Hollow spherical nano-traps using pillararene-based polymer for efficient uranium extraction from seawater.

Herein, a hollow spherical pillar[5]arene-based polymer (P5-AO) adsorbent was synthesized. The P5-AO adsorbent was capable of effectively capturing uranium from simulated seawater (139.5 mg g) and real seawater (8.

Highly efficient removal of rare earth elements by two-dimensional titanium carbide nanosheets as impacted via water chemistry.

The separation and recycling of rare earth elements (REEs) are very important owing to the high demand, limited resource, specific usages, and environmental issues. In this work, two-dimensional TiCT MXene was introduced to remove REEs (Nd(III) and La(III)) from water, and its physicochemical properties were conducted by HRTEM, SEM-EDS, XRD, FTIR, and XPS. Various parameters, such as initial pH, REEs initial concentration, contact time, and temperature, were investigated by batch experiment, respectively.

Preparation and evaluation of celite decorated iron nanoparticles for the sequestration performance of hexavalent chromium from aqueous solution.

The increasing usage of an important heavy metal chromium for industrial purposes, such as metallurgy, electroplating, leather tanning, and other fields, has contributed to an augmented level of hexavalent chromium (Cr(VI)) in watercourses negatively impacting the ecosystems and significantly making Cr(VI) pollution a serious environmental issue. In this regard, iron nanoparticles exhibited great reactivity in remediation of Cr(VI)-polluted waters and soils, but, the persistence and dispersion of the raw iron should be improved. Herein, this article utilized an environment-friendly celite as a modifying reagent and described the preparation of a novel composites namaly celite decorated iron nanoparticles (C-Fe) and evaluation of C-Fe for the sequestration performance of Cr(VI) from aqueous solution.

Geochemical and U-Th isotopic insights on uranium enrichment in reservoir sediments.

Uranium (U) geochemistry and its isotopic compositions of reservoir sediments in U mine area were poorly understood. Herein, U and Th isotopic compositions were employed to investigate source apportionment and geochemical behavior of U in 41 reservoir sediments from a U mining area, Guangdong, China. The remarkably high contents of both total U (207.

Adsorption and mechanistic study of the invasive plant-derived biochar functionalized with CaAl-LDH for Eu(III) in water.

Herein, we developed the invasive plant-derived biochar (IPB) functionalized with CaAl-LDH at five mass ratios using a physical mixture method, assessed their adsorption perform for Eu(III), and explored the relative mechanisms. Results show that the IPB successfully loaded CaAl-LDH in five composites and their Eu(III) sorption affinities were strongly affected by solution pH, contact time, temperature, and the mass ratio of LDH and IPB. All the sorpiton process for Eu(III) occurred on the heterogeneous surface of five composites and the boundary layer diffusion limited the chemical sorption rate.

Is the interaction between graphene oxide and minerals reversible?

The increased applications and production of graphene oxide (GO) make the necessity to study information on the interaction of GO with minerals. In this work, adsorption and desorption were used to study the reversibility of interaction between GO and goethite/kaolinite. Result showed that the pH value, ionic strength, and temperature had significant effects on the adsorption and desorption behavior of GO.

Thallium pollution in China and removal technologies for waters: A review.

Thallium (Tl) is a typical toxic metal, which poses a great threat to human health through drinking water and the food chain (biomagnification). China has rich Tl-bearing mineral resources, which have been extensively explored and utilized, leading to release of large amounts of Tl into the environment. However, research on Tl pollution and removal techniques is relatively limited, because Tl has not been listed within the scope of environmental monitoring in China for several decades.

Enhanced Photocatalytic Simultaneous Removals of Cr(VI) and Bisphenol A over Co(II)-Modified TiO.

To enhance the electron-hole separation and boost the practical performance of commercial titania (Degussa P25) under natural solar light, in this work, P25 was modified with Co(II) species (CoP25) through post-treatment with decomposition of Co-ethylenediaminetetraacetic acid precursors in a wet chemical anchoring process. With appropriate Co(II) loading amount as molecular cocatalyst, the resulted CoP25-4 showed significantly improved photocatalytic performance for Cr(VI) reduction and bisphenol A (BPA) oxidation under UV-light irradiation. The coexistence of Cr(VI) and BPA promoted mutually the degradation of both pollutants.

Mechanistic insights into sequestration of U(VI) toward magnetic biochar: Batch, XPS and EXAFS techniques.

The magnetic iron oxide (FeO) nanoparticles stabilized on the biochar were synthesized by fast pyrolysis of Fe(II)-loaded hydrophyte biomass under N conditions. The batch experiments showed that magnetic biochar presented a large removal capacity (54.35mg/g) at pH3.

Enhanced immobilization of U(VI) on Mucor circinelloides in presence of As(V): Batch and XAFS investigation.

The combined pollution of radionuclides and heavy metals has been given rise to widespread concern during uranium mining. The influence of As(V) on U(VI) immobilization by Mucor circinelloides (M. circinelloides) was investigated using batch experiments.

Adsorption and co-adsorption of graphene oxide and Ni(II) on iron oxides: A spectroscopic and microscopic investigation.

Graphene oxide (GO) may strongly interact with toxic metal ions and mineral particles upon release into the soil environment. We evaluated the mutual effects between GO and Ni (Ni(II)) with regard to their adsorption and co-adsorption on two minerals (goethite and hematite) in aqueous phase. Results indicated that GO and Ni could mutually facilitate the adsorption of each other on both goethite and hematite over a wide pH range.

The enhancement roles of layered double hydroxide on the reductive immobilization of selenate by nanoscale zero valent iron: Macroscopic and microscopic approaches.

Herein, we utilized nanoscale zero-valent iron loaded on layered double hydroxide (NZVI/LDH) to immobilize Se(VI) and evaluated the enhancement role of LDH in the NZVI reaction system. The structural characterization indicated that LDH could stabilize and disperse NZVI as well as prevent NZVI from oxidation, thereby increasing iron reactivity. Batch experiments displayed that, compared with those by NZVI, both extent and rate of Se(VI) immobilized by NZVI/LDH significantly increased, owing to the prominent synergistic effect ascribing from adsorption and reduction.

Macroscopic and spectroscopic studies of the enhanced scavenging of Cr(VI) and Se(VI) from water by titanate nanotube anchored nanoscale zero-valent iron.

Herein, a promising titanate nanotubes (TNT) anchored nanoscale zero-valent iron (NZVI) nanocomposite (NZVI/TNT) was synthesized, characterized and used for the enhanced scavenging of Cr(VI) and Se(VI) from water. The structural identification indicated that NZVI was uniformly loaded on TNT, thereby, the oxidation and aggregation of NZVI was significantly minimized. The macroscopic experimental results indicated that NZVI/TNT exhibited higher efficiency as well as rate on Cr(VI) and Se(VI) scavenging resulted from the good synergistic effect between adsorption and reduction.

Thallium contamination in arable soils and vegetables around a steel plant-A newly-found significant source of Tl pollution in South China.

Thallium (Tl) is a highly toxic rare element. Severe Tl poisoning can cause neurological brain damage or even death. The present study was designed to investigate contents of Tl and other associated heavy metals in arable soils and twelve common vegetables cultivated around a steel plant in South China, a newly-found initiator of Tl pollution.

Enhanced sequestration of Cr(VI) by nanoscale zero-valent iron supported on layered double hydroxide by batch and XAFS study.

Herein, the reduction of nanoscale zero-valent iron (NZVI) and adsorption of layered double hydroxides (LDH) to sequester Cr(VI) were well combined by the immobilization of NZVI onto LDH surface (NZVI/LDH). The characterization results revealed that LDH decreased NZVI aggregation and thus increased Cr(VI) sequestration. The batch results indicated that Cr(VI) sequestration by NZVI/LDH was higher than that of NZVI, and superior to the sum of reduction and adsorption.

The roles of a pillared bentonite on enhancing Se(VI) removal by ZVI and the influence of co-existing solutes in groundwater.

The zero-valent iron permeable reactive barrier (ZVI-PRB) is a promising technology for in-situ groundwater remediation. However, its long-term performance often declined due to the blocked reactive sites by corrosion products and by interference of co-existing solutes. In order to address these issues, a pillared bentonite (Al-bent) was homogeneously mixed with ZVI for removing selenate (Se(VI)) from simulated groundwater in column experiments.

Enhanced reduction of chlorophenols by nanoscale zerovalent iron supported on organobentonite.

The reactivity of nanoscale zerovalent iron (NZVI) on removing chlorophenols (2-chlorophenol, 2,4-dichlorophenol, 2,4,6-trichlorophenol and pentachlorophenol) was remarkably enhanced by using a hydrophobic support of organobentonite (CTMA-Bent), namely the bentonite modified with organic cetyltrimethylammonium (CTMA) cations. The complete dechlorination of chlorophenols and total conversion into phenol using this novel NZVI/CTMA-Bent combination was observed in batch experiments. The kinetic studies suggested that the reduction of chlorophenols by NZVI was accelerated due to the enhanced adsorption onto CTMA-Bent, which facilitated the mass transfer of chlorophenols from aqueous to iron surface.

Colloidal diatomite, radionickel, and humic substance interaction: a combined batch, XPS, and EXAFS investigation.

This work determined the influence of humic acid (HA) and fulvic acid (FA) on the interaction mechanism and microstructure of Ni(II) onto diatomite by using batch experiments, X-ray photoelectron spectroscopy (XPS), and extended X-ray absorption fine structure (EXAFS) methods. Macroscopic and spectroscopic experiments have been combined to see the evolution of the interaction mechanism and microstructure of Ni(II) in the presence of HA/FA as compared with that in the absence of HA/FA. The results indicated that the interaction of Ni(II) with diatomite presents the expected solution pH edge at 7.

Mutual effects of copper and phosphate on their interaction with γ-Al2O3: combined batch macroscopic experiments with DFT calculations.

The mutual effects of Cu(II) and phosphate on their interaction with γ-Al(2)O(3) are investigated by using batch experiments combined with density functional theory (DFT) calculations. The results of batch experiments show that coexisting phosphate promotes the retention of Cu(II) on γ-Al(2)O(3), whereas phosphate retention is not affected by coexisting Cu(II) at low initial phosphate concentrations (≤ 3.6 mg P/L).

Application of a novel plasma-induced CD/MWCNT/iron oxide composite in zinc decontamination.

Herein, β-cyclodextrin (β-CD) was grafted onto magnetic MWCNT/iron oxide particles by using low temperature plasma-induced technique to synthesize a novel nanocomposite. The prepared composite (denoted as CD/MWCNT/iron oxide) exhibited high magnetic property (saturation magnetization M(s)=37.8 emu/g) and good dispersion property in aqueous solution.

Characterization of diatomite and its application for the retention of radiocobalt: role of environmental parameters.

Clay minerals have been extensively studied because of their strong sorption and complexation ability. In this work, diatomite was characterized by using acid-base titration. Retention of radionuclide (60)Co(II) from aqueous solution by sorption onto diatomite was investigated by using batch technique under various environmental conditions such as pH, ionic strength, humic acid (HA), fulvic acid (FA), and temperature.

Investigation of the sequestration mechanisms of Cd(II) and 1-naphthol on discharged multi-walled carbon nanotubes in aqueous environment.

The increasing exploitation of multi-walled carbon nanotubes (MWCNTs) into many industrial processes has raised considerable concerns as they are likely to be released into the environment. The interactions of the pollutants in water with discharged MWNCTs will further influence the environmental behavior and fate of these contaminants. In this context, our work aims to quantify the sequestration mechanisms and species distribution of Cd(II) and 1-naphthol on discharged MWCNTs by using batch technique.

The removal of U(VI) from aqueous solution by oxidized multiwalled carbon nanotubes.

Multiwalled carbon nanotubes (MWCNTs) have exhibited high sorption capacity for radionuclides due to the unique hollow structure and large surface area. In this study, surface properties of oxidized MWCNTs were characterized by using XRD, SEM, FTIR and potentiometric acid-base titration. The sorption of U(VI) on oxidized MWCNTs as a function of contact time, U(VI) concentration, pH, ionic strength, humic acid/fulvic acid (HA/FA) and carbonate was investigated by using batch technique.

Impact of water quality parameters on the sorption of U(VI) onto hematite.

In this study, the sorption of U(VI) from aqueous solution on hematite was studied as a function of various water quality parameters such as contact time, pH, ionic strength, soil humic acid (HA) or fulvic acid (FA), solid content and temperature by using a batch technique. The results demonstrated that the sorption of U(VI) was strongly dependent on ionic strength at pH<6.0, and outer-sphere surface complexation may be the main sorption mechanism.