“第七届全国绿色环保肥料(农药)新技术、新产品交流会”专题报告

本次会议有27个专题报告,各具特色、异彩纷呈,突出展现了腐植酸肥料(农药)领域开发应用的最新研究和开发进展。为了让读者了解本次会议取得的成果,本栏目按会议专题报告顺序,将报告提要、报告中具有代表性的图或表、报告人简介和报告评价等内容编辑刊出。见21～45页。

大兴安岭北坡火烧迹地森林景观恢复及其影响因子——以郁闭度指标为例

1987年发生在大兴安岭北坡的特大火灾造成了森林资源的巨大损失,森林景观恢复一直是人们关注的热点.本研究选取与森林生产力密切相关的郁闭度因子作为研究对象,以ArcView、ArcGIS等地理信息系统软件为研究平台,采用1987年和2000年两期森林资源二类调查数据,对郁闭度、火烧强度、抚育类型和地形因子等进行分级,利用Kendall等级相关分析、相似性分析等方法,探讨了森林郁闭度格局的恢复状况以及火烧强度、更新类型、地形因子对郁闭度恢复的影响.结果表明,2000年郁闭度等级构成与1987年火前相比发生了明显变化,无林地以及高郁闭度等级比重明显下降,较低郁闭度等级比重显著上升;火烧强度对火后恢复的影响最为关键,火烧强度与郁闭度等级呈负相关;更新措施短期内对郁闭度恢复影响不显著,但可以缩短森林演替的周期,对未来针叶林群落生产力恢复具有重要的促进作用;地形因子中坡度对郁闭度恢复影响最为明显,其次为坡位,坡向影响最弱.

菱镁矿粉尘污染土壤机理及其植物修复

综述了菱镁矿粉尘对土壤的污染和植物的毒害作用机理,分析了镁粉尘污染土壤的改良途径,探讨了植物修复的可行性和关键技术。菱镁矿在开采、生产加工过程中产生的大量粉尘,主要成分为MgCO3和MgO,镁粉尘对土壤的污染和植物的毒害作用主要是通过碱化、板结土壤,以及使土壤中的水溶性钙、镁离子比例失调而造成的。虽然菱镁矿粉尘污染土壤的植物修复研究鲜见报道,但通过植物吸收、植物代谢和植物积累等作用去除土壤中的过量镁具有较强的可行性。

沈阳城市森林绿量测算

借助ARC/GIS地理信息系统,以“平面量推算平面量”的方法,测算了沈阳市城市森林的绿量.结果表明:沈阳市城市森林不同类型单位面积绿量以风景游憩林最高,为3·86m2·m-2;生态公益林最低,为2·27m2·m-2;城市森林分布区单位面积绿量为2·99m2·m-2;城区单位面积绿量为0·25m2·m-2.沈阳城市森林总体绿量约为1·13×108m2·其中,附属林为4·15×107m2,占36·64%;生态公益林2·72×107m2,占23·99%;风景游憩林2·20×107m2,占19·38%;道路林1·84×107m2,占16·20%;生产经营林0·43×107m2,占3·79%.经检验,平面量推算平面量方法测算精度达到91·81%(α=0·05).

Facile preparation of macroscopic soft colloidal crystals with fiber symmetry

A facile, efficient way to fabricate macroscopic soft colloidal crystals with fiber symmetry by drying a latex dispersion in a tube is presented. A transparent, stable colloidal crystal was obtained from a 25 wt % latex dispersion by complete water evaporation for 4 days. The centimeter-long sample was investigated by means of synchrotron small-angle X-ray diffraction (SAXD). Analysis of a large number of distinct Bragg peaks reveals that uniaxially oriented colloidal crystals with face-centered cubic lattice structure were formed.

Synthesis, characterization and optical property of flower-like indium tin sulfide nanostructures

We report a simple method for novel flower-like In4SnS8 nanostructure synthesis. A flower-like In4SnS8 nanostructure was synthesized via a one-pot hydrothermal route using the biomolecule L-cysteine as a sulfur source. The structure was characterized using X-ray powder diffraction (XRPD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), nitrogen adsorption analysis and photoluminescence spectra. This flower-like structure consists of crosslinked nanoflakes and possesses good thermostability and a high BET surface area.

The effect of multiwall carbon nanotube on the crystallization, morphology, and rheological properties of nylon1010 nanocomposites

Nanocomposites based on poly(iminosebacoyl imino-decamethylene) (PA1010) and multiwall carbon nanotubes (MWNTs) were successfully prepared by melt blending technique. environmental scanning electron microscope micrographs of the fracture surfaces showed that not only is there an evenly dispersion of MWNTs throughout the PA1010 matrix but also a strongly interfacial adhesion with the matrix. The combined effect of more defects on MWNTs and low temperature buckling fracture is mainly responsible for the broken tubes. Differential scanning calorimeter results showed that the MWNTs acted as a nucleation agent and increased the crystallization rate and decreased crystallite size. In the linear region, rheological measurements showed a distinct change in the frequency dependence of storage modulus, loss modulus, and complex viscosity particularly at low frequencies. We conclude that the rheological percolation threshold might occur when the content of MWNTs is over 2 wt% in the composites.

Syntheses and crystal structures of mononuclear rhodium hydrido complexes from the reactions of [Rh(H)(2)(PPh3)(2)(EtOH)(2)]ClO4 with various nitrogen ligands

Reactions of the Rh hydrido complex [Rh(H)(2)(PPh3)(2)(EtOH)(2)]ClO4 (1) With nitrogen ligands such as 2-(4-thiazolyl)benzimidazole (tbz). pyridazine (pdz), imidazole (im) and pyrimidine (pmd) in CH,Cl, afforded Various mononuclear Rh hydrido complexes, [Rh(H)(2)(PPh3)(2)(tbz)]CIO4 (2), [Rh(H)(2)(PPh3)(2)(pdZ)(2)]ClO(4)(.)2CH(2)Cl(2) (3). [Rh(H)Cl(PPh3)(2)(pdz)(2)](ClO4CH2Cl2)-C-. (4). [Rh(H)(2)(PPh3)(2)(im)(2)]ClO(4)(.)2CH(2)Cl(2) (5). [Rh(H)Cl(PPh3)(2)(im)(2)](ClO4CH2Cl2)-C-. (6). [Rh(H)(2)(PPh3)(2)(pmd)(2)](ClO4CH2Cl2)-C-. (7) and the Rh non-hydrido complex [RhCl2(pmd)(4)]ClO4 (8). The Rh complexes 2. 3, 5 and 6 were crystallographically characterized. The formation process was monitored by H-1 NMR and UV-Vis spectra. In all the Rh hydrido complexes, the Rh atom is coordinated by two PPh3. ligands in trans-positions and two nitrogen ligands in the cis-positions. The remaining sites Lire occupied by one or two hydride atoms to form a saturated 18-electron framework in a slightly distorted octahedral geometry. For complex 2 an appreciable inter-molecular pi interaction is observed between planes of tbz and PPh3 ligands, while an intra-molecular hydrogen bonding interaction between C-H and Cl atoms is found in complex 6.

Vibronic transitions and site substitution of Eu2+ and codoped ions in KMgF3 : Eu-X (X=Ce, Cr, Gd, Cu) system

The high-resolution emission spectra of KMgF3 : Eu and KMgF3 : Eu-X(X = Ce, Cr, Gd, Cu) single crystals were measured at 300 and 77 K. The vibronic side bands of Eu2+ were characterized and an assignment of the normal mode frequencies to particular vibrations has been made. The correlation between the vibronic frequencies of Eu2+ and the site substitution of other co-dopcd ions was first found. The relationship between vibronic intensity of Eu2+ and other doped ions concentration showed that Cr3+, Gd3+ ions competed K+ sites with Eu2+ ions. Ce3+ and Eu3+ occurred the electron transference. The introduction of Cu+ made for Eu2+ substuting for K+ sites.

KMgF_3∶Eu,X(X=Ce,Cr,Gd,Cu)体系中Eu~(2+)振动光谱和共掺离子的格位取代

测定了一系列单掺杂 Eu2 +和双掺杂 Eu,X( X=Ce,Cr,Gd,Cu)的 KMg F3晶体在 30 0 K和 77K的高分辨发射光谱以及伴随的振动光谱 ,据此研究了 Eu2 + 在这些体系中的振动跃迁特征 ,并指认了每一振动峰所对应的正则振动模式 .首次发现了在共掺杂体系中 Eu2 +振动频率与其它掺杂离子格位取代间的相关性