(My dumb ass forgot to tag)

Hello Fediverse, I have a bit of a technical question about the chemistry of resins, drying oils and their polymerisation. Related to an ink-making project of mine, I'll tell more about that later. The thing is, I am *absolutely not* a chemist, so I turn to the Internet with the hope of finding the knowledge I am lacking! I explain more in the following thread, thanks in advance for reading and feel free to answer in either French or English.

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#chemistry #ink

So, I'm a pen and paper lover, and I wanted to make a durable ink of (most importantly) open composition, preferably plant-based. Resins and drying oils have caught my interest for two reasons : the firsts have an ability to set quickly, however they remain soluble in their solvent, the others… well, *dry* (although they actually cross-link) in a longer period of time (about a week for raw flaxseed oil, can be brought to under a day). Let me get into a few details here.

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Resins, at least natural ones, are essentially made of two compounds : long, acyclic chains or carbons, and another cyclic aliphatic, with several cycles, both compounds bearing a carboxylic (R-C(O)OH) and a few alcohol (R-OH) groups. When the solvent evaporates, intermolecular forces make the resin set, and the whole thing may take years to cure, if untreated.

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Drying oils are made of unsaturated fats. The more double bonds they have, the more “drying” they are.

I am not sure what happens with the double bonds, however dioxygen from the air will create a hydroperoxyde (R-O-OH) that will allow the cross-linking of two carbon chains as an ether (R1-O-R2) and release water. Siccatives (metallic soaps) catalyse these reactions, and interestingly, they can also catalyse the polymerisation of resins (this time, through esterification).

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Now that all this is said, I believe it would be… *mechanically* beneficial to use both resin and oil, for flow at first, then for the plasticity of the dried ink film. But anyway, if I want rapid setting, I will need resin, and if I want curing, I will need the addition of siccatives. However, contrary to drying oils, resins molecules all have oxygen atoms in carboxylic and alcohol groups.

(Question coming, finally!)

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So my question is : *in solvent* (I think I'll use ethanol) and with the addition of a siccative, should the molecules of resin cross-link? And if so, can the reaction be prevented by the addition of an antioxydant (say, eugenol)?

Thanks again for your time.

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(What would be a long thread without a post scriptum?)

PS : It is going to be an artistic, small scale and artisanal process, so I do not expect to get an exact theory and there will be a lot of testing to get the recipe right, but I would like to confirm that my expectations are correct, otherwise… well, if it dries in the pot, it is not going to work!

Also, I'm a very *safety first* person, so I will be careful.

@machinart The oxygen in the resin will not interact with the double bonds in the oils. That is done only by O2 and some other not so common oxidisers.
An antioxidant will not help in any way. Could even prevent the curing.
@rstein Thank you for your answers! Out of curiosity, may I ask what these “not so common oxidisers” are? And, as I asked in another answer, if the antioxidant is volatile enough to evaporate with the solvent, it won't prevent the curing?