Zinc oxide-decorated multiwalled carbon nanotubes: a selective electrochemical sensor for the detection of Pb(II) ion in aqueous media

Journal of Materials Science: Materials in Electronics - Multiwalled carbon nanotubes, due to high conductivity, stability, and large specific surface area, have a potential ability to promote...     

Effect of Li<Subscript>2</Subscript>O on the Refractive Index and Optical Band Gap of Cadmium Phosphate Glasses

A series of lithium cadmium phosphate glasses having composition (mol %) xLi₂O-(50 ? x)CdO-50P₂O₅ were prepared in a platinum crucible by the melt quenching technique. The quantity x varies in the range 0–40. The mass density and refractive index of these glasses were found in the ranges 3.95–2.89 g/cm₃ and 1.55–1.40, respectively. The optical absorbance studies were also carried out on these glasses to measure their energy gaps. The absorption spectra of these glasses were recorded in the UV-visible range. No sharp edges were found in the optical spectra, which verifies the amorphous nature of these glasses. The optical band gap energies for these glasses were found to be in the range 2.58–3.5 eV. It was observed that the density, the refractive index, and the optical band gap energy decrease with increasing amount of lithium oxide. The band tailing, worked out from the Urbach plots, shows an increase with increasing Li₂O content and lies in the range 0.47–0.78 eV. The absorption coefficient is observed to show an exponential dependence on the photon energy.     

Synthesis and evaluating of carbon nanoallotrope-biomacromolecule gel composites as drug delivery systems

This work was done to assess the role of precursors (agro and graphite) on performance of carbon nanoallotropes-biomacromolecules composite as drug delivery for controlling the release of niacin. In this respect graphene oxide and bagasse-based carbon oxide were synthesized and chelated with chitosan (Cs-GO and Cs-Co). These gel composites were characterized by many techniques [morphology, differential scanning calorimetry, Fourier-transform infrared spectroscopy, swelling, encapsulation efficiency (EE) and loading (L) % of niacin. Another series of experiments was carried out for studying the role of replacing part of carbon nanoallotrope by carboxymethyl cellulose (CMC) on performance of produced drug carries, these systems were coded as Cs-GO-CMC and Cs-Co-CMC. The data showed that, the Cs-GO gel composite provided maximum release of NA, at 5 h, for pH's simulated gastric and intestinal fluids; pH. 2.1 and pH 7.4 (1120 mg/L and 757 mg/L). The incorporation of CMC is not acceptable as it provided low drug release together with burst release of NA-drug, and consequently possible caused tissue irritation or toxicity in the human body. The Cs-GO and Cs-CO systems with relatively low drug loading were recommended for their better controllability system to NA release, which prolonging benefit of human with niacin. The NA release from all investigated gels followed Fickian and non-Fickian diffusion mechanisms.     

Remote sensing of canopy light use efficiency in temperate and boreal forests of North America using MODIS imagery

Light use efficiency (LUE) is an important variable characterizing plant eco-physiological functions and refers to the efficiency at which absorbed solar radiation is converted into photosynthates. The estimation of LUE at regional to global scales would be a significant advantage for global carbon cycle research. Traditional methods for canopy level LUE determination require meteorological inputs which cannot be easily obtained by remote sensing. Here we propose a new algorithm that incorporates the enhanced vegetation index (EVI) and a modified form of land surface temperature (T_m) for the estimation of monthly forest LUE based on Moderate Resolution Imaging Spectroradiometer (MODIS) imagery. Results demonstrate that a model based on EVI × T_m parameterized from ten forest sites can provide reasonable estimates of monthly LUE for temperate and boreal forest ecosystems in North America with an R² of 0.51 (p < 0.001) for the overall dataset. The regression coefficients (a, b) of the LUE–EVI × T_m correlation for these ten sites have been found to be closely correlated with the average EVI (EVI_ave, R² = 0.68, p = 0.003) and the minimum land surface temperature (LST_min, R² = 0.81, p = 0.009), providing a possible approach for model calibration. The calibrated model shows comparably good estimates of LUE for another ten independent forest ecosystems with an overall root mean square error (RMSE) of 0.055 g C per mol photosynthetically active radiation. These results are especially important for the evergreen species due to their limited variability in canopy greenness. The usefulness of this new LUE algorithm is further validated for the estimation of gross primary production (GPP) at these sites with an RMSE of 37.6 g C m^? 2 month^? 1 for all observations, which reflects a 28% improvement over the standard MODIS GPP products. These analyses should be helpful in the further development of ecosystem remote sensing methods and improving our understanding of the responses of various ecosystems to climate change.     

Synthesis and characterization of niobium-doped potassium tetragonal tungsten bronzes, KxNbyW1?yO3

Needle-shaped crystals of sizes up to 5 μm × 5 μm × 40 μm of nominal composition K _x Nb _y W_1−y O₃ were synthesized by solid state method at 800 °C using appropriate amount of WO₃, WO₂, Nb₂O₅, and K₂WO₄. The samples were characterized with XRD, SEM, microprobe analysis, optical spectroscopy, and Raman spectroscopy. The XRD patterns of the samples show single phase of tetragonal tungsten bronze (TTB) type (P4/mbm, No. 127) up to y = 0.07. Structure refinements reveal an increase in cell parameter with increasing nominal niobium content within the TTB phase. The elemental compositions of the crystals determined by electron microprobe analysis also show an increase in Nb content with increasing y. With increasing Nb content the reflectivity minimum in the near infrared spectral range shifts towards lower wavenumber indicating the effect of decreasing carrier concentration. Pyrochlore type phase (KNbWO₆) is obtained as a second phase when nominal composition y > 0.07.     

Comparative Study of the Kinetic Degradation of Differently Decrystallized Cotton Linters Using Nonisothermal DTA Curves

Cellulose samples of different degree of decrystallization were subjected to differential thermal analysis (DTA) technique under nonisothermal conditions. The samples were prepared by preswelling the cotton linters in 24-Baumé NaOH followed by the use of direct or indirect methods to dry the mercerized cotton. The thermal stabilities of the samples were estimated taking into account the values of initial decomposition temperature, maximum decomposition temperature, and activation energy. The activation energy preexponential constant, order of reaction, and other thermodynamic parameters (ΔH, ΔS, and ΔG) associated with each stage were derived by applying integrated peak areas (Satava and Skvara), the Borchart—Daniels general method, and the Prount—Tompkins equation. The results showed that the cellulose pyrolysis process cannot be described as having a single value of E _a over the entire pyrolysis range. Also, the decrystallization caused by destruction of the formed alkali cellulose complex with a isopropanol—water (WAN) system was found to be the most pronounced change in pyrolytic parameters (i.e., less thermal stability) compared with native and other decrystallized samples. The dependence of E _a on IR measurements is also discussed.     

Transitional Phases at Ceramic–Metal Interfaces: Orthorhombic, Cubic, and Hexagonal Ti-Si-Cu-N Compounds

Reaction products at the boundary between Si₃N₄ and Ag-Cu-Ti braze alloy have been characterized by transmission electron microscopy. Beyond the TiN adjoining the Si₃N₄ substrate is a continuous layer of a previously unreported, orthorhombic Ti-Si-Cu-N compound. Evidence of additional cubic and hexagonal Ti-Si-Cu-N phases is also found; these exist as isolated grains farther from the substrate. The cubic compound is probably an η-type M₆X phase of the sort observed at other ceramic-metal interfaces. These "dilute ceramics," in which metallic constituents dominate, are common transitional phases in ceramic-metal systems.     

Structural Studies of Anomalous Behavior in the Silica-Alumina Gel System

This paper compares the structure ofAl₂O₃-SiO₂ xerogels prepared with Al₂O₃ contents ranging from 21 to 75 wt% (13 to 64 mol%). The 47 wt% Al₂O₃ xerogel (Al/Si ≅ 1) exhibits anomalously low surface area (≅1 m²/g) and skeletal density compared with other Al₂O₃-Si₂ compositions. Based on the results of nitrogen adsorption/condensation, helium displacement, high-resolution transmission electron microscopy (HRTEM), small-angle X-ray scattering (SAXS), and small-angle neutron scattering (SANS), we attribute the low surface area and skeletal density (density of the solid phase which is inaccessable to helium) to the formation of closed micropores, whereas the higher surface area materials exhibit a slightly coarser texture comprising open pores with radii of ≅1 nm. X-ray diffraction (XRD) and ²⁹SI and ²⁷Al magic-angle spinning nuclear magnetic resonance (MASNMR) indicate no anomalous behavior in the 47% sample on molecular length scales. HRTEM indicates the presence of a small fraction of crystallites which is supported by the SAXS results, but it is unknown if this crystallinity is related to low surface area. Low-field ¹H NMR spin-lattice relaxation measurements show that the physical structure of all of the 'wet' gels is similar implying that pore closure occurs during drying. Consistent with this idea, gel surface area and density increased significantly when the pore fluid (water) was replaced with a lower surface tension fluid (formamide, dioxane, ethanol. water/surfactant).     

Some Semiconductor Properties of Carboxymethyl Cellulose-Copper Complexes

Metal chelates of three grades of carboxymethyl cellulose (CMC) (LI-L3) with Cu(II) ions, either originating from CuCl₂ or CuSO₄, were prepared and characterized by elemental analysis, infrared spectra, and electrical conductivity studies. The results showed that the degree of substitution of CMCs and the origin of the Cu(II) ion have a profound effect on the amount of metal included in the polymer complexes and the structure and the electrical conductivity of the prepared complexes. CMC acts as a uninegatively charged bidentate ligand when it is chelated with Cu(II) of CuCl₂ via the carboxymethyl group and exhibits the formula Cu(L)₂, whereas it acts as a binegatively charged bitentate ligand when it is chelated with CuSO₄ via the carboxymethyl and secondary hydroxyl groups and exhibits the formula CuL.2H₂O. The investigation revealed that the electrical conductivity depends on the temperature and has two maximum peaks. The values of the activation energy for the conductivity of CMC and their complexes indicated that the samples changed from a low-semiconductor to a high-semiconductor property with heating. It is found that CMC-Cu(II) complexes formed from CuSO₄ exhibit a high-semiconductor property compared to complexes derived from CuCl₂.