接种外源微生物菌剂对香蕉茎秆堆肥的影响

为了研究接种外源微生物菌剂对香蕉茎秆堆肥的影响,本实验采用高温好氧堆肥技术,设计了对照（不接菌）、接种白腐菌及棱盖多孔菌3个处理,探讨了不同处理堆肥过程中堆体温度、水分、pH值、电导率、有机碳、C/N、发芽指数及堆肥质量的变化情况。结果表明,接种微生物菌剂处理的温度均高于对照,且高温期持续时间相对较长,以接种白腐菌处理的高温持续时间最长;接种外源微生物菌剂对堆肥含水率、pH、EC、全碳、C/N变化影响不大;与对照相比,接种白腐菌可增加全氮及全钾的含量,有利于提高堆肥产品质量;接种白腐菌处理在36 d（GI〉50%）就达到腐熟,比对照提前8 d腐熟,明显缩短堆肥腐熟时间;而接种棱盖多孔菌处理比对照推迟10 d腐熟,共需54 d不利于香蕉茎秆堆肥的进行。     

不同接种量的微生物秸秆腐熟剂对蔬菜副产物堆肥效果的影响

为了明确不同接种量的微生物秸秆腐熟剂对蔬菜副产物堆肥效果的影响,以玉米秸秆为调理剂,在调节初始物料含水率为63％和C/N为28的条件下,设置了B1(堆肥混合物+1％秸秆腐熟剂)、B2(堆肥混合物+3％秸秆腐熟剂)、B3(堆肥混合物+5％秸秆腐熟剂)和CK(堆肥混合物+3％灭菌惰性载体)4个处理,测定不同堆肥处理对温度、含水率、碳氮比(C/N)、半纤维素、纤维素、木质素、总养分含量、发芽指数等指标的影响.结果表明,蔬菜副产物堆肥接种微生物秸秆腐熟剂均能够使堆肥周期缩短,有效降低堆肥含水率,提高有机质的降解幅度,并且使堆肥中半纤维素、纤维素、木质素降解率分别提高1.03％、1.16％和1.47％;氮磷钾养分含量也比不接种处理平均提高0.48％.4个处理的总体堆肥效果表现为:B2＞B1 ＞B3＞CK.     

牛粪与小麦秸秆混合高温堆肥的腐熟进程研究

通过研究牛粪与小麦秸秆混合高温堆肥的腐熟进程,寻求最佳的堆肥体积比,旨在为农业废弃物快速资源化利用提供科学依据。将牛粪与小麦秸秆分别按体积比10∶0、8∶2、6∶4、4∶6、2∶8混合,高温堆肥64d,研究各种处理下堆肥进程。结果表明,与纯牛粪高温堆肥相比,添加小麦秸秆可以加快堆肥升温速度,抑制高温堆肥前期pH的升高和氨气挥发,减少氮素损失,加速堆肥内有毒有害物质分解,加快C/N降低速率。其中牛粪和小麦秸秆以6∶4的体积比混合高温堆肥时效果最好,堆肥结束时有机质和速效氮下降幅度最小,分别为31.84%和18.18%,全氮、全磷、全钾、速效磷和速效钾的提高幅度最大,分别为15.86%、13.64%、9.42%、22.73%和29.30%。若以种子发芽指数80%作为堆肥腐熟的评价指标,牛粪和小麦秸秆按6∶4体积比混合高温堆肥43d即可腐熟,比纯牛粪腐熟提前了12d。综合判断,实际应用中牛粪与小麦秸秆按6∶4体积比进行高温堆肥较为适宜。     

微生物生理群在猪粪秸秆高温堆肥碳氮转化中的作用

在自制的强制通风静态堆肥反应箱中,猪粪与秸秆以鲜重7∶1的比例进行了堆肥化实验,在堆制的23 d里根据堆温变化分阶段采集堆肥样品,利用MPN法测定了堆料中纤维素分解菌和氮素微生物生理群的数量变化,同时测定了相应的碳、氮含量。结果表明,纤维素分解菌在稳定腐熟阶段较多,对于后期有机碳的降解和腐殖质含量的增大起了很大的作用,在堆制的23 d里,腐殖质增加了2.4%。整个堆制过程中,氨化细菌的数量最大且与氨气释放浓度和铵态氮含量呈显著正相关,都在高温期增加,降温期后减少,氨化细菌的数量在高温期的增加率远高于降温期后的减少率,而铵态氮在高温期的增加率远低于在降温后期的减少率,铵态氮总体上减少了74.1%;亚硝化细菌数量与硝态氮呈正相关;反硝化细菌数量在降温期上升幅度较大,堆制结束时为堆制初期的13倍,且与堆肥中硝态氮含量呈正相关;硝态氮含量增加了87.5%;堆肥后期硝态氮的增加可能与堆肥中存在能进行硝化作用的反硝化细菌有关。固氮菌数量在堆制结束时达堆制初期的2.61倍,主要在降温期增加较多,对堆肥中有机氮的形成起很大作用。     

添加VT菌剂和有机物料腐熟剂对堆肥的影响

通过在高温好氧堆肥中分别添加VT菌剂和有机物料腐熟剂,研究接种3‰的VT菌剂和有机物料腐熟剂促进堆肥的作用效果。结果表明,接种VT菌剂的处理与空白和接种有机物料腐熟剂的处理相比,堆肥初期升温更快;高温期更长;堆肥结束时,C/N降低的多,NO3-N增加的多,NH4+-N挥发的少,接种VT菌剂和VT有机物料腐熟剂都可促进有机质的充分降解,缩短堆肥时间,加快堆肥腐熟,提高堆肥肥力。     

添加VT菌剂和有机物料腐熟齐对堆肥的影响

通过在高温好氧堆肥中分别添加VT菌剂和有机物料腐熟剂，研究接种3％o的VT菌剂和有机物料腐熟剂促进堆肥的作用效果。结果表明，接种VT菌剂的处理与空白和接种有机物料腐熟剂的处理相比，堆肥初期升温更快；高温期更长；堆肥结束时，C／N降低的多，NO3-N增加的多，NH4-N挥发的少，接种VT菌剂和VT有机物料腐熟剂都可促进有机质的充分降解，缩短堆肥时间，加快堆肥腐熟，提高堆肥肥力。     

微生物菌剂强化餐厨垃圾和污泥联合堆肥

为探究微生物菌剂对餐厨垃圾和污泥联合好氧堆肥的影响,以餐厨垃圾和污泥(湿重1∶1)混合原料为堆肥底物,添加底物总湿重30％的废木屑作为膨胀剂,向底物中分别加入微生物菌剂和腐熟堆肥为处理组,并以不添加外源物作为对照,通过测定堆肥过程中的理化性质、腐熟效果和营养元素的变化,考察菌剂和腐熟堆肥对联合堆肥的促进作用.结果表明,...     

城市生活垃圾和污泥混合堆肥中氮素变化规律研究

进行了不同比例的垃圾和污泥混合的高温好氧静态堆肥小试试验,主要研究了堆肥过程中全氮、氨氮、硝态氮、水溶性氮以及有机碳等的变化.结果表明,堆肥过程中有机碳、全氮和碳氮比呈下降趋势;堆肥产品中全氮与其初始浓度成正比,初始浓度越高,结束时全氮越高;碳氮比在整个堆肥过程中变化不大;氨氮的变化显著,堆肥23 d,3种比例的混合样品(垃圾和污泥体积比分别为9∶1、5∶1和3∶1)中的氨氮分别由堆肥前的11.1、10.9、10.5 g/kg下降到1.1、2.1、3.1 g/kg;水溶性全氮和水溶性氨氮的下降趋势明显,水溶性氨氮是构成水溶性全氮的主要成分,堆肥前期温度的上升引起水溶性全氮和水溶性氨氮的迅速下降;硝态氮和水溶性硝态氮的浓度低,变化小;氮素损失主要在第3～10天的堆肥高温期,污泥量越大,氮素损失越严重,氮素损失率最高达45%.     

快腐剂对畜禽粪便堆肥过程中腐熟度的影响

以牛粪、菌糠和鸡粪等为材料按照两种比例调配为混合基质,在添加或不添加快腐剂的条件下在发酵桶中进行为期38 d的堆肥发酵实验,通过对发酵产物的温度、p H值、总有机碳、C/N、硝铵态氮含量和种子发芽指数等指标变化的研究,揭示了快腐剂对发酵过程的影响。结果表明,虽然快腐剂对有机物料的温度、C/N比无显著的影响,但可以促进铵态氮向硝态氮的转化,在16 d时使发酵产物NH+4-N/NO-3-N比值降为0.15,达到腐熟标准(0.16);提升种子发芽指数,在腐解29 d时使种子发芽指数达到82.76%,达到完全腐熟指标(0.8),比不添加快腐剂的处理提前了4 d左右。快腐剂的作用效果受腐解物料配比的影响。     

堆肥过程中腐殖酸的生成演化及应用研究进展

腐殖酸是堆肥过程中生成的最具代表性的次生产物,对堆肥的稳定性、腐熟度等性质有重要影响。介绍了堆肥过程中腐殖酸的生成及动态变化,分析了堆肥腐殖酸的结构特性,归纳了堆肥过程中腐殖酸生成机制,并在此基础上探讨了影响堆肥腐殖酸生成演化的主要影响因素,总结了堆肥腐殖酸作为堆肥腐熟度指标、表面活性物质、吸附剂等的应用情况,最后提出了当前堆肥腐殖酸研究中存在的主要问题,并对未来的研究方向进行了展望。     

A new approach for the fractionation of water-soluble organic carbon in atmospheric aerosols and cloud drops

A novel approach is described for the fractionation of water-soluble organic carbon (WSOC) in atmospheric aerosols and cloud drops. The method is based on the preliminary adsorption of the sample, acidified at pH 2, on a polymeric styrene-divinylbenzene resin (XAD-2) and subsequent elution with a series of solvents, which leads to the fractionation of the sample into three classes of compounds. The method was set up using synthetic mixtures of organic compounds and then applied to selected samples of atmospheric aerosols and cloud drops. All samples and collected fractions were analysed using size exclusion chromatography (SEC). This method proved particularly useful both in providing information on the organic content of the samples and for the characterisation of the macromolecular compounds (MMCs) in the samples. Synthetic samples were prepared using humic, fulvic and tannic acid to simulate naturally occurring MMCs. In the first fraction, eluted with HCl, only the most soluble organic compounds (oxalic acid, formic acid and acetic acid) were collected. In the second fraction, eluted with methanol, the major part of the organic material was collected together with the more hydrophilic constituents of the humic substances. In the third fraction, it was possible to separately recover the more hydrophobic component of the humic substances. A large number of atmospheric samples (fog, aerosol, cloud) were then analysed using SEC. Most of these samples evidenced a noteworthy chromatogram at 254 nm. Moreover, the chromatographic area evidenced a clear linear correlation with the total organic carbon (TOC) values. The fractionation method on XAD-2 was finally applied to selected atmospheric samples, yielding three classes of organic compounds. In each sample, a non-negligible amount of compounds with dimensional and chemical properties similar to humic substances were collected in the third fraction. The carbon content in this latter fraction was estimated both by TOC and by means of the correlation between TOC and SEC area.     

矿物复合PAC混凝去除给水中腐殖酸的研究

为了降低饮用水中有机微污染物的浓度，对矿物高岭土复配聚合氯化铝（PAC）吸附混凝共沉降去除腐殖酸进行了研究，结果表明：矿物高岭土与PAC复配的最佳量均为12 mg/L，此时水样浊度、腐殖酸去除率分别达到98.9%和97.9%，出水残余铝浓度0.16 mg/L。高岭土复配对于处理后水中铝形态也产生了影响，与单独使用PAC相比，总铝浓度降低了24%，特别是对人体毒害较强的溶解态铝浓度降低了71%。     

The effect of pH, ion strength and reactant content on the complexation of Cu2+ by various natural organic ligands from water and soil in Hong Kong

The complexation constants for copper associated with different natural organic ligands, including dissolved organic carbon (DOC) extracted from water, water soluble organic carbon (WSOC), fulvic acid (FA) and humic acid (HA) from soil, were determined and then compared based on discrete single site model. Both ion-selective electrode (ISE) and anodic stripping voltammetry were used to determine the content of free copper ions, while the relative number of complexation sites was estimated using a fluorescence quenching (FQ) at the same time. ISE proved to be the most applicable technique when the concentration of copper was above 10(-7) moll(-1). The logk values for two WSOC sample sites (Song Ziyuan and Xin Niangtan) were 4.64 and 4.66; higher than both the DOC and HA values yet lower than the FA values, which were unusually high due to unavoidable pollution from the cation exchange resin used during the purification process. Binding affinities between the copper ions and the organic ligands obtained from streams in Yong Wei (DOC) and Song Ziyuan (WSOC) were influenced by pH, ion strength, and reactant concentration. Values for logk increased with increases in pH (ion strength of 0.1 N). At pH 4, the logk values decreased with increases in the supporting electrolyte concentration and total copper ion additions.     

新型水处理活性炭选型技术

活性炭依其原料不同、生产工艺不同,而有不同的吸附性能.使用简易的活性炭选型方法,可以减少应用测试时的备选炭型,从而大大降低活性炭水处理技术的运行成本.以碘值、甲基蓝值、苯酚值和丹宁酸值4种吸附容量性能指标为依据的活性炭选型技术,可以有效地预测活性炭对于水中各种大小不同污染物的去除能力.BET测试结果证明了这4项指标数据对于活性炭孔径分布预测的准确性.2,4-二氯苯酚和腐殖酸等目标化合物的吸附容量实验结果也都验证了这4项指标的预测功用,说明这种简便的活性炭选型技术有着广泛的应用价值.     

Effect of soil and sediment composition on acetochlor sorption and desorption

Background, aim, and scope  Herbicide fate and its transport in soils and sediments greatly depend upon sorption–desorption processes. Quantitative determination of herbicide sorption–desorption is therefore essential for both the understanding of transport and the sorption equilibrium in the soil/sediment–water system; and it is also an important parameter for predicting herbicide fate using mathematical simulation models. The total soil/sediment organic carbon content and its qualitative characteristics are the most important factors affecting sorption–desorption of herbicides in soil or sediment. Since the acetochlor is one of the most frequently used herbicides in Slovakia to control annual grasses and certain annual broad-leaved weeds in maize and potatoes, and posses various negative health effects on human beings, our aim in this study was to investigate acetochlor sorption and desorption in various soil/sediment samples from Slovakia. The main soil/sediment characteristics governing acetochlor sorption–desorption were also identified. Materials and methods  The sorption–desorption of acetochlor, using the batch equilibration method, was studied on eight surface soils, one subsurface soil and five sediments collected from the Laborec River and three water reservoirs. Soils and sediments were characterized by commonly used methods for their total organic carbon content, distribution of humus components, pH, grain-size distribution, and smectite content, and for calcium carbonate content. The effect of soil/sediment characteristics on acetochlor sorption–desorption was examined by simple correlation analysis. Results  Sorption of acetochlor was expressed as the distribution coefficient (K _d). K _d values slightly decreased as the initial acetochlor concentration increased. These values indicated that acetochlor was moderately sorbed by soils and sediments. Highly significant correlations between the K _d values and the organic carbon content were observed at both initial concentrations. However, sorption of acetochlor was most closely correlated to the humic acid carbon, and less to the fulvic acid carbon. The total organic carbon content was found to also significantly influence acetochlor desorption. Discussion  Since the strong linear relationship between the K _d values of acetochlor and the organic carbon content was already released, the corresponding K _oc values were calculated. Considerable variation in the K _oc values suggested that other soil/sediment parameters besides the total soil organic carbon content could be involved in acetochlor sorption. This was revealed by a significant correlation between the K _oc values and the ratio of humic acid carbon to fulvic acid carbon (C_HA/C_FA). Conclusions  When comparing acetochlor sorption in a range of soils and sediments, different K _d values which are strongly correlated to the total organic carbon content were found. Concerning the humus fractions, the humic acid carbon content was strongly correlated to the K _d values, and it is therefore a better predictor of the acetochlor sorption than the total organic carbon content. Variation in the K _oc values was attributed to the differences in distribution of humus components between soils and sediments. Desorption of acetochlor was significantly influenced by total organic carbon content, with a greater organic carbon content reducing desorption. Recommendations and perspectives  This study examined the sorption–desorption processes of acetochlor in soils and sediments. The obtained sorption data are important for qualitative assessment of acetochlor mobility in natural solids, but further studies must be carried out to understand its environmental fate and transport more thoroughly. Although, the total organic carbon content, the humus fractions of the organic matter and the C_HA/C_FA ratio were sufficient predictors of the acetochlor sorption–desorption. Further investigations of the structural and chemical characteristics of humic substances derived from different origins are necessary to more preciously explain differences in acetochlor sorption in the soils and sediments observed in this study.     

Influence of suspended clay minerals and humic matter on the solid phase extraction efficiency of selected pesticides from water

The purpose of this investigation was to determine the influence of humic acids (HA) and Ca-montmorillonite (CaM) on the solid-phase extraction (SPE) efficiency of atrazine, alachlor and alpha-cypermethrin from water samples at various pH-values. The nature and intensity of binding of the studied pesticides to CaM were determined by X-ray diffraction analysis and termogravimetric analysis (TGA) test. The studied pesticides eluted from discs were analysed by thin-layer chromatography (TLC). The effects of CaM and humic acid were generally pH-dependent and acted independently in extraction efficiency influence. Lower recovery of pesticides was observed at higher pH values when CaM was > or =0.1 g and was attributed to greater dispersion of clay, increased surface area and subsequent adsorption. Concentrations of dissolved organic carbon (DOC) in humic acid had less effect on the extraction efficiency when water was at pH 8 compared to water at pH 2, which was probably due to greater nonpolar interactions of the pesticides to the charge-neutralized humic acid molecule.     

Influence of Suspended Clay Minerals and Humic Matter on the Solid Phase Extraction Efficiency of Selected Pesticides from Water

The purpose of this investigation was to determine the influence of humic acids (HA) and Ca-montmorillonite (CaM) on the solid-phase extraction (SPE) efficiency of atrazine, alachlor and α-cypermethrin from water samples at various pH-values. The nature and intensity of binding of the studied pesticides to CaM were determined by X-ray diffraction analysis and termogravimetric analysis (TGA) test. The studied pesticides eluted from discs were analysed by thin-layer chromatography (TLC). The effects of CaM and humic acid were generally pH-dependent and acted independently in extraction efficiency influence. Lower recovery of pesticides was observed at higher pH values when CaM was ≥0.1 g and was attributed to greater dispersion of clay, increased surface area and subsequent adsorption. Concentrations of dissolved organic carbon (DOC) in humic acid had less effect on the extraction efficiency when water was at pH 8 compared to water at pH 2, which was probably due to greater nonpolar interactions of the pesticides to the charge-neutralized humic acid molecule.     

Influences of adding easily degradable organic waste on the minimization and humification of organic matter during straw composting

To find a better composting process with low greenhouse gas emission and high humus production, the effect of adding kitchen waste on reduction and humification of organic matter during straw composting was studied. Three processes were compared, consisting of different ratios of straw and kitchen waste (1:2, 1:1, and 2:1). At four time points over a 62-d incubation, the reduction and humification of compost was evaluated by measuring the total mass, carbon content, and humic material content of the compost. Treatment 1 (straw/kitchen waste ratio of 1:2) reduced the total mass of compost the most. Treatment 2 (straw/kitchen waste ratio of 1:1) reduced the total carbon content the most, reflecting the highest emission of greenhouse gas. Treatment 3 produced the most humic acid material and released the lowest amount of carbon. Hence, from the point of view of reducing greenhouse gas emissions and increasing stable organic matter such as humus and humic acid during composting, treatment #3 was optimal. The three treatments resulted in significant differences in microbial biomass and enzyme activity during composting. The highest amount of active microbial biomass was associated with the largest reduction in compost mass (treatment 1). Higher proportions of straw (treatments 2 and 3), which contains more lignin, were associated with greater β-glycosidase activity, which may generate more humus that can improve soil quality. Dehydrogenase activity seemed to be the most important microbial factor in organic carbon catabolism or humification.     

Characterization of surface marine sediments from Ría de Arousa estuary according to extractable humic matter content

Surface marine sediments from Ría de Arousa estuary were analyzed for humic and fulvic acids by UV-visible spectrometry and have been characterized using elemental analysis (carbon, hydrogen and nitrogen elemental composition) and spectrometric data (A2/A4 ratio, absorbancies at 270 and 407 nm and E4/E6 ratio, absorbancies at 465 and 665 nm). These variables have been used as discriminating factors to distinguish of marine and terrestrial origin of humic and fulvic acids in Ría de Arousa surface marine sediments. Principal component analysis, PCA, and cluster analysis, CA, have been used as unsupervised pattern recognition procedures. The half-range central value transformation was used as data pre-treatment to homogenize data. After a Varimax rotation, PCA applied to humic acid data has reveled that spectrometric A2/A4 and E4/E6 ratios are the main dominating features in the first principal component (48.6% of total variance), the humic acid content is the feature with the highest weight in the second principal component (22.9% of the total variability) and the carbon elemental composition domain in the third principal component (13.3% of total variance). Results from PCA have revealed that surface sediments collected at inner-left part of the estuary and at the mouth of the river Ulla belong to the same group. Similarly, PCA has shown that surface sediments from the right mouth of the estuary form a compact group. Taking in account the water circulation in Ría de Arousa estuary, these findings mean that the organic matter in surface sediments from the inner-left part of the estuary derived mainly from terrestrial organic matter while the organic matter in surface sediments from the right mouth of the estuary is mainly derived from marine sources. Finally, it must be noticed that any classification of surface sediments was assessed when applying of PCA and CA from fulvic acids data.     

Organic compounds adsorption onto activated carbon: the effect of association between dissolved humic substances and pesticides

The quantitative determination of pesticide binding to dissolved humic substances is relevant to both water treatment operation using activated carbon adsorption process and the application of transport models that predict the environmental distribution patterns of a given hydrophobic contaminant. In this study and in a first set of experiments, the extent of binding between (i) three pesticides of environmental concern, aldicarb, lindane and pentachlorophenol, and (ii) dissolved commercial humic acid and soil extracted fulvic acid, was determined using dialysis experiments and water solubility enhancement tests. In a second set of experiments, the influence of dissolved humic substances or pesticide on the retention of the other co-adsorbate onto activated carbon was investigated in binary systems. It was found that association was negligible for aldicarb and that the pesticide sorption onto activated carbon was not affected by humic acid (8.5 mg liter(-1) DOC). The association constants K for lindane and pentachlorophenol were identical in the presence of fulvic acid (logK=4.1) but lower than that observed with humic acid. In the presence of humic acid, binding affinity for pentachlorophenol (logK=4.6) was higher than the one observed for lindane (logK=4.4), despite its much higher water solubility. This observation suggests that the aromatic character of the pentachlorophenol molecule contributes to association interactions with humic acid. From co-adsorption experiments onto activated carbon it was found that fulvic acid (7.7 mg litre(-1) DOC) slightly enhances sorption kinetics of pentachlorophenol. Lindane (1 mg litre(-1)) does not affect sorption kinetics for fulvic acid but markedly enhances both the sorption kinetics and adsorptive capacity for humic acid. Activated carbon retention of dissolved humic substances or pesticide appears to be enhanced by the association potential that exists between these co-adsorbates in some binary systems.