Effective Adsorption of Colorants from Sugarcane Juice by Bagasse-Based Biochar-Hydroxyapatite Composite
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ABSTRACT:
SUBMITTER: Wang C
PROVIDER: S-EPMC9322621 | biostudies-literature |
REPOSITORIES: biostudies-literature
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Project description:The highly efficient removal of uranium from mine tailings effluent, radioactive wastewater and enrichment from seawater is of great significance for the development of nuclear industry. In this work, we prepared an efficient U(VI) adsorbent by EDTA modified sugarcane bagasse (MESB) with a simple process. The prepared adsorbent preserves high adsorptive capacity for UO22+ (pH 3.0) and uranyl complexes, such as UO2(OH)+, (UO2)2(OH)22+ and (UO2)3(OH)5+ (pH 4.0 and pH 5.0) and good repeatability in acidic environment. The maximum adsorption capacity for U(VI) at pH 3.0, 4.0 and 5.0 is 578.0, 925.9 and 1394.1 mg/g and the adsorption capacity loss is only 7% after five cycles. With the pH from 3.0 to 5.0, the inhibitive effects of Na+ and K+ decreased but increased of Mg2+ and Ca2+. MESB also exhibits good adsorption for [UO2(CO3)3]4- at pH 8.3 from 10 mg/L to 3.3 μg/L. Moreover, MESB could effectively extract U(VI) from simulated seawater in the presence of other metals ions. This work provided a general and efficient uranyl enriched material for nuclear industry.
| S-EPMC5768879 | biostudies-literature
Project description:Herein, biochar was produced by the slow pyrolysis of sugarcane bagasse at 500 °C in absence of oxygen. The resulting sugarcane bagasse biochar (SB500) was characterized and used for aqueous carbofuran sorptive removal. Batch carbofuran sorption studies were accomplished to ascertain the influence of solution pH, contact time, temperature (25, 35 and 45 °C) and adsorbate/adsorbent concentration. SB500 adsorbed more carbofuran at low pH values and less carbofuran at high pH values. The necessary sorption equilibrium, kinetic and thermodynamic parameters were determined. The equilibrium isotherm data were fitted to the Freundlich, Langmuir and Temkin models. The Langmuir equation best fitted the experimental sorption data. The maximum Langmuir adsorption capacity of 18.9 mg g-1 was obtained at pH 6.0 and 45 °C. The enthalpy change (ΔH°), entropy change (ΔS°) and Gibbs free energy (ΔG°) were evaluated. The fixed-bed carbofuran sorption studies were carried out using the optimum parameters determined via the batch studies. The necessary fixed-bed design parameters were obtained. Carbofuran desorption and SB500 regeneration were successfully achieved. About 96% of the total carbofuran was successfully desorbed from the exhausted biochar using 20 mL ethanol in 10 mL increments. Moreover, a possible carbofuran adsorption mechanism has been proposed. A number of interactions including (1) hydrogen bonding of the protonated and neutral carbofuran to biochar, (2) carbofuran sorption onto biochar via π-π electron donor-acceptor interactions and (3) carbofuran diffusion into the biochar pores were considered to explain the sorption mechanism. The batch and fixed-bed sorption results demonstrate that the sugarcane bagasse biochar (SB500) can be effectively used for the sustainable removal and recovery of carbofuran from water.
| S-EPMC9070364 | biostudies-literature
Project description:Today, sugarcane bagasse (SB) is used for bioethanol and biodiesel production, energy generation, and adsorbent synthesis. The goal of this project is to determine the optimized conditions for producing adsorbent from sugarcane bagasse using hydrothermal carbonization (HTC) and KOH activation. To optimize process parameters such as reaction temperature, residence time, ZnCl2/SB mixing ratios, and water/SB mixing ratios, response surface methodology was used. The results revealed that the optimum modified adsorption occurred at 180 °C, 11.5 h, a water to biomass ratio of (5:1), and a ZnCl2 to precursor ratio of (3.5:1). The physicochemical features of optimum activated hydrochar were investigated, as well as batch adsorption experiments. The pseudo-second-order kinetic model and the Langmuir isotherm model were found to fit the experimental results in batch adsorption studies [[Formula: see text] (mg/g)]. Thermodynamic experiments further confirmed the spontaneous and exothermic adsorption mechanism.
| S-EPMC8595365 | biostudies-literature
Project description:Sugarcane bagasse fly ash, a residual product resulting from the incineration of biomass to generate power and steam, is rich in SiO2. Sodium silicate is a fundamental material for synthesizing highly porous silica-based adsorbents to serve circular practices. Aflatoxin B1 (AFB1), a significant contaminant in animal feeds, necessitates the integration of adsorbents, crucial for reducing aflatoxin concentrations during the digestive process of animals. This research aimed to synthesize aluminosilicate and zinc silicate derived from sodium silicate based on sugarcane bagasse fly ash, each characterized by a varied molar ratio of aluminum (Al) to silicon (Si) and zinc (Zn) to silicon (Si), respectively. The primary focus of this study was to evaluate their respective capacities for adsorbing AFB1. It was revealed that aluminosilicate exhibited notably superior AFB1 adsorption capabilities compared to zinc silicate and silica. Furthermore, the adsorption efficacy increased with higher molar ratios of Al:Si for aluminosilicate and Zn:Si for zinc silicate. The N2 confirmed AFB1 adsorption within the pores of the adsorbent. In particular, the aluminosilicate variant with a molar ratio of 0.08 (Al:Si) showcased the most substantial AFB1 adsorption capacity, registering at 88.25% after an in vitro intestinal phase. The adsorption ability is directly correlated with the presence of surface acidic sites and negatively charged surfaces. Notably, the kinetics of the adsorption process were best elucidated through the application of the pseudo-second-order model, effectively describing the behavior of both aluminosilicate and zinc silicate in adsorbing AFB1.
| S-EPMC11196643 | biostudies-literature
Project description:This research details the synthesis and application of a novel pectin-hydroxyapatite (PHAp) composite for fluoride (F-) adsorption from aqueous solutions. To determine the efficiency of the adsorption process parameters, i.e., adsorbent dose (0.1-0.4 g), initial fluoride concentration (10-30 mg/L), and temperature (298-313 K), the Box-Behnken design with three levels and three factors have been utilized. The quadratic model was established on 27 batch runs by regression analysis of the experimental data of these runs. The efficacy of adsorption was observed using the Langmuir and Freundlich models. The adsorption rate was found at 3.17 mg g-1min-1, and adsorption kinetics followed pseudo-second order (PSO) for PHAp. The significant novelty of this work is the synthesis of unique cubical-shaped rods biopolymer composite from hydroxyapatite. Additionally, this composite showed high adsorption capacity for F- compared to other hydroxyapatite adsorbents, and the improved adsorption capacity is attributed to its unique shape which provides a larger surface area. It can be reused for up to six cycles, which makes this method environment-friendly. The economic viability of the synthesized PHAp composite, in comparison to other adsorbents, is evident from the cost-benefit analysis.
| S-EPMC6644855 | biostudies-literature
Project description:Bagasse-derived carbon electrodes were developed by doping with nitrogen functional groups and compositing with high-capacity MnO2 nanoparticles (MnO2/NBGC). The bagasse-derived biochar was N-doped by refluxing in urea, followed by the deposition of MnO2 nanoparticles onto its porous surface via the hydrothermal reduction of KMnO4. Different initial KMnO4 loading concentrations (i.e. 5, 10, 40, and 100 mM) were applied to optimize the composite morphology and the corresponding electrochemical performance. Material characterization confirmed that the carbon composite has a mesoporous structure along with the dispersion of MnO2 nano-particles on the N-containing carbon surface. It was found that the 5-MnO2/NBGC sample exhibited the highest electrochemical performance with a reversible capacity of 760 mA h g-1 at a current density of 186 mA g-1. It delivered reversible capacities of 488 and 390 mA h g-1 in cycle tests at 372 and 744 mA g-1, respectively, for 150 cycles and presented good reversibility with nearly 100% coulombic efficiency. In addition, it could exert high capacities up to 388 and 301 mA h g-1 even under high current densities of 1860 and 3720 mA g-1, respectively. Moreover, most of the prepared composite products showed high rate capability with great reversibility up to more than 90% after testing at a high current density of 3720 mA g-1. The great electrochemical performance of the MnO2/NBGC nanocomposite electrode can be attributed to the synergistic impact of the hierarchical architecture of the MnO2 nanocrystals deposited on porous carbon and the capacitive effect of the N-containing defects within the carbon material. The nanostructure of the MnO2 particles deposited on porous carbon limits its large volume change during cycling and promotes good adhesion of MnO2 nanoparticles with the substrate. Meanwhile, the capacitive effect of the exposed N-functional groups enables fast ionic conduction and reduces interfacial resistance at the electrode interface.
| S-EPMC10782432 | biostudies-literature
Project description:A novel cost-effective and multifunctional nanocomposite was developed based on sustainable macroalgae biomass. The brown seaweed Sargassum latifolium was utilized for alginate extraction and the calcareous red seaweed Tricleocarpa fragilis was utilized as CaCO3 source for nanohydroxyapatite synthesis. The developed Zn2+-crosslinked alginate/nanohydroxyapatite (ZA/nHA) beads were characterized by FT-IR, XRD, and TEM. The antimicrobial potential of ZA/nHA to disinfect synthetic Escherichia coli-contaminated water was evaluated at different bacterial load and composite concentrations. The developed ZA/nHA effectively inactivated bacteria at initial concentration ≤ 105 CFU mL-1 and 0.5-1% (w/v) of ZA/nHA within 300-360 min. The kinetics of bacterial disinfection exhibited better fitting to Weibull model than Log-liner model, which confirmed the disinfection process. Furthermore, treatment of the cyanobacterium (Chroococcus sp.) and the microalga (Chlorella sp.) with ZA/nHA showed promising antialgal properties as indicated by reductions in chlorophyll a. The treatment indicated 100% and 90% removal of Chroococcus sp. and Chlorella sp. within 2 and 4 days, respectively. The developed ZA/nHA also exhibited a promising application as a biosorbent for crystal violet (CV). The adsorption process was very fast (0.171 mg CV g-1 adsorbent was removed within 7 min at pH 6.0). The adsorption kinetics exhibited better fitting to the pseudo-second order and Elovich models than the pseudo-first order equation. Besides, Sips model better represented the isotherm data of CV adsorption. The thermodynamic analysis indicated exothermic adsorption, which became more favorable at low temperature and high CV concentration. The developed nanocomposite is eco-friendly and suitable for multiple environmental applications.
| S-EPMC10644496 | biostudies-literature
Project description:LaFeO3/biochar composite is prepared by cellulose-modified microwave-assisted method at 450 °C. The structure is identified by Raman spectrum which, consists of characteristics biochar bands and octahedral perovskite chemical shifts. The morphology is examined by scanning electron microscope (SEM); two phases are observed, rough microporous biochar and orthorhombic perovskite particles. The BET surface area of the composite is 57.63 m2/g. The prepared composite is applied as a sorbent for the removal of Pb2+, Cd2+, and Cu2+ ions from aqueous solutions and wastewater. The adsorption ability reaches a maximum at pH > 6 for Cd2+, and Cu2+ ions, and is pH-independent for Pb2+ ions adsorption. The adsorption follows pseudo 2nd order kinetic model, Langmuir isotherm for Pb2+ ions, and Temkin isotherms for Cd2+, and Cu2+ ions. The maximum adsorption capacities, qm, are 606, 391, and 112 mg/g for Pb2+, Cd2+, and Cu2+ ions, respectively. The electrostatic interaction is responsible for the adsorption of Cd2+, and Cu2+ ions on LaFeO3/biochar composite. In case of Pb2+ ions form a complex with the surface functional groups of the adsorbate. LaFeO3/biochar composite shows high selectivity for the studied metal ions and excellent performance in real samples. The proposed sorbent can be easily regenerated and effectively reused.
| S-EPMC10257711 | biostudies-literature
Project description:Citric acid-based polymer/hydroxyapatite composites (CABP-HAs) are a novel class of biomimetic composites that have recently attracted significant attention in tissue engineering. The objective of this study was to compare the efficacy of using two different CABP-HAs, poly (1,8-octanediol citrate)-click-HA (POC-Click-HA) and crosslinked urethane-doped polyester-HA (CUPE-HA) as an alternative to autologous tissue grafts in the repair of skeletal defects. CABP-HA disc-shaped scaffolds (65 wt.-% HA with 70% porosity) were used as bare implants without the addition of growth factors or cells to renovate 4 mm diameter rat calvarial defects (n = 72, n = 18 per group). Defects were either left empty (negative control group), or treated with CUPE-HA scaffolds, POC-Click-HA scaffolds, or autologous bone grafts (AB group). Radiological and histological data showed a significant enhancement of osteogenesis in defects treated with CUPE-HA scaffolds when compared to POC-Click-HA scaffolds. Both, POC-Click-HA and CUPE-HA scaffolds, resulted in enhanced bone mineral density, trabecular thickness, and angiogenesis when compared to the control groups at 1, 3, and 6 months post-trauma. These results show the potential of CABP-HA bare implants as biocompatible, osteogenic, and off-shelf-available options in the repair of orthopedic defects.
| S-EPMC4220725 | biostudies-literature
Project description:BACKGROUND:Considering that the costs of cellulases and hemicellulases contribute substantially to the price of bioethanol, new studies aimed at understanding and improving cellulase efficiency and productivity are of paramount importance. Aspergillus niger has been shown to produce a wide spectrum of polysaccharide hydrolytic enzymes. To understand how to improve enzymatic cocktails that can hydrolyze pretreated sugarcane bagasse, we used a genomics approach to investigate which genes and pathways are transcriptionally modulated during growth of A. niger on steam-exploded sugarcane bagasse (SEB). RESULTS:Herein we report the main cellulase- and hemicellulase-encoding genes with increased expression during growth on SEB. We also sought to determine whether the mRNA accumulation of several SEB-induced genes encoding putative transporters is induced by xylose and dependent on glucose. We identified 18 (58% of A. niger predicted cellulases) and 21 (58% of A. niger predicted hemicellulases) cellulase- and hemicellulase-encoding genes, respectively, that were highly expressed during growth on SEB. CONCLUSIONS:Degradation of sugarcane bagasse requires production of many different enzymes which are regulated by the type and complexity of the available substrate. Our presently reported work opens new possibilities for understanding sugarcane biomass saccharification by A. niger hydrolases and for the construction of more efficient enzymatic cocktails for second-generation bioethanol.
| S-EPMC3219568 | biostudies-literature