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Synthesis, structure, and characterization of glyoxal‐urea‐formaldehyde cocondensed resins
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Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/(sici)1097-4628(20000307)75:10<1243::aid-app5>3.0.co;2-fopenalex-snapshot
Examination of selected synthesis parameters for typical wood adhesive-type urea-formaldehyde resins by13C-NMR spectroscopy. II
inferredcites →https://doi.org/10.1002/(sici)1099-0518(19990401)37:7<995::aid-pola14>3.0.co;2-6openalex-snapshot
Examination of selected synthesis parameters for typical wood adhesive-type urea-formaldehyde resins by13C NMR spectroscopy. I
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Reactivity, chemical structure, and molecular mobility of urea–formaldehyde adhesives synthesized under different conditions using FTIR and solid‐state 13C CP/MAS NMR spectroscopy
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Ester acceleration mechanisms in phenol–formaldehyde resin adhesives
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inferredcites →https://doi.org/10.1007/s10973-010-1143-8openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.indcrop.2010.10.007openalex-snapshot
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inferredcites →https://doi.org/10.1016/j.polymer.2004.08.019openalex-snapshot
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inferredcites →https://doi.org/10.1016/s0143-7496(03)00089-7openalex-snapshot
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NTIS (National Technical Information Service)
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Innovative and multifunctional bio-based resins for the durability of wood and wood-based composites.
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