Aqueous Polymer Modification of Cellulose Nanofibrils by Grafting‐Through a Reactive Methacrylate Group

The rheological and mechanical properties of crosslinked polymer gels arise from the structure of the gel network. In turn, the structure of the gel network results from: thermodynamically determined interactions between the polymer chain segments, the interactions of the crosslinking metal ion with the polymer, and the deformation history of the network. Interpretations of mechanical and rheological measurements on polymer gels invariably begin with a conceptual model of,the microstructure of the gel network derived from polymer kinetic theory. In the present work, we use freeze-etch replication TEM to image the polymer network morphology of titanium crosslinked hydroxypropyl guars in an attempt to directly relate macroscopic phenomena with network structure.

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Facile preparation of nanofiller-paper using mixed office paper without deinking

TAPPI Journal ◽

10.32964/tj14.3.167 ◽

2015 ◽

Vol 14 (3) ◽

pp. 167-174 ◽

Cited By ~ 8

Author(s):

QIANQIAN WANG ◽

J.Y. ZHU

Keyword(s):

Cellulose Nanofibrils ◽

Ash Content ◽

Raw Material ◽

Mechanical Grinding ◽

Microscope Imaging ◽

Facile Preparation ◽

Electron Microscope Imaging ◽

Thermal Stability Of ◽

Scanning Electron ◽

Office Paper

Mixed office paper (MOP) pulp without deinking with an ash content of 18.1 ± 1.5% was used as raw material to produce nanofiller-paper. The MOP pulp with filler was mechanically fibrillated using a laboratory stone grinder. Scanning electron microscope imaging revealed that the ground filler particles were wrapped by cellulose nanofibrils (CNFs), which substantially improved the incorporation of filler into the CNF matrix. Sheets made of this CNF matrix were densified due to improved bonding. Specific tensile strength and modulus of the nanofiller-paper with 60-min grinding reached 48.4 kN·m/kg and 8.1 MN·m/kg, respectively, approximately 250% and 200% of the respective values of the paper made of unground MOP pulp. Mechanical grinding duration did not affect the thermal stability of the nanofiller-paper.

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An effective method for determining the retention and distribution of cellulose nanofibrils in paper handsheets by dye labeling

TAPPI Journal ◽

10.32964/tj17.03.157 ◽

2018 ◽

Vol 17 (03) ◽

pp. 157-164 ◽

Cited By ~ 3

Author(s):

Shengdan Wang ◽

Wenhua Gao ◽

Kefu Chen ◽

Jinsong Zeng ◽

Jun Xu ◽

...

Keyword(s):

Correlation Coefficient ◽

Congo Red ◽

Kraft Pulp ◽

Cellulose Nanofibrils ◽

Standard Curve ◽

Congo Red Dye ◽

Mechanical Disintegration ◽

Softwood Kraft Pulp ◽

White Water ◽

Red Dye

Cellulose nanofibrils (CNF) were prepared by cellulase in conjunction with mechanical disintegration from the bleached softwood kraft pulp and labelled by Congo red dye. The labelled CNF were used to investigate the retention and distribution of CNF in paper handsheets. The retention of the labelled CNF was obtained by measuring the absorbance of white water using an ultraviolet-visible spectrophotometer. The results showed that this method for measuring the retention was rapid, feasible, and sensitive, owing to the high correlation coefficient R2 (0.9993) of the standard curve. The labelled CNF showed even distribution in paper handsheets. The colorimetric values of paper handsheets were explored with a residual ink analyzer.

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Functional Poly(p-Xylylene)s via Chemical Reduction of Poly(p-Phenylene Vinylene)s

10.26434/chemrxiv.9868196.v1 ◽

2019 ◽

Cited By ~ 1

Author(s):

Ain Uddin ◽

Weifan Sang ◽

Yong Gao ◽

Kyle Plunkett

Keyword(s):

Film Formation ◽

Chemical Reduction ◽

Water Soluble ◽

Phenylene Vinylene ◽

Polymer Modification ◽

Polymer Backbone ◽

Crosslinking Process ◽

Conducting Membranes ◽

In Situ Crosslinking

The synthesis of poly(p-xylylene)s (PPXs) with sidechains containing alkyl bromide functionality, and their post-polymer modification, is described. The PPXs were prepared by a diimide hydrogenation of poly(p-phenylene vinylene)s (PPVs) that were originally synthesized by a Gilch polymerization. The polymer backbone reduction was carried out with hydrazine hydrate in toluene at 80 °C to provide polymers with the sidechain-containing bromide functionality intact. To demonstrate post-polymer modification of the sidechains, the resulting PPX polymers were modified with trimethylamine to form tetraalkylammonium ion functionality and were evaluated as anion conducting membranes. While PPX homopolymers containing tetralkylammonium ions were completely water soluble and not able to form valuable films, PPX copolymers containing mixed tetraalkylammonium ions and hydrophobic chains were capable of film formation and alkaline stability. In addition, an in situ crosslinking process that used N,N,N',N'-tetramethyl-1,6-hexanediamine during the tetraalkylammonium formation of brominated PPX polymers was also evaluated and gave reasonable films with conductivities of ~10 mS-cm-1.

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Functional Poly(p-Xylylene)s via Chemical Reduction of Poly(p-Phenylene Vinylene)s

10.26434/chemrxiv.9868196 ◽

2019 ◽

Author(s):

Ain Uddin ◽

Weifan Sang ◽

Yong Gao ◽

Kyle Plunkett

Keyword(s):

Film Formation ◽

Chemical Reduction ◽

Water Soluble ◽

Phenylene Vinylene ◽

Polymer Modification ◽

Polymer Backbone ◽

Crosslinking Process ◽

Conducting Membranes ◽

In Situ Crosslinking

The synthesis of poly(p-xylylene)s (PPXs) with sidechains containing alkyl bromide functionality, and their post-polymer modification, is described. The PPXs were prepared by a diimide hydrogenation of poly(p-phenylene vinylene)s (PPVs) that were originally synthesized by a Gilch polymerization. The polymer backbone reduction was carried out with hydrazine hydrate in toluene at 80 °C to provide polymers with the sidechain-containing bromide functionality intact. To demonstrate post-polymer modification of the sidechains, the resulting PPX polymers were modified with trimethylamine to form tetraalkylammonium ion functionality and were evaluated as anion conducting membranes. While PPX homopolymers containing tetralkylammonium ions were completely water soluble and not able to form valuable films, PPX copolymers containing mixed tetraalkylammonium ions and hydrophobic chains were capable of film formation and alkaline stability. In addition, an in situ crosslinking process that used N,N,N',N'-tetramethyl-1,6-hexanediamine during the tetraalkylammonium formation of brominated PPX polymers was also evaluated and gave reasonable films with conductivities of ~10 mS-cm-1.

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Cellulose Nanofibrils-based Hydrogels for Biomedical Applications: Progresses and Challenges

Current Medicinal Chemistry ◽

10.2174/0929867327666200303102859 ◽

2020 ◽

Vol 27 (28) ◽

pp. 4622-4646 ◽

Cited By ~ 1

Author(s):

Huayu Liu ◽

Kun Liu ◽

Xiao Han ◽

Hongxiang Xie ◽

Chuanling Si ◽

...

Keyword(s):

Mechanical Properties ◽

Metal Ion ◽

Biomedical Applications ◽

Biomedical Application ◽

Cellulose Nanofibrils ◽

Wound Dressings ◽

Preparation Methods ◽

Tissue Scaffold ◽

Surface Areas ◽

Mechanical Methods

Background: Cellulose Nanofibrils (CNFs) are natural nanomaterials with nanometer dimensions. Compared with ordinary cellulose, CNFs own good mechanical properties, large specific surface areas, high Young's modulus, strong hydrophilicity and other distinguishing characteristics, which make them widely used in many fields. This review aims to introduce the preparation of CNFs-based hydrogels and their recent biomedical application advances. Methods: By searching the recent literatures, we have summarized the preparation methods of CNFs, including mechanical methods and chemical mechanical methods, and also introduced the fabrication methods of CNFs-based hydrogels, including CNFs cross-linked with metal ion and with polymers. In addition, we have summarized the biomedical applications of CNFs-based hydrogels, including scaffold materials and wound dressings. Results: CNFs-based hydrogels are new types of materials that are non-toxic and display a certain mechanical strength. In the tissue scaffold application, they can provide a micro-environment for the damaged tissue to repair and regenerate it. In wound dressing applications, it can fit the wound surface and protect the wound from the external environment, thereby effectively promoting the healing of skin tissue. Conclusion: By summarizing the preparation and application of CNFs-based hydrogels, we have analyzed and forecasted their development trends. At present, the research of CNFs-based hydrogels is still in the laboratory stage. It needs further exploration to be applied in practice. The development of medical hydrogels with high mechanical properties and biocompatibility still poses significant challenges.

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Humidity‐Induced Nanoscale Restructuring in PEDOT:PSS and Cellulose Nanofibrils Reinforced Biobased Organic Electronics

Advanced Electronic Materials ◽

10.1002/aelm.202100137 ◽

2021 ◽

pp. 2100137

Author(s):

Calvin J. Brett ◽

Ola K. Forslund ◽

Elisabetta Nocerino ◽

Lucas P. Kreuzer ◽

Tobias Widmann ◽

...

Keyword(s):

Organic Electronics ◽

Cellulose Nanofibrils

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Superelastic and flexible 3D printed waterborne polyurethane/cellulose nanofibrils structures

Additive Manufacturing ◽

10.1016/j.addma.2021.102107 ◽

2021 ◽

pp. 102107

Author(s):

Yuan Chen ◽

Zhengyang Yu ◽

Hale Oguzlu ◽

Jungang Jiang ◽

MiJung Cho ◽

...

Keyword(s):

Cellulose Nanofibrils ◽

Waterborne Polyurethane ◽

3D Printed

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Thermal Behaviour of Common Thermoresponsive Polymers in Phosphate Buffer and in Its Salt Solutions

Polymers ◽

10.3390/polym13010090 ◽

2020 ◽

Vol 13 (1) ◽

pp. 90

Author(s):

Łukasz Otulakowski ◽

Maciej Kasprów ◽

Aleksandra Strzelecka ◽

Andrzej Dworak ◽

Barbara Trzebicka

Keyword(s):

Thermal Behaviour ◽

Phosphate Buffer ◽

Pure Water ◽

Thermal Response ◽

The Body ◽

Solution Temperature ◽

Thermoresponsive Polymers ◽

Aqueous Polymer ◽

Cloud Point Temperature ◽

Size Of Particles

Thermoresponsive polymers are a promising material for drug nanocarrier preparation, which makes the study of their aggregation in physiological conditions very important. In this paper, the thermal behaviour of the thermoresponsive polymers poly(N-isopropylacrylamide), poly(2-isopropyl-2-oxazoline-co-2-n-propyl-2-oxazoline) and poly[(2-hydroxyethyl methacrylate)-co-oligo(ethylene glycol) methyl ether methacrylate] were studied in phosphate buffer (PBS) and solutions of its salts in concentration as in PBS. The thermal response of the polymers was measured using UV-Vis and dynamic light scattering (DLS). The salts shifted the cloud point temperature (TCP) of the (co)polymers to higher values compared to the TCP of aqueous polymer solutions. In PBS and NaCl solutions, all polymers exhibited an unexpected and previously unreported transmittance profile. During heating, an additional aggregation of polymers appeared above the TCP accompanied by the formation of a precipitate. In monosodium phosphate solutions and pure water, the studied polymers showed lower critical solution temperature (LCST-type) behaviour. DLS measurements showed that a salt influenced the size of the resulting polymer particles. The sizes and stability of particles depended on the heating rate. In PBS and NaCl solutions, the size of particles in the dispersion decreased above 60 °C, and the precipitate appeared on the bottom of the cuvette. The additional aggregation of polymer and its falling out of solution may hinder the removal of carriers from the body and has to be taken into account when preparing nanocarriers.

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Layer-by-Layer Spray-Coating of Cellulose Nanofibrils and Silver Nanoparticles for Hydrophilic Interfaces

ACS Applied Nano Materials ◽

10.1021/acsanm.0c02819 ◽

2021 ◽

Author(s):

Qing Chen ◽

Calvin J. Brett ◽

Andrei Chumakov ◽

Marc Gensch ◽

Matthias Schwartzkopf ◽

...

Keyword(s):

Silver Nanoparticles ◽

Cellulose Nanofibrils ◽

Spray Coating ◽

Layer By Layer

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