The textile industries have incorporated perfume microencapsulation technology to improve their products. However, certain industrial microcapsules show low encapsulation capacity and low material stability. In this study, vanillin/chitosan microcapsules were prepared via spray‐drying, and the encapsulation efficiency and loading capacity of the microcapsule were 50.69% and 30.31%, respectively. Quantum–chemical calculations confirm the interactions of hydrogen bonds between vanillin and chitosan. Their applicability to the cotton fabric with citric acid as the cross‐linking reagent has been investigated. The structure of the microcapsule‐treated cotton fabric has been characterized with various physico‐chemical techniques. The results confirm the microcapsules have been successfully grafted onto the cotton fabrics. The release experiments show that 21.9% vanillin was retained under 65°C and 80% humidity conditions and 8.6% vanillin still existed after 14 washes. Copyright © 2013 John Wiley & Sons, Ltd.
Terpinen‐4‐ol has several biological properties, but its low stability and water‐solubility limit its use. This study reports the formation of a solid terpinen‐4‐ol/β‐cyclodextrin (β‐CD) inclusion complex via lyophilization. Release experiments were performed at various temperatures (40, 60, 80, and 100°C) with humidity of 70%. The release of terpinen‐4‐ol was significantly increased with rising temperature. Avrami's equation was used to analyse release kinetics and a good fit was observed for terpinen‐4‐ol release. In addition, the complex enhanced antibacterial activity against Staphylococcus aurueus, Pseudomonas aeruginosa and Escherichia coli, with concentration ranging from 1.25 mg/ml to 5 mg/ml. To explain the experimental data, physico‐chemical techniques have been utilized to investigate the inclusion complex of terpinen‐4‐ol with β‐CD. Finally, the possible structure of the complex was proposed by quantum chemical calculations. The results indicated that enhanced thermal stability and antibacterial activity of terpinen‐4‐ol could be attributed to the weak interactions of hydrogen bonds between terpinen‐4‐ol and β‐CD. Copyright © 2014 John Wiley & Sons, Ltd.
We report an efficient, reusable, and selective 6-aminothiouracil (ATA)-modified Zr(IV)-based adsorbent (defined as UiO-66-ATA(Zr)) for lead ion removal in water. The adsorption equilibrium time and the maximum sorption capacity of UiO-66-ATA(Zr) for Pb(II) are, respectively, 120 min and 386.98 mg/g at pH 4 and 298 K. The Pb(II) removal rate reaches 96% at 60 min and exceeds 99% at the equilibrium state in the pH range of 2.0–5.8. Hill and pseudo-second-order models can well describe the sorption process. Pb(II) adsorbing onto UiO-66-ATA(Zr) is an irreversible, favorable chemisorption process with multimolecule participation and film diffusion control. The calculations of density functional theory, the experimental results, and the characterization analyses suggest that the binding mechanisms are the chelation and ion-exchange/electrostatic interactions between hydroxyl/amino/sulfhydryl groups of UiO-66-ATA(Zr) and Pb(II). Besides, UiO-66-ATA(Zr) has a better affinity to Pb(II) than the coexisting ions in water and an excellent repeatability at eight cycles of adsorption. Moreover, the thermodynamic study shows that UiO-66-ATA(Zr) adsorbing Pb(II) is an endothermic reaction. Thus, UiO-66-ATA(Zr) is a prospective sorbent for Pb(II) removal under the initiative of environmental protection and water purification, and this work may also provide an idea for industrial catalysis.
The exploration of high-performance cathode candidates is of great significance for aqueous aluminum-metal batteries (AAMBs). Here, we, for the first time, report tetrachloro-1,4-benzoquinone (TCQ) as a superior organic AAMBs cathode....
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