Influence of carboxymethylation on the gelling capacity,rheological properties,and antioxidant activity of feruloylated arabinoxylans from different sources

Feruloylated arabinoxylans (FAX) are gelling polysaccharides presenting antioxidant activity (AC) and potential application as delivery systems. The influence of carboxymethylation on the gelling capacity, rheological properties, and AC of FAX from wheat flour (FAX1) and maize distillers grains (FAX2) was analyzed. The degree of substitution of carboxymethyl groups was 0.27 and 1.77 for carboxymethylated FAX1 (CFAX1) and FAX2 (CFAX2), which presented a change in M _n from 446 to 362 kDa and from 120 to 180 kDa, and a loss in FA content from 1.05 to traces and from 10.13 to 0.12, respectively, after carboxymethylation. G′ value at the end of rheological tests for FAX1 (71 Pa) and FAX2 (726 Pa) was higher than the corresponding G″ value. In contrast, G″ value for CFAX1 (0.35 Pa) and CFAX2 (0.03 Pa) was higher than the respective G′ value, indicating that they do no form gels. The AC increased in CFAX1 in relation to FAX1 from 4.49 to 8.30 mmol Trolox equivalent antioxidant capacity (TEAC) kg⁻¹, respectively, while it decreased in CFAX2 with regard to FAX2 from 11.31 to 9.43 mmol TEAC kg⁻¹, respectively. Carboxymethylation could be a path to design FAX derivatives offering alternative potential applications. © 2019 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2020 , 137, 48325.     

Jute sticks derived novel graphitic porous carbon nanosheets as Li-ion battery anode material with superior electrochemical properties

Graphitic porous carbon sheets (GPCS), which were synthesized at a low temperature of 900°C by KOH chemical activation technique, possess a specific surface area of 1246 m² g^-1 with high pore volume. The size of the pores varied in micro-mesopore regions and exhibited three-dimensional sheet-like morphology composed of multilayered graphene sheets with an inter planar distance of 0.360 nm. The GPCS material was tested as anode for Li-ion battery (LIB) application in half cell mode (vs Li⁺/Li). The fabricated GPCS electrode shows excellent electrochemical properties in comparison with commercial graphite such as a high discharge specific capacity of 1022 mA h g^-1 after 10 cycles at 100 mA g^-1 and excellent specific capacity retention of 170 mA h g^-1 at a very high current rate of 8000 mA g^-1 and also retains a high capacity of 541 mA h g^-1 after 250 cycles at 500 mA g^-1, which suggests that GPCS material can be a promising electrode for LIB application. A brief comparison with commercial graphite and various carbonaceous materials from literature demonstrated that the GPCS electrode was potential material for high rate LIBs.     

Sulfur-doped shaddock peel–derived hard carbons for enhanced surface capacity and kinetics of lithium-ion storage

Sulfur doping has been regarded an energetic route to optimize the lithium storage properties of carbon-based electrode materials. In this work, sulfur-doped shaddock peel–derived hard carbon is successfully prepared by a KOH- and C₂H₅NS-assisted pyrolysis procedure. It is demonstrated that sulfur doping has strong effect on surface activation and graphitization enhancement, which results in the significant enhancement of the surface adsorption capacity and reaction kinetics of the hard carbon materials. When employed as a lithium ion batteries (LIBs) anode, the as-obtained hard carbon demonstrates excellent cycling and rate properties, presenting a great specific capacity of 738 mAhg⁻¹ at 50 mAg⁻¹ after 200 cycles, as well as 491 mAhg⁻¹ at 200 mAg⁻¹ after 300 cycles. Even at 1000 and 2000 mAg⁻¹, the hard carbon provides a large rate capacity of 283 and 179 mAhg⁻¹, respectively. Besides, it is revealed that the Li⁺ storage process is determined by the surface-induced pseudocapacitive process, whose capacitive proportion reach 60% at 0.5 mVs⁻¹. This work suggests that the low cost and eco-friendly sulfur-doped shaddock peel–derived hard carbon is a very prospective LIB anode material.     

Solution blow spun nickel oxide/carbon nanocomposite hollow fibres as an efficient oxygen evolution reaction electrocatalyst

The development of efficient electrocatalysts for slow reaction of the oxygen evolution reaction (OER) is fundamental for viability of the electrochemical water splitting technologies. Here we report for the first time the synthesis of NiO/carbon hollow fibres (NiO-HF) by the Solution Blow Spinning (SBS) technique, and a study of their catalytic activity towards the OER in alkaline medium. The hollow fibres were obtained with ca. 300 nm in diameter consisting of agglomerated NiO nanoparticles with an average size of 50 nm which is close to the tubular wall thickness. The formation mechanism of the hollow structure was discussed. It was revealed that the carbon from polyenic branch of polyvinylpyrrolidone (PVP) resists the firing treatment and acts as an agglomerating agent, thus ensuring a conductive and percolating path between NiO nanoparticles along the fibres. A battery of electrochemical tests of NiO-HF supported by commercial Ni foam reveals excellent electrochemical activity for OER in 1 M KOH, in comparison with reference NiO nanoparticles (NiO-NP, diameter ca. 23 nm). NiO-HF attains an overpotential of 340 mV vs. RHE at a current density of 10 mA cm⁻², which is amongst the lowest values reported in the literature for undoped NiO. Chronopotentiometry reveals stable NiO-HF electrodes over 15 h under an electrolysis current of 25 mA cm⁻². Microscopic analysis shows that the fibrillar morphology is completely preserved after the electrolysis test. The remarkable performance of the NiO-HF catalyst is ascribed to the enhanced electronic conductivity resulting from the interpenetrating NiO-HF/carbon microstructure.     

The dual capacity of the NiSn alloy/MWCNT nanocomposite for sodium and hydrogen ions storage using porous Cu foam as a current collector

A nanostructured NiSn alloy/multi-walled carbon nanotube (MWCNT) composite was successfully synthesized for highly reversible sodium and hydrogen ions storage by using an electrochemical deposition process on porous Cu foam. The surface morphology of the resulting NiSn alloy/MWCNT nanocomposite was characterized using a field-emission scanning electron microscope, indicating the formation of sphere-like NiSn alloy nanoparticles with an average size of 190 nm. On the other hand, X-ray diffraction analysis, energy dispersive and Fourier transform infrared spectroscopies were employed to determine the crystalline structure, elemental surface and chemical composition of the nanocomposite electrode. The initial sodium discharge capacity of the electrode was maximized at ∼550 mAh g⁻¹ under the current density of 1000 mA g⁻¹, and a high hydrogen discharge capacity of 5200 mAh g⁻¹ was obtained at 1100 mA g⁻¹ after 20 cycles. A comprehensive comparison between the sodium and hydrogen ions capacities in this study and those of the literature for different materials and structures was also performed. Accordingly, the resulting nanocomposite electrode with dual capacity may offer promising applications in both sodium-ion battery and hydrogen storage.     

Preparation and characterisation of a novel copper‐imprinted polymer based on β‐cyclodextrin copolymers for selective determination of Cu2+ ions

A novel ion‐imprinted polymer (IIP) using (6‐O‐butene diacid ester)‐β‐cyclodextrin (β‐CD‐MAH) as the functional monomer and copper ions as the template was developed for Cu²⁺ sensing. First, reactive β‐cyclodextrin (β‐CD) monomers with vinyl carboxylic acid functional groups were synthesised and were co‐polymerised with styrene via radical polymerisation. Then, the β‐CD copolymers were complexed with Cu²⁺ in order to obtain the IIP. The imprinting effect was realised by removing the template ions from the imprinted polymer. The structure, composition and morphology of the IIP were characterised by Fourier transform IR spectroscopy, energy‐dispersive spectroscopy and field‐emission SEM. The adsorption capacity was investigated by UV–visible spectroscopy in batch operation mode. The maximum adsorption capacity for the Cu²⁺ template ions was 28.91 mg g^?1, and the adsorption selectivity was clearly illustrated from the increased sorption affinity towards Cu²⁺ ions over other competing ions. The adsorption was affected by the pH of the aqueous medium, and enhanced adsorption capacity was observed at pH 5. The prepared IIP could be used 10 times after its regeneration without significant loss of the adsorption capacity. © 2018 Society of Chemical Industry     

Estimation of maximum available capacity of lithium-ion battery based on multi-view features extracted from reconstructed charging curve

A new method is developed in the paper to estimate the maximum available capacity which is an important basis for indicating the State of Health (SOH) of lithium-ion batteries. Firstly, a data reconstruction approach is proposed to pre-process the acquired data to suppress the influence of measurement noise and reduce the negative impact on estimation precision when measuring equipment adopts different sampling frequencies. Then, the variation trend of the incremental capacity curve obtained based on the reconstructed data with the battery aging is analyzed, and a health indicator (HI) including multi-view features is put forward to characterize the battery degradation more comprehensively. The multi-view features are coming from the capacity increment curve versus voltage and time, including the maximum value of the capacity increment curve, the voltage corresponding to the maximum value, other values surrounding the maximum value and so on. Finally, Support Vector Regression is used to establish a model between the extracted HI and the maximum available capacity, and two types of open source data are used to verify the performance. The experimental results show that the data reconstruction method and multi-view health indicator proposed in the paper can obtain high precision estimation results.     

Thermodynamic properties of sodium pyrovanadate (Na4V2O7) at high temperature (298.15–873 K)

The sodium pyrovanadate (Na₄V₂O₇) powder was synthesized by solid-state reaction using sodium carbonate (Na₂CO₃) and vanadium pentoxide (V₂O₅) as raw materials. X-ray powder diffraction (XRD), scanning electron microscope (SEM), and differential scanning calorimeter (DSC) were used to accurately characterize the synthesized sample. The solid-state phase transformation from α-Na₄V₂O₇ to β-Na₄V₂O₇ occurs at the temperature 696 K and the enthalpy is equals to 1.03 ± 0.01 kJ/mol, the endothermic effect at 931 K and the enthalpy is equals to 31.35 ± 0.31 kJ/mol, which is related to the melting of Na₄V₂O₇. The high-temperature heat capacity of Na₄V₂O₇ was measured using a Multi-high temperature calorimeter 96 line and DSC. The obtained high-temperature heat capacity of Na₄V₂O₇, as a function of temperature, was modeled as: Cp=314.62+0.05T-5494390T^-2 J·mol^-1·K^-1 (298.15-873 K). The temperature dependence on heat capacity was then used for computing changes in the enthalpy, entropy, and Gibbs free energy at the specific temperature internal.     

Phytochemical Composition and in Vitro Analysis of Nopal (O. Ficus-Indica) Cladodes at Different Stages of Maturity

This study aimed to determine the phytochemical profile and nutraceutical properties of nopal cladodes (Opuntia ficus-indica) at different stages of maturity. Medium-age cladodes showed the highest total saponins, phytosterols, and indigestible fiber, as well as the highest in vitro antioxidant capacity and digestive enzymes inhibitory activity. Furthermore, these cladodes presented the highest content of p-hydroxybenzoic acid, p-coumaric acid, rutin, narcissin, nicotiflorin, β-sitosterol, and sitosteryl-3-β-glucopyranoside, as well as several amino acids, organic acids, and fatty acids. Whereas young cladodes contained the highest concentration of condensed and hydrolyzable tannins. These results demonstrated that maturity affects the nutritional and nutraceutical properties of nopal cladodes.