TY - JOUR
T1 - Oxidation of drying oils containing non-conjugated and conjugated double bonds catalyzed by a cobalt catalyst
AU - Oyman, Z.O.
AU - Ming, W.
AU - Linde, van der, R.
PY - 2005
Y1 - 2005
N2 - The oxidation of drying oil containing non-conjugated (linseed oil) and conjugated (tung oil) double bonds catalyzed by Co(II)-2-ethylhexanoate (Co-EH) is investigated. There is distinctive difference in the oxidation mechanism between the two model oils. For the non-conjugated linseed oil, H-abstraction occurs via the most susceptible double allylic H atom. A large amount of oxygen is taken up, leading to the formation of hydroperoxides; the hydroperoxides are then decomposed into alkoxy and peroxy free radicals, followed by the formation of cross-links and byproducts. In contrast, for the mainly conjugated tung oil, the oxidation has to start with H-abstraction from the monoallylic position. In comparison with linseed oil, a lower amount of oxygen is consumed, and much less hydroperoxides and byproducts are formed. It indicates that, once free radicals are formed, they tend to directly add to a conjugated double bond, instead of abstracting a monoallylic H atom. A tentative explanation is given in terms of bond dissociation energy of related bonds.
AB - The oxidation of drying oil containing non-conjugated (linseed oil) and conjugated (tung oil) double bonds catalyzed by Co(II)-2-ethylhexanoate (Co-EH) is investigated. There is distinctive difference in the oxidation mechanism between the two model oils. For the non-conjugated linseed oil, H-abstraction occurs via the most susceptible double allylic H atom. A large amount of oxygen is taken up, leading to the formation of hydroperoxides; the hydroperoxides are then decomposed into alkoxy and peroxy free radicals, followed by the formation of cross-links and byproducts. In contrast, for the mainly conjugated tung oil, the oxidation has to start with H-abstraction from the monoallylic position. In comparison with linseed oil, a lower amount of oxygen is consumed, and much less hydroperoxides and byproducts are formed. It indicates that, once free radicals are formed, they tend to directly add to a conjugated double bond, instead of abstracting a monoallylic H atom. A tentative explanation is given in terms of bond dissociation energy of related bonds.
U2 - 10.1016/j.porgcoat.2005.06.004
DO - 10.1016/j.porgcoat.2005.06.004
M3 - Article
SN - 0300-9440
VL - 54
SP - 198
EP - 204
JO - Progress in Organic Coatings
JF - Progress in Organic Coatings
IS - 3
ER -