CN111644123A - Microwave-responsive additive active-release capsule and preparation method thereof - Google Patents
Microwave-responsive additive active-release capsule and preparation method thereof Download PDFInfo
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- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J13/00—Colloid chemistry, e.g. the production of colloidal materials or their solutions, not otherwise provided for; Making microcapsules or microballoons
- B01J13/02—Making microcapsules or microballoons
- B01J13/20—After-treatment of capsule walls, e.g. hardening
- B01J13/22—Coating
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B20/00—Use of materials as fillers for mortars, concrete or artificial stone according to more than one of groups C04B14/00 - C04B18/00 and characterised by shape or grain distribution; Treatment of materials according to more than one of the groups C04B14/00 - C04B18/00 specially adapted to enhance their filling properties in mortars, concrete or artificial stone; Expanding or defibrillating materials
- C04B20/10—Coating or impregnating
- C04B20/1018—Coating or impregnating with organic materials
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B20/00—Use of materials as fillers for mortars, concrete or artificial stone according to more than one of groups C04B14/00 - C04B18/00 and characterised by shape or grain distribution; Treatment of materials according to more than one of the groups C04B14/00 - C04B18/00 specially adapted to enhance their filling properties in mortars, concrete or artificial stone; Expanding or defibrillating materials
- C04B20/10—Coating or impregnating
- C04B20/1018—Coating or impregnating with organic materials
- C04B20/1022—Non-macromolecular compounds
- C04B20/1025—Fats; Fatty oils; Ester type waxes; Higher fatty acids; Derivatives thereof
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
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- C04B20/00—Use of materials as fillers for mortars, concrete or artificial stone according to more than one of groups C04B14/00 - C04B18/00 and characterised by shape or grain distribution; Treatment of materials according to more than one of the groups C04B14/00 - C04B18/00 specially adapted to enhance their filling properties in mortars, concrete or artificial stone; Expanding or defibrillating materials
- C04B20/10—Coating or impregnating
- C04B20/1018—Coating or impregnating with organic materials
- C04B20/1029—Macromolecular compounds
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B20/00—Use of materials as fillers for mortars, concrete or artificial stone according to more than one of groups C04B14/00 - C04B18/00 and characterised by shape or grain distribution; Treatment of materials according to more than one of the groups C04B14/00 - C04B18/00 specially adapted to enhance their filling properties in mortars, concrete or artificial stone; Expanding or defibrillating materials
- C04B20/10—Coating or impregnating
- C04B20/1018—Coating or impregnating with organic materials
- C04B20/1029—Macromolecular compounds
- C04B20/1044—Bituminous materials
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B20/00—Use of materials as fillers for mortars, concrete or artificial stone according to more than one of groups C04B14/00 - C04B18/00 and characterised by shape or grain distribution; Treatment of materials according to more than one of the groups C04B14/00 - C04B18/00 specially adapted to enhance their filling properties in mortars, concrete or artificial stone; Expanding or defibrillating materials
- C04B20/10—Coating or impregnating
- C04B20/1055—Coating or impregnating with inorganic materials
- C04B20/1066—Oxides, Hydroxides
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- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K5/00—Heat-transfer, heat-exchange or heat-storage materials, e.g. refrigerants; Materials for the production of heat or cold by chemical reactions other than by combustion
- C09K5/02—Materials undergoing a change of physical state when used
- C09K5/06—Materials undergoing a change of physical state when used the change of state being from liquid to solid or vice versa
- C09K5/063—Materials absorbing or liberating heat during crystallisation; Heat storage materials
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Abstract
The invention relates to the field of additives for building materials, in particular to a microwave-responsive additive active-release capsule and a preparation method thereof. The active release capsule consists of a capsule wall, a capsule core and an encapsulating material, wherein the capsule wall is porous ceramsite; the capsule core is an additive needing to control active release; the packaging material is doped with Fe3O4The organic phase change material of (1). The method is rapid, simple and convenient, the used materials have wide sources, can stably exist in building materials, and the additive loading capacity is strong, so the method can be widely applied to loading of various additives. In addition, the Fe in the packaging material is utilized3O4The microwave responsiveness and the wave-absorbing heat-generating function of the composite material can be realized by applyingThe external microwave signal triggers the capsule to respond so that the capsule actively releases the additive, the problems of low utilization efficiency, even possible negative effects and the like caused by the fact that the additive is directly doped into the building material are effectively solved, and further the active control on the performance of the building material is realized.
Description
Technical Field
The invention relates to the field of additives for building materials, in particular to a microwave-responsive additive active-release capsule and a preparation method thereof.
Background
In the conventional concrete performance improvement method, the use of the admixture is a very efficient, economical and environment-friendly method, and thus is widely used. However, the admixture is usually directly mixed in the concrete casting process to participate in the whole process of the cement hydration reaction, which has direct influence on the action effect of the admixture: such as rust inhibitor, the effective components of the rust inhibitor are easy to bury by cement hydration products and cannot fully play a role; tackifiers and the like can increase the solution viscosity, reduce the fluidity of free water in the concrete and lose the workability, and delay the hydration of cement; expanding agents, etc. are not expected to act immediately after the cement begins to hydrate and the concrete has not yet shrunk, otherwise the active ingredients are consumed in large amounts at an early stage. This not only increases the construction cost of the concrete structure, but may even have a negative impact on the properties of strength, durability, etc. Therefore, there is a need to research a new mixing method of an additive in concrete, which can ensure that the action effect of the additive is not influenced by factors such as hydration reaction of cement and the like, and can improve the performance of the new mix-hardened concrete by using the additive.
In recent years, microcapsule controlled release technology has been widely studied and applied in the fields of medicine, agriculture, food and the like, and with the inspiration, researchers assume that microcapsule controlled release technology is applied in the field of concrete, so as to achieve the purpose that the admixture does not lose efficiency prematurely and can improve the performance of newly mixed and hardened concrete. At present, the microcapsule controlled release technology is mainly applied to self-repairing concrete and internal curing concrete in the field of concrete: the patent CN 110510910A introduces a self-repairing material of a concrete micro-crack microcapsule with a capsule wall easy to degrade, wherein the capsule wall is made of a cellulose material easy to oxidize and degrade under the action of illumination, has a light-oxygen degradation effect, and can break at the crack of the concrete to release a self-repairing agent in the microcapsule; in patent CN 108609880A, a microcapsule is prepared aiming at the corrosion of reinforced concrete, when the reinforced concrete is corroded, the pH value of the concrete is reduced, and the capsule wall is locally damaged under the conditions of alkalescence and neutrality, so that the capsule core rust inhibitor is released, and the corrosion of reinforcing steel bars is inhibited; patent CN 108947341A introduces a microbial microcapsule capable of continuously repairing and solving the water seepage problem of underground engineering, when the water seepage problem occurs to concrete, the capsule wall with water seepage and air permeability enables water and oxygen to permeate into the microbial capsule, and activates strains to metabolize to generate carbon dioxide, and the carbon dioxide can react with calcium ions in the concrete to generate calcium carbonate precipitate to fill concrete cracks. The application is based on a passive control release mechanism, namely, the microcapsules loaded with the admixture are triggered to respond when the environmental condition of the concrete matrix changes, so that the admixture is released, and the release mechanism can well cope with the application conditions similar to repair and the like; however, when the conditions of the concrete matrix are not changed greatly and the admixture is needed, the admixture is difficult to be released actively to exert the effect. The microcapsule prepared and applied based on the active control release mechanism can realize that an external signal is artificially controlled and applied to release the additive at any time, namely no matter the concrete is in a fresh-mixed state or a hardened state, so that the active release of the additive and the active control of the performance of the concrete are realized.
Disclosure of Invention
Aiming at the problems, the invention provides a microwave-responsive additive active-release capsule and a preparation method thereof. Adding the capsule into concrete, applying microwave, and Fe3O4Absorbing microwave to generate heat when Fe3O4When the temperature of the organic phase-change material is higher than the phase-change temperature of the organic phase-change material, the organic phase-change material is melted, thereby releasing the admixture.
The first purpose of the invention is to provide a microwave response additive active release capsule. The second purpose is to provide a preparation method of the microwave response additive active release capsule. The third purpose is to provide the application of the preparation method of the microwave response additive active release capsule.
Firstly, the invention discloses a microwave loudspeakerThe additive actively releases the capsule, the capsule consists of a capsule wall, a capsule core and an encapsulating material, and the capsule wall is porous ceramsite; the capsule core is an additive needing to be controlled to release; the packaging material is doped with Fe3O4The organic phase change material of (1).
Further, the capsule wall is porous ceramsite, the particle size is 1.0-1.5 cm, the porosity is 30-45%, and the crushing resistance is 450-600N.
Further, the additive active release capsule is characterized in that the core material is a concrete additive such as an additive, a rust inhibitor, a water reducing agent or a tackifier.
Furthermore, the packaging material is doped with Fe3O4In which Fe3O4The grain diameter is 20nm, and the purity is 99.5%; the organic phase-change material is paraffin, stearic acid, hydrogel or polymer gel and the like, and the phase-change temperature is 55-60 ℃.
Further, said Fe3O4The mixing amount in the organic phase change material is 10-30%.
Secondly, the invention discloses a preparation method of the microwave response additive active release capsule, which comprises the following steps:
(1) loading an additive into the packaging material porous ceramsite:
immersing the porous ceramsite in the additive, and carrying out vacuum treatment to fully load the additive into the porous ceramsite; wherein the vacuum pumping condition of the vacuum treatment is less than 20KPa, and the time is 24 h.
(2) By doping with Fe3O4The paraffin-encapsulated porous ceramsite is as follows:
heating the organic phase change material to melt it, adding Fe3O4And slowly stirring to make Fe3O4Uniformly distributing the mixture in a molten organic phase-change material, quickly putting the porous ceramsite loaded with the additive into the molten organic phase-change material, quickly rolling for a plurality of circles to uniformly coat a layer of packaging material on the surface of the porous ceramsite, taking out the porous ceramsite, and cooling the porous ceramsite to room temperature to obtain the active release capsule.
The phase-change material is organic phase-change material such as paraffin, stearic acid, hydrogel or polymer gel, and the phase-change temperature is 55-60 ℃;
the temperature for heating the organic phase change material is 70-80 ℃;
said added Fe3O4The mixing amount is 10-30%.
The active release capsule is spherical or ellipsoidal, and the particle size is 1.0-1.7 cm.
The invention principle of the invention is as follows: loading the additive into the porous ceramsite through vacuum treatment, packaging the porous ceramsite by using an organic phase-change material to prevent the additive from flowing out, and simultaneously doping a wave-absorbing material Fe into the organic phase-change material3O4Preparing an active release capsule; adding the capsule into concrete, applying microwave, and Fe3O4Absorbing microwave to generate heat when Fe3O4When the temperature of the organic phase-change material is higher than the phase-change temperature of the organic phase-change material, the organic phase-change material is melted, thereby releasing the admixture.
The invention has the beneficial effects that:
compared with the prior art, the invention has the advantages that: (1) the raw materials of the additive active release capsule have wide sources, can stably exist in concrete, have strong additive loading capacity, and can be widely applied to loading of various additives; (2) the active additive release capsule prepared by the preparation method can trigger the capsule to respond by applying an external microwave signal so as to actively release the additive, effectively solve the problem of reduced action effect caused by directly doping the additive into the building material, and further realize the active control of the performance of the building material.
Drawings
FIG. 1 is a schematic view of an additive active-release capsule prepared according to the present invention.
Fig. 2 shows the release of the external agent active release capsule under the action of microwaves in example 2.
Fig. 3 is a release profile of the external agent active release capsule under the action of microwaves in example 3.
Wherein, 1-additive, 2-porous ceramsite, 3-paraffin and 4-Fe3O4And (3) powder.
The specific implementation mode is as follows:
the following examples are intended to illustrate the present invention and should not be construed as limiting the scope of the invention. All technical and scientific terms used herein have the same meaning as commonly understood by one of ordinary skill in the art to which this invention belongs.
Example 1
And (3) immersing the porous ceramsite with the particle size of 1.0cm in the polycarboxylate superplasticizer (the mass fraction is 20%), and carrying out vacuum treatment for 24 hours to ensure that the porous ceramsite is fully loaded with the polycarboxylate superplasticizer. Heating paraffin (phase transition temperature 55-60 ℃) at 70 ℃ to melt the paraffin, and adding 10% of Fe3O4And slowly stirring to make Fe3O4Uniformly distributed in the molten paraffin, and quickly putting the porous ceramsite loaded with the polycarboxylate superplasticizer into the molten paraffin and doped with Fe3O4The molten paraffin is quickly rolled for a plurality of circles to enable the surface of the porous ceramsite to be uniformly coated with a layer of paraffin, and the porous ceramsite is taken out and cooled to room temperature to obtain the active release capsule.
The loading capacity of an active release capsule is defined as: the mass of the loaded polycarboxylate superplasticizer accounts for the percentage of the total mass of the active release capsule. The loading capacity of the active release capsule was measured to be 71%.
Example 2
And immersing the porous ceramsite with the particle size of 1.2cm in a carboxyl amino alcohol rust inhibitor (yellow liquid, the mass fraction of which is 30 percent), and carrying out vacuum treatment for 24 hours to ensure that the porous ceramsite is fully loaded with the carboxyl amino alcohol rust inhibitor. Heating paraffin (phase transition temperature 55-60 ℃) at 70 ℃ to melt the paraffin, adding 15% of Fe3O4, and slowly stirring to enable Fe3O4Evenly distributed in the molten paraffin, and the porous ceramsite loaded with the carboxyl amino alcohol rust inhibitor is quickly put into the molten paraffin and doped with Fe3O4The molten paraffin is quickly rolled for a plurality of circles to enable the surface of the porous ceramsite to be uniformly coated with a layer of paraffin, and the porous ceramsite is taken out and cooled to room temperature to obtain the active release capsule.
Putting the active release capsule into a concrete simulation solution3.5% NaCl saturated Ca (OH)2The volume ratio of the solution to the concrete simulation solution to the active release capsule is 4: 1, applying microwave with power of 500W to treat Fe for 90s3O4Absorbing microwave to generate heat when Fe3O4When the temperature is higher than the paraffin phase transition temperature, the paraffin is melted, and the release of a light yellow liquid in the solution can be observed, namely the carboxyl amino alcohol rust inhibitor is released, as shown in figure 2.
Example 3
Immersing the porous ceramsite with the particle size of 1.1cm into a polyethylene glycol tackifier (with the molecular weight of 1000 and the mass fraction of 20%), and carrying out vacuum treatment for 24 hours to fully load the polyethylene glycol tackifier on the porous ceramsite. Heating stearic acid (phase transition temperature 55-60 ℃) at 70 ℃ to melt the stearic acid, and adding 25% of Fe3O4And slowly stirring to make Fe3O4Uniformly distributed in molten stearic acid, and quickly putting the porous ceramsite loaded with the polyethylene glycol tackifier into the porous ceramsite mixed with Fe3O4And (3) rapidly rolling for a plurality of circles in the molten stearic acid to uniformly coat a layer of stearic acid on the surface of the porous ceramsite, taking out the porous ceramsite, and cooling the porous ceramsite to room temperature to obtain the active release capsule.
Placing the active release capsules into a concrete simulation solution, wherein the concrete simulation solution is a 3.5% NaCl saturated Ca (OH)2 solution, and the volume ratio of the concrete simulation solution to the active release capsules is 6: 1, applying microwave with power of 600W to treat Fe for 60s3O4Absorbing microwave to generate heat when Fe3O4Above the stearic acid phase transition temperature, the stearic acid melts, thereby releasing the polyethylene glycol tackifier.
The concentration of the released polyethylene glycol tackifier is tested by using an ultraviolet-visible spectrophotometer, the release rate of the active release capsule is defined as the percentage of the mass of the tackifier released into an external medium to the mass of the tackifier in the active release capsule, the release rate of the active release capsule at a given time (0h, 2h, 4h, … …, 10h, 12h, 24h, 48h and 72h) is calculated, and the release behavior of the active release capsule is characterized, as shown in fig. 3.
Example 4
And immersing the porous ceramsite with the particle size of 1.0cm in the alcamines rust inhibitor (the mass fraction is 20%), and performing vacuum treatment for 24 hours to fully load the alcamines rust inhibitor into the porous ceramsite. Heating paraffin (the phase transition temperature is 55-60 ℃) at 70 ℃ to melt the paraffin, adding 30% of Fe3O4, slowly stirring to ensure that Fe3O4 is uniformly distributed in the molten paraffin, quickly putting the porous ceramsite loaded with the alcamines rust inhibitor into the molten paraffin doped with Fe3O4, quickly rolling for a plurality of circles to uniformly coat a layer of paraffin on the surface of the porous ceramsite, taking out the porous ceramsite, and cooling the porous ceramsite to room temperature to obtain the active release capsule.
Forming 150mm concrete test pieces (water cement ratio 0.53; cement 223kg, water 118kg, medium sand 840kg, continuous graded broken stone 1260kg of 5-20mm per cubic meter), fixing a smooth Q235 reinforcing steel bar (coated with epoxy resin except exposed surfaces) with the diameter of 12mm and the length of 200mm at the center of a concrete pouring surface, doping an alcamine rust inhibitor with the mass of 2% of the cement into an experimental group to actively release capsules in the forming process, and doping Fe with the same amount as that of the experimental group into a blank group3O4. And (3) standard maintenance for 28d, applying a 800W microwave signal, processing for 120s to control the release of the alcohol amine rust inhibitor in the concrete, testing the corrosion degree of the steel bars in the concrete of the experimental group and the blank group by using an electrochemical method, and indirectly reflecting the release effect of the alcohol amine rust inhibitor in the concrete by comparing the corrosion degrees.
The above examples illustrate the technical solution of the present invention in detail. It will be clear that the invention is not limited to the described embodiments. Various changes may be made by those skilled in the art based on the embodiments of the invention, and any changes which are equivalent or similar to the embodiments of the invention are intended to fall within the scope of the invention.
Claims (8)
1. The microwave-responsive additive active-release capsule is characterized by comprising a capsule wall, a capsule core and an encapsulating material, wherein the capsule wall is porous ceramsite; the capsule core is an additive needing to control active release; the packaging material is doped with Fe3O4The organic phase change material of (1).
2. The admixture active-release capsule according to claim 1, wherein the capsule wall is porous ceramsite, the particle size is 1.0-1.5 cm, the porosity is 30-45%, and the crushing resistance is 450-600N.
3. The admixture active release capsule of claim 1, wherein the capsule core is a concrete admixture.
4. The admixture active release capsule of claim 1, wherein the encapsulating material is doped with Fe3O4Of an organic phase-change material of, Fe3O4The grain diameter is 20nm, and the purity is 99.5%; the organic phase change material is one of paraffin, stearic acid, hydrogel or polymer gel, and the phase change temperature is 55-60 ℃.
5. The admixture active release capsule of claim 1, wherein said Fe is3O4The doping amount in the organic phase change material is 10% -30%.
6. The method for preparing the microwave-responsive additive active-release capsule according to any one of claims 1 to 5, comprising the steps of:
(1) loading an additive into the packaging material porous ceramsite:
immersing the porous ceramsite in the additive, and carrying out vacuum treatment, wherein the negative pressure pumping condition of the vacuum treatment is less than 20KPa, and the time is 24 hours, so that the additive is fully loaded on the porous ceramsite;
(2) by doping with Fe3O4The paraffin-encapsulated porous ceramsite is as follows:
heating the organic phase change material to melt it, adding Fe3O4And slowly stirring to make Fe3O4Uniformly distributing the mixture in a molten organic phase-change material, quickly putting the porous ceramsite loaded with the additive into the molten organic phase-change material, quickly rolling for a plurality of circles to uniformly coat a layer of packaging material on the surface of the porous ceramsite, taking out the porous ceramsite, and cooling the porous ceramsite to room temperature to obtain the active release capsule.
7. The method for preparing an active release capsule according to claim 6, wherein the temperature for heating the organic phase change material in the step (2) is 70 to 80 ℃.
8. The method for preparing an active release capsule according to claim 6, wherein in the step (2), the active release capsule is spherical or ellipsoidal and has a particle size of 1.0 to 1.7 cm.
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Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN112094069A (en) * | 2020-09-17 | 2020-12-18 | 山东大学 | Self-repairing microcapsule internally doped with paraffin powder and microwave-assisted self-repairing method |
| CN114111458A (en) * | 2021-11-24 | 2022-03-01 | 安徽理工大学 | Device and method for activating expansion performance of static crushing agent by temperature control |
| CN115073055A (en) * | 2022-07-11 | 2022-09-20 | 中建商品混凝土有限公司 | Preparation method of concrete self-repairing microcapsule |
Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH03126650A (en) * | 1989-10-12 | 1991-05-29 | Shimizu Corp | Microencapsulated cement admixture responding to electrical impulse and control method for setting of cement |
| CN1450141A (en) * | 2003-04-10 | 2003-10-22 | 同济大学 | Phase-changing energy-storage composite material for building and preparation process thereof |
| CN106747653A (en) * | 2017-02-07 | 2017-05-31 | 山东科技大学 | A kind of one-component healing capsule and self union concrete |
| CN107875390A (en) * | 2017-10-31 | 2018-04-06 | 青岛大学 | A kind of shell contains micro- organogel of load medicine of ferroso-ferric oxide and its preparation method and application |
| WO2018226315A1 (en) * | 2017-06-06 | 2018-12-13 | Xinova, LLC | Releasable agent apparatus and methods for manufacturing and using the same |
-
2020
- 2020-05-08 CN CN202010382083.0A patent/CN111644123B/en active Active
Patent Citations (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPH03126650A (en) * | 1989-10-12 | 1991-05-29 | Shimizu Corp | Microencapsulated cement admixture responding to electrical impulse and control method for setting of cement |
| CN1450141A (en) * | 2003-04-10 | 2003-10-22 | 同济大学 | Phase-changing energy-storage composite material for building and preparation process thereof |
| CN106747653A (en) * | 2017-02-07 | 2017-05-31 | 山东科技大学 | A kind of one-component healing capsule and self union concrete |
| WO2018226315A1 (en) * | 2017-06-06 | 2018-12-13 | Xinova, LLC | Releasable agent apparatus and methods for manufacturing and using the same |
| CN107875390A (en) * | 2017-10-31 | 2018-04-06 | 青岛大学 | A kind of shell contains micro- organogel of load medicine of ferroso-ferric oxide and its preparation method and application |
Cited By (3)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN112094069A (en) * | 2020-09-17 | 2020-12-18 | 山东大学 | Self-repairing microcapsule internally doped with paraffin powder and microwave-assisted self-repairing method |
| CN114111458A (en) * | 2021-11-24 | 2022-03-01 | 安徽理工大学 | Device and method for activating expansion performance of static crushing agent by temperature control |
| CN115073055A (en) * | 2022-07-11 | 2022-09-20 | 中建商品混凝土有限公司 | Preparation method of concrete self-repairing microcapsule |
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