CN108587265A - A kind of high activity functional form diatom ooze and preparation method thereof - Google Patents

A kind of high activity functional form diatom ooze and preparation method thereof Download PDF

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CN108587265A
CN108587265A CN201810360674.0A CN201810360674A CN108587265A CN 108587265 A CN108587265 A CN 108587265A CN 201810360674 A CN201810360674 A CN 201810360674A CN 108587265 A CN108587265 A CN 108587265A
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parts
diatomite
diatom ooze
functional form
high activity
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肖力光
庞博
赵壮
张艺超
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Jilin Jianzhu University
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    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09DCOATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
    • C09D1/00Coating compositions, e.g. paints, varnishes or lacquers, based on inorganic substances
    • C09D1/10Coating compositions, e.g. paints, varnishes or lacquers, based on inorganic substances lime
    • C09D1/12Coating compositions, e.g. paints, varnishes or lacquers, based on inorganic substances lime with organic additives
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/02Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols by adsorption, e.g. preparative gas chromatography
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    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/74General processes for purification of waste gases; Apparatus or devices specially adapted therefor
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D53/00Separation of gases or vapours; Recovering vapours of volatile solvents from gases; Chemical or biological purification of waste gases, e.g. engine exhaust gases, smoke, fumes, flue gases, aerosols
    • B01D53/34Chemical or biological purification of waste gases
    • B01D53/74General processes for purification of waste gases; Apparatus or devices specially adapted therefor
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    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/60Additives non-macromolecular
    • C09D7/61Additives non-macromolecular inorganic
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    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/60Additives non-macromolecular
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    • C09D7/62Additives non-macromolecular inorganic modified by treatment with other compounds
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    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
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    • C09D7/00Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
    • C09D7/40Additives
    • C09D7/70Additives characterised by shape, e.g. fibres, flakes or microspheres
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2255/00Catalysts
    • B01D2255/80Type of catalytic reaction
    • B01D2255/802Photocatalytic
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    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2257/00Components to be removed
    • B01D2257/70Organic compounds not provided for in groups B01D2257/00 - B01D2257/602
    • B01D2257/702Hydrocarbons
    • B01D2257/7022Aliphatic hydrocarbons
    • B01D2257/7025Methane
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    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
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    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
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    • Y02CCAPTURE, STORAGE, SEQUESTRATION OR DISPOSAL OF GREENHOUSE GASES [GHG]
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    • Y02C20/20Capture or disposal of greenhouse gases of methane

Abstract

The invention discloses a kind of high activity functional form diatom oozes and preparation method thereof, by grinding, two three-level diatomite after acidleach carry out low temperature oxygen-free thermal activation treatment, it is combined with negative pressure load method using collosol and gel, it is prepared for tripolite loading nano zinc oxide composite photocatalyst material, improve the functional performance of diatom ooze, then by the diatomite base optic catalytic material and white cement of above-mentioned preparation, coarse whiting, talcum powder, sand, grey calcium, bentonite, polymer dispersion powder, polypropylene fibre, polyvinyl alcohol, antifoaming agent uniformly mixes, add water to stir into body of paste and is prepared into functional form diatom ooze.The problems such as high activity functional form diatom ooze in the present invention is high to the purification efficiency of room air, both solves picking, and durability is poor also ensures the diatomaceous reasonable utilization of two three-levels.

Description

A kind of high activity functional form diatom ooze and preparation method thereof
Technical field
The present invention discloses a kind of high activity functional form diatom ooze and preparation method thereof, is related to a kind of for indoor high activity Functional form diatom ooze and preparation method thereof belongs to indoor wall technical field of coatings.
Background technology
Problem of environmental pollution have become the whole society face with significant problem urgently to be resolved hurrily, with outdoor PM2.5 values It is continuously increased, the indoor environment of a health environment-friendly is particularly important, currently, people study indoor air quality and environment energetically Harmony, development function environmental protection become hot spot in the indoor air purification new material of one.Diatom ooze is with its safety and environmental protection, color It is abundant, functional performance is good, it is decorative favored by consumers in general by force, by the end of in May, 2017, there is the diatom of brand in the country Mud manufacturing enterprise is up to more than 500 families, but on the one hand entire diatom ooze industry does not account for the diatomaceous activity of functional stuffing and asks Topic, most enterprises have lost the diatomite of pozzolanic activity for use as the diatomite of filter aid or using high-temperature calcination Diatom ooze production is carried out, not only production cost is made to increase substantially, and cause the serious wasting of resources, two three-level diatomite do not have It is effectively used.Also cause diatom ooze durability poor simultaneously, hardness is insufficient;On the other hand there is no explore new method to make Photochemical catalyst and the progress of low-grade diatomite are compound, and the photocatalytic nanometer particle that most enterprises use is easy reunion, bad dispersibility, Cannot preferably load causes to achieve the effect that degradation of contaminant over celite, often appears as to air purification effect It is bad, do not reach the functional performance etc. publicized in the market.
Invention content
The present invention provides a kind of high activity functional form diatom oozes and preparation method thereof, are activated to low-grade diatomite Processing makes photochemical catalyst be carried out with low-grade diatomite compound, prepares functional form diatom ooze, improve low-grade diatomaceous comprehensive It closes and utilizes.
A kind of high activity functional form diatom ooze of the present invention, it is characterised in that mainly by following weight part ratio Made of raw material:
Diatomite/nano zine oxide composite photocatalyst material(10-50 parts), white cement(10-60 parts), coarse whiting(10-60 parts), it is sliding Mountain flour(5-40 parts), sand(10-100 parts), grey calcium(10-50 parts), bentonite(5-60 parts), polymer dispersion powder(0.1-2 parts)、 Polypropylene fibre(0.1-2 parts), polyvinyl alcohol(0.1-1 parts).
The preparation method of a kind of high activity functional form diatom ooze of the present invention, it is characterised in that include the following steps:
1)The vitriol lixiviation 1-5h processing of two three-level diatomite of 100-200 mesh addition 30-80% is placed in high temperature furnace and is calcined, Initial temperature is set as 50 DEG C, 5 DEG C/min of heating rate, anaerobic thermal activation treatment temperature is 300-800 DEG C, the thermal activation time For 1-5h, it is cooled to room temperature to get to the diatomite after activation;
2)After mixing by the citric acid of the zinc nitrate of 15-25mol and 1mol, the distilled water of 100-500mol is added;By its It stirs evenly, while instilling the absolute ethyl alcohol of 10-40mol slowly, then instill the ammonium hydroxide of 1-10mol slowly, be secondly added The polyethylene glycol of 0.01-0.1mol after being then ultrasonically treated 40-80min, is placed in 60-100 DEG C of water temperature and carries out magnetic current stirring 1- 6h obtains suspension;Diatomite after activation is pressed 4 with suspension:1 molar ratio mixing.It is uniformly mixed, stands 1-8h, dry Dry, grinding obtains diatomite/nano zine oxide composite photocatalyst material powder in high temperature furnace after 200-800 DEG C of calcining 2-8h Body;
3)By step 2)Middle diatomite/nano zine oxide composite photocatalyst material(10-50 parts)With white cement(10-60 parts), again Calcium(10-60 parts), talcum powder(5-40 parts), sand(10-100 parts), grey calcium(10-50 parts), bentonite(5-60 parts), dispersible breast Rubber powder(0.1-2 parts), polypropylene fibre(0.1-2 parts), polyvinyl alcohol(0.1-1 parts)Mixing, according to turning for 300-900r/min Speed is stirred, and is kept color stuffing evenly dispersed, is slowly added into water(40-100 parts), antifoaming agent(0.01-0.05 parts), according to The rotating speed of 1000-3000r/min is stirred, and obtains stable uniformly mixed paste diatom ooze.
The present invention improves diatomaceous pozzolanic activity using low temperature oxygen-free thermal activation method, and being used as active blend can Hydration reaction occurs with hydrated products such as cement, grey calcium in diatom ooze, improves durability, then negative pressure load method is used to prepare Diatomite/nano zine oxide composite photocatalyst material realizes adsorption and enrichment using the synergistic effect of diatomite and nano zine oxide Degradation harmful substance reaches the functional purpose such as purification.
The positive effect of the present invention is:By carrying out low temperature oxygen-free thermal activation to the diatomite after purification, by nano oxygen Change zinc load on it, regulating and controlling effect on the one hand is played to diatomaceous aperture, more multi-stage porous is produced, is conducive to water On the other hand the absorption of molecule and pollutant makes tripolite loading nano zinc oxide photocatalysis material pair using negative pressure load method Pollutant can effectively degrade, and the diatom ooze durability not only prepared is high, functional performance is good, and improves low-grade silicon The comprehensive utilization of diatomaceous earth.Not only fundamentally solve the diatomite used in diatom ooze do not have activity cause hardness deficiency picking, The problems such as PARA FORMALDEHYDE PRILLS(91,95) absorption degradation rate is low, and ensure that low-grade diatomaceous reasonable utilization, resource are not wasted.
Specific implementation mode
Discussed below specific examples are only used to explain the present invention, does not limit the invention in any way, not Under the premise of technical solution of the invention, those of ordinary skill in the art made for the present invention are easy to implement to be appointed What, which is changed or changes, falls within scope of the presently claimed invention.
Embodiment 1
1)The vitriol lixiviation 3h processing of 150 mesh, two three-level diatomite addition 60% is placed in high temperature furnace, at anaerobic thermal activation It is 600 DEG C to manage temperature, and the thermal activation time is 2h, is cooled to room temperature to get to the diatomite after activation;
2)After mixing by the citric acid of the zinc nitrate of 20mol and 1mol, the distilled water of 200mol is added.It is stirred for It is even, while the absolute ethyl alcohol of 20mol is instilled slowly, then the ammonium hydroxide of 2mol is instilled slowly, the poly- second of 0.05mol is secondly added Glycol after being then ultrasonically treated 60min, is placed on progress magnetic current stirring 5h in 80 DEG C of water temperatures and obtains suspension;By the silicon after activation Diatomaceous earth presses 4 with suspension:1 molar ratio mixing.It is uniformly mixed, stands 1h, dry, grinding, 600 DEG C of calcining 2h in high temperature furnace Afterwards, diatomite/nano zine oxide composite photocatalyst material powder is obtained;
3)By step 2)In obtained diatomite/nano zine oxide composite photocatalyst material 25kg and white cement 15kg, coarse whiting 20kg, talcum powder 10kg, sand 20kg, grey calcium 20kg, bentonite 10kg, 0.5 kg of polymer dispersion powder, polypropylene fibre 0.2 Kg, 0.3 kg of polyvinyl alcohol, are stirred according to the rotating speed of 500r/min, keep color stuffing evenly dispersed, be slowly added into water 80 Kg, 0.02 kg of antifoaming agent, is stirred according to the rotating speed of 2000r/min, obtains stable uniformly mixed paste diatom ooze.
Embodiment 2:
The embodiment selects diatomite in the market to prepare diatom ooze, is blank control group
1)Select diatomite general in the market(By 1000 DEG C or more of temperature calcination)As functional filler;
2)After mixing by the citric acid of the zinc nitrate of 25mol and 1mol, the distilled water of 230mol is added.It is stirred for It is even, while the absolute ethyl alcohol of 30mol is instilled slowly, then the ammonium hydroxide of 5mol is instilled slowly, the poly- second of 0.03mol is secondly added Glycol after being then ultrasonically treated 60min, is placed on progress magnetic current stirring 2h in 80 DEG C of water temperatures and obtains suspension;By the silicon after activation Diatomaceous earth presses 6 with suspension:1 molar ratio mixing.It is uniformly mixed, stands 4h, dry, grinding, 600 DEG C of calcining 2h in high temperature furnace Afterwards, diatomite/nano zine oxide composite photocatalyst material powder is obtained;
3)By step 2)In obtained diatomite/nano zine oxide composite photocatalyst material 25kg and white cement 15kg, coarse whiting 20kg, talcum powder 10kg, sand 20kg, grey calcium 20kg, bentonite 10kg, polymer dispersion powder 0.5kg, polypropylene fibre 0.2kg, Polyvinyl alcohol 0.3kg is stirred according to the rotating speed of 500r/min, keeps color stuffing evenly dispersed, is slowly added into water 80kg, defoaming Agent 0.02kg is stirred according to the rotating speed of 2000r/min, obtains stable uniformly mixed paste diatom ooze.
Embodiment 3:
The embodiment selects the diatomite of common law supported nano zinc oxide to prepare diatom ooze
1)The vitriol lixiviation 2h processing of 180 mesh, two three-level diatomite addition 40% is placed in high temperature furnace, at anaerobic thermal activation It is 600 DEG C to manage temperature, and the thermal activation time is 2h, is cooled to room temperature to get to the diatomite after activation;
2)After mixing by the citric acid of the zinc nitrate of 25mol and 1mol, the distilled water of 280mol is added.It is stirred for It is even, while the absolute ethyl alcohol of 40mol is instilled slowly, then the ammonium hydroxide of 3mol is instilled slowly, the poly- second of 0.05mol is secondly added Glycol after being then ultrasonically treated 60min, is placed on progress magnetic current stirring 2h in 100 DEG C of water temperatures and obtains suspension;By the silicon after activation Diatomaceous earth presses 5 with suspension:1 molar ratio mixing.It is uniformly mixed, stands 5h, dry, grinding, 600 DEG C of calcining 2h in high temperature furnace Afterwards, diatomite/nano zine oxide composite photocatalyst material powder is obtained;
3)By step 2)In obtained diatomite/nano zine oxide composite photocatalyst material 30kg and white cement 15kg, coarse whiting 20kg, talcum powder 10kg, sand 30kg, grey calcium 20kg, bentonite 10kg, polymer dispersion powder 0.5kg, polypropylene fibre 0.2kg, Polyvinyl alcohol 0.3kg is stirred according to the rotating speed of 500r/min, keeps color stuffing evenly dispersed, is slowly added into water 80kg, defoaming Agent 0.02kg is stirred according to the rotating speed of 2500r/min, obtains stable uniformly mixed paste diatom ooze.
Embodiment 4:
1)The vitriol lixiviation 1h processing of 200 mesh, two three-level diatomite addition 80% is placed in high temperature furnace, at anaerobic thermal activation It is 600 DEG C to manage temperature, and the thermal activation time is 2h, is cooled to room temperature to get to the diatomite after activation;
2)After mixing by the citric acid of the zinc nitrate of 35mol and 1mol, the distilled water of 350mol is added.It is stirred for It is even, while the absolute ethyl alcohol of 20mol is instilled slowly, then the ammonium hydroxide of 5mol is instilled slowly, the poly- second of 0.08mol is secondly added Glycol after being then ultrasonically treated 60min, is placed on progress magnetic current stirring 2h in 100 DEG C of water temperatures and obtains suspension;By the silicon after activation Diatomaceous earth presses 5 with suspension:1 molar ratio mixing.It is uniformly mixed, stands 7h, dry, grinding, 600 DEG C of calcining 2h in high temperature furnace Afterwards, diatomite/nano zine oxide composite photocatalyst material powder is obtained;
3)By step 2)In obtained diatomite/nano zine oxide composite photocatalyst material 15kg and white cement 15kg, coarse whiting 20kg, talcum powder 10kg, sand 20kg, grey calcium 20kg, bentonite 15kg, polymer dispersion powder 0.5kg, polypropylene fibre 0.2kg, Polyvinyl alcohol 0.3kg is stirred according to the rotating speed of 500r/min, keeps color stuffing evenly dispersed, is slowly added into water 90kg, defoaming Agent 0.01kg is stirred according to the rotating speed of 2000r/min, obtains stable uniformly mixed paste diatom ooze.
Test example
Table 1 is the Indexs measure to the diatom ooze items general performance prepared by embodiment 1-4, and table 2 is made to embodiment 1-4 The Indexs measure of standby diatom ooze various functions performance, table 3 are to be surveyed to the diatom ooze limits of harmful substances prepared by embodiment 1-4 Test result, wherein the detection of diatomaceous pozzolanic activity index is carried out according to GB/T12957-2005 regulations, diatom ooze General performance index, functional performance index and harmful substance, which are detected, to be carried out according to JC/T2177-2013 professional standards regulation.
The general performance index of 1 diatom ooze of table
The various functions performance indicator of 2 diatom ooze of table
3 diatom ooze limits of harmful substances test result of table
Conclusion:It is satisfied by professional standard, work(according to the general specification of the prepared diatom ooze of above-mentioned table 1,2,3 Energy property technology requires to be far above required by standard, and unharmful substance detection.By the experimental data of table 2 it is found that implementing From the point of view of example 1 is compared with embodiment 2, pozzolanic activity index improves 14.2%, illustrates diatomite under the conditions of low temperature oxygen-free thermal activation Pozzolanic activity be more than pozzolanic activity of diatomite under the conditions of high temperature thermal activation, can be with according to the picking situation after 30 days Find out, diatomaceous pozzolanic activity has strong influence to the durability of diatom ooze;Embodiment 4 can with the comparison of embodiment 1 :Diatom soil matrix composite photocatalyst material content has certain influence, content increase appropriate, silicon to the functional performance of diatom ooze The functional performance of algal gel is also correspondingly improved.
In conclusion the diatom ooze prepared by the present invention adequately considers diatomaceous activity and uses new method system The problem of standby diatomite/nano zine oxide composite photocatalyst material, achieves and improves hardness, the high effect of the activity that do not lose powder, institute A kind of high activity functional form diatom ooze and preparation method thereof has been obtained with the present invention.

Claims (2)

1. a kind of high activity functional form diatom ooze, it is characterised in that mainly made of the raw material of following weight part ratio:
Diatomite/nano zine oxide composite photocatalyst material(10-50 parts), white cement(10-60 parts), coarse whiting(10-60 parts)、
Talcum powder(5-40 parts), sand(10-100 parts), grey calcium(10-50 parts), bentonite(5-60 parts)、
Polymer dispersion powder(0.1-2 parts), polypropylene fibre(0.1-2 parts), polyvinyl alcohol(0.1-1 parts).
2. a kind of preparation method of high activity functional form diatom ooze according to claim 1, it is characterised in that including following Step:
1)The vitriol lixiviation 1-5h processing of two three-level diatomite of 100-200 mesh addition 30-80% is placed in high temperature furnace and is calcined, Initial temperature is set as 50 DEG C, 5 DEG C/min of heating rate, anaerobic thermal activation treatment temperature is 300-800 DEG C, the thermal activation time For 1-5h, it is cooled to room temperature to get to the diatomite after activation;
2)After mixing by the citric acid of the zinc nitrate of 15-25mol and 1mol, the distilled water of 100-500mol is added;By its It stirs evenly, while instilling the absolute ethyl alcohol of 10-40mol slowly, then instill the ammonium hydroxide of 1-10mol slowly, be secondly added The polyethylene glycol of 0.01-0.1mol after being then ultrasonically treated 40-80min, is placed in 60-100 DEG C of water temperature and carries out magnetic current stirring 1- 6h obtains suspension;Diatomite after activation is pressed 4 with suspension:1 molar ratio mixing;
It is uniformly mixed, stands 1-8h, dry, grinding obtains diatomite/nanometer in high temperature furnace after 200-800 DEG C of calcining 2-8h Zinc oxide composite photocatalyst material powder;
3)By step 2)Middle diatomite/nano zine oxide composite photocatalyst material(10-50 parts)With white cement(10-60 parts), again Calcium(10-60 parts), talcum powder(5-40 parts), sand(10-100 parts), grey calcium(10-50 parts), bentonite(5-60 parts), dispersible breast Rubber powder(0.1-2 parts), polypropylene fibre(0.1-2 parts), polyvinyl alcohol(0.1-1 parts)Mixing, according to turning for 300-900r/min Speed is stirred, and is kept color stuffing evenly dispersed, is slowly added into water(40-100 parts), antifoaming agent(0.01-0.05 parts), according to The rotating speed of 1000-3000r/min is stirred, and obtains stable uniformly mixed paste diatom ooze.
CN201810360674.0A 2018-04-20 2018-04-20 A kind of high activity functional form diatom ooze and preparation method thereof Pending CN108587265A (en)

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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN113244887A (en) * 2021-05-17 2021-08-13 吉林建筑大学 Preparation method of high-functionality graphene diatomite composite material

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Application publication date: 20180928