JOURNAL OF ELECTROANALYTICAL CHEMISTRY
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2018
·
IF 3.235
Hongrui Wang,Min Gao,Yan-an Zhu,Huawei Zhou,Huating Liu,Lin Gao,Mingxing Wu
Carbon molecular sieve is introduced as flexible supercapacitor electrode for the first time. The carbon molecular sieve electrode generates a specific capacitance of 108.0 F·g −1 and demonstrates an excellent stability with 98.5% preservation of its initial capacitance after 10,000 charging-discharging cycles. To further enhance the electrochemical performance, a flexible 3-D structured composite electrode is synthesized via an electrochemical polymerization method by depositing poly 3,4‑ethylenedioxythiophene film on the carbon molecular sieve surface, denoted as carbon molecular sieve@poly 3,4‑ethylenedioxythiophene. The specific capacitance of the composite electrode is up to 126.0 F·g −1 , higher than both poly 3,4‑ethylenedioxythiophene (115.7 F·g −1 ) and carbon molecular sieve (108.0 F·g −1 ). Moreover, the flexible composite electrode preserves 96.0% of its initial capacitance after 10,000 charging-discharging cycles at 1.00 A·g −1 . The superior performance of the composite electrode is attributed to the combined merits of the superior conductivity and excellent cycle stability of the carbon molecular sieve and 3-D porous network configuration of the poly 3,4‑ethylenedioxythiophene.
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FOOD CHEMISTRY
·
2017
·
IF 4.529
Ting Hu,Qilin Huang,Kahing Wong,Hong Yang,Jingsi Gan,Yanru Li
An alkali-soluble polysaccharide was extracted from Lignosus rhinocerotis sclerotia (LRP). Its structural characteristics were determined by GC–MS, FT-IR, GC, 1D and 2D NMR combined with Smith degradation and methylation analysis. The LRP had a (1 → 3)-β- d -Glcp backbone with every three residues bearing a (1 → 6)-linked and hyperbranched side chain that contained three (1 → 6)-β- d -Glcp residues as secondary main chain and two terminal β- d -Glcp residues linked at O3. The degree of branching was 0.76 from GC–MS analysis, implying a highly branched structure for LRP. The M w , < S 2 > z 1/2 , R h and [ η ] values of LRP in 0.25 M LiCl/DMSO were measured by SEC-MALLS-Vis-RI combination technology to be 2.88 × 10 5 g/mol, 30.36 nm, 22.34 nm and 131.50 ml/g, respectively. Furthermore, the exponent α of [ η ] –M w , β of < S 2 > z 1/2 –M w , the fractal dimension d f and molecular parameter ρ were determined to be 0.20, 0.33, 2.50 and 1.36, demonstrating that the LRP was a hyperbranched polysaccharide and adopted a compact coil conformation in LiCl/DMSO.
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JOURNAL OF PHYSICAL CHEMISTRY B
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2013
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IF 3.607
Jingjing Li,Kaiqi Fan,Libo Niu,Yuanchao Li,Jian Song
The effect of salt on the gelatinization of 2,4-(3,4-dichlorobenzylidene)-d-sorbitol (DCBS), a novel low-molecular-weight gelator, was studied. DCBS showed pronounced hydrogelation and the electron micrographs indicated that the hydrogels consists of globular aggregates. Addition of NaCl to the aqueous medium accelerated the gelation process and also caused the gel’s morphology to change from globular to long fibers. In addition, the thermal properties of the hydrogels were improved with the addition of NaCl. UV–vis and fluorescence emission spectra showed that extensive aggregation of the phenyl rings was responsible for the gelation. The presence of NaCl induced a red shift in the emission peaks of DCBS and a decrease of the pyrene polarity index I1/I3 in the gels, which indicated that there was more π–π stacking in the hydrogels with NaCl than in the gels without NaCl. Variable-temperature 1H NMR spectra further demonstrated that the π–π interactions were enhanced by NaCl. FTIR studies showed that hydrogen bonding was also a contributing factor in the gelation process. Wide-angle X-ray diffraction (WXRD) showed that the hydrogels had a layered structure which did not change with the addition of NaCl. Density functional theory (DFT) calculations indicated the possible molecular packing of the gelator in the nanofibers.
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Bioengineered
·
2017
·
IF 1.691
Wen-Bin Zhou,Jin-Song Gong,Hai-Juan Hou,Heng Li,Zhen-Ming Lu,Hong-Yu Xu,Zheng-Hong Xu,Jin-Song Shi
Phosphatidylserine (PS) is useful as the additive in industries for memory improvement, mood enhancement and drug delivery. Conventionally, PS was extracted from soybeans, vegetable oils, egg yolk, and biomass; however, their low availability and high extraction cost were limiting factors. Phospholipase D (PLD) is a promising tool for enzymatic synthesis of PS due to its transphosphatidylation activity. In this contribution, a new and uncharacterized PLD was first obtained from GenBank database via genome mining strategy. The open reading frame consisted of 1614 bp and potentially encoded a protein of 538-amino-acid with a theoretical molecular mass of 60 kDa. The gene was successfully cloned and expressed in Escherichia coli. Its enzymatic properties were experimentally characterized. The temperature and pH optima of PLD were determined to be 60°C and 7.5, respectively. Its hydrolytic activity was improved by addition of Ca2+ at 5 mM as compared with the control. The enzyme displayed suitable transphosphatidylation activity and PS could be synthesized with L-serine and soybean lecithin as substrates under the catalysis of PLD. This PLD enzyme might be a potential candidate for industrial applications in PS production. To the best of our knowledge, this is the first report on genome mining of PLDs from GenBank database.
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FOOD CHEMISTRY
·
2024
·
IF 8.5
Jing Sun,Zaixu Wang,Yongjin Dai,Moran Zhang,Xinyi Pang,Xiangfei Li,Yingjian Lu
Molds and mycotoxins pose severe threats to health. Bacillomycin D (BD) can effectively inhibit mold growth. Attapulgite (ATP) can provide a good carrier for antimicrobial agents. Natural ATP was acid-modified to obtain H-ATP. It was used to load BD to obtain a novel composite material (H-ATP-BD). The results showed H-ATP had better adsorption performance than ATP. BD was adsorbed up to 93.13 % by adding 30 mg H-ATP and stirring at 40 ℃ for 120 min. Fourier transform infrared spectra (FTIR), size and zeta potential, X-ray diffraction (XRD), and X-ray photoelectron spectroscopy (XPS) results confirmed successful loading of BD onto H-ATP. The composite showed good inhibition of Aspergillus and adding 0.6 % H-ATP-BD composite was effective in removing 89.06 % of aflatoxin B 1 (AFB 1 ) at 50 °C. Model fitting indicated that AFB 1 removal was a spontaneous exothermic reaction. This research will lay the foundation for the development of efficient and green antimicrobial and toxin-reducing materials.
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Polymer-Plastics Technology and Materials
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2024
·
IF 2.6
Jingwen Lan,Rukuan Liu,Sisi Liu,Airong Xu
Eco-friendly silk fibroin/poly(D,L-lactide-co-glycolide) (SF/PLGA) materials were successfully fabricated using a facile strategy. The materials were characterized by scanning electron micrograph (SEM), X-ray diffraction (XRD) and infrared spectra (IR). Systematic investigations were completed to examine the degradation rates in natural soil, cytocompatibility and thermostability of the materials. It is interesting to find that after SF was hybridized by PLGA, the thermostability and degradation rate increased. Meanwhile, the materials show good cytocompatibility. SEM, IR and XRD results reveal that there is hardly any interaction between SF and PLGA in the SF/PLGA material, and SF is physically mixed with PLGA. This study opens up a new horizon in the design and preparation of SF-based materials for promising applications in medical and biodegradable material fields.
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ACS Nano
·
2025
·
IF 16
Juexin Huang,Jingyi Xia,Sravan Baddi,Yu Zhao,Chuan-liang Feng
Piezoelectric biomaterials hold immense potential for next-generation microdevices, yet their piezoelectric performance often trails behind that of conventional synthetic counterparts. This study demonstrates a dual-scale polarization strategy to significantly enhance the piezoelectric response of d-phenylalanine derivatives (d-PheAD). Molecular-level polarization is amplified through ionic interactions with l-glutamic acid-modified Fe3O4 magnetic nanoparticles, while macroscopic alignment of d-PheAD nanoarrays under magnetic fields optimizes collective dipole orientation. This synergistic approach elevates the effective piezoelectric coefficient (deff) from 10.4 to 121.9 pm V–1, outperforming most biomaterial-based piezoelectric systems and many inorganic piezoelectric systems. Integrating these engineered assemblies into a triboelectric-enhanced piezoelectric nanogenerator yields unprecedented electrical outputs (2853 nA, 51.9 V), a 25-fold improvement over baseline configurations. The device achieves real-time detection of trace HCl gas at low concentrations, demonstrating superior sensitivity compared to commercial electrochemical sensors. By bridging molecular design and macroscopic engineering, this work establishes a scalable paradigm for deploying eco-friendly piezoelectric biomaterials in high-performance microelectronics and environmental monitoring technologies.
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Nano-Micro Letters
·
2023
·Vol. 16
·期 1
·1-18
·
IF 26.6
Li Xudong,Qiang Zhuomin,Han Guokang,Guan Shuyun,Zhao Yang,Lou Shuaifeng,Zhu Yongming
High-entropy catalysts featuring exceptional properties are, in no doubt, playing an increasingly significant role in aprotic lithium-oxygen batteries. Despite extensive effort devoted to tracing the origin of their unparalleled performance, the relationships between multiple active sites and reaction intermediates are still obscure. Here, enlightened by theoretical screening, we tailor a high-entropy perovskite fluoride (KCoMnNiMgZnF 3 -HEC) with various active sites to overcome the limitations of conventional catalysts in redox process. The entropy effect modulates the d -band center and d orbital occupancy of active centers, which optimizes the d – p hybridization between catalytic sites and key intermediates, enabling a moderate adsorption of LiO 2 and thus reinforcing the reaction kinetics. As a result, the Li–O 2 battery with KCoMnNiMgZnF 3 -HEC catalyst delivers a minimal discharge/charge polarization and long-term cycle stability, preceding majority of traditional catalysts reported. These encouraging results provide inspiring insights into the electron manipulation and d orbital structure optimization for advanced electrocatalyst.
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Scientific Reports
·
2020
·Vol. 10
·期 1
·1-12
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IF 3.998
Wu Yifan,Li Lingtong,Chen Shaopeng,Qin Jun,Chen Xiaolang,Zhou Dengfeng,Wu Hong
Poly( D -lactic acid) (PDLA) with different polyethylene glycol (PEG) segment synthesized PDLA-PEG-PDLA triblock copolymer through the ring-opening reaction of D -LA and PEG will be used as a toughening modifier. The microstructure, crystal structures and crystallization behaviors of this triblock copolymer were investigated by Fourier transform infrared (FTIR) spectroscopy, nuclear magnetic resonance (NMR) spectroscopy, X-ray diffraction (XRD), differential scanning calorimetry (DSC) and polarized optical microscopy (POM). The triblock copolymer is synthesized from the appearance of CH 2 stretching vibration peak at 2910 cm −1 and C-O stretching vibration peak at 1200 cm −1 from PEG in FTIR spectra. Moreover, the chemical shift that is about 3.6 ppm in 1 H NMR and 68.8ppm in 13 C NMR proves this matter. The results of XRD and DSC reveal that PDLA and PEG are crystallized separately, and are not fully compatible, and microphase separation has occurred in this triblock copolymer. PEG can induce the triblock copolymer to accelerate the rate of crystallization, allowing it to crystallize more completely in the same amount of time. When the molecular weight of PEG is 6000 or the ratio of D -LA/PEG is 1/1, the crystallizability of PDLA-PEG-PDLA triblock copolymer is the best.
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GREEN CHEMISTRY
·
2015
·Vol. 18
·期 7
·2147-2154
·
IF 8.02
Alei Zhang,Cong Gao,Jing Wang,Kequan Chen,Pingkai Ouyang
In this study, we present an efficient affinity adsorption–enzymatic reaction integrated approach to produce N-acetyl-D-glucosamine (GlcNAc) from crude chitin powders (CP). Chitinase was first purified from the crude enzyme mixture by affinity adsorption on the CP substrate, with ∼92.7% recovery of the enzyme achieved within 10 minutes in the presence of 20 g L−1 of CP under optimized conditions. The chitinase then efficiently converted 40 g L−1 of CP to 39.3 g L−1 of GlcNAc in a batch enzymatic reaction for 4 days, achieving nearly 100% conversion of the substrate CP. The product GlcNAc was easily separated from hydrolysates after destaining, concentrating, crystallizing and drying processes with a high purity of 98%. In addition, the chitinase can be conveniently reused for several batches by the affinity adsorption–enzymatic reaction approach, giving an average yield of 29.6 g L−1 of GlcNAc based on 30 g L−1 of CP as the substrate.
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FOOD CONTROL
·
2014
·
IF 2.819
Mohamed Reda Zahi,Hao Liang,Qipeng Yuan
The purpose of this research was to develop a novel antimicrobial delivery system by encapsulating d -limonene into an organogel-based nanoemulsion and investigating its antimicrobial activity. The d -limonene organogel-based nanoemulsion was prepared by high pressure homogenization method. The surfactant concentration had a major impact on the droplets' formation and distribution. At the optimal condition (10% w/w Tween 80, 100 Mpa, and 10 Cycles) the smallest droplet size ( d ≈ 36 nm) could be obtained, which has shown a narrow structure and good stability. Results from the antimicrobial activity have shown the encapsulation of d -limonene (4% w/w) into the organogel-based nanoemulsion contributed to the increase of its antimicrobial activity. In addition, the mechanism of d -limonene organogel-based nanoemulsion against the tested microorganisms was studied by the electronic microscope observation and the cell constituent release. This research would have an important implication for the design of more efficient antimicrobial systems for food preservation and production.
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ORGANIC PROCESS RESEARCH & DEVELOPMENT
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2024
·
IF 3.1
Yuan Li,Chun You,Yi-Heng P. Job Zhang
d-Glucaric acid (GA), one of the polyhydroxy dicarboxylic acids, is known for its great potentials in the polymer, food, detergent, and pharmaceutical industries. Here, we presented a highly efficient synthesis of GA from starch by in vitro biotransformation (ivBT). This one-pot ivBT was composed of five thermophilic enzymes (i.e., isoamylase, α-glucan phosphorylase, phosphoglucomutase, inositol 1-phosphate synthase, and inositol monophosphatase) responsible for the synthesis of myo-inositol (MI) from starch, followed by three mesophilic enzymes (i.e., myo-inositol oxygenase (MIOX), uronate dehydrogenase (UDH), and H2O-forming NADH oxidase (NOX)) responsible for the synthesis of GA from inositol. Also, a stepwise-added enzyme cocktail strategy was employed to circumvent the inhibition of GA on MIOX and mismatches in enzymes’ properties, such as temperature and pH. The three-step cascade bioprocessing in one pot resulted in the concentration of disodium glucarate of approximately 9.66 g/L (i.e., 38 mM) from 10 g/L maltodextrin with an atom efficiency of 96.6%. Up to 52.1 g/L disodium d-glucarate, the highest titer reported, was produced in a stirred bioreactor operated in two-reaction temperature ranges, featured with the stepwise addition of enzyme cocktails, and equipped with a constant pH controller and stirring for enough oxygen supplies. This study could open a new door to the industrial biomanufacturing of GA by ivBT.
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