Enhanced hydrogen sorption in single walled carbon nanotube incorporated MIL-101 composite metal-organic framework

Metal-Organic Frameworks (MOFs) have emerged as potential hydrogen storage media due to their high surface area, pore volume and adjustable pore sizes. The large void space generated by cages in MOFs is not completely utilized for hydrogen storage application owing to weak interactions between the walls of MOFs and H₂ molecules. These unutilized volumes in MOFs can be effectively utilized by incorporation of other microporous materials such as single walled carbon nanotubes into the pores of MOFs which could effectively tune the pore size and pore volume of the material towards hydrogen sorption. Single walled carbon nanotubes (SWNT) incorporated MIL-101 composite MOF material (SWNT@MIL-101) was synthesized by adding purified single walled carbon nanotube (SWNT) in situ during the synthesis of MIL-101. The powder X-ray diffraction patterns of SWNT@MIL-101 showed the structure of MOF was not disturbed by SWNT incorporation. Hydrogen sorption capacities of MIL-101 was observed to increase from 6.37 to 9.18 wt% at 77 K up to 60 bar and from 0.23 to 0.64 wt% at 298 K up to 60 bar. The increment in the hydrogen uptake capacities of composite MOF materials was attributed to the decrease in the pore size and enhancement of micropore volume of MIL-101 by single walled carbon nanotube incorporation.     

Synthesis of submicron size hollow carbon spheres by a chemical reduction — solvothermal method using carbon tetrachloride as carbon source

A simple, rapid and energy efficient approach based on copper mediated chemical reduction — solvothermal method was employed to prepare submicron size hollow carbon spheres (SHCS) using carbon tetrachloride as carbon source. The obtained SHCS were characterized by means of various physico-chemical techniques like nitrogen adsorption-desorption measurements at 77 K, XRD, SEM, TEM, EDX and FT-Raman techniques. Thus characterized samples displayed macroporous nature of carbon with carbon and chloride contents of about 73% and 12% on atomic basis respectively. The presence of chloride content may open new avenues for surface modifications of SHCS in the area of catalysis and separation science.     

Molecular beam epitaxial HgCdTe material characteristics and device performance: Reproducibility status

Extensive material, device, and focal plane array (FPA) reproducibility data are presented to demonstrate significant advances made in the molecular beam epitaxial (MBE) HgCdTe technology. Excellent control of the composition, growth rate, layer thickness, doping concentration, dislocation density, and transport characteristics has been demonstrated. A change in the bandgap is readily achieved by adjusting the beam fluxes, demonstrating the flexibility of MBE in responding to the needs of infrared detection applications in various spectral bands. High performance of photodiodes fabricated on MBE HgCdTe layers reflects on the overall quality of the grown material. The photodiodes were planar p-on-n junctions fabricated by As ion-implantation into indium doped, n-type, in situ grown double layer heterostructures. At 77K, diodes fabricated on MBE Hg_1−xCd_xTe with x ≈ 0.30 (λ_co ≈ 5.6 μm), x ≈ 0.26 (λ_co ≈ 7 μm), x ≈ 0.23 (λ_co ≈ 10 μm) show R₀A products in excess of 1 x 10⁶ ohm-cm², 7 x 10⁵ ohm-cm², and 3 x 10² ohm-cm², respectively. These devices also show high quantum efficiency. As a means to assess the uniformity of the MBE HgCdTe material, two-dimensional 64 x 64 and 128 x 128 mosaic detector arrays were hybridized to Si multiplexers. These focal plane arrays show an operability as high as 97% at 77K for the x ≈ 0.23 spectral band and 93% at 77K for the x ≈ 0.26 spectral band. The operability is limited partly by the density of void-type defects that are present in the MBE grown layers and are easily identified under an optical microscope.     

Automatic classification of sleep stages based on the time-frequency image of EEG signals

In this paper, a new method for automatic sleep stage classification based on time-frequency image (TFI) of electroencephalogram (EEG) signals is proposed. Automatic classification of sleep stages is an important part for diagnosis and treatment of sleep disorders. The smoothed pseudo Wigner–Ville distribution (SPWVD) based time-frequency representation (TFR) of EEG signal has been used to obtain the time-frequency image (TFI). The segmentation of TFI has been performed based on the frequency-bands of the rhythms of EEG signals. The features derived from the histogram of segmented TFI have been used as an input feature set to multiclass least squares support vector machines (MC-LS-SVM) together with the radial basis function (RBF), Mexican hat wavelet, and Morlet wavelet kernel functions for automatic classification of sleep stages from EEG signals. The experimental results are presented to show the effectiveness of the proposed method for classification of sleep stages from EEG signals.     

Cobalt catalyzed hydroformylation of higher olefins in the presence of chemically modified cyclodextrins

The cobalt catalyzed hydroformylation of higher olefins in the presence of chemically modified cyclodextrins was investigated in an aqueous biphasic system. The effect of various parameters, such as the nature of the cyclodextrin and olefin, the temperature, the CO/H₂ pressure, the concentration of the cyclodextrin and TPPTS was studied. The results demonstrate that the partially methylated β-cyclodextrin gives good conversion (>92%) and selectivity (>92%) for the hydroformylation of higher olefins without impeding the recovery of the catalytic system.     

Influences of Mesoporosity Generation in ZSM-5 and Zeolite Beta on Catalytic Performance During <Emphasis Type="Italic">n</Emphasis>-Hexane Isomerization

Abstract  

Catalytic performance of Pt impregnated parent and desilicated nano-crystalline zeolites, ZSM-5 and Beta for n-hexane isomerization was studied. Difference in channel systems of the zeolites and absence/presence of mesopores therein were found to be reflected in product distributions. ZSM-5 was desilicated by NaOH and zeolite Beta with tetramethylammonium hydroxide (TMAOH.) Desilication was found to afford comparable catalytic performance to that of the parent counterpart at reaction temperature lower by 25 °C. Observed product distributions could be substantiated with characterizations such as ammonia TPD, surface area determination and SEM. Desilicated zeolite Beta was seen to be less prone to coking as deduced from the TGA study. Location of Pt with reference to proton sites within the channels and that inside the pores viz a viz external surface also have been discussed briefly.     

Effects of Doping Trivalent Ions in Bismuth Borate Glasses

Bismuth borate glasses from the system: 40Bi₂O₃–59B₂O₃–1Tv₂O₃ (where Tv=Al, Y, Nd, Sm, and Eu) and three glasses of composition: 40Bi₂O₃–60B₂O₃, 37.5Bi₂O₃–62.5B₂O₃ and 38Bi₂O₃–60B₂O₃–2Al₂O₃ were prepared by melt quenching and characterized by density, UV-visible absorption spectroscopy and differential thermal analysis (DTA) studies. Bismuth borate glasses exhibit a very strong optical absorption band just below their absorption edge. Glasses were devitrified by heat treatment at temperatures above their glass transition temperatures and the crystalline phases produced in them were characterized by Fourier transform infrared (FTIR) absorption spectroscopy and X-ray diffraction (XRD). Bi₃B₅O₁₂ was found to be the most abundant phase in all devitrified samples. DTA studies on glasses and FTIR and XRD analysis on crystallized samples revealed that very small amounts of trivalent ion doping causes significant changes in the devitrification properties of bismuth borate glasses; rare-earth ions promote the formation of metastable BiBO₃–I and BiBO₃–II phases during glass crystallization.     

Study of uranium sorption using D2EHPA‐impregnated polymeric beads

The extractant‐impregnated polymeric beads (EIPBs), containing Di(2‐ethylhexyl) phosphonic acid (D2EHPA) as an extractant and polyethersulfone as base polymer, were prepared by phase‐inversion method. These beads were characterized by fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), and scanning electron microscope (SEM) analysis to gain insight into the composition and morphology of beads. The beads exhibited good acid stability as no significant structural deformation or leaching out of the extractant was observed in 6M HNO₃ solution, up to the studied equilibration time of 15 days. The synthesized EIPBs were evaluated, for their ability to absorb uranium from aqueous solution, at different concentration and pH values. The kinetics measurement showed that about 90 min of equilibration time was enough to remove saturation amount of uranium from the solution. Kinetic modeling analysis of the extraction results was carried out using pseudo‐first‐order, pseudo‐second‐order, and intraparticle diffusion equations and the corresponding rate constants were determined. The equilibrium data were fitted into different isotherm models and were found to be represented well by the Freundlich isotherm equation. Reusability of the beads was also established by multiple sorption–desorption experiments. © 2013 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 130: 3355–3364, 2013