Volatile Organic Compound Gas-Sensing Properties of Bimodal Porous α-Fe2O3 with Ultrahigh Sensitivity and Fast Response.

Porous solid with multimodal pore size distribution provides plenty of advantages including large specific surface area and superior mass transportation to achieve high gas-sensing performances. In this study, α-Fe2O3 nanoparticles with bimodal porous structures were prepared successfully through a nanocasting pathway, adopting the bicontinuous 3D cubic symmetry mesoporous silica KIT-6 as the hard template. Its structure and morphology were characterized by X-ray diffraction, nitrogen adsorption-desorption, transmission electron microscopy, and so on. Furthermore, the gas sensor fabricated from this material exhibited excellent gas-sensing performance to several volatile organic compounds (acetone, ethyl acetate, isopropyl alcohol, n-butanol, ethanol, and methanol), such as ultrahigh sensitivity, rapid response speed (less than 10 s) and recovery time, good reproducibility, as well as stability. These would be associated with the desirable pore structure of the material, facilitating the molecules diffusion toward the entire sensing surface, and providing more active sensing sites for analytical gas.

Ordered Large-Pore Mesoporous Cr2O3 with Ultrathin Framework for Formaldehyde Sensing.

A series of ordered mesoporous chromium oxides (Cr2O3) were synthesized by first replicating bicontinuous cubic Ia3d mesoporous silica (KIT-6), then a controlled mesostructural transformation from Ia3d to I4132 symmetry during the replication from KIT-6 to Cr2O3 was achieved by reducing the pore size and interconnectivities of KIT-6, accompanied with an increase in pore size from 3 to 12 nm and a decrease in framework thickness from 8.6 to 5 nm of the resultant Cr2O3 replicas. The gas-sensing behavior of the Cr2O3 replicas toward formaldehyde (HCHO) was systematically investigated. Ordered mesoporous Cr2O3 with both large accessible pores (12 nm) and an ultrathin framework (5 nm) exhibits the best sensing performance, with a response (Rgas/Rair = 119) toward 9 ppm of HCHO 4.4 times higher than that (Rgas/Rair = 27) of its counterpart with small pores and a thick framework. Moreover, it possesses excellent selectivity for detecting HCHO over other interference gases such as CO, benzene, toluene, p-xylene, NH3, H2S, and moisture. The significantly enhanced sensing performance of ordered large-pore mesoporous Cr2O3 with ultrathin framework suggests its great potential for the selective detection of HCHO.

Synthesis of poly (methyl methacrylate)-b-polystyrene with high molecular weight by DPE seeded emulsion polymerization and its application in proton exchange membrane.

In this article, we present poly (methyl methacrylate)-b-polystyrene (PMMA-b-PS) with different block ratios and high molecular weight, which was synthesized by environmentally friendly seeded emulsion polymerization with 1,1-diphenylethylene (DPE) as a chain transfer agent. Polymerization kinetics in the first and second stage was investigated. Stable latex and homogeneous latex particles were obtained with the characterization of laser light scattering (LLS) and transmission electron microscopy (TEM). SEC and (1)H NMR revealed the successful preparation of block copolymers with high molecular weight and two different block ratios. The morphology of microphase separation of block copolymer thin films was investigated by AFM, and long-range order lamellar morphology was observed after vapor-annealing. The block copolymer with block ratio of almost 1:1 and higher molecular weight than that of previous PMMA-b-PS was sulfonated with acetyl sulfate, and the sulfonation was confirmed by FTIR, (1)H NMR, and TGA. Then, the sulfonated PMMA-b-PS was casted as membranes. The electrochemical impedance spectroscopy displayed that membranes possessed favorable proton conductivity and fine dimensional stability, and they could be candidates as proton exchange membranes.

Effect of large pore size of multifunctional mesoporous microsphere on removal of heavy metal ions.

Pore size of mesoporous materials is crucial for their surface grafting. This article develops a novel multifunctional microsphere with a large pore size mesoporous silica shell (ca. 10.3 nm) and a magnetic core (Fe3O4), which is fabricated using cetyltrimethylammonium bromide (CTAB) as pore-forming agents, tetraethyl orthosilicate (TEOS) as silicon source through a sol-gel process. Compared with small pore size mesoporous silica magnetic microspheres (ca. 2-4 nm), the large pore size one can graft 447 mg/g amino groups in order to adsorb more heavy metal ions (Pb(2+): 880.6 mg/g, Cu(2+): 628.3mg/g, Cd(2+): 492.4 mg/g). The metal-loaded multifunctional microspheres could be easily removed from aqueous solution by magnetic separation and regenerated easily by acid treatment. The results suggest that the large pore size multifunctional microspheres are potentially useful materials for high effectively adsorbing and removing different heavy metal ions in aqueous solution.

Fabrication of one-dimensional Fe3O4/P(GMA-DVB) nanochains by magnetic-field-induced precipitation polymerization.

One-dimensional (1D) magnetic Fe(3)O(4)/P(GMA-DVB) peapod-like nanochains have been successfully synthesized by magnetic-field-induced precipitation polymerization using Fe(3)O(4) as building blocks and P(GMA-DVB) as linker. The Fe(3)O(4) microspheres without surface modification can be arranged with the direction of the external magnetic field in a line via the dipolar interaction between Fe(3)O(4) microspheres and linked permanently via P(GMA-DVB) coating during precipitation polymerization. The length of peapod-like nanochains can be controlled by magnetic field intensity, and the thickness of polymer shell can be tuned by the amount of monomers. Magnetic measurement revealed that these 1D peapod-like nanochains showed highly magnetic sensitivity. In the presence of magnetic field, 1D magnetic Fe(3)O(4)/P(GMA-DVB) peapod-like nanochains can be oriented and aligned along the direction of external magnetic field.

Comprehensive study of mesoporous carbon functionalized with carboxylate groups and magnetic nanoparticles as a promising adsorbent.

Highly ordered mesoporous carbon functionalized with carboxylate groups and magnetic nanoparticles has been successfully synthesized. By oxidative treatment using (NH(4))(2)S(2)O(8) and H(2)SO(4) mixed solution, numerous hydrophilic groups were created in the mesopores without destroying the ordered mesostructure of CMK-3. Through the in situ reduction in Fe(3+), magnetic nanoparticles were successfully introduced into the mesopores, resulting in the multifunctional mesoporous carbon Fe-CMK-3. The obtained hybrid carbon material possesses ordered mesostructure, high Brunauer-Emmett-Teller (BET) surface area up to 1013 m(2)/g, large pore volume of about 1.16 cm(3)/g, carboxylic surface, and excellent magnetic property. When used as an adsorbent, Fe-CMK-3 exhibits excellent performances for removing toxic organic compounds from waster-water, with a high adsorption capacity, an extremely rapid adsorption rate, and an easy magnetically separable process. In the case of requiring emergency removal of large amount of organic pollutants in aqueous, the hybrid carbon adsorbent would be an ideal choice.