1997
DOI: 10.1002/(sici)1097-4628(19971107)66:6<1183::aid-app18>3.0.co;2-2
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Phenol-formaldehyde resol resins studied by13C-NMR spectroscopy, gel permeation chromatography, and differential scanning calorimetry

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Cited by 72 publications
(22 citation statements)
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“…, the relatively low‐intensity peak at 39.8–40.2 ppm in the spectrum of the phenolic resin corresponded to the phenol para / para ‐connected methylene carbon ( p , p ‐Ph–CH 2 –Ph); there were no peaks detected at 29–30 or 34–36 ppm, suggesting the complete absence of both the phenol ortho / ortho ‐ ( o,o ‐Ph–CH 2 –Ph) and phenol para / ortho ‐methylene carbon ( o,p ‐Ph–CH 2 –Ph), respectively, in the phenolic resin. There are some differences in these results compared to those obtained by Holopainen et al, who concluded that p , p ‐Ph–CH 2 –Ph and o,p ‐Ph–CH 2 –Ph groups were present in phenolic resin . This difference can be attributed to the resin synthesis temperature employed; the study conducted by Timo Holopainen used a temperature of 80°C, while the present experiment used a temperature of 75°C, with mainly p , p ‐Ph‐CH 2 ‐Ph produced at this lower temperature.…”
Section: Resultscontrasting
confidence: 81%
See 1 more Smart Citation
“…, the relatively low‐intensity peak at 39.8–40.2 ppm in the spectrum of the phenolic resin corresponded to the phenol para / para ‐connected methylene carbon ( p , p ‐Ph–CH 2 –Ph); there were no peaks detected at 29–30 or 34–36 ppm, suggesting the complete absence of both the phenol ortho / ortho ‐ ( o,o ‐Ph–CH 2 –Ph) and phenol para / ortho ‐methylene carbon ( o,p ‐Ph–CH 2 –Ph), respectively, in the phenolic resin. There are some differences in these results compared to those obtained by Holopainen et al, who concluded that p , p ‐Ph–CH 2 –Ph and o,p ‐Ph–CH 2 –Ph groups were present in phenolic resin . This difference can be attributed to the resin synthesis temperature employed; the study conducted by Timo Holopainen used a temperature of 80°C, while the present experiment used a temperature of 75°C, with mainly p , p ‐Ph‐CH 2 ‐Ph produced at this lower temperature.…”
Section: Resultscontrasting
confidence: 81%
“…Initial F/P value is an important factor influencing the properties of the phenolic resin . Astarloa‐Aierbe et al studied the effects of different F/P ratios on the synthesis of phenolic resins ; their results indicated that the concentration of residual formaldehyde and phenol relied on both the initial F/P value and catalytic loading and that, with an increase in the F/P molar ratio, the bridging bonds between hydroxymethyl groups and benzene rings (methylene and ether) increased as well.…”
Section: Introductionmentioning
confidence: 99%
“…8d. It seems that the small shear forces exerted on PheMMT agglomerates during polymerization are able to overcome the attraction forces between the layers due to the weak forces that stack them together [9, 45], thus exfoliating the smaller stacks. Thereby, Fig.…”
Section: Resultsmentioning
confidence: 99%
“…[8][9][10][11][12][13][14][15][16][17][18] The kinetic analysis of DSC thermograms gives dynamic information during curing because it provides the quantitative heat flow associated with the polymerization process. [8][9][10][11][12][13][14][15][16][17][18] The kinetic analysis of DSC thermograms gives dynamic information during curing because it provides the quantitative heat flow associated with the polymerization process.…”
Section: Introductionmentioning
confidence: 99%
“…[8][9][10][11][12][13][14][15][16][17][18] The kinetic analysis of DSC thermograms gives dynamic information during curing because it provides the quantitative heat flow associated with the polymerization process. 9 The kinetics of complex processes such as the curing reaction for PF can be described by model-free kinetics. These peaks have been interpreted using the structural information provided by nuclear magnetic resonance and gel permeation chromatography.…”
Section: Introductionmentioning
confidence: 99%