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ACS Applied Nano Materials · 2021 · IF 5.097

Selective Photothermal Reduction of CO2 to CO over Ni-Nanoparticle/N-Doped CeO2 Nanocomposite Catalysts

Zewei Jia,Shangbo Ning,Yuxin Tong,Xin Chen,Huilin Hu,Lequan Liu,Jinhua Ye,Defa Wang

Photothermal reverse water gas shift reaction is one of the promising methods to palliate global energy and environmental issues. Searching for catalysts with high activity and CO selectivity for CO2 conversion has been attracting extensive attention. In this work, Ni nanoparticle-loaded N-doped CeO2 (Ni/N-CeO2) composite catalysts were synthesized using a three-step method. Under light irradiation, the optimal Ni/N5.0-CeO2 exhibited a CO yield rate of 20.9 mmol·gcat–1·h–1 with almost 100% of CO selectivity via photothermal CO2 reduction. As a comparison, Ni/CeO2, without nitrogen doping, showed a high CH4 selectivity. The strong light absorption of Ni/N5.0-CeO2 mainly by loading of Ni nanoparticles and the enhanced adsorption/activation of CO2 molecules due to increased oxygen vacancies in N5.0-CeO2 by N-doping were supposed to account for the excellent catalytic performances. The doping of nitrogen was of particular importance for the formation of N–H bonds, which could modulate the reaction pathway for promoting the reduction of CO2 toward CO while suppressing the undesirable CO2 methanation process.

研究领域: 化学工程 · 环境科学 · 材料科学
✓ 已验证 DOI 高影响因子
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MICROCHEMICAL JOURNAL · 2024 · IF 4.9

Synthesis of the immobilized laccase on N-doped carbon nanonets for photothermal detection of hydroquinone

Xinyue Wang,Li Liu,Binbin Jiang,Weiwei Xie,Qingyang Chong,Song Li,Zhiming Chen

The rapid and sensitive detection of hazardous substances is essential for safeguarding human health. This work presented the synthesis of laccase immobilized on N-doped carbon nanonets (N-doped carbon nanonets-lac) biosensor and its application for the photothermal detection of hydroquinone. The N-doped carbon nanonets-lac biosensor demonstrated rapid response and precise detection of hydroquinone in 5 s, along with excellent sensitivity, good tolerance to metal ions and organic compounds, outstanding selectivity, and storage stability. Thanks to the photothermal effect of N-doped carbon nanonets, the N-doped carbon nanonets-lac biosensor was demonstrated as a photothermal biosensor for hydroquinone detection. The N-doped carbon nanonets-lac biosensor exhibits a highly sensitive current response under illumination, with a detection limit as low as 0.14 μM (S/N = 3) and an extensive response range of 1–1000 μM. Furthermore, the N-doped carbon nanonets-lac biosensor showed reliable performance in photothermal analysis of tap and Yangtze River water samples, highlighting its technical effectiveness in detecting contamination of toxic compounds in real water samples.

研究领域: 环境科学 · 生物化学 · 分析化学
✓ 已验证 DOI 高影响因子
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AICHE JOURNAL · 2020 ·Vol. 66 ·期 11 ·e17023 · IF 3.519

Bipolar membrane electrodialysis for cleaner production of N-methylated glycine derivative amino acids

Yaoming Wang,Xiaoli Wang,Haiyang Yan,Chenxiao Jiang,Liang Ge,Tongwen Xu

In this study, cleaner production of N -methylglycine (NMG), N , N -dimethylglycine (DMG), and N , N , N -trimethylglycine (TMG) with similar structures but different methylate groups was performed using bipolar membrane electrodialysis (BMED). The effects of the feed mass concentration and current density on the separation performance were intensively analysed in terms of the molecular size, molecular structure, ion concentration, and interaction between amino acids and membranes. The results indicated that the optimal recovery performance was achieved at a current density of 200 A/m 2 and feed mass concentration of 6%. Under the optimal conditions, the energy consumption and current efficiencies were 2.3 kWh/kg and 78% for NMG, 2.49 kWh/kg and 69.5% for DMG, and 3.52 kWh/kg and 39.6% for TMG, respectively. It was speculated a competition for water splitting occurs between the bipolar membranes and anion exchange membranes when BMED is used for the separation and purification of large-sized bioproducts.

研究领域: 生物工程 · 化学工程 · 环境科学
✓ 已验证 DOI 高影响因子
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JOURNAL OF NANOPARTICLE RESEARCH · 2023 ·Vol. 25 ·期 8 ·1-10 · IF 2.5

Fast degradation of rhodamine B by peroxymonosulfate activated with Fe–N carbon nanotubes

Cui Wei,Fang Jiahui,Wan Yuanyuan,Tao Xueyu,Guo Litong,Feng Qiyan

In this study, Fe–N co-doped carbon nanotubes (Fe–N-CNTs) were prepared and used to activate peroxymonosulfate (PMS) for advanced oxidation removal of Rhodamine B (RhB). The XRD, XPS, SEM and EDS results revealed that the Fe, N, O co-doped carbon nanotubes (Fe–N-CNTS) coated with FeO(OH) nanosheets were successfully synthesized by a simple pyrolyzing process. The large BET specific surface area (286.42 m 2 /g) and hybrid pore structure of micropores and mesopores (3–10 nm) of the Fe–N-CNTS ensured its good RhB degradation performance (98% in 30 min) by activatting PMS. The Fe–N-CNTS-1.5 had the best degradation performance, which could be attributed to the synergy effect between FeO(OH) nanosheets and Fe–N-CNTS. The 1 O 2 , O 2 •, •OH and SO 4 −• were formed during the PMS activating process and involved in the RhB degradation. The reaction constant of 0.5483 min −1 could be obtained by adding 1.5 mM PMS, which is about 12 and 24 times of the reaction constant of PMS only (0.0458 min −1 ) and FeN-CNTS only (0.0226 min −1 ), respectively. This work provides new insight into the mechanism of PMS activation by carbon-based catalysts for the efficient degradation of RhB.

研究领域: 环境科学 · 材料科学
✓ 已验证 DOI 高影响因子
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RSC Advances · 2013 ·Vol. 4 ·期 12 ·6048-6054 · IF 2.562

Eco-friendly synthesis of regenerable antimicrobial polymeric resin with N-halamine and quaternary ammonium salt groups

Zhiqiang Jie,Xiufang Yan,Lianhong Zhao,Shelby Davis Worley,Jie Liang

An effective macroporous cross-linked antimicrobial polymeric resin containing N-halamine and quaternary ammonium salt moieties was synthesized in an eco-friendly and economical way. Commercially available macroporous crosslinked chloromethylated polystyrene (CMPS) resin reacted with the salt of 5,5-dimethylhydantoin (DMH) and trimethylamine (TMA) in water to produce a polymeric resin containing hydantoinyl and quaternary ammonium salt moieties, poly(p-methylstyrene)-3-(5,5-dimethylhydantoin)-co-trimethyl ammonium chloride (PSHTMA). The hydantoinyl groups in PSHTMA were converted to an antimicrobial N-halamine structure by a facile chlorination reaction in dilute NaOCl solution. The as-synthesized antimicrobial polymeric resin (Cl-PSHTMA) was characterized by FT-IR, X-ray photoelectron spectroscopy, and zeta-potential measurement. The antimicrobial tests showed that the as-synthesized antimicrobial polymeric resin was capable of 7-log inactivation of S. aureus and 8-log inactivation of E. coli within 1 minute contact time. Moreover, the N-halamine moieties in Cl-PSHTMA exhibited excellent regenerability.

研究领域: 材料科学 · 微生物学 · 环境科学
✓ 已验证 DOI 高影响因子
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CHINESE JOURNAL OF CATALYSIS · 2019 · IF 4.914

In situ synthesis of Fe-N-C catalysts from cellulose for hydrogenation of nitrobenzene to aniline

Hao Wang,Xiaohao Liu,Guangyue Xu,Ziwei Guo,Ying Zhang

ABSTRACT Owing to Fe being the most abundant and least expensive transition metal on the earth, the utilization of Fe-based catalysts for catalytic hydrogenation has attracted worldwide attention. In this work, a series of N-doped C supported Fe catalysts (Fe-N-C) were prepared by co-pyrolysis of cellulose and ferric chloride under ammonia atmosphere. Characterization methods such as elemental analysis, atomic absorption spectroscopy, nitrogen adsorption-desorption isotherms, transmission electron microscopy, high-resolution transmission electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy were carried out to explore the physicochemical properties of the catalysts. Using hydrogenation of nitrobenzene as a model reaction, the catalysts prepared at different pyrolysis temperatures displayed different activities. Fe-N-C-700 exhibited the best activity among these catalysts, with the yield of aniline being up to 98.0% under 5 MPa H 2 at 120 °C after 12 h. Combined with the results of catalyst characterization and comparative tests, the transformation of Fe species and the generation of N-doped C, especially graphitized N-doped C, in the catalyst may be the main factors affecting the activity. A kinetic study was carried out and the apparent activation energy was obtained as 31.53 kJ/mol. The stability of the catalyst was also tested and no significant decrease in the activity was observed after 5 runs.

研究领域: 化学工程 · 材料科学
✓ 已验证 DOI 高影响因子
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MICROCHIMICA ACTA · 2021 ·Vol. 188 ·期 8 ·1-9 · IF 5.833

Glutathione-functionalized two-dimensional cobalt sulfide nanosheets for rapid and highly efficient enrichment of N-glycopeptides

Gao Wenjie,Bai Yu,Liu Huwei

Protein glycosylation plays pivotal role in a variety of biological processes and has association with many diseases. The highly efficient glycopeptide enrichment is essential for the mass spectrometry–based glycoproteome research to reduce interference from non-glycopeptides. In this study, novel glutathione-functionalized two-dimensional cobalt sulfide nanosheets (Co-S@Au-GSH) were synthesized for rapid and highly effective enrichment of glycopeptides. By using this nanomaterial, 34 and 21 N-glycopeptides were effectively captured from human serum immunoglobulin G (IgG) and horseradish peroxidase (HRP) digests, respectively. In addition, the Co-S@Au-GSH showed remarkable performance in N-glycopeptide extraction with high selectivity (HRP: BSA = 1:500), low limit of detection (0.5 fmol/μL), high binding capacity (150 mg/g), good reusability, and great robustness. Moreover, it was successfully applied in complex serum samples, demonstrating its excellent enrichment performance. These results indicated that this nanomaterial has great potential in complicated practice samples in glycoproteome determination. Graphical abstract

研究领域: 蛋白质组学 · 生物化学 · 分析化学
✓ 已验证 DOI PubMed 高影响因子
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SYNTHESIS-STUTTGART · 2023 ·Vol. 55 ·期 20 ·3393-3401 · IF 2.6

Copper-Catalyzed Coupling of N-Phenoxyacetamides and 2H-Azirines for Synthesis of α-Amino Oxime Ethers

Yue-Lu Zhu,Jie Yan,Xiu-Xuan Xu,Zong-Yu Sun,Jiao Chen

Copper-catalyzed coupling reaction involving N-phenoxyacetamides and 2H-azirines is described, in which N–O and C–N bonds are broken and restructured. This protocol provides an efficient strategy for the highly regioselective synthesis of racemic α-amino oxime ethers. In addition, this strategy can be used to modify natural products and is gram-scale compatible.

研究领域: 有机化学 · 合成化学
✓ 已验证 DOI 高影响因子
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MICROCHEMICAL JOURNAL · 2025 · IF 5.1

An ultrasensitive fluorescence immunosensor for SCCA detection based on Ag NPs@N-doped carbon quantum dots

Zhirou Xu,Zhengtong Wu,Xuyang Sun

An ultrasensitive fluorescence immunosensor based on silver nanoparticles@ nitrogen-doped carbon quantum dots (Ag NPs@N/CQDs) and exploiting the quenching effect of gold nanoparticles (Au NPs) was fabricated for squamous cell carcinoma antigen (SCCA) detection. Ag NPs@N/CQDs were immobilized on the surface of an indium tin oxide (ITO) electrode and then coupled with the primary antibody of SCCA. The primary antibody captured SCCA on the ITO electrode, forming an immune complex with the secondary antibody labeled with gold nanoparticles, thereby constructing a sandwich-structured fluorescent sensor. Using the prepared sensor, a new method for detecting trace amounts of SCCA in human serum was established. Owing to the effective quenching of fluorescence intensity of Ag NPs@N/CQDs by Au NPs, combined with the presence of a sandwich immune structure, the sensor exhibits high sensitivity and selectivity. The method demonstrates a linear range of 2 − 4000 fg mL −1 and a detection limit of 0.87 fg mL −1 . The the recovery rate for real serum samples was between 94.45 % to 103.43 %.

研究领域: 生物医学工程 · 肿瘤学 · 纳米技术
✓ 已验证 产品关联 DOI 高影响因子
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TRANSACTIONS OF NONFERROUS METALS SOCIETY OF CHINA · 2025 · IF 4.7

Selective flotation separation of ilmenite from titanaugite using n-octylphosphonic acid as collector in acidic pulp

Pan CHEN,Jia-yan LIU,Ji-hua ZHAI,Yao-hui YANG,Wei SUN

n-octylphosphonic acid (OPA) was introduced as a novel collector for ilmenite flotation and its effectiveness was compared with the conventional chelating collector, benzohydroxamic acid (BHA). Micro-flotation tests demonstrated that OPA was a highly effective and selective collector for separating ilmenite from titanaugite over acidic conditions (optimal pH around 3), which was also supported by adsorption amount measurements. X-ray photoelectron spectroscopy (XPS) tests indicated that the chemisorption of OPA onto ilmenite surface was much stronger than that of BHA. Solution chemistry diagram analyses indicated that OPA could dissociate well at pH 3.0 and mostly exist in anion form. DFT calculations further confirmed that OPA was much easier to adsorb onto ilmenite surface with shorter bond length and lower adsorption energy in comparison with BHA. Therefore, OPA maintained good collecting ability and selectivity for ilmenite flotation in the strongly acidic pulp, providing valuable insights into new collector design and development.

CAS / MDL: 25013-16-5 643-79-8
研究领域: 矿物加工工程 · 表面化学
✓ 已验证 产品关联 DOI 高影响因子
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POLYMER INTERNATIONAL · 2014 ·Vol. 64 ·期 4 ·563-570 · IF 2.247

Homopolymerization and copolymerization of N-substituted maleimides with chiral anionic initiators

Yi-Ling Huang,Jing Cao,Wei Hu,Sai Liang

Novel optically active anionic initiators bearing a chiral oxazole substituent on the fluorene ring, ( S )-1-(9H-fluoren-2-yl)-4-isopropyl-4,5-dihydrooxazole lithium (Li-( S )-1-FIDH) and ( S )-2-(9H-fluoren-2-yl)-4-isopropyl-4,5-dihydrooxazole lithium (Li-( S )-2-FIDH), were prepared. Anionic homopolymerizations of achiral N -substituted maleimide (RMI) with the chiral initiators were investigated. The optically active polymers obtained were attributed to asymmetric induction of the chiral initiators. The very crowded chiral initiator Li-( S )-1-FIDH was found to play a better asymmetric induction role in the polymers than Li-( S )-2-FIDH. Anionic copolymerization of ( R )-(+)- N -1-phenylethyl maleimide and optically inactive RMI with Li-( S )-1-FIDH were also studied. © 2014 Society of Chemical Industry

研究领域: 高分子化学 · 有机化学
✓ 已验证 DOI 高影响因子
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JOURNAL OF MOLECULAR STRUCTURE · 2023 · IF 3.8

Stable tetranuclear copper cage as efficient heterogeneous catalyst for C−C and C−N bond forming reactions

Peng Xiong,Tong-Wei Zhang,Shi-Ming Li,Mei-Yu Xu,Guang-Ming -Liang,Liu-Cheng Gui,Xiu-Jian Wang

Two tetranuclear copper cages with tubular type, [Cu 4 (BMBA) 4 ((CH 3 ) 2 N) 2 (H 2 O) 2 ] ( 1 ) and [Cu 4 (BMBA) 4 (Bipy)(H 2 O) 2 ] ( 2 ), were successfully constructed by the reaction of Cu(NO 3 ) 2 with dicarboxylic acid 4,4′-[( ethylazanediyl ) bis ( methylene )]-bis[(1,1′-biphenyl)-2-carboxylic acid] (H 2 BMBA) under solvothermal conditions. The complexes 1 and 2 exhibit a similar cage structure, formed by four ligands connecting two binuclear copper paddle-wheel secondary building units (SBUs). Interestingly, the complex 2 was obtained by appropriately binding of 4, 4′-bipyridine (Bipy) molecule on the axial positions of two Cu paddle-wheels inside the cage. For this reason, the complex 2 exhibits excellent stability in some common organic solvents at room temperature and aqueous solutions with a pH of 2 to 12. Upon thermal activation of complex 2 , the coordinated water molecules can be removed, and its exposed metal active-sites show Lewis acid character, which can be used an efficient heterogeneous catalysis of Knoevenagel condensation (C C) and Clauson-Kaas (C N) reactions.

研究领域: 化学 · 材料科学 · 催化反应
✓ 已验证 DOI 高影响因子
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