RESEARCH ON CHEMICAL INTERMEDIATES
·
2018
·Vol. 44
·期 5
·3455-3474
·
IF 1.674
Sun Xiao,Guo Rui-tang,Li Ming-yuan,Sun Peng,Pan Wei-guo,Liu Shu-ming,Liu Jian,Liu Shuai-wei
Fe was used as the modifier to improve the performance of CeZr 2 O
x
catalyst for the selective catalytic reduction (SCR) reaction with ammonia. Experimental results revealed that proper Fe species (Fe/Ce molar ratio = 2) could effectively improve the SCR activity of CeZr 2 O
x
, along with the elevated resistance to SO 2 and H 2 O. The characterization results including BET, XRD, H 2 -TPR and NH 3 -TPD confirmed that Fe species in Fe 2 CeZr 2 O
x
catalyst could inhibit the formation of ZrO 2 crystals and lead to higher reducibility and surface acidity. In addition, more Ce 3+ and surface active oxygen species could be detected on Fe 2 CeZr 2 O
x
compared with CeZr 2 O
x
. By means of in situ DRIFT technique, it could be deduced that the SCR reaction process over Fe 2 CeZr 2 O
x
was accelerated mainly through theL–H pathway due to the advanced adsorption of NH 3 and NO
x
species, along with the promoted NO conversion to NO 2 . Therefore, the modification of CeZrO
x
catalyst by Fe had a significant stimulation effect on its low-temperature SCR performance.
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CHEMICAL PAPERS
·
2017
·Vol. 72
·期 1
·51-56
·
IF 1.258
Wei Mengyi,Qian Chao,Chen Xinzhi
Based on the recycling of NO
x
, the Cu(I)- and HNO 3 -catalyzed oxidation of 2-chloro-4-(methylsulfonyl)toluene to 2-chloro-4-(methylsulfonyl)benzoic acid has been developed with an excellent yield of 84.2% and a purity of 99.7%. The optimized reaction conditions (160 °C, oxygen pressure 1.5 MPa, HNO 3 concentration 25 wt%, HNO 3 : substrate 0.5:1) use 1.0 mol% CuI as catalyst. The dosage of HNO 3 in the new process is only 25% of the stoichiometric amount and 12.5% of the amount of the traditional process. The NO
x
emission is 5% amount of the traditional process. The oxidation of several additional toluene derivatives with comparable yields demonstrates the generality to these reaction conditions.
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Frontiers of Chemical Science and Engineering
·
2025
·Vol. 19
·期 4
·1-12
·
IF 4.5
Xing Xiangwen,Jiang Jingxuan,Liu Jing,Zhao Pei,Cui Lin,Dong Yong
The sodium persulfate (Na 2 S 2 O 8 )-urea system has been proven to be an excellent scrubbing solution for the wet removal of NO. Commonly, seawater is used as a wet carrier in marine applications. To further explore the feasibility of marine denitrification using Na 2 S 2 O 8 -urea system, this study proposed the Na 2 S 2 O 8 -urea-seawater composite redox system for NO removal from the marine exhaust gas. The effects of seawater carrier, reaction temperature, Na 2 S 2 O 8 concentration, urea concentration, pH value, and NO concentration on NO removal were investigated. Additionally, the NO 3 − concentration in the solution was measured. Results showed that the lowest normalized NO concentration was 0.099, with the corresponding mass of NO absorbed per unit volume of solution reaching 0.108 g·L −1 . The addition of seawater carrier and incremental reaction temperature, Na 2 S 2 O 8 , and urea concentration promoted the NO removal performance. When the pH value increased within the range of 4–7, the NO removal performance decreased. The NO removal performance increased as the pH value further increased to 8, but decreased again when the pH value increased to 11. An increase in NO concentration was detrimental to NO removal. The Cl − , HCO 3 − , and CO 3 2− in seawater could augment the total concentration of active free radicals to improve denitrification performance.
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ChemCatChem
·
2020
·Vol. 13
·期 1
·438-444
·
IF 4.853
Xianwei Wang,Nobutaka Maeda,Daniel M. Meier,Alfons Baiker
Graphical Potassium titanate (K 2 Ti 8 O 17 ) nanobelts (KTN) are a unique support for Au and bimetallic AuRh nanoparticles showing strong enhancement of the catalytic reduction of NO with CO to N 2 .The KTN support facilitates the formation of surface nitrate, carbonate and isocyanide species, resulting in superior catalytic activity compared to corresponding TiO 2 -supported catalysts. The catalytic reduction of NO with CO was examined over monometallic Au and bimetallic AuRh nanoparticles supported on potassium titanate (K 2 Ti 8 O 17 ) nanobelts (KTN) and TiO 2 . The highly crystalline KTN, prepared from TiO 2 by a hydrothermal process using KOH, were several μm long and ca. 8 nm wide. Both Au and bimetallic AuRh catalysts showed a striking enhancement of the catalytic performance with KTN as support, compared to corresponding TiO 2 -supported catalysts. The reasons for this behavior could be traced back using in situ diffuse reflectance infrared Fourier transform spectroscopy in tandem with modulation excitation spectroscopy, which proved that the KTN support promotes the formation of surface nitrate (−NO 3 − ), carbonate (−CO 3 2− ), and isocyanide (−NCO) species. In particular, the combination of KTN with bimetallic AuRh nanoparticles results in the facile formation of isocyanide, which is a pivotal intermediate for producing dinitrogen molecules via the reaction with NO; NCO (a) +NO (a) →N 2 +CO 2 .
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Separations
·
2025
·Vol. 12
·期 8
·215
·
IF 2.7
Jiuquan Qi,Qianwen Chen,Chuanying Liu,Chengliang Xiao,Shuainan Ni
Due to the nearly identical chemical properties of Lu and Yb, the production of no-carrier-added (NCA)177Lu faces significant challenges in their separation. Achieving efficient and streamlined separation of Lu and Yb is crucial for the production of NCA177Lu. This study systematically investigated the separation performance of the commercial Rext-P350 extraction resin for Lu and Yb. Static adsorption experiments revealed that, at a solid–liquid ratio of 8 g/L, both Lu3+and Yb3+were nearly completely adsorbed, with saturation adsorption capacities of 25.8 mg/g and 21.5 mg/g, respectively. An increase in the nitric acid concentration in the aqueous phase significantly inhibited adsorption, but the separation factor for Lu3+/Yb3+remained above 1.88. The adsorption kinetics followed a pseudo-second-order model (R2> 0.99), with equilibrium reached within 15 min, demonstrating fast adsorption kinetics. Characterization by SEM, FT-IR, and XPS confirmed the chemical coordination between the resin and Lu3+/Yb3+. Dynamic chromatographic separation experiments showed that the Rext-P350 resin exhibited significantly better separation performance for Lu3+/Yb3+compared to 2-ethylhexylphosphoric acid mono-2-ethylhexyl ester (P507) extraction resin. Leveraging the excellent performance of Rext-P350 resin, a two-stage continuous extraction chromatography process was designed, achieving efficient separation of 0.045 mg of Lu3+from 200 mg of Yb3+with a Lu3+purity of 90.9% and a yield of 98.4%. This study provides a feasible separation technique for the purification of NCA177Lu.
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International Journal of Nanomedicine
·
2024
·
IF 6.6
Junjuan Li,Yue Tian,Qi Qin,Zhaolei Ding,Xue Zhao,Wei Tan
Purpose: Owing to its noninvasive nature, broad-spectrum effectiveness, minimal bacterial resistance, and high efficiency, phototherapy has significant potential for antibiotic-free antibacterial interventions and combating antibacterial biofilms. However, finding effective strategies to mitigate the detrimental effects of excessive temperature and elevated concentrations of reactive oxygen species (ROS) remains a pressing issue that requires immediate attention.Methods: In this study, we designed a pH-responsive cationic polymer sodium nitroside dihydrate/branched polyethylenimine–indocyanine green@polyethylene glycol (SNP/PEI-ICG@PEG) nanoplatform using the electrostatic adsorption method and Schiff’s base reaction. Relevant testing techniques were applied to characterize and analyze SNP/PEI-ICG@PEG, proving the successful synthesis of the nanomaterials. In vivo and in vitro experiments were performed to evaluate the antimicrobial properties of SNP/PEI-ICG@PEG.Results: The morphology and particle size of SNP/PEI-ICG@PEG were observed via TEM. The zeta potential and UV-visible (UV‐vis) results indicated the synthesis of the nanomaterials. The negligible cytotoxicity of up to 1 mg/mL of SNP/PEI-ICG@PEG in the presence or absence of light demonstrated its biosafety. Systematic in vivo and in vitro antimicrobial assays confirmed that SNP/PEI-ICG@PEG had good water solubility and biosafety and could be activated by near-infrared (NIR) light and synergistically treated using four therapeutic modes, photodynamic therapy (PDT), gaseous therapy (GT), mild photothermal therapy (PTT, 46 °C), and cation. Ultimately, the development of Gram-positive (G+) Staphylococcus aureus (S. aureus) and Gram-negative (G−) Escherichia coli (E. coli) were both completely killed in the free state, and the biofilm that had formed was eliminated.Conclusion: SNP/PEI-ICG@PEG demonstrated remarkable efficacy in achieving controlled multimodal synergistic antibacterial activity and biofilm infection treatment. The nanoplatform thus holds promise for future clinical applications.
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BIOMATERIALS
·
2025
·
IF 12.9
Fang Zhang,Bingbing Zhao,Keqiang Lu,Xueping Zeng,Zikun Wang,Wei Chen,Yunyun Zhou,Juanjuan Peng,Lingzhi Zhao
Oxidative stress and fibrosis are core drivers of post-myocardial infarction dysfunction. Conventional therapies predominantly address either acute oxidative damage or chronic fibrosis, lacking strategies that concurrently target the two interconnected processes. Here, a microenvironment-responsive nanomedicine delivering nitric oxide (NO) and curcumin specifically to the infarcted heart is presented (named C@Si-NM). Constructed from glutathione-sensitive cyclic nitrate-trimethylene carbonate-polyethylene glycol block copolymer micelles crosslinked with silica, the system releases both NO and the encapsulated curcumin upon encountering elevated glutathione levels at the infarction site. In cardiomyocytes, NO suppresses the opening of mitochondrial permeability transition pore, inhibiting the release of reactive oxygen species, while curcumin directly acts as an antioxidant. In fibroblasts, NO inhibits the TGF-β/Smad pathway and curcumin downregulates the production of TGF-β, jointly suppressing fibrosis. The combined nanomedicine C@Si-NM significantly improved cardiac function in a rat model of MI after four weeks of treatment, resulting in an ejection fraction of 74 %. This value approached the normal range of 81 % and was superior to the outcomes observed with NO monotherapy at 62 % or curcumin monotherapy at 63 %. This strategy effectively mitigates both oxidative damage and fibrosis, bridging the gap between acute and chronic therapeutic interventions of myocardial infarction.
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高影响因子
JOURNAL OF COLLOID AND INTERFACE SCIENCE
·
2025
·
IF 9.7
Shengyong Lu,Xuanhao Guo,Manting Chen,Guanjie Wang,Juan Qiu,Jiaming Ding,Minghui Tang,Zhengdong Han,Yaqi Peng,Jianhua Yan
The synergistic removal of multiple pollutants from flue gas has attracted growing interest in recent years. In this study, Cu-doped MnCeO x catalysts were synthesized via an impregnation method and integrated into PTFE fibers using a split-film process to enable the simultaneous removal of chlorobenzene (CB) and nitrogen oxide (NO). Among the catalysts tested, Mn 2 Ce 1 Cu 0.6 O x exhibited the highest performance, achieving 90 % CB degradation and 100 % NO conversion at 180 °C. The PTFE-based catalytic fibers also demonstrated excellent removal efficiency, reaching 83.7 % for dioxins at the same temperature. A possible reaction mechanism is proposed in which the NH 3 -SCR process facilitates CB oxidation by generating reactive intermediates. Cu doping was found to enhance the density of acid sites and promote the ring-opening of CB, thereby suppressing chlorine accumulation and improving catalyst stability. These findings provide valuable insights for the development and optimization of catalytic bag filters for the efficient, synergistic removal of multiple pollutants from industrial emissions.
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CHEMICAL ENGINEERING JOURNAL
·
2017
·
IF 6.216
Hailong Li,Weilin Zhang,Jun Wang,Zequn Yang,Liqing Li,Kaimin Shih
Simultaneous nitrogen monoxide (NO) reduction and elemental mercury (Hg 0 ) oxidation in the presence of ammonia (NH 3 ) was for the first time studied on a copper oxide/titanium dioxide (CuO/TiO 2 ) catalyst at low flue gas temperatures. More than 80% NO reduction and 90% Hg 0 oxidation were concurrently achieved on the CuO/TiO 2 catalyst at 250 °C under a simulated NH 3 selective catalytic reduction (SCR) atmosphere. NO was likely oxidized on the CuO/TiO 2 catalyst to form active nitrogenous species, particularly with the aid of oxygen. The active nitrogenous species then significantly promoted Hg 0 oxidation. NH 3 itself did not affect Hg 0 conversion on the CuO/TiO 2 catalyst. The co-occurrences of NO and NH 3 led to a reduction in oxidized mercury (HgO in this work), which partially offset the Hg 0 oxidation and therefore resulted in a relatively lower Hg 0 conversion efficiency. However, compared to flue gas without NO and NH 3 , the combined presence of NO and NH 3 still enhanced Hg 0 oxidation over the CuO/TiO 2 catalyst, primarily because of the overwhelming benefit from NO. This is superior to many other SCR catalysts, including commercial vanadia-based SCR catalysts, on which an SCR atmosphere generally inhibits Hg 0 conversion.
研究领域:
环境催化
·
大气污染控制
·
化学工程
·
材料科学
·
环境化学
·
工业生态学
·
能源与环境技术
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INTERNATIONAL JOURNAL OF BIOLOGICAL MACROMOLECULES
·
2026
·
IF 8.5
Hongchao Deng,Zikang Wang,Shoumiao Peng,Shunyu Yao,Yiwang Zhao,Huiling Guo
Bacterial-infected wound healing still faces substantial challenges, including multidrug-resistance, uncontrollable bleeding, long-term inflammation, and impaired angiogenesis. However, current treatment strategies cannot meet the complex demands of skin wound healing. We here developed a dual dynamic CFP hydrogel based on Schiff base and borate ester bonds between carboxymethyl chitosan (CMCS), polyvinyl alcohol (PVA), and 2-formylphenylboronic acid (2-FPBA). Meanwhile, customized L-arginine/epigallocatechin-3-gallate/ferric ion (EAF) nanoparticles and the thermal-labile 2,2′-azobis[2-(2-imidazolin-2-yl) propane] dihydrochloride (AIPH) initiator were embedded into the CFP hydrogel for healing infected wound. The EAF/A/CFP hydrogel could create a protective barrier on bleeding wounds and reduced blood loss. Under 808 nm laser irradiation, the hydrogel exhibited excellent photothermal, alkyl free radical production ability, and continuous release of nitric oxide (NO) to effectively eradiate the bacteria, including mature biofilms. In addition, NO release regulated inflammation and promoted angiogenesis, thus significantly promoting the wound healing. The EAF/A/CFP hydrogel successfully achieved rapid wound repair in a full-thickness skin wound model. Consequently, this study provides a potential dressing for comprehensive management of skin wound healing.
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Bioengineering-Basel
·
2026
·Vol. 13
·期 8
·908
·
IF 4.4
Dandan Zhang,Zhigang Zhang,Dingxing Huang,Zhuoran Sun,Jiamin Huang,Chi Zhang,Qingyang Zeng,Qiling Liu,Wenzhuo Chen
Osteoarthritis is an irreversible degenerative joint disease driven by sustained NF-κB-mediated inflammatory responses, and conventional intra-articular hyaluronic acid or small-molecule NF-κB inhibitors cannot achieve targeted on-demand treatment due to poor solubility, rapid clearance and lack of lesion microenvironment responsiveness. OA with inherent anti-chondrolytic activity can self-assemble into nanocarriers in water, yet it lacks stimuli-responsive capacity. Herein, we rationally designed and synthesized an OA-Der by covalently conjugating o-phenylenediamine fragments to the OA backbone.1H NMR and HRESI-MS spectra fully verified the accurate chemical structures of intermediate and final OA-Der. Blank OA-Der micelles exhibited uniform spherical core–shell nanostructures (50–150 nm) under TEM and AFM, while pathological high NO triggered complete disassembly of micellar assemblies. We further co-assembled OA-Der with NF-κB inhibitor BAY 11-7082 to construct NO-responsive BAY@OA-Der supramolecular micelles. In vitro experiments using human C28/I2 chondrocytes with LPS-induced inflammatory injury demonstrated that BAY@OA-Der significantly improved cell viability and reduced apoptotic chondrocyte proportion. At mRNA and protein levels, the supramolecular micelle formulation remarkably suppressed NF-κB p65 phosphorylation, downregulated cartilage-degrading ADAMTS5, and upregulated ACAN compared with free BAY or blank OA-Der. Collectively, this natural bioactive self-assembled NO-responsive delivery platform achieves synergistic anti-inflammatory and matrix-protective effects by precisely releasing drugs at NO-overexpressed osteoarthritis inflammatory sites and offers an in vitro design strategy for osteoarthritis responsive delivery systems.
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Applied Materials Today
·
2026
·
IF 7
Huixing Li,Jiaxing Xiong,Fangwei Qi,Jun Zan,Xiuwen Gao,Wenjie Ma,Kunlong Li,Gao Pan,Pan He,Dongan Wang,Yang Shuai,Shuping Peng
Biomimetic hierarchical bone scaffold: outer Haversian canals and inner Gyroid pores for high memchanical strength. • Cascade antibacterial: thermal cleaves biofilms and Fe-NO bonds, releasing NO into bacteria to kill S. aureus and E. coli • Synergistic osteogenesis: thermal activates HSP70, synergizing with Ca 2+ and PO 4 3- to boost osteogenic differentiation. • pH regulation: amine groups from oxidative self-polymerization increase the pH value, enhancing scaffold stability. Poly- L -lactic acid (PLLA) is widely used in bone scaffold engineering due to its favorable biocompatibility, biodegradability, and processability. However, its mechanical properties are limited by insufficient crystallinity during fabrication. Moreover, bone repair is often accompanied by early bacterial infection and local pH reduction, which challenge the antibacterial effect, osteogenic capacity and structural stability of PLLA scaffolds. Herein, PLLA and hydroxyapatite (HA) are melt-blended into PLLA/HA (PHA). followed by self-polymerization of polydopamine (PDA) and electrostatic adsorption sodium nitroprusside of (SNP). The composite is then prepared into a PHA@PDA-SNP scaffold, with an outer Haversian canal layer and inner Gyroid-perforated. Ingeniously, the scaffold utilizes photothermal produced by near-infrared light to cleave biofilm and the Fe-NO bond in SNP, promoting NO release and entry into bacteria. Meanwhile, thermal can activate HSP70, synergizing with Ca 2+ and PO 4 3- released by PHA to boost osteogenic differentiation. Moreover, the amine groups retained during the oxidation process of PDA can weaken the acidic environment and enhance scaffold stability. Results show that the bone scaffold mimics the natural bone structure with high compressive strength (162.9 MPa) by biomimetic manufacturing. Scaffold exhibits cell osteogenic differentiation as evidenced by a 70% upregulation of HSP70 and Ca 2+ influx, and a 4.5-fold increase of ALP and ARS. Scaffold utilizes photothermal and NO to achieve antibacterial rates of 97.4% and 98.2% against S. aureus and E. coli , respectively. Download: Download high-res image (194KB) Download: Download full-size image
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