Metabolites changes of a low-temperature and low-salt fermented Chinese kohlrabi during fermentation based on non-targeted metabolomic analysis

A low-temperature and low-salt industrially fermented Chinese kohlrabi (LSCK) was developed in this study, with the salt usage decreased by approximately 70% compared to the traditional high-salt fermented Chinese kohlrabi (HSCK). The differences in physicochemical properties, metabolites and overall flavors during LSCK fermented for 0, 45 and 90 days (d) were analyzed by gas chromatography-time-of-flight mass spectrometry (GC-TOF-MS), electronic nose (E-nose) and other techniques. The results showed that the total acid content increased significantly from 3.68 to 8.59 g/kg. However, the protein content significantly decreased from 2.52/100 to 0.66 g/100 g. The number of lactic acid bacteria cells increased significantly from 3.69 to 4.46 log10CFU/g. Based on multivariate statistical analysis, 21, 14, and 15 differential metabolites were identified in the three treatment groups A1 (0 and 45 days), A2 (45 and 90 days), and A3 (0 and 90 days) respectively (VIP > 1, p < 0.05, |log2FC| ≥ 1.1). Carbohydrates, sugar alcohols, amino acids and their derivatives were the main differential metabolites in the LSCKs fermented for different periods. Aminoacyl−tRNA biosynthesis and glycine, serine and threonine metabolism pathways significantly correlated with the differential metabolites based on Kyoto Encyclopedia of Genes and Genomes (KEGG) analysis (p < 0.05). Furthermore, the overall odors were significantly different among the LSCKs with different fermentation periods, as detected by E-nose. The present study describes the change trend of metabolites during LSCK fermentation and elucidates important metabolic pathways in LSCK, providing a theoretical basis for the target regulation of functional metabolites in kohlrabi and the optimization of LSCK processing

Comparative Study of Pile Pillared Support and Pile-anchor Retaining in Deep Pit

Support pattern is the most important factor affecting the stability of foundation pit. In order to study the stable state of deep foundation pit, this paper selects pile pillared support and pile-anchor retaining which are high accident rate for comparison, and optimizes the construction scheme combined with the actual deep foundation pit project. The deformation of the supporting structure and the settlement of the foundation pit of Huiquan Square are used to analyze by FLAC3D. The variation range and trend of the internal force of the steel support and the axial force of the anchor cable are analyzed under the different values of the soil layer parameters, such as elastic modulus, cohesion and internal friction angle. The results show that the internal force of pile pillared support is greatly affected by the change of cohesion and the anchor axial force is greatly affected by the change of elastic modulus and internal friction angle. Meanwhile, the influence degree of each soil layer parameter on the internal force of support structure is different, which provides reference suggestions for the selection of support pattern of deep foundation pit

High interfacial charge storage capability of carbonaceous cathodes for Mg batteries

A rechargeable Mg battery where the capacity mainly originates from reversible reactions occurring at the electrode/electrolyte interface efficiently avoids the challenge of sluggish Mg intercalation encountered in conventional Mg batteries. The interfacial reactions in a cell based on microwave-exfoliated graphite oxide (MEGO) as the cathode and all phenyl complex (APC) as electrolyte are identified by quantitative kinetics analysis as a combination of diffusion-controlled reactions involving ether solvents (esols) and capacitive processes. During magnesiation, esols in APC electrolytes can significantly affect the electrochemical reactions and charge transfer resistances at the electrode/electrolyte interface and thus govern the charge storage properties of the MEGO cathode. In APC–tetrahydrofuran (THF) electrolyte, MEGO exhibits a reversible capacity of ∼220 mAh g–1 at 10 mA g–1, while a reversible capacity of ∼750 mAh g–1 at 10 mA g–1 was obtained in APC-1,2-dimethoxyethane (DME) electrolyte. The high capacity improvement not only points to the important role of the esols in the APC electrolytes but also presents a Mg battery with high interfacial charge storage capability as a very promising and viable competitor to the conventional intercalation-based batteries.acceptedVersio

Effects of Low-Temperature and Low-Salt Fermentation on the Physicochemical Properties and Volatile Flavor Substances of Chinese Kohlrabi Using Gas Chromatography–Ion Mobility Spectrometry

To explore the effect of low-temperature and low-salt fermentation on the volatile flavor substances of Chinese kohlrabi, low-temperature and low-salt fermented Chinese kohlrabi (LSCK) and traditional high-salt fermented Chinese kohlrabi (HSCK) were produced. The physicochemical and texture properties of the two kinds of Chinese kohlrabies were evaluated. Headspace gas chromatography-ion mobility spectrometry (GC-IMS) and electronic nose (E-nose) were used to analyze the volatile flavor substances of the kohlrabi. The results showed that the total acid content significantly decreased (p p p 1, including tetrahydrothiophene, ethyl 3-(methylthio)propanoate, 3-methylbutyric acid, hexanenitrile, and 3-methyl-3-buten-1-ol, could be used as potential biomarkers for identifying LSCK and HSCK. The E-nose analysis further demonstrated that there was a significant difference in overall flavor between the LSCK and HSCK. The present study provides support for the development of green processing technology and new low-salt Chinese kohlrabi products

High interfacial charge storage capability of carbonaceous cathodes for Mg batteries

A rechargeable Mg battery where the capacity mainly originates from reversible reactions occurring at the electrode/electrolyte interface efficiently avoids the challenge of sluggish Mg intercalation encountered in conventional Mg batteries. The interfacial reactions in a cell based on microwave-exfoliated graphite oxide (MEGO) as the cathode and all phenyl complex (APC) as electrolyte are identified by quantitative kinetics analysis as a combination of diffusion-controlled reactions involving ether solvents (esols) and capacitive processes. During magnesiation, esols in APC electrolytes can significantly affect the electrochemical reactions and charge transfer resistances at the electrode/electrolyte interface and thus govern the charge storage properties of the MEGO cathode. In APC–tetrahydrofuran (THF) electrolyte, MEGO exhibits a reversible capacity of ∼220 mAh g–1 at 10 mA g–1, while a reversible capacity of ∼750 mAh g–1 at 10 mA g–1 was obtained in APC-1,2-dimethoxyethane (DME) electrolyte. The high capacity improvement not only points to the important role of the esols in the APC electrolytes but also presents a Mg battery with high interfacial charge storage capability as a very promising and viable competitor to the conventional intercalation-based batteries

Impact of mesoporous structure of acid-treated clay on nickel dispersion and carbon deposition for CO methanation

Nickel catalysts supported on different acid-treated clays were prepared by the impregnation method in order to investigate the effect of the pore structures of supports on the dispersion and the chemical states of nickel species, and thus on the carbon depositions resulted from the dissociation of the CO molecules adsorbed on different active nickel sites. The catalysts and supports were characterized by the X-ray diffraction (XRD), the transmittance electron microscopy (TEM), the H-2 temperature-programmed reduction (H-2-TPR), the nitrogen adsorption-desorption, and the thermogravimetry and differential thermal analysis (TG-DTA). The CO methanation performance of the catalyst was investigated at a temperature range from 300 degrees C to 500 degrees C. The results indicated that the dispersion and the states of the nickel species on the support were influenced strongly by the pore structures of the acid-treated clays, and only the mesopores composed by partly damaged clay layers were conducive to forming the active nickel species, and thus reducing the deposition of the inactive carbon and improving the stability of the catalyst. The carbon species deposited on different active sites was slightly different in the oxidative properties when it was oxidized in air. A fraction of aluminum in the clays was leached out by acid, which decreased the possibility of forming the spinel phase of nickel aluminate in the catalyst. The highly dispersed nickel species showed little relevance to the high activity of the catalyst, but it exhibited a strong relation to the nickel sites from the bulk nickel species. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved