CN1747897A - Manufacturing method of activated carbon structure having a frame - Google Patents
Manufacturing method of activated carbon structure having a frame Download PDFInfo
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- CN1747897A CN1747897A CNA2004800039773A CN200480003977A CN1747897A CN 1747897 A CN1747897 A CN 1747897A CN A2004800039773 A CNA2004800039773 A CN A2004800039773A CN 200480003977 A CN200480003977 A CN 200480003977A CN 1747897 A CN1747897 A CN 1747897A
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B38/00—Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof
- C04B38/06—Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof by burning-out added substances by burning natural expanding materials or by sublimating or melting out added substances
- C04B38/063—Preparing or treating the raw materials individually or as batches
- C04B38/0635—Compounding ingredients
- C04B38/069—Other materials, e.g. catalysts
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- B—PERFORMING OPERATIONS; TRANSPORTING
- B01—PHYSICAL OR CHEMICAL PROCESSES OR APPARATUS IN GENERAL
- B01D—SEPARATION
- B01D39/00—Filtering material for liquid or gaseous fluids
- B01D39/02—Loose filtering material, e.g. loose fibres
- B01D39/06—Inorganic material, e.g. asbestos fibres, glass beads or fibres
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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
- C01B32/354—After-treatment
- C01B32/382—Making shaped products, e.g. fibres, spheres, membranes or foam
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B38/00—Porous mortars, concrete, artificial stone or ceramic ware; Preparation thereof
- C04B38/0006—Honeycomb structures
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/00474—Uses not provided for elsewhere in C04B2111/00
- C04B2111/00793—Uses not provided for elsewhere in C04B2111/00 as filters or diaphragms
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- C—CHEMISTRY; METALLURGY
- C04—CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
- C04B—LIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
- C04B2111/00—Mortars, concrete or artificial stone or mixtures to prepare them, characterised by specific function, property or use
- C04B2111/00474—Uses not provided for elsewhere in C04B2111/00
- C04B2111/0081—Uses not provided for elsewhere in C04B2111/00 as catalysts or catalyst carriers
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- F—MECHANICAL ENGINEERING; LIGHTING; HEATING; WEAPONS; BLASTING
- F23—COMBUSTION APPARATUS; COMBUSTION PROCESSES
- F23J—REMOVAL OR TREATMENT OF COMBUSTION PRODUCTS OR COMBUSTION RESIDUES; FLUES
- F23J2219/00—Treatment devices
- F23J2219/30—Sorption devices using carbon, e.g. coke
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- Engineering & Computer Science (AREA)
- Ceramic Engineering (AREA)
- Organic Chemistry (AREA)
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- Solid-Sorbent Or Filter-Aiding Compositions (AREA)
Abstract
The invention discloses a manufacturing method for active carbon with strong adsorption function and strength. The method of the invention comprises the following steps that: carbon fibers are added and taken as reinforcing materials of the active carbon; active carbon compounds (the compounds consist of the active carbon which is provided with the carbon fibers and asphalt which is used as adhesives) are molded into a framework die; the active carbon compounds are converted into carbonates so as to make an active carbon structure receive a framework. The framework is made of metal and can be resistant to corrosion during the process of conversion of the active carbon compounds into the carbonates, and the shape of the framework can be diversified according to different purposes.
Description
Technical field
The present invention relates to a kind of method of making activated carbon structure, this is a kind of framework that can make a good job of absorption and intensity function.
Background technology
Activated carbon has a huge accurate surface-area (about 1500 meters squared per gram), and because of containing many micropores, it is widely used for dispeling the organic substance that is present in the middle of the fluidity substances such as air, water.
Many drawbacks are arranged when using activated carbon.At first, use a parcel or filter cylinder, activated carbon is fixed on particle state by reticulation and similar thing.Can produce the pressure whereabouts that adsorptive power and conversion unit are caused in this case, be very difficult because will control activated carbon certain parcel factor in parcel or filter cylinder.Then, it is interior as sorbing material or catalyzer that activated carbon should be filled in a filter cylinder, and can be dispelled under wind action easily.Secondly, when being used continuously, activated carbon generally is filled in the special instrument, so that carry out the separation after the passivation, still, because activated carbon particle is so little, the pressure that generally can produce instrument falls phenomenon after rise.
In order to overcome above-mentioned drawback, many tests were all carried out, such as: use tackiness agent to make the filterableness structure of likeness in form honeycomb; Increase the volume of activated carbon particle.When using tackiness agent to make activated carbon structure, tackiness agent may stop up its micropore, reduces certain surface-area of this structure, and adsorptive power is had a greatly reduced quality.For example, activated carbon power and water-soluble starch are mixed, form activated carbon structure, and oven dry activated carbon tissue, even these steps all can be very useful when forming a special construction, but tackiness agent has stopped up the micropore of activated carbon structure, cause certain low surface area to dwindle.And in the process of water is arranged, or when surpassing the temperature of combustion of starch, the mode of using starch to make tackiness agent is impracticable.
The bounding force of tackiness agent (such as starch) and activated carbon is very weak, and when the tackiness agent capacity was on the low side, the activated carbon structure that contains starch and activated carbon was easy to destroyed.When the tackiness agent capacity is higher, certain concrete surface meeting step-down of activated carbon, thus destroy adsorptive power.
Therefore, in the carbonate switching process, the tamanori that can change charcoal mixes with activated carbon power or particle, thereby the whole tackiness agent and activated carbon power or particulate material of containing changed into carbon.This method can be carried out under higher relatively temperature, so the reduction of the concrete surface-area of activated carbon is then lower.That is to say, tackiness agent in the carbonate conversion process by carbonating and kept its state, like this since, the steadiness of structure can remain unchanged, the concrete surface area minimizing degree of structure is also low, because the volatile matter of tackiness agent has produced some micropores in the high temperature evaporation process.In a word, tackiness agent serves as thermoplastic resin exactly in this purpose.
The 303rd, No. 239 Korean Patent has disclosed a kind of tackiness agent, is used to make the pitch or the thermoplastic resin of carbon optical fiber filtering type sorbent material such as being used for fixing activated carbon.
When pitch is used as tackiness agent, generally about 400 degrees centigrade, carry out with the postheat treatment of carbon fiber mix.In heat treatment process, pitch is become meso-phase and is attached on the carbon optical fiber.Yet in heat treatment process, because pitch can be transformed into a kind of heat-proof polymer, it does not have micropore is in accordance with expectation.Therefore, just in case certain piece bituminous amount thickness excessive or carbon optical fiber is excessive, the original micropore of carbon optical fiber can stop up, but therefore more further carbon optical fiber micropore may lose activity.Thus, increasing certain concrete surface area is very difficult thing.If dosed that small portion activated carbon powder, just tension intensity increases, but the reduction of concrete surface area is very high.
In addition, the 302nd, No. 472 Korean Patent disclosed and a kind ofly by high-temperature heat treatment tackiness agent has been transformed into the method for carbon, and wherein, thermo-elasticity or thermoplastic polymer be as tackiness agent, and activated carbon powder by this adhesive attachment on inorganic filter or wire netting.In this case, be conditional attached to the activated carbon powder amount on wire netting or the inorganic filter.In addition, owing to can stablize heating at back thermoplastic polymer that thermoplastic polymer is hardened, therefore stable thermoplastic polymer is carried out carbonization may need lot of energy and time.And lower as the output of the thermo-elasticity of tackiness agent or thermoplastic polymer, therefore when increasing binder dosage, specific surface area can reduce.That is to say that although the intensity of activated carbon structure increases along with the increase of tackiness agent, specific surface area can reduce.
As mentioned above, use the tackiness agent that meets conventional related can easily carry out mold.If as tackiness agent, then this tackiness agent may block some micropores with starch, and can reduce the adsorptive power of activated carbon structure.If by as tackiness agent activated carbon powder being adhered to structurally thermoplastic polymer, then by the thermal pretreatment of low temperature more, thermoplastic polymer can decompose, and temperature more Gao Shihui carry out carbonization.In the previous case (use starch), thermal treatment temp may be different because of the characteristic of tackiness agent.And in latter event (use thermoplastic resin), the carbonization meeting consumes plenty of time and energy.
In addition, because the viscosity of this tackiness agent is higher, be difficult to make activated carbon to mix mutually with this tackiness agent, therefore temperature is higher when using traditional method to make activated carbon structure.But also used solvent to dilute the tackiness agent that uses traditional method to make.When using solvent, carburising step can be comparatively complicated.In addition, in heat treatment process, can produce bubble, therefore may not can form activated carbon structure well.Along with adhesive consumption increases, the intensity of activated carbon structure also improves constantly.But tackiness agent may block the micropore of activated carbon, thereby has reduced specific surface area.
Therefore, need a kind of activated carbon structure with high-tensile of design strongly, this structure can be resisted high temperature, and has high absorption capacity, can prolong the commutation period of new texture.
Summary of the invention
Therefore, target of the present invention provides the activated carbon structure with following framework: activated carbon structure has outstanding adsorptive power and intensity in this framework.
Therefore, another target of the present invention provides the activated carbon structure that can make such as different shapes such as honeycomb type, collar plate shape or anchor chain types.
For realizing above-mentioned target, made the activated carbon structure that in structure, has the enhancing framework, so that can make large scale structure, and the intensity that improves structure.In addition, by using the specific surface area that can reduce activated carbon structure as the mixture of the pitch of tackiness agent and activated carbon powder slightly.
In embodiment of the present invention, introduced the making method of the activated carbon structure of band framework, step is as follows: at first, make activated carbon mixture in this ratio of reinforcement material of the activated carbon powder of about 100 weight (wt), the tackiness agent of about 5~40wt, about 5~30wt.Secondly, the framework with predetermined shape is installed in the mold.Then, activated carbon mixture is filled between mold and the framework; Moreover, under 50 ℃~300 ℃ temperature, to activated carbon mixture preheating 10~30 minutes.Then, under rare gas element, put in the smelting furnace activated carbon mixture into (temperature is 400 ℃~1000 ℃) carbonization 1~15 hour.At last, under rare gas element, input steam or carbonic acid gas are with cooling of carbonization mixture and activation.
According to first-selected embodiment of the present invention, tackiness agent is a kind of in pitch, creosote, viscid bitumen and the gilsonite.Containing in the reinforcement material that length gives is the carbonizedfibres of 1~20mm.Framework is a kind of in iron, stainless steel, nickel, nickelalloy, aluminium, copper and composition thereof.Framework is to be formed by uneven surface, helps strengthening adhesion strength, and its surface is made of the thick pitch of about 0.1mm.Activated carbon mixture also comprises a kind of precursor substance, can be used as precious metal or metal oxide catalyst and uses in making the activated carbon mixture step.Activated carbon structure is supported precious metal or metal oxide catalyst.
Description of drawings
By describing first-selected embodiment with reference to the accompanying drawings in detail, above-mentioned target of the present invention and other advantage just clearly: Fig. 1 is the skeleton view that contains the part vertical view, has shown the structure that adopts the honeycomb type activated carbon that metal porous match plate dies makes; Fig. 2 is a skeleton view, has shown the structure of the honeycomb type activated carbon that has metal bar; Fig. 3 is a skeleton view, the structure of the fixing most honeycomb type activated carbon of example explanation; Fig. 4 is a skeleton view, and display layer stacks the structure of long-pending excellent type activated carbon; Fig. 5 is a separate perspective view, has shown the bottom mold and the top mold of honey comb structure respectively, and metal porous match plate dies; Fig. 6 is an assembled perspective view, has shown bottom mold and the top mold and the metal porous match plate dies of honey comb structure, and wherein, activated carbon mixture is mixed mutually with activated carbon, carbonizedfibres, and tackiness agent is filled in the combination mold; Fig. 7 is the explanation skeleton view of the excellent type activated carbon structure of a manufacturing.
Embodiment
Hereinafter, will with reference to the accompanying drawings best mode and the first-selected embodiment of the present invention that carries out an invention be elaborated.It should be noted that for graphic simplicity and explanation, can use some reference numbers to come part or like product are marked.
In embodiment of the present invention, introduced the making method of the activated carbon structure of band framework, step is as follows: at first, make activated carbon mixture, this mixture by about 100 weight (wt) in the activated carbon powder partly, the 5~40wt part in the tackiness agent, 5~30wt in the reinforcement material partly form.Secondly, the framework with predetermined shape is installed in the mold.Then, activated carbon mixture is filled between mold and the framework; Moreover, under 50 ℃~300 ℃ temperature, to activated carbon mixture preheating 10~30 minutes.Then, under rare gas element, put in the smelting furnace activated carbon mixture into (temperature is 400 ℃~1000 ℃) carbonization 1~15 hour.At last, under rare gas element, input steam or carbonic acid gas are with cooling of carbonization mixture and activation.
Pre-heating step is in order better tackiness agent to be put in the middle of the reinforcement material.Carburising step must be carried out under rare gas element, and as nitrogen, argon gas etc., this helps preventing fire.If in oxygen, carry out, the thermal treatment meeting danger close in the carburising step.Moreover, by activation carbonization mixture, can enlarge the micropore of activated carbon structure, or remove the material that the activated carbon structure surface does not react, so just can increase concrete surf zone, heat up the activatory step thereby saved passing through in the traditional method.Tackiness agent is a kind of of pitch, creosote, viscid bitumen, gilsonite and their mixtures, can be solid shape or aqueous, can be solid and liquid mixture during use, also can be independent solid or liquid.
Generally speaking, preferably adopt softening temperature to be higher than the Powdered pitch of room temperature.If adopt aqueous pitch, viscosity is an important processing factors.Mix with heavy oil (aqueous creosote wet goods) by intensification or with pitch, may command bituminous viscosity, thus the flowability between control activated carbon and the tackiness agent also is easier to mixed active carbon and tackiness agent.
Embodiment in according to the present invention, when tackiness agent was put into activated carbon powder equably, intensity was constant, and the reduction of concrete surface area can be very low.The intensity height of the part that amount of binder is higher, the reduction of concrete surface area is also very high.The intensity of the part that amount of binder is less is low, and the reduction of concrete surface area is also low.According to embodiment of the present invention, when softening temperature is higher than 60 ℃ pitch when the tackiness agent, pitch is easy to mix with activated carbon and reinforcement material, because pitch is Powdered; When mixed uniformly activated carbon mixture was kept in the environment that is higher than softening temperature, the asphalt powder of uniformly distributing in activated carbon mixture can liquefy, and after the liquefaction, and can be applied to the surface of activated carbon, framework and reinforcement material.Therefore compare with the structure that adopts liquid adhesive to form, this kind texture quality is better, mainly is because adopted uniform mixing.
Coal tar pitch has one 60 to 100 ℃ softening temperature, at room temperature keeps solid state, also has a kind of hydrocarbon mixture of fragrance.This and mixture have polymer weight, so boiling point is very high.And, when the coal tar pitch adstante febre, easy polymerization reaction take place.Coal tar pitch contains phenyl ring on three and carbon one carbochains, so that hydrocarbon ratio uprises, about 1.6-1.9.Therefore, when it is decomposed by thermal treatment, can produce wide variation; Wedding agent is suitable for activated carbon structure.When pitch was used as wedding agent, volatile quantity was very little, thereby made pitch almost become carbon, and carbon transforms power and just increased.So even only use a spot of pitch, the power of activated carbon structure has also increased, carbonization just can take place at short notice.In addition, in the process of carbonization, because the formation effect of volatile component, the decrement of certain surface areas is very little,
According to a function mode of the present invention, the activated carbon structure that has framework comprises the carbon fiber reinforcement material that a length is 1~20mm.Because carbon fiber as reinforcement material, is compared with the situation of only using wedding agent, and activated carbon structure has higher intensity.
According to a function mode of the present invention, framework mainly is steel, stainless steel, nickel, nickelalloy, aluminium, copper and composition thereof.In addition, framework is made of a coarse surface, to strengthen bounding force; Also comprise the asphalt surface course of a thickness more than 0.1mm.Therefore coarse surface has increased surface area, has also increased the bounding force between framework and the activated carbon.Upper layer is to form by the road oil on the framework, and becomes carbon surface layer in carbonization process, thus keep and activated carbon mixture 12 between bounding force.
If framework is a rod-type 31, the diameter of bar is approximately 1~20mm so.If framework is the net formula, Wang thickness is about 0.1mm so, and circle or rectangular opening are about 10mm.
In addition, in the process of making activated carbon mixture, can be supported by activated carbon structure as the precursor of precious metal or golden oxygen catalyst.The consumption of precursor can be controlled according to the purpose of reaction, and has temperature meeting increase in the process of carbonization of the activated carbon of precursor.Then, precursor is decomposed, and activated carbon structure has also just comprised and also just comprised catalyzer.In other words, the step of the activeconstituents of support catalyst can be eliminated, to increase output and to save energy and cost.
After this, demonstration of the present invention is described in detail by Fig. 1 to Fig. 7.
Demonstration 1: rod-type activated carbon structure.The invention provides a kind of method of using rod-type framework 31 to make activated carbon structure.According to this demonstration of the present invention, framework is that a diameter is 1 to 20 millimeter rectangle or a circle.At first, framework is installed on 32 or 33 the mould.The second, on 32 or 33 mould, insert activated carbon mixture, mixture is mixed by about 100 minutes heavy activated carbon, 15 to 20 fens heavy wedding agents and 10 to 15 fens heavy reinforcement materials.The 3rd, remove 32 or 33 moulds and activated carbon mixture was heated 10 minutes in advance with about 100 ℃ temperature.Then, with about 400 ℃ temperature pre-heated activated carbon mixture is carried out carbonization and activate reaching 1 hour, the rod-type activated carbon structure has just been made.
According to an operation demonstration of the present invention, must provide an absorption instrument.As shown in Figure 4, the rod-type activated carbon structure crosses one another in adsorber, thereby reduces the pressure drop of adsorber and increase adsorptive capacity.
Example 2: honeycomb type activated carbon structure.The honeycomb type activated carbon structure.Honeycomb type activated carbon structure 10 with holes or 20 the method for making is provided in specific examples of the present invention.
The metal sheet 13 of wire netting or 13b with holes (as shown in Figure 5) at first, is provided.
According to a function mode of the present invention, the size of each hole 13b and the eyelet of activated carbon structure or pore 11 (as shown in Figure 1, 2, 3) size are basic identical or bigger.Secondly, have therein in the honeycomb type mold 61,63 of a plurality of bars, filled activated carbon mixture according to 100wt activated carbon, about 15~20wt tackiness agent and this mixed of 10~15wt reinforcement material.Each bar will be as the pore of this structure.The 3rd, removed mold 61,63, and activated carbon mixture has been carried out preheating in 10 minutes with the temperature of 100C.Then, the activated carbon mixture of preheating 1 hour carbonization and activation have been carried out, so that make the honeycomb type activated carbon structure (20 among 10 among Fig. 1 and Fig. 2) that has 1 pore 11 at least with the temperature of 400C.
According to a function mode of the present invention, a plurality of bars 62 that can form in honeycomb type activated carbon structure 10,20 in the honeycomb type mold 61,63 of pore can be attached on bottom mold that comprises a plurality of holes (63a) (61) and the top mold (63).A plurality of bars 62 can sting thoroughly portion's mold (63) and pass a plurality of holes (63a), thereby are fixed on the bottom mold (61).According to a first-selected function mode of the present invention, a plurality of bars (62) and a plurality of hole (63a) are rectangle.
Owing to can therefore can make large, honeycomb type activated carbon structure 10 according to the big or small manufacturing structure 10 of wire netting or metal sheet 13.
As shown in Figure 5, by the hole on the fixed metal plate 13 (13a among Fig. 5) but fixed sturcture 10 therefore can easily this structure be fixed in the conduit of an adsorption device, on the wall or the like.
Although with reference to incidental sketch legend of the present invention is described in this article, but should understand, the present invention is not limited to these accurate examples, and on top of the personnel of this technology can carry out other various changes or modifications under the situation that does not depart from scope of the present invention or spirit.
According to a function mode of the present invention, activated carbon mixture comprises activated carbon powder or carbon granules, as the carbonizedfibres of reinforcement material, as the pitch that activated carbon powder or carbon granules is adhered to the tackiness agent on the metal frame.Activated carbon mixture is attached to metal frame and carry out carbonization, thereby makes the activated carbon structure sclerosis with mixture and framework.Can make large-scale activated carbon structure according to the shape of framework in addition.
And this does not need the fixedly frame of activated carbon structure, the pressure decline of therefore having saved manufacturing cost and having prevented to be caused by frame.Activated carbon structure can have different shape, can easily append on an adsorption device or from an adsorption device to separate, and have outstanding intensity, has therefore saved manufacturing cost by the weight and the simplification an adsorption device that reduce an adsorption device.
Claims (7)
1. a manufacturing has the method for the activated carbon structure of framework, and it comprises following steps:
At first, make activated carbon mixture in this ratio of reinforcement material of the activated carbon powder of about 100 weight (wt), the tackiness agent of about 5~40wt, about 5~30wt;
Secondly, the framework with predetermined shape is installed in the mold;
Then, activated carbon mixture is filled between mold and the framework;
Moreover, under 50 ℃~300 ℃ temperature, to activated carbon mixture preheating 10~30 minutes;
Then, under rare gas element, put in the smelting furnace activated carbon mixture into (temperature is 400 ℃~1000 ℃) carbonization 1~15 hour;
At last, under rare gas element, input steam or carbonic acid gas are with cooling of carbonization mixture and activation.
2. the method for claim 1 is characterized by: tackiness agent is a kind of in tar, pitch, creosote, viscid bitumen and the gilsonite.
3. the method for claim 1 is characterized by: containing in the reinforcement material that length gives is the carbonizedfibres of 1~20mm.
4. the method for claim 1 is characterized by: framework is a kind of in iron, stainless steel, nickel, nickelalloy, aluminium, copper and composition thereof.
5. the method for claim 1, it is characterized by: framework is to be formed by uneven surface, helps strengthening adhesion strength, its surface is made of the thick pitch of about 0.1mm.
6. the method for claim 1, it is characterized by: activated carbon mixture also comprises a kind of precursor substance, can be used as precious metal or metal oxide catalyst and use in making the activated carbon mixture step, activated carbon structure is supported precious metal or metal oxide catalyst.
7. as claim 1 or 2 or 3 or 4 or 5 or 6 described methods, it is characterized by: activated carbon mixture comprises the tackiness agent of the activated carbon powder of 100wt, about 5~40wt and the strongthener of about 5~30wt, wherein, tackiness agent is a kind of in tar, pitch, creosote, viscid bitumen and the gilsonite, and reinforcement material comprises the carbonizedfibres that length is about 1~20mm.
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JP3610208B2 (en) * | 1997-11-12 | 2005-01-12 | 京セラ株式会社 | Activated carbon honeycomb structure |
US6599856B1 (en) * | 1999-10-21 | 2003-07-29 | Tennex Corporation | Formed activated carbon and process for producing the same |
CN1114481C (en) * | 2000-05-11 | 2003-07-16 | 中国科学院山西煤炭化学研究所 | Method for preparing active carbon for storing methane |
CN1367038A (en) * | 2001-01-22 | 2002-09-04 | 中国石油化工股份有限公司 | Formed active carbon and its production method |
-
2003
- 2003-09-04 KR KR10-2003-0061671A patent/KR100509348B1/en active IP Right Grant
-
2004
- 2004-02-16 CN CNB2004800039773A patent/CN1330567C/en not_active Expired - Fee Related
- 2004-02-16 JP JP2006502710A patent/JP4776530B2/en not_active Expired - Fee Related
Cited By (6)
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CN105342756A (en) * | 2015-10-21 | 2016-02-24 | 芜湖悠派护理用品科技股份有限公司 | Nursing mat |
CN105964221A (en) * | 2016-05-25 | 2016-09-28 | 绍兴文理学院 | Composite carbon rod based on waste wool granular active carbon and preparation method for composite carbon rod |
CN105964221B (en) * | 2016-05-25 | 2018-07-31 | 绍兴文理学院 | A kind of composite carbon rod and preparation method thereof based on discarded hair granular activated carbon |
CN107570114A (en) * | 2017-09-18 | 2018-01-12 | 惠州市银嘉环保科技有限公司 | A kind of super passage ultrafiltration effect active carbon stick and preparation method thereof |
CN109453745A (en) * | 2018-12-28 | 2019-03-12 | 苏州班顺工业气体设备有限公司 | High strength carbon molecular sieve and preparation method thereof |
CN113816376A (en) * | 2021-09-30 | 2021-12-21 | 国家能源集团宁夏煤业有限责任公司 | Binder special for coal-based activated carbon and preparation method thereof |
Also Published As
Publication number | Publication date |
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KR20040074211A (en) | 2004-08-23 |
JP2006517901A (en) | 2006-08-03 |
JP4776530B2 (en) | 2011-09-21 |
KR100509348B1 (en) | 2005-08-22 |
CN1330567C (en) | 2007-08-08 |
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