A method was developed for the determination of tetraethyl ammonium （TEA） by reversed-phase ion- pair chromatography with indirect ultraviolet detection, Chromatographic separation was achieved on a reversed-phase C...A method was developed for the determination of tetraethyl ammonium （TEA） by reversed-phase ion- pair chromatography with indirect ultraviolet detection, Chromatographic separation was achieved on a reversed-phase C18 column using background ultraviolet absorbing reagent - ion-pair reagent - organic solvent as mobile phase. The effects of the background ultraviolet absorbing reagents, detection wavelength, ion-pair reagents, organic solvents and column temperature on the determination method were investigated and the retention rules discussed. Results found that TEA could be successfully analyzed by using 0.7 mmol/L 4-aminophenol hydrochloride and 0.15 mmol/L 1-heptanesulfonic acid sodium mixed with 20% （v/v） methanol as mobile phase at a UV detection wavelength of 230 nm. Under these conditions, the retention time of tetraethyl ammonium was 2.85 min. The detection limit （S/N = 3） for TEA was 0.06 mg/L. The relative standard deviations （n = 5） for peak area and retention time were 0.35% and 0.02%, respectively. The method has been successfully applied to the determination of synthesized tetraethyl ammonium bromide. Recovery of tetraethyl ammonium after spiking was 99.1%.展开更多
A coordinated ionic liquid [3(CH3CH2)4N+Cl-·(NH2)2CO] was synthesized from urea and tetraethyl ammonium chloride,and its structure was characterized by IR and XRD.The results showed that the IR absorption peak of...A coordinated ionic liquid [3(CH3CH2)4N+Cl-·(NH2)2CO] was synthesized from urea and tetraethyl ammonium chloride,and its structure was characterized by IR and XRD.The results showed that the IR absorption peak of carbonyl was at 1619.10 cm-1 compared with that of urea at 1690.72cm-1,which was due to reaction of urea and tetraethyl ammonium chloride.There was a new peak at 2θ=30.37° in the XRD pattern.The range of thermal stability is from room temperature to about 250℃,and is higher than other common organic solvents.展开更多
The eutectic ionic liquid （EIL） tetraethyl ammonium bromide-malonic acid （TEAB-Mal） was synthesized, with its structure characterized by the FT-IR spectroscopy and the 1H NMR spectrometry. The performance for remo...The eutectic ionic liquid （EIL） tetraethyl ammonium bromide-malonic acid （TEAB-Mal） was synthesized, with its structure characterized by the FT-IR spectroscopy and the 1H NMR spectrometry. The performance for removal of basic nitrogen compounds by EIL was studied using coker diesel as the feedstock. Experimental results showed that the EIL （TEAB-Mal） exhibited a good denitrogenation performance, leading to a 93.6% of basic N-removal efficiency under reaction conditions covering： a temperature of 30 ℃, an EIL to oil mass ratio of 1：1, an extraction time of 30 min, and a settling time of 120 min, while the basic nitrogen content in diesel dropped from 580 μg/g to 37 gg/g. In addition, the efficiency for extraction of basic N-compounds could still reach 62.9% at am EIL/oil mass ratio of 1：7 after four recycles of the EIL.展开更多
基金supported by the Natural Science Foundation of Heilongjiang Province(Grant No.B201307)the Ministry of Education of Heilongjiang Province(No.12531192)the Program for Scientific and Technological Innovation Team Construction in Universities of Heilongjiang Province(No. 2011TD010)
文摘A method was developed for the determination of tetraethyl ammonium （TEA） by reversed-phase ion- pair chromatography with indirect ultraviolet detection, Chromatographic separation was achieved on a reversed-phase C18 column using background ultraviolet absorbing reagent - ion-pair reagent - organic solvent as mobile phase. The effects of the background ultraviolet absorbing reagents, detection wavelength, ion-pair reagents, organic solvents and column temperature on the determination method were investigated and the retention rules discussed. Results found that TEA could be successfully analyzed by using 0.7 mmol/L 4-aminophenol hydrochloride and 0.15 mmol/L 1-heptanesulfonic acid sodium mixed with 20% （v/v） methanol as mobile phase at a UV detection wavelength of 230 nm. Under these conditions, the retention time of tetraethyl ammonium was 2.85 min. The detection limit （S/N = 3） for TEA was 0.06 mg/L. The relative standard deviations （n = 5） for peak area and retention time were 0.35% and 0.02%, respectively. The method has been successfully applied to the determination of synthesized tetraethyl ammonium bromide. Recovery of tetraethyl ammonium after spiking was 99.1%.
文摘A coordinated ionic liquid [3(CH3CH2)4N+Cl-·(NH2)2CO] was synthesized from urea and tetraethyl ammonium chloride,and its structure was characterized by IR and XRD.The results showed that the IR absorption peak of carbonyl was at 1619.10 cm-1 compared with that of urea at 1690.72cm-1,which was due to reaction of urea and tetraethyl ammonium chloride.There was a new peak at 2θ=30.37° in the XRD pattern.The range of thermal stability is from room temperature to about 250℃,and is higher than other common organic solvents.
基金the financial support from the Doctoral Funds of Liaoning Provincial Natural Science Foundation(201601323)
文摘The eutectic ionic liquid （EIL） tetraethyl ammonium bromide-malonic acid （TEAB-Mal） was synthesized, with its structure characterized by the FT-IR spectroscopy and the 1H NMR spectrometry. The performance for removal of basic nitrogen compounds by EIL was studied using coker diesel as the feedstock. Experimental results showed that the EIL （TEAB-Mal） exhibited a good denitrogenation performance, leading to a 93.6% of basic N-removal efficiency under reaction conditions covering： a temperature of 30 ℃, an EIL to oil mass ratio of 1：1, an extraction time of 30 min, and a settling time of 120 min, while the basic nitrogen content in diesel dropped from 580 μg/g to 37 gg/g. In addition, the efficiency for extraction of basic N-compounds could still reach 62.9% at am EIL/oil mass ratio of 1：7 after four recycles of the EIL.
