A Review of Current Achievements and Recent Challenges in Bacterial Medium-Chain-Length Polyhydroxyalkanoates: Production and Potential Applications.

Using petroleum-derived plastics has contributed significantly to environmental issues, such as greenhouse gas emissions and the accumulation of plastic waste in ecosystems. Researchers have focused on developing ecofriendly polymers as alternatives to traditional plastics to address these concerns. This review provides a comprehensive overview of medium-chain-length polyhydroxyalkanoates (mcl-PHAs), biodegradable biopolymers produced by microorganisms that show promise in replacing conventional plastics. The review discusses the classification, properties, and potential substrates of less studied mcl-PHAs, highlighting their greater ductility and flexibility compared to poly(3-hydroxybutyrate), a well-known but brittle PHA. The authors summarize existing research to emphasize the potential applications of mcl-PHAs in biomedicine, packaging, biocomposites, water treatment, and energy. Future research should focus on improving production techniques, ensuring economic viability, and addressing challenges associated with industrial implementation. Investigating the biodegradability, stability, mechanical properties, durability, and cost-effectiveness of mcl-PHA-based products compared to petroleum-based counterparts is crucial. The future of mcl-PHAs looks promising, with continued research expected to optimize production techniques, enhance material properties, and expand applications. Interdisciplinary collaborations among microbiologists, engineers, chemists, and materials scientists will drive progress in this field. In conclusion, this review serves as a valuable resource to understand mcl-PHAs as sustainable alternatives to conventional plastics. However, further research is needed to optimize production methods, evaluate long-term ecological impacts, and assess the feasibility and viability in various industries.

A novel route to the synthesis of α-Fe2O3@C@SiO2/TiO2 nanocomposite from the metal-organic framework as a photocatalyst for water treatment.

In this study, an attempt was made to synthesize metal-organic frameworks (MOFs) based magnetic iron particles as photocatalysts for textile dye wastewater. Improvement strategy was a novel two-step dry method without using conventional methods to eliminate the consumption of chemical reagents. First, the heterogeneous photocatalyst of Fe-MOFs derived magnetic carbon nanocomposite with carboxylic acid surface functional groups (Fe@C-COOH) was achieved. Next, the α-Fe2O3@C@SiO2/TiO2 was successfully synthesized followed by a sol-gel method to coat the SiO2 shell and a solvothermal method to coat the surface of the intermediate TiO2 particles. The as-synthesized nanocomposite materials were characterized and physicochemical analytical equipment. Further, the investigation on magnetic photocatalytic nanocomposite α-Fe2O3@C@SiO2/TiO2 performance of dye degradation and photocatalytic activity on Reactive yellow 145 (RY145), using as an indicator was conducted. The as-synthesized nanocomposite particles were characterized using X-ray powder diffraction (XRD), thermogravimetric analysis (TGA), Fourier-transform infrared spectroscopy (FT-IR), vibrating sample magnetometer (VSM), X-ray energy dispersive spectroscopy (EDX), and scanning electron microscopy (SEM) techniques. The structural characterization of the as-synthesized materials proved that these methods generate oxygen-containing functional groups, such as, -OH, -CO, and -COOH, which increases the polarity and hydrophilicity of the photocatalyst. The photocatalytic oxidation of RY145 dye under UVc light was discussed by the apparent first-order reaction rate and the kinetic model of the Langmuir-Hinshelwood followed a better fitting. The optimal performance of the composite is at pH = 2, 15 mg/100 mL of photocatalyst dose, 150 mg/L concentration of the dye RY145 at 25 °C temperature under UVc lamp irradiation for 90 min, and with the apparent reaction rate constant was 0.0165 min-1. The thermodynamic analysis of activation parameters computed by the Eyring model and based on transition state theory (TST), an endothermic reaction with a positive value for Δ‡Ho (50.16 kJ mol-1) and a negative value for Δ‡So (-153 J/mol K) both contribute toward achieving positive values for Δ‡Go and a nonspontaneous process. The proposed α-Fe2O3@C@SiO2/TiO2 demonstrated a high capability of photocatalytic degradation up to 97% after five successive cycles at the optimal condition compared to that of Fe3O4@C (18.74%) and Fe@C-COOH (77.9%) without reusability.

A new anti-fouling polysulphone nanofiltration membrane blended by amine-functionalized MCM-41 for post treating waste stabilization pond's effluent.

Developing an effective and stable separation membrane for water treatment is of much interest while challenging because of the restrictions of membrane fouling and water flux reduction. To minimize this problem, in this work, highly porous and hydrophilic nanostructure of NH2-modified MCM-41 (NH2-MCM-41) was embedded successfully into the nanofiltration (NF) membrane body via commonly used phase inversion method. The unmodified and modified nanofiller was analyzed by Fourier Transform Infrared (FTIR) spectroscopy, X-Ray powder diffractometry (XRD), field emission scanning electron microscopy (FE-SEM), thermogravimetric analysis (TGA), and nitrogen adsorption-desorption. Furthermore, the modified membranes were characterized through surface and cross section FE-SEM images, the membrane surface roughness, hydrophilicity, antifouling properties and dye rejection. Benefiting from porous networks and enhanced hydrophilicity, the mixed matrix membranes (MMMs) revealed more prominent hydrophilic property as well as higher pure water flux (PWF) compared with naked membrane. The polysulphone (PSf) membrane modified with NH2-MCM-41-1.0 exhibited the highest pure water flux (PWF) of 65.43 kg/m2.h and superior antifouling characteristics with a flux recovery ratio (FRR) of around 97.0% and an irreversible fouling resistance (Rir) of 3.2%. Furthermore, the optimal membrane possessed high dye rejection (100%) and antifouling capacity (FRR of 97%) while filtering a field sample, effluent from a local stabilization pond treating municipal wastewater. The fabricated membrane in this study is believed to pave pathways for constructing NF membranes with superior effectiveness for other municipal and industrial wastewaters treatment.

Assessment of resistance and biosorption ability of Lactobacillus paracasei to remove lead and cadmium from aqueous solution.

Since heavy metals have been regarded as ubiquitous environmental pollutants, the exploitation of bacterial biosorption has been suggested as an applicable method for being employed for heavy metal depletion. The present study aimed to characterize the function of Lactobacillus paracasei in the presence of Pb (II) and Cd (II). The simultaneous effect of pH, initial metal concentration, and inoculum size demonstrated the Pb (II) removal of 85.77% at the lowest pH, while the inoculum size was enhanced to 45 CFU/100 ml. The maximum Cd (II) removal was obtained at a high level of pH and inoculum size, while the metal concentration was reduced to 30 ppb. The addition of Cd (II) concentration in access led to the 10% drop in Cd (II) removal efficiency attributed to the metal toxicity and pH. Additionally, the slight variation in the amount of inoculum size caused the decreasing trend in the Cd (II) removal. According to the obtained results, the benefit of L. paracasei in the biosorption of heavy metals was well-recognized, which could be suggested as an alternative candidate. PRACTITIONER POINTS: Strain of Lactobacillus paracasei as potential probiotics was tested for biosorption. A successful response surface method was proposed. L. paracasei showed a good efficiency for the lead and cadmium biosorption. Biosorption process was effective in removing low metal level from drinking water. The maximum biosorption was found to be 85.77% for Pb (II) obtained from the experiment.

Graphene quantum dots based on maltose as a high yield photocatalyst for efficient photodegradation of imipramine in wastewater samples.

PURPOSE: In this work, for the first time, graphene quantum dots (GQDs) based on maltose were fabricated as a new photocatalytic material to the photodegradation of imipramine (as a persistence organic pollutant) under light irradiation. METHODS: The synthesized GQDs were characterized by different instrumentation approaches such as X-ray diffraction (XRD), Fourier transform-infrared spectroscopy (FT-IR), scanning electron microscopy (SEM), nitrogen adsorption/desorption, and transmission electron microscopy (TEM). A Box-Behnken design (BBD) and the response surface methodology (RSM) were applied for the optimization of different factors that affect the overall photocatalytic yield. RESULTS: Under the optimized conditions (pH of the sample solution: 2.0; photocatalyst dosage: 0.1 mg mL-1; UV exposure time: 80 min), the highest achievable reduction efficiency was obtained about 80%. The stability and reusability of the synthesized photocatalytic material were investigated in four reaction cycles (80 min), which showed only a 15% photo-activity loss after the fourth photocatalytic runs. CONCLUSIONS: The proposed method was successfully applied to degrade the mentioned drug in the real wastewater samples by about 70%. Regarding the mentioned advantages by the proposed method, this new kind of photocatalytic material possesses a strong potential for photodegradation of pollutants in industrial wastewater samples. GRAPHICAL ABSTRACT: Photodegradation of imipramine using graphene quantum dots based on maltose.

Field measurement of effects of individual and combined application of biochar and polyacrylamide on erosion variables in loess and marl soils.

Controlling soil erosion, especially in its initial stages, is greatly important in natural resources management. Consequently, the present research aimed to control splash and interrill erosion in two soil types (marl at Marzan-Abad and loess at Maraveh-Tapeh sites in northern Iran) using biochar (BC) and polyacrylamide (PAM). We established 0.5 × 0.5-m plots and applied BC (800 g·m-2), PAM (2 g·m-2), and BC + PAM (800 g·m-2 + 2 g·m-2) with control plots and three replications on a slope of ~25%. We used a rainfall simulator to achieve rainfall intensity of 50 mm·h-1 with 30-min duration in the experiments. Analysis of the results obtained from the variables of splash and interrill erosion during the rainfall-runoff process showed that the PAM significantly (p ≤ 0.05) increased all study variables of splash erosion. For interrill erosion, it reduced the variables of soil loss and sediment concentration. However, the difference was not significant (p > 0.05) compared to the control plot and runoff from the two treatment sites increased relative to that from the control plots. The plot treated with BC showed decreased runoff volume, runoff coefficient, and soil loss compared to the control plot at the Marzan-Abad site, but the differences were not statistically significant (p > 0.05). However, the plot in which loess soil was treated with BC at the Maraveh-Tapeh site exhibited considerably (p ≤ 0.05) increased runoff and soil loss compared to the control plot. The entire results verified a wide range for benefit reduction of study treatments from +25.09 to -37.49% for runoff and from +38.59 to -231% for soil loss with more effectiveness for Maraveh-Tapeh Loess soil as well as combined application of BC and PAM. These findings contribute to improved understanding of proper application of soil amendments to control runoff and soil loss in loam and loess soils.

Preparation and surface engineering of CM-ß-CD functionalized Fe3O4@TiO2 nanoparticles for photocatalytic degradation of polychlorinated biphenyls (PCBs) from transformer oil.

The aim of the present research is to investigate the efficiency of surface-modified magnetic nanoparticles for photocatalytic degradation of PCBs from transformer oil. Therefore, CMCD-Fe3O4@TiO2 was successfully produced via grafting of carboxymethyl-ß-cyclodextrin (CM-ß-CD) onto the core-shell titania magnetic nanoparticles surface. The photocatalytic efficiency of CMCD-Fe3O4@TiO2 for degradation of PCBs was systematically evaluated using an experimental design and the process parameters were optimized by response surface methodology (RSM). The central composite design (CCD) with four experimental parameters was used successfully in the modeling and optimization of photocatalytic efficiency in removing PCBs from transformer oil. ANOVA analysis confirmed a high R-squared value of 0.9769 describing the goodness of fit of the proposed model for the significance estimation of the individual and the interaction effects of variables. The optimal degradation yields of PCBs was achieved 83 % at a temperature of 25 °C, time of 16 min, the dosage of the catalyst of 8.35 mg and oil: ethanol ratio of 1:5. These findings encourage the practical use of CM-ß-CD-Fe3O4@TiO2 as a promising and alternative photocatalyst on an industrial scale for the cleaning of organic pollutants such as PCBs due to its environmental friendliness, the benefit of magnetic separation and good reusability after five times.

The feasibility of cost-effective manufacturing activated carbon derived from walnut shells for large-scale CO2 capture.

The economic potential of activated carbon (AC) synthesis from walnut shell biomass for CO2 capture was evaluated in the present study. For this purpose, the chemical activation was employed to manufacture ACs and the effect of different impregnation ratios of activation agents, comprising KOH (KH) and H3PO4 (HP), onto the properties of fabricated ACs was examined. The obtained results demonstrated that the synthesized AC by HP activation with an impregnation ratio of 1:2.5, which was identified as HP2.5, possesses the highest surface area (1512.6 m2/g), micropore volume percentage (74.65%), and CO2 adsorption (3.55 mmol/g) at 1 bar and 30 °C. Moreover, the equilibrium CO2 adsorption data for HP2.5 were better fitted with the Freundlich model, indicating the multilayer CO2 adsorption onto the heterogeneous AC surface dominantly through a physisorption process. In addition, the economic estimations revealed a cost of about $1.83/kg for the ultimate production that was significantly lower than the most of available CACs in the market. Therefore, walnut shells can be considered as a cost-effective and promising biomass source from a scale-up point of view.

Synthesis, characterization and photocatalytic application of Ag-doped Fe-ZSM-5@TiO2 nanocomposite for degradation of reactive red 195 (RR 195) in aqueous environment under sunlight irradiation.

BACKGROUND: Most dyes have aromatic rings in their structures, which make them highly toxic for human being and aquatic life. Heterogeneous photodegradation using TiO2 nanoparticles is one of the most applied methods used for dye removal. The wide band gap of TiO2 nanoparticles disables its use of the visible light and thus the vast potential of sunlight. To overcome this deficiency, Ag doped TiO2 nanoparticles were loaded on Fe-ZSM-5. METHODS: Fe-ZSM-5@TiO2-Ag photocatalyst was synthesized through sol-gel and hydrothermal methods to remove hazardous Reactive Red 195 (RR 195) from aqueous solution. RESULTS: Pure phase of Fe-ZSM-5@TiO2-Ag with specific surface area of 332 m2/g was successfully synthesized. Formation of Ti-O-Ag functional group in the photocatalyst structure confirmed the nanocomposite form of the product. SEM and TEM images portrayed the synthesized zeolite and photocatalyst NPs in a size range of ≤100 nm with homogenous distribution of Ag doped TiO2 on Fe-ZSM-5 surface. The band-gap energy of Fe-ZSM-5@TiO2-Ag was calculated 1.97 eV at λ = 630 nm. Photocatalytic activity of the photocatalyst under natural sunlight was investigated through photodecomposition of RR 195 in an aqueous solution. The dye photodecomposition of about 98% was achieved at photocatalyst concentration of 400 mg/L, pH of 3, and dye concentration of 50 mg/L at ambient temperature after 120 min under sunlight using 0.5 ml of TiO2 and silver ammonium nitrate. The photocatalyst reusability was found significant after 5 frequent cycles. CONCLUSION: The novel Ag-doped TiO2-Fe-ZSM-5 nanocomposite with sunlight sensitivity can be a promising candidate to purify wastewater containing organic pollutants.

A novel facile synthesis of the amine-functionalized magnetic core coated carboxylated nanochitosan shells as an amphoteric nanobiosupport.

We developed a novel synthesis method for a multifunctional nanocomposite with amine-functionalized Fe3O4 core coated with carboxylated nanochitosan shells (NH2-Fe3O4@NCS-COOH) via carbodiimide activation. The chemical structures of chitosan and carboxylated nanochitosan (NCS-COOH) were verified by 1H NMR which confirmed the incorporation of citric acid by the formation of the new signal of the CH2 H-atoms. TEM image displayed the synthesized NH2-Fe3O4@NCS-COOH nanoparticles were in a spherical shape with an average size of 100 nm. The results of XRD revealed that NH2-Fe3O4@NCS-COOH have a good crystalline nature with the face center cubic structure and with the average crystallite size of 17 nm. The characterization using VSM showed that the magnetic nanoparticle had superparamagnetic behavior and the saturation magnetization was up to 30 emu/g. The BET specific surface area of NH2-Fe3O4@NCS-COOH was 45.18 m2/g. The synthesized nanostructure was found to be stable in different ranges of pH due to covalent bonds between nanochitosan and Fe3O4.

The impact of nanoparticles zero-valent iron (nZVI) and rhizosphere microorganisms on the phytoremediation ability of white willow and its response.

Soil contaminated with heavy metals (HMs) is a serious problem throughout the world that threatens all living organisms in the soil. Therefore, large-scale remediation is necessary. This study investigated a new combination of remediation techniques on heavy metal contaminated soil, phytoremediation, and soil amendment with nano-sized zero-valent iron (nZVI) and rhizosphere microorganisms. White willow (Salix alba L.) was grown for 160 days in pots containing Pb, Cu, and Cd and amended with 0, 150, and 300 (mg kg-1) of nZVI and rhizosphere microorganisms, including the arbuscular mycorrhizal fungus (AMF), Rhizophagus irregularis, and the plant growth promoting rhizobacteria (PGPR), Pseudomonas fluorescens. The results showed that inoculation with PGPR and AMF, particularly dual inoculation, improved plant growth as well as the physiological and biochemical parameters of white willow, and increased the bioconcentration factor (BCF) of Pb, Cu, and Cd. The low dose of nZVI significantly increased the root length and the leaf area of the seedlings and increased the BCF of Cd. In contrast, the high dose of nZVI had negative effects on the seedlings growth and the BCF of Pb and Cu, about - 32% and - 63%, respectively. Our results demonstrate that nZVI at low doses can improve plant performance in a phytoremediation context and that the use of beneficial rhizosphere microorganisms can minimize nZVI stress in plants and make them less susceptible to stress even under high dose conditions.

Biological CNP removal from meat-processing wastewater in an innovative high rate up-flow A2O bioreactor.

A high rate up-flow anaerobic, anoxic and oxic (A2O) bioreactor was designed and operated for meat-processing wastewater (MPW) treatment as a single cost-effective system with the aim of simultaneous CNP removal. The influence of three essential factors, HRT, COD/TN ratio and aerated volume fraction on the reactor performance was assessed using response surface methodology (RSM). The required HRT to reach 98.5% COD removal was achieved at 7.5 h. Simultaneous CNP removal under denitrification rate of 199.4 mg/l.d gave high nitrate to nitrogen gas conversion of 74.6 mg/l. An HRT, COD/TN ratio and aerated volume fraction of 10 h, 100:20 and 60%, respectively, was a favored condition for an efficient nitrogen removal with effluent total Kjeldahl nitrogen (TKN) less than 70 mg/l. Under optimum condition, an HRT, COD/TN and aerated volume fraction of 8 h, 100:14 and 65%, respectively, resulted an effluent phosphorus of 43 mg/l, but 93.97 mg/l phosphorus was released in an anaerobic condition at 6 h. An effluent with a low turbidity of about 1.5 NTU and a sludge volume index (SVI) of 75.9 ml/g was achieved using at HRT of 12.5 h, COD/TN ratio of 100: 8 and aerated volume fraction of 50%. Under these conditions, the removal efficiencies for COD, TKN, nitrate-nitrogen (NO3--N), total nitrogen (TN) and phosphorus (PO43--P) were obtained to be 98.33, 92.06, 91.97, 90.48 and 83.48%, respectively. As a result, the application of the up-flow A2O bioreactor is a promising configuration to get hygienic water from wastewater.

Drinking water treatment sludge as an effective additive for biogas production from food waste; kinetic evaluation and biomethane potential test.

The effect of drinking water treatment sludge (DWTS) as a mixture additive, on biogas and methane production from food waste was studied. Mesophilic anaerobic digestion of food waste with 5 concentrations of DWTS (0, 2, 6, 12, and 18 ppm) was carried out. It was found that DWTS can significantly enhance biogas and methane yield. The highest biogas (671 Nml/g VS) as well as methane yield (522 Nml/g VS) was observed when 6 mg/kg DWTS was added. This is equal to 65 and 58 percent increase in comparison with the control digester. The calculated lag time for methane was found to be in between 3.3 and 4.7 days. The DWTS also reduced the lag phase and retention time. The biogas experimental data was fitted with the modified Gompertz and the first-order kinetic models with R2 higher than 0.994 and 0.949, respectively. The ratio of the experimental biogas production to the theoretical biogas production (ɛ) for control sample was 0.53 while for other samples containing additive were higher than 0.78.

Acid pretreatment and enzymatic saccharification of brown seaweed for polyhydroxybutyrate (PHB) production using Cupriavidus necator.

The brown seaweed Sargassum sp. was used as a feedstock to produce polyhydroxybutyarte (PHB) using Cupriavidus necator PTCC 1615. In order to release monomeric sugars, dilute acid hydrolysis of Sargassum sp. biomass was followed by enzymatic saccharification. In addition, the effect of different nitrogen sources was evaluated for PHB production. The fermentation of hydrolysate with the ammonium sulfate as selected nitrogen source resulted PHB yield of 0.54±0.01g/g reducing sugar. Then, NaCl was used as external stress factor which was added to the media. Addition of 8g/L NaCl had a positive impact on high PHB yield of 0.74±0.01g/g reducing sugar. Increasing trend of NaCl concentration to 16g/L was found to inhibit the production of PHB. Based on obtained results using 20g/L of reducing sugar, at desired condition the highest cell dry weight and PHB concentrations were 5.36±0.22 and 3.93±0.24g/L, respectively. The findings of this study reveal that Sargassum sp. is a promising feedstock for biopolymer production. The characteristics of produced PHB were analyzed by FTIR, differential scanning calorimetry and 1H NMR.

Evaluation of antibacterial efficiency of chitosan and chitosan nanoparticles on cariogenic streptococci: an in vitro study.

BACKGROUND AND OBJECTIVES: The most prevalent and worldwide oral disease is dental caries that affects a significant proportion of the world population. There are some classical approaches for control, prevention and treatment of this pathologic condition; however, the results are still not completely successful. Therefore new methods are needed for better management of this important challenge. Chitosan is a natural and non-toxic polysaccharide with many biological applications, particularly as an antimicrobial agent. Chitosan nanoparticle is a bioactive and environment friendly material with unique physicochemical properties. The aim of the present study was to investigate the antimicrobial effect of chitosan and nano-chitosan on the most important cariogenic streptococci. MATERIALS AND METHODS: For evaluation of antimicrobial effect of chitosan and nano-chitosan against oral streptococci broth micro-dilution method was carried out for four bacterial species; Streptococcus mutans, Streptococcus sobrinus, Streptococcus sanguis and Streptococcus salivarius. Also the effect of these materials on adhesion of above bacteria was evaluated. One-way ANOVA and post hoc Tukey test were used for statistical analysis. RESULTS: The MICs of chitosan for S. mutans, S. sanguis, S. salivarius and S. sobrinus were 1.25, 1.25, 0.625 and 0.625 mg/mL, respectively. The MIC of chitosan nanoparticle for S. mutans, S. salivarius and S. sobrinus was 0.625 mg/mL and for S. sanguis was 0.312 mg/mL. Chitosan and chitosan nanoparticles at a concentration of 5 mg/mL also reduced biofilm formation of S. mutans up to 92.5% and 93.4%, respectively. CONCLUSION: The results of this study supported the use of chitosan and chitosan nanoparticles as antimicrobial agents against cariogenic Streptococci.

Electricity generation through degradation of organic matters in medicinal herbs wastewater using bio-electro-Fenton system.

In the present study, the potential application of the bio-electro-Fenton (BEF) process for the treatment of medicinal herbs wastewater in a mediator-less microbial fuel cell (MFC) system is investigated. This process is operated in a dual-chamber MFC with anaerobic seed sludge as biocatalyst in an anode chamber under conditions of neutral pH, an aerobic cathode chamber equipped with a Fe@Fe2O3/graphite composite cathode and a Nafion membrane as a separator. The performance of the MFC is determined in three different mixed liquor suspended solids (MLSS) loadings, Nafions (112, 115) and a salt bridge in an air-cathode BEF process, in terms of power generation, chemical oxygen demand (COD) removal efficiency, columbic and energy efficiencies. Under optimal conditions, the batch experiment results show that the cathode chamber of the BEF reactor, equipped with Nafion 112 and inoculated with seed sludge at 3000 mg L(-1) MLSS concentration, produces the maximum power density of 49.76 mW m(-2), 0.56 mg L(-1) and 29 mol L(-1) of H2O2 and Fe(2+), respectively. Under these conditions, the MFC achieves COD removal 78.05% in the anaerobic anode chamber and 84.02% as a result of aerobic processes from the air-cathode BEF chamber, whilst the maximum voltage εcb and εE values are 600 mV, 4.09% and 1.37%, respectively.

Preparation, characterization and photocatalytic application of TiO2/Fe-ZSM-5 nanocomposite for the treatment of petroleum refinery wastewater: Optimization of process parameters by response surface methodology.

Photocatalytic degradation of organic contaminants from petroleum refinery wastewater under UV and sunlight was investigated by immobilizing nanosized TiO2 photocatalyst into the structure of as-synthesized Fe-ZSM-5 zeolite via sol-gel method. Pure phase of TiO2/Fe-ZSM-5 photocatalyst with specific surface area of 304.6 m(2) g(-1) and loaded TiO2 of 29.28% was successfully synthesized. Effects of various operational parameters on treatment process were investigated by use of Response Surface Methodology (RSM). Maximum reduction of 80% COD was achieved at pH of 4, a photocatalyst concentration of 2.1 g l(-1), temperature of 45 °C and UV exposure time of 240 min. Gas chromatography-mass demonstrated an apparent shift in molecular weight from a higher fraction to a lower fraction even under sunlight. It is expected that the prepared photocatalyst is able to use ultraviolet and visible light energy. Results indicated that removal of COD degradation did not decrease as the reuse cycle of photocatalyst increased. Moreover, the potential to use sunlight energy and the simplicity of operation make photocatalysis an attractive prospect in terms of petroleum refinery wastewater treatment.

Application of integrated ozone and granular activated carbon for decolorization and chemical oxygen demand reduction of vinasse from alcohol distilleries.

This study investigates the treatment of the distilleries vinasse using a hybrid process integrating ozone oxidation and granular activated carbons (GAC) in both batch and continuous operation mode. The batch-process studies have been carried out to optimize initial influent pH, GAC doses, the effect of the ozone (O3) and hydrogen peroxide (H2O2) concentrations on chemical oxygen demand (COD) and color removal of the distilleries vinasse. The continuous process was carried out on GAC and ozone treatment alone as well as the hybrid process comb both methods to investigate the synergism effectiveness of the two methods for distilleries vinasse COD reduction and color removal. In a continuous process, the Yan model described the experimental data better than the Thomas model. The efficiency of ozonation of the distilleries vinasse was more effective for color removal (74.4%) than COD removal (25%). O3/H2O2 process was not considerably more effective on COD and color removal. Moreover, O3/GAC process affected negatively on the removal efficiency by reducing COD and color from distilleries vinasse. The negative effect decreased by increasing pH value of the influent.

Application of chitosan-citric acid nanoparticles for removal of chromium (VI).

In the present study, CS-CA nanoparticle was prepared for forming a new amide linkage, by grafting the amino groups of CS in the presence of carboxylic groups of CA that acts as cross-linking agent. The as-prepared CS-CA nanoparticle samples were characterized by use of dynamic light scattering (DLS), scanning electron microscopy (SEM), Fourier-transformed infrared spectroscopy (FTIR), X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS) techniques, which showed that the cross-linking agent preserved during the chemical modifications. The adsorption capacity of the CS-CA nanoparticles for the removal of Cr (VI) in aqueous solution was studied. The adsorption equilibrium data taken at the optimized condition, i.e., 25 °C and pH of 3, were analyzed with the Langmuir, Freundlich and Redlich-Peterson isotherm models. The kinetics of Cr (VI) adsorption on CS-CA nanoparticles obtained at different initial concentrations were also analyzed using the pseudo-second-order model.

Kinetic studies on fermentative production of biofuel from synthesis gas using Clostridium ljungdahlii.

The intrinsic growth, substrate uptake, and product formation biokinetic parameters were obtained for the anaerobic bacterium, Clostridium ljungdahlii, grown on synthesis gas in various pressurized batch bioreactors. A dual-substrate growth kinetic model using Luong for CO and Monod for H2 was used to describe the growth kinetics of the bacterium on these substrates. The maximum specific growth rate (µ(max) = 0.195 h(-1)) and Monod constants for CO (K s,CO = 0.855 atm) and H2 (K(s,H2) = 0.412 atm) were obtained. This model also accommodated the CO inhibitory effects on cell growth at high CO partial pressures, where no growth was apparent at high dissolved CO tensions (P(CO)(∗) > 0.743 atm). The Volterra model, Andrews, and modified Gompertz were, respectively, adopted to describe the cell growth, substrate uptake rate, and product formation. The maximum specific CO uptake rate (q(max) = 34.364 mmol/g cell/h), CO inhibition constant (K(I) = 0.601 atm), and maximum rate of ethanol (R(max) = 0.172 mmol/L/h at P(CO) = 0.598 atm) and acetate (R(max) = 0.096 mmol/L/h at P(CO) = 0.539 atm) production were determined from the applied models.