文献检索

查找使用阿拉丁产品的科研文献

检索与阿拉丁产品相关的同行评审论文、DOI、PubMed 编号、期刊、作者、CAS 号及研究领域。

科研影响力快照

与阿拉丁产品相关的已发表科研成果

在搜索之前,这些指标可帮助访客快速了解产品关联科研的规模与质量。

346,438+ SCI 论文 与阿拉丁产品引用相关
2,295,919.25 总影响因子 匹配文献记录中影响因子的总和
81.20 最高期刊影响因子 匹配期刊中的最高 IF
6.63 平均期刊影响因子 匹配文献的平均 IF

参考指标 指标基于阿拉丁文献引用数据库及期刊影响因子记录。文献关联仅供科研参考,请以原始文献为准。

产品列表

视图 列表 网格

显示第373至384个,产品总数1,277个

设置提升方向
MIL
ENERGY & FUELS · 2017 · IF 3.091

Enhanced Adsorption Performance of Aromatics on a Novel Chromium-Based MIL-101@Graphite Oxide Composite

Xuejiao Sun,Daofei Lv,Yongwei Chen,Ying Wu,Qihui Wu,Qibin Xia,Zhong Li

Chromium-based MIL-101 and graphite oxide (GO) composite (MIL-101@GO) was synthesized and applied for adsorption performances toward a series of aromatics (benzene, toluene, and ethylbenzene). Desorption activation energies of aromatics on this composite were evaluated based on temperature-programmed desorption (TPD) experiments. The results indicated that the aromatic uptakes on the composite increase with the carbon number at low pressure. In contrast, at high pressure, their adsorption capacities exhibit an opposite trend. The composite possesses high uptakes of the aromatics, which are approximately 1.8–6.0 times higher compared with conventional adsorbents. The desorption activation energies of the aromatics increase with the carbon number of aromatics. Additionally, the adsorption of ethylbenzene on the composite is highly reversible. More importantly, the MIL-101@GO composite exhibits enhanced thermal conductivity up to 0.369 W/mK at 303 K. The MIL-101@GO composite with high adsorption capacity, enhanced thermal conductivity, and efficient recyclability provided a promising candidate for practical applications in field of volatile organic compounds adsorption.

CAS / MDL: 100-41-4
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
ENVIRONMENTAL SCIENCE & TECHNOLOGY · 2024 · IF 10.8

Dose-Dependent Effect on Plant Growth of Exposure to Metal–Organic Framework MIL-101(Cr)

Yacong Liu,Yue Lin,Weichao Wang,Ke Min,Weibo Ling,Wende Ma,Weican Zhang,Xingwang Hou,Linfeng Wei,Qian Liu,Guibin Jiang

With the increasing use of metal–organic frameworks (MOFs), they will inevitably enter the environment intentionally or unintentionally. However, the effects of MOFs on plant growth are poorly understood. Here, we investigated the effects of exposure of the rhizosphere to MOFs on plant growth. MIL-101(Cr) was selected as a research model due to its commercial availability and wide use. Soybean plants at the two-leaf stage were subjected to various durations (1–7 days) and concentrations (0–1000 mg/L) of exposure in hydroculture with a control group treated with ultrapure water. We found that MIL-101(Cr) had a positive effect on soybean growth at a lower dose (i.e., 200 mg/L); however, at higher doses (i.e., 500 and 1000 mg/L), it exhibited significant toxicity to plant growth, which is evidenced by leaf damage. To investigate the mechanism of this effect, we used Cr as an indicator to quantify, track, and image MIL-101(Cr) in the plant with laser ablation inductively coupled plasma mass spectrometry (LA-ICP-MS). Results indicated that MIL-101(Cr) primarily accumulated in the cortex of roots (up to 40 times higher than that in stems), with limited translocation to stems and negligible presence in leaves and cotyledons. In addition, metabolomic analysis of soybeans indicated that low-dose MIL-101(Cr) could increase the sucrose content of soybean roots to promote plant growth, while a high dose could induce lipid oxidation in roots. This study provides valuable insights into the ecological toxicology of MOFs and underscores the importance of assessing their environmental impact for sustainable agricultural practices.

✓ 已验证 产品关联 DOI PubMed 高影响因子
查看原文 查看 PubMed
JOURNAL OF NANOPARTICLE RESEARCH · 2024 ·Vol. 26 ·期 9 ·1-15 · IF 2.1

Catalytic degradation of rhodamine B by α-DMACoPc/TiO2/MIL-101 (Fe) enhanced catalytic system

Yin Yanbing,Zhang Xueli,Jiang Bei,Wang Zhou,Feng Yongming,Li Xueying

Developing efficient catalysts for visible light reactions is vital in the field of photocatalysis. This study focuses on the synthesis of novel ternary composites (α-DMACoPc/TiO 2 /MIL-101 (Fe)) by leveraging the excellent adsorption properties of MIL-101 (Fe), the photosensitizing capabilities of phthalocyanine, and the photocatalytic potential of TiO 2 . The nanocomposites’ structural and optical attributes were thoroughly analyzed. X-ray powder diffraction (XRD) was utilized to showcase the crystalline nature of the composites. Furthermore, Fourier transform infrared (FT-IR) studies confirmed the formation of ternary nanocomposites. Optical absorption investigations demonstrated the tuning of the optical band gap from the UV to the visible range. The results indicated that nearly 94% of the organic material was decomposed after 150 min of exposure to simulated sunlight from a xenon lamp. This high efficiency can be attributed to the synergistic interaction among the composites, enhancing light absorption. The composite’s robust stability was evidenced through cyclic tests. Valuable information was provided to advance the design and synthesis of photocatalysts consisting of metal–organic frameworks synergized with semiconductors. Exploring the possibility of mesoporous materials was based on MOFs for photodegradation of organic pollutants. The photocatalytic degradation of organic pollutants by MOFs mesoporous materials was also investigated. The potential of composite materials in the field of dye degradation of industrial waste is confirmed. The good recycling photocatalytic reusability indicates the promising application of this photocatalyst. Graphical Abstract

CAS / MDL: 10026-22-9 10025-77-1
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
JOURNAL OF HAZARDOUS MATERIALS · 2024 · IF 12.2

Co-adsorption performance of iodine and NOX in iodine exhaust gas by NH2-MIL-125

Xuanhao Liang,Guangyuan Chen,Hao Zhang,Ling Zhang,Tao Duan,Lin Zhu

Ti-based MOFs exhibit ultra-high stability in radioactive waste gases containing nitrogen oxides (NO X ) and are effective in capturing radioactive iodine. In this study, NH 2 -MIL-125 was synthesized via a one-pot solvothermal method and its adsorption performance for iodine was investigated using batch adsorption experiments, the stability of materials was tested by simulating post-processing conditions. The results indicated that NH 2 -MIL-125 had a maximum iodine adsorption capacity of 1.61 g/g at 75 ℃ and reached adsorption equilibrium within 60 min, and the adsorption capacity of methyl iodine reached 776.9 mg/g. The material also exhibited excellent stability and iodine adsorption performance in the presence of NO X . After soaking in NO 2 for 24 h, its structure remained stable and the adsorption capacity for iodine remained at 231.5 mg/g. The excellent co-adsorption performance of NH 2 -MIL-125 on iodine and NO X was attributed to the synergistic effects of Ti-OH groups and amino functional groups. These findings provide a reference for the capture of radioactive iodine and also demonstrate the potential of NH 2 -MIL-125 for iodine capture during spent fuel reprocessing .

✓ 已验证 产品关联 DOI PubMed 高影响因子
查看原文 查看 PubMed
Surfaces and Interfaces · 2024 · IF 5.7

Boosting photothermal CO2 hydrogenation with H2O by MIL-100(Fe) derived Fe@C confined Ni2P

Pengfei Zhu,Mengrong Geng,Shuang Qin,Heyang Cao,Zhenhong He,Xinhua Gao,Chuanyi Wang

The conversion of CO 2 into chemical products or fuels of great value always remains an outstanding challenge. Here, we report a heterojunction Fe@C/Ni 2 P composite catalyst obtained by preparing MIL-100(Fe) derived Fe@C confined Ni 2 P nanoparticles, which is applied to photothermal catalytic CO 2 hydrogenation with H 2 O. Without adding any sacrificial agents or co-catalysts, the optimal Fe@C/Ni 2 P sample shows higher yields for CO 2 -to-C 2 H 6 and CO 2 -to-CO yield of 5.83 μmol g −1 h −1 and 179.9 μmol g −1 h −1 than that of pristine Fe@C and Ni 2 P, respectively. The experimental results indicated that the obtained Fe@C/Ni 2 P can act as catalytic sites to adsorb, activate, and convert CO 2 under low-intensity LED light irradiation (420 nm) with a temperature of 200 ℃. The physical structure, photochemical properties and energy band structure of the Fe@C/Ni 2 P composite catalysts were investigated by XRD, XPS, FT-IR, TEM, BET, respectively. Furthermore, the reaction pathway of Fe@C/Ni 2 P photothermal catalytic CO 2 hydrogenation with H 2 O to C2 products and CO were systematically analyzed by in situ infrared spectroscopy (DRIFTS).

CAS / MDL: 7723-14-0
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
JOURNAL OF MATERIALS CHEMISTRY · 2012 ·Vol. 22 ·期 15 ·7449-7455 · IF 5.968

Metal–organic framework MIL-100(Fe) for the adsorption of malachite green from aqueous solution

Shu-Hui Huo,Xiu-Ping Yan

The adsorption of malachite green from aqueous solution on a highly porous metal–organic framework MIL-100(Fe) was studied in view of the adsorption isotherm, thermodynamics, kinetics, and regeneration of the sorbent. The adsorption isotherms of malachite green on MIL-100(Fe) followed the Freundlich model, and MIL-100(Fe) possessed heterogeneous surface caused by the presence of different functional groups on the surface. The adsorption of malachite green on MIL-100(Fe) is controlled by an entropy effect rather than an enthalpy change, and obeyed a pseudo-second-order kinetics. Analysis of the intraparticle diffusion plots revealed that more than one process affected the adsorption, and film (boundary layer) diffusion controlled the adsorption rate at the beginning. Evidence from zeta potential and X-ray photoelectron spectroscopic data showed that the adsorption of malachite green was also driven by electrostatic attraction and the interaction between the Lewis base –N(CH3)2 in malachite green and the water molecule coordinated metal sites of MIL-100(Fe). MIL-100(Fe) gave much higher adsorption capacity for malachite green than other conventional adsorbents such as activated carbon and natural zeolite. The high adsorption capacity, good solvent stability, and excellent reusability make MIL-100(Fe) attractive for the removal of MG from aqueous solution.

✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
JOURNAL OF CHROMATOGRAPHY A · 2017 · IF 3.981

Pyrolytic in situ magnetization of metal-organic framework MIL-100 for magnetic solid-phase extraction

Shu-Hui Huo,Hai-Yan An,Jing Yu,Xue-Feng Mao,Zhe Zhang,Lei Bai,Yan-Feng Huang,Peng-Xin Zhou

In this study, we report a facile, environmental friendly fabrication of a type of magnetic metal-organic framework (MOF) MIL-100 that can be used for magnetic solid-phase extraction (MSPE). The magnetic MOF composites were fabricated using in situ calcination method. The as-synthesized materials exhibited both high porosity and magnetic characteristics. They used for the MSPE of polycyclic aromatic hydrocarbons (PAHs) from water samples. Such MOF-based magnetic solid-phase extraction in combination with gas chromatography equipped with a flame ionization detector (GC-FID), exhibited wide linearity (0.02–250   μ g   L −1 ), low detection limits (4.6-8.9   ng   L −1 ), and high enrichment factors (452–907) for PAHs. The relative standard deviations (RSDs) for intra- and inter-day extractions of PAHs were ranging from 1.7% to 9.8% and 3.8% to 9.2%, respectively. The recoveries for spiked PAHs (1   μ g   L −1 ) in water samples were in the range of 88.5% to 106.6%. The results showed that the special anion-π orbital (electron donor-acceptor) interaction and π-π stacking between magnetic MIL-100 and PAHs play an important role in the adsorption of PAHs.

CAS / MDL: 7439-89-6
✓ 已验证 产品关联 DOI PubMed 高影响因子
查看原文 查看 PubMed
APPLIED SURFACE SCIENCE · 2025 · IF 6.9

The type II MIL-100/BiOBr heterojunctions promote efficient photo-Fenton degradation of tetracycline hydrochloride

Bo Xue,Chuanruo Yang,Pengtao Guo,Ting Wang,Gan Li,Dahuan Liu

The low efficiency of photogenerated carriers separation and slow cycling of Fe 2+ /Fe 3+ in Fe-based metal–organic frameworks (MOFs) have limited the improvement of their photo-Fenton activity. Therefore, in this work, MIL-100/BiOBr heterogeneous photo-Fenton catalyst was constructed by compositing MIL-100 with BiOBr nanosheets through a simple solvent evaporation method. In this system, the type II heterojunctions formed by the close contact of MIL-100 and BiOBr can promote the separation of photogenerated carriers and accelerate the redox cyclic of Fe 2+ /Fe 3+ , thereby significantly enhancing the photo-Fenton activity. Under visible light irradiation for 60 min, the best removal rate of tetracycline hydrochloride (TCH) by MIL-100/BiOBr is 94.3 %. Remarkably, the MIL-100/BiOBr exhibits a nearly fourfold increase in degradation rate constant compared to MIL-100 at photo-Fenton system. In addition, the catalysts can maintain high degradation performance over a wide pH range (3–9) and the co-existence of different anions. An in-depth investigation of the degradation mechanism reveals that superoxide radicals ( · O 2 – ) and hydroxyl radicals (·OH) play major roles in the photo-Fenton system. Based on this, the possible degradation pathways were proposed. Therefore, this study provides a new strategy for Fe-based MOFs to remove emerging pollutants from wastewater by photo-Fenton reaction.

✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
CARBON · 2024 · IF 10.5

Synergistic NH2-MIL-88B/Ta4C3TX/graphene aerogels for sustainable wastewater treatment and thermal energy storage

Jiarong Zhang,Long Yu,Ya'nan Zhao,Tianran Zhao,Yi'na Yang,Chunna Yu,Chang Zhao,Guangjian Xing

The urgent need for multifunctional, high-performance materials is critical in addressing environmental pollution and energy shortages faced by contemporary society. This research presents innovative NH 2 -MIL-88B/Ta 4 C 3 T X /graphene aerogels that exhibit exceptional capabilities in photocatalysis and thermal energy storage utilizing solar energy. Synthesized through a combination of hydrothermal and freeze-drying methods, these aerogels feature unique structural characteristics, including a hierarchical porous structure, low density, and a large specific surface area. Furthermore, the synergistic effects of NH 2 -MIL-88B, Ta 4 C 3 T X MXene, and the aerogel matrix contribute to remarkable physicochemical properties, such as high sunlight absorptivity and an optimal optical band gap that aligns well with the solar spectrum. These attributes enable the aerogels to photodegrade various dye and antibiotic drug solutions with high concentrations. The photodegradation efficiencies achieved were 75.57 % for Congo red, 61.56 % for methylene blue, and 58.57 % for tetracycline hydrochloride. Additionally, these aerogels exhibit significant adsorption capacities for various dyes and drugs. Moreover, when the phase change material polyethylene glycol is successfully integrated into the aerogels, they exhibit excellent thermal energy storage performance with leak-proof capabilities. A high photothermal conversion efficiency of 90.15 %, a phase enthalpy of 202.13 J g −1 , and an enthalpy efficiency of 98.55 % provide evidence for this. This work provides valuable insights into the development of multifunctional aerogels aimed at addressing the challenges of wastewater treatment and energy shortages.

CAS / MDL: 10424-65-4
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
MATERIALS CHEMISTRY AND PHYSICS · 2025 · IF 4.7

The electrochemical performance of MoO2@FeMoO4 composites derived from PMo12@MIL-101(Fe) for supercapacitors

Ziwei Chen,JinChang Zhao,Qing Li,Rufen Chen,HuiJiao Zhang,Hui Zhao,Kezhong Wu

The synergistic coupling of different metal species endows mixed transition metal oxides (MTMOs) as electrode materials for supercapacitors with multiple redox reaction pathways and enhances the electronic conductivity. In this study, three MoO 2 @FeMoO 4 electrode materials were derived from the precursor PMo 12 @MIL-101(Fe) by pyrolysis at 600 °C, 700 °C, and 800 °C under an O 2 atmosphere. The precursor was composed of polyoxomolybdate (H 3 PMo 12 O 40 , PMo 12 ) and Fe-based metal-organic frameworks (MOFs) MIL-101(Fe). The structural characteristics of the three obtained MoO 2 @FeMoO 4 composites were characterized by XRD, XPS, SEM, and N 2 adsorption measurement. Then, the effects of the pyrolysis preparation temperature for the MoO 2 @FeMoO 4 composites on the energy storage performance of the supercapacitor electrode were evaluated by cyclic voltammetry (CV) and galvanostatic charge/discharge tests. Among three electrodes, the specific capacitance of 339.6 F g −1 of the obtained MoO 2 @FeMoO 4 (700 °C) electrode was the highest compared to 291.2 F g −1 of MoO 2 @FeMoO 4 (600 °C) and 209.7 F g −1 of MoO 2 @FeMoO 4 (800 °C) at a current density of 0.5 A g −1 in 1.0 M NaOH electrolyte. As a result, the different pyrolysis preparation temperatures can alter the atomic microelectronic state and geometric configuration of the MoO 2 @FeMoO 4 , which can construct a high-density Fe–Mo bimetallic multicatalytic active site, thus affecting the activity of the composites. The excellent pseudo-supercapacitance response of the MoO 2 @FeMoO 4 (700 °C) electrode can be ascribed to its larger S BET and greater number of voids, which can generate more Fe–Mo bimetallic active sites and facilitate the electrolyte diffusion, indicating high energy conversion efficiency for potential application in supercapacitors.

✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
MICROCHEMICAL JOURNAL · 2025 · IF 5.1

A highly sensitive photoelectrochemical aptamer sensor based on MIL-101(Cr)&Bi2S3 for chlorpyrifos detection

Zhaoxiang Zhong,Bochi Pan,Yi Xing,Hanlin Xu,Min Zhang,Lei Ding,Faliang Cheng

The extensive global application of chlorpyrifos (CPF) has led to significant environmental accumulation through aquatic systems, presenting substantial risks to ecological integrity and public health. This urgency necessitates advanced detection methodologies with enhanced sensitivity and operational efficiency to ensure environmental safety. Here, we developed a novel photoelectrochemical aptamer sensor utilizing a MIL-101(Cr)&Bi 2 S 3 heterostructure composite. This architecture synergistically integrates the broad-spectrum photon absorption capability of Bi 2 S 3 with the hierarchical porosity and structural stability of MIL-101(Cr), achieving remarkable enhancement in both electron-hole separation efficiency and interfacial charge transfer. The sensing platform was further optimized through aptamer functionalization, which confers precise molecular recognition capabilities while maintaining optimal charge transfer dynamics at the electrode interface. Systematic evaluation demonstrated exceptional analytical performance: a linear detection range spanning four orders of magnitude (0.05–10 μg/mL), ultralow detection limit of 0.022 ng/mL (S/N = 3). The developed methodology provides a versatile framework for adapting to other organophosphorus pesticide detection requirements through modular aptamer replacement.

✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
JOURNAL OF SOLID STATE CHEMISTRY · 2024 · IF 3.2

High efficiency degradation of RhB by MIL-88A(Fe)/MoS2 activated persulfate and its mechanism

Xuechang Ren,Ju An,Suying Ding,Zhenyu Yang,Miao Tian,Ning Fu

MoS 2 /MIL-88A (Fe) composite catalyst was prepared by in-situ formation method. The material was characterized by SEM, TEM, XRD and XPS, and the Rhodamine B(RhB) was activated and degraded by persulfate (PMS). The results showed that M-10/M 1:2 had the best degradation effect on RhB, the rate constant was 0.66420 min −1 , and the degradation rate could reach 1.89–14 times that of other doped composite catalysts. The SEM results showed that M − 10 had the least sulfur content, fewer MoS 2 flower layers and more exposed Mo 4+ atoms, which improved the electron transfer efficiency and accelerated the degradation reaction. The XPS spectra before and after M-10/M 1:2 reaction showed that the REDOX reaction of Fe 3+ /Fe 2+ and Mo 4+ /Mo 6+ on the catalyst surface played an important role in the activation of PMS. The results of free radical capture experiment and ESR test showed that the main active substances in M-10/M 1:2 /PMS reaction system were SO 4 •− , 1 O 2 , •O 2 − , and •OH, which only played a role in the degradation of RhB. Finally, based on the ESR results of M-10/M 1:2 /PMS system and the changes of Fe and Mo elements in XPS characterization before and after the reaction, the degradation mechanism of M-10/M 1:2 /PMS system was proposed.

✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
已复制

文献关联基于可获得的产品、CAS、DOI 及引用记录。收录不代表作者或出版方对阿拉丁产品的背书,请以原始文献为准。