2013
DOI: 10.1016/j.indcrop.2012.08.033
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Hydroxyalkylated xylans – Their synthesis and application in coatings for packaging and paper

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Cited by 95 publications
(84 citation statements)
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“…The 1 H NMR spectrum of HPX (Fig. 2) showed a very intense signal at 1.13 ppm clearly attributed to the methyl protons of the substituent hydroxypropyl groups [21]. From the comparison of the integrated area of this signal and that of anomeric H-1, a DS of 1.07 was determined for HPX (Section 2.3.2).…”
Section: U N C O R R E C T E D P R O O Fmentioning
confidence: 98%
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“…The 1 H NMR spectrum of HPX (Fig. 2) showed a very intense signal at 1.13 ppm clearly attributed to the methyl protons of the substituent hydroxypropyl groups [21]. From the comparison of the integrated area of this signal and that of anomeric H-1, a DS of 1.07 was determined for HPX (Section 2.3.2).…”
Section: U N C O R R E C T E D P R O O Fmentioning
confidence: 98%
“…Hydroxypropyl xylan (HPX) synthesis was carried out according to the method used by Laine et al [21]. Briefly, 13 g of 50% aqueous sodium hydroxide was added to 3.25 g of BX dispersed in distilled water (16.3%, w/w) was added and the mixture vigorously stirred in a Scheme 1.…”
Section: Hydroxypropylationmentioning
confidence: 99%
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