2009
DOI: 10.1295/polymj.pj2008199
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Synthesis and Properties of a High-Molecular-Weight Organosoluble Bisphenol A Novolac

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Cited by 17 publications
(10 citation statements)
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“…These groups were easier to be decomposed by heating than protected hydroxyl groups; therefore, the thermal stability of unprotected LP was less than those of alkoxylated LP (2-5). In our previous report, 20 the weight decrease of a conventional phenol novolac (ca. M n ¼1500) started below 150 1C due to degradation around the phenolic hydroxy groups.…”
Section: Thermal Properties Of Lp and 2-5mentioning
confidence: 90%
“…These groups were easier to be decomposed by heating than protected hydroxyl groups; therefore, the thermal stability of unprotected LP was less than those of alkoxylated LP (2-5). In our previous report, 20 the weight decrease of a conventional phenol novolac (ca. M n ¼1500) started below 150 1C due to degradation around the phenolic hydroxy groups.…”
Section: Thermal Properties Of Lp and 2-5mentioning
confidence: 90%
“…34 The phenolic resin with a low-molecular weight (4) was prepared according to the previous report. [12][13][14][15][16][17] Addition-condensation of 2,2-bis(4-methoxyphenyl)propane (1) with formaldehyde. To a mixture of 1 (1.28 g, 5 mmol) and paraformaldehyde (0.30 g, 10 mmol as a formaldehyde unit) were added acetic acid (AcOH, 2 ml) and chloroform (CHCl 3 , 3 ml).…”
Section: Methodsmentioning
confidence: 99%
“…These resins have interesting properties that make them suitable for industrial use, such as thermostability and mechanical strength. [2][3][4][5][6][7][8][9][10][11][12][13][14][15][16][17] During the curing of novolacs, hexamethylenetetramine (HMTA) is frequently used as the curing agent; 1 however, the resultant curing products usually tend to contain amine derivatives and the unreacted curing agent as impurities, which often lead to coloration and degradation of the products.…”
mentioning
confidence: 99%
“…We succeeded in developing a phase‐separation system (2‐step process II) that can produce processable and organosoluble lignophenol (LP) 21–26. The structure of LP is similar to that of artificial phenolic resins,27–37 which are often used as plastics, adhesives, cures, etc. Being a natural polymer‐based plastic, LP is considered to be a substitute for commodity polymers derived from fossil fuels.…”
Section: Introductionmentioning
confidence: 99%