scholarly journals A multi-step reaction scheme to simulate self-heating ignition of coal: Effects of oxygen adsorption and smouldering combustion

Author(s):  
Han Yuan ◽  
Franz Richter ◽  
Guillermo Rein
2011 ◽  
Vol 704-705 ◽  
pp. 897-902
Author(s):  
Xiao Xing Zhong ◽  
De Ming Wang ◽  
Wei Lu ◽  
Hai Hui Xin

In different conditions (time, temperature and coal particle size), oxygen physisorption of different coal samples were tested by a oxygen adsorption detection instrument with chromatograph, followed by the analysis of the relation between oxygen physisorption in coal self-heating and the propensity of coal to spontaneous combustion. The results indicate that the physisorption reaches 80% of the saturate amount in several seconds, and then with the rapid decline of the sorption rate takes about 1 min to get saturated. The physisorption decreases with the temperature rise, and increases then drops with decreasing coal particle size, only playing a role in oxygen transportation, physisorption heat generation and the first motivation for coal to self-ignite. The content of oxygen physisorption cannot reflect the capacity of chemisorption and chemical reaction during spontaneous combustion. It is concluded that the sole oxygen physisorption cannot identify the oxidation reactivity of coal effectively.


2020 ◽  
Vol 56 (6) ◽  
pp. 2603-2621 ◽  
Author(s):  
Zhenwen Hu ◽  
Xuanze He ◽  
Francesco Restuccia ◽  
Guillermo Rein

Abstract Many thermal events have been reported during storage and transport of large numbers of Lithium-ion batteries (LIBs), raising industry concerns and research interests in its mechanisms. Apart from electrochemical failure, self-heating ignition, driven by poor heat transfer could also be a possible cause of fire in large-scale ensembles of LIBs. The classical theories and models of self-heating ignition assume a homogeneous lumped system, whereas LIBs storage involves complex geometry and heterogeneous material composition due to the packaging and insulation, which significantly changes the heat transfer within the system. These effects on the self-heating behaviour of LIBs have not been studied yet. In this study, the self-heating ignition behaviour of a box containing 100 LiCoO2 (LCO) type of cylindrical cells with different insulation is numerically modelled using COMSOL Multiphysics with a multi-step reaction scheme. The model predicts that the critical ambient temperature triggering self-ignition of the box is 125°C, which is 30°C lower than that for a single cell, and the time to thermal runaway is predicted to be 15 times longer. The effects of different insulating materials and packing configurations are also analysed. This work provides novel insights into the self-heating of large-scale LIBs.


Author(s):  
Mohit Pushp ◽  
Anders Lönnermark ◽  
Mikael Hedenqvist ◽  
Peter Vikegard

AbstractSelf-ignited fires at municipal solid waste (MSW) storage sites are relatively common. The minimization of the phenomenon of self-heating in the waste can reduce the risks for smouldering combustion. The purpose of this work was to develop a method that can be used to measure and characterize the heat production in MSW. The method is based on isothermal heat conduction microcalorimetry (IMC). The heat production in MSW was determined based on sampling from two sites in two different geographical locations in Sweden. Both the original waste and milled/homogenised waste were tested. The heat production was measured at different temperatures together with gas analysis using micro-gas chromatography. The activity in the waste, in terms of its heat flow, increased when the temperature increased up to 60 °C and decreased at higher temperatures, e.g., 70 and 80 °C. The consumption of oxygen and the production of carbon dioxide, together with the heat production, indicated that aerobic metabolism was responsible for the heat production. This is further strengthened by the marginal heat production observed for ultraviolet treated waste. The results showed that IMC is a valuable tool for characterising the self-heating in municipal and industrial waste.


Author(s):  
Eva-Maria Mandelkow ◽  
Ron Milligan

Microtubules form part of the cytoskeleton of eukaryotic cells. They are hollow libers of about 25 nm diameter made up of 13 protofilaments, each of which consists of a chain of heterodimers of α-and β-tubulin. Microtubules can be assembled in vitro at 37°C in the presence of GTP which is hydrolyzed during the reaction, and they are disassembled at 4°C. In contrast to most other polymers microtubules show the behavior of “dynamic instability”, i.e. they can switch between phases of growth and phases of shrinkage, even at an overall steady state [1]. In certain conditions an entire solution can be synchronized, leading to autonomous oscillations in the degree of assembly which can be observed by X-ray scattering (Fig. 1), light scattering, or electron microscopy [2-5]. In addition such solutions are capable of generating spontaneous spatial patterns [6].In an earlier study we have analyzed the structure of microtubules and their cold-induced disassembly by cryo-EM [7]. One result was that disassembly takes place by loss of protofilament fragments (tubulin oligomers) which fray apart at the microtubule ends. We also looked at microtubule oscillations by time-resolved X-ray scattering and proposed a reaction scheme [4] which involves a cyclic interconversion of tubulin, microtubules, and oligomers (Fig. 2). The present study was undertaken to answer two questions: (a) What is the nature of the oscillations as seen by time-resolved cryo-EM? (b) Do microtubules disassemble by fraying protofilament fragments during oscillations at 37°C?


2020 ◽  
Vol 6 (8(77)) ◽  
pp. 21-23
Author(s):  
S.N. Sarmasov ◽  
R.Sh. Rahimov ◽  
T.Sh. Abdullayev

The effect of oxygen adsorption on the conductivity of PbTe films is studied. Pn junctions based on PbTe films are photosensitive in the IR spectral region with a maximum photosensitivity of 𝜆𝑚𝑎𝑥 microns. The tunneling mechanism of current flow through the pn junction is shown.


2020 ◽  
Vol 492 (1) ◽  
pp. 57-59
Author(s):  
S. L. Bazhenov ◽  
I. V. Sosnovskii ◽  
A. S. Kechek’yan

1980 ◽  
Vol 45 (9) ◽  
pp. 2391-2399 ◽  
Author(s):  
Miroslav Kašpar ◽  
Jiří Trekoval

The polymerization kinetics of isoprene (2-methyl-1,3-butadiene) in benzene with butyllithium as the initiator was investigated by the gas chromatographic method. After completion of the initial period of the reaction, its order with respect to the initial concentration of initiator is negative at the concentrations of the latter between 0.01 and 0.25 mol/l, and positive at higher concentrations. A reaction scheme has been suggested with respect to the "cross" association of butyllithium and of the "living" oligoisoprene.


1981 ◽  
Vol 46 (3) ◽  
pp. 561-572 ◽  
Author(s):  
Karel Komers

The author derived theoretical dependences of preasymptotic slopes of the currentless E-t curves (potential of an indicator redox electrode against time) on the number of equivalents, n, of added oxidation agent, assuming a reaction scheme of two consecutive concurrent second-order reactions involving the formation of intermediate products ( a side reaction of the starting compound with the final oxidation product leading to an adduct, which undergoes consecutive bimolecular oxidations leading again to the final product). The dependences enable to determine the type of the relatively stable intermediate products and the ratios of the rate constants. The theory was applied to the oxidation of four symmetrically disulphonated naphthidines with cerium(IV) sulphate in aqueous sulphuric acid and the results were substantiated spectrophotometrically


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