journal article·2015-12

Physical–chemical properties of xylan/PAAc magnetic semi‐interpenetrating network hydrogel

Xiao‐Feng Sun, Zhanxin Jing, Haihong Wang, Yuyang Liu

Polymer Composites· Volume 36· Issue 12
Publisher page

Abstract

A novel magnetic semi‐IPN hydrogel based on xylan and poly(acrylic acid) was prepared, and the prepared hydrogels had excellent thermal stability, magnetic‐, and pH‐ sensitive properties. The physical‐chemical properties of the prepared hydrogels depended on the contents of xylan and Fe3O4 nanoparticles. The thermal stability of the hydrogels enhanced as the contents of xylan and Fe3O4 nanoparticles increased; however, the equilibrium swelling ratio decreased with increasing the contents of Fe3O4 nanoparticles and xylan. The interconnected pore channels were formed in the hydrogels and the amount of the channels increased with an increase in xylan content. The prepared hydrogels had a super‐paramagnetic property, and the magnetization increased with an increase in the content of Fe3O4 nanoparticles. The superior characteristics of the xylan/PAAc magnetic semi‐IPN hydrogel would expand its applications in drug delivery and magnetic separation aspects. POLYM. COMPOS., 36:2317–2325, 2015. © 2014 Society of Plastics Engineers
Source: crossref · Quality: baseline

Research context

OpenAlex topics: Hydrogels: synthesis, properties, applications · Characterization and Applications of Magnetic Nanoparticles · Nanoparticle-Based Drug Delivery

SciVX discovery tags are terminology-based. OpenAlex topics are source-provided classifications.

Affiliations

Department of Chemistry, MOE Key Lab of Space Applied Physics and Chemistry College of Science, Northwestern Polytechnical University Xian 710072 China

Funding

National Natural Science Foundation of China · Shaanxi Science and Technology Research Project for Young Scientist · Fund for Fundamental Research of Northwestern Polytechnical University

References (28)

Show source-provided references
1. 10.1021/jf071893i10.1021/jf071893i ↗
2. 10.1038/nbt0886-73110.1038/nbt0886-731 ↗
3. 10.1007/b13681610.1007/b136816 ↗
4. 10.1016/j.biortech.2010.01.13710.1016/j.biortech.2010.01.137 ↗
5. 10.1002/1521-3927(20000601)21:9<542::AID-MARC542>3.0.CO;2-710.1002/1521-3927(20000601)21:9<542::AID-MARC542>3.0.CO;2-7 ↗
6. 10.1002/pc.2104610.1002/pc.21046 ↗
7. 10.1002/macp.20090065710.1002/macp.200900657 ↗
8. 10.1016/j.watres.2011.07.01810.1016/j.watres.2011.07.018 ↗
9. 10.1016/j.jallcom.2011.01.01810.1016/j.jallcom.2011.01.018 ↗
10. 10.1016/j.jmmm.2011.11.03910.1016/j.jmmm.2011.11.039 ↗
11. 10.1016/j.biomaterials.2009.01.04010.1016/j.biomaterials.2009.01.040 ↗
12. 10.1016/j.carbpol.2010.01.02010.1016/j.carbpol.2010.01.020 ↗
13. 10.1016/j.cej.2014.01.06510.1016/j.cej.2014.01.065 ↗
14. 10.1016/j.carres.2007.07.00710.1016/j.carres.2007.07.007 ↗
15. 10.1016/j.cej.2011.10.06610.1016/j.cej.2011.10.066 ↗
16. 10.1016/j.polymer.2006.08.05610.1016/j.polymer.2006.08.056 ↗
17. Xiang M. · Acta Phys. Chim. Sin. · 2011 · 27 · 126710.3866/PKU.WHXB20110429 ↗
18. 10.1016/j.indcrop.2010.12.00510.1016/j.indcrop.2010.12.005 ↗
19. 10.1039/b900103d10.1039/b900103d ↗
20. 10.1016/j.mseb.2012.01.00310.1016/j.mseb.2012.01.003 ↗
21. 10.1016/j.apsusc.2009.11.07910.1016/j.apsusc.2009.11.079 ↗
22. 10.1016/j.carbpol.2008.07.02410.1016/j.carbpol.2008.07.024 ↗
23. 10.1016/j.polymdegradstab.2007.02.01110.1016/j.polymdegradstab.2007.02.011 ↗
24. 10.1016/j.eurpolymj.2007.02.02310.1016/j.eurpolymj.2007.02.023 ↗
25. 10.1016/j.polymdegradstab.2007.02.02510.1016/j.polymdegradstab.2007.02.025 ↗
26. 10.1002/app.218010.1002/app.2180 ↗
27. 10.1021/bm100642y10.1021/bm100642y ↗
28. 10.1016/j.carbpol.2007.02.01610.1016/j.carbpol.2007.02.016 ↗