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Journal of Cleaner Production · 2024 · IF 9.7

Molecular dissociation of DTMS tailoring cellulose regeneration and hydrophobic modification for building highly transparent cellulose films

Chengling Huang,Youjie Gao,Yi Chen,Yunfei Shen,Hou-Yong Yu

Earth has become depleted of oil and has suffered from the misuse of non-biodegradable plastics. Significant efforts have been dedicated to addressing the application flaws of cellulose as a substitute for plastics derived from petroleum. One of key defects was non-hydrophobic nature which highly influenced the mechanical properties of cellulose material during practical uses. Here, an innovative method was proposed to achieve hydrophobic modification of cellulose films through the molecular dissociation of dodecyltrimethoxysilane (DTMS) without the use of any toxic agents during the cellulose regeneration process. The hydrophobic (water contact angle of 118°), transparent (transmittance of 85%), and high-strength (70 MPa) DC films (cellulose films modified by DTMS) were successfully fabricated via cellulose regeneration process tailored by DTMS after molecular dissociation. The DC films stood out in both hydrophobicity and strength compared with several commercial plastics and the possible hydrophobic mechanism was proposed. Furthermore, the obsession with smart sensing abilities in DC films has made it a potential tool for monitoring baby diapers. Therefore, unlike conventional concepts, the methodology we adopted is simple and efficient, and it also eliminates the need for cellulose and replaces it with plastics.

研究领域: 材料科学 · 化学工程
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Polymers · 2025 ·Vol. 17 ·期 16 ·2179 · IF 4.9

Tough Hydrogel Reinforced by Meta-Aramid Nanofibers for Flexible Sensors

Zhiwen Hou,Yongzheng Li,Donghao Zhang,Cun Peng,Yan Wang,Kunyan Sui

Hydrogels exhibit significant promise for advanced flexible sensing applications owing to their intrinsic softness, biocompatibility, and customizable functionalities. Nevertheless, their limited mechanical strength poses a critical barrier to practical implementation. In this study, we engineered a mechanically robust alginate/chitosan (SA/CS) hydrogel reinforced with meta-aramid (PMIA) nanofibers. The resulting composite hydrogel achieves a tensile strength of 16.8 MPa, substantially exceeding the performance of conventional biomass-derived hydrogels. When employed as a flexible sensor, the hydrogel demonstrates exceptional pressure-sensing capabilities, featuring high sensitivity (178.41 MΩ/MPa below 5 kPa), rapid response kinetics (0.4–0.8 s), and sustained stability (>200 cycles). Leveraging these properties, we successfully monitored vocal cord vibrations and finger motion trajectories, highlighting their potential for biomechanical sensing applications.

CAS / MDL: 127-19-5
研究领域: 生物医学工程 · 材料科学 · 柔性电子器件
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Journal of Materials Chemistry A · 2022 ·Vol. 10 ·期 40 ·21379-21389 · IF 14.511

Ultrastrong, flame-retardant, intrinsically weldable, and highly conductive metallized Kevlar fabrics

Xi Lu,Yusheng Ye,Wenhui Shang,Simin Huang,Haifei Wang,Tiansheng Gan,Guokang Chen,Libo Deng,Qixing Wu,Xuechang Zhou

Conductive textiles are promising components for next-generation wearable electronics. However, it is still a challenge for current conductive textiles and wearable electronic devices to survive in harsh environments, such as extreme mechanical damages and low/high-temperature stresses. Herein, we report ultrastrong, flame-retardant, intrinsically weldable, and highly conductive metallized Kevlar fabrics (MKFs) fabricated via polymer-assisted electroless deposition (ELD) and electrodeposition (ED) techniques. The combination of ELD and ED techniques effectively metallizes the Kevlar fabrics, enabling ultrahigh conductivity (sheet resistance <0.007 Ω sq−1). More importantly, the deposited metal layers significantly enhance the anti-impact properties of Kevlar fabrics by 2–3 times. Due to the inherent properties of Kevlar and effective metal coatings, the MKFs maintain conductivity while suffering various mechanical damages (GPa-scale tensile strength, cutting, sticking, etc.), high temperatures (∼300 °C), and even flame stresses. Surprisingly, the MKFs show intrinsic weldability with traditional solder materials. The multifunctional applications of such high-performance metallized fabrics are demonstrated as textile-based conductors, heaters, and supercapacitors, all of which could survive in extremely harsh conditions.

研究领域: 材料科学 · 纺织工程 · 电子工程
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ADVANCED MATERIALS · 2024 · IF 27.4

Hydrogen Bond Mediated Strong Plasticization for High Performance Alginate Plastics

Hao Yan,Junsheng Wang,Cong Du,Zheng Li,Hua Yuan,Zhen Xu,Yeqiang Tan

The increasingly severe plastic pollution has urged an inevitable trend to develop biodegradable plastic products that can take over synthetic plastics. As one of the most abundant natural polymers, polysaccharides is an ideal candidate to substitute synthetic plastics. The rigidity of polysacchride chains principally allows high strength and stiffness of their materials, however, challenges the facile orientation in material processing. Here, a general hydrogen bond mediated plasticization strategy to regulate isotropic sodium alginate (SA) chains to highly ordered state is developed, and alginate plastics with high performances is fabricated. It is revealed that hydroxyl groups in glycerol modulate the viscoelasticity of SA solids by forming strong hydrogen bonds with SA chains, achieving a large stretchability at high solid content. Highly orientated alginate films exhibit superior tensile strength of 575 MPa and toughness of 60.7 MJ/m 3 , outperforming most regenerated biomass films. The high solid content and large stretchability mediated by strong hydrogen bonding ensure plastic molding of solid-like SA with high fidelity. This hydrogen bond mediated plasticity provides a facile but effective method to justify the high performances of polysaccharide-based plastics. This article is protected by copyright. All rights reserved

研究领域: 材料科学 · 生物学
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CARBOHYDRATE POLYMERS · 2017 · IF 4.811

High strength, biocompatible hydrogels with designable shapes and special hollow-formed character using chitosan and gelatin

Shuiping Wu,Hua Dong,Qingtao Li,Gang Wang,Xiaodong Cao

Hydrogels with good mechanical properties, excellent biocompatibility and designable shapes are of great importance for their biomedical applications. Herein, a series of high strength, biocompatible hydrogels have been synthesized by integrating sodium citrate into the thermally reversible chitosan/gelatin to form multiple physically crosslinking networks. Besides the ideal formability, a thermal etching or welding method has been developed to program the surface morphology and fabricate hydrogels with complicated shapes freely. More impressively, the special hollow “cup-shaped and tubular” structure has also been constructed by applying an interrupted gelation process in controlled ion crosslinking time and the subsequent dissolving process at 37   °C in deionized water. The high strength, biocompatible hydrogels with special internal and external shape adjustable characters, potentially useful in vascular repair and substitutes of cartilage, may further broaden our understanding of the plasticity of the hydrogels.

CAS / MDL: 9012-76-4
研究领域: 生物材料学 · 组织工程学
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Journal of Asian Ceramic Societies · 2020 · IF 2.653

A three-dimensional mullite-whisker network ceramic with ultra-light weight and high-strength prepared by the foam-gelcasting method

Mengmeng Yang,Jijia Li,Yiran Man,Zijun Peng,Xiaofang Zhang,Xudong Luo

A three-dimensional mullite-whiskers network ceramic with ultra-light weight and high-strength was obtained by the foaming gel-casting method with active mulllite powders and NH4F. Ultrafine active mullite powder was used as the raw material and SDS (sodium dodecyl sulfate) as a pore-forming agent. The effects of sintering temperature on the microstructure, flexural strength and thermal conductivity of the porous ceramics were systematically investigated. The mullite-whisker network porous ceramic has a fibrous-framework structure composed of interweaving mullite-whiskers. Because the pore-walls are composed of interlacing whiskers and the pores are filled with whiskers, the porous ceramics exhibited good mechanical properties and low thermal conductivity. The flexural strength of the obtained mullite-whisker porous ceramic sintered at 1500°C was up to 1.45 Mpa, while the porosity was as high as 89%. In addition, the thermal conductivity of the porous ceramic at room temperature was as low as 0.045 W/m⋅K.

CAS / MDL: 10043-01-3 13517-24-3
研究领域: 材料科学 · 陶瓷工程
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Journal of Materials Research and Technology-JMR&T · 2021 · IF 5.039

Hydrogel with high toughness and strength for fabricating high performance stab-resistant aramid composite fabric

Xiayun Zhang,Ting-Ting Li,Yuxiao Wang,Bing-Chiuan Shiu,Hao-Kai Peng,Ching-Wen Lou,Jia-Horng Lin

In order to prepare a new high-performance and flexibility stab-resistant composite material, one type of high-toughness and high-strength hydrogel is combined with aramid fabric. In this paper, the nanocomposite (NC) hydrogels are prepared using Pluronic F127 Diacrylate (PF127DA) as the crosslinking agent, acrylamide as the monomer and nano-silica as nano additive. The influence of the addition amount of nano-silica on the toughness and strength of nano-composite hydrogels is discussed. The strength and toughness of the NC hydrogels with nano silica are higher than that of the acrylamide hydrogel without nano particles. The NC hydrogel with the best strength is made as a composite with aramid fabric and the effect of nanocomposite hydrogel on the stab resistance of the stab-resistant composite material is studied. The research shows that the stab resistance performance of the composite material prepared by aramid fabric and nanocomposite hydrogel is effectively improved in comparison with aramid fabric, and the yarn pulling force is also improved. The composite material with high stab resistance can be used as the stab-resistant layer of armor, cut-resistant gloves and stab-resistant base material of shoes. This work provided a possibility for preparing a kind of lightweight composite material with high stab resistance.

研究领域: 材料科学 · 复合材料
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ACS Omega · 2020 · IF 2.87

Light, Strong, and Ductile Architectures Achieved by Silk Fiber “Welding” Processing

Dinghao Wu,Chao Ye,Yawen Liu,Jing Ren,Yuan Yao,Shengjie Ling

Light, strong, and ductile materials (LSDMs) are desired in many emerging fields, such as biomedicine, aerospace industries, and structural engineering materials. However, producing such materials remains a significant challenge because their structures cannot confer the desired mechanical properties. In this study, we developed a silk fiber “welding” strategy to construct bioinspired LSDMs. The key to the welding process is to etch the surface of silk fiber through a partial dissolution process. The dissolved silk proteins further serve as welding materials or glues to bond the silk fibers together. Remarkably, these silk-LSDMs are not only lightweight (with the densities of around 0.28 g cm–3) but also strong and tough. Their compression strength reaches up to 13.8 ± 3.4 MPa, which is higher than those of most natural and engineered porous materials. These favorable structural and mechanical characteristics, together with outstanding biocompatibility of silk proteins, render these silk-LSDMs applicable in regenerated engineered tissues and water treatment materials.

研究领域: 材料科学 · 生物医学工程 · 结构工程
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CHEMICAL ENGINEERING JOURNAL · 2021 · IF 13.273

High strength, recyclable, anti-swelling and shape-memory hydrogels based on crystal microphase crosslinking and their application as flexible sensor

Shuwei Cai,Ben Niu,Xinyu Ma,Songhan Wan,Xianru He

To develop high strength, anti-swelling, and sustainable hydrogels, acrylonitrile copolymer hydrogels are prepared based on the structural characteristics of microphase separation and physical crosslinking of thermoplastic elastomers. The hydrogel can be recycled and reprocessed into any desired shape and can withstand the maximum tensile stress of about 23 MPa, the maximum fracture energy is as high as 7592 J/m 2 . The hydrogels exhibit strain hardening behavior at low strain. In addition, the high strength can be maintained stably for more than 60 days in an aqueous environment and the hydrogel has pH-induced shape memory property. The hydrogel can be further strengthened by the introduction of zinc ions, and its toughness and elongation at break are greatly improved, which is mainly based on the dynamic balance between free zinc ions and conjunct zinc ions in the gel. In addition, the introduction of zinc ions also greatly improves the electrical conductivity of the gel. The strain sensor prepared by this gel has high sensitivity, good linear response, and stability, and is expected to be a promising candidate material for flexible electronic products and strain sensors.

研究领域: 材料科学 · 生物医学工程
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INDUSTRIAL CROPS AND PRODUCTS · 2024 · IF 5.6

Formaldehyde-free biomass adhesive based on industrial alkali lignin with high strength and toughness

Ying Zhu,Fudong Zhang,Ruohong Bian,Guodong Zeng,Jiongjiong Li,Yan Lyu,Jianzhang Li

The preparation of industrial lignin-based adhesives generally requires the use of large amounts of petrochemical products or toxic and hazardous reagents, which severely limits their widespread application in the wood-based panel industry. In this study, we present a novel approach for synthesizing an eco-friendly lignin-based wood adhesive using aminated alkali lignin (AAL) and epoxy-terminated hyperbranched polyester (EHBP). The AAL was prepared by aminating alkali lignin through a green and formaldehyde-free method. The EHBP was synthesized by grafting epichlorohydrin onto biomass-derived hyperbranched polyester. The resulting adhesive performed excellent bonding strength of 2.41 MPa and debonding work of 0.711 J, which were 3.63 and 15.2 times higher than those of the pure lignin adhesive, respectively. This exceptional bonding strength surpassed that of most previously reported biomass adhesives. The moisture uptake value of the adhesive decreased by 75.6 % and the residual rate increased by 239.2 %. In addition, the prepared adhesive exhibited enhanced mold resistance. Importantly, the adhesive was primarily composed of biomass materials and their derivatives and was less costly than most commercial formaldehyde-based and bio-based adhesives. This work presents new possibilities for the high-value utilization of industrial lignin and the development of formaldehyde-free and environmentally friendly adhesives.

研究领域: 材料科学 · 环境科学 · 林业工程
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Journal of Materials Research and Technology-JMR&T · 2022 · IF 6.267

Fabrication of ionic wood crosslinked by Ca2+ with high strength, toughness, and weather resistance

Xuefeng Zhang,Huanbo Wang,Zhijun Chen,Shiyu Guo,Yuan Fu,Tian Liu

Fast-growing natural poplar wood is not meet with in many requirements such as high strength and flame retardant due to its porous structure and loose materials. In this study, we established a simple and feasible method that includes delignification, ionic bond formation via the crosslinking of carboxyl groups in TEMPO-oxidized wood after delignification with calcium ions , and hot-pressing of stacked veneers to improve the quality, density, strength, toughness, and weather resistance of natural wood (NW). This method has the following advantages: The inner cellulose microfiber is highly aligned, thus closely cross-linking and tightly bonding cellulose microfibers and nanofibers between the interfaces and inner layers of the wood boards via hydrogen bonding and ionic bonding. A laminated densified TEMPO-oxidized ionic wood (IW) showed substantially higher specific strength (∼196.9 MPa cm3 g−1), higher tensile strength (∼246 MPa), higher flexural strength (∼257 MPa), higher flexural modulus (∼36 GPa), higher impact toughness (∼42.34 kJ m−2), and superior fire retardancy, UV resistance, water resistance, and also higher density (∼1.25 g cm−3) than NW. Larger-size laminated densified structural materials with satisfactory thermal stability can also be fabricated using the proposed method.

研究领域: 材料科学 · 林业工程
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ULTRASOUND IN MEDICINE AND BIOLOGY · 2022 · IF 3.694

Enhanced Sonothrombolysis Induced by High-Intensity Focused Acoustic Vortex

Shifang Guo,Zhen Ya,Pengying Wu,Lei Zhang,Mingxi Wan

High-intensity focused ultrasound (HIFU) thrombolysis provides a targeted and non-invasive therapy for thrombosis-related diseases. Rapid thrombolysis and restoration of blood flow are vital to reduce the disability and death rate . The objective of this study was to explore the feasibility of using a high-intensity focused acoustic vortex (HIFAV) to enhance sonothrombolysis. The in vitro clots were treated with HIFU with a peak negative pressure (PNP) of 2.86 MPa (HIFU A) or 3.27 MPa (HIFU B) or HIFAV with a PNP of 2.14 MPa. The results revealed that HIFAV thrombolysis could achieve a significantly higher efficiency than HIFU (HIFAV: 65.4%, HIFU A: 24.1%, HIFU B: 31.6%, p < 0.01), even at a lower intensity. The average size of the debris particles generated in HIFAV thrombolysis was similar to that in HIFU. Additionally, the cavitation activities were found to be more intense in HIFAV thrombolysis. Although the efficiency of HIFAV thrombolysis was higher when the pulse repetition frequency increased from 100 to 500 Hz (41.4% vs. 65.4%, p < 0.05), it decreased when the PRF reached 1000 Hz (29.9%). Lastly, it was found that increasing the duty cycle from 5% to 15% led to a higher efficiency in HIFAV thrombolysis (40.3% vs. 75.2%, p < 0.001). This study illustrated that HIFAV provided enhanced thrombolysis and that its efficiency could be further increased by optimizing the ultrasound parameters.

研究领域: 生物医学工程 · 超声治疗 · 血栓性疾病
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