04 October 2023 3 458 Report

Hi all, I've read hundreds of articles on the use of TiO2 as a photocatalyst to degrade Methylene Blue from water. I have also conducted my own work on this particularly via the sol-gel route as well as nano powder slurries and nano powder immobilised in PVA crosslinked with PEG. I've replicated 10 or so methods from various papers, often with completely different results than they had. Actually with failures. The one thing I did not replicate, is when they specify they used a UVC (254nm) light, I did not. I always used an 11W UVA (385nm) light (replacing the bulb often for certainty. In trying to find what my error was, I switched to a UVC light and got the same results as the authors. I then removed the catalyst and also still got the same results, with a UVC light only. Indicating Methylene Blue was being degraded via Photolysis. My results always checked on a Thermo Helios Spectrophotometer with an absorbance peak of 664. My question is, are these research articles, none of whom described running a control without the catalyst, actually achieving photocatalysis in their lab reactors? Or are they being led to believe they've succeeded due to Photolysis? Why is no-one talking about removal of Methylene Blue via 254nm UVC light? My reactor is Quartz glass with the UVC light sitting externally and the reaction occurring under stirring. I have replicated it 8 times with the same results. When I switch to 385nm only, I get no removal of MB. When I install a TiO2 catalyst, I also get no changes. Clearly my catalysts are flawed but I've asked that in another question with no real answers so far.

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