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Journal articles on the topic 'Thermal decomposition products'

Author: Grafiati

Published: 4 June 2021

Last updated: 12 February 2022

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1

Lin, Ai Jeng, Anthony D. Theoharides, and Daniel L. Klayman. "Thermal decomposition products of dihydroahtemisinin ()." Tetrahedron 42, no. 8 (1986): 2181–84. http://dx.doi.org/10.1016/s0040-4020(01)90596-4.

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2

Hatten, Courtney D., Kevin R. Kaskey, Brian J. Warner, Emily M. Wright, and Laura R. McCunn. "Thermal decomposition products of butyraldehyde." Journal of Chemical Physics 139, no. 21 (2013): 214303. http://dx.doi.org/10.1063/1.4832898.

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3

Tsuchiya, Yoshio, and Kikuo Sumi. "Thermal decomposition products of polyvinyl chloride." Journal of Applied Chemistry 17, no. 12 (2007): 364–66. http://dx.doi.org/10.1002/jctb.5010171207.

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4

Baev, Alekseiy K. "THERMAL DECOMPOSITION OF TRIMETHYLINDIUM." IZVESTIYA VYSSHIKH UCHEBNYKH ZAVEDENIY KHIMIYA KHIMICHESKAYA TEKHNOLOGIYA 59, no. 2 (2018): 30. http://dx.doi.org/10.6060/tcct.20165902.52431.

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The thermal decomposition of trimethylindium was studied. The kinetic parameters, composition of gaseous products and activation energy were established. The mechanism of proceeding reactions was proposed.

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5

Lesnikovich, A. I., O. A. Ivashkevich, G. V. Printsev, P. N. Gaponik, and S. V. Levchik. "Thermal decomposition of tetrazole Part III. Analysis of decomposition products." Thermochimica Acta 171 (November 1990): 207–13. http://dx.doi.org/10.1016/0040-6031(90)87020-d.

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6

Barontini, Federica, Valerio Cozzani, and Luigi Petarca. "Thermal Stability and Decomposition Products of Hexabromocyclododecane." Industrial & Engineering Chemistry Research 40, no. 15 (2001): 3270–80. http://dx.doi.org/10.1021/ie001002v.

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7

Panasyuk, G. P., L. A. Azarova, G. P. Budova, and A. P. Savost’yanov. "Copper terephthalate and its thermal decomposition products." Inorganic Materials 43, no. 9 (2007): 951–55. http://dx.doi.org/10.1134/s0020168507090075.

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8

Kennah, Harold Edwin, Maryanne F. Stock, and Yves Alarie. "Toxicity of Thermal Decomposition Products from Composites." Journal of Fire Sciences 5, no. 1 (1987): 3–16. http://dx.doi.org/10.1177/073490418700500101.

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9

Shishlov, N. M., Sh S. Akhmetzyanov, and S. L. Khursan. "Radical products of thermal decomposition of polydiphenylenesulfophthalide." Russian Chemical Bulletin 62, no. 7 (2013): 1614–24. http://dx.doi.org/10.1007/s11172-013-0234-7.

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10

Morin, Julien, and Yuri Bedjanian. "Thermal Decomposition of Isopropyl Nitrate: Kinetics and Products." Journal of Physical Chemistry A 120, no. 41 (2016): 8037–43. http://dx.doi.org/10.1021/acs.jpca.6b06552.

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11

Lin, Ai Jeng, Daniel L. Klayman, James M. Hoch, James V. Silverton, and Clifford F. George. "Thermal rearrangement and decomposition products of artemisinin (qinghaosu)." Journal of Organic Chemistry 50, no. 23 (1985): 4504–8. http://dx.doi.org/10.1021/jo00223a017.

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12

Morgan, D. J., S. St. J. Warne, S. B. Warrington, and P. H. A. Nancarrow. "Thermal decomposition ractions of caledonite and their products." Mineralogical Magazine 50, no. 357 (1986): 521–26. http://dx.doi.org/10.1180/minmag.1986.050.357.16.

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AbstractThe thermal decomposition of caledonite has been examined by simultaneous differential thermal analysis, thermogravimetry and mass spectrometry. Structural H2O and CO2 are liberated endothermically between 300 and 400°C leaving a residue of lead sulphate, oxysulphate, and Cu(I) and Cu(II) oxides. A series of sharp endothermic peaks between 850 and 950°C correspond to phase transition and melting reactions of the PbO-PbSO4 mixture. The sulphate anion breaks down above 880 °C. Mass spectra of the gaseous decomposition products show SO2, SO, and O2, although SO is an artefact arising from

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13

Vasiliou, AnGayle, Krzysztof M. Piech, Xu Zhang, et al. "The products of the thermal decomposition of CH3CHO." Journal of Chemical Physics 135, no. 1 (2011): 014306. http://dx.doi.org/10.1063/1.3604005.

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14

Wójcik, M. A. "The thermal decomposition of the carbonate reaction products." Journal of Thermal Analysis 43, no. 1 (1995): 149–56. http://dx.doi.org/10.1007/bf02635977.

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15

Huneck, Siegfried, Jürgen Schmidt, and Raffaele Tabacchi. "Thermal Decomposition of Lichen Depsides." Zeitschrift für Naturforschung B 44, no. 10 (1989): 1283–89. http://dx.doi.org/10.1515/znb-1989-1023.

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The thermal decomposition of the following lichen depsides has been described: lecanoric acid, gyrophoric acid, evernic acid, perlatolic acid, planaic acid, confluentic acid, atranorin, 4-O-de-methylbarbatic acid, and sekikaic acid. Main reaction products are decarboxylated compounds, phenolic units, rearranged depsides, and xanthones. Triethylammonium salts of depside carboxylic acids decompose at reasonably lower temperature than the corresponding free acids.

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16

Pieczara, Gabriela, Maciej Manecki, Grzegorz Rzepa, Olaf Borkiewicz, and Adam Gaweł. "Thermal Stability and Decomposition Products of P-Doped Ferrihydrite." Materials 13, no. 18 (2020): 4113. http://dx.doi.org/10.3390/ma13184113.

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This work aimed to determine the effect of various amounts of P admixtures in synthetic ferrihydrite on its thermal stability, transformation processes, and the properties of the products, at a broad range of temperatures up to 1000 °C. A detailed study was conducted using a series of synthetic ferrihydrites Fe5HO8·4H2O doped with phosphates at P/Fe molar ratios of 0.2, 0.5, and 1.0. Ferrihydrite was synthesized by a reaction of Fe2(SO4)3 with 1 M KOH at room temperature in the presence of K2HPO4 at pH 8.2. The products of the synthesis and the products of heating were characterized at various

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17

Mineely, PJ. "Thermal Decomposition of Some Iron(III) Chromates." Australian Journal of Chemistry 41, no. 2 (1988): 263. http://dx.doi.org/10.1071/ch9880263.

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The thermal decomposition of the chromates FeOHCrO4, KFe3(CrO4)2(OH)6, Fe2(CrO4)3.H2O and Fe2(CrO4)3.3H2O have been studied by thermal analysis and Mossbauer spectroscopy. The possible presence of Fe2O(CrO4)2 as a second phase formed during the decomposition is discussed. Final products in all reactions were oxides of iron(III) and chromium(III). In addition K2Cr2O7 Was present in the reaction products for KFe3(CrO4)2(OH)6.

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18

Jakoubková, Marie, and Josef Pola. "CO2 laser induced decomposition of propylene oxide." Collection of Czechoslovak Chemical Communications 55, no. 10 (1990): 2455–59. http://dx.doi.org/10.1135/cccc19902455.

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The continuous-wave (cw) CO2 laser induced decomposition of propylene oxide yields propanal, propanone and methyl vinyl ether as primary isomerization products. The absence of allylol and great amounts of ethene among products of ensuing fragmentation of primary products make the reaction different from conventional thermal decomposition of propylene oxide. CW CO2 laser induced decomposition of methyl vinyl ether affords propanal as isomerization product and shows thermal interconvertibility of propylene oxide and methyl vinyl ether.

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19

Kopylov, N. I. "Chemical, phase composition and properties of products of thermal decomposition of coal of Tavantolgoy deposit of Mongolia." Bulletin of the Karaganda University. "Chemistry" series 95, no. 3 (2019): 88–95. http://dx.doi.org/10.31489/2019ch3/88-95.

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20

Inoue, H., T. Nakazawa, T. Mitsuhashi, T. Shirai, and E. Fluck. "Characterization of Prussian blue and its thermal decomposition products." Hyperfine Interactions 46, no. 1-4 (1989): 723–31. http://dx.doi.org/10.1007/bf02398265.

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21

Uchiyama, Shigehisa, Mayumi Noguchi, Ayana Sato, Miho Ishitsuka, Yohei Inaba, and Naoki Kunugita. "Determination of Thermal Decomposition Products Generated from E-Cigarettes." Chemical Research in Toxicology 33, no. 2 (2020): 576–83. http://dx.doi.org/10.1021/acs.chemrestox.9b00410.

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22

Knutsson, A., M. P. Johansson, P. O. Å. Persson, L. Hultman, and M. Odén. "Thermal decomposition products in arc evaporated TiAlN/TiN multilayers." Applied Physics Letters 93, no. 14 (2008): 143110. http://dx.doi.org/10.1063/1.2998588.

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23

Kopelev, N. S., A. I. Popov, and M. D. Val'kovskii. "Properties of the products of CsxFeO2+0.5x thermal decomposition." Journal of Radioanalytical and Nuclear Chemistry Letters 188, no. 2 (1994): 99–108. http://dx.doi.org/10.1007/bf02164943.

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24

Vogt, Jürgen. "Thermal analysis of epoxy-resins: Identification of decomposition products." Thermochimica Acta 85 (April 1985): 411–14. http://dx.doi.org/10.1016/0040-6031(85)85611-2.

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25

Chen, P. C., W. Lo, and K. H. Hu. "Molecular structures of mononitroanilines and their thermal decomposition products." Theoretica Chimica Acta 95, no. 3-4 (1997): 99–112. http://dx.doi.org/10.1007/bf02341695.

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26

Chen, P. C., W. Lo, and K. H. Hu. "Molecular structures of mononitroanilines and their thermal decomposition products." Theoretica Chimica Acta 95, no. 3 (1997): 99. http://dx.doi.org/10.1007/s002140050187.

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27

Mahapatra, Sipra, T. P. Prasad, K. K. Rao, and R. Nayak. "Thermal decomposition of hydrolysis products of Fe(OH)SO4." Thermochimica Acta 161, no. 2 (1990): 279–85. http://dx.doi.org/10.1016/0040-6031(90)80309-m.

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28

Johnston, P. K., E. Doyle, and R. A. Orzel. "Acrylics: A Literature Review of Thermal Decomposition Products and Toxicity." Journal of the American College of Toxicology 7, no. 2 (1988): 139–200. http://dx.doi.org/10.3109/10915818809014519.

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A comprehensive literature review on the thermal decomposition products and combustion toxicity of acrylics is presented. The types of products produced by the thermal decomposition of acrylic polymers vary widely. At lower temperatures, simple methacrylate polymers are degraded almost entirely to monomer, whereas simple acrylate polymers are degraded primarily to chain fragments and the alcohols corresponding to the ester groups. More complex methacrylate and acrylate polymers appear to be degraded primarily to the olefins corresponding to the ester groups. The major products formed through t

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29

Kinsella, Karen, James R. Markham, Chad M. Nelson, and Thomas R. Burkholder. "Thermal Decomposition Products of Fiberglass Composites: A Fourier Transform Infrared Analysis." Journal of Fire Sciences 15, no. 2 (1997): 108–25. http://dx.doi.org/10.1177/073490419701500203.

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Decomposition products of fiberglass composites used in construc tion were identified using Fourier transform infrared (FT-IR) spectroscopy. This bench-scale study concentrated on identification and quantification of toxic species. Identifying compounds evolved during thermal decomposition provides data to develop early fire detection systems as well as evaluate product fire safety performance. Material fire behavior depends on many factors. Ventila tion, radiant heat flux, and chemical composition are three factors that can be modeled. Physical observations of composites during thermal decomp

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30

Tao, Neng, Changcheng Liu, Haoran Xing, Song Lu, Siuming Lo, and Heping Zhang. "Experimental and Density Functional Theory Studies on 1,1,1,4,4,4-Hexafluoro-2-Butene Pyrolysis." Molecules 25, no. 17 (2020): 3799. http://dx.doi.org/10.3390/molecules25173799.

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A series of thermal decomposition experiments were conducted over a temperature range of 873–1073 K to evaluate the thermal stability of 1,1,1,4,4,4-hexafluoro-2-butene (HFO-1336mzz(Z)) and the production of hydrogen fluoride (HF). According to the detected products and experimental phenomena, the thermal decomposition of HFO-1336mzz(Z) could be divided into three stages. Our experimental results showed that HF concentration gradually increased with the elevation of thermal decomposition temperature. In this present study, a total of seven chemical reaction pathways of HFO-1336mzz(Z) pyrolysis

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31

Johnston, P. K., E. Doyle, and R. A. Orzel. "Phenolics: A Literature Review of Thermal Decomposition Products and Toxicity." Journal of the American College of Toxicology 7, no. 2 (1988): 201–20. http://dx.doi.org/10.3109/10915818809014520.

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A comprehensive literature review on the thermal decomposition products and combustion toxicity of phenolics is presented. The major decomposition products of phenolics appear to be CO, CO2, H2O, and methane. Smaller quantities of H2, formaldehyde, and other volatile organics, including phenol, methylphenols, and dimethylphenols, also appear to be produced. The types and quantities of thermal decomposition products and the temperatures at which they are produced depend on numerous factors, including the resin structure and formulation and the conditions of degradation. Phenolics produced produ

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32

Yang, Chang Yan, Yun Wei, Fa Bin Ye, Yi Gang Ding, and Yuan Xin Wu. "Effect of Additives on Thermal Decomposition of Phosphogypsum." Advanced Materials Research 415-417 (December 2011): 735–40. http://dx.doi.org/10.4028/www.scientific.net/amr.415-417.735.

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The effect of different additives on thermal decomposition of phosphogypsum was investigated by means of a thermogravimetry coupled with a Fourier transform infra-red spectroscopy. These additives included C, CaO, Al2O3 and S. The temperature of thermal decomposition of phosphogypsum is about 1100~1320°C without any additives under the background of nitrogen. The temperature of the thermal decomposition of phosphogypsum decreased obviously with the addition of CaO, C and S. No influence was found for the thermal decomposition of phosphogypsum with the addition of Al2O3. As one of evolved produ

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33

Trif, László, Fernanda P. Franguelli, György Lendvay, et al. "Thermal analysis of solvatomorphic decakis (dimethylammonium) dihydrogendodecatungstate hydrates." Journal of Thermal Analysis and Calorimetry 144, no. 1 (2021): 81–90. http://dx.doi.org/10.1007/s10973-020-10494-4.

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AbstractThis study aims to describe the thermal decomposition of two solvatomorphs of decakis(dimethylammonium) dihydrogendodecatungstate ((Me2NH2)10H2W12O42·10H2O and 11 H2O) under inert and oxidizing atmospheres. Thermal studies have been done by TG-MS, TG-DSC-MS, XRD and IR methods in both synthetic air and helium atmospheres. The general characteristics of thermal decomposition are similar for both solvatomorphs. Minor differences could be observed in the resolution and shifting of the decomposition peak temperatures depending on the heating rate or atmosphere used. The first step of decom

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34

de Bakker, P. M. A., E. De Grave, R. E. Vandenberghe, L. H. Bowen, R. J. Pollard, and R. M. Persoons. "Mössbauer study of the thermal decomposition of lepidocrocite and characterization of the decomposition products." Physics and Chemistry of Minerals 18, no. 2 (1991): 131–43. http://dx.doi.org/10.1007/bf00216606.

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35

Domonov, Denis P., and S. I. Pechenyuk. "Thermal decomposition of double complex compounds of 3D metals." Herald of Kola Science Centre of the RAS 12, no. 3-2020 (2020): 5–15. http://dx.doi.org/10.37614/2307-5228.2020.12.3.001.

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The paper is devoted to the study of thermolysis of double complex compounds (DCС) of metalsin the I transition series. 30 DCСwith various combinations of metal-central atoms (Co-Fe, Cu-Fe, Ni-Fe Cr-Fe, Cr-Co,) and ligands (ammonia, urea (ur), ethylenediamine (en), 1,3-diaminopropane (tn), cyanide, oxalate and nitrite anions) were synthesized and characterized. A complete study of the thermal proper-ties of these DCCs in three atmospheres was carried out: oxidizing (air), inert (Ar, N2, partly He) and re-ducing (H2), in the temperature range of 20–1000°Cand at constant heating rate of 10°C/min

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36

Sozinov, S. A., L. V. Sotnikova, A. N. Popova, and L. M. Hitsova. "Thermal-Decomposition Products of Hexane-Insoluble Asphaltenes from Coal Pitch." Coke and Chemistry 61, no. 11 (2018): 447–52. http://dx.doi.org/10.3103/s1068364x1811008x.

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37

Antoš, K., and J. Sedlář. "Influence of brominated flame retardant thermal decomposition products on HALS." Polymer Degradation and Stability 90, no. 1 (2005): 188–94. http://dx.doi.org/10.1016/j.polymdegradstab.2005.03.008.

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38

Altarawneh, Mohammednoor, Anam Saeed, Mohammad Al-Harahsheh, and Bogdan Z. Dlugogorski. "Thermal decomposition of brominated flame retardants (BFRs): Products and mechanisms." Progress in Energy and Combustion Science 70 (January 2019): 212–59. http://dx.doi.org/10.1016/j.pecs.2018.10.004.

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39

Beirakhov, A. G., A. V. Rotov, N. N. Efimov, E. G. Il’in, and A. E. Gekhman. "Thermal Stability and Products of Decomposition of Hydroxylaminate Uranyl Complexes." Russian Journal of Inorganic Chemistry 64, no. 2 (2019): 185–89. http://dx.doi.org/10.1134/s0036023619020025.

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40

Barontini, Federica, Katia Marsanich, Luigi Petarca, and Valerio Cozzani. "Thermal Degradation and Decomposition Products of Electronic Boards Containing BFRs." Industrial & Engineering Chemistry Research 44, no. 12 (2005): 4186–99. http://dx.doi.org/10.1021/ie048766l.

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41

L’abbé, (The late) Gerrit, Leonard K. Dyall, Kathleen Meersman, and Wim Dehaen. "Rates and Products of the Thermal Decomposition of 5-Azidoisothiazoles." Journal of Chemical Research, no. 7 (1997): 226. http://dx.doi.org/10.1039/a701866e.

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42

Ilhan, Sedat, Cem Kahruman, and Ibrahim Yusufoglu. "Characterization of the thermal decomposition products of ammonium phosphomolybdate hydrate." Journal of Analytical and Applied Pyrolysis 78, no. 2 (2007): 363–70. http://dx.doi.org/10.1016/j.jaap.2006.09.009.

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43

Simionescu, Cr I., C. Vasile, P. Onu, et al. "Modification in thermal decomposition products of polymers by catalytic pyrolysis." Thermochimica Acta 134 (October 1988): 301–5. http://dx.doi.org/10.1016/0040-6031(88)85251-1.

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44

Zhang, Qing, Ahmed S. M. Saleh, Jing Chen, Peiran Sun, and Qun Shen. "Monitoring of thermal behavior and decomposition products of soybean oil." Journal of Thermal Analysis and Calorimetry 115, no. 1 (2013): 19–29. http://dx.doi.org/10.1007/s10973-013-3283-0.

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45

Williams, Brent J., Yaping Zhang, Xiaochen Zuo, et al. "Organic and inorganic decomposition products from the thermal desorption of atmospheric particles." Atmospheric Measurement Techniques 9, no. 4 (2016): 1569–86. http://dx.doi.org/10.5194/amt-9-1569-2016.

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Abstract. Atmospheric aerosol composition is often analyzed using thermal desorption techniques to evaporate samples and deliver organic or inorganic molecules to various designs of detectors for identification and quantification. The organic aerosol (OA) fraction is composed of thousands of individual compounds, some with nitrogen- and sulfur-containing functionality and, often contains oligomeric material, much of which may be susceptible to decomposition upon heating. Here we analyze thermal decomposition products as measured by a thermal desorption aerosol gas chromatograph (TAG) capable o

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46

Williams, B. J., Y. Zhang, X. Zuo, et al. "Organic and inorganic decomposition products from the thermal desorption of atmospheric particles." Atmospheric Measurement Techniques Discussions 8, no. 12 (2015): 13377–421. http://dx.doi.org/10.5194/amtd-8-13377-2015.

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Abstract. Atmospheric aerosol composition is often analyzed using thermal desorption techniques to evaporate samples and deliver organic or inorganic molecules to various designs of detectors for identification and quantification. The organic aerosol (OA) fraction is composed of thousands of individual compounds, some with nitrogen- and sulfur-containing functionality, and often contains oligomeric material, much of which may be susceptible to decomposition upon heating. Here we analyze thermal decomposition products as measured by a thermal desorption aerosol gas chromatograph (TAG) capable o

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47

Sheng, Su, Shengming Jin, and Kuixin Cui. "Thermal Decomposition of Nanostructured Bismuth Subcarbonate." Materials 13, no. 19 (2020): 4287. http://dx.doi.org/10.3390/ma13194287.

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Nanostructured (BiO)2CO3 samples were prepared, and their thermal decomposition behaviors were investigated by thermogravimetric analysis under atmospheric conditions. The method of preparation and Ca2+ doping could affect the morphologies of products and quantity of defects, resulting in different thermal decomposition mechanisms. The (BiO)2CO3 nanoplates decomposed at 300–500 °C with an activation energy of 160–170 kJ/mol. Two temperature zones existed in the thermal decomposition of (BiO)2CO3 and Ca-(BiO)2CO3 nanowires. The first one was caused by the decomposition of (BiO)4(OH)2CO3 impurit

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48

Czech, Zbigniew, Robert Pełech, and Krzysztof Zych. "Thermal decomposition of acrylic pressure-sensitive adhesives." Polish Journal of Chemical Technology 11, no. 4 (2009): 7–12. http://dx.doi.org/10.2478/v10026-009-0036-8.

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Thermal decomposition of acrylic pressure-sensitive adhesives The general aim of this article is to review the state of knowledge on pressure-sensitive adhesives (PSAs) and pyrolysis. Recent research data in the field of pyrolysis gas- chromatography (Py-GC) analysis of acrylic PSAs are presented. First, PSA characteristics and applications, pyrolysis (including Py-GC) as an analytical method, and system solutions, are described. The latest scientific achievements in the analysis of thermal degradation products of acrylic PSAs are then presented.

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49

Cong, Zhang, Chen Xiang, Hu Yongpeng, et al. "A series of guanidine salts of 3,6-bis-nitroguanyl-1,2,4,5-tetrazine: green nitrogen-rich gas-generating agent." RSC Advances 10, no. 60 (2020): 36287–94. http://dx.doi.org/10.1039/d0ra06766k.

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50

Atamanov, M., R. Amrousse, J. Jandosov, et al. "Combustion Characteristics of HAN-based Green Propellant Assisted with Nanoporous Active Carbons." Eurasian Chemico-Technological Journal 19, no. 3 (2017): 215. http://dx.doi.org/10.18321/ectj665.

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Combustion of hydroxylammonium nitrate (95 wt.% HAN) ‒ water solution in presence of high specific surface area activated carbons is investigated in a constant-pressure bomb within the pressure range of 1‒6 MPa. The linear burning rate increased for the system of HAN admixed with activated carbons compared to those of the HAN alone. Moreover, the thermal decomposition of HAN (95 wt.%) ‒ water solution spiked with activated carbons was assessed by DTA – TG method. In the presence of activated carbons, the ability to trigger the decomposition at a lower temperature (86 °C vs 185 °C) was observed

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