方面,在进水C/N较低的工况1(C/N平均为2.3)、工况2(C/N平均为2.2)和工况4(C/N平均为2.0)下,1~#IASBR的出水氨氮质量浓度明显比2~#IASBR更低,而在进水C/N相对较高时两者无显著差异。TN去除与氨氮去除有类似规律。构建以进水TOC、氨氮、TN、TP、C/N和HRT、缺氧/好氧循环次数为输入的反向传播人工神经网络(BP-ANN)模型,对TOC、氨氮、TN、TP的去除率进行模拟预测,结果显示以上4个输出参数在训练组中的预测结果和实际检测结果之间绝对平均误差分别为2.65%、5.27%、3.56%、34.56%,在测试组中的预测结果和实际检测结果之间绝对平均误差分别为2.74%、3.40%、5.13%、28.32%。     

低C/N比水产养殖废水生物脱氮实验研究

随着短程硝化-反硝化理论研究的发展,在低C/N比条件下,实现污水的生物脱氮处理已成为可能。为此,设计了水产养殖用水的三级生物膜短程硝化-反硝化处理工艺,并对该工艺在去除模拟水产养殖废水主要污染物的作用进行了初步研究。研究结果表明,在进水pH值7.5~8.5,温度为28~32℃,溶解氧为0.5~1 mg/L,游离氨浓度为5~10 mg/L的条件下,模拟废水的COD、NH4+-N和TN的平均去除率分别达到94.4%、91.6%和70.1%;并且低C/N比对出水氨氮NH4+-N的去除率影响不大,NO2--N的平均浓度控制在5.2 mg/L以下,低于鱼类的耐受浓度。表明该短程硝化-反硝化工艺设计,可用于低C/N比水产养殖废水主要污染物的生物处理,尤其是可消除NO2--N对水产养殖的潜在威胁,基本达到养鱼回用标准。     

水洗碳氢溶剂废气的废水生物降解效能及影响因素研究

采用厌氧折流板反应器(ABR)/连续搅拌反应器(CSTR)组合工艺,通过构建共基质体系对水洗碳氢溶剂废气的废水(简称水洗废水)进行处理研究,探讨了共基质体系可行性,考察了水力停留时间(HRT)、硝化液回流比(R,%)、COD和氨氮质量比(C/N)、pH等对水洗废水处理效率的影响。结果表明:(1)共基质体系对去除水洗废水中难降解有机物效果显著。水洗废水占总废水的体积分数≤60%时共代谢效果最佳,COD平均去除率高于84%,氮污染物的去除受该体系影响小。(2)HRT=12h时碳污染物去除效果最佳,COD平均去除率为89.40%。较长的HRT利于脱氮,HRT=24h时氨氮平均去除率达98%,平均出水氨氮为0.87mg/L。R=300%(体积分数)时碳氮污染物去除效果最优。(3)C/N=10时组合装置对废水的脱氮除碳性能最好,COD、总有机碳(TOC)、氨氮和TN平均去除率分别为87.93%、93.11%、95.94%和77.29%。除碳最适pH为6.7,脱氮偏好碱性环境(pH=8.6)。     

有效微生物菌与水生植物联合净化珍珠蚌养殖废水

以无有效微生物(EM)菌与水生植物的珍珠蚌养殖水体(NSE)作为对照组,对EM菌(EM)、苦草+菹草(VP)、水芹菜+水葱(OS)、苦草+菹草+EM菌(VPE)以及水芹菜+水葱+EM菌(OSE)净化珍珠蚌养殖废水的效果进行了对比研究。实验结果表明,EM、VP、OS对珍珠蚌养殖水体N、P均有较好的净化效果,VPE与OSE去N、P效果更佳。净化28 d后5组合中VPE对NH4+-N的去除效果最好,去除率达98.79%;OSE对NO2-N与TN的去除效果最佳,去除率分别达88.09%和91.53%;TP的去除率VPE最高,达91.75%;而COD的去除率以VP最高,达94.97%,效果好于VPE与OSE;EM池水体DO质量浓度第8天达到峰值(9.88±0.61)mg/L,VP、OS、VPE与OSE均在第16天左右达到峰值。实验数据还表明,EM净化水体效果与VP、OS、VPE和OSE均存在显著性差异,对照组NSE对水体的净化效果不明显。     

混凝-IBAC深度处理焦化废水的试验研究

以哈尔滨某气化厂焦化废水为目标,探讨混凝-固定化生物活性炭(IBAC)工艺对哈尔滨气化厂焦化废水进行深度处理的净化效能及其可行性.采用筛选、驯化的脱酚菌,对活性炭(GAC)进行固定,使之形成固定化生物活性炭.当该工艺进水COD＜800 mg/L时,出水COD在100 mg/L以下,平均去除率在80%左右;当进水总酚在200 mg/L以下时,出水的总酚含量基本在20 mg/L以下;当进水氨氮浓度在75 mg/L以下时,出水氨氮浓度在25 mg/L以下.焦化废水中各污染物指标经混凝-IBAC工艺深度处理后可达污水综合排放标准(GB 8978-1996)的二级标准.     

组合工艺处理猪场废水中试实验研究

采用改良UASB-MAP氮磷回收-动态膜好氧-水平潜流人工湿地组合工艺对某猪场废水进行了中试实验研究,重点研究了改进UASB和MAP工艺启动条件参数,并考察了组合工艺稳定运行条件下对猪场废水的COD、N和P等污染物的去除效果。结果表明,该集成工艺启动速度快,污染物去除效果稳定(COD、氨氮和TP的去除率分别为99%、90%和97%)。中试实验结果可为进一步的工程推广应用奠定基础。     

一株高效硝化菌的鉴定及其特性

本研究通过测定菌株ABT01在不同初始氮浓度、pH、C/N、温度和溶氧条件下对氨氮的去除效果,获得该菌株的最佳应用条件。实验结果表明,当初始氨氮浓度低于40 mg/L时,该菌株的氨氮去除率高达85%以上。该菌株最适脱氨氮条件均为：pH 5.0-7.0、C/N=5、35℃、摇床转速150 r/min（溶解氧5.1 mg/L）,氨氮去除率最高达96.8%。同时该菌株经16S rDNA测序、细胞壁脂肪酸组成等鉴定方法,确定ABT01为枯草芽孢杆菌（Bacillus subtilis）。研究表明,枯草芽孢杆菌ABT01具有较好的氨氮去除能力,对水产养殖水质调控有潜在的应用价值。     

生物生态耦合系统对分散式农村生活污水的深度净化

针对分散式农村生活污水排放标准的提升,通过集约式立体生物生态耦合系统对农村生活污水二级处理出水进行深度净化,采用国家标准方法对系统进出水中的COD、氨氮、TN和TP进行了测定,评价了系统对各污染物质的去除效果。结果表明:在实验进水COD,氨氮,TN和TP均属于《城镇污水处理厂污染物排放标准》(GB 18918-2002)一级B标准时,系统稳定后实验出水的COD,氨氮,TN和TP的浓度分别可降至9～35、1～7、8.0～14.9、0.20～0.47 mg·L~(-1),均满足一级A标准。随着流水分区不同,COD,氨氮,TN和TP的浓度逐渐降低。采用集约式立体生物生态耦合系统可使农村生活污水二级处理出水水质达到一级A排放标准,实现深度净化的需求。     

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     

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.     

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.     

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.     

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.     

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.     

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。     

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.     

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     

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.