Microporous activated carbon fiber and preparation method thereof

An activated carbon fiber and microporous technology, which is applied in the field of microporous activated carbon fiber and its preparation, can solve the problems of reducing fiber strength, low carbonization temperature, and reducing yield, and achieves enhanced adsorption force, large specific surface area, and high yield. high effect

Active Publication Date: 2020-12-11
QINGDAO HSJ ENVIRONMENTAL PROTECTION TECH CO LTD
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Problems solved by technology

There are following problems in this activated carbon fiber preparation technology: (1) the physical activation method needs to use the oxidizing property of activated gas to erode the surface of activated carbon fiber at high temperature, remove tar and uncarbonized matter, and produce new pores, thereby causing huge Ratio of material ablation and dimensional shrinkage, reducing yield and increasing production cost
(2) The activation process inevitably causes the loss of carbon components and reduces the fiber strength
[0004] However, the existing phosphoric acid chemical activation method ACF products usually have the following problems: (1) the oxidation of phosphoric acid in the preparation process of the chemical activation method ACF will increase the content of oxygen-containing functional groups on the surface of the material
Oxygen-containing functional groups, acidic functional groups and other strong hydrophilic functional groups lead to poor hydrophobicity of the material, and it is easy to adsorb water molecules, so that the adsorption sites are occupied and the adsorption force on pollutants is reduced.
(2) The pore size of the ACF product prepared by the physical method is concentrated below 0.8nm, and the adsorption force on VOCs is much higher than that on water. Although the activated carbon fiber prepared by the chemical method has a large specific surface area and a wide range of pore size distribution, it is beneficial Desorption, but its adsorption force of VOCs is weaker than the physical method ACF, resulting in the material's adsorption performance on VOCs being greatly affected by the water content and the humidity of the exhaust gas
(3) The final carbonization temperature in the preparation process of chemical activation method ACF is low, resulting in incomplete removal of H and O elements, and its ignition point is lower than that of physical method ACF

Method used

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  • Microporous activated carbon fiber and preparation method thereof
  • Microporous activated carbon fiber and preparation method thereof
  • Microporous activated carbon fiber and preparation method thereof

Examples

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Effect test

Embodiment 1

[0039] A microporous activated carbon fiber, the ash content of the activated carbon fiber is 1.25wt%, the ignition point is 413°C, and the specific surface area is 2089m 2 / g, no sticking problem, the wicking height is 15cm, the O element content accounts for 13.41%, the C element content accounts for 69.86%, and the H element content accounts for 1.95%; the pore size distribution is as follows figure 2 As shown, the proportion of pores below 0.8nm is about 45%, and the proportion of pores of 0.8-2nm is about 55%.

[0040]The preparation method is: mix viscose fiber mat with 12% phosphoric acid solution according to the ratio of fiber to phosphoric acid mass ratio of 1:0.6, impregnate at 40°C for 30min, dry with hot air at 50°C for 5 hours, and then carbonize under nitrogen atmosphere Treatment, carbonization selects the gradient heating process, that is, the temperature of the first gradient is 90°C and the time is 20min, the temperature of the second gradient is 220°C and ...

Embodiment 2

[0043] A microporous activated carbon fiber, the ash content of the activated carbon fiber is 1.93wt%, the ignition point is 435°C, and the specific surface area is 1966m 2 / g, no sticking and filament problem, the wicking height is 13cm, the O element content accounts for 8.05%, the C element content accounts for 89.03%, and the H element content accounts for 1.61%; the pore size distribution is as follows image 3 As shown, the proportion of pores below 0.8nm is about 48%, and the proportion of pores of 0.8-2nm is about 52%.

[0044] The preparation method is as follows: solvent method cellulose fiber mat and 7% phosphoric acid solution are mixed according to the ratio of fiber to phosphoric acid mass ratio of 1:0.8, soaked at 50°C for 30min, dried at 30°C for 7 hours, and then carried out in air atmosphere Carbonization treatment, carbonization selects a gradient heating process, that is, the temperature of the first gradient is 100°C and the time is 30min, the temperature ...

Embodiment 3

[0047] A microporous activated carbon fiber, the ash content of the activated carbon fiber is 1.14wt%, the ignition point is 445°C, and the specific surface area is 1655m 2 / g, no sticking and filament problem, the wicking height is 9cm, the O element content accounts for 5.07%, the C element content accounts for 85.55%, and the H element content accounts for 1.13%; the pore size distribution is as follows Figure 4 As shown, the proportion of pores below 0.8nm is about 50%, and the proportion of pores of 0.8-2nm is about 50%.

[0048] The preparation method is: mix cupro ammonia fiber cloth with 15% phosphoric acid solution according to the mass ratio of fiber and phosphoric acid of 1:0.2, soak at 60°C for 60min, dry at 60°C for 3 hours, and then carbonize under nitrogen atmosphere , the carbonization selects the gradient heating process, that is, the temperature of the first gradient is 120°C and the time is 40min, the temperature of the second gradient is 180°C and the time...

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Abstract

The invention provides a microporous activated carbon fiber and a preparation method thereof, and belongs to the field of activated carbon fibers. The ash content of the microporous activated carbon fiber is 1.1 wt%-2.0 wt%, the specific surface area is 1500 m < 2 >/g-2100 m < 2 >/g, the proportion of pores below 0.8 nm is 40-50%, the proportion of pores of 0.8-2 nm is 50-60%, no mesopores above 2nm exist, the O element content is 5%-15%, the C element content is 65%-90%, the H element content is 1%-2%, and the ignition point is 300-450 DEG C. The preparation method comprises the following steps: impregnating raw materials with a phosphoric acid aqueous solution, drying, carbonizing, washing with water, and carrying out high-temperature modification to obtain the activated carbon fiber. Wherein the raw materials are artificial fibers and/or natural fibers; the mass fraction of the phosphoric acid aqueous solution is 5%-15%. The microporous activated carbon fiber has the advantages ofno mesopore, high proportion of 0.8-2 nm micropores, large specific surface area, high strength and no sticking problem; meanwhile, the ignition point is high, the hydrophobicity is high, and the VOCsadsorption acting force is enhanced; the preparation method is low in cost and high in product yield.

Description

technical field [0001] The invention relates to the field of activated carbon fibers, in particular to a microporous activated carbon fiber and a preparation method thereof. Background technique [0002] The physical activation method is the preparation method of activated carbon fiber commonly used in industrial production at present. After pretreatment and carbonization of the activator, the carbon monoxide or carbon dioxide gas generated by the reaction with the physical activator (carbon dioxide, water vapor, etc.) Many micropores are produced. There are following problems in this activated carbon fiber preparation technology: (1) the physical activation method needs to use the oxidizing property of activated gas to erode the surface of activated carbon fiber at high temperature, remove tar and uncarbonized matter, and produce new pores, thereby causing huge The proportion of material ablation and the shrinkage rate of size will reduce the yield and increase the produc...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): B01J20/20B01J20/28B01D53/02D01F9/16B01J20/30
CPCB01J20/20B01J20/28023D01F9/16B01D53/02B01D2257/708Y02A50/20
Inventor 万月亮陈保磊梁鹏王玲玲迟淑丽
Owner QINGDAO HSJ ENVIRONMENTAL PROTECTION TECH CO LTD
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