土壤有机碳同位素样品制备过程的影响因素讨论

IEECAS SKLLQG

板栗内皮对酸性废水中重金属的吸附

选取板栗内皮作为吸附剂,在实验室条件下,通过振荡吸附的方法研究了板栗内皮对pH 2.0的酸性废水中,镉、铅、铜、锌4种重金属离子的吸附特性。研究结果表明,当板栗内皮的加入量为30 g/L,反应时间1 h,达到对溶液中4种重金属离子的最大去除率,分别为Cd 98.9%、Pb 99.6%、Zn 98.9%、Cu 98.7%;热力学实验结果表明,板栗内皮对4种重金属离子的吸附容量分别为Cd 3.2、Pb 90.8、Zn 27.3、Cu 52.4 mg/g;动力学实验结果表明,吸附反应在60 min内可以达平衡。Elovich方程最适合描述板栗内皮吸附重金属离子的动力学行为,板栗内皮对镉、铅、铜、锌4种重金属的吸附速率和吸附时间成反比,同一时刻对4种重金属离子吸附速率大小依次是Pb2+>Cd2+>Cu2+>Zn2+。

凋落叶多样性对杉木幼苗生长及吸收~(15)N标记硫铵的影响

利用15N硫铵研究了凋落叶多样性对杉木幼苗生长及养分吸收的影响 .结果表明 ,凋落叶多样性的增加有利于盆栽杉木幼苗的生长 .杉木、火力楠、红栲和刺楸 4种凋落叶混合处理后 ,杉木幼苗的生长量最大 ;杉木、火力楠、刺楸 3种凋落叶混合处理后的杉木幼苗生长量次之 ,其它依次为杉木、火力楠、红栲 3种凋落叶混合处理 >杉木和刺楸凋落叶处理 >杉木和红栲凋落叶处理 >对照 >杉木和火力楠 2种凋落叶混合处理 >杉木凋落叶处理 .就杉木幼苗对硫铵氮的吸收率而言 ,不作任何处理的杉木幼苗吸收率最高 ,其次为杉木、火力楠、红栲和刺楸 4种凋落叶混合处理 ,其它依次为杉木、火力楠、刺楸 3种凋落叶混合处理和杉木、火力楠、红栲 3种凋落叶混合处理 >杉木和刺楸凋落叶处理 >杉木和红栲凋落叶处理>杉木和火力楠 2种凋落叶混合处理 >杉木凋落叶处理 .另外 ,用凋落叶处理后 ,土壤中硫铵氮的残留量比不作凋落叶处理的土壤多 ,硫铵氮的总回收量也比不作凋落叶处理的土壤大幅增加 ,而且凋落叶多样性的增加也会增加硫铵氮的残留量 .

栽培模式、施氮和品种对冬小麦冠层结构和产量的影响

在黄土高原南部半湿润易旱区土垫旱耕人为土上进行大田试验,研究氮肥、品种和栽培模式对冬小麦叶面积指数(LAI)和透光率(DIFN)及产量的影响。结果表明,小麦生长过程中LAI先增大后减小,在开花期最大,成熟期最小,施氮能够显著增加LAI;DIFN的变化规律与LAI相反。不同品种间LAI和DIFN差异显著。全程覆膜和覆膜150 d的LAI极显著大于常规栽培、集雨面栽培和三密一稀栽培模式,DIFN与此相反;施氮后籽粒产量极显著增加。在不同栽培模式下,以全程覆膜、覆膜150 d和集雨面栽培模式的产量较高,但从维持土壤质量角度考虑,则覆膜150 d和集雨面2种栽培模式优于其它几种栽培模式;从冠层结构特征分析,这2种栽培模式更有利于增加群体光合能力。

一种基于粒子的牛顿流体与粘弹性流体统一模拟方法

在越来越受到人们关注的基于物理流体动画领域,目前分别模拟牛顿流体或粘弹性流体的方法很多,但很少有统一模拟两者的方法.文中基于光滑粒子流体动力学方法,通过对传统纳维-斯托克斯方程添加弹性应力项,提出了一种新的统一模拟牛顿流体和粘弹性流体的方法.通过实验说明该方法不仅有效,易于实现,而且具有良好的可控性,仅仅通过调节参数就可以模拟不同粘弹性、不同类型的流体现象.

Evaluation of Effects of Bivalent Cations on the Formation of Purine-rich Triple-Helix DNA by ESI-FT-MS

The GGA triplet repeats are widely dispersed throughout eukaryotic genomes. (GGA)n or (GGT)n oligonucleotides can interact with double-stranded DNA containing (GGA:CCT)n to form triple-stranded DNA. The effects of 8 divalent metal ions (3 alkaline-earth metals and 5 transition metals) on formation of these purine-rich triple-helix DNA were investigated by electrospray ionization Fourier transform ion cyclotron resonance mass spectrometry (ESI-FT-MS). In the absence of metal ions, no triplex but single-strand, duplex, and purine homodimer ions were observed in mass spectra. The triple-helix DNA complexes were observed only in the presence of certain divalent ions. The effects of different divalent cations on the formation of purine-rich triplexes were compared. Transition-metal ions, especially Co2+ and Ni2+, significantly boost the formation of triple-helix DNA, whereas alkaline-earth metal ions have no positive effects on triplex formation. In addition, Ba2+ is notably beneficial to the formation of homodimer instead of triplex.

电荷转移配合物薄膜制备方法和结构表征的研究进展

回顾了与Langmuir-Blodgett(LB)技术有关的电荷转移配合物薄膜的各类制备方法、结构表征结果,并比较了制备方法对薄膜结构的影响.例如,将LB膜C18H37TCNQ(电子受体)插入到电子给体3,3',5,5'-tetramethylbenzidine(四甲基联苯胺,TMB)的石油醚溶液中进行掺杂,制备了TMB·C18H37TCNQ电荷转移配合物薄膜.在这种薄膜中,给体和受体以面对面的方式堆积,两者的环平面与基片平面接近垂直.而采用硬脂酸和C18H37TCNQ的混合LB膜通过类似的掺杂路线制备的TMB·C18H37TCNQ薄膜的结构发生了一些变化,例如其长的烃链C18H37更加垂直于基片平面.通过比较以前的各种实验结果可以得出以下结论:电荷转移配合物的结构可以通过制备方法得到控制.

Novel chemical synthesis of Pt-Ru-P electrocatalysts by hypophosphite deposition for enhanced methanol oxidation and CO tolerance in direct methanol fuel cell

A novel method was developed to prepare the highly active Pt-Ru-P/C catalyst. The deposition of phosphorus significantly increased electrochemical active surface (EAS) area of catalyst by reduces Pt-Ru particle size. TEM images show that Pt-Ru-P nanoparticles have an uniform size distribution with an average diameter of 2 nm. Cyclic voltammetry (CV), Chronoamperometry (CA), and CO stripping indicate that the presence of non-metal phosphorus as an interstitial species Pt-Ru-P/C catalyst shows high activity for the electro-oxidation of methanol, and exhibit enhanced performance in the oxidation of carbon monoxide compared with Pt-Ru/C catalyst. At 30 degrees C and pure oxygen was fed to the cathode, the maximum power density of direct methanol fuel cell (DMFC) with Pt-Ru-P/C and Pt-Ru/C catalysts as anode catalysts was 61.5 mW cm(-2) and 36.6 mW cm(-2), respectively. All experimental results indicate that Pt-Ru-P/C catalyst was the optimum anode catalyst for direct methanol fuel cell.

Oxythiamine hexafluorophosphate monohydrate, a thiamine antagonist with the same conformation as thiamine

In the title compound, 3-[(3,4-dihydro-2-methyl-4-oxopyrimidin-5-yl)methyl]-5-(2-hydroxyethyl)-4-methylthiazolium hexafluorophosphate monohydrate, C12H16N3O2S+. PF6-.H2O, oxythiamine is a monovalent cation with a neutral oxopyrimidine ring. The molecule assumes the F conformation, which is a common form for thiamine but which is substantially different from the unusual V conformation found in the chloride and hydrochloride salts of oxythiamine. The anion-bridging interaction, C-H . . . anion . . . pyrimidine, is emphasized as being important for stabilization of the F conformation.

Rapid identification of saponins in plant extracts by electrospray ionization multi-stage tandem mass spectrometry and liquid chromatography/tandem mass spectrometry

Electrospray ionization multi-stage tandem mass spectrometry (ESI-MSn) and liquid chromatography coupled with on-line mass spectrometry (LC/MS/MS) were applied to characterize saponins in crude extracts from Panax ginseng. The MSn data of the [M - H](-) ions of saponins can provide structural information on the sugar sequences of the saccharide chains and on the sapogins of saponins. By ESI-MSn, non-isomeric saponins and isomeric saponins with different aglycones can be determined rapidly in plant extracts. LC/MS/MS is a good complementary analytical tool for determination of isomeric saponins. These approaches constitute powerful analytical tools far rapid screening and structural assignment of saponins in plant extracts. Copyright (C) 2000 John Wiley & Sons, Ltd.