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The adsorption of dimethylamine on Cu(1 1 0) and Ni(1 1 1) has been studied by reflection absorption infrared spectroscopy. For Cu(1 1 0), adsorption was molecular at 80 and 300 K and for submonolayer dimethylamine the appearance of A′ and not A″ modes indicated Cs symmetry. Similar bonding was found for Ni(1 1 1) at 170 K. Annealing the adlayer to 350 K resulted in the formation of a new species on Ni(1 1 1), similar to that which has been identified as methylaminocarbyne on Pt(1 1 1). In contrast only molecular dimethylamine was identified on Cu(1 1 0), with H-bonded interactions at high coverage and a potential surface dimer. 相似文献
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In this article, the simultaneous determination of primary and secondary aliphatic amines including dimethylamine (DMA), diethylamine and eleven primary aliphatic amines by high performance liquid chromatography (HPLC) with fluorescence detection has been achieved using a BODIPY-based fluorescent derivatization reagent, 1,3,5,7-tetramethyl-8-(N-hydroxysuccinimidyl butyric ester)-difluoroboradiaza-s-indacene (TMBB-Su). The derivatization reaction of TMBB-Su with aliphatic amines was optimized with orthogonal design experiment and the derivatization reaction proceeded at 15 °C for 25 min. The baseline separation of these derivatives was carried out on a C8 column with methanol-tetrahydrofuran-50 mM pH 6.50 HAc-NaAc buffer (55/5/40, v/v/v) as a mobile phase. Detected at the excitation and emission of 490 and 510 nm, respectively, the detection limits were obtained in the range of 0.01-0.04 nM (signal-to-noise ratio = 3). The proposed method has been applied to the determination of trace aliphatic amines in viscera samples from mice without complex pretreatment or enrichment method. The recoveries ranged from 95.1% to 106.8%, depending on the samples investigated. 相似文献
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胺基化合物修饰戊二醛交联壳聚糖树脂的合成及其红外光谱研究 总被引:6,自引:0,他引:6
研究了以三聚氯氰为活化剂,正丁胺、二甲胺、三甲胺、三乙胺、苯甲胺、对甲基苯胺、对氨基苯磺酸修饰戊二醛交联壳聚糖的制备及其红外光谱。壳聚糖1 155 cm-1的糖苷键ν(C—O—C)吸收峰、899 cm-1的环振动吸收峰和1 030 cm-1的伯羟基ν(C—OH)吸收峰基本不变。在3 430~3 440 cm-1的ν(O—H)和ν(N—H)吸收峰稍有变化,1 400~1 384 cm-1的δ(C—H)吸收峰变化较明显。氨基化修饰交联壳聚糖仲羟基的ν(C—OH)吸收峰由1 095 cm-1移至1 060~1 070 cm-1。三聚氯氰活化交联壳聚糖在803~812 cm-1和1 584~1 590 cm-1出现均三嗪环骨架振动吸收峰。随取代度和脱乙酰度不同,壳聚糖的酰胺Ⅰ,Ⅱ,Ⅲ峰强度变化明显。伯仲胺修饰交联壳聚糖在1 517~1 530 cm-1出现质子化氨基δ(N—H)吸收峰,三甲胺、三乙胺修饰交联壳聚糖此峰消失或减弱,但在1 400~1 500 cm-1出现一组ν(C—N)吸收峰。 相似文献
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ar Ceylan KOAK KOAK Süleyman ükriye KARABBEROLU Zekerya DURSUN 《Turkish Journal of Chemistry》2020,44(1):125
Dimethylamine borane (DMAB) is a promising fuel alternative for fuel cell applications. In this work cyclic voltammetric behavior of DMAB was investigated on the polymerized aminophenol film decorated with Ag nanoparticles in alkaline media. The polymer film was formed on the glassy carbon electrode by electrochemical technique and then, the surface was modified with Ag nanoparticles. The surface of the modified electrode was identified by scanning electron microscopy, transmission electron microscopy, X-ray photoelectron spectroscopy, and electrochemical impedance spectroscopy techniques. The developed electrode has displayed high electrocatalytic activity for DMAB oxidation in alkaline media depending on the supporting electrolyte concentration. Experimental parameters such as cycle number used in electropolymerization of p-aminophenol, deposition of Ag nanoparticles and supporting electrolyte were optimized. 相似文献
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Summary A TLC method has been developed for separating Th4+, UO2
2+ and Zr4+ in the presence of some common anions using a dimethylamine/acetone/formic acid mobile phase. Capacity factors, separation
factors and resolution for the separation of Th4+ from UO2
2+ have been evaluated. The effect of the pH of the sample on RF values of Th4+, UO2
2+, Ni2+ and Cu2+ has also been examined. 相似文献
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A new method is presented for the determination of DMA in water as its 9-fluorenylmethyl chloroformate (FMOC) derivative using solid-phase microextraction (SPME) and liquid chromatography. The method is based on the employment of SPME fibres coated with carbowax-templated resin (CW-TR) for analyte extraction and derivatization. The fibres were successively immersed in the samples, in a solution of o-phthalaldialdehyde and N-acethyl-l-cysteine (OPA–NAC) and finally, in a solution of FMOC. OPA–NAC reacted on the fibre with possible primary aliphatic amines present in the samples, particularly with PA which is a direct interferent in the determination of DMA with FMOC. In such a way, the formation of PA–FMOC during the second stage was prevented, and thus the method was selective for DMA. The proposed procedure was applied to the determination of DMA in the 1.0–10.0 μg/mL range. The method provided suitable linearity, accuracy and reproducibility, and limits of detection and quantification of 0.3 and 1.0 μg/mL, respectively. The applicability of the method for the determination of DMA in different types of water is shown. 相似文献
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The use of contactless conductivity detection for the determination of different organic amines in CE was successfully demonstrated. Aliphatic non UV-absorbing species could be determined along absorbing compounds by measuring the conductivity of their protonated forms. The species tested included short-chained aliphatic primary, secondary and tertiary amines, branched aliphatic amines, diamines, hydroxyl-substituted amines as well as species incorporating aromatic and non-aromatic cyclic moieties. Highest sensitivity was obtained with BGE solutions containing solely acetic acid. A concentration of 0.5 M at a pH value of 2.5 was used. Detection limits were in the order of 1 microM. Complete separation of cis- and trans-1,2-diaminocyclohexane could be achieved by adding 18-crown-6 as modifier to the electrolyte solution. 相似文献