MnO is a common material for the fabrication and design of capacitive deionization (CDI) devices but there is little information on the role of MnO crystal phase on CDI performance. A series of MnO (α, β, γ, and δ phase) were synthesized and fabricated as cathodes for studying the CDI performance as affected by pH in simple batch mode experiments. Our results revealed that the deionization efficiency decreased with increased negative surface charge as a result of the deprotonated surface. Importantly, this correlation was pH independent and the surface heterogeneity due to different MnO phase was likely responsible for the different degree of surface ionization and consequently the CDI efficiency. Results of electrochemical impedance spectroscopy analyses further implicated that a highly ionized surface would result in a diffusion layer with a great resistance that conversely inhibited the access of co-ions in the CDI process. This indicated the applied potential was mainly responsible for driving ions transporting through the double layer resistance instead of accommodating them (electrosorption). Based on our results, the surface heterogeneity as a result of different spatially distributed MnO octahedral would be accounted for the varying degree of surface ionization and consequently the discrepancy in CDI efficiency among different MnO phases.
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http://dx.doi.org/10.1016/j.scitotenv.2019.04.172 | DOI Listing |
ACS Appl Mater Interfaces
January 2025
School of Materials Science and Engineering, Henan Key Laboratory of Advanced Nylon Materials and Application, Zhengzhou University, Zhengzhou 450001, China.
Piezoelectric polymer textiles offer distinct advantages in the fabrication of wearable nanogenerators (NGs). One effective strategy to enhance the output capacity of NGs is to modulate the piezoelectric performance of the textiles. This paper focuses on further improving the piezoelectric properties of nylon-11,11 textiles through post-drawing and annealing treatments.
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January 2025
Rheology Department, Polymat Institute, University of the Basque Country, 20018 Donostia-San Sebastian, Euskadi, Spain.
This paper addresses the author's current understanding of the physics of interactions in polymers under a voltage field excitation. The effect of a voltage field coupled with temperature to induce space charges and dipolar activity in dielectric materials can be measured by very sensitive electrometers. The resulting characterization methods, thermally stimulated depolarization (TSD) and thermal-windowing deconvolution (TWD), provide a powerful way to study local and cooperative relaxations in the amorphous state of matter that are, arguably, essential to understanding the glass transition, molecular motions in the rubbery and molten states and even the processes leading to crystallization.
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January 2025
Departamento de Química Física, Facultad de Ciencias Químicas, Universidad Complutense de Madrid, Ciudad Universitaria, Plaza de la Ciencias s/n, 28040 Madrid, Spain.
This study examines the adsorption and bulk assembly behaviour of quaternized hydroxyethylcellulose ethoxylate (QHECE)-sodium dodecyl sulphate (SDS) complexes on negatively charged substrates. Due to its quaternized structure, QHECE, which is used in several industries, including cosmetics, exhibits enhanced electrostatic interactions. The phase behaviour and adsorption mechanisms of QHECE-SDS complexes are investigated using model substrates that mimic the wettability and surface charge of damaged hair fibres.
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January 2025
Department of Forest and Fire Sciences, University of Idaho, Moscow, ID 83844-1132, USA.
This study investigated the valorization of industrial lignin for producing biodegradable polybutylene succinate (PBS)-lignin copolymers. PBS was blended with varying lignin contents (0-45 wt. %) and crosslinked/grafted using dicumyl peroxide (DCP).
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January 2025
Department of Organic Chemistry and Technology, Faculty of Chemical Technology and Biotechnology, Budapest University of Technology and Economics, Műegyetem rkp. 3., 1111 Budapest, Hungary.
A series of α-hydroxy-alkylphosphonates and α-hydroxy-alkylphosphine oxides were synthesized by the Pudovik reaction of acetaldehyde and acetone with dialkyl phosphites or diarylphosphine oxides. The additions were performed in three different ways: in liquid phase using triethylamine as the catalyst (1), on the surface of AlO/KF solid catalyst (2), or by a MW-assisted NaCO-catalyzed procedure (3). In most of the cases, our methods were more efficient and more robust than those applied in the literature.
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