Add like
Add dislike
Add to saved papers

Magnetic cellulose nanocrystal nanocomposites for the development of green functional materials.

Carbohydrate Polymers 2017 November 2
A magnetic cellulosic material composed of cellulose nanocrystals (CNC) and cobalt ferrite (CoFe2 O4 ) nanoparticles was developed through evaporation-induced self-assembly (EISA). Nanoparticles demonstrated good dispersibility within the cellulose nanocrystal template. The addition of glucose to CNC network allows the development of homogeneous crack-free CNC-based films and does no modify neither the morphology nor the optical properties. In contrast, the introduction of CoFe2 O4 nanoparticles produces a marked decrease in the amount of the transmitted light. 20wt.% of CoFe2 O4 nanoparticles inside the CNC matrix induced a maximum magnetization value of 12.96emug-1 , increased the real part of the dielectric constant (permittivity) from 10 (pure CNC film) to 12 and improved the thermostability of the nanocomposite as evidenced by the increase of the onset temperature from 165.1 to 220.4°C. Those features obtained in a non-petroleum-based composite provide insight into the development of the next generation of functional materials from natural origin.

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