材料期刊网

Phosphorus Removal of High Phosphorus Iron Ore byGasBased Reduction and Melt Separation

TANG Huiqing , GUO Zhancheng , ZHAO Zhilong

钢铁研究学报(英文版)

A large deposit of high phosphorus iron ore in China contains an average of 1.2% phosphorus and 50% iron and it has not been utilized. In current work, a novel process to remove phosphorus of the ore has been proposed. The novel process has been demonstrated theoretically and experimentally. The theoretical work (numerical simulation) was carried out with HSC chemistry package and a mathematical model developed using the coexistence theory of slag structure. Gas-based reduction and melt separation experiments were then designed and conducted. Simulation results shows that that all iron compounds in the ore could be reduced to metallic iron using CO/ H2 under temperature above 1000K and the yield of iron is more than 90% under either atmosphere; P can not be reduced and exists as Ca3(PO4)2; in the melt separation process, iron metallization ratio, melting temperature and CaO-adding ratio affect the phosphorus partition between slag and molten metal and CaO-adding ratio is the most distinguished parameter. Results of gas-based reduction agreed well with the simulation except for iron metallization ratio being less than predicted. This difference is mainly attributed to kinetic condition. Results of melt separation experiment show most P is left in the slag sample and some P in the metal sample exists as slag inclusion..

关键词: High phosphorus iron ore;Numerical simulation;Gas-based reduction;Melt separation

预测复合材料非线性有效介电系数的割线方法

周萧明 , 胡更开

复合材料学报 doi:10.3321/j.issn:1000-3851.2004.06.026

提出了预测复合材料非线性电位移和电场强度关系的一种解析方法,该方法基于各向材料的割线介电常数,将非线性问题转化成一系列线性问题来求解.该方法适用于任意各向异性复合材料和组分材料的非线性性质,而常用的Stroud和Hui的模型只适用于各向同性复合材料和组分材料的弱线性.证明了本文方法具有Ponte Castaneda提出的变分结构.计算结果表明,当基体非线性较小时,本文模型的预测与Stroud和Hui的模型一致,但当基体非线性系数增大时,本文模型能给出合理的预测结果,而Stroud和Hui的模型则会超出基体和夹杂的性能范围.

关键词: 复合材料 , 介电常数 , 非线性 , 割线方法

Molecular dynamics studies on vacancy-interstitial annihilation in silicon

Acta Physica Sinica

Molecular dynamics (MD) simulation is performed to study the vacancy-interstitial annihilation in crystalline silicon. We choose the Stillinger-Weber potential, which is commonly used for silicon, to describe the interaction between atoms. The system is relaxed under 300K and 1400K respectively. We have found that < 111 > is the preferred recombination direction and propose the presence of an energy barrier in the < 110 > direction. From the calculated value of energy barrier along < 110 > we give a reasonable explanation for the difference between Tang's and Zawadzki's data.

关键词: molecular dynamics;vacancy and interstitial;diffusion;point-defects;diffusion;mechanisms

ELECTRONIC-PROPERTIES OF ONE-DIMENSIONAL QUASI-LATTICES

Zeitschrift Fur Physik B-Condensed Matter

we study the on-site model of a new class of one-dimensional quasiperiodic lattices, for which the substitution rules are B --> BA, and A --> BAB. By means of the renormalization-group approach, a interesting multifractal spectral behavior has been found, which has been confirmed by numerical simulation. A Cantor-like energy spectra is obtained by using the Kohmoto-Kadanaff-Tang (KKT) renormalization-group method. Three kinds of wave-function behavior (extended, localized, and intermediate states) are definitely found.

关键词: energy-spectrum;quasiperiodic lattices;localization problem;trace;maps;fibonacci;quasicrystal;systems;tilings

铜催化炔丙醇酯与β-羰基膦酸酯的不对称[3+2]环加成反应合成手性膦酰化2,3-二氢呋喃

陈修帅 , 侯传金 , 李晴 , 刘彦军 , 杨瑞丰 , 胡向平

催化学报 doi:10.1016/S1872-2067(16)62488-9

手性2,3-二氢呋喃衍生物是一类重要的杂环化合物,广泛存在于天然产物和生物活性分子中.它们也经常被用于手性四氢呋喃化合物的不对称合成.因此,人们发展了很多合成手性2,3-二氢呋喃化合物的方法,如有机小分子催化的多米诺迈克尔-烷基化反应、“中断的”Feist-Bénary反应或改进的 Feist-Bénary反应.此外,过渡金属催化的手性2,3-二氢呋喃的不对称合成在近些年引起了人们的极大关注. Ozawa等通过 Pd-催化2,3-二氢呋喃的动力拆分方法获得了手性2-芳基-2,3-二氢呋喃. Evans发展了一种 Sc-催化联烯硅和乙醛酸乙酯的[3+2]环加成反应合成手性2,3-二氢呋喃的方法.最近, Fu和 Tang等发展了 Cu催化烯酮和重氮化合物的[4+1]环加成反应合成手性2,3-二氢呋喃的方法.在 Nishibayashi和 van Maarseveen的开创性工作之后, Cu催化的不对称炔丙基转化反应取得了很大的进展.最近,我们发展了一类新的三齿手性 P,N,N-配体,在 Cu催化不对称炔丙基取代、脱羧炔丙基取代、[3+2]、[3+3]和[4+2]环加成反应中表现出优秀的对映和非对映选择性.其中,我们发现采用 Cu催化炔丙醇酯和β-酮酯的[3+2]环加成反应,能高对映选择性地获得手性2,3-二氢呋喃.我们设想,采用β-羰基膦酸酯代替β-酮酯,通过这种 Cu催化[3+2]环加成反应,将可以合成一类具有重要生物活性的手性膦酰化2,3-二氢呋喃化合物.基于这种设想,本文使用手性 P,N,N-配体,通过 Cu催化炔丙醇酯与β-羰基膦酸酯的不对称[3+2]环加成反应,以很好的收率和最高92% ee的对映选择性获得了一系列光学活性的膦酰化2,3-二氢呋喃化合物.我们以炔丙醇酯1a与β-羰基膦酸酯2a为标准底物,优化了反应条件,考察了配体、Cu盐、碱和反应温度等对反应收率和对映选择性的影响.我们确定了最佳的反应条件：以4b为配体,以 Cu(OTf)2为铜盐,以t-BuOK为碱,以 MeOH为溶剂,–20oC反应24 h.在此条件下,我们对β-羰基磷酸酯2的适用范围进行了考察.结果表明,各种苯基取代的β-羰膦磷酸酯均能得到很好的收率和对映选择性.苯环上取代基的空间效应对反应的对映选择性影响不大,但对反应收率影响较大,与相应3-取代或4-取代底物相比较,2-取代的底物获得的收率较低.苯环对位取代基的电子效应对反应的影响不大,给电子基或吸电子基的底物,均得到了较好的收率和对映选择性.杂环取代的底物同样适用于该反应,以90%的收率和89% ee的对映选择性获得了相应的[3+2]环加成产物.对于烷基底物,虽然反应的产率略低,但是得到了高达92% ee的产物.此外,我们对炔丙醇酯底物的适用范围也进行了考察.结果表明,该体系对于各种取代的炔丙醇酯底物均可以获得较高的收率和良好的对映选择性.总之,本文发展了一种铜催化炔丙醇酯与β-羰基膦酸酯的不对称[3+2]环加成反应的方法,成功合成了手性膦酰化2,3-二氢呋喃化合物.通过使用一个结构刚性的酮亚胺三齿 P,N,N-配体,以很好的收率和最高92% ee的对映选择性获得了一系列光学活性的膦酰化2,3-二氢呋喃化合物.

关键词: 铜 , 不对称合成 , 3+2环加成 , β-羰基膦酸酯 , 膦酰化 2,3-二氢呋喃