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Tetraphenyldithiodiphosphonate is synthesized by polymerization precipitation. The P = S bond of the material has strong polarity, which is conducive to improving the electron mobility of the complex and inhibiting the accumulation between molecules. The synthesized tetraphenyldithiodiphosphonate is characterized by FT-IR, SEM, XPS and XRD. In addition, the pseudo-second-order kinetic model is used to simulate the experimental data well, and the adsorption process conforms to the Langmuir isotherm model. Thermodynamic studies of adsorption have shown that the adsorption process is essentially a spontaneous endothermic process. At room temperature, tetraphenyldithiodiphosphonate demonstrates a maximum adsorption capacity for uranium(VI) reaching 398.8 mg g−1. [ABSTRACT FROM AUTHOR]

In this study, amino modified mesoporous silica (HMS-TEEPA-TEA) was used for the first time to remove uranium (VI) from aqueous solution. The synthesized HMS-TEEPA-TEA was characterized by SEM, EDS, FTIR, BET and XPS techniques. The present work attempted to optimize and compare the adsorption process parameters like pH, adsorbate concentration, and adsorbent dose using Box-Behnken designs of response surface methodology. The adsorption amount and removal rate reached 337.26 mg/g and 99.57%, respectively. Model P> F < 0.0001 in this experiment (generally P > F < 0.05 is considered significant), indicating that the model is extremely significant and can be considered as highly referable for its predicted response values. The fit of the data to the Langmuir isotherm and the proposed secondary kinetics indicates that the adsorption process is monolayer and chemical in nature. The effect of copper on HMS-TEEPA-TEA adsorption is more complex than other background ions. The removal of uranium (VI) by HMS-TEEPA-TEA remained above 80% for four consecutive experiments with repeated adsorbent use. The results indicate that HMS-TEEPA-TEA is an effective adsorbent for the removal of uranium (VI) from aqueous solutions with the advantages of low cost, high availability and easy production. [ABSTRACT FROM AUTHOR]

In this work, a new material containing chitosan(CS)-hexachlorocyclotriphosphazene (HP) composite was synthesized with polyphosphoric acid as the cross-linking agent for the effective removal of uranium(VI) from aqueous solution. The prepared material was characterized by FTIR, EDS, SEM, BET and XPS. According to batch experiments, its adsorption equilibrium (Qe = 398.8 mg g−1) was reached within 50 min at pH 6.0. The adsorption process could be well fitted to the pseudo-second-order model and the Langmuir model. The thermodynamic analysis indicated that the adsorption was an exothermic and spontaneous process. Furthermore, the CS-HP has superior absorption reusability. This study proved that CS-HP could be considered as the highly efficient and sustainable material for removal of uranium(VI) from aqueous solution. [ABSTRACT FROM AUTHOR]

Bis(diphenyl phosphate) imine(Htpop) was synthesized as an adsorbent for the effective removal of U(VI) from aqueous solutions using triphenyl phosphate(TPP) as the starting material. Htpop possesses notable polarity, characterized by the presence of -P O(phosphoryl) and -N-H(imino) functional groups, along with other bulky substituents. It has the capability to form chelates with metal ions, thus enabling the removal of radionuclide U(VI) from aqueous solution. The overall adsorption experiment shows that both phosphoryl and imino groups interact with uranyl ions, and the removal rate reaches 99.53 % at pH 6.0. The adsorption process conforms to the Pseudo-second-order kinetic model and Langmuir isotherm model. [ABSTRACT FROM AUTHOR]

The preparation of easily synthesized and cheap composite materials for the efficient removal of toxic oxoanions still remains challenging in sewage treatment. Herein, a new carbonized manganese-crosslinked sodium alginate (Mn/SA-C) was fabricated for the removal of arsenite (As(III)), arsenate (As(V)) and hexavalent chromium (Cr(VI)) in water. The results indicated that the Mn/SA-C pretreated with MnSO 4 solution (Mn/SA-C-S) exhibited a rapid adsorption toward As(III) and As(V) with the removal efficiency of >98% within 10 min, and had a high adsorption capacity toward As(III), As(V), and Cr(VI) with the maximum value of 189.29, 193.29, and 104.50 mg/g based on the Langmuir model, respectively. The removal efficiency of As(III), As(V), and Cr(VI) could be further significantly enhanced by coupling a photocatalytic process. For example, the time in which >98% of Cr(VI) (10 mg/L) was removed dramatically shortened from 360 min (adsorption) to 45 min (adsorption-photocatalysis), and the removal efficiency of As(III) increased by ∼10% within initial 5 min. This was primarily attributed to the Mn-catalyzed production of the photocatalytic excitons for Cr(VI) reduction, and the superoxide (•O 2 −) and hydroxyl (•OH) radicals for As(III) oxidation. The adsorption removal of arsenic (As) was primarily ascribed to surface complexation with MnO and precipitation by MnS 2 , and oxidative adsorption because of Mn valence cycle. The removal mechanisms of Cr(VI) mainly contained reduction by MnO and MnS 2 , complexation with MnO and carboxyl/hydroxyl groups as well as Cr(OH) 3 precipitation. Our research provides a promising Mn/SA-C-S material for rapid and efficient removal of As(III), As(V), and Cr(VI) in contaminated water through an adsorption-photocatalysis synergistic strategy. [Display omitted] • A novel carbonized manganese-crosslinked sodium alginate (Mn/SA-C) was prepared. • >98% of As(III) and As(V) was rapidly adsorbed within 10 min under dark condition. • As(III), As(V) and Cr(VI) adsorption fitted well to pseudo-second-order models. • The removal of As(III), As(V) and Cr(VI) was enhanced by coupling a photocatalysis. • Adsorption-photocatalysis mechanisms of As(III), As(V) and Cr(VI) were proposed. [ABSTRACT FROM AUTHOR]