Simultaneous S-scheme promoted Ag@AgVO3/g-C3N4/CeVO4 heterojunction with enhanced charge separation and photo redox ability towards solar photocatalysis.

Photocatalytic removal of toxic contaminants is one of the emerging techniques for water remediation, but it suffers from low redox ability, charge recombination and poor light harvesting efficiency. The present work reports a simultaneous S-scheme promoted by CeVO4/g-C3N4/Ag@AgVO3. The formation of the S-scheme mechanism enhanced the generation of photogenerated carriers and also improved the redox ability of the electrons and holes in the reduction and oxidation photocatalysts. The ternary demonstrated remarkable photo switching properties along with efficient charge separation which was achieved through dual interfacial interaction within the ternary (Ag@AgVO3/g-C3N4 and CeVO4/g-C3N4). The heterojunction formation was verified through the shift in binding energy spectra in the X-ray Photoelectron spectroscopy (XPS), and high-resolution transmission electron microscopy analysis (HR-TEM). The ternary demonstrated reduced PL intensity, width of space charge region and an upsurge in photogenerated current density in the order of 93 µA/cm2 (∼6X higher than all the pristine). This resulted in efficient removal of methyl orange, methylene blue and endocrine disruptive bisphenol-A with a removal rate of 0.02 min-1, 0.03 min-1 and 0.0087 min-1 and an apparent quantum yield of 4.6 × 10-9 (Methylene Orange), 6.89 × 10-9 (Methylene Blue) and 2 × 10-9 (Bisphenol A/H2O2).

ZIF-67 blended PVDF membrane for improved Congo red removal and antifouling properties: A correlation establishment between morphological features and ultra-filtration parameters.

Dye effluents from various sectors have constantly imperilled the environment and ecosystem. Nano-composite membrane technology incorporating metal-organic frameworks (MOFs) has shown tremendous potential for toxic pollutant remediation. This study details the impact of ZIF-67 MOF nanoparticles on the structural properties of polyvinylidene fluoride (PVDF) ultrafiltration membrane during the non-solvent induced phase separation (NIPS) process. In order to outline the properties that determine the performance parameters in a MOF-modified mixed matrix membrane, the corresponding changes in mean pore size (MPS), surface porosity, solvent viscosity, and hydrophilicity have been discussed with appropriate surface characterization analysis. The suitability of ZIF-67 as filler nanoparticles were established based on polymer compatibility, dispersibility, and water stability studies. The ZIF-67 incorporated PVDF mixed matrix membranes (MMM) showed 99.5% CR dye removal with 2.6 times DI water permeability than the neat. The flux recovery ratio (FRR) improved by 1.9 times and the membranes were found suitable for up to 5 filtration cycles. Based on the overall results, a correlation analysis between the MMM surface properties and membrane performance parameters were established to determine the key performance parameters. It was observed that in comparison to MPS, surface porosity was more correlated to Jd/Jw (r = 0.96) and FRR (r = 0.95).

Z-scheme promoted heterojunction photocatalyst (Ag@AgVO3 /rGO/CeVO4) with improved interfacial charge transfer for efficient removal of aqueous organics irradiated under LED light.

A facile hydrothermal route was followed to obtain a ternary composite Ag@AgVO3/rGO/CeVO4 with in-situ deposition of Ag nanoparticles over the AgVO3 nano-belts. The in-situ deposition was promoted and enhanced with the introduction of GO. The as-synthesized composite demonstrated remarkable visible light harvesting efficiency greater than 75% in the visible region. The charge separation and light harvesting properties were achieved through the Z-scheme mechanism mediated through rGO and the electron trapping/Schottky barrier effect from Ag nanoparticles. The reduction in the width of space charge region (∼2.5 times) and simultaneous increase in the density of charge carriers (2.3∗1018) promoted the LED irradiated photocatalytic performance. The decay time of the charge carriers were prolonged in the order of 4.46 s implying the enhancement in the charge separation. The studies were extended to charge trapping and the band structure modelling. The later emphasized on the prominence of Z-scheme mechanism with hole mediated degradation pathway. The LED photocatalysis demonstrated a removal efficiency of 87.20% for MB and 55.51% for phenol with a average AQE of 29.28% (MB) and 13.90% (phenol) for the ternary. The mineralization efficiency determined through TOC analysis was found to be 71.72%, and 66.43% for MB and phenol system respectively.

LED-light-activated photocatalytic performance of metal-free carbon-modified hexagonal boron nitride towards degradation of methylene blue and phenol.

The present study outlines the transformation of non-photoresponsive hexagonal boron nitride (HBN) into a visible-light-responsive material. The carbon modification was achieved through a solid-state reaction procedure inside a tube furnace under nitrogen atmosphere. In comparison to HBN (bandgap of 5.2 eV), the carbon-modified boron nitride could efficiently absorb LED light irradiation with a light harvesting efficiency of ≈90% and a direct bandgap of 2 eV. The introduction of carbon into the HBN lattice led to a significant change in the electronic environment through the formation of C-B and C-N bonds which resulted in improved visible light activity, lower charge transfer resistance, and improved charge carrier density (2.97 × 1019 cm-3). This subsequently enhanced the photocurrent density (three times) and decreased the photovoltage decay time (two times) in comparison to those of HBN. The electronic band structure (obtained through Mott-Schottky plots) and charge trapping analysis confirmed the dominance of e-, O2 -•, and •OH as dominant reactive oxygen species. The carbon modification could effectively remove 93.83% of methylene blue (MB, 20 ppm solution) and 48.56% of phenol (10 ppm solution) from the aqueous phase in comparison to HBN which shows zero activity in the visible region.

Facile monomer interlayered MOF based thin film nanocomposite for efficient arsenic separation.

The thin film nanocomposites (TFN) based membranes are sensitive to the synergy between the polymer and nanoparticles. TFN incorporating metal-organic frameworks (MOFs) have shown tremendous enhancement in permeability. This study investigates alternate MOF positioning during TFC fabrication for a highly selective membrane. Co-Zn-based mixed metal-organic framework (mMOF) was interlayered between m-phenylenediamine (MPD) and trimesoyl chloride (TMC) to form a polyamide (PA) selective layer. The practiced method conveniently allowed exact loading of mMOF and thus prevented the loss. Owing to the mMOF's placement between MPD and TMC, an increase in PA cross-linking was observed. The mMOF-MPD monomer compatibility allowed homogeneous distribution and formation of a defect-free PA layer. The surface morphology showed a more pronounced formation of leaves-like features due to interfacial degassing. Neutral solute-based filtration tests determined mean pore size, probability distribution, and MWCO. The incorporation of mMOF led to formation of additional nanochannels in the membrane surface. The perm-selectivity studies performed on a dead-end filtration unit resulted in 94% As5+ retention with 2.5 times higher permeance than the control. The current study pronounced the viability of the monomer interlayer method to form a highly selective TFN for water separation and related applications.

Heterojunction formation between AgNbO3 and Co3O4 for full solar light utilization with improved charge-carrier separation.

In the present study, the charge-carrier recombination of visible light active perovskite silver niobate (AgNbO3) was reduced by forming heterojunction with Co3O4 through simple impregnation and calcination route. The loading percentage of Co3O4 was varied as 2, 5, and 10 wt.%. The XRD study revealed reduced interlayer spacing in the composite due to the replacement of the bigger Ag+ ions by the smaller Co2+ and Co3+ ions of Co3O4. It was observed that the light harvesting efficiency of the materials was increased with increased loading of Co3O4. The TEM and XPS analysis confirmed the presence of Ag nanoparticles over the perovskite in the composite. The electrochemical analysis revealed enhanced charge-carrier number density and increased charge-carrier lifetime in the composite as a result of the presence of both silver and cobalt ions in the lattice. Further this enhanced charge-carrier separation of the composites was established through photocatalysis of Bisphenol-A under both solar and LED light. Charge-trapping study indicated *O2- and *OH as the major radicals involved and Z-scheme as the predominant charge transfer pathway for generation of these reactive oxygen species.

Accelerated sunlight photocatalysis through improved electron mobility between g-C3N4 and BiPO4 nanomaterial.

Herein, we report a detailed study on creating heterojunction between graphitic carbon nitride (g-C3N4) and bismuth phosphate (BiPO4), enhancing the unpaired free electron mobility. This leads to an accelerated photocatalysis of 2,4-dichlorophenols (2,4-DCPs) under sunlight irradiation. The heterojunction formation was efficaciously conducted via a modest thermal deposition technique. The function of g-C3N4 plays a significant role in generating free electrons under sunlight irradiation. Together, the generated electrons at the g-C3N4 conduction band (CB) are transferred and trapped by the BiPO4 to form active superoxide anion radicals (•O2-). These active radicals will be accountable for the photodegradation of 2,4-DCPs. The synthesized composite characteristics were methodically examined through several chemical and physical studies. Due to the inimitable features of both g-C3N4 and BiPO4, its heterojunction formation, 2.5wt% BiPO4/g-C3N4 achieved complete 2,4-DCP removal (100%) in 90 min under sunlight irradiation. This is due to the presence of g-C3N4 that enhanced electron mobility through the formation of heterojunctions that lengthens the electron-hole pairs' lifetime and maximizes the entire solar spectrum absorption to generate active electrons at the g-C3N4 conduction band. Thus, this formation significantly draws the attention for future environmental remediation, especially in enhancing the entire solar spectrum's harvesting.

Nanoremediation: Sunlight mediated dye degradation using electrospun PAN/CuO-ZnO nanofibrous composites.

This work demonstrated the development of nanofiber templated metal oxide nanocomposites by hydrothermal and calcination methods for photocatalytic degradation using Congo red (CR) as model pollutant. Herein, we developed PAN/CuO-ZnO nanocomposites by the electrospinning technique followed by heat treatment process i.e hydrothermal and calcination. The obtained nanofibrous composites were characterized by various analytical techniques such as X-Ray Diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), Thermogravimetric analysis (TG), High-resolution transmission electron microscopy (HRTEM), X-ray photoelectron spectroscopy (XPS), Photoluminescence (PL) and UV-Vis diffuse reflectance spectroscopy (DRS) studies. The results demostrated that the nanocomposites obtained through calcination possess better optical response with robust electronic structures. This is due to the better charge separation of excited electron-hole pairs of p-n heterostructured PAN/CuO-ZnO hybrid nanocomposites. The photocatalytic efficiency is found to be 98% and 93% for nanocomposites obtained through calcination and hydrothermal methods respectively. The reusability studies confirmed the stability and viability of multiple utilizations of photocatalysts. Furthermore, the photocatalytic mechanism corroborated the photocatalytic properties of the integrated facile nanofibrous-metallic (PAN/CuO-ZnO) composites and hence can be implemented in water remediation effectively.

Granular Mg-Fe layered double hydroxide prepared using dual polymers: Insights into synergistic removal of As(III) and As(V).

Controlling the particle size and aggregation of nanosheet layers in layered double hydroxides (LDHs) is critical for their application. Herein, we report the preparation of Mg-Fe LDH through a co-precipitation method. The LDH was embedded using polyacrylamide (PAM) and polyvinyl alcohol (PVA; the LDH was designated as PAM/PVA-LDH) for As(III) and As(V) removal. We found that doping with 0.3 mL PVA (2 g L-1) and 0.4 mL (20 g L-1) PAM solution delaminated the nanosheet layers of 1 g of the LDH (PAM40/PVA30-LDH) and restructured the crystal phase from monoclinic to orthorhombic. This increased the surface area and pore volume. Furthermore, PAM40/PVA30-LDH exhibited higher affinity for As(III) and As(V) removal with maximum adsorption capacities of 14.1 and 22.8 mg g-1, respectively, compared to LDH alone with adsorption capacities of 7.1 and 7.9 mg g-1, respectively. It was found that the highest adsorption capacities of As(III) and As(V) using PAM40/PVA30-LDH occurred at pH ∼7 and pH 2.5, respectively. X-ray photoelectron spectroscopy analysis revealed that the removal of As(III) and As(V) on PAM40/PVA30-LDH was mainly attributable to ion exchange with intercalated SO42-, hydrogen bonding, and complexation mechanisms. These findings illustrate that PAM40/PVA30-LDH would be an excellent adsorbent for the remediation of arsenic-polluted wastewater.

C-Dot TiO2 nanorod composite for enhanced quantum efficiency under direct sunlight.

C-Dots obtained from a sustainable route (melon-rinds were used as the source) were combined with TiNRs to create a composite via a simple hydrothermal technique. The obtained materials were subjected to analyses viz. FESEM, XRD, Raman spectroscopy, XPS, PL, FTIR and UV-vis-DRS for understanding their intrinsic nature. The solar photocatalytic performance was evaluated by the degradation of methyl orange (MO) as a model pollutant. The optical properties indicated that there was a clear redshift in the composite with a band gap of 2.49 eV, while the XRD results corresponded to a calculated crystalline size of 24.80 nm. The PL analysis proved the role of C-dots as an electron surge to the TiNRs. The photocatalytic reaction was faster with C-dots as compared to the solo TiNR with a higher degradation of 93.3% within 150 min obeying pseudo-first order kinetics with a rate constant k = 0.01723 min-1. The charge carrier scavenging investigation showed the role of numerous reactive oxygen species (ROS) on the degradation of MO. The formulated composite has demonstrated its ability in effectively handling the contaminants in water. Thus, this study establishes the two-step thermal method as an easy, facile, environmentally-friendly, and low-cost synthesis method for the large-scale production of a photocatalyst.

Amalgamation of N-graphene quantum dots with nanocubic like TiO2: an insight study of sunlight sensitive photocatalysis.

In this work, a sunlight-sensitive photocatalyst of nanocubic-like titanium dioxide (TiO2) and N-doped graphene quantum dots (N-GQDs) is developed through a simple hydrothermal and physical mixing method. The successful amalgamation composite photocatalyst characteristics were comprehensively scrutinized through various physical and chemical analyses. A complete removal of bisphenol A (BPA) is attained by a synthesized composite after 30 min of sunlight irradiation as compared to pure TiO2. This clearly proved the unique contribution of N-GQDs that enhanced the ability of light harvesting especially under visible light and near-infrared region. This superior characteristic enables it to maximize the absorbance in the entire solar spectrum. However, the increase of N-GQDs weight percentage has created massive oxygen vacancies that suppress the generation of active radicals. This resulted in a longer duration for a complete removal of BPA as compared to lower weight percentage of N-GQDs. Hence, this finding can offer a new insight in developing effective sunlight-sensitive photocatalysts for various complex organic pollutants degradation.

Sonocatalytic reduction of nitrate using magnetic layered double hydroxide: Implications for removal mechanism.

In this study, magnetic layered double hydroxides (mag-LDHs) were synthesized through compositing magnetite with three different metals (Mg, Cu and Al) under ultrasound (US, 100 kHz frequency and 50 W power). For the first time, mag-LDHs were applied to sonocatalytic reduction of nitrate (NO3-) and the reduction mechanism were determined by conducting kinetic tests and various spectroscopic analyses. Based on the kinetic data, NO3- reduction and the selectivity for N2 highly depends on the ratio between Mg/Al, solution pH and sonication frequency. The best condition for sonocatalytic denitrification was found to be pH 7 operated under 100 kHz (50% power) using the catalyst with lowest amount of Al (mag-LDH-Al0.3Mg1.5). As a proposed mechanism, NO3- is initially reduced to NO2- by Cu0, and then further reduced to N2/NH4+ by Mg0. Hypothetically Al0 could provide sorption sites for hydrogen radicals (·H) dissociated from ultrasound, hence served as reducing sites in denitrification process. The XPS analysis showed an increased peak of Cu0 after the sonocatalytic reduction when catalyst has lower amount of Al. The excessive hydrogen adsorbed on Al0 might spill-over to the adjacent Cu, thus reducing the CuO into Cu0 at high temperature created by the implosion of the microbubbles. Without the use of consumable reducing agents (i.e. H2 gas), sonocatalytic reduction could be a potential candidate of remediation method to treat NO3- polluted water with high N2 selectivity and easy magnetic recovery.

M/g-C3N4 (M=Ag, Au, and Pd) composite: synthesis via sunlight photodeposition and application towards the degradation of bisphenol A.

In this work, natural sunlight successfully induced the deposition of gold (Au), silver (Ag), and palladium (Pd) nanoparticles (NPs) with 17.10, 9.07, and 12.70 wt% onto the surface of graphitic carbon nitride (g-C3N4). The photocatalytic evaluation was carried out by adopting Bisphenol A (BPA) as a pollutant under natural sunlight irradiation. The presence of noble metals was confirmed by EDX, HRTEM, and XPS analysis. The deposition of Ag NPs (7.9 nm) resulted in the degradation rate which was 2.15-fold higher than pure g-C3N4 due to its relatively small particle size, contributing to superior charge separation efficiency. Au/g-C3N4 unveiled inferior photoactivity because the LSPR phenomenon provided two pathways for electron transfer between Au NPs and g-C3N4 further diminished the performance. The improved degradation lies crucially on the particle size and Schottky barrier formation at the interface of M/g-C3N4 (M=Au, Ag, and Pd) but not the visible light harvesting properties. The mechanism insight revealed the holes (h+) and superoxide radical (•O2-) radical actively involved in photocatalytic reaction for all composites.

Sugarcane juice derived carbon dot-graphitic carbon nitride composites for bisphenol A degradation under sunlight irradiation.

Carbon dots (CDs) and graphitic carbon nitride (g-C3N4) composites (CD/g-C3N4) were successfully synthesized by a hydrothermal method using urea and sugarcane juice as starting materials. The chemical composition, morphological structure and optical properties of the composites and CDs were characterized using various spectroscopic techniques as well as transmission electron microscopy. X-ray photoelectron spectroscopy (XPS) results revealed new signals for carbonyl and carboxyl groups originating from the CDs in CD/g-C3N4 composites while X-ray diffraction (XRD) results showed distortion of the host matrix after incorporating CDs into g-C3N4. Both analyses signified the interaction between g-C3N4 and CDs. The photoluminescence (PL) analysis indicated that the presence of too many CDs will create trap states at the CD/g-C3N4 interface, decelerating the electron (e-) transport. However, the CD/g-C3N4(0.5) composite with the highest coverage of CDs still achieved the best bisphenol A (BPA) degradation rate at 3.87 times higher than that of g-C3N4. Hence, the charge separation efficiency should not be one of the main factors responsible for the enhancement of the photocatalytic activity of CD/g-C3N4. Instead, the light absorption capability was the dominant factor since the photoreactivity correlated well with the ultraviolet-visible diffuse reflectance spectra (UV-vis DRS) results. Although the CDs did not display upconversion photoluminescence (UCPL) properties, the π-conjugated CDs served as a photosensitizer (like organic dyes) to sensitize g-C3N4 and injected electrons to the conduction band (CB) of g-C3N4, resulting in the extended absorption spectrum from the visible to the near-infrared (NIR) region. This extended spectral absorption allows for the generation of more electrons for the enhancement of BPA degradation. It was determined that the reactive radical species responsible for the photocatalytic activity were the superoxide anion radical (O2•-) and holes (h+) after performing multiple scavenging tests.

Mechanistic insights into plasmonic photocatalysts in utilizing visible light.

The utilisation of sunlight as an abundant and renewable resource has motivated the development of sustainable photocatalysts that can collectively harvest visible light. However, the bottleneck in utilising the low energy photons has led to the discovery of plasmonic photocatalysts. The presence of noble metal on the plasmonic photocatalyst enables the harvesting of visible light through the unique characteristic features of the noble metal nanomaterials. Moreover, the formation of interfaces between noble metal particles and semiconductor materials further results in the formation of a Schottky junction. Thereby, the plasmonic characteristics have opened up a new direction in promoting an alternative path that can be of value to the society through sustainable development derived through energy available for all for diverse applications. We have comprehensively prepared this review to specifically focus on fundamental insights into plasmonic photocatalysts, various synthesis routes, together with their strengths and weaknesses, and the interaction of the plasmonic photocatalyst with pollutants as well as the role of active radical generation and identification. The review ends with a pinnacle insight into future perspectives regarding realistic applications of plasmonic photocatalysts.

Mechanistic Characteristics of Surface Modified Organic Semiconductor g-C3N4 Nanotubes Alloyed with Titania.

The visible-light-driven photocatalytic degradation of Bisphenol A (BPA) was investigated using the binary composite of alkaline treated g-C3N4 (HT-g-C3N4) deposited over commercial TiO2 (Evonik Degussa GmbH, Essen, Germany). The existence and contribution of both TiO2 and g-C3N4/HT-g-C3N4 in the composite was confirmed through various analytical techniques including powder X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), field emission scanning electron microscopy (FESEM), Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), ultraviolet-visible diffuse reflectance spectra (UV-vis-DRS), and photoluminescence (PL) analysis. The results showed that the titania in the binary composite exhibited both pure rutile and anatase phases. The morphological analysis indicated that the spongy "morel-like" structure of g-C3N4 turned to nanotube form after alkaline hydrothermal treatment and thereby decreased the specific surface area of HT-g-C3N4. The low surface area of HT-g-C3N4 dominates its promising optical property and effective charge transfer, resulting in a deprived degradation efficiency of BPA two times lower than pure g-C3N4. The binary composite of HT-g-C3N4/TiO2 exhibited excellent degradation efficiency of BPA with 2.16 times higher than the pure HT-g-C3N4. The enhanced photocatalytic activity was mainly due to the promising optical band gap structure with heterojunction interface, favorable specific surface area, and good charge separation.

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

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.

Synthesis, features and solar-light-driven photocatalytic activity of TiO2 nanotube arrays loaded with SnO2.

In the present study TiO2 nanotube arrays (TNTs) were loaded with a post-transition metal oxide particles namely SnO2 via incipient wet impregnation method by varying its concentration (1.59 wt%, 2.25 wt% and 2.84 wt%). The photocatalytic activity of the prepared photocatalyst was evaluated for the degradation of methylene blue (MB) in presence of natural solar light irradiation. The morphological analyses revealed that the prepared TNTs had average inner diameter of 109 nm, wall thickness of 15 nm and tube length of 7-10 µm, respectively, while the crystalline phase and Raman spectra confirmed the 100% anatase mineral form of TiO2. Further, the presence of SnO2 in TNTs was confirmed by high resolution transmission electron microscopy (HRTEM) and X-ray photoelectron spectroscopy (XPS). The visible light absorption properties of TNTs improved drastically with increasing SnO2 loadings. The coupling effect of SnO2 and TiO2 significantly enhanced degradation efficiency of MB. An 84% degradation of MB was achieved in 6 h of irradiation under clear sky condition.

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.

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.