Randy Holmes-Farley
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My Tank Thread
Thanks. 

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Yes. The sintering of microcrystalline anatase is possible and has already been done on several surfaces, heating the deposited film of a suspension of TiO2 at a maximum of 400ºC, above that the change to rutile can occur. The problem is to be able to coat the interior of the tube uniformly with the anatase film, and then heat it. On flat surfaces it is much easier.AOP=Advanced oxidation processes. Its a term of art in the water treatment industry.
I think a better approach to creating the TiO2 surface would be to coat the inside of a tube with powdered anatase and then sinter it in place rather than chemically create a oxide layer. You'd have better control of crystalline form although I think some of the anatase would undergo a phase change to rutile at temperatures high enough to sinter. Rutile still has reasonable catalytic efficiency though.
You'd likely want a coating thick enough to be periodically resurfaced as the catalyst will likely eventually foul.
Yes. The sintering of microcrystalline anatase is possible and has already been done on several surfaces, heating the deposited film of a solution of TiO2 at a maximum of 400ºC, above that the change to rutile can occur. The problem is to be able to coat the interior of the tube uniformly with the anatase film, and then heat it. On flat surfaces it is much easier.
But again, if the anatase coating is obtained and kept permanently irradiated, it will hardly accumulate debris due to its "self-cleaning" effect and maintenance may perhaps be given with periodic flow increases on the reaction surface, para drag larger particles eventually adhered.
Regards
In order for there to be a real detriment to the catalytic action of the irradiated anatase, the carbonate deposit would have to be thick enough to be opaque to UV light and impervious to water, otherwise it would continue to function.It is self cleaning to organics, but what about deposition of inorganic minerals, such as calcium carbonate, or, if you accept that it happens even in seawater, the calcium hydroxyapatite?
Yea, I agree. I'd expect a decrease in efficiency due to fouling from abiotic sources but also perhaps some organics that are refractory to degredation by hydroxyl radicals. From prior lab research I worked on, I know things with aromatics like humic/fulvic acid can be pretty stubborn toward reactive oxygen species.It is self cleaning to organics, but what about deposition of inorganic minerals, such as calcium carbonate, or, if you accept that it happens even in seawater, the calcium hydroxyapatite?
There might be problems with the hydroxyl radicals attacking the PVC over time. Incorporation in a ceramic sleeve might work, but the process of firing the ceramic might cause a phase change to a crystal form with a lower catalytic efficiency. It depends on the temperature at which the ceramic is fired. I would not expect titanium sheet to exhibit this sort of chemistry to any appreciable extent.How about putting the titanium dioxide in a pvc Binder. The surface would be less reactive but you’d have a reactive surface of oxide. Can the oxide be formed into a ceramic sleeve? I just added titanium sheet to my UV to stop the plastic breaking down. So far it works for that purpose and I see no other changes.
I assume the titanium sheet you added would probably be fine to just shield the housing from UV. I have the same problem of the plastic breaking down in my UV unit. I've seen a bunch of different methods of immobilizing TiO2: sintering, impregnating concrete, etc.So then what would be a good sleeve material to block uv and not get killed itself and also not poison the tank.
how about this https://www.ebay.com/i/111815964657?chn=ps
Or can i just run the output over GAC.
If you find any pelletized anatase, let me know. All I've ever seen is powdered/granular.Couldnt you buy titanium pellets of the kind you need and just run a uv light over the pellets?
If you find any pelletized anatase, let me know. All I've ever seen is powdered/granular.

