水相合成CdTe量子点测定海藻中微量碲

以亚碲酸钠(Na2TeO3)为Te源,CdCl2为Cd源,水合肼(SHJ)为还原剂,3-巯基丙酸(3-MPA)为稳定剂,制得λEX=380 nm和λEM=608 nm的CdTe量子点(CdTe QDs),该量子点的荧光强度与合成前Na2TeO3浓度呈线性关系.在n(Cd)/n(SHJ)=1∶0.04,n(Cd)/n(3-MPA)=1∶2.7,温度为100℃,反应时间为120m in,溶液pH 10.5的最佳条件下,可制备荧光量子产率为65％的CdTe QDs,该量子点的荧光强度与含碲物质的浓度符合较宽的线性范围(1.0～300 μmol/L),相关系数为0.9982,检测限为38 nmol/L.方法 用于测定微波消解下的海藻样品,加标回收率为106.0％ ～ 112.0％,RSD为5.4％ ～6.1％.     

羟基磷灰石/聚乙烯醇/壳聚糖水凝胶在模拟体液中的力学性能

从仿生学角度出发,将自制的人工角膜支架材料羟基磷灰石/聚乙烯醇/壳聚糖(n-HA/PVA/CS)浸泡在模拟体液中,对材料的含水率及力学性能进行了测试,并利用扫描电镜、X射线衍射仪、电感耦合等离子体原子发射光谱仪及热重分析仪研究了材料在模拟体液中的形貌、晶体结构、元素组成及热稳定性.结果表明,在模拟体液中,n-HA/PVA/CS复合水凝胶的含水率为80%~86%,具有较高的拉伸强度,能承受正常眼压,且热稳定性较好.在浸泡后期,n-HA/CS/PVA复合材料对Ca2+的吸附和释放达到动态平衡;而其表面含有微量的纳米羟基磷灰石沉积,有利于纤维细胞的长入.     

Water Catalysis of the Reaction of Methanol with OH Radical in the Atmosphere is Negligible

Faced with the contradictory results of two recent experimental studies [Jara‐Toro et al., Angew. Chem. Int. Ed. 2017 , 56, 2166 and Chao et al., Angew. Chem. Int. Ed. 2019 , 58, 5013] of the possible catalytic effect of water vapor on CH₃OH + OH reaction, we report calculations that corroborate the conclusion made by Chao et al. and extend the rate constant evaluation down to 200 K. The rate constants of the CH₃OH + OH reaction catalyzed by a water molecule are computed as functions of temperature and relative humidity using high‐level electronic structure and kinetics calculations. The Wuhan–Minnesota Scaling (WMS) method is used to provide accurate energetics to benchmark a density functional for direct dynamics. Both high‐frequency and low‐frequency anharmonicities are included. Variational and tunneling effects are treated by canonical variational transition state theory with multidimensional small‐curvature tunneling. And, most significantly, we include multistructural effects in the rate constant calculations. Our calculations show that the catalytic effect of water vapor is not observable at 200–400 K.     

Water-dispersible hydroxyapatite nanorods synthesized by a facile method

A simple and effective method, using calcium nitrate and triammonium phosphate as starting materials, for the preparation of water-dispersible hydroxyapatite nanorods (HAp) was reported. The process primarily involves the preparation of HAp with the addition of sodium citrate (NaC) and the exchange of absorbed ions (NaC) with sodium hexame taphosphate (NaP). The end products were investigated using various means in order to confirm the particles’ crystal phase and morphology and to understand how to improve their stability. The results demonstrate that the resulting HAp at 90 °C is rod-like with length of 300-400 nm and width of 40-60 nm. The zeta potential values of pure HAp, HAp-NaC, HAp-NaC/NaP are from −15.20, −30.89 to −44.84 mV. The settling time test shows the HAp-NaC/NaP could keep stable above 7 months without any creaming or visible sedimentation. The amount of NaC and the reaction temperature play significant roles in the whole process due to the formation of Ca containing precipitates.     

隔离式协议转换器在压变并行温补系统上的研发与应用

文章提出隔离式协议转换器在压力变送器并行温压补偿系统上的研发与应用,其目的是替换现存以HART总线[1]为基础的并行温压补偿系统的补偿电路,进而简化了补偿电路,提高了主站与工位采集板之间的通讯速率,使系统的维护和维修简单,以及令PCI总线驱动控制PIO数字I/O电路[2]完全的独立出来,只用于温压补偿中气路的切换选择控制;隔离式协议转换器是一款自主研发、自拟协议的独立模块,经压力变送器生产企业的应用与验证,该研发成果能够较好地解决现在温压补偿系统存在的问题,同时易移植于其它温压补偿系统上,并满足压力变送器生产客户的需求。     

Phosphine-catalyzed [4 + 1] annulation between α,β-unsaturated imines and allylic carbonates: synthesis of 2-pyrrolines

In this report, a phosphine-catalyzed [4 + 1] annulation between α,β-unsaturated imines and allylic carbonates is described. This reaction represents the first realization of catalytic [4 + 1] cyclization of 1,3-azadienes with in situ formed phosphorus ylides, which provides highly efficient and diastereoselective synthesis of 2-pyrrolines.     

Tin (IV) chloride-promoted one-pot synthesis of novel tacrine analogues

A facile synthesis of potential acetylcholinesterase (AChE) inhibitors, the tacrine analogues 3a-p, has been accomplished by direct cyclocondensation of 1-aryl-4-cyano-5-aminopyrazole with β-ketoesters using tin(IV) chloride as catalyst. The structures of all the compounds have been confirmed by IR, 1H- and 13C-NMR.     

Exponential synchronization of complex networks with nonidentical time-delayed dynamical nodes

In this Letter, exponential synchronization of a complex network with nonidentical time-delayed dynamical nodes is considered. Two effective control schemes are proposed to drive the network to synchronize globally exponentially onto any smooth goal dynamics. By applying open-loop control to all nodes and adding some intermittent controllers to partial nodes, some simple criteria for exponential synchronization of such network are established. Meanwhile, a pinning scheme deciding which nodes need to be pinned and a simply approximate formula for estimating the least number of pinned nodes are also provided. By introducing impulsive effects to the open-loop controlled network, another synchronization scheme is developed for the network with nonidentical time-delayed dynamical nodes, and an estimate of the upper bound of impulsive intervals ensuring global exponential stability of the synchronization process is also given. Numerical simulations are presented finally to demonstrate the effectiveness of the theoretical results.     

激光辐照绝缘样品不同位置的沿面闪络性能

绝缘体沿面闪络是制约脉冲功率技术发展的瓶颈之一。为了能对沿面闪络机理有更深的认识,通过在沿面闪络过程中引入激光辐照的作用,考察了绝缘样品上不同的辐照位置对于沿面闪络性能的影响。实验结果表明:辐照位置越靠近闪络起始的地方,对沿面闪络性能的影响越大;在沿面闪络的过程中,不同的阶段如闪络起始阶段及电子倍增阶段在整个闪络过程中所起的作用不同。