2003
DOI: 10.2115/fiber.59.465
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Thermal and Mechanical Properties of Sodium Lignosulfonate-based Rigid Polyurethane Foams Prepared with Three Kinds of Polyols

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Cited by 7 publications
(5 citation statements)
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“…The peaks with a maximum intensity between 320 and 345°C in the dTG curves of the composites reinforced with curaua [Figure 4(b)] and coir fibers (figure not shown) were related to the mass loss associated with the break‐up of urethane bonds, i.e., the degradation of the hard segments in the PU matrix 14, 61. In addition, the moieties typical of NaLS present in the matrix began to decompose at this temperature, and the cellulose present in the fibers used as reinforcement also decomposes.…”
Section: Resultsmentioning
confidence: 99%
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“…The peaks with a maximum intensity between 320 and 345°C in the dTG curves of the composites reinforced with curaua [Figure 4(b)] and coir fibers (figure not shown) were related to the mass loss associated with the break‐up of urethane bonds, i.e., the degradation of the hard segments in the PU matrix 14, 61. In addition, the moieties typical of NaLS present in the matrix began to decompose at this temperature, and the cellulose present in the fibers used as reinforcement also decomposes.…”
Section: Resultsmentioning
confidence: 99%
“…In neat lignopolyurethanes (nonreinforced), the Izod impact strength increased with increasing chain length of the polyol used: the lignopolyurethane prepared from CO [Figure 1(b)] exhibited higher impact strength than that of PEG [Figure 1(d)], which had higher impact strength than that of DEG [Figure 1(c)]. The use of polyols with longer chains may lead to a lower degree of crosslinking and a material with more elastomeric characteristics and high molecular mobility, resulting in higher impact strength 14…”
Section: Resultsmentioning
confidence: 99%
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“…Polyols, except lignin, can affect the mechanical and thermal properties of polyurethane foams. Hatakeyama et al [169,170] investigated the mechanical and thermal properties of lignin-based polyurethane foams derived from sodium lignosulfonate mixed with diethylene glycol, triethylene glycol, and PEG. The glass transition temperatures and thermal stability increased with decreasing oxyethylene chain lengths, and the compression strength and compression modulus increased with increasing oxyethylene chain lengths.…”
Section: Urethanizationmentioning
confidence: 99%
“…63,65,66 The KL had a higher content of phenolic hydroxyl groups (Online Supplemental Table S2) which form less stable urethane bonds than aliphatic hydroxyl groups, which were predominant in the OL and LS. 63,67 In the range 280–350°C, the rate of weight loss in the KL PUF was lower than in the other materials (DTG). Once the more labile urethane bonds were broken, a lower rate in the KL PUF due to a higher thermal stability in the remaining urethane network caused by higher cross-link density or a differing biopolyol structure was possible.…”
Section: Resultsmentioning
confidence: 90%