Porous carbons prepared from a novel hard wood composite waste for effective adsorption of Pb(ii) and Cd(ii) ions.

In our previous investigations, a hard wood composite (HWC) was formulated by adding rice straw, as a filler to the recycled polystyrene foam waste at mass ratio (50/50) at 170 °C and pressed under 40 kPa. Here, the disposed HWC product as a model scrap was applied for production of porous carbons enclosed with graphene sheets. To attain this approach, HWC was hydrothermally carbonized (S1) followed by either post-heat treatment (S2) or potassium hydroxide (KOH, S3) activation at 750 °C for 2 hours. The properties of prepared samples were evaluated using SEM, ATR-IR, and porosity measurements. The adsorption performance of the obtained porous carbons toward removal of lead (Pb(ii)) and cadmium (Cd(ii)) ions from aqueous solutions was investigated under different operating conditions like contact time, initial pH, initial metal ions concentration and adsorbent dose. Kinetic models such as pseudo-first order, pseudo-second order and intraparticle diffusion were used to analyze the adsorption data. Langmuir, Freundlich, Dubinin-Radushkevich and Redlich-Peterson isotherms were applied. Thermodynamics and regeneration studies were performed. The sample (S3) comprised a micro-mesoporous carbon structure encompassed by graphene sheets, with the largest total surface area (422 m2 g-1) and adsorption capacities for Pb(ii) and Cd(ii) ions of 207.9 and 119.6 mg g-1, respectively. The experimental adsorption data were best elucidated using Langmuir and pseudo second-order kinetic models. Thermodynamic experiments confirmed that adsorption is an endothermic and spontaneous process. Conclusively, the investigated HWC waste is a promising carbonaceous precursor for preparing effective porous graphene-carbons used in the removal heavy metals from their aqueous stream.

Preparation and characterization of chemically cross-linked zwitterionic copolymer hydrogel for direct dye and toxic trace metal removal from aqueous medium.

In this work, a zwitterionic copolymer hydrogel with adsorption affinity toward anionic dye and cationic trace metal was prepared by a free radical copolymerization of cationic ([3-(methacryloylamino)propyl] trimethylammonium chloride (MPTC)) and anionic (sodium 4-vinylbenzenesulfonate (SVBS)) monomers. Bis[2-(methacryloyloxy)ethyl] phosphate was used as a cross-linker and its effect on the adsorption properties of the prepared hydrogel was evaluated. The prepared materials were characterized by FTIR, XRD, SEM, EDX, and N2 adsorption at 77 K analysis. FTIR and EDX analysis demonstrated the successful preparation of poly(MPTC-co-VBS). XRD and SEM analysis showed that the poly (MPTC-co-VBS) is amorphous and has quasi-honeycomb morphology with large pores. Increasing the amount of the cross-linker enhanced the adsorption of direct blue 71 dye (DB71) and Pb(II) ions. The highest removal of DB71 and Pb(II) was achieved after 2 h using 1.5 g/L of poly(MPTC-co-VBS); however, the optimum solution pH was 3 for DB71 and 5 for Pb(II). The kinetics and isotherm studies illustrated that the surface of poly(MPTC-co-VBS) is heterogenous with small-sized homogenous pitches and the DB71 and Pb(II) adsorption onto poly(MPTC-co-VBS) is favorable. Finally, poly(MPTC-co-VBS) is more efficient in removing DB71 and Pb(II) from aqueous solutions than many other reported adsorbents.

One-Step Room-Temperature Synthesis of Bimetallic Nanoscale Zero-Valent FeCo by Hydrazine Reduction: Effect of Metal Salts and Application in Contaminated Water Treatment.

The effect of initial salt composition on the formation of zero-valent bimetallic FeCo was investigated in this work. Pure crystalline zero-valent FeCo nanoparticles (NPs) were obtained using either chloride or nitrate salts of both metals. Smaller NPs can be obtained using nitrate salts. Comparing the features of the FeCo prepared at room temperature and the solvothermal method revealed that both materials are almost identical. However, the room-temperature method is simpler, quicker, and saves energy. Energy-dispersive X-ray (EDX) analysis of the FeCo NPs prepared using nitrate salts at room temperature demonstrated the absence of oxygen and the presence and uniform distribution of Fe and Co within the structure with the atomic ratio very close to the initially planned one. The particles were sphere-like with a mean particle size of 7 nm, saturation magnetization of 173.32 emu/g, and surface area of 30 m2/g. The removal of Cu2+ and reactive blue 5 (RB5) by FeCo in a single-component system was conformed to the pseudo-first-order and pseudo-second-order models, respectively. The isotherm study confirmed the ability of FeCo for the simultaneous removal of Cu2+ and RB5 with more selectivity toward Cu2+. The RB5 has a synergistic effect on Cu2+ removal, while Cu2+ has an antagonistic effect on RB5 removal.

Simultaneous removal of Pb2+ and direct red 31 dye from contaminated water using N-(2-hydroxyethyl)-2-oxo-2H-chromene-3-carboxamide loaded chitosan nanoparticles.

This study reports the preparation of a new material that can remove synthetic dyes and trace metals simultaneously. A new coumarin derivative was synthesized and its chemical structure was inferred from spectral data (FT-IR, 1H-NMR, 13C-NMR). Meanwhile, chitosan nanoparticles (CsNPs) were prepared then used as a carrier for two different concentrations of the coumarin derivative (C1@CsNPs and C2@CsNPs). The TEM, SEM and DLS findings illustrated that the prepared nanocomposites exhibited spherical shape and small size (less than 200 nm). The performance of the prepared material for the removal of an anionic dye (direct red 31, DR31) and cationic trace metal (Pb2+) was evaluated in unary and binary systems. The results revealed that complete removal of 10 mg L-1 of DR31 and Pb2+ in unary system was achieved at pHo 3.0 and 5.5 using 0.5 and 2.0 g L-1, respectively, of C2@CsNPs. The adsorption of DR31 and Pb2+ followed different mechanisms as deduced from the effect of pHo, kinetic, isotherm and binary adsorption studies. The adsorption of DR31 followed the Langmuir isotherm model and the pseudo-first-order kinetic model. While, the adsorption of Pb2+ followed Freundlich isotherm model and Elovich kinetic model. In the binary system, the co-presence of DR31 and Pb2+ did not affect the adsorption of each other's. Overall, the prepared material showed promising results for the removal of anionic dyes and cations trace metals from contaminated water.

Development of Ag-dendrites @Cu nanostructure for removal of selenium (IV) from aqueous solution.

Removal of selenite (Se (IV)) from wastewater is vital due to its more toxic and mobile properties. In this study, a novel dendritic silver-dendrites@ copper with hierarchical side-branches were synthesized through a two-pot rapid, facile, and green precipitation route. Characterization of the dendrites by transmission electron microscope (TEM), scanning electron microscope (SEM), dynamic light scattering (DLS), and X-ray diffraction spectroscopy (XRD) confirmed the proper preparation of dendritic AgCu nanostructure. Significantly, the Ag@Cu nanostructure has high specific surface area (150 m2 /g) and excellent adsorption activity toward selenite. The adsorption rate of Se (IV) on the dendritic AgCu reaches 94% within 60 min under normal adsorption procedures. Both adsorption kinetics and isotherms have been described well by the pesudo-second order model and Langmuir model, respectively. The noticeable high adsorption capabilities can mainly accredit to the effect of the hierarchical side-branched structure. Therefore, the dendritic AgCu nanostructure has a room of treating heavy metals-contaminated industrial wastewater streams. PRACTITIONER POINTS: Silver-dendrites@ copper with hierarchical side-branches were synthesized through a rapid and green precipitation route using copper nanoparticles. The prepared nanostructure was applied for Se (IV) adsorption at varying operational conditions (contact time, pH, and dose). High adsorption capacity for Se (IV) up to 173.1 mg/g was achieved using the prepared nanoparticles applying Langmuir isotherm model.

Bioremediation of potentially toxic metal and reactive dye-contaminated water by pristine and modified Chlorella vulgaris.

This is the first study on the biosorption of Cu2+ and reactive yellow 145 (RY145) dye by citric acid (CA), NaOH, and heat-treated Chlorella vulgaris (Cv). Influence of contact time, initial adsorptive concentration, and biomass dosage on the biosorption process was explored. The biosorption kinetics and isotherm were comprehensively investigated as well. The Fourier transform infrared analysis proved the successful insertion of carbonyl groups on Cv surface by CA modification and the intensification of all Cv functional groups by heat treatment. CA modified Cv was the best biosorbent for RY145, 0.5 g/L removes 97% of 10 mg/L solution (pHi 2) in 40 min. The biosorption was favorable, occurred via the formation of a monolayer of RY145 on the homogenous surface of CA-modified Cv and followed the pseudo-second-order kinetics. On the other hand, heat-treated Cv was the best biosorbent for Cu2+, 0.5 g/L removes 92% of 10 mg/L solution (pHi 5) in 5 min. The biosorption of Cu2+ on heat-treated Cv was complex and involves more than one mechanism. The Langmuir theoretical monolayer saturation capacity of RY145 on CA-modified Cv was comparable to other biosorbents, while that of Cu2+ on heat-treated Cv was drastically superior.

Removal of Hazardous Contaminants from Water by Natural and Zwitterionic Surfactant-modified Clay.

In this study, natural clay (NC) was collected from Saudi Arabia and modified by cocamidopropyl betaine (CAPB) at different conditions (CAPB concentration, reaction time, and reaction temperature). NC and modified clay (CAPB-NC) were characterized using X-ray diffraction, thermogravimetric analysis, Fourier transform infrared spectroscopy, field-emission scanning electron microscopy, and N2 adsorption at 77 K. The adsorption efficiency of NC and CAPB-NC toward Pb2+ and reactive yellow 160 dye (RY160) was evaluated. The adsorption process was optimized in terms of solution initial pH and adsorbent dosage. Finally, the adsorption kinetics and isotherms were studied. The results indicated that NC consists of agglomerated nonporous particles composed of quartz and kaolinite. CAPB modification reduced the specific surface area and introduced new functional groups by adsorbing on the NC surface. The concentration of CAPB affects the adsorption of RY160 tremendously; the optimum concentration was 2 times the cation exchange capacity of NC. The equilibrium adsorption capacity of CAPB-NC toward RY160 was about 6 times that of NC and was similar for Pb2+. The adsorption process followed the pseudo-second-order kinetics for both adsorptive. RY160 adsorption on CAPB-NC occurs via multilayer formation while Pb2+ adsorption on NC occurs via monolayer formation..

Silver/quartz nanocomposite as an adsorbent for removal of mercury (II) ions from aqueous solutions.

Silver nanoparticles (AgNPs) and silver/quartz nanocomposite (Ag/Q)NPs)) were synthesized by sol-gel method using table sugar as chelating agent. The synthesized nanosized materials were used for mercury ions adsorption from aqueous solutions. The materials were characterized by X-ray diffraction (XRD), Transmission Electron microscope (TEM), and surface area (BET). Adsorption of Hg2+ (10 mg/l) is strongly dependent on time, initial metal concentration, dose of adsorbent and pH value. Silver/quartz nanocomposite ((Ag/Q)NPs)) shows better efficiency than individual silver nanoparticles (AgNPs). This composite removed mercury ions from the aqueous solution with efficiency of 96% at 60 min with 0.5g adsorbent dosage at pH 6. The adsorption process explained well by the pseudo-second-order kinetic model. In conclusion silver/quartz nanocomposite (Ag/Q)NPs)) shows higher removal efficiency for mercury ions from aqueous solutions than individual silver naoparticles (AgNPs) or quartz (Q).

Mn0.2Co0.8Fe2O4 and encapsulated Mn0.2Co0.8Fe2O4/SiO2 magnetic nanoparticles for efficient Pb2+ removal from aqueous solution.

Sol-gel auto-combustion technique was used to synthesize spinel ferrite nanoparticles of Mn0.2Co0.8Fe2O4 (MCF). Using the modified Stöber method, these magnetic nanoparticles were encapsulated with silica to form the core/shell Mn0.2Co0.8Fe2O4/SiO2 (MCFS). The phase composition, morphology, particle size, and saturation magnetization of the encapsulated nanoparticles were studied using X-ray diffraction (XRD), high resolution-transition electron microscopy (HR-TEM), and vibrating sample magnetometer (VSM). HR-TEM images indicated that particle size of the nanoparticles ranged from 15 to 40 nm, and VSM measurements showed that Ms of uncoated and coated samples were 65.668 emu/g and 61.950 emu/g and the Hc values were 2,151.9 Oe and 2,422.0 Oe, respectively. The effects of metal concentration, solution pH, contact time, and adsorbent dose of the synthesized nanoparticles on lead (Pb2+) ions removal from an aqueous solution were investigated. Based on Langmuir isotherm model, the results for peak adsorption capacity of the adsorbent under optimal conditions was 250.5 mg/g and 247 mg/g for MCF and MCFS, respectively. We concluded that Pb2+ adsorption occurred via a chemisorption mechanism based on the analysis of adsorption kinetics. The adsorbents displayed consistent adsorption efficiencies following three cycles of regeneration, indicating that these magnetic nanoparticles are promising candidates for wastewater purification.

Adsorption of Methylene Blue and Pb2+ by using acid-activated Posidonia oceanica waste.

Dead leaves of seagrass Posidonia oceanica were activated by using one mol L-1 acetic acid and used as an eco-adsorbent for the removal of methylene blue (MB) and Pb2+ from aqueous solutions. The seagrass was characterized by chemical and physical measurements that confirmed the acid-activation of seagrass. The favourable conditions for MB and Pb2+ adsorption onto the activated seagrass (SGa) were determined to be a pH range of 2-12 and ≥6, an adsorbent dosage of 3.0 and 0.5 g L-1, respectively, and a shaking time of 30 min, which are suitable for a wide range of wastewaters. The equilibrium data were analysed using the Langmuir, Freundlich and Dubinin-Raduskavich-Kaganer (DRK) adsorption isotherm models. The Freundlich and DRK models best describe the adsorption processes of MB and Pb2+, on SGa with capacities of 2681.9 and 631.13 mg g-1, respectively. The adsorption isotherm fitting and thermodynamic studies suggest that the adsorption mechanism of MB may combine electrostatic and physical multilayer adsorption processes, in which MB may be present as monomers as well as dimers and trimers which were confirmed from UV spectroscopy whereas Pb2+ is chemically adsorbed onto SGa. The pseudo-2nd-order kinetic model was utilized to investigate the kinetics of adsorption processes. The removal process was successfully applied for MB-spiked brackish waste water from Manzala Lake, Egypt, with removal efficiencies of 91.5-99.9%.

Synthesis, characterization and adsorption properties of microcrystalline cellulose based nanogel for dyes and heavy metals removal.

Recently, naturally occurring biopolymers have attracted the attention as potential adsorbents for the removal of water contaminants. In this work, we present the development of microcrystalline cellulose (MCC)-based nanogel grafted with acrylamide and acrylic acid in the presence of methylene bisacrylamide and potassium persulphate as a crosslinking agent and initiator, respectively. World-class facilities such as X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), surface analysis, field emission scanning electron microscopy (FE-SEM), high resolution transmission electron microscopy (HR-TEM) and zeta sizer were used to characterize the synthesized MCC based nanogel. The prepared nanogel was applied to remove reactive red 195 (RR195) dye and Cd (II) from aqueous medium at different operational conditions. The adsorption experiments showed that the feed concentration of monomers has a significant effect on the removal of RR195 which peaked (93% removal) after 10min of contact time at pH2 and a dose of 1.5g/L. On contrary, the feed concentration has insignificant effect on the removal of Cd (II) which peaked (97% removal) after 30min of contact time at pH6 and a dose of 0.5g/L. The adsorption equilibrium data of RR195 and Cd (II) was best described by Freundlich and Langmuir, respectively. Conclusively, the prepared MCC based nanogels were proved as promising adsorbents for the removal of organic pollutants as well as heavy metals.