CN103643351A - Method for producing active carbon fiber in salt dip pretreatment mode - Google Patents

Method for producing active carbon fiber in salt dip pretreatment mode Download PDF

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Publication number
CN103643351A
CN103643351A CN201310669896.8A CN201310669896A CN103643351A CN 103643351 A CN103643351 A CN 103643351A CN 201310669896 A CN201310669896 A CN 201310669896A CN 103643351 A CN103643351 A CN 103643351A
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raw material
salt pretreatment
salt
solution
carbon fiber
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CN201310669896.8A
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CN103643351B (en
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杨学斌
杨学彦
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Suzhou Shengze science and Technology Pioneer Park Development Co.,Ltd.
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杨学斌
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Abstract

The invention discloses a method for producing an active carbon fiber in a salt dip pretreatment mode. The method comprises the following steps: cutting and flattening a viscose fiber (felt or cloth) as a raw material, subsequently performing three times of continuous salt dip pretreatment, namely spraying and dipping the viscose fiber into a 7-8% (NH4)2HPO3 solution, a 6-7% (NH4)2HPO3 solution and 5-6% of (NH4)2HPO3 solution in a salt dip pretreatment device under the condition of 40-60 DEG C, after dipping, dehydrating and drying by using an extruder, subsequently drying in a wind type drier, and finally settling and rolling the dried raw material and continuously performing a carbonization process on the dried raw material to be carbonize the dried raw material. By adopting the method disclosed by the invention, not only can the raw material be uniformly and sufficiently dipped, but also the concentration of the (NH4)2HPO3 solution is not diluted, the weight is increased, and moisture is not carried away, so that a prepared product is low in moisture content, high in carbon content, high in adsorption pertinence and large in effective specific surface area.

Description

A kind of method of producing activated carbon fiber salt pretreatment
technical field:
The present invention relates to activated carbon fiber preparation method technical field, particularly a kind of method of producing activated carbon fiber salt pretreatment.
background technology:
At present, prior art is the salt pretreatment methods that adopt in producing the pretreated process of activated carbon fiber more, be that raw fiber is fully immersed in salt (phosphate, carbonate, sulfate etc.) solution, carry out carbonization after then making it dehydrate, activated carbon fiber is prepared in activation.And the salting liquid (as 6% ~ 8%) that mostly adopts single concentration in impregnation technology floods raw fiber certain hour, after dry, carry out carbonization-activation, although the production yield to the performance of product and product makes moderate progress and improves, but it is insufficient that salting liquid soaks, and takes away large quantity of moisture, make carbon fiber meeting fusion and decomposition when high temperature cabonization, cause the carbon content of product low, thereby effective ratio area is little, adsorption desorption capacity is low, therefore in Application Areas, can be subject to certain restrictions.
summary of the invention:
In view of this, the object of the present invention is to provide a kind ofly to make organic solution by raw fiber dipping fully, do not take away moisture, products obtained therefrom phosphorus content is high, adsorb method with strong points, to have the salt pretreatment that effective ratio area is large.
For achieving the above object, the present invention by the following technical solutions: a kind of method of producing activated carbon fiber salt pretreatment, comprises the steps:
S1: take viscose felt, cloth is raw material, carries out salt pretreatment by raw material cutting, after planishing;
S2: the raw material after planishing is carried out to salt pretreatment for the first time, in salt pretreatment device in 7% ~ 8% (NH 4) 2hPO 3solution sprays rear immersion 1 ~ 2h under the condition of 40 ℃ ~ 60 ℃, after immersion, by extruder, dehydrates;
S3: after salt pretreatment, carry out continuously for the first time salt pretreatment for the second time, in salt pretreatment device in 6% ~ 7% (NH 4) 2hPO 3solution sprays rear immersion 1 ~ 2h under the condition of 40 ℃ ~ 60 ℃, after immersion, by extruder, dehydrates;
S4: after salt pretreatment, carry out continuously for the second time salt pretreatment for the third time, in salt pretreatment device in 5% ~ 6% (NH 4) 2hPO 3solution sprays rear immersion 1 ~ 2h under the condition of 40 ℃ ~ 60 ℃, after immersion, by extruder, dehydrates;
S5: the raw material after salt pretreatment is for the third time dried in dryer, and temperature is controlled at 120 ~ 140 ℃, and pressure is 0.2 ~ 0.4 Mpa;
S6: enter continuously carbonization technique after raw material arrangement, volume after drying is flat and carry out carbonization.
Above-mentioned salt pretreatment device is that top is provided with eight spray equipments, and bottom is for soaking position, and it is highly 1 ~ 1.5m that solution soaks.
Above-mentioned dryer adopts wind formula dryer, in the middle of it, is three-layer network band, is inside provided with two three-dimensional rollings of rod, heats rod heat conduction make raw material stoving by steam, and effectively drying length is 36m.
Viscose (felt or cloth) by three salt pretreatments is in (NH 4) 2hPO 3in solution, through three continuous sprays, dry after soaking, dehydrating, raw material can not only be soaked evenly, fully again, and (NH 4) 2hPO 3the concentration of solution is not diluted, and weight increases, and do not take away moisture, thereby the product moisture content of gained is low, and phosphorus content is high, it is with strong points to adsorb, effective ratio area is large.
the specific embodiment:
The invention will be further described by the following examples, take viscose felt, cloth as raw material is prepared active carbon fiber felt, cloth is example, and the method step of salt pretreatment is as follows:
A) take viscose felt, cloth is raw material, by raw material cutting, after planishing, carries out salt pretreatment;
B) raw material after planishing is carried out to salt pretreatment for the first time, in salt pretreatment device in 7% ~ 8% (NH 4) 2hPO 3solution sprays rear immersion 1 ~ 2h under the condition of 40 ℃ ~ 60 ℃, after immersion, by extruder, dehydrates;
C) after salt pretreatment, carry out continuously salt pretreatment for the second time for the first time, in salt pretreatment device in 6% ~ 7% (NH 4) 2hPO 3solution sprays rear immersion 1 ~ 2h under the condition of 40 ℃ ~ 60 ℃, after immersion, by extruder, dehydrates;
D) after salt pretreatment, carry out continuously salt pretreatment for the third time for the second time, in salt pretreatment device in 5% ~ 6% (NH 4) 2hPO 3solution sprays rear immersion 1 ~ 2h under the condition of 40 ℃ ~ 60 ℃, after immersion, by extruder, dehydrates;
E) raw material after salt pretreatment is for the third time dried in dryer, temperature is controlled at 120 ~ 140 ℃, and pressure is 0.2 ~ 0.4 Mpa;
F) raw material arrangement, volume after drying are entered to carbonization technique after putting down continuously and carry out carbonization.
Described salt pretreatment device is that top is provided with eight spray equipments, and bottom is for soaking position, and it is highly 1 ~ 1.5m that solution soaks.
Described dryer adopts wind formula dryer, in the middle of it, is three-layer network band, is inside provided with two three-dimensional rollings of rod, heats rod heat conduction make raw material stoving by steam, and effectively drying length is 36m.
The present invention produces the active carbon fiber felt obtaining, the various performance parameters of cloth, after testing as following table 1:
Table 1
Sequence number Project Parameter
1 Specific area (㎡/g) 800~2500
2 Filament diameter (μ m) 10~20
3 Bulk density (g/cm2) 0.04~0.10
4 Phosphorus content (%) >95
5 Moisture (%) <5
6 Burning-point (℃) >500
7 PH value 5.0~7.0
Various performance parameters by above-mentioned table 1 active carbon fiber felt, cloth is analyzed, Product Activity carbon fiber felt, cloth phosphorus content be up to more than 95%, guaranteed its more by force, more lasting adsorption capacity, and effectively increase the service life; Can be according to the molecular size deisgn product micropore of institute's adsorbent, aperture and the ratio thereof of mesopore, thus reach targetedly optimal adsorption effect; Moisture is low, when caning be controlled in effective high-specific surface area below 5%, still can control the accounting of micropore, mesopore, thereby guarantee the effective adsorption effect of product.

Claims (3)

1. a method of producing activated carbon fiber salt pretreatment, comprises the steps:
Take viscose felt, cloth is raw material, by raw material cutting, after planishing, carries out salt pretreatment;
Raw material after planishing is carried out to salt pretreatment for the first time, in salt pretreatment device in 7% ~ 8% (NH 4) 2hPO 3solution sprays rear immersion 1 ~ 2h under the condition of 40 ℃ ~ 60 ℃, after immersion, by extruder, dehydrates;
After salt pretreatment, carry out continuously for the first time salt pretreatment for the second time, in salt pretreatment device in 6% ~ 7% (NH 4) 2hPO 3solution sprays rear immersion 1 ~ 2h under the condition of 40 ℃ ~ 60 ℃, after immersion, by extruder, dehydrates;
After salt pretreatment, carry out continuously for the second time salt pretreatment for the third time, in salt pretreatment device in 5% ~ 6% (NH 4) 2hPO 3solution sprays rear immersion 1 ~ 2h under the condition of 40 ℃ ~ 60 ℃, after immersion, by extruder, dehydrates;
Raw material after salt pretreatment is for the third time dried in dryer, and temperature is controlled at 120 ~ 140 ℃, and pressure is 0.2 ~ 0.4 Mpa;
After raw material arrangement, volume after drying is flat, enter continuously carbonization technique and carry out carbonization.
2. the method for production activated carbon fiber salt pretreatment according to claim 1, is characterized in that, described salt pretreatment device top is provided with eight spray equipments, and bottom is for soaking position, and it is highly 1 ~ 1.5m that solution soaks.
3. the method for production activated carbon fiber salt pretreatment according to claim 1, it is characterized in that, described dryer adopts wind formula dryer, centre is three-layer network band, inside be provided with two three-dimensional rollings of rod, by steam, heat rod heat conduction and make raw material stoving, effectively drying length is 36m.
CN201310669896.8A 2013-12-11 2013-12-11 A kind of method of producing activated carbon fiber salt pretreatment Active CN103643351B (en)

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Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105064031A (en) * 2015-08-20 2015-11-18 北京化工大学 Method for preparing high-modulus carbon fibers at low temperature
CN113913969A (en) * 2021-11-18 2022-01-11 因达孚先进材料(苏州)有限公司 Method for preparing hydrophobic activated carbon fiber from carbon felt leftover material

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1114633A (en) * 1994-07-03 1996-01-10 中国科学院长春应用化学研究所 Method for preparation of viscose fibre active carbon
CN1204622A (en) * 1998-06-20 1999-01-13 中山大学 Treatment of waste water containing dye using activated carbon fiber adsorption process
JP2002038334A (en) * 2000-07-28 2002-02-06 Nokia Mobile Phones Ltd Method for producing fine activated carbon fiber and fine activated carbon fiber produced thereby
US6383972B1 (en) * 1997-11-24 2002-05-07 Messier-Bugatti Preparation of a catalyst support in activated carbon fibres
CN1632199A (en) * 2004-11-29 2005-06-29 东华大学 Process for preparing big aperture active carbon fibers

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1114633A (en) * 1994-07-03 1996-01-10 中国科学院长春应用化学研究所 Method for preparation of viscose fibre active carbon
US6383972B1 (en) * 1997-11-24 2002-05-07 Messier-Bugatti Preparation of a catalyst support in activated carbon fibres
CN1204622A (en) * 1998-06-20 1999-01-13 中山大学 Treatment of waste water containing dye using activated carbon fiber adsorption process
JP2002038334A (en) * 2000-07-28 2002-02-06 Nokia Mobile Phones Ltd Method for producing fine activated carbon fiber and fine activated carbon fiber produced thereby
CN1632199A (en) * 2004-11-29 2005-06-29 东华大学 Process for preparing big aperture active carbon fibers

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN105064031A (en) * 2015-08-20 2015-11-18 北京化工大学 Method for preparing high-modulus carbon fibers at low temperature
CN113913969A (en) * 2021-11-18 2022-01-11 因达孚先进材料(苏州)有限公司 Method for preparing hydrophobic activated carbon fiber from carbon felt leftover material

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