Predictive modeling of copper (II) adsorption from aqueous solutions by sawdust: a comparative analysis of adaptive neuro-fuzzy interference system (ANFIS) and artificial neural network (ANN) approaches.

Heavy metal ions are considered to be the most prevalent and toxic water contaminants. The objective of thois work was to investigate the effectiveness of employing the adsorption technique in a laboratory-size reactor to remove copper (II) ions from an aqueous medium. An adaptive neuro-fuzzy inference system (ANFIS) and a feed-forward artificial neural network (ANN) were used in this study. Four operational factors were chosen to examine their influence on the adsorption study: pH, contact duration, initial Cu (II) ions concentration, and adsorbent dosage. Using sawdust from wood, prediction models of copper (II) ions adsorption were optimized, created, and developed using the ANN and ANFIS models for tests. The result indicates that the determination coefficient for copper (II) metal ions in the training dataset was 0.987. Additionally, the ANFIS model's R2 value for both pollutants was 0.992. The findings demonstrate that the models presented a promising predictive approach that can be applied to successfully and accurately anticipate the simultaneous elimination of copper (II) and dye from the aqueous solution.

A Comparison of the Effect of Cellulose Nanocrystals (CNCs) and Polyethylene Glycol (PEG) as Additives in Ultrafiltration Membranes (PES-UF): Characterization and Performance.

This work demonstrated the potential of CNC as a substitute for PEG as an additive in ultrafiltration membrane fabrication. Two sets of modified membranes were fabricated using the phase inversion technique, with polyethersulfone (PES) as the base polymer and 1-N-methyl-2 pyrrolidone (NMP) as the solvent. The first set was fabricated with 0.075 wt% CNC, while the second set was fabricated with 2 wt% PEG. All membranes were characterized using SEM, EDX, FTIR, and contact angle measurements. The SEM images were analyzed for surface characteristics using WSxM 5.0 Develop 9.1 software. The membranes were tested, characterized, and compared for their performance in treating both synthetic and real restaurant wastewater. Both membranes exhibited improved hydrophilicity, morphology, pore structure, and roughness. Both membranes also exhibited similar water flux for real and synthetic polluted water. However, the membrane prepared with CNC gave higher turbidity removal and COD removal when raw restaurant water was treated. The membrane compared well with the UF membrane containing 2 wt% PEG in terms of morphology and performance when synthetic turbid water and raw restaurant water were treated.

Preparation of Copper-Decorated Activated Carbon Derived from Platamus occidentalis Tree Fiber for Antimicrobial Applications.

This study focuses on a greener approach to synthesizing activated carbon by carbonizing Platamus occidentalis tree fibers (TFSA) with 98% H2SO4 at 100 °C. The resulted TFSA was employed as an effective adsorbent for copper ions in aqueous media, yielding copper decorated TFSA (Cu@TFSA). The successful adsorption of copper onto the TFSA was proven through extensive characterization techniques. Herein, the TEM and XPS showed that copper nanoparticles were formed in situ on the TFSA surface, without the use of additional reducing and stabilizing agents nor thermal treatment. The surface areas of TFSA and Cu@TFSA were 0.0150 m2/g and 0.3109 m2/g, respectively. Applying the Cu@TFSA as an antimicrobial agent against Escherica coli ( E. coli) and Salmonella resulted in the potential mitigation of complex secondary pollutants from water and wastewater. The Cu@TFSA exhibited outstanding antimicrobial activity against E. coli and Salmonella in both synthetic and raw water samples. This demonstrated a complete growth inhibition observed within 120 min of exposure. The bacteria inactivation took place through the destruction of the bacteria cell wall and was confirmed by the AFM analysis technique. Cu@TFSA has the potential to be used in the water and wastewater treatment sector as antimicrobial agents.

Preparation of Nanofiltration Membrane Modified with Sawdust-Derived Cellulose Nanocrystals for Removal of Nitrate from Drinking Water.

In this work, cellulose nanocrystals (CNC) derived from sawdust were successfully incorporated into a nanofiltration membrane produced by the interfacial polymerization of piperazine (PIP) and trimesoyl chloride (TMC). The characteristics of unmodified and CNC-modified membranes were investigated using scanning electron microscopy (SEM), Atomic Force Microscopy (AFM), zeta potential measurement, X-ray photoelectron spectroscopy (XPS), and contact angle measurement. The performance of the membranes in terms of nitrate removal and water flux was investigated using 60 mg/L of potassium nitrate solution in a dead-end test cell. The characteristics of the modified membrane revealed a more nodular structure, higher roughness, increased negative surface charge, and higher hydrophilicity than the pristine membrane, leading to nitrate rejection of 94%. In addition, the membrane gave an average water flux of 7.2 ± 1.8 L/m2/h/bar. This work implies that nanofiltration, a relatively low-pressure process compared to reverse osmosis, can be used for improved nitrate removal from drinking water using an NF membrane modified with sawdust-derived cellulose nanocrystals.

A Comparison of Unmodified and Sawdust Derived-Cellulose Nanocrystals (CNC)-Modified Polyamide Membrane Using X-ray Photoelectron Spectroscopy and Zeta Potential Analysis.

Cellulose nanocrystals (CNC) obtained from waste sawdust were used to modify the polyamide membrane fabricated by interfacial polymerization of m-phenylene-diamine (MPDA) and trimesoyl chloride (TMC). The efficiency of the modification with sawdust-derived CNC was investigated using zeta potential and X-ray photoelectron spectroscopy (XPS). The effect of the modification on membrane mechanical strength and stability in acidic and alkaline solutions was also investigated. Results revealed that the negative zeta potential decreased at a high pH and the isoelectric point shifted into the acidic range for both modified and unmodified membranes. However, the negative charges obtained on the surface of the modified membrane at a pH lower than 8 were higher than the pristine membrane, which is an indication of the successful membrane modification. The XPS result shows that the degree of crosslinking was lowered due to the presence of CNC. Enhanced stability in solution in all pH ranges and the increase in mechanical strength, as indicated by higher Young's modulus, maximum load, and tensile strength, confirmed the robustness of the modified membrane.

Numerical Modelling Assisted Design of a Compact Ultrafiltration (UF) Flat Sheet Membrane Module.

The increasing adoption of ultra-low pressure (ULP) membrane systems for drinking water treatment in small rural communities is currently hindered by a limited number of studies on module design. Detailed knowledge on both intrinsic membrane transport properties and fluid hydrodynamics within the module is essential in understanding ULP performance prediction, mass transfer analysis for scaling-up between lab-scale and industrial scale research. In comparison to hollow fiber membranes, flat sheet membranes present certain advantages such as simple manufacture, sheet replacement for cleaning, moderate packing density and low to moderate energy usage. In the present case study, a numerical model using computational fluid dynamics (CFD) of a novel custom flat sheet membrane module has been designed in 3D to predict fluid flow conditions. The permeate flux through the membrane decreased with an increase in spacer curviness from 2.81 L/m2h for no (0%) curviness to 2.73 L/m2h for full (100%) curviness. A parametric analysis on configuration variables was carried out to determine the optimum design variables and no significant influence of spacer inflow or outflow thickness on the fluid flow were observed. The numerical model provides the necessary information on the role of geometrical and operating parameters for fabricating a module prototype where access to technical expertise is limited.

Facile synthesis and application of cellulosic coagulant from banana peels in cadmium-spiked water.

Cellulosic coagulant with low crystallinity and surface charge of -19.2 mV were extracted from wet banana peels (WBE) using kitchen-blending method. Functionalization with ferric chloride and aluminium chloride yielded higher surface charge of -23.8 mV (mWBE). Both WBE and mWBE coagulants were used to target cadmium ions from aqueous solution. Coagulants and the floccules (WBEA and mWBEA) were characterized by XRD, FT-IR, zeta sizer nano series, and SEM/EDs. The amount of cadmium ion coagulated was determined using ICP-OES. The FTIR analysis revealed the functional groups involved in the coordination and subsequent removal of the metals ions around 1634 cm-1, ascribed to the C = O vibrational band of carbonyl group. Microscopic analysis revealed that the mWBE is porous and exhibited microfibers with rod-like morphology. The effects of parameters such as the initial concentration, coagulant dosage and solution pH were investigated. Coagulation results showed that 10 mg of WBE and mWBE could remove about 80% and 90% of the Cd2+ ions respectively. However; the difference in the performance of both materials does not justify the essence of surface modification. Therefore, WBE is considered more efficient and environmentally friendly. Notwithstanding, the performance of these coagulants in real environmental samples will confirm their robustness.

Metal oxide-cellulose nanocomposites for the removal of toxic metals and dyes from wastewater.

Waste water remediation of toxic metals and dyes could be complex to achieve owing to several factors. Various techniques have been developed for the removal of these pollutants. However, the success of these water treatment techniques mainly depends on the choice of appropriate media. Most of the commercial and chemically synthesized materials for water treatment create additional hazards due to the leaching of toxic chemicals into the process water. Consequently, studies on the development of better materials which could achieve high efficiency without posing any health risk led to the exploration of non-toxic composite materials such as those composed of cellulose and metal oxides. The focus is on the choice of materials and the best methods that allows their combination in order to address the pollution caused by heavy metals and dyes. This review critically analyses or assess the use of cellulose incorporated with metal oxides in the removal of toxic metals and dyes from industrial effluent. The nanocomposites have been accepted as a technique that circumvents the problems associated with the use of only metal oxides in water purification. They provide a platform for an improvement in the hydrophobicity of the composite with concomitant efficiency in adsorption and photocatalysis.

Sawdust-Based Cellulose Nanocrystals Incorporated with ZnO Nanoparticles as Efficient Adsorption Media in the Removal of Methylene Blue Dye.

The continuous increase in the wastes generated from forestry, timber, and paper industries has engendered the need for their transformation into economically viable materials for the benefit of mankind. This study reports the preparation and application of sawdust-derived cellulose nanocrystals (CNC) incorporated with zinc oxide as a novel adsorbent for the removal of methylene blue (MB) from water. The CNC/ZnO nanocomposite was characterized using Fourier transform infrared, X-ray diffraction (XRD), and scanning electron microscopy. The amount of MB adsorbed was determined by a UV-vis spectrophotometer. The microscopic analysis revealed that the nanocomposite had a narrow particle size range and exhibited both spherical and rod-like morphologies. The XRD analysis of the nanocomposite showed characteristic high-intensity peaks in the range of 30-75° attributed to the presence of ZnO nanoparticles, which were responsible for the enhancement of the crystallinity of the nanocomposite. The results revealed a relationship between the MB removal efficiency and changes in solution pH, nanocomposite dosage, initial concentration, temperature, and reaction time. The adsorption equilibrium isotherm, measured in the temperature range of 25-45 °C and using a concentration of 20-100 mg/L, showed that the MB sorption followed the Langmuir isotherm with a maximum adsorption capacity of 64.93 mg/g. A pseudo-second-order kinetic model gave the best fit to the experimental data. Based on adsorption performance, the CNC/ZnO nanocomposite offers prospects for further research and application in amelioration of dye-containing effluent.

Synthesis and application of alginate immobilised banana peels nanocomposite in rare earth and radioactive minerals removal from mine water.

This study describes the preparation, characterisation and application of pelletised immobilised alginate/montmorillonite/banana peels nanocomposite (BPNC) in a fixed-bed column for continuous adsorption of rare earth elements and radioactive minerals from water. The materials was characterised by Fourier transform infrared, X-ray diffraction and scanning electron microscopy analyses. Analyses indicated that the pellets are porous and spherical in shape. FT-IR analysis showed that the functional groups responsible for the coordination of metal ions were the carboxylic (-COO-) and siloxane (Si-O-Si and Si-O-Al) groups. XRD analysis showed two additional peaks which were attributed to alginate and montmorillonite. The influence of the initial concentration, bed depth and flow rate were investigated using synthetic and real mine water in order to determine the breakthrough behaviour of both minerals. The processed bed volume, adsorbent exhaustion rate and service time, were also explored as performance indices for the adsorbent material. Furthermore, the breakthrough data were fitted to both the Thomas and Bohart-Adams models. The BPNC exhibited high affinity for U, Th, Gd and La in the real mine water sample. However, studies may still be required using waters from different environments in order to determine the robustness of BPNC.

Fixed-bed operation for manganese removal from water using chitosan/bentonite/MnO composite beads.

In the present study, a new composite adsorbent, chitosan/bentonite/manganese oxide (CBMnO) beads, cross-linked with tetraethyl-ortho-silicate (TEOS) was applied in a fixed-bed column for the removal of Mn (II) from water. The adsorbent was characterised by scanning electron microscopy (SEM), Fourier transform infra-red (FT-IR), N2 adsorption-desorption and X-ray photoelectron spectroscopy (XPS) techniques, and moreover the point of zero charge (pHpzc) was determined. The extend of Mn (II) breakthrough behaviour was investigated by varying bed mass, flow rate and influent concentration, and by using real environmental water samples. The dynamics of the column showed great dependency of breakthrough curves on the process conditions. The breakthrough time (tb), bed exhaustion time (ts), bed capacity (qe) and the overall bed efficiency (R%) increased with an increase in bed mass, but decreased with the increase in both influent flow rate and concentration. Non-linear regression suggested that the Thomas model effectively described the breakthrough curves while large-scale column performance could be estimated by the bed depth service time (BDST) model. Experiments with environmental water revealed that coexisting ions had little impact on Mn (II) removal, and it was possible to achieve 6.0 mg/g breakthrough capacity (qb), 4.0 L total treated water and 651 bed volumes processed with an initial concentration of 38.5 mg/L and 5.0 g bed mass. The exhausted bed could be regenerated with 0.001 M nitric acid solution within 1 h, and the sorbent could be reused twice without any significant loss of capacity. The findings advocate that CBMnO composite beads can provide an efficient scavenging pathway for Mn (II) in polluted water.

Photocatalytic degradation of P-Cresol using TiO2/ZnO hybrid surface capped with polyaniline.

This study evaluated the photocatalytic activity of polyaniline (PANI)-capped titanium dioxide and zinc oxide (TiO2/ZnO) hybrid, for the degradation of P-Cresol. The hybrid was synthesized by precipitating ZnO on the surface of commercial TiO2. An "in situ" chemical oxidative polymerization method was used to prepare the PANI capped hybrid (TiO2/ZnO/PANI). The photocatalysts were characterized by powder X-ray diffraction (XRD), a Brunauer Emmett Teller (BET) analyzer, Fourier-transform infrared (FTIR) and photoluminescence spectroscopies, high resolution-transmission electron microscopy (HR-TEM) and thermogravimetric analysis (TGA). During photodegradation under ultraviolet (UV) irradiation, ZnO, TiO2, TiO2/ZnO hybrid and TiO2/ZnO/PANI composite had P-Cresol removal of 43%, 50%, 61% and 99%, respectively. The higher activity of the TiO2/ZnO hybrid as compared to TiO2 and ZnO was attributed to a reduced electron-hole pair recombination. The recombination was further significantly reduced upon introduction of PANI; hence, the highest activity observed with TiO2/ZnO/PANI. The initial reaction rate constant for TiO2/ZnO/PANI (0.9679 min-1) was more than twice compared to that for TiO2/ZnO hybrid (0.1259 min-1). A synergistic effect between PANI and TiO2/ZnO resulted in a highly efficient charge separation caused by the transfer of photogenerated holes from the hybrid to highest occupied molecular orbitals (HOMO) of PANI. The best TiO2/ZnO/PANI (PANI to TiO2/ZnO) ratio observed was 0.5:2 for the photodegradation of P-Cresol. Total organic carbon (TOC) analysis indicated a 97.4% mineralization of P-Cresol with PANI/TiO2/ZnO.

Ultraviolet and solar photocatalytic ozonation of municipal wastewater: Catalyst reuse, energy requirements and toxicity assessment.

The present study evaluated the treatment of municipal wastewater containing phenol using solar and ultraviolet (UV) light photocatalytic ozonation processes to explore comparative performance. Important aspects such as catalyst reuse, mineralization of pollutants, energy requirements, and toxicity of treated wastewater which are crucial for practical implementation of the processes were explored. The activity of the photocatalysts did not change significantly even after three consecutive uses despite approximately 2% of the initial quantity of catalyst being lost in each run. Analysis of the change in average oxidation state (AOS) demonstrated the formation of more oxidized degradation products (ΔAOS values of 1.0-1.7) due to mineralization. The energy requirements were determined in terms of electrical energy per order (EEO) and the collector area per order (ACO). The EEO (kWh m-3 Order-1) values were 26.2 for ozonation, 38-47 for UV photocatalysis and 7-22 for UV photocatalytic ozonation processes. On the other hand, ACO (m2 m-3 order-1) values were 31-69 for solar photocatalysis and 8-13 for solar photocatalytic ozonation. Thus photocatalytic ozonation processes required less energy input compared to the individual processes. The cytotoxicity of the wastewater was analysed using the 3-(4, 5-dimethylthiazol-2-yl)-2, 5-diphenyltetrazolium bromide (MTT) assay with Vero cells. The cell viability increased from 28.7% in untreated wastewater to 80% in treated wastewater; thus showing that the treated wastewater was less toxic. The effectiveness of photocatalytic ozonation, recovery and reusability of the photocatalysts, as well as detoxification of the wastewater make this low energy consumption process attractive for wastewater remediation.

Evaluation of synergy and bacterial regrowth in photocatalytic ozonation disinfection of municipal wastewater.

The use of solar and ultraviolet titanium dioxide photocatalytic ozonation processes to inactivate waterborne pathogens (Escherichia coli, Salmonella species, Shigella species and Vibrio cholerae) in synthetic water and secondary municipal wastewater effluent is presented. The performance indicators were bacterial inactivation efficiency, post-disinfection regrowth and synergy effects (collaboration) between ozonation and photocatalysis (photocatalytic ozonation). Photocatalytic ozonation effectively inactivated the target bacteria and positive synergistic interactions were observed, leading to synergy indices (SI) of up to 1.86 indicating a performance much higher than that of ozonation and photocatalysis individually (SI≤1, no synergy; SI>1 shows synergy between the two processes). Furthermore, there was a substantial reduction in contact time required for complete bacterial inactivation by 50-75% compared to the individual unit processes of ozonation and photocatalysis. Moreover, no post-treatment bacterial regrowth after 24 and 48h in the dark was observed. Therefore, the combined processes overcame the limitations of the individual unit processes in terms of the suppression of bacterial reactivation and regrowth owing to the fact that bacterial cells were irreparably damaged. The treated wastewater satisfied the bacteriological requirements in treated wastewater for South Africa.

Batch equilibrium and kinetics of mercury removal from aqueous solutions using polythiophene/graphene oxide nanocomposite.

Polythiophene/graphene oxide (PTh/GO) nanocomposite (NC) was prepared through polymerisation of thiophene in the presence of GO and was used for mercury ions (Hg2+) adsorption in aqueous solutions. Equilibrium studies showed that mercury removal was strongly influenced by solution pH and GO composition in the NC. The equilibrium data were well described by both Langmuir and Freundlich isotherm models, with a Langmuir maximum adsorption capacity of 113.6 mg/g. Adsorption kinetics were rapid and correlated well with the pseudo-second-order model. The thermodynamic studies indicated that the adsorption was spontaneous and endothermic in nature, and occurred through a physicochemical mechanism. Desorption studies revealed that PTh/GO NC could be used repeatedly for three adsorption-desorption cycles without a significant loss in its capacity. Competing ions reduced mercury uptake although considerable values were still attained. The findings of this study suggest that PTh/GO NC is a potential adsorbent for Hg2+ removal from aqueous solutions.

Impact of ozonation in removing organic micro-pollutants in primary and secondary municipal wastewater: effect of process parameters.

The study investigates the influence of process parameters on the effectiveness of ozonation in the removal of organic micro-pollutants from wastewater. Primary and secondary municipal wastewater containing phenol was treated. The effect of operating parameters such as initial pH, ozone dosage, and initial contaminant concentration was studied. An increase in contaminant decomposition with pH (3-11) was observed. The contaminant removal efficiencies increased with an increase in ozone dose rate (5.5-36.17 mg L(-1) min(-1)). Furthermore, the ultraviolet absorbance (UV 254 nm) of the wastewater decreased during ozonation indicating the breakdown of complex organic compounds into low molecular weight organics. Along the reaction, the pH of wastewater decreased from 11 to around 8.5 due to the formation of intermediate acidic species. Moreover, the biodegradability of wastewaters, measured as biological and chemical oxygen demand (BOD5/COD), increased from 0.22 to 0.53. High ozone utilization efficiencies of up to 95% were attained thereby increasing the process efficiency; and they were dependent on the ozone dosage and pH of solution. Ozonation of secondary wastewater attained the South African water standards in terms of COD required for wastewater discharge and dissolved organic carbon in drinking water and increased significantly the biodegradability of primary wastewater.

Application of banana peels nanosorbent for the removal of radioactive minerals from real mine water.

Transformation of agricultural waste such as banana peels into a valuable sorbent material has been proven effective and efficient in wastewater treatment. Further, transformation into nanosorbent to enhance the removal capacity of actinides (uranium and thorium) from synthetic and real mine water is extensively investigated in this study. The nanosorbent samples before and after adsorption were characterised by X-ray diffraction (XRD), Fourier transform infra-red (FTIR), zetasizer nanoseries and scanning electron microscopy (SEM) while the amount of radioactive substances adsorbed was determined by inductively coupled plasma optical emission spectroscopy. Results revealed that there was a crystallite size and particle size reduction from 108 to 12 nm and <65,000 nm to <25 nm respectively as a function of milling time. Furthermore, appearance and disappearance of nanofibers via milling was noticed during structural analysis. The functional groups responsible for the banana peels capability to coordinate and remove metal ions were identified at absorption bands of 1730 cm-1 (carboxylic groups) and 889 cm-1 (amine groups) via FTIR analysis. Equilibrium isotherm results demonstrated that the adsorption process was endothermic for both uranium and thorium. The Langmuir maximum adsorption capacity was 27.1 mg g-1, 34.13 mg g-1 for uranium and 45.5 mg g-1, 10.10 mg g-1 for thorium in synthetic and real mine water, respectively. The results obtained indicate that nanostructured banana peels is a potential adsorbent for the removal of radioactive substances from aqueous solution and also from real mine water. However, the choice of this sorbent material for any application depends on the composition of the effluent to be treated.

Modelling energy efficiency of an integrated anaerobic digestion and photodegradation of distillery effluent using response surface methodology.

Anaerobic digestion (AD) is efficient in organic load removal and bioenergy recovery when applied in treating distillery effluent; however, it is ineffective in colour reduction. In contrast, ultraviolet (UV) photodegradation post-treatment for the AD-treated distillery effluent is effective in colour reduction but has high energy requirement. The effects of operating parameters on bioenergy production and energy demand of photodegradation were modelled using response surface methodology (RSM) with a view of developing a sustainable process in which the biological step could supply energy to the energy-intensive photodegradation step. The organic loading rate (OLRAD) and hydraulic retention time (HRTAD) of the initial biological step were the variables investigated. It was found that the initial biological step removed about 90% of COD and only about 50% colour while photodegradation post-treatment removed 98% of the remaining colour. Maximum bioenergy production of 180.5 kWh/m(3) was achieved. Energy demand of the UV lamp was lowest at low OLRAD irrespective of HRTAD, with values ranging between 87 and 496 kWh/m(3). The bioenergy produced formed 93% of the UV lamp energy demand when the system was operated at OLRAD of 3 kg COD/m(3) d and HRT of 20 days. The presumed carbon dioxide emission reduction when electricity from bioenergy was used to power the UV lamp was 28.8 kg CO2 e/m(3), which could reduce carbon emission by 31% compared to when electricity from the grid was used, leading to environmental conservation.

Microwave-assisted synthesis, characterization and antibacterial activity of Ag/ZnO nanoparticles supported bentonite clay.

Composites of silver-zinc oxide nanoparticles supported on bentonite clay were synthesized by the microwave-assisted synthesis method for use as an antibacterial material. Silver nitrate was used as the precursor of silver nanoparticles while zinc oxide nanoparticles were commercially sourced. The composites were characterized by powder X-ray diffraction (XRD), transmission electron microscope (TEM), Fourier transform infrared (FTIR) and BET surface area measurements. XRD spectra showed peaks of silver confirming the formation of the silver and not of the silver nitrate or any other impurity of the metal. Meanwhile TEM confirmed the formation of silver and zinc oxide nanoparticles on the clay layers, with particle sizes ranging from 9-30 nm and 15-70 nm, respectively. The antibacterial activities of the composites were evaluated against Gram negative Escherichia coli bacteria and Gram positive Enterococcus faecalis bacteria by the disc diffusion method. Whereas both composites of Ag-clay and ZnO-clay showed good antibacterial activity against bacteria, a better antibacterial activity was observed with Ag/ZnO-clay composite. The results therefore reveal that Ag/ZnO-clay composite is a promising bactericide that can be used for deactivating microbes in water.

An integrated anaerobic digestion and UV photocatalytic treatment of distillery wastewater.

Anaerobic up-flow fixed bed reactor and annular photocatalytic reactor were used to study the efficiency of integrated anaerobic digestion (AD) and ultraviolet (UV) photodegradation of real distillery effluent and raw molasses wastewater (MWW). It was found that UV photodegradation as a stand-alone technique achieved colour removal of 54% and 69% for the distillery and MWW, respectively, with a COD reduction of <20% and a negligible BOD reduction. On the other hand, AD as a single treatment technique was found to be effective in COD and BOD reduction with efficiencies of above 75% and 85%, respectively, for both wastewater samples. However, the AD achieved low colour removal efficiency, with an increase in colour intensity of 13% recorded when treating MWW while a colour removal of 51% was achieved for the distillery effluent. The application of UV photodegradation as a pre-treatment method to the AD process reduced the COD removal and biogas production efficiency. However, an integration in which UV photodegradation was employed as a post-treatment to the AD process achieved high COD removal of above 85% for both wastewater samples, and colour removal of 88% for the distillery effluent. Thus, photodegradation can be employed as a post-treatment technique to an AD system treating distillery effluent for complete removal of the biorecalcitrant and colour imparting compounds.