SENSORS AND ACTUATORS B-CHEMICAL
·
2022
·
IF 9.221
Xian-En Zhao,Ya-Nan Zuo,Yinghui Xia,Jing Sun,Shuyun Zhu,Guobao Xu
Although fluorescent nanozymes exhibit great potential in sensing fields, few current nanozyme-based sensors are designed to discriminate catechol (CC) from its two isomers. Herein, fluorescent metal-organic framework (MOF)-based nanozyme is utilized for ratiometric and selective detection of CC without the interferences of hydroquinone (HQ) and resorcinol (RC). NH 2 -Cu-MOF plays multiple roles: (1) it exhibits excellent photoluminescence at 435 nm owing to the 2-amino-1,4-benzenedicarboxylic acid ligand; (2) Cu 2+ imparts MOF oxidase activity to trigger the oxidation of o -phenylenediamine (OPD) into luminescent products (oxOPD) with emissive peak at 571 nm, which quenches the intrinsic fluorescence of NH 2 -Cu-MOF (435 nm) through inner filter effect (IFE); (3) Cu 2+ can complex with CC specifically to produce complex containing o -semiquinone, which not only inhibits MOF’s oxidase-like activity but also quenches the fluorescence of MOF. Therefore, the presence of CC induces the decrease of fluorescence at 571 nm followed by the slight recovery of fluorescence at 435 nm. Notably, HQ and RC have negligible influences on the fluorescence of NH 2 -Cu-MOFs/OPD system. Based on these facts, a ratiometric fluorescence platform for CC has been constructed. It exhibits high sensitivity towards CC with LOD of 0.1 μM.
研究领域:
分析化学
·
生物传感
·
材料科学
✓ 已验证
DOI
高影响因子
ACS Applied Materials & Interfaces
·
2020
·
IF 8.758
Yixing Luo,Qifeng Yang,Wendan Nie,Qilu Yao,Zhujun Zhang,Zhang-Hui Lu
Hydrogen (H2), a regenerable and promising energy carrier, acts as an essential role in the construction of a sustainable energy system. Formic acid (HCOOH, FA), a natural biological metabolic products and also accessible through carbon dioxide (CO2) reduction, has a great potential to serve as a prospective H2 supplier for the fuel cell. Herein, ultrafine and electron-rich IrPdAu alloy nanoparticles with a size of 1.4 nm are highly dispersed on amine-modified mesoporous SiO2 (NH2-SBA-15) and used as a highly active and selective catalyst for fast H2 production from FA. The as-synthesized IrPdAu/NH2-SBA-15 possesses superior catalytic activity and 100% H2 selectivity with initial turnover frequency values of 6316 h–1 with the additive of sodium formate (SF) and 4737 h–1 even without SF at 298 K, comparable to the most effective heterogeneous catalysts ever published. The excellent performance of IrPdAu/NH2-SBA-15 was not only ascribed to the combination of the electronic synergistic effect of trimetallic alloys and the strong metal–support interaction effect but also attributed to the amine (−NH2) alkaline groups grafted on SBA-15, which is beneficial to boost the split of the O–H bond of FA.
研究领域:
材料科学
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催化化学
·
能源化学
✓ 已验证
DOI
高影响因子
JOURNAL OF CHROMATOGRAPHY B-ANALYTICAL TECHNOLOGIES IN THE BIOMEDICAL AND LIFE SCIENCES
·
2025
·
IF 2.8
Yingxia Guo,Meichen Liu,Jiye Tian,Chunpeng Feng,Qingbin Wang,Xuan Zhao,Lei Yin
As an important chemical reagent, methoxy polyethylene glycol amine (mPEG-NH 2 ) is widely used in biomedical field. Unraveling the pharmacokinetic behavior of mPEG-NH 2 polymers is essential for revealing the toxicity and efficiency of mPEG-NH 2 related drug delivery systems. In this study, a simple analytical assay based on mass spectrometry (MS) was first established and validated for quantification of mPEG 5 -NH 2 in biological matrix. The multiple reaction monitoring (MRM) transitions at m / z 252.2 (precursor ions) → 87.7 (fragment ions) and m / z 371.2 (precursor ions) → 89.2 (fragment ions) were chosen to determine mPEG 5 -NH 2 and OH-PEG 8 -OH, respectively. The UHPLC-MS/MS assay showed excellent linearity over the range of 0.01–10 μg/mL. Intra-day and inter-day accuracies and precisions of the assay were all within ± 6.44 %. The analytical assay was successfully applied to reveal the in vivo pharmacokinetic behavior of mPEG 5 -NH 2 in rats.
研究领域:
药理学
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分析化学
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生物医学工程
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产品关联
DOI
PubMed
高影响因子
SEPARATION AND PURIFICATION TECHNOLOGY
·
2025
·
IF 9
Guowei Shan,Xiao Xiao,Hong Gao,Qi Zhang,Houyi Peng,Weixing Li
Heavy metal ion (HMI)-contaminated wastewater is a great threat to public health. Membrane separation is an efficient and green technology for HMI removal. Here, the strategy of nanoparticle in-situ growth combined with molecule grafting was proposed to fabricate the UiO-66-NH 2 -g-DTPA/PES composite membrane. The UiO-66-NH 2 nanoparticles bound within the PES membrane substrate uniformly brought a significant number of primary amino groups, providing abundant graft sites for DTPA molecule. Numerous carboxyl groups and tertiary amine groups were introduced as the result of DTPA grafting, enabling the formation of M−DTPA complexes with HMIs. The fabricated UiO-66-NH 2 -g-DTPA/PES membranes exhibited excellent performances. The pure water flux arrived at 6208 L·m −2 ·h −1 and the efficiencies of removing Cu 2+ , Pb 2+ , Cr 3+ and Cd 2+ were 99.73%, 99.79%, 96.91% and 98.33%, respectively. Moreover, the UiO-66-NH 2 -g-DTPA/PES membrane also showed a remarkable stability in pH conditions ranging from 3 to 10 and remained a relatively high performance in the cyclic test.
研究领域:
环境科学
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材料科学
✓ 已验证
产品关联
DOI
高影响因子
INTERNATIONAL JOURNAL OF HYDROGEN ENERGY
·
2025
·
IF 8.3
Jun-Qing Ye,Bin Cheng,Yunfei Bu,Jun-Feng Qian,Qian Liang,Ming-Yang He,Qun Chen
The development of high-efficiency photocatalysts for water splitting to hydrogen (H 2 ) is crucial for alleviating energy crisis and environmental problems. In this study, a novel type-II ternary heterojunction photocatalyst, CDs/NH 2 -MIL-125 (Ti)/Cu 2 O, was fabricated through the integration of NH 2 -MIL-125 (Ti) with Cu 2 O and carbon dots (CDs), exhibited excellent photocatalytic H 2 production rate of 12817.1 μmol/g/h with apparent quantum efficiency (AQE) of 17.13 % under visible light irradiation. Characterization revealed a uniform and dense structural integration with a high Brunauer-Emmett-Teller (BET) surface area of 275.9 m 2 g −1 and a suitable energy band gap of 2.18 eV. Furthermore, the heterostructures promoted efficient photo-generated carrier separation and enhanced reduction capabilities . Notably, CDs, serving as cocatalysts or electron acceptors, improved visible light utilization and electron migration, significantly boosting H 2 production. Insights from electron spin resonance (ESR) and density functional theory (DFT) calculations supported the migration mechanisms of electrons. This work presents a significant advance in photocatalytic technology for sustainable energy by designing high-performance CDs-modified heterojunction photocatalysts.
研究领域:
材料科学
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能源科学
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF ALLOYS AND COMPOUNDS
·
2024
·
IF 5.8
Qingqing Wang,Wei Zhou,Claudia Li,Sibudjing Kawi,Yinhui Li
The application of photocatalysts in environmental field has emerged as a prominent research topic. Nevertheless, the efficiency of photocatalysts is reduced as the recombination of photogenerated chargers significantly, restricting their extensive use in this domain. In the present study, photocatalysts composed of bismuth molybdate/NH 2 -UiO-66(Zr) (Bi 2 MoO 6 /NH 2 -UiO-66(Zr)) featuring Z-scheme heterojunctions were effectively synthesized using a two-step hydrothermal technique. These photocatalysts exhibit remarkable photocatalytic degradation under visible light conditions. Notably, the broad planar configuration of Bi 2 MoO 6 sheets improves the separation of the photogenerated charge carriers. NH 2 -UiO-66(Zr) layered atop Bi 2 MoO 6 sheets enhances the availability of catalytically active sites, reduces charge recombination, and promotes charge transfer through the interface. The kinetic rate constant for Bi 2 MoO 6 /NH 2 -UiO-66(Zr) is around 0.00329 L mg −1 min −1 , indicating the increase of 3.78 and 41.13 times compared with pure Bi 2 MoO 6 and NH 2 -UiO-66(Zr), respectively. The efficiency for photocatalytic degradation of tetracycline using Bi 2 MoO 6 /NH 2 -UiO-66(Zr) reaches 81.72 % under visible light. Importantly, this efficiency exhibits a reduction of 10 % after five recycling cycles, demonstrating notable stability. The photocatalytic mechanism involved in tetracycline degradation was uncovered through trapping experiments and EPR, indicating that it is predominantly facilitated by the active oxidation of ·O 2 - and ·OH. The intermediates of the photocatalytic process as well as the possible degradation pathways were discussed. The creation of Bi 2 MoO 6 sheets/NH 2 -UiO-66(Zr) heterojunction photocatalysts provides a fresh approach to the development of novel catalysts, which may lead to significant advancements in environmental remediation efforts.
研究领域:
环境科学
·
材料科学
✓ 已验证
产品关联
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2020
·
IF 10.652
Qiuzheng Du,Pu Wu,Yiyang Sun,Jingyi Zhang,Hua He
A simple and recyclable imprinted catalytic composite (ZnO@NH 2 -UiO-66, ZUM) was synthesized by postsynthetic modification method with tetracycline (TC) as molecular template. A series of ZUM-n composites with different NH 2 -UiO-66 dopants from 0.1 to 0.7 g had been prepared and compared. The characterization results showed that ZUM-1 possessed the advantages of uniform size, high surface area and wide absorption spectrum. Further research results indicated that ZUM-1 composite has the ability of selective adsorption and the higher photocatalytic degradation efficiency to TC without secondary pollution. Under visible light irradiation, the ZUM-1 could degrade 61.9% of TC within 30 min, which may relate to the inhibition effect of composite materials on electron-hole recombination. The degradation selectivity of ZUM-1 was investigated by comparing the degradation efficiency of TC, tetracycline hydrochloride and ciprofloxacin. The high degradation efficiency and selectivity of ZUM-1 were also confirmed in real samples. The stability experiments showed that the ZUM-1 possessed excellent recyclability and stability in the photocatalytic degradation process, and the recycled process was environmentally friendly. The mechanism of TC photodegradation by ZUM-1 was investigated by UV–vis spectra, photoelectrochemical and radical scavenger experiment. And the possible degradation products were analyzed by HPLC-MS. All in all, this method provided a simple and promising perspective for preparing visible-light-responsive molecular imprinting composites with high specificity and photocatalytic activity.
研究领域:
环境科学
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材料科学
·
光催化
✓ 已验证
产品关联
DOI
高影响因子
JOURNAL OF PHYSICAL CHEMISTRY B
·
2021
·
IF 2.991
Minjun Ma,Xueke Gao,Zhaohui Guo,Yan Qiao
Biotin–dendrimer conjugates (such as biotin-PAMAMs-NH2) are important macromolecules in the field of host–guest chemistry and widely used systems for delivery. The similar chemical structures of the inner and outer layers of PAMAM-NH2 make it difficult to illuminate the interaction and the binding affinity of biotin-PAMAMs-NH2. By utilizing NMR techniques including 1H NMR titration, CSSF-TOCSY, STDD methods, and 2D DOSY analysis, we demonstrate a method to sort out these interactions. The methylene protons of the inner and outer layers of PAMAM-NH2 are successfully identified and accurately positioned so that the carboxylic acid groups of biotins are having ionic interactions with the outermost amine groups of PAMAM-NH2. The inner PAMAM-NH2 is protonated when reaching the isoelectric point of PAMAM-NH2, increasing the hydrodynamic radius. On the basis of the NMR experiments, a model is proposed, where the carboxylic acid groups and heterocyclic skeleton of biotin arched over the outer layers of PAMAM-NH2 like a bridge. Furthermore, using STDD epitope mapping, the binding affinity between biotin and PAMAM-NH2 was quantified. The diffusion behavior of biotin-G5 PAMAM-NH2 complex is more complicated than that of biotin-G3 PAMAM-NH2 complex due to steric hindrance. The results provide a theoretical basis for understanding these complicated drug delivery systems.
研究领域:
化学
·
药物递送系统
·
分子相互作用
✓ 已验证
DOI
高影响因子
Biosensors-Basel
·
2024
·Vol. 14
·期 10
·512
·
IF 4.9
Jiawen Fan,Junjie Qi,Jingkun Li,Fuwei Pi
Arginine has been widely applied in the food industry as coloring agents, flavoring agents, and nutritional fortifiers. It is also one of the major components of feed additives. Currently, methods for the highly selective detection of arginine remain absent. For accurate and sensitive detection of L−arginine, a novel ratiometric fluorescence assay based on Ru@UiO-66-NH2was developed and demonstrated in this study. Under optimized detection conditions, the limit of detection (LOD) of this assay for L-arginine was 2.32 μM, which is superior to most assays reported to date. Meanwhile, Ru@UiO-66-NH2showed good stability within 30 days, demonstrating the wide applicability of the proposed assay. The spike-and-recovery rates of the proposed assay for L-arginine in real samples (e.g., tea, grape juice, and serum) were 84.27–113.09%. Overall, the proposed assay showed high sensitivity, good reproducibility, and excellent stability in the detection of L-arginine in both buffer and real samples.
研究领域:
分析化学
·
食品科学
·
生物化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Nanoscale
·
2025
·
IF 5.1
Zuyao Fu,Lingfeng Yang,Zhaoyang Ding,Jing Xie
Immobilized enzymes play a crucial role in analytical sensing due to their exceptional stability and considerable commercial importance. In this study, a stable Zr-based metal–organic framework (UiO-66-NH2) was prepared as an immobilization platform for horseradish peroxidase (HRP) through covalent binding. HRP@UiO-66-NH2 retained 75% of its activity after 10 cycles. Subsequently, a colorimetric/fluorometric dual-mode sensing strategy using HRP@UiO-66-NH2 was developed for nitrite detection. HRP@UiO-66-NH2 facilitated the transformation of the non-colored compound 3,3′,5,5′-tetramethylbenzidine (TMB) into its blue oxidized form. When nitrite is added, oxidized TMB (ox-TMB) specifically engaged with nitrite (NO2−) to generate diazotized TMB, leading to a color shift from blue to yellow. Concurrently, NO2− reacted with the amino groups of HRP@UiO-66-NH2, forming diazonium compounds and suppressing the fluorescence of HRP@UiO-66-NH2. The limits of detection were 0.21 μM and 0.19 μM for the colorimetric and fluorometric strategies, respectively. Furthermore, a portable kit for detecting nitrite was created by integrating gelatin with HRP@UiO-66-NH2. The kit could visually identify nitrite from 10–400 μM in colorimetric mode and 0–400 μM in fluorometric mode. This method provides an innovative approach for nitrite sensing, paving the way for new research into multifunctional immobilized enzymes and their potential uses in biochemical sensing applications.
研究领域:
生物化学
·
分析化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Foods
·
2024
·Vol. 13
·期 17
·2736
·
IF 4.7
Shibing Zhang,Yiran Wang,Chunyu Yang,Xi Wang,Siyi Wang,Jiping Yin,Yinan Du,Di Wu,Jiangning Hu,Qi Zhao
In this study, amino-modified micro-mesoporous silica (NH 2 -MMS) with hierarchical pores was prepared by modifying micro-mesoporous silica ZSM-5 with 3-aminopropyltriethoxysilane and used as an adsorbent in solid-phase extraction to analyze free fatty acids (FFAs) in krill oil during storage for an initial time. The Brunner Emmet Teller adsorption experiment and Fourier transform infrared spectroscopy demonstrate that NH 2 -MMS, with a hierarchical pore structure, was successfully synthesized. The adsorption experiments, especially static adsorption, indicate that the absorption ability of the prepared NH 2 -MMS, with a hierarchical pore structure, toward FFAs was better than that of traditional amino-modified mesoporous silica (SBA-15) with a mesoporous structure at all temperature and concentrations. Fairly low limits of detection (0.06–0.15 μg g −1 ), acceptable recoveries (85.16–94.31%), and precision (0.08–5.26%) were attained under ideal circumstances. Moreover, NH 2 -MMS has the advantages of easy preparation and being environmentally friendly. As a result, this method offers an alternative to the current method for determining FFAs in different kinds of oil specimens.
研究领域:
食品科学
·
分析化学
✓ 已验证
产品关联
DOI
PubMed
高影响因子
JOURNAL OF HAZARDOUS MATERIALS
·
2024
·
IF 12.2
Jiami Ma,Zhixin Hu,Weihong Guo,Cheng Ni,Pan Li,Bosheng Chen,Songhua Chen,Jinlong Wang,Yanbing Guo
Ground−level ozone (O 3 ) pollution poses a significant threat to both ecosystem sustainability and human health. The catalytic decomposition of O 3 presents as a promising technology to address the issues of O 3 pollution. This study undertook the synthesis of various functionalized metal−organic framework (MOF) catalysts ( i.e., X-MIL-53(Fe) (X = H, NH 2 , NO 3 )) to delve into the influence of ligand functional groups on skeletal structure and catalytic efficacy, particularly focusing on unraveling the mechanism of O 3 catalytic decomposition under humid conditions. NH 2 -MIL-53(Fe) catalyst achieved complete O 3 decomposition under ambient temperature and high humidity conditions (RH=75 %), exhibiting a reaction rates (mol·m −2 ·s −1 ) 129 and 10.5 times greater than that of MIL-53(Fe) and NO 2 -MIL-53(Fe). The NH 2 group promotes electron flow within the backbone towards the hydroxyl group (OH) linked to Fe atom. In humid O 3 , H 2 O molecules augment the interaction between O 3 and NH 2 -MIL-53(Fe), and OH is converted to·O 2 − after deprotonation, promoting O 3 decomposition. Additionally, leveraging three−dimensional (3D) printing technology, a monolithic catalyst for O 3 decomposition was prepared for application. This study not only advances understanding of the mechanisms underlying O 3 decomposition but also offers practical solutions for addressing O 3 pollution at humid conditions.
研究领域:
环境科学
·
材料科学
✓ 已验证
DOI
PubMed
高影响因子
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