Cathode-anode reaction products interplay enabling high performance of LiNi0.8Co0.1Mn0.1O2/artificial graphite pouch batteries at elevated temperature

2021 ◽  
Vol 514 ◽  
pp. 230583
Author(s):  
Huajun Zhao ◽  
Yunxian Qian ◽  
Guangfu Luo ◽  
Jian Chang ◽  
Chaoyang Wang ◽  
...  
Keyword(s):  
Elevated Temperature ◽  
High Performance ◽  
Reaction Products ◽  
Artificial Graphite ◽  
Anode Reaction

scholarly journals Achieving High-Performance Spherical Natural Graphite Anode through a Modified Carbon Coating for Lithium-Ion Batteries

Energies ◽  
2021 ◽  
Vol 14 (7) ◽  
pp. 1946 ◽  
Author(s):  
Hae-Jun Kwon ◽  
Sang-Wook Woo ◽  
Yong-Ju Lee ◽  
Je-Young Kim ◽  
Sung-Man Lee
Keyword(s):  
High Performance ◽  
Carbon Coating ◽  
Coulombic Efficiency ◽  
Rate Capability ◽  
Lithium Ion ◽  
Rate Performance ◽  
Natural Graphite ◽  
Artificial Graphite ◽  
Ag Electrodes ◽  
Natural Graphite Anode

The electrochemical performance of modified natural graphite (MNG) and artificial graphite (AG) was investigated as a function of electrode density ranging from 1.55 to 1.7 g∙cm−3. The best performance was obtained at 1.55 g∙cm−3 and 1.60 g∙cm−3 for the AG and MNG electrodes, respectively. Both AG, at a density of 1.55 g∙cm−3, and MNG, at a density of 1.60 g∙cm−3, showed quite similar performance with regard to cycling stability and coulombic efficiency during cycling at 30 and 45 °C, while the MNG electrodes at a density of 1.60 g∙cm−3 and 1.7 g∙cm−3 showed better rate performance than the AG electrodes at a density of 1.55 g∙cm−3. The superior rate capability of MNG electrodes can be explained by the following effects: first, their spherical morphology and higher electrode density led to enhanced electrical conductivity. Second, for the MNG sample, favorable electrode tortuosity was retained and thus Li+ transport in the electrode pore was not significantly affected, even at high electrode densities of 1.60 g∙cm−3 and 1.7 g∙cm−3. MNG electrodes also exhibited a similar electrochemical swelling behavior to the AG electrodes.

On the Chemistry of Tetrabenzyl Thiuram Disulfide and Tetramethyl Thiuram Disulfide with Bis (Triethoxysilylpropyl) Tetrasulfide in Silica Compounds

2003 ◽  
Vol 76 (4) ◽  
pp. 876-891 ◽  
Author(s):  
R. N. Datta ◽  
A. G. Talma ◽  
S. Datta ◽  
P. G. J. Nieuwenhuis ◽  
W. J. Nijenhuis ◽  
...  
Keyword(s):  
High Performance ◽  
Room Temperature ◽  
Succinic Anhydride ◽  
Dynamic Properties ◽  
The Other ◽  
Resonance Spectroscopy ◽  
Reaction Products ◽  
Negative Effect ◽  
Higher Temperature ◽  
Analytical Tools

Abstract The use of thiurams such as Tetramethyl thiuram disulfide (TMTD) or Tetrabenzyl thiuram disulfide (TBzTD) has been explored to achieve higher cure efficiency. The studies suggest that a clear difference exists between the effect of TMTD versus TBzTD. TMTD reacts with Bis (triethoxysilylpropyl) tetrasulfide (TESPT) and this reaction can take place even at room temperature. On the other hand, the reaction of TBzTD with TESPT is slow and takes place only at higher temperature. High Performance Liquid Chromatography (HPLC) with mass (MS) detection, Nuclear Magnetic Resonance Spectroscopy (NMR) and other analytical tools have been used to understand the differences between the reaction of TMTD and TESPT versus TBzTD and TESPT. The reaction products originating from these reactions are also identified. These studies indicate that unlike TMTD, TBzTD improves the cure efficiency allowing faster cure without significant effect on processing characteristics as well as dynamic properties. The loading of TESPT is reduced in a typical Green tire compound and the negative effect on viscosity is repaired by addition of anhydrides, such as succinic anhydride, maleic anhydride, etc.

scholarly journals Preparation of isocyanates by carbamates thermolysis on the example of butyl isocyanate

2019 ◽  
Vol 58 (4) ◽  
pp. 40-47
Author(s):  
Ratmir R. Dashkin ◽  
◽  
Dmitry A. Gordeev ◽  
Khusrav Kh. Gafurov ◽  
Sergey N. Mantrov ◽  
...  
Keyword(s):  
Gas Phase ◽  
High Performance ◽  
Gas Flow ◽  
Flow Reactor ◽  
Packed Column ◽  
Biologically Active ◽  
Dibutyltin Dilaurate ◽  
Reaction Products ◽  
Uv Detector ◽  
Laboratory Setup

Butyl isocyanate is widely distributed as a precursor for the production of a number of biologically active substances: fungicides, preservatives, insecticides, personal care products, etc. Nowadays, there are a number of methods for the preparation of isocyanates, which can be divided into liquid phase and gas phase. One of the perspective methods for the production of isocyanates is the thermolysis of carbamate and/or the actions of various reaction activating agents, accompanied by the elimination of alcohol, but this process is reversible, which greatly complicates its use in industry. The paper presents the results of studies of non-catalytic thermal decomposition of N-alkylcarbamates with the formation of alkylisocyanates on the example of butylisocyanate in the gas phase, flow reactor in a wide temperature range (200 to 450 °C). In addition, a series of experiments was carried out using a catalyst, dibutyltin dilaurate, in order to reduce the thermolysis temperature and increase the yield of the final product. To implement the isocyanate production process, an experimental laboratory setup, consisting of a gas flow meter (argon) regulator, a packed column (for heating) and a sorption solution tank, was developed and tested. The thermolysis of N-n-butylcarbamate was carried out in two variations: the preparation of an individual n-butylisocyanate and the passage of reaction products through a sorption solution linking the n-butyl isocyanate to N-n-butyl-N '-(1-phenylethyl)urea, which allows to estimate the yield of the target n-butylisocyanate without additional losses. The analysis of the obtained substances was carried out by high performance liquid chromatography with a UV detector (target product) and a mass detector (analysis of by-products). According to the results of research, a modification of the laboratory facility was proposed, as well as n-butylisocyanate was obtained with a yield of 49% on the basis of a new technique.

Simultaneous Determination and Identification of Penicillin Residues by High-Performance Liquid Chromatographic Analysis

1997 ◽  
Vol 60 (8) ◽  
pp. 1006-1009 ◽  
Author(s):  
CHIH-CHUN HONG ◽  
FUSAO KONDO
Keyword(s):  
Simultaneous Determination ◽  
Bovine Serum ◽  
High Performance ◽  
Gradient Flow ◽  
Correlation Coefficients ◽  
High Performance Liquid Chromatographic ◽  
Penicillin G ◽  
Reaction Products ◽  
Liquid Chromatographic Analysis ◽  
Liquid Chromatographic

A new method was developed for simultaneous determination and identification of seven penicillins (amoxicillin, ampicillin, methicillin, penicillin G, oxacillin, cloxacillin, and dicloxacillin) in bovine serum. Each sample was simply extracted with acetonitrile, and identification of the reaction products of penicillins after treatment with 1,2,4-triazole-HgCl2 solution was then carried out by high-performance liquid chromatography (HPLC) with on ultraviolet spectrophotometric detector at 325 nm. Separation of the penicillin reaction products by HPLC was carried out by using a mobile phase of 0.1 M phosphate buffer and acetonitrile in ratios of 85:15 and 60:40 (vol/vol) in a gradient flow. The retention times of the seven penicillins ranged from 4.3 to 24.6 min, and the detection limits of penicillin concentration ranged from 0.04 to 0.2 μg/ml. The calibration curves for individual penicillins extracted from bovine serum were linear, and the correlation coefficients for each of the drugs were over 0.99. The determination of penicillins extracted from bovine serum spiked with each drug gave a recovery rate from 82.0 ± 5.6% to 105.6 ± 4.6%. This detection method may be useful for routine laboratory testing of residual penicillins.

Designing a Multifunctional Separator for High‐Performance Li–S Batteries at Elevated Temperature

Small ◽  
2019 ◽  
Vol 15 (47) ◽  
pp. 1904332 ◽  
Author(s):  
Yibo He ◽  
Shichao Wu ◽  
Qi Li ◽  
Haoshen Zhou
Keyword(s):  
Elevated Temperature ◽  
High Performance

Developing high performance mechanical properties at elevated temperature in squeeze cast Al-Cu-Mn-Fe-Ni alloys

2019 ◽  
Vol 150 ◽  
pp. 128-137 ◽  
Author(s):  
Bo Lin ◽  
Wenxin Zhang ◽  
Xiaoping Zheng ◽  
Yuliang Zhao ◽  
Zhaohui Lou ◽  
...  
Keyword(s):  
Mechanical Properties ◽  
Elevated Temperature ◽  
High Performance ◽  
Ni Alloys ◽  
Squeeze Cast

Induction and Transcription Studies of the Dextransucrase Gene in Leuconostoc mesenteroides NRRL B-512F

1999 ◽  
Vol 65 (12) ◽  
pp. 5504-5509 ◽  
Author(s):  
M. Quirasco ◽  
A. López-Munguía ◽  
M. Remaud-Simeon ◽  
P. Monsan ◽  
A. Farrés
Keyword(s):  
High Performance ◽  
Leuconostoc Mesenteroides ◽  
Carbon Sources ◽  
Promoter Sequence ◽  
Culture Conditions ◽  
Start Codon ◽  
Reaction Products ◽  
Product Specificity ◽  
First Time

ABSTRACT Dextransucrase production by Leuconostoc mesenteroidesNRRL B-512F in media containing carbon sources other than sucrose is reported for the first time. Dextransucrases were analyzed by gel electrophoresis and by an in situ activity assay. Their polymers and acceptor reaction products were also compared by 13C nuclear magnetic resonance and high-performance liquid chromatography techniques, respectively. From these analyses, it was found that, independently of the carbon source, L. mesenteroides NRRL B-512F produced dextransucrases of the same size and product specificity. The 5′ ends of dextransucrase mRNAs isolated from cells grown under different culture conditions were identical. Based on this evidence, we conclude that dextransucrases obtained from cells grown on the various carbon sources result from the transcription of the same gene. The control of expression occurs at this level. The low dextransucrase yields from cultures in d-glucose ord-fructose and the enhancement of dextransucrase gene transcription in the presence of sucrose suggest that an activating phenomenon may be involved in the expression mechanism. Dextransucrase mRNA has a size of approximately 4.8 kb, indicating that the gene is located in a monocistronic operon. The transcription start point was localized 34 bp upstream from the ATG start codon. The −10 and −35 sequences found, TATAAT and TTTACA, were highly homologous to the only glycosyltransferase promoter sequence reported for lactic acid bacteria.

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