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Nanomaterials · 2020 ·Vol. 10 ·期 4 ·755 · IF 4.324

Preparation and Properties of Cassava Residue Cellulose Nanofibril/Cassava Starch Composite Films

Lijie Huang,Hanyu Zhao,Tan Yi,Minghui Qi,Hao Xu,Qi Mo,Chongxing Huang,Shuangfei Wang,Yang Liu

Because of its non-toxic, pollution-free, and low-cost advantages, environmentally-friendly packaging is receiving widespread attention. However, using simple technology to prepare environmentally-friendly packaging with excellent comprehensive performance is a difficult problem faced by the world. This paper reports a very simple and environmentally-friendly method. The hydroxyl groups of cellulose nanofibrils (CNFs) were modified by introducing malic acid and the silane coupling agent KH-550, and the modified CNF were added to cassava starch as a reinforcing agent to prepare film with excellent mechanical, hydrophobic, and barrier properties. In addition, due to the addition of malic acid and a silane coupling agent, the dispersibility and thermal stability of the modified CNFs became significantly better. By adjusting the order of adding the modifiers, the hydrophobicity of the CNFs and thermal stability were increased by 53.5% and 36.9% ± 2.7%, respectively. At the same time, the addition of modified CNFs increased the tensile strength, hydrophobicity, and water vapor transmission coefficient of the starch-based composite films by 1034%, 129.4%, and 35.95%, respectively. This material can be widely used in the packaging of food, cosmetics, pharmaceuticals, and medical consumables.Keywords:cassava residue;cellulose nanofibril;modified;cassava starch;composite film;nanocomposite

CAS / MDL: 97-67-6
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CARBOHYDRATE POLYMERS · 2020 · IF 7.182

Boron nitride–nanosheet enhanced cellulose nanofiber aerogel with excellent thermal management properties

Ya Liu,Yipeng Zhang,Tougen Liao,Li Gao,Meng Wang,Xu Xu,Xinxin Yang,He Liu

Boron nitride nanosheets (BNNSs) are desirable materials for thermal management applications owing to their excellent thermal conductivity. Such property also related to the increased thermal transfer efficiency per unit mass, which can be improved by constructing three-dimensional (3D) structures. Cellulose nanofibers (CNFs) are often used to prepare 3D skeletons and stabilize the dispersion of inorganic fillers. Therefore, CNF/BNNS aerogels were prepared to disperse BNNS in a 3D network. CNF/BNNS aerogel exhibited a thermal conductivity of 0.57 W m −1  K −1 , which is an enhancement of 443 % compared to 0.105 W m −1  K −1 of CNF aerogel. The surface temperature changes of the aerogels were confirmed a strong thermal management capacity. The BNNSs also resulted in the compressive strength increased from 0.25 MPa (CNF aerogel) to 0.37 MPa (CNF/BNNS aerogel). This study provides an effective strategy for the preparation of cellulose-based nanocomposite aerogels with excellent thermal management properties and mechanical properties.

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CHINESE JOURNAL OF CHEMISTRY · 2020 ·Vol. 38 ·期 5 ·494-500 · IF 3.826

Reinforcement of Self-Healing Polyacrylic Acid Hydrogel with Acrylamide Modified Microcrystalline Cellulose†

Changzhuang Bai,Qiuhua Huang,Xiaopeng Xiong

Summary of main observation and conclusion Self-healing hydrogel such as polyacrylic acid (PAA) hydrogel has attracted increasing attention based on its promising potential applications. However, it usually suffers from low strength especially as mechanical device. Herein, a commercial microcrystalline cellulose (MCC) was modified with acrylamide to graft polyacrylamide (PAM) chains on the particle surface. The acrylamide-modified MCC (AM-MCC) was then dispersed in monomer solution of acrylic acid to prepare composite hydrogel. The mechanical properties of the obtained composite hydrogels and the self-healed hydrogels were carefully measured by compressive and tensile tests, and by dynamic mechanical analysis. Our results demonstrate that introduction of a small amount of AM-MCC such as 3 wt% can not only reinforce the original hydrogel and the healed hydrogel markedly, but also improve self-healing efficiency obviously. The analyses indicate that in addition to the reversible multi-interactions such as hydrogen bonding and ionic interactions, the entanglements between the PAA chains of the hydrogel matrix and the PAM chains grafted on the MCC particles have also played an important role on the improvement in mechanical performances and the healing ability of the hydrogel. Moreover, the responsiveness to exterior ion has been tested to indicate potential application of the composite hydrogel as self-healable sensor.

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BIOMACROMOLECULES · 2020 · IF 6.092

Effect of Sugars on the Real-Time Adsorption of Expansin on Cellulose

Peiqian Zhang,Yuanyuan Ma,Mei Cui,Jieying Wang,Renliang Huang,Rongxin Su,Wei Qi,Zhimin He,Wim Thielemans

Biological pretreatment is a safe and environmentally friendly method for disrupting recalcitrant lignocellulose structures. Expansin and expansin-like proteins are used to open up the cellulose structure and display significant synergism when mixed with cellulases that catalyze the breakdown of (hemi)cellulose into sugars. However, the adsorption behavior of expansin in the presence of sugar products is yet unknown. In this work, we monitored the effects of various sugars on the real-time adsorption of Bacillus subtilis expansin (BsEXLX1) onto cellulose films using a quartz crystal microbalance with dissipation. Cellobiose and xylose at low concentrations enhanced BsEXLX1 adsorption, whereas they disrupted adsorption at higher concentrations. Arabinose and mannose continuously inhibited expansin adsorption with increasing concentration. No obvious influence of glucose and galactose on BsEXLX1 adsorption was found. Contact angle measurements and atomic force microscopy of cellulose upon BsEXLX1 adsorption in the presence of sugars showed that both hydrophilicity and roughness increased with BsEXLX1 treatment. These results give us the ability to modulate and control expansin adsorption and provide insights into effective expansin use during enzymatic hydrolysis of lignocellulose in biorefineries.

CAS / MDL: 528-50-7 28072-80-2
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2020 · IF 5.162

N-halamine modified multiporous bacterial cellulose with enhanced antibacterial and hemostatic properties

Shumin Zhang,Lin Li,Xuehong Ren,Tung-Shi Huang

Bacterial cellulose (BC) is a natural polymer with remarkable superiority for fabricating biomaterials. In this study, a multiporous bacterial cellulose (MBC) film was modified with N-isopropylacrylamide (NIPAM), and the modified MBC film was imbued with antibacterial properties after chlorination. The dried chlorinated samples showed superb antibacterial efficacy and could inactivate 6.19 log of inoculated S. aureus and 6.29 log of E. coli within 1 min of contact. After releasing active chlorine for 12 h, 3.67 log of S. aureus and 3.97 log of E. coli were inactivated within 30 min of contact. The prepared films displayed high porous and layered structures with a resultant excellent water retention which can be applied as material for wound dressings. In addition, the chlorinated films showed hemostatic ability on wound bleeding and good biocompatibility. The prepared N-halamine functionalized MBC films might have great potential applications as wound dressings.

CAS / MDL: 7758-19-2
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Journal of Materials Chemistry C · 2020 ·Vol. 8 ·期 24 ·8234-8242 · IF 7.059

A transparent and adhesive carboxymethyl cellulose/polypyrrole hydrogel electrode for flexible supercapacitors

Ya Cheng,Xiuyan Ren,Lijie Duan,Guanghui Gao

Flexible supercapacitors have attracted increasing attention due to their unique soft and capacitive properties. However, for a conductive polymer-based electrode material, the mechanical properties, conductivity and the interface bonding with the electrolyte are all challenging. Here, polypyrrole (PPy) hydrogel electrodes with high stretchability (over 700%), electrical conductivity (11.07 S m−1) and interfacial bonding properties were prepared by doping carboxymethyl cellulose (CMC). Due to the emulsification effect of CMC, PPy could form hydrophilic CMC/PPy fibers in aqueous solutions. Moreover, during the formation process of the PPy hydrogel, uniformly distributed CMC/PPy particles were obtained in situ, resulting in the unique visible light transmission and ultraviolet shielding characteristics of the PPy hydrogel. As a flexible electrode, the PPy hydrogels were assembled into an all-solid-state supercapacitor, which exhibited a specific capacitance of 126.38 F g−1 and excellent cyclic stability (capacitance retention of 82% after 1000 cycles). This facile method of preparing transparent PPy hydrogels can pave a new way for constructing capacitive electronic skins.

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Nano-Micro Letters · 2020 ·Vol. 12 ·期 1 ·1-17 · IF 12.264

An Ultra-microporous Carbon Material Boosting Integrated Capacitance for Cellulose-Based Supercapacitors

Ding Chenfeng,Liu Tianyi,Yan Xiaodong,Huang Lingbo,Ryu Seungkon,Lan Jinle,Yu Yunhua,Zhong Wei-Hong,Yang Xiaoping

An ultra-microporous carbon material simultaneously with high specific surface area (1554 m 2  g −1 ) and packing density (1.18 g cm −3 ) is designed and fabricated. The resulting carbon material integrates the high gravimetric and volumetric capacitance (430 F g −1 and 507 F cm −3 at 0.5 A g −1 ) and thereof provides the robust all-solid-state cellulose supercapacitor with high areal and volumetric density.

CAS / MDL: 872-50-4 24937-79-9
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International Journal of Bioprinting · 2021 · IF 6.638

Cellulose Nanocrystal-Enhanced Thermal-Sensitive Hydrogels of Block Copolymers for 3D Bioprinting

Yuecheng Cui,Ronghua Jin,Yifan Zhang,Meirong Yu,Yang Zhou,Li-Qun Wang

The hydrogel formed by polyethylene glycol-aliphatic polyester block copolymers is an ideal bioink and biomaterial ink for three-dimensional (3D) bioprinting because of its unique temperature sensitivity, mild gelation process, good biocompatibility, and biodegradability. However, the gel forming mechanism based only on hydrophilic-hydrophobic interaction renders the stability and mechanical strength of the formed hydrogels insufficient, and cannot meet the requirements of extrusion 3D printing. In this study, cellulose nanocrystals (CNC), which is a kind of rigid, hydrophilic, and biocompatible nanomaterial, were introduced to enhance the hydrogels so as to meet the requirements of extrusion 3D printing. First, a series of poly( ε -caprolactone/lactide)- b -poly(ethylene glycol)- b -poly( ε -caprolactone/lactide) (PCLA-PEG-PCLA) triblock copolymers with different molecular weights were prepared. The thermodynamic and rheological properties of CNC-enhanced hydrogels were investigated. The results showed that the addition of CNC significantly improved the thermal stability and mechanical properties of the hydrogels, and within a certain range, the enhancement effect was directly proportional to the concentration of CNC. More importantly, the PCLA-PEG-PCLA hydrogels enhanced by CNC could be extruded and printed through temperature regulation. The printed objects had high resolution and fidelity with effectively maintained structure. Moreover, the hydrogels have good biocompatibility with a high cell viability. Therefore, this is a simple and effective strategy. The addition of the hydrophilic rigid nanoparticles such as CNC improves the mechanical properties of the soft hydrogels which made it able to meet the requirements of 3D bioprinting.

CAS / MDL: 502-44-3 9001-62-1
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Polymers · 2021 ·Vol. 13 ·期 13 ·2142 · IF 4.329

Fabrication and Application of SERS-Active Cellulose Fibers Regenerated from Waste Resource

Shengjun Wang,Jiaqi Guo,Yibo Ma,Alan X. Wang,Xianming Kong,Qian Yu

The flexible SERS substrate were prepared base on regenerated cellulose fibers, in which the Au nanoparticles were controllably assembled on fiber through electrostatic interaction. The cellulose fiber was regenerated from waste paper through the dry-jet wet spinning method, an eco-friendly and convenient approach by using ionic liquid. The Au NPs could be controllably distributed on the surface of fiber by adjusting the conditions during the process of assembling. Finite-difference time-domain theoretical simulations verified the intense local electromagnetic fields of plasmonic composites. The flexible SERS fibers show excellent SERS sensitivity and adsorption capability. A typical Raman probe molecule, 4-Mercaptobenzoicacid (4-MBA), was used to verify the SERS cellulose fibers, the sensitivity could achieve to 10−9M. The flexible SERS fibers were successfully used for identifying dimetridazole (DMZ) from aqueous solution. Furthermore, the flexible SERS fibers were used for detecting DMZ from the surface of fish by simply swabbing process. It is clear that the fabricated plasmonic composite can be applied for the identifying toxins and chemicals.Keywords:regenerated cellulose fiber;Au NP;controllably assembled;SERS;dimetridazole

CAS / MDL: 551-92-8
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CELLULOSE · 2021 ·Vol. 28 ·期 12 ·7735-7748 · IF 5.044

Degradation mechanism of green biopolyester nanocomposites with various cellulose nanocrystal based nanohybrids

Lu Gaojun,Zhu Jingli,Yu Houyong,Jin Meijin,Abdalkarim Somia Yassin Hussain,Wei Yong

Oceans and soils have been contaminated with traditional plastic due to its lack of degradability. Therefore, green biopolymer composites reinforced with cellulose nanocrystal-zinc oxide hybrids (ZnO hybrids) with good biodegradation ability provided a positive impact on reducing environmental challenges. In this work, the effect of various morphologies of ZnO hybrids on the biodegradation ability of poly(butylene adipate-co-terephthalate), PBAT) under seawater, soil burial, and UV aging conditions were investigated. Sheet-like ZnO hybrids (s-ZnO hybrid) efficiently enhanced the mechanical, UV-blocking properties and biodegradation ability of PBAT nanocomposite films. Compared to neat PBAT, the best tensile strength of PBAT nanocomposite with 2 wt% s-ZnO hybrid was increased by 15.1%, meanwhile this nanocomposite films showed the highest biodegradation rate after 80 days of soil degradation and 90 days of seawater degradation. Besides, three possible biodegradation mechanisms of green PBAT nanocomposite films were presented, hinting that such PBAT nanocomposite have great promising packaging applications. Graphic abstract

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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES · 2021 · IF 6.953

Facile transformation of carboxymethyl cellulose beads into hollow composites for dye adsorption

Hua-Rong Yang,Shan-Shan Li,Qing-Da An,Shang-Ru Zhai,Zuo-Yi Xiao,Li-Ping Zhang

Novel millimeter hollow microspheres were fabricated from carboxymethyl cellulose microspheres and polyethyleneimine using glutaraldehyde as a crosslinking agent. The hollow microspheres prepared with different polyethyleneimine usages and different polyethyleneimine treatment time were investigated deeply and characterized via SEM-EDX, FT-IR, and BET surface area analysis. It was shown that polyethyleneimine could break the coordination bonds between the carboxyl and Al (III) in carboxymethyl cellulose microspheres, leading to the formation of hollow structures. Most importantly, the usage and treatment time of polyethyleneimine can distinctly tailor the structure of the carboxymethyl cellulose microspheres, resulting in the formation of different hollow microspheres with varied shell thickness and size. Most importantly, we found that the prepared hollow microspheres have excellent adsorption performance toward targeted methyl blue under testing conditions. By virtue of the large accessible amount of -NH 2 groups and its unique hollow structure, this type of millimeter hollow microspheres have broad application prospects in the treatment of emerging contaminants in wastewater.

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MOLECULES · 2021 ·Vol. 26 ·期 16 ·5003 · IF 4.412

Fabrication and Evaluation of Alginate/Bacterial Cellulose Nanocrystals–Chitosan–Gelatin Composite Scaffolds

Zhengyue Li,Xiuqiong Chen,Chaoling Bao,Chang Liu,Chunyang Liu,Dongze Li,Huiqiong Yan,Qiang Lin

It is common knowledge that pure alginate hydrogel is more likely to have weak mechanical strength, a lack of cell recognition sites, extensive swelling and uncontrolled degradation, and thus be unable to satisfy the demands of the ideal scaffold. To address these problems, we attempted to fabricate alginate/bacterial cellulose nanocrystals-chitosan-gelatin (Alg/BCNs-CS-GT) composite scaffolds using the combined method involving the incorporation of BCNs in the alginate matrix, internal gelation through the hydroxyapatite-d-glucono-δ-lactone (HAP-GDL) complex, and layer-by-layer (LBL) electrostatic assembly of polyelectrolytes. Meanwhile, the effect of various contents of BCNs on the scaffold morphology, porosity, mechanical properties, and swelling and degradation behavior was investigated. The experimental results showed that the fabricated Alg/BCNs-CS-GT composite scaffolds exhibited regular 3D morphologies and well-developed pore structures. With the increase in BCNs content, the pore size of Alg/BCNs-CS-GT composite scaffolds was gradually reduced from 200 μm to 70 μm. Furthermore, BCNs were fully embedded in the alginate matrix through the intermolecular hydrogen bond with alginate. Moreover, the addition of BCNs could effectively control the swelling and biodegradation of the Alg/BCNs-CS-GT composite scaffolds. Furthermore, the in vitro cytotoxicity studies indicated that the porous fiber network of BCNs could fully mimic the extracellular matrix structure, which promoted the adhesion and spreading of MG63 cells and MC3T3-E1 cells on the Alg/BCNs-CS-GT composite scaffolds. In addition, these cells could grow in the 3D-porous structure of composite scaffolds, which exhibited good proliferative viability. Based on the effect of BCNs on the cytocompatibility of composite scaffolds, the optimum BCNs content for the Alg/BCNs-CS-GT composite scaffolds was 0.2% (w/v). On the basis of good merits, such as regular 3D morphology, well-developed pore structure, controlled swelling and biodegradation behavior, and good cytocompatibility, the Alg/BCNs-CS-GT composite scaffolds may exhibit great potential as the ideal scaffold in the bone tissue engineering field.Keywords:alginate;bacterial cellulose nanocrystals;internal gelation;layer-by-layer electrostatic assembly;composite scaffolds;bone tissue engineering

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