AlCl_3对细颗粒泥沙絮凝沉降的影响

铝类絮凝剂对细颗粒泥沙絮凝沉降有重要作用 ,常应用于浑水澄清、农业污水处理等研究中。在AlCl3 浓度为 0～ 1 7mmol/L ,泥沙浓度为 1 0g/L时 ,用吸管法研究了AlCl3 对细颗粒泥沙絮凝沉降的影响 ,结果表明 :在液面下同一深度 ,泥沙浓度随时间呈指数衰减 ;悬液经多次搅拌后再沉降 ,其沉速减缓 ;当AlCl3 浓度为 0 9～ 1 7mmol/L时 ,出现明显的清浑水交界面 ,交界面随时间等速下降 ,平均沉速为 4 75 6cm/min ,对应的絮团平均粒径为 0 0 31 5mm ;土娄土絮凝临界粒径为 0 0 2 7mm。

石油烃、Cu~(2+)单一与复合污染对沙蚕的毒性效应

在实验室模拟条件下研究了石油烃、Cu2+单一与复合污染对沙蚕的毒性效应.试验的结果表明,沙蚕的死亡率与石油烃、Cu2+的浓度呈显著相关关系.其半数致死浓度LC50分别为:30.2～116.26μg/L(石油烃);449.52～1130.34μg/L(Cu2+).沙蚕体内Cu2+的积累量随着暴露溶液中Cu2+浓度的上升而增加,当Cu2+的浓度>500μg/L时,这一变化十分显著;而沙蚕体内石油烃的含量随着暴露溶液中石油烃浓度的升高无显著变化.而Cu2+和石油烃复合污染对沙蚕的毒性作用较为复杂,在不同的处理中,表现出了协同和拮抗两种作用方式.同时,在Cu2+与石油烃复合污染条件下,沙蚕体内Cu2+的积累量也有显著变化.在复合处理组中,当Cu2+的浓度达到500μg/L时,Cu2+在沙蚕体内的积累量与Cu2+单一污染相比,Cu2+在沙蚕体内积累量相比显著降低.

苔藓植物对植物天然更新的影响

种子是天然更新的基础,幼苗和幼树的生长是天然更新过程中最敏感的阶段。苔藓植物作为许多生态系统的主要地被物,在维管植物天然更新过程中发挥着不容忽视的作用。在许多植被类型中,都有发育良好的苔藓群落,大量的研究证明它们的存在影响到维管植物的萌发、建成和生长,并且可能进一步影响到物种的共生,有一些种类甚至可能指示树种的更新。本文就苔藓植物对物种更新早期阶段的作用和影响进行了综述。包括苔藓植物的生理特性造成的微气候变化;苔藓群落对种子传播、萌发及幼苗建成的影响。并讨论了苔藓植物与更新物种的种间关系及其对幼苗生长的化感作用。

一种测量林窗面积的改良方法:等角椭圆扇形法

目前测量林窗面积较精确的方法为:测量从林窗中心沿8或16个罗盘方向到林窗林冠边缘的距离,再将林窗近似成等角8或16边形估测其面积(本文称这类方法为等角多边形法)。研究表明,等角8或16边形法均会低估林窗面积,本文提出一种改良方法:等角椭圆扇形法,野外测量与前者相同,计算时将相邻距离间的部分近似为椭圆扇形,以所有椭圆扇形面积之和估测林窗面积。用配对t检验对等角多边形法和等角椭圆扇形法的林窗面积进行比较,结果表明:(1)等角16边形法与等角8或4边形法存在极显著差异(P<0.001),比后两者,分别高10.96%和61.66%,这表明等角条边形法均会低估林窗面积;(2)等角椭圆扇形16分法比等角16边形法大10.16%,且二者之间存在极显著差异(P<0.001),因此,等角16边形法的测量值位于等角椭圆扇形16分法和等角8边形法之间;由(1)和(2)可推断等角椭圆扇形16分法比等角8边形法更准确;(3)等角椭圆扇形8分法与等角椭圆扇形16分法没有显著差异(P=0.715),但与等角8边形法存在显著差异(P<0.05),因此,等角椭圆扇形8分法比等角8边形法更准确。另外,本文的两个等角8边形法(基于两组不同罗盘方位的测量距离)求得的林窗面积之间存在极显著差异(P<0.01),而两个等角椭圆扇形8分法之间却没有差异(P=0.778),这表明等角椭圆扇形8分法的结果更稳定。

过去2000年中国温度变化研究的几个问题

根据最近重建的中国东部地区过去2000年冬半年温度距平序列,结合最近其他一些相关研究结果,对过去2000年中国温度变化序列的重建方法、小冰期及魏晋南北朝冷期的起迄时间与寒冷状况、中世纪暖期与隋唐暖期的温暖程度、过去2000年中国冷暖变化的幅度与速率、温度变化的千年波动周期、20世纪气候增暖是否超出过去2000年气候波动的最大范围及20世纪暖期历史相似型等几个问题进行了综合评述.

经济改革背景下中国城市用地扩展的时空格局及其驱动因素分析

改革开放以来,中国进入了快速城市化发展时期。本文利用高分辨率陆地卫星(LandsatTM/ETM)遥感影像数据,监测了中国城市用地扩展态势,并分析了影响中国城市用地扩展的驱动因素。研究表明:1990～2000年,中国城市用地扩展表现出明显的时空分异态势,城市用地增长了近82万hm~2,其中前5年的扩展占80.8%,后5年的扩展占19.2%,后5年的扩展规模明显低于前5年。研究还发现,城市用地主要以同心圆模式、飞地模式、轴向扩展模式与多极核扩展模式以及4种扩展模式的组合模式扩张。本文选取13个特大城市作为典型案例,对其城市用地扩展的驱动机制进行了研究,研究发现,人口增长、经济发展以及土地管理法规政策的变化是影响城市用地扩展的主要因素。

Synthesis and properties of soluble poly[bis(benzimidazobenzisoquinolinones)] based on novel aromatic tetraamine monomers

Four aromatic tetraamine monomers possessing flexible ether linkages were successfully synthesized by nucleophilic aromatic substitution of hydroquinone, 4,4'-dihydroxybiphenyl, 2,2'-bis(4-hydroxyphenyl)propane, and 2,7-dihydroxynaphthalene with 5-chloro-2-nitroaniline, followed by reduction, respectively. With these monomers, a new class of soluble poly[ bis(benzimidazobenzisoquinolinones)] was prepared by a one-step, high-temperature solution polycondensation. The resulting polymers were completely soluble in phenolic solvents and had high inherent viscosities ranging from 1.2 to 1.5 g dL(-1). These polymers had glass transition temperatures in the range of 427-449 degrees C. Thermogravimetric analysis showed that all polymers were thermally stable, with 5% weight loss recorded above 510 degrees C in nitrogen.

Synthesis, photophysical and electrophosphorescent properties of mononuclear Pt(II) complexes with arylamine functionalized cyclometalating ligands

Four cyclometalated Pt(II) complexes, i.e., [(L-2)PtCl] (1b), [(L-3)PtCl] (1c), [(L-2)PtC CC6H5] (2b) and [(L-3)PtC CC6H5] (2c) (HL2 = 4-[p-(N-butyl-N-phenyl)anilino]-6-phenyl-2,2'-bipyridine and HL3 = 4-[p(-N,N'-dibutyl-N'-phenyl)phenylene-diamino]-phenyl-6-phenyl-2,2'-bipyridine), have been synthesized and verified by H-1 NMR, C-13 NMR and X-ray crystallography. Unlike previously reported complexes [(L-1)PtCl] (1a) and [(L-1)PtC CC6H5] (2a) (HL1 = 4,6-diphenyl-2,2'-bipyridine), intense and continuous absorption bands in the region of 300-500 nm with strong metal-to-ligand charge transfer ((MLCT)-M-1) (d pi(Pt) -> pi*(L)) transitions (epsilon similar to 2 x 10(4) dm(3) mol (1) cm (1)) at 449-467 nm were observed in the UV-Vis absorption spectra of complexes 1b, 1c, 2b and 2c.

First-principles investigation on the elastic, magnetic and electronic properties of MFe3N (M = Fe, Ru, Os)

The elastic, magnetic and electronic properties of MFe3N (M = Fe, Ru, Os) are investigated via first-principles calculations. The calculated results are in agreement with the experimental and other theoretical data. The high ratios of bulk modulus to shear modulus 2.7, 2.0, and 1.8 for gamma'-Fe4N, RuFe3N, and OsFe3N, respectively, indicate that they have good ductility. gamma'-Fe4N possesses the largest B/C-44 (3.41) ratio, which suggests that it is much prone to shearing. The net magnetic moment per formula unit decreases from 9.90 for gamma'-Fe4N, 7.66 for RuFe3N, to 6.80 mu(B) for OsFe3N.

Polypropylene as a carbon source for the synthesis of multi-walled carbon nanotubes via catalytic combustion

Multi-walled carbon nanotubes (MWCNTs) were efficiently synthesized by catalytic combustion of polypropylene (PP) using nickel compounds (such as Ni2O3, NiO, Ni(OH)(2) and NiCO3 (.) 2Ni(OH)(2)) as catalysts in the presence of organic-modified montmorillonite (OMMT) at 630-830 degrees C. Morphologies of the sample undergoing different combustion times were observed to investigate actual process producing MWCNTs by this method. The obtained MWCNTs were characterized by X-ray diffraction (XRD), transmission electron microscope and Raman spectroscopy. The yield of MWCNTs was affected by the composition of PP mixtures with OMMT and nickel compounds and the combustion temperature. The proton acidic sites from the degraded OMMT layers due to the Hoffman reaction of the modifiers at high temperature played an important role in the catalytic degradation of PP to supply carbon sources that are easy to be catalyzed by nickel catalyst for the growth of MWCNTs. The XRD measurements demonstrated that the nickel compounds were in situ reduced into the Ni(0) state with the aid of hydrogen gas and/or hydrocarbons in the degradation products of PP, and the Ni(O) was really the active site for the growth of MWCNTs. The combination of nickel compounds with OMMT was a key factor to efficiently synthesize MWCNTs via catalytic combustion of PP.

Structure identification of a prenylflavonol glycoside from Epimedium koreanum by electrospray ionization tandem mass spectrometry

A novel prenylflavonol glycoside, named acetylicariin, has been isolated from the aerial parts of Epimedium koreanum Nakai. The structure has been identified by electrospray ionization multi-stage tandem mass spectrometry (ESI-MSn) and other chemical evidence, which has been elucidated as 8-prenylkaempferol-4'-methoxyl-3-O-alpha-L-rhamnopyranosyl-7-O-beta-D-(2''-O-acetyl)glucopyranoside.

Calculation of the thermal expansion coefficient for Bi2Sr2CaCu2O8

An estimation method of thermal expansion coefficient in term of lattice energy which was developed earlier for simple materials is extended to a complex material of Bi2Sr2CaCu2O8 (Bi-2212). The calculation of the chemical bond property and thermal expansion coefficient of Bi-2212 has been carried out and the theoretical values were in good agreement with the corresponding experimental results. The dependence of the thermal expansion coefficient on the different structures and on the flexible oxidation states of Bi and Cu are investigated. The results indicate that the thermal expansion coefficients of Bi-2212 are insensitive to the low lattice distortion of the average structure and the changes of formal valences of Bi and Cu ions.

Hydrothermal synthesis and characterization of bimetallic cluster complex [{Mn(phen)(2)}(2)V4O12]center dot 1/2 H2O

A new bimetallic cluster complex with the formula [(Mn(phen)(2))(2)V4O12].1/2 H2O has been synthesized through hydrothermal reaction of vanadate staring material with manganese cation in the presence of nitrogen donor chelating ligand and characterized by single-crystal X-ray diffraction, elemental analysis, IR UV-vis, ESR spectrum and thermal analysis. The compound crystallize in the monoclinic space group P2(1)/c with a = 18.475(4) Angstrom, b = 11.473(2) Angstrom, c = 23.667(5) Angstrom, beta = 97.76(3)degrees, V = 4971(2) Angstrom(3) and Z = 4. The structure of [{Mn(phen)(2)}(2)V4O12].1/2 H2O is composed of a discrete V4O124- cluster covalently attached to two [Mn(phen)(2)](2+) fragments.