人工湿地基质净化磷素的吸附剂性能

通过基质磷素等温吸附实验,研究了砂子、水淬渣、钢渣3种人工湿地基质净化磷素的效果.结果表明:Freundlich和Langmuir等温吸附曲线方程均能较好地描述上述基质磷素吸附的过程,其磷素理论饱和吸附量依次为钢渣12 500 mg.kg-1,水淬渣3 333 mg.kg-1,砂子270 mg.kg-1.基质吸附饱和后,磷素解吸实验表明:水淬渣磷素解吸率最低,为0.68%;砂子的解吸率最高,为7.59%.虽然钢渣的吸附量最大,但其水溶液pH显强碱性,不适合湿地植物的生长;水淬渣作为一种工业废料,磷素吸附量为砂子的12倍左右,解吸率为砂子的1/10,而且对植物生长无明显危害,是一种比较有应用前景的湿地除磷材料.

WEPP模型的最新研究进展

WEPP(Water Soil Loss Equation)作为新一代水蚀预报模型,是指导水土保持措施优化配置、水土资源保护与持续利用的有效工具。近年来,遥感和GIS技术为WEPP快速获取所需资料、处理数据、图像编辑和输出等提供可靠的技术支撑;同时,区域化、尺度概念的引入,为WEPP应用于大尺度提供技术保障。为借鉴WEPP模型的优点,促进我国水蚀预报模型的发展,对WEPP模型的最新发展进行了详尽的介绍,并对WEPP应用到我国时可能存在的问题进行了初步分析。

沙地云杉生态型同工酶研究

沙地云杉是内蒙古地区特有树种,只分布于浑善达克沙地东部边缘;由于长期适应干旱生态条件,分化出3种土壤生态型,即紫果型、红果型和绿果型沙地云杉,并在很多生态、生理特征上表现出明显的差异.本文采用聚丙烯酰胺凝胶电泳技术,分析了3种生态型沙地云杉的过氧化物同工酶和酯酶同工酶的酶谱特征.结果表明:不管是过氧化物同工酶还是酯酶同工酶,紫果型沙地云杉的酶带条数最多,红果型其次,绿果型酶带条数最少.在酶带强度方面也有类似的结果,紫果型沙地云杉具有较多的强、次强、中带,红果型其次,绿果型最少.这在一定程度上表明,在干旱条件下产生的3种不同生态型沙地云杉,以紫果型对干旱抗性最强,绿果型最弱,红果型居于二者之间,这一结论将为沙地云杉的经营管理及品种选择提供科学依据. 图2参21

沈阳市域森林生态系统服务功能价值评估

采用费用支出法、机会成本法、替代成本法等方法对沈阳市森林生态系统的涵养水源、调节气候、固碳释氧、保持土壤、净化环境、旅游等生态功能价值进行了初步估算。结果表明,沈阳市森林生态系统服务功能总价值为359.631亿元,其中,直接经济价值为4.374亿元、涵养水源价值为3.652亿元、调节气候价值为281.5亿元、固碳释氧价值为34.194亿元、保持土壤价值为0.699亿元、净化环境价值为35.133亿元、旅游价值为800万元。

受干扰长白山阔叶红松林林分组成及冠层结构特征

通过样地调查对不同干扰方式产生的过伐天然林、次生白桦林和人工落叶松林等群落的结构组成进行分析和分类探讨 ,并选取了林窗片断和叶面积指数两个能表示群落冠层结构的指标进行分析。结果表明 ,林窗片断值分别为 :原始阔叶红松林 0 194、原始阔叶类 0 185、结构转换型 0 315、结构保留型 0 36 3、结构破坏型 0 2 35、严重干扰类型 0 5 5 0、次生白桦林0 2 13和人工落叶松林 0 2 2 7;叶面积指数分别为 :原始阔叶红松林 1 76 6、原始阔叶类 1 6 80、结构转换型 1 2 5 0、结构保留型 1 0 2 8、结构破坏型 1 5 5 0、严重干扰类型 0 6 35、次生白桦林1 731和人工落叶松林 1 4 73。

影响土壤N_2O排放和CH_4吸收的主控因素的研究(英文)

本文于2000年7月,在实验室模拟条件下,以长白山阔叶红松林鲜土壤为对象,采用正交试验设计法对土壤进行培养实验,研究了影响土壤N2O排放和CH4吸收的主要因素。考察了温度、水分、pH值、NH4+及NO3-五因素对森林土壤N2O排放和CH4吸收的影响。实验结果显示:在本试验设计的因素、水平条件下,N2O排放速率、CH4吸收速率二者均与土壤pH值和温度这两个因素呈显著正相关。并且N2O排放速率与CH4吸收速率间呈显著线性正相关关。

一种资源敏感的Web应用性能诊断方法

提出一种资源敏感的性能诊断方法.对于Web应用事务,该方法利用资源服务时间对于不同负载特征相对稳定的特点建立性能特征链,并依据运行时资源服务时间异常实现性能异常的有效检测、定位和诊断.实验结果表明,该方法可适应系统负载特征变化,诊断各种资源使用相关的性能异常.

海洋渔业遥感地理信息系统应用服务技术和方法

全面概要地介绍具有自主知识产权、可业务化运行的海洋渔业遥感、地理信息系统技术应用服务系统的研制技术方法和功能特点

Synthesis and Characterization of Urea Bridged Hybrid Periodic Mesoporous Organosilica Materials

Urea bridged organic-inorganic hybrid mesoporous SiO2 materials (U-BSQMs) were synthesized through a sol-gel procedure by co-condensation of bis(triethoxysilyl propyl) urea (BSPU) under basic conditions using cetyltrimethylammonium bromide (CTAB) as organic template. X-ray diffraction (XRD) and transmission electron microscopy (TEM) confirmed the mesoporous structure of the sample. Fourier-transform infrared spectroscopy (FT-IR), solid state CP-MAS NMR spectroscopy of Si-29 (Si-29, CP-MAS NMR) and C-13 (C-13 CP NMR) indicated that most of the Si-C bonds are unbroken during the synthesis process.

Effect of Y for enhanced age hardening response and mechanical properties of Mg-Ho-Y-Zr alloys

In this study, compositional dependence of age hardening characteristics and tensile properties were investigated for Mg-4Ho-xY-0.6Zr alloys (x = 0, 3 5, and 7 wt%). The result showed that with increasing Y content, the hardness of the alloys increased in the as-quenched and aged-peak conditions. Considerable age hardening response was recognized for the alloys. When the alloy containing 7% Y showed the most remarkable age hardening response at aging temperature of 250 degrees C.

毛细管电泳及液相色谱法研究黄连黄芩配伍过程化学成分的变化

对黄连与黄芩的不同比例配伍进行定量研究。黄连与黄芩按6∶1、6∶4、6∶7、6∶10、6∶13比例配伍,采用高效毛细管电泳法测定了黄连单煎液、黄连黄芩共煎液中生物碱的含量;采用高效液相色谱法测定了黄芩单煎液、黄连黄芩共煎液中黄酮的含量。结果显示,黄连黄芩共煎产生沉淀,使有效成分的含量降低。

Implantation of Nafion (R) ionomer into polyvinyl alcohol/chitosan composites to form novel proton-conducting membranes for direct methanol fuel cells

A series of cost-effective, proton-conducting composite membranes, comprising of Nafion (R) ionomer, chitosan (CS). and polyvinyl alcohol (PVA), is successfully prepared. By taking advantage of the strong electrostatic interactions between Nafion (R) ionomer and CS component, Nafion ionomer is effectively implanted into the PVA/CS composite membranes, and improves proton conductivity of the PVA/CS composite membranes. Furthermore, this effect dramatically depends on the composition ratio of PVA/CS, and the optimum conductivity is obtained at the PVA/CS ratio of 1:1. The developed composite membranes exhibit much lower methanol permeability compared with the widely used Nafion (R) membrane, indicating that these novel membranes have great potential for direct methanol fuel cells (DMFCs).

Highly conductive, methanol resistant fuel cell membranes fabricated by layer-by-layer self-assembly of inorganic heteropolyacid

Layer-by-layer (LBL) self-assembly is a simple and elegant method of constructing organic-inorganic composite thin films from environmentally benign aqueous solutions. In this paper, we utilize this method to develop proton-exchange membranes for fuel cells. The multilayer film is constructed onto the surface of sulfonated poly(arylene ether ketone) (SPAEK-COOH) membrane by LBL self-assembly of polycation chitosan (CTS) and negatively charged inorganic particle phosphotungstic acid (VIA). The highly conductive inorganic nanoparticles ensure SPAEK-COOH-(CTS/PTA)(n) membranes to maintain high proton conductivity values up to 0.086 S cm(-1) at 25 degrees C and 0.24S cm(-1) at 80 degrees C, which are superior than previous LBL assembled electrolyte systems.

Direct electrochemistry and electrocatalysis of glucose oxidase immobilized on glassy carbon electrode modified by Nafion and ordered mesoporous silica-SBA-15

In this paper, it was found that glucose oxidase (GOD) has been stably immobilized on glassy carbon electrode modified by ordered mesoporous silica-SBA-15 and Nafion. The sorption behavior of GOD immobilized on SBA-15 matrix was characterized by transmission electron microscopy (TEM), ultraviolet-visible (UV-vis), FTIR, respectively, which demonstrated that SBA-15 can facilitate the electron exchange between the electroactive center of GOD and electrode. The direct electrochemistry and electrocatalysis behavior of GOD on modified electrode were characterized by cyclic voltammogram (CV) which indicated that GOD immobilized on Nafion and SBA-15 matrices displays direct, nearly reversible and surface-controlled redox reaction with an enhanced electron transfer rate constant of 3.89 s(-1) in 0.1 M phosphate buffer solution (PBS) (pH 7.12).