Synthesis of graphitic carbon nitride-based nanocomposites and their mechanical properties in epoxy compositions.

Thermoset epoxy resins are widely used in research and commercial applications. Zeolite imidazole framework-8 (ZIF-8), graphitic carbon nitride (GCN, g-CN), and S-doped graphitic carbon nitride (SCN, S-g-CN) composites were synthesized as accelerators and their effects on the physical properties of epoxies were examined. An ultrasound-assisted method was used to prepare ZIF-8/GCN and ZIF-8/SCN nanocomposites while g-CN and S-g-CN were prepared from the calcination of melamine and thiourea, respectively.

Synthesis of Waterborne Polyurethane Using Phosphorus-Modified Rigid Polyol and its Physical Properties.

In this study, a phosphorous-containing polyol (P-polyol) was synthesized and reacted with isophorone diisocyanate (IPDI) to produce water-dispersed polyurethane. To synthesize waterborne polyurethanes (WPUs), mixtures of P-polyol and polycarbonate diol (PCD) were reacted with IPDI, followed by the addition of dimethylol propionic acid, to confer hydrophilicity to the produced polyurethane. An excess amount of water was used to disperse polyurethane in water, and the terminal isocyanate groups of the resulting WPUs were capped with ethylene diamine.

Preparation of C60 Nanowhiskers-SnO2 Nanocomposites and Photocatalytic Degradation of Organic Dyes.

C60 nanowhiskers were prepared using a liquid-liquid interfacial precipitation (LLIP) method. Tin oxide (SnO2) nanoparticles were synthesized by a reaction of tin (IV) chloride pentahydrate with ammonium nitrate in an electric furnace. The C60 nanowhiskers-SnO2 nanocomposites were calcined in an electric furnace at 700 °C under an inert argon gas atmosphere for 2 h.

Preparation of ZnS-graphene nanocomposites under electric furnace and photocatalytic degradation of organic dyes.

Zinc sulfide (ZnS) nanoparticles were synthesized from zinc nitrate hexahydrate and thiourea under microwave irradiation. The ZnS-graphene nanocomposites were calcined in an electric furnace at 700 degrees C under an inert argon gas atmosphere for 2 hr. The heated ZnS-graphene nanocomposites were characterized by X-ray diffraction, scanning electron microscopy, transmission electron microscopy and UV-vis spectrophotometry.

Preparation of graphene-ZrO2 nanocomposites by heat treatment and photocatalytic degradation of organic dyes.

ZrO2 nanoparticles were synthesized by combining a solution containing zinconyl chloride in distilled water with a NH4OH solution under microwave irradiation. Graphene and ZrO2 nanocomposites were synthesized in an electric furnace at 700 degrees C for 2 hours. The heated graphene-ZrO2 nanocomposites were characterized by X-ray diffraction, scanning electron microscopy and transmission electron microscopy.

Preparation of C60(O)n-ZnO nanocomposite under electric furnace and photocatalytic degradation of organic dyes.

Zinc oxide (ZnO) nanoparticles were synthesized sonochemically by applying ultrasonic irradiation to a mixed aqueous-alcoholic solution of zinc nitrate with sodium hydroxide at room temperature. The morphology and optical properties of the ZnO nanoparticles were examined by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and UV-vis spectroscopy. The C60(O)n nanoparticles were synthesized by heating a mixture of C60 and 3-chloroperoxybenzoic acid in a benzene solvent under the reflux system.

Synthesis of [60]fullerene-ZnO nanocomposite under electric furnace and photocatalytic degradation of organic dyes.

Zinc oxide (ZnO) nanoparticles were synthesized by a reaction between an aqueous-alcoholic solution of zinc nitrate and sodium hydroxide under ultrasonic irradiation at room temperature. The morphology, optical properties of the ZnO nanoparticles were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and UV-vis spectroscopy. The [60]fullerene and zinc oxide nanocomposite were synthesized in an electric furnace at 700 degrees C for two hours.

Synthesis of gold nanoparticles using pluronic F127NF under microwave irradiation and catalytic effects.

This study examined the synthesis of gold nanoparticles with pluronic F127NF and KAuCl4 in water under non-classical conditions. The gold nanoparticle products were well dispersed in water and characterized by ultraviolet-visible spectroscopy and transmission electron microscopy. The reaction time for the synthesis was investigated by monitoring the change in color and the peak of the UV-vis spectra under microwave conditions.

Preparation of self-assembled zinc oxide nanoparticles multilayer films under ultrasonic irradiation.

Zinc oxide nanoparticles were synthesized and self-assembled on the reactive surface of a glass slide functionalized with (3-mercaptopropyl)-trimethoxysilane under ultrasonic irradiation. The structure, morphology, and optical property of the zinc oxide nanoparticles were investigated by TEM, XRD, and UV-vis spectroscopy. The functionalized glass slide was soaked in an aqueous solution which dispersed zinc oxide nanoparticles under ultrasonic irradiation.

Sonochemical reaction of fullerene[C60] with several 2'-azidoethyl per-O-acetyl glycosides.

Cycloadditive reaction of fullerene[C60] with various 2'-azidoethyl per-O-acetyl glycopyranoside of D-mannose, D-galactose, D-glucose, D-xylose and D-maltose, respectively gave the glycosyl fullerene[C60] derivatives 2a-2e such as alpha-D-mannosyl fullerene[C60] under ultrasonication. Based on analyses using 1H- and 13C-NMR, UV-vis, FT-IR, and FAB-MS spectroscopies of the glycosyl fullerene[C60] derivatives, the products were composed of a mixture of [5,6]- and [6,6]-junction isomers which were predominantly the closed [5,6]-junction isomer.

Preparation of a water-soluble fullerene [C70] under ultrasonic irradiation.

A water-soluble fullerene [C(70)] is prepared with fullerene [C(70)] and a mixture of concd. sulfuric acid (H(2)SO(4)) and concd. nitric acid (HNO(3)) at the ratio (v/v) of 3:1 under ultrasonic irradiation at 25-43 degrees C.

Ultrasonic, chemical stability and preparation of self-assembled fullerene[C60]-gold nanoparticle films.

C(60)-functionalized gold nanoparticle films were self-assembled on the reactive surface of glass slides functionalized with 3-aminopropyltrimethoxysilane. The functionalized glass slides were alternately soaked in the solutions containing unmodified C(60) and 4-aminothiophenoxide/hexane thiolate-protected gold nanoparticles. Organic reaction (amination) facilitated the layer-by-layer multilayer film assembly.

The oxidation of fullerene[C60] with various amine N-oxides under ultrasonic irradiation.

The reaction of C60 with various amine N-oxides such as 3-picoline N-oxide (Aldrich 98.0%), pyridine N-oxide hydrate (Aldrich 95.0%), quinoline N-oxide (Aldrich 97.

Synthesis of a water-soluble fullerene [C60] under ultrasonication.

A water-soluble fullerene [C60] is prepared with fullerene [C60] and a mixture of strong inorganic acids at the ratio (v/v) of 3:1 under ultrasonic condition at 25-43 degrees C. The MALDI-TOF MS and 13C-NMR spectra confirmed that the product of a water-soluble fullerene compound was C60.

The oxidation of fullerene [C70] with various oxidants by ultrasonication.

The reaction of C70 by ultrasonication with various oxidants such as 3-chloroperoxy benzoic acid (Fluka 99%), 4-methyl morpholine N-oxide (Aldrich 97%), chromium (VI) oxide (Aldrich 99.9%), and oxone monopersulfate compound, at room temperature causes the oxidation of fullerene [C70(O)n] (n = 1-2 or n = 1). The FAB-MS, UV-visible, FT-IR spectra, and HPLC analysis confirmed that products of fullerene oxidation are [C70(O)n] (n = 1-2 or n = 1).