酸化餐厨垃圾厌氧消化产氢研究

分析了餐厨垃圾酸化过程中的pH、挥发性脂肪酸(VFA)产量及含水量等参数的变化,考察了酸化餐厨垃圾厌氧消化过程中的产氢情况,并探讨了调节初始pH对酸化餐厨垃圾产氢的影响.结果表明,餐厨垃圾的酸化是一个前期极为快速的过程,经过1d的酸化,新鲜餐厨垃圾的pH就从6.0左右下降到4.5左右,而后pH缓慢下降,经过5～6 d的酸化,pH下降到4.0以下;餐厨垃圾酸化过程中,产生的VFA主要是异戊酸,其浓度变化与VFA的浓度变化趋势较为一致;酸化时间为1、3、4、5、6d的餐厨垃圾体系产生的氢气的最高体积分数呈递减趋势,产氢量也呈现出相同的变化趋势;初始pH对酸化餐厨垃圾体系的产氢影响是很大的,调节到相同初始pH的不同体系,产氢的结果可以相近.因此,pH是酸化餐厨垃圾厌氧消化产氢过程中必须控制的关键因素之一.     

温度和物料配比对餐厨垃圾与果蔬垃圾协同厌氧产氢的影响研究

采用餐厨垃圾和果蔬垃圾协同厌氧产氢工艺,通过pH、氨氮、还原糖、溶解性COD(SCOD)等指标变化规律、产氢动力学和相关性分析,研究不同温度和物料配比(餐厨垃圾与果蔬垃圾的湿质量比)对协同厌氧产氢潜力的影响。结果表明,温度和物料配比对餐厨垃圾和果蔬垃圾协同厌氧产氢均有显著影响。高温组(55℃)物料配比为1∶4时累积产气量和氢气体积分数最大,分别为510mL和52.57%;中温(35℃)组物料配比为1∶2时累积产气量最大为200mL,物料配比为1∶1时氢气体积分数最大为5.45%。相关性分析表明,pH与累积产气量呈显著负相关,氨氮与累积产气量呈显著正相关。高温协同厌氧产氢可有效提高微生物活性和产氢潜力,促进餐厨垃圾和果蔬垃圾的有效利用,实现有机废弃物的绿色能源化。     

竹叶与餐厨垃圾厌氧共消化工艺

将黄金竹和毛竹的竹叶分别与餐厨垃圾厌氧共消化,通过分析消化过程中的产气量、pH、COD、NH4+-N和VFAs变化,探讨添加不同竹叶对餐厨垃圾厌氧消化效果的影响。实验结果表明,添加毛竹叶显著增强了餐厨垃圾的厌氧消化能力。毛竹叶+餐厨垃圾组的总产气量是餐厨垃圾对照组单独厌氧消化总产气量的3.28倍,甲烷总产量为10.1 L,COD去除率高达83.0%。而添加黄金竹叶对餐厨垃圾厌氧消化的影响则不明显,可能因为黄金竹叶在消化过程中释放了大量挥发性脂肪酸(VFAs),造成体系酸中毒。     

脂肪酶强化餐厨垃圾厌氧产甲烷及其影响因素研究

油脂降解缓慢是影响餐厨垃圾厌氧发酵的重要原因。应用脂肪酶强化餐厨垃圾厌氧产甲烷,探究了脂肪酶投加量、温度和pH对产甲烷的影响。结果表明,脂肪酶能够促进餐厨垃圾厌氧发酵的水解和酸化,为产甲烷菌提供物质基质,还能提高脱氢酶的活性。脂肪酶最佳投加量为0.4g/L,最适温度为35℃,最适pH为7.0。     

餐厨垃圾生化产甲烷潜力的数学模拟

为资源化回收利用餐厨垃圾,采用BMP实验对其产甲烷潜力进行了研究,测定了不同厌氧消化时间内的沼气产量及COD、VFA浓度,并在此基础上对餐厨垃圾产甲烷潜力进行了数学模拟。结果表明,混合液COD浓度变化曲线呈逐渐下降的趋势,VFA出现短暂积累,应调控厌氧消化系统的碱度。餐厨垃圾经40 d厌氧消化后,实际生物化学产沼气及产甲烷潜力分别可达559.1、349.7 mL·g-1 VS,第20天后累积产气量增加不显著。数学模拟结果表明,餐厨垃圾最初7 d的平均水解常数为0.244 d-1,模拟产沼气及甲烷潜力分别可达578.36和363.72 mL·g-1 VS,实际产沼气及甲烷潜力分别占模拟产沼气及甲烷潜力的96.7%、96.1%,采用固体停留时间为25~30 d进行厌氧消化较为合理。     

污泥基生物炭对餐厨垃圾厌氧消化产甲烷及微生物群落结构的影响

为考察污泥基生物炭对餐厨垃圾厌氧消化的影响,以餐厨垃圾为基质,设置4种不同接种比(inoculum to substrate ratio, ISR)的批次实验,以得到不同酸化程度的厌氧消化体系;检测空白组、餐厨垃圾对照组和生物炭实验组的产甲烷情况和微生物群落结构的变化。结果表明：当ISR=2时,生物炭对餐厨垃圾厌氧消化效果不明显;当ISR=0.5时,生物炭使其停滞期缩短28.9%左右;ISR越小,生物炭对酸化停滞时间缩短以及产甲烷速率提高的效果越明显。同时,生物炭可以促进Chloroflex,Proteobacteria,Bacteroidetes的生长,从而提高厌氧消化中间产物的产生。当ISR较大时,厌氧消化系统的产甲烷途径以乙酸利用型为主,投加生物炭可以促进乙酸型产甲烷;随着ISR减小,产甲烷途径有逐渐向氢利用型转变的趋势,同时Methanosacrina逐渐替代Methanosaeta利用乙酸产甲烷。本研究结果可为污泥基生物炭在餐厨垃圾厌氧消化的实际应用提供参考。     

餐厨垃圾单相厌氧酸化系统恢复参数

针对现今餐厨垃圾单相厌氧酸化系统缺乏有效的恢复性监控指标,提出可有效表征酸化系统恢复的监控指标。在中温条件下,连续对餐厨垃圾单相厌氧消化系统进行负荷冲击及恢复,分别对pH、沼气产率及成分、挥发性脂肪酸组成成分、总碱度(TA)和碳酸氢盐碱度(BA)及其组合指标进行监测分析。结果表明,传统单因子参数不能有效地指示系统恢复,选取VFA/BA和丙酸/乙酸的比值作为餐厨垃圾单相厌氧酸化系统恢复指示性参数。在酸化系统恢复过程中,当丙酸/乙酸≤1.4、VFA/BA≤0.4时,表明系统中各种挥发酸浓度值已恢复正常,且具有足够的缓冲能力,可提高反应器负荷,保证反应器恢复启动运行。     

餐厨垃圾高温厌氧消化

在中试规模下,研究餐厨垃圾高温厌氧消化试验,通过监测餐厨垃圾厌氧消化过程中产气量、气体组成等产气情况和消化液中pH值、SCOD、NH4+-N、VFAs等化学指标含量变化,确定餐厨垃圾厌氧消化的最大有机负荷,并分析餐厨垃圾高温厌氧消化技术的可行性,结果表明,在工程上餐厨垃圾单独进行高温厌氧消化产甲烷具有技术可行性,但难以保证系统长时间安全稳定运行;餐厨垃圾厌氧消化正常运行时最大有机负荷可达2.551 kg VS/(m3.d);当系统有机负荷为2.551 kg VS/(m3.d)时,每天每千克VS最高可产生甲烷量0.622 m3;氨氮对餐厨垃圾厌氧消化产甲烷影响明显;餐厨垃圾中固有Na+含量对厌氧消化产甲烷影响不明显。     

不同来源污泥接种餐厨垃圾厌氧发酵产氢效果研究

在相同接种配比(接种污泥占餐厨垃圾的质量分数为30%)条件下,研究了4种不同来源污泥(压滤污泥、厌氧污泥、曝气污泥和河底淤泥)添加或不添加缓冲剂时对餐厨垃圾厌氧发酵产氢效果的影响.结果发现,在不添加缓冲剂时.4种污泥接种餐厨垃圾厌氧发酵平均产氢量依次为厌氧污泥>河底淤泥>压滤污泥>曝气污泥,接种厌氧污泥的餐厨垃圾平均产氢量最高,达10.11mL(以每克挥发性固体(VS)计,下同);而添加缓冲剂时.4种污泥接种餐厨垃圾厌氧发酵平均产氢量依次为厌氧污泥>曝气污泥>压滤污泥>河底淤泥,接种厌氧污泥的餐厨垃圾平均产氢量也最高,为33.72 mL,且体系pH得以缓冲.     

零价铁对餐厨垃圾厌氧消化产甲烷的影响研究

针对餐厨垃圾厌氧消化酸抑制而造成的消化效率低和产气量低等问题,在中温((37±1)℃)条件下,通过向厌氧消化器中投加不同量的零价铁(Fe~0),考察其对餐厨垃圾厌氧消化过程中pH、挥发性脂肪酸(VFAs)、日产气量、COD及累计产气量的影响。结果表明,投加1 000mg/L Fe~0对餐厨垃圾厌氧消化酸抑制的缓冲作用最好,可保证厌氧系统的稳定及最佳运行,第10天的VFAs转化率比对照组(CK组)提高了36.21%;COD去除率比CK组高13.10百分点;日产气量峰值为1 728mL;25d的累积产气量为10 108mL,比CK组高35.01%。     

Sorption and desorption of Cu and Cd by macroalgae and microalgae

The sorption and desorption of Cu and Cd by two species of brown macroalgae and five species of microalgae were studied. The two brown macroalgae, Laminaria japonica and Sargassum kjellmanianum, were found to have high capacities at pHs between 4.0 and 5.0 while for microalgae, optimum pH lay at 6.7. The presence of other cations in solution was found to reduce the sorption of the target cation, suggesting a competition for sorption sites on organisms. Sorption isotherms obeyed the Freundlich equation, suggesting involvement of a multiplicity of mechanisms and sorption sites. For the microalgae tested, Spirulina platensis had the highest capacity for Cd, followed by Nannochloropsis oculata, Phaeodactylum tricornutum, Platymonas cordifolia and Chaetoceros minutissimus. The reversibility of metal sorption by macroalgae was examined and the results show that both HCl and EDTA solutions were very effective in desorbing sorbed metal ions from macroalgae, with up to 99.5% of metals being recovered. The regenerated biomass showed undiminished sorption performance for the two metals studied, suggesting the potential of such material for use in water and wastewater treatment.     

Kinetic and structural relationships of transition monomeric and oligomeric carboxyl- and choline-esterases

The kinetic and structural relationships of eight electrophoretically pure mammalian serum and liver serine carboxylesterases (CE) and cholinesterases (ChE) have been studied. Eight CE's and ChE's, which were fully resolved but only partially purified, provided additional information. Five of the electrophoretically pure esterases were monomeric, and of these, four belonged to a new and widely distributed class. These four monomeric esterases hydrolyzed choline esters, but at widely differing rates. Thus two were termed monomeric butyrylcholinesterases, mBuChE I and II, and two were monomeric CE's (mCE). The rabbit liver mCE was not a subunit of the oligomeric CE (oCE), although the oCE also hydrolyzed choline esters at a very low rate. The complex kinetics of the mCE's, mBuChE's, oCE's, and of the oligomeric BuChE's of horse and human serum could be interpreted according to a single reaction scheme involving an allosteric site and the equation derived from it. Thus activation and inhibition at high substrate concentrations, together with sigmoidal activity versus substrate concentration plots, all of which characterize the reactions of these esterases, could be interpreted by a single scheme and equation. Structural and kinetic comparisons showed a progressive transition of properties from the oCE's through the mCE's to the oBuChE's. One of the purified mCE's was from horse serum, and it exhibited physical and kinetic properties unlike those of the liver mCE's or oCE's.     

Persistence and dissipation kinetics of trifloxystrobin and tebuconazole in onion and soil

The persistence and dissipation kinetics of trifloxystrobin and tebuconazole on onion were studied after application of their combination formulation at a standard and double dose of 75 + 150 and 150 + 300 g a.i. ha^?1. The fungicides were extracted with acetone, cleaned-up using activated charcoal (trifloxystrobin) and neutral alumina (tebuconazole). Analysis was carried out by gas chromatograph (GC) and confirmed by gas chromatograph mass spectrometry (GC-MS). The recovery was above 80% and limit of quantification (LOQ) 0.05 mg kg^?1 for both fungicides. Initial residue deposits of trifloxystrobin were 0.68 and 1.01 mg kg^?1 and tebuconazole 0.673 and 1.95 mg kg^?1 from standard and double dose treatments, respectively. Dissipation of the fungicides followed first-order kinetics and the half life of degradation was 6–6.6 days. Matured onion bulb (and field soil) harvested after 30 days was free from fungicide residues. These findings suggest recommended safe pre-harvest interval (PHI) of 14 and 25 days for spring onion consumption after treatment of Nativo 75 WG at the standard and double doses, respectively. Matured onion bulbs at harvest were free from fungicide residues.     

Sorption and Desorption Behavior of Chloroanilines and Chlorophenols on Montmorillonite and Kaolinite

The bioavailability of pollutants, pesticides and/or their degradation products in soil depends on the strength of their sorption by the different soil components, particularly by the clay minerals. This study reports the sorption-desorption behavior of the environmentally hazardous industrial pollutants and certain pesticides degradation products, 3-chloroaniline, 3,4-dichloroaniline, 2,4,6-trichloroaniline, 4-chlorophenol, 2,4-dichlorophenol and 2,4,6-trichlorophenol on the reference clays kaolinite KGa-1 and Na-montmorillonite SWy-l. In batch studies, 2.0 g of clay were equilibrated with 100.0 mL solutions of each chemical at concentrations ranging from 10.0 to 200.0 mg/L. The uptake of the compounds was deduced from the results of HPLC-UV-Vis analysis. The lipophilic species were best retained by both clay materials. The most lipophilic chemical used in the study, 2,4,6-trichloroaniline, was also the most strongly retained, with sorption of up to 8 mg/g. In desorption experiments, which also relied on HPLC-UV-Vis technique, 2,4,6-trichloroaniline was the least desorbed from montmorillonite. However, on kaolinite all of the compounds under study were irreversibly retained. The experimental data have been modelled according to the Langmuir and Freundlich isotherms. A hypothesis is proposed concerning the sorption mechanism and potential applications of the findings in remediation strategies have been suggested.     

Sorption and desorption behavior of chloroanilines and chlorophenols on montmorillonite and kaolinite

The bioavailability of pollutants, pesticides and/or their degradation products in soil depends on the strength of their sorption by the different soil components, particularly by the clay minerals. This study reports the sorption-desorption behavior of the environmentally hazardous industrial pollutants and certain pesticides degradation products, 3-chloroaniline, 3,4-dichloroaniline, 2,4,6-trichloroaniline, 4-chlorophenol, 2,4-dichlorophenol and 2,4,6-trichlorophenol on the reference clays kaolinite KGa-1 and Na-montmorillonite SWy-l. In batch studies, 2.0 g of clay were equilibrated with 100.0 mL solutions of each chemical at concentrations ranging from 10.0 to 200.0 mg/L. The uptake of the compounds was deduced from the results of HPLC-UV-Vis analysis. The lipophilic species were best retained by both clay materials. The most lipophilic chemical used in the study, 2,4,6-trichloroaniline, was also the most strongly retained, with sorption of up to 8 mg/g. In desorption experiments, which also relied on HPLC-UV-Vis technique, 2,4,6-trichloroaniline was the least desorbed from montmorillonite. However, on kaolinite all of the compounds under study were irreversibly retained. The experimental data have been modelled according to the Langmuir and Freundlich isotherms. A hypothesis is proposed concerning the sorption mechanism and potential applications of the findings in remediation strategies have been suggested.     

Bacterial and archaeal diversity in oil fields and reservoirs and their potential role in hydrocarbon recovery and bioprospecting

Environmental Science and Pollution Research - Hydrocarbon is a primary source of energy in the current urbanized society. Considering the increasing demand, worldwide oil productions are declining...     

畜禽养殖业污染与循环经济

解决畜禽养殖业的污染问题要以充分利用资源为根本出发点，通过对污染全过程控制及废物综合利用，达到畜禽粪便的减量化、无害化、资源化，走循环经济的发展道路。     

Degradation in soil and water and ecotoxicity of rimsulfuron and its metabolites.

The degradation and ecotoxicity of sulfonylurea herbicide rimsulfuron and its major metabolites were examined in batch samples of an alluvial sandy loam and in freshwater. An HPLC-DAD method was adapted to simultaneously identify and quantify rimsulfuron and its metabolites, which was successfully validated by GC-MS analysis. In aqueous solutions, pure rimsulfuron was rapidly hydrolyzed into metabolite 1 (N-(4,6-dimethoxypyrimidin-2-yl)-N-(3-(ethylsulfonyl)-2-pyridinylurea)), which itself was transformed into the more stable metabolite 2 (N-((3-(ethylsulfonyl)-2-pyridinyl)-4,6-dimethoxy-2-pyrimidineamine)), with half-life (t(1/2)) values of 2 and 2.5 days, respectively. Hydrolysis was instantaneous under alkaline conditions (pH = 10). In aqueous suspensions of the alluvial soil (pH = 8), formulated rimsulfuron had a half-life of 7 days, whereas that of metabolite 1 was similar to that in water (about 3.5 days). The degradation of the two major metabolites was also studied in soil suspensions with the pure compounds at concentrations ranging from 1 to 10 mg l(-1). The half-life of metabolite 1 ranged from 3.9 to 5 days, close to the previous values. Metabolite 2 was more persistent and its degradation is strongly dependent on the initial concentration (C0): half-life values ranged from 8.1 to 55 days at 2-10 mg l(-1), respectively. These values are higher than those determined from the kinetics of metabolite 1 transformation into metabolite 2 (t(1/2) = 8-19 days). The ecotoxicity of the three chemicals was evaluated through their effect on Daphnia magna and Vibrio fischeri (Microtox bioassay). No effect was observed on D. magna with 24 and 48 h acute toxicity tests. Similarly, no toxic effect was observed with the Microtox test for the three chemicals in the range of concentrations tested that included the field application dose. Thus, being of low persistence and lacking acute toxicity, these chemicals present a low environmental risk. However, chronic effects should be studied in order to confirm the safety of rimsulfuron and its major metabolites.     

Isocyanatocyclohexane and isothiocyanatocyclohexane levels in urban and industrial areas and possible emission-related activities

Isocyanatocyclohexane and isothiocyanatocyclohexane are becoming relevant compounds in urban and industrial air, as they are used in important amounts in automobile industry and building insulation, as well as in the manufacture of foams, rubber, paints and varnishes. Glass multi-sorbent tubes (Carbotrap, Carbopack, Carboxen) were connected to LCMA-UPC pump samplers for the retention of iso- and isothiocyanatocyclohexanes. The analysis was performed by automatic thermal desorption (ATD) coupled with capillary gas chromatography (GC)/mass spectrometry detector (MSD). TD-GC/MS was chosen as analytical method due to its versatility and the possibility of analysis of a wide range of volatility and polarity VOC in air samples. The method was satisfactory sensitive, selective and reproducible for the studied compounds. The concentrations of iso- and isothioisocyanatocyclohexanes were evaluated in different urban, residential and industrial locations from extensive VOC air quality and odour episode studies in several cities in the Northeastern edge of Spain. Around 200–300 VOC were determined qualitatively in each sample. Higher values of iso- and isothiocyanatocyclohexane were found in industrial areas than in urban or residential locations. The concentrations ranged between n.d.−246 and n.d.−29 μg m⁻³ for isocyanatocyclohexane and isothiocyanatocyclohexane, respectively, for industrial areas. On the other hand, urban and residential locations showed concentrations ranging between n.d.−164 and n.d.−29 μg m⁻³ for isocyanatocyclohexane and isothiocyanatocyclohexane, respectively. The site location (urban or industrial), the kind and nearness of possible iso- and isothiocyanatocyclohexane emission activities (industrial or building construction) and the changes of wind regimes throughout the year have been found the most important factors influencing the concentrations of these compounds in the different places.