Determination of seven nitrobenzene compounds in mainstream cigarette smoke with heart-cutting two-dimensional gas chromatography

A heart-cutting two-dimensional gas chromatography (GC) method was developed for the determination of nitrobenzene compounds (NBCs) in mainstream cigarette smoke. For the method, the particulate matter of cigarette smoke was extracted with cyclohexane, purified with a silica solid-phase extraction (SPE) cartridge and analyzed by heart-cutting two-dimensional GC equipped with two electron capture detectors. The heart-cutting two-dimensional GC was achieved by a single-column GC oven equipped with a microfluidic pressure balanced device (Deans switch). Two-dimensional GC was compared to single-dimensional GC and found to be clearly better for the separation of seven NBCs from a complex smoke matrix. The limits of detection ranged from 1.28 to 9.83 ng/mL, spiked recoveries were between 88.3 and 106.8% and relative standard deviation ranged from 2.79 to 12.78%. The NBCs yields of six kinds of Chinese and international cigarettes brands, which were all smoked according to two smoking protocols (International Organization for Standardization and Health Canada Intense smoking regimens), were determined and compared.     

Rapid and sensitive analysis of three polyphenols in tobacco by CE using homemade C(4) D with a mini detection cell

A rapid, sensitive, and practical CE with C(4) D detection was developed for the analysis of three polyphenols (rutin, scopoletin, and chlorogenic acid) in tobacco samples. The constructed mini detection cell (12 mm × 10 mm × 10 mm) of C(4) D featured with small inner cell volume (～2 nL), smaller noise (<0.9 mV), repeatability, high strength and durableness. Three polyphenols were ultrasonically extracted with methanol-water (70:30, v/v) solution following SPE cleanup. The CE method was optimized with the running buffer of 150 mmol L(-1) 2-amino-2-methyl-1-propanol (pH 11.2), and the applied separation voltage of +20 kV over a capillary of 50 μm id × 375 μm od × 50 cm (38 cm to the C(4) D window, 41.5 cm to the UV detector window), which gave a baseline separation of three polyphenols within ca. 6 min. The method provided the limits of quantification (S/N = 10) at about 0.08-0.15 μg g(-1) for three polyphenols, whereas the overall recoveries ranged from 82% to 88%. The proposed method has been successfully applied to measure three polyphenols in the actual tobacco samples, and their contents were calculated and evaluated.     

A general method for palladium-catalyzed direct carbonylation of indole with alcohol and phenol

A novel strategy involving a first oxidative iodination and subsequent Pd(0)-catalyzed carbonylation to yield indole-3-carboxylate has been developed. It showed perfect generality to indole, alcohol, and phenol. The current methodology could also be conveniently applied to the synthesis of biologically active tropisetron from simple indole and tropine.     

Detection of L‐phenylalanine using molecularly imprinted solid‐phase extraction and flow injection electrochemiluminescence

A novel flow injection electrochemiluminescence method combined with molecularly imprinted solid‐phase extraction was developed for the determination of L ‐phenylalanine, in which was used as the luminophor and indium tin oxide glass was modified as the working electrode. Molecularly imprinted polymers, synthesized by self‐assembly with functional monomer and crossing linker, were used for the selective extraction of L ‐phenylalanine. In order to overcome the drawbacks of traditional electrochemiluminescence cells such as high IR drop, high over‐potential and so on, a novel electrochemiluminescence cell was developed. The enhanced electrochemiluminescence intensity was linearly related with the concentration of L ‐phenylalanine in the range from 1.0×10^?7 to 5.0×10^?5 g/mL with a detection limit of 2.59×10^?8 g/mL. The relative standard deviation for the determination of 1.0×10^?6 g/mL L ‐phenylalanine was 1.2% (n=11). The method showed higher sensitivity and good repeatability, and was successfully applied for the determination of L ‐phenylalanine in egg white, chicken and serum samples. A possible mechanism for the enhanced electrochemiluminescence response on indium tin oxide glass is proposed.     

从FeSe0.5Te0.5的V～I曲线论磁通动力学的诸模型（英文）

高温超导体的发现动摇了支配磁通动力学二十几年的Kim-Anderson模型.于是人们提出了新的涡旋玻璃态模型,集体钉扎模型和U～j对数关系模型来描述高温超导体的磁通动力学.其中,涡旋玻璃态模型已被人们广泛接受.Fe基超导体发现后,人们它行为十分类似于高温超导体.我们实验上仔细研究了FeSe0.5Te0.5单晶的V～I关系曲线,发现上述诸模型均不能很好的解释我们的实验结果,而张的反跳模型恰能很好的拟合实验结果.本文讨论了诸模型对高温超导体磁通动力学描述的适用性并给出合理的解释.     

Cooling of Akmal-Pandharipande-Ravenhall neutron stars with a rotochemical heating source

Employing phenomenological density-dependent critical temperatures of strong singlet-state proton pairing and of moderate triplet-state neutron pairing, we investigate the effects of rotochemical heating on the thermal evolution of superfluid neutron stars whose cores consist of npe matter with the Akmal-Pandharipande-Ravenhall equation of state. Since the star is not quite in the weak interaction equilibrium state during spin-down, the departure from the chemical equilibrium leads to the rotochemical heating in a rotating NS which will increase the stellar＇s temperature. Our calculations show that the rotochemical heating delays the cooling of superfluid neutron stars considerably and makes the previous classification of NS cooling ambiguous. What＇s more, our model is currently consistent with all the observational data, and in particular some middle-aged and cold NSs （PRS J0205＋6449 in 3C 58, PRS J1357-6429, RX J007.0＋7303 in CTA 1, Vela） can be better explained when taking into account rotochemical heating.     

Cooling of Akmal-Pandharipande-Ravenhall neutron stars with a rotochemical heating source

Employing phenomenological density-dependent critical temperatures of strong singlet-state proton pairing and of moderate triplet-state neutron pairing, we investigate the effects of rotochemical heating on the thermal evolution of superfluid neutron stars whose cores consist of npe matter with the Akmal-Pandharipande-Ravenhall equation of state. Since the star is not quite in the weak interaction equilibrium state during spin-down, the departure from the chemical equilibrium leads to the rotochemical heating in a rotating NS which will increase the stellar's temperature. Our calculations show that the rotochemical heating delays the cooling of superfluid neutron stars considerably and makes the previous classification of NS cooling ambiguous. What's more, our model is currently consistent with all the observational data, and in particular some middle-aged and cold NSs (PRS J0205+6449 in 3C 58, PRS J1357-6429, RX J007.0+7303 in CTA 1, Vela) can be better explained when taking into account rotochemical heating.     

超声乳化溶剂扩散法制备阿奇霉素超细粉体

采用超声乳化溶剂扩散法制备了阿奇霉素超细粉体，讨论了溶剂、温度、阿奇霉素浓度以及稳定剂种类和用量等条件对微粉粒径及形貌的影响．实验结果表明，在实验选定的最佳实验条件下(结晶温度0～5℃，阿奇霉素浓度0．03mol／L，1％聚乙二醇(PEG)、乙醇为溶剂)，可制备出平均粒径为500nm的均匀分散阿奇霉素超细粉体。     

Synthesis and Crystal Structure of N,N′-4-aminomethyl-pyromellitic diimide

1 INTRODUCTION N,N?-4-aminomethyl-pyromellitic diimide (4-pmpmdwas firstly obtained[1] in 1989 as one of the bypro-ducts by refluxing equimolar quantities of pyrome-llitic anhydride, n-hexylamine and 4-aminomethyl py-ridine in dry DMF to assemble electronic donor-spa-cer-acceptor systems, but its structure and coordina-tion chemistry did not receive attention at that time.For 4-pmpmd, the entity of two methylene groups(-CH2-) between the rigid pyromellitic diimide (PMDcore and two fre…     

富氧燃烧条件下煤焦的燃尽特性

本文利用平面火焰携带流反应器研究了DT烟煤在富氧燃烧条件下的燃烧实验。采用灰示踪法分析煤焦的燃尽和元素释放特性,并采用等密度模型计算了基于氧化反应C+0.5O_2→CO的表观反应动力学参数。研究结果表明;煤粉在富氧燃烧条件下的燃尽慢于空气燃烧;富氧燃烧条件下,煤焦与CO_2的气化反应会导致煤焦表面对O的化学吸附,进而导致氧元素释放速率减慢;高氧浓度条件下,高浓度CO_2对煤焦燃尽的抑制作用大于CO_2气化反应对煤焦燃尽的促进作用,降低环境氧浓度可以逐步提高CO_2气化反应对煤焦燃尽的贡献。