Pichiah Saravanan

Graphene oxide and Ag engulfed TiO2 nanotube arrays for enhanced electron mobility and visible-light-driven photocatalytic performance

The visible-light-driven photocatalytic degradation of Methylene Blue (MB) and 2-chlorophenol (2-CP) were investigated using the composite of Ag nanoparticles (Ag NPs) and graphene oxide (GO) deposited over TiO2 nanotube arrays (TNTs). The resulting TNTs in the composite showed 100% anatase phase with no occurrence of the rutile phase. An implicit microscopic and spectroscopic technique (FESEM, HRTEM, FTIR and Raman analysis) confirmed the presence of Ag NPs and GO in the composite photocatalyst. It also exhibited an evident shift of the absorption edge in the visible range. The successful depositions of Ag contributed to improved photocatalytic activity in the visible spectrum owing to the existence of localized surface plasmon resonance (LSPR), and further the deposition of GO minimized the recombination of electron–hole pairs. The photocatalytic degradation of both MB and 2-CP followed pseudo-second order kinetics. In the primary run, both MB and 2-CP exhibited almost similar degradation efficiency of 68.3 and 66.8%, respectively. The reusability studies showed a deprived performance for MB degradation than that of 2-CP, due to chemisorption of MB. The prepared composite exhibited significantly larger enhancement in the photocatalytic oxidation of pollutants with greater electrons mobility to reactive sites of GO and Ag.

Palladium nanoparticles anchored to anatase TiO2 for enhanced surface plasmon resonance-stimulated, visible-light-driven photocatalytic activity

Summary Freely assembled palladium nanoparticles (Pd NPs) on titania (TiO2) nano photocatalysts were successfully synthesized through a photodeposition method using natural sunlight. This synthesized heterogeneous photocatalyst (Pd/TiO2) was characterized through field emission scanning electron microscopy (FESEM), high resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD), BET surface area, UV–vis diffuse reflectance spectra (UV-DRS), Raman and photoluminescence (PL) analyses. The simple and smart synthesis anchored well the deposition with controlled Pd NPs size ranging between 17 and 29 nm onto the surface of TiO2. Thus, it gives the characteristic for Pd NPs to absorb light in the visible region obtained through localized surface plasmon resonance (LSPRs). Apparently, the photocatalytic activity of the prepared photocatalysts was evaluated by degrading the endocrine disrupting compound (EDC) amoxicillin (AMX) excited under an artificial visible light source. In the preliminary run, almost complete degradation (97.5%) was achieved in 5 h with 0.5 wt % Pd loading and the degradation followed pseudo-first-order kinetics. The reusability trend proved the photostability of the prepared photocatalysts. Hence, the study provides a new insight about the modification of TiO2 with noble metals in order to enhance the absorption in the visible-light region for superior photocatalytic performance.

Biodegradation of phenol and m-cresol in a batch and fed batch operated internal loop airlift bioreactor by indigenous mixed microbial culture predominantly Pseudomonas sp.

An internal loop airlift reactor (ILALR) is developed and studied for biodegradation of phenol/m-cresol as single and dual substrate systems under batch and fed batch operation using an indigenous mixed microbial strain, predominantly Pseudomonas sp. The results showed that the culture could degrade phenol/m-cresol completely at a maximum concentration of 600mgl(-1) and 400mgl(-1), respectively. Batch ILALR study has revealed that phenol has been preferentially degraded by the microbial culture rather than m-cresol probably owing to the toxic effect of the later. Sum kinetic model evaluated the interaction between the phenol/m-cresol in dual substrate system, which resulted in a high coefficient of determination (R(2)) value >0.98). The fed batch results showed that the strain was able to degrade phenol/m-cresol with maximum individual concentrations 600mgl(-1) each in 26h and 37h, respectively. Moreover for fed batch operation, degradation rates increased with increase in feed concentration without any lag in the degradation profile.

Batch growth kinetics of an indigenous mixed microbial culture utilizing m-cresol as the sole carbon source

An indigenous mixed microbial culture, isolated from a sewage treatment plant located in Guwahati was used to study biodegradation of m-cresol in batch shake flasks. m-Cresol concentration in the growth media was varied from 100mg/L to 900mg/L. The degradation kinetics was found to follow a three-half-order model at all initial m-cresol concentrations with regression values greater than 0.97. A maximum observed specific degradation rate of 0.585h(-1) was observed at 200mg/L m-cresol concentration in the medium. In the range of m-cresol concentrations used in the study, specific growth rate of the culture and specific degradation rates were observed to follow substrate inhibition kinetics. These two rates were fitted to kinetic models of Edward, Haldane, Luong, Han-Levenspiel, and Yano-Koga that are used to explain substrate inhibition on growth of microbial culture. Out of these models Luong and Han-Levenspiel models fitted the experimental data best with lowest root mean square error values. Biokinetic constants estimated from these two models showed good potential of the indigenous mixed culture in degrading m-cresol in wastewaters.

Kinetics of phenol and m-cresol biodegradation by an indigenous mixed microbial culture isolated from a sewage treatment plant

An acclimatized mixed microbial culture, predominantly Pseudomonas sp., was enriched from a sewage treatment plant, and its potential to simultaneously degrade mixtures of phenol and m-cresol was investigated during its growth in batch shake flasks. A 2(2) full factorial design with the two substrates at two different levels and different initial concentration ranges (low and high), was employed to carry out the biodegradation experiments. The substrates phenol and m-cresol were completely utilized within 21 h when present at low concentrations of 100 mg/L for each, and at high concentration of 600 mg/L for each, a maximum time of 187 h was observed for their removal. The biodegradation results also showed that the presence of phenol in low concentration range (100-300 mg/L) did not inhibit m-cresol biodegradation. Whereas the presence of m-cresol inhibited phenol biodegradation by the culture. Moreover, irrespective of the concentrations used, phenol was degraded preferentially and earlier than m-cresol. A sum kinetics model was used to describe the variation in the substrate specific degradation rates, which gave a high coefficient of determination value (R2 > 0.98) at the low concentration range of the substrates. From the estimated interaction parameter values obtained from this model, the inhibitory effect of phenol on m-cresol degradation by the culture was found to be more pronounced compared to that of m-cresol on phenol. This study showed a good potential of the indigenous mixed culture in degrading mixed substrate of phenolics.

Reduced graphene oxide and Ag wrapped TiO2 photocatalyst for enhanced visible light photocatalysis

A well-organised reduced graphene oxide (RGO) and silver (Ag) wrapped TiO2 nano-hybrid was successfully achieved through a facile and easy route. The inherent characteristics of the synthesized RGO-Ag/TiO2 were revealed through crystalline phase, morphology, chemical composition, Raman scattering, UV-visible absorption, and photoluminescence analyses. The adopted synthesis route significantly controlled the uniform formation of silver nanoparticles and contributed for the absorption of light in the visible spectrum through localized surface plasmon resonance effects. The wrapped RGO nanosheets triggered the electron mobility and promoted visible light shift towards red spectrum. The accomplishment of synergised effect of RGO and Ag well degraded Bisphenol A under visible light irradiation with a removal efficiency of 61.9%.

Treatment of phenolics containing synthetic wastewater in an internal loop airlift bioreactor (ILALR) using indigenous mixed strain of Pseudomonas sp. under continuous mode of operation

The scope of this study is to evaluate the performance of internal loop airlift bioreactor (ILALR) in treating synthetic wastewater containing phenol and m-cresol, in single and multi component systems. The microbe utilized in the process was an indigenous mixed strain of Pseudomonas sp. isolated from a wastewater treatment plant. The reactor was operated at both lower and higher hydraulic retention times (HRTs) i.e., 4.1 and 8.3 h, respectively, by providing an inlet feed flow rate of 5 and 10 mL/min. Shock loading experiments were also performed up to a maximum concentration of 800 mg/L for phenol at 8.3 h HRT and 500 mg/L for m-cresol at 4.1 h HRT. The study showed complete degradation of both phenol and m-cresol, when they were degraded individually at a HRT of 8.3 h. Experiments with both phenol and m-cresol present as mixtures were performed based on the 2(2) full factorial design of experiments.

Preparation of Improved p-n Junction NiO/TiO2 Nanotubes for Solar-Energy-Driven Light Photocatalysis

Self-organized TiO2 nanotubes (TNTs) with average inner diameter of 109 nm, wall thickness of 15 nm, and tube length of 7–10 μm were loaded with nickel oxide (NiO) nanoparticles via incipient wet impregnation method. The molar concentration of Ni(NO3)2·6H2O aqueous solution varied in a range of 0.5 M–2.5 M. The samples were characterized for crystalline phase, morphology, topography, chemical composition, Raman shift, and UV-Vis diffusion reflection properties. The finding shows that the loading of NiO did not influence the morphology, structure, and crystalline phase of TNTs but it exhibited significant effect on crystallite size and optical absorption properties. Further, the solar-energy-driven the photocatalytic activity of NiO/TNTs and pure TNTs was evaluated by degrading methylene blue (MB). The results confirm that photocatalytic efficiency of NiO/TNTs is higher than that of TNTs.

Surface chemistry and adsorption mechanism of cadmium ion on activated carbon derived from Garcinia mangostana shell

A detailed surface characterizations and adsorption mechanism of Cd2+ on chemical activated carbon (CAC) prepared from Garnicia mangostana shell were investigated. The activation is accomplished in self-generating atmosphere using phosphoric acid as activating agent. The characterizations performed are elemental analysis, functional group identification, N2 adsorption isotherm and surface charges. Adsorption mechanism of metal ion was tested using Cd2+ as model ion. CAC achieved BET surface area of 1,498 m2/g with a mixture of micro and mesopores. The point of zero charge is observed to be at pH 2.8 and the optimum pH for Cd2+ adsorption on CAC is 12. The adsorption isotherm followed the Freundlich model, and the adsorption kinetics was explained by pseudo-second order kinetic model. From thermodynamic studies, the adsorption was found to be physical adsorption. X-ray photoelectron spectroscopy (XPS) confirmed the adsorption of Cd2+ onto CAC as +2 oxidation state.

Preparation, characterisation and solar photoactivity of titania supported strontium ferrite nanocomposite photocatalyst

Enhanced ferromagnetic and visible light active titanium dioxide (TiO2) photocatalyst was synthesised by depositing a hard ferromagnet strontium ferrite (SrFe12O19) onto TiO2 via an effortless hydrothermal and poly-condensation method. The catalysts were characterised by X-ray diffraction (XRD), transmission electron microscope (TEM), energy dispersive X-ray spectroscopy (EDS), BET surface analysis, vibrating sample magnetometer (VSM), X-ray photon spectroscopy (XPS), Fourier transform infrared spectroscopy (FT-IR) and UV-visible light spectroscopy analysis. The prepared nanocomposite photocatalyst exhibited physically a powerful ferromagnetic property with significant stability against the loss of its magnetic property (coercivity ≈2200 G). The catalyst can be fluidised and recovered by an external magnetic field enhancing separation and mixing efficiency. Furthermore, it resulted in a reduced band gap (≈2.3 eV) which resulted in enhanced visible light absorption compared with unsupported TiO2. The photocatalytic activity was investigated by degrading a recalcitrant phenolic compound, viz., 2, 4-dichlorophenol (2,4-DCP) as model pollutant under different illuminance of daylight. Complete degradation of 2,4-DCP (50 mg/L initial concentration in 0.25 L) was achieved in 120 min (supported photocatalyst) and 180 min (unsupported TiO2) under higher illuminance of sunlight. Likewise under diffused sunlight, 100% degradation of 2,4-DCP was achieved in 240 min for the supported TiO2, while ≥90% degradation could be achieved in 300 min for the unsupported TiO2. The supported nanocomposite was recycled under a permanent magnetic field with a mass recovery of 98% and reused.