CERAMICS INTERNATIONAL
·
2026
·
IF 6
WANG Wei,WANG Song,Y.U. Yiping,L.I. Wei
Conventional granular catalysts exhibit insufficient stability in high-temperature N 2 O catalysis, suffering from issues such as significant bed pressure drop and particle sintering/agglomeration. While light curing molding offers an effective approach for fabricating novel monolithic catalysts to reduce pressure drop and prevent sintering, this method necessitates high-temperature calcination for carrier stabilization, inevitably creating a trade-off between specific surface area and mechanical strength. This study proposes a novel LaMgAl 11 O 19 (LMA) carrier preparation method combining light curing molding with in-situ solid-state synthesis. This approach achieves both precise macro-geometric structuring through light curing molding and simultaneous regulation of LMA crystallization, coarsening, and carrier stabilization via in-situ solid-state reaction, thereby balancing the conflict between carrier strength and specific surface area. The resulting 3D-LMA carrier demonstrates superior performance compared to those produced by traditional 3D-printing methods, maintaining a specific surface area of 10.20 m 2 /g after sintering at 1350 °C with compressive strength reaching 97.62 ± 22.20 MPa. When loaded with Ir to form 3D-Ir/LMA, the catalyst outperforms granular LMA catalysts in N 2 O decomposition tests, exhibiting enhanced catalytic activity and stability. This breakthrough provides new possibilities for meeting the demands of high-temperature N 2 O catalysis.
✓ 已验证
产品关联
DOI
高影响因子
INORGANIC CHEMISTRY
·
2018
·
IF 4.7
Sheng-Ping Guo,Zong-Dong Sun,Yang Chi,Huai-Guo Xue
A noncentrosymmetric adduct, SbI3·(S8)3, is obtained by a facile solution method. It crystallizes in the trigonal space group R3m, and its structure features van der Waals force connected, isolated trigonal-pyramidal SbI3 and chairlike S8 units. SbI3·(S8)3 exhibits strong second-harmonic-generation responses around 4 times that of KH2PO4 (1.064 μm) and 1 times that of AgGaS2 (AGS; 2.1 μm) at 210–250 μm, respectively. Under both laser-radiation wavelengths, it exhibits type I phase-matching behavior. Its laser-induced damage threshold is measured to be around 26 times that of AGS under 1.064 μm. To better understand these optical data, theoretical calculations are performed to address its electronic structure and optical properties.
研究领域:
材料科学
·
光学
·
无机化学
·
非线性光学
·
晶体工程
✓ 已验证
DOI
高影响因子
FUEL
·
2026
·
IF 7.5
Wen Tang,Jing-Pei Cao,Xiao-Yan Zhao,Dan Xie,Kai-Rui Luan,Chang-Jiang Li,Qi-Ming She,Tungalagtamir Bold
Research on pressurized methane dry reforming (DRM) is of great significance for the integration with downstream F-T synthesis processes and reducing gas compression costs. However, the increase in pressure leads to severe coking, which limits the stable operation of the process. Developing Co-based bimetallic catalysts doped with a small amount of noble metals is one of the important approaches to improving the catalysts’ coking resistance and catalytic performance, thereby alleviating this issue. In this work, a carbon-supported Co-Ir bimetallic catalyst doped with 0.2 wt% Ir (denoted as Co-0.2Ir/C) was developed. Structural characterizations confirmed the formation of Co-Ir alloy, with the metal particles on the catalyst being highly dispersed and having an average particle size of 4.82 nm. Under the reaction conditions of 800 °C, 0.5 MPa, and 30,000 mL g cat -1 h −1 , the incorporation of Ir effectively enhanced the initial catalytic activity of the catalyst and achieved stable operation for 100 h, with final CH 4 and CO 2 conversion reaching 73.9 % and 82.8 %, respectively. In addition, this study focused on the structural changes of the catalyst during the induction period, confirming the dynamic evolution laws of metal particle redispersion and amorphous carbon graphitization. These findings explain the dynamic variation phenomenon where the conversion of CH 4 and CO 2 first increased significantly and then gradually stabilized during the reaction. This study provides certain guiding significance for the development of relatively low-cost carbon-supported metal catalysts, the realization of stable operation of DRM under pressurized conditions, and the clarification of the structure–activity relationship of such catalysts in the DRM reaction.
✓ 已验证
产品关联
DOI
高影响因子
MICROCHIMICA ACTA
·
2020
·Vol. 187
·期 7
·1-8
·
IF 6.232
Li Shuhuai,Pang Chaohai,Ma Xionghui,Zhao Min,Li Haibo,Wang Mingyue,Li Jianping,Luo Jinhui
A luminescent double recognition nanoprobe is described as a new strategy for the selective determination of chiral molecules. C-dots/Ir/Au fluorescent nanoparticles, synthesised under hydrothermal conditions, are used as a high-performance probe in combination with a molecularly imprinted polymer (MIP) and calix[6]arene as a double recognition element. Thiolated calix[6]arene is grafted on C-dots/Ir/Au as the first recognition element, which then forms a host–guest complex with the target molecule levodopa (L-DOPA). Subsequently, an MIP is prepared on the C-dots/Ir/Au (MIP/C-dots/Ir/Au) by chemical polymerisation. After the removal of L-DOPA, double recognition imprinting cavities are formed. The fluorescence intensity at 478 nm of the nanoprobe is effectively quenched by adsorption of L-DOPA on MIP/C-dots/Ir/Au, which provides a method for L-DOPA determination. Owing to the double recognition strategy, this method has excellent selectivity which can effectively avoid interference from enantiomer D-DOPA, and a imprinting factor of 7.1 is obtained for L-DOPA. This accurate and reliable method, with a wide linear range (5 × 10 −10 to 1.2 × 10 −7 mol L −1 ) and a low limit of detection (1.45 × 10 −10 mol L −1 ), was successfully applied to the determination of L-DOPA in real samples, giving standard recoveries of 89.7–110.0%. Thus, the proposed sensing method provides a viable approach for the determination of a single enantiomer.
Schematic presentation of the MIP/C-dots/Ir/Au for L-DOPA detection. A fluorescence double chiral recognition nanoprobe is prepared of C-dots/Ir/Au nanoparticles as signal probe, and a molecularly imprinted polymer (MIP) and calix[6]arene as a double recognition element. Owing to the double recognition strategy, this method has strong specificity and can effectively avoid interference from enantiomers and racemates.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Acta Biomaterialia
·
2019
·
IF 6.638
Fangfang Xia,Jiaqi Niu,Yuping Hong,Chenlu Li,Wen Cao,Lirui Wang,Wenxiu Hou,Yanlei Liu,Daxiang Cui
Nanotheranostics has gained increasing interest, as it offers a great potential to realize personalized diagnostics and therapy. In this work, we report a facile approach of the fabrication of gold nanostars (GNS) attached with matrix metalloproteinases (MMP2) polypeptides (Ac-GPLGIAGQ) and IR-780 iodide through bovine serum albumin (BSA) for targeted dual-modal photoacoustic (PA)/near-infrared (NIR) fluorescence imaging and enhanced photothermal therapy (PTT)/photodynamic therapy (PDT) for lung cancer. MMP2 polypeptides served as the targeting ligand, IR-780 iodide functioned as the NIR fluorescence imaging agent as well as PTT/PDT agent, and GNS acted as the carrier of IR-780 molecules and performed PA imaging and PTT. DLS and CCK-8 assay demonstrated that the nanoprobes (GNS@BSA/I-MMP2) exhibited excellent stability and biocompatibility under physiological conditions. Subsequent in vitro studies verified that GNS@BSA/I-MMP2 nanoparticles (NPs) were effectively internalized by A549 cancer cells and exhibited remarkable antitumor efficacy. Furthermore, GNS@BSA/I-MMP2 NPs could specifically target the tumor and significantly suppress the tumor growth, and their antitumor effects were mainly through the synergistic effects of PDT and PTT based on IR-780 and GNS. These findings imply the potential of GNS@BSA/I-MMP2 NPs as a targeting PA/NIR probe in tumor diagnosis and combined therapy with a single light source. Statement of Significance We reported a convenient and facile approach to load IR-780 iodides in gold nanostars (GNS). This material could simultaneously perform near-infrared imaging/photoacoustic imaging and thermotherapy/photodynamic therapy. MMP2 coating on the surface of GNS@BSA/IR-780 promoted the prepared nanoparticles (GNS@BSA/I-MMP2) to target the tumor region. The heat generated by the synergistic effect of the GNS and IR-780 molecules resulted in the high temperature of the GNS@BSA/I-MMP2 NPs, which efficiently suppressed the growth of tumor, and the tumor volume decreased by 93% compared with that in the PBS groups with laser irradiation.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
ELECTROCHIMICA ACTA
·
2015
·
IF 4.504
Shuhuai Li,Guihao Yin,Xuejin Wu,Chunhua Liu,Jinhui Luo
A novel supramolecular imprinted electrochemical sensor was developed for carbofuran (CBF) determination based on a multiwalled carbon nanotube-supported Pd-Ir nanocomposite catalyst (MWCNT/Pd-Ir) with methylene blue (MB) signal amplification. First, MWCNT/Pd-Ir composite nanoparticles were synthesized and used to modify the surface of a glassy carbon electrode; then, a molecular imprinted polymer for CBF was prepared by electropolymerization , with MB-doped o -phenylenediamine as the functional monomer and a 4-tert-butylcalix[8]arene-CBF (4TB[8]A-CBF) supramolecular complex as the template. The electrical signals were controlled though the elution and re-adsorption of CBF. Due to the double catalysis by the MWCNT/Pd-Ir and MB, the current intensity for CBF was obviously amplified. Additionally, because of the double recognition by the 4TB[8]A and MIP, the sensors showed outstanding CBF identification properties. The method was applied to detect CBF in agricultural products, and the satisfactory results were obtained.
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF MOLECULAR LIQUIDS
·
2017
·
IF 3.648
Yaran Yin,Taotao Fu,Chunying Zhu,Youguang Ma
Densities and viscosities of binary mixtures {[Bmim][BF 4 ] + MDEA}, {MDEA + H 2 O} and ternary mixture {[Bmim][BF 4 ] + MDEA + H 2 O} were measured at T = (293.15–333.15) K. The volumetric and viscometric properties of binary and ternary mixtures, such as excess molar volume ( V E ), viscosity deviation (Δ η ), excess Gibbs energy of activation of viscous flow (Δ G ⁎E ), and Grunberg-Nissan interaction parameter ( G 12 ), were deduced from experimental data. The excess molar volumes and viscosities data were used to calculate the Redlich-Kister and Jouyban-Acree equations coefficients for binary mixtures , and Singh et al. and Jouyban-Acree extended equations coefficients for ternary mixtures. The intermolecular interactions in binary and ternary mixtures were discussed through volumetric and viscometric properties and FT-IR spectroscopic analysis .
✓ 已验证
产品关联
DOI
高影响因子
Theranostics
·
2020
·
IF 8.579
Wanbing Qin,Guilan Quan,Ying Sun,Minglong Chen,Peipei Yang,Disang Feng,Ting Wen,Xinyu Hu,Xin Pan,Chuanbin Wu
High aggressiveness and recurrence of melanoma tumors require multiple systemic drug administrations, causing discomfort and severe side effects to the patients. Topical treatment strategies that provide repetitively controllable and precise drug administrations will greatly improve treatment effects. Methods: In this study, a spatiotemporally controlled pulsatile release system, which combined dissolving microneedles (DMNs) and thermal-sensitive solid lipid nanoparticles (SLNs), was constructed to realize multiple doses of dual-modal chemo-photothermal therapy in a single administration. Paclitaxel (PTX) and photothermal agent IR-780 were encapsulated into SLNs and were concentrated in the tips of DMNs (PTX/IR-780 SLNs @DMNs). Equipped with several needles, the DMN patch could be directly inserted into the tumor site and provide a stable “Zone accumulation” to constrain the PTX/IR-780 SLNs at the tumor site with uniform distribution. Results: In vitro experiments showed that after irradiation with near-infrared light, the PTX/IR-780 SLNs gradually underwent phase transition, thereby accelerating the release of PTX. When irradiation was switched off, the PTX/IR-780 SLNs cooled to re-solidify with limited drug release. Compared with intravenous and intratumoral injections, very few SLNs from PTX/IR-780 SLNs @DMNs were distributed into other organs, resulting in enhanced bioavailability at the tumor site and good safety. In vivo analysis revealed that PTX/IR-780 SLNs @DMNs exhibited significant anti-tumor efficacy. In particular, the primary tumor was completely eradicated with a curable rate of 100% in 30 days and the highest survival rate of 66.67% after 100 days of treatment. Conclusion: Herein, we developed a DMN system with a unique spatiotemporally controlled pulsatile release feature that provides a user-friendly and low-toxicity treatment route for patients who need long-term and repeat treatments.
研究领域:
药学
·
癌症治疗
·
纳米技术
·
生物医学工程
✓ 已验证
产品关联
DOI
PubMed
高影响因子
ACS Sensors
·
2022
·
IF 9.618
Yue Xu,Haiyan Chen,Shufen Xu,Ji Liu,Yang Chen,Lijuan Gui,Hua Li,Ruixi Li,Zhenwei Yuan,Bowen Li
Several photosensitizers have recently been proposed as novel approaches against β-lactamase-producing drug-resistant bacteria. However, these reported photosensitizers are rarely used for accurate recognition of drug-resistant bacteria. To tackle this challenge, the structurally modified photosensitizer CySG-2 based on a lipophilic cationic heptamethine indocyanine near-infrared (NIR) dye (IR-780) and an important synthesis intermediate of cephalosporin antibiotic (GCLE) not only achieved the accurate recognition of TEM-1 methicillin-resistant Staphylococcus aureus (MRSA) successfully but also achieved antimicrobial photodynamic therapy (aPDT) in animal models infected by drug-resistant bacteria. Accurate enzyme recognition and efficient photodynamic therapy capabilities allow CySG-2 to achieve one stone with two birds. In addition, CySG-2 could also promote the eradication of internalized MRSA by facilitating the autophagy process, which is synergistic with its capacity of inducing reactive oxygen species generation under NIR laser irradiation for aPDT. Collectively, it is an effective multifunctional photosensitizer with the potential ability to guide the optimal use of different antibiotics and apply them in clinical treatment.
研究领域:
药学
·
微生物学
·
生物医学工程
·
传染病学
✓ 已验证
DOI
PubMed
高影响因子
NEW JOURNAL OF CHEMISTRY
·
2024
·
IF 2.7
Qihong Xue,Zhikui Jiang,Chao Wang,Xian Kan,Jiaming Wang,Jiangang Chen
13-Ni/ZrO2, 13-Ni3P/ZrO2, 13-Ni/SiO2, and 13-Ni3P/SiO2 catalysts were used in the hydrogenation of diethyl oxalate (DEO) to ethyl glycolate (Egly) to investigate the modulating effect of phosphorus. XRD, TEM and FT-IR results show that phosphorus act as a divider of Ni metallic particle and shows a segregation effect. The presence of P transformed the linkage of surface metals from the original -Ni-Ni-Ni-Ni- to the P-Ni-P-Ni-P state, and FT-IR shows that the former adsorbed CO in a combination of linear and bridging adsorption mode, whereas the latter predominantly in CO linear adsorption. Bridging adsorption is via dual sites and makes the preliminary hydrogenation products less likely to detach from the catalyst surface thus facilitating deep hydrogenation, while linear adsorption facilitates partial hydrogenation by a rapid detachment of intermediate product like Egly. The various loading Ni3P/SiO2 catalysts show incomplete phosphorylation with increasing nickel loading, giving rise to a state of coexistence of Ni and Ni3P crystalline phases. This may lead to a coexistence of surface -Ni-Ni-Ni-Ni- and P-Ni-P-Ni-P and the corresponding assort of adsorption, e.g. bridging/linear ones, making deep hydrogenation occur partially besides stepwise hydrogenation.
研究领域:
催化
·
材料科学
·
化学工程
✓ 已验证
DOI
高影响因子
PHYSICAL CHEMISTRY CHEMICAL PHYSICS
·
2024
·Vol. 26
·期 9
·7855-7864
·
IF 2.9
Yao Wang,Ziqi Wang,Lujuan Yang,Wenkai Zhang,Gang Ma
Understanding the amyloid nucleation mechanism is fundamentally important for the development of diagnostics and therapeutics of amyloid-related diseases and for the design and application of amyloid-based materials. To this end, we here explore the use of atomic force microscopy (AFM) and a side-chain-based infrared (IR) probe technique to investigate the amyloid nanosheet formation mechanism of an Aβ16–22 variant, KLVFXAK, where X is p-cyanophenylalanine with its side-chain cyano group being an infrared probe. Using AFM, we reveal that the formation of KLVFXAK amyloid nanosheets follows a two-step non-classical nucleation mechanism. The first step is the rapid formation of a metastable fibrillar intermediate and the second step is slow transformation to the final nanosheet. Using the side-chain-based IR probe technique, we obtain spectroscopic evidence for the proposed nucleation mechanism of the amyloid nanosheet as well as the structural details for the intermediate and amyloid nanosheet. By using the structural constraints set by the two techniques, we propose the structural models for both the fibrillar intermediate and the amyloid nanosheet. In addition, we further investigated the amyloid nanosheet formation mechanism of a similar Aβ16–22 variant, KLVFXAE, and showed the impact of mutation on the amyloid nucleation mechanism. Our work also provides a nice example of how to use the combined approach of AFM and a side-chain-based IR probe technique to unravel the complex nucleation mechanism of amyloid formation.
研究领域:
生物物理学
·
结构生物学
·
材料科学
·
蛋白质化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2024
·
IF 13.3
Wei Zhou,Wenwei Zhang,Xueqin Ma,Haichen Lai,Xingguang Zhang
Metal-zeolites catalysts are of great importance in selective organic conversions. Zeolites possess features of highly-ordered porous network, adjustable acidic properties (Brønsted/Lewis), spatial nanoconfinement effects, unique shape selectivity and the strong (hydrothermal-) stability. The role of zeolite hydroxyl (z-OH) groups, such as bridging ones in Si-O(H)-Al (B acids) and terminal ones in Al-OH and Si-OH (silanols), in catalysis is an interesting topic, particularly when they are not catalytic active sites, while they affect the catalytic performances. This study comprehensively investigated series of Au/USY catalysts in the selective oxidation of benzyl alcohol to benzaldehyde and clarified the dominating contributions of Al-associated z-OH groups to affecting catalytic conversions and selectivity via altering the Si/Al ratio and reducing z-OH groups by amorphous silica species derived from diethoxydimethylsilane under high-temperature calcination. The catalysts were characterized by XRD, BET, TEM, XPS, UV/Vis, FT-IR and in-situ DRIFT to investigate crystal structures, textural properties, morphologies, size distribution, chemical state of gold, acidity, and adsorptive properties. The experimental results proved that zeolites with a higher amount of z-OH groups tuned by Si/Al ratios or by diethoxydimethylsilane silylation exhibited higher catalytic activity because of the adsorption effect. Finally, a possible mechanism was discussed based on the experimental results and literature.
研究领域:
催化
·
材料科学
·
化学工程
✓ 已验证
产品关联
DOI
高影响因子
危险品化学品经营许可证（带存储）