2004
DOI: 10.1016/j.porgcoat.2004.08.006
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Development of a fast drying lacquer based on raw lacquer sap

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Cited by 99 publications
(86 citation statements)
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“…The peaks at the m/z ¼ 370 (C 17 -triene type), 372 (C 17 -diene type), 374 (C 17 -monoene type), 376 (C 17 -saturated type), and 382 [C 6 H 5 -(CH 2 ) 12 C 6 H 3 -(OH) 2 (figure not shown). The peaks at the m/z-range of 684-692 correspond to O-dimethyl ethers of urushiol dimers, whereas the peaks in the m/z-range of 724-752 correspond to O-dimethyl ethers of thitsiol dimers.…”
Section: Fd-ms Measurementmentioning
confidence: 99%
See 1 more Smart Citation
“…The peaks at the m/z ¼ 370 (C 17 -triene type), 372 (C 17 -diene type), 374 (C 17 -monoene type), 376 (C 17 -saturated type), and 382 [C 6 H 5 -(CH 2 ) 12 C 6 H 3 -(OH) 2 (figure not shown). The peaks at the m/z-range of 684-692 correspond to O-dimethyl ethers of urushiol dimers, whereas the peaks in the m/z-range of 724-752 correspond to O-dimethyl ethers of thitsiol dimers.…”
Section: Fd-ms Measurementmentioning
confidence: 99%
“…Previously, we developed a series of fast-drying lacquers using kurome, 2 hybridized, [3][4][5] and blended methods. 6 Using these techniques to improve the slow drying time of thitsiol, in this study, we tried blending urushiol with thitsiol to make a new blended lacquer.…”
Section: Introductionmentioning
confidence: 99%
“…1). All of these components have been separated and purified [1,5] and some of the components have been studied individually, such as the structural analysis of urushiols and laccols [6][7][8][9][10][11]; lacquer polysaccharides [4,[12][13][14]; fast drying lacquer [15][16][17][18][19], and the morphology and components of lacquer film [20][21][22][23], however, their interactions have been scarcely investigated due to their complexity [24]. Some interesting phenomena have been observed, for example lacquer polysaccharides in the surface of the lacquer film act as a barrier layer against oxygen diffusion [25].…”
Section: Introductionmentioning
confidence: 99%
“…www.intechopen.com In order to reveal the enzymatic polymerization mechanism of thitsiol, we reinvestigated the dimer structures produced in the initial stage of enzymatic polymerization by using modern techniques including 1H-1H and 1H-13C correlation two-dimensional NMR measurements [18][19]. The structures of thitsiol dimers from Melanorrhoea (Gluta) usitata were characterized by means of high-resolution NMR spectroscopy involving twodimensional NMR measurements using field gradient DQF-COSY, HMQC, and HMBC.…”
Section: Drying Mechanismmentioning
confidence: 99%