Scavenging of hexavalent chromium from aqueous solution by Macadamia nutshell biomass modified with diethylenetriamine and maleic anhydride.

Based on the premise that aqueous anions of hexavalent chromium (Cr(VI)) are capable of electrostatic interaction with cationic and polar active sites, acid-washed Madacamia nutshell biomass was sequentially treated with diethylenetriamine (DETA) and maleic anhydride (MA) to graft poly(diethylenetriamine-co-maleic anhydride). By displaying a new peak at 1685 cm-1 ascribed to amide CO stretching vibrations, Fourier transform infrared spectroscopy highlighted the formation of amide groups through reaction of DETA with carboxyl groups on the biomass surface. Scanning electron microscopic images of the MA-modified biomass displayed polymeric growths attributed to copolymerization of DETA with MA. The polar and ionizable amide and amine groups of the grafted copolymer endowed the adsorbent with Cr(VI) removal capabilities over a wide pH range demonstrated by removal efficiencies between 70.9% and 81.7% in the pH 1.6 to pH 10.0 range for the treatment of 20 mL solutions containing 100 mg L-1 Cr(VI) with 200 mg of adsorbent. Conformity of the adsorption isotherm data to the Freundlich model revealed the heterogeneous nature of the adsorbent surface, which comprised a variety of functional groups capable of interaction with Cr(VI) species in solution. The Sips isotherm model provided the best fit to the equilibrium experimental data, and the adsorption capacity was 779.1 mg g-1 at pH 1.6, room temperature and an adsorbent dosage of 5.0 g L-1. The findings indicate that Cr(VI) adsorption onto diethylenetriamine and maleic anhydride modified Madacamia nutshell biomass is a promising option for Cr(VI) removal from aqueous solutions.

Synthesis, Characterization and Antimicrobial Activity of Zinc Oxide Nanoparticles against Selected Waterborne Bacterial and Yeast Pathogens.

The disinfection of wastewater using nanoparticles (NPs) has become a focal area of research in water treatment. In this study, zinc oxide (ZnO) NPs were synthesized using the microwave heating crystallization technique and characterized using transmission electron microscopy (TEM), Fourier transform infrared (FTIR) spectroscopy and X-ray diffraction (XRD). Qualitative well diffusion and quantitative minimum inhibitory concentration (MIC) tests were conducted to determine the antimicrobial activity of ZnO NPs against selected waterborne pathogenic microbes. FTIR spectral studies confirmed that the binding of urea with Zn occurs through Zn-O stretching. XRD confirmed the crystallized identity in a hexagonal ZnO wurtzite-type structure. The formation of zones of inhibition and low MIC values in the antimicrobial analysis were indicative of the effective antimicrobial activity of zinc oxide nanoparticles against the test microorganisms. The application of metallic nanoparticles in water treatment could curb the spread of waterborne microbial diseases.

Quantification of some ARVs' removal efficiency from wastewater using a moving bed biofilm reactor.

To date, in South Africa alone, there are an estimated 4.5 million people receiving antiretroviral (ARV) therapy. This places South Africa as the country with the largest ARV therapy programme in the world. As a result, there are an increasing number of reports on the occurrence of ARVs in South African waters. Achieving efficient and bio-friendly methods for the removal of these pollutants is considered as a concern for environmental researchers. This study aims at studying the efficiency of a moving bed biofilm reactor (MBBR) system for removing ARVs from wastewater. A continuous-flow laboratory scale system was designed, built, installed, and operated at a carrier filling rate of 30%, an organic loading rate of 0.6 kg COD/m3.d-1 OLR, a hydraulic retention time of 18h, and a 27.8 mL/min flow rate. The systems were monitored over time for the elimination of conventional wastewater parameters i.e., Biological Oxygen Demand, Chemical Oxygen Demand, and nutrients. The results showed that the MBBR system as a bio-friendly method has high efficiency in removing Nevirapine, Tenofovir, Efavirenz, Ritonavir and Emtricitabine from the synthetic influent sample with an average removal of 62%, 74%, 94%, 94% and 95%, respectively, after 10 days of operation.

Comparative study of the photocatalytic degradation of 2-chlorophenol under UV irradiation using pristine and Ag-doped species of TiO2, ZnO and ZnS photocatalysts.

A comparative photocatalytic degradation of 2-chlorophenol (2CP) in aqueous solution was investigated using pristine and Ag-doped semiconductor photocatalysts obtained from TiO2, ZnO and ZnS. Varying percentages (1, 3 and 5%) of Ag nanoparticles were doped on the semiconductor photocatalysts via the sol-gel method. The pristine and Ag-doped photocatalysts were characterized using UV-Vis diffuse reflectance spectroscopy, photo-luminescence spectroscopy, X-Ray diffractometry, Fourier transform infrared spectroscopy and transmission electron microscopy; and these techniques confirmed the successful syntheses of the pristine and Ag-doped species. The photocatalytic activities of all species for the degradation of 2CP were carried in photo-reactor using UV irradiation intensity of 1.4 mW/cm2 for 150 min; and the effects of various operating parameters (such as catalyst loading, pH and 2CP initial concentrations) were studied. The results showed enhanced 2CP degradation in the Ag-doped species in comparison to the pristine species while alkaline pH region was most suitable for 2CP degradation especially at low concentration. Lower loadings of the photocatalysts were usually more effective for the 2CP degradation and the degradation trend in the TiO2 and ZnS species was 5% Ag-doped >3% Ag-doped >1% Ag-doped > Pristine, while it was 1% Ag-doped >3% Ag-doped >5% Ag-doped > Pristine in the ZnO. Thus, although the Ag doping enhanced 2CP by all semiconductor photocatalysts, the Ag-doped TiO2 was more effective than the ZnO and ZnS species.

Removal of tetracycline from the aquatic environment using activated carbon: A comparative study of adsorption performance based on the activator agents.

This research focus endeavour to compare the remediation of tetracycline (TC) through activated carbon (AC), crafted utilizing two distinct chemical activators: zinc chloride (ACZ), and potassium hydroxide (ACK), using pine cone biowaste as an effective carbon precursor, followed by microwave-assisted activation. The impact of TC removal by ACZ and ACK adsorbents was thoroughly examined. The influence of pH, adsorbent mass, adsorption isotherms, kinetics, and inclusive thermodynamics were studied. Our results revealed that the interaction between TC and ACZ or ACK adsorbents aligned well with the model of pseudo-second-order kinetics, whilst the Langmuir model fitted the adsorption isotherm data of ACZ and ACK. The ACZ have a maximum adsorption capacity of 327.87 mg/g compared to that of the ACK (283.29 mg/g). Adsorption of TC was facilitated by the suitable pore volume, abundant microporous, and mesoporous structure of these adsorbents. The ACZ adsorbent is abundant in oxygen-containing functional groups, compared to ACK with minimized reactive sites, in bonding with the TC molecules through hydrogen bonding, for faster removal of TC. Our finding from this work further highlights that the synthesized ACZ from pine cones evidenced significant environmental potentials in the elimination of antibiotics from aqueous solution, to promote clean application perspectives.

Adsorption of Cr(VI) and phosphate anions by amino-functionalized palm oil fibers.

This work developed a novel sustainable adsorbent (PF-Aq) prepared by the amino-functionalization of palm oil fibers (PF). XPS, SEM/EDS, TGA/DSC, and FT-IR techniques proved the successful functionalization of the PF with the amino group. The PF-Aq adsorbent presents a high adsorption capacity for phosphate and Cr(VI) ions. Adsorption kinetics of the ions onto the PF-Aq followed the general-order models, with 240- and 300-min equilibrium times for phosphate and Cr(VI), respectively. The Freundlich equilibrium model can explain the adsorption of phosphate and Cr(VI) on the PF-Aq. Besides, the maximum adsorption capacities were 151.07 mg g-1 for phosphate and 206.08 mg g-1 for Cr(VI). The best pH for the adsorption of both ions on PF-Aq was 4.0. Interestingly, adsorption was exothermic for phosphate and endothermic for Cr(VI). The adsorption capacities were reduced by 16% for phosphate and 10% for Cr(VI) after 5 adsorption-desorption cycles, demonstrating the good recyclability of the PF-Aq. It can be concluded that PF-Aq is a relevant adsorbent to uptake phosphate and Cr(VI) from water due to its high adsorption capacity, low cost, recyclability, availability, and fast kinetics. Finally, the excellent adsorption potential results from inserting amino groups in the PF, allowing electrostatic interactions between adsorbent and adsorbate.

Molecular imprinted polymer for solid-phase extraction of flavonol aglycones from Moringa oleifera extracts.

Molecular imprinted polymer produced using quercetin as the imprinting compound was applied for the extraction of flavonol aglycones (quercetin and kaempferol) from Moringa oleifera methanolic extracts obtained using heated reflux extraction method. Identification and quantification of these flavonols in the Moringa extracts was achieved using high performance liquid chromatography with ultra violet detection. Breakthrough volume and retention capacity of molecular imprinted polymer SPE was investigated using a mixture of myricetin, quercetin and kaempferol. The calculated theoretical number of plates was found to be 14, 50 and 8 for myricetin, quercetin and kaempferol, respectively. Calculated adsorption capacities were 2.0, 3.4 and 3.7 µmol/g for myricetin, quercetin and kaempferol, respectively. No myricetin was observed in Moringa methanol extracts. Recoveries of quercetin and kaempferol from Moringa methanol extracts of leaves and flowers ranged from 77 to 85% and 75 to 86%, respectively, demonstrating the feasibility of using the developed molecularly imprinted SPE method for quantitative clean-up of both of these flavonoids. Using heated reflux extraction combined with molecularly imprinted SPE, quercetin concentrations of 975 ± 58 and 845 ± 32 mg/kg were determined in Moringa leaves and flowers, respectively. However, the concentrations of kaempferol found in leaves and flowers were 2100 ± 176 and 2802 ± 157 mg/kg, respectively.

Trends in removal of pharmaceuticals in contaminated water using waste coffee and tea-based materials with their derivatives.

The introduction of large amounts of pharmaceuticals into the environmental waters is well-documented in literature with their occurrence reported in all different water matrices accessible to humans and animals. At the same time, the increasing consumption of coffee and tea-based beverages results in the generation of solid waste, which is mostly disposed-off in the environment. To minimize environmental pollution, coffee and tea-based materials have been proposed as suitable options to remove pharmaceuticals in environmental waters. Therefore, this article provides a critical review on the preparation and applications of coffee and tea-based materials in removing pharmaceuticals from contaminated water. In this context, most studies in literature focused on the applications of these materials as adsorbents, while only limited work on their role in degradation of pharmaceuticals is discussed. The successful application in adsorption studies is attributed to high surface areas of adsorbents and the ability to easily modify the adsorbent surfaces by incorporating functional groups that provide additional oxygen atoms, which promote easy interactions with pharmaceuticals. Hence, the adsorption mechanisms are mostly described by hydrogen bonding, electrostatic and π-π interactions with sample pH playing a dominant role in the adsorption process. Overall, the present article focused on the developments, trends and future research direction on the preparations and applications of coffee and tea-based materials for efficient removal of pharmaceuticals in water. PRACTITIONER POINTS: Review of tea and coffee wastes application for removal of pharmaceuticals in water Key applications in adsorption and degradation of pharmaceuticals in water Removal mostly explained by hydrogen bonding, electrostatic, and π-π interactions Trends, gaps, and future research to be explored are reviewed and highlighted.

Synthesis of molecularly imprinted polymers for extraction of fluoroquinolones in environmental, food and biological samples.

In recent years, fluoroquinolones have been found present in important water resources and food sources which compromises the food quality and availability, thereby, causing risks to the consumer. Despite the recent advancement in the development of analytical instrumentation for routine monitoring of fluoroquinolones in water, food, and biological samples, sample pre-treatment is still a major bottleneck of the analytical methods. Therefore, fast, selective, sensitive, and cost-effective sample preparation methods prior to instrumental analysis for fluoroquinolones residues in environmental, food and biological samples are increasingly important. Solid-phase extraction using different adsorbents is one of the most widely used pre-concentration/clean-up techniques for analysis of fluoroquinolones. Molecularly imprinted polymers (MIPs) serve as excellent effective adsorbent materials for selective extraction, separation, clean-up and preconcentration of various pollutants in different complex matrices. Therefore, synthesis of MIPs remains crucial for their applications in sample preparation as this offers much-needed selectivity in the extraction of compounds in complex samples. In this study, the progress made in the synthesis of MIPs for fluoroquinolones and their applications in water, food and biological samples were reviewed. The present review discusses the selection of all the elements of molecular imprinting for fluoroquinolones, polymerization processes and molecular recognition mechanisms. In conclusion, the related challenges and gaps are given to offer ideas for future research focussing on MIPs for fluoroquinolones.

Trace Metals, Crude Protein, and TGA-FTIR Analysis of Evolved Gas Products in the Thermal Decomposition of Roasted Mopane Worms, Sweet Corn, and Peanuts.

The thermal behavior of mopane worms (Imbrasia belina), roasted peanuts (Arachis hypogaea L.), and sweet corn (Zea mays L. saccharata) was investigated under inert conditions using the TGA-FTIR analytical technique heated from 64 to 844°C at a heating rate of 20°C/min. The degradation patterns of the food samples differed as sweet corn and peanuts exhibited four degradation stages 188, 248, 315, and 432°C and 145, 249, 322, and 435°C, respectively. Mopane worms displayed three (106, 398, and 403°C). The different decomposition patterns together with the types of evolved gases shown by FTIR analysis justified the varied biochemical and chemical composition of foods. The common evolved gas species between the food samples were H2O, CO2, P=O, CO, and CH4 but mopane worms showed two extra different bands of C-N and N-H. Higher volumes of evolved gases were recorded at temperatures between 276 and 450°C, which are higher than the usual cooking temperature of 150°C. This means that the food maintained its nutritional value at the cooking temperature. Mopane worms were found to contain twice and four times crude protein content than peanuts and corn, respectively. Only total arsenic metal was reported to be above threshold limits.

Determination of furanic compounds in Mopane worms, corn, and peanuts using headspace solid-phase microextraction with gas chromatography-flame ionisation detector.

A headspace-solid phase microextraction - gas chromatography-flame ionisation detector (HS-SPME-GC/FID) method was developed for the simultaneous determination of furan, 2-methylfuran and 2-furaldehyde in thermally processed Mopane worms, corn, and peanuts. The optimal HS-SPME conditions with polydimethylsiloxane/carboxen/divinylbenzene (PDMS/CAR/DVB) fiber were 30 °C, 40 min and 600 rpm stirring speed. The recoveries, detection and quantification limits for the analytes in food samples were 67-106%, 0.54-3.5 µg kg-1, and 1.8-12 µg kg-1, respectively. These results showed that the developed method was accurate, reproducible, and sensitive for the determination of furan, 2-methylfuran and 2-furaldehyde in complex food matrices with limited interference from other components. The optimised analytical method was applied for monitoring the presence of the furanic compounds in heat-processed South African foods. Although 2-furaldehyde was not detected in food samples, the maximum concentrations of 24 and 95 µg kg-1 were found for furan and 2-methylfuran, respectively.

A Critical Review on the Synthesis and Application of Ion-Imprinted Polymers for Selective Preconcentration, Speciation, Removal and Determination of Trace and Essential Metals from Different Matrices.

The presence of toxic trace metals and high concentrations of essential elements in the environment presents a serious threat to living organism. Various methods have been used for the detection, preconcentration and remediation of these metals from biological, environmental and food matrices. Owing to the complexicity of samples, methods with high selectivity have been used for detection, preconcentration and remediation of these trace metals. These methods are achieved by the use of ion-imprinted polymers (IIPs) due to their impressive properties such as selectivity, high extraction efficiency, speciation capability and reusability. Because of the increase of toxic trace and essential metals in the environment, IIPs have attracted great use in analytical chemistry. This review, provide a brief background on IIPs and polymerization method that are used for their preparation. Recent applications of IIPs as adsorbents for preconcentration, removal, speciation and electrochemical detection of trace and essential metal is also discussed.

Application of polymer-coated Macadamia integrifolia nutshell biomass impregnated with palladium for chromium(VI) remediation.

Freely suspended and porous basket restrained granules of palladium nanoparticles supported on polymer-grafted Macadamia nutshell biomass (Pd@Polym-MNS) composite were used for the treatment chromium(VI)-containing water. In the presence of formic acid, the Pd@Polym-MNS demonstrated its activity in the adsorption-reduction-based conversion of noxious chromium(VI) to less toxic chromium(III) with a low activation energy of 13.4 kJ mol-1, ΔH0 (+ 10.8 kJ mol-1), ΔS0 (-270.0 J mol-1 K-1), and ΔG0 (+ 91.3 to + 98.0 kJ mol-1) indicated the exothermic, endergonic and non-spontaneous nature of the catalytic redox reaction. In addition to facilitating easy recovery, rinsing, and reuse, restraining the Pd@Polym-MNS in the basket reactor helped maintain the integrity of the catalysts by preventing violent collisions of suspended granules with the mixing apparatus and the walls of the reaction vessel. Whereas the pseudo-first-order rate constant was recorded as 0.157 min-1 upon initial use, values of the mean and relative standard deviation for the second, third and fourth consecutive uses were found to be 0.219 min-1 and 1.3%, respectively. According to a response surface methodological approach to batch experimentation, the initial concentration of chromium(VI) and catalyst dosage had the greatest impact on the redox reaction rate, accounting for 85.7% and 11.6% of the variability in the value of the pseudo-first-order rate constant, respectively. Mutually beneficial effects of the combinations of high formic acid and low chromium(VI) concentration, high temperature and catalyst dosage as well as high formic acid and catalyst dosage were recorded.

Magnetic Ion Imprinted Polymers (MIIPs) for Selective Extraction and Preconcentration of Sb(III) from Environmental Matrices.

Antimony(III) is a rare element whose chemical and toxicological properties bear a resemblance to those of arsenic. As a result, the presence of Sb(III) in water might have adverse effects on human health and aquatic life. However, Sb(III) exists at very ultra-trace levels which may be difficult for direct quantification. Therefore, there is a need to develop efficient and reliable selective extraction and preconcentration of Sb(III) in water systems. Herein, a selective extraction and preconcentration of trace Sb(III) from environmental samples was achieved using ultrasound assisted magnetic solid-phase extraction (UA-MSPE) based on magnetic Sb(III) ion imprinted polymer-Fe3O4@SiO2@CNFs nanocomposite as an adsorbent. The amount of antimony in samples was determined using inductively coupled plasma optical emission spectrometry (ICP-OES). The UA-MSPE conditions were investigated using fractional factorial design and response surface methodology based on central composite design. The Sb(III)-IIP sorbent displayed excellent selectivity towards Sb(III) as compared to NIIP adsorbent. Under optimised conditions, the enrichment factor, limit of detection (LOD) and limit of quantification (LOQ) of UA-MSPE/ICP-OES for Sb(III) were 71.3, 0.13 µg L-1 and 0.44 µg L-1, respectively. The intra-day and inter-day precision expressed as relative standard deviations (%RSDs, n = 10 and n = 5) were 2.4 and 4.7, respectively. The proposed analytical method was applied in the determination of trace Sb(III) in environmental samples. Furthermore, the accuracy of the method was evaluated using spiked recovery experiments and the percentage recoveries ranged from 95-98.3%.

Multi-ion imprinted polymers (MIIPs) for simultaneous extraction and preconcentration of Sb(III), Te(IV), Pb(II) and Cd(II) ions from drinking water sources.

Simultaneous extraction and preconcentration of several potentially toxic metal ions have received great attention because of their toxicological effects on aquatic life and human beings. Multi-ion imprinted polymers (MIIP) have proved to be promising adsorbents with excellent specific recognition performance than single-ion imprinted polymer. Therefore, in this study, the MIIP strategy was employed for simultaneous extraction and enrichment of Sb(III), Cd(II), Pb(II) and Te(IV) ions from drinking water sources. MIIPs was used as a sorbent material in ultrasound-assisted dispersive solid phase extraction combined with inductively coupled plasma optical emission spectrometry (UA-DSPE/ICP-OES). The experimental parameters that affect the extraction efficiency and recovery of Sb(III), Cd(II), Pb(II) and Te(IV) were investigated using response surface methodology. Under optimum conditions, the enhancement factors, linear range, limit of detection (LOD) and limit of quantification (LOQ) were 37.7-51.1, 0.04-100 µg L-1, 0.011-0.28 µg L-1, 0.037-093 µg L-1, respectively. The intra-day (n = 10) and inter-day (n = 5) precision expressed as relative standard deviations (%RSDs,) were 3% and 5%, respectively. The proposed UA-DSPE/ICP-OES method was applied for preconcentration and determination of the trace metal ions in environmental samples. Furthermore, the accuracy of the method was evaluated using spiked recovery experiments and the percentage recoveries ranged from 95% to 99.3%.

A comparative study of acid-treated, base-treated, and Fenton-like reagent-treated biomass for Cr(VI) sequestration from aqueous solutions.

A wide variety of biomass materials have been used for the removal of toxic chromium(VI) by biosorption. The current study investigated the efficacy of Macadamia nutshells treated with sodium hydroxide, nitric acid, and the Fenton-like reagent in the removal of Cr(VI). The adsorbents were characterized by FTIR, SEM, TGA, and elemental analysis. Effects of functional parameters influencing the adsorption of Cr(VI), solution pH (pH 1-11), contact time (5-250 min), concentration of adsorbent (1-10 g/L), and adsorbate concentration (10-200 mg/L) were investigated. The optimum conditions for biosorption were pH 1.4, adsorbent dose of 5 g/L, and 160 min of contact time. In all cases, the base-treated adsorbent displayed superior performance compared to others, with highest percent removal of 98%. The adsorbate-adsorbent interactions were better explained by the Freundlich isotherm and the pseudo-first-order rate model. The Macadamia-based adsorbents are potentially useful for Cr(VI) removal from aqueous solutions. PRACTITIONER POINTS: Three different chemical activators were investigated for the modification of Macadamia surface. The base-treated material exhibited the highest specific surface area of 12.1 m2 /g. The Cr(VI) adsorption performance for the base-treated material dwarfed the other materials. Excellent Cr(VI) removal efficiency in the presence of competitors was achieved.

Palladium nanoparticles dispersed on functionalized macadamia nutshell biomass for formic acid-mediated removal of chromium(VI) from aqueous solution.

Driven by the need for sustainably sourced catalysts and the use of reaction systems that generate environmentally benign by-products, the present study aimed to deposit stable, dispersed palladium (Pd) nanoparticles on the modified surfaces of granular macadamia nutshell (MNS) biomass for catalytic reduction of hexavalent chromium (Cr(VI)) to trivalent chromium (Cr(III)). Through wet impregnation with Pd(II) ions and subsequent hydrazine-mediated reduction to Pd(0), Pd nanoparticles were embedded in a scaffold of polyethyleneimine grafted on bleached MNS previously coated with a chemically bound layer of polyglycidyl methacrylate. Imagery from scanning electron microscopy showed the formation of different layers of the polymeric coating and dispersed palladium resulting from surface modification and palladium nanoparticle synthesis, respectively. X-ray diffraction analysis confirmed the formation of Pd on the modified MNS surface and suggested an estimated crystallite size of 5.0 nm. The supported nanoparticles exhibited catalytic activity in formic acid-mediated Cr(VI) reduction and showed promising stability with consecutive reuse. These findings set the stage for advanced studies into performance optimization.

Application of Hollow Fibre-Liquid Phase Microextraction Technique for Isolation and Pre-Concentration of Pharmaceuticals in Water.

In this article, a comprehensive review of applications of the hollow fibre-liquid phase microextraction (HF-LPME) for the isolation and pre-concentration of pharmaceuticals in water samples is presented. HF-LPME is simple, affordable, selective, and sensitive with high enrichment factors of up to 27,000-fold reported for pharmaceutical analysis. Both configurations (two- and three-phase extraction systems) of HF-LPME have been applied in the extraction of pharmaceuticals from water, with the three-phase system being more prominent. When compared to most common sample preparation techniques such as solid phase extraction, HF-LPME is a greener analytical chemistry process due to reduced solvent consumption, miniaturization, and the ability to automate. However, the automation comes at an added cost related to instrumental set-up, but a reduced cost is associated with lower reagent consumption as well as shortened overall workload and time. Currently, many researchers are investigating ionic liquids and deep eutectic solvents as environmentally friendly chemicals that could lead to full classification of HF-LPME as a green analytical procedure.

Recent advances in hexavalent chromium removal from aqueous solutions by adsorptive methods.

Chromium exists mainly in two forms in environmental matrices, namely, the hexavalent (Cr(vi)) and trivalent (Cr(iii)) chromium. While Cr(iii) is a micronutrient, Cr(vi) is a known carcinogen, and that warrants removal from environmental samples. Amongst the removal techniques reported in the literature, adsorption methods are viewed as superior to other methods because they use less chemicals; consequently, they are less toxic and easy to handle. Mitigation of chromium using adsorption methods has been achieved by exploiting the physical, chemical, and biological properties of Cr(vi) due to its dissolution tendencies in aqueous solutions. Many adsorbents, including synthetic polymers, activated carbons, biomass, graphene oxide, and nanoparticles as well as bioremediation, have been successfully applied in Cr(vi) remediation. Initially, adsorbents were used singly in their natural form, but recent literature shows that more composite materials are generated and applied. This review focused on the recent advances, insights, and project future directions for these adsorbents as well as compare and contrast the performances achieved by the mentioned adsorbents and their variants.

Adsorptive Removal of Hexavalent Chromium by Diphenylcarbazide-Grafted Macadamia Nutshell Powder.

Macadamia nutshell powder oxidized by hydrogen peroxide solutions (MHP) was functionalized by immobilizing 1,5'-diphenylcarbazide (DPC) on its surface. The effectiveness of grafting was confirmed by the Fourier transform infrared spectrum due to the presence of NH and C=C stretches at 3361, 1591, and 1486 cm-1, respectively, on the grafted material which were absent in the nongrafted material. Thermogravimetric analysis revealed that the presence of DPC on the surface of Macadamia shells lowered the thermal stability from 300°C to about 180°C owing to the volatile nature of DPC. Surface roughness as a result of grafting was appreciated on the scanning electron microscopy images. Parameters influencing the adsorptive removal of Cr(VI) were examined and found to be optimal at pH 2, 120 min, 150 mg/L, and 2.5 g/L. Grafting MHP with DPC leads to an increase in the Langmuir monolayer capacity from 37.74 to 72.12 mg/g. Grafting MHP with DPC produced adsorbent with improved removal efficiency for Cr(VI).