Photoinduced Metal-Free Atom Transfer Radical Polymerization for the Modification of Cellulose with Poly(-isopropylacrylamide) to Create Thermo-Responsive Injectable Hydrogels.

Photoinduced metal-free ATRP has been successfully applied to fabricate thermo-responsive cellulose graft copolymer (PNIPAM--Cell) using 2-bromoisobuturyl bromide-modified cellulose as the macroinitiator. The polymerization of N-isopropylacrylamide (NIPAM) from cellulose was efficiently activated and deactivated with UV irradiation in the presence of an organic-based photo-redox catalyst. Both FTIR and C NMR analysis confirmed the structural similarity between the obtained PNIPAM--Cell and that synthesized via traditional ATRP methods.

Structural changes of hemicellulose during pulping process and its interaction with nanocellulose.

It is believed that hemicellulose plays a crucial role in binding cellulose and lignin in plant cells. It may provide significant implications through figuring out the interaction between hemicellulose and microfibers and gaining insights how the structure of hemicellulose affects its association with cellulose nanofibers. Herein, the hemicellulose and nanocellulose fractions from pulps obtained by controlling the H-factors of kraft pulping process were quantitatively evaluated for their adsorption behavior using QCM-D.

Fabrication of Low-Temperature Fast Gelation β-Cyclodextrin-Based Hydrogel-Loaded Medicine for Wound Dressings.

β-Cyclodextrin (β-CD) is often used as a drug carrier for biomedical materials due to its unique cavity structure. Herein, β-CD was modified by acryloyl chloride and further copolymerized with -isopropylacrylamide (NIPAM) and acrylic acid (AA) to obtain PNIPAMβ-CD-AC. The results showed that the critical phase transition temperature of PNIPAM/β-CD-AC could be controlled at 19 °C, and the fast sol-gel phase transition was realized in 2-10 s.

Core-Shell Structured Magnetic Carboxymethyl Cellulose-Based Hydrogel Nanosorbents for Effective Adsorption of Methylene Blue from Aqueous Solution.

This article reports effective removal of methylene blue (MB) dyes from aqueous solutions using a novel magnetic polymer nanocomposite. The core-shell structured nanosorbents was fabricated via coating FeO nanoparticles with a layer of hydrogel material, that synthesized by carboxymethyl cellulose cross-linked with poly(acrylic acid-co-acrylamide). Some physico-chemical properties of the nanosorbents were characterized by various testing methods.

Cellulose-based thermo-enhanced fluorescence micelles.

Recently, cellulose-based stimuli-responsive nanomaterials have received significant attention because of its natural source and biocompatibility. In this study, cellulose-graft-poly(nisopropylacrylamide)-co-2-methyl-acrylic acid 2-carbazol-9-yl-ethyl ester (cellulose-g-(PNIPAAm&PCz)) block polymers were successfully synthesized by homogeneous atom transfer radical polymerization (ATRP) in LiCl/N,N-dimethylacetamide (DMAc) dissolution system. The block polymers showed different properties due to the different PCz content.

Enhanced degradation of Acid Red 73 by using cellulose-based hydrogel coated FeO nanocomposite as a Fenton-like catalyst.

Carboxymethyl cellulose-based hydrogel coated FeO magnetic nanoparticles were prepared using a coprecipitation combining graft copolymerization method, and characterized by various techniques to study their structure-property relationships. The nanocomposite was used as a heterogeneous Fenton-like catalyst for Acid Red 73 degradation. The effects of several key parameters, solution pH, HO concentration, catalyst dosage, and temperature of the reaction medium on the pseudo-first-order kinetics of dye degradation was evaluated.