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INTERNATIONAL JOURNAL OF HYDROGEN ENERGY · 2020 · IF 4.939

Electrolysis of waste water containing aniline to produce polyaniline and hydrogen with low energy consumption

Shenglin Lu,Bin Zhao,Mingxing Chen,Lei Wang,Xian-Zhu Fu,Jing-Li Luo

Hydrogen generation from water electrolysis is attempted to be one of the replacement of sources as a clean fuel with high energy density . However, its application is limited by the high overpotential of oxygen evolution reaction (OER). Herein, hydrogen fuel is obtained from waste water by replacing OER with aniline electrochemical polymerization . Compared to the OER, the potential of aniline electro-polymerization greatly decreases 1240 mV at the current density of 30 mA cm −2 even using carbon paper electrode. Moreover, the Faradaic efficiency of hydrogen production is close to 100%. The as-prepared polyaniline demonstrates good performance as electrochemical capitative materials. This work provides efficient and lower energy consumed access to co-generate hydrogen and polyaniline in a convenient step by starting from the toxic and environmental-unfriendly wastewater.

CAS / MDL: 62-53-3 7664-93-9
研究领域: 环境科学 · 能源科学
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Materials Today Physics · 2021 · IF 9.298

Interfacial polymerized copolymers of aniline and phenylenediamine with tunable magnetoresistance and negative permittivity

Feichong Yao,Wenhao Xie,Ming Yang,Hang Zhang,Hongbo Gu,Ai Du,Nithesh Naik,David P. Young,Jing Lin,Zhanhu Guo

With the purpose of ameliorating the electrical property, permittivity and magnetoresistance of polyaniline (PANI) nanofibers , three types of phenylenediamine (PDA), including o -PDA, m -PDA, and p -PDA, and different contents of PDA have been incorporated into the PANI polymer backbone by the interfacial copolymerization of aniline with PDA. The results demonstrate that different types and contents of PDAs could disclose the distinct effects on the chemical structures , crystalline structures, and morphologies for copolymers of aniline with PDA affirmed by Fourier transform infrared (FTIR) spectroscopy, solid-state 13 C nuclear magnetic resonance ( 13 C NMR), X-ray diffraction (XRD), scanning electron microscope (SEM) and transmission electron microscopy (TEM). The molecular weight of all copolymers is reduced by several orders of magnitude relative to pure PANI nanofibers confirmed by gel permeation chromatography (GPC). The resistivity variations for the copolymers of aniline with different types of PDAs are well explained from the point view of their molecular structures based on the first-principle simulations (i.e. intrachain electrical conductivity) and degree of crystallinity gained from XRD (i.e. interchain electrical conductivity). A tunable room-temperature magnetoresistance (MR) and a controllable negative permittivity are discovered in the copolymers of aniline with different types and contents of PDAs. This work provides a new insight for the manipulation of electrical transport for PANI nanofibers and helps seek the new applications of conductive polymer .

CAS / MDL: 62-53-3
研究领域: 材料科学 · 化学
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Molecular Catalysis · 2021 · IF 5.062

Conversion of aniline contaminant to valuable polyaniline polymers from wastewater under alkaline conditions

Chang Bai,Yong Liu,Cong Wang,Xiao-Cong Zhang,Jia-Xuan Wu,Hai-Tao Ren,Xu Han

Although the oxidation processes mediated by persulfate (PS) and peroxymonosulfate (PMS) attract more attention in the degradation of various recalcitrant contaminants, the high concentrations of oxidants required for the low concentrations of contaminants always limit their large-scale applications. In this work, aniline can be effectively oxidized by CuO and PS under pH-neutral and alkaline conditions. The increased observed rate constant ( k obs ) values with increasing pHs indicate that the oxidation of aniline is facilitated by solution OH − . Meanwhile, the low ratios between the removed PS and aniline (1.19 at pH 7.0 and 1.68 at pH 12.0) indicate the high catalytic oxidation efficacy of the CuO-PS system. The insignificant contributions of SO 4 − , OH, 1 O 2 and O 2 − to aniline oxidation in quenching experiments and EPR analysis suggest that PS is likely activated on the surface of CuO via the non-radical pathway. The presence of carbon-centered radicals (CCRs), as well as UV and GC MS analysis, indicates the important intermediates of PhNH 2 + and PhNH radicals during the oxidation process, revealing that separate transfer of an electron from aniline to the activated PS, followed by subsequent abstraction of a H + by OH − to form PhNH are two important steps in the oxidation process. Further coupling of PhNH radicals results in the formation of insoluble polyaniline polymers at pHs 7.0 and 12.0. The high thermal stability and ideal pseudo-capacitive properties of the insoluble products indicate that the polyaniline produced from aniline wastewater can be used for high-temperature-resistant materials or capacitors. This study provides an efficient alternative to turn aniline waste to polyaniline polymers.

研究领域: 环境科学 · 材料科学
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JOURNAL OF INDUSTRIAL AND ENGINEERING CHEMISTRY · 2021 · IF 6.064

Electronic effects on protective mechanism of electropolymerized coatings based on N-substituted aniline derivatives for mild steel in saline solution

Hao Liu,Baomin Fan,Zining Liu,Xiaoqi Zhao,Biao Yang,Xingwen Zheng,Hua Hao

Polyaniline (PANI), poly( N -methylaniline) (PNMA) and poly( N- formylanilide) (PNFA) coatings were fabricated over mild steel via chronoamperometric strategy in oxalate electrolyte. Scanning electron microscope (SEM), attenuated total reflection infrared spectroscopy (ATR-IR) and X-ray photoelectron spectroscopy (XPS) evidenced the polymerization of monomers . Anticorrosive effects of PANI, PNMA and PNFA coatings for steel substrate were evaluated during long-term immersion in 3.5% NaCl solution by potentiodynamic polarization , electrochemical impedance spectroscopy (EIS) and frequency modulation (EFM). Morphological variation for coated specimens before and after immersion in NaCl solution was also monitored by SEM and atomic force microscope (AFM). Differentiated protection capability were observed for three coatings following the sequence of PNFA > PNMA > PANI. Through electrochemical and interfacial analyses, electroactivity and physical barrier were ascertained as the critical factors, especially the former one, in the long-term protection capacity. Electroactivity was distinguished by the elevated apparent current density from non-destructive EFM measurements. Furthermore, electron-donation and -withdrawal effects of N -substituents played an essential role in coating electroactivity. In detail, N -substituents improved the anodic protection and physical barrier of PNMA and PNFA coatings. Particularly, formyl with electron-withdrawal effect reinforced the anodic protection and thus the superior the anticorrosion efficiency of PNFA for underlying steel.

CAS / MDL: 62-53-3 79-16-3
研究领域: 材料科学 · 腐蚀与防护 · 电化学
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Materials Today Communications · 2023 · IF 3.8

Synthesis of hypercross-linked hybrid polyanilines from hollow spherical polyaniline and octavinylsilsesquioxane and its dye adsorption performance

Qinghu Meng,Lu Yu,Xue Yang,Rui Gao,Hejia Chang,Yue Wu,Zhizhou Yang,Anhou Xu,Sheng Gao,Fang Liu

In this manuscript, a series of functionalized PS microsphere (FPS), FPS@polyaniline (FPS@PANI) composite, hollow polyaniline sphere (HPANis), hypercross-linked hybrid polyanilines (HHPs) were prepared. The resulting polymers were well characterized. The results indicated that FPS was a uniform and well-defined sphere with rough and reticulate surface. The diameter of FPS was about 250 nm. FPS@PANI composite possessed well-defined spherical appearance, and its size was about 300~500 nm. The resultant HHP-1, HHP-2, and HHP-3 displayed higher specific surfaces of 153, 274 and 342 m 2 g —1 , respectively. They are mainly composed of micropores and mesopores. The adsorption experiments revealed that the computed maximum adsorbed quantities of malachite green (MG) and rhodamine B (RhB) for HHP-3 were 495.04 and 826.44 mg g —1 at 298 K and pH= 4, respectively, which were higher than many developed adsorbents. The regeneration experiments exhibited that after four cycles’ regeneration, the reusability performances of MG and RhB were still up to 92.19% and 88.05% respectively, suggesting that HHP-3 possessed wide prospect to be a promising adsorbent for dye waste water treatment and ecological environment restoration.

CAS / MDL: 62-53-3 78-08-0
研究领域: 材料科学 · 环境科学
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Environmental Chemistry · 2012 ·Vol. 9 ·期 6 ·558-563 · IF 2.57

Photochlorination of aniline in Fe3+-containing saline water under simulated solar light irradiation

Lei Wu,Xuefeng Hu,Lei Wu,Xuefeng Hu

Environmental context Aromatic amines are widely used chemicals, which show enhanced toxicity and longer environmental persistence when halogenated. We investigated the chlorination of aniline in seawater and in natural aqueous solutions containing Fe3+ and Cl–, under simulated sunlight irradiation. The results increase our understanding of the transformation pathway of typical nitrogen-containing aromatic contaminants in the environment. Photochlorination of aniline was observed in aqueous solutions containing dissolved FeIII and chloride ions under simulated solar light irradiation. Effects of O2, Cl–, Fe3+ and pH on the formation of chloroanilines (CAs) were investigated. para-chloroaniline (4CA) was identified as the main chlorinated product. The formation of 4CA is enhanced with increased concentrations of Cl– or Fe3+, and decreased pH, whereas oxygen plays a negligible role in the process. The results indicate that, Cl• is formed mainly by the photodissociation of FeCl2+–FeCl2+ complexes, and reacts with Cl– to produce Cl2•–. Aniline is then oxidised by Cl2•– into an anilino radical cation, which further reacts with Cl2•– to generate CAs. The photochlorination of aniline in natural seawater was also observed. Other phototransformation products of aniline were detected and a transformation pathway was proposed. This work provides evidence for the photochemical chlorination path of aniline-based aromatic amines in aqueous solutions.

研究领域: 环境科学 · 化学
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MOLECULES · 2019 ·Vol. 24 ·期 20 ·3718 · IF 3.06

Metal-Organic Frameworks of MIL-100(Fe, Cr) and MIL-101(Cr) for Aromatic Amines Adsorption from Aqueous Solutions

Mao-Long Chen,Shu-Yang Zhou,Zhou Xu,Li Ding,Yun-Hui Cheng

MIL-100(Fe, Cr) and MIL-101(Cr) were synthesized by the hydrothermal method and applied to the adsorptions of five aromatic amines from aqueous solutions. These three metal-organic frameworks (MOFs) were well characterized by powder X-ray diffraction (PXRD), scanning electron microscope (SEM), transmission electron microscope (TEM), thermogravimetric analysis (TGA) and surface area analysis. The adsorption mechanism of three MOFs and the effects of the structures of MOFs on the adsorption of aromatic amines were discussed. The results show that the cavity system and suitable hydrogen bond acceptor were important factors for the adsorption for five aromatic amines of aniline, 1-naphthalamine, o-toluidine, 2-amino-4-nitrotoluene and 2-nitroaniline: (a) the saturated adsorption capacity of aniline, 1-naphthylamine and o-toluidine on MIL-100(Fe) were 52.0, 53.4 and 49.6 mg/g, respectively, which can be attributed to the intermolecular hydrogen bond interaction and cavity system diffusion. (b) The adsorption capacity of 2-nitroaniline and 2-amino-4-nitrotoluene on MIL-101(Cr) were 54.3 and 25.0 mg/g, respectively, which can be attributed to the more suitable pore size of MIL-101(Cr) than that of MIL-100(Fe, Cr). The MOFs of MIL-100(Fe) and MIL-101(Cr) can be potential materials for removing aromatic amines from aqueous solutions.Keywords:metal-organic framework;adsorption;aromatic amines;aniline;1-naphthalamine;o-toluidine;2-amino-4-nitrotoluene;2-nitroaniline

CAS / MDL: 100-21-0 554-95-0
研究领域: 材料科学 · 环境科学
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POLYMER · 2017 · IF 3.684

Electrochromic and electrofluorochromic behavior of novel polyurea bearing oligoaniline and triphenylamine units

Ying Yan,Ningwei Sun,Xiaoteng Jia,Xincai Liu,Ce Wang,Danming Chao

Electroactive materials have gained increasing attention for their intelligent applications. In this work, we report the design and synthesis of a novel electrochromic and electrofluorochromic dual-switching polyurea bearing oligoaniline and fluorescent triphenylamine units (PUOT). Cyclic voltammogram of PUOT exhibits two reversible redox couples at 0.96 V/0.73 V and 1.36 V/1.11 V (vs. Ag/AgCl reference electrode), ascribed to the redox transformation of oligoaniline and triphenylamine groups, respectively. In this wide potential window (0–1.6 V), the PUOT film reveals a unique multistage regulated electrochromic behavior with maximal transmittance contrast value of 38% switching from 0.0 V to 1.0 V, and partial transmittance contrast value of 14% (0–1.6 V) and 24% (1.0–1.6 V). Furthermore, its electrofluorochromic behavior has also been disclosed at the potential range of 0–1.0 V, which demonstrates that the oligoaniline groups should be served as electroactive units in this electrofluorochromic system. Our research not only presents a deep understanding of the optical-electrical modulation mechanism but also paves the way for their future applications.

CAS / MDL: 7727-54-0 10217-52-4
研究领域: 材料科学 · 化学
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Journal of Water Process Engineering · 2024 · IF 6.3

Electrosorption approach removing PFOA from wastewater using a MXene-polyaniline film

Jinfeng Zhao,Yuntong Fan,Jiaqi Zhangle,Congcong Ni

Perfluorooctanoic acid (PFOA) is a persistent organic pollutant found in various industrial effluents, posing significant environmental and health risks. Electrosorption of PFOA on MXene-polyaniline film from water was studied. The results of electrosorption kinetics showed that the functionalized MXene film with polyaniline resulting in an approximately 100 % increase in electrosorption capacitance for PFOA due to increasing of the MXene film's volumetric capacitance and modifying of surface chemistry of MXene. The maximum adsorption of PFOA on MXene and MXene-polyaniline films were 358.5 mg/g and 966.1 mg/g, respectively, at an initial concentration of 100 mg/L upon application of +1.0 V. Moreover, humic acid (HA) competing with the adsorption sites, sodium chloride through the double-layer compression effect, and pH affecting the amine or amide functional groups on MXene-polyaniline which inhibited PFOA adsorption onto MXene-polyaniline film were thoroughly examined. Lastly, the reversible adsorption–desorption cycles show that the MXene–polyaniline film possesses the potential to be used continuously. To address PFAS pollution in water sources, we think our approach can help build effective and long-lasting technology.

研究领域: 环境科学 · 材料科学
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APPLIED SURFACE SCIENCE · 2016 · IF 3.15

Dual-shell hollow polyaniline/sulfur-core/polyaniline composites improving the capacity and cycle performance of lithium–sulfur batteries

Yanling An,Pan Wei,Meiqiang Fan,Da Chen,Haichao Chen,QiangJian Ju,Guanglei Tian,Kangying Shu

In this study, a dual-shell hollow polyaniline/sulfur-core/polyaniline (hPANI/S/PANI) composite was prepared by successively depositing PANI, S, and PANI on the surface of a template silicon sphere. The electrochemical properties of this composite were evaluated using a lithium plate as an anode in lithium/sulfur cells. The hPANI/S/PANI composite showed a discharge capacity of 572.2   mAh   g −1 after 214 cycles at 0.1   C, and the Coulombic efficiency was above 87% in the whole charge/discharge cycle. The improved cycle property of the hPANI/S/PANI composite can be ascribed to the fine sulfur particles homogeneously deposited on the PANI surface and sprawled inside the two PANI layers during the charge/discharge cycle. This behavior stabilized the nanostructure of sulfur and enhanced its conductivity.

研究领域: 材料科学 · 电化学
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Foods · 2023 ·Vol. 12 ·期 15 ·2875 · IF 5.2

Development of Simultaneous Determination Method of Pesticide High Toxic Metabolite 3,4-Dichloroaniline and 3,5 Dichloroaniline in Chives Using HPLC-MS/MS

Yibo Dong,Xiaolong Yao,Wanping Zhang,Xiaomao Wu

3,4-dichloroaniline (3,4-DCA) and 3,5-dichloroaniline (3,5-DCA) are, respectively, the primary metabolites deriving from the breakdown of phenylurea herbicides and dicarboximide fungicides in both soils and plants, whose residues in vegetable products have a heightened concern considering their higher health risks to humans and greater toxicity than the parent compounds in the environment. In this study, a sensitive high-performance liquid chromatography-tandem mass spectrometry (HPLC-MS/MS) method was developed for the simultaneous determination of 3,4-DCA and 3,5-DCA residues in chive products based on the optimization of HPLC-MS/MS chromatographic and mass-spectrometric conditions using the standard substances and the modified QuEChERS preparation technique. The preparation efficiency of 3,4-DCA and 3,5-DCA from chive samples showed that acetonitrile was the best extractant. The combination of the purification agent graphite carbon black + primary secondary amine and the eluting agent acetonitrile + toluene (4:1,v/v) had a satisfactory purification effect. The linear correlation coefficients (R2) were more than 0.996 with the six concentration range of 0.001–1.000 mg/L for 3,4-DCA and 3,5-DCA. The limit of detection and limit of quantitation of this method was 0.6 and 2.0 µg/kg for 3,4-DCA, as well as 1.0 and 3.0 µg/kg for 3,5-DCA, respectively. The matrix effect range of 3,4-DCA and 3,5-DCA in chive tissues was from −9.0% to −2.6% and from −4.4% to 2.3%, respectively. The fortified recovery of 3,4-DCA and 3,5-DCA in chive samples at four spiked levels of 0.001–1.000 mg/kg was 75.3–86.0% and 78.2–98.1%, with the relative standard deviation of 2.1–8.5% and 1.4–11.9%, respectively. The limit of detection (LOD) and limit of quantification (LOQ) of the method were 0.6, 2.0, and 1.0, 3.03 for 4-DCA and 3,5-DCA, respectively. This study highlights that the analytical method established here can efficiently and sensitively detect residues of 3,4-DCA and 3,5-DCA residues for monitoring chive products. The method was successfully applied to 60 batches of actual vegetable samples from different regions.Keywords:3,4-dichloroaniline;3,5-dichloroaniline;simultaneous determination;UPLC-MS/MS;chive

CAS / MDL: 95-76-1 626-43-7
研究领域: 分析化学 · 食品安全 · 环境科学
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JOURNAL OF POROUS MATERIALS · 2021 ·Vol. 29 ·期 1 ·103-110 · IF 2.496

β Zeolite/bentonite composite as a novel catalyst for condensation of aniline to diphenylamine

Yang Yeqing,Liao Yingling,Liu Naiwang,Shi Li,Meng Xuan

β Zeolite/bentonite composite was synthesized by simple kneading as catalyst for condensation reaction of aniline to diphenylamine. The experiment which was conducted at 320 °C under 2 MPa with a liquid hourly space velocity (LHSV) of 2 h −1 showed that the Hβ zeolite loading 25% clay exhibited the highest activity (9.9% aniline conversion) and selectivity. Pilot experiments (315–320 °C, 2 MPa, LHSV of 0.20–0.22 h −1 ) have also confirmed that the catalyst had good stability. The crystalline structure, acidic property and textural property of the catalysts were characterized by XRD, Py-IR, N 2 adsorption–desorption. Moreover, according to the thermodynamic analysis, the condensation of aniline to diphenylamine is an exothermic reaction, indicating that too high temperature operation is unfavorable for the reaction. The studied β zeolite/bentonite composite is of promising efficiency in condensation of aniline to diphenylamine.

研究领域: 催化化学 · 材料科学
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