Ferromagnetic iron oxide–cellulose nanocomposites prepared by ultrasonication

Literature Information

Publication Date 2017-10-27
DOI 10.1039/C7PY01587A
Impact Factor 5.582
Authors

Razvan Rotaru, Marcela Savin, Nita Tudorachi, Cristian Peptu, Petrisor Samoila, Liviu Sacarescu, Valeria Harabagiu


View Original

Abstract

This paper highlights the efficiency of ultrasonication, as a clean and energy-saving method for the preparation of cellulose–iron oxide ferromagnetic composites in two steps. Hydroxyl-functionalized maghemite–goethite nanoparticles (MG) having a saturation magnetization of 56.9 emu g−1 at room temperature were first synthesized by a one-pot procedure involving ultrasonication of an aqueous alkaline Fe2+ salt solution. Organic–inorganic nanocomposites were obtained by a second ultrasonication step of an aqueous suspension of micronized cellulose and MG nanoparticles. The cumulative effect of ultrasonication and MG nano-projectiles was found to strongly decrease the degree of crystallinity of cellulose. The microstructural characterisation of the resulting composite evidenced its size polydispersity, with small nanoparticles uniformly attached on the surface of cellulose microfibrils. Vibrating sample magnetic measurement indicated a hysteresis curve specific to ferromagnetic materials and the appearance of a superparamagnetic phenomenon at low temperature (a blocking temperature of 62 K). Cellulose/iron oxide clusters with an average size around 7 nm and characterized by high decomposition temperatures (around 645 °C) were proven to be responsible for the observed superparamagnetic phenomenon. The superiority of the ultrasonication process versus a procedure involving simple mechanical stirring, in terms of composite yield, dispersion uniformity of MG nanoparticles and magnetic properties is discussed.

Related Literature

Composition space of PtIrPdRhRu high entropy alloy nanoparticles synthesized by solvothermal reactions

Andreas Dueholm Bertelsen, Alexander Reinhardt Hansen, Nils Lau Nyborg Broge, Aref Mamakhel, Martin Bondesgaard, Bo Brummerstedt Iversen

2022-10-14 Communication

DOI: 10.1039/D2CC04827B

Synthesis of glycerol 1,2-carbonate by transesterification of glycerol with dimethyl carbonate using triethylamine as a facile separable homogeneous catalyst

Olga Gómez-Jiménez-Aberasturi, Camilo Ramírez-López, Belén Maestro-Madurga

2012-10-02 Paper

DOI: 10.1039/C2GC35992H

Facile access to 2-hydroxy-2-substituted indole-3-ones via a copper-catalyzed oxidative cyclization of 2-arylethynylanilines

Weiqiang Sun, Xueli Cui, Jing Qu, Xiaojia Cai, Jinhui Hu, Zhuang Xiong, Suqin Guo, Wen-Hua Chen, Jia-Qiang Wu

2023-05-15 Communication

DOI: 10.1039/D3CC01390A

Inside back cover

2023-09-27 Cover

DOI: 10.1039/D3SC90189K

C–H bond chlorination using nickel(ii) complexes of tetradentate amido-quinoline ligands

Sanjay Adhikari, Aniruddha Sarkar, Basab Bijayi Dhar

2022-02-28 Communication

DOI: 10.1039/D2CC00639A

Highly-oxidised, sulfur-rich, mixed-valence vanadium(iv/v) complexes

Michelle K. Taylor, David J. Evans, Charles G. Young

2006-09-05 Communication

DOI: 10.1039/B610036H

Machine learning for non-additive intermolecular potentials: quantum chemistry to first-principles predictions

Richard S. Graham, Richard J. Wheatley

2022-05-24 Communication

DOI: 10.1039/D2CC01820A

Water-in-salt electrolytes – molecular insights to the high solubility of lithium-ion salts

Aleksandar Tot, Lars Kloo

2022-08-01 Communication

DOI: 10.1039/D2CC03062D

Growing Co–Ni–Se nanosheets on 3D carbon frameworks as advanced dual functional electrodes for supercapacitors and sodium ion batteries

Mingyue Gao, Yanchun Xue, Yutang Zhang, Chengxing Zhu, Haiwei Yu, Xingmei Guo, Shasha Sun, Shenglin Xiong, Qinghong Kong, Junhao Zhang

2022-06-13 Research Article

DOI: 10.1039/D2QI00695B

You might also like

Compound Q&A

What are the main uses of 4-Nitrophenyl phosphate disodium salt hexahydrate (CAS: 333338-18-4)?

4-Nitrophenyl phosphate disodium salt hexahydrate is primarily used as a substra...

333338-18-44-Nitrophenyl phosph...
Compound Q&A

What are the main uses of 2-(Trifluoromethyl)-1,3-oxazole-4-carboxylic Acid (CAS: 1060816-01-4)?

2-(Trifluoromethyl)-1,3-oxazole-4-carboxylic Acid (CAS: 1060816-01-4) is widely ...

1060816-01-42-(Trifluoromethyl)-...
Compound Q&A

How should 2-Fluoro-4-biphenylcarboxylic acid (CAS: 137045-30-8) be stored?

2-Fluoro-4-biphenylcarboxylic acid should be stored in a cool, dry place at room...

137045-30-82-Fluoro-4-biphenylc...
Compound Q&A

What industries use Prednisolone-21-Carboxylic Acid (CAS: 61549-70-0)?

Prednisolone-21-Carboxylic Acid is primarily used in the pharmaceutical industry...

61549-70-0Prednisolone-21-Carb...
Compound Q&A

How should 4-(Hydrazinomethyl)-1,2,3-benzenetriol (CAS: 3614-72-0) be stored?

4-(Hydrazinomethyl)-1,2,3-benzenetriol (CAS: 3614-72-0) should be stored in a co...

3614-72-04-(Hydrazinomethyl)-...
Compound Q&A

What industries use 4-Amino-1-methyl-1H-pyrazole-5-carboxylic acid hydrochloride (CAS: 92534-70-8)?

4-Amino-1-methyl-1H-pyrazole-5-carboxylic acid hydrochloride (CAS: 92534-70-8) i...

92534-70-84-Amino-1-methyl-1H-...
Compound Q&A

What regulatory guidelines apply to dehydropachymic acid (CAS: 77012-31-8)?

Dehydropachymic acid (CAS: 77012-31-8) is regulated by various agencies. It fall...

77012-31-8Dehydropachymic acid
Compound Q&A

What is the market or research trend for 6-[(2,2-Dimethylpropanoyl)amino]nicotinic acid (CAS: 898561-66-5)?

The market and research trends for 6-[(2,2-Dimethylpropanoyl)amino]nicotinic aci...

898561-66-56-[(2,2-Dimethylprop...
Compound Q&A

How should 1,10-Phenanthroline-2,9-dicarbaldehyde (CAS: 57709-62-3) be stored?

1,10-Phenanthroline-2,9-dicarbaldehyde should be stored in a cool, dry place awa...

57709-62-31,10-Phenanthroline-...
Compound Q&A

How is 5-Carbamoyl-11-oxo-10,11-dihydro-5H-dibenzo[b,f]azepin-10-yl acetate (CAS: 113952-21-9) typically synthesized?

5-Carbamoyl-11-oxo-10,11-dihydro-5H-dibenzo[b,f]azepin-10-yl acetate can be synt...

113952-21-95-Carbamoyl-11-oxo-1...

Source Journal

Polymer Chemistry

Polymer Chemistry
CiteScore: 8.6
Self-citation Rate: 7.3%
Articles per Year: 457

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.

Recommended Compounds

Recommended Suppliers

Disclaimer
This page provides academic journal information for reference and research purposes only. We are not affiliated with any journal publishers and do not handle publication submissions. For publication-related inquiries, please contact the respective journal publishers directly.
If you notice any inaccuracies in the information displayed, please contact us at support@chemtradehub.com. We will promptly review and address your concerns.