化学发光分析法测定绿原酸

本文基于碱性介质中绿原酸对鲁米诺-铁氰化钾化学发光体系的抑制作用,首次建立了绿原酸的化学发光分析法,并探讨了其作用机理。方便简便、迅速、重复性好、灵敏度高。采用该法可测定1.0×10-8g/ml～1.0×10-5g/ml范围内的绿原酸,其检出限达到5.2×10-9g/ml,回收率为104%.     

酸性高锰酸钾-高良姜素化学发光体系的发光光谱

在多聚磷酸介质条件下,对酸性高锰酸钾和高良姜素化学发光新体系的发光现象进行了研究,并通过测定反应的化学发光光谱、紫外吸收光谱、荧光光谱和微量电位滴定曲线对其发光体的确定提供了实验依据。实验数据表明,在0.1mol·L-1多聚磷酸溶液中,当高锰酸钾和高良姜素的量比为6∶5时,体系有最强的化学发光,在氧化剂过量的条件下,化学发光强度与高良姜素浓度在一定范围成正比关系。此外,由体系的化学发光光谱与高锰酸根离子的电子吸收光谱之间有镜像对称性关系的现象,证明了主发光体应来源于高锰酸钾;发光动力学实验还证明该发光体不是单一型体,伴随发光过程发光体有歧化反应现象。根据实验结果,对该体系可能的发光机理进行了讨论,提出高锰酸钾和高良姜素化学发光的主要发光体来源于高锰酸根离子的还原产物且为氧化还原反应过程中产生的激发态Mn(Ⅱ)和Mn(Ⅲ)型体,通过高良姜素氧化生成的活性游离基产物而产生激发态的Mn(Ⅱ)型体是生成发光体的主要途径。该化学发光强度与高良姜素含量成线性关系,以此可以进行定量分析;而由歧化过程形成的激发态Mn(Ⅲ)的发光行为却会干扰高良姜素含量与总发光强度之间的线性关系,不利于定量分析。     

Potassium Sensing by Using a Newly Synthesized Squaraine Dye in Sol-Gel Matrix

Squaraines are a group of fluorescent dyes and pigments derived from squaric acid and dialkylanilines well known in applications such as photoreceptors, organic solar cells, optical recording media, and non-linear optics. Their very promising spectral properties, long wavelength absorption and emission, and high absorptivity and quantum yields have not been exploited so far in relation to optical sensor design. They exhibit excellent solubility in sol-gel matrices, and the ligand is an integral part of the fluorophore system, which makes the molecule a fluoroionophore. In this work, potassium-sensing agent, bis[4-N-(1-aza-4,7,10,13,16-pentaox acyclooctadecyl)-3,5-dihydroxyphenyl] squaraine has been used for potassium sensing in a sol-gel matrix. The spectrofluorimetric response of dye-doped tetraethyl ortosilicate (TEOS) film after exposure to certain concentrations of K⁺ has been investigated, and 62% of relative signal change was achieved. The dynamic working range of the sensor membrane has been found between 10^–9 and 10^–6 M K⁺, in other terms from nanomolar to micromolar levels, which is an advantage over flame emission spectroscopy, in view of detection limit. The sensor is fully reversible within the dynamic range and the response time (₉₀) is found to be 2 min under batch conditions. The cross-sensitivity of the molecule to Na⁺, Ba²⁺, Ca²⁺, and NH⁺ ₄ was also tested in separate solutions.     

大口径氘化磷酸二氢钾晶体离线亚纳秒激光预处理技术

大口径氘化磷酸二氢钾(DKDP)晶体抗激光损伤性能偏低严重地制约着大型高功率激光装置输出水平.本研究利用离线亚纳秒激光预处理技术有效地提升了大口径DKDP晶体抗激光损伤性能.实际使用情况表明,采用离线亚纳秒激光预处理后,DKDP晶体在9 J/cm2激光通量辐照下的表面平均损伤密度得到大幅下降,由未处理前的5.02 pp...     

新疆玛纳斯湖水蒸发过程研究

本文依据Na^ ,K^ ,Mg^2 //Cl^-,SO4^2--H2O五元水盐体系相图，对新疆玛纳斯盐湖水进行原料分析、理论研究、25℃等温蒸发实验和自然蒸发实验，研究了该湖水蒸发过程中盐类的析出规律及湖水中各组分浓度变化的规律，为进行工艺实验及将来的综合开发利用提供了可靠依据。     

Synergistic effects on iodine release in potassium iodide solution by combination of ultrasound and visible light irradiations

Iodine release in potassium iodide solution has been investigated under the irradiations of ultrasound and visible light respectively and simultaneously. We have observed that the amount of iodine liberated under the combined irradiation of ultrasound and visible light is larger than the sum of that under the respective irradiations of ultrasound and visible light, indicating a synergistic effect of ultrasound and visible light irradiations. Based on the investigation of the reaction kinetics of iodine liberated, we have ascribed the synergistic effect to the perfect stirring of the photochemical reactor induced by the applying simultaneous ultrasound. The ideal stirring can result in the homogenization of the primary light effect in the whole reaction medium, which induces the acceleration of the photochemical reaction. On behavior of our knowledge, there are few reports on the investigations of utilizing the combination of ultrasonic energy and light energy to accelerate the reaction yield and rate as well as the kinetics of the reaction.     

Radiation induced polymerization of Vinylbenzoate–II. Study of the molecular weights of polymers

Abstract

In this study, the molecular weights of the polymer from vinyl benzoate has been reported for different dose rates and different temperatures. The mol.wt. remains around 4000. With increasing dose, the molecular weight increases to about 14,000. The degrees of polymerization and the kinetic chain lengths calculated from the experimentally determined G _R values have been compared which show that the kinetic chain length is larger than the D ^? Pn.

From a plot of the (D ^? Pn)^?1 vs. R _p , an intercept is obtained which is equal to 3.25 × 10^?2 which is higher than obtained in conventional polymerization. By examining the effect of temperature on mol.wt., the dependence of R _p on dose rate and the absence of induction period it has been concluded that chain transfer occurs to impurities that are generated during radiolysis.     

High Tc superconductors with different Cu2+/Cu3+ ratios in the Y–Ba–Cu–O system

Studies on different phases in the Y-Ba-Cu-O system have revealed that T_C around 90 K is obtainable with different Cu /Cu ratios provided the correct oxygen proportion is maintained.     

Anisotropic electrical properties of Bi0.5(Na0.75K0.25)0.5TiO3 ceramics fabricated by reactive templated grain growth (RTGG)

We have fabricated lead-free Bi_0.5(Na_0.75K_0.25)_0.5TiO₃ (BNKT) ceramics by a conventional process (CP) and reactive templated grain growth (RTGG) methods. The effect of grain orientation on structure, dielectric, complex impedance and electrical properties was investigated. The phase formation and grain morphology of BNKT ceramics were examined by X-ray diffraction (XRD) and scanning electron microscope (SEM), respectively. High dielectric constant and low dielectric loss was observed for grain oriented (textured) BNKT ceramics. Complex impedance, temperature dependent ac and dc conductivity were performed to explore the conduction behavior of the prepared BNKT ceramics.     

Polyethylene Glycol–Enhanced Chemoselective Synthesis of Organic Carbamates from Amines,CO2, and Alkyl Halides

An efficient and environmentally benign method for the synthesis of organic carbamates was developed. Amines, CO₂, and alkyl halides underwent a three-component reaction with the aid of K₂CO₃ and polyethylene glycol (PEG, MW = 400), affording the organic carbamates under ambient conditions. PEG could presumably act as a solvent and phase-transfer catalyst (PTC). Notably, the presence of PEG could also depress the alkylation of both the amine and the carbamate, thus resulting in enhanced selectivity toward the target carbamate.

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