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Examination of selected synthesis parameters for wood adhesive-type urea–formaldehyde resins by 13C NMR spectroscopy. III

✍ Scribed by Moon G. Kim


Publisher
John Wiley and Sons
Year
2001
Tongue
English
Weight
254 KB
Volume
80
Category
Article
ISSN
0021-8995

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✦ Synopsis


Abstract

The varying polymer structures of wood adhesive‐type urea–formaldehyde resins resulting from different formaldehyde/first urea (F/U~1~) mole ratios used in the first step of resin manufacture were investigated using ^13^C. As the F/U~1~ mole ratio decreased progressively from 2.40 to 2.10 and to 1.80, the viscosity increase due to polymerization during resin synthesis became faster and resulted in decreasing side‐chain branches and increasing free urea amide groups in the resin structure. The resultant UF resins, with the second urea added to an overall F/(U~1~ + U~2~) of 1.15, showed viscosity decreases when heated with stirring or allowed to stand at room temperature that were also characteristic with the F/U~1~ mole ratios used in resin synthesis. The formaldehyde emission levels of particleboards bonded with the freshly made UF resins showed relatively small but similarly characteristic variations. © 2001 John Wiley & Sons, Inc. J Appl Polym Sci 80: 2800–2814, 2001


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Selected synthesis parameters of typical wood adhesive-type urea-formaldehyde (UF) resins were examined using the 13 C NMR spectroscopy. The monomeric hydroxymethylureas and methylene-ether derivatives formed in the initial alkaline reaction polymerize in the subsequent acidic reaction by forming me