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Adsorption behaviour of hydrogarnet for humic acid.

ABSTRACT: Discharge of humic acid (HA) in aqueous environments is a key health and aesthetic issue. The present work investigates the use of hydrogarnet as a novel adsorbent for HA. Hydrogarnet was hydrothermally synthesized with different solvents to control the chemical composition. Hydrogarnet with three types of chemical compositions had better adsorption properties for HA than hydrogarnet with a single chemical composition. Controlling the chemical composition of hydrogarnet increased the number of hydroxyl groups and the overall binding energy of the system, leading to changes in the zeta potential. The enhancement of these adsorption properties is related to the increased numbers of hydroxyl groups on the surface and their diverse binding energies.

SUBMITTER: Maeda H

PROVIDER: S-EPMC5936920 | biostudies-literature | 2018 Apr

REPOSITORIES: biostudies-literature

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Adsorption behaviour of hydrogarnet for humic acid.

Maeda Hirotaka H Kurosaki Yuichi Y Nakayama Masanobu M Ishida Emile Hideki EH Kasuga Toshihiro T

Royal Society open science 20180411 4

Discharge of humic acid (HA) in aqueous environments is a key health and aesthetic issue. The present work investigates the use of hydrogarnet as a novel adsorbent for HA. Hydrogarnet was hydrothermally synthesized with different solvents to control the chemical composition. Hydrogarnet with three types of chemical compositions had better adsorption properties for HA than hydrogarnet with a single chemical composition. Controlling the chemical composition of hydrogarnet increased the number of h ...[more]

PMID: 29765655

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humic acid

Project description:humic acid Raw sequence reads

| PRJNA953493 | ENA

Study of Humic Acid Adsorption Character on Natural Maifan Stone: Characterization, Kinetics, Adsorption Isotherm, and Thermodynamics.

Project description:In this paper, the adsorption of humic acid (HA) on natural maifan stone (MS) in aqueous medium was investigated. The changes in MS after adsorption have been characterized explicitly. The adsorption behavior was studied by varying the factors of pH (5-10), reaction time (10-180 min), initial HA concentration (5-50 mg/L), adsorbent dosage (0.1-1.2 g), and temperature (25-45 °C). The kinetics of the adsorption process of HA was fitted well with the pseudo-second-order model (R 2 = 0.99). The isothermal results revealed that the adsorption process is favorable, and highly fitting Langmuir models (R 2 > 0.99) were used. Additionally, the obtained maximum adsorption capacity of MS for HA was approximately 1 mg/g. The adsorption process of HA onto MS was endothermic according to the thermodynamic study. The changes in the excitation-emission-matrix of HA and the X-ray diffraction of MS after adsorption indicate the interaction of HA and MS. However, the reason for these changes is still unclear. Thus, the results show that the natural MS exhibited a certain adsorption capacity for HA. It is promising to develop novel natural MS-based materials for adsorption of HA.

| S-EPMC7144149 | biostudies-literature

Development of Lignin-Based Mesoporous Carbons for the Adsorption of Humic Acid.

Project description:There is an increasing urge to make the transition toward biobased materials. Lignin, originating from lignocellulosic biomass, can be potentially valorized as humic acid (HA) adsorbents via lignin-based mesoporous carbon (MC). In this work, these materials were synthesized for the first time starting from modified lignin as the carbon precursor, using the soft-template methodology. The use of a novel synthetic approach, Claisen rearrangement of propargylated lignin, and a variety of surfactant templates (Pluronic, Kraton, and Solsperse) have been demonstrated to tune the properties of the resulting MCs. The obtained materials showed tunable properties (BET surface area: 95-367 m2/g, pore size: 3.3-36.6 nm, V BJH pore volume: 0.05-0.33 m3/g, and carbon and oxygen content: 55.5-91.1 and 3.0-12.2%, respectively) and good performance in terms of one of the highest HA adsorption capacities reported for carbon adsorbents (up to 175 mg/g).

| S-EPMC8210454 | biostudies-literature

Incorporation of humic acid into biomass derived carbon for enhanced adsorption of phenol.

Project description:In the present work, the biomass derived carbon decorated with humic acid (HC), was synthesized through impregnation method for the adsorption of phenol from water environment. Humic acids contain more oxygen-containing functional groups and hydrogen bonds, which promotes the binding between HC and phenol molecules. The results indicated that the adsorption performance of HC to phenol was better than that of commercial activated carbon. Moreover, in addition to physical absorption, the chemical reaction between carboxylic groups on the carbon surface and hydroxyl in phenol also played an important role during the process. The adsorption behavior of HC was described by equilibrium and kinetics parameters. Pseudo-second order model can describe the adsorption process well. Langmuir model was more suitable for the equilibrium adsorption data fitting, indicating that the adsorption mechanism of phenol on carbon surface tends to be monolayer adsorption. Considering practical application, UV254, chemical oxygen demand (COD) and ammonia from raw wastewater were selected as target contaminants and the corresponding adsorption experiments were carried out. The results displayed that HC exhibited excellent adsorption performance, especially for UV254, indicating that as-prepared carbon material had potential application for the control of certain organic pollutants in actual wastewater.

| S-EPMC6934675 | biostudies-literature

Tetracycline Adsorption on Magnetic Sludge Biochar: Effects of pH, Humic Acid (HA), and Fulvic Acid (FA).

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| S-EPMC9318179 | biostudies-literature

Changes in the Aggregation Behaviour of Zinc Oxide Nanoparticles Influenced by Perfluorooctanoic Acid, Salts, and Humic Acid in Simulated Waters.

Project description:The increasing utilization of zinc oxide nanoparticles (ZnO-NPs) in many consumer products is of concern due to their eventual release into the natural environment and induction of potentially adverse impacts. The behaviour and environmental impacts of ZnO-NPs could be altered through their interactions with environmentally coexisting substances. This study investigated the changes in the behaviour of ZnO-NPs in the presence of coexisting organic pollutants (such as perfluorooctanoic acid [PFOA]), natural organic substances (i.e., humic acid [HA]), and electrolytes (i.e., NaCl and CaCl2) in simulated waters. The size, shape, purity, crystallinity, and surface charge of the ZnO-NPs in simulated water after different interaction intervals (such as 1 day, 1 week, 2 weeks, and 3 weeks) at a controlled pH of 7 were examined using various characterization techniques. The results indicated alterations in the size (such as 162.4 nm, 1 day interaction to >10 µm, 3 weeks interaction) and zeta potential (such as -47.2 mV, 1 day interaction to -0.2 mV, 3 weeks interaction) of the ZnO-NPs alone and when PFOA, electrolytes, and HA were present in the suspension. Different influences on the size and surface charge of the nanoparticles were observed for fixed concentrations (5 mM) of the different electrolytes. The presence of HA-dispersed ZnO-NPs affected the zeta potential. Such dispersal effects were also observed in the presence of both PFOA and salts due to their large aliphatic carbon content and complex structure. Cation bridging effects, hydrophobic interactions, hydrogen bonding, electrostatic interactions, and van der Waals forces could be potential interaction forces responsible for the adsorption of PFOA. The presence of organic pollutants (PFOA) and natural organic substances (HA) can transform the surface characteristics and fate of ZnO-NPs in natural and sea waters.

| S-EPMC11359926 | biostudies-literature

Effect of Tube Diameters and Functional Groups on Adsorption and Suspension Behaviors of Carbon Nanotubes in Presence of Humic Acid.

Project description:The adsorption and suspension behaviors of carbon nanotubes (CNTs) in the water environment determine the geochemical cycle and ecological risk of CNTs and the compounds attached to them. In this study, CNTs were selected as the research object, and the effect of tube diameters and functional groups (multiwall CNTs (MWNTs) and hydroxylated MWNTs (HMWNTs)) on the adsorption and suspension behaviors of the CNTs in the presence of humic acid (HA) was systematically analyzed. The results indicate that HA adsorption decreased with the increase in the solution pH, and the adsorption amount and rate were negatively correlated with the tube diameter of the CNTs. The surface hydroxylation of the CNTs prevented the adsorption of HA, and the maximum adsorption amounts on the MWNTs and HMWNTs were 195.95 and 74.74 mg g-1, respectively. HA had an important effect on the suspension of the CNTs, especially for the surface hydroxylation, and the suspension of the CNTs increased with the increase in the tube diameter. The characteristics of the CNTs prior to and after adsorbing HA were characterized by transmission electron microscopy, fluorescence spectroscopy, Fourier-transform infrared spectroscopy and Raman spectroscopy. The results indicate that surface hydroxylation of the CNTs increased the adsorption of aromatic compounds, and that the CNTs with a smaller diameter and a larger specific surface area had a disordered carbon accumulation microstructure and many defects, where the adsorption of part of the HA would cover the defects on the CNTs' surface. Density functional theory (DFT) calculations demonstrated that HA was more easily adsorbed on the CNTs without surface hydroxylation. This investigation is helpful in providing a theoretical basis for the scientific management of the production and application of CNTs, and the scientific assessment of their geochemical cycle and ecological risk.

| S-EPMC9100522 | biostudies-literature

Effects of humic acid on Pb2+ adsorption onto polystyrene microplastics from spectroscopic analysis and site energy distribution analysis.

Project description:Microplastics (MPs), act as vectors of heavy metal pollutants in the environment, is of practical significance to study the adsorption process and mechanism on heavy metals. In this study, polystyrene microplastics (PSMPs) were used as model MPs to study the adsorption of Pb2+ on PSMPs and the effects of humic acid (HA) on the adsorption process. The results showed that HA promoted the adsorption of Pb2+ on PSMPs, and the higher the concentration of HA, the greater the adsorption of Pb2+. With the increase of pH value and decrease of ionic strength, the adsorption capacity of PSMPs for Pb2+ increased. The scanning electron microscope equipped with the energy dispersive spectroscope (SEM-EDS), fourier transform-infrared spectra (FT-IR) and X-ray photoelectron spectroscopy (XPS) analysis showed that Pb2+ could be adsorbed directly onto PSMPs and also indirectly by HA. The higher KSV values in the PSMPs-HA-Pb2+ system than PSMPs-HA system by fluorescence analysis of HA suggested that HA acted as a bridging role in the adsorption of Pb2+ on PSMPs. The site energy distribution analysis further revealed that HA increased the average site energy μ(E*) and its standard deviation σe* of PSMPs by introducing more adsorption sites, thus enhanced the adsorption affinity of PSMPs. This study provided more thoughts and insights into the adsorption behavior and mechanism of MPs for Pb2+ in aquatic environments.

| S-EPMC9142603 | biostudies-literature

Influence of Zinc and Humic Acids on Dye Adsorption from Water by Two Composts.

Project description:Searching for alternative low-cost biosorbents for the removal of textile dyes from wastewater is currently an important subject of research. In this work, we have investigated how the presence of other contaminants in textile wastewaters can affect dye adsorption by biosorbents. We tested the adsorption of three dyes of different types: Basic Violet 10 (BV10), Acid Blue 113 (AB113) and Direct Blue 71 (DB71) by two different composts-municipal solid waste compost and pine bark compost-in the presence of Zn (5 mg L-1) or dissolved organic matter (100 mg humic acids L-1) in batch experiments. Dye adsorption capacity for both composts followed the following sequence: BV10 > AB113 > DB71. In general, dye sorption at the equilibrium was adequately described by the Freundlich model, but not always by the Langmuir model, which did not allow for the estimation of maximum retention capacities in all cases. In general, these were around 1 mg g-1 for DB71, 2 mg g-1 for AB113, and 40 mg g-1 for BV10. Municipal solid waste compost had slightly higher affinity than pine bark compost for the anionic dyes AB113 and DB71, whereas for the cationic dye BV10, pine bark compost presented a much higher adsorption capacity (41.7 mg g-1 versus 6.8 mg g-1). The presence of Zn or dissolved organic matter in the solutions at typical wastewater concentrations did not decrease the dye adsorption capacity of the composts. This result is positive both for the real application of composts to real textile wastewaters and for the validity of the results of biosorbent performance obtained with single-dye solutions.

| S-EPMC10094621 | biostudies-literature

Effect of dissolved humic acids and coated humic acids on tetracycline adsorption by K2CO3-activated magnetic biochar.

Project description:Humic acids (HAs) widely exist in water environment, and has an important impact on the adsorption of pollutants. Herein, HAs (both dissolved and coated) was employed to assess the effect on the removal of the organic contaminant tetracycline (TC) by K2CO3 modified magnetic biochar (KMBC). Results showed that low concentration of dissolved HAs promoted TC removal, likely due to a bridging effect, while higher concentration of dissolved HAs inhibited TC adsorption because of the competition of adsorption sites on KMBC. By characterization analysis, coated HAs changed the surface and pore characteristics of KMBC, which suppressed the TC removal. In a sequential adsorption experiment involving dissolved HAs and TC, the addition of HAs at the end of the experiment led to the formation of HAs-TC ligands with free TC, which improved the adsorption capacity of TC. TC adsorption by KMBC in the presence of dissolved HAs and coated HAs showed a downward trend with increasing pH from 5.0 to 10.0. The TC adsorption process was favorable and endothermic, and could be better simulated by pseudo-second-order kinetics and Freundlich isotherm model. Hydrogen bonds and π-π interactions were hypothesized to be the underlying influencing mechanisms.

| S-EPMC9643364 | biostudies-literature

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