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Materials · 2017 ·Vol. 10 ·期 1 ·84 · IF 2.654

Synthesis of Magnetic Microspheres with Sodium Alginate and Activated Carbon for Removal of Methylene Blue

Chaodao Li,Jianjiang Lu,Shanman Li,Yanbin Tong,Bangce Ye

Based on the adsorption performance of composite microspheres with activated carbon (AC) and sodium alginate (SA), as well as the magnetic property of Fe3O4, we designed and explored an efficient strategy to prepare a unique, multifunctional Fe3O4/AC/SA composite absorbent (MSA-AC) that extracted dye from aqueous solution. The composite exhibited the following advantages: rapid and simple to prepare, environmentally friendly process, low-cost, recyclability, and multi-functionality. The physicochemical properties of the prepared magnetic microspheres were measured, and methylene blue (MB) was selected to investigate the performance of the magnetic absorbent. The results showed a maximum adsorption capacity of 222.3 mg/g for MB. Adsorption studies revealed that the data of adsorption isotherms and kinetics fit the pseudo-second-order kinetic model and Langmuir isotherm model.Keywords:magnetic microsphere;methylene blue;adsorption properties

CAS / MDL: 107-15-3
研究领域: 环境科学 · 材料科学
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Journal of Central South University · 2024 ·Vol. 31 ·期 4 ·1292-1305 · IF 3.7

Adsorption performance and mechanistic study of Pb, Cd and As by CaAl-LDH in wastewater

Hou Jin-feng,Sun Qian,Hao Xiu-zhen

Heavy metal composite pollution is becoming increasingly serious. In this study, CaAl-layered double hydroxide (CaAl-LDH) was prepared using the facile co-precipitating method, and was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), fourier transform infrared (FTIR) spectroscopy and X-ray photoelectron spectroscopy (XPS). Lead(II), Cd(II), and As(V) were selected as the representative heavy metals to evaluate the adsorption capability of the synthesized CaAl-LDH by the batch experiments. The maximal adsorption capability of CaAl-LDH for Pb(II), Cd(II), and As(V) was 786.6, 437.2 and 72.9 mg/g, respectively. The adsorption mechanism of Pb, Cd and As may be surface precipitation, isomorphic substitution and ion exchange within the interlayer spaces of LDH, respectively. In conclusion, this experiment provides a LDH material with fast and efficient adsorption performance for both anionic and cationic metals, indicating its potential for practical application in the remediation of heavy metal composite pollution.

CAS / MDL: 7784-27-2 7631-99-4
研究领域: 环境科学 · 材料科学
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CRYSTENGCOMM · 2024 · IF 2.6

Study on acid-modulated UiO-66-NH2 and its adsorption performance and mechanism for OTC

Hao He,Xiao-kai Liu,Bai-yun Zhao,Li-juan Zhou,Xuan Zhao,Chen-xu Wang,Ji-yuan Zhang,Yuan-fang Zhang,Li Wang

In this study, UiO-66-NH2 nanoparticles were synthesized via a hydrothermal method, using acetic acid and hydrochloric acid as modulators to optimize the specific surface area and pore width. Oxytetracycline (OTC) was chosen as the test compound to evaluate the adsorption efficiency of UiO-66-NH2.The material was thoroughly characterized under varying conditions, and the adsorption mechanism was systematically explored through adsorption kinetics, isotherms, and thermodynamic analyses. The results demonstrated that UiO-66-NH2 exhibited a high OTC adsorption capacity, achieving a maximum of 312.5 mg g−1 under optimal conditions. XRD, TGA, and BET analyses revealed that acetic acid and hydrochloric acid significantly improved the crystallinity and thermal stability of UiO-66-NH2, increasing the specific surface area from 8.023 m2 g−1 to 998.663 m2 g−1 and reducing the pore width from 18.783 nm to 2.129 nm. FTIR, XPS, adsorption kinetics, and isotherm studies indicated that the main forces driving OTC adsorption by CMC-Fe were hydrogen bonding, π–π stacking, weak electrostatic interactions, and pore filling. Cyclic adsorption experiments further demonstrated the excellent reusability of UiO-66-NH2. In summary, the use of acetic acid and hydrochloric acid significantly increased the specific surface area of UiO-66-NH2, exposing more adsorption sites and playing a critical role in pollutant removal.

研究领域: 材料科学 · 环境科学 · 化学工程
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Polymers · 2023 ·Vol. 15 ·期 8 ·1879 · IF 5

Green Preparation of Lightweight, High-Strength Cellulose-Based Foam and Evaluation of Its Adsorption Properties

Yongxing Zhou,Wenbo Yin,Yuliang Guo,Chenni Qin,Yizheng Qin,Yang Liu

In recent years, the application scope of most cellulose-based foams is limited due to their low adsorbability and poor recyclability. In this study, a green solvent is used to extract and dissolve cellulose, and the structural stability of the solid foam is enhanced by adding a secondary liquid via the capillary foam technology, and the strength of the solid foam is improved. In addition, the effects of the addition of different gelatin concentrations on the micro-morphology, crystal structure, mechanical properties, adsorption, and recyclability of the cellulose-based foam are investigated. The results show that the cellulose-based foam structure becomes compact, the crystallinity is decreased, the disorder is increased, and the mechanical properties are improved, but its circulation capacity is decreased. When the volume fraction of gelatin is 2.4%, the mechanical properties of foam are the best. The stress of the foam is 55.746 kPa at 60% deformation, and the adsorption capacity reaches 57.061 g/g. The results can serve as a reference for the preparation of highly stable cellulose-based solid foams with excellent adsorption properties.Keywords:cellulose-based foam;gelatin;adsorption

研究领域: 材料科学 · 环境科学
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APPLIED CLAY SCIENCE · 2021 · IF 5.467

Aggregated germanium saponite: Removal and retention of polymeric thorium and uranium complexes

Baihui Zhai,Shan Zhu,Qiang Tian,Na Li,Minhao Yan,Mark J. Henderson

The present study concerns the removal of thorium and uranium from aqueous solution, and particularly the effect of clay particle size and morphology on the adsorption of polynuclear actinide complexes by synthetic saponite nanoscale powders. Saponites were synthesized from a reactant mixture containing aluminum nitrate, magnesium nitrate, and either sodium silicate or sodium germanate . The saponite powders were analyzed by TEM , XRD , SAXS , N 2 -adsorption-desorption isotherms and FT-IR. Ge-saponite contained randomly stacked platelets ≈ 100 nm long and 80 nm wide, while Si-saponite showed roughly spherical agglomerates ≈ 60–80 nm in size. Small-angle X-ray scattering measurements indicated a hierarchical pore network among the plates and their agglomerates. Thorium polymers composed of fractal aggregates of branched filaments were characterized by synchrotron radiation-SAXS. The distribution coefficient ( K d mL/g) values for thorium (20 μg/mL) at pH 4 were: Ge-saponite (10 5 ) ≈ Si-saponite (10 5 ) > raw saponite (10 4 ) ≈ raw saponite (washed) (10 4 ). The K d values for uranium (20 μg/mL) at pH 5.5 were: Ge-saponite (10 3 ) ≈ raw saponite (washed) (10 3 ) ≈ Si-saponite (10 3 ) ≈ raw saponite (10 3 ). The difference in uranyl adsorption performance observed between the two nanoparticle forms of saponite was attributed to a larger pore width for Ge-saponite (3.5 nm) compared with Si-saponite (0.8 nm). The results have implications for mineral ore tailings containing thorium(IV) and, by analogy, Pu(IV) in a clay buffer environment within a geological repository for high-level nuclear waste .

研究领域: 环境科学 · 放射化学
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WATER AIR AND SOIL POLLUTION · 2018 ·Vol. 229 ·期 4 ·1-10 · IF 1.769

Sorption of Uranium on a Bifunctional Polymer of Diethylenetriaminepentaacetic Acid Cross-Linked β-Cyclodextrin in the Presence of Humic Acid: Kinetics, Isotherms, and Thermodynamics

Dai Ying,Lv Riwen,Huang Dejuan,Tao Qinqin

Humic acid (HA) plays an important role in the migration and transformation of uranium in natural waters. To effectively remove uranium in the presence of HA, a bifunctional polymer, diethylenetriaminepentaacetic acid cross-linked β -cyclodextrin (DTPA- β -CD), was synthesized by polycondensation reaction. The sorption performance of DTPA- β -CD in functions of pH, ionic strength, contact time, initial time, and temperature were explored batch wise. Experimental results showed that DTPA- β -CD could concurrently sorb uranium and HA around pH of 3.0. The sorption strongly depended on pH and on ionic strength, demonstrating outer-sphere surface complex in nature. Two sorption kinetics well followed pseudo-second-order model. Sorption isotherm accorded with Sips model. Increasing temperature facilitated uranium and restrained HA sorption. This work demonstrated that DTPA- β -CD was a promising material for sorbing uranium in the presence of HA.

CAS / MDL: 7585-39-9
研究领域: 环境科学 · 化学工程
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2019 · IF 4.784

Phosphorus removal and recovery from water with macroporous bead adsorbent constituted of alginate-Zr4+ and PNIPAM-interpenetrated networks

Huayong Luo,Xueyang Zeng,Peng Liao,Hongwei Rong,Tian C. Zhang,Z. Jason Zhang,Xiangchao Meng

Currently, there is a growing trend in employing natural biomaterials (e.g., alginate) to prepare a novel bead adsorbent for phosphorus (P) elimination. However, the utilization of alginate beads to remove and recover P from effluents possesses limitations associated with its physical characteristics such as a dense gel layer, poor mechanical strength and low stability. To overcome the limitations and improve the adsorption performances, we synthesized a novel alginate-derived bead constituted of PNIPAM network interpenetrated in alginate-Zr 4+ network (PNIPAM/SA-Zr) decorated with polyethylene glycol as a pore-forming agent, and then investigated its ability to remove and recover P from effluents. The morphology, functional groups, surface area, and mechanical strength of the beads were evaluated by SEM, FTIR , BET, and swelling analysis. The adsorption of P was investigated by varying various factors. The adsorption kinetics , isotherms, and thermodynamics were studied. Particularly, the P-loaded beads exhibited a faster desorption rate under thermal stimulus, and remained good desorption efficiency and reusability within five consecutive cycles. Zeta-potential and XPS results revealed that the adsorption mechanisms were related to electrostatic interactions, ligand exchange, and the formation of inner-sphere complexes. The beads possessed favorable fixed-bed column operation performances for P removal and recovery from real wastewater.

研究领域: 环境科学 · 材料科学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2022 · IF 9.136

Insights into enhanced elimination of U(VI) and Eu(III) by amidoxime-functionalized Ti3C2Tx MXenes

Di Zhang,Bing Zhao,Lijie Liu,Hao Tang,Xiangxue Wang,Shujun Yu

Although two-dimensional transition metal carbides and carbonitrides (MXenes) are becoming increasingly popular in contaminant remediation field, the preparation of MXene nanosheets that can efficiently eliminate the target pollutants still deserves in-depth investigation. Here we produced amidoxime Ti 3 C 2 T x nanosheets (TC-AO), which were efficient radionuclide adsorbents with high stability and positive affinity, by introducing the amidoxime group into the Ti 3 C 2 T x MXene surface through grafting by diazonium salt. The high stability and abundant functional groups of TC-AO were demonstrated by different characterization techniques such as scanning electron microscope (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FT-IR), thermogravimetric analyzer (TGA), and X-ray photoelectron spectroscopy (XPS). Multiple factors affecting the radionuclide removal performance were explored, including reaction time, temperature, pH, ionic strength, anions and cations. The experimental results demonstrated that the radionuclide uptake by TC-AO was a heat-absorbing, spontaneous single-molecule chemisorption process and was consistent with the pseudo-secondary and Langmuir models. When pH < 6, the mechanism of uranium removal was inner complexation, and as the pH continued to increase, uranium removal shifted to outer complexation. Furthermore, the results certificated that TC-AO exhibited fast reaction kinetics (reaching equilibrium in about 20 min), excellent removal efficiency (279.57 mg U·g −1 and 73.99 mg Eu·g −1 ), outstanding selectivity and good stability. The studies showed that TC-AO had good stability and functionality, which was not only valuable for the design of MXene based adsorbents, but also provided a meaningful option for the extraction of radioactive pollutants from wastewater.

研究领域: 材料科学 · 环境科学
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Journal of Environmental Chemical Engineering · 2023 · IF 7.7

Insights into the performance and mechanism of Cr(VI) and U(VI) removal in water using innovative cross-linked chitosan adsorbent

Peng Cheng,Zhiyang Wei,Yara Arbid,Tengfei Fu,Xiaowei Liu,Olivier Monfort

The primary aim of this work is to test a novel adsorbent prepared by cross-linking of tetrafluoroterephthalonitrile with chitosan (CS-TFT) for the removal of Cr(VI) and U(VI). The CS-TFT is stable until 250 °C and possesses amino functional groups due to the presence of CS that remain intact even after the cross-linking reaction, thus being a benefit for adsorption properties; while the TFT brought roughness to CS-TFT that keeps its high porosity. The adsorption efficiency of CS-TFT is evaluated in the batch experiment of Cr(VI) and U(VI) adsorption along with the effect of different experimental parameters (pH, time, temperature, initial concentrations, and co-existing inorganic cations). The maximum adsorption capacity of CS-TFT for adsorption of Cr(VI) and U(VI) was 265.96 mg·g -1 at pH = 3 and 346.06 mg·g -1 at pH = 5, respectively, at 298 K and the corresponding partition coefficients were 12,454 and 6181 mg g -1 mM -1 , respectively. The kinetics of the adsorption process is identified as a pseudo-second-order model and the Langmuir isotherm model is considered. The CS-TFT shows satisfactory reusability since it can be used after 6 cycles of regeneration with a removal efficiency of Cr(VI) and U(VI) higher than 90 %. The adsorption mechanism is also proposed based on investigation of CS-TFT by FTIR, XPS and SEM-EDS before and after adsorption. The results show that hydroxy (–OH) and amino (–NH 2 ) groups play a key role in the chemical adsorption . All these findings suggest that CS-TFT could be a promising adsorbent for wastewaters treatment .

CAS / MDL: 9012-76-4 1835-49-0
研究领域: 环境科学 · 材料科学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2024 · IF 8.1

Construction of hydrophobic HKUST-1 in wood with selective adsorption performance for toluene and moisture blends

Zhu Liu,Shoulu Yang,Zhongwei Wang,Ning Ji,Xingong Li,Yingfeng Zuo

The effect of moisture on the volatile organic compound (VOC) adsorption on biomass-derived metal–organic framework composites is significant in practical applications. In this study, wood-based metal organic frameworks (MOF199-W) and hydrophobic MOF199-W (HMOF199-W) were developed using HKUST-1 (MOF199) and long alkyl chains to investigate the adsorption performance of toluene and enhance the selectivity of adsorption under high humidity conditions. The results demonstrated that HKUST-1 could be anchored onto the surface of wood vessels and fibers through coordination with Cu 2+ , resulting in an improved surface area in comparison to natural wood. The toluene adsorption capacity of MOF199-W with a 20 % loading was comparable to that of an equivalent amount of MOF199, with adsorption capacities of 323.5 mg/g and 369.9 mg/g, respectively. Further, the Yoon-Nelson model was found to adequately describe the dynamic adsorption process. Following the introduction of long alkyl chains, MOF199 and MOF199-W were endowed with strong hydrophobic character (water contact angle of 107.0 ◦ , 104.0 ◦ , and water uptake of 30.5 mL/g, 55.3 mL/g). With the increase in humidity, the adsorption performance of MOF199 and MOF199-W for toluene sharply decreased, but HMOF199 and HMOF199-W still maintained the adsorption capacities at 304.7 mg/g and 226.7 mg/g, even under 80 % RH conditions. Therefore, HMOF199-W has shown great potential in wooden building materials with the ability for toluene capture under humid conditions.

研究领域: 材料科学 · 环境科学
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ACS Applied Polymer Materials · 2024 · IF 4.4

Efficient Separation of Uranium(VI) by CaCO3-Doped Chitosan with PO43– Modification: Adsorption Behaviors and Mechanism Study

Jun Liao,Congcong Ding,Junping Shi,Liang Jiang,Qiuyi Wang,Lielin Wang

The application of chitosan-based materials for the separation of uranium from wastewater was limited due to the lack of active sites. In this work, a chitosan-based composite (CaCO3@aCS/PA) was effectively created by modifying chitosan with CaCO3 and phytic acid to enhance the adsorption performance of chitosan materials. CaCO3@aCS/PA showed no significant changes and no Ca2+ was detected in the solution after stirring for 10 h in a solution with pH > 3, indicating good stability of CaCO3@aCS/PA, which was beneficial for use in adsorption. Moreover, the adsorption capacity and adsorption percentage of CaCO3@aCS/PA for uranium reached 842.0 mg/g (298 K, pH = 4) and 95.4% (C0 = 10 mg/L, pH = 4) and the adsorption equilibrium time was significantly shortened, indicating that the modification with CaCO3 and phytic acid enhanced the adsorption ability of chitosan for uranium, which was related to the synergistic effect of various active sites (CO32–, PO43–, −OH, and –NH2) on CaCO3@aCS/PA for uranium adsorption.

研究领域: 环境科学 · 材料科学
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SCIENCE OF THE TOTAL ENVIRONMENT · 2021 · IF 7.963

Development of an acidized biochar-supported hydrated Fe(III) oxides for highly efficient cadmium and copper sequestration from water

Yan Li,Liangmin Gao,Yu Wang,Shuo Cheng,Guowei Wu,Xuan Yang,Shunli Wan

Biochar-supported metallic oxides are attractive adsorbents for heavy metal cleanup, but the adsorption performance is still unsatisfactory as a result of the self-aggregation of the incorporated metallic oxides. A new hybrid nano-material was prepared through impregnating hydrated ferric oxide (HFO) nanoparticles within biochar bearing high-density charged oxygen-containing groups (e.g., carboxyl and hydroxyl groups) (ABC) derived from HNO 3 treatment. The as-made adsorbent, denoted as HFO-ABC, possesses highly dispersed HFO nanoparticles with typical size lower than 20 nm, and exhibits greater sorption capacity for Cd(II) and Cu(II) than the pristine biochar-supported HFO. It also shows great sorption preference toward Cd(II) and Cu(II) in co-presence of high levels of Ca 2+ , Mg 2+ and humic acid (HA). Such prominent performance is put down to the high-density charged functional groups on the host ABC, which not only promote the dispersion of the immobilized HFO nanoparticles but also generate the potential Donnan membrane effect, i.e., the pre-concentration and permeation of target metals prior to their preferable adsorption by nano-HFO. The predicted effective coefficients of intra-particle diffusion for Cu(II) and Cd(II) are 3.83 × 10 −9 and 4.33 × 10 −9 cm 2 /s, respectively. HFO-ABC exhibits excellent performance for fixed-bed column application, and yields 513 and 990 BV effluents for Cd(II) and Cu(II) to achieve their discharge standards, respectively. The spent HFO-ABC could be in situ regenerated using binary HCl-CaCl 2 solution with desorption efficiency higher than 95%. All results manifest that increasing charged functional groups via HNO 3 treatment is an effective measure for boosting sorption performance of biochar-based nanocomposites.

研究领域: 环境科学 · 材料科学
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