CN112979985A - Composite metal organic framework material and preparation method thereof - Google Patents

Composite metal organic framework material and preparation method thereof Download PDF

Info

Publication number
CN112979985A
CN112979985A CN202110293513.6A CN202110293513A CN112979985A CN 112979985 A CN112979985 A CN 112979985A CN 202110293513 A CN202110293513 A CN 202110293513A CN 112979985 A CN112979985 A CN 112979985A
Authority
CN
China
Prior art keywords
organic framework
framework material
metal organic
composite metal
reaction
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN202110293513.6A
Other languages
Chinese (zh)
Inventor
陈焕新
胡军
温慧敏
廖才俊
戴广林
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Ningbo Zhetie Jiangning Chemical Co ltd
Zhejiang University of Technology ZJUT
Original Assignee
Ningbo Zhetie Jiangning Chemical Co ltd
Zhejiang University of Technology ZJUT
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Ningbo Zhetie Jiangning Chemical Co ltd, Zhejiang University of Technology ZJUT filed Critical Ningbo Zhetie Jiangning Chemical Co ltd
Priority to CN202110293513.6A priority Critical patent/CN112979985A/en
Publication of CN112979985A publication Critical patent/CN112979985A/en
Pending legal-status Critical Current

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08GMACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
    • C08G83/00Macromolecular compounds not provided for in groups C08G2/00 - C08G81/00
    • C08G83/008Supramolecular polymers
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/22Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising organic material
    • B01J20/223Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising organic material containing metals, e.g. organo-metallic compounds, coordination complexes
    • B01J20/226Coordination polymers, e.g. metal-organic frameworks [MOF], zeolitic imidazolate frameworks [ZIF]
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01JCHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
    • B01J20/00Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
    • B01J20/28Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties
    • B01J20/28002Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof characterised by their form or physical properties characterised by their physical properties
    • B01J20/28009Magnetic properties
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/28Treatment of water, waste water, or sewage by sorption
    • C02F1/285Treatment of water, waste water, or sewage by sorption using synthetic organic sorbents
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F2101/00Nature of the contaminant
    • C02F2101/30Organic compounds
    • C02F2101/308Dyes; Colorants; Fluorescent agents
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K3/00Use of inorganic substances as compounding ingredients
    • C08K3/18Oxygen-containing compounds, e.g. metal carbonyls
    • C08K3/20Oxides; Hydroxides
    • C08K3/22Oxides; Hydroxides of metals
    • C08K2003/2265Oxides; Hydroxides of metals of iron
    • C08K2003/2275Ferroso-ferric oxide (Fe3O4)
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00Specific properties of additives
    • C08K2201/01Magnetic additives
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08KUse of inorganic or non-macromolecular organic substances as compounding ingredients
    • C08K2201/00Specific properties of additives
    • C08K2201/011Nanostructured additives

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Polymers & Plastics (AREA)
  • Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Analytical Chemistry (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Hydrology & Water Resources (AREA)
  • Engineering & Computer Science (AREA)
  • Environmental & Geological Engineering (AREA)
  • Water Supply & Treatment (AREA)
  • Inorganic Chemistry (AREA)
  • Compounds Of Iron (AREA)

Abstract

The invention discloses a composite metal organic framework material, which is Fe3O4@ MIL-100 (Fe), molecular formula: fe3C18H10O16. The preparation method comprises the step one of adding FeCl3·6H2Dissolving O and anhydrous sodium acetate in ethylene glycol, transferring the ethylene glycol into a polytetrafluoroethylene reaction kettle, sealing the reaction kettle, and placing the reaction kettle in a constant-temperature drying oven for solvothermal reaction to obtain a solid product; drying in a vacuum drying oven at 60 deg.C for 12 hr to obtain ferroferric oxide nanoparticles; step two, mixing the trimesic acid,ferroferric oxide nanoparticles and H2O reacts under microwave to generate orange brown solid which is collected by a magnet; washing with hot water and hot ethanol, and vacuum drying at 60 deg.C overnight to obtain composite metal organic framework material Fe3O4@ MIL-100 (Fe). The advantages are that: simple preparation process, low preparation cost, good stability and strong adsorption force.

Description

Composite metal organic framework material and preparation method thereof
Technical Field
The invention relates to the technical field of metal organic framework material preparation, in particular to a composite metal organic framework material and a preparation method thereof.
Background
The metal organic framework Material (MOF) is a novel porous crystal material formed by combining metal ions and organic ligands through coordination bonds, has the characteristics of large specific surface area, high porosity, adjustable pore diameter, functionalization and the like, and is widely applied to the fields of selective adsorption separation, storage, sensing, catalysis and the like of gases.
In recent years, with the rapid development of industry, the problem of water pollution has become one of the serious problems that must be controlled. The water contaminants mainly include: organic dyes, antibiotics, cyanides, and the like; among the numerous water contaminants, the organic contaminants are the most harmful. The application range of the dye is wider and wider, and the dye not only meets the material requirements of people, but also brings no small burden to the environment. Organic dyes have carcinogenic and teratogenic hazards, and once a large amount of organic dyes are discharged into water, the organic dyes not only pollute the environment, but also cause certain social effects.
Various methods are currently used to remove water contaminants, including adsorption, membrane separation, precipitation, oxidation, biological treatment, and electrochemical techniques. However, these techniques have certain limitations and disadvantages, such as high cost and poor contaminant removal. In addition, some technologies only have adsorption effect on specific pollutants, and cannot deal with the increasingly serious problem of environmental water pollution. Among these techniques, the adsorption method is considered to be more suitable for the removal of organic dyes due to its effectiveness and economy. Therefore, it is an important problem to be solved to find a fast and efficient method and adsorbent for removing water pollutants.
Disclosure of Invention
The invention aims to make up the defects and discloses a composite metal organic framework material which is simple in preparation process, low in preparation cost, good in stability and strong in adsorption force and a preparation method thereof to the society.
The technical scheme of the invention is realized as follows:
a composite metal-organic skeleton material is prepared from Fe3O4@ MIL-100 (Fe), the molecular formula of which is: fe3C18 H10O16
A preparation method of a composite metal organic framework material is characterized by comprising the following steps: the method comprises the following steps:
step one, FeCl is firstly added3·6H2Dissolving O and anhydrous sodium acetate in ethylene glycol, transferring the ethylene glycol into a polytetrafluoroethylene reaction kettle, sealing the reaction kettle, placing the reaction kettle in a constant-temperature drying box, and carrying out solvothermal reaction to obtain a solid product; washing the solid product with ethanol and high-purity water respectively to remove impurities, and then drying in a vacuum drying oven at 60 ℃ for 12 hours to obtain ferroferric oxide nanoparticles;
step two, trimesic acid, ferroferric oxide nano particles and H2O reacts under microwave to generate orange brown solid which is collected by a magnet; washing the collected product with hot water and hot ethanol for multiple times, and finally vacuum drying at 60 ℃ overnight to obtain the composite metal organic framework material Fe3O4 @ MIL-100(Fe)。
The measures for further optimizing the technical scheme are as follows:
in the first step, FeCl3·6H2The molar ratio of O to anhydrous sodium acetate is 1: 1-1: 2.5.
in the step one, the average diameter of the obtained ferroferric oxide nano particles is 470-530 nm.
In the first step, the constant temperature of the solvothermal reaction is 200 ℃, and the reaction time is 5 to 8 hours. Preferably, it is
The reaction time was 7 h.
In the second step, the molar ratio of the trimesic acid to the ferroferric oxide nanoparticles is 2: 1.
In the second step, the reaction is carried out under the microwave condition of 150-180 ℃ for 15-30 min by a microwave method. The reaction is preferably carried out under microwave conditions at 150 ℃ for 30 min.
Compared with the prior art, the invention has the advantages that:
the invention relates to a composite metal organic framework material and a preparation method thereof, wherein an MIL-100 (Fe) metal organic framework which has a stable structure and coordination unsaturated metal ions is selected. At the same time, magnetic Fe3O4The addition of the nano particles further improves the recoverable convenience of the composite metal organic framework material, removes the complicated recovery process of centrifugal collection, and increases the absorption and degradation capacity of the material to organic dyes due to the coordination unsaturated metal ions in the MOF structure. The composite metal organic framework material of the invention integrates the adsorption and degradation capacities of MOF porous material to organic dye and Fe3O4The magnetic property of the nano particles enables the nano particles to have stronger chemical stability, quick separation and reusability. The raw materials used in the preparation method are low in cost, wide in source, simple and easy to operate in the preparation process, low in requirement on equipment and short in reaction time.
Drawings
FIG. 1 is a scanning electron microscope image of the composite metal organic framework material of the present invention.
Detailed Description
A composite metal-organic skeleton material is prepared from Fe3O4@ MIL-100 (Fe), the molecular formula of which is: fe3C18 H10O16
A preparation method of a composite metal organic framework material comprises the following steps:
step one, FeCl is firstly added3·6H2O and anhydrousDissolving sodium acetate in ethylene glycol, transferring the ethylene glycol into a polytetrafluoroethylene reaction kettle, sealing the reaction kettle, placing the reaction kettle in a constant-temperature drying box, and carrying out solvothermal reaction to obtain a solid product; washing the solid product with ethanol and high-purity water respectively to remove impurities, and then drying in a vacuum drying oven at 60 ℃ for 12 hours to obtain ferroferric oxide nanoparticles; wherein FeCl3·6H2The molar ratio of O to anhydrous sodium acetate is 1: 1-1: 2.5, the average diameter of the obtained ferroferric oxide nano particles is 470-530 nm, the constant temperature of the solvothermal reaction is 200 ℃, the reaction time is 5-8 h, and the preferable reaction time is 7 h.
Step two, trimesic acid (H)3BTC), ferroferric oxide nanoparticles and H2O reacts under microwave to generate orange brown solid which is collected by a magnet; washing the collected product with hot water and hot ethanol for multiple times, and finally vacuum drying at 60 ℃ overnight to obtain the composite metal organic framework material Fe3O4@ MIL-100 (Fe); wherein the molar ratio of the trimesic acid to the ferroferric oxide nanoparticles is 2:1, and the reaction is carried out under the microwave condition of 150-180 ℃ for 15-30 min by a microwave method, preferably at 150 ℃ for 30 min.
Composite metal organic framework material Fe prepared by the preparation method3O4FIG. 1 shows a scanning electron micrograph of @ MIL-100 (Fe).
This is further illustrated by the specific examples below.
Example 1
A preparation method of a composite metal organic framework material comprises the following steps:
step one, Fe3O4Preparation of nanoparticles: first 3.46g of FeCl3·6H2Completely dissolving O and 2.66g of anhydrous sodium acetate in 80mL of ethylene glycol, transferring the ethylene glycol into a polytetrafluoroethylene reaction kettle, sealing the reaction kettle, placing the reaction kettle into an electric heating blowing constant-temperature drying oven, and carrying out solvothermal reaction for 7 hours at the temperature of 200 ℃ to obtain a solid product; washing the solid product with ethanol and high purity water respectively for 3 times to remove impurities, and vacuum drying the sampleDrying at 60 ℃ for 12 hours to obtain the ferroferric oxide nano particles. The average diameter of the obtained ferroferric oxide nano particles is 500 nm.
Step two, Fe3O4Preparation of @ MIL-100 (Fe) composite: fe3O4@ MIL-100 (Fe) is synthesized by a simple and rapid microwave method, and H is specifically synthesized3BTC (1.05 g), ferroferric oxide nanoparticles (0.58 g) and H2O (12.5 mL) was reacted at 150 ℃ for 30min under microwave to give an orange-brown solid which was collected with a magnet. In order to remove unreacted ions and H3BTC washing the collected product with hot water and hot ethanol for multiple times, and finally vacuum drying at 60 deg.C overnight to obtain composite metal organic framework material Fe3O4 @ MIL-100(Fe)。
Example 2
A preparation method of a composite metal organic framework material comprises the following steps:
step one, Fe3O4Preparation of nanoparticles: first 3.46g of FeCl3·6H2Completely dissolving O and 2.66g of anhydrous sodium acetate in 80mL of ethylene glycol, transferring the ethylene glycol into a polytetrafluoroethylene reaction kettle, sealing the reaction kettle, placing the reaction kettle into an electric heating blowing constant-temperature drying oven, and carrying out solvothermal reaction for 5 hours at the temperature of 200 ℃ to obtain a solid product; and (3) washing the solid product respectively with ethanol and high-purity water, washing for 3 times respectively to remove impurities, and finally drying the sample in a vacuum drying oven at 60 ℃ for 12 hours to obtain the ferroferric oxide nanoparticles. The average diameter of the obtained ferroferric oxide nano particles is 470 nm.
Step two, Fe3O4Preparation of @ MIL-100 (Fe) composite: fe3O4@ MIL-100 (Fe) is synthesized by a simple and rapid microwave method, and H is specifically synthesized3BTC (1.05 g), ferroferric oxide nanoparticles (0.58 g) and H2O (12.5 mL) was reacted at 150 ℃ for 30min under microwave to give an orange-brown solid which was collected with a magnet in order to remove unreacted ions and H3BTC washing the collected product with hot water and hot ethanol for several times, and vacuum drying at 60 deg.C overnight to obtain composite metal organic boneFrame material Fe3O4 @ MIL-100(Fe)。
Example 3
A preparation method of a composite metal organic framework material comprises the following steps:
step one, Fe3O4Preparation of nanoparticles: first 3.46g of FeCl3·6H2Completely dissolving O and 2.66g of anhydrous sodium acetate in 80mL of ethylene glycol, transferring the ethylene glycol into a polytetrafluoroethylene reaction kettle, sealing the reaction kettle, placing the reaction kettle into an electric heating blowing constant-temperature drying oven, carrying out solvothermal reaction for 6 hours at the temperature of 200 ℃ to obtain solid products, respectively washing the solid products with ethanol and high-purity water for 3 times to remove impurities, and finally placing a sample into a vacuum drying oven to be dried for 12 hours at the temperature of 60 ℃ to obtain the ferroferric oxide nanoparticles. The average diameter of the obtained ferroferric oxide nano particles is 490 nm.
Step two, Fe3O4Preparation of @ MIL-100 (Fe) composite: fe3O4@ MIL-100 (Fe) is synthesized by a simple and rapid microwave method, and H is specifically synthesized3BTC (1.05 g), ferroferric oxide nanoparticles (0.58 g) and H2O (12.5 mL) was reacted at 150 ℃ for 30min under microwave to give an orange-brown solid which was collected with a magnet. In order to remove unreacted ions and H3BTC washing the collected product with hot water and hot ethanol for multiple times, and finally vacuum drying at 60 deg.C overnight to obtain composite metal organic framework material Fe3O4 @ MIL-100(Fe)。
Example 4
A preparation method of a composite metal organic framework material comprises the following steps:
step one, Fe3O4Preparation of nanoparticles: first 3.46g of FeCl3·6H2Completely dissolving O and 2.66g of anhydrous sodium acetate in 80mL of ethylene glycol, transferring the ethylene glycol into a polytetrafluoroethylene reaction kettle, sealing the reaction kettle, placing the reaction kettle into an electric heating blowing constant-temperature drying oven, and carrying out solvothermal reaction for 7 hours at the temperature of 200 ℃ to obtain a solid product; washing the solid product with ethanol and high purity water respectively for 3 times to remove impurities, and washing with ethanol and high purity water respectivelyAnd (3) drying the sample in a vacuum drying oven at 60 ℃ for 12 hours to obtain the ferroferric oxide nanoparticles. The average diameter of the obtained ferroferric oxide nano particles is 530 nm.
Step two, Fe3O4Preparation of @ MIL-100 (Fe) composite: fe3O4@ MIL-100 (Fe) is synthesized by a simple and rapid microwave method, and H is specifically synthesized3BTC (1.05 g), ferroferric oxide nanoparticles (0.58 g) and H2O (12.5 mL) was reacted at 150 ℃ for 15min under microwave to give an orange-brown solid which was collected with a magnet. In order to remove unreacted ions and H3BTC the collected product was washed several times with hot water and hot ethanol. Finally vacuum drying overnight at 60 ℃ to obtain the composite metal organic framework material Fe3O4 @ MIL-100(Fe)。
Example 5
The preparation process is basically the same as that of the example 1, except that: in the second step, the reaction is carried out for 15min at 180 ℃ under microwave.
Example 6
The preparation process is basically the same as that of the example 1, except that: in the second step, the reaction is carried out for 30min at 180 ℃ under microwave.
The composite metal organic framework material Fe prepared by the invention3O4The @ MIL-100 (Fe) combines the excellent properties of the MOF, such as overlarge specific surface area, high porosity and superparamagnetism of magnetic nanoparticles, so that the composite metal organic framework material has good adsorption property and magnetic responsiveness, the problem that practical application is limited due to the fact that most of conventional adsorbents are not easy to separate from an aqueous solution can be effectively solved, and the application of the adsorbent in the field of water treatment is expanded. The composite metal organic framework material Fe of the invention3O4The @ MIL-100 (Fe) can be used for treating organic dyes in sewage, has large absorption capacity on rhodamine B, methylene blue and the like, has degradation capability and is compounded with magnetic Fe3O4The nano particle material has the characteristics of simple and convenient recovery and high reuse rate.
The magnetic nanoparticles and the metal organic framework material are compounded, the respective advantages of the magnetic nanoparticles and the metal organic framework material are fully exerted, the synergistic effect on performance is generated, and the magnetic metal organic framework material has the characteristics of good adsorption performance, simplicity and rapidness in synthesis, capability of being quickly recovered, high repeated utilization rate, wide raw material source and the like, so that the magnetic metal organic framework material has wider application in the field of water treatment.
While the preferred embodiments of the present invention have been illustrated, various changes and modifications may be made by one skilled in the art without departing from the scope of the present invention.

Claims (9)

1. A composite metal organic framework material is characterized in that: the organic framework material is Fe3O4@ MIL-100 (Fe), the molecular formula of which is: fe3C18 H10O16
2. The method for preparing a composite metal organic framework material according to claim 1, which is characterized in that: the method comprises the following steps:
step one, FeCl is firstly added3·6H2Dissolving O and anhydrous sodium acetate in ethylene glycol, transferring the ethylene glycol into a polytetrafluoroethylene reaction kettle, sealing the reaction kettle, placing the reaction kettle in a constant-temperature drying box, and carrying out solvothermal reaction to obtain a solid product; washing the solid product with ethanol and high-purity water respectively to remove impurities, and then drying in a vacuum drying oven at 60 ℃ for 12 hours to obtain ferroferric oxide nanoparticles;
step two, trimesic acid, ferroferric oxide nano particles and H2O reacts under microwave to generate orange brown solid which is collected by a magnet; washing the collected product with hot water and hot ethanol for multiple times, and finally vacuum drying at 60 ℃ overnight to obtain the composite metal organic framework material Fe3O4 @ MIL-100(Fe)。
3. A composite metal organic framework material according to claim 2, wherein: in the first step, FeCl3·6H2The molar ratio of O to anhydrous sodium acetate is 1: 1-1: 2.5.
4. a composite metal organic framework material according to claim 2, wherein: in the step one, the average diameter of the obtained ferroferric oxide nano particles is 470-530 nm.
5. A composite metal organic framework material according to claim 2, wherein: in the first step, the constant temperature of the solvothermal reaction is 200 ℃, and the reaction time is 5 to 8 hours.
6. A composite metal organic framework material according to claim 5, wherein: the reaction time is 7 h.
7. A composite metal organic framework material according to claim 2, wherein: in the second step, the molar ratio of the trimesic acid to the ferroferric oxide nanoparticles is 2: 1.
8. A composite metal organic framework material according to claim 2, wherein: in the second step, the reaction is carried out under the microwave condition of 150-180 ℃ for 15-30 min by a microwave method.
9. A composite metal organic framework material according to claim 8, wherein: in the second step, the reaction is carried out under the microwave condition of 150 ℃ for 30 min.
CN202110293513.6A 2021-03-19 2021-03-19 Composite metal organic framework material and preparation method thereof Pending CN112979985A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202110293513.6A CN112979985A (en) 2021-03-19 2021-03-19 Composite metal organic framework material and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202110293513.6A CN112979985A (en) 2021-03-19 2021-03-19 Composite metal organic framework material and preparation method thereof

Publications (1)

Publication Number Publication Date
CN112979985A true CN112979985A (en) 2021-06-18

Family

ID=76332712

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202110293513.6A Pending CN112979985A (en) 2021-03-19 2021-03-19 Composite metal organic framework material and preparation method thereof

Country Status (1)

Country Link
CN (1) CN112979985A (en)

Cited By (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113952935A (en) * 2021-11-19 2022-01-21 中国农业科学院蔬菜花卉研究所 Magnetic MOFs composite material and preparation method and application thereof
CN115254071A (en) * 2022-08-04 2022-11-01 华侨大学 Magnetic metal organic framework composite material and preparation method and application thereof
CN115779685A (en) * 2023-02-10 2023-03-14 北京理工大学 Preparation method of photo-Fenton film based on metal organic framework material
CN116444809A (en) * 2023-03-23 2023-07-18 河南大学 Hollow nano flower-like double MOF-based heterojunction material and preparation method and application thereof

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103657596A (en) * 2013-12-13 2014-03-26 天津工业大学 Synthesis method of magnetic metal organic framework composite material
CN105597686A (en) * 2016-01-12 2016-05-25 郑州轻工业学院 Preparation method and application of Fe3O4@MIL-100 (Fe)
CN105833915A (en) * 2015-01-14 2016-08-10 同济大学 Core/shell-type iron-based metal organic framework photo-Fenton catalyst, preparation and application thereof
CN107042087A (en) * 2017-01-19 2017-08-15 中国石油大学(华东) A kind of method that Situ Hydrothermal prepares magnetic metal organic framework core-shell material
CN109908871A (en) * 2019-03-21 2019-06-21 沈阳药科大学 A kind of magnetic Fe3O4The preparation method and applications of@MIL-100

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103657596A (en) * 2013-12-13 2014-03-26 天津工业大学 Synthesis method of magnetic metal organic framework composite material
CN105833915A (en) * 2015-01-14 2016-08-10 同济大学 Core/shell-type iron-based metal organic framework photo-Fenton catalyst, preparation and application thereof
CN105597686A (en) * 2016-01-12 2016-05-25 郑州轻工业学院 Preparation method and application of Fe3O4@MIL-100 (Fe)
CN107042087A (en) * 2017-01-19 2017-08-15 中国石油大学(华东) A kind of method that Situ Hydrothermal prepares magnetic metal organic framework core-shell material
CN109908871A (en) * 2019-03-21 2019-06-21 沈阳药科大学 A kind of magnetic Fe3O4The preparation method and applications of@MIL-100

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
MINGFEI SHAO ET AL.: ""Preparation of Fe3O4@SiO2@Layered Double Hydroxide Core−Shell Microspheres for Magnetic Separation of Proteins"", 《JOURNAL OF THE AMERICAN CHEMICAL SOCIETY》 *
SOBIA ASLAM ET AL.: ""In situ one-step synthesis of Fe3O4@MIL-100(Fe) core-shells for adsorption of methylene blue from water"", 《JOURNAL OF COLLOID AND INTERFACE SCIENCE》 *

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113952935A (en) * 2021-11-19 2022-01-21 中国农业科学院蔬菜花卉研究所 Magnetic MOFs composite material and preparation method and application thereof
CN115254071A (en) * 2022-08-04 2022-11-01 华侨大学 Magnetic metal organic framework composite material and preparation method and application thereof
CN115779685A (en) * 2023-02-10 2023-03-14 北京理工大学 Preparation method of photo-Fenton film based on metal organic framework material
CN116444809A (en) * 2023-03-23 2023-07-18 河南大学 Hollow nano flower-like double MOF-based heterojunction material and preparation method and application thereof
CN116444809B (en) * 2023-03-23 2023-12-08 河南大学 Hollow nano flower-like double MOF-based heterojunction material and preparation method and application thereof

Similar Documents

Publication Publication Date Title
CN112979985A (en) Composite metal organic framework material and preparation method thereof
Lv et al. Ball milling synthesis of covalent organic framework as a highly active photocatalyst for degradation of organic contaminants
Lei et al. Fabrication of metal-organic frameworks@ cellulose aerogels composite materials for removal of heavy metal ions in water
Lu et al. Photoredox catalysis over graphene aerogel-supported composites
Hou et al. Polymer brushes on metal–organic frameworks by UV-induced photopolymerization
CN110586041B (en) Perfluoroalkyl compound extraction and analysis method based on MOFs stripping graphite phase nitrogen carbide adsorbent
Azhar et al. Cascade applications of robust MIL-96 metal organic frameworks in environmental remediation: Proof of concept
CN110560001B (en) Preparation method and application of Fe-MOFs nano material containing ionic liquid
Yan et al. L-Lysine-grafted graphene oxide as an effective adsorbent for the removal of methylene blue and metal ions
CN110746608A (en) Nitrogen-containing cyclodextrin polymer porous material and preparation method and application thereof
CN115970656A (en) Amino acid covalent grafting cyclodextrin-metal organic framework material and application thereof
CN110639474B (en) Adsorbent for separating propylene and propane and preparation method thereof
Lv et al. Preparation of β-CD and Fe3O4 integrated multifunctional bioadsorbent for highly efficient dye removal from water
CN109092245A (en) A kind of tripolite loading carbon nanotube adsorption agent and preparation method thereof
CN110523398B (en) Carbon nano-sheet layer loaded TiO2Molecularly imprinted material and preparation method and application thereof
CN104258827B (en) Magnetic mesoporous carbon of Polyaniline-modified and its preparation method and application
Xu et al. Selective CO2 photoreduction into CO over Ti3C2 quantum dots decorated NH2-MIL-101 (Fe) heterostructures
CN111569944A (en) Manganese ion doped metal organic framework material and preparation method thereof
CN108499534B (en) Compact gas separation hybrid material containing graphene metal organic framework and preparation method thereof
Xing et al. The fabrication of dendrimeric phenylboronic acid-functionalized magnetic graphene oxide nanoparticles with excellent adsorption performance for the separation and purification of horseradish peroxidase
CN108786493B (en) Filter membrane for sewage treatment or seawater desalination and preparation method and application thereof
CN113600150B (en) Method for preparing magnetic super-crosslinked polymer from vacuum residue
CN105536738B (en) A kind of MAR and MIL 53(Al)Composite adsorbing material of combination and preparation method thereof
CN110975841B (en) Magnetic polymer nano-adsorption material LM-MP and preparation method and application thereof
CN113105024A (en) Method for removing organic pollutants in water body by using three-dimensional aerogel composite material

Legal Events

Date Code Title Description
PB01 Publication
PB01 Publication
SE01 Entry into force of request for substantive examination
SE01 Entry into force of request for substantive examination
RJ01 Rejection of invention patent application after publication

Application publication date: 20210618

RJ01 Rejection of invention patent application after publication