Synthesis of Sulfonated Carbon Nanocage and Its Performance as Solid Acid Catalyst

Abstract  

A carbon nanocage material (CKT) was first successfully sulfonated by introducing sulfophenyl groups on the surface of pore channels through benzenesulfonic acid-containing aryl radical in situ generated from the reaction of 4-aminobenzenesulfonic acid and isoamyl nitrite in water. The sulfonated carbon nanocage material (S-CKT) was characterized by Fourier transform infrared spectroscopy, transmission electron microscopy, powder small-angle X-ray diffraction and nitrogen sorption measurements. The results showed that the S-CKT still possess the high specific surface area (787 m²/g) and uniform mesoporous (pore diameter 4.7 nm) structures, although the structure of S-CKT is slightly disorder, compared with its unsulfonated precursor. S-CKT, as a carbon-based solid acid catalyst, showed good catalytic performance and reusability in the cross-Aldol condensation of ketones with aromatic aldehydes under solvent-free condition.     

Nanosized Mn(acac)<Subscript>3</Subscript> Anchored on Amino Functionalized Silica for the Selective Oxidative Synthesis of 2-arylbenzimidazoles, 2-arylbenzothiazoles and Aerobic Oxidation of Benzoins in Water

Abstract  

Silica functionalized Mn(acac)₃ was prepared and employed for the one-pot oxidative synthesis of 2-arylbenzimidazoles, 2-arylbenzothiazoles; and oxidation of benzoins to benzils under air atmosphere using water as the reaction medium. Environmentally friendly procedure, chemoselectivity and excellent yields are main advantages of this procedure. In all the cases, the catalyst was found to be highly active and selective; passes hot filtration test successfully; and could be recycled several times with a slight loss of activity.     

Selective Oxidation of Glycerol Catalyzed by Rh/Activated Carbon: Importance of Support Surface Chemistry

Abstract  

Noble metal catalysts (Pt, Ir, Pd, Rh, Au) supported on activated carbon were assessed for glycerol oxidation. Rhodium is a highly efficient catalyst when the support has neutral or basic properties. The surface chemistry of activated carbon plays a key role in the performance.     

Gas-phase Photocatalytic Oxidation of Acrylonitrile on Sulphated TiO<Subscript>2</Subscript>: Continuous Flow and Transient Study

Abstract  

The gaseous products of photocatalytic oxidation (PCO) of acrylonitrile on sulphated P25 in concentrations from 10 to 100 ppm at 60 to 130 °C were CO₂, HCN and HNCO. This photocatalyst showed disproportionally improved performance at higher temperature and longer retention times. The temperature-programmed oxidation (TPO) after PCO disclosed possible reaction routes.     

Hyperbranched poly (amine-ester)-poly(ε-caprolactone) copolymer and their nanoparticles as camptothecin delivery system

A new amphiphilic hyperbranched poly (amine-ester)-poly(ε-caprolactone) copolymer (HPAE-co-PCL) was synthesized by ring-opening polymerization of ε-caprolactone and branched poly (amine-ester) (HPAE-OHs) with Sn(Oct)₂ as catalyst. The chemical structures of copolymers were determined by FT-IR, ¹H-NMR (¹³C-NMR), thermo gravimetric analysis apparatus (TGA) and differential scanning calorimetry (DSC). Camptothecin (CPT)-loaded copolymer nanoparticles were prepared by the oil-in water (o/w) emulsion technique method. Their physicochemical characteristics, e.g. morphology and nanoparticles size distribution were then evaluated by means of fluorescence spectroscopy, environmental scanning electron microscopy (ESEM), and dynamic light scattering (DLS). CPT-loaded nanoparticles assumed a spherical shape and have unimodal size distribution. It was found that the chemical composition of the nanoparticles was a key factor in controlling nanoparticles size, drug-loading content, and drug release behavior. As the molar ratio of ε-caprolactone to HPAE increased, the nanoparticles size and drug-loading content increased, and the drug release rate decreased. The antitumor activity of the CPT-loaded HPAE-co-PCL nanoparticles against human hepatoma HEPG2 cells was evaluated by 3-(4, 5-Dimethylthiazol-2-yl)-2,5-diphenyl tetrazolium bromide (MTT) method. The CPT-loaded HPAE-co-PCL nanoparticles showed comparable anticancer efficacy with the free drug.     

Resolution of a Five-Component Mixture of Quaternary Ammonium Surfactants on Silica Gel 60 <Emphasis Type=Italic>F</Emphasis><Subscript>254</Subscript> High Performance Thin Layer Chromatographic Plates

The mutual separation of a mixture of cetyltrimethyl ammonium chloride (CTAC), methyl trioctyl ammonium bromide (MTOB), dodecyltrimethyl ammonium chloride (DTAC), benzyltrimethyl ammonium chloride (BTAC) and tetrabutyl ammonium bromide (TBAB), was achieved on silica high performance thin layer chromatographic plates using dimethyl sulfoxide with aqueous sodium-l-tartrate dibasic dihydrate as the solvent system. The effect of concentration of sodium-l-tartrate dibasic dihydrate on the mobility of all the five quaternaries was examined. The limit of detection of CTAC, MTOB, DTAC, BTAC and TBAB was estimated as 0.6, 0.6, 0.3, 0.6 and 0.3 μg/zone, respectively. The method developed was utilized to identify these surfactants in different spiked water samples after their preliminary separation.     

Performance and Microstructural Study on Soap Using Different Fatty Acids and Cations

The desired benefits of the finished soap product are governed by a professional selection of appropriate raw materials, the manufacturing process or both. A better understanding of the crystallization of the soap microstructure is needed which has direct effects on the properties of final products. Soap microstructures and soap composition are not only determined by the length of hydrophobic fatty chain, saturation extent of fatty acid chain, fatty acid distribution but also by the cation effect. Thus, four different fatty acid compositions and the effect of sodium and potassium cations were studied. The performance of the potassium and sodium bar soaps prepared was monitored and was correlated with solid phase thermal analysis. The microstructural effect was examined using ATR-FTIR, FESEM and XRD. The specific ion effect and ion interaction involving both cations and carboxylate anions on different chemical compositions was correlated.     

Effects of Reaction Parameters in Catalysis of Glycerol Oxidation by Citrate-Stabilized Gold Nanoparticles

Abstract  

This work describes a catalytic oxidation of glycerol using citrate-stabilized gold nanoparticles (citrate-AuNPs) having a mean diameter of 22 ± 3 nm. A careful product analysis was performed by mean of high-performance liquid chromatography, liquid chromatography–mass spectrometry and nuclear magnetic resonance spectroscopy. Effects of reaction temperature, oxygen pressure, catalyst and reactant concentration, and NaOH/glycerol molar ratio on glycerol conversion, and product yields were investigated. The glycerol conversion and glyceric acid yield were optimum when the oxidation was performed using 0.6 M glycerol and NaOH at 80 °C under 3 bar of O₂ pressure in the presence of 50 ppm citrate-AuNPs catalyst for 3 h.