ANALYTICAL CHEMISTRY
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2022
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IF 8.008
Changxiang Fang,Junying Li,Zhihao Feng,Xiaoyi Li,Min Cheng,Yan Qiao,Weihua Hu
Extracellular electron transfer (EET) is a critical process involved in microbial fuel cells. Spatially resolved mapping of EET flux is of essential significance due to the inevitable spatial inhomogeneity over the bacteria/electrode interface. In this work, EET flux of a typical bioanode constructed by inhabiting Shewanella putrefaciens CN32 on a porous polyaniline (PANI) film was successfully mapped using a newly established oblique incident reflectivity difference (OIRD) technique. In the open-circuit state, the PANI film was reduced by the electrons released from the bacteria via the EET process, and the resultant redox state change of PANI was sensitively imaged by OIRD in a real-time and noninvasive manner. Due to the strong correlation between the EET flux and OIRD signal, the OIRD differential image represents spatially resolved EET flux, and the in situ OIRD signal reveals the dynamic behavior during the EET process, thus providing important spatiotemporal information complementary to the bulky electrochemical data.
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高影响因子
JOURNAL OF APPLIED POLYMER SCIENCE
·
2022
·Vol. 139
·期 35
·e52822
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IF 3.057
Hejia Chang,Qinghu Meng,Defa Liu,Yue Wu,Zhizhou Yang,Bin Sun,Fang Liu,Yu Liu
Synthesis of hollow spherical polyaniline (HSPANI) with the merits of facile strategy, low cost, low safety risk and high adsorption capacity of Cr(VI) is always a big challenge. In this manuscript, we proposed a facile way to preparation of HSPANI by using the poly(styrene-co-acrylic acid) sphere as template. The results indicated that HSPANI was emeraldine comprised of lots of basically uniform hollow spheres, and its average pore diameter was about 300 nm. HSPANI displayed high adsorption capacity of Cr(VI), and its value arrived at 601.3, 347.8, 235 mg g −1 at pH = 1, 2, and 3, respectively, which were high than many other adsorbents. The endothermic, spontaneous and chemical adsorption process was responsible for this adsorption. The Cr(VI) adsorption capacity was significant relied on its pH, contact time, Cr(VI) concentration and adsorption temperature. The adsorption behavior was well agreed with pseudo second-order equation and Redlich–Peterson isotherm models. HSPANI exhibited remarkable selectivity for adsorption of Cr(VI) even if the K + , Cu 2+ , NO 3 − and SO 4 2− were coexisted. HSPANI also displayed excellent regeneration performance. Therefore, this work not only provided a facile way to synthesis of hollow spherical polyaniline, but also supplied a potential adsorbent for adsorption of Cr(VI) from the industrial wastewater.
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COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
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2022
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IF 5.518
Lichang Zhang,Kaiyun Wu,Yaxin Chen,Ren Liu,Jing Luo
A novel kind of graphene/polyaniline hybrid microcapsules loaded with self-healing agent (linseed oil, LO) were synthesized by Pickering emulsion template method in this work. In our strategy, graphene oxide (GO) was used as Pickering emulsifier to stabilize emulsion droplet containing aniline and linseed oil . After the polymerization of aniline, graphene/polyaniline microcapsules loaded with linseed oil (LO@GO/PANI) were prepared. By adjusting GO concentration and oil-water ratio, the size of the emulsion droplet and LO@GO/PANI microcapsule can be controlled at about 15–20 µm. The successful synthesis of LO@GO/PANI microcapsules was proved by SEM, FT-IR and TGA . The unique GO/PANI hybrid shell combined the outstanding barrier property of GO and anti-corrosion function of PANI. The solvent resistance results showed that the as-prepared microcapsules possessed stronger resistance to organic solvents . A smart coating with dual functions of anti-corrosion and self-healing was prepared by dispersing the as-prepared LO@GO/PANI microcapsule in waterborne epoxy resin . As the contents of microcapsules was 10 wt%, the scratch of the coating was completely healed after 12 h observed from the microscope images. The electrochemical impedance spectroscopy (EIS) and salt spray test all verified that the incorporation of microcapsules could significantly improve the anti-corrosion performance of the water-borne coatings. After 40 days' immersion, the low frequency modulus of the composite coating was almost 2 orders of magnitude higher than that of pure epoxy coating, and no obvious corrosion product was observed after 500 h salt spray test.
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JOURNAL OF HAZARDOUS MATERIALS
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2022
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IF 14.224
Tong Liu,Yang Liu,Peng Zhou,Zhaokun Xiong,Heng Zhang,Chuanshu He,Ye Du,Gang Yao,Bo Lai
As one of the most promising advanced oxidation processes , the activation of S(IV) by iron-based materials to produce SO 4 •− has become a hot technology for the degradation of organic pollutants . However, the mechanism of radical chain reactions has not been clearly explored. Herein, we established a novel AOP system based on the combination of zero-valent iron (ZVI) and potassium pyrosulfite (PPS). Combined with the degradation trends of CBZ and the change of DO concentration, the system was proposed to be divided into a slow initiation stage in 5 min and a rapid degradation stage in 5 − 10 min. Through a series of quenching experiments, electron paramagnetic resonance tests and several probe experiments, the mechanisms of two radical chain reactions were proposed between ZVI and PPS: the first one produced O 2 •− and HO • , and the other produced SO 3 •− , SO 5 •− , SO 4 •− and HO • . The two-stage reaction and two radical production paths of the ZVI/PPS system were proposed for the first time, which provided theoretical guidance for the practical application of the ZVI/PPS system. The ZVI/PPS system has been found to have excellent environmental adaptability in the treatment of industrial wastewater .
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JOURNAL OF HAZARDOUS MATERIALS
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2022
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IF 14.224
Hao Wang,Hui Yun,Minghan Li,Hanlin Cui,Xiaodan Ma,Yanqing Zhang,Xuanyuan Pei,Liying Zhang,Ke Shi,Zhiling Li,Bin Liang,Aijie Wang,Jizhong Zhou
Triclocarban (TCC), one of the typical antimicrobial agents, is a contaminant of emerging concern commonly found in high concentration in water environments. However, the fate and toxicity of TCC in wastewater treatment systems remain poorly understood. Here, we investigated how TCC impacts chemical oxygen demand and inorganic nitrogen transformation in a hydrolytic anaerobic-anoxic/oxic process. In the anaerobic section, the transformation of TCC was dominated by reductive dechlorination and supplemented by two amid bonds hydrolysis. In the anoxic and oxic sections, the hydrolysis of amid bonds dominated. The toxicity was reduced after the treatment (IC 50 from 0.09 to 0.54). TCC inhibited NH 4 + -N removal in the anaerobic section and led to the NO 3 - -N accumulation (2.84–4.13 mg/L) after treatment, with the abundance of N-removal bacteria decreased by 6%. Furthermore, the original ecological niche was gradually replaced by TCC-resistant/degradative bacteria, formating new microbial modules to resist the TCC stress. Importantly, fourteen genera including Methanosaeta , Longilinea , Dokdonella and Mycobacterium as potential bioindicators warning TCC and its intermediates were proposed. Overall, this study provides new insights into the fate of TCC in biological wastewater treatment systems and suggests a great importance for TCC control to ensure the health and resilience of ecosystems.
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TALANTA
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2022
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IF 6.556
Hao-Fei Sun,Yuan-Yuan Cui,Chang-Qing Zhen,Cheng-Xiong Yang
Microporous organic networks (MONs) are promising in high performance liquid chromatography (HPLC) with large specific surface area, good hydrophobicity and stability. However, their superhydrophobic structures restrict MONs-based HPLC only in reversed-phase mode. To decrease the hydrophobicity of pristine MONs and to expand their broad application in HPLC, here we described the monomer-mediated fabrication of core-shell MON-2COOH@SiO 2 microspheres for reversed-phase liquid chromatography (RPLC)/hydrophilic interaction liquid chromatography (HILIC) mixed-mode chromatography for the first time. The –COOH groups were introduced into MONs’ skeleton to improve their hydrophilicity and to provide hydrophilic interaction sites. The MON-2COOH was grafted onto silica via a monomer mediated method to produce monodispersed core-shell microspheres. By adjusting the concentration of reactants, the thickness of MON-2COOH shell was easily manipulated. The packed MON-2COOH@SiO 2 column showed high resolution and selectivity for separating both hydrophobic (alkylbenzenes, polycyclic aromatic hydrocarbons , anilines and phenols) and hydrophilic (nucleoside and nucleic bases) probes, highlighting the promise of MONs in mixed-mode HPLC. The MON-2COOH@SiO 2 column also achieved good separation to sulfonamides, nonsteroidal anti-inflammatory drugs, flavonoids and phenylurea herbicides , and offered better resolution than commercial C18 and pristine SiO 2 column. Multiple retention mechanisms were also found on MON-2COOH@SiO 2 packed column, underlining the great potential of MONs in mixed-mode HPLC.
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ACS Applied Polymer Materials
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2022
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IF 4.855
Shanjin Hu,Xiaoxue Du,Yanhui Bi,Ping-Ping He,Yali Mu,Chang Liu,Qi Gao,Mengyuan Yin,Weiwei Guo
As smart soft materials with programmable functions and excellent biocompatibility, DNA hydrogels have great potential in a variety of application fields, such as in the fabrication of soft biosensing devices. However, most DNA hydrogels are formed by self-assembly of multibranched DNA structures or with the assistance of enzymatic processes or chemical modifications, which significantly increases the complexity of material designing and the cost of construction. Herein, we report on the construction of responsive DNA hydrogel based on the self-assembly of one short single-stranded DNA (ssDNA), and the self-assembly can also occur within a polymeric matrix to construct interpenetrating network (IPN) hydrogel. Mechanism investigation reveals that the self-assembly between the short ssDNA strands leads to the formation of long linear DNA structures and looped structures, and the entanglement between these DNA assemblies at high concentrations results in the formation of three-dimensional hydrogel networks. By programming the sequence of the ssDNA strand, pH-responsive DNA hydrogel or catalytic DNA hydrogel can be constructed. Furthermore, the interpenetration of the catalytic DNA networks within a polyacrylamide hydrogel matrix leads to the formation an IPN hydrogel with higher structure stability and with excellent catalytic activity on the polymerization of aniline into conductive polyaniline (PANI). The successful construction of conductive PNAI patterns templated by the IPN hydrogel films is further achieved, which may hold potential in soft electronic and biosensing applications.
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JOURNAL OF ALLOYS AND COMPOUNDS
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2022
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IF 6.371
Xing Wu,Wenxuan Hu,Jiahuan Qiu,Biao Geng,Miao Du,Qiang Zheng
MXene , a kind of booming two-dimensional (2D) nanomaterials , has exhibited a promising application on free-standing high-performance supercapacitors. However, researches on MXene-based cathodes are still under development because its susceptibility to oxidation . Herein, a flexible free-standing polyaniline@MXene-carbon nanotubes (CNTs) film was prepared by a delicately-designed solvent-assisted self-assembly method followed with a vacuum filtration process. The zero-dimensional (0D) polyaniline (PANI) nanoparticle , which is often used as a cathode nanomaterial, was coated on the surface of 2D MXene nanosheets by solvent-assisted self-assembly to prevent MXene from oxidation and provide high specific capacitance simultaneously. The one-dimensional (1D) CNTs were introduced to endow the composite with well mechanical strength and flexibility. The ternary composite film delivers an excellent mechanical performance with a tensile strength of 99.4 MPa, a high specific capacitance of 463 F g −1 at 5 mV s −1 , and good cyclic stability with 92 % capacitance retention after 10,000 cycles. The asymmetric supercapacitor device assembled with the ternary composite film as cathode and the prepared free-standing MXene-CNTs as anode achieves a high energy density of 10 Wh kg −1 and an exceptional power density of 2808 W kg −1 .
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ENVIRONMENTAL SCIENCE & TECHNOLOGY
·
2022
·
IF 11.357
Honglong Zhang,Zhenyu Shi,Jun Ma,Fuyi Cui,Jing Zhang,Timothy J. Strathmann
In this study, a representative redox mediator, 2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPO), and its para-substituted derivatives (TEMPOs: 4-hydroxyl-TEMPO, 4-acetylamino-TEMPO, and 4-amino-TEMPO) significantly accelerated the abatement of trace organic contaminants (TrOCs, i.e., bisphenol-A (BPA), phenol, amines, and phenylbutazone) by Mn(VII) over a wide pH range of 4.0–9.0. The addition of substituents at para to the > N–O• moiety significantly influenced the degradation kinetics of TrOCs by changing the reduction potentials of TEMPOs and the corresponding oxoammonium cations (TEMPOs+); a linear relationship was observed between the substituents’ para Hammett sigma constants and the reduction potentials of TEMPOs and TEMPOs+. Pseudo-first-order reaction rate constants (kobs, min–1) of TrOC degradation by Mn(VII)/TEMPOs were also affected by the pKa of the TrOCs. Generally, the highest kobs values for individual TrOCs were observed at pH near the pKa even for TEMPOs+ with relatively pH-invariant reduction potentials. Overall, TrOC abatement kinetics were related to a combination of reactive species (Mn(VII), in situ formed MnO2, and TEMPOs+). For BPA, the relative contributions (R) of reactive species ranked as R(TEMPOs+) > R(Mn(VII)) > R(in situ formed MnO2) at pH 4.0–8.0, whereas R(Mn(VII)) > R(TEMPOs+) at pH 9.0 mainly owing to a change in BPA speciation as the pH approached the pKa1 value for BPA. The results of this study are useful for the development of heterogeneous TEMPO-based redox mediators and future applications of TEMPO-mediated oxidation systems for accelerated abatement of TrOCs in water.
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高影响因子
ChemElectroChem
·
2022
·Vol. 9
·期 12
·e202200082
·
IF 4.782
Jian Liu,Xiaohang Ma,Zhenfa Zi
Graphical Flower power : Polyaniline nano-flowers doped with L-phenylalanine (PANI-NF) porous structures were prepared. The supercapacitor assembled with PANI-NF symmetrical electrode showed maximum specific capacitance of 580 F g −1 (I=0.5 A g −1 ), a maximum energy density of 53.9 Wh kg −1 , and excellent cycle stability at high current density. It made an LED work continuously for more than 600 seconds after charging for 10 seconds. In this work, three-dimensional (3D) nanostructures of polyaniline nano-sheets, nano-particles, nano-nets and nano-flowers were synthesized with valine, sulfuric acid, sodium acetate and L-phenylalanine as doping acids, respectively. Conductive polyaniline with 3D nanostructure was proven as an excellent energy storage material because of its superior electrical properties and unique structure. The porous structure not only greatly improved the charge transfer efficiency and reduced the resistance, but also improved the cycle stability and energy storage of the electrode material. Polyaniline nano-flowers doped with L-phenylalanine (PANI-NF) showed a maximum specific capacitance of 580 F g −1 (I=0.5 A g −1 ), a maximum energy density of 53.9 Wh kg −1 , and excellent cycle stability at high current density.
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JOURNAL OF CATALYSIS
·
2022
·
IF 8.047
Lihua Zhu,Huan Zhang,Huaze Zhu,Huan Fu,Anna Kroner,Zhiqing Yang,Hengqiang Ye,Bing Hui Chen,Rafael Luque
Herein, we report a simple synthesis of PtNiCo trimetallic nanoparticles (NPs) loaded on carbon black (PtNiCo/C) via ambient-temperature chemical reduction and galvanic replacement reaction. The influence of thermal treatment temperature in 10 %H 2 /N 2 on PtNiCo NPs in PtNiCo/C-X nanostructures is revealed, where, X = 200 °C, 500 °C. XRD, XPS, TEM, HAADF-STEM, HRTEM, STEM-EDX elemental line-scanning (mapping), HS-LEIS, H 2 -TPR, atomic resolution aberration-corrected STEM (AC-STEM), XANES and EXAFS have been employed to characterize various nanostructures of PtNiCo NPs in PtNiCo/C-X. We established the relationship of nanostructure-reducing temperature thus catalytic behavior of PtNiCo/C-X: PtNiCo/C-200 ∼ Pt island (single atom and cluster)-on-NiCo alloy NP, PtNiCo/C-500 ∼ PtNiCo alloy NPs. PtNiCo/C-200 provides much improved catalytic activity and selectivity to target products ( NO 2 group hydrogenation) as compared to PtNiCo/C-500 for nitroarenes selective hydrogenation under mild reaction conditions (1.0 MPa-H 2 pressure, 18 °C or 40 °C-reaction temperature). That is considered to be closely correlated with the synergy effect of Pt islands and NiCo alloy nanoparticles in PtNiCo/C-200.
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Journal of Engineered Fibers and Fabrics
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2022
·
IF 2
Yu Wu,Sihao Zhou,Jie Yi,Dongsheng Wang,Wen Wu
Continuous production of conductive hydrogel fibers has received extensive interests due to their wide application in strain sensors. In this paper, we report on the fabrication of continuous alginate/polyaniline/graphene hydrogel fibers by the in situ polymerization and wet spinning methods. The obtained hydrogel fiber with good flexibility, high water absorbability (11.37 g/g), proper resistivity (220 Ω·m ) and stable resistance changes at both low strain (10%) and high strain (20% and 50%) could be used as a working strain sensor for a wearable human movements monitor. The conductive alginate/polyaniline/graphene hydrogel fiber shows highly sensitive, flexible, and recoverable (90% retention after five cycles) properties when monitoring palm, elbow, and knee movements. This kind of hydrogel with high elasticity and high sensitivity provides a possibility for the preparation of electromechanical sensors.
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