A novel method of the separation/preconcentration and determination of trace molybdenum(VI) in water samples using microcrystalline triphenylmethane loaded with salicyl fluorone

It is the first time that triphenylmethane was used as an adsorbent to preconcentrate and separate trace amount of molybdenum in water samples. The effects of different parameters, such as acidity, stirring time and various metal ions, the amounts of triphenylmethane and salicyl fluorine, etc. on the enrichment yield of molybdenum have been studied to optimize the experimental conditions. Under the optimum conditions, molybdenum can be adsorbed on the surface of microcrystalline triphenylmethane loaded with salicyl fluorone by the intermolecular action strength. The possible reaction mechanism for the enrichment of molybdenum was discussed in detail in this paper. Mo(VI) can be completely separated from Pb(II), Co(II), Cu(II), Cr(III), Ni(II), Hg(II), Zn(II), Cd(II), Fe(III) and Al(III) in the solution. The proposed method was successfully applied to the determination of trace amount of molybdenum in various water samples by spectrophotometry after preconcentration using microcrystalline triphenylmethane. The preconcentration factor is from 83 (500 ml water sample was enriched to 6.0 ml) to 166 (1000 ml water sample was enriched to 6.0 ml). The detection limit is 1.3 × 10⁻⁵ mg l⁻¹ and the linearity is maintained in the concentration range 3.8 × 10⁻³ to 0.36 mg l⁻¹ with a correlation coefficient of 0.9998. The recoveries are in the range of 93.5-104%. The relative standard deviation is 1.8-2.9%. Analytical results obtained with this novel method are very satisfactory.     

Reaction of alkenes with hydrogen peroxide and sodium iodide: a nonenzymatic biogenic-like approach to iodohydrins

An efficient protocol to synthesize iodohydrins from alkenes is presented. Reactions were conducted in aqueous media using safe and readily available sodium iodide (the most abundant form of the element), and a highly convenient oxidant such as hydrogen peroxide. Addition of a protic acid triggers a faster and efficient process, a role formally related to that played by haloperoxidase enzymes in naturally occurring transformations. The successful application of these conditions to multigram scale preparations and over natural products derivatives is also discussed.     

干摩擦和水润滑条件下芳纶浆粕/环氧树脂复合材料摩擦磨损性能研究

研究了芳纶浆粕纤维增强环氧复合材料在干摩擦和水润滑条件下的摩擦磨损性能,探讨了纤维含量对复合材料摩擦磨损性能的影响,并分析了复合材料的磨损机理.结果表明:芳纶浆粕纤维能够大幅度提高环氧树脂的摩擦磨损性能;当纤维体积分数为40%时,复合材料的比磨损率最小;在水润滑条件下,复合材料的摩擦系数和磨损率均比干摩擦下的明显降低,这是由于水起到了润滑和冷却作用;干摩擦时的磨损机理为粘着磨损和塑性变形,水润滑时主要为犁削和轻微的磨粒磨损.     

CdS nanocrystallites sensitized ZnO nanorods with plasmon enhanced photoelectrochemical performance

A sandwiched structure of CdS/Ag/ZnO nanorod photoanode exhibits greatly enhanced photoelectrochemical activity for solar hydrogen generation, due to synergistic effect of CdS nanocrystallites and plasmonic Ag nanoparticles for the enhanced optical absorption and the promoted charge carrier separation.     

343 nm飞秒激光制备微孔阵列以增强聚氨酯合成革透湿性

为了提高聚氨酯(PU)合成革透湿性,分别使用343 nm飞秒激光和作为对比的1030 nm飞秒激光及1064 nm纳秒激光制备微孔阵列。采用扫描电镜(SEM)和3D激光扫描显微镜对比研究了微孔形貌。结果表明,343 nm飞秒激光可以制备出效果最佳的微孔。此外,分析了3种激光与PU涂层的作用机理,揭示了343 nm飞秒激光合成革微钻孔过程仅表现为光化学烧蚀,光化学和光热烧蚀同时发生于1030 nm飞秒激光钻孔过程,而1064 nm纳秒激光只显示了光热烧蚀。激光合成革表面钻孔后,测量其透湿性和抗张力。结果显示: 微孔密度越大,皮革透湿性(WVP)越大而抗张力越低,脉冲重叠的增加会导致WVP的增加和抗张力的下降;同时,随着脉冲重叠从91.7%降到50%,微孔直径从45 μm降低到30 μm,而微孔锥度从0.7°增加到12.1°;当脉冲重叠率为91.7%,微孔密度为2550/cm²时,最大的WVP增长率为306%。     

环境水样中硒形态分析的样品预处理

综述了近几年来测定环境水样中硒的样品前处理方法,主要包括样品消解,加入基体改进剂和分离富集3个方面。消解法中主要使用湿法消解;加入基体改进剂适用于石墨炉原子吸收光谱法的样品预处理,可以提高硒的灰化温度,减少硒的损失以及样品中基体的干扰;固相萃取法是萃取法的主要使用手段。     

火焰原子吸收光谱法测定饮用水中铜和锶的研究

实验的主要目的是对火焰原子吸收光谱法测定饮用水中铜和锶的方法进行研究。其中对火焰原子吸收光谱法测定锶的两种方法均进行了研究。在选定的最佳仪器条件下,测定铜、锶(方法 1)和锶(方法 2)RSD分别为0.65%、2.67%、1.01%。饮用水中铜、锶(方法 1)和锶(方法2)的回收率分别为95.00%、95.00%、91.00%。实验表明,该法操作简单、测试快速、结果准确稳定。     

Deprotection of Oximes using Iodosobenzene in the Presence of β‐Cyclodextrin in Water

A mild and efficient method for the regeneration of carbonyl compounds from oximes at room temperature in impressive yields has been developed using iodosobenzene/KBr in the presence of β‐cyclodextrin in water.     

丙烯腈、己二腈和丙腈与水的二元体系液-液相平衡数据的测定和关联(英文)

采用平衡法测定了丙烯腈+水、己二腈+水、丙腈+水三个二元体系在不同温度(303.15、313.15、323.15、333.15K)下的液-液相平衡数据;并采用NRTL(α=0.2,α=0.3)模型和UNIQUAC模型对液-液平衡数据进行了关联.结果显示,NRTL和UNIQUAC模型对三个二元体系在不同温度下的互溶度关联的目标函数值均小于1×10-17,实验值与计算值吻合较好,绝对偏差小于0.009,关联精度较高.该研究结果可为丙烯腈、丙腈和水三元平衡溶解度数据的模拟和预测提供可靠的基础数据,并对电解二聚法生产己二腈中电解液的分离提纯工艺具有一定的指导意义.     

Rhodium(I)‐Catalyzed Regiospecific Dimerization of Aromatic Acids: Two Direct CH Bond Activations in Water

2,2′‐Diaryl acids are key building blocks for some of the most important and high‐performance polymers such as polyesters and polyamides (imides), as well as structural motifs of MOFs (metal–organic frameworks) and biological compounds. In this study, a direct, regiospecific and practical dimerization of simple aromatic acids to generate 2,2′‐diaryl acids has been discovered, which proceeds through two rhodium‐catalyzed C? H activations in water. This reaction can be easily scaled up to gram level by using only 0.4–0.6 mol % of the rhodium catalyst. As a proof‐of‐concept, the natural product ellagic acid was synthesized in two steps by this method.