Add like
Add dislike
Add to saved papers

Effects of calcination temperature and heating rate on the photocatalytic properties of ZnO prepared by pyrolysis.

A series of ZnO nanorods were prepared by pyrolysis of zinc acetate at different calcination temperatures and heating rates under ambient atmosphere. The as-prepared ZnO nanorods were characterized by X-ray diffractometer (XRD), scanning electron microscopy (SEM), UV-visible diffuse reflectance spectroscopy (DRS) and X-ray photoelectron spectroscopy (XPS). The photocatalytic performances of the ZnO nanorods were evaluated by the photodegradation of methyl orange (MO) and 4-nitrophenol (4-NP). The morphology, optical property, surface composition, and photocatalytic performance of the ZnO samples were affected by both calcination temperature and heating rate. The photocatalytic activity of the ZnO sample was obviously decreased with increased heating rate, which might be ascribed to the simultaneous decrease of oxygen vacancies and surface adsorption oxygen species. The ZnO nanorods prepared at 300°C with a heating rate of 1°C/min exhibited good photocatalytic activity and photochemical stability, allowing good potential practical application in environmental remediation.

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