CN1648040A - Method for directly preparing honeycomb active carbon from coal - Google Patents
Method for directly preparing honeycomb active carbon from coal Download PDFInfo
- Publication number
- CN1648040A CN1648040A CN 200410092429 CN200410092429A CN1648040A CN 1648040 A CN1648040 A CN 1648040A CN 200410092429 CN200410092429 CN 200410092429 CN 200410092429 A CN200410092429 A CN 200410092429A CN 1648040 A CN1648040 A CN 1648040A
- Authority
- CN
- China
- Prior art keywords
- coal
- activated carbon
- tar
- carbon capable
- alveolate activated
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Granted
Links
Landscapes
- Carbon And Carbon Compounds (AREA)
- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Abstract
In the preparation of honeycomb active carbon directly with coal, coal powder, emulsified coal tar, water soluble adhesive, lubricant and water are produced into honeycomb active carbon through crushing, compounding, kneading, extruding, drying, carbonizing and activating. The present invention has low cost and simple production apparatus, and the prepared honeycomb active carbon has great specific surface area, high porosity, high resistance to water, acid and alkali, high compression strength, high heat resistance, and easy heat or washing regeneration.
Description
Technical field
The invention belongs to a kind of manufacture method of Alveolate activated carbon capable, relate in particular to a kind of method that directly prepares Alveolate activated carbon capable by coal.
Background technology
China is coal-fired big country, and coal accounts for 75% of primary energy source total quantity consumed.Along with the continuous growth of consumption of coal, coal fire discharged sulfurous gas, oxynitride also constantly increase, and surpass 2000 and 9,100,000 tons for years, occupy first place in the world, cause China's acid rain and sulfur dioxide pollution to be on the rise.According to the estimation of relevant research, by 2000 and 2010, the NOx quantity discharged of China will reach 1,561 ten thousand tons and 2,194 ten thousand tons respectively.China has begun to mention agenda to the NOx discharging and the control of polluting, and clearly proposes in " the atmosphere method " of nineteen ninety-five revision " oxynitride that enterprise should progressively produce fire coal take control measure ".Therefore, strengthen the research of oxynitride control techniques in the fire coal boiler fume, exploitation is fit to the control techniques of China's national situation, and strengthen environmental protection work is the important assurance that China implements the strategy of sustainable development.
Honeycombed catalyst has the advantages that geometrical surface is big, voidage is high, bed pressure drop is low, and therefore, the preparation of honeycombed catalyst and utilisation technology become in recent years scientific worker's research focus both at home and abroad.At present, main two classes of Alveolate activated carbon capable technology of preparing of patent documentation report: the method for forming and dip coating.U.S.Pat.No.3,825,460 reports use the papery honeycomb to be parent, by dip-coating powdered carbon (as carbon black, natural or graphous graphite powder, coke powder, coal dust) or sugar, phenol-formaldehyde resin powder, cacao shell powder, walnut parting and solution, suspension or emulsion natural or staple fibre and organic bond (as coal-tar pitch, resol, Resins, epoxy) configuration, through 110 ℃ of dryings, 600-1000 ℃ inert atmosphere charing, 700-1000 ℃ of activation obtains specific surface area 300-800m
2/ g Alveolate activated carbon capable.U.S.Pat.No.4; 399; 052 employing phenol-formaldehyde resin powder, powdered carbon are activated carbon precursor, and silicon carbide, titanium carbide are toughener, and carboxymethyl cellulose is the temporary adhesion agent; water soluble phenol resin is a binding agent; material is by mixing, kneading, extrusion moulding, then under the argon shield condition in 750 ℃ of charings 5 hours, 900-950 ℃ steam activation 3-5 hour; the Alveolate activated carbon capable malleation intensity 6.5-8.25Mpa, the side pressure strength 0.8-2.8Mpa that make, specific surface area 920-1120m
2/ g, heat shock resistance 400-900 ℃.U.S.Pat.No.4,992,319 use the glass fibre corrugation paper of high voidage to be parent, the suspension that dip-coating gac and vinylformic acid or vinylidene resin are made, and the Alveolate activated carbon capable that obtains after the drying can be used for filtering ozone, foul smell and support of the catalyst.U.S.Pat.No.5; 356; 852, E.P.Pat.No.492081A1 adopts multipolymer, the silicone resin of activity charcoal powder and Vltra tears, polyvinyl alcohol or polyvinyl alcohol and poly-ethylene methacrylic ester to add water or ethanol to make and plastify mud cream; pass through extrusion moulding then, 100 ℃ or 200 ℃ of (carbon-dioxide protecting) dryings make ultimate compression strength 1.13-6.88Mpa, specific surface area 646-1300m
2/ g.E.P.Pat.No.728, the 521B1 report uses resol to be activated carbon precursor, Mierocrystalline cellulose, kaolin, trichroite are filler, MC or cellulose ester are temporary transient tamanori, soap or linolic acid are lubricant, add suitable quantity of water and be mixed with plastic mud material, honeycomb steel die hole density is 16-32 hole/cm
2The time extrusion pressure between 3.7-7.6Mpa, honeycomb solidifies 3 hours, 900 ℃ charings 5 hours, 800-900 ℃ carbonic acid gas activation 1 hour, the Alveolate activated carbon capable benzene adsorptive capacity 213-601mg/g that makes at 150 ℃.U.S.Pat.No.6,284,705B1, U.S.Pat.No.6,171,373B1 has reported a kind of method of utilizing gac and mineral binder bond to prepare Alveolate activated carbon capable.Specific surface area 600-2000m
2The 50-30 in proportion of the gac of/g and mineral binder bond: 50-70 configuration, mineral binder bond is suitably allocated by clay, kaolin, nepheline and water glass and is formed.Mentioned component additionally adds the methylcellulose gum of 2.5-3% again and the water of 66-102% is made plasticity mud cream, and the extrusion moulding honeycomb is through freezing or vacuum-drying, inert atmosphere protection high-temperature calcination, and ultimate compression strength can reach 1.4-8.9Mpa.U.S.Pat.No.6,699,561B2 proposed another kind of direct usefulness 34 ~ 37% activity charcoal powders and 11-12% phenol-formaldehyde resin powder, 5-10% clay, 2-3% cellulose ester, 7-8% starch paste, 0.5-0.9% polyacrylamide, 4-5% paraffin, 1.5-1.7% soap, 27-31% water through mixing, extrude, shaping, drying and 650-850 ℃ charing 5-30 minute, the cellular activated carbon that obtains can be used as adsorption filter, and available electrically heated regeneration.In sum, in order to improve the ultimate compression strength of Alveolate activated carbon capable, a kind of way is to adopt mineral binder bond to realize in high-temperature calcination, and another kind of way is to utilize resin that can charing and add the carbide toughener and realize.Must cause the effectively reduction of carbon content in the honeycomb like this, and the production cost increase, be difficult to industrialization promotion and use.
Summary of the invention
What the purpose of this invention is to provide that a kind of production cost is low, ultimate compression strength is high directly prepares the method for Alveolate activated carbon capable by coal
The preparation method of Alveolate activated carbon capable of the present invention is obtained through raw material pulverizing, batching, kneading, extrusion moulding, drying, charing, activation by coal dust, emulsification coal tar, water-soluble binder, lubricant and water.Concrete preparation method may further comprise the steps:
(1) coal dust configuration: brown coal or bituminous coal and coking coal are crushed to respectively≤2mm, then by quality than brown coal or bituminous coal: after coking coal=1: the 0.2-0.5 mixing, be ground to below the 74 μ m coal dust that obtains mixing again;
(2) emulsification coal tar: the first step, asphalt content 〉=55% coal-tar heavy oil is preheated to 120-150 ℃; Second step, the preparation of emulsifier aqueous solution, the stablizer of the 0.5-2% of the 2-6% tensio-active agent of adding coal-tar heavy oil quality and coal-tar heavy oil quality in water, and be preheated to 80-90 ℃ of formation emulsifier aqueous solution; The 3rd step was a coal-tar heavy oil by mass ratio: emulsifier aqueous solution=1: 0.3-0.7 under agitation condition, adds coal-tar heavy oil and makes emulsification coal tar in the emulsifier aqueous solution;
(3) processing of plasticity-coal slime: by mass ratio is coal dust: emulsification coal tar: water: water-soluble binder: lubricant=34-57: 30-36: 6-29: 3-5: 2-3, with stirring in its adding kneader, make plastic coal slime;
(4) pugging: the plasticity-coal slime is handled through vacuum deairing machine or extrusion shaping machine, and coal slime is mixed, and removes large particulate matter with 60 to 100 purpose silk screen filter then in shaper;
(5) extrusion moulding: the coal slime adding after pugging is handled is equipped with in the extrusion shaping machine of honeycomb steel die, carries out moulding, the honeycomb that obtains wetting;
(6) drying: wet honeycomb is dried to moisture and is lower than 2%;
(7) charing and activation: as protection gas, be heated to 600-800 ℃ with rare gas element by heat-up rate 3-5 ℃/min, and under this temperature charing 2-3 hour; Be warmed up to 750-850 ℃ by heat-up rate 5-15 ℃/min then, use steam activation 3-15 hour, obtain Alveolate activated carbon capable.
Aforesaid tensio-active agent is sodium lignosulfonate, humate, sodium formaldehyde condensation products or polymethylene anthracene sulfonic acid sodium.
Aforesaid stablizer can be selected divalence or trivalent soluble metallic salt, as calcium chloride, ferric sulfate or iron nitrate etc.
Aforesaid water-soluble binder is to select starch, polyvinyl alcohol (PVA), cellulose ester (comprising methylcellulose gum, ethyl cellulose, Vltra tears), Natvosol and Xylo-Mucine (CMC) etc.
Aforesaid lubricant can be the saponification material that tung oil, oleum lini or edible oil and production process thereof produce.
Aforesaid steel die can adopt 8-16 hole/cm
2Square hole honeycomb steel die
Aforesaid forming pressure is 7-14Mpa.
Aforesaid rare gas element is nitrogen or argon gas.
The Alveolate activated carbon capable of the present invention's preparation is specially adapted to the purification of fire coal, oil-firing boiler tail gas clean-up and the indoor harmful gas of electric power, chemical fertilizer, metallurgy industry, technical fields such as Treatment of Industrial Water, support of the catalyst.
Compared with the prior art the present invention has the following advantages:
(1) be that the Alveolate activated carbon capable cost made of activated carbon precursor is extremely low with cheap bituminous coal or brown coal;
(2) use coal-tar heavy oil as binding agent, and carried out emulsification, kneading, moulding process can be finished at normal temperatures, make kneading, extrusion not need the insulation measure, production unit is simplified greatly.
(3) absorption of Alveolate activated carbon capable, catalytic performance and physical property (as geometrical shape, size, pore size distribution, intensity etc.) can be carried out cutting as required.
(4) this Alveolate activated carbon capable has the advantages that the unit volume specific surface area is big, voidage is high, bed pressure drop is low, can prevent the latch up phenomenon that particulate matter causes in dust or the water.
(5) the water-fast acid-fast alkali-proof of this Alveolate activated carbon capable, ultimate compression strength height, good heat resistance, heat regeneration or regenerated from washing easily.
Embodiment
Embodiment 1:
(1) coal dust configuration: brown coal and coking coal are crushed to respectively≤2mm, then by quality than brown coal: after coking coal=mixing in 1: 0.3, be ground to below the 74 μ m coal dust that obtains mixing again.
(2) emulsification coal tar: the first step, asphalt content are that 57% coal-tar heavy oil is preheated to 120 ℃; Second step, the preparation emulsifier aqueous solution.Add 4% tensio-active agent (is benchmark with coal tar) and 0.5% stablizer (is benchmark with coal tar) in the water, and be preheated to 80 ℃ and form emulsifier aqueous solutions; In the 3rd step, press coal-tar heavy oil: emulsifier aqueous solution (mass ratio)=1: 0.5 slowly adds coal tar under agitation condition and makes emulsification coal tar in the emulsifier aqueous solution.The tensio-active agent of emulsification coal-tar heavy oil is a sodium lignosulfonate, and stablizer is a calcium chloride.
(3) processing of plasticity-coal slime: coal dust in proportion: emulsification coal tar: water: polyvinyl alcohol: tung oil=38: 36: 20: add in kneaders at 4: 2 and to stir, make plastic coal slime.
(4) pugging: the plasticity-coal slime is handled through vacuum deairing machine or extrusion shaping machine, and coal slime is mixed, and removes the large particulate matter that above-mentioned operation may be brought into 60 purpose silk screen filter then in shaper.
(5) extrusion moulding: the coal slime adding after pugging is handled is equipped with in the extrusion shaping machine of honeycomb steel die, is to carry out moulding, the honeycomb that obtains wetting under the 7Mpa in forming pressure.
(6) drying: wet honeycomb is dried to moisture and is lower than 2%.
(7) charing and activation: as protection gas, be heated to 600 ℃ with nitrogen or argon gas by 3 ℃/min of heat-up rate, and charing 2 hours under this temperature; Being warmed up to 800 ℃ by 5 ℃/min of heat-up rate then, is activated media activation 3 hours with water vapour, obtains Alveolate activated carbon capable.The cellular activated carbon performance index see Table 1
Embodiment 2:
(1) coal dust configuration: brown coal and coking coal are crushed to respectively≤2mm, then by quality than brown coal: after coking coal=mixing in 1: 0.2, be ground to below the 74 μ m coal dust that obtains mixing again.
(2) emulsification coal tar: the first step, asphalt content be 58% be preheated to 140 ℃ from warm coal tar; Second step, the preparation emulsifier aqueous solution.Add 5% tensio-active agent (is benchmark with coal tar) and 2% stablizer (is benchmark with coal tar) in the water, and be preheated to 85 ℃ and form emulsifier aqueous solutions; In the 3rd step, press coal-tar heavy oil: emulsifier aqueous solution (mass ratio)=1: 0.6 slowly adds coal tar under agitation condition and makes emulsification coal tar in the emulsifier aqueous solution.The tensio-active agent of emulsification coal-tar heavy oil is a humate, and stablizer is a ferric sulfate.
(3) processing of plasticity-coal slime: coal dust in proportion: emulsification coal tar: water: W-Gum: oleum lini=40: 30: 25: add in kneaders at 5: 3 and to stir, make plastic coal slime.
(4) pugging: the plasticity-coal slime is handled through vacuum deairing machine or extrusion shaping machine, and coal slime is mixed, and removes the large particulate matter that above-mentioned operation may be brought into 80 purpose silk screen filter then in shaper.
(5) extrusion moulding: the coal slime adding after pugging is handled is equipped with in the extrusion shaping machine of honeycomb steel die, is to carry out moulding, the honeycomb that obtains wetting under the 7Mpa in forming pressure.
(6) drying: the honeycomb of extruding is dried to moisture and is lower than 2%.
(7) charing and activation: as protection gas, be heated to 700 ℃ with nitrogen or argon gas, and under this temperature, be incubated 3 hours by 5 ℃/min of heat-up rate; Being warmed up to 800 ℃ by 10 ℃/min of heat-up rate then, is activated media activation 5 hours with water vapour, obtains Alveolate activated carbon capable.The cellular activated carbon performance index see Table 1
Embodiment 3:
(1) coal dust configuration: bituminous coal and coking coal are crushed to respectively≤2mm, then by quality than bituminous coal: after coking coal=mixing in 1: 0.5, be ground to below the 74 μ m coal dust that obtains mixing again.
(2) emulsification coal tar: the first step, asphalt content are that 55% coal-tar heavy oil is preheated to 140 ℃; Second step, the preparation emulsifier aqueous solution.Add in stablizer (is benchmark with the coal tar) water of 2% tensio-active agent (is benchmark with coal tar) and 0.5%, and be preheated to 85 ℃ and form emulsifier aqueous solutions; In the 3rd step, press coal-tar heavy oil: emulsifier aqueous solution (mass ratio)=1: 0.3 slowly adds coal tar under agitation condition and makes emulsification coal tar in the emulsifier aqueous solution.The tensio-active agent of emulsification coal-tar heavy oil is the sodium formaldehyde condensation products, and stablizer is a ferric sulfate.
(3) processing of plasticity-coal slime: coal dust in proportion: emulsification coal tar: water: methylcellulose gum: tung oil oil=57: 30: 8: add in kneaders at 3: 2 and to stir, make plastic coal slime.
(4) pugging: the plasticity-coal slime is handled through vacuum deairing machine or extrusion shaping machine, and coal slime is mixed, and removes the large particulate matter that above-mentioned operation may be brought into 80 purpose silk screen filter then in shaper.
(5) extrusion moulding: the coal slime adding after pugging is handled is equipped with in the extrusion shaping machine of honeycomb steel die, is to carry out moulding, the honeycomb that obtains wetting under the 14Mpa in forming pressure.
(6) drying: wet honeycomb is dried to moisture and is lower than 2%.
(7) charing and activation: as protection gas, be heated to 800 ℃ with nitrogen or argon gas by 3 ℃/min of heat-up rate, and charing 2 hours under this temperature; Being warmed up to 750 ℃ by 10 ℃/min of heat-up rate then, is activated media activation 15 hours with water vapour, obtains Alveolate activated carbon capable.The cellular activated carbon performance index see Table 1
Embodiment 4:
(1) coal dust configuration: bituminous coal and coking coal are crushed to respectively≤2mm, then by quality than bituminous coal: after coking coal=mixing in 1: 0.4, be ground to below the 74 μ m coal dust that obtains mixing again.
(2) emulsification coal tar: the first step, asphalt content are that 56% coal-tar heavy oil is preheated to 140 ℃; Second step, the preparation emulsifier aqueous solution.Add 4% tensio-active agent (is benchmark with coal tar) and 1% stablizer (is benchmark with coal tar) in the water, and be preheated to 85 ℃ and form emulsifier aqueous solutions; In the 3rd step, press coal-tar heavy oil: emulsifier aqueous solution (mass ratio)=1: 0.3 slowly adds coal tar under agitation condition and makes emulsification coal tar in the emulsifier aqueous solution.The tensio-active agent of emulsification coal-tar heavy oil is the sodium formaldehyde condensation products, and stablizer is a calcium chloride.
(3) processing of plasticity-coal slime: coal dust in proportion: emulsification coal tar: water: ethyl cellulose: soya-bean oil=50: 30: 13: add in kneaders at 4: 3 and to stir, make plastic coal slime.
(4) pugging: the plasticity-coal slime is handled through vacuum deairing machine or extrusion shaping machine, and coal slime is mixed, and removes the large particulate matter that above-mentioned operation may be brought into 80 purpose silk screen filter then in shaper.
(5) extrusion moulding: the coal slime adding after pugging is handled is equipped with in the extrusion shaping machine of honeycomb steel die, is to carry out moulding, the honeycomb that obtains wetting under the 12Mpa in forming pressure.
(6) drying: wet honeycomb is dried to moisture and is lower than 2%.
(7) charing and activation: as protection gas, be heated to 700 ℃ with nitrogen or argon gas by 3 ℃/min of heat-up rate, and charing 2 hours under this temperature; Being warmed up to 800 ℃ by 10 ℃/min of heat-up rate then, is activated media activation 10 hours with water vapour, obtains Alveolate activated carbon capable.The cellular activated carbon performance index see Table 1
Embodiment 5:
(1) coal dust configuration: bituminous coal and coking coal are crushed to respectively≤2mm, then by quality than bituminous coal: after coking coal=mixing in 1: 0.3, be ground to below the 74 μ m coal dust that obtains mixing again.
(2) emulsification coal tar: the first step, asphalt content are that 56% coal-tar heavy oil is preheated to 140 ℃; Second step, the preparation emulsifier aqueous solution.Add 5% tensio-active agent (is benchmark with coal tar) and 0.5% stablizer (is benchmark with coal tar) in the water, and be preheated to 85 ℃ and form emulsifier aqueous solutions; In the 3rd step, press coal-tar heavy oil: emulsifier aqueous solution (mass ratio)=1: 0.5 slowly adds coal tar under agitation condition and makes emulsification coal tar in the emulsifier aqueous solution.The tensio-active agent of emulsification coal-tar heavy oil is a polymethylene anthracene sulfonic acid sodium, and stablizer is an iron nitrate.
(3) processing of plasticity-coal slime: coal dust in proportion: emulsification coal tar: water: Vltra tears: soya-bean oil saponification material=45: 33: 15: add in kneaders at 5: 2 and to stir, make plastic coal slime.
(4) pugging: the plasticity-coal slime is handled through vacuum deairing machine or extrusion shaping machine, and coal slime is mixed, and removes the large particulate matter that above-mentioned operation may be brought into 100 purpose silk screen filter then in shaper.
(5) extrusion moulding: the coal slime adding after pugging is handled is equipped with in the extrusion shaping machine of honeycomb steel die, is to carry out moulding, the honeycomb that obtains wetting under the 10Mpa in forming pressure.
(6) drying: wet honeycomb is dried to moisture and is lower than 2%.
(7) charing and activation: as protection gas, be heated to 600 ℃ with nitrogen or argon gas by 4 ℃/min of heat-up rate, and charing 2 hours under this temperature; Being warmed up to 800 ℃ by 10 ℃/min of heat-up rate then, is activated media activation 8 hours with water vapour, obtains Alveolate activated carbon capable.The cellular activated carbon performance index see Table 1
Embodiment 6:
(1) coal dust configuration: bituminous coal and coking coal are crushed to respectively≤2mm, then by quality than bituminous coal: after coking coal=mixing in 1: 0.2, be ground to below the 74 μ m coal dust that obtains mixing again.
(2) emulsification coal tar: the first step, asphalt content are that 60% coal-tar heavy oil is preheated to 140 ℃; Second step, the preparation emulsifier aqueous solution.Add 6% tensio-active agent (is benchmark with coal tar) and 2% stablizer (is benchmark with coal tar) in the water, and be preheated to 85 ℃ and form emulsifier aqueous solutions; In the 3rd step, press coal-tar heavy oil: emulsifier aqueous solution (mass ratio)=1: 0.7 slowly adds coal tar under agitation condition and makes emulsification coal tar in the emulsifier aqueous solution.The tensio-active agent of emulsification coal-tar heavy oil is a polymethylene anthracene sulfonic acid sodium, and stablizer is an iron nitrate.
(3) processing of plasticity-coal slime: coal dust in proportion: emulsification coal tar: water: Natvosol: tung oil oil=34: 36: 22: add in kneaders at 5: 3 and to stir, make plastic coal slime.
(4) pugging: the plasticity-coal slime is handled through vacuum deairing machine or extrusion shaping machine, and coal slime is mixed, and removes the large particulate matter that above-mentioned operation may be brought into 60 purpose silk screen filter then in shaper.
(5) extrusion moulding: the coal slime adding after pugging is handled is equipped with in the extrusion shaping machine of honeycomb steel die, is to carry out moulding, the honeycomb that obtains wetting under the 7Mpa in forming pressure.
(6) drying: wet honeycomb is dried to moisture and is lower than 2%.
(7) charing and activation: as protection gas, be heated to 700 ℃ with nitrogen or argon gas by 3 ℃/min of heat-up rate, and charing 2 hours under this temperature; Being warmed up to 850 ℃ by 15 ℃/min of heat-up rate then, is activated media activation 6 hours with water vapour, obtains Alveolate activated carbon capable.The cellular activated carbon performance index see Table 1
Embodiment 7:
(1) coal dust configuration: bituminous coal and coking coal are crushed to respectively≤2mm, then by quality than bituminous coal: after coking coal=mixing in 1: 0.2, be ground to below the 74 μ m coal dust that obtains mixing again.
(2) emulsification coal tar: the first step, asphalt content are that 60% coal-tar heavy oil is preheated to 140 ℃; Second step, the preparation emulsifier aqueous solution.Add 6% tensio-active agent (is benchmark with coal tar) and 2% stablizer (is benchmark with coal tar) in the water, and be preheated to 85 ℃ and form emulsifier aqueous solutions; In the 3rd step, press coal-tar heavy oil: emulsifier aqueous solution (mass ratio)=1: 0.7 slowly adds coal tar under agitation condition and makes emulsification coal tar in the emulsifier aqueous solution.The tensio-active agent of emulsification coal-tar heavy oil is a polymethylene anthracene sulfonic acid sodium, and stablizer is an iron nitrate.
(3) processing of plasticity-coal slime: coal dust in proportion: emulsification coal tar: water: Xylo-Mucine: tung oil=34: 36: 22: add in kneaders at 5: 3 and to stir, make plastic coal slime.
(4) pugging: the plasticity-coal slime is handled through vacuum deairing machine or extrusion shaping machine, and coal slime is mixed, and removes the large particulate matter that above-mentioned operation may be brought into 60 purpose silk screen filter then in shaper.
(5) extrusion moulding: the coal slime adding after pugging is handled is equipped with in the extrusion shaping machine of honeycomb steel die, is to carry out moulding, the honeycomb that obtains wetting under the 7Mpa in forming pressure.
(6) drying: wet honeycomb is dried to moisture and is lower than 2%.
(7) charing and activation: as protection gas, be heated to 650 ℃ with nitrogen or argon gas by 5 ℃/min of heat-up rate, and charing 2 hours under this temperature; Being warmed up to 850 ℃ by 15 ℃/min of heat-up rate then, is activated media activation 3 hours with water vapour, obtains Alveolate activated carbon capable.The cellular activated carbon performance index see Table 1
Table 1 cellular activated carbon performance index table look-up
Performance | Embodiment 1 | Embodiment 2 | Embodiment 3 | Embodiment 4 | Embodiment 5 | Embodiment 6 | Embodiment 7 |
Specific surface area, m 2/g | ?284 | ?235 | ?1040 | ?812 | ?412 | ?578 | ?286 |
Pore volume, ml/g | ?0.31 | ?0.42 | ?0.86 | ?0.63 | ?0.56 | ?0.57 | ?0.34 |
Ultimate compression strength, Mpa | ?13 | ?3 | ?16 | ?24 | ?2 | ?29 | ?36 |
Point of ignition, ℃ | ?400 | ?450 | ?500 | ?500 | ?480 | ?450 | ?400 |
Claims (10)
1, a kind ofly directly prepares the method for Alveolate activated carbon capable, it is characterized in that comprising the steps: by coal
(1) coal dust configuration: brown coal or bituminous coal and coking coal are crushed to respectively≤2mm, then by quality than brown coal or bituminous coal: after coking coal=1: the 0.2-0.5 mixing, be ground to below the 74 μ m coal dust that obtains mixing again;
(2) emulsification coal tar: the first step, asphalt content 〉=55% coal-tar heavy oil is preheated to 120-150 ℃; Second step, the preparation of emulsifier aqueous solution, the stablizer of the 0.5-2% of the 2-6% tensio-active agent of adding coal-tar heavy oil quality and coal-tar heavy oil quality in water, and be preheated to 80-90 ℃ of formation emulsifier aqueous solution; The 3rd step was a coal-tar heavy oil by mass ratio: emulsifier aqueous solution=1: 0.3-0.7 under agitation condition, adds coal-tar heavy oil and makes emulsification coal tar in the emulsifier aqueous solution;
(3) processing of plasticity-coal slime: by mass ratio is coal dust: emulsification coal tar: water: water-soluble binder: lubricant=34-57: 30-36: 6-29: 3-5: 2-3, with stirring in its adding kneader, make plastic coal slime;
(4) pugging: the plasticity-coal slime is handled through vacuum deairing machine or extrusion shaping machine, and coal slime is mixed, and removes large particulate matter with 60 to 100 purpose silk screen filter then in shaper;
(5) extrusion moulding: the coal slime adding after pugging is handled is equipped with in the extrusion shaping machine of honeycomb steel die, carries out moulding, the honeycomb that obtains wetting;
(6) drying: wet honeycomb is dried to moisture and is lower than 2%;
(7) charing and activation: as protection gas, be heated to 600-800 ℃ with rare gas element by heat-up rate 3-5 ℃/min, and under this temperature charing 2-3 hour; Be warmed up to 750-850 ℃ by heat-up rate 5-15 ℃/min then, use steam activation 3-15 hour, obtain Alveolate activated carbon capable.
2, as claimed in claim 1ly a kind ofly directly prepare the method for Alveolate activated carbon capable, it is characterized in that described tensio-active agent is sodium lignosulfonate, humate, sodium formaldehyde condensation products or polymethylene anthracene sulfonic acid sodium by coal.
3, as claimed in claim 1ly a kind ofly directly prepare the method for Alveolate activated carbon capable, it is characterized in that described stablizer selects divalence or trivalent soluble metallic salt by coal.
4, as claimed in claim 3ly a kind ofly directly prepare the method for Alveolate activated carbon capable, it is characterized in that described divalence or trivalent soluble metallic salt are calcium chloride, ferric sulfate or iron nitrate by coal.
5, as claimed in claim 1ly a kind ofly directly prepare the method for Alveolate activated carbon capable, it is characterized in that described water-soluble binder is starch, polyvinyl alcohol, cellulose ester, Natvosol or Xylo-Mucine by coal.
6, as claimed in claim 5ly a kind ofly directly prepare the method for Alveolate activated carbon capable, it is characterized in that described cellulose ester is methylcellulose gum, ethyl cellulose or Vltra tears by coal.
7, as claimed in claim 1ly a kind ofly directly prepare the method for Alveolate activated carbon capable, it is characterized in that described lubricant is the saponification material that tung oil, oleum lini or edible oil and production process thereof produce by coal.
8, as claimed in claim 1ly a kind ofly directly prepare the method for Alveolate activated carbon capable, it is characterized in that described steel die adopts 8-16 hole/cm by coal
2Square hole honeycomb steel die.
9, as claimed in claim 1ly a kind ofly directly prepare the method for Alveolate activated carbon capable, it is characterized in that described forming pressure is 7-14Mpa by coal.
10, as claimed in claim 1ly a kind ofly directly prepare the method for Alveolate activated carbon capable, it is characterized in that described rare gas element is nitrogen or argon gas by coal.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN 200410092429 CN1288077C (en) | 2004-12-21 | 2004-12-21 | Method for directly preparing honeycomb active carbon from coal |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN 200410092429 CN1288077C (en) | 2004-12-21 | 2004-12-21 | Method for directly preparing honeycomb active carbon from coal |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1648040A true CN1648040A (en) | 2005-08-03 |
CN1288077C CN1288077C (en) | 2006-12-06 |
Family
ID=34869346
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN 200410092429 Active CN1288077C (en) | 2004-12-21 | 2004-12-21 | Method for directly preparing honeycomb active carbon from coal |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN1288077C (en) |
Cited By (32)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100408474C (en) * | 2006-08-01 | 2008-08-06 | 长春惠工净化工业有限公司 | Production method of desulfur denitrate dust collecting active coke |
CN101766991A (en) * | 2010-02-11 | 2010-07-07 | 赵建勋 | Unshaped activated coke adsorption catalyst |
CN101766990A (en) * | 2010-02-11 | 2010-07-07 | 赵建勋 | Wastewater purification active coke adsorbent and preparation method thereof |
CN101857224A (en) * | 2010-06-11 | 2010-10-13 | 清华大学 | Preparation method of phenolic resin combined honeycomb activated carbon |
CN102674341A (en) * | 2012-05-14 | 2012-09-19 | 李钱胜 | Columnar activated carbon based on coal pitch binders and preparation method of columnar activated carbon |
CN102976321A (en) * | 2012-12-07 | 2013-03-20 | 淮北市森化碳吸附剂有限责任公司 | Manufacturing method of flue gas desulfurization/denitrification activated carbon |
CN103060053A (en) * | 2013-01-11 | 2013-04-24 | 蔡京鹏 | Waterproofing binder of coal |
CN104549370A (en) * | 2014-12-26 | 2015-04-29 | 江苏高淳陶瓷股份有限公司 | Photocatalytic cellular activated carbon net |
CN103787329B (en) * | 2014-01-17 | 2015-10-28 | 张双全 | A kind of method of compound preparation of binder gac |
CN106241807A (en) * | 2016-08-05 | 2016-12-21 | 王毅 | A kind of Powdered Activated Carbon prepares the method for granular active carbon |
CN106395817A (en) * | 2016-08-26 | 2017-02-15 | 广东韩研活性炭制造有限公司 | Honeycomb-type active carbon, and preparation method thereof |
CN106479587A (en) * | 2015-08-24 | 2017-03-08 | 陆乃昌 | Boiler of power plant biomass composite fuel |
CN106479588A (en) * | 2015-08-24 | 2017-03-08 | 陆乃昌 | Molded coal boiler biomass fuel and its manufacture method |
CN106629719A (en) * | 2016-09-21 | 2017-05-10 | 广东美的制冷设备有限公司 | Preparation technology for activated carbon |
CN106865542A (en) * | 2017-02-23 | 2017-06-20 | 成都国化环保科技有限公司 | A kind of activated carbon with hollow morphology |
CN107235489A (en) * | 2017-06-27 | 2017-10-10 | 南京林业大学 | A kind of preparation method of high-specific surface area Alveolate activated carbon |
CN109179406A (en) * | 2018-10-23 | 2019-01-11 | 西安交通大学 | A kind of coal slime activation prepares the method for active carbon and its application in supercapacitor |
CN109248540A (en) * | 2018-09-30 | 2019-01-22 | 江苏斯沃得环保科技有限公司 | A kind of Alveolate activated carbon absorbing unit |
CN109305682A (en) * | 2018-09-30 | 2019-02-05 | 江苏斯沃得环保科技有限公司 | A kind of honeycombed absorbent charcoal material and preparation method thereof |
CN109499351A (en) * | 2019-01-11 | 2019-03-22 | 四川大学 | Cross-flow type drips the preparation method of filter box and bio-trickling filter and cellular activated carbon |
CN109970057A (en) * | 2019-04-30 | 2019-07-05 | 陕西师范大学 | Cellular activated carbon based on coal liquefaction residue and semi-coke end |
CN110451491A (en) * | 2019-08-20 | 2019-11-15 | 中国航发北京航空材料研究院 | A kind of preparation method of porous graphene granular materials |
CN110872120A (en) * | 2018-08-31 | 2020-03-10 | 中车大同电力机车有限公司 | Preparation method of activated carbon |
CN111908469A (en) * | 2020-07-13 | 2020-11-10 | 宁夏新龙蓝天科技股份有限公司 | Preparation method of special adsorption activated carbon |
CN111908467A (en) * | 2019-06-28 | 2020-11-10 | 大同中车煤化有限公司 | Activated carbon and preparation method thereof |
CN112142372A (en) * | 2020-07-21 | 2020-12-29 | 中欣环保科技有限公司 | Preparation method of active carbon capable of generating negative oxygen ions |
CN112661976A (en) * | 2020-12-21 | 2021-04-16 | 安徽工业大学 | Preparation method of low-rank coal-based high-efficiency water reducing agent |
CN112811410A (en) * | 2021-01-12 | 2021-05-18 | 陕西科技大学 | Recyclable biochar block and preparation method thereof |
CN112938972A (en) * | 2021-04-01 | 2021-06-11 | 淮北市大华环保科技有限公司 | Production method of coal-based molded activated carbon integrated with carbon activation |
CN114752349A (en) * | 2022-04-18 | 2022-07-15 | 宁夏西泰煤化工有限公司 | Coal-based activated carbon binder based on high-temperature coal tar and modified asphalt, and production method and system thereof |
CN114988406A (en) * | 2022-07-26 | 2022-09-02 | 龙岩市华研活性炭科技有限公司 | Preparation process of water-resistant honeycomb activated carbon |
CN117261337A (en) * | 2023-11-18 | 2023-12-22 | 山西立恒焦化有限公司 | Honeycomb activated carbon preparation forming die |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101214957B (en) * | 2008-01-15 | 2011-09-21 | 青岛华世洁环保科技有限公司 | Water-resistant high mechanical strength honeycomb activated carbon and preparation method thereof |
-
2004
- 2004-12-21 CN CN 200410092429 patent/CN1288077C/en active Active
Cited By (39)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN100408474C (en) * | 2006-08-01 | 2008-08-06 | 长春惠工净化工业有限公司 | Production method of desulfur denitrate dust collecting active coke |
CN101766991A (en) * | 2010-02-11 | 2010-07-07 | 赵建勋 | Unshaped activated coke adsorption catalyst |
CN101766990A (en) * | 2010-02-11 | 2010-07-07 | 赵建勋 | Wastewater purification active coke adsorbent and preparation method thereof |
CN101766991B (en) * | 2010-02-11 | 2012-06-13 | 赵建勋 | Unshaped activated coke adsorption catalyst |
CN101857224A (en) * | 2010-06-11 | 2010-10-13 | 清华大学 | Preparation method of phenolic resin combined honeycomb activated carbon |
CN101857224B (en) * | 2010-06-11 | 2012-10-24 | 清华大学 | Preparation method of phenolic resin combined honeycomb activated carbon |
CN102674341A (en) * | 2012-05-14 | 2012-09-19 | 李钱胜 | Columnar activated carbon based on coal pitch binders and preparation method of columnar activated carbon |
CN102976321A (en) * | 2012-12-07 | 2013-03-20 | 淮北市森化碳吸附剂有限责任公司 | Manufacturing method of flue gas desulfurization/denitrification activated carbon |
CN103060053A (en) * | 2013-01-11 | 2013-04-24 | 蔡京鹏 | Waterproofing binder of coal |
WO2014107914A1 (en) * | 2013-01-11 | 2014-07-17 | Cai Jingpeng | Water-blocking binder for coal |
CN103787329B (en) * | 2014-01-17 | 2015-10-28 | 张双全 | A kind of method of compound preparation of binder gac |
CN104549370A (en) * | 2014-12-26 | 2015-04-29 | 江苏高淳陶瓷股份有限公司 | Photocatalytic cellular activated carbon net |
CN104549370B (en) * | 2014-12-26 | 2016-09-14 | 江苏高淳陶瓷股份有限公司 | Photocatalysis cellular activated carbon net |
CN106479587A (en) * | 2015-08-24 | 2017-03-08 | 陆乃昌 | Boiler of power plant biomass composite fuel |
CN106479588A (en) * | 2015-08-24 | 2017-03-08 | 陆乃昌 | Molded coal boiler biomass fuel and its manufacture method |
CN106241807A (en) * | 2016-08-05 | 2016-12-21 | 王毅 | A kind of Powdered Activated Carbon prepares the method for granular active carbon |
CN106395817A (en) * | 2016-08-26 | 2017-02-15 | 广东韩研活性炭制造有限公司 | Honeycomb-type active carbon, and preparation method thereof |
CN106629719A (en) * | 2016-09-21 | 2017-05-10 | 广东美的制冷设备有限公司 | Preparation technology for activated carbon |
CN106865542A (en) * | 2017-02-23 | 2017-06-20 | 成都国化环保科技有限公司 | A kind of activated carbon with hollow morphology |
CN107235489A (en) * | 2017-06-27 | 2017-10-10 | 南京林业大学 | A kind of preparation method of high-specific surface area Alveolate activated carbon |
CN110872120A (en) * | 2018-08-31 | 2020-03-10 | 中车大同电力机车有限公司 | Preparation method of activated carbon |
CN109248540A (en) * | 2018-09-30 | 2019-01-22 | 江苏斯沃得环保科技有限公司 | A kind of Alveolate activated carbon absorbing unit |
CN109305682A (en) * | 2018-09-30 | 2019-02-05 | 江苏斯沃得环保科技有限公司 | A kind of honeycombed absorbent charcoal material and preparation method thereof |
CN109179406A (en) * | 2018-10-23 | 2019-01-11 | 西安交通大学 | A kind of coal slime activation prepares the method for active carbon and its application in supercapacitor |
CN109499351A (en) * | 2019-01-11 | 2019-03-22 | 四川大学 | Cross-flow type drips the preparation method of filter box and bio-trickling filter and cellular activated carbon |
CN109970057A (en) * | 2019-04-30 | 2019-07-05 | 陕西师范大学 | Cellular activated carbon based on coal liquefaction residue and semi-coke end |
CN111908467A (en) * | 2019-06-28 | 2020-11-10 | 大同中车煤化有限公司 | Activated carbon and preparation method thereof |
CN110451491A (en) * | 2019-08-20 | 2019-11-15 | 中国航发北京航空材料研究院 | A kind of preparation method of porous graphene granular materials |
CN111908469A (en) * | 2020-07-13 | 2020-11-10 | 宁夏新龙蓝天科技股份有限公司 | Preparation method of special adsorption activated carbon |
CN112142372A (en) * | 2020-07-21 | 2020-12-29 | 中欣环保科技有限公司 | Preparation method of active carbon capable of generating negative oxygen ions |
CN112661976A (en) * | 2020-12-21 | 2021-04-16 | 安徽工业大学 | Preparation method of low-rank coal-based high-efficiency water reducing agent |
CN112811410A (en) * | 2021-01-12 | 2021-05-18 | 陕西科技大学 | Recyclable biochar block and preparation method thereof |
CN112811410B (en) * | 2021-01-12 | 2022-08-23 | 陕西科技大学 | Recyclable biochar block and preparation method thereof |
CN112938972A (en) * | 2021-04-01 | 2021-06-11 | 淮北市大华环保科技有限公司 | Production method of coal-based molded activated carbon integrated with carbon activation |
CN114752349A (en) * | 2022-04-18 | 2022-07-15 | 宁夏西泰煤化工有限公司 | Coal-based activated carbon binder based on high-temperature coal tar and modified asphalt, and production method and system thereof |
CN114752349B (en) * | 2022-04-18 | 2023-09-26 | 宁夏西泰煤化工有限公司 | Coal-based activated carbon binder based on high-temperature coal tar and modified asphalt, and production method and system thereof |
CN114988406A (en) * | 2022-07-26 | 2022-09-02 | 龙岩市华研活性炭科技有限公司 | Preparation process of water-resistant honeycomb activated carbon |
CN117261337A (en) * | 2023-11-18 | 2023-12-22 | 山西立恒焦化有限公司 | Honeycomb activated carbon preparation forming die |
CN117261337B (en) * | 2023-11-18 | 2024-02-27 | 山西立恒焦化有限公司 | Honeycomb activated carbon preparation forming die |
Also Published As
Publication number | Publication date |
---|---|
CN1288077C (en) | 2006-12-06 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN1288077C (en) | Method for directly preparing honeycomb active carbon from coal | |
CN1272241C (en) | Shaped activated carbon | |
CN1200769C (en) | Mercury removal catalyst and method of making and using same | |
CN1146469C (en) | Method for making mesoporous carbon | |
CN107029668B (en) | A kind of honeycomb type molecular sieve-active carbon compound adsorbent, preparation method and applications | |
CN105944665A (en) | Preparation method of molecular sieve concentration rotating wheel adsorption packing for treating VOCs | |
CN108439403B (en) | Method for preparing biomass-formed activated carbon by low-temperature pre-pyrolysis and superfine raw materials | |
CN102431992A (en) | Method for preparing porous carbon material by using magnesium oxide template in cooperation with activation of potassium hydroxide | |
CN109160512A (en) | A kind of gasification of biomass residue pressed active carbon and preparation method thereof | |
CN101961644B (en) | Chloride-carbonaceous skeleton composite adsorbent and preparation method thereof | |
CN105148843A (en) | Active carbon granule, preparing method thereof and carbon tank | |
CN107235489A (en) | A kind of preparation method of high-specific surface area Alveolate activated carbon | |
CN112125306B (en) | Activated carbon and preparation method thereof | |
CN111661846B (en) | Method for preparing activated carbon | |
CN104069690A (en) | Zeolite ceramisite filter material prepared by gangue and preparation method of zeolite ceramisite filter material | |
CN111389382B (en) | Preparation method and application of lanthanum-iron oxide modified nano inorganic material straw porous carbon | |
CN103641507A (en) | Zeolite-attapulgite composite honeycomb body and preparation method thereof | |
CN1290606C (en) | Vehicular wood active carbon and preparing method tehreof | |
CN114988406A (en) | Preparation process of water-resistant honeycomb activated carbon | |
CN1072975C (en) | Alumina-based catalyst for the treatment of gases containing sulphur compounds, use of these catalysts for the treatment and processes for treatment of the said gases | |
CN112939583B (en) | RTO honeycomb ceramic heat accumulator prepared from bauxite tailings and preparation method thereof | |
CN1054015A (en) | Handle gaseous effluent catalyst of using and the method for handling these gaseous effluents | |
CN101016154A (en) | Method of preparing active carbon for gas cleaning and environmental protection by crop straw | |
CN110255554A (en) | A kind of novel desulphurization denitration activity charcoal | |
CN108588882A (en) | A kind of industrial residue based composite fibre and preparation method thereof |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant |