The Adsorption Capacity of GONs/CMC/Fe₃O₄ Magnetic Composite Microspheres and Applications for Purifying Dye Wastewater.
Ontology highlight
ABSTRACT:
SUBMITTER: Lv S
PROVIDER: S-EPMC5344555 | biostudies-other | 2017 Jan
REPOSITORIES: biostudies-other
Similar Datasets
Project description:Polyamine chelating adsorbents have a good removal effect on dye wastewater. In this study, small molecule triethylenetetramine and macromolecular poly(ethylene imine) were selected as aminated reagent, and two kinds of aminated chitosan microspheres, TETA-CTSms and PEI-CTSms, were obtained by emulsion cross-linking method. The microspheres were fully characterized by FTIR, SEM, XRD, EDS and TGA. EDS results showed that the N content of the PEI-CTSms and TETA-CTSms microspheres increased significantly after the cross-linking reaction and can reach 5.7 wt% and 7.3 wt%, respectively. Adsorption experiments confirmed that TETA-CTSms and PEI-CTSms showed greater adsorption characteristics for anionic dye reactive yellow (RY) in aqueous solutions compared with CTSms, and the adsorption capacity per unit area was increased by 39.11% and 88.56%, respectively. The adsorption capacity of aminated microspheres for RY decreased with the increase of pH. The adsorption kinetics conformed to the pseudo-second-order model, and the adsorption process was in accordance with the Langmuir isotherm model. The negative value of ΔG confirmed that the adsorption process was spontaneous, and the dye adsorption was a multiple process dominated by chemical chelating and physical adsorption.
| S-EPMC6549955 | biostudies-literature
Project description:Systematic investigations involving laboratory, analytical, and field trials were carried out to obtain the most efficient adsorbent for the removal of congo red (CR) dye from industrial effluent. Modification of the zeolite (Z) by the Acanthophora Spicifera algae (AS; marine algae) was evaluated in terms of adsorption capability of the zeolite to remove CR dye from aqueous solution. The zeolite/algae composite (ZAS) was fabricated using the wet impregnation technique. The AS, Z, and the synthesized ZAS composite were analyzed utilizing various characterization techniques. The newly synthesized ZAS composite has an adsorption capacity that is significantly higher than that of Z and AS, particularly at low CR concentrations. Batch experiments were carried out to explore the effects of different experimental factors, as well as the dye adsorption isotherms and kinetics. Owing to the presence of intermolecular interactions, the computational analysis showed that the adsorption of the CR molecule on zeolite surfaces is exothermic, energetically favorable, and spontaneous. Furthermore, growing the zeolite surface area has no discernible effect on the adsorption energies in all configurations. The ZAS composite may be used as a low-cost substitute adsorbent for the removal of anionic dyes from industrial wastewater at lower dye concentrations, according to the experimental results. Adsorption of CR dye onto Z, AS, and ZAS adsorbents was adequately explained by pseudo-second-order kinetics and the Langmuir isotherm. The sorption mechanism was also evaluated using Weber's intra-particle diffusion module. Finally, field testing revealed that the newly synthesized adsorbent was 98.0% efficient at extracting dyes from industrial wastewater, proving the foundation of modern eco-friendly materials that aid in the reuse of industrial wastewater.
| S-EPMC8464800 | biostudies-literature
Project description:Methods to remove dye pollutants with natural enzyme, like horseradish peroxidase (HRP), are still limited due to high costs and low stability levels. The development of such a method with similar enzymatic activity is important and could be helpful in wastewater disposal. A metal organic framework material, Fe-loaded MOF-545 (Fe), was synthesized in our study as a new way to remove dyes due to its peroxidase-like activity. The structural characterizations of Fe-loaded MOF-545(Fe) was investigated using scanning electron microscopy (SEM), UV-Vis absorption spectra, and X-ray diffraction (XRD). The peroxidase-like (POD-like) activity of Fe-loaded MOF-545(Fe) was investigated under different pH and temperature conditions. Because of the Fe added into the MOF-545 structure, the absorption of Fe-loaded MOF-545(Fe) for acid (anionic) dyes (methyl orange (MO)) was better than for basic (cationic) dyes (methylene blue (MB)). The Fe-loaded MOF-545(Fe) could give a significant color fading for MO and MB over a short time (about two hours) with peroxidase-like activity. The remarkable capacity of Fe-loaded MOF-545(Fe) to remove the MO or MB is due to not only physical adsorption, but also degradation of the MO and MB with POD-like activity. Therefore, Fe-loaded MOF-545(Fe) has significant potential regarding dye removal from wastewater.
| S-EPMC6983047 | biostudies-literature
Project description:Groundwater treatment sludge is a Fe/Mn-bearing waste that is mass produced in groundwater treatment plant. In this study, sludge was converted to a magnetic adsorbent (MA) by adding ascorbate. The sludge was weakly magnetised in the amorphous form with Fe and Mn contents of 28.8% and 8.1%, respectively. After hydrothermal treatment, Fe/Mn oxides in the sludge was recrystallised to siderite and rhodochrosite, with jacobsite as the intermediate in the presence of ascorbate. With an increment in ascorbate dosage, the obtained magnetic adsorbent had a significant increase in chromate adsorption but a decrease in magnetisation. When the Mascorbate/MFe molar ratio was 10, the produced MA-10 was a dumbbell-shaped nanorod with a length of 2-5 ?m and a diameter of 0.5-1 ?m. This MA-10 showed 183.2 mg/g of chromate adsorption capacity and 2.81 emu/g of magnetisation. The mechanism of chromate adsorption was surface coprecipitation of the generated Cr3+ and Fe3+/Mn4+ from redox reaction between chromate and siderite/rhodochrosite on MA-10, separately. This study demonstrated an efficient recycling route of waste sludge from groundwater treatment to produce MA for treating chromate-bearing wastewater.
| S-EPMC7286529 | biostudies-literature
Project description:The availability and quality of water resources is currently the primary concern in Southern Africa. The challenge is to improve or develop water treatment materials or methods to solve this problem of potable water scarcity. Hence, this article presents the analyzed data, which are supplementary data information on the study of bio nanosponge phosphorylated-carbon nanotube/nanoparticles polyurethane composite (pMWCNT/β-CD/TiO2-Ag) as polymeric nanobiosorbent, for water treatment. The developed polymeric nanobiosorbent (pMWCNT/β-CD/TiO2-Ag) was synthesized using combined methods of amidation reaction, cross polymerization, and sol-gel process. The removal of water pollutants (trichloroethylene (TCE) and Congo red (CR) dye) was conducted by the batch adsorption method. The conditions used during the adsorption experiments and methods (applied to quantify the water samples after adsorption studies) are described. Additional data obtained on the effect of pH, isotherm, kinetic, and thermodynamic studies are also illustrated.
| S-EPMC8027523 | biostudies-literature
Project description:Monodisperse polyvinyl alcohol (PVA) microspheres have been widely used for targeted drug delivery, embolization, and templates. However, the fast and facile fabrication of PVA microspheres with uniform size and internal structure and good sphericity remains a challenge. In this study, the PVA microspheres with uniformity in the size, shape, and internal structure were rapidly fabricated, using single-emulsion droplet templates by an on-chip approach. First, we designed a polydimethylsiloxane (PDMS) microfluidic chip integrated with three functional units, used for the droplet generation, mixing of reagents, and pre-curing of PVA microspheres, respectively. Then, we precisely controlled the generation of PVA aqueous droplets, mixing of reagents, and the gelation rate for the production of high-quality microspheres by adjusting the pH value, flow rate, and the channel structure. The prepared PVA microspheres are characterized with good sphericity, uniform internal structure, and narrow size distribution. The microspheres have good adsorption capacity and recyclability for small-molecule drugs, as demonstrated by the adsorption and desorption of methylene blue (MB). The adsorption behavior is well described by the pseudo-second-order model, and intraparticle diffusion is as fast as the external film diffusion.
| S-EPMC6888467 | biostudies-literature
Project description:In this study, we report the synthesis and application of mesoporous CoFe2O4@MIL-100(Fe) hybrid magnetic nanoparticles (MNPs) for the simultaneous removal of inorganic arsenic (iAs). The hybrid adsorbent had a core-shell and mesoporous structure with an average diameter of 260 nm. The nanoscale size and mesoporous character impart a fast adsorption rate and high adsorption capacity for iAs. In total, 0.1 mg L-1 As(V) and As(III) could be adsorbed within 2 min, and the maximum adsorption capacities were 114.8 mg g-1 for As(V) and 143.6 mg g-1 for As(III), higher than most previously reported adsorbents. The anti-interference capacity for iAs adsorption was improved by the electrostatic repulsion and size exclusion effects of the MIL-100(Fe) shell, which also decreased the zero-charge point of the hybrid absorbent for a broad pH adsorption range. The adsorption mechanisms of iAs on the MNPs are proposed. An Fe-O-As structure was formed on CoFe2O4@MIL-100(Fe) through hydroxyl substitution with the deprotonated iAs species. Monolayer adsorption of As(V) was observed, while hydrogen bonding led to the multi-layer adsorption of neutral As(III) for its high adsorption capacity. The high efficiency and the excellent pH- and interference-tolerance capacities of CoFe2O4@MIL-100(Fe) allowed effective iAs removal from natural water samples, as validated with batch magnetic separation mode and a portable filtration strategy.
| S-EPMC5244426 | biostudies-literature
Project description:The present work demonstrates the development of hydroxyapatite (HA)/gold (Au) nanocomposites to increase the adsorption of methylene blue (MB) dye from the wastewater. HA nanopowder was prepared via a wet chemical precipitation method by means of Ca(OH)2 and H3PO4 as starting materials. The biosynthesis of gold nanoparticles (AuNPs) has been reported for the first time by using the plant extract of Acrocarpus fraxinifolius. Finally, the as-prepared HA nanopowder was mixed with an optimized AuNPs solution to produce HA/Au nanocomposite. The prepared HA/Au nanocomposite was studied by using Fourier transform infrared spectroscopy (FTIR), X-ray diffraction (XRD), and Scanning Electron Microscopy (SEM) with Energy Dispersive X-Ray Analysis (EDX) analysis. Adsorption studies were executed by batch experiments on the synthesized composite. The effect of the amount of adsorbent, pH, dye concentration and temperature was studied. Pseudo-first-order and pseudo-second-order models were used to fit the kinetic data and the kinetic modeling results reflected that the experimental data is perfectly matched with the pseudo-first-order kinetic model. The dye adsorbed waste materials have also been investigated against Pseudomonas aeruginosa, Micrococcus luteus, and Staphylococcus aureus bacteria by the agar well diffusion method. The inhibition zones of dye adsorbed samples are more or less the same as compared to as-prepared samples. The results so obtained indicates the suitability of the synthesized sample to be exploited as an adsorbent for effective treatment of MB dye from wastewater and dye adsorbed waste as an effective antibacterial agent from an economic point of view.
| S-EPMC8227305 | biostudies-literature
Project description:The sensitive electronic environment at the quantum dot (QD)-dye interface becomes a roadblock to enhancing the energy conversion efficiency of dye-functionalized quantum dots (QDs). Energy alignments and electronic couplings are the critical factors governing the directions and rates of different charge transfer pathways at the interface, which are tunable by changing the specific linkage groups that connect a dye to the QD surface. The variation of specific anchors changes the binding configurations of a dye on the QD surface. In addition, the presence of a co-adsorbent changes the dipole-dipole and electronic interactions between a QD and a dye, resulting in different electronic environments at the interface. In the present work, we performed density functional theory (DFT)-based calculations to study the different binding configurations of N719 dye on the surface of a Cd33Se33 QD with a co-adsorbent D131 dye. The results revealed that the electronic couplings for electron transfer were greater than for hole transfer when the structure involved isocyanate groups as anchors. Such strong electronic couplings significantly stabilize the occupied states of the dye, pushing them deep inside the valence band of the QD and making hole transfer in these structures thermodynamically unfavourable. When carboxylates were involved as anchors, the electronic couplings for hole transfer were comparable to electron transfer, implying efficient charge separation at the QD-dye interface and reduced electron-hole recombination within the QD. We also found that the electronic couplings for electron transfer were larger than those for back electron transfer, suggesting efficient charge separation in photoexcited QDs. Overall, the current computational study reveals some fundamental aspects of the relationship between the interfacial charge transfer for QD@dye composites and their morphologies which benefit the design of QD-based nanomaterials for photovoltaic applications.
| S-EPMC8452815 | biostudies-literature
Project description:This study prepared iron-manganese oxide-modified biochar (FM-BC) by impregnating rice straw biochar (BC) with a mixed solution of ferric nitrate and potassium permanganate. The effects of pH, FM-BC dosage, interference of coexisting ions, adsorption time, incipient Pb(II) concentration, and temperature on the adsorption of Pb(II) by FM-BC were investigated. Moreover, the Pb(II) adsorption mechanism of FM-BC was analyzed using a series of characterization techniques. The results showed that the Fe-Mn oxide composite modification significantly promoted the physical and chemical functions of the biochar surface and the adsorption capacity of Pb(II). The specific surface area of FM-BC was 18.20 times larger than that of BC, and the maximum Pb(II) adsorption capacity reached 165.88 mg/g. Adsorption kinetic tests showed that the adsorption of Pb(II) by FM-BC was based on the pseudo-second-order kinetic model, which indicated that the adsorption process was mainly governed by chemical adsorption. The isothermal adsorption of Pb(II) by FM-BC conformed to the Langmuir model, indicating that the adsorption process was spontaneous and endothermic. Characterization analyses (Fourier transform infrared spectroscopy and X-ray photoelectron spectroscopy) showed that the adsorption mechanism of Pb(II) by FM-BC was mainly via electrostatic adsorption, chemical precipitation, complexation, ion exchange, and the transformation of Mn2O3 into MnO2. Therefore, FM-BC is a promising adsorbent for Pb(II) removal from wastewater.
| S-EPMC9316531 | biostudies-literature