Properties of raw sawdust ofParkia biglobosa, as a biosorbent for the removal of Acid Blue 161 dye in single, binary, and ternary dye systems with Rhodamine B and Methylene Blue dyes in aqueous solution, were investigated. The sawdust was characterized using Scanning Electron Microscopy, Fourier Transform Infrared spectrophotometry, X-ray diffraction, and pH point of zero charge. Batch adsorption experiments were carried out to determine the equilibrium characteristics, thermodynamics, and kinetics of the sorption processes. The data obtained were subjected to various isotherm and kinetics equations. The results showed that the adsorption processes were described by different isotherm models depending on the composition of the system; they were all spontaneous (ΔGranges from −0.72 to −5.36 kJ/mol) and endothermic (range ofΔHis 11.37–26.31 kJ/mol) and with increased randomness withΔSvalues of 55.55 and 98.78 J·mol/K for single and ternary systems, respectively. Pseudo-second-order kinetics model gave better fit for all the sorption systems studied irrespective of the differences in composition, with the initial and overall rate constants higher for the mixtures than for the single system (6.76 g·mg−1min−1). The presence of Rhodamine B and Methylene Blue had a synergetic effect on the maximum monolayer capacity of the adsorbent for Acid Blue 161 dye.
Linear low density polyethylene (LLDPE) exhibits a complex molecular structure that is characterized by molar mass and chemical composition distributions. Both molecular parameters complementarily influence the final application properties. Typically, the molecular structure of commercial polyolefins is characterized by a set of technical parameters including the melt flow index, the crystallization and melting temperatures and the comonomer content as obtained using Fourier transform infrared or NMR spectroscopy. LLDPEs with high comonomer contents are typically regarded as plastomers or elastomers. Due to their low crystallinities, characterization of these materials using crystallization‐based analytical techniques is of limited use since the majority of the material is rather amorphous. Such materials need specific alternative analytical methods that may be based on molar mass and/or chemical composition fractionation. Here it is shown that for a comprehensive analysis of LLDPEs with similar bulk properties, preparative molar mass fractionation (pMMF) and advanced analysis of the fractions are required. The pMMF fractions are comprehensively analyzed using size exclusion chromatography, differential scanning calorimetry and high‐temperature high‐performance liquid chromatography to provide detailed information on molar mass and copolymer composition. Correlated information of these molecular parameters is obtained by comprehensive two‐dimensional liquid chromatography. © 2019 Society of Chemical Industry
The photocatalytic activities of TiO2 have been limited mainly to absorbing in the ultraviolet spectrum which accounts for only 5% of solar radiation. High energy band gap and electron recombination in TiO2 nanoparticles are responsible for its limitations as a photocatalyst. An oxygen deficient surface can be artificially created on the titanium oxide by zero valent nano iron through the donation of its excess electrons. A visible light active TiO2 nanoparticle was synthesized in the current investigation through simple chemical reduction using sodium boro-hydride. The physical and textural properties of the synthesized oxygen deficient TiO2 photocatalyst was measured using scanning/ transmission electron microscopy while FTIR, XRD and nitrogen sorption methods (BET) were employed for its further characterizations. Photochemical decoloration of orange II sodium dye solution in the presence of the synthesized TiO2 was measured using an UV spectrophotometer. The resulting oxygen deficient TiO2 has a lower energy band-gap, smaller pore sizes, and enhanced photo-catalytic properties. The decoloration (88%) of orange (II) sodium salt solution (pH 2) under simulated solar light was possible at 20 min. This study highlights the effect of surface oxygen defects, crystal size and energy band-gap on the photo-catalytical property of TiO2 nanoparticles as impacted by nano zero valent iron. It opens a new window in the exploitation of instability in the dopant ions for creation of a visible light active TiO2 photocatalyst.
The spatial and seasonal distribution of eight US Environmental Protection Agency priority poly aromatic hydrocarbons (PAHs); namely benzo(b)fluoranthene, benzo(a)pyrene, indeno(1,2,3-cd)pyrene, benzo(k)fluoranthene, chrysene, benzo(a)anthracene, dibenz(a,h)anthracene and fluoranthene were investigated in 35 soil samples. Gas chromatography with flame ionization detection was used for the quantification of the PAHs in the residential, roadside and industrial soil samples collected in proximity to an industrial area, including a petrochemical plant, in Cape Town. The sum of the concentrations of the detected PAHs (RPAHs) in winter ranged between nd (not detected) and 13.88 mg/kg, with a mean concentration of 4.08 mg/kg and a standard deviation of distribution of 2.64 mg/kg, while in summer, RPAHs ranged between nd and 10.43 mg/kg, with a mean concentration of 0.50 mg/kg and standard deviation of distribution 1.83 mg/kg. The presence and concentration level of the PAHs detected in the soil samples vary significantly under climatic change (p \ 0.05). The maximum concentrations of individual PAHs in the soil samples were higher in winter compared to the maximum concentrations of the PAHs detected in summer. The diagnostic ratios of selected PAH compounds showed that petrogenic processes were the most likely sources of the PAH compounds in the soil samples. In summer and winter, the total PAH concentration increased in order of residential soil \ industrial soil B roadside soil.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.
hi@scite.ai
10624 S. Eastern Ave., Ste. A-614
Henderson, NV 89052, USA
Copyright © 2024 scite LLC. All rights reserved.
Made with 💙 for researchers
Part of the Research Solutions Family.