Adsorption mechanism of Ca2+, Mg2+, Fe3+, and Al3+ ions in phosphoric acid-nitric acid solution on 001 × 7 and S957 resins.

Selective removal of Ca2+ and Mg2+ ions using the 001 × 7 resin and Fe3+ and Al3+ ions using the S957 resin is able to achieve the deep purification of the phosphoric acid-nitric acid solution, but the adsorption behaviors of Fe3+ and Al3+ ions are seriously suppressed by phosphoric acid. In order to understand the interaction mechanism of separation processes and the influence of phosphoric acid, we first studied the bonding form of Ca2+, Mg2+, Fe3+, and Al3+ ions on 001 × 7 and S957 resins using FT-IR and XPS techniques; subsequently, quantum chemistry computation was carried out to further explore the bonding mechanism between the functional groups on resins and metal ions. FT-IR and XPS results reveal that for the adsorption process on the 001 × 7 resin, hydroxyls from sulfonic acid groups combine with Ca2+ and Mg2+ ions. Whereas Fe3+ and Al3+ ions are adsorbed on the S957 resin through an exchange reaction with hydroxyls on the phosphonic acid group but not on the sulfonic acid group. Quantum chemistry computation results reveal that the phosphonic acid group has a larger binding energy with Fe3+ and Al3+ ions. Thus, the S957 resin still presents great adsorption performance for Fe3+ and Al3+ ions despite the influence of dihydrogen phosphate ions in the phosphoric acid-nitric acid solution.

One-step synthesis of a benzothiadiazole-based nonbranching functionalized covalent organic framework and its application in efficient removal of Hg2.

In recent years, a variety of adsorbents have been developed for Hg2+ removal. However, these adsorbents are unsatisfactory for adsorption due to narrow and irregular pore channels or poor adsorption capacity and low stability. Therefore, it is worth exploring a porous Hg2+ adsorbent material with high adsorption performance and stability. In this study, a benzothiadiazole-based nonbranching functionalized covalent organic framework (COF) material (TPS-COF) by one-step synthesis was reported, which exhibited a high specific surface area of 1564 m2 g-1, high crystallinity and stability attributed to its high conjugated linkage structure of benzothiadiazole. In addition, due to the rich S and N elements of the benzothiadiazole unit, it exhibited excellent adsorption performance on Hg2+, including excellent adsorption amount (1040 mg g-1), high initial adsorption rate (448 mg g-1 min-1) and very short adsorption equilibrium time (10 min), with an efficient removal rate of Hg2+ in the pH range of 2-8. After desorption, the TPS-COF still retained good pore stability, adsorption capacity, and reusability. Such a one-step synthetic unbranched functionalization strategy provides further insights to achieve a good balance between the high crystallinity, functionality and stability of COFs.

Comparison of Salvianolic Acid A Adsorption by Phenylboronic-Acid-Functionalized Montmorillonites with Different Intercalators.

Due to its success in treating cardio-cerebrovascular illnesses, salvianolic acid A (SAA) from Salvia miltiorrhiza is of major importance for effective acquisition. For the adsorption of salvianolic acid, cationic polyelectrolytes, and amino-terminated silane intercalated with phenylboronic-acid-functionalized montmorillonites, known as phenylboronic-acid-functionalized montmorillonites with PEI (PMP) and phenylboronic-acid-functionalized montmorillonites with KH550 (PMK), respectively, were produced. In this paper, detailed comparisons of the SAA adsorption performance and morphology of two adsorbents were performed. PMP showed a higher adsorption efficiency (>88%) over a wide pH range. PMK showed less pH-dependent SAA adsorption with a faster adsorption kinetic fitting in a pseudo-second-order model. For both PMP and PMK, the SAA adsorption processes were endothermic. Additionally, it was clearer how temperature affected PMP adsorption. PMK has a higher adsorption selectivity. This study demonstrates how the type of intercalator can be seen to have an impact on adsorption behavior through various structural variations and offers an alternative suggestion for establishing a dependable method for the synthesis of functional montmorillonite from the intercalator's perspective.

One-step synthesis of cyclic compounds towards easy room-temperature phosphorescence and deep blue thermally activated delayed fluorescence.

With the advantages of facile one-pot synthesis and THF-irrigating purification, we first developed novel cyclic compounds with deep blue thermally activated delayed fluorescence (TADF) and room-temperature phosphorescence (RTP) dual emission even in the as-spun films. Careful crystal analysis, combined with theoretical calculations, reveal that abundant inter- and intra-molecular interactions, whatsoever the molecular packing, are obligated to unique RTP properties. These results open up a new study of compounds with multiple acceptors and donors, and represent an important step in the further development of deep blue TADF and easy RTP emission.