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Zhicun WANG Xiaoman HAN Yixi WANG Kenan MEN Lin CUI Jianning WU Guihua MENG Zhiyong LIU Xuhong GUO 《材料科学前沿(英文版)》2019,13(1):54-63
A polyacrylic acid(PAA)/gelatin(Gela)/polyvinyl alcohol(PVA)hydrogel was prepared by copolymerization,cooling,and freezing/thawing methods.This triplenetwork(TN)structure hydrogel displayed superior mechanical properties,low swelling ratio and self-healing properties,The superior mechanical properties are attributed to the triple helix association of Gela and PVA crystallites by reversible hydrogen bonding.The characterization results indicated that the fracture stress and the strain were 808 kPa and 370% respectively,while the compression strength could reach 4443 kPa and the compressive modulus was up to 39 MPa under the deformation of 90%.The hydrogen bonding in PVA contributed to maintain and improve the self-healing ability of hydrogels.Every type of hydrogels exhibited a higher swelling ratio under alkaline conditions,and the swelling ratios of PAA,PAA/PVA and PAA/Gela hydrogels were 27.71,12.30 and 9.09,respectively.The PAA/Gela/PVA TN hydrogel showed the lowest swelling ratio(6.57)among these hydrogels.These results indicate that the novel TN hydrogels possess good environmental adaptability and have potential applications in the biomedical engineering and sensor field. 相似文献
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目前对卧螺离心机内部流场的数值模拟大多采用传统欧拉模型,考虑其内部伴有盐析等固相粒子微观行为过程的研究少有报道。本文应用计算流体力学软件Fluent,基于群体平衡模型与多相流Eulerian模型、RNG k-ε模型耦合方法,对卧螺离心机内部盐析两相流场进行三维数值模拟,通过仿真与实验相结合的方式,得到卧螺离心机内盐析流场的晶体颗粒粒径分布、组分数分布和浓度分布及其变化规律,初步揭示了卧螺离心机内伴有盐析的流场晶体颗粒分布特性。研究结果表明:卧螺离心机内盐析晶体粒径的分布随液环半径的增大而增大,螺旋叶片正壁面粒径明显较背面大,从排液端至排渣端的晶体粒径分布有整体逐渐变大的轴向粒径梯度;流道内晶体粒径随转鼓转速的增大而减小,随进口固相体积分数的增大而增大;大粒径晶体的组分数在液环外侧及螺旋叶片正面附近相对较大,而中、小粒径晶体组分数的分布规律则与之相反;盐析颗粒浓度在液环外侧较高且分布均匀,且随转鼓转速的提高而提高,PBM模型与Euler模型计算结果有一定的相似与差异。 相似文献
134.
研究了纤维素酶和木聚糖酶对速生杨枝桠材P—RCAPMP酶促磨浆性能的影响。实验结果表明酶预处理可以改善P—RCAPMP浆的磨浆性能和成浆质量。纤维素酶和木聚糖酶预处理纸浆打浆度提高3-11°SR,磨浆能耗明显降低。最佳酶用量为25IU/g。与未经过酶预处理速生杨枝桠材P—RCAPMP浆相比,纤维素酶预处理纸浆裂断长提高12%,撕裂指数提高13%,耐破指数提高14%,耐折度提高50%,白度提高1.2%ISO。木聚糖酶预处理纸浆裂断长略有提高,撕裂指数提高15%,耐破指数提高12%,耐折度提高75%,白度提高1.9%ISO。酶预处理可抑制纸浆返黄。纤维素酶的酶促磨浆效果好于木聚糖酶。 相似文献
135.
Guihua Liu Dan Luo Rui Gao Yongfeng Hu Aiping Yu Zhongwei Chen 《Small (Weinheim an der Bergstrasse, Germany)》2020,16(37)
The practical application of lithium–sulfur (Li–S) batteries is hindered by the “shuttle” of lithium polysulfides (LiPS) and sluggish Li–S kinetics issues. Herein, a synergistic strategy combining mesoporous architecture design and defect engineering is proposed to synthesize multifunctional defective 3D ordered mesoporous cobalt sulfide (3DOM N‐Co9S8?x) to address the shuttling and sluggish reaction kinetics of polysulfide in Li–S batteries. The unique 3DOM design provides abundant voids for sulfur storage and enlarged active interfaces that reduce electron/ion diffusion pathways. Meanwhile, X‐ray absorption spectroscopy shows that the surface defect engineering tunes the CoS4 tetrahedra to CoS6 octahedra on Co9S8, endowing abundance of S vacancies on the Co9S8 octahedral sites. The ever‐increasing S vacancies over the course of electrochemical process further promotes the chemical trapping of LiPS and its conversion kinetics, rendering fast and durable Li–S chemistry. Benefiting from these features, the as‐developed 3DOM N‐Co9S8?x/S cathode delivers high areal capacity, superb rate capability, and excellent cyclic stability with ultralow capacity fading rate under raised sulfur loading and low electrolyte content. This design strategy promotes the development of practically viable Li–S batteries and sheds lights on the material engineering in related energy storage application. 相似文献
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138.
Conductive hydrogels are attracting tremendous interest in the field of flexible and wearable soft strain sensors because of their great potential in electronic skins, and personalized healthcare monitoring. However, conventional conductive hydrogels using pure water as the dispersion medium will inevitably freeze at subzero temperatures, resulting in the diminishment of their conductivity and mechanical properties; meanwhile, even at room temperature, such hydrogels suffer from the inevitable loss of water due to evaporation, which leads to a poor shelf‐life. Herein, an antifreezing, self‐healing, and conductive MXene nanocomposite organohydrogel (MNOH) is developed by immersing MXene nanocomposite hydrogel (MNH) in ethylene glycol (EG) solution to replace a portion of the water molecules. The MNH is prepared from the incorporation of the conductive MXene nanosheet networks into hydrogel polymer networks. The as‐prepared MNOH exhibits an outstanding antifreezing property (?40 °C), long‐lasting moisture retention (8 d), excellent self‐healing capability, and superior mechanical properties. Furthermore, this MNOH can be assembled as a wearable strain sensor to detect human biologic activities with a relatively broad strain range (up to 350% strain) and a high gauge factor of 44.85 under extremely low temperatures. This work paves the way for potential applications in electronic skins, human?machine interactions, and personalized healthcare monitoring. 相似文献
139.
Dezhang Ren Jie Ying Meiling Xiao Ya‐Ping Deng Jiahua Ou Jianbing Zhu Guihua Liu Yi Pei Shuang Li Altamash M. Jauhar Huile Jin Shun Wang Dong Su Aiping Yu Zhongwei Chen 《Advanced functional materials》2020,30(7)
The lack of efficient strategies to address the intrinsic activity, site accessibility, and structural stability issues of metal‐carbon hybrid catalysts is restricting their real‐world implementation on the basis of rechargeable zinc–air batteries. Herein, a dual metal–organic frameworks (MOFs) pyrolysis strategy is developed to regulate the intrinsic activity and porous structure of the derived catalysts, where a Fe2Ni_MIL‐88@ZnCo_zeolitic imidazolate framework (ZIF), with a hierarchically porous structure, multifunctional components, and an integrated architecture, acts as an ideal precursor to obtain multimetal based porous nanorod (FeNiCo@NC‐P). Benefitting from the synergetic effect of the multimetal components, facilitated reactant accessibility, and the well‐retained integrated structure, the resultant FeNiCo@NC‐P catalyst exhibits an oxygen reduction reaction half‐wave potential of 0.84 V as well as an oxygen evolution reaction potential of 1.54 V at 10 mA cm–2. Furthermore, the practical application of FeNiCo@NC‐P in the zinc–air battery displays a low voltage gap and long‐term durability (over 130 h at a current density of 10 mA cm–2), which outperforms the commercial noble metal benchmarks. This work not only affords a competitive bifunctional oxygen electrocatalyst for zinc–air batteries but also paves a new way to design and fabricate MOF‐derived materials with tunable catalytic properties. 相似文献
140.
Solar‐Powered Redox Cells: Efficient Solar Energy Harvesting and Storage through a Robust Photocatalyst Driving Reversible Redox Reactions (Adv. Mater. 31/2018)
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