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。

347,358+ SCI 论文 与阿拉丁产品引用相关
2,303,472.95 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1225至1236个,产品总数1,251个

设置提升方向
immobilization
MICROCHIMICA ACTA · 2021 ·Vol. 188 ·期 6 ·1-11 · IF 5.833

Immobilization of cellulase on monolith supported with Zr(IV)-based metal-organic framework as chiral stationary phase for enantioseparation of five basic drugs in capillary electrochromatography

Ma Mingxuan,Zhang Jian,Li Peipei,Du Yingxiang,Gan Jie,Yang Jiangxia,Zhang Liu

Metal-organic framework (UiO-66-NH 2 )-incorporated organic polymer monolith was prepared by thermal polymerization. By virtue of the superior physical and chemical properties, the UiO-66-NH 2 -modified organic monolith was then functionalized by chiral selector cellulase via the condensation reaction between the primary amino groups and aldehyde groups. The synthesized materials were characterized by Fourier transform infrared spectroscopy, high-resolution transmission electron microscopy, scanning electron microscopy, X-ray photoelectron spectrometry, thermogravimetric analysis, and nitrogen sorption isotherm. The cellulase@poly(glycidyl methacrylate-UiO-66-NH 2 -ethylene glycol dimethacrylate) (cellulase@poly(GMA-UiO-66-NH 2 -EDMA)) monolith was applied to enantiomerically separate the basic racemic forms of metoprolol, atenolol, esmolol, bisoprolol, and propranolol. In contrast to the cellulase@poly(GMA-co-EDMA) monolith without UiO-66-NH 2 , the cellulase@poly(GMA-UiO-66-NH 2 -EDMA) monolith reveals significantly improved enantiodiscrimination performance for metoprolol (Rs: 0 → 1.67), atenolol (Rs: 0 → 1.50), esmolol (Rs: 0 → 1.52), bisoprolol (Rs: 0 → 0.36), and propranolol (Rs: 0 → 0.44). The immobilization pH of cellulase, buffer pH, UiO-66-NH 2 concentration, and the proportion of organic modifier were evaluated in detail with enantiomerically separating chiral molecules. The intra-day, inter-day, column-to-column, and inter-batch precision have been discussed, the result was preferable, and the relative standard deviation (RSD) of separation parameters was <4.3%. Graphical abstract Schematic representation of the preparation of a UiO-66-NH 2 -modified organic polymer monolith for enantioseparating five racemic β-blockers. UiO-66-NH 2 was synthesized and converted into a monolith as the stationary phase. Then, the modified monolith containing cellulase as the chiral selector was applied in a capillary electrochromatography system for enantioseparating chiral drugs.

✓ 已验证 DOI PubMed 高影响因子
查看原文 查看 PubMed
INDUSTRIAL & ENGINEERING CHEMISTRY RESEARCH · 2020 · IF 3.573

Preparation of Highly Uniform Polyurethane Microspheres by Precipitation Polymerization and Pd Immobilization on Their Surface and Their Catalytic Activity in 4-Nitrophenol Reduction and Dye Degradation

Xingjie Yang,Xubao Jiang,Muhammad Sohail Bashir,Xiang Zheng Kong

Polyurethanes (PUNs) have been widely used in many fields. However, there are few reports on their microsphere preparation through precipitation polymerization. Herein, uniform PUN microspheres are prepared by precipitation polymerization of toluene diisocyanate and trimethylolpropane, without any surfactant and stabilizer. Under optimized conditions, monomers are fully polymerized within 2 h at a monomer concentration as high as 25.0 wt %, with a high yield of the microspheres (96.9%). By loading Pd on their surface, composite microspheres Pd@PUN are obtained and used as catalysts. 4-Nitrophenol is completely reduced within 1 min, with a kinetic constant of 4.96 min–1, significantly higher than many reported Pd-loaded catalysts, and with comparable reusability. Used in degradation of dye molecules, the catalytic performance is practically unchanged after 20 recycled uses. This work provides a simple method for the preparation of highly uniform PUN microspheres with a high yield and their Pd-loaded catalysts, both of great potential for various applications.

✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
Bioresources and Bioprocessing · 2024 ·Vol. 11 ·期 1 ·1-14 · IF 4.3

Immobilization of Thermomyces lanuginosus lipase in a novel polysaccharide-based hydrogel by a two-step crosslinking method and its use in the lauroylation of α-arbutin

Chen Ming,She Weina,Zhao Xin,Chen Cheng,Zhu Benwei,Sun Yun,Yao Zhong

The Thermomyces lanuginosus lipase (TLLs) was successfully immobilized within a novel hydrogel matrix through a two-step crosslinking method. TLLs were initially crosslinked through the Schiff base reaction by oxidized carboxymethyl cellulose (OCMC). The water-soluble OCMC@TLLs complex was subsequently crosslinked by carboxymethyl chitosan (CMCSH) in a microfluidic apparatus to form the CMCHS/OCMC@TLLs microspheres. The CD (Circular Dichroism, CD) and FT-IR (Fourier Transform infrared spectroscopy, FT-IR) spectra demonstrated that the crosslinking of TLLs with OCMC resulted in a less significant impact on their structure compared to that with glutaraldehyde. CMCHS/OCMC@TLLs showed decreased catalytic performance due to the mass transfer resistance, while its thermal stability was greatly improved. The CMCHS/OCMC@TLLs were used to catalyze the lauroylation of arbutin in tetrahydrofuran. After 12 h of reaction under optimal conditions, the yield of 6′-O-lauryl arbutin reached an impressive 92.12%. The prepared 6′-O-lauryl arbutin has high lipophilicity and exhibits similar tyrosinase inhibitory activity and higher antioxidant activity compared to its parent compound.

✓ 已验证 DOI PubMed 高影响因子
查看原文 查看 PubMed
INDUSTRIAL CROPS AND PRODUCTS · 2022 · IF 6.449

Lipase immobilization on multi-walled carbon nanotubes used as a target fishing tool and followed by molecular docking technique to analyze lipase inhibitor from Robinia pseudoacacia L.

Shuai Wang,Yunxiao Wang,Shunxin Wang,Shuang Guo,Dongyu Gu,Jifeng Wang,Yi Yang

In this study, R. pseudoacacia flowers exhibited potential lipase ( Aspergillus niger ) inhibitory activity. To quickly explore the active compound, ligand fishing was adopted for screening the ligand from R. pseudoacacia flowers by lipase immobilized on magnetic polyamidoamine dendrimer-coated multi-walled carbon nanotubes . After ligand fishing, the target compound was separated purposefully by optimizing the separation conditions of high-speed counter-current chromatography (HSCCC). As results, kaempferol with the IC 50 of 327.64 ± 15.33 μg/mL was separated and identified. The further molecular docking results indicated that kaempferol was interacted with amino acid residue in the active site of lipase through van der Waals force, hydrogen bonds and Pi-Pi T-shaped interactions, yielding the binding energy of − 6.43 kcal/mol. The present method not only revealed the lipase inhibitory substances in R. pseudoacacia , but also provided an effective means for the screening of other natural substances.

CAS / MDL: 6104-58-1
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
JOURNAL OF MATERIALS SCIENCE · 2022 ·Vol. 57 ·期 4 ·2483-2501 · IF 4.682

In-situ immobilization of titanium dioxide on poly (ether ether ketone) hollow fiber membranes and the effect of pH level on the photo-removal process of dyes

Chen Yuan,Zhang Shengchang,Jiang Chunhui,Zhong Tianhaoyue,Su Zexi,Xu Qibin,Jiang Mengjin,Liu Pengqing

In order to prevent secondary pollution due to the photocatalyst titanium dioxide (TiO 2 ) used in industrial wastewater treatment, and to boost the photo-removal efficiency TiO 2 was immobilized on the surface of high-performance poly (ether ketone) (PEEK) hollow fiber membrane via an in-situ grafting reaction. γ -Methylacryloyloxypropyltrimethoxysilane (MAPS) was used as a coupling agent to link the PEEK hollow fiber membranes with TiO 2 under UV radiation and hydrothermal treatment. The surface chemical structure, surface morphologies, and permeability of the PEEK-PMAPS-TiO 2 membranes were characterized using Fourier transform infrared spectroscopy (FTIR), X-ray photoelectron spectroscopy (XPS), scanning electron microscopy (SEM), and the water flux test. The performance of PEEK-PMAPS-TiO 2 membranes in terms of their ability to accelerate the photo-removal of different dyes was investigated under a range of pH conditions. Experimental results showed that the photo-degradation efficiency for tartrazine can be reached 100% (after 4 h of UV radiation at pH of 3.5) with a TiO 2 grafting degree of 15.56 wt% on the composite membranes. We also find that the acidic/alkaline condition accelerates the processes of absorption and photo-removal of negatively/positively charged dyes. In addition, the recyclability of the PEEK-PMAPS-TiO 2 membrane was also investigated. After refreshing treatment, the second photo-removal efficiency still reached over 95%. Graphical abstract

CAS / MDL: 129-17-9
✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
BIOPROCESS AND BIOSYSTEMS ENGINEERING · 2021 ·Vol. 44 ·期 8 ·1781-1792 · IF 3.21

Immobilization of recombinant Escherichia coli cells expressing glucose isomerase using modified diatomite as a carrier for effective production of high fructose corn syrup in packed bed reactor

Jin Li-Qun,Chen Xian-Xiao,Jin Yi-Ting,Shentu Jun-Kang,Liu Zhi-Qiang,Zheng Yu-Guo

To improve the operational stability of glucose isomerase in E. coli TEGI-W139F/V186T, the immobilized cells were prepared with modified diatomite as a carrier and 74.1% activity of free cells was recovered after immobilization. Results showed that the immobilized cells still retained 86.2% of the initial transformational activity after intermittent reused 40 cycles and the yield of D-fructose reached above 42% yield at 60 °C. Moreover, the immobilized cells were employed in the continuous production of High Fructose Corn Syrup (HFCS) in a recirculating packed bed reactor for 603 h at a constant flow rate. It showed that the immobilized cells exhibited good operational stability and the yield of D-fructose retained above 42% within 603 h. The space–time yield of high fructose corn syrup reached 3.84 kg L −1  day −1 . The investigation provided an efficient immobilization method for recombinant cells expressing glucose isomerase with higher stability, and the immobilized cells are a promising biocatalyst for HFCS production.

CAS / MDL: 9002-98-6
✓ 已验证 产品关联 DOI PubMed 高影响因子
查看原文 查看 PubMed
Journal of the Taiwan Institute of Chemical Engineers · 2018 · IF 3.849

Fabrication of three functionalized silica adsorbents: Impact of co-immobilization of imidazole, phenyl and long-chain alkyl groups on bisphenol A adsorption from high salt aqueous solutions

Zhike Wang,Yunyi Zhu,Haitian Chen,Haili Wu,Cunling Ye

Based on the physicochemical properties of bisphenol A (BPA), chemical co-immobilizations of imidazole, phenyl and hexadecyl were done onto silica to obtain three functionalized silica adsorbents. Accordingly, the combinations of hexadecyl and imidazole, hexadecyl and phenyl, and phenyl and imidazole were named as Sil-(HDTMS-MPS)-VIm, Sil-(HDTMS-MPS)-S and Sil-MPS-(S-VIm), respectively. The composites were characterized by FTIR, TGA and SEM. The aim of this work was to explore how these typical functional groups affect the adsorption behavior of BPA. Experiments demonstrated that alkaline imidazole would play a key role for the BPA adsorption, and the synergy of imidazole and hexadecyl exhibited the highest adsorption affinities for BPA in the pH range of 4.0–9.0 due to the high K ow value of BPA. The maximum adsorption capacity of Sil-(HDTMS-MPS)-VIm for BPA obtained from Langmuir model was 89.6 mg/g at 293 K. Furthermore, the prepared three functionalized silicas retained their good adsorption capacities of BPA in high salt solutions, and the adsorption behaviors of BPA for these adsorbents were well described by the pseudo-second-order kinetic model and the Freundlich model. This work suggests that the synergy of hydrogen bond-forming alkaline functional group and hydrophobic long-chain alkyl group benefits BPA removal from aqueous solutions.

✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
ANALYTICAL AND BIOANALYTICAL CHEMISTRY · 2015 ·Vol. 408 ·期 3 ·805-814 · IF 3.436

Penetrable silica microspheres for immobilization of bovine serum albumin and their application to the study of the interaction between imatinib mesylate and protein by frontal affinity chromatography

Ma Liyun,Li Jing,Zhao Juan,Liao Han,Xu Li,Shi Zhi-guo

In the current study, novel featured silica, named penetrable silica, simultaneously containing macropores and mesopores, was immobilized with bovine serum albumin (BSA) via Schiff base method. The obtained BSA-SiO 2 was employed as the high-performance liquid chromatographic (HPLC) stationary phase. Firstly, d - and l -tryptophan were used as probes to investigate the chiral separation ability of the BSA-SiO 2 stationary phase. An excellent enantioseparation factor was obtained up to 4.3 with acceptable stability within at least 1 month. Next, the BSA-SiO 2 stationary phase was applied to study the interaction between imatinib mesylate (IM) and BSA by frontal affinity chromatography. A single type of binding site was found for IM with the immobilized BSA, and the hydrogen-bonding and van der Waals interactions were expected to be contributing interactions based on the thermodynamic studies, and this was a spontaneous process. Compared to the traditional silica for HPLC stationary phase, the proposed penetrable silica microsphere possessed a larger capacity to bond more BSA, minimizing column overloading effects and enhancing enantioseparation ability. In addition, the lower running column back pressure and fast mass transfer were meaningful for the column stability and lifetime. It was a good substrate to immobilize biomolecules for fast chiral resolution and screening drug-protein interactions. The preparation of BSA-SiO2 column based on the penetrable silica and its application in chiral separation and frontal analysis

✓ 已验证 产品关联 DOI PubMed 高影响因子
查看原文 查看 PubMed
TALANTA · 2019 · IF 4.916

Covalent immobilization of covalent organic framework on stainless steel wire for solid-phase microextraction GC-MS/MS determination of sixteen polycyclic aromatic hydrocarbons in grilled meat samples

Tian-Tian Ma,Xiao-Fang Shen,Cheng Yang,Hai-Long Qian,Yue-Hong Pang,Xiu-Ping Yan

Covalent organic framework TpBD was grafted on stainless steel wire with polydopamine as a linker. The fabricated TpBD bonded stainless steel wire was used as the solid-phase microextraction fiber to extract sixteen polycyclic aromatic hydrocarbons (PAHs) for subsequent GC-MS/MS determination in grilled meat samples. The developed method gave the limits of detection ( S/N  = 3) from 0.02 (pyrene)-1.66 (naphthalene) ng L −1 and enhancement factors from 1069 (naphthalene)-10879 (benz(a)anthracene). The relative standard deviations (RSDs) for intra-day and inter-day study are in the range of 2.6%–8.5% and 4.5%–9.4%, respectively. The fiber-to-fiber RSDs for three parallel prepared fibers were 5.3%–10.0%. One TpBD bonded fiber can stand at least 200 cycles without significant loss of extraction efficiency. The developed method was successfully applied for the determination of trace PAHs in grilled meat samples with recoveries from 85.1% to 102.8%.

✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
JOURNAL OF ALLOYS AND COMPOUNDS · 2026 · IF 6.7

Insights into the Structural Evolution and Heavy Metal Immobilization in a CaO–Fe₂O₃–SiO₂ System during Multi-Source Solid Waste Co-Vitrification: Integrated Experimental and Theoretical Study

Hao Liu,Yaji Huang,Huikang Song,Tianhang Tang,Hao Shi,Lang Kai,Chenlu Yang

A novel pathway for the co-disposal of municipal solid waste incineration fly ash (MFA) and bottom slag (BS) with waste glass (WG) was proposed. Combined melting experiments and theoretical calculation were employed, which revealed the structural evolution of the CaO-Fe₂O₃-SiO₂ system and the underlying mechanisms of heavy metal immobilization. It was demonstrated that stable glassy products were obtained within a CaO/(Fe₂O₃+SiO₂) mass ratio ( M C / ( SF ) MC/(SF) ) range of 0.13~0.41. The leaching concentrations of heavy metals in these vitrified products were suppressed to the relevant regulatory standards. With an increasing M C / ( SF ) MC/(SF) , the glass network became more depolymerized, as evidenced by a higher population of low-connectivity Qⁿ units in the structure. However, under Fe₂O₃-enriched system, the Fe coordination shifted from solely tetrahedral [FeO₄] towards a mixed tetrahedral/octahedral environment. Moreover, Pb and Cd were incorporated into the glass matrix via interstitial doping. The depolymerized network dominated by CaO favored the Pb enrichment. Cd tended to be stabilized in the Fe-rich structure, facilitated by the formation of highly localized Cd-O bonds. This study elucidated the coupling effects of oxide composition on glass structure and heavy metal immobilization behavior, providing a fundamental theoretical basis for understanding and optimizing the vitrification process for solid waste treatment.

✓ 已验证 产品关联 DOI 高影响因子
查看原文 查看 PubMed
COLLOIDS AND SURFACES A-PHYSICOCHEMICAL AND ENGINEERING ASPECTS · 2026 · IF 5.4

Simultaneously selective adsorption and effective immobilization of p-arsanilic acid (p-ASA) and roxarsone (ROX) from water by utilizing novel double-template molecularly imprinted polymers: Performance and mechanism

Runqiao Chen,Shuheng Yi,Zhipan Wen,Han Feng,Xing Yin,Lingyue Shu,Yalei Zhang

To enhance the special selectivity and recognizability of two kinds of typical phenylarsonic compounds ( p -arsanilic acid ( p -ASA) and roxarsone (ROX)) in complicated water bodies, novel double-template molecularly imprinted polymers (DMIPs) were successfully synthesized via the suspension polymerization method. Subsequently, laboratory scale tests were carried out to systematically investigate the adsorption behavior and performance of p -ASA and ROX by using polymers. The result indicated that DMIPs exhibited super p -ASA/ROX sequestration and immobilization compared with non-imprinted polymers (DNIPs), which was associated with imprinting effect of polymers. The better removal efficiency of p -ASA/ROX by DMIPs were occurred in a broad pH region (3.0–9.0), whereas solution pH severely affected the uptake of DNIPs for organic arsenic compounds. According to the remarkable binding selectivity and special recognizability of DMIPs, common inorganic ions and natural organic matters (NOM) were negligible influence on targeted pollutants removal, and excellent adsorption capacity could still maintain even in the presence of interfering substances that displayed similar chemical structure with templates to a certain extent. Finally, the remarkable reusability and stable performance in continuous flow studies demonstrated the obtained DMIPs were promising candidates for simultaneously and effectively eliminating these multiple organic arsenic pollutants in harsh and complicated aquatic environment.

✓ 已验证 DOI 高影响因子
查看原文 查看 PubMed
JOURNAL OF COLLOID AND INTERFACE SCIENCE · 2024 · IF 9.4

Construction of direct Z-scheme Co9S8/CdS with tubular heterostructure through the simultaneous immobilization and in-situ reduction strategy for enhanced photocatalytic Cr(VI) reduction under visible light

Luping Feng,Jianghong Wang,Lixiang Zhang,Jiadong Li,Yifan Zhang,Minghong Xu,Peisong Tang,Hua Wang

Tubular Co 9 S 8 /CdS heterostructures have been successfully synthesized by in-situ growing CdS onto Co 9 S 8 nanotubes through a simultaneous immobilization and in-situ reduction strategy. It turned out that the so-obtained heterostructure with Co 9 S 8 /CdS molar ratio of 1/10 can display a broad light absorption edge and especially much enhanced capacity for photocatalytic reduction of Cr(VI) under visible light . The characterization analysis and experimental results suggested that an interfacial electrostatic field between Co 9 S 8 and CdS elements in the heterostructure could be constructed due to their different Fermi levels , allowing for more quantities of highly reductive electrons to participate in the photocatalytic reaction. Therefore, the so-obtained Co 9 S 8 /CdS (1/10) heterostructures could achieve the photocatalytic reduction efficiency of 100% within 20 min, which was more than two and four times larger than that of pristine CdS and Co 9 S 8 , respectively. Moreover, the possible photocatalytic reaction mechanism for reducing Cr(VI) was investigated and found to follow the direct Z-scheme charge transfer pathway. This novel fabrication route for composite photocatalysts with tubular heterostructures could lead to the widespread implementations for the elimination of various harmful pollutants in the process of environmental governance.

✓ 已验证 产品关联 DOI PubMed 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。