ACS Applied Materials & Interfaces
·
2024
·
IF 8.3
Shuchao Jiang,Hongqi Shi,Yuzhe Xu,Jiaojiao Liu,Tie Yu,Guoqing Ren
Formic acid (FA, HCOOH) is regarded as one of the most promising carriers for hydrogen storage. However, the catalyst design for FA dehydrogenation into H2 with high efficiency is not clear. Here, we elucidate the rationale of size effect over the most commonly used Pd-based catalyst through supporting different Pd species, including single atoms, nanoclusters, and nanoparticles, on amine-functionalized active carbon (Pd/AC-NH2). The activity test presents that Pd/AC-NH2 with Pd nanoclusters exhibits the best turnover frequency (TOF) value of 40856 h–1 for 1 M FA at 328 K and even 1504 h–1 for neat FA at 308 K, which is comparable to the homogeneous catalysts and has been the first heterogeneous catalyst used in neat FA dehydrogenation under mild conditions. The comprehensive characterizations reveal that the size of Pd species affects the ratios of Pd0/Pd2+ and hydrogen spillover effect, which is crucial for the C–H cleavage and H2 desorption. Besides, the influences of amine groups on catalytic performance were further examined. This work provided an ingenious guideline to design efficient and practical catalysts for hydrogen storage under ambient conditions.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Journal of Materials Chemistry A
·
2017
·Vol. 5
·期 30
·15797-15807
·
IF 8.867
Dan Zhao,Xiao-Hui Liu,Yue Zhao,Peng Wang,Yi Liu,Mohammad Azam,Saud I. Al-Resayes,Yi Lu,Wei-Yin Sun
Excess and deficiency of iron(III) and antibiotics from normal permissible limits will induce serious disorders, so their detection is important but challenging. In this work, by introducing a new amino triazole ligand N1-(4-(1H-1,2,4-triazole-1-yl)benzyl)-N1-(2-aminoethyl)ethane-1,2-diamine (L), a series of Cd(II)-based metal–organic frameworks (MOFs) [Cd3(BDC)3(DMF)2] (1), [Cd(L)(BDC)]2·2DMF·H2O (2), [NaCd2(L)(BDC)2.5]·9H2O (3), [Cd2(L)(2,6-NDC)2]·DMF·5H2O (4) and [Cd2(L)(BPDC)2]·DMF·9H2O (5) were synthesized. MOFs 1, 2 and 3 obtained under the same conditions with the same auxiliary ligand (H2BDC) but different amounts of alkali (NaOH) show distinct 3D, 1D and 3D framework structures, respectively, in which L and BDC2− exhibit varied coordination modes. 4 and 5 with 3D structures were isolated by using longer auxiliary ligands of 2,6-H2NDC and H2BPDC. The porosity and excellent fluorescence performance of 3, 4 and 5 make them potential luminescent sensors for Fe(III) and antibiotics. The results show that 3, 4 and 5 represent high sensitivity for the detection of Fe(III) ions with detection limits of 155 ppb for 3, 209 ppb for 4 and 297 ppb for 5 due to the existence of open channels and chelating NH2 sites. In addition, the strong emissions of 3, 4 and 5 can be quenched efficiently by trace amounts of NFs (nitrofurazone, NZF; nitrofurantoin, NFT; furazolidone, FZD) antibiotics even in the presence of other competing antibiotics such as β-lactams (penicillin, PCL). They are responsive to NZF with detection limits of 162 ppb for 3, 75 ppb for 4 and 60 ppb for 5.
✓ 已验证
DOI
高影响因子
CHEMICAL ENGINEERING JOURNAL
·
2012
·
IF 3.461
Jianming Zhang,Shangru Zhai,Shi Li,Zuoyi Xiao,Yu Song,Qingda An,Ge Tian
Contamination of natural water with heavy metals (especially lead ions) is a problem of major concern and thus great demand of effective adsorbents for removal of toxic ions is increasing. Due to the task-specific properties of amino groups, core–shell nanostructures of Fe 3 O 4 @SiO 2 –NH 2 have been extensively investigated as advanced adsorbents; however, most studies on surface modification of Fe 3 O 4 @SiO 2 substances were of environmentally inefficient grafting methods. Herein, we demonstrated that mono-dispersed and spherical Fe 3 O 4 @SiO 2 –NH 2 nanomaterials can be facilely prepared by co-condensation of TEOS with APTMS employing a green sol–gel process. The as-prepared Fe 3 O 4 @SiO 2 –NH 2 magnetic nanoparticles (MNPs) prepared under optimum conditions possessing uniform core–shell structure (∼200 nm in diameter), relatively high loading of amino-functionality (∼5.45 wt%), easy recovery by external magnet and effective removal of Pb(II) ( q m = 243.9 mg/g, 25 °C). The adsorption was shown to be effective and a higher temperature was more favorable for the adsorption. The adsorption equilibrium data obeyed the Langmuir model and the kinetic data were well fitted to the pseudo-second-order model. Thermodynamic studies revealed the feasibility and endothermic nature of the system. These results demonstrated that the sol–gel produced Fe 3 O 4 @SiO 2 –NH 2 , due to its easy synthesis and recovery and eco-friendliness, can be a potential adsorbent for Pb(II) removal.
✓ 已验证
产品关联
DOI
高影响因子
ACS Applied Materials & Interfaces
·
2014
·
IF 5.9
Cheng Sun,Yuanfu Deng,Lina Wan,Xusong Qin,Guohua Chen
There is a great interest in the utilization of silicon-based anodes for lithium-ion batteries. However, its poor cycling stability, which is caused by a dramatic volume change during lithium-ion intercalation, and intrinsic low electric conductivity hamper its industrial applications. A facile strategy is reported here to fabricate graphene oxide-immobilized NH2-terminated silicon nanoparticles (NPs) negative electrode (Si@NH2/GO) directed by hydrogen bonding and cross-linked interactions to enhance the capacity retention of the anode. The NH2-modified Si NPs first form strong hydrogen bonds and covalent bonds with GO. The Si@NH2/GO composite further forms hydrogen bonds and covalent bonds with sodium alginate, which acts as a binder, to yield a stable composite negative electrode. These two chemical cross-linked/hydrogen bonding interactions—one between NH2-modified Si NPs and GO, and another between the GO and sodium alginate—along with highly mechanically flexible graphene oxide, produced a robust network in the negative electrode system to stabilize the electrode during discharge and charge cycles. The as-prepared Si@NH2/GO electrode exhibits an outstanding capacity retention capability and good rate performance, delivering a reversible capacity of 1000 mAh g–1 after 400 cycles at a current of 420 mA g–1 with almost 100% capacity retention. The results indicated the importance of system-level strategy for fabricating stable electrodes with improved electrochemical performance.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
Journal of Materials Chemistry B
·
2015
·Vol. 3
·期 9
·2006-2011
·
IF 4.726
Na Li,Yaoguang Wang,Wei Cao,Yunhui Zhang,Tao Yan,Bin Du,Qin Wei
The excellent catalytic activity of a novel nanomaterial was introduced to ultrasensitive sandwich-type electrochemical immunosensor applications for detection of carcinoembryonic antigen (CEA). Amino-functionalized multi-walled carbon nanotube (MWCNT-NH2) supported PdPt nanocages were used as catalytic labels of secondary anti-CEA. PdPt nanocages with hollow interiors and porous walls could efficiently enhance electrocatalysis for reduction of H2O2. Meanwhile, with good dispersion, large specific surface area and amino groups, MWCNT-NH2 can immobilize a large amount of PdPt nanocages to improve the sensitivity and amplify the signal of the immunosensor. For the immobilization of primary antibodies, 3-aminopropyltriethoxysilane functionalized graphene sheets were used as transducing materials to modify glassy carbon electrodes and to enhance the electron transfer efficiently. Under the optimal conditions, the electrochemical immunosensor exhibited a wide linear range of 0.001–20 ng mL−1 with a low detection limit of 0.2 pg mL−1 for CEA. The proposed sensing strategy enriches electrochemical immunoassays and may have a promising application in bioassay analysis.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
APPLIED CATALYSIS B-ENVIRONMENTAL
·
2024
·
IF 20.2
Yinghao Li,Ying Li,Qinglong Meng,Ke Jing,Jingyi Zhang,Qingyu Guan
Achieving efficient phosphorus recovery and reuse from wastewater presents formidable challenges. In this study, a synergistic adsorption photocatalysis process was successfully constructed. 0.1Bi-MIL-101-NH 2 showed the maximum phosphorus adsorption performance of 112 mg/g. After phosphorus adsorption, photoelectrochemical measurements confirmed that the photoelectric properties of the 0.1Bi-MIL-101-NH 2 -P sample was improved, and the degradation efficiency of SMX was increased by 20 % within 120 min. Meanwhile, the mineralization rate reached 91 %. The incorporation of Bi significantly enhanced the adsorption energy of the 0.1Bi-MIL-101-NH 2 sample. Notably, the presence of phosphorus on the surface of 0.1Bi-MIL-101-NH 2 -P enhanced the adsorption of water molecules by the material, thereby augmenting the generation of •OH. •O 2 - and •OH played dominant roles in the photodegradation of SMX. Finally, the degradation pathways of intermediates were further studied by Density functional theory (DFT) calculations and LC-MS analysis. This study provides a new avenue for phosphorus recovery and organic pollutant degradation.
✓ 已验证
产品关联
DOI
高影响因子
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH
·
2024
·
IF 3.8
Douhao Yang,Ruiting Jian,Jianjun Yan,Ao Zhang,Bowen Liu,Zhongwei Liu
Defect engineering has a great effect on the properties of metal–organic frameworks (MOFs). In this study, the defective UiO-66-NH2 MOFs are successfully prepared by a rapid Ar plasma modification method. At certain experimental conditions (15 W radio frequency input power, 20 Pa working pressure, and 120 s Ar plasma modification time), the afforded UiO-66-NH2 shows significant enhancement in photocatalytic reduction of Cr(VI), and a maximum reduction efficiency of 68.5% is obtained. Advanced characterizations show that the plasma treatment generates missing-linker defects within the UiO-66-NH2 structure, which can enhance the separation of photogenerated electrons and holes and improve the photoreduction capability. The findings not only contribute to a better understanding of the relationship between the structure and performance of MOFs but also provide a simple approach for defect engineering of MOFs.
✓ 已验证
产品关联
DOI
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.
✓ 已验证
产品关联
DOI
高影响因子
LANGMUIR
·
2024
·
IF 3.7
Jing Zhang,Changhua Li,Xiaofeng Zhang,Hao Chen,Rui Gou,Chao Zhang,Dan Sun,Yi He
The use of graphene-based materials as anticorrosion coatings to protect metals is always a topic of discussion. In this work, silicon nitride (Si3N4) was aminated to improve its water dispersibility. Then it is attached to the graphene oxide (GO) surface to improve compatibility with epoxy (EP) resin as well as conductivity. The results of Fourier transform infrared (FTIR) spectroscopy, transmission electron microscopy (TEM), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and zeta potentials test analyses indicated that Si3N4–NH2@GO with a layer-point structure has been successfully prepared. The corrosion resistance of the composite coatings was characterized by electrochemical impedance spectroscopy (EIS) and polarization curve analysis, and the wear resistance of the composite coatings was tested by friction and wear tests. The results showed that 1.0% Si3N4–NH2@GO has excellent corrosion and wear resistance. The use of Si3N4–NH2@GO layer point structures in this study broadens the way for GO applications.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS
·
2024
·
IF 4.9
Qin Cheng,Jinping Gan,Kai Cai,Ming Xia,Yi Wu,Shanshan He,Pan Cheng,Qihao Guo,Ke Liu,Dong Wang
High-quality polyamide (PA) nanofiltration (NF) membrane with excellent selectivity and permeability is of great research significant because of their high practical application value, especially for the precise separation of divalent and monovalent ions, such as Mg 2+ and Li + . Herein, UiO-66-NH 2 nanoparticles (NPs) decorated ethylene vinyl alcohol copolymer (EVOH) nanofiber substrate (M-NFM) was utilized to construct high-quality Janus NF membrane through interfacial polymerization (IP) reaction using polyethyleneimine (PEI) and piperazine (PIP) as aqueous phase monomers and trimesoyl chloride (TMC) as organic phase monomers. The incorporation of UiO-66-NH 2 NPs significantly influenced the hydrophilicity, surface morphology, and pore structure of the substrate, thereby enhancing the properties of the resulting NF. Optimally prepared membranes demonstrated improved separation performance, permeability, stability, and antifouling characteristics compared to the unmodified substrate. Notably, at a Mg 2+ /Li + ratio of 30, the resultant NF membrane achieved a separation factor (S Mg 2+ /Li + ) of 28.4 and a salt permeation flux of 156.8 L·m -2 ·h -1 ·MPa -1 . Additionally, the membrane exhibited over 98% rejection rates for FeCl 3 , CuSO 4 , CaCl 2 , MgSO 4 , MgCl 2 and Na 2 SO 4 with fluxes exceeding 150 L·m -2 ·h -1 ·MPa -1 , highlighting its effectiveness in rejecting multivalent ions. This research presents a simpler and more reliable approach to the fabrication of high-quality Janus PA NF membrane, offering promising potential for industrial-scale applications.
✓ 已验证
产品关联
DOI
高影响因子
RSC Advances
·
2024
·Vol. 14
·期 38
·28148-28159
·
IF 3.9
Lidi Gao,Xinran Qu,Shuang Meng,Mo Chen,Yuxin He,Fuquan Zhao,Hongtao Chu,Shili Qin,Fenglong Jin
The excellent stability of covalent organic frameworks (COFs) and the diversity of metal organic frameworks (MOFs) make MOF/COF hybrid materials promising candidates for chromatographic stationary phases. In this paper, a TpBD/UiO-66-NH2 hybrid material was synthesized through a Schiff-base reaction between TpBD COFs and UiO-66-NH2 MOFs; characterized using Fourier-transform infrared spectroscopy, X-ray diffraction, and X-ray photoelectron spectroscopy; and bonded to a capillary to prepare a TpBD/UiO-66-NH2-bonded open tubular capillary electrochromatography (OT-CEC) column. Results suggested that the hybrid material had the crystal morphology of a single COF and MOF, a micro–mesoporous structure, and good thermal stability. The inner surface of the OT-CEC column was tightly and uniformly distributed with the stationary phase (∼1.5 μm). The baseline separation of 13 amino acids and three families (4 acidic antibiotics, 4 preservatives and 6 sulfonamides) of emerging pollutant mixtures was achieved due to the synergistic effect of TpBD and UiO-66-NH2 in the stationary phase. The OT-CEC column showed good reproducibility and stability with relative standard deviations of migration time and resolutions in the range of 1.17–3.93% and 1.79–4.31%, respectively.
✓ 已验证
产品关联
DOI
PubMed
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.
✓ 已验证
产品关联
DOI
PubMed
高影响因子
危险品化学品经营许可证（带存储）