Transparent and flexible films of new segmented polyurethane nanocomposites incorporated by NH2-functionalized TiO2 nanoparticles

In this work, TiO₂ nanoparticles are surface modified by NH₂-terminated organic moieties arised from 4,4′-methylene diphenyl diisocyanate (MDI). These nanoparticles are incorporated into ether-based segmented polyurethane (SPU) matrix. MDI is utilized as monomer together with poly(tetramethylene oxide) (PTMO) comonomer for preparing the final polymer as well. The NH₂-functionalized TiO₂ nanoparticles are covalently linked to the NCO terminals of the resulting SPU macromolecules during film preparation stage. Therefore, in addition to butylene glycol, these surface modified nanoparticles with enhanced organophilicity could play the role of the second chain extender of NCO-capped SPU macromolecules through formation of urea linkages. Optical and thermal behaviors of the transparent and flexible film (SPU/TiO₂–MDI) is compared with those of unmodified TiO₂ (SPU/TiO₂) and TiO₂-unloaded SPU films. Though the particle loading is only 5 wt.%, incorporation of TiO₂ and TiO₂–MDI nanoparticles into the SPU polymer enhances significantly the light absorption in UV region at 300–400 nm. SEM images of the prepared films clearly show a considerable decrease in particle aggregation for TiO₂–MDI into SPU matrix compared to that of unmodified TiO₂. TG analyses indicate a one-step decomposition pattern with onset temperatures of about 360 and 380 °C for neat SPU and SPU/TiO₂–MDI, respectively. Moreover, DTA thermograms of both nanocomposites show obviously two exothermic phase transitions in the thermal range of 330–440 °C.     

一种轻小型四极杆质谱仪射频电源的研制

四极杆结构是四极杆质谱仪的核心结构，由射频电源分别施加两组高压高频信号进行驱动，利用电场的变化和输入离子的质荷比差异对离子进行筛选。针对四极杆质谱仪小型化的研制需求，以信号调制模块、放大模块、反馈电路和直流模块为基本构型，设计了一种应用于轻小型四极杆质谱仪的射频驱动电源。经实际测试，该电源可以在谐振频率1.33 MHz、扫描频率10 Hz的输入条件下，输出峰 峰值电压最高可达3.33 kV的调幅射频高压信号并驱动四极杆结构，扫描切换时间不高于1 ms。射频电源输出信号稳定、波动小、交直比的波动为0.1%。该射频电源相较于常规的四极杆射频电源具有更高的扫描范围，体积小巧，功耗仅30 W，接口简单，有较高的实用价值。     

Synthesis,thermal stability and unknown properties of Fe1–xAlxVO4 solid solution

A continuous solid solution Fe_1-xAl_xVO₄ was synthesized by conventional ceramic method and characterized by DTA, XRD, IR, UV–vis/DRS and Mössbauer spectroscopy. Fe_1-xAl_xVO₄ crystallizes in a triclinic system and is isostructural with FeVO₄ and AlVO₄. With increasing content of Al³⁺ ions substituted for Fe³⁺ in the matrix structure of FeVO₄ a contraction of crystal lattice was observed, accompanied by shifts of IR absorption bands towards higher wavenumbers and shifts of UV absorption bands towards shorter wavelength. On the basis of the results of UV–vis investigations, the band gap energies were calculated. The solid solution sample of composition Fe_0.67Al_0.33VO₄ was found to have the highest melting point from among all examined samples, which equals to 870?°C. Moreover, the solid product of incongruent melting of Fe_1-xAl_xVO₄ for 0.75?>?x?≥?0.5 is Fe_1-xAl_xVO₄ solid solution, richer in iron. On the grounds of Mössbauer investigation, the partition of iron and aluminum ions over three accessible crystallographic sites was established. Fe_0.5Al_0.5VO₄ sample was successfully used as a reactant for Fe₄Al₄V₁₀W₁₆O₈₅ preparation.     

Synthesis and spectroscopic studies of some new azobenzenesulfonamide

Abstract

Diazotized sulfadiazine derivative (1) was coupled with some nitrogen heterocyclic namely (thiazolone derivatives 2a–c, thiazole derivatives 4a–c and barbituric acid derivatives 6a,b) to give the corresponding azo compounds 3a–c, 5a–c and 7a,b in good yields. The newly synthesized azo benzene sulfonamide dyes were recorded their UV visible spectra in the region 200–600?nm in four different solvents and discussed the effect of solvents, substituent and effect of acid and base on the absorption values of these dyes.     

Effect of vinyl acetate content on the photovoltaic-encapsulation performance of ethylene vinyl acetate under accelerated ultra-violet aging

The vinyl acetate (VA) content in ethylene vinyl acetate (EVA) can significantly affect its performance as an encapsulant in photovoltaic modules under field conditions. EVA films of varying VA content (18, 24, 33, and 40%) have been prepared using twin screw extruder with the necessary additives and subsequently cured at 150 °C. All the EVA films have been subjected to UV radiation at a wavelength of 340 nm for 1000 and 2000 h to simulate accelerated field aging. The effects of accelerated aging on the gel content, mechanical properties, transmittance, Fourier transform infra-red (FTIR) spectra, thermal stability, degree of crystallinity, and yellowness have been studied. The observations made in this study of UV aging up to 2000 h suggests that the optimum range of VA content in EVA should be between 18 and 33% by weight. VA content beyond 40% degrades almost all properties needed for an encapsulate material after aging of only 2000 h. VA content of around 18% is the most stable under UV aging conditions but has a slightly lower value of transmittance for the unaged sample although the difference in transmittance between different specimens decreases with UV aging. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48268.     

不同有机物对硝酸盐氮测试的影响

研究了红糖、葡萄糖、乙酸钠、甲醇、乙醇、乙酸、丙酸、丁酸、正戊酸、混合有机溶剂等10种不同有机物对麝香草酚光谱法和离子色谱法测试硝酸盐氮的影响。结果表明,溶液中含有红糖或葡萄糖时,均会对麝香草酚法测试硝酸盐氮造成影响,使得测试结果偏大;在无硝酸根离子存在时,红糖和葡萄糖的质量浓度与硝酸盐氮的测试浓度非线性相关;而乙酸钠、甲醇、乙醇、乙酸、丙酸、丁酸、正戊酸和混合有机溶剂则对麝香草酚法测试硝酸盐氮没有影响。实验发现,红糖和葡萄糖在浓硫酸的作用下与麝香草酚发生Molisch反应,形成有色复合物和红棕色不溶性沉淀。实验采用离子色谱法测试硝酸盐氮时,红糖和葡萄糖等糖类有机物对测试结果均无影响。     

紫外分光光度法测定核酸含量的影响因素分析

选择寡聚核苷酸、鲑鱼精单链DNA、小牛胸腺双链DNA标准物质为样本,系统研究了溶液pH、苯酚、丙酮、蛋白质、多糖等对紫外分光光度法测量结果的影响情况,另外考察了核糖核酸(RNA)和脱氧核糖核酸(DNA)的相互影响情况。研究发现基于分光光度法的核酸定量分析,易受溶液pH、苯酚、丙酮、蛋白质、多糖等的影响,另外,DNA和RNA之间也会相互干扰。因此,紫外分光光度法测定核酸含量时,特别是该方法用于核酸标准物质特性量值确定时,需要样品高度纯化,pH确定的条件下才能保证测量结果的准确可靠。