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Oxidation kinetics of YBaCo4O7+? and substituted oxygen carriers.

ABSTRACT: In this paper, the relaxation kinetics of the oxidation process of the YBaCo4O7+? , Y0.95Ti0.05BaCo4O7+? and Y0.5Dy0.5BaCo4O7+? oxygen carriers is studied with isothermal reaction data. XRD analysis for fresh samples shows that all the samples have YBaCo4O7+? structure. Scanning electron microscopy images of samples show that the samples consist of porous agglomerates of primary particles. Isothermal TG experiments are conducted with temperatures of 290°C, 310°C, 330°C and 350°C, respectively. It is found that the Avrami-Eroféev model describes solid-phase changes in the oxygen absorption process adequately. The results show that the distributed activation energies of the oxidation process obtained by the Avrami-Eroféev model are 42.079?kJ?mol-1, 42.944?kJ?mol-1 and 41.711?kJ?mol-1 for the YBaCo4O7+? , Y0.95Ti0.05BaCo4O7+? and Y0.5Dy0.5BaCo4O7+? oxygen carriers, respectively. The kinetic model was obtained to predict the oxygen carrier conversion of oxygen absorption for different time durations. The kinetic parameters obtained here are quite vital when this material is used in reactors.

SUBMITTER: Hou L

PROVIDER: S-EPMC6030326 | biostudies-literature | 2018 Jun

REPOSITORIES: biostudies-literature

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Oxidation kinetics of YBaCo4O7+δ and substituted oxygen carriers.

Hou Limin L Yu Qingbo Q Wang Kun K Qin Qin Q Wei Mengqi M Yang Fan F

Royal Society open science 20180620 6

In this paper, the relaxation kinetics of the oxidation process of the YBaCo4O7+δ , Y0.95Ti0.05BaCo4O7+δ and Y0.5Dy0.5BaCo4O7+δ oxygen carriers is studied with isothermal reaction data. XRD analysis for fresh samples shows that all the samples have YBaCo4O7+δ structure. Scanning electron microscopy images of samples show that the samples ...[more]

PMID: 30110463

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Project description:Purpose:The present study aimed to determine whether whole-body fat oxidation and muscle deoxygenation kinetics parameters during exercise were related in individuals with different aerobic fitness levels. Methods:Eleven cyclists [peak oxygen uptake ( V.O2?p?e?a?k ): 64.9 ± 3.9 mL?kg-1?min-1] and 11 active individuals ( V.O2?p?e?a?k : 49.1 ± 7.4 mL?kg-1?min-1) performed a maximal incremental cycling test to determine V.O2?p?e?a?k and a submaximal incremental cycling test to assess whole-body fat oxidation using indirect calorimetry and muscle deoxygenation kinetics of the vastus lateralis (VL) using near-infrared spectroscopy (NIRS). A sinusoidal (SIN) model was used to characterize fat oxidation kinetics and to determine the intensity (Fatmax) eliciting maximal fat oxidation (MFO). The muscle deoxygenation response was fitted with a double linear model. The slope of the first parts of the kinetics (a 1) and the breakpoint ([HHb]BP) were determined. Results:MFO (p = 0.01) and absolute fat oxidation rates between 20 and 65% V.O2?p?e?a?k were higher in cyclists than in active participants (p < 0.05), while Fatmax occurred at a higher absolute exercise intensity (p = 0.01). a 1 was lower in cyclists (p = 0.02) and [HHb]BP occurred at a higher absolute intensity (p < 0.001) than in active individuals. V.O2?p?e?a?k was strongly correlated with MFO, Fatmax, and [HHb]BP (r = 0.65-0.88, p ? 0.001). MFO and Fatmax were both correlated with [HHb]BP (r = 0.66, p = 0.01 and r = 0.68, p < 0.001, respectively) and tended to be negatively correlated with a 1 (r = -0.41, p = 0.06 for both). Conclusion:This study showed that whole-body fat oxidation and muscle deoxygenation kinetics were both related to aerobic fitness and that a relationship between the two kinetics exists. Individuals with greater aerobic fitness may have a delayed reliance on glycolytic metabolism at higher exercise intensities because of a longer maintained balance between O2 delivery and consumption supporting higher fat oxidation rates.

Project description:Lecithin:cholesterol acyltransferase (LCAT) has been shown to play a role in the depletion of lipid oxidation products, but this has so far not been studied in humans. In this study, we investigated processes and parameters relevant to lipid oxidation in carriers of functional LCAT mutations.In 4 carriers of 2 mutant LCAT alleles, 63 heterozygotes, and 63 family controls, we measured activities of LCAT, paraoxonase 1, and platelet-activating factor-acetylhydrolase; levels of lysophosphatidylcholine molecular species, arachidonic and linoleic acids, and their oxidized derivatives; immunodetectable oxidized phospholipids on apolipoprotein (apo) B-containing and apo(a)-containing lipoproteins; IgM and IgG autoantibodies to malondialdehyde-low-density lipoprotein and IgG and IgM apoB-immune complexes; and the antioxidant capacity of high-density lipoprotein (HDL). In individuals with LCAT mutations, plasma LCAT activity, HDL cholesterol, apoA-I, arachidonic acid, and its oxidized derivatives, oxidized phospholipids on apo(a)-containing lipoproteins, HDL-associated platelet-activating factor-acetylhydrolase activity, and the antioxidative capacity of HDL were gene-dose-dependently decreased. Oxidized phospholipids on apoB-containing lipoproteins was increased in heterozygotes (17%; P<0.001) but not in carriers of 2 defective LCAT alleles.Carriers of LCAT mutations present with significant reductions in LCAT activity, HDL cholesterol, apoA-I, platelet-activating factor-acetylhydrolase activity, and antioxidative potential of HDL, but this is not associated with parameters of increased lipid peroxidation; we did not observe significant changes in the oxidation products of arachidonic acid and linoleic acid, immunoreactive oxidized phospholipids on apo(a)-containing lipoproteins, and IgM and IgG autoantibodies against malondialdehyde-low-density lipoprotein. These data indicate that plasma LCAT activity, HDL-associated platelet-activating factor-acetylhydrolase activity, and HDL cholesterol may not influence the levels of plasma lipid oxidation products.

Dataset Information

Oxidation kinetics of YBaCo4O7+? and substituted oxygen carriers.

Publications

Oxidation kinetics of YBaCo<sub>4</sub>O<sub>7+<i>δ</i></sub> and substituted oxygen carriers.

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