96 resultados para Physico-chemical properties
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水土保持工程及植被措施实施,对土壤形成条件、土壤特征及土壤发育产生一定影响,而侵蚀土壤发育程度是评价土壤质量变化及其生态环境效应的重要基础。研究黄土高原水土保持措施对侵蚀土壤理化性质、发育和功能的影响,可为水土保持综合治理,改善黄土高原生态环境提供依据。评述长期定位试验的方法及以空间代替时间的原理,研究了在实施不同水土保持措施后,土壤基本理化性状的变化特征。结果表明:随着措施实施年限的增加,土壤的水分环境和土壤有机碳含量发生了明显改善,对土壤结构和功能产生了影响。证明水土保持措施对侵蚀土壤的发育有一定促进作用。
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通过野外调查和室内分析相结合的方法,研究子午岭次生林区不同土地利用方式下的土壤性质状况,分析土地利用状况与土壤质量之间的关系,结果表明:不同土地利用方式表层土壤有机质、全氮、全磷、pH值、脲酶、蔗糖酶和碱性磷酸酶含量或活性差异显著,农地主要土壤养分含量和酶活性较低,林地则较高。除pH值外,不同利用方式下土壤养分和酶活性均随土层深度的增加而逐渐减小。除土壤pH值外,不同利用方式下土壤有机质、全氮、全磷、铵态氮、脲酶、蔗糖酶、碱性磷酸酶和过氧化氢酶之间呈显著或极显著正相关性。以林地为对照的土壤退化指数表明农用地和撂荒翻耕地土壤质量退化显著,其表层(0~20cm)土壤退化指数分别为44.86%和43.10%;撂荒未翻耕地深层(20~130cm)土壤质量则有所提高。
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研究了陕北农牧交错带荒漠化土地上种植人工植被后,在不同的植被恢复类型和生长状态下土壤物理、化学和生物学性状的特征。结果表明,随着人工植被的建立与生长,土壤肥力总体趋于好转,土壤理化性质得到显著改善,土壤质地变细,微生物数量增加,土壤酶活性增强;同时,使流动沙地向半固定、固定沙丘方向转化。但随着植被盖度和植被种类的不同,不同样地土壤肥力差异很大;多年生乔木林改良土壤肥力的潜力最高,耕作粗放的农地土壤肥力有所下降。
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To explore the changes of soil chemical properties in vegetable greenhouse,a comparative study was carried out with the samples gathered from vegetable greenhouse fields and their adjacent upland fields in Damintun Town,Xinming County,Liaoning Province.The results showed that compared with upland fields,the contents of soil organic carbon and total nitrogen in greenhouse fields increased significantly.At the depth of 0~30 cm,soil organic carbon in greenhouses of 1-,4-and 10-year increased by 31.09%,35.44%,and 66.80%,respectively,compared with the upland soil.Soil nitrate content at the depth of 0~30 cm in greenhouse fields was 5.05~12.49 times as much as that in upland fields.The nitrate content in different soil layers increased with the increasing age of greenhouse field.,e.g.,at the depth of 20~30 cm,soil nitrate content was significantly higher in 10-year than in 1-and 4-year greenhouse field,with an increase of 65.73% and 50.89%,respectively,and 6.55 times as much as that in upland field,which indicated that soil nitrate transported downwards,and obviously enriched in deeper soil layers under heavy application of fertilizer.Also with the increasing age of greenhouse field,soil pH decreased,while soil soluble salts accumulated.
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This review focuses on the synthesis, assembly, surface functionalization, as well as application of inorganic nanostructures. Electrochemical and wet- chemical methods are demonstrated to be effective approaches to make metal nanostructures under control without addition of a reducing agent or protecting agent. Owing to the unique physical and chemical properties of the nano-sized materials, novel applications are introduced using inorganic nanomaterials, such as electrocatalysis, photoelectricity, spectrochemistry, and analytical chemistry.
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The measured results of thermal analysis depend on experimental conditions. The international and national organizations have constituted a series of methods to characterize the physical and chemical properties for substances. The applications to physical transition, chemical reaction, and characteristic parameters of substances are given in the article as examples.
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Intelligent polymers or stimuli-responsive polymers may exhibit distinct transitions in physical-chemical properties, including conformation, polarity, phase structure and chemical composition in response to changes in environmental stimuli. Due to their unique 'intelligent' characteristics, stimuli-sensitive polymers have found a wide variety of applications in biomedical and nanotechnological fields. This review focuses on the recent developments in biomedical application of intelligent polymer systems, such as intelligent hydrogel systems, intelligent drug delivery systems and intelligent molecular recognition systems. Also, the possible future directions for the application of these intelligent polymer systems in the biomedical field are presented.
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Gas-phase ion-molecule reactions of buckminsterfullerene (C-60) with the ion systems generated from the self-chemical-ionization of alkyl methyl ethers(CH3OCnH2n+1, n =2 , 3, 4) were studied in the ion source of a mass spectrometer. The adduct cation [C60C2H5O](+) and protonated molecular ion [C60H](+) were observed as the major products, The former was produced by the reactions.of C-60 with the methoxymethyl ion [CH3O = CH2](+) , the latter corresponded to the proton transfer reactions from the protonated alkyl methyl ethers to C60 It is suggested that the [3+2] cycloadduct is the most favorable structure among the probable isomers with special chemical properties, Our investigation provides the guidance for the synthesis of this compound in condensed phase.
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Heteropoly acids (HPAs), such as dodecatungstosilicic acid (SiW12), adsorb strongly on to activated carbons. The surface chemical properties of the activated carbons have a pronounced effect on the adsorption of HPAs. To obtain activated carbons with the desired surface chemical properties, modification with mineral acids has been applied. The adsorption isotherms of SiW12 from aqueous solution and various acidic media on to the various carbons have been studied. On the basis of the results obtained, an adsorption model for HPAs from acidic media is presented.
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The DCI MS of C-60 with the reactions of gaseous cyclohexane and cyclohexene have been studied. Several kinds reactions of C-60 have been observed. The results show that the gasphase C-60 has very active chemical properties. The adduct ions of [C60C4H7](+) and [C60C5H7](+) may be formed by [2+4] cycloaddition where one of double bonds of C-60 acted as a dienophilic unit.
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In this paper, three new topological indices, A(x1), A(x2), and A(x3), have been developed for use in multivariate analysis in structure-property relationship (SPR) and structure-activity relationship (SAR) studies. Good results have been obtained by using them to predict the physical and chemical properties and biological activities of some organic compounds.
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in this Raper, based on distance matrix and branch vertex of atomes in a molecule, a new topological index (Y(x)) has been developed to be used in research on physical and chemical properties of alkanes. It is concluded that this index bears good structure selectivity and relativity when the results from index were compared with that of other ones.
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随着全球生态环境的恶化,各国日益重视对水体中各种污染物的治理。利用藻类的吸收、富集和降解作用,可以去除污水中的营养物质、重金属离子和有机污染物,与其他物理、化学及工程的方法相比,该技术具有以下优点:成本低、能耗小、治理效果较好,对环境污染小,有利于资源化,有利于整体生态环境的改善,是治理水质污染的新途径。 本文利用几种大型海藻对富营养化海水进行处理,结果发现孔石莼、刚毛藻均有很强的吸收N、P的能力,吸收能力依次为褶曲刚毛藻>束生刚毛藻>孔石莼。水体中褶曲刚毛藻3 g/L含量,在3~5小时之内,可把中等以上富营养化海水中的N、P降低至一类海水水平。利用刚毛藻处理富营养化地下海水和养殖废水,进行海参和大菱鲆养殖试验,探索藻类净化水质和废水循环利用的新模式,使水体保持较低的营养盐状态,减轻养殖废水对环境的影响,实现了海水养殖业与环境的可持续发展。 刚毛藻在我国近海滩涂分布广泛,利用它来处理富营养化水体,并和水产养殖业相结合,既净化水体,使养殖废水能循环利用,满足水产养殖的需求,又改善水产业生态环境。同时,将回收藻体生产优质饲料、食品和药物等,实现藻类资源的高值利用。刚毛藻营养丰富,用其替代鼠尾藻作海参饲料,资源丰富,成本低,效果好,是一种值得加以开发利用的宝贵资源,具有广泛的应用前景。 生物吸附法是一种经济有效的移除废水中有害重金属离子的方法。由于藻类细胞壁中的多聚糖可提供吸附重金属的位点,廉价而蕴藏丰富的海藻对多种重金属表现出很强的吸附能力。所以本文通过分批实验,研究了非活体刚毛藻对水体中重金属Cu2+、Pb2+和Cd2+的吸附影响因子、吸附热力学、吸附动力学及吸附机理,得到了平衡等温线及动力学数据。吸附过程的最佳pH值为5.0,吸附量随温度的升高而增加,水体中常见的Na+、K+、Ca2+、Mg2+阳离子及Cl-、NO3-、SO42-、C2O42-等阴离子的存在对吸附的影响并不显著。EDTA存在时,吸附百分率大大降低。吸附等温线符合Langmuir和Freundlich方程。刚毛藻对重金属Cu2+、Pb2+和Cd2+的吸附容量很高,25℃时,对Cu2+、Pb2+和Cd2+的最大吸附容量分别为1.61 mmol/g、0.96 mmol/g和0.98 mmol/g,且吸附过程为吸热反应。刚毛藻对重金属Cu2+、Pb2+和Cd2+的吸附过程为化学吸附,在吸附过程中藻体表面的官能团可能与金属离子发生了螯合作用。吸附动力学过程符合pseudo-二级动力学模型,在初始的30min内,吸附速率很快,随后速率逐渐降低。解吸试验表明,用EDTA可以对重金属进行回收,刚毛藻可以循环利用。实验结果表明刚毛藻是一种高效、经济实用的生物吸附材料,可用来吸附回收水体中的重金属Cu2+、Pb2+和Cd2+等。 通过非活体刚毛藻对重金属Cr6+的吸附影响因子、吸附动力学、吸附机理的研究发现,刚毛藻对Cr6+具有很强的还原能力,对电镀废水中的Cr6+的还原去除提供了非常好的方法。吸附过程的最佳pH值为2~3,实际电镀废水通常在此pH范围,因此处理实际废水时,首先在原酸性条件下,对Cr6+进行还原去除,然后调废水pH至5.0,继续进行吸附,去除其他二价离子及被还原的三价Cr离子,实现了利用同一材料还原Cr6+为Cr3+,并将Cr3+和其他重金属离子同时去除。通过对机理的讨论,认为刚毛藻对Cr6+的生物吸附过程不是一个简单的“离子交换过程”,而是一个“吸附还原过程”。在海藻量足够的前提下,只要时间足够长,Cr6+可被彻底还原去除。 利用工业废弃物褐藻渣,对水体中重金属离子Cu2+、Pb2+、Cd2+及Cr6+的生物吸附特性分别进行了讨论,结果表明褐藻渣对重金属离子的吸附特性与刚毛藻一致,吸附等温线符合Langmuir和Freundlich方程,在25℃时,pH为5.0时,由Langmuir方程求出褐藻渣对Cu2+、Pb2+和Cd2+的最大吸附容量分别为4.20 mmol/g、3.13 mmol/g和2.97 mmol/g。褐藻渣对低、高浓度的重金属Cr6+都具有很强的吸附能力,且移除效果比较彻底。实际应用结果表明,褐藻渣是一种高效、经济实用的生物吸附材料,可用来吸附回收水体中的重金属离子,具有广泛的应用前景。
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Fish Lateolabrax japonicus were exposed to anion surfactant sodium dodecylbenzene sulfonate (SDBS) and sodium dodecyl sulfate (SDS) at 1 mg/l, respectively, for 6, 12 and 18 d, with one control group. Liver antioxidant enzymes, including superoxide dismutase (SOD), catalase (CAT), glutathione peroxidase (GPx), reduced glutathione (GSH) and glutathione S-transferase (GST) were determined; brain acetylcholinesterase (AChE) and liver inducible nitric oxide synthase (NOS) activities were also measured. The results of the study indicated that these parameters made different, sometimes, adverse responses to SDBS and SDS exposure, such as the activity of NOS can be inhibited by SDBS and induced by SDS, the different physico-chemical characteristics of SDBS and SDS should be responsible for their effects on enzyme activities. (c) 2005 Elsevier B.V. All rights reserved.
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Organic carbon (OC) in definitely small area sediments(according to marine dimension)off the Huanghe River Estuary is investigated in order to evaluate the feature of regional difference of physical and chemical properties in marginal sea sediments. The distributions of OC in sediments with natural grain size and the relationship with the pH, Eh,Es and Fe3+/Fe2+ are discussed. In addition,OC decomposition rates in surfacial/subsurfacial sediments are estimated. OC concentrations range from 0.26% to 1.8%(wt)in the study area. Significant differences in OC content and in horizontal distribution as well as various trends in surfacial/subsurfacial sediments exhibit the feature of regional difference remarkably in marginal sea sediments. The complicated distribution of OC in surface sediments is due to the influence of bacterial activity and abundance, bioturbation of benthos and physical disturbance. The OC decomposition rate constant in surfacial/subsurfacial sediments ranges from 0.0097 to 0.076 a(-1) and the relatively high values may be mainly related to bacteria that are mainly responsible for OC mineralization;meio-and macrofauna affect OC degradation both directly, through feeding on it, and indirectly through bioturbation and at the same time coarse sediments are also disadvantageous to OC preservation. In almost all the middle and bottom sediments the contents of OC decrease with the increase of deposition depth, which indicates that mineralization of OC in the middle and bottom sediments has occurred via processes like SO42- reduction and Fe-oxide reduction.