沉积物性质对沉积物微生物燃料电池产电性能的影响

沉积物微生物燃料电池(SMFC)作为一种原位修复手段,既能降解沉积物中有机污染物,又可同时输出电能,具有广阔的应用前景.沉积物的来源和特性对于SMFC的产电及污染物降解性能具有重要影响.本研究采用了不同环境的6种沉积物(VS质量分数为3.1%~12.6%)构建SMFC反应器,研究不同沉积物构建的SMFC的产电性能、有机物去除率以及SMFC液相p H值的变化.实验结果显示,在不外加有机碳源的条件下,只有当沉积物的VS含量较高(12.6%)时,SMFC才可实现稳定产电,最大功率密度为39.6 m W·m-2.而当沉积物的VS含量较低(12%)时,SMFC不能实现自发产电.向6种沉积物中投加乙酸钠作为外加碳源,可明显促进产电.在有外加碳源的条件下,具有较高含盐量的沉积物构建的SMFC产电性能较好,其最大功率密度可达到142.3 m W·m-2.试验还发现,以土壤与厌氧污泥为混合底物的SMFC系统的产电功率密度明显低于纯土壤SMFC系统,显示了厌氧污泥对SMFC产电有抑制作用.     

Effects of introducing energy recovery processes to the municipal solid waste management system in Ulaanbaatar, Mongolia

Currently, most developing countries have not set up municipal solid waste management systemswith a viewof recovering energy fromwaste or reducing greenhouse gasemissions. In this article, we have studied the possible effects of introducing three energy recovery processes either as a single or combination approach, refuse derived fuel production, incineration and waste power generation, and methane gas recovery from landfill and power generation in Ulaanbaatar, Mongolia, as a case study. We concluded that incineration process is the most suitable as first introduction of energy recovery. To operate it efficiently, 3Rs strategies need to be promoted. And then, RDF production which is made of waste papers and plastics in high level of sortingmay be considered as the second step of energy recovery. However, safety control and marketability of RDF will be required at that moment.     

Distributed generation by energy from waste technology: A life cycle perspective

Municipal Solid Waste in general and its organic fraction in particular is a potential renewable and non-seasonal resource. In this work, a life cycle assessment has been performed to evaluate the environmental impacts of two future scenarios using biogas produced from the organic fraction of municipal solid waste (OFMSW) to supply energy to a group of dwellings, respectively comprising distributed generation using solid oxide fuel cell (SOFC) micro-CHP systems and condensing boilers. The London Borough of Greenwich is taken as the reference case study. The system is designed to assess how much energy demand can be met and what is the best way to use the digestible waste for distributed energy purposes.The system is compared with two alternative scenarios fuelled by natural gas: a reference scenario, where the electricity is supplied by the grid and the heat is supplied from condensing boilers, and a fuel cell micro-CHP system. The results show that, although OFMSW alone can only supply between 1% and 4% of the total energy demand of the Borough, a saving of ∼130 tonnes of CO₂ eq per year per dwelling equipped with micro-CHP is still achievable compared with the reference scenario. This is primarily due to the surplus electricity produced by the fuel cell when the micro-CHP unit is operated to meet the heat demand. Use of biogas to produce heat only is therefore a less desirable option compared with combined heat and power production. Further investigation is required to identify locally available feedstock other than OFMSW in order to increase the proportion of energy demand that can be met in this way.     

消油剂与120#燃料油对马粪海胆(Hemicentrotus pul-cherrimus)抗氧化酶活性的影响

在溢油事故应急处置中,消油剂的使用备受争议。为探究消油剂和溢油对海洋底栖模式生物海胆(Hemicentrotus pulcherrimus)复合毒性效应,通过WAFs(Water-accommodated fractions)和CEWAFs(Chemically enhanced water-accommodated fractions)的96 h暴露实验,测定海胆肠和性腺中过氧化氢酶(CAT)、超氧化物歧化酶(SOD)、谷胱甘肽硫转移酶(GST)、谷胱甘肽过氧化物酶(GPx)活性的变化。实验结果表明:随油水配比浓度的增加,4种酶活性呈现先升高后降低趋势,且酶活性峰值均极显著高于海水对照组水平(P0.01)。肠中4种酶活性最大诱导倍数均高于性腺。相同暴露浓度下,CEWAFs组4种酶活性诱导程度均高于WAFs组。消油剂对照组和海水对照组间4种酶活性则无显著性差异(P0.05)。     

处理垃圾渗滤液的Fe/C空气阴极MFC性能研究

用浸渍法制得硝酸铁/活性炭粉催化剂,通过吸附法将催化剂吸附到碳毡上制作Fe/C催化剂碳毡空气阴极电极.通过改变初始活性炭粉投加量和硝酸铁浓度,考察了两者对以垃圾渗滤液为燃料的MFC产电性能影响;通过循环伏安测试,对不同硝酸铁浓度下自制阴极电极性能进行了评价;在最佳催化条件下考察了装置运行稳定性;并对不同进水COD浓度下同步产电和污水净化性能进行了研究.结果表明,随着活性炭粉投加量或硝酸铁浓度的增加,MFC产电性能均呈现先升高后降低的趋势;当活性炭粉投加量为1 g且硝酸铁浓度为0.25 mol.L-1时,电池性能最佳,功率密度为4 199.8 mW.m-3,表观内阻为465Ω;在硝酸铁和活性炭粉最佳比范围内,MFC的内阻和功率密度分别随着催化剂量的增加而减小和增加;循环伏安测试进一步表明,硝酸铁浓度为0.25 mol.L-1时放电容量最大,且性能稳定;在最佳催化条件下,随着进水COD浓度的增加,MFC产电性能增加,功率密度达5 478.92 mW.m-3,同时COD去除量也增加,最大为1 505.2 mg.L-1,垃圾渗滤液的COD去除率最大达89.1%.     

柴油轿车燃用煤基F-T合成油的排放特性

依据GB 18352.3-2005Ⅰ型试验循环,对帕萨特柴油轿车燃用沪四柴油、煤基F-T合成油、体积混合比例分别为10%和50%的煤基F-T合成油-沪四柴油混合燃料的CO、NOx、HC、PM和CO2排放特性进行了试验研究,分析了该车燃用F-T合成油尾气污染物排放的环境影响特性.结果表明,GB 18352.3-2005Ⅰ型试验循环中,该车燃用煤基F-T合成油-沪四柴油混合燃料城区行驶循环排放的CO、HC、PM和CO2相对较高,城郊行驶循环排放的NOx相对较高;与沪四柴油比较,该柴油轿车燃用煤基F-T合成油-沪四柴油混合燃料后,其CO、NOx、HC、PM和CO2排放均有不同程度的降低,且产生气溶胶、酸化、全球变暖等环境影响的潜力减小.煤基F-T合成油是一种较理想的柴油替代/补充燃料.     

硫氰酸根在粒状镁铝复合氧化物上的吸附性能

以镁铝水滑石(Mg/Al-LDH)为前驱物制备了粒状镁铝复合氧化物(G-Mg3.3AlO4.8),采用BET、XRD、SEM和FT-IR方法对其结构进行了表征,考察了这种新材料对硫氰酸根(SCN-)的吸附性能.G-Mg3.3AlO4.8的比表面积和平均孔径分别为269.4 m2.g-1和13.25 nm,成型造粒保留了层状结构且无新相生成.Freundlich等温式和准二级动力学方程能很好地描述SCN-在G-Mg3.3AlO4.8上的静态吸附过程,25℃初始浓度为500 mg.L-1时静态吸附量可达165.8 mg.g-1;Yoon-Nelson模型能很好地预测SCN-在G-Mg3.3AlO4.8上的穿透曲线,初始浓度100 mg.L-1、流速5 mL.min-1、床层高度10 cm和pH=6时穿透点吸附量可达50.73 mg.g-1,重复使用4次对SCN-的脱除率均保持在98%以上,是一种可重复利用的高效吸附剂.     

高温纤维素降解菌群筛选及产酶特性

从园林废弃物鸡粪混合堆肥的高温期堆肥样品中,筛选出6株具有高效纤维素降解性的高温菌.通过16S rRNA基因序列比对和构建系统发育树分析,初步鉴定这6种菌株为高温紫链霉菌(Streptomyces thermoviolaceus)、嗜热淀粉酶链霉菌(S.thermodiastaticus)、嗜热一氧化碳链霉菌(S.thermocarboxydus)、黄白链霉菌(S.albidoflavus)、热普通链霉菌(S.thermovulgaris)和波茨坦短芽孢杆菌(Brevibacillus borstelensis).目前为止,国内外对纤维素降菌群的研究较少,本研究将6种菌株1∶1等体积混合制成混合菌群M-1,利用DNS法比较混合菌群M-1和单一菌株的产羧甲基纤维素酶(CMCase)能力.结果表明,混合菌群M-1比单一菌株产CMCase能力强.对混合菌群M-1产CMCase活力特性进行研究,确定混合菌群M-1的最佳产酶条件.结果表明,混合菌群M-1以体积分数1%接种量接种于初始p H为4的以麸皮+淀粉混合物为碳源,玉米粉为有机氮源,KNO_3为无机氮源的培养基中,45℃条件下培养,能够有最大的酶活,达135.9 U·m L~(-1).条件优化后,产酶能力提高1.8倍.     

微生物燃料电池浸取废旧锂电池的影响因素分析

将MFC的阴极还原能力应用于废旧锂电池正极材料LiCoO_2的还原浸取.构建了以弱酸中LiCoO_2作为化学阴极电子受体的双室MFC,探讨了MFC阴极浸取还原LiCoO_2的可行性,并研究了浸取还原过程中阴极液pH、离子强度、固液比等因素对MFC的产电性能与LiCoO_2浸取效果的影响.实验结果表明:MFC阴极还原LiCoO_2使得固相中Co(III)被还原为液相中Co(II)是可行的,MFC能够持续地输出电压,且MFC优于弱酸浸取效果.阴极液pH值越低,MFC的产电性能和LiCoO_2的浸取效果越明显,阴极液pH为1.0时,MFC的最大输出电压为600 m V,60 h时浸取率达到86.5%;随着阴极液中KCl浓度和固液比(S/L)的增加,MFC输出电压和浸取效率也越高;对影响MFC的影响因素分析讨论得出,阴极液pH值是LiCoO_2还原过程中重要影响因素,因此,在后续的实验设计中要重点考虑pH的影响.     

非离子型表面活性剂强化混合菌降解间二甲苯的性能研究

从焦化废水厂的活性污泥中筛选间二甲苯混合降解菌,并研究非离子型表面活性剂吐温80(C_(64)H_(124)O_(26))对混合菌降解间二甲苯的强化作用.研究结果表明:驯化后的间二甲苯混合降解菌以产黄杆菌属(Rhodanobacter sp.)为主,占比41.2%;仅存在吐温80作为单一碳源时,高浓度的吐温80对混合降解菌没有明显的抑制作用;吐温80与间二甲苯共存时,当吐温80浓度为2 CMC,反应72 h后间二甲苯的降解率达到最高,为76%;提前12 h(较混合降解菌)投加浓度为2 CMC的吐温80,最利于菌种的生长繁殖及间二甲苯的降解.