秸秆发酵产氢的影响因素研究

以加热预处理的厌氧活性污泥为接种物,以秸秆（稻草、麦杆）为发酵底物进行微生物产氢实验,研究了不同秸秆粒径、纤维素酶用量、预处理方法、发酵液pH值对秸秆发酵产氢速率以及产氢气量的影响.其中颗粒粒径为170 μm的稻草经过NaOH预处理,按照底物与纤维素酶用量1∶1的比例酶解,进而发酵产氢的单位总产氢量为90.5 mL/g,最大单位产氢速率为0.58 mL/(h·g).     

水稻秸秆厌氧发酵制氢技术研究

以水稻秸秆为研究原料,用牛粪为接种物,采用稀硫酸预处理方法来提高秸秆纤维素的降解率,从而提高其发酵产氢的能力,并且进一步考察了发酵初始pH、发酵温度、牛粪与秸秆的质量比和底物浓度四个条件对发酵产氢的影响。实验结果表明:在接种100g/L牛粪的条件下,以1.8%的硫酸加热30min预处理秸秆产氢效果最佳,为19.64mL/gTS,是未经过预处理的秸秆产氢量(0.1mL/gTS)的196倍,粗纤维含量由未处理前的36.7%下降到酸处理后的31.5%。在pH8.0、温度为37℃、牛粪与秸秆质量比为2.5∶1、底物浓度为50g/L时的产氢效果最好,累计产氢量为29.14mL/gTS,此时生物气中没有检测到甲烷气体,氢气浓度达到63.88%。     

NaOH预处理对香蕉秸秆厌氧发酵产沼气的影响

以农村废弃资源香蕉秸秆为原料,采用试验室自制的厌氧发酵装置,在恒温35℃和发酵料液总固体质量分数为6%的条件下进行沼气发酵试验,研究不同质量分数(2%、4%、6%、8%) NaOH的预处理对香蕉秸秆厌氧发酵产气效果的影响。研究结果表明:香蕉秸秆经过NaOH预处理后与对照组(未经NaOH预处理)相比产气量明显增加,其中,NaOH预处理浓度为6%的处理组,发酵58 d时的总产沼气量、总产甲烷量、总固体(TS)产气量、总固体(TS)产甲烷量均最高,分别为21581. 00 mL、11878. 30 mL、548. 87 mL/g、302. 10 mL/g。经过NaOH预处理后的香蕉秸秆发酵过程中pH值在适宜的范围内波动,发酵前后发酵液中COD的降解率均达到60%以上。故综合来看,NaOH预处理能缩短香蕉秸秆厌氧发酵的启动时间,增加发酵体系的缓冲性和稳定性,提高产气效果,且NaOH预处理浓度为6%时,香蕉秸秆厌氧发酵效果最优。     

不同湿热预处理条件对餐厨垃圾厌氧发酵产氢的影响

采用湿热水解技术处理餐厨垃圾,研究不同湿热预处理温度与时间下餐厨垃圾w(VS)(VS为挥发性固体)、ρ(CODs_Cr)(CODs为溶解性化学需氧量)、ρ(TOC)、ρ(TN)等指标的变化,以评价湿热预处理对餐厨垃圾厌氧产氢效能的影响. 在此基础上,结合厌氧产氢动力学分析,确定厌氧发酵产氢的最佳湿热预处理条件. 结果表明:湿热预处理温度、时间对餐厨垃圾可浮油脱出量、w(VS)具有显著影响. 餐厨垃圾湿热预处理后ρ(CODs_Cr)、ρ(TOC)、ρ(TN)变化情况与w(VS)呈负相关. 餐厨垃圾经90℃湿热预处理30min后,可浮油脱出量为37.5mL/kg,w(VS)/w(TS)为95.12%,最大比产氢量达242.1mL/g,最大产氢速率为12.46mL/h,累积产氢率达0.88mol/mol,厌氧产氢启动时间为12.85h. 说明对餐厨垃圾进行适度的湿热预处理可有效提高有机物溶解性与生物可利用效率,进而提高厌氧发酵累积产氢量与产氢速率. 综合能耗、产出等因素,湿热预处理温度90℃,处理时长30min,为餐厨垃圾厌氧发酵产氢的最佳湿热预处理条件.      

初始pH对酸性预处理污泥厌氧发酵产氢的影响

对污泥进行不同pH值的酸性预处理,用HCl将污泥pH值分别调到2.0、3.0、4.0、5.0,在4℃条件下放置24 h,然后再用NaOH分别调到2.0～12.0用于批量试验,系统考察了不同初始pH值对酸性预处理污泥厌氧发酵产氢的影响.研究表明,初始pH为2.0～4.0以及12.0时对产氢菌及耗氢菌有抑制作用,总体产氢量少;初始pH为5.0～9.0时,甲烷菌及产氧菌均活跃,产氢滞后时间短.但总体产氢量少;初始pH为11.0时,甲烷菌受到明显抑制,而产氢菌仍然活跃,总体产氢量较高,发酵后期pH恒定在7.0～8.0,经pH为2.0、3.0、4.0和5.0酸性预处理的污泥(干重)累积产氢量分别为0.59、1.83、0.50和0.56 mL/g.     

湿热预处理对餐厨废弃物厌氧产氢发酵类型的影响

通过批试验分析湿热预处理前后餐厨废弃物CODs(溶解性化学需氧量)、CODt(总化学需氧量)、粗蛋白浓度、碳氮比(C/N)等指标及代谢产物的变化,研究湿热预处理对餐厨废弃物厌氧发酵类型和产氢效能的影响。采用Gompertz动力学模型分析经湿热预处理后厌氧发酵系统启动速度、累积产氢量、产氢速率的变化。结果表明,餐厨废弃物经150℃湿热预处理30 min后,可浮油脱出量高达97.5 mL/kg,CODs和C/N变化显著;VFAs(挥发性有机酸)和乙醇浓度分析表明,湿热预处理可使餐厨废弃物厌氧发酵产氢的产酸类型从丙酸型发酵转变为丁酸型发酵。在微生物的作用下,湿热预处理时间为30 min时,经90℃处理后餐厨废弃物中的丁酸等VFAs进一步降解转化为乙酸、CO2和H2,比产氢量最高为242.1 mL/g(以VSS计)。湿热预处理可以改变餐厨废弃物中碳水化合物、蛋白质和脂肪的理化性质,影响其厌氧发酵产氢产酸类型,达到改善餐厨废弃物厌氧发酵产氢效能的目的。     

Pseudomonas sp. GL1利用不同预处理污泥产氢及其底物变化研究

采用厌氧发酵的方法研究Pseudomonas sp.GL1利用灭菌、微波和超声波预处理污泥产氢效果,讨论3种预处理污泥产氢效果的差异,并对污泥发酵过程中底物性质变化(SCOD、可溶性蛋白质、总糖和pH值等)进行了探讨.实验结果显示,产氢菌Pseudomonas sp.GL1发酵各预处理污泥过程中均只有H2和CO2产生,无CH4产生.3种不同预处理污泥同等条件下发酵,灭菌污泥的产氢效果最佳,氢气含量高达81.45%,产氢率为30.07mL·g-1.超声波处理污泥产氢延迟时间最短(3 h);灭菌污泥最长(15 h);微波预处理污泥为12 h.在预处理污泥发酵产氢过程中,各种污泥性质变化情况各不相同,尤其是灭菌污泥,这说明不同的预处理方法影响Pseudomonas sp.GL1发酵过程对污泥中营养物质的利用.     

水稻秸秆经漆酶预处理后产沼气研究

利用秸秆产沼气是秸秆无害化处理解决环境污染问题的可行手段.本研究针对秸秆特殊结构而导致产沼气少、启动慢、利用率低等问题,采用自培养漆酶预处理水稻秸秆,提高了秸秆产气率及利用率.通过研究发现,当漆酶添加量为40 mL、发酵温度为35℃、预处理7d的条件下,秸秆的产气量最高;同时发现,金属离子的添加对沼气产量有很大影响,其中Cu2添加后产气量提高最多.另外,研究发现预处理天数为24 d的秸秆木质素纤维素降解率最高.     

外加淀粉酶预处理污泥厌氧发酵产氢研究

通过外加淀粉酶预处理剩余污泥,考察了淀粉酶对污泥的破解效果,研究了接种产氢菌(Enterococcus sp.LG1)和未接种产氢菌两种状况下,污泥厌氧发酵产氢效果,并与相应温度(60℃)热预处理污泥的发酵产氢效果进行对比,同时分析探讨了污泥发酵产氢过程中底物和pH值的变化.结果表明,淀粉酶预处理污泥4h后水解效果最佳...     

污泥厌氧发酵产氢的影响因素

污水生物处理过程中产生大量剩余污泥, 通常采用厌氧发酵处理并获取甲烷气体. 产氢产酸是污泥厌氧消化过程中的一个中间阶段. 本研究考察了原污泥和经碱处理的污泥在不同初始pH(3.0～12.5)条件下的产氢效果, 以及污泥性质和污泥浓度等对产氢效果的影响. 结果表明, 当初始pH为11.0时污泥发酵的产氢率达到最大值.采用原污泥发酵产氢时, 在初始pH为11.0的条件下发酵产氢获得的最大产氢率为8.1 mL/g, 而经碱处理的污泥在同样初始pH的条件下发酵产氢可将其产氢率提高一倍左右, 达到16.9 mL/g. 污泥经碱处理后厌氧发酵4d无甲烷产生, 且可有效地降低氢气消耗的速率. 另外, 污泥的VSS/SS值过低时会大大降低污泥的产氢率, 而污泥浓度对产氢率无明显影响.     

Distribution and ecological effect of mercury in Laogang landfill, Shanghai, China

Laogang landfill near Shanghai is the largest landfill in China, and receives about 10000 t of daily garbage per day, Samples of topsoil and plants were analyzed to evaluate mercury pollution from the landfill. For topsoil samples, there were significant correlations among total mercury （HgT）, combinative mercury （Hgc） and gaseous mercury （HgG）, and content of total organic carbon （TOC）, but, no significantly relationship was found between Hg content and filling time. Hg content changes in vertical profiles with time showed that the average Hgv of profiles 1992, 1996, and 2000 was similar, but their average HgG was quite different. HgT was significantly correlated with Hgc in profile 1992 and 2000, and Hgv was significantly correlated with Hg6 in profile 1996. HgG/Hgv ratio in profile samples decreased in the order of （HgG,/HgT）1992〉（HgG/HgT）1996〉〉（HgG/HgT）2000. A simple outline of Hg release in landfill could be drawn： with increasing of filling time, degradation undergoes different biodegradation, accordingly, gaseous mercury goes through small, more, and small proportion to total mercury. Distribution of Hg in plants was inhomogeneous, following the order of leaf〉root〉stem. The highest value of leaf may be associated with higher atmospheric Hg from landfill. Ligneous plants （e.g. Phyllostachys glanca, Prunus salicina and Ligustrum lucidum） are capable of enriching more Hg than herbaceous plants.     

EDTA-enhanced phytoremediation of lead contaminated soil by Bidens maximowicziana

Phytoremediation is a potential cleanup technology for the removal of heavy metals from contaminated soils.Bidens maximowicziana is a new Pb hyperaccumulator,which not only has remarkable tolerance to Pb but also extraordinary accumulation capacity for Pb.The maximum Pb concentration was 1509.3 mg/kg in roots and 2164.7 mg/kg in overground tissues.The Pb distribution order in the B. maximowicziana was:leaf>stem>root.The effect of amendments on phytoremediation was also studied.The mobility of soil Pb and the Pb concentrations in plants were both increased by EDTA application.Compared with CK(control check),EDTA application promoted translocation of Pb to overground parts of the plant.The Pb concentrations in overground parts of plants was increased from 24.23-680.56 mg/kg to 29.07-1905.57 mg/kg.This research demonstrated that B.maximowicziana appeared to be suitable for phytoremediation of Pb contaminated soil,especially,combination with EDTA.     

Decomposition of alachlor by ozonation and its mechanism

Decomposition and corresponding mechanism of alachlor, an endocrine disruptor in water by ozonation were investigated. Results showed that alachlor could not be completely mineralized by ozone alone. Many intermediates and final products were formed during the process, including aromatic compounds, aliphatic carboxylic acids, and inorganic ions. In evoluting these products, some of them with weak polarity were qualitatively identified by GC-MS. The information of inorganic ions suggested that the dechlorination was the first and the fastest step in the ozonation of alachlor.     

Enzymatic oxidation of aqueous pentachlorophenol

The influence of the nonionic surfactant Tween 80 on pentachlorophenol （PCP） oxidation catalyzed by horseradish peroxidase was studied. The surfactant was tested at concentrations below and above its critical micelle concentration （CMC）. Enhancement of PCP removal was observed at sub-CMCs. The presence of Tween 80 in the reaction mixture reduced enzyme inactivation which occurred through a combination of free radical attack and sorption by precipitated products. A simple first-order model was able to simulate time profiles for enzyme inactivation in the presence or absence of Tween 80. At supra-CMCs, the surfactant caused noticeable reductions in PCP removal, presumably through micelle partitioning of PCP which precluded the hydrophobic PCP molecule from interacting with the enzyme.     

基于综合水质标识指数和对应分析法的校园河道水质评价

以三峡大学的校园河道求索溪为研究对象,利用综合水质标识指数法确定求索溪水质类别,分析其水质时空变化规律,并利用对应分析法得出求索溪中不同监测点的主要污染因子.研究结果表明:求索溪整体的综合水质标识指数为7.423,整体水质为劣V类(地表水环境质量标准GB 3838-2002)且黑臭.从时间变化来看,求索溪4月份的水质最差,5月份次之,4、5月份所有监测点的水质都劣于V类且黑臭;8月份水质最好,水质为Ⅳ类;从空间分布来看,8个监测点综合水质标识指数均超过6.0,水质为劣V类,其中6号监测点的水质相对最好,监测点3号的水质相对最差;对应分析法得出求索溪的整体水体污染程度受总氮因子的影响最大,其次为总磷.该研究拟为求索溪及类似校园河道的水环境治理研究提供基础依据和参考.     

Effects of chitosan on growth of an aquatic plant (Hydrilla verticillata) in polluted waters with different chemical oxygen demands

Effects of chitosan on a submersed plant, Hydrilla verticillata, were investigated. Results indicated that H. venicillata could prevent ultrastructure phytotoxicities and oxidativereaction from polluted water with high chemical oxygen demand (COD). Superoxide dismutase (SOD) activity and malondialdehyde (MDA) contents in H. verticillata treated with 0.1% chitosan in wastewater increased with high COD (980 mg/L) and decreased with low COD (63 mg/L), respectively. Ultrastructural analysis showed that the stroma and grana of chloroplast basically remained normal. However, plant cells from the control experiment (untreated with chitosan) were vacuolated and the cell interval increased. The relict of protoplast moved to the center, with cells tending to disjoint. Our findings indicate that wastewater with high COD concentration can cause a substantial damage to submersed plant, nevertheless, chitosan probably could alleviate the membrane lipid peroxidization and ultrastructure phytotoxicities, and protect plant cells from stress of high COD concentration polluted water.     

Removal of cadmium using MnO2 loaded D301 resin

MnO2 loaded weak basic anion exchange resin D301 （Anion exchange resin, macroreticular weak basic styrene） as adsorbent has been prepared and applied to the removal of cadmium. The adsorption characteristics have been investigated with respect to effect of pH, equilibrium isotherms, removal kinetic data, and interference of the coexisting ions. The results indicated that the Cd^2＋ could be efficiently removed using MnO2 loaded D301 resin in the pH range of 3-8 from aqueous solutions with the co-existence of high concentration of alkali and alkaline-earth metals ions. The saturate adsorption capacity of the Cd^2＋ was 77.88 mg/g. The adsorption process followed the pseudo first-order kinetics. The equilibrium data obtained in this study accorded excellently with the Langmuir adsorption isotherm.     

Effect of coagulation pretreatment on the fouling of ultrafiltration membrane

The purpose of this study is to understand the effect and mechanism of preventing membrane fouling, by coagulation pretreatment, in terms of fractional component and molecular weight of natural organic matter （NOM）. A relatively higher molecular weight （MW） of hydrophobic compounds was responsible for a rapid decline in the ultrafiltration flux. Coagulation could effectively remove the hydrophobic organics, resulting in the increase of flux. It was found that a lower MW of neutral hydrophilic compounds, which could remove inadequately by coagulation, was responsible for the slow declining flux. The fluxes in the filtration of coagulated water and supernatant water were compared and the results showed that a lower MW of neutral hydrophilic compounds remained in the supernatant water after coagulation could be rejected by a membrane, resulting in fouling. It was also found that the coagulated flocs could absorb neutral hydrophilic compounds effectively. Therefore, with the coagulated flocs formed on the membrane surface, the flux decline could be improved.     

Penetration analysis of elements and bioleaching treatment of spent refractory for recycling

Acidithiobacillus ferrooxidans ATCC23270 and Acidithiobacillus thiooxidans TM-32 were used for bioleaching of spent refractories of aluminium and copper melting furnaces for their recycling.Firstly,penetration of elements into aluminium melting furnace refractory was investigated and it was found that up to 7 cm from surface was contaminated.Comparison on leaching efficiency by the strains ATCC23270 and TM-32 found that the strain ATCC23270 could treat larger amount of the refractories than the strain TM-32 could do.In the experiment of bioleaching of spent refractory aluminium melting furnace by the strain ATCC23270,high leaching efficiency were obtained on Al,Si,and Ca,and extremely low leaching performance was,however,shown on the rest of elements i.e.,Na,Mn,and Zn.Under the strain TM-32 use,relatively high leaching performance was recognized on Al,Si,Ca,Na,Mn,and Zn.In the experiment of bioleaching for spent refractory copper melting furnace,almost the same leaching trends were shown on Cu,Zn,Al,and Si under the strains ACTT23270 and TM-32 uses.     

Simultaneous removal of ammonium and phosphate by zeolite synthesized from coal fly ash as influenced by acid treatment

Zeolite synthesized from fly ash （ZFA） without modification is not efficient for the purification of NH4＋ and phosphate at low concentrations that occur in real effluents, despite the high potential removal capacity. To develop an effective technique to enhance the removal efficiency of ammonium and phosphate at low concentrations, ZFA was modified with acid treatment and the simultaneous removal of ammonium and phosphate in a wide range of concentration was investigated. It was seen that when compared with untreated ZFA, only the treatment by 0.01 mol/L of H2SO4 significantly improved the removal efficiency of ammonium at low initial concentrations. The behavior was well explained by the pH effect. Treatment by more concentrated H2SO4 led to the deterioration of the ZFA structure and a decrease in the cation exchange capacity. Treatment by 0.01 mol/L H2SO4 improved the removal efficiency of phosphate by ZFA at all initial P concentrations, while the treatment by concentrated H2SO4 （≥0.9 mol/L） resulted in a limited maximum phosphate immobilization capacity （PIC）. It was concluded that through a previous mild acid treatment （e.g. 0.01 mol/L of H2SO4）, ZFA can be used in the simultaneous removal of NH4＋ and P at low concentrations simulating real effluent.