Pinecone biochar for the Adsorption of chromium (VI) from wastewater: Kinetics, thermodynamics, and adsorbent regeneration.

High concentration of chromium in aquatic environments is the trigger for researchers to remediate it from wastewater environments. However, conventional water treatment methods have not been satisfactory in removing chromium from water and wastewater over the last decade. Similarly, many adsorption studies have been focused on one aspect of the treatment, but this study dealt with all aspects of adsorption packages to come up with a concrete conclusion. Therefore, this study aimed to prepare pinecone biochar (PBC) via pyrolysis and apply it for Cr(VI) removal from wastewater. The PBC was characterized using FTIR, SEM-EDX, BET surface area, pHpzc, Raman analyses, TGA, and XRD techniques. Chromium adsorption was studied under the influence of PBC dose, solution pH, initial Cr(VI) concentration, and contact time. The characteristics of PBC are illustrated by FTIR spectroscopic functional groups, XRD non-crystallite structure, SEM rough surface morphology, and high BET surface area125 m2/g, pore volume, 0.07 cm3/g, and pore size 1.4 nm. On the other hand, the maximum Cr (VI) adsorption of 69% was found at the experimental condition of pH 2, adsorbent dosage 0.25 mg/50 mL, initial Cr concentration 100 mg/L, and contact time of 120 min. Similarly, the experimental data were well-fitted with the Langmuir adsorption isotherm at R2 0.96 and the pseudo-second-order kinetics model at R2 0.99. This implies the adsorption process is mainly attributed to monolayer orientation between the adsorbent and adsorbate. In the thermodynamics study of adsorption, ΔG was found to be negative implying the adsorption process was feasible and spontaneous whereas the positive values of ΔH and ΔS indicated the adsorption process was endothermic and increasing the degree of randomness, respectively. Finally, adsorbent regeneration and reusability were successful up to three cycles. In conclusion, biochar surface modification and reusability improvements are urgently required before being applied at the pilot scale.

The removal of pathogenic bacteria and dissolved organic matter from freshwater using microporous membranes: insights into biofilm formation and fouling reversibility.

Pathogenic bacteria in drinking-water pose a health risk to consumers, as they compromise the quality of portable water. Chemical disinfection of water containing dissolved organic matter (DOM) causes harmful disinfection by-products. In this work, 4-hydroxybenzoic acid (4-HBA) blended polyethersulfone membranes were fabricated and characterised using microscopic and spectroscopic techniques. The membranes were evaluated for the removal of bacteria and DOM from synthetic and environmental water. Permeate flux increased from 287.30 to 374.60 l m-2 h-1 at 3 bars when 4-HBA increased from 0 to 1.5 wt.%, suggesting that 4-HBA influenced the membrane's affinity for water. Furthermore, 4-HBA demonstrated antimicrobial properties by inhibiting bacterial growth. The membrane with 1 wt.% 4-HBA recorded 99.4 and 100% bacteria removal in synthetic and environmental water, respectively. Additionally, DOM removal of 55-73% was achieved. A flux recovery ratio (FRR) of 94.6% was obtained when a mixture of bacteria and humic acid was filtered, implying better fouling layer reversibility during cleaning. Furthermore, 100% FRR was achieved when a multimedia granular filtration step was installed prior to membrane filtration. The results illustrated that the membranes had a high permeate flux with low irreversible fouling. This indicated the potential of the membranes in treating complex feed streams using simple cleaning protocols.

Detection and Quantification of Bisphenol A in Surface Water Using Absorbance-Transmittance and Fluorescence Excitation-Emission Matrices (A-TEEM) Coupled with Multiway Techniques.

In the present protocol, we determined the presence and concentrations of bisphenol A (BPA) spiked in surface water samples using EEM fluorescence spectroscopy in conjunction with modelling using partial least squares (PLS) and parallel factor (PARAFAC). PARAFAC modelling of the EEM fluorescence data obtained from surface water samples contaminated with BPA unraveled four fluorophores including BPA. The best outcomes were obtained for BPA concentration (R2 = 0.996; standard deviation to prediction error's root mean square ratio (RPD) = 3.41; and a Pearson's r value of 0.998). With these values of R2 and Pearson's r, the PLS model showed a strong correlation between the predicted and measured BPA concentrations. The detection and quantification limits of the method were 3.512 and 11.708 micro molar (µM), respectively. In conclusion, BPA can be precisely detected and its concentration in surface water predicted using the PARAFAC and PLS models developed in this study and fluorescence EEM data collected from BPA-contaminated water. It is necessary to spatially relate surface water contamination data with other datasets in order to connect drinking water quality issues with health, environmental restoration, and environmental justice concerns.

Emerging remediation potentiality of struvite developed from municipal wastewater for the treatment of acid mine drainage.

The valorisation of wastewaters for minerals recovery and their potential beneficiation has gained enormous attention recently. In this study the removal of phosphate and ammonia from municipal wastewater using activated magnesite resulted in the formation of struvite. The optimum conditions for the synthesis of struvite were 60 min of mixing, 300 rpm mixing speed, 1 g of activated magnesite and room temperature, whilst optimum conditions for the treatment of acid mine drainage (AMD) using the synthesized struvite were 45 min of mixing, 20 g of struvite dosage, 1000 mL, and 300 rpm mixing speed. The efficacy of struvite for neutralisation of AMD and attenuation of inorganic contaminants were ≥98.99% for metals (Al3+, Fe3+, and Mn2+) and ≥30% for SO42-. Traces of other metals such as Zn, Cu, Ni, Pb, and Cr were significantly attenuated. Phosphate was fully attenuated from the aqua-sphere. PHREEQC predicted the removal of minerals as oxy-(hydro)-sulphates, oxy-(hydro)-phosphate, metals hydroxides, and other complexes. FE-SEM equipped with FIB and an EDX, XRD, XRF, and FTIR confirmed the synthesis of struvite and fate of chemical species after treatment. This study confirmed the feasibility of recovering phosphate and ammonia as struvite which can be employed for the treatment of AMD.

Modeling the antifouling properties of atomic layer deposition surface-modified ceramic nanofiltration membranes.

This work investigates the enhancement of antifouling properties of ceramic nanofiltration membranes by surface modification via atomic layer deposition (ALD) of TiO2. Feed solutions containing bovine serum albumin (BSA), humic acid (HA) and sodium alginate (SA) were used as model foulants. The classic fouling mechanism models and the modified fouling indices (MFI) were deduced from the flux decline profiles. Surface roughness values of the ALD coated and uncoated membranes were 63 and 71 nm, respectively, while the contact angles were 34.2 and 59.5°, respectively. Thus, coating increased the water affinity of the membrane surfaces and consequently improved the anti-fouling properties. The MFI values and the classic fouling mechanism correlation coefficients for cake filtration for the ALD coated and the uncoated membrane upon SA fouling were 42,963 (R2 = 0.82) and 143,365 sL-2 (R2 = 0.98), respectively, whereas the correlation coefficients for the combined foulants (SA + BSA + HA) were 267,185 (R2 = 0.99) and 9569 sL-2 (R2 = 0.37), respectively. The study showed that ALD can effectively enhance the antifouling properties of ceramic membranes.

The application of GO-Fe3O4 nanocomposite for chromium adsorption from tannery industry wastewater.

The discharge of untreated tannery industrial wastewater into the environment has resulted in an adverse effect on the ecosystem and public health. Therefore, this work aimed to remove chromium ions from tannery wastewater through magnetite graphene oxide-nanocomposite (GO-Fe3O4). The experimental design of the study was a full factorial 24 approach using pH, adsorbent dose, contact time, and initial chromium concentrations. The results of FTIR analysis revealed the presence of functional groups such as hydroxyl (3438 cm-1), alcohol (1230 cm-1), aromatic (1467 cm-1), ketone (1629 cm-1), and ether (1120 cm-1). Similarly, GO-Fe3O4 acquired a high surface area of 296.2 m2/g whereas the XRD analysis showed the presence of predominant peaks which are attributed to the magnetite component. Moreover, the SEM image showed many ups and downs on the surface of the adsorbent. These cracks of morphology can create a conducive environment for the interaction of adsorbent and adsorbate. The maximum chromium removal of 95.9% was achieved at the optimum conditions of the initial chromium concentration of 40 mg/L, pH 4, adsorbent dose 1 g/100 mL, and contact time of 120 min whereas the removal of chromium from real tannery wastewater was found to be 90.3%. Based on the adsorption isotherm, the Langmuir model was the best fit for experimental data at R2 0.99, indicating homogeneous and monolayer adsorption. Finally, it can be concluded that GO-Fe3O4 was effective for chromium removal, which is a promising technology to be scaled up at the industrial level for wastewater treatment.

Synthesis of biochar-CoFe2O4 nanocomposite for adsorption of methylparaben from wastewater under full factorial experimental design.

The presence of endocrine-disrupting chemicals in municipal wastewater has emerged as a threat to human health and the environment. Therefore, this study aimed to develop biochar-cobalt ferrite (BCF) nanocomposite for the removal of methylparaben from water under the full factorial experimental design of 4 factors with 3 levels (34). The biochar-CoFe2O4 nanocomposite was developed by co-precipitation method from cobalt ferrite and biochar of Eucalyptus tree bark. Adsorbent surface morphology and functional and elemental composition were carried out by scanning electron microscopy (SEM), Fourier transform infrared (FTIR) spectroscopy, and energy-dispersive X-ray spectroscopy (EDS) techniques which showed the presence of cracks with a rough surface, reasonable surface chemical composition, and many chemical functional groups, respectively. The experimental and predicted adsorption efficiencies ranged from 25.3 to 85.6% and 21.8 to 80.3%, respectively. The maximum adsorption performance (85.6%) reduced the methylparaben concentration from 27.5 to 4.0 mg/L at the optimum condition of adsorbent dose of 55 mg/100 mL, pH 6, contact time 90 min, and the initial methylparaben concentration of 27.5 mg/L. However, the adsorbent dose was the most influential main factor whereas the least influential was the interaction between solution pH and contact time under the regression model. The model also showed that 69% methylparaben removal was described by the regression model. The experimental data best fitted with the Freundlich model indicate multilayer adsorption which is the implication of physisorption. The sorption mechanism is attributed to Vander Waals forces, H-bonding, and dipole interaction. This BCF nanocomposite adsorbent appears to be promising for the removal of methylparaben from wastewater, but a further optimization process is essential to boost the treatment performance.

Detection of humic acid in water using flat-sheet and folded-rod viscous alkaline glucose syrups.

The utility of a low-cost biocompatible material for the detection of pollutants in water is highly essential to ensure safety and economic efficiency. In this paper, solutions of two viscous alkaline glucose syrups (AGS@22-sheet and AGS@60-rod), obtained under two different temperature conditions (22 °C and 60 °C) were used to detect low levels of humic acid (HA), a carcinogen pro-molecule and metal-complexing agent in an aqueous solution. The AGS materials were characterized using ultraviolet-visible spectroscopy (UV-Vis), Fourier transform infrared spectroscopy and scanning electron microscopy (SEM). By evaluation, a detection limit (LOD) as low as 4.6 × 10-5 mg L-1 was obtained. The sensing capability of the new technology was further extended to the detection of HA in a real water sample (tap water) using the standard addition method with 98 and 100.05% recoveries. The sensing was improved in the presence of sodium acetate and sodium citrate and was found to follow a pseudo-first order reaction. These findings show that the as-synthesized glucose syrups have the potential to detect humic acid in water and thus may be employed for the quantification of HA in water treatment plants or textile industry.

PARAFAC model as an innovative tool for monitoring natural organic matter removal in water treatment plants.

The increase of fluorescent natural organic matter (fNOM) fractions during drinking water treatment might lead to an increased coagulant dose and filter clogging, and can be a precursor for disinfection by-products. Consequently, efficient fNOM removal is essential, for which characterisation of fNOM fractions is crucial. This study aims to develop a robust monitoring tool for assessing fNOM fractions across water treatment processes. To achieve this, water samples were collected from six South African water treatment plants (WTPs) during winter and summer, and two plants in Belgium during spring. The removal of fNOM was monitored by assessing fluorescence excitation-emission matrices datasets using parallel factor analysis. The removal of fNOM during summer for South African WTPs was in the range 69-85%, and decreased to 42-64% in winter. In Belgian WTPs, fNOM removal was in the range 74-78%. Principal component analysis revealed a positive correlation between total fluorescence and total organic carbon (TOC). However, TOC had an insignificant contribution to the factors affecting fNOM removal. Overall, the study demonstrated the appearance of fNOM in the final chlorinated water, indicating that fNOM requires a customised monitoring technique.

Interactions between Organic Model Compounds and Ion Exchange Resins.

Ion exchange (IEX) can successfully remove natural organic matter (NOM) from surface water. However, the removal mechanism is not well understood due to the complexity and variability of NOM in real source waters as well as the influence of multiple parameters on the removal behavior. For example, this includes the physicochemical properties of the NOM and IEX resin, and the presence of competing anions. Model compounds with a range of physical and chemical characteristics were therefore used to determine the mechanisms of NOM removal by IEX resins. Fifteen model compounds were selected to evaluate the influence of hydrophobicity, size, and charge of organic molecules on the removal by ion exchange, both individually and in mixtures. Three different resins, comprising polystyrene and polyacrylic resin of macroporous and gellular structure, showed that charge density (CD) was the most important characteristic that controlled the removal, with CD of >5 mequiv mgDOC-1 resulting in high removal (≥89%). Size exclusion of compounds with high MW (≥8 kDa) was evident. The hydrophobicity of the resin and model compound was particularly important for removal of neutral molecules such as resorcinol, which was best removed by the more hydrophobic polystyrene resin. Relationships were identified that provided explanations of the interactions observed between NOM and IEX resin in real waters.

Fundamental fouling mechanisms of dissolved organic matter fractions and their implications on the surface modifications of ceramic nanofiltration membranes: insights from a laboratory scale application.

This work reports on the fundamental factors influencing inter-foulant and foulant-membrane interactions during simulated dissolved organic matter removal using ceramic nanofiltration. Fouling tests were performed using sodium alginate (SAL), humic acid (HA) and bovine serum albumin (BSA) as model foulants. Fouling potentials of each foulant and their mixtures were investigated using feed solutions containing fixed concentrations of K+, Na+, Mg2+ and Ca2+ with a total ionic strength of 10 mM. The impact of modification by atomic layer deposition on fouling mitigation was also assessed. The flux decline in the first 100 min for single foulants was 4.16 × 10-2, 2.69 × 10-2 and 1.60 × 10-2 Lm-2 for SAL, HA and BSA, respectively. These results demonstrated that for the single foulants, deposition on the membrane surface in the early stages of filtration was primarily governed by membrane-foulant interactions. Interestingly, cake filtration was the least fouling mechanism in feed solutions composed of BSA and SAL (R2 = 0.519, 0.374 for BSA + SAL and BSA + SAL + HA, respectively) and the most favorable fouling mechanism of feed solution which included HA and SAL (R2 = 0.972). The water contact angle dropped from 58o to 35° after coating, thus improving its anti-fouling properties.

An optimised and validated surrogate analyte A-TEEM-PARAFAC-PLS technique for detecting and quantifying the biological oxygen demand in surface water.

A 5-day test duration makes BOD5 measurement unsatisfactory and hinders the development of a quick technique. Protein-like fluorescence peaks show a strong correlation between the BOD characteristics and the fluorescence intensities. For identifying and measuring BOD in surface water, a simultaneous absorbance-transmittance and fluorescence excitation-emission matrices (A-TEEM) method combined with PARAFAC (parallel factor) and PLS (partial least squares) analyses was developed using a tyrosine and tryptophan (tyr-trpt) mix as a surrogate analyte for BOD. The use of a surrogate analyte was decided upon due to lack of fluorescent BOD standards. Tyr-trpt mix standard solutions were added to surface water samples to prepare calibration and validation samples. PARAFAC analysis of excitation-emission matrices detected the tyr-trpt mix in surface water. PLS modelling demonstrated significant linearity (R2 = 0.991) between the predicted and measured tyr-trypt mix concentrations, and accuracy and robustness were all acceptable per the ICH Q2 (R2) and ASTM multivariate calibration/validation procedures guidelines. Based on a suitable and workable surrogate analyte method, these results imply that BOD can be detected and quantified using the A-TEEM-PARAFAC-PLS method. Very positive comparability between tyr-trypt mix concentrations was found, suggesting that tyr-trypt mix might eventually take the place of a BOD-based sampling protocol. Overall, this approach offers a novel tool that can be quickly applied in water treatment plant settings and is a step in supporting the trend toward rapid BOD determination in waters. Further studies should demonstrate the wide application of the method using real wastewater samples from various water treatment facilities.

Utilization of biochar for remediation of heavy metals in aqueous environments: A review and bibliometric analysis.

Biochar usage for removing heavy metals from aqueous environments has emerged as a promising research area with significant environmental and economic benefits. Using the PICO approach, the research question aimed to explore using biochar to remove heavy metals from aqueous media. We merged the data from Scopus and the Web of Science Core Collection databases to acquire a comprehensive perspective of the subject. The PRISMA guidelines were applied to establish the search parameters, identify the appropriate articles, and collect the bibliographic information from the publications between 2010 and 2022. The bibliometric analysis showed that biochar-based heavy metal remediation is a research field with increasing scholarly attention. The removal of Cr(VI), Pb(II), Cd(II), and Cu(II) was the most studied among the heavy metals. We identified five main clusters centered on adsorption, water treatment, adsorption models, analytical techniques, and hydrothermal carbonization by performing keyword co-occurrence analysis. Trending topics include biochar reusability, modification, acid mine drainage (AMD), wastewater treatment, and hydrochar. The reutilization of heavy metal-loaded spent biochar includes transforming it into electrodes for supercapacitors or stable catalyst materials. This study provides a comprehensive overview of biochar-based heavy metal remediation in aquatic environments and highlights knowledge gaps and future research directions.

Electrocatalytic oxidation of pyrrole on a quasi-reversible silver nanodumbbell particle surface for supramolecular porphyrin production.

Photoactive supramolecular porphyrin assemblies are attractive molecules for light-harvesting applications. This is due to their relatively non-toxicity, biological activities and charge and energy exchange characteristics. However, the extreme cost associated with their synthesis and requirements for toxic organic solvents during purification pose a challenge to the sustainability characteristics of their applications. This work presents the first report on the sustainable synthesis, spectroscopic and photophysical characterizations of a near-infrared (NIR) absorbing Ca(II)-meso-tetrakis (4-hydroxyphenyl)porphyrin using an electrolyzed pyrrole solution. The latter was obtained by cycling the pyrrole solution across the silver nanodumbbell particle surface at room temperature. The electrolyzed solution condensed readily with acidified p-hydroxybenzaldehyde, producing the targeted purple porphyrin. The non-electrolyzed pyrrole solution formed a green substance with significantly different optical properties. Remarkable differences were observed in the voltammograms of the silver nanodumbbell particles and those of the conventional gold electrode during the pyrrole cycling, suggesting different routes of porphyrin formation. The rationale behind these formations and the associated mechanisms were extensively discussed. Metalation with aqueous Ca2+ ion caused a Stokes shift of 38.75 eV. The current study shows the advantage of the electrochemical method towards obtaining sustainable light-harvesting porphyrin at room temperature without the need for high-energy-dependent conventional processes.

Optimization of Cr (VI) removal from aqueous solution with activated carbon derived from Eichhornia crassipes under response surface methodology.

Tannery industries' effluent contains a high concentration of Cr (VI) which has the potential to affect the environment and public health. Therefore, this study aimed to investigate the optimization of Cr (VI) adsorption by activated carbon (AC) derived from Eichhornia crassipes from an aqueous solution. The adsorbent was activated with dilute sulfuric acid followed by thermal activation. AC was characterized using proximate analysis, SEM, FTIR, X-ray diffraction, and the BET method. The Cr (VI) removal optimization process was performed using a central composite design under the response surface methodology. The proximate analysis showed that the moisture content, volatile matter, ash content, and fixed carbon of the activated carbon were 5.6%, 18.2%, 14.4%, and 61.8% respectively. The surface areas of the Eichhornia crassipes before activation, after activation, and after adsorption were 60.6 g/m2, 794.2 g/m2, and 412.6 g/m2 respectively. A highly porous structure with heterogeneous and irregular shapes was observed in the SEM micrograph. In the FTIR analysis, different peaks are indicated with various functional groups. The intensity of XRD peaks decreased as 2 theta values increased, which indicates the presence of an amorphous carbon arrangement. The point of zero charge (pHpzc) of the activated carbon was found to be 5.20. A maximum Cr (VI) removal of 98.4% was achieved at pH 5, contact time 90 min, adsorbent dose 2 g, and initial Cr (VI) concentration of 2.25 mg/L. Statistically significant interactions (P < 0.05) were observed between the initial Cr (VI) concentration and adsorbent dose as well as the initial Cr (VI) concentration and contact time. Langmuir adsorption isotherm fitted the experimental data best, with an R2 value of 0.99. The separation constant (RL) indicates that the adsorption process is favorable. The kinetic experimental data were best fitted with the pseudo-second-order model with an R2 value of 0.99 whereas the adsorption rate is controlled by intraparticle and extragranular diffusion processes. Generally, the AC has the potential to be a strong adsorbent candidate for wastewater treatment at the industrial level.

Advances in polymer-based detection of environmental ibuprofen in wastewater.

Globally, ibuprofen is the third most consumed drug and its presence in the environment is a concern because little is known about its adverse effects on humans and aquatic life. Environmentalists have made monitoring and the detection of ibuprofen in biological and environmental matrices a priority. For the detection and monitoring of ibuprofen, sensors and biosensors have provided rapid analysis time, sensitivity, high-throughput screening, and real-time analysis. Researchers are increasingly seeking eco-friendly technology, and this has led to an interest in developing biodegradable, bioavailable, and non-toxic sensors, or biosensors. The integration of polymers into sensor systems has proven to significantly improve sensitivity, selectivity, and stability and minimize sample preparation using bioavailable and biodegradable polymers. This review provides a general overview of perspectives and trends of polymer-based sensors and biosensors for the detection of ibuprofen compared to non-polymer-based sensors.

Understanding the Principles and Applications of Dual Z-Scheme Heterojunctions: How Far Can We Go?

In the past seven years, dual Z-scheme heterojunctions evolved as favorable approaches for enhanced charge carrier separation through direct or indirect charge transfer transportation mechanisms. The dynamics of the charge transfer is the major strategy for understanding their photoactivity and stability through the formation of distinctive redox centers. The understanding of currently recognized principles for successful fabrication and classification in different energy and pollution remediation strategies is discussed, and a universal charge transfer-type-based classification of dual Z-schemes that can be adopted for Z-scheme and S-scheme heterojunctions is proposed. Methods used for determining the charge transfer as proof of dual Z-scheme existence are outlined. Most importantly, a new macroscopic N-scheme and a triple Z-scheme that can also be adopted as triple S-scheme heterostructures composed of four semiconductors are proposed for generating both oxidatively and reductively empowered systems. The proposed systems are expected to possess properties that enable them to harvest solar light to drive important chemical reactions for different applications.

Adsorption of chromium from electroplating wastewater using activated carbon developed from water hyacinth.

Industrial wastewater polluted with high concentrations of Cr is commonly discharged into water resources without proper treatment. This gives rise to the deterioration of water quality and imposes adverse effects on public health. Therefore, this study is aimed at removing Cr from electroplating wastewater using activated carbon produced from water hyacinth under a full factorial experimental design with three factors and three levels (pH,2,5 and 8, adsorbent dose 0.5,1and1.5 in 100 mL and contact time 30, 60 and120 min). A phosphoric acid solution of 37% was used to activate the carbon, which was then subjected to thermal decomposition for 15 min at 500 °C. The activated carbon was characterized by the presence of a high surface area (203.83 m2/g) of BET, cracking of adsorbent beads of SEM morphology, amorphous nature of XRD, and many functional groups of FTIR such as hydroxyl (3283 cm-1), alkane (2920 cm-1), nitrile (2114 cm-1) and aromatics (1613 cm-1). The minimum Cr adsorption performance of 15.6% was obtained whereas maximum removal of 90.4% was recorded at the experimental condition of pH 2, adsorbent dose of 1.5 g/100 mL, and contact time of 120 min at a fixed value of initial Cr concentration of 100 mg/L. Similarly, the maximum Cr removal from real electroplating wastewater was 81.2% at this optimum point. Langmuir's model best described the experimental value at R2 0.96 which implies the adsorption is chemically bonded, homogeneous, and monolayer. Pseudo-second-order model best fits with the experimental data with R2 value of 0.99. The adsorbent was regenerated for seven cycles and the removal efficiency decreased from 93.25% to 21.35%. Finally, this technology is promising to be scaled up to an industrial level.

Electrochemical, surface morphological and computational evaluation on carbohydrazide Schiff bases as corrosion inhibitor for mild steel in acidic medium.

Anticorrosion and adsorption behaviour of synthesized carbohydrazide Schiff bases, namely (Z)-N'-(4-hydroxy-3-methoxybenzylidene)-6-methyl-2-oxo-4-phenyl-1,2,3,4-tetrahydropyrimidine-5-carbohydrazide(MBTC) and (Z)-N'-(3,4-dichlorobenzylidene)-6-methyl-2-oxo-4-phenyl-1,2,3,4-tetrahydropyrimidine-5-carbohydrazide (CBTC) was examined for mild steel (MS) in 15% HCl medium. The corrosion inhibition study was performed by using gravimetric, thermodynamic, electrochemical and theoretical studies including density functional theory (DFT), molecular dynamic simulation (MDS) and Monte Carlo simulations (MCS). The outcomes in terms of corrosion inhibition efficiency using electrochemical impedance spectroscopy (EIS) method at 303 K and 150 ppm concentration were 96.75% for MBTC and 95.14% for CBTC. Both inhibitors adsorbed on the MS surface through physical as well as chemical adsorption and followed the Langmuir isotherm. The mixed-type nature of both inhibitors was identified by polarization results. Surface analysis was done using FESEM, EDX, AFM and XPS studies and results showed that a protective layer of inhibitor molecules was developed over the surface of MS. The results of DFT, MCS and MDS are in accordance with experimental results obtained by weight loss and electrochemical methods.

The potential of biochar-photocatalytic nanocomposites for removal of organic micropollutants from wastewater.

Biochar (BC)-photocatalyst nanocomposites have emerged as appealing water and wastewater treatment technology. Such nanocomposite materials benefit from the synergistic effect of adsorption and photocatalysis to attain improved removal of pollutants from water and wastewater. Under this review, three BC-based nanocomposite photocatalysts such as BC-TiO2, BC-ZnO, and BC-spinel ferrites were considered. These nanocomposites acquire intrinsic properties to improve the practical limitations of the pristine BC and photocatalysts. The BC-based nanocomposites attained high photocatalytic activity, mechanical hardness, thermal stability, chemically non-reactive, magnetically permeable, reduced energy band gaps, improved reusability, and simplified recovery. Moreover, BC-based photocatalytic nanocomposites showed reduced recombination rates of the electron-hole pairs which are desirable for photocatalytic applications. However, the surface areas of the composites are usually smaller than that of the BC but higher than those of the pristine photocatalysts. Practically, the performances of the nanocomposites are much superior to those of the corresponding pristine components. This hybrid treatment technology is an emerging field and its industrial application is still at an early stage of the investigation. Therefore, exploring the full potential and practical applications of this technology is highly encouraging. Hence, this review focused on the critical evaluation of the most recent research on the synthesis, characterization, and photocatalytic treatment efficiency of the BC photocatalyst nanocomposites towards emerging pollutants in the aqueous medium. Moreover, the influence of various sources of BC feedstocks and their limitations on adsorption and photodegradation activities are discussed in detail. Finally, concluding remarks and future research directions are given to assist and shape the exploration of BC-based nanocomposite photocatalysts in water treatment.