Production of nano‐calcium carbonate from shells of the freshwater channeled applesnail,Pomacea canaliculata,by hydrothermal treatment and its application with polyvinyl chloride

The use of naturally renewable shells of the freshwater channeled applesnail, Pomacea canaliculata, as a filler to replace commercial calcium carbonate (CaCO₃) was investigated in this study. Ground P. canaliculata shell particles were converted to nano‐CaCO₃ particles by the displacement reaction of calcium chloride in sodium carbonate solution followed by hydrothermal treatment at 100°C for 1 h to synthesize nano‐CaCO₃ with particle sizes of 30–100 nm in diameter. The mechanical properties, in terms of the tensile strength, elongation at brake and impact strength, of polyvinyl chloride (PVC) were greatly improved by mixing with nano‐CaCO₃ at 5–10 parts per hundred of resin. Additionally, the presence of nano‐CaCO₃ at the same levels increased the flame resistance and thermal stability of the PVC composite materials. POLYM. COMPOS., 36:1620–1628, 2015. © 2014 Society of Plastics Engineers     

Dye-sensitized solar cell made of mesoporous titania by surfactant-assisted templating method

Nanocrystalline mesoporous titania was obtained by surfactant-assisted templating method using tetraisopropyl orthotitanate modified with acethylacetone and laurylamine hydrochloride as template. This material was applied for the electrode of dye-sensitized solar cell. The mesoporous TiO₂ (MP-TiO₂) cells exhibited higher short-circuit photocurrent density and solar energy conversion efficiency compared to P25 (a typical commercial titania powder) cells. The incident photon to current conversion efficiency spectrum of MP-TiO₂ can be improved by using the cell made with 5% P25 additive. Double-layer titania cells were fabricated to further improve cell performance by increasing the film thickness and light scattering. The solar conversion efficiency up to 8.06% was obtained by using the double-layer titania cell sintered at 450 °C for 2 h.     

Hydrothermal synthesis, characterization, photocatalytic activity and dye-sensitized solar cell performance of mesoporous anatase TiO2 nanopowders

Mesoporous anatase TiO₂ nanopowder was synthesized by hydrothermal method at 130 °C for 12 h. The samples were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM), selected-area electron diffraction (SAED), HRTEM, and Brunauer-Emmett-Teller (BET) surface area. The as-synthesized sample with narrow pore size distribution had average pore diameter about 3-4 nm. The specific BET surface area of the as-synthesized sample was about 193 m²/g. Mesoporous anatase TiO₂ nanopowders (prepared by this study) showed higher photocatalytic activity than the nanorods TiO₂, nanofibers TiO₂ mesoporous TiO₂, and commercial TiO₂ nanoparticles (P-25, JRC-01, and JRC-03). The solar energy conversion efficiency (η) of the cell using the mesoporous anatase TiO₂ was about 6.30% with the short-circuit current density (Jsc) of 13.28 mA/cm², the open-circuit voltage (Voc) of 0.702 V and the fill factor (ff) of 0.676; while η of the cell using P-25 reached 5.82% with Jsc of 12.74 mA/cm², Voc of 0.704 V and ff of 0.649.     

An approach for preparing an absorbable porous film of silk fibroin–rice starch modified with trisodium trimetaphosphate

The absorbable porous material, especially gelatin porous film, is widely used for surgical use to stop bleeding, but its price is quite high. Thus, a new material at lower price with desirable properties is required. This article presents an approach to prepare a porous film of silk fibroin–rice starch (SF–RS) modified with trisodium trimetaphosphate (STMP). The preparation was performed using freeze‐drying method aiming to increase the porosity and improve some other properties of the modified porous film. The solutions of SF and RS (5 : 95 weight ratio) and STMP were mixed and adjusted to pH 12 before being neutralized to pH 7 and freeze‐dried for 48 h. Result from the SEM images showed that the average pore size of the SF–RS film increased from 17 to 126 μm after STMP was added up to 5.0% w/w. Similar to the SF–RS–STMP hydrogel, the linkages within the modified SF–RS porous film also occurred mainly between the O? H groups of RS and the triphosphate group of STMP. Moreover, cross‐linking density of the porous film increased with the increasing content of STMP, evidenced from the increase of relative methylene blue adsorption. The addition of STMP also affected the physical properties of the modified porous film such as degree of swelling, oxygen permeability, but not the water solubility. Whereas, the residual ash of the modified porous films was lower than 2.0% and the degradation of the film ceased after soaking in 0.01M PBS solution for about 2 weeks. © 2014 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2015 , 132, 41517.     

Low temperature hydrothermal synthesis of monodispersed flower-like titanate nanosheets

Monodispersed flower-like titanate superstructure was successfully prepared by simple hydrothermal process without any surfactant or template. N₂-sorption analysis, scanning electron microscopy (SEM), and X-ray diffraction (XRD) observation of as-synthesized product revealed the formation of flower-like titanate with diameter of about 250–450 nm and BET surface area (S_BET) of 350.7 m² g^?1. Upon thermal treatment at 500 °C, the titanate nanosheets were converted into anatase TiO₂ with moderate deformation of their structures. The as-prepared flower-like titanate showed high photocatalytic activity for H₂ evolution from water splitting reaction. Moreover, the sample heat treated at 500 °C exhibited higher photocatalytic activity than that of commercial TiO₂ anatase powder (ST-01).     

Simple hydrothermal preparation of nanofibers from a natural ilmenite mineral

Titanate nanofibers were synthesized by a simple hydrothermal method using a natural ilmenite mineral as the starting material. The chemical composition, crystalline structure, shape, size, and specific surface area of the prepared samples were characterized by X-ray fluorescence (XRF), X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and the Brunauer–Emmett–Teller analysis (BET). The crystalline structure of the as-synthesized nanofibers demonstrated a layered titanate form, H₂Ti_xO_2x+1. The length of the prepared nanofibers ranged from 2 to 7 μm with diameters ranging from 20 to 90 nm. The as-synthesized nanofibers were solids with BET surface areas of approximately 50 m²/g. This synthetic method provides a simple route for the fabrication of one-dimensional (1-D) nanostructured materials from a low-cost natural mineral.     

Synthesis and dye-sensitized solar cell performance of nanorods/nanoparticles TiO2 from high surface area nanosheet TiO2

High surface area nanosheet TiO2 with mesoporous structure were synthesized by hydrothermal method at 130 degrees C for 12 h. The samples characterized by XRD, SEM, TEM, SAED, and BET surface area. The nanosheet structure was slightly curved and approximately 50-100 nm in width and several nanometers in thickness. The as-synthesized nanosheet TiO2 had average pore diameter about 3-4 nm. The BET surface area and pore volume of the sample were about 642 m(2)/g and 0.774 cm(3)/g, respectively. The nanosheet structure after calcinations were changed into nanorods/nanoparticles composite with anatase TiO2 structure at 300-500 degrees C (10-15 nm in rods diameter and about 5-10 nm in particles diameter). The solar energy conversion efficiency (eta) of the cell using nanorods/nanoparticles TiO2 (from the nanosheet calcined at 450 degrees C for 2 h) with mesoporous structure was about 7.08% with Jsc of 16.35 mA/cm(2), Voc of 0.703 V and ff of 0.627; while eta of the cell using P-25 reached 5.82% with Jsc of 12.74 mA/cm(2), Voc of 0.704 V, and ff of 0.649.