Following on from MIGNAL's post.
This will get increasingly chemical, so I apologise if it bamboozles anyone just ask and I'll try to make a more detailed less technical explanation.
Shelac is composed of long chain organic acids, they're almost insoluble in "Non-Polar Solvents" i.e. Mineral Spirits, Natural Turpentine etc.
But, subject to pH effects they're very soluble in "Polar Protic Solvents" i.e. Ethanol (Grain Alcohol) and Methanol (Wood Alcohol), which are infinately miscable with non-polar solvents.
Linseed Oil and Rosin are miscable with both Polar and Non-Polar Solvents, (It's possible, but not easy to solvate the Rosin in hot linseed directly, much easier to use a Non-Polar solvent to help it along).
The trick is to find a solvent, or solvent blend which will happily solvate both the Shelac and Rosin, and remain miscable with the linseed oil, a "Mutual Solvent".
I've experimented with various mixes, and it's not always worked smoothly either, as you can unwittingly drop the shellac solids out as a precipitate if you don't have enough of the mutual solvent in the mix, but too much solvent will leave insufficient linseed relative to the solids to polymerise into a matrix which bonds to the surface, rather than just dry onto the surface as a deposited coating.
Interestingly, the components of linseed oil and shellac are structurally quite simmilar and both undergo some degree of cross linking with exposure to oxidative processes, via different chemical reactions.
Rosin is the odd one out structurally, with a rather different structure which is not as conducive to cross linking in its natural form; however when esterified with by acid catylised reaction with an alcohol it develops that property, as 'ester gum' which is important in commercially available varnishes, (when reacted with a polyol, it would be a form of Alkyd), this polymerisation is chemically simmilar to the one which shellac can undergo.
With regards to drying, there are a couple of ways to achieve the same effect, UV will increase the frequency of the Free-radical reactions which integrate oxygen (as hydroperoxy groups) into the unsaturated tails of the fatty acids making up the oil, a catalyst (moden drying agents) will reduce the energy needed for that to happen increasing frequency, and finally introducing more oxygen will increase the frequency by providing the reactant where it's needed (this is what older drying agents, like lead dioxide or chromium trioxide did).
MIGNAL":21w7y7jm said:I wasn't aware that Shellac would go into an oil based varnish.
How are you making the Shellac, rosin and linseed oil varnish? Are you heating this until you reach the long string stage? You will also need to add a drier and/or subject it to lots of UV to get it to dry and harden in a reasonable time.
Any resin/oil varnish should be able to produce a pretty glossy surface if you go through the grits/polishes, providing the oil to resin ration isn't too high. In any case these sorts of varnishes aren't what one call hard wearing. You really have to go to the short amber/copal varnishes or the harder synthetic resin varnishes to get hard wearing. Behlens used to do a synthetic oil varnish that was really hard and tough. Dried fast too. I suspect that a lot of the stuff sold as 'table top' or 'bar top' varnishes will be very similar too.
This will get increasingly chemical, so I apologise if it bamboozles anyone just ask and I'll try to make a more detailed less technical explanation.
Shelac is composed of long chain organic acids, they're almost insoluble in "Non-Polar Solvents" i.e. Mineral Spirits, Natural Turpentine etc.
But, subject to pH effects they're very soluble in "Polar Protic Solvents" i.e. Ethanol (Grain Alcohol) and Methanol (Wood Alcohol), which are infinately miscable with non-polar solvents.
Linseed Oil and Rosin are miscable with both Polar and Non-Polar Solvents, (It's possible, but not easy to solvate the Rosin in hot linseed directly, much easier to use a Non-Polar solvent to help it along).
The trick is to find a solvent, or solvent blend which will happily solvate both the Shelac and Rosin, and remain miscable with the linseed oil, a "Mutual Solvent".
I've experimented with various mixes, and it's not always worked smoothly either, as you can unwittingly drop the shellac solids out as a precipitate if you don't have enough of the mutual solvent in the mix, but too much solvent will leave insufficient linseed relative to the solids to polymerise into a matrix which bonds to the surface, rather than just dry onto the surface as a deposited coating.
Interestingly, the components of linseed oil and shellac are structurally quite simmilar and both undergo some degree of cross linking with exposure to oxidative processes, via different chemical reactions.
Rosin is the odd one out structurally, with a rather different structure which is not as conducive to cross linking in its natural form; however when esterified with by acid catylised reaction with an alcohol it develops that property, as 'ester gum' which is important in commercially available varnishes, (when reacted with a polyol, it would be a form of Alkyd), this polymerisation is chemically simmilar to the one which shellac can undergo.
With regards to drying, there are a couple of ways to achieve the same effect, UV will increase the frequency of the Free-radical reactions which integrate oxygen (as hydroperoxy groups) into the unsaturated tails of the fatty acids making up the oil, a catalyst (moden drying agents) will reduce the energy needed for that to happen increasing frequency, and finally introducing more oxygen will increase the frequency by providing the reactant where it's needed (this is what older drying agents, like lead dioxide or chromium trioxide did).