林可霉素菌(Streptomyces lincolnensis)利用吡唑酮废水的研究

采用被吡唑酮废液驯化、分离、筛选后的林可霉素菌,并对其在摇瓶上利用吡唑酮废液中的硫酸铵发酵(7 d)生产林可霉素进行了研究。实验结果表明,废液加入培养基体积比都为1∶10,实验1中菌丝代谢和对照比正常,其中还原糖利用最快,在发酵后期为0.24 mg/L,林可霉素起步效价最低为2 100 IU/mL,与对照相比最后发酵效价降低了70 IU/mL;实验2发酵过程pH值偏低,全程为5.86～6.50,氨基氮代谢缓慢为40 mg/100 mL,最后林可霉素效价最低为4 480 IU/mL;实验3中废液在发酵进入48 h中后期的时候补入能促进菌丝体分泌,最后林可霉素为5 180 IU/mL,比对照发酵水平高出8.82%。可见实验3的实验设计有利于林可霉素菌利用吡唑酮废液生产林可霉素,为废物循环利用、变废为宝的可行性作了有意义尝试。     

铁盐和铝盐混凝对印染废水生化出水中溶解性有机污染物的去除特性

以三氯化铁和硫酸铝为混凝剂,印染废水二级生化出水为研究对象,并利用XAD-8/XAD-4吸附树脂联用技术将印染废水生化出水中溶解性有机物分为疏水酸、非酸疏水物质、弱疏水物质及亲水物质4类有机物,通过小试实验探讨了2种混凝剂对生化出水中各类溶解性有机物的去除效果及特点。实验结果表明,对于该印染废水的生化出水,溶解性有机物的主要成分是疏水性物质,以DOC表征时占总DOC的75%,其中疏水酸约占41%,疏水性物质也是引起色度的主要物质,所占比例以ADMI7.6表征时为89%,其中以非酸疏水物质的贡献最大,达到52%,并且非酸疏水物质中不饱和双键或芳香环有机物的含量较高。在三氯化铁和硫酸铝各自最佳的混凝条件下,均能够有效去除由疏水性物质（疏水酸和非酸疏水物质）引起的色度,但三氯化铁对弱疏水性物质以及亲水物质的去除率高于硫酸铝,这使得三氯化铁对印染废水生化出水中的溶解性有机物的去除效果优于硫酸铝。并且三氯化铁和硫酸铝混凝工艺均能明显降低生化出水的毒性。     

质子化改性交联壳聚糖的制备及其吸附硫酸根离子的性能

以壳聚糖为原料,甲醛为氨基保护剂,戊二醛为交联剂,采用反相悬浮交联法制备交联壳聚糖,再对其进行质子化改性得到质子化改性交联壳聚糖吸附剂。通过正交实验对该吸附剂的制备条件进行优化,并对其吸附水中硫酸根（SO₄^2-）的吸附等温特性和动力学进行研究,最后对制备和吸附过程进行能谱分析（EDS）并对吸附剂进行了再生实验。实验结果表明,交联反应的优化条件为：反应温度50℃、反应时间6 h、甲醛：戊二醛：壳聚糖为4.5：0.5：3（质量比）;该吸附过程符合Langmuir吸附等温模型,在25℃（298 K）下,吸附容量最大可达133.87 mg/g;吸附过程较好地符合拟二级动力学模型;EDS分析表明了交联反应、质子化改性和吸附反应均已发生;该吸附剂的再生性能良好,可以重复使用。     

ABR处理硫酸盐有机废水的BP神经网络建模

通过厌氧折流板反应器(ABR)处理硫酸盐有机废水的实验数据对BP神经网络进行训练,建立了ABR处理硫酸盐有机废水的BPNN模型,通过测试对比,找出了较优训练函数为traingda,较优训练次数为1 900.利用分割连接权值法(PCW)对影响出水SO42-和COD的主要因素进行分析,结果显示进水COD、SO42-、pH、COD/SO42-和HRT对出水SO42-和COD均产生一定影响,其中进水pH对出水SO42-和COD的影响最大,相对重要性(RI)指数分别为30.79％和23.44％;并通过样本试验数据分别建立了对SO42-和COD去除率的限制因子仿真模型,为预测硫酸盐有机废水的厌氧处理过程提供指导.     

碱式硫酸铝溶液中SO42-的测定

建立了以铬黑T为指示剂,乙二胺四乙酸二钠反滴定过量BaCl₂的碱式硫酸铝溶液中SO₄^2-的测定方法。实验确定的操作条件为：待测试样稀释后ρ（SO_4^2-）为0.025 ~0.100 g/L,BaCl₂过量率为25%~100%,并且在加入BaCl₂前将试样煮沸,三乙醇胺加入量为0.10 L/L。该法回收率在98.90%~100.72%,相对标准偏差小于1%。测定方法准确,可靠,且操作简便、快速。     

O3-H2O2氧化法处理印染废水

采用O₃-H₂O₂氧化法对印染废水进行氧化处理,比较了O₃氧化法和O₃-H₂O₂氧化法对印染废水的处理效果,考察了初始废水pH、H₂O₂加入量、O₃流量和反应时间对废水的色度去除率和COD去除率的影响。实验结果表明：O₃-H₂O₂氧化法对废水的COD和色度的去除效果比O₃氧化法更好;在初始废水pH为11、H₂O₂加入量为13mmol/L、O₃流量为6g/h、反应时间为60min的最佳工艺条件下,处理后废水COD为61.50mg/L,COD去除率为95.73%,废水色度为5倍,色度去除率为99.75%,TOC为37.84mg/L,TOC去除率为85.10%,BOD₅为22.76mg/L,BOD₅去除率为90.20%,BOD₅/COD为0.37。     

Hydrogen Sulfide Gas Treatment by a Chemical‐Biological Process: Chemical Absorption and Biological Oxidation Steps

In order to remove high concentrations of hydrogen sulfide (H₂S) gas from anaerobic wastewater treatments in livestock farming, a novel process was evaluated for H₂S gas abatement involving the combination of chemical absorption and biological oxidation processes. In this study, the extensive experiments evaluating the removal efficiency, capacity, and removal characteristics of H₂S gas by the chemical absorption reactor were conducted in a continuous operation. In addition, the effects of initial Fe^2 + concentrations, pH, and glucose concentrations on Fe^2 + oxidation by Thiobacillus ferrooxidans CP9 were also examined. The results showed that the chemical process exhibited high removal efficiencies with H₂S concentrations up to 300 ppm, and nearly no acclimation time was required. The limitation of mass‐transfer was verified as the rate‐determining step in the chemical reaction through model validation. The Fe^2 + production rate was clearly affected by the inlet gas concentration as well as flow rate and a prediction equation of ferrous production was established. The optimal operating conditions for the biological oxidation process were below pH 2.3 and 35°C in which more than 90% Fe^3 + formation ratio was achieved. Interestingly, the optimal glucose concentration in the medium was 0.1%, which favored Fe^2 + oxidation and the growth of T. ferrooxidans CP9.     

Ti（Ⅳ）催化臭氧／过氧化氢预处理酸性难降解废水

在Ti（Ⅳ）和过氧化氢存在条件下,考察了臭氧化酸性苯乙酮溶液、硝基苯溶液和垃圾渗滤液（浙江衢州某垃圾填埋场）的预处理效能。结果表明,在pH2．86条件下,单独臭氧化处理对苯乙酮、硝基苯和垃圾渗滤液的COD去除率分别为10．1％、44％和28．6％。BOD,／COD值分别从原来的0．039、0．060和0．085提高到了0．130、0．158和0．174,仍属生化难降解废水。当体系加入Ti（Ⅳ）后,臭氧化苯乙酮和硝基苯的COD去除率分别达到了75．5％和65％,BOD;／COD则提高到了0．679和0．314,可生化性提升明显。对于垃圾渗滤液,只有当体系加入Ti（Ⅳ）和H22后,臭氧化COD的去除率达到66．6％,BOD、／COD提高至0．425。上述结果对酸性难降解废水的处理实际意义非常突出。     

Matrix based fertilizers reduce nitrogen and phosphorus leaching in three soils

We compared the efficacy of matrix based fertilizers (MBFs) formulated to reduce NO3-, NH4+, and total phosphorus (TP) leaching, with Osmocoate 14-14-14, a conventional commercial slow release fertilizer (SRF) and an unamended control in three different soil textures in a greenhouse column study. The MBFs covered a range of inorganic N and P in compounds that are relatively loosely bound (MBF 1) to more moderately bound (MBF 2) and more tightly bound compounds (MBF 3) mixed with Al(SO4)3H2O and/or Fe2(SO4)3 and with high ionic exchange compounds starch, chitosan and lignin. When N and P are released, the chemicals containing these nutrients in the MBF bind N and P to a Al(SO4)3H2O and/or Fe2(SO4)3 starch-chitosan-lignin matrix. One milligram (8000 spores) of Glomus intradices was added to all formulations to enhance nutrient uptake. In all three soil textures the SRF leachate contained a higher amount of NH4+, NO3- and TP than leachate from all other fertilizers. In all three soils there were no consistent differences in the amount of NH4+, NO3- and TP in the MBF leachates compared to the control leachate. Plants growing in soils receiving SRF had greater shoot, root and total biomass than all MBFs regardless of Al(SO4)3H2O or Fe2(SO4)3 additions. Arbuscular mycorrhizal infection in plant roots did not consistently differ among plants growing in soil receiving SRF, MBFs and control treatments. Although the MBFs resulted in less plant growth in this experiment they may be applied to soils growing plants in areas that are at high risk for nutrient leaching to surface waters.     

Seasonal Differences in the Levels of Gaseous Air Pollutants in the Vicinity of a Waste Dump

Hydrogen sulphide, ammonia, nitrogen dioxide, mercaptans and sulphur dioxide (H₂S, NH₃, NO₂, R-SH, SO₂) concentrations were measured at the location in the vicinity of the waste dump to determine the air pollution level of these pollutants prior to the operation of the Mobile Thermal Treatment Plant. Samples were collected over one year period. Seasonal differences, and the influence of meteorological parameters (temperature, relative humidity, pressure and wind direction) on the air pollution levels were studied. Results show relatively low concentrations of H₂S, NO₂, R-SH and SO₂, while NH₃ levels were higher compared to the guideline values. Good weather conditions (high air pressure and low relative humidity) are connected to long range transport of NO₂, while higher temperatures result in elevated NH₃ and R-SH concentrations. Because of the predominant northeast wind direction (the same as the waste dump direction), the contribution of air pollution from the direction of the waste dump at the measuring site is significant, but that does not necessarily mean that the pollutants originated from that source.