模拟酸雨对污泥堆肥中重金属形态转化及其环境行为的影响

通过模拟酸雨淋溶土柱的方法,研究了酸雨（pH=5．0和2．9）作用下污泥堆肥中Zn、Cu和Ni的溶出和迁移性。分析了酸雨对重金属形态分布规律的影响。结果表明,在相同酸雨强度下,淋出液中重金属含量与其在土柱中迁移距离大小次序为Zn〉Cu〉Ni;重金属在相同深度的土层中含量大小次序为Zn〉Ni〉Cu。淋溶液pH的降低和污泥堆肥施加比例的提高均会增加重金属在淋出液和土柱中的含量,但不影响重金属在土柱中的迁移距离。土壤酸化会促使土壤中重金属形态向活性形态转化,而且迁移距离增加。     

添加污泥对尾矿砂理化性质及香樟生理特性的影响

以香樟作为指示植物,选取黄岩、临海和路桥地区污水处理厂污泥,将污泥与尾矿砂按(污泥质量比例为0%对照、25%、50%和75%)配比进行栽培试验。测定添加污泥对尾矿砂理化性质以及香樟生理特性的影响。结果表明:随着污泥比例的增加,混合基质中的有机质、全氮、全磷明显增加,pH值明显降低,离子交换量明显减少,Cu和Cd总量明显增加,而Pb总量明显减少,Zn总量没有明显变化,Cu、Cd和Zn的DTPA提取量明显增加,而Pb的DTPA提取量明显减少。黄岩和临海污泥在25%和50%比例时,香樟叶和茎的生物量和叶绿素含量明显增加,而根的生物量没有明显变化,在75%比例时,生物量和叶绿素含量均明显减少;而添加路桥污泥使香樟叶、茎和根的生物量和叶绿素含量明显减少。丙二醛含量则与生物量和叶绿素含量呈现相反的变化特征。黄岩和临海污泥在25%和50%比例时,根和叶的Cu、Cd、Pb和Zn含量明显减少,在75%比例时,Cu、Cd和Zn含量则明显增加;而添加路桥污泥使叶和根的Cu、Cd和Zn含量明显增加,Pb含量明显减少。研究表明添加污泥提高了尾矿砂的养分含量,同时改变了其重金属组成,对污泥重金属含量和有机质组成的监控可以准确地预测污泥改良后尾矿砂对植物毒性的变化。     

污泥与园林废弃物混合堆肥对波斯菊生长及重金属积累的影响

随着城镇人口增加和城市化的快速发展,每天产生大量的污泥和园林废弃物,而厌氧消化的污泥与园林废弃物的混合堆肥产品应用于林地土壤改良,是城市废弃物循环利用的一种经济有效的方式。本研究在北京平原造林区开展试验,探讨混合堆肥对波斯菊的生长及对重金属元素吸收的影响。结果表明:施用堆肥对土壤全氮和有机质含量无显著影响; Cu、Zn、Cd三种重金属元素在土壤中主要以残渣态的形态存在;施用堆肥提高了土壤Cu、Zn含量,但Zn总量未超过土壤环境质量标准(GB 15618—2018)中的土壤污染风险筛选值300 mg·kg-1,Cu在施肥量较高时超过土壤污染风险筛选值100 mg·kg-1;土壤背景值中Cd含量已经高于土壤污染风险管制值4.0 mg·kg-1,施用堆肥对Cd含量的影响无明显规律;波斯菊株高、生物量和花数均随着堆肥施用量的增加而增加;波斯菊对重金属元素的富集性表现为CuCdZn。本研究表明,北京平原造林区的人工林生态系统可以忍受一定浓度的污泥和园林废弃物混合堆肥,并利用其中的营养物质,提高土壤肥力,促进植物生长。     

灞河流域溶解性有机质分子量分级表征及其与水质的相关性

溶解性有机质是水体中有机质分解与营养盐再生的核心载体之一,是碳、氮等生源要素生物地球化学循环的重要环节,也是水环境科学研究的重点内容.本研究应用液相-有机碳-有机氮检测(LC-OCD-OND)技术研究了西安市灞河流域水体中溶解性有机质(DOM)不同分子量组分特征,分析其与河水水质的相关性.结果表明: 河水DOM按照分子量分布,主要由生物大分子、腐殖质类物质、腐殖质降解产物、低分子中性物质和低分子酸组成,各组分平均浓度分别为0.15、1.75、0.48、0.36和0.002 mg·L^-1,河水中DOM总体含量水平由高到低的顺序为城市河段＞城镇河段＞源区河段.组分中分子量介于1000~20000 Da的腐殖质类物质占DOM总量的49.0%,含量及丰度从高到低依次为中游城镇段＞污水厂出口段＞污水厂下游河口段＞上游源头段;分子量＞20000 Da的生物大分子约占DOM总量的5.1%,丰度由高到低依次为污水厂出口＞污水厂下游河口＞上游源头＞中游城镇段,污水处理厂出水所产生的外生源有机质对河流DOM的贡献最大.DOM不同分子量组分与水质的相关性明显,表明基于LC-OCD-OND分级表征的DOM各分子量组分和丰度不仅可以作为水质监测的一个综合性指标,也可以用来表征河流水质的空间异质性,并能对污染物各组分进行定量化判别和来源解析.     

物料预处理对堆肥减量化、腐殖化和稳定化的影响及其微生物机制

堆肥是有机固体废弃物处理与资源化的主要途径之一,包括矿化和腐殖化两个过程,且都和微生物活动有关。矿化过程会产生二氧化碳(CO2)等温室气体,是一个典型的温室气体释放过程。腐殖化过程则会产生稳定的腐殖质,则是优良的土壤改良剂。在堆肥稳定化的前提下,如何有效减少堆肥过程中的CO2释放,强化堆肥的腐殖化过程,增加作为优良土壤改良剂的腐殖质产量,对于发展低碳化堆肥技术,实现堆肥的资源化利用具有重要意义。本文选取水稻秸秆和餐厨垃圾作为堆肥原料,研究不同预处理对堆肥过程中矿化和腐殖化过程的影响,并探讨了不同预处理影响矿化和腐殖化过程的微生物机理。结果表明堆料加热预处理后,堆肥的矿化作用被明显削弱,总碳(TC)减量率仅为23.4%,并且最后形成了可观产量的稳定腐殖质(每kg堆料70 d后腐殖质含量为22.09 g±0.35 g,腐殖化系数达2.0),因此加热预处理后的堆肥过程在保证稳定腐殖质的产量前提下更低碳化。预处理通过影响堆料的性质和初始状态下堆料中微生物的种类和数量从而影响堆肥的矿化和腐殖化过程。活性微生物量与脱氢酶活性是矿化过程的主要决定因素,而多酚氧化酶活性主要影响堆肥的稳定腐殖化过程。     

牛脑海马NGF分离纯化及微量元素含量检测

将牛脑海马粗提物经盐析、透析、CM-离子交换层析分离纯化得到2个洗脱峰,其中CM2峰含有NGF。利用Western Blot检测结果表明,NGF的分子量约为55 KD和70 KD;PC12细胞法检测其生物学活性,在CM2分离组分作用下,PC12细胞轴突生长效果优于2 ng/mL标准品NGF;原子吸收分光光度法检测脑海马结构微量元素含量,Zn与Cu无差别,Fe与Zn、Cu有差异(P<0.01);CM2组分中Fe与Cu含量无差异,Zn远高于Fe、Cu含量(P<0.01)。     

翻堆频率对堆肥减量化、腐殖化和稳定化的影响

好氧堆肥是有机固体废弃物处理处置的有效手段之一,堆肥还田也是贫瘠土壤改良的常用措施。但好氧堆肥是一个典型的CO_2等温室气体的释放过程。如何减少堆肥过程中的CO_2释放,强化堆肥的腐殖化过程对于实现有机固体废弃物的低碳化堆肥、提高作为优良土壤改良剂的腐殖质产量具有重要意义。本文选取农林秸秆和餐厨垃圾作为堆肥原料,研究不同翻堆频率对堆肥过程中的物料减量化、腐殖化和稳定化的影响,以期发现一个较低碳的堆肥工艺,并从微生物角度初步探索了其影响机制。研究结果显示,不同的翻堆频率(分别为每2 d、4 d和6 d翻堆一次),堆料的减量化和腐殖化程度有一定差异,翻堆频率为4 d的堆肥工艺物料减量率最高为50.5%,但碳减量率最低为77.4%;而翻堆频率为2 d的堆肥工艺腐殖质产量最高;3种堆肥工艺经62 d堆肥都达到了腐熟程度,翻堆频率为4 d的堆肥工艺腐熟化程度最高。不同的翻堆频率可能通过影响堆肥过程中堆料的温度、含氧量等因素从而改变堆料中活性微生物量、种类和生物酶活性,进而影响堆料的矿化和腐殖化进程。     

好氧高温猪粪堆肥中重金属砷、铜、锌的形态变化及钝化剂的影响

采用连续提取法研究了猪粪好氧堆肥处理中重金属浓度和形态的变化以及添加不同比例的重金属钝化剂对其浓度和形态的影响.结果表明：经过堆肥处理后,猪粪中重金属As、Cu和Zn的总浓度均有所增加.从重金属结合形态的变化来看,可交换态As和Zn含量降低,残渣态As和Zn含量升高,表明As和Zn存在着向有效性相对较低的形态转化的趋势;重金属Cu则表现出不同的变化趋势,即可交换态与残渣态Cu含量下降,而碳酸盐结合态、铁锰结合态及有机结合态Cu含量有所增加,在今后的堆肥利用中应注意其可能带来的环境风险;3种重金属钝化剂及不同添加比例的处理中,5.0%的海泡石和2.5%的膨润土分别对重金属As、Zn表现出较好的钝化效果,堆肥后残渣态As和Zn的增幅分别达到79.8%和158.6%,均高于不加钝化剂处理.与对照相比,堆肥后7.5%的海泡石对残渣态Cu的降低幅度最小,为39.3%.猪粪堆肥中添加适量的重金属钝化剂,可以在一定程度上降低重金属的有效性以及猪粪堆肥利用中重金属污染的风险.     

城市污泥对作物种子发芽及幼苗生长影响的初步研究

不同类型污泥及其堆肥对通菜、菜心种子发芽和幼苗生长影响的研究表明 ,深圳生污泥、佛山生污泥和广州生污泥及其堆肥对通菜种子的发芽率有明显的影响 ,前者仅为73% ,其余的在 85%左右 ,均低于对照处理 ( 93% ) .而它们对菜心种子的发芽率 ,除了深圳生污泥有抑制作用外 ( 75% ) ,其余均表现为促进作用 ( 90 % ) ,均高于对照处理 ( 85% ) .它们对于两种作物幼苗的生长则均表现为不同程度的抑制作用甚至是损害作用 .污泥及其堆肥中抑制作物种子发芽和幼苗生长的物质主要是有机酸和醛类等有机物 .生污泥经过消化作用或适当的堆沤作用可降解这些有机物 ,从而减弱或消除这种抑制作用 .因此 ,生污泥经过消化作用或适当的堆沤作用后用于农业生产更为安全 .但对刚施用污泥或污泥堆肥的耕地最好不要直接播种 .     

堆肥对土壤重金属垂直分布的影响与污染评价

对不同畜禽粪便堆肥与土壤重金属垂直分布的关系进行了研究．结果表明,在畜禽粪便堆肥过程中,粪堆下土壤pH值和有机质显著增加,其pH和有机质含量的垂直分布表现为从表层到底层逐渐降低．各种畜禽粪便粪堆下土壤Zn、Cd含量明显增高,且从表层到底层呈逐渐减小的趋势．鸡粪和猪粪堆下土壤Cu含量随土层深度增加而降低;牛粪堆下土壤Cu含量随土层深度增加没有明显的变化．自然条件下Cd和Zn在土壤系统中的迁移能力大于Cu．各粪堆下的部分土层Cu、Zn、Cd含量超过我国土壤环境质量一级标准．应用地质积累指数法对各土层污染评价的结果表明,只有肉鸡粪堆下0～10cm土壤和蛋鸡粪堆下0～40cm土壤受到轻度Zn污染,其它粪堆下各土层均未受到Cu、Zn、Pb和Cd污染．     

The influence of humic substances on the molecular weight distributions of phosphate and iron in epilimnetic lake waters

1. The influence of humic substances on the association of free inorganic iron and phosphate with material of larger molecular weight was investigated in epilimnetic samples from two humus‐rich lakes of contrasting ionic strength. After modification of the molecular weight distribution of the humic substances in the samples using dialysis and ultrafiltration, the molecular weight distribution of added radioisotopes ( Fe3+ and PO43?) was assessed using gel filtration chromatography.
2. The association of Fe3+ and PO43? with larger molecular weight fractions (>50 000 and 10 000–50 000 Da) was not in general related to the quantity of humic substances of the same molecular weight in the samples. However, the proportions of Fe3+ and PO43? observed in higher molecular weight peaks were strongly correlated to the quantity of humic substances of the same molecular weight in (a) the 10 000–50 000 Da peak in the sample of low ionic strength at pH 5.5 and pH 7.0, and (b) the> 50 000 Da peak in the sample of higher ionic strength at pH 4.0.
3. It was concluded that humic substances promote the association of Fe3+ and PO43? with higher molecular weight fractions primarily by acting as peptizing agents for inorganic colloids containing Fe and P. Association of Fe3+ and PO43? with material of higher molecular weight via the formation of humic substance‐Fe3+–PO43? complexes was identified but only at specific pH and within specific molecular weight ranges for each of the epilimnetic lake water samples studied.     

Influence of humic substances on bioavailability of Cu and Zn during sewage sludge composting

Influence of humic substances (HS) on bioavailability of Cu and Zn was characterized during 120 days co-composting of sewage sludge and maize straw. At the initial stage of composting, Cu and Zn in sewage sludge were released as organic matter was degraded, and water soluble Cu and Zn increased markedly. Water soluble Cu and FA content decreased after 21 days whereas water soluble Zn increased during the whole process. Both HA-Cu and HA-Zn were significantly and positively correlated with HA and H/F, respectively. At the end of composting, the distribution coefficients of HA-Cu and HA-Zn reached 27.50% and 3.33% respectively with HA-Cu/HA-Zn ratio increased from 1.29 to 2.73. The results suggest that Cu combined with HA more strongly than Zn, and composting treatment could decrease bioavailability of Cu markedly.     

Identification of Pt and Pd bound to humic acid species in spiked soils and street dusts by size exclusion chromatography and ICP-MS

Abstract

The formation of PGE-humic acid (HA) complexes in soil and street dust samples was investigated. In order to assess the distribution of Pt and Pd among molecular weight fractions of humic substances, the HA extracts (extracted by 0.1 mol L^?1 sodium pyrophosphate) were analysed by size exclusion chromato-graphy coupled on-line with UV-Vis detection. Similar chromatograms were obtained for soils and street dust samples (254 nm, 280 nm) and two size fractions were operationally defined as high (1600–5000 Da) and low molecular (< 1600 Da) HA fractions. The concentration of Pt and Pd in the separated extracts was determined by ICP-MS. The results indicate that up to 43% of Pt is in the high molecular and up to 52% in the low molecular HA fraction. In both type of soil samples, Pd is preferentially bound to the low molecular HA fraction. Dependence of Pd–HA and Pt–HA formation on the sample type both in the soils and in the street dust sample as well as on Pt oxidation state was established. Metallic Pt shows a tendency for complexation with the fractions of HA higher than 5000 Da. In the street dust samples, the distribution of Pt and Pd is similar and is strongly dependent on the sample type, being bound mainly to the fractions: higher than 5000 Da, 1600–5000 Da and the fraction lower than 1600 Da.     

Humic substances change during the co-composting process of municipal solid wastes and sewage sludge

The change of the degree of stability of compost during the composting process was a kind of guideline for our study. This stability was estimated by monitoring the chemical fractionation (extraction of humic and fulvic acids, and humin) during two cycles of composting. Change of humin (H), humic-like acid carbon (CHA) and fulvic-like acid carbon (CFA) fractions during the composting process of municipal solid wastes were investigated using two windrows W1 (100% of municipal solid wastes) and W2 (60% of municipal solid wastes and 40% of dried sewage sludge). Humin and fulvic acid fractions in the two windrows decreased since the start of composting process and tend to stabilize. At the end of composting process, humic acid fraction is more important in the windrow without sludge (W1) than the one with sludge (W2). The humification indexes used in this study showed that the humic-like acid carbon fraction production takes place largely during the phase of temperature increase (thermophilic phase), and it appeared very active in the windrow W2. At the end of composting process, the E₄/E₆ ratio value indicated that the compost of W1 is more mature than the compost of W2. The humification ratio (HR) allowed a correct estimation of compost organic matter stabilization level.     

Electrofocusing the compost organic matter obtained by coupling SEC-PAGE

Humic acids (HA)-like extracted from compost at the beginning (t(0)) and after 130 days of composting (t(130)) were fractionated by coupling size exclusion chromatography to polyacrylamide gel electrophoresis (SEC-PAGE). HA-like fractions with the same molecular size (MS) and electrophoretic mobility were pooled and further characterised by analytical polyacrylamide gel electrofocusing (EF) and compared with HA separated from a Typic Chernozem soil. During the composting process all fractions were subjected to quantitative and qualitative modifications: the high MS fraction was degraded, the mid MS fractions were qualitatively changed, the content of low MS fractions increased and changed qualitatively. The main changes in EF pattern of the non fractionated HA-like t(130) were associated to low MS fractions. Such data seem to be reliable for explanation what mechanisms and monitoring of the evolution of the compost organic matter for their agricultural uses.     

Interaction of platinum with metallothionein-like ligands in the rat kidney after administration of cis-dichlorodiammine platinum II

After the administration of the anticancer drug cis-dichlorodiammine platinum II (cisplatin) to male rats, the Pt in the soluble fraction of the kidney is isolated, by gel filtration, in association with a high molecular weight component and a low molecular weight fraction. At 24 h, Pt is also recovered in a metallothionein-like fraction which elutes from Sephadex G-50 with a lower apparent molecular weight than endogenous (Cu, Zn)-thionein or Cd-thionein isolated from the kidneys of Cd2+-treated rats. None of these low molecular weight metal-binding fractions binds to Octyl Sepharose CL-4B. On DE-52 ion exchange chromatography, Cd-thionein is resolved into two isometallothioneins whereas the low molecular weight Pt-binding fraction is only partially purified and contains at least six components which elute at higher gradient concentrations than metallothionein. Pretreatment with Cd2+ which stimulates the synthesis of renal and hepatic metallothionein has no effect on the uptake and subcellular distribution of Pt in the liver and kidneys. Cisplatin treatment reduces the concentration of Cu and Zn in the renal metallothionein and other soluble protein fractions in the kidney. When administered to Cd2+-pretreated rats, cisplatin promotes the loss of Zn from the soluble protein fractions but causes the redistribution of Cd from the metallothionein to the high molecular weight fraction and fails to inhibit the Cd2+-induced accumulation of Cu in the kidneys and the binding of Cu to the soluble protein fractions. It is suggested that metallothionein probably does not have a significant role in the renal metabolism of Pt following the administration of cisplatin to rats.     

The effects of humic substances within the Ah horizon of a Calcic Luvisol on morphological changes related to invertase and peroxidase activities in wheat roots

The chemical and biological characteristics of humus within the Ah horizon (Calcic-Luvisol) have been studied. Attention was paid to variation in the NMR spectra of humic fractions and ¹³C values and to how these changes are related to different biological humic fraction activities.The chemical changes in particular involve the decrease of the aromatic component and the increase of the non-aromatic component within the horizon and the different ¹³C value not only within the horizon but also among the humic fractions distinctive of different molecular sizes.An attempt has been made to explain the vertical chemical changes in terms of processes affecting the biological characteristics of the high and low molecular size humic fractions. The main conclusions are that the low molecular size humic fractions, in the upper part of the horizon, are of greater importance with respect to the other humic fractions in influencing the enzyme activities linked to growth metabolism. The biological role of the high molecular size humic fractions characterised by a relevant content of peptidic- and carbohydratic-C is also presented.     

Copper and zinc fractions affecting microorganisms in long-term sludge-amended soils

The influences of Zn and Cu on soil enzyme activities (acid phosphatase, alkaline phosphatase, arylsulfatase, cellulase, dehydrogenase, protease (z-FLase), urease, beta-D-glucosidase and beta-D-fructofuranosidase (invertase)) and microbial biomass carbon were investigated in agricultural soils amended with municipal sewage sludge or compost since 1978. The trace metals in the soils were fractionated using a sequential extraction method. Long-term application of the sewage sludge and composts caused accumulations of Cu and Zn in the soils, ranging from 140 to 144 and from 216 to 292 mg kg(-1), respectively. The percentage of Cu was highest in the NaOH- and HNO3-extractable fractions (44-51% and 38-46%, respectively), while the percentage of Zn was highest in the HNO3- and EDTA-extractable fractions (65-83% and 11-32%, respectively). Although the percentage of the bioavailable fractions (sum of KNO3 + H2O-, NaOH-, and EDTA-extractable amounts) of Cu (53-64%) was higher than that of Zn (15-37%), the percentage of the most labile fractions (KNO3 + H2O) of Zn (2.1-5.9%) was larger than that of Cu (1.1-2.4%). The size of the microbial biomass carbon increased with the application of sewage sludge or compost. For some enzymes, however, the ratio of the enzyme activity to microbial biomass was lower in the soils amended with sewage sludge or compost than that in the control soil. The soil enzyme activities were more adversely affected by Zn than by Cu. From a multiple regression analysis, it was found that dehydrogenase, urease, and beta-D-glucosidase activities were reduced by the KNO3 + H2O-extractable fraction of Zn in the soils. These microbial activities seem to be sensitive to Zn stress, indicating the possibility that they might be useful bioindicators for evaluation of the toxic effects of Zn on microorganisms in the soils.     

Characterization of natural organic matter (NOM) derived from sewage sludge compost. Part 1: chemical and spectroscopic properties

In this study changes in the properties of natural organic matter (NOM) were studied during composting of sewage sludge in a laboratory experiment using the pile method. Typical physicochemical parameters were measured during 53 days of composting including humic fractions. The effects of humification on the molecular properties of humic acids (HA) were investigated by 13C CP/MAS NMR spectroscopy. On the basis of chemical analyses, 53 days of composting sewage sludge with structural material can be divided into three phases: (i) domination of rapid decomposition of non-humic, easily biodegradable organic matter (two to three weeks), (ii) domination of organic matter humification and formation of polycondensed, humic-like substances (the next two weeks), (iii) stabilization of transformed organic material and weak microbial activity. Spectroscopic characterization (13C NMR) of compost humic acids reveals changes in their structures during maturation. The changes are highly correlated with the processes taking place in bulk compost.     

Chemical and structural evolution of humic acids during organic waste composting

The effects of the composting process on the chemical and structural properties of humic acids have been studied in seven different organic waste mixtures from different origin. Only slight changes in elemental composition have been found in the humic acids after the composting process pointing to a more aromatic structure with higher proportions of oxygen and nitrogen. Functional groups were the most sensitive to the changes caused by the composting process showing a marked increase in the total acidity and phenolic, carboxyl and carbonyl groups. Gel permeation chromatography showed a slight increase in the average molecular weight of the humic acids. Infrared spectroscopy did not show important differences in humic acid structure but a clear decrease in the intensity of the bands in the region 3000–2850 cm^-1 corresponding to the aliphatic fractions. As a general result, the composting process yields humic acids in which the elemental and functional composition are closer to that of the more humified soil humic acids.