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POLYMER BULLETIN · 2024 ·Vol. 81 ·期 11 ·10175-10185 · IF 3.1

Ductile polylactic acid/poly(butylene diglycolate): structures and properties

Hu Jing,Wang Guoqiang

Polylactic acid (PLA) is a kind of polyester from biomass. To increase the ductility of PLA, melt blending was used to prepare the polylactic acid/poly(butylene diglycolate) blends in this study. The effect of poly(butylene diglycolate) (PBD) on the thermal, crystallization, tensile, and dynamic mechanical properties of PLA was investigated. The blend containing 30 wt% PBD has a substantially improved elongation at break (79%) due to the lower glass transition temperature of PBD compared to PLA. The results indicated that PLA and PBD exhibited partial compatibility, which was confirmed by dynamic mechanical analysis (DMA) and scanning electron microscope (SEM). Fourier transform infrared spectroscopy (FTIR) analysis showed there is the interaction between PLA and PBD. In summary, the incorporation of PBD resulted in improved mechanical properties, indicating potential for applications requiring enhanced ductility.

研究领域: 高分子材料科学 · 生物医用材料 · 聚合物共混 · 材料力学性能 · 可降解高分子
✓ 已验证 DOI 高影响因子
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JOURNAL OF FOOD PROTECTION · 2018 ·Vol. 81 ·期 10 ·1643-1650 · IF 1.51

Effect of Carnauba Wax–Based Coating Containing Glycerol Monolaurate on Decay and Quality of Sweet Potato Roots during Storage

Huqing Yang,Xia Li,Guoquan Lu

Because of high water loss and rot observed in postharvest sweet potato ( Ipomoea batatas (L.) Lam.) roots, a carnauba wax (CW)–based nanoemulsion without or with glycerol monolaurate (CW-GML) was developed by a high-energy emulsification approach. The effects of the two coatings on decay, respiration rate, weight loss, surface color, total soluble sugar, and starch content as well as the sensory quality of sweet potato roots were investigated during storage at 20°C for 50 days. Compared with the control treatment (water) and CW coating alone, CW-GML coating exhibited higher emulsion stability and antifungal activity, and treatment resulted in a uniform and continuous coating on roots. The CW-GML and CW coatings both effectively reduced root weight loss and respiration rate and inhibited decay incidence compared with control roots during storage. The CW-GML coating showed markedly stronger inhibition of root rot than the CW coating. Both the CW-GML and CW coatings promoted an increase in root sweetness but did not negatively impact perceived flavor. The overall results demonstrate that the CW-GML coating holds great promise as an effective postharvest technology to preserve food quality and extend shelf life of sweet potato roots.

研究领域: 食品科学 · 采后生物学 · 农产品贮藏 · 食品保鲜技术 · 应用植物学
✓ 已验证 DOI 高影响因子
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JOURNAL OF HAZARDOUS MATERIALS · 2019 · IF 7.65

Composite nanofiltration membrane with asymmetric selective separation layer for enhanced separation efficiency to anionic dye aqueous solution

Zhenhua Lü,Feng Hu,Haiyan Li,Xiru Zhang,Sanchuan Yu,Meihong Liu,Congjie Gao

The development of high performance membrane is crucial for enhanced separation efficiency of nanofiltration process in treating wastewaters from dye and textile industries. In this work, a novel thin-film composite nanofiltration membrane with an asymmetric separation layer composed of relatively compact skin and loose body was designed and fabricated for improved perm-selectivity and antifouling property. Nascent composite membrane with loose poly(piperazine amide) (PA) separation layer was interfacially synthesized and performed with secondary surface reaction using an aqueous tannic acid (TA) solution. Membrane characterizations verified the formation of compact TA skin on top of the loose PA layer through forming covalent bonds via esterification reaction. Compared with the composite nanofiltration membrane with PA symmetric separation layer having the same glucose rejection of about 82.0%, the permeability to pure water of the composite membrane with PA/TA asymmetric separation layer was higher by 28.0%, the water fluxes to aqueous solutions dissolved with model anionic dyes of alizarin yellow R, sunset yellow and Congo red under steady state were higher by 50.3, 43.9 and 36.1%, and the steady-state flux declines were lowered by 27.8, 43.4 and 23.5%, respectively. Furthermore, the PA/TA-based membrane also exhibited better antifouling property and rejection ability to alizarin yellow R.

研究领域: 材料科学 · 环境工程 · 膜分离技术 · 高分子化学 · 水处理
✓ 已验证 DOI 高影响因子
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JOURNAL OF POWER SOURCES · 2015 · IF 6.217

One-pot synthesis of carbon-coated nanosized LiTi2(PO4)3 as anode materials for aqueous lithium ion batteries

Zhantao Liu,Xusong Qin,Hui Xu,Guohua Chen

In this study, a one-pot sintering process incorporating sol–gel preparation route and in-situ carbon coating was proposed for the synthesis of carbon-coated nanosized LiTi 2 (PO 4 ) 3 . Experimental results show that the prepared LiTi 2 (PO 4 ) 3 particles are of high crystallinity and well-coated by turbostratic carbon. Attributed to nanosized particles and enhanced conductivity provided by turbostratic carbon coating, the carbon-coated LiTi 2 (PO 4 ) 3 showed high rate performance and good cycling life in aqueous electrolyte. Particularly, the carbon-coated LiTi 2 (PO 4 ) 3 exhibited initial specific capacities of 103 and 89 mAh g −1 , and retained 80.6% and 97% of the initial capacities after 120 cycles at 1C and 10C in aqueous electrolyte, respectively. The high rate performance and good cycling life of carbon-coated LiTi 2 (PO 4 ) 3 in aqueous electrolyte reveal its potential as negative electrode in aqueous lithium-ion batteries for electric vehicles and industrial-scale energy storage systems .

研究领域: 材料科学 · 电化学 · 能源存储 · 纳米技术 · 无机化学
✓ 已验证 DOI 高影响因子
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Journal of Coatings Technology and Research · 2017 ·Vol. 15 ·期 3 ·505-514 · IF 1.557

Barrier functionality of SiO x layers and their effect on mechanical properties of SiO x /PLA composite films

Zhao Yuan,Huang Chongxing,Bei Ronghua,Su Hongxia,Wang Shuangfei

Silicon oxide (SiO x ) films are widely used as barrier layers in different types of commodity packaging and have caught the interest of manufacturers and researchers alike owing to their high barrier functionality, good acid and alkali resistance, ability to withstand high-temperature and microwave treatments, and good transparency. In this study, we first synthesized polylactic acid (PLA) films by extrusion calendaring and then deposited a SiO x layer on the PLA films by plasma-enhanced chemical vapor deposition to prepare SiO x /PLA composite films. We then evaluated the barrier functionality of the SiO x layer and elucidated its underlying mechanism. We also analyzed its effect on the mechanical properties of the composite films by comparing the oxygen and water vapor transmission rates, soil degradation performances, and surface morphologies of the two types of synthesized films (uncoated and coated with SiO x ). The results showed that, because of the SiO x layer, the barrier properties and mechanical properties of the SiO x /PLA composite films were better than those of the uncoated films. In particular, the oxygen and water vapor transmission rates of the composite films were approximately 8–10 and 6–8 times lower, respectively, than those of the uncoated PLA films. In addition, the SiO x layer lowered the rate of soil degradation of the composite films, owing to which the weight-loss rates of the composite films were also lower than those of the uncoated films. Further, the tensile strengths and elongations at break of the composite films were higher because of the SiO x layer. Graphical

研究领域: 材料科学 · 高分子材料 · 包装工程 · 表面改性 · 生物降解材料
✓ 已验证 DOI 高影响因子
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APPLIED SURFACE SCIENCE · 2019 · IF 5.155

Surface-fluorinated Li4Ti5O12 nanowires/reduced graphene oxide composite as a high-rate anode material for Lithium ion batteries

Guorong Hu,Jilin Wu,Ke Du,Zhongdong Peng,Ming Jia,Hao Yang,Yanbing Cao

The surface-fluorinated Li 4 Ti 5 O 12 nanowires/reduced graphene oxide composite is synthesized through a hydrothermal procedure. Lithium ion transport is promoted by forming a special morphology of lithium titanate nanowires, meanwhile, electronic transmission is facilitated by surface fluorination and conductive network of graphene coating. These three kinds of synergistic effects greatly improve the rate performance of lithium titanate . The surface-fluorinated Li 4 Ti 5 O 12 nanowires/reduced graphene oxide composite exhibits high specific capacities (167.5 mAh g −1 at 1 C and even 132.6 mAh g −1 at 10 C) and good cyclic stability (95% capacity remain after 300 cycles at 5 C). The influences of surface fluorination and graphene coating on electrochemical performance of lithium titanate are investigated in detail in terms of reversible capacity, cyclability and rate capability. Its excellent electrochemical properties make it become possible to be a potential anode material for high-rate lithium-ion batteries applied in high power facilities.

研究领域: 材料科学 · 电化学 · 纳米科技 · 能源存储 · 锂离子电池
✓ 已验证 DOI 高影响因子
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POWDER TECHNOLOGY · 2019 · IF 3.413

Hybrid humics/sodium carboxymethyl cellulose water-soluble binder for enhancing the electrochemical performance of a Li-ion battery cathode

Shuzhen Yang,Yanfang Huang,Shengpeng Su,Guihong Han,Jiongtian Liu

A hybrid water-soluble humics-based binder (humics/sodium carboxymethyl cellulose (CMC)) was studied to enhance the electrochemical performance of a Li-ion battery cathode (LiFePO 4 ) in this work. Molecular dynamics simulations of binder active fractions with related materials (LiFePO 4 and Al) were performed to explore the binding mechanisms. Humics serve to connect the active material and provide a conducting bridge in the cathode. To improve the adhesion between the particles and current collector, CMC is added as an auxiliary fraction with a mass ratio of humics to CMC of 3:1. The scanning electron microscope results indicate that the morphology of the electrode with the hybrid humics/CMC binder is more uniform than that of electrodes with conventional polyvinylidene fluoride and CMC binders. The electrochemical performance and cycling stability of the cathode materials are obviously enhanced. The reversible specific capacity can reach 152.3 mAh g −1 at 0.5 °C after 100 cycles. The rate capability is greatly improved, with a specific capacity as high as 105 mAh g −1 at 8 °C. The humics/CMC composite can be regarded as a novel, environmentally friendly and high-efficiency binder for application in Li-ion batteries.

研究领域: 电化学 · 材料科学 · 能源存储 · 纳米材料 · 可持续能源技术
✓ 已验证 DOI 高影响因子
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JOURNAL OF HAZARDOUS MATERIALS · 2017 · IF 6.065

Preparation of a surface-grafted imprinted ceramic membrane for selective separation of molybdate anion from water solutions

Jianxian Zeng,Zhihui Dong,Zhe Zhang,Yuan Liu

A surface-grafted imprinted ceramic membrane (IIP-PVI/CM) for recognizing molybdate (Mo(VI)) anion was prepared by surface-initiated graft-polymerization. Firstly, raw alumina ceramic membrane (CM) was deposited with SiO 2 active layer by situ hydrolysis deposition method. Subsequently, γ-methacryloxy propyl trimethoxyl silane (MPS) was used as a coupling agent to introduce double bonds onto the SiO 2 layer (MPS-CM). Then, 1-vinylimidazole (VI) was employed as a functional monomer to graft-polymerization onto the MPS-CM (PVI-CM). During the graft-polymerization, the influence factors of grafting degree of PVI were investigated in detail. Under optimum conditions (monomer concentration 20   wt%, temperature 70   °C, initiator amount 1.1   wt% and reaction time 8   h), the grafting degree of 20.39   g/100   g was obtained. Further, Mo(VI) anion was used as a template to imprint in the PVI-CM by employing 1,6-dibromohexane as a cross-linking agent, and then Mo(VI) was removed, obtaining the IIP-PVI/CM with many imprinted cavities for Mo(VI). Thereafter, static adsorption and dynamic separation properties of IIP-PVI/CM for Mo(VI) were studied. Results indicate that IIP-PVI/CM shows a specific selectivity for Mo(VI) with the adsorption capacity of 0.69   mmol/100   g, and the selectivity coefficient of IIP-PVI/CM is 7.48 for molybdate to tungstate anions. During the dynamic separation, IIP-PVI/CM has also good selectivity for separation of Mo(VI) and W(VI) anions.

研究领域: 环境化学 · 材料科学 · 分离科学 · 高分子化学 · 无机分析化学
✓ 已验证 DOI 高影响因子
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JOURNAL OF MOLECULAR LIQUIDS · 2019 · IF 4.561

Experiment and model for surface tensions of 2‑diethylaminoethanol‑N‑(2‑aminoethyl)ethanolamine, 2‑diethylaminoethanol‑N‑methyl‑1,3‑propane‑diamine and 2‑diethylaminoethanol‑1,4‑butanediamine aqueous solutions

Pan Zhang,Lemeng Wang,Chunjie Lu,Mengying Li,Shujun Yu,Dong Fu

The surface tensions of 2‑diethylaminoethanol (DEAE)‑ N ‑(2‑aminoethyl)ethanolamine (AEEA), DEAE‑ N ‑methyl‑1,3‑propane‑diamine (MAPA) and DEAE‑1,4‑butanediamine (BDA) aqueous solutions have been measured by using the BZY-1 surface tension meter. The mass fractions of DEAE and AEEA/MAPA/BDA respectively ranged from 0.300 to 0.500 and 0.050 to 0.150. The temperature ranged from 303.2 K to 323.2 K. A thermodynamic equation was proposed to model the surface tension and the calculated results agreed well with the experiments. The effects of temperature and mass fraction of amines on the surface tension were demonstrated on the basis of experiments and calculations. The surface thermodynamics including surface enthalpy and surface entropy of blended amine aqueous solutions were also determined, and their temperature and mass fraction dependences were analyzed.

研究领域: 物理化学 · 溶液化学 · 热力学 · 表面科学 · 化工材料
✓ 已验证 DOI 高影响因子
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Sustainable Energy & Fuels · 2021 ·Vol. 5 ·期 5 ·1538-1547 · IF 6.367

A facile preparation of PEO–LiClO4–fumed SiO2 composite solid-state electrolyte with improved electrochemical performance for lithium-metal batteries

Ruyan Lei,Yanping Yang,Chenjuan Yu,Yinsi Xu,Yuanzhuo Li,Jun Li

In order to improve the electrochemical performance and efficiently prepare a solid polymer electrolyte (SPE) for the lithium-metal battery (LMB), a fumed SiO2 (FS) with surface Si–OH group was used to fabricate FS-modified poly(ethylene oxide) (PEO)–LiClO4-based SPE by a facile preparation process. The influences of the FS content on the morphological properties, thermal properties, lithium salt dissociation, mechanical properties, and electrochemical properties of SPE were systematically analyzed. Results indicate that FS with the hydrophilic property was widely distributed throughout the amorphous phase of SPE, thus the crystallinity of SPE was reduced to 25.83% when the FS mass loading was 6.85 wt%. In addition, a greater dissociation degree of lithium salt was achieved after the addition of FS, and a higher ion conductivity of 3.03 × 10−4 S cm−1 and Li-ion migration number of 0.396 were recorded at 60 °C. The all-solid-state Li/SPE/Li coin cell showed excellent stable cyclability (380 h) and the LiFePO4 (LFP)/SPE/Li coin cell demonstrated good discharge specific capacity and coulomb efficiency of 96 mA h g−1 and 100.2%, respectively, after 100 cycles of galvanostatic charge–discharge operation under 0.5C at 60 °C. Thus, based on collective results, it is expected that SPE presented in this work is a promising electrolyte for next-generation high-energy all-solid-state LMB with enhanced safety.

研究领域: 材料科学 · 电化学 · 能源存储 · 高分子化学 · 固态离子学
✓ 已验证 DOI 高影响因子
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JOURNAL OF SOL-GEL SCIENCE AND TECHNOLOGY · 2013 ·Vol. 66 ·期 1 ·133-138 · IF 1.66

Preparation of anticorrosion hybrid silica sol–gel coating using Ce(NO3)3 as catalyst

Peng Shusen,Zhao Wenjie,Zeng Zhixiang,Li He,Xue Qunji,Wu Xuedong

In this report, hybrid silica sol–gel coating was prepared using Ce(NO 3 ) 3 (Sol-Ce) as catalyst. Structure, surface morphology and anticorrosion ability of Sol-Ce solution/coating were studied by infrared spectroscopy (IR), scanning electron microscopy, energy dispersive spectrometer (EDS), potentiodynamic scan (PDS) and electrochemical impedance spectroscopy (EIS). IR results showed that Ce(NO 3 ) 3 had a stronger influence on reactivity of alkoxysilane. EDS results revealed that the fraction of Fe in Sol-Ce coating was significantly lower than regular acid-catalyzed hybrid silica sol–gel coating (Sol-Ac) and Sol-Ac with Ce(NO 3 ) 3 -doped coating (Sol-Ac/Ce). The results of PDS and EIS demonstrated that Sol-Ce coating had better anticorrosion ability than Sol-Ac and Sol-Ac/Ce on carbon steel. The enhanced anticorrosion performance of the Sol-Ce coating might result from the following two reasons: (a) Ce(NO 3 ) 3 as a catalyst could alleviate the negative effects of low pH with using acid catalyst (dissolution of carbon steel) and (b) Ce(NO 3 ) 3 could impede corrosion of carbon steel as corrosion inhibitor.

研究领域: 材料科学 · 表面工程 · 腐蚀与防护 · 无机化学 · 电化学
✓ 已验证 DOI 高影响因子
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JOURNAL OF ALLOYS AND COMPOUNDS · 2022 · IF 6.371

Enhanced energy harvesting performances of flexible piezoelectric nanocomposite based on CNTs@PZT nanofibers network

Xiaofei Liu,Jian Wang,Zhonghui Shen,Hongjian Zhang,Baowen Li,Yong Zhang,Xin Zhang

Flexible organic/inorganic piezoelectric nanocomposites are highly demanded for flexible wearable electronic devices due to their excellent mechanical flexibility and high piezoelectric performance. However, the output performance of ceramic-polymer-based piezoelectric nanogenerators (PENGs) is restricted by the poor electrical conductivity of the organic matrix and the distinct discrepancy in mechanical strength between inorganic filler and organic matrix. Herein, we propose a flexible piezoelectric polymer nanocomposite based on CNTs@PZT nanofibers (NFs) network where the carbon nanotubes (CNTs) were introduced into the piezoelectric lead zirconate titanate (PZT) NFs to simultaneously improve the electrical conductivity and mechanical strength of nanocomposites. When subjected to a periodical bending deformation , the CNTs@PZT NFs network-based PENG with optimal addition of CNTs (0.6 wt%) generates a maximum electrical output up to ∼12.5 V and ∼80 nA cm −2 which is four times higher than that of PENGs without CNTs doping. An ultrahigh power density of 91.7 nW cm −2 is obtained with an external load resistance of 40 MΩ when pressed via a 10 N compressive force , and furthermore, the generated power could charge a capacitor and further light a commercial LED. This work may pave a new way for the development of high-output nanocomposite-type PENGs.

研究领域: 材料科学 · 纳米科技 · 能源材料 · 柔性电子学 · 功能材料
✓ 已验证 DOI 高影响因子
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