Maskless Preparation of Spatially-Resolved Plasmonic Nanoparticles on Polydimethylsiloxane via In Situ Fluoride-Assisted Synthesis

Here, a fluoride-assisted route for the controlled in-situ synthesis of metal nanoparticles (NPs) (i.e., AgNPs, AuNPs) on polydimethylsiloxane (PDMS) is reported. The size and coverage of the NPs on the PDMS surface are modulated with time and over space during the synthetic process, leveraging the improved yield (10×) and faster kinetics (100×) of NP formation in the presence of F⁻ ions, compared to fluoride-free approaches. This enables the maskless preparation of both linear and step gradients and patterns of NPs in 1D and 2D on the PDMS surface. As an application in flexible plasmonics/photonics, continuous and step-wise spatial modulations of the plasmonic features of PDMS slabs with 1D and 2D AgNP gradients on the surface are demonstrated. An excellent spatially resolved tuning of key optical parameters, namely, optical density from zero to 5 and extinction ratio up to 100 dB, is achieved with AgNP gradients prepared in AgF solution for 12 minutes; the performance are comparable to those of commercial dielectric/interference filters. When used as a rejection filter in optical fluorescence microscopy, the AgNP-PDMS slabs are able to reject the excitation laser at 405 nm and retain the green fluorescence of microbeads (100 µm) used as test cases.     

醇镁还原法一步制取对氯苯胺的研究

醇镁还原法一步制取对氯苯胺是一种新的方法 ,研究发现最佳反应温度为 80℃～ 85℃ ,反应时间为4h ,对氯硝基苯与镁粉的用量 (物质的量比 )为 1∶3,产率为 80 %。     

Novel application of radiotracer techniques for corrosion studies of zinc and aluminium in acidic medium

The adsorption of sulphate ions on Zn and Al was studied in 0.5 M NaClO₄ supporting electrolyte at various pH values in the range of pH=2-7 by radiotracer techniques. It was found in both cases that the adsorption of sulphate passes over maximum in the pH range studied.The phenomena observed are interpreted by the assumption that the main component of the overall process is anion adsorption on the protonated oxides/hydroxides formed as a result of corrosion. At low pH values the steady state coverage with respect to these products should be very low owing to their dissolution; consequently the extent of anion adsorption induced must also be very low. At higher pH values where no protonation occurs the adsorption of anions decreases significantly.     

Kinetics study of Ti[O(CH2)4OCHCH2]4 initiated ring‐opening polymerization of ε‐caprolactone by differential scanning calorimetry

Chemical shrinkage was used for the in situ measurement of the progressing chemical stabilization reactions and the influence of ozone during the stabilization of polyacrylonitrile. A method for evaluating the activation energy through the sensitivity temperature is presented. The calculated results show that the activation energies were 161.57 kJ/mol in air and 181.23 kJ/mol in ozone-enriched air. Therefore, the chemical reactions were postponed during stabilization in ozone-enriched air. Ozone seemed to act in three ways: first, ozone promoted the formation of the serious skin–core structure. Second, ozone accelerated the chemical reactions and shortened the stabilization time at lower heating rates. Third, ozone postponed the chemical reactions. © 2008 Wiley Periodicals, Inc. J Appl Polym Sci 2008     

掺杂改性对聚苯乙烯性能影响的研究

文章阐述了掺杂烷氧金属的聚苯乙烯的制备以及用红外光谱、扫描电镜和热分析分析其微观结构和热性能的部分研究结果。     

卤素离子对铝合金阳极的活化作用

镓锡合金沉积子铝阳极表面，形成活化点，是含镓、锡铝合金阳极活化的根本原因。溶液中的卤素离子在氧化膜上的吸附及在其中的扩散也促进了铝电极的阳极溶解。合金元素及溶液中的阴离子通过改变铝电极表面的零电荷，影响着合金元素在铝电极表面的沉积的难易程度，从而影响着铝合金阳极的活化性能。     

几种无机阴离子对TiO_2催化活性影响的实验研究

以N掺杂TiO2试剂为催化剂,降解偶氮直接耐酸大红4BS溶液,同时外加4种浓度不同的阴离子溶液,探讨了HCO3-,F-,NO3-,H2PO4-等阴离子对N/TiO2化学试剂催化活性的影响。实验表明,HCO3-,F-,NO3-,H2PO4-等阴离子对N/TiO2化学试剂的催化活性有显著影响。因此,可以通过外加不同的离子来提高或降低N/TiO2的活性。     

Characterization and Sintering Behavior of Alkoxide-Derived Aluminosilicate Powders

Submicrometer SiO₂-Al₂O₃ powders with compositions of 46.5 to 76.6 wt% Al₂O₃ were prepared by hydrolysis of mixed alkoxides. Phase change, mullite composition, and particle size of powders with heating were analyzed by DTA, XRD, IR, BET, and TEM. As-produced amorphous powders partially transformed to mullite and Al-Si spinel at around 980°C. The compositions of mullite produced at 1400° and 1550°C were richer in Al₂O₃ than the compositions of stable mullite solid solutions predicted from the phase diagram of the SiO₂-Al₂O₃ system. Particle size decreased with increasing Al₂O₃ content. The sintered densities depended upon the amount of SiO₂-rich glassy phase formed during sintering and the green density expressed as a function of particle size.     

Equilibrium and kinetic studies of the extraction of chelated copper(II) anions with Aliquat 336

The equilibrium and kinetics of solvent extraction of Cu²⁺ from aqueous solutions containing equimolar EDTA with Aliquat 336 in n‐decanol and kerosene at 298 K were investigated. The concentrations of Cu²⁺ (8–50 mol m^?3), Cl^? (5–60 mol m^?3), and Aliquat 336 (20–100 mol m^?3) were varied. A semi‐empirical model with three parameters was proposed to describe the equilibrium behavior, in which the non‐idealities in both aqueous and organic phases were considered. Over the ranges studied, the model agreed reasonably well with the experimental data (standard deviation, 15%). The forward and backward reaction rate constants were determined as (5.31 ± 0.16)×10^?6 m^9/4 mol^?3/4 s^?1 and (2.62 ± 0.09)×10^?7 s^?1, respectively, at 298 K. An interfacial reaction mechanism was proposed, which revealed that the reaction between the chelated anions and trimeric amine molecules at the interface was rate limiting. The derived rate laws were consistent with the experimental results. © 2002 Society of Chemical Industry     

共存阴离子对核酸阻锈剂在模拟混凝土孔溶液中钢筋阻锈作用的影响

将一种含有长度在20～80个碱基的各种引物的混合溶液溶解在核酸缓冲液中作为核酸阻锈剂,通过线性极化和电化学阻抗谱(EIS)两种电化学手段分别研究共存阴离子HCO_3~-和SO_4~(2-)对核酸阻锈剂在模拟混凝土孔溶液中对钢筋氯盐腐蚀的影响。利用X射线光电子能谱(XPS)分析了在有共存阴离子存在的模拟混凝土孔溶液中钢筋电极在核酸阻锈剂作用下表面膜的组成结构。结果表明:核酸阻锈剂具有良好的钢筋防腐蚀效果,共存阴离子HCO_3~-的存在使钢筋的腐蚀速率加快,但核酸的加入能明显减弱钢筋腐蚀倾向,具有和商用阻锈剂(主要成分为磷酸钠)基本相同的阻锈效率;共存阴离子SO_4~(2-)的存在加快了钢筋的腐蚀速率,且SO_4~(2-)的浓度较低时核酸阻锈剂的阻锈效率已经超过了同等条件下的商用阻锈剂。