Highly selective synthesis of single-walled carbon nanotubes from methane in a coupled Downer-turbulent fluidized-bed reactor

For the synthesis of single-walled carbon nanotubes (SWCNTs) from CH₄ over a Fe/MgO catalyst, we proposed a coupled Downer-turbulent fluidized-bed (TFB) reactor to enhance the selectivity and yield (or production rate) of SWCNTs. By controlling a very short catalyst residence time (1–3 s) in the Downer, only part of Fe oxides can be reduced to form Fe nano particles (NPs) available for the growth of SWCNTs. The percentage of unreduced Fe oxides increased and the yield of SWCNTs decreased accordingly with the increase of catalyst feeding rate in Downer. SWCNTs were preferentially grown on the catalyst surface and inhibited the sintering of the Fe crystallites which would be formed thereafter in the downstream TFB, evidenced by TEM, Raman and TGA. The coupled Downer-turbulent fluidized-bed reactor technology allowed higher selectivity and higher production rate of SWCNTs as compared to TFB alone.     

An Efficient Separation Method of Polysaccharides: Preparation of an Antitumor Polysaccharide APS-2 from Auricularia polytricha by Radial Flow Chromatography

Auricularia polytricha is an edible mushroom, quite popular in China. Modern pharmacology research indicate that A. polytricha polysaccharides possess antitumor and immunomodulatory activities. In this paper, an antitumor Auricularia polytricha polysaccharide (APS)-2 was purified by radial flow chromatography (RFC) in a column of 500 mL bed-volume (40 cm i.d × 15 cm) packed with DEAE52-cellulose anion ion-exchange resin. The optimal separation conditions were: sample flow-velocity 15–20 mL min^?1, sample volume 160–200 mL, and elution with distilled water and 0.2 M NaCl at a velocity of 35–45 mL min^?1. The yield and content of APS-2 obtained under these conditions were 182 mg g^?1 total polysaccharides and 98.35 %, respectively. The study provides guidelines for the separation and purification of polysaccharides using a radial flow chromatography column.     

Size-Exclusion Chromatography of Asphaltenes: An Experimental Comparison of Commonly Used Approaches

Asphaltenes, the heaviest and most polar fraction of crude oil, are responsible for the clogging of oil pipelines and of underground reservoir rocks. Asphaltenes are defined as a solubility class (toluene- or benzene-soluble, n-alkane insoluble), and a consensus is still lacking on the molar mass (M) averages, distribution, and range of these materials. Size-exclusion chromatography (SEC) is among the most widely employed methods for characterizing the M averages and distributions of both natural and synthetic polymers and, as such, has seen widespread application in the study of asphaltenes. SEC analysis of asphaltenes presents a number of challenges, however, some inherent to all low-M materials and some unique to these particular analytes. Here, we have experimentally compared several of the most commonly used approaches to SEC of asphaltenes, in hope of both demonstrating the influence of experimental conditions upon the results obtained as well as to determine optimal conditions of analysis. In the end, while the former goal was met, the latter one remains an open challenge in the field.     

Mild and Efficient Syntheses of 1-Aryl-3,4-dihydroisoquinolines and 1-Aryl-3,4-dihydro-β-carbolines via Regiospecific β-Eliminations of the Corresponding N-Tosyl-1,2,3,4-tetrahydroisoquinolines and N-Tosyl-1,2,3,4-tetrahydro-β-carbolines

Treatment of N-tosyl-1-aryl-1,2,3,4-tetrahydro-isoquinolines or N-tosyl-1-aryl-1,2,3,4-tetrahydro-β-carbolines with a strong base such as NaOH or KOH at 70 °C in dimethylsulfoxide (DMSO) produced 1-aryl-3,4-dihydroisoquinolines or 1-aryl-3,4-dihydro-β-carbolines in good yields via mild and regiospecific β-eliminations. A dramatic solvent effect was observed, DMSO was crucial for the reactions. The temperature is also crucial for the reactions and should be kept between 60 and 80 °C.     

Hydrogen Peroxide–Promoted Transformation of Thioureas/Thiosemicarbazides to Related Ureas/Semicarbazides at Room Temperature via Grinding

A novel and environmentally benign synthetic method for ureas through hydrogen peroxide–promoted desulfurization of thioureas at room tepemperature via grinding is reported. As compared with the traditional method, this one is manipulatively simple and the oxidant is low cost, highly active, and environmentally friendly.     

Dispersion Mechanism of Superfine SiC Particles in the Different Condition Liquid

SiC@A1(OH)₃-Y(OH)₃ core-shell composite particles are synthesized by co-precipitation method for strengthening the antioxidation of SiC at high temperature. To reach better A1(OH)₃-Y(OH)₃ composite shell and higher coating ratio on the SiC particles surfaces, SiC particles must be adequately dispersed in the SiC suspension during the coating process. The dispersion mechanism of SiC particles is investigated by the sedimentation method. Through test and analysis, the optimum conditions of the dispersion of SiC particles in the SiC suspension are sedimentating for 10 minutes, ultrasonic dispersion for 10 minutes, the lower SiC concentration, pH = 9, the dispersant content for the 2% volume of SiC suspension and using the polyelectrolyte dispersant, respectively.     

Optical and Electronic Properties of Different Kinds of Water‐Soluble Porphyrin Films

Water‐soluble porphyrin‐porphyrin and porphyrin‐CdSe nanoparticle monolayer films were self‐assembled on different substrates. The influence of substrates, types of films, and heat treatment temperature on fluorescence of different kinds of porphyrin films was investigated. The SEM images showed the formation of monolayer films on porous alumina foil. The films assembled on porous alumina foil possessed higher fluorescence intensity and thermal stability. The result of conductance measurement indicated that the interaction of trimethylamidophenylporphyrin iodide (TAPPI) molecules with hydroxyl groups on porous alumina foil was weakened after CdSe nanoparticles assembled with TAPPI.