2004
DOI: 10.1016/j.jcis.2003.12.029
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Comparative study of carbon dioxide and nitrogen atmospheric effects on the chemical structure changes during pyrolysis of phenol–formaldehyde spheres

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Cited by 59 publications
(51 citation statements)
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“…2 indicate that there are no significant variations between the RG samples prepared using different vacuum time. For all the resin gel samples, it is observed that there are four decomposition steps of the gels, which is in line with reports elsewhere [38,39]. The first step occurs at temperatures up to 200 °C, and the second step between 250 and 330 °C with mass losses of ~8 and ~13 wt% for each step, respectively.…”
Section: Materials Characterisationsupporting
confidence: 90%
“…2 indicate that there are no significant variations between the RG samples prepared using different vacuum time. For all the resin gel samples, it is observed that there are four decomposition steps of the gels, which is in line with reports elsewhere [38,39]. The first step occurs at temperatures up to 200 °C, and the second step between 250 and 330 °C with mass losses of ~8 and ~13 wt% for each step, respectively.…”
Section: Materials Characterisationsupporting
confidence: 90%
“…Tp1 = Peak temperature of first thermal event; Tp2 = Peak temperature of second thermal event; Tp3 = Peak temperature of third thermal event; Tmaxd = Temperature of maximum decomposition Table 5, Table 6, and Fig. 3, which show the effects of incorporation of bio-oil on thermal profiles of the resin samples, indicate that generally the resin samples exhibited three major decomposition events in temperature zones of 200 to 300 °C, 350 to 500 °C, and 500 to 700 °C, a pattern which is consistent with earlier reports (Kim et al 2004;Chen et al 2008;Wang et al 2009a;Cheng et al 2011;. This pattern may be termed as: postcuring, thermal reforming, and ring stripping (Khan and Ashraf 2007).…”
Section: Thermal Degradation Properties Of the Synthesized Resinssupporting
confidence: 89%
“…The variation in relative intensities of these peaks clearly indicates different extent of (tri-vs. tetra-) substitutions of the aromatic rings caused by crosslinking through acidification with HCl, and formation of methylol groups by addition of formaldehyde. [38] Thermogravimetric analysis of the samples under air showed distinct degradation profiles (Figure S5 a). All three samples show a weight loss of around 5 % below 160 8C, attributed to the loss of adsorbed moisture and other volatile organics.…”
mentioning
confidence: 99%