CN105498710A - Preparation method for preparing modified compound calcium-based carbon dioxide adsorbent through fishbone - Google Patents

Preparation method for preparing modified compound calcium-based carbon dioxide adsorbent through fishbone Download PDF

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CN105498710A
CN105498710A CN201510952347.0A CN201510952347A CN105498710A CN 105498710 A CN105498710 A CN 105498710A CN 201510952347 A CN201510952347 A CN 201510952347A CN 105498710 A CN105498710 A CN 105498710A
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carbon dioxide
container
calcium
fish
subsequently
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高大元
宋国
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    • 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
    • B01J20/24Naturally occurring macromolecular compounds, e.g. humic acids or their derivatives
    • 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
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2253/00Adsorbents used in seperation treatment of gases and vapours
    • B01D2253/20Organic adsorbents
    • BPERFORMING OPERATIONS; TRANSPORTING
    • B01PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
    • B01DSEPARATION
    • B01D2257/00Components to be removed
    • B01D2257/50Carbon oxides
    • B01D2257/504Carbon dioxide
    • 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02CCAPTURE, STORAGE, SEQUESTRATION OR DISPOSAL OF GREENHOUSE GASES [GHG]
    • Y02C20/00Capture or disposal of greenhouse gases
    • Y02C20/40Capture or disposal of greenhouse gases of CO2

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  • Analytical Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
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  • Oil, Petroleum & Natural Gas (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)

Abstract

The invention discloses a preparation method for preparing modified compound calcium-based carbon dioxide adsorbent through fishbone, and belongs to the technical field of environment protection. For the problem that at present, because the repeated utilization adsorption rate of calcium-based carbon dioxide adsorbent in the carbon dioxide adsorption process is decreased and the calcium-based carbon dioxide adsorbent can not be used any more, cost is increased, the internal structures of fishbone are protected through liquid nitrogen first, high-temperature processing is then conducted, impurities in fishbone are removed through instantaneous high temperature, preliminary enzymolysis is then conducted on fishbone so that polypeptide and amino acid substances can be attached to the inner portions of fishbone, calcium inside fishbone is protected and then react with acid substances, an initial body for compounding and modifying the compound calcium-based carbon dioxide adsorbent is formed and mixed with sodium silicate and the like, and laser strengthening is conducted so that the internal structures of the modified compound calcium-based carbon dioxide adsorbent can be expanded; meanwhile, silicon salt, aluminum and other substances are adsorbed to the inner portion of the modified compound calcium-based carbon dioxide adsorbent, the carbon dioxide adsorption capacity of the modified compound calcium-based carbon dioxide adsorbent is increased, and then the modified compound calcium-based carbon dioxide adsorbent which can be repeatedly used and has the carbon dioxide adsorption rate of 75% or above is prepared.

Description

A kind of preparation method utilizing fish-bone to prepare modification composite calcium-base carbon dioxide absorber
Technical field
The invention discloses a kind of preparation method utilizing fish-bone to prepare modification composite calcium-base carbon dioxide absorber, belong to environmental technology field.
Background technology
At present, with CO 2global warming caused by main greenhouse gases has been subject to the common concern of countries in the world.The data display of U.S.'s announcement in 2004, the global CO from 2000 to 2004 2emission level increases by 3% every year---and this speed is that nineteen ninety was to CO in 1999 2discharge gather way (1.1%) nearly 3 times.This will cause migrating of vegetation and species extinction, and climate zone moves, and sea level rise floods with land, the phenomenons such as ocean current changes and EI Nino takes place frequently.China is CO 2discharge big country, especially coal fired power plant CO 2emission control arrived instant stage.
The technology of calcium oxide-based Capture by Sorbents carbon dioxide is mainly based on the thought (CalciumCarbonateLooping) of Calcium Carbonate Cyclic, carbon dioxide is separated from flue gas with the chemical reaction of carbon dioxide by adsorbent, then under carbon dioxide enriched environment by absorption product high-temperature calcination, obtain the carbon dioxide of high concentration, and then carry out again compressing, transporting and storage work.Technique early-stage Study, mainly in natural limestone, because it has cheap, widely distributed feature, and is widely used; But, due to the restriction of the architectural characteristic of natural limestone own, cause it when recycling, sorption enhanced rate (sorption enhanced rate=be converted into the calcium oxide-based adsorbent/adsorbent total amount of calcium carbonate) for carbon dioxide acutely declines along with the increase of cycle-index, thus considerably increases cost absorption.In recent years, increasing researcher starts the modification work paying close attention to calcium oxide base class adsorbent, thus improves its absorptivity to carbon dioxide (conversion ratio of natural limestone is about 60%) and the rate that can be recycled.
Summary of the invention
The technical problem that the present invention mainly solves: for Ca-base adsorbent traditional at present in absorbing carbon dioxide process, sharply decline owing to reusing adsorption rate, and can not re-use, increase the problem of cost, first the present invention uses liquid nitrogen to protect fish-bone internal structure, carry out high-temperature process subsequently, instantaneous high-temperature removes the inner impurity of fish-bone, carried out preliminary enzymolysis again, make its inner attachment polypeptide and amino acid material, the calcium of inside is protected, then react with acidic materials, form composite modified composite calcium-base carbon dioxide absorber just body, finally it is mixed with sodium metasilicate etc., carry out laser reinforcing, its internal structure is expanded, make its inner material such as absorption silicon salt and aluminium etc. simultaneously, increase its adsorption capacity to carbon dioxide, prepare a kind of reusable, carbon dioxide absorption rate reaches the modification composite calcium-base carbon dioxide absorber of more than 75%.
In order to solve the problems of the technologies described above, the technical solution adopted in the present invention is:
(1) 600 ~ 900g fish-bone is got, remove surface impurity, use liquid nitrogen to be cooled to-10 ~-5 DEG C to fish-bone, after then keeping temperature 2 ~ 4min, pulverizer is put in fish-bone taking-up pulverize, sieve to obtain 30 ~ 50 order fish-bone powder, puts it into subsequently in Muffle furnace, design temperature 500 ~ 600 DEG C, keep temperature, preliminary pyrolysis 3 ~ 6min, then taken out, obtain pre-treated fish bone powder;
(2) the fish-bone powder of gained is put into container, add 20 ~ 30g compound fertilizer production and 10 ~ 15g laccase wherein, mix, then the hydrochloric acid solution that mass fraction is 5 ~ 10% is added wherein, flood mixture 2 ~ 3cm, moved in water-bath by container subsequently and heat, temperature is set as 35 ~ 40 DEG C, with rotating speed 130 ~ 150r/min, stir enzymolysis 1 ~ 2h;
(3) filtration under diminished pressure after above-mentioned stirring terminates, collect filtrate, the filtrate of gained is put into baking oven dry, put it into subsequently in container, add the alcohol solution dipping filtrate that mass fraction is 30 ~ 50% wherein, then respectively to wherein adding 50 ~ 60mL acetic acid and 40 ~ 50mL lactic acid, stir, then 40 ~ 50 DEG C are heated to container, keep temperature ageing 12 ~ 15h;
(4) after above-mentioned ageing terminates, add 4 ~ 6mL methyl acrylate wherein, after mixing, container is lowered the temperature, with rotating speed 100 ~ 110r/min, slow stirring, cooling, until produce without white precipitate, keeps 1 ~ 3min, filters subsequently, collecting filtrate carries out air-dry, obtains composite calcium-base carbon dioxide absorber just body;
(5) by the composite calcium-base carbon dioxide absorber of above-mentioned gained, sodium acid carbonate and Aluminate, 5:2:1 in mass ratio, mix, the mixture of gained is put into glass container, adds soaked in absolute ethyl alcohol mixture wherein, then add the sodium metasilicate of Aluminate quality 5 ~ 10% wherein, stir, subsequently by container until 50 ~ 80s in laser reinforcing device, pulse width set is 20 ~ 25ns, and repetition rate is 4 ~ 8Hz;
(6) after above-mentioned laser reinforcing, container is taken out, adds 100 ~ 150mL distilled water wherein, be heated to 80 ~ 90 DEG C, keep temperature 2 ~ 3h, then add calcium hydroxide wherein, pH is regulated to be 6.5 ~ 7.0, subsequently it is cooled to and produces without precipitation, then the mixture in container is put into centrifuge carry out centrifugation, collect centrifugal thing, dry, pulverize, sieve to obtain 90 ~ 100 order particles, can obtain modification composite calcium-base carbon dioxide absorber.
Application process of the present invention: in a calcining furnace, first pass into N 2, make in calcining furnace, to be full of protective gas N 2, in order to avoid the existence of air, weigh 10g modification composite calcium-base carbon dioxide absorber and be placed in sample tray, calcining is by 200 DEG C, temperature rises to 800 ~ 950 DEG C, when in pallet, sample quality no longer changes, extend calcination time 5 ~ 10min, it is made to activate completely, after its activation, taking 5g modification composite calcium-base carbon dioxide absorber is respectively positioned in pallet, with being placed in two containers, one uses carbon dioxide to protect container, one uses nitrogen to protect it, when in pallet, sample quality no longer changes, taken out respectively, take quality to obtain, the quality using the modification composite calcium-base carbon dioxide absorber of carbon-dioxide protecting is 8.6 ~ 9.1g, the quality of the modification composite calcium-base carbon dioxide absorber of nitrogen protection is used to remain unchanged, quality is taken after repeating test 170 ~ 190 times, the modification composite calcium-base carbon dioxide absorber detecting use carbon-dioxide protecting obtains its conversion ratio and reaches 30 ~ 35%.
The invention has the beneficial effects as follows:
(1) adsorbent obtained by the made the present invention of the present invention, absorbing carbon dioxide that can be permanent, compared with traditional, persistence adds 20 ~ 30%;
(2) adsorbent obtained by the present invention is easy to operation, and cost is low.
Detailed description of the invention
Get 600 ~ 900g fish-bone, remove surface impurity, use liquid nitrogen to be cooled to-10 ~-5 DEG C to fish-bone, after then keeping temperature 2 ~ 4min, pulverizer is put in fish-bone taking-up pulverize, sieve to obtain 30 ~ 50 order fish-bone powder, puts it into subsequently in Muffle furnace, design temperature 500 ~ 600 DEG C, keep temperature, preliminary pyrolysis 3 ~ 6min, then taken out, obtain pre-treated fish bone powder; The fish-bone powder of gained is put into container, add 20 ~ 30g compound fertilizer production and 10 ~ 15g laccase wherein, mix, then the hydrochloric acid solution that mass fraction is 5 ~ 10% is added wherein, flood mixture 2 ~ 3cm, moved in water-bath by container subsequently and heat, temperature is set as 35 ~ 40 DEG C, with rotating speed 130 ~ 150r/min, stir enzymolysis 1 ~ 2h;
Filtration under diminished pressure after above-mentioned stirring terminates, collect filtrate, the filtrate of gained is put into baking oven dry, put it into subsequently in container, add the alcohol solution dipping filtrate that mass fraction is 30 ~ 50% wherein, then respectively to wherein adding 50 ~ 60mL acetic acid and 40 ~ 50mL lactic acid, stir, then 40 ~ 50 DEG C are heated to container, keep temperature ageing 12 ~ 15h; After above-mentioned ageing terminates, add 4 ~ 6mL methyl acrylate wherein, after mixing, container is lowered the temperature, with rotating speed 100 ~ 110r/min, slow stirring, cooling, until produce without white precipitate, keeps 1 ~ 3min, filters subsequently, collecting filtrate carries out air-dry, obtains composite calcium-base carbon dioxide absorber just body; By the composite calcium-base carbon dioxide absorber of above-mentioned gained, sodium acid carbonate and Aluminate, 5:2:1 in mass ratio, mix, the mixture of gained is put into glass container, adds soaked in absolute ethyl alcohol mixture wherein, then add the sodium metasilicate of Aluminate quality 5 ~ 10% wherein, stir, subsequently by container until 50 ~ 80s in laser reinforcing device, pulse width set is 20 ~ 25ns, and repetition rate is 4 ~ 8Hz; After above-mentioned laser reinforcing, container is taken out, adds 100 ~ 150mL distilled water wherein, be heated to 80 ~ 90 DEG C, keep temperature 2 ~ 3h, then add calcium hydroxide wherein, pH is regulated to be 6.5 ~ 7.0, subsequently it is cooled to and produces without precipitation, then the mixture in container is put into centrifuge carry out centrifugation, collect centrifugal thing, dry, pulverize, sieve to obtain 90 ~ 100 order particles, can obtain modification composite calcium-base carbon dioxide absorber.
Example 1
Get 700g fish-bone, remove surface impurity, use liquid nitrogen to be cooled to-8 DEG C to fish-bone, after then keeping temperature 3min, pulverizer is put in fish-bone taking-up pulverize, sieve to obtain 40 order fish-bone powder, puts it into subsequently in Muffle furnace, design temperature 550 DEG C, keep temperature, preliminary pyrolysis 5min, then taken out, obtain pre-treated fish bone powder; The fish-bone powder of gained is put into container, add 25g compound fertilizer production and 12g laccase wherein, mix, then the hydrochloric acid solution that mass fraction is 8% is added wherein, flood mixture 2cm, moved in water-bath by container subsequently and heat, temperature is set as 38 DEG C, with rotating speed 140r/min, stir enzymolysis 2h; Filtration under diminished pressure after above-mentioned stirring terminates, collect filtrate, the filtrate of gained is put into baking oven dry, put it into subsequently in container, add the alcohol solution dipping filtrate that mass fraction is 40% wherein, then respectively to wherein adding 55mL acetic acid and 45mL lactic acid, stir, then 45 DEG C are heated to container, keep temperature ageing 14h; After above-mentioned ageing terminates, add 5mL methyl acrylate wherein, after mixing, container is lowered the temperature, with rotating speed 105/min, slow stirring, cooling, until produce without white precipitate, keeps 2min, filters subsequently, collecting filtrate carries out air-dry, obtains composite calcium-base carbon dioxide absorber just body; By the composite calcium-base carbon dioxide absorber of above-mentioned gained, sodium acid carbonate and Aluminate, 5:2:1 in mass ratio, mix, the mixture of gained is put into glass container, adds soaked in absolute ethyl alcohol mixture wherein, then add the sodium metasilicate of Aluminate quality 8% wherein, stir, subsequently by container until 70s in laser reinforcing device, pulse width set is 205ns, and repetition rate is 6Hz; After above-mentioned laser reinforcing, container is taken out, adds 120mL distilled water wherein, be heated to 85 DEG C, keep temperature 2h, then add calcium hydroxide wherein, pH is regulated to be 7.0, subsequently it is cooled to and produces without precipitation, then the mixture in container is put into centrifuge carry out centrifugation, collect centrifugal thing, dry, pulverize, sieve to obtain 90 order particles, can obtain modification composite calcium-base carbon dioxide absorber.
In a calcining furnace, first pass into N 2, make in calcining furnace, to be full of protective gas N 2, in order to avoid the existence of air, weigh 10g modification composite calcium-base carbon dioxide absorber and be placed in sample tray, calcining is by 200 DEG C, temperature rises to 800 DEG C, when in pallet, sample quality no longer changes, extend calcination time 5min, it is made to activate completely, after its activation, taking 5g modification composite calcium-base carbon dioxide absorber is respectively positioned in pallet, with being placed in two containers, one uses carbon dioxide to protect container, one uses nitrogen to protect it, when in pallet, sample quality no longer changes, taken out respectively, take quality to obtain, the quality using the modification composite calcium-base carbon dioxide absorber of carbon-dioxide protecting is 8.6g, the quality of the modification composite calcium-base carbon dioxide absorber of nitrogen protection is used to remain unchanged, quality is taken after repeating test 170 times, the modification composite calcium-base carbon dioxide absorber detecting use carbon-dioxide protecting obtains its conversion ratio and reaches 30%.
Example 2
Get 900g fish-bone, remove surface impurity, use liquid nitrogen to be cooled to-5 DEG C to fish-bone, after then keeping temperature 4min, pulverizer is put in fish-bone taking-up pulverize, sieve to obtain 50 order fish-bone powder, puts it into subsequently in Muffle furnace, design temperature 600 DEG C, keep temperature, preliminary pyrolysis 6min, then taken out, obtain pre-treated fish bone powder; The fish-bone powder of gained is put into container, add 30g compound fertilizer production and 15g laccase wherein, mix, then the hydrochloric acid solution that mass fraction is 10% is added wherein, flood mixture 3cm, moved in water-bath by container subsequently and heat, temperature is set as 40 DEG C, with rotating speed 150r/min, stir enzymolysis 2h; Filtration under diminished pressure after above-mentioned stirring terminates, collect filtrate, the filtrate of gained is put into baking oven dry, put it into subsequently in container, add the alcohol solution dipping filtrate that mass fraction is 50% wherein, then respectively to wherein adding 60mL acetic acid and 50mL lactic acid, stir, then 50 DEG C are heated to container, keep temperature ageing 15h; After above-mentioned ageing terminates, add 6mL methyl acrylate wherein, after mixing, container is lowered the temperature, with rotating speed 110r/min, slow stirring, cooling, until produce without white precipitate, keeps 3min, filters subsequently, collecting filtrate carries out air-dry, obtains composite calcium-base carbon dioxide absorber just body; By the composite calcium-base carbon dioxide absorber of above-mentioned gained, sodium acid carbonate and Aluminate, 5:2:1 in mass ratio, mix, the mixture of gained is put into glass container, adds soaked in absolute ethyl alcohol mixture wherein, then add the sodium metasilicate of Aluminate quality 10% wherein, stir, subsequently by container until 80s in laser reinforcing device, pulse width set is 25ns, and repetition rate is 8Hz; After above-mentioned laser reinforcing, container is taken out, adds 150mL distilled water wherein, be heated to 90 DEG C, keep temperature 3h, then add calcium hydroxide wherein, pH is regulated to be 7.0, subsequently it is cooled to and produces without precipitation, then the mixture in container is put into centrifuge carry out centrifugation, collect centrifugal thing, dry, pulverize, sieve to obtain 100 order particles, can obtain modification composite calcium-base carbon dioxide absorber.
In a calcining furnace, first pass into N 2, make in calcining furnace, to be full of protective gas N 2, in order to avoid the existence of air, weigh 10g modification composite calcium-base carbon dioxide absorber and be placed in sample tray, calcining is by 200 DEG C, temperature rises to 950 DEG C, when in pallet, sample quality no longer changes, extend calcination time 5 ~ 10min, it is made to activate completely, after its activation, taking 5g modification composite calcium-base carbon dioxide absorber is respectively positioned in pallet, with being placed in two containers, one uses carbon dioxide to protect container, one uses nitrogen to protect it, when in pallet, sample quality no longer changes, taken out respectively, take quality to obtain, the quality using the modification composite calcium-base carbon dioxide absorber of carbon-dioxide protecting is 9.1g, the quality of the modification composite calcium-base carbon dioxide absorber of nitrogen protection is used to remain unchanged, quality is taken after repeating test 190 times, the modification composite calcium-base carbon dioxide absorber detecting use carbon-dioxide protecting obtains its conversion ratio and reaches 35%.
Example 3
Get 600g fish-bone, remove surface impurity, use liquid nitrogen to be cooled to-10 DEG C to fish-bone, after then keeping temperature 2min, pulverizer is put in fish-bone taking-up pulverize, sieve to obtain 30 order fish-bone powder, puts it into subsequently in Muffle furnace, design temperature 500 DEG C, keep temperature, preliminary pyrolysis 3min, then taken out, obtain pre-treated fish bone powder; The fish-bone powder of gained is put into container, add 20g compound fertilizer production and 10g laccase wherein, mix, then the hydrochloric acid solution that mass fraction is 5% is added wherein, flood mixture 2cm, moved in water-bath by container subsequently and heat, temperature is set as 35 DEG C, with rotating speed 130r/min, stir enzymolysis 1h; Filtration under diminished pressure after above-mentioned stirring terminates, collect filtrate, the filtrate of gained is put into baking oven dry, put it into subsequently in container, add the alcohol solution dipping filtrate that mass fraction is 30% wherein, then respectively to wherein adding 50mL acetic acid and 40mL lactic acid, stir, then 40 DEG C are heated to container, keep temperature ageing 12h; After above-mentioned ageing terminates, add 4mL methyl acrylate wherein, after mixing, container is lowered the temperature, with rotating speed 100r/min, slow stirring, cooling, until produce without white precipitate, keeps 1min, filters subsequently, collecting filtrate carries out air-dry, obtains composite calcium-base carbon dioxide absorber just body; By the composite calcium-base carbon dioxide absorber of above-mentioned gained, sodium acid carbonate and Aluminate, 5:2:1 in mass ratio, mix, the mixture of gained is put into glass container, adds soaked in absolute ethyl alcohol mixture wherein, then add the sodium metasilicate of Aluminate quality 5% wherein, stir, subsequently by container until 50s in laser reinforcing device, pulse width set is 20ns, and repetition rate is 4Hz; After above-mentioned laser reinforcing, container is taken out, adds 100mL distilled water wherein, be heated to 80 DEG C, keep temperature 2h, then add calcium hydroxide wherein, pH is regulated to be 6.5, subsequently it is cooled to and produces without precipitation, then the mixture in container is put into centrifuge carry out centrifugation, collect centrifugal thing, dry, pulverize, sieve to obtain 80 order particles, can obtain modification composite calcium-base carbon dioxide absorber.
In a calcining furnace, first pass into N 2, make in calcining furnace, to be full of protective gas N 2, in order to avoid the existence of air, weigh 10g modification composite calcium-base carbon dioxide absorber and be placed in sample tray, calcining is by 200 DEG C, temperature rises to 900 DEG C, when in pallet, sample quality no longer changes, extend calcination time 8min, it is made to activate completely, after its activation, taking 5g modification composite calcium-base carbon dioxide absorber is respectively positioned in pallet, with being placed in two containers, one uses carbon dioxide to protect container, one uses nitrogen to protect it, when in pallet, sample quality no longer changes, taken out respectively, take quality to obtain, the quality using the modification composite calcium-base carbon dioxide absorber of carbon-dioxide protecting is 8.8, the quality of the modification composite calcium-base carbon dioxide absorber of nitrogen protection is used to remain unchanged, quality is taken after repeating test 180 times, the modification composite calcium-base carbon dioxide absorber detecting use carbon-dioxide protecting obtains its conversion ratio and reaches 32%.

Claims (1)

1. utilize fish-bone to prepare a preparation method for modification composite calcium-base carbon dioxide absorber, it is characterized in that concrete preparation process is:
(1) 600 ~ 900g fish-bone is got, remove surface impurity, use liquid nitrogen to be cooled to-10 ~-5 DEG C to fish-bone, after then keeping temperature 2 ~ 4min, pulverizer is put in fish-bone taking-up pulverize, sieve to obtain 30 ~ 50 order fish-bone powder, puts it into subsequently in Muffle furnace, design temperature 500 ~ 600 DEG C, keep temperature, preliminary pyrolysis 3 ~ 6min, then taken out, obtain pre-treated fish bone powder;
(2) the pre-treated fish bone powder of gained is put into container, add 20 ~ 30g compound fertilizer production and 10 ~ 15g laccase wherein, mix, then the hydrochloric acid solution that mass fraction is 5 ~ 10% is added wherein, flood mixture 2 ~ 3cm, moved in water-bath by container subsequently and heat, temperature is set as 35 ~ 40 DEG C, with rotating speed 130 ~ 150r/min, stir enzymolysis 1 ~ 2h;
(3) filtration under diminished pressure after above-mentioned stirring terminates, collect filtrate, the filtrate of gained is put into baking oven dry, put it into subsequently in container, add the alcohol solution dipping filtrate that mass fraction is 30 ~ 50% wherein, then respectively to wherein adding 50 ~ 60mL acetic acid and 40 ~ 50mL lactic acid, stir, then 40 ~ 50 DEG C are heated to container, keep temperature ageing 12 ~ 15h;
(4) after above-mentioned ageing terminates, add 4 ~ 6mL methyl acrylate wherein, after mixing, container is lowered the temperature, with rotating speed 100 ~ 110r/min, slow stirring, cooling, until produce without white precipitate, keeps 1 ~ 3min, filters subsequently, collecting filtrate carries out air-dry, obtains composite calcium-base carbon dioxide absorber just body;
(5) by the composite calcium-base carbon dioxide absorber of above-mentioned gained, sodium acid carbonate and Aluminate, 5:2:1 in mass ratio, mix, the mixture of gained is put into glass container, adds soaked in absolute ethyl alcohol mixture wherein, then add the sodium metasilicate of Aluminate quality 5 ~ 10% wherein, stir, subsequently by container until 50 ~ 80s in laser reinforcing device, pulse width set is 20 ~ 25ns, and repetition rate is 4 ~ 8Hz;
(6) after above-mentioned laser reinforcing, container is taken out, adds 100 ~ 150mL distilled water wherein, be heated to 80 ~ 90 DEG C, keep temperature 2 ~ 3h, then add calcium hydroxide wherein, pH is regulated to be 6.5 ~ 7.0, subsequently it is cooled to and produces without precipitation, then the mixture in container is put into centrifuge carry out centrifugation, collect centrifugal thing, dry, pulverize, sieve to obtain 90 ~ 100 order particles, can obtain modification composite calcium-base carbon dioxide absorber.
CN201510952347.0A 2015-12-20 2015-12-20 Preparation method for preparing modified compound calcium-based carbon dioxide adsorbent through fishbone Pending CN105498710A (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110721664A (en) * 2019-10-10 2020-01-24 浙江海洋大学 Preparation method of mussel shell powder/carboxymethyl cellulose composite gel adsorbent
CN111389366A (en) * 2020-04-20 2020-07-10 南华大学 Modification method of activated carbon, modified activated carbon and application thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN101269320A (en) * 2008-05-16 2008-09-24 东南大学 Method for preparing calcium group carbonic anhydride adsorption agent
US20090084731A1 (en) * 2007-10-01 2009-04-02 Talley Jeffrey W Biogenic template for enhanced sorption of contaminants
CN104923159A (en) * 2015-06-15 2015-09-23 武汉理工大学 Fish bone charcoal adsorbent and preparation method and application thereof
CN104959132A (en) * 2015-06-16 2015-10-07 昆明理工大学 Preparation method of carbon dioxide calcium-based adsorbent

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20090084731A1 (en) * 2007-10-01 2009-04-02 Talley Jeffrey W Biogenic template for enhanced sorption of contaminants
CN101269320A (en) * 2008-05-16 2008-09-24 东南大学 Method for preparing calcium group carbonic anhydride adsorption agent
CN104923159A (en) * 2015-06-15 2015-09-23 武汉理工大学 Fish bone charcoal adsorbent and preparation method and application thereof
CN104959132A (en) * 2015-06-16 2015-10-07 昆明理工大学 Preparation method of carbon dioxide calcium-based adsorbent

Non-Patent Citations (4)

* Cited by examiner, † Cited by third party
Title
EHAB M.ZAYED ET AL: "Potential use of novel modified fishbone for anchoring hazardous metal ions from their solutions", 《ECOLOGICAL ENGINEERING》 *
SARA CASTILHO ET AL: "Sorbents for CO2 capture from biogenesis calcium wastes", 《CHEMICAL ENGINEERING JOURNAL》 *
吴嵘等: "包硅改性纳米碳酸钙应用于高温CO2吸附的性能", 《化工学报》 *
夏文水等: "《大宗淡水鱼贮运保鲜与加工技术》", 30 April 2014 *

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN110721664A (en) * 2019-10-10 2020-01-24 浙江海洋大学 Preparation method of mussel shell powder/carboxymethyl cellulose composite gel adsorbent
CN110721664B (en) * 2019-10-10 2021-12-17 浙江海洋大学 Preparation method of mussel shell powder/carboxymethyl cellulose composite gel adsorbent
CN111389366A (en) * 2020-04-20 2020-07-10 南华大学 Modification method of activated carbon, modified activated carbon and application thereof

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