Materials Today Energy
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2021
·
IF 7.311
Xin Li,Quan Feng,Dingsheng Wu,Alfred Mensah,Wei Li,Yibing Cai,Dawei Li,Qufu Wei
The rise of energy harvesting textiles opens up an emerging path to prospective energy solutions for the next generation of wearable electronics. Flexible electrodes as the core link in enzymatic biofuel cell (EBFC) should be stretchable while using enzyme molecules to transfer the energy from chemical of green fuels into electricity, which is beneficial to meet the key requirements of practical applications and shows considerable potential in wearable electronics. As a result, we develop a single EBFC based on intramolecular electron transfer using a stretchable electrode made of polyurethane/zeolitic imidazolate framework-8@laccase/carbon nanotubes (PU/ZIF-8@LAC/CNTs), which encapsulates LAC into ZIF-8 crystals during ZIF-8 in-situ growth on PU nanofibers . The maximal power density output of single-EBFC reached 1.33 W m −3 . More importantly, after multiple deformations of 75 stretching cycles, continuously stretching and holding and 180° twisting cycles, the single-EBFC retains an E OCV of more than 50%, which exhibits stable energy output, thus the stretchability of PU/ZIF-8@LAC/CNTs are proved. This stretchable electrode can establish a stable platform of power devices and will be potentially integrated into wearable electronics.
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Defence Technology
·
2021
·
IF 3.172
Wissam Bessa,Djalal Trache,Mehdi Derradji,Ahmed Fouzi Tarchoun
The design of astonishing combinations of benzoxazine resins with various fillers is nowadays of great interest for high quality products, especially in ballistic armors. The objective of this study is to investigate a new hybrid material prepared as multi-layered composite plate by hand lay-up technique. Different composites were manufactured from Kevlar fabrics reinforced polybenzoxazine, which was filled with silane treated microcrystalline cellulose (MCC Si) at various amounts in the interlayers. The developed materials were tested for their flexural, dynamic mechanical and ballistic performance. The aim was to highlight the effect of adding different amounts of MCC Si on the behavior of the different plates. Compared to the baseline, the dynamic mechanical and bending tests revealed an obvious decrease of the glass transition of 21 °C and a notable increase in storage modulus and flexural strength of about 180 %and17%, respectively, upon adding 1% MMC Si as filler. Similarly, the ballistic test exhibited an enhancement in kinetic energy absorption for which the composite supplemented with 1% MCC Si had the maximal energy absorption of 166.60 J. These results indicated that the developed panels, with interesting mechanical and ballistic features, are suitable to be employed as raw materials to produce body armor.
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SEPARATION AND PURIFICATION TECHNOLOGY
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2021
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IF 7.312
Chuankun Yin,Qianna Xia,Jiao Zhou,Bowen Li,Yu Guo,Aimal Khan,Xiaoxia Li,Aihua Xu
The development of efficient and eco-friendly Mn-based catalysts for peroxymonosulfate (PMS) activation and revealing the mechanism are highly desired for pollutants removal in wastewater. In this study, a ternary mullite oxide YMn 2 O 5 (YMO) was synthesized for bisphenol A (BPA) degradation in the presence of PMS for the first time. Combined with XPS, EPR and TG, abundant surface labile oxygen species (O lab ) with a ratio of 39.7% were identified in the mullite materials, which was higher than that for α-, β-, γ- and δ-MnO 2 . YMO also exhibited higher interfacial conductivity and stronger interactions among the catalyst, PMS and BPA than other MnO 2 . Superior performance in BPA degradation was observed with YMO, and O lab was suggested as the main active sites, for the normalized first-order rate constant was linearly dependent on the ratio of the oxygen species. Chemical quenching experiments, EPR and open circuit potential suggested that the degradation of BPA was mainly caused by the direct electron transfer process through the reactive O lab -PMS complexes. The influence of YMO concentration, PMS concentration, solution pH, different anions and reaction temperature was thoroughly studied. Moreover, the intermediates were identified and the possible degradation pathways were proposed. This work demonstrated that mullite oxide YMO with enriched O lab species can be used as eco-friendly catalysts for efficient PMS activation to remove recalcitrant organic compounds in wastewater.
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JOURNAL OF HAZARDOUS MATERIALS
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2021
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IF 10.588
Xuan-Yuan Pei,Hong-Yu Ren,Guo-Shuai Liu,Guang-Li Cao,Guo-Jun Xie,De-Feng Xing,Nan-Qi Ren,Bing-Feng Liu
Bisphenols (BPs) are distributed in worldwide as typical environmental hormones, which potentially harm the ecological environment and human health. In this study, four BPs, i.e., bisphenol A, bisphenol F, bisphenol S, and bisphenol AF, were used as prototypes to identify the intrinsic differences in degradation mechanisms correlated with the molecular structures in peroxydisulfate (PDS)-based advanced oxidation processes (AOPs). Electron transfer was the main way of modified biochar to trigger the heterogenous catalysis of PDS, which can cause the degradation of BPs. Phenolic hydroxyl groups on bisphenol pollutants were considered as possible active sites, and the existence of substituents was the main reason for the differentiation in the degradation efficiency of various bisphenols. Results of ecotoxicity prediction showed that most intermediates produced by the degradation of BPs in the β-SB/PDS system, which was dominated by the electron transfer pathway, had a lower toxicity than the parent molecules, while the toxicity of several ring cleavage intermediates was higher. This study presents a simple modification scheme for the conversion of biochar into functional catalysts and provides insights into the mechanism of heterogeneous catalytic degradation mediated by modified biochar as well as the degradation differences of bisphenol pollutants and their potential ecotoxicity.
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CHEMICAL ENGINEERING JOURNAL
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2021
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IF 13.273
Pingping Yang,Xuejiao Hu,Yizhou Tu,Guizhou Xu,Lin Sun,Xianchuan Xie
Organic micropollutant in the aquatic environment has become a worldwide problem. In this study, a new DMpillar[5]arene-based porous organic polymer (DMPBP[5]) with the highest surface area of 1347.4 ± 39.3 m 2 g −1 is developed through Friedel-Crafts alkylation reaction between DMpillar[5]arene (DMP5) and 4,4′-bis(chloromethyl)-1,1′-biphenyl (BCMBP) to remove a wide range of organic micropollutants with fast removal rate and large uptake amounts. The synthesized DMPBP[5] can capture many types of organic pollutants in water including positively charged, negatively charged and neutral ones and those with different hydrophilicity, through host–guest interaction, hydrophobic interaction, electrostatic interaction and π-π interaction. For some pollutants, the adsorption kinetic constants of DMPBP[5] are thousands of times larger than that of activated carbon (AC) and even 10 4 -10 5 times larger than that of resin (XAD-4), and the adsorption capacities of DMPBP[5] are about 3 and 4 times higher than that of AC and XAD-4, respectively. The superior adsorption performance of DMPBP[5] is attributed to permanent porosity and accessible binding sites because of the introduction of rigid structure. Even at environmentally relevant concentrations, DMPBP[5] can quickly remove the pollutants simultaneously and can be easily regenerated with methanol under ambient conditions. In short, due to the wide adsorption range, excellent adsorption performance, and easy recyclability, DMPBP[5] is an excellent adsorbent for wastewater treatment with great application potential.
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CHEMICAL ENGINEERING JOURNAL
·
2021
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IF 13.273
Hengyu Cai,Jing Zou,Jinbin Lin,Jiawen Li,Yixin Huang,Shuyin Zhang,Baoling Yuan,Jun Ma
Owing to the high peroxide bond dissociation energy (377 kJ mol −1 ), peroxymonosulfate (PMS) is rather difficult to be activated by heat for degrading organic pollutants. This work is the first to add sodium hydroxide (NaOH) to enhance the elimination of acetaminophen in heat/PMS system. Heat/PMS system even possessed a better Performance than heat/peroxydisulfate (PDS) system with the addition of NaOH. Quenching experiments and electron paramagnetic resonance tests demonstrated that singlet oxygen and hydroxyl radical were the primary reactive oxygen species responsible for acetaminophen elimination in NaOH-enhanced heat/PMS system. Singlet oxygen mainly came from the alkaline activation of PMS, while hydroxyl radical was generated from the thermolysis of peroxide bond. Increasing PMS concentration and reaction temperature favored the production of reactive oxygen species and the elimination of acetaminophen. Nine degradation intermediates of acetaminophen were identified by LC/TOF/MS and the corresponding degradation pathways were proposed. Chloride ion significantly accelerated the elimination of acetaminophen, while humic acid and carbonate ion slightly retarded acetaminophen removal. NaOH-enhanced heat/PMS system was highly efficient in eliminating many organic pollutants and more prone to degrading electron-rich organics. This study developed a simple and efficient approach to strengthening the oxidation capacity of heat-activated PMS and highlighted the superiority of PMS to PDS in thermolysis under alkaline conditions.
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SPECTROCHIMICA ACTA PART A-MOLECULAR AND BIOMOLECULAR SPECTROSCOPY
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2019
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IF 2.931
Song Wang,Lantian Su,Lumei Wang,Dongwei Zhang,Guoqing Shen,Yun Ma
This paper proposes the idea of establishing carbendazim (CBZ) colorimetric determination in spiked water samples by specific aptamers of unlabeled carbendazim (CBZ), gold nanoparticles (AuNPs) and cationic polymer poly-diallyldimethylammonium chloride (PDDA). In the absence of CBZ, the CBZ aptamer will react with the cationic polymer PDDA by electrostatic interaction to form a complex structure. Therefore, the gold nanoparticles will remain dispersed due to the lack of PDDA. However, when CBZ is added into the sensory system, the CBZ-specific aptamer can selectively capture CBZ to form a stable complex structure. Due to the consumption of the aptamer, PDDA is unable to interact with the aptamer and begins to induce aggregation of AuNPs, thereby causing the color of the solution to change from red to blue. Colorimetric determination of CBZ based on the specific recognition of aptamer and the PDDA-induced aggregation of AuNPs has a detection limit of 2.2 nM, a linear range (R = 0.9960) from 2.2 to 500 nM. The method has good sensitivity and specificity, and the average recovery of CBZ is 94.9–104.8% in the application of actual water samples. This colorimetric method is simple, time-saving and low requirements for equipment, therefore, it holds great potential for CBZ detection in the environmental water samples.
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BIOSENSORS & BIOELECTRONICS
·
2019
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IF 9.518
Jian Zhang,Xiaobo Fang,Jayne Wu,Zhiwen Hu,Yu Jiang,Haochen Qi,Lei Zheng,Xiaofeng Xuan
With increasing industrialization of food production, residues of organophosphorus pesticides (OPs) are more frequently found in the environment including rivers, lakes and soils. Extended exposure to OPs, even at a level below 1 nM, may lead to liver and central nervous system damages in humans and animals, while existing detection methods are not sensitive enough to detect OPs at trace levels. We presented a simple-to-use aptasensor to rapidly detect broad-spectrum OPs with high sensitivity. DNA aptamer was modified on the surface of a micro interdigitated electrode chip, and AC electrokinetics was employed to accelerate the binding of OP molecules to the aptamer probe. The sensing strategy directly measured the interfacial capacitance whose change rate was adopted as a quantitative indicator of recognition events, with a sample to result detection time of 30 s. This aptasensor had a wide linear range of (fM ~ nM), and the detection limit reached (0.24–1.67) fM for four highly-toxic OPs, with good specificity. It still showed good activity after being stored in non-refrigerated environment for at least 14 days. This aptasensor as well as the detection method offer a promising solution for on-site and real-time sensitive OP detection.
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Journal of Materials Chemistry C
·
2019
·Vol. 8
·期 1
·303-309
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IF 6.641
Shuai Yang,Yang He,Yanju Liu,Jinsong Leng
In this paper, a series of shape-memory poly(arylene ether ketone)s (PAKEs) with various flexible groups (i.e., carbolic bonds, ether, and ketone linkages) and entangled crystalline polymeric structures were synthesized by combining different bisphenol monomer (bisphenol A monomer and methyl hydroquinone monomer) proportions with a 4,4′-difluorobenzophenone monomer. The flexible parts and the entangled parts acted as a reversible phase and permanent phase, respectively. The prepared PAEK films exhibited excellent heat-triggered shape-memory behaviors with tunable glass transition temperatures (Tg) from 116 °C to 140.5 °C including an extremely high fixity ratio (over 98%), high recovery ratio (over 92%), and fast recovery rate (within 7.0 s). As increasing the content of the methyl hydroquinone monomer in the structural unit, the recovery ratio showed a downward trend, whereas the recovery time increased gradually. In addition, the electric-triggered shape-memory effect of the PAEK films was achieved via the introduction of carbon nanotubes (CNTs). Upon applying a voltage of 25 V, the recovery ratios of the composite films containing 10 wt% and 15 wt% CNTs were all over 80% (of 83.0% and 87.6%, respectively), indicating a great electric-triggered shape-memory behavior. The recovery ratio increased and the triggered voltage decreased as increasing the content of CNTs. The heat and electric dual-triggered shape-memory PAEK composites could be important smart materials possessing wide application prospects.
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APPLIED SURFACE SCIENCE
·
2019
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IF 5.155
Hongjie Zhu,Lingxuan Gong,Zhengkui Li
There is a great need to design a new method for fabricating efficient and cheap Z-scheme photocatalysts. For this reason, we synthesized a novel Z-scheme photocatalyst α-Fe 2 O 3 /P3HT with O-Ti-O charge transfer mediator. The effective compounding of each part was confirmed by different characterization methods. The charge transfer mechanism was confirmed to obey the Z-scheme mechanism by measuring the valence band value and by ESR experiments. Moreover, the Z-scheme mechanism in this system was further discussed based on the observed changes in the chemical structure and the theoretical calculation. Based on the characterization of the optical properties, this novel catalyst exhibited better charge transfer and separation abilities under visible light conditions due to its unique architecture. Additionally, this novel Z-scheme photocatalyst showed enhancement in the bisphenol A degradation effect, the degradation reaction was pseudo-first-order kinetics, a removal rate of up to 90% was maintained after four cycles. The BPA degradation pathway was also discussed in this study. This study provides a new approach for the construction of Z-scheme photocatalysts.
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ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH
·
2019
·Vol. 26
·期 36
·36410-36422
·
IF 2.914
Latif Abdul,Kai Sun,Si Youbin
This study demonstrated, for the first time, Fe(III)/peroximonosulphate (PMS) could be an efficient advanced oxidation process (AOP) for wastewater treatment. Bisphenol A (BPA) was chosen as a model pollutant in the present study. Fe(III)-activated PMS system proved very effective to eliminate 92.18% of BPA (20 mg/L) for 30-min reaction time at 0.50 mM PMS, 1.5 g/L Fe(III), pH 7.0. The maximum degradation of BPA occurred at neutral pH, while it was suppressed at both strongly acidic and alkaline conditions. Organic and inorganic ions can interfere with system efficiency either positively or negatively, so their interaction was thoroughly investigated. Furthermore, the presence of organic acids also affected BPA degradation rate, especially the addition of 10 mM citric acid decreased the degradation rate from 92.18 to 66.08%. Radical scavenging experiments showed that SO 4 •– was the dominant reactive species in Fe(III)/PMS system. A total of 5 BPA intermediates were found by using LC/MS. A possible degradation pathway was proposed which underwent through bridge cleavage and hydroxylation processes. Acute toxicity of the BPA degradation products was assessed using Escherichia coli growth inhibition test . These findings proved to be promising and economical to deal with wastewater using iron mineral for the elimination of organic pollutants.
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Materials Science & Engineering C-Materials for Biological Applications
·
2019
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IF 4.959
Zhu Mengting,Tonni Agustiono Kurniawan,You Yanping,Ram Avtar,Mohd Hafiz Dzarfan Othman
Bisphenol A (BPA) is a refractory pollutant presents in water body that possesses serious threats to living organisms. To deal with it, we investigate and evaluate the effectiveness of GO@BiOI/Bi 2 WO 6 composite as a novel photocatalyst for BPA removal from aqueous solutions under UV–vis irradiation. To enhance its removal for BPA, the surface of BiOI/Bi 2 WO 6 is modified with graphene oxide (GO). This composite is named as ‘GO@BiOI/Bi 2 WO 6 ’. Changes in its physico-chemical properties after surface modification with GO are characterized by XRD, FTIR, FESEM-EDS, XPS, PL, and BET methods. Optimized conditions of BPA degradation by the composite are determined under identical conditions. Photodegradation pathways of BPA and its removal mechanisms by the same composite are presented. It is obvious that the GO@BiOI/Bi 2 WO 6 has demonstrated its potential as a promising photocatalyst for BPA removal under UV–vis irradiation. About 81% of BPA removal is attained by the GO@BiOI/Bi 2 WO 6 under optimized conditions (10 mg/L of BPA, 0.5 g/L of dose, pH 7 and 5 h of reaction time). The oxidation by-products of BPA degradation include p -hydroquinone or 4-(1-hydroxy-1-methyl-ethyl)-phenol. In spite of its performance, the treated effluents are still unable to meet the maximum discharge limit of <1 mg/L set by national legislation. Therefore, subsequent biological processes are essential to maximize its biodegradation in the wastewater samples before their discharge into waterbody.
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