Browse
Submit Data
Databases
API
Help

Dataset Information

0 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Adsorption Removal of Environmental Hormones of Dimethyl Phthalate Using Novel Magnetic Adsorbent.

ABSTRACT: Magnetic polyvinyl alcohol adsorbent M-PVAL was employed to remove and concentrate dimethyl phthalate DMP. The M-PVAL was prepared after sequential syntheses of magnetic Fe3O4 (M) and polyvinyl acetate (M-PVAC). The saturated magnetizations of M, M-PVAC, and M-PVAL are 57.2, 26.0, and 43.2 emu g(-1) with superparamagnetism, respectively. The average size of M-PVAL by number is 0.75 μm in micro size. Adsorption experiments include three cases: (1) adjustment of initial pH (pH0) of solution to 5, (2) no adjustment of pH0 with value in 6.04-6.64, and (3) adjusted pH0 = 7. The corresponding saturated amounts of adsorption of unimolecular layer of Langmuir isotherm are 4.01, 5.21, and 4.22 mg g(-1), respectively. Values of heterogeneity factor of Freundlich isotherm are 2.59, 2.19, and 2.59 which are greater than 1, revealing the favorable adsorption of DMP/M-PVAL system. Values of adsorption activation energy per mole of Dubinin-Radushkevich isotherm are, respectively, of low values of 7.04, 6.48, and 7.19 kJ mol(-1), indicating the natural occurring of the adsorption process studied. The tiny size of adsorbent makes the adsorption take place easily while its superparamagnetism is beneficial for the separation and recovery of micro adsorbent from liquid by applying magnetic field after completion of adsorption.

SUBMITTER: Chang CC

PROVIDER: S-EPMC4519534 | biostudies-other | 2015

REPOSITORIES: biostudies-other

ACCESS DATA

Json Xml

Similar Datasets

A Magnetic Adsorbent for the Removal of Cationic Dyes from Wastewater.

Project description:In this article, a study was presented on the adsorption activity of a new nanocomposite particle Fe₃O₄@1, which was synthesized by combining [Cu(HL)₂]₂H₂[P₂Mo₅O23]·10H₂O (1) (HL = 2-acetylpyridine semicarbazone) and Fe₃O₄ nanoparticles. Transmission electron microscopy and X-ray powder diffraction analyses revealed that Fe₃O₄@1 possessed high crystallinity with an average particle size of 19.1 nm. The adsorption activity of the as-prepared Fe₃O₄@1 was investigated by photometrically monitoring the removal of methylene blue, rhodamine B, safranine T, gentian violet, fuchsin basic, and methyl orange from aqueous solutions. Significantly, we could easily separate Fe₃O₄@1 from the reaction media by applying an external magnet. Furthermore, the recycling performance was observed using methylene blue, revealing the recyclability and high stability of Fe₃O₄@1. It was shown that Fe₃O₄@1 is a promising candidate material for adsorbing cationic dyes in aqueous media.

| S-EPMC6163381 | biostudies-literature

Optimization by Box-Behnken design for environmental contaminants removal using magnetic nanocomposite.

Project description:In this study, a CoO-Fe2O3/SiO2/TiO2 (CIST) nanocomposite was synthesized and utilized as an adsorbent to remove methylene blue (MB), malachite green (MG), and copper (Cu) from aqueous environments. The synthesized nanocomposite was characterized using field emission scanning electron microscopy (FE-SEM), Fourier-transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), and X-ray diffraction (XRD). Input parameters included pH (3-10), contact time (10-30 min), adsorbent amount (0.01-0.03 g), and pollutant concentration (20-60 mg L-1). The effects of these parameters on the removal process efficiency were modeled and optimized using the response surface methodology (RSM) based on the Box-Behnken design (BBD). The RSM-BBD method demonstrated the capability to develop a second-degree polynomial model with high validity (R2 ˃ 0.99) for the removal process. The optimization results using the RSM-BBD method revealed a removal efficiency of 98.01%, 93.06%, and 88.26% for MB, MG, and Cu, respectively, under optimal conditions. These conditions were a pH of 6, contact time of 10 min, adsorbent amount of 0.025 g, and concentration of 20 mg L-1. The synthesized adsorbent was recovered through five consecutive adsorption-desorption cycles using hydrochloric acid. The results showed an approximately 12% reduction from the first to the seventh cycle. Also, MB, MG, and Cu removal from real water samples in optimal conditions was achieved in the range of 81.69-98.18%. This study demonstrates the potential use of CIST nanocomposite as an accessible and reusable option for removing MB, MG, and Cu pollutants from aquatic environments.

| S-EPMC10960869 | biostudies-literature

Magnetic Polypyrrole-Gelatin-Barium Ferrite Cryogel as an Adsorbent for Chromium (VI) Removal.

Project description:Polypyrrole-gelatin aerogels, containing magnetic barium ferrite (BaFe) particles, (PPy-G-BaFe) were synthesized by oxidative cryopolymerization and used as adsorbents for the removal of Cr(VI) from aqueous media. The removal was performed at pH 4, which was shown to be the optimal value, due to HCrO4- being the dominant species in these conditions and its more favorable adsorption and reduction compared to CrO42-, present at pH > 4. It was found that the presence of magnetic BaFe particles had no effect on the adsorption performance of PPy aerogels in terms of capacity and kinetics, which was attributed to its relatively low content in the composite. After the adsorption, the presence of chromium in the composites was confirmed by EDX and its electrostatic interaction with the adsorbent was pointed at by vibrational spectroscopy, corresponding to the accepted adsorption mechanism. The adsorption kinetics followed the pseudo-second-order model pointing at chemisorption being the rate-limiting step. The adsorption isotherm data was best fitting with the Temkin model. The maximum adsorption capacity, calculated using the Langmuir model, was 255.8 mg g-1 (the maximum experimental value was 161.6 mg g-1). Additionally, the possibility of Cr(VI) adsorption in the presence of Cl-, Br-, NO3- and SO42- as interfering ions was shown.

| S-EPMC10606301 | biostudies-literature

A facile calcination conversion of groundwater treatment sludge (GTS) as magnetic adsorbent for oxytetracycline adsorption.

Project description:In this paper, groundwater treatment sludge (GTS) was recycled as a magnetic adsorbent via a facile calcination process without adding any reductant. The prepared magnetic adsorbents (MAs) were characterized by scanning electron microscopy (SEM), X-ray diffractometer (XRD) and X-ray photoelectron spectroscopy (XPS), vibrating sample magnenometer (VSM) and Mössbauer spectroscopy. The results showed that GTS comprised 33.2% Fe, 1.4% Al and 6.2% Si, and exhibited a weak saturation magnetization of 0.0008 emu/g. Without NaOH, the GTS calcinated at 700 and 500 °C were well magnetized with Ms of 20.1 and 7.1 emu/g, separately, but exhibited a low Ms of 0.43 emu/g at 300 °C. By adding NaOH powder, the Ms of GTS apparently increased to 4.9 emu/g after calcination at 300 °C, and further to 8.5 emu/g at 500 °C. In GTS, about 96.1% Fe was involved in ferrihydrite form. The Ms of calcinated GTS was accompanied with the phase transformation of ferrihydrite to maghemite. Si/Al oxides in GTS coordinated on the surface sites of ferrihydrite and inhibited the conjunction and phase transformation of adjacent ferrihydrite particles, but were effectively desorbed as in the presence of NaOH. Na500, preparing by calcinating GTS at 500 °C with NaOH, showed an optimal total surface sites (Hs) of 0.65 mmol/g. Oxytetracycline (OTC) was used as a target for studying the adsorption characteristics of synthetic magnetic adsorbents and a high adsorption capacity of oxytetracycline of 862.1 mg/g in comparison with the other calcinated GTS, and the adsorption data was consistent with the Langmuir model. By adding 6 g/L Na-500, approximately 100% of oxytetracycline and tetracycline and nearly 40% total organic carbon were removed from real pharmaceutical wastewater. With the method, GTS can be converted in mass production to magnetic adsorbent that exhibits effective application in pharmaceutical wastewater treatment.

| S-EPMC7935931 | biostudies-literature

Molecular insights into the pH-dependent adsorption and removal of ionizable antibiotic oxytetracycline by adsorbent cyclodextrin polymers.

Project description:Effects of pH on adsorption and removal efficiency of ionizable organic compounds (IOCs) by environmental adsorbents are an area of debate, because of its dual mediation towards adsorbents and adsorbate. Here, we probe the pH-dependent adsorption of ionizable antibiotic oxytetracycline (comprising OTCH2 (+), OTCH(±), OTC(-), and OTC(2-)) onto cyclodextrin polymers (CDPs) with the nature of molecular recognition and pH inertness. OTCH(±) commonly has high adsorption affinity, OTC(-) exhibits moderate affinity, and the other two species have negligible affinity. These species are evidenced to selectively interact with structural units (e.g., CD cavity, pore channel, and network) of the polymers and thus immobilized onto the adsorbents to different extents. The differences in adsorption affinity and mechanisms of the species account for the pH-dependent adsorption of OTC. The mathematical equations are derived from the multiple linear regression (MLR) analysis of quantitatively relating adsorption affinity of OTC at varying pH to adsorbent properties. A combination of the MLR analysis for OTC and molecular recognition of adsorption of the species illustrates the nature of the pH-dependent adsorption of OTC. Based on this finding, γ-HP-CDP is chosen to adsorb and remove OTC at pH 5.0 and 7.0, showing high removal efficiency and strong resistance to the interference of coexisting components.

| S-EPMC3897700 | biostudies-literature

Removal of bisphenol A from aqueous media using a highly selective adsorbent of hybridization cyclodextrin with magnetic molecularly imprinted polymer.

Project description:In this study, a unique magnetic molecularly imprinted polymer (MMIP) adsorbent towards bisphenol A (BPA) as a template molecule was developed by bulk polymerization using β-cyclodextrin (β-CD) as a co-monomer with methacrylic acid (MAA) to form MMIP MAA-βCD as a new adsorbent. β-CD was hybridized with MAA to obtain water-compactible imprinting sites for the effective removal of BPA from aqueous samples. Benzoyl peroxide and trimethylolpropane trimethacrylate were used as the initiator and cross-linker, respectively. The adsorbents were characterized by Fourier transform infrared spectroscopy, scanning electronic microscopy, transmission electron microscopy, vibrating sample magnetometer, Brunauer-Emmett-Teller and X-ray diffraction. 1H nuclear magnetic resonance spectroscopy was used to characterize the MAA-βCD and BPA-MAA-βCD complex. Several parameters influencing the adsorption efficiency of BPA such as adsorbent dosage, pH of sample solution, contact time, initial concentrations and temperature as well as selectivity and reusability study have been evaluated. MMIP MAA-βCD showed significantly higher removal efficiency and selective binding capacity towards BPA compared to MMIP MAA owing to its unique morphology with the presence of β-CD. The kinetics data can be well described by the pseudo second-order kinetic and Freundlich isotherm and Halsey models best fitted the isotherm data. The thermodynamic studies indicated that the adsorption reaction was a spontaneous and exothermic process. Therefore, MMIP based on the hybrid monomer of MAA-βCD shows good potential of a new monomer in molecularly imprinted polymer preparation and can be used as an effective adsorbent for the removal of BPA from aqueous solutions.

| S-EPMC8074973 | biostudies-literature

Efficient removal of crystal violet dye using EDTA/graphene oxide functionalized corncob: a novel low cost adsorbent.

Project description:In this study, EDTA functionalized corncob (EDTA-corncob) and EDTA/graphene oxide functionalized corncob (EDTA-GO/corncob) were prepared using disodium ethylenediamine tetraacetic acid and the graphene oxide immersion method. EDTA-corncob and EDTA-GO/corncob were characterized by SEM and FTIR spectroscopy. On this basis, the adsorption properties of EDTA-corncob and EDTA-GO/corncob were studied with crystal violet as the adsorbate. The optimum adsorption conditions were determined by the effect of samples on the adsorption properties of crystal violet at different times, temperatures and pH, and the reusability of the samples was studied. The results showed that adsorption capacity of crystal violet on EDTA-GO/corncob was higher compared with natural corncob and EDTA-corncob. The most suitable pH value of the solution is about 6.0, the adsorption equilibrium time is 200 min. EDTA-GO/corncob can be reused eight times. This study indicated that EDTA-GO/corncob is a reusable adsorbent for rapid, low-cost, and efficient removal of dye from waste water.

| S-EPMC9066744 | biostudies-literature

Efficient removal of pharmaceuticals from water using graphene nanoplatelets as adsorbent.

Project description:Recently, pharmaceutical pollutants in water have emerged as a global concern as they give threat to human health and the environment. In this study, graphene nanoplatelets (GNPs) were used to efficiently remove antibiotics sulfamethoxazole (SMX) and analgesic acetaminophen (ACM) as pharmaceutical pollutants from water by an adsorption process. GNPs; C750, C300, M15 and M5 were characterized by high-resolution transmission electron microscopy, Raman spectroscopy, X-ray diffraction and Brunauer-Emmett-Teller. The effects of several parameters viz. solution pH, adsorbent amount, initial concentration and contact time were studied. The parameters were optimized by a batch adsorption process and the maximum removal efficiency for both pharmaceuticals was 99%. The adsorption kinetics and isotherms models were employed, and the experimental data were best analysed with pseudo-second kinetic and Langmuir isotherm with maximum adsorption capacity (Qm) of 210.08 mg g-1 for SMX and 56.21 mg g-1 for ACM. A regeneration study was applied using different eluents; 5% ethanol-deionized water 0.005 M NaOH and HCl. GNP C300 was able to remove most of both pollutants from environmental water samples. Molecular docking was used to simulate the adsorption mechanism of GNP C300 towards SMX and ACM with a free binding energy of -7.54 kcal mol-1 and -5.29 kcal mol-1, respectively, which revealed adsorption occurred spontaneously.

| S-EPMC7890490 | biostudies-literature

Metal Removal from Nickel-Containing Effluents Using Mineral-Organic Hybrid Adsorbent.

Project description:Nickel is one of the most dangerous environmental pollutants and its removal from wastewater is an important task. The capacity of a mineral-organic hybrid adsorbent, consisting of Shewanella xiamenensis biofilm and zeolite (clinoptilolite of the Chola deposit), to remove metal ions from nickel-containing batch systems under different experimental conditions was tested. The obtained biosorbent was characterized using neutron activation, SEM, and FTIR techniques. It was established that maximum removal of cations, up to 100%, was achieved at pH 6.0. Several mathematical models were applied to describe the equilibrium and kinetics data. The maximum adsorption capacity of the hybrid biosorbent, calculated using the Langmuir model, varied from 3.6 to 3.9 mg/g. Negative Gibbs energy values and positive ∆H° values indicate the spontaneous and endothermic character of the biosorption process. The effects of several parameters (pH and biosorbent dosage) on Ni(II) removal from real effluent, containing nickel with a concentration of 125 mg/L, were investigated. The optimal pH for Ni(II) removal was 5.0-6.0 and an increase of sorbent dosage from 0.5 to 2.0 led to an increase in Ni(II) removal from 17% to 27%. At two times effluent dilution, maximum Ni(II) removal of 26% was attained at pH 6.0 and sorbent dosage of 1.0 g. A 12-fold effluent dilution resulted in the removal of 72% of Ni(II) at the same pH and sorbent dosage values. The obtained hybrid biosorbent can be used for Ni(II) removal from industrial effluents with low Ni(II) concentrations.

| S-EPMC7578995 | biostudies-literature

Adsorption of basic yellow dye dataset using Ethiopian kaolin as an adsorbent.

Project description:This article presents batch experimental data describing the main batch adsorption operation parameters. Also the adsorption models (adsorption isotherm, adsorption kinetics and thermodynamic studies) of basic yellow dye on to the raw and treated kaolin adsorbents. Besides, instrumental analyses were recorded to characterize kaolin adsorbent. Such as, thermogravimetric analyzer, Fourier transformation infrared and scanning electroscope with energy dispersion spectroscopy were used. UV-Visible spectrometer was used throughout the experimental study for the determination of absorbance. The effect of adsorption temperature (30 °C, 50 °C 70 °C), PH (3, 7, 9), initial dye concentration (20 mg/l, 40 mg/l, 60 mg/l), contact time (20 min, 40 min, 60 min, 80 min, 100 min) and adsorbent dosage (0.1, 0.5, 1, 1.5, 2 g/100ml) have been well determined. For adsorbent characteristics, we provide dataset regarding (i) thermogravimetery with differential scanning calorimetery, (ii) Fourier transform infrared spectral data before and after basic yellow dye adsorption process, (iii) scanning electroscope with energy dispersion spectroscopy image at ×500 resolution, (iv) X-ray diffraction and, (v) batch adsorption experimental parameters records. Regarding scanning electroscope with energy dispersion spectroscopy image, we provide data of three surface morphology image and three elemental distribution spectra for raw and treated kaolin adsorbent.

| S-EPMC6811902 | biostudies-other

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data