Removal of Arsenic in Groundwater Using Fe(III) Oxyhydroxide Coated Sand: A Case Study in Mekong Delta, Vietnam

Because of its threat to the quality of freshwater resources and human health, arsenic (As) pollution is important to scientific communities and policymakers around the world. The Mekong Delta, Vietnam, is one hotspot of As pollution. Its risk assessment of different environmental components has been well documented; however, very few studies focus on As removal techniques. Considering this information gap, this study aimed to investigate the performance of an innovative and low-cost treatment system using Fe(III)-oxyhydroxide (FeOOH) coated sand to remove As(III) from aqueous solution. Batch and column experiments were conducted at a laboratory scale in order to study removal kinetics and efficiency. Experimental results indicated that the adsorption isotherm of As(III) on FeOOH coated sand using Langmuir and Freundlich models have high regression factors of 0.987 and 0.991, respectively. The batch adsorption experiment revealed that contact time was approximately 8 h for rough saturation (kinetic test). The concentration of As(III) in effluents at flow rates of 0.6 L/h, 0.9 L/h, and 1.8 L/h ranged from 1.1 µg/L to 1.7 µg/L. Results from this study indicated that FeOOH coated sand columns were effective in removing As(III) from water, with a removal efficiency of 99.1%. Ultimately, FeOOH coated sand filtration could be a potential treatment system to reduce As(III) in the domestic water supply in remote areas of the Vietnamese Mekong Delta.

Rice Straw Biochar and Magnetic Rice Straw Biochar for Safranin O Adsorption from Aqueous Solution

This study investigates the adsorption of Safranin O (SO) from aqueous solution by both biochar and magnetic biochar derived from rice straw. Rice straw biochar (RSB) was made by pyrolysis in a furnace at 500 °C, using a heating rate of 10 °C·min−1 for 2 h in an oxygen-limited environment, whilst the magnetic rice straw biochar (MRSB) was produced via the chemical precipitation of Fe2+ and Fe3+. The physicochemical properties of the synthesized biochars were characterized using SEM, SEM- EDX, XRD, FTIR techniques, and N2 adsorption (77 K) and pHpzc measurements. Batch adsorption experiments were used to explore the effect of pH, biochar dosage, kinetics, and isotherms on the adsorption of SO. Experimental data of RSB and MRSB fit well into both Langmuir and Freundlich isotherm models, and were also well-explained by the Lagergren pseudo-second-order kinetic model. The maximum SO adsorption capacity of MRSB was found to be 41.59 mg/g, while for RSB the figure was 31.06 mg/g. The intra-particle diffusion model indicated that the intra-particle diffusion may not be the only rate-limiting step. The collective physical and chemical forces account for the adsorption mechanism of SO molecules by both RSB and MRSB adsorbents. The obtained results demonstrated that the magnetic biochar can partially enhance the SO adsorption capacity of its precursor biochar and also be easily separated from the solution by using an external magnet.

Kinetics Studies of Metallic Ions Adsorption by Immobilised Chitosan

Immobilised chitosan on glass plates was used as an adsorbent for metallic ions from aqueous solutions in a batch adsorption system. Experiments were carried out as a function of contact time and initial metallic ions concentration. The adsorption efficiency increased with increasing initial metallic ions concentration (5 – 20 mg L-1) and the observed trend was: Ag2+ > Cu2+ > Ni2+ > Fe3+ > Cd2+ > Zn2+. The experimental data were fitted to pseudo-first, pseudo-second-order, intra-particle, and liquid film diffusion kinetic models. The applicability of the pseudo-second-order kinetic model indicated that the adsorption behaviour was ascribed by chemisorption. Further data analysis by the diffusion kinetic models suggested that the metallic ions adsorption was controlled by more than one step; adsorption at the active sites, intra-particle, and liquid film diffusion.

A Novel Geopolymer Foam Based On ZSM-5 Zeolite Fabricated Using Templating Emulsion/Chemical Foaming Method and Its Application in Batch and Continuous Dye Removal Systems

Geopolymers as sustainable and environmentally friendly “green materials”, can be synthesized by utilizing waste material and by-products. A porous geopolymer foam adsorbent based on ZSM-5 zeolite was prepared using templating emulsion/chemical foaming method in different conditions and used for dye removal in batch and continuous systems. The parameters affecting the dye adsorption including temperature, concentration, and pH, kinetics, isotherm, and thermodynamics of the process were investigated. The results of the geopolymer foam synthesis showed that thermal pretreatment of the zeolite has a positive effect on the strength and adsorption capacity. Moreover, the increase in sodium silicate more than the stoichiometric reduces the strength and adsorption capacity. The findings obtained from the batch adsorption process showed that the adsorption kinetics of the pseudo-second-order model and the adsorption isotherm of the Temkin model is adjusted with the experimental data. Thermodynamic results indicated that the process of dye adsorption with geopolymer foam is exothermic. The results from continuous experiments indicated more compatibility of the adsorption process with the models of Thomas and Bohart-Adams. The maximum adsorption capacity of methylene blue in batch and continuous processes was 9.82 and 8.17 mg/g. The adsorbent reduction was performed successfully by chemical and thermal processes.

From Waste to Waste: Iron Blast Furnace Slag for Heavy Metal Ions Removal from Aqueous System

Blast furnace slag (BFS) is considered a cheap sorbent for the get rid of Co2+ and Pb2+ ions from an aqueous medium. The slag is characterized using X-ray diffraction (XRD), X-ray fluorescence (XRF), N2 adsorption-desorption isotherms, energy dispersive X-ray analysis (EDX), scanning electron microscopy (SEM), and zeta potential. The removal of Co2+ and Pb2+ ions was carried out using batch adsorption experiments from an aqueous medium. The influence of several variables as pH, duration, sorbent quantity, temperature, and preliminary ions concentration was considered. The isotherm, kinetic, thermodynamic, and recyclability were also conducted. The maximum uptake capacity for Co2+ and Pb2+ was 43.8 and 30.2 mg g-1 achieved at pH 6 after 60 min. contact duration. The adsorption kinetics and isotherms of BFS for Co2+ and Pb2+ fitted well to Avrami and Freundlich models, respectively. The main sorption mechanism between BFS and the metal ions was ion exchange. The regeneration of the used slag was studied for reuse many cycles. In terms of economics and scalability, the treatment with the unmodified BFS has great potentials.

The Performance of Different AgTiO2 Loading into Poly(3-Nitrothiophene) for Efficient Adsorption of Hazardous Brilliant Green and Crystal Violet Dyes

The in-situ polymerization technology was used to successfully produce nanostructured binary nanocomposites (NCs) made from a poly (3-nitrothiophen) matrix (P3NT) that were loaded effectively with nanoparticles (NPs) of silver titanium dioxide (AgTiO2), of varying percentages (10%, 20%, and 30%). A uniform coating of P3NT covers the AgTiO2 NPs. Various methods were performed to confirm the fabrication of the binary P3NT/AgTiO2 NCs adsorbents, such as FTIR, XRD, SEM, and EDX. Both dyes (brilliant green (B.G.) and crystal violet (C.V.)) were removed from liquid media by using the binary P3NT/AgTiO2 NCs. A range of batch adsorption studies was used to optimize various factors that impact the elimination of B.G. or C.V. dyes, including the pH, weight of the binary P3NT/AgTiO2 NC, proportion of AgTiO2 NP, time, and temperature. The pseudo-second-order kinetics ( R 2 = 0.999 ) was better adapted for the adsorption procedure’s empirical data whereby the maximum adsorption capacity of the C.V. dye was 43.10 mg/g and ( R 2 = 0.996 ) the maximum adsorption potential was 40.16 mg/g for B.G. dye, succeeded by the pseudo-second-order kinetics. Moreover, the adhesion of B.G. and C.V. pigments on the layers of NCs involves an endothermic reaction. In addition, the concocted adsorbent not only exhibited strong adsorption characteristics during four consecutive cycles but also possessed a higher potential for its reuse. According to the findings, the NCs might possibly be used as a robust and reusable adsorbent to remove B.G. and C.V. pigments from an aqueous medium.

MAGNETICALLY MODIFIED SUGARCANE BAGASSE BIOCHAR AS CADMIUM REMOVAL AGENT IN WATER

Heavy metals are hazardous to health at certain levels. Currently, heavy metals are removed by physicochemical treatments, such as adsorption, flotation, and electrochemical deposition, and also biological treatments, such as algal biofilm reactor and anaerobic ammonium oxidation. In this study, magnetic biochar was produced to enhance the effectiveness and performance of the adsorbent for heavy metal removal. This study aimed to synthesise high-performance magnetic biochar, to determine the optimum parameters and conditions for high yield of magnetic biochar and high removal of cadmium (Cd2+) from aqueous solution, and to determine the adsorption kinetics and isotherms for Cd2+ removal. Nickel oxide (NiO)-impregnated sugarcane bagasse was subjected to slow pyrolysis to produce magnetic biochar. The impregnated metal, pyrolysis temperature, and pyrolysis time were varied to determine the optimum parameters and conditions to produce high-performance magnetic biochar. The removal of Cd2+ from aqueous solution and batch adsorption study were conducted. The synthesised magnetic biochar was characterised using field-emission scanning electron microscopy (FESEM), energy dispersive X-ray (EDX), X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) surface area, Fourier transform infrared (FTIR), and vibrating sample magnetometer (VSM). The adsorption data agreed well with the pseudo-second-order model and followed the Langmuir isotherm model. This study achieved 88.47% removal efficiency of Cd2+ from aqueous solution. Thus, the removal of this heavy metal as a human carcinogen reduces the hazardous effects on human health and reduces the toxicity in the environment. ABSTRAK: Logam berat adalah berbahaya bagi kesihatan di peringkat tertentu. Pada masa ini, logam berat disingkirkan melalui rawatan fizikokimia, seperti penyerapan, pengapungan, dan deposit elektrokimia, dan rawatan biologikal, seperti reaktor biofilem alga dan oksidasi ammonium anerobik. Kajian ini menghasilkan biochar magnetik bagi meningkatkan keberkesanan dan prestasi penyerapan penyingkiran logam berat. Kajian ini bertujuan bagi mengsintesis biochar magnetik pada prestasi tinggi, bagi menghasilkan parameter optimum dan keadaan pengeluaran tinggi biochar magnetik dan penyingkiran tinggi kadmium (Cd2+) daripada larutan akues, dan bagi mendapatkan penyerapan kinetik dan isoterma penyingkiran Cd2+. Nikel oksida (NiO)-impregnat hampas tebu adalah berdasarkan pirolisis perlahan bagi menghasilkan biochar magnetik. Logam yang terimpregnat, suhu pirolisis dan tempoh pirolisis dipelbagaikan bagi mendapatkan parameter optimum dan keadaan bagi menghasilkan biochar magnetik berprestasi-tinggi. Penyingkiran Cd2+ daripada larutan akues dan kajian penyerapan berkumpulan telah dibuat. Biochar magnetik yang disentisis diklasifikasikan menggunakan mikroskopi elektron imbasan medan-pancaran (FESEM), tenaga sebaran X-ray (EDX), pembelauan X-ray (XRD), kawasan permukaan Brunauer-Emmett-Teller (BET), Penjelmaan Fourier inframerah (FTIR), dan sampel getaran magnetometer (VSM). Data penyerapan menunjukkan persetujuan dengan model aturan-kedua-pseudo dan mengikuti model isoterma Langmuir. Kajian ini mencapai 88.47% keberkesanan penyingkiran Cd2+ daripada larutan akues. Oleh itu, penyingkiran logam berat ini sebagai karsinogen manusia mengurangkan kesan teruk pada kesihatan manusia dan pengurangan toksik pada alam sekitar.

Adsorption of Anionic Dye Onto ZSM-5 Zeolite-based Bio Membrane: Characterizations, Kinetics and Adsorption Isotherm

In this study, we report polyvinyl alcohol/carboxymethyl cellulose/gelatin/ZSM-5 zeolite (PVA/CMC/GEL/ZSM-5) membrane for anionic dye (rhodamine B, Rh B) removal from aqueous solution. The prepared membrane was characterized using different techniques such as Fourier transform infrared spectroscopy (FT-IR), X-ray diffraction (XRD), scanning electron microscopy (SEM), optical microscopy (OM), universal testing machine (UTM) and water contact angle respectively. XRD, FT-IR and SEM analysis indicates successful incorporation of zeolite into PVA/CMC/GEL membrane. The improved hydrophobicity of the zeolite loaded membrane was confirmed by contact angle analysis. The Rh B removal efficiency of zeolite loaded PVA/CMC/GEL membrane was investigated through batch adsorption technique. The effect of different parameters such as initial dye concentration, zeolite dosage, contact time, temperature and pH on the adsorption was examined. Rh B dye adsorption onto the membrane followed Freundlich isotherm model. The kinetic studies revealed that Rh B dye adsorption on the membrane could be explained using pseudo-second-order model. Finally, the recyclability test revealed that the membrane exhibits good recycle efficiency and is stable after 6 recycle.

Single-Step Hydrothermal Synthesis of Biochar from H3PO4-Activated Lettuce Waste for Efficient Adsorption of Cd(II) in Aqueous Solution

Developing an ideal and cheap adsorbent for adsorbing heavy metals from aqueous solution has been urgently need. In this study, a novel, effective and low-cost method was developed to prepare the biochar from lettuce waste with H3PO4 as an acidic activation agent at a low-temperature (circa 200 °C) hydrothermal carbonization process. A batch adsorption experiment demonstrated that the biochar reaches the adsorption equilibrium within 30 min, and the optimal adsorption capacity of Cd(II) is 195.8 mg∙g−1 at solution pH 6.0, which is significantly improved from circa 20.5 mg∙g−1 of the original biochar without activator. The fitting results of the prepared biochar adsorption data conform to the pseudo-second-order kinetic model (PSO) and the Sips isotherm model, and the Cd(II) adsorption is a spontaneous and exothermic process. The hypothetical adsorption mechanism is mainly composed of ion exchange, electrostatic attraction, and surface complexation. This work offers a novel and low-temperature strategy to produce cheap and promising carbon-based adsorbents from organic vegetation wastes for removing heavy metals in aquatic environment efficiently.