CN115504811A - Permanent CO sequestration utilizing solar photo-thermal catalysis of minerals 2 Method (2) - Google Patents

Permanent CO sequestration utilizing solar photo-thermal catalysis of minerals 2 Method (2) Download PDF

Info

Publication number
CN115504811A
CN115504811A CN202211104000.7A CN202211104000A CN115504811A CN 115504811 A CN115504811 A CN 115504811A CN 202211104000 A CN202211104000 A CN 202211104000A CN 115504811 A CN115504811 A CN 115504811A
Authority
CN
China
Prior art keywords
minerals
reactor
carbon dioxide
fixing agent
silicate mineral
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.)
Granted
Application number
CN202211104000.7A
Other languages
Chinese (zh)
Other versions
CN115504811B (en
Inventor
田森林
朱娴
李晨
赵群
谢明军
宁平
崔祥芬
黄建洪
胡学伟
李英杰
刘树根
史建武
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.)
Kunming University of Science and Technology
Original Assignee
Kunming University of Science and Technology
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 Kunming University of Science and Technology filed Critical Kunming University of Science and Technology
Priority to CN202211104000.7A priority Critical patent/CN115504811B/en
Publication of CN115504811A publication Critical patent/CN115504811A/en
Application granted granted Critical
Publication of CN115504811B publication Critical patent/CN115504811B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Images

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/45Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements
    • C04B41/50Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with inorganic materials
    • C04B41/5007Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with inorganic materials with salts or salty compositions, e.g. for salt glazing
    • C04B41/501Coating or impregnating, e.g. injection in masonry, partial coating of green or fired ceramics, organic coating compositions for adhering together two concrete elements with inorganic materials with salts or salty compositions, e.g. for salt glazing containing carbon in the anion, e.g. carbonates
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B41/00After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone
    • C04B41/009After-treatment of mortars, concrete, artificial stone or ceramics; Treatment of natural stone characterised by the material treated

Landscapes

  • Chemical & Material Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Ceramic Engineering (AREA)
  • Materials Engineering (AREA)
  • Structural Engineering (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Physical Or Chemical Processes And Apparatus (AREA)
  • Carbon And Carbon Compounds (AREA)

Abstract

The invention discloses a method for permanently sealing CO by utilizing solar photo-thermal catalysis mineral 2 The method comprises the following steps: s1, absorbing sunlight in a photo-thermal device and converting light energy into heat energy; s2, filling a silicate mineral carbon dioxide fixing agent and a catalyst into a reactor after mixing; s3, mixing CO 2 Introducing into a reactor; s4, continuously introducing the heat energy obtained in the step S1 into a reactor to perform mineral carbonization reaction; s5, after the reaction is finished, separating the saturated silicate mineral carbon dioxide fixing agent from the catalyst, carrying out subsequent treatment on the carbon dioxide fixing agent, and returning the catalyst to the step S2 for recycling; and S6, permanently sealing the silicate mineral generated after the reaction. The invention uses solar energy as energy source to carry out CO 2 The permanent storage of the minerals, the sustainable utilization of energy, the sustainable execution of the mineral storage process, permanent fixation, no limitation of regions and spaces and no pollution to the environment.

Description

Permanent CO sequestration utilizing solar photo-thermal catalysis of minerals 2 Method (2)
Technical Field
The invention belongs to the technical field of environmental protection, and particularly relates to permanent CO sequestration by utilizing solar photothermal catalysis of minerals 2 The method of (1).
Background
Currently the most common removal of CO 2 The method is a carbon capture and sequestration technology, which adopts the carbon capture technology to capture CO discharged by the industry or related energy industries 2 Separated, transported and sealed to the seabed or underground. Wherein CO is 2 Mineral sequestration is considered to be the most promising sequestration technology. CO 2 2 The mineral sealing technology is to simulate and accelerate the weathering process of rock in nature, and utilizes the reaction of carbon dioxide and calcium-magnesium-containing silicate mineral to make it react with stable carbonate (CaCO) 3 /MgCO 3 ) Form and permanent sealing.
However, the sequestration process requires the consumption of large amounts of energy to remove the CO 2 Meanwhile, the environment is polluted, so people begin to seek a sustainable, efficient and green environmental solution. Wherein the environmental problem is solved by degrading environmental pollution and developing green energy to replace fossil energyBecome two mainstream schemes at present. Solar energy is a green, sustainable energy source. Therefore, the research on the relevant technology for realizing carbon emission reduction by utilizing natural energy is very important.
Disclosure of Invention
The invention aims to provide a method for permanently sealing CO by utilizing solar photo-thermal catalysis of minerals 2 The method of (1).
The object of the invention is achieved by the following steps:
s1, absorbing sunlight in a photo-thermal device and converting light energy into heat energy;
s2, filling a silicate mineral carbon dioxide fixing agent and a catalyst into a reactor after mixing;
s3, mixing CO 2 Introducing into a reactor;
s4, continuously introducing the heat energy obtained in the step S1 into a reactor to perform mineral carbonization reaction; in the process of CO capture 2 The reaction with natural mineral or industrial waste (silicate mineral carbon dioxide fixing agent) rich in Ca, mg and other elements in a reactor under a proper temperature condition to generate a stable carbonate product;
s5, after the reaction is finished, separating the saturated silicate mineral carbon dioxide fixing agent from the catalyst, carrying out subsequent treatment on the carbon dioxide fixing agent, and returning the catalyst to the step S2 for recycling;
and S6, permanently storing the silicate mineral generated after the reaction or using the silicate mineral as a building raw material.
Preferably, the photothermal device comprises a quartz tube, a film and a vacuum layer, wherein the film covers the outer surface of the quartz tube, the vacuum layer covers the film, the film is a Cr film, and the pressure of the vacuum layer is 1.2 x 10 -3 Pa; the Cr film can be a commercial Cr film, and the Cr film covers the outer surface of the quartz tube in a coating mode, so that the quartz tube can completely absorb sunlight, simultaneously radiate a small amount of infrared light, convert the sunlight into heat energy and localize the heat energy; the vacuum layer is used for reducing heat loss, and the temperature is 1KW m under the condition that the ambient temperature is 30 DEG C -2 The photo-thermal device has an internal temperature as high as 305 ℃.
Preferably, the silicate mineral carbon dioxide fixing agent in the step S2 is one of wollastonite, olivine, serpentine, talc and basalt which contain calcium and magnesium elements.
Preferably, the reactor in the step S2 is a reactor of a solid particle bed, and is one of a fixed bed reactor, a fluidized bed reactor, a moving bed reactor and a trickle bed reactor.
Preferably, CO is said in step S3 2 The concentration is 50% -100%.
Preferably, the heat energy in the step S4 is controlled to be 600K-1000K.
Preferably, the S4 step mineral carbonization reaction directly carbonizes the dry-method carbon fixation in the route, wherein the liquid-solid ratio of the dry-method carbon fixation is lower than 0.2, and the carbonization rate is 50% -90% under the 673K reaction condition.
Preferably, the particle size of the catalyst is 50-200 μm, the particle size of the silicate mineral carbon dioxide fixing agent is 50-100 μm, and the separation method of the catalyst and the silicate mineral carbon dioxide fixing agent in the step S5 is one of screening, gravity separation and magnetic separation.
Preferably, the permanent sealing in step S6 is one of sea filling, landfill and mine piling.
Compared with the prior art, the invention has the following technical effects:
1. according to the invention, a silicate mineral carbon dioxide fixing agent and a catalyst react with carbon dioxide in a reactor to generate a stable carbonate product, the heat energy required by the reaction is the heat energy obtained by converting light energy by a photo-thermal device, the catalyst can be separated and reused after the reaction, and the carbonate product can be permanently sealed and can also be used as a building raw material;
2. the method of the invention utilizes solar energy as CO 2 The energy in the mineral sealing and storing process can reduce energy consumption cost, the energy can be continuously utilized, the whole sealing and storing process can be continuously carried out without reversion, and CO can be treated 2 The resource utilization is carried out, the waste is changed into valuable, and the environment benefit is good; the environment is not polluted; without regional and spatial restrictions, at any rateCO 2 The mineral is sealed and stored without worrying about the problems of insufficient energy supply and energy transportation; the solar energy is used as renewable energy, so that the utilization of non-renewable energy is reduced, and the non-renewable energy is protected.
Drawings
FIG. 1 is a schematic flow diagram of the process of the present invention;
in the figure: 1-quartz tube, 2-film, 3-vacuum layer, 4-reactor.
Detailed Description
The invention is further illustrated by the following examples, but is not intended to be limited in any way, and any modifications or alterations based on the teachings of the invention are intended to fall within the scope of the invention.
Example 1
Permanent CO sequestration by utilizing solar photo-thermal catalysis of minerals 2 The method comprises the following steps:
s1, absorbing sunlight in a photo-thermal device and converting light energy into heat energy;
s2, mixing a silicate mineral carbon dioxide fixing agent and a catalyst and filling the mixture into a reactor, wherein the silicate mineral carbon dioxide fixing agent is wollastonite containing calcium and magnesium elements, the particle size of the silicate mineral carbon dioxide fixing agent is 50 micrometers, and the particle size of the catalyst is 50 micrometers;
s3, mixing CO 2 Introducing into a fixed bed reactor, CO 2 The concentration is 50%;
s4, continuously introducing the heat energy obtained in the step S1 into a fixed bed reactor to carry out mineral carbonization reaction, wherein the heat energy is controlled at 600K;
s5, after the reaction is finished, separating the saturated silicate mineral carbon dioxide fixing agent from the catalyst by adopting a screening method, subsequently treating the carbon dioxide fixing agent, and returning the catalyst to the step S2 for recycling;
and S6, filling the silicate mineral generated after the reaction into the sea.
Example 2
This example utilizes solar photothermal catalysis of minerals to permanently sequester CO 2 The photo-thermal device comprises a quartz tube 1, a film 2 and a vacuum layer 3 except the step S1, wherein the outer surface of the quartz tube 1A film 2 is covered on the vacuum layer 3, the film 2 is a Cr film, the pressure of the vacuum layer 3 is 1.2 multiplied by 10 -3 Pa; s2, the silicate mineral carbon dioxide fixing agent is olivine containing calcium and magnesium elements, the particle size of the silicate mineral carbon dioxide fixing agent is 200 mu m, and the particle size of the catalyst is 200 mu m; the reactor in the step S3 is a fluidized bed reactor, and CO 2 The concentration is 100%; s4, controlling the heat energy to be 1000K; s5, reselection separation is adopted for separation; the procedure of example 1 was repeated except that the silicate mineral was buried in the landfill at step S6.
Example 3
This example utilizes solar photothermal catalysis of minerals for permanent CO sequestration 2 The method comprises the steps except the step S2, wherein the silicate mineral carbon dioxide fixing agent is serpentine containing calcium and magnesium, the particle size of the silicate mineral carbon dioxide fixing agent is 125 mu m, and the particle size of the catalyst is 75 mu m; s3 step the reactor is a moving bed reactor, CO 2 The concentration is 75%; s4, controlling the heat energy at 800K, and performing dry carbon fixation in a direct carbonization route of mineral carbonization reaction, wherein the liquid-solid ratio of the dry carbon fixation is 0.10; s5, magnetic separation is adopted for separation in the step; the silicate minerals are deposited outside the mine in the step S6, and the procedure is the same as in example 1.
Example 4
This example utilizes solar photothermal catalysis of minerals to permanently sequester CO 2 The method of (3), except for the step (S2), the silicate mineral carbon dioxide fixing agent is talc containing calcium and magnesium, the particle size of the silicate mineral carbon dioxide fixing agent is 130 μm, and the particle size of the catalyst is 60 μm; the reactor in the step S3 is a trickle bed reactor and CO 2 The concentration is 70%; s4, controlling the heat energy at 900K, and directly carbonizing the dry-method solid carbon in the direct carbonization route of the mineral carbonization reaction, wherein the liquid-solid ratio of the dry-method solid carbon is 0.15; s5, magnetic separation is adopted for separation in the step; step S6 silicate minerals were used as building raw materials, and the rest was the same as in example 1.
Example 5
This example utilizes solar photothermal catalysis of minerals to permanently sequester CO 2 The method comprises the steps except the step S2, wherein the silicate mineral carbon dioxide fixing agent is basalt containing calcium and magnesium, the particle size of the silicate mineral carbon dioxide fixing agent is 120 mu m, and the catalyst is preparedThe grain diameter is 80 μm; s3, the reactor is a fixed bed reactor, CO 2 The concentration is 60%; s4, controlling the heat energy at 700K, and directly carbonizing the dry-method solid carbon in the route of mineral carbonization reaction, wherein the liquid-solid ratio of the dry-method solid carbon is 0.19; s5, screening separation is adopted in the separation in the step; step S6 the silicate mineral was used as a building material, and the rest was the same as in example 1.

Claims (9)

1. Permanent CO sequestration utilizing solar photo-thermal catalysis of minerals 2 The method is characterized by comprising the following steps:
s1, absorbing sunlight in a photo-thermal device and converting light energy into heat energy;
s2, filling a silicate mineral carbon dioxide fixing agent and a catalyst into a reactor after mixing;
s3, mixing CO 2 Introducing into a reactor;
s4, continuously introducing the heat energy obtained in the step S1 into a reactor to perform mineral carbonization reaction;
s5, after the reaction is finished, separating the saturated silicate mineral carbon dioxide fixing agent from the catalyst, carrying out subsequent treatment on the carbon dioxide fixing agent, and returning the catalyst to the step S2 for recycling;
and S6, permanently storing the silicate mineral generated after the reaction or using the silicate mineral as a building raw material.
2. The method of claim 1, wherein the solar photothermal catalysis of minerals is utilized to permanently sequester CO 2 The method is characterized in that the photo-thermal device comprises a quartz tube (1), a film (2) and a vacuum layer (3), the film (2) covers the outer surface of the quartz tube (1), the vacuum layer (3) covers the film (2), the film (2) is a Cr film, and the pressure of the vacuum layer (3) is 1.2 multiplied by 10 -3 Pa。
3. The method of claim 1, wherein the solar photothermal catalysis of minerals is utilized to permanently sequester CO 2 The method is characterized in that the silicate mineral carbon dioxide fixing agent in the step S2 is wollastonite, olivine, serpentine, talc and brown stone containing calcium and magnesium elementsOne kind of Wuyan rock.
4. The method of claim 1, wherein the solar photothermal catalysis of minerals is utilized to permanently sequester CO 2 The method is characterized in that the reactor in the step S2 is a reactor of a solid particle bed layer and is one of a fixed bed reactor, a fluidized bed reactor, a moving bed reactor and a trickle bed reactor.
5. The method of claim 1, wherein the solar photothermal catalysis of minerals is utilized to permanently sequester CO 2 Characterized in that CO as described in step S3 2 The concentration is 50% -100%.
6. The method of claim 1, wherein the solar photothermal catalysis of minerals is utilized to permanently sequester CO 2 The method is characterized in that the heat energy in the step S4 is controlled to be 600K-1000K.
7. The method of claim 1, wherein the solar photothermal catalysis of minerals is utilized to permanently sequester CO 2 The method is characterized in that dry carbon fixation in a direct carbonization route of mineral carbonization reaction in the step S4 is performed, wherein the liquid-solid ratio of the dry carbon fixation is lower than 0.2, and the carbonization rate is 50-90% under the 673K reaction condition.
8. The method of claim 1, wherein the solar photothermal catalysis of minerals is utilized to permanently sequester CO 2 The method is characterized in that the particle size of the catalyst is 50-200 mu m, the particle size of the silicate mineral carbon dioxide fixing agent is 50-100 mu m, and the separation method of the catalyst and the silicate mineral carbon dioxide fixing agent in the S5 step is one of screening, gravity separation and magnetic separation.
9. The method of claim 1, wherein the solar photothermal catalysis of minerals is utilized to permanently sequester CO 2 The method of (2), wherein the permanent sealing in step (S6) is one of sea filling, landfill, and mine piling.
CN202211104000.7A 2022-09-09 2022-09-09 Solar photo-thermal catalytic mineral permanent CO sealing 2 Is a method of (2) Active CN115504811B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN202211104000.7A CN115504811B (en) 2022-09-09 2022-09-09 Solar photo-thermal catalytic mineral permanent CO sealing 2 Is a method of (2)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN202211104000.7A CN115504811B (en) 2022-09-09 2022-09-09 Solar photo-thermal catalytic mineral permanent CO sealing 2 Is a method of (2)

Publications (2)

Publication Number Publication Date
CN115504811A true CN115504811A (en) 2022-12-23
CN115504811B CN115504811B (en) 2023-09-22

Family

ID=84504623

Family Applications (1)

Application Number Title Priority Date Filing Date
CN202211104000.7A Active CN115504811B (en) 2022-09-09 2022-09-09 Solar photo-thermal catalytic mineral permanent CO sealing 2 Is a method of (2)

Country Status (1)

Country Link
CN (1) CN115504811B (en)

Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090169452A1 (en) * 2007-12-28 2009-07-02 Constantz Brent R Methods of sequestering co2
US20100221163A1 (en) * 2009-02-27 2010-09-02 Caterpillar Inc. Method to sequester co2 as mineral carbonate
CN101902167A (en) * 2009-05-28 2010-12-01 北京智慧剑科技发展有限责任公司 Butterfly-type black body solar photovoltaic/thermal converter
CN101902163A (en) * 2009-05-28 2010-12-01 北京智慧剑科技发展有限责任公司 Solar photoelectric light-heat converter for flat black body
CN102198367A (en) * 2011-03-17 2011-09-28 青岛科技大学 Technology for carbon solidification, base manufacture, soil make and sand control
CN104383811A (en) * 2014-11-17 2015-03-04 南京朗洁环保科技有限公司 Method for removing carbon dioxide by semidry method based on straw ash
CN105567325A (en) * 2014-10-11 2016-05-11 中国科学院大连化学物理研究所 Spinel compound-carbonate mixture system for solar energy photo-thermal chemical conversion, preparation and application thereof
CN107744722A (en) * 2017-11-14 2018-03-02 西安交通大学 Collecting carbonic anhydride and recycling system and method based on Driven by Solar Energy
CN114751372A (en) * 2022-03-12 2022-07-15 昆明理工大学 Method for fixing carbon dioxide in water-gas shift process by utilizing real-time carbonization of silicate

Patent Citations (9)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090169452A1 (en) * 2007-12-28 2009-07-02 Constantz Brent R Methods of sequestering co2
US20100221163A1 (en) * 2009-02-27 2010-09-02 Caterpillar Inc. Method to sequester co2 as mineral carbonate
CN101902167A (en) * 2009-05-28 2010-12-01 北京智慧剑科技发展有限责任公司 Butterfly-type black body solar photovoltaic/thermal converter
CN101902163A (en) * 2009-05-28 2010-12-01 北京智慧剑科技发展有限责任公司 Solar photoelectric light-heat converter for flat black body
CN102198367A (en) * 2011-03-17 2011-09-28 青岛科技大学 Technology for carbon solidification, base manufacture, soil make and sand control
CN105567325A (en) * 2014-10-11 2016-05-11 中国科学院大连化学物理研究所 Spinel compound-carbonate mixture system for solar energy photo-thermal chemical conversion, preparation and application thereof
CN104383811A (en) * 2014-11-17 2015-03-04 南京朗洁环保科技有限公司 Method for removing carbon dioxide by semidry method based on straw ash
CN107744722A (en) * 2017-11-14 2018-03-02 西安交通大学 Collecting carbonic anhydride and recycling system and method based on Driven by Solar Energy
CN114751372A (en) * 2022-03-12 2022-07-15 昆明理工大学 Method for fixing carbon dioxide in water-gas shift process by utilizing real-time carbonization of silicate

Also Published As

Publication number Publication date
CN115504811B (en) 2023-09-22

Similar Documents

Publication Publication Date Title
CN102527225B (en) A kind of method using reproducible carbide slag collecting carbon dioxide from fuel gas
KR101464010B1 (en) Integrated chemical process
EP2833062B1 (en) Municipal solid waste treatment and utilization system
US10790525B2 (en) Systems for storing, distributing and dispatching energy on demand using and recycling carbon
Morales-Flórez et al. Artificial weathering pools of calcium-rich industrial waste for CO2 sequestration
JP2012500718A (en) Improved integrated chemistry
CN107098323A (en) A kind of g C3N4Nanometer sheet and preparation method and application
CN106590702B (en) A kind of house refuse low temperature pyrogenation electricity generation system and method
CN110698087B (en) Device and method for comprehensively utilizing thermal-state steel slag
CN101898087A (en) Method and device for converting and absorbing carbon dioxide and comprehensively utilizing waste heat of steel slag
KR101636674B1 (en) Apparatus and method for mineralizing carbon dioxide using 3-phase fluidized bed system
CN115504811A (en) Permanent CO sequestration utilizing solar photo-thermal catalysis of minerals 2 Method (2)
CN206449652U (en) A kind of house refuse low temperature pyrogenation electricity generation system
CN112850644A (en) Device and method for preparing high-purity hydrogen by gasifying household garbage through plasma
CN1196750C (en) Carbon producing apparatus utilizing biomass
US20150044757A1 (en) Methods and Systems for Capturing and Storing Carbon Dioxide
Su et al. Modification and resource utilization of coal gasification slag-based material: A review
CN114768501A (en) Carbon dioxide mineralization coupling system for capturing carbon dioxide in flue gas and based on industrial solid waste
CN114620963A (en) Method for completely carbonizing reclaimed powder
CN114751372A (en) Method for fixing carbon dioxide in water-gas shift process by utilizing real-time carbonization of silicate
CN113340105A (en) Method for decomposing and disposing phosphogypsum by using sintering machine and recycling phosphogypsum
Imoisili et al. Microwave-assisted synthesis and characterization of zeolite prepared from south africa coal fly ash
Martins et al. An inter-loop approach for hydrothermal carbonization of sewage sludge to produce hydrochars and their use as an adsorbent for iron removal from spent sulfuric acid
Burra et al. Thermochemical Solutions for CO 2 Utilization to Fuels and Value-Added Products
JP2000119049A (en) Production of cement

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
GR01 Patent grant
GR01 Patent grant