Add like
Add dislike
Add to saved papers

Thermal decomposition of bimetallic titanium complexes: A new method for synthesizing doped titanium nano-sized catalysts and photocatalytic application.

In this study, synthesis of bimetallic (Co, Mn, and Ni) complexes of salicylic acid (L1 ) and 1,2 dihydroxybenzene (L2 ) based on titanium(IV) were investigated, then the samples were decomposed by thermal method to obtain Mx Tiy Oz nanoparticles (M = Ni, Co, and Mn). The samples in complexes mode were analyzed by UV-Vis (200-800 nm), FT-IR (4000-400 Cm-1 ), CHN analysis and the structure of the bimetallic compounds also were investigated by the Quantum-chemical modelling. In addition, the samples in nanoparticles mode were studied by thermal analysis (to obtain DTA curves), XRD, FESEM image and EDX analyzing. BET surface analysis was carried out to analyze active surface, pore diameter and porosity of the Mx Tiy Oz nanoparticles. Based on the results, obtained samples as catalysts were able to absorb not just UV but also visible light. Catalysts were able to degrade bromophenol blue as a harmful organic substance under UV and visible lights, although, this ability was more significant when the samples were used under visible light.

Full text links

We have located links that may give you full text access.
Can't access the paper?
Try logging in through your university/institutional subscription. For a smoother one-click institutional access experience, please use our mobile app.

Related Resources

For the best experience, use the Read mobile app

Mobile app image

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app

All material on this website is protected by copyright, Copyright © 1994-2024 by WebMD LLC.
This website also contains material copyrighted by 3rd parties.

By using this service, you agree to our terms of use and privacy policy.

Your Privacy Choices Toggle icon

You can now claim free CME credits for this literature searchClaim now

Get seemless 1-tap access through your institution/university

For the best experience, use the Read mobile app