真实火箭射流冲击流场中激波结构的实验研究

本文采用一种有效的激光-莫瑞光栅干涉系统首次拍摄到真实火箭燃气射流冲击流场的激波结构.解决了长期以来无法拍摄到高温、高速、强火焰光的火箭射流流场图像的问题。利用这一系统,研究了射流冲击流场中激波结构的一些变化规律,发现了一些新的激波结构。较系统地研究了欠膨胀射流冲击各种锥体的激波形态。     

葫芦脲[7]的包结作用对亚甲基蓝和吖啶橙吸收光谱的影响

利用密度泛函方法对吖啶橙和亚甲基蓝与主体葫芦脲[7]分子作用的内、外包结物结构进行了理论计算.亚甲基蓝与葫芦脲[7]的内包结构型最稳定,吖啶橙与葫芦脲[7]的内、外包结构型的热稳定性相当.在相同的理论水平上利用时间相关的密度泛函方法计算了客体分子及其各构型包结物的激发态性质预测相应的吸收光谱.比较了客体分子的跃迁轨道组成及其性质的变化,预测葫芦脲[7]的包结作用对吖啶橙和亚甲基蓝分子的轨道能级和电子跃迁性质使其吸收光谱性质的影响.     

Sensory Response and Two-Photon-Fluorescence Study of Regioregular Polythiophene Nanoparticles

Nanoparticles of a regioregular and soluble polythiophene were fabricated by mini-emulsion technique. The fabricated nanoparticles were characterized by optical spectroscopy and dynamic light scattering. The fluorescence quenching of these fabricated nanoparticles with 2,4-dinitrotolune (DNT) in aqueous and organic solutions was investigated. Significant fluorescence quenching was observed. The Stern-Volmer constants were determined to be higher than that of the bulk polymer in solution, indicating that the nanoparticles provide better sensitivity in DNT sensing. Strong two-photon-induced fluorescence was measured from these nanoparticles.     

中药柴胡总皂苷急性肝毒性的代谢组学研究

运用UPLC-MS联用技术对空白对照组、柴胡总皂苷(SS)组大鼠在给药后第3天和第5天的尿液样本进行分析检测,获得了以质荷比和保留时间为变量的矩阵数据。据此建立各组大鼠的尿液代谢轮廓图,并利用主成分分析(PCA)建立了SS的代谢组学毒性模型。结合肝组织病理,探讨了柴胡总皂苷的急性肝毒性。对于SS组与正常组,大鼠尿液代谢轮廓图表现出了一定的差异。在代谢组学毒性模型中,给药第3天和第5天的PCA分类均偏离正常组,而第5天的偏离程度强于第3天。同时,在第5天的肝组织病理切片中发现了组织病变。由此表明,给药组大鼠的代谢组偏离了正常组,这种偏离正是肝急性毒性的表现,且给药到第5天的肝毒性强于第3天,表明肝毒性与给药累积剂量呈正相关,表现出了明显的急性和累积肝毒性。     

Three New C19‐Diterpenoid Alkaloids from Aconitum forrestii

A further study of the alkaloid constituents of Aconitum forrestii led to the isolation of three new C₁₉‐diterpenoid alkaloids, named 14‐acetoxy‐8‐O‐methylsachaconitine ( 1 ), 14‐acetoxyscaconine ( 2 ), and 8‐O‐ethylcammaconine ( 3 ). Their structures were determined by UV, IR, and MS, 1D‐ and 2D‐NMR analyses.     

Prenylated Benzene Metabolites from Melicope pteleifolia

Chemical investigation on the stem and root of Melicope pteleifolia afforded three new prenylated benzene metabolites as racemic mixtures, named pteleifolins A–C ( 1 – 3 , resp.). Their gross structures were elucidated on the basis of spectroscopic analysis, especially 2D‐NMR experiments. An enantiomer resolution of (±)‐ 1 using chiral HPLC was performed, and the absolute configuration of the enantiomers were determined to be (+)‐(S)‐ 1 and (?)‐(R)‐ 1 by means of circular‐dichroism analysis.     

The slagging propensity of Zn-rich scrap tyre ash in reducing environments consisting of CO and CO2 and its promotion of the slagging of Si-rich coal ash

This study includes a comprehensive investigation on the ash slagging characteristics of zinc (Zn)-rich tyre ash and its interaction with silica (Si)-rich coal ash blended at different ratios in a 5% CO in CO₂ reducing environment. Such an environment is expected to occur near the burner in a combustor, as well as serves as a fundamental study on the slagging propensity upon the effect of CO, which is a principal reducing agent in a gasifier. An approach consisting of experimental studies using modified inclined plane (M-IP) methodology, advanced analytical techniques including the scanning electron microscopy (SEM) and x-ray photoelectron (XPS) spectroscopy, and thermodynamic equilibrium calculations were used to elaborate the slagging propensities of the single and blended ashes. Furthermore, the fate of Zn within tyre ash and its potential implications on the slagging properties were evaluated. Tyre ash easily melts to liquid slag upon increasing temperature compared to the silica-rich coal ash. Zinc does not evaporate but rather remains within tyre slag mostly as a hemimorphite (Zn₄(Si₂O₇)(OH))-like coordination structure attributing to the characteristic blue colour of tyre slag. The low ionic potential value of 2.7 for Zn²⁺ is characteristic of basic ions that have a greater tendency to depolymerise the Si-rich ash slag matrix and acts as a fluxing agent in ash slag. Moreover, it was proven that Zn²⁺ plays a synergistic role with Ca²⁺ in enhancing the flowability of the Si-rich slag remarkably. Furthermore, for the pure tyre slag, Zn was found to preferentially deposit at the corundum (Al₂O₃) substrate interface and even penetrate/react with the porous corundum, causing a strong corrosion on the substrate. However, blending of tyre ash with coal ash alleviates this problem by a preferred scavenging of Zn into the entire Si matrix, which in turn protects the corundum plate.     

Synthesis,isolation and characterization of methyl levulinate from cellulose catalyzed by extremely low concentration acid

A direct synthesis of methyl levulinate from cellulose alcoholysis in methanol medium under mild condition (180–210 °C) catalyzed by extremely low concentration sulfuric acid (≤0.01 mol/L) and the product isolation were developed in this study. Effects of different process variables towards the catalytic performance were performed as a function of reaction time. The results indicated that sulfuric acid concentration, temperature and initial cellulose concentration had significant effects on the synthesis of methyl levulinate. An optimized yield of around 50% was achieved at 210 °C for 120 min with sulfuric acid concentration of 0.01 mol/L and initial cellulose concentration below 100 g/L. The resulting product mixture was isolated by a distillation technique that combines an atmospheric distillation with a vacuum distillation where n-dodecane was added to help distill the heavy fraction. The light fraction including mainly methanol could be reused as the reaction medium without any substantial change in the yield of methyl levulinate. The chemical composition and structural of lower heavy fraction were characterized by GC/MS, FTIR, ¹H-NMR and ¹³C-NMR techniques. Methyl levulinate was found to be a major ingredient of lower heavy fraction with the content over 96%. This pathway is efficient, environmentally benign and economical for the production of pure levulinate esters from cellulose.     

Removal of carbonyl sulfide from CO2 stream using AgNO3-modified NaZSM-5

Removal of carbonyl sulfide (COS) from CO₂ stream is significant for the production and utilization of food grade CO₂. This study investigates the adsorption performance of Ag/NaZSM-5 as adsorbent prepared by incipient wetness impregnation for the removal of COS from a CO₂ stream in a fixed-bed adsorption apparatus. Effects of various conditions on the preparation of adsorbent, adsorption and desorption were intensively examined. The results revealed that COS can be removed to below 1×10^?9 from a CO₂ stream (1000 ppm COS/CO₂) using Ag/NaZSM-5 (10 wt% AgNO₃) with an adsorption capacity of 12.86 mg-g^?1. The adsorbent can be fully regenerated using hot air at 450 °C. The adsorption ability remained stable even after eight cycles of regeneration.