Synthesis and characterization of thorium phosphate phases by spray pyrolysis: chemistry of thorium phosphates

This paper describes the synthesis of some thorium phosphate compounds with different Th/P ratio (1/2, 2/3 and 3/4) by a spray pyrolysis technique. The so-prepared rough compounds were annealed at different temperatures for 2 h and then analyzed by mainly X-ray diffraction on powder and infrared spectroscopy. Every rough compound is composed by very badly crystallized ThO₂ phase polluted by carbon residue. An annealing treatment at 800 °C leads to the thorium diphosphate phase, α-ThP₂O₇ in every case. At 900 °C, such a phase is decomposed into a thorium phosphate diphosphate phase (Th₄(PO₄)₄P₂O₇, called TPD). However, a thorium excess in the initial mixture (Th/P = 3/4) leads also to observe the ThO₂ phase. The TPD phase is stable up to 1200 °C and does not react with the ThO₂ compound. Beyond 1200 °C, the TPD phase is slowly decomposed into a thorium phosphate compound which should be a thorium oxide phosphate; this compound does not contain any diphosphate species.     

A numerical study of the heterogeneous porosity effect on self-propagating high-temperature synthesis (SHS)

Self-propagating high-temperature synthesis (SHS), or the so-called micropyretic/combustion synthesis, is a technique whereby a material is synthesized by the propagation of a combustion front across a powder. Heterogeneous distributions of porosities are common during self-propagating high-temperature synthesis when powders are pressed and the conventional modeling treatments thus far have only considered uniform systems. Heterogeneities in the porosity are thought to result in local variations of such thermophysical/chemical parameters for the reactants as density and thermal conductivity further changing the combustion temperature, the propagation velocity, and the propagation pattern of a combustion front. This study investigates the impact of porosity variations during self-propagating high-temperature synthesis with Ti + 2B. In addition, the simulations for the propagation of combustion fronts across a non-uniform compact where the porosity is monotonically decreased or increased along the specimens due to die wall friction are also carried out.     

Synthesis and characteristics of SiC whiskers with “rosary bead” morphology

SiC whiskers with ″rosary bead″ morphology were synthesized using suitable silicon source and carbon source through solid reaction at the temperature above 1537 K. The diameter and length of the SiC whiskers were about 0.1-1.0 μm and 20-100 μm,respectively. The largest diameter of their enlarged ends of the whiskers was about 0.2-1.0 μm, and it gradually and smoothly decreased to the size of the plain part of the whiskers. The results of X-ray diffraction analysis show that the crystalline structure of the obtained SiC whiskers is β-SiC. It is considered that the SiC whiskers grow via a vapor-solid mechanism.     

金属硫族化合物晶体的研究进展

金属硫族化合物具有特殊的物理化学性质，在半导体材料、催化剂载体、固体化学、电磁及光学特性等高科技领域具有不可替代的重要性．近10年来人们竞相研究，用各种方法合成了成百上千新的金属硫化物、硒化物和碲化物，形成0～3维多硫金属材料，其晶体合成方法有：电化学法、固相合成法、溶剂热法等．文章综述了金属硫族化合物几种合成方法、介绍了晶体的结构特征及其新进展．     

Hydrothermal Synthesis and Crystal Structure of a New Dimeric Lanthanum(Ⅲ) Complex

A new dimeric lanthanum(Ⅲ) complex [La2(phen)2(C7H3N2O6)6](phen=1,10-phenanthroline) was synthesized by the hydrothermal method and determined by single crystal X-ray diffraction analysis. The La(Ⅲ) ion is coordinated to seven oxygen atoms from five carboxylate groups and two nitrogen atoms from a phen ligand,forming a monocapped square antiprismatic geometry. Six carboxylate groups coordinate to two La(Ⅲ) ions in three modes which are chelating bidentate,bridging bidentate and bridging tridentate. The crystal is triclinic with space group P-1,a=1.2030(4) nm,b=1.2962(5) nm,c=1.3330(5) nm,α=104.410(5)°,β=114.048(4)°,γ＝100.054(4)°,V=1.7467(10) nm3,Mr=952.46,Z=2,Dc=1.811 g·cm-3,F(000)=944,S=1.017,μ=1.320 mm-1,with R1=0.0298 and wR2=0.0625.     

基于深度特征合成和关联规则的数据库异常访问检测

企业或组织内部的重要数据都存储在数据库中,因此数据库经常成为恶意入侵者的攻击目标。传统防火墙对于来自外部的入侵者有着很好的抵御作用,但无法检测来自系统内部人员的异常访问。针对数据库异常访问检测中存在的不足和缺陷,提出了一种基于深度特征合成(DFS)和关联规则(Apriori)算法的异常检测方法。通过对比BP神经网络、随机森林和C4.5决策树等3种其他检测算法表明,新提出的方法能够更加高效地提取用户特征,从而使检测的精准率和效率有显著提升。     

三次样条函数在假设模态综合法中的应用

对复杂结构进行振动分析的模态综合法已发展得较为成熟,它在应用上的限制主要是部件模态假设的困难(尤其是非规则部件),而综合结果的可信度在相当程度上取决于是否能得到一组合理的假设模态 。本文介绍的利用三次样条函数插值法求取转轴耦合系统各部件连续主模态的方法,有效地解决了这个问题。     

Mo~( 6)掺杂制备SO_4~(2-)/TiO_2/MoO_3固体超强酸催化合成氯乙酸异辛酯

以氯乙酸和异辛醇为原料,用Mo 6掺杂制备SO2-4/TiO2/MoO3的固体超强酸催化剂催化合成氯乙酸异辛酯,研究了酯化反应的优化条件。当n(异辛醇):n(氯乙酸)为1.1∶1;催化剂用量为反应物料质量的2.0%时,反应时间90min,氯乙酸异辛酯的收率达到95.5%。     

Constrained pole-placement using transformation and LQ-design

A new procedure for constrained pole-placement is presented. The poles of the closed loop system are placed within a circle in the left half plane. The design procedure is noniterative and the solution is obtained via linear quadratic (LQ) design for a transformed system. The circle can be chosen in order to obtain good transient properties of the closed loop system. The method combines the properties of pole-placement and LQ-design.     

ADS熔盐散裂靶中子学性能研究

与传统加速器驱动次临界系统（ADS）采用金属靶作为散裂中子靶的设计不同,加速器驱动次临界熔盐堆（AD-MSRs）采用靶堆一体的设计,直接使用燃料熔盐作为散裂中子靶。由于熔盐靶的中子学性能直接影响AD MSRs的能量放大系数、核废物的嬗变和核燃料增殖的效率,所以本研究基于MCNPX程序,详细计算了高能质子轰击氟盐和氯盐两种熔盐靶产生的散裂中子产额、散裂中子能谱、能量沉积分布以及散裂产物等中子学性能,并与液态Pb和铅铋共熔体（LBE）两种液态金属靶进行了对比。计算结果表明,熔盐靶在散裂中子产额上与液态金属靶有一定的差距,但熔盐靶内能量沉积分布的梯度较小,更有利于靶区的热量导出。与液态Pb和LBE靶相比,熔盐靶的散裂产物中包含更多的气体以及高质量数的α发射体核素。