Thermal and photoluminescence properties of hydrated YPO4:Eu nanowires

In this work, we used the solution precipitation route to synthesize Eu³⁺-doped YPO₄·nH₂O nanowires. The structure, morphology, composition, thermal behavior, and photoluminescence of as-synthesized product were characterized by X-ray diffraction (XRD), thermogravimetric and differential thermal analysis (TG/DTA), energy-dispersive X-ray spectroscopy (EDS), Fourier transform infrared spectroscopy (FT-IR), field emission scanning electron microscopic (FE-SEM) and photoluminescence (PL) spectra. The dependence of the structure, morphology, composition and luminescent properties on the thermal treatment was investigated. The results indicate that the aqueous synthesis has a better control on the structure, morphology, composition of the products, and that the heat treatment induces the transitions of the structure, composition, and luminescent properties.     

Insights into the cycloaddition reaction mechanism between ketenimine and unsaturated hydrocarbon: A theoretical study

The cycloaddition reaction mechanisms between interstellar molecule ketenimine and unsaturated hydrocarbon (ethyne and ethylene) have been systematically investigated employing the second-order Møller-Plesset perturbation theory (MP2) method. Geometry optimizations and vibrational analyses have been performed for the stationary points on the potential energy surfaces of the system. The calculated results show that it can be produced the five-membered cyclic carbene intermediates through pericyclic reaction processes between ketenimine and ethyne (or ethylene). For the reaction between ketenimine and ethyne, through the following H-transferred processes, carbene intermediate can be isomerized to the pyrrole compounds. For the reaction between ketenimine and ethylene, carbene intermediate can be isomerized to the pyrroline compounds. The present study is helpful to understand the reactivity of nitrogenous cumulene ketenimine and the formation of prebiotic species in interstellar space.     

溴化锌-季(鎓)三溴盐催化二氧化碳和环氧化合物偶联反应

研究了溴化锌-季鎓三溴盐催化二氧化碳和环氧化合物偶联反应,考察了反应温度、压力和不同金属盐对反应的影响以及催化剂的循环使用性能.结果表明,在413 K和1.0 MPa条件下,以溴化锌为催化剂,苯基三甲基三溴化铵为共催化剂,无需加入任何溶剂就可以使二氧化碳和环氧化合物发生偶联反应,并以很高的收率得到环碳酸酯.     

正庚烷在β沸石负载碳化钼催化剂上的异构化研究

利用程序升温还原法制备了β沸石负载碳化钼催化剂。XRD表征显示,利用正戊烷作为碳源得到了对异构化具有活性的βMo2C。以正庚烷为模型反应物,在连续流动固定床反应装置上考察了温度、压力、空速和氢烃比对βMo2C/β沸石催化剂临氢异构化反应性能的影响。获得了β沸石负载碳化钼催化剂上正庚烷异构化的最佳反应条件温度270℃～275℃,压力1.0MPa～1.5MPa,体积空速1.0h－1,氢烃体积比200∶1。在最佳条件下反应物转化率为82%,选择性和异构产物收率分别达到71%和58%。     

凝胶渗透色谱和气相色谱-质谱法测定动物食品中27种有机氯和15种拟除虫菊酯类农药残留量

有机氯农药虽已被世界各国禁止使用,但由于其化学性质稳定和难以降解,在环境中仍然存在有机氯农药残留,并通过食物链的富集作用,造成对食物的污染.     

赖氨酸修饰壳聚糖磁性超微载体的制备和表征

本文设计并合成了良好水溶性的赖氨酸修饰壳聚糖,并对制备工艺进行了优化.产物通过红外(FTIR)和核磁(1H-NMR)进行了表征,并将其作为壳层材料制备了赖氨酸修饰壳聚糖磁性超微载体.通过光电能谱(XPS)、透射(TEM)、激光粒度仪、X射线衍射(XRD)、磁性能测试(VSM)对载体进行了表征.结果表明,制备的赖氨酸修饰壳聚糖磁性超微载体表面带有大量的氨基(-NH2),粒径分布较为均一(100nm左右),形貌较为规则,并具有良好的超顺磁性,因而该载体具有更加良好的性能.     

Pd_2(dba)_3/BINAP催化合成1,4-双-(4′-苯胺基苯酰基)苯

以Pd2(dba)3/BINAP催化1,4-双-(4′-溴苯酰基)苯和苯胺反应,合成了1,4-双-(4′-苯胺基苯酰基)苯,其结构经UV,1HNMR,13CNMR和元素分析表征。     

F-T合成校正综合动力学模型

考虑了烯烃、醇与酸的再吸附及其非本征效应(烯烃、醇与酸在催化剂孔道中的扩散作用、物理吸附及溶解度效应)对产物分布的影响,推导了基于详细反应机理的亚甲基插入的烷基机理F-T合成校正综合动力学模型.利用文献数据对动力学模型进行了回归,获得了与文献报道结果相一致的动力学参数.由校正动力学模型计算的烷烃、烯烃、醇与酸产物分布及烯烃比、醇烃比及酸烃比与实验数据较好地吻合.动力学计算结果表明,在铁锰催化剂上,烷烃、烯烃、醇与酸生成的反应是平行竞争反应,烯烃、醇与酸在催化剂表面的再吸附及二次反应导致产物分布偏离了ASF分布.动力学研究还表明,相同碳数的醇与酸产物在催化剂表面上再吸附及二次反应的机会比相同碳数的烯烃大.通过比较相同碳数的烯烃、醇与酸的分子体积及沸点,指出了在铁锰催化剂上,低碳数的烯烃、醇与酸的再吸附及二次反应对产物分布影响的非本征效应中,烯烃、醇与酸的扩散阻力不是主导效应.     

无焰燃烧烟密度标准物质的研制

介绍无焰燃烧烟密度标准物质的研制方法。选用合适的α-纤维素作为原材料,经打浆造纸后,作为标准物质候选物,经均匀性检验和稳定性考察合格后,对标准物质进行定值。在无焰燃烧条件下烟密度标准物质的标准值为175,扩展不确定度为8;校正烟密度标准物质的标准值为166,扩展不确定度为8。