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MCM-41
FUEL · 2016 · IF 3.611

Template method for a hybrid catalyst material POM@MOF-199 anchored on MCM-41: Highly oxidative desulfurization of DBT under molecular oxygen

Si-Wen Li,Rui-Min Gao,Rong-Lan Zhang,Jian-she Zhao

A catalyst system designed by a kind of hybrid material POM@MOF-199@MCM-41 (PMM) was found by a one pot and POM template self-construction of MOF-199 in the pore of MCM-41. This catalyst was exploited to act as a stable heteropolyacid-based one in the direct oxidative desulfurization process with a feedstock of model oil under O 2 as oxidant. Based on optimal conditions, the DBT conversion reached up to 98.5% and the PMM could be recycled ten times with a slight decrease, which was compared with heteropolyacid only based on MOF-199 and MCM-41, respectively. Additionally, the structure of ordered nano-sized pores of MOF-199 with POM encapsulated in was clear under crystal analysis, which offered strong evidences for the further movement into the MCM-41.

CAS / MDL: 10213-10-2 75-59-2
研究领域: 化学 · 催化材料科学
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ChemCatChem · 2021 ·Vol. 13 ·期 17 ·3772-3780 · IF 5.686

A Novel Gemini Sulfonic Ionic Liquid Immobilized MCM-41 as Efficient Catalyst for Doebner-Von Miller Reaction to Quinoline

An Li,Xinyang Wang,Yuhang Li,Caiwu Luo,Jiance Zhang,Kun Liu,Cen Zhang,Congshan Zhou

Graphical Quinoline synthesis : A novel gemini sulfonic acidic pyridiniumium ionic liquid immobilized MCM-41 was successfully prepared as a green heterogeneous catalyst, which exhibited high catalytic activity and excellent reusability in quinoline synthesis. A novel 2,2′-bipyridine-based gemini sulfonic ionic liquid was first synthesized and then immobilized on MCM-41 support (named IL1/MCM-41), which was further characterized using XRD, FT-IR, SEM, TEM, N 2 -physisorption, XPS and TG techniques. These characterization results revealed that the IL1/MCM-41 presented a whole ordered mesoporous structure, excellent thermal stability as well as the interaction between ionic liquid with MCM-41. Catalytic activity of the obtained IL1/MCM-41 was systematically evaluated for the Doebner-Von Miller reaction to generate quinoline. Compared to conventional imidazole-type single sulfonic ionic liquid supported on MCM-41 (named IL2/MCM-41), IL1/MCM-41 exhibited higher catalytic activity and better reusability, which was probably due to the synergistic catalytic effect of the dual sulfonic acid group on IL2 and the stronger interaction between dipyridine ring of ionic liquid with MCM-41 support, respectively. Meanwhile, a plausible reaction routes for the synergistic catalytic action of dual sulfonic acid to quinoline over the IL1/MCM-41 catalyst was also proposed in this paper.

研究领域: 化学工程 · 材料科学
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MICROPOROUS AND MESOPOROUS MATERIALS · 2016 · IF 3.349

Construction of Solely Lewis acidic sites on Zr-MCM-41 and the catalytic activity for the Prins condensation of β-pinene and paraformaldehyde to nopol

Xing Chu,Dan Zhou,Dan Li,Kun Xia,Ning Gan,Xinhuan Lu,Renfeng Nie,Qinghua Xia

This work has firstly constructed purely Lewis acidic sites on MCM-41 successfully, for which Zr-MCM-41 catalysts with different Zr contents are prepared through the hydrolysis of ZrOCl 2 on MCM-41, followed by calcination . Thus-prepared materials possess typical hexagonal mesostructures, irregular morphologies, large surface areas, and large pore sizes, as revealed by XRD , SEM, TEM, N 2 adsorption, and DRIFT FTIR. UV–vis, Raman and XPS spectra prove the formation of isolated species in high dispersion on the surface of MCM-41. NH 3 -TPD analysis shows that the acid intensity of the catalysts is proportional to the content of Zr, and the acidity of Zr-MCM-41 with the Zr content of <0.5% is very weak. Pyridine-IR spectra show that the surface acidity is mainly consisted of Lewis acidity, and solely Lewis acidic sites are constructed on Zr-MCM-41(550) with a low Zr content < 0.5 wt%. More Lewis acidic sites exposed on the surface of Zr-MCM-41 are considerably important for promoting the titled Prins condensation.

研究领域: 催化化学 · 材料科学
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CHEMICAL ENGINEERING SCIENCE · 2025 · IF 4.3

Ti/MCM-41 with highly active Si-O-Ti structures for efficient extraction and oxidative desulfurization of fuel oil

Jianyun Yang,Yaoxing Xiang,Jisheng Xu,Chengxiang Shi,Lun Pan,Xiangwen Zhang,Ji-Jun Zou

Oxidative desulfurization (ODS) is a promising technology for removing sulfur compounds from fuel oil under mild conditions. This study prepared Ti/MCM-41 catalyst using a simple adsorption-hydrolysis-argon calcination method and applied it to ODS. Carbon introduced by tetrabutyl titanate (TBOT) and generated by calcination in inert atmosphere restrains the growth of TiO 2 , thereby promoting the formation of a high-activity Si-O-Ti structure. By using the optimal Ti/MCM-41 catalyst, desulfurization rate of model oil (dibenzothiophene dissolved in decalin, 500 ppm of sulfur) as high as 99.8 % was achieved at 40 °C with methanol as extractant and H 2 O 2 as oxidant (O/S = 4). After six recycles, the S removal rate was still 97.9 %. Reaction conditions like reaction temperature and extractant were carefully analyzed to explore the active structure and reaction mechanism, deducing that Si-O-Ti species promote the reaction probably by forming highly active bis-hydroperoxo Ti species with five-membered ring structure. Moreover, the promotion of methanol effect was found and reasonably explained. This work provides important guidance to the design of new catalysts, selection of extractant and optimization of oxidant for more efficient phase-transfer extractive and catalytic oxidation desulfurization (ECODS) process.

研究领域: 催化化学 · 环境工程 · 化学工程 · 材料科学
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Engineering · 2025 · IF 11.6

Two Birds with One Stone: Enzymatic Degumming and Deacidification for Arachidonic Acid-Enriched Algae Oil Using PLA1@MCM-41-C8

Zhonghui Liu,Yi Zhang,Tieliang Liu,Qi Zhou,Yandaizi Zhou,Kheng-Lim Goh,Siew-Young Quek,Fenghong Huang,Mingming Zheng

Algae oil contains polyunsaturated fatty acids (PUFAs) that are beneficial to human health and development. Enzymatic refining is a sustainable approach that can improve the quality and nutritional value of algae oil. However, this approach involves the use of specific enzymes to remove unwanted impurities such as phospholipids (PLs) and free fatty acids (FFAs). This study proposes a novel immobilized phospholipase, immobilized phospholipase A1 (PLA1@MCM-41-C 8 ), which serves a dual purpose: it is effective for both degumming arachidonic acid (ARA)-enriched algal oil and its subsequent deacidification. The use of PLA1@MCM-41-C 8 achieved a degumming rate of 95.9% for crude algal oil, with an ARA retention rate of up to 97.3%. The acidity of the degummed oil decreased from 14.5 to 1.1 mg KOH∙g −1 , while simultaneously producing 29.2% high-value diacylglycerol (DAG). By comparing enzymatically degummed and deacidified ARA-enriched algae oil (EDDO) with crude ARA-enriched algae oil (CO), commercialized refining algae oil (CRO), it was found that enzymatic refining had minimal impact on antioxidant stability, fatty acid composition, and oil content. In particular, the flavor characteristics of algal oil before and after enzymatic refining with PLA1@MCM-41-C 8 remained unchanged and were dominated by the main volatile compounds: alcohols and aldehydes. Compared with free phospholipase A1 (PLA1), PLA1@MCM-41-C 8 exhibited significantly improved thermostability, pH tolerance, solvent tolerance, and long-term reusability. These characteristics make it a promising candidate for complex oil refining in industrial applications.

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CHEMICAL ENGINEERING JOURNAL · 2025 · IF 13.2

Ga-Ni modified MCM-41@HZSM-5 core-shell zeolite for catalytic fast pyrolysis of wheat straw to produce monocyclic aromatics

Hong Tian,Huimin Mao,Jiawei Wang,Yi Cheng

The HZSM-5 zeolite was modified through alkali treatment (NaOH) and metal loading (Ga, Ni), followed by constructing an MCM-41 layer to create a core–shell molecular sieve catalyst. With the feedstock of wheat straw, this work investigated the effects of various catalysts on pyrolysis product distribution and bio-oil composition with a tubular furnace and Py-GC/MS. The results showed that with the alkali-treated HZSM-5, the yield of monocyclic aromatic hydrocarbons (MAHs) in the bio-oil reached 40.35%, with an overall bio-oil yield of 21.16%. Metal-modified zeolites, exhibiting enhanced acidity, further optimized the bio-oil composition, producing an MAH yield of 61.48% and 27.31% bio-oil yield. Bimetal loading with Ga and Ni further enhanced MAH selectivity, delivering an MAH yield of 69.48% and a bio-oil yield of 27.79%. The synergy between Ga and Ni suppressed excessive aromatization and polymerization into polycyclic aromatic hydrocarbons (PAHs), favouring MAH formation. Constructing an MCM-41 layer further promotes the selectivity of MAHs. Compared to uncoated catalysts, those coated with MCM-41 significantly improved monocyclic aromatic yields, achieving the highest MAH yield of 83.61%.

研究领域: 能源化学 · 催化材料科学
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MICROPOROUS AND MESOPOROUS MATERIALS · 2018 · IF 3.649

Beta-MCM-41 micro-mesoporous catalysts in the hydroisomerization of n-heptane: Definition of an indexed isomerization factor as a performance descriptor

Li Gao,Zhiyuan Shi,Ubong Jerome Etim,Pingping Wu,Dezhi Han,Wei Xing,Svetlana Mintova,Peng Bai,Zifeng Yan

Beta-MCM-41(BM) composites consisting of Beta zeolite grown on MCM-41 type mesoporous structure were prepared. The composite materials were used as a support for stabilization of Pt. The Pt containing catalysts (Pt/HBM) were applied in n-heptane hydroisomerization reaction. The Pt/HBM catalysts showed higher n-heptane conversion and higher selectivity to isoheptanes in comparison to pure Beta and MCM-41. The results were explained by the accelerated diffusion of isoheptanes in the Pt/HBM composites, and the high concentration of acid sites with a moderate strength in the composites, which reduced the cracking of reactants and products. Based on the experimental results, an indexed isomerization factor (IIF) was deduced, which is correlated with the physical properties of the supports. The results indicated that the isoheptane yield of the catalysts is strongly dependent on the support (IIF). The general IIF descriptor for predicting the isomerization performance of support materials can provide precise guidance for the design of new micro-mesoporous composites.

CAS / MDL: 77-98-5
研究领域: 催化化学 · 材料科学
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SEPARATION AND PURIFICATION TECHNOLOGY · 2022 · IF 9.136

Insights into the different catalytic behavior between Ce and Cr modified MCM-41 catalysts: Cr2S3 as new active species for CH3SH decomposition

Xiaohua Cao,Tianhao Ai,Zhizhi Xu,Jichang Lu,Dingkai Chen,Dedong He,Jiangping Liu,Rui Tian,Yutong Zhao,Yongming Luo

High sulfur resistance and high stability of catalysts are crucial for the catalytic decomposition of sulfur-containing volatile organic compounds. In this work, compared to 5Ce-MCM-41, the 5Cr-MCM-41 catalyst exhibited ultra-stability (no activity loss at 600 h) and higher sulfur resistance. The physical structure and chemical characteristics of the catalysts were analyzed by XRD , H 2 -TPR, NH 3 -TPD, CO 2 -TPD, XPS , and TEM. Combining the characterization results, we found that the 5Cr-MCM-41 catalyst presented outstanding catalytic performance due to superior reducibility and appropriate acidity, which results in the conversion of most of the C and S elements in the CH 3 SH to the gas-phase coke- and sulfur-containing products rather than accumulating on the catalyst surface. Meanwhile, the catalytic performance, reaction path, and deactivation mechanism of rare earth metal (Ce) and transition metal (Cr) modified MCM-41 catalysts were systematically investigated by in situ DRIFTS and DFT calculations. Additionally, a new active phase (sulfide state Cr 2 S 3 ) was proposed and proved via accurately designed experiments, which plays a significant role in the collaborative removal of CH 3 SH with hexavalent chromium (Cr(VI)). These findings are beneficial for designing high sulfur resistance catalysts for the removal of CH 3 SH and other sulfur-containing products.

研究领域: 催化化学 · 环境科学 · 材料科学
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INTERNATIONAL JOURNAL OF MOLECULAR SCIENCES · 2021 ·Vol. 22 ·期 12 ·6540 · IF 5.924

Efficient Activation of Coal Fly Ash for Silica and Alumina Leaches and the Dependence of Pb(II) Removal Capacity on the Crystallization Conditions of Al-MCM-41

Xu Zhang,Tao Du,He Jia

In this study, four different coal fly ashes (CFAs) were used as raw materials of silica and alumina for the preparation of the alumina-containing Mobil Composition of Matter No. 41 (Al-MCM-41) and the exploration of an activation strategy that is efficient and universal for various CFAs. Alkaline hydrothermal and alkaline fusion activations proceeded at different temperatures to determine the best treatment parameters. We controlled the pore structure and surface hydroxyl density of the CFA-derived Al-MCM-41 by changing the crystallization temperature and aging time. The products were characterized by small-angle X-ray diffraction, nitrogen isotherms, Fourier-transform infrared spectroscopy,29Si silica magic-angle spinning nuclear magnetic resonance, and transmission electron microscopy, and they were then grafted with thiol groups to remove Pb(II) from aqueous solutions. This paper innovatively evaluates the CFA activation strategies using energy consumption analysis and determines the optimal activation methodology and parameters. This paper also unveils the effect of the crystallization condition of Al-MCM-41 on its subsequent Pb(II) removal capacity. The results show that the appropriate selection of crystallization parameters can considerably increase the removal capacity over Pb(II), providing a new path to tackle the ever-increasing concern of aquic heavy-metal pollution.Keywords:coal fly ash;CFA activation;Al-MCM-41;crystallization parameters;Pb(II) removal capacity

研究领域: 环境科学 · 材料科学
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APPLIED CATALYSIS B-ENVIRONMENTAL · 2022 · IF 24.319

Synthesis of high-grade Jet fuel blending precursors by aldol condensation of lignocellulosic ketones using HfTPA/MCM-41 with strong acids and enhanced stability

Qi Li,Genkuo Nie,Hongyu Wang,Ji-Jun Zou,Shitao Yu,Hailong Yu,Xin Jin,Dongpei Zhang,Huibing Shi,Deming Zhao

Upgrading lignocellulosic ketones to Jet fuel precursors by aldol condensation is the key step for the synthesis of high-grade bio-Jet fuels. State-of-art works are confined in pure feedstock used, catalysis sites leaching and coking. Therefore, we synthesized a strong solid acid HfTPA/MCM-41 and used it to catalyze aldol condensation of lignocellulosic ketone mixture to bio-jet fuel blending precursors, where 80 %Hf 1.5 TPA/MCM-41 shows better activity than 80 %HPW/MCM-41 and commercial zeolites with 66.8 % yield of products obtained. The good performance of the catalyst is ascribed to good acid properties, large surface area and especially new strong L acids and good stability based on anti-coking and water tolerance by Hf doping, which changes the electronic structure of the catalyst surface to efficiently activate C O bond of ketones to form a metal enolate intermediate and anchoring HPW from leaching. This work demonstrates an efficient way to synthesize high-performance acid catalyst applied in bio-jet fuel synthesis.

CAS / MDL: 39389-20-3
研究领域: 化学工程 · 可再生能源
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Molecular Catalysis · 2024 · IF 3.9

Producing (alkyl-)cyclohexane diols using lignin derived phenols over Nb2O5 and Ni/MCM-41

Guili Luan,Guihua Yang,Hongyu Wang,Jiaxuan Li,Haojie Sun,Mengyao Sun,Changfei Shi,Shitao Yu,Ji-Jun Zou,Genkuo Nie

(Alkyl-)cyclohexane diols are of high value as industrial reagents and resources, but current producing methods are still unsustainable. Herein, a new method of producing (alkyl-)cyclohexane diols using lignin derived phenols with yield as high as 91.2 % by selective hydrogenolysis is firstly achieved over Nb 2 O 5 and Ni/MCM-41. The hydrogenolysis is completed by designing two-step reactions compositing of selective crack of C(sp 3 )-O bond and selective hydrogenation of benzene ring of lignin derived phenols to achieve a high selectivity. Nb 2 O 5 demonstrates superior activity and long-life time in C(sp 3 )-O bond cleavage compared to commercial solid acids. The robust catalytic performance was thoroughly analyzed through detailed characterization and attributed to the abundant oxygen vacancies produced, which lead more strong L acids and adsorb the methoxy group in lignin derived phenols and at the same time interact with the acid sites to facilitate the cleavage of the C(sp 3 )-O bond. The consequent selective hydrogenation of benzene ring is completed by Ni/MCM-41 easily. More lignin derived phenols are explored in this reaction with (alkyl-)cyclohexane diols universally synthesized. This work provides a new application of lignin derived phenols to synthesize value-added chemicals and makes contribution to sustainable development by biorefineries.

CAS / MDL: 120-80-9 21348-59-4
研究领域: 化学工程 · 催化 · 可持续化学 · 生物化学
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JOURNAL OF MOLECULAR LIQUIDS · 2021 · IF 6.165

Surface modification of MCM-41 by chain transfer free radical polymerization and their utilization for intracellular pH-responsive delivery of curcumin

Wenfeng Yan,Junmao Li,Wei Long,Yulin Feng,Mingzhen He,Weifeng Zhu,Meiying Liu,Hui Ouyang,Xiaoyong Zhang,Yen Wei

In this paper, a simple method that relied on direct chain transfer free radical polymerization was reported to synthesize MSNs based polymeric composites (named as MCM-41-SH-poly (PEGMA- co -VPA)) using poly (ethylene glycol) monomethyl ether (PEGMA) and 4-vinyl phenylboric acid (VPA) as monomers. The utilization of MCM-41-SH-poly (PEGMA- co -VPA) to load and delivery curcumin (CUR) was also evaluated in detail. The structure, properties, drug loading and release behaviors were evidenced by various characterization techniques. The results from biological studies have shown that CUR can be effectively loaded on MCM-41-SH-poly (PEGMA- co -VPA) with high drug loading rate through formation of borate bond between CUR and VPA. More importantly, resultant drug-loading complexes displayed excellent water dispersibility and CUR could be released from complexes with pH responsiveness. Taken together, we have developed a simple method for surface modification MCM-41 and resultant composites could display improved properties for intracellular controlled drug delivery applications.

研究领域: 材料科学 · 纳米医学 · 药物递送系统
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