CN108636355A - A kind of preparation method from regeneration activity filtration core - Google Patents
A kind of preparation method from regeneration activity filtration core Download PDFInfo
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- CN108636355A CN108636355A CN201810568092.1A CN201810568092A CN108636355A CN 108636355 A CN108636355 A CN 108636355A CN 201810568092 A CN201810568092 A CN 201810568092A CN 108636355 A CN108636355 A CN 108636355A
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/02—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material
- B01J20/20—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof comprising inorganic material comprising free carbon; comprising carbon obtained by carbonising processes
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/30—Processes for preparing, regenerating, or reactivating
- B01J20/34—Regenerating or reactivating
- B01J20/3416—Regenerating or reactivating of sorbents or filter aids comprising free carbon, e.g. activated carbon
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01J—CHEMICAL OR PHYSICAL PROCESSES, e.g. CATALYSIS OR COLLOID CHEMISTRY; THEIR RELEVANT APPARATUS
- B01J20/00—Solid sorbent compositions or filter aid compositions; Sorbents for chromatography; Processes for preparing, regenerating or reactivating thereof
- B01J20/30—Processes for preparing, regenerating, or reactivating
- B01J20/34—Regenerating or reactivating
- B01J20/345—Regenerating or reactivating using a particular desorbing compound or mixture
- B01J20/3475—Regenerating or reactivating using a particular desorbing compound or mixture in the liquid phase
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- C—CHEMISTRY; METALLURGY
- C01—INORGANIC CHEMISTRY
- C01B—NON-METALLIC ELEMENTS; COMPOUNDS THEREOF; METALLOIDS OR COMPOUNDS THEREOF NOT COVERED BY SUBCLASS C01C
- C01B32/00—Carbon; Compounds thereof
- C01B32/30—Active carbon
- C01B32/312—Preparation
- C01B32/318—Preparation characterised by the starting materials
- C01B32/324—Preparation characterised by the starting materials from waste materials, e.g. tyres or spent sulfite pulp liquor
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Abstract
The present invention relates to a kind of preparation methods from regeneration activity filtration core, belong to water-purifying material preparing technical field.The present invention will digest filtrate and fermentation is blended in coconut husk crushed material,It will be reacted after reaction filter cake charing and after potassium rhodanate and the mixing of amino trimethyl phosphonic acids again,Note film is fired after the mixing of final and polyethylene,It obtains from regeneration activity filtration core,The present invention obtains the enzymolysis liquid rich in amino acid by enzymolysis first,Porous cocoanut shell particle by enzymolysis liquid and after crushing is blended in rich in being sealed by fermentation under microbial action,Then by the cocoanut shell containing carboxyl and amino and iron salt solutions hybrid reaction,Obtain activated carbon,Then activated carbon is blended with potassium rhodanate and amino trimethyl phosphonic acids,So that part metals ion removes in activated carbon,The generation in hole makes activated carbon oxidation produced by the present invention greatly improve,Activated carbon and water reaction generate the extremely strong hydroxyl radical free radical OH of oxidisability,It is finally reached voluntarily regenerated purpose,It has broad application prospects.
Description
Technical field
The present invention relates to a kind of preparation methods from regeneration activity filtration core, belong to water-purifying material preparing technical field.
Background technology
As the improvement of people's living standards, the requirement to water quality is also gradually increased, the quality of Drinking Water water quality with
Human health is closely related.But serious environmental disruption and pollution so that water quality also changes, and then influences the body of people
Body health, causes a series of vicious circle, seriously affects social progress and the health of the mankind.
Filter medium refer to it is all can make working media pass through and will wherein solid particle or drop retention with reach separation or
Purify the porosity of purpose.Currently, the filter core that water purification industry mostly uses greatly can be divided into three kinds of different roles:
(1)Filter the substances such as water body recovery technology macromolecular particle object and colloid;
(2)Organic chemical pollutant in adsorbed water body, such as remaining pesticide, biochemical fertilizer, herbicide, synthetic detergent and originally
The harmful substances such as water sterilization by-product chlorine residue;
(3)Filtering intercepts the halfway residual poisonous and harmful substance of pre-treatment and microorganism etc..
It has been the most commonly used means for the purification of water body currently with activated carbon, activated carbon fibre possesses flourishing
Specific surface area and narrow pore-size distribution have the function of to adsorb heterochromatic, peculiar smell and chlorine residue etc. in water, and removal effect is preferable, therefore
And it is widely used in during the water treatment of the various fields such as food, medicine, chemical industry, environmental protection.But active Carbon fibe
Easy saturation, intensity difference, dust are more, and adsorption capacity can successively decrease with usage time, cause effluent quality uneven, use is short
Adsorption function is lost after time, needs to be replaced frequently, involves great expense.Especially for the water body of high-content heavy metal ion
In, saturation is easily reached using activated carbon adsorption, and very high adsorption efficiency is not achieved.Cannot have in purification process simultaneously
The bacterium in water body is killed and inhibited to effect, limited to the detergent power of water body.
Therefore just need to develop a kind of material with efficient absorption amount to meet the needs of application.
Invention content
Present invention mainly solves the technical issues of, for current active filtration core absorption easily reach saturation, and
And adsorption capacity can successively decrease with usage time, cause effluent quality uneven, using after a short while i.e. lose adsorption function,
The defect needed to be replaced frequently provides a kind of preparation method from regeneration activity filtration core.
In order to solve the above-mentioned technical problem, the technical solution adopted in the present invention is:
A kind of preparation method from regeneration activity filtration core, it is characterised in that specifically preparation process is:
(1)20~30min is crushed with tissue pulverizer after agrocybe, soybean and pineapple are mixed, mixed powder is obtained and minces, it will
Mixed powder, which minces, to be fitted into after protease and water mixing in enzymatic vessel, is digested, is separated by filtration to obtain enzymolysis filtrate;
(2)Weigh cocoanut shell be put into pulverizer crush 2~3h after obtain pulverized particles, by pulverized particles and above-mentioned enzymolysis filtrate
It is fitted into fermentation tank as fermentation substrate after mixing, then bed-silt is added into fermentation tank, stirred evenly with stirring rod rear close
Sealed cans mouth is sealed by fermentation;
(3)Wait for it is above-mentioned be separated by filtration to obtain fermentation filter residue after fermentation, the nitric acid for being 30% by ferment filter residue and mass fraction
Ferrous solution mixes, and is put into the reaction of sonic oscillation instrument sonic oscillation, filters after reaction, isolated reaction filter cake;
(4)Above-mentioned reaction filter cake is put into retort, carbonization reaction is kept the temperature under nitrogen protection state, is gone out after charing
Material, obtains from preparing active carbon, will be mixed to get pre-reaction from preparing active carbon and potassium rhodanate and amino trimethyl phosphonic acids and water
Object;
(5)Above-mentioned pre-reaction object is fitted into autoclave, high-temperature high-voltage reaction, takes out reaction product mistake after reaction
Filter, isolated filter cake are from regenerated carbon;
(6)Count in parts by weight, weigh 15~20 parts of polyethylene, 50~60 parts it is above-mentioned from regenerated carbon be mixed 30~
Mixed material after stirring is placed in mold, and moves into baking furnace by 40min, forms by a firing and comes out of the stove, is cooled to 40~60
DEG C demoulding is to get from regeneration activity filtration core.
Step(1)Described in agrocybe, soybean and pineapple mass ratio be 5:2:7, mixed powder minces and protease
And the mass ratio of water is 10:1:100, the temperature of enzymolysis is 25~28 DEG C, and enzymolysis time is 6~8h.
Step(2)Described in pulverized particles and enzymolysis filtrate mass ratio be 1:3, the addition of bed-silt is fermentation
The temperature of the 5% of substrate quality, sealing and fermenting is 30~40 DEG C, and the time of sealing and fermenting is 3~5 days.
Step(3)Described in fermentation filter residue and mass fraction be 30% the mass ratio of iron nitrate solution be 1:10, ultrasound
The frequency of oscillating reactions is 25~30kHz, and the time of sonic oscillation reaction is 1~2h.
Step(4)Described in heat preservation carbonization reaction temperature be 300~400 DEG C, keep the temperature carbonization reaction time be 2~
3h is 10 from preparing active carbon and potassium rhodanate and the mass ratio of amino trimethyl phosphonic acids and water:1:1:5.
Step(5)Described in the pressure of high-temperature high-voltage reaction be 2.3~2.5MPa, the temperature of high-temperature high-voltage reaction is
200~220 DEG C, the time of high-temperature high-voltage reaction is 8~10h.
Step(6)Described in the temperature formed by a firing be 200~250 DEG C, the time formed by a firing be 1~2h.
The beneficial effects of the invention are as follows:
The present invention digests first using the biomass rich in amino acid as raw material after co-grinding, then will enzymolysis filtrate and coconut shell flour
Mince blending fermentation, will fermentation filter residue and iron nitrate solution mix carry out sonic oscillation reaction, then will reaction filter cake charing after and
It is reacted under high-temperature and high-pressure conditions after potassium rhodanate and the mixing of amino trimethyl phosphonic acids, note film is burnt after the mixing of final and polyethylene
System is obtained from regeneration activity filtration core, and the present invention obtains the enzymolysis liquid rich in amino acid by enzymolysis first, by enzymolysis liquid and powder
Porous cocoanut shell particle after broken is mixed and is sealed by fermentation in the case where being acted on rich in the bed-silt of microorganism and humic acid, is passed through
Amino acid and humic acid degradation are generated a large amount of pendant carboxylic groups and amino and other active groups by microorganism, and in microorganism
These pendant carboxylic groups and amino and other active groups are introduced into pore interior and the surface of cocoanut shell particle under effect,
Then by the cocoanut shell containing carboxyl and amino and iron salt solutions hybrid reaction, the metal ion chela of pendant carboxylic group and amino is utilized
Iron ion chelating is anchored at internal void and the surface of cocoanut shell particle by conjunction property, and the introducing of other active groups increases coconut palm
Activated adoption bit number of points in shell particle, then through high temperature carbonization, the activated carbon containing metal ion is obtained, it will then contain metal
The activated carbon of ion is blended with potassium rhodanate and amino trimethyl phosphonic acids, under conditions of high temperature and pressure so that in activated carbon
Part metals ion removes, and generates metal cavity in activated carbon internal void and surface, the generation in these holes makes this hair
Bright activated carbon oxidation obtained greatly improves, and after active carbon filter core use, organic impurities reaches absorption in the water of absorption
After saturation, activated carbon and the water reaction being in contact with it generate the extremely strong hydroxyl radical free radical OH of oxidisability, it can be with activated carbon
The organic matter adsorbed in filter core generates organic free radical and is allowed to structure destruction, and oxygenolysis is finally reached voluntarily regenerated purpose,
So that active carbon filter core absorption property produced by the present invention is lasting, effluent quality is lasting, without often replacing, has wide
Application prospect.
Specific implementation mode
It is 5 in mass ratio by agrocybe, soybean and pineapple:2:20~30min is crushed with tissue pulverizer after 7 mixing,
It obtains mixed powder to mince, it is 10 in mass ratio that mixed powder, which is minced with protease and water,:1:It is packed into enzymatic vessel after 100 mixing
In, 6~8h is digested at 25~28 DEG C, is separated by filtration to obtain enzymolysis filtrate;It weighs cocoanut shell and is put into 2~3h of crushing in pulverizer
After obtain pulverized particles, be 1 in mass ratio by pulverized particles and above-mentioned enzymolysis filtrate:After 3 mixing hair is packed into as fermentation substrate
In fermentation tank, then the bed-silt of fermentation substrate quality 5% is added into fermentation tank, tank mouth is sealed after being stirred evenly with stirring rod,
It is sealed by fermentation 3~5 days at 30~40 DEG C;It waits for after fermentation, being separated by filtration to obtain fermentation filter residue, by fermentation filter residue and quality point
Number is 1 in mass ratio for 30% iron nitrate solution:10 mixing are put into sonic oscillation instrument and are vibrated with the frequency ultrasound of 25~30kHz
1~2h is reacted, is filtered after reaction, isolated reaction filter cake;Reaction filter cake is put into retort, in nitrogen protection shape
It is heated to 300~400 DEG C under state, keeps the temperature 2~3h of carbonization reaction, discharges, obtained from preparing active carbon after charing, it will be certainly
Preparing active carbon and potassium rhodanate and amino trimethyl phosphonic acids and water are 10 in mass ratio:1:1:5 are mixed to get pre-reaction object;It will
Pre-reaction object is fitted into autoclave, is heated to 200~220 DEG C under conditions of pressure is 2.3~2.5MPa, high temperature
8~10h of reaction under high pressure, takes out reaction product filtering after reaction, and isolated filter cake is from regenerated carbon;By weight
Number meter, weigh 15~20 parts of polyethylene, 50~60 parts 30~40min is mixed from regenerated carbon, will be after stirring it is mixed
It closes material to be placed in mold, and moves into baking furnace, 1~2h is kept the temperature under conditions of temperature is 200~250 DEG C, is formed by a firing
And come out of the stove, 40~60 DEG C of demouldings are cooled to get from regeneration activity filtration core.
It is 5 in mass ratio by agrocybe, soybean and pineapple:2:20min is crushed with tissue pulverizer after 7 mixing, is obtained
Mixed powder minces, and it is 10 in mass ratio that mixed powder, which is minced with protease and water,:1:It is fitted into enzymatic vessel after 100 mixing,
6h is digested at 25 DEG C, is separated by filtration to obtain enzymolysis filtrate;Weigh cocoanut shell be put into pulverizer crush 2h after obtain pulverized particles,
It is 1 in mass ratio by pulverized particles and above-mentioned enzymolysis filtrate:It is fitted into fermentation tank as fermentation substrate after 3 mixing, then to fermentation
The bed-silt of fermentation substrate quality 5% is added in tank, seals tank mouth after being stirred evenly with stirring rod, 3 is sealed by fermentation at 30 DEG C
It;It waits for after fermentation, being separated by filtration to obtain fermentation filter residue, the iron nitrate solution that ferment filter residue and mass fraction are 30% is pressed
Mass ratio is 1:10 mixing, are put into sonic oscillation instrument with the frequency ultrasound oscillating reactions 1h of 25kHz, filter after reaction, point
From obtain reaction filter cake;Reaction filter cake is put into retort, 300 DEG C are heated under nitrogen protection state, keeps the temperature charcoal
Change reaction 2h, discharges, obtained from preparing active carbon after charing, it will be from preparing active carbon and potassium rhodanate and amino trimethyl-phosphine
Acid and water are 10 in mass ratio:1:1:5 are mixed to get pre-reaction object;Pre-reaction object is fitted into autoclave, is in pressure
It is heated to 200 DEG C, high-temperature high-voltage reaction 8h under conditions of 2.3MPa, takes out reaction product filtering, separation after reaction
It is from regenerated carbon to obtain filter cake;Count in parts by weight, weigh 15 parts of polyethylene, 50 parts from regenerated carbon be mixed
Mixed material after stirring is placed in mold, and moves into baking furnace by 30min, is kept the temperature under conditions of temperature is 200 DEG C
1h is formed by a firing and is come out of the stove, and is cooled to 40 DEG C of demouldings to get from regeneration activity filtration core.
It is 5 in mass ratio by agrocybe, soybean and pineapple:2:25min is crushed with tissue pulverizer after 7 mixing, is obtained
Mixed powder minces, and it is 10 in mass ratio that mixed powder, which is minced with protease and water,:1:It is fitted into enzymatic vessel after 100 mixing,
7h is digested at 27 DEG C, is separated by filtration to obtain enzymolysis filtrate;Weigh cocoanut shell be put into pulverizer crush 2h after obtain pulverized particles,
It is 1 in mass ratio by pulverized particles and above-mentioned enzymolysis filtrate:It is fitted into fermentation tank as fermentation substrate after 3 mixing, then to fermentation
The bed-silt of fermentation substrate quality 5% is added in tank, seals tank mouth after being stirred evenly with stirring rod, 4 is sealed by fermentation at 35 DEG C
It;It waits for after fermentation, being separated by filtration to obtain fermentation filter residue, the iron nitrate solution that ferment filter residue and mass fraction are 30% is pressed
Mass ratio is 1:10 mixing, are put into sonic oscillation instrument with the frequency ultrasound oscillating reactions 1h of 27kHz, filter after reaction, point
From obtain reaction filter cake;Reaction filter cake is put into retort, 350 DEG C are heated under nitrogen protection state, keeps the temperature charcoal
Change reaction 2h, discharges, obtained from preparing active carbon after charing, it will be from preparing active carbon and potassium rhodanate and amino trimethyl-phosphine
Acid and water are 10 in mass ratio:1:1:5 are mixed to get pre-reaction object;Pre-reaction object is fitted into autoclave, is in pressure
It is heated to 210 DEG C, high-temperature high-voltage reaction 9h under conditions of 2.4MPa, takes out reaction product filtering, separation after reaction
It is from regenerated carbon to obtain filter cake;Count in parts by weight, weigh 17 parts of polyethylene, 55 parts from regenerated carbon be mixed
Mixed material after stirring is placed in mold, and moves into baking furnace by 35min, is kept the temperature under conditions of temperature is 225 DEG C
1h is formed by a firing and is come out of the stove, and is cooled to 50 DEG C of demouldings to get from regeneration activity filtration core.
It is 5 in mass ratio by agrocybe, soybean and pineapple:2:30min is crushed with tissue pulverizer after 7 mixing, is obtained
Mixed powder minces, and it is 10 in mass ratio that mixed powder, which is minced with protease and water,:1:It is fitted into enzymatic vessel after 100 mixing,
8h is digested at 28 DEG C, is separated by filtration to obtain enzymolysis filtrate;Weigh cocoanut shell be put into pulverizer crush 3h after obtain pulverized particles,
It is 1 in mass ratio by pulverized particles and above-mentioned enzymolysis filtrate:It is fitted into fermentation tank as fermentation substrate after 3 mixing, then to fermentation
The bed-silt of fermentation substrate quality 5% is added in tank, seals tank mouth after being stirred evenly with stirring rod, 5 is sealed by fermentation at 40 DEG C
It;It waits for after fermentation, being separated by filtration to obtain fermentation filter residue, the iron nitrate solution that ferment filter residue and mass fraction are 30% is pressed
Mass ratio is 1:10 mixing, are put into sonic oscillation instrument with the frequency ultrasound oscillating reactions 2h of 30kHz, filter after reaction, point
From obtain reaction filter cake;Reaction filter cake is put into retort, 400 DEG C are heated under nitrogen protection state, keeps the temperature charcoal
Change reaction 3h, discharges, obtained from preparing active carbon after charing, it will be from preparing active carbon and potassium rhodanate and amino trimethyl-phosphine
Acid and water are 10 in mass ratio:1:1:5 are mixed to get pre-reaction object;Pre-reaction object is fitted into autoclave, is in pressure
It is heated to 220 DEG C, high-temperature high-voltage reaction 10h under conditions of 2.5MPa, takes out reaction product filtering, separation after reaction
It is from regenerated carbon to obtain filter cake;Count in parts by weight, weigh 20 parts of polyethylene, 60 parts from regenerated carbon be mixed
Mixed material after stirring is placed in mold, and moves into baking furnace by 40min, is kept the temperature under conditions of temperature is 250 DEG C
2h is formed by a firing and is come out of the stove, and is cooled to 60 DEG C of demouldings to get from regeneration activity filtration core.
The active carbon filter core that comparative example is produced with Nanjing company is as a comparison case
Active carbon filter core produced by the present invention from regeneration activity filtration core and comparative example is detected, testing result such as table
1, table 2, shown in table 3:
1 performance measurement result of table
Test event | Detection method | Example 1 | Example 2 | Example 3 | Comparative example |
Specific surface area(m2/g) | Absorption method | 1659 | 1275 | 1693 | 1028 |
Void content(cm3/g) | Mercury displacement method | 1.53 | 1.58 | 1.63 | 0.89 |
Mesoporous(%) | N2 method | 99.1 | 99.1 | 99.3 | 94.3 |
Iodine sorption value(mg/g) | ASTM4607 methods | 5.6 | 5.7 | 5.9 | 2.5 |
Methylene blue adsorption(mL/g) | Absorption method | 149 | 154 | 157 | 112 |
Adsorption rate(%) | Absorption method | 96.4 | 96.7 | 97.2 | 86.9 |
By active carbon filter core made from example 1~3 produced by the present invention and comparative example, it is added separately to a concentration of 50mg/L's of 1L
Lead ion, copper ion, arsenic ion, cadmium ion, nickel ion and cobalt ions solution in, at 25 DEG C after shaking table concussion for 24 hours, detection
The residual concentration of heavy metal ion in each solution, and calculate active carbon filter core to lead ion, copper ion, arsenic ion, cadmium from
The adsorption rate of son, nickel ion and cobalt ions, acquired results are shown in Table 2.
2 performance measurement result of table
By made from example 1~3 produced by the present invention and comparative example active carbon filter core carry out it is heavy metal ion adsorbed after, be placed in 4%
Alkaline permanganate solution in be stirred continuously, impregnate 4~6 hours, filter, be washed with deionized to neutrality, be dried to perseverance
Weight can utilize again, retest the adsorption rate of going to heavy metal ion, testing result is as shown in table 3.
3 performance measurement result of table
By table 1, table 2,3 data of table it is found that active carbon filter core produced by the present invention, have adsorption capacity it is big, to heavy metal ion
Strong adsorption, cyclic utilization rate height, environmentally safe feature, have good market prospects.
Claims (7)
1. a kind of preparation method from regeneration activity filtration core, it is characterised in that specifically preparation process is:
(1)20~30min is crushed with tissue pulverizer after agrocybe, soybean and pineapple are mixed, mixed powder is obtained and minces, it will
Mixed powder, which minces, to be fitted into after protease and water mixing in enzymatic vessel, is digested, is separated by filtration to obtain enzymolysis filtrate;
(2)Weigh cocoanut shell be put into pulverizer crush 2~3h after obtain pulverized particles, by pulverized particles and above-mentioned enzymolysis filtrate
It is fitted into fermentation tank as fermentation substrate after mixing, then bed-silt is added into fermentation tank, stirred evenly with stirring rod rear close
Sealed cans mouth is sealed by fermentation;
(3)Wait for it is above-mentioned be separated by filtration to obtain fermentation filter residue after fermentation, the nitric acid for being 30% by ferment filter residue and mass fraction
Ferrous solution mixes, and is put into the reaction of sonic oscillation instrument sonic oscillation, filters after reaction, isolated reaction filter cake;
(4)Above-mentioned reaction filter cake is put into retort, carbonization reaction is kept the temperature under nitrogen protection state, is gone out after charing
Material, obtains from preparing active carbon, will be mixed to get pre-reaction from preparing active carbon and potassium rhodanate and amino trimethyl phosphonic acids and water
Object;
(5)Above-mentioned pre-reaction object is fitted into autoclave, high-temperature high-voltage reaction, takes out reaction product mistake after reaction
Filter, isolated filter cake are from regenerated carbon;
(6)Count in parts by weight, weigh 15~20 parts of polyethylene, 50~60 parts it is above-mentioned from regenerated carbon be mixed 30~
Mixed material after stirring is placed in mold, and moves into baking furnace by 40min, forms by a firing and comes out of the stove, is cooled to 40~60
DEG C demoulding is to get from regeneration activity filtration core.
2. a kind of preparation method from regeneration activity filtration core according to claim 1, it is characterised in that:Step(1)In
The mass ratio of the agrocybe, soybean and pineapple is 5:2:7, mixed powder minces is with the mass ratio of protease and water
10:1:100, the temperature of enzymolysis is 25~28 DEG C, and enzymolysis time is 6~8h.
3. a kind of preparation method from regeneration activity filtration core according to claim 1, it is characterised in that:Step(2)In
The mass ratio of the pulverized particles and enzymolysis filtrate is 1:3, the addition of bed-silt is the 5% of fermentation substrate quality, sealing
The temperature of fermentation is 30~40 DEG C, and the time of sealing and fermenting is 3~5 days.
4. a kind of preparation method from regeneration activity filtration core according to claim 1, it is characterised in that:Step(3)In
The mass ratio for the iron nitrate solution that the fermentation filter residue and mass fraction are 30% is 1:10, sonic oscillation reaction frequency be
The time of 25~30kHz, sonic oscillation reaction are 1~2h.
5. a kind of preparation method from regeneration activity filtration core according to claim 1, it is characterised in that:Step(4)In
The temperature of the heat preservation carbonization reaction is 300~400 DEG C, and the time for keeping the temperature carbonization reaction is 2~3h, from preparing active carbon and sulphur
Potassium cyanide and the mass ratio of amino trimethyl phosphonic acids and water are 10:1:1:5.
6. a kind of preparation method from regeneration activity filtration core according to claim 1, it is characterised in that:Step(5)In
The pressure of the high-temperature high-voltage reaction is 2.3~2.5MPa, and the temperature of high-temperature high-voltage reaction is 200~220 DEG C, high temperature and pressure
The time of reaction is 8~10h.
7. a kind of preparation method from regeneration activity filtration core according to claim 1, it is characterised in that:Step(6)In
The temperature formed by a firing is 200~250 DEG C, and the time formed by a firing is 1~2h.
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Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
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CN110013832A (en) * | 2019-03-18 | 2019-07-16 | 贵州万峰湖智慧水产科技有限公司 | A kind of cultivation water process carbon fiber modifying material and preparation method thereof |
CN111334318A (en) * | 2020-03-18 | 2020-06-26 | 重庆三峡学院 | Method for preparing plant-based biochar from single component through biological activation and modification |
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2018
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Cited By (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN110013832A (en) * | 2019-03-18 | 2019-07-16 | 贵州万峰湖智慧水产科技有限公司 | A kind of cultivation water process carbon fiber modifying material and preparation method thereof |
CN110013832B (en) * | 2019-03-18 | 2022-03-04 | 广州誉隆智慧科技有限公司 | Carbon fiber modified material for aquaculture water treatment and preparation method thereof |
CN111334318A (en) * | 2020-03-18 | 2020-06-26 | 重庆三峡学院 | Method for preparing plant-based biochar from single component through biological activation and modification |
CN111334318B (en) * | 2020-03-18 | 2021-07-27 | 重庆三峡学院 | Method for preparing plant-based biochar from single component through biological activation and modification |
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