柳枝稷的生长发育与土壤水分特征

1992—1998年中国科学院安塞水土保持综合试验站在山地、川地引种10份原产美国的柳枝稷(Panicum virgatum)材料,经过7 a测定,数据表明柳枝稷在3～5 a生长高峰期对土壤水分需求最大,产量最高。从土壤水分含量的变化来看,柳枝稷草地在80—200 cm土层已经形成土壤干层,而且在经过生长季节降雨和休闲期的雨雪水分补充不能够补偿,这主要是维持较大的生产力造成。柳枝稷在半干旱黄土丘陵区有较强的适应性,这对当地人工草地建造、天然草地改良具有重要意义。通过对柳枝稷驯化栽培的人工草地在黄土丘陵半干旱地区立地条件下生产力与土壤水分特征的比较,以揭示柳枝稷的生态适应性对其地上生物量形成规律的影响,为该地区合理利用牧草资源、提高草地的生产能力提供依据与参考。

土壤结构改良剂在节水农业中的研究与应用

amendment; Water-saving agriculture; Research prospect; 【摘要】 为了充分了解土壤结构改良剂在节水农业中的研究应用现状,本文从作用机理、田间应用技术和效果等几个方面介绍土壤改良剂的应用现状。在此基础上,提出了土壤改良剂在节水农业应用中需要进一步解决的问题,指出了必须深入系统地研究不同土壤结构改良剂的田间实际应用效果,进一步研究有关土壤结构改良剂尤其是残留单体对环境的负面影响。

流动注射氢化物发生-原子吸收分光光度法测定血清中的硒

<正> 硒是人体健康必需的微量元素之一。对维持正常代谢起着重要的调节作用。长期缺硒可导致克山病发生,会使受孕率显著下降,频繁出现流产、难产和死胎,还会并发贫血症等。然而,过量的硒对人体也有害,能导致胃肠疾病,神经过敏和紫斑病的发生。由此可见,硒和人体健康有着十分密切的关

温度和脲酶抑制剂影响下的土壤脲酶动力学行为

为了揭示脲酶抑制剂对土壤脲酶动力学特性的影响,采用模拟试验方法,获得了HQ、PPD和NBPT在温度梯度(10℃、20℃、30℃)作用下的土壤脲酶动力学行为。结果表明,对照处理白浆土脲酶Km和Vmax大于褐土,而Vmax/Km小于褐土。随温度升高,土壤脲酶Km和Vmax增加,Vmax/Km先增加后降低。与对照相比,HQ、PPD和NBPT均使Km增加,Vmax降低,表明其作用机理均属于混合型抑制。与HQ相比,PPD和NBPT对动力学参数的影响强度较大,持续作用时间较长,表明PPD和NBPT更有效的抑制脲酶活性。统计分析显示,土壤脲酶Km、Vmax和Vmax/Km均土壤理化指标存在显著的相关性。

Selective hydrogenation of maleic anhydride to gamma-butyrolactone in supercritical carbon dioxide

The reaction rates of the hydrogenation of maleic anhydride (MAH) and succinic anhydride (SAH) were significantly accelerated and the selectivity to gamma-butyrolactone (GBL) was enhanced largely when the reaction mixture was pressurized by a non-reactant of CO2. Above 99% selectivity to GBL was achieved in 14 MPa CO2, the superior selectivity in scCO(2) was attributed to that MAH and/or SAH could be extracted to CO2 phase and separated from H2O, the hydrolysis were thus minimized and so the selectivity to GBL was improved.

The relationship between the thermal expansions and structures of ABO(4) oxides

The linear thermal expansion coefficients of ABO(4) compounds are determined and the expansion tendency is analyzed from the chemical bond viewpoint. All chemical bonds contributions are involved. The contributions from different chemical bonds are compared with each other and the origin of the expansion behavior of ABO(4) oxides is revealed that the A-O bonds expansions dominate the compound expansion. The calculated expansion coefficients agree satisfactorily with the experimental data. By analyzing the expansion regularity the range of the expansion coefficients can be qualified. The thermal expansion coefficients of some ABO(4) compounds having not been measured are predicted and discussed.

Preparation and characterization of W-Type hexaferrite doped with La3+

A series of W-type ferrites with the composition of Ba1-xLaxCo2Fe16O27 (where, x = 0.0, 0.05, 0.10, 0.15, 020 and 0.25) were prepared by solid-state reaction method. The structure transformations of the ferrites were examined by XRD, DTA-TG and XPS, and the microwave-absorbing properties were investigated by evaluating the permeability and permittivity of materials (mu(r), epsilon(r)). The results showed that the phase-transition temperature increased with the addition of La2+ content, and a single-phase was formed at 1250 degrees C at last. Microwave properties were obviously improved as a result of the substitution of La3+ for Ba2+ at the frequency range of 0.5 similar to 18.0 GHz.

Crystal structures of EtEDTB center dot 1.4C(2)H(5)OH center dot 5H(2)O and H4EtEDTB(ClO4)(4)center dot C2H5OH (EtEDTB=N, N, N ', N '-tetrakis[2-(1-ethylbenzimidazolyl)methyl]-1,2-ethanediamine)

The crystal structures of EtEDTB.1.4C(2)H(5)OH.5H(2)O 1 and H4EtEDTB(ClO4)(4).C2H5OH 2 (EtEDTB = N, N,N',N'-tetrakis[2-(1-ethylbenzimidazolyl)methyl]-1,2-ethanediamine) have been determined by single-crystal X-ray diffraction method. Compound 1 crystallizes in the space group P(1) over bar with a = 11.489(2), b = 11.866(3), c = 12.002(3) Angstrom, alpha = 97.47(2), beta = 114.564(13), gamma = 114.11(2)degrees, V = 1266.6(5) Angstrom(3), Z = 1, M-r = 847.48, D-c = 1.111 g/cm(3), F(000) = 456 and mu(MoKalpha) = 0.076 mm(-1). A total of 5207 reflections were measured for 1, of which 4323 were independent. The structure of 1 was solved by direct methods and refined by full-matrix least-squares technique to the final R = 0.0706 and wR = 0.1802 for 1318 observed reflections with I > 2sigma(I). In the structure of 1, centrosymmetric EtEDTB molecules are linked by hydrogen bonds through water and ethanol to form 2-dimensional network. Compound 2 crystallizes in the space group C2/c with a = 24.260(5), b = 13.040(3), c = 17.680(4) Angstrom, beta = 97.50(3)degrees, V = 5545.2(2) Angstrom(3), Z = 4, M-r = 1140.80, D-c = 1.366 g/cm(3), F(000) = 2384 and mu(MoKalpha) = 0.289 mm(-1).

High PL quantum efficiency of poly(phenylene vinylene) systems through exciton confinement

Photoluminescence (PL) quantum efficiency is a key issue in designing successful light-emitting polymer systems. Exciton relaxation is strongly affected by exciton quenching at nonradiative trapping centers and the formation of excimers. These factors reduce the PL quantum yield of light-emitting polymers. In this work, we have systematically investigated the effects of exciton confinement on the PL quantum yield of an oligomer, polymer, and alternating block copolymer (ABC) PPV system. Time-resolved and temperature-dependent luminescence studies have been performed. The ABC design effectively confine photoexcitations within the chromophores, preventing exciton migration and excimer formation. An unusually high (PL) quantum yield (above 90%) in the solid state is reported for the alternating block copolymer PPV, as compared to that of similar to 30% of the polymer and oligomer model compounds. (C) 2000 Elsevier Science S.A. All rights reserved.

Synthesis and crystal structure of a novel compound: [H3PMo12O40][CO(NH2)(2)](3)center dot-5H(2)O

The title compound, [H3PMo12O40][CO(NH2)(2)](3). 5H(2)O, was synthesized and characterized by IR, C-13 NMR and X-ray diffraction. This is the first example of a urea-heteropoly acid species. Crystal data: monoclinic, C2/c, a = 17.790(4) Angstrom, b = 17.158(3) Angstrom, e = 25.512(5) Angstrom, beta = 100.65(3)degrees, V = 8514(3) Angstrom (3), Z = 6, R-1 = 0.0437, wR2 = 0. 1092. In the unit cell, the urea molecules occupy cavities in the polyoxometalate lattice ordered along b-axis. Water molecules occupy the space left by polyoxometalates, and urea. Polyoxometalate O atoms, the N atoms of urea and O atoms of water molecules are involved in hydrogen bonding. (C) 2001 Elsevier Science B.V. All rights reserved.

Metal ion adducts in the structural analysis of ginsenosides by electrospray ionization with multi-stage mass spectrometry

The effect of metal (Li+, Na+, K+, Ag+) cationization on collision-induced dissociation of ginsenosides was investigated by electrospray ionization mass spectrometry combined with multi-stage mass spectrometry (ESI-MSn). The fragments of sodiated and lithiated molecules give valuable structural information regarding the nature of the aglycone and the sequence and linkage information of sugar moieties. However, the number and relative abundances of fragment ions from lithiated ginsenosides are significantly greater than for the sodiated species, The K+ adducts undergo glycosidic cleavages and very limited cross-ring reactions. The silver ion adducts fragment mainly through glycosidic cleavages. Copyright (C) 2001 John Wiley & Sons, Ltd.

The exciplex as an intermediate for photocycloaddition of 9-vinyl anthracene and p-N, N-dimethylamino styrene

The appearence of the new fluorescence peak at about 570 nm demonstrates exciplex formation between the singlet states of 9-vinyl anthracene and p-N, N-dimethylamino stytene. With increasing the polarity of solvents t the red-shift of the emission wavelength occurs and the fluorescence quantum yield of the exciplex decreases. For example t the fluorescence peak is at 550 nm in totuene and at 595 nm in butanone. The fluorescence quatum yields in totuene and in butanone are 0.053 and O respectively. Both the relative yield of the photocycloaddition dimer and the ratio of the relative yields of the trans and cis dimers decrease with increasing the polarity of solvents. For example, the relative yields of the dimer are 1.0 in totuene and 0.04 in butanone respectively. The ratio of the relative yields of traits and cis dimers are 0.54 and 0 in totuene and butanones t respectively. In addition, the exciplex intermediate mechanism was suggested for the photocycloaddition between 9-vinyl anthracene and 9-N, N-dimethylamino styrene.

PROBABILISTIC ESTIMATION OF THE STRUCTURE SEMINVARIANTS IN THE MONOCLINIC AND ORTHORHOMBIC SYSTEMS WHEN ANOMALOUS SCATTERERS ARE PRESENT

The estimate formulas for the two-phase structure seminvariants (TPSSs) in the presence of anomalous scattering are obtained from the estimate of the two-phase structure invariants [Hauptman (1982). Acta Cryst. A38, 632-641; Giacovazzo (1983). Acta Cryst.

含膨润土的部分水解交联聚丙烯酰胺高吸水性树脂的研究

高吸水性树脂是近年来迅速发展起来的一类新型功能高分子材料,其应用十分广泛,但该类材料尚需急待解决三大问题,即降低成本,提高吸水后凝胶强度,提高凝胶耐盐性,后者已有文献报道,而前两个问题还没有得以解决.作者于1978年曾用丙烯酰胺(AM)和甲叉基双丙烯酰胺碱水溶液共聚交联,水解、造粒、烘干、粉碎,研制出吸水膨胀