Sol-Gel to Prepare Nickel Doped TiO2 Nanoparticles for Photocatalytic Treatment of E 131 VF Food Dye Wastewater

Sol–gel method was applied for synthesis of TiO2 nanoparticles in the existence of different volumes of ethanol (10–50 mL) with the purpose to find optimized synthesis conditions. Also, nickel doped TiO2 nanoparticles (Ni/TiO2 molar ratio: 0.1-1.0%) were prepared by the similar technique but in the existence of 10 mL ethanol and heated at different temperatures (300 °C –600 °C). XRD, SEM/EDX, UV-Vis DRS, FTIR and Raman spectroscopy were applied to identify the structural and morphological characteristics of the as-synthesized samples. XR diffraction results verified that TiO2 samples prepared with various volumes of ethanol (10–50 mL) consist of anatase and brookite phases up to 500 °C and rutile phase at 600 °C. The intensity of brookite diffraction decreased with the increase of calcination temperatures. Also, the low ethanol volume favored for formation of rutile phase at 600 °C. The addition of Ni(II) during the preparation of TiO2 nanoparticles prevented the formation of rutile phase. The undoped samples were synthesized with 10 and 20 mL ethanol and treated at 500 °C displayed the best catalytic performance for photocatalytic treatment of E 131 VF dye solution (rate constant: 0.051 and 0.061 (a.u) respectively). Ni doped TiO2 samples displayed lower photoactivity and rate constant

Photocatalytic Treatment of Synthetic Wastewater Containing 2,4 dichlorophenol by Ternary MWCNTs /Co-TiO2 Nanocomposite Under Visible Light

In this work, multi-walled carbon nanotubes (MWCNTs)/Co-TiO2 nanocomposites were synthesized and investigated for photocatalytic degradation of 2,4-dichlorophenol (2,4-DCP) under visible light. Characterization of photocatalysts was done by means of XRD, FT-IR and SEM/EDX techniques. Obtained results showed cobalt doping can inhibit phase transformation from anatase to rutile and eliminate the recombination of electron-hole pairs. The presence of MWCNTs can both increase the photoactivity and change surface properties to achieve sensitivity to visible light. The optimum mass ratio of MWCNTs and cobalt (Co) dopant in TiO2 was the prominent factor to harvest MWCNTs/Co-TiO2 photocatalyst. The sample containing 3.13 wt% cobalt exhibited the highest activity under visible light for 2,4-DCP degradation, which was completed within 180 min using a 0.1 g/L dose of this photocatalyst in a 40 mg/L solution of the 2,4-DCP. The reactions follow the first-order kinetics. The reaction intermediates were identified by GC–MS technique. GC–MS analysis showed the major intermediates of 2,4-DCP degradation are simple acids like oxalic acid, acetic acid, etc. as the final products

Silver Doped TiO2 Nanoparticles: Preparation, Characterization and Efficient Degradation of 2,4-dichlorophenol Under Visible Light

Hydrothermally synthesized TiO2 nanoparticles containing different amounts of silver were characterized by X-Ray diffraction (XRD), Fourier transform infrared (FT-IR) and scanning electron microscopy equipped with energy dispersive X-ray microanalysis (SEM/EDX) techniques. XRD results showed prepared samples include 100% anatase phase. The presence of silver in TiO2 nanoparticle network was established by XRD, SEM/EDX and FT-IR techniques. The photocatalytic performance of the prepared catalysts was tested for the degradation of 2,4-dichlorophenol (2,4-DCP) under visible light.. The experiments demonstrated that 2,4-DCP was effectively degraded in the presence of Ag/TiO2 samples. It was confirmed that the presence of Ag on TiO2 catalysts could enhance the photocatalytic degradation of 2,4-DCP in aqueous suspension. It was found that an optimal dosage of 1.68 wt% Ag in TiO2 achieved the fastest 2,4-DCP degradation (95% after 180 min irradiation) under the experimental conditions. On the basis of various characterizations of the photocatalysts, the reactions involved to explain the photocatalytic activity enhancement due to Ag doping include a better separation of photogenerated charge carriers. GC-MS analysis showed the major intermediates of 2,4-DCP degradation are simple acids like oxalic acid, acetic acid, etc. as the final products

Alkali treated Foumanat tea waste as an efficient adsorbent for methylene blue adsorption from aqueous solution

The adsorption of methylene blue (MB) from aqueous solution by alkali treated Foumanat tea waste (ATFTW) from agriculture biomass was investigated. The adsorbent was characterized by Scanning Electron Microscopy (SEM), Fourier Transform-Infrared Spectroscopy (FT-IR) and nitrogen physisorption. FTIR results showed complexation and ion exchange appear to be the principle mechanism for MB adsorption. The adsorption isotherm data were fitted to Langmuir, Sips, Redlich-Peterson and Freundlich equations, and the Langmuir adsorption capacity, Qmax was found to be 461 mgg−1. It was found that the adsorption of MB increases by increasing temperature from 303 to 323 K and the process is endothermic in nature. The removal of MB by ATFTW followed pseudo-second order reaction kinetics based on Lagergren equations. Mechanism studies indicated that the adsorption of MB on the ATFTW was mainly governed by external mass transport where particle diffusion was the rate limiting step

Efficient removal of tizanidine and tetracycline from water: A single and competitive sorption approach using carboxymethyl cellulose granulated iron-pillared clay

This study deals with the development of a granulated Fe-pillared clay (Fe-PC) using carboxymethylcellulose (CMC) as a binder to present it as an innovative adsorbent for the individual and competitive adsorption of tetracycline (Tc) and tizanidine (Tz) from water. An optimum pH value of 7 was determined for both individual and multi-component adsorption. The optimal dosage of granulated Fe-PC was determined to be 1.5 g/L for Tz and 3 g/L for Tc, resulting in constant removal rates of 80 % for Tc and 90 % for Tz. Tizanidine showed a higher affinity for powdered or granulated Fe-PC compared to tetracycline, due to its smaller molecular size and increased amine functional groups. Consequently, Tz showed improved kinetic rates (initial pseudo-second order sorption rates of 170.79 and 25.62 mg/g.h for Tz and Tc, respectively) and equilibrium capacities (maximum monolayer adsorption capacity of granulated Fe-PC at room temperature over Tc and Tz, 54.89 mg/g and 66.40 mg/g). Granulation affected the kinetic rate for both adsorbates, albeit with a more pronounced effect for Tc. The adsorption of Tz was less sensitive to temperature changes, indicating a lower enthalpy change of adsorption (14.24 and 77.91 kJ/mol for Tz and Tc, respectively). HCl for Tc and NaCl for Tz were identified as optimal desorption eluents, confirming the involvement of cation exchange in Tz adsorption. Surface functional group analysis confirmed the proposed complexation mechanisms. Tz consistently showed a higher affinity for granular Fe-PC than Tc, especially at lower adsorbent dosages. This article provides a comprehensive insight into the characterization of the prepared adsorbents and their cyclic adsorption-desorption performance for Tc and Tz