CN1895768A - Production of carbon fibre regular corrugation filler - Google Patents
Production of carbon fibre regular corrugation filler Download PDFInfo
- Publication number
- CN1895768A CN1895768A CN 200610014352 CN200610014352A CN1895768A CN 1895768 A CN1895768 A CN 1895768A CN 200610014352 CN200610014352 CN 200610014352 CN 200610014352 A CN200610014352 A CN 200610014352A CN 1895768 A CN1895768 A CN 1895768A
- Authority
- CN
- China
- Prior art keywords
- ripple
- carbon
- carbon fibre
- carbon fiber
- fibre web
- 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
Images
Abstract
A corrugated carbon fiber filler is prepared from the polyacrylonitrile based carbon fibers through weaving to become mesh or fabric, gas-phase oxidizing, drying, immersing in epoxy resin, bimaleimide resin, or caprolactam resin, putting it in corrugating mould, demoulding, and carbonizing.
Description
Technical field
The present invention relates to a kind of manufacture method of carbon fibre regular corrugation filler, belong to the manufacturing technology of high-performance filler.
Background technology
In departments such as petrochemical industry, fine chemistry industry, light industry, food, pharmacy, environmental protection and atomic energy, packed tower is indispensable visual plant, is widely used in unit processes in chemical synthesis such as distillation, absorption, washing, cooling.Packed tower is compared with plate column has outstanding features such as flux is big, efficient is high, pressure is little.Use the old plate column of high efficiency packing technological transformation, generally can make output improve 30-100%, energy consumption reduces 20-50%, and properties of product are obviously improved.In recent years, the appearance of novel packed tower and the successful Application in main equipment have obtained huge economic benefit and social benefit in China.
Filler (being divided into dumped packing and structured packing) is the core component of packed tower, and it has determined the performance of packed tower with tower internals.Filler provides the surface of gas-liquid two-phase contact mass transfer and heat exchange.Because the progress of industrial technology, production scale maximizes, and requires tower to have big flux, and liquid is evenly distributed, and reduces the packing layer resistance, improves separative efficiency, reaches energy-saving effect.Structured packing can be satisfied the requirement of major diameter tower, and therefore the development of all kinds of structured packings is rapid.Compare with dumped packing, structured packing can be arranged more large tracts of land, does not almost have enlarge-effect, compound with regular structure, and the efficient height, energy-saving effect is remarkable.
By the material classification, structured packing comprises metal, plastics, pottery etc.
Above-mentioned various filler in strong corrosive medium, particularly hydrofluoric acid, chloric acid, formic acid, acetate, monoxone, etc. poor corrosion resistance, life cycle is short, causes the waste that causes resource, and the cost of producing product is improved.
Summary of the invention
The object of the present invention is to provide a kind of preparation method of carbon fibre regular corrugation filler.Regular corrugation filler with this method manufacturing has the strong corrosion resistant performance, can be suitable for working under various corrosive medium conditions.
The present invention is realized by following technical proposals.A kind of preparation method of carbon fibre regular corrugation filler is characterized in that comprising following process:
(1) with the diameter is 7-9 μ m, every bundle carbon fiber is 4000,6000 or 8000, polyacrylonitrile-based carbon fibre is a raw material, adopts through compiling multi-axial fabric technology or woven technology, and it is the carbon cloth of 0.1-0.35mm that carbon fiber knit is become 20-40 purpose carbon fibre web or thickness.
(2) step (1) is knitted carbon fibre web or carbon cloth carry out surface clean, decontamination with acetone and deionized water; Then in 400-500 ℃ of gaseous oxidation, drying; Dried carbon fibre web or carbon cloth are immersed among epoxy resin, BMI or the caprolactam resin that viscosity is 300-600cP, 10-30 minute; The carbon fibre web or the carbon cloth that are impregnated with resin are placed in the mould with ripple bar, solidify between 60-200 ℃, be 0.5-2 hour hardening time, forms carbon fiber ripple net or carbon fiber corrugated plating behind the holder mould.
(3) carbon fiber ripple net or the carbon fiber corrugated plating that step (2) is made places vacuum furnace, under 1-3KPa vacuum and nitrogen protection condition, with 5-10 ℃/min heating rate, rises to 950-1200 ℃ and gives carbonization, is incubated 2-5 hour, comes out of the stove after the cooling.
(4) ripple carbon fibre web or the ripple carbon fiber board that step (3) is made axially is mutually the rule of 90 ° of angles by the ripple of adjacent two ripple carbon fibre webs or ripple carbon fiber board, and ripple carbon fibre web or ripple carbon fiber board are assembled into the filler block.
The invention has the advantages that process conditions are easy to accurate control, carrier performance is easy to adjust.The specific area of modified carbon fiber structured packing is 350-1500m
2/ m
3, and mechanical property is not less than stainless steel and the netted porous aggregate of titanium alloy.Particularly outstanding is, the modified carbon fiber structured packing has free from corrosion substantially characteristic, can realize the high purity material manufacturing feasibility, thereby it is short to have overcome active time in the deep-etching tower such as titanium material, stainless steel, and shut-down (breakdown) mainteance is frequent, the shortcoming that resource consumption is high.
Description of drawings
The carbon fibre web structural representation that Fig. 1 adopts for the present invention;
The carbon fibre web structural representation that Fig. 2 adopts for the present invention;
Fig. 3 is two 90 ° crossing ripple carbon fiber board schematic diagrames of the present invention.
The specific embodiment
Example 1
With the diameter is 7-9 μ m, and every bundle carbon fiber is that 4000 polyacrylonitrile-based carbon fibre is a raw material, adopts 4 * 4 through compiling multiaxis to technology, is woven into 40 purpose carbon fibre webs.Clean through acetone then and washed with de-ionized water removal dirt, the carbon fibre web of removing dirt places drying oven to carry out gaseous oxidation, drying at 400 ℃.It is to reach 10 minutes in the 400cP epoxy resin that dried carbon fibre web is immersed in viscosity, the carbon fibre web that is impregnated with epoxy resin is placed mould, mould offers equilateral continuous triangle shape, place the carbon fibre web that is impregnated with epoxy resin of mould, solidify through 0.5 hour at 60 ℃, the vertical direction up and down that makes leg-of-mutton axis and carbon fibre web through the demoulding is the ripple carbon fibre web of 30 ° of angles; The ripple carbon fibre web is placed vacuum furnace, under 1KPa vacuum and nitrogen protection,, rise to 950 ℃ and carry out carbonization, be incubated 2 hours, come out of the stove after being cooled to room temperature with 5 ℃/min heating rate; The ripple carbon fibre web of carbonization is assembled into the filler block by the rule that the ripple axis of adjacent two ripple carbon fibre webs is mutually 90 ° of angles.
Example 2
With the diameter is 7-9 μ m, and the polyacrylonitrile-based carbon fibre that every bundle carbon fiber is 6000 is a raw material, adopts 4 * 4 through compiling multiaxis to technology, is woven into 20 purpose carbon fibre webs.Clean through acetone then and washed with de-ionized water removal dirt, the carbon fibre web of removing dirt places drying oven to carry out the gaseous oxidation drying at 500 ℃.Dried carbon fibre web is immersed in the BMI that viscosity is 300cP and reaches 20 minutes, the carbon fibre web that is impregnated with BMI is placed mould, mould offers equilateral continuous triangle shape, place the carbon fibre web that is impregnated with BMI of mould, solidify through 1 hour at 150 ℃, the vertical direction up and down that makes leg-of-mutton axis and carbon fibre web through the demoulding is the ripple carbon fibre web of 45 ° of angles; The ripple carbon fibre web is placed vacuum furnace, under 2KPa vacuum and nitrogen protection,, rise to 1200 ℃ and carry out carbonization, be incubated 5 hours, come out of the stove after being cooled to room temperature with 10 ℃/min heating rate; The ripple carbon fibre web of carbonization is assembled into the filler block by the rule that the ripple axis of adjacent two ripple carbon fibre webs is mutually 90 ° of angles.
Example 3
With the diameter is 7-9 μ m, and every bundle carbon fiber is that 6000 polyacrylonitrile-based carbon fibre is a raw material, adopts 4 * 4 through compiling through compiling the multiaxis technology, is woven into 20 purpose carbon fibre webs.Clean through acetone then and washed with de-ionized water removal dirt, the carbon fibre web of removing dirt places drying oven to carry out the gaseous oxidation drying at 450 ℃.Dried carbon fibre web is immersed in the caprolactam that viscosity is 600cP and reaches 30 minutes, the carbon fibre web that is impregnated with caprolactam is placed mould, mould offers equilateral continuous triangle shape, place the carbon fibre web that is impregnated with caprolactam of mould, solidify through 2 hours at 200 ℃, the vertical direction up and down that makes leg-of-mutton axis and carbon fibre web through the demoulding is the ripple carbon fibre web of 45 ° of angles; The ripple carbon fibre web is placed vacuum furnace, under 2KPa vacuum and nitrogen protection,, rise to 1000 ℃ and carry out carbonization, be incubated 4 hours, come out of the stove after being cooled to room temperature with 8 ℃/min heating rate; The ripple carbon fibre web of carbonization is assembled into the filler block by the rule that the ripple axis of adjacent two ripple carbon fibre webs is mutually 90 ° of angles.
Example 4
With the diameter is 7-9 μ m, and every bundle carbon fiber is that 4000 polyacrylonitrile-based carbon fibre is a raw material, adopts woven technology, and thickness is the carbon cloth of 0.1mm.Clean through acetone then and washed with de-ionized water removal dirt, the carbon cloth of removing dirt places drying oven to carry out the gaseous oxidation drying at 400 ℃.It is to reach 10 minutes in the 400cP epoxy resin that dried carbon cloth is immersed in viscosity, the carbon cloth that is impregnated with epoxy resin is placed mould, mould offers equilateral continuous triangle shape, place the carbon cloth that is impregnated with epoxy resin of mould, solidify through 0.5 hour at 60 ℃, the vertical direction up and down that makes leg-of-mutton axis and carbon cloth through the demoulding is the ripple carbon fiber board of 30 ° of angles; The ripple carbon fiber board is placed vacuum furnace, under 1KPa vacuum and nitrogen protection,, rise to 950 ℃ and carry out carbonization, be incubated 2 hours, come out of the stove after being cooled to room temperature with 5 ℃/min heating rate; The ripple carbon fiber board of carbonization is assembled into the filler block by the rule that the ripple axis of adjacent two ripple carbon fiber boards is mutually 90 ° of angles.
Example 5
With the diameter is 7-9 μ m, and every bundle carbon fiber is that 6000 polyacrylonitrile-based carbon fibre is a raw material, adopts woven technology, and thickness is the carbon cloth of 0.15mm.Clean through acetone then and washed with de-ionized water removal dirt, the carbon cloth of removing dirt places drying oven to carry out the gaseous oxidation drying at 450 ℃.It is to reach 20 minutes in the 450cP BMI that dried carbon cloth is immersed in viscosity, the carbon cloth that is impregnated with BMI is placed mould, mould offers equilateral continuous triangle shape, place the carbon cloth that is impregnated with BMI of mould, solidify through 1 hour at 150 ℃, the vertical direction up and down that makes leg-of-mutton axis and carbon cloth through the demoulding is the ripple carbon fiber board of 30 ° of angles; The ripple carbon fiber board is placed vacuum furnace, under 2KPa vacuum and nitrogen protection,, rise to 1200 ℃ and carry out carbonization, be incubated 3 hours, come out of the stove after being cooled to room temperature with 8 ℃/min heating rate; The ripple carbon fiber board of carbonization is assembled into the filler block by the rule that the ripple axis of adjacent two ripple carbon fiber boards is mutually 90 ° of angles.
Example 6
With the diameter is 7-9 μ m, and every bundle carbon fiber is that 6000 polyacrylonitrile-based carbon fibre is a raw material, adopts woven technology, the carbon cloth of 0.15mm.Clean through acetone then and washed with de-ionized water removal dirt, the carbon cloth of removing dirt places drying oven to carry out the gaseous oxidation drying at 500 ℃.It is to reach 30 minutes in the 500cP caprolactam that dried carbon cloth is immersed in viscosity, the carbon cloth that is impregnated with caprolactam is placed mould, mould offers equilateral continuous triangle shape, place the carbon cloth that is impregnated with caprolactam of mould, solidify through 2 hours at 1200 ℃, the vertical direction up and down that makes leg-of-mutton axis and carbon cloth through the demoulding is the ripple carbon fiber board of 30 ° of angles; The ripple carbon fiber board is placed vacuum furnace, under 3KPa vacuum and nitrogen protection,, rise to 1000 ℃ and carry out carbonization, be incubated 5 hours, come out of the stove after being cooled to room temperature with 10 ℃/min heating rate; The ripple carbon fiber board of carbonization is assembled into the filler block by the rule that the ripple axis of adjacent two ripple carbon fiber boards is mutually 90 ° of angles.
Claims (1)
1, a kind of preparation method of carbon fibre regular corrugation filler is characterized in that comprising following process:
(1) with the diameter is 7-9 μ m, every bundle carbon fiber is 4000,6000 or 8000, polyacrylonitrile-based carbon fibre is a raw material, adopts through compiling multi-axial fabric technology or woven technology, becomes order to count 20-40 purpose carbon fibre web carbon fiber knit or thickness is the carbon cloth of 0.1-0.15mm;
(2) step (1) is knitted carbon fibre web or carbon cloth cleans with acetone and deionized water carries out surface clean, decontamination; Then 400-500 ℃ of gaseous oxidation drying; Dried carbon fibre web or carbon cloth are immersed in epoxy resin, BMI or the caprolactam resin that viscosity is 300-600cP 10-30 minute, the carbon fibre web or the carbon cloth that are impregnated with resin are placed in the mould with ripple bar, between 60-200 ℃, solidify, be 0.5-2 hour hardening time, forms carbon fiber ripple net or carbon fiber corrugated plating behind the holder mould;
(3) carbon fiber ripple net or the carbon fiber corrugated plating that step (2) is made places vacuum furnace, under 1-3KPa vacuum and nitrogen protection condition, with 5-10 ℃/min heating rate, rises to 950-1200 ℃ and carries out carbonization, is incubated 2-5 hour, comes out of the stove after the cooling;
(4) ripple carbon fibre web or the ripple carbon fiber board that step (3) is made axially is mutually the rule of 90 ° of angles by the ripple of adjacent two ripple carbon fibre webs or ripple carbon fiber board, and ripple carbon fibre web or ripple carbon fiber board are assembled into the filler block.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2006100143528A CN1895768B (en) | 2006-06-15 | 2006-06-15 | Production of carbon fibre regular corrugation filler |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN2006100143528A CN1895768B (en) | 2006-06-15 | 2006-06-15 | Production of carbon fibre regular corrugation filler |
Publications (2)
Publication Number | Publication Date |
---|---|
CN1895768A true CN1895768A (en) | 2007-01-17 |
CN1895768B CN1895768B (en) | 2010-11-10 |
Family
ID=37608496
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN2006100143528A Expired - Fee Related CN1895768B (en) | 2006-06-15 | 2006-06-15 | Production of carbon fibre regular corrugation filler |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN1895768B (en) |
Cited By (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101870800A (en) * | 2010-05-27 | 2010-10-27 | 哈尔滨工业大学 | Hollow carbon cloth epoxy resin composite material and preparation method thereof |
CN103240834A (en) * | 2012-02-03 | 2013-08-14 | 南京润泰科技有限公司 | Preparation method of carbon fiber resin matrix composite material |
CN103465486A (en) * | 2013-09-02 | 2013-12-25 | 大连塑料研究所有限公司 | Continuous production method of reinforced high-strength plastic plate |
CN103921439A (en) * | 2014-03-20 | 2014-07-16 | 张�杰 | Sheet material production equipment and method |
CN105016192A (en) * | 2015-06-09 | 2015-11-04 | 云南电网有限责任公司曲靖供电局 | Carbon fiber plate horizontal double-fission wire lifting hook clamp for 220 kV hot-line work |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102756479B (en) * | 2012-07-27 | 2014-04-16 | 宜兴市飞舟高新科技材料有限公司 | Resin-based carbon fiber damping material and preparation method thereof |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN1127675A (en) * | 1994-12-27 | 1996-07-31 | 天津市乾隆科技开发公司 | Wave ring packing |
CN1089028C (en) * | 1997-12-24 | 2002-08-14 | 冯天扬 | Carbon and/or graphite board corrugated regular filler for packed column |
-
2006
- 2006-06-15 CN CN2006100143528A patent/CN1895768B/en not_active Expired - Fee Related
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101870800A (en) * | 2010-05-27 | 2010-10-27 | 哈尔滨工业大学 | Hollow carbon cloth epoxy resin composite material and preparation method thereof |
CN101870800B (en) * | 2010-05-27 | 2011-11-23 | 哈尔滨工业大学 | Hollow carbon cloth epoxy resin composite material and preparation method thereof |
CN103240834A (en) * | 2012-02-03 | 2013-08-14 | 南京润泰科技有限公司 | Preparation method of carbon fiber resin matrix composite material |
CN103465486A (en) * | 2013-09-02 | 2013-12-25 | 大连塑料研究所有限公司 | Continuous production method of reinforced high-strength plastic plate |
CN103921439A (en) * | 2014-03-20 | 2014-07-16 | 张�杰 | Sheet material production equipment and method |
CN103921439B (en) * | 2014-03-20 | 2016-09-14 | 张�杰 | Board production equipment and method |
CN105016192A (en) * | 2015-06-09 | 2015-11-04 | 云南电网有限责任公司曲靖供电局 | Carbon fiber plate horizontal double-fission wire lifting hook clamp for 220 kV hot-line work |
Also Published As
Publication number | Publication date |
---|---|
CN1895768B (en) | 2010-11-10 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN1895768B (en) | Production of carbon fibre regular corrugation filler | |
CN103833549B (en) | A kind of preparation method of polyol esters of fatty acids | |
CN105063571B (en) | The preparation method of three-dimensional grapheme in a kind of stainless steel base | |
CN101077980A (en) | Method for preparing light oil from supercritical water modified vacuum residuum | |
CN1291956C (en) | Method and apparatus for preparing isolongifolene from longifolene | |
Zhang et al. | One-step hydrothermal synthesis of the modified carbon cloth membrane: Towards visible light driven and self-cleaning for efficient oil-water separation | |
CN1943840A (en) | Method for producing anti corrosion composite filtering material | |
CN102689014A (en) | Preparation method of metal fiber porous surface heat exchange tube | |
CN1948147A (en) | Preparation method of high specific surface area coal mass active carbon | |
CN111841592A (en) | In-situ derivatization synthesis of TiO by using Ti-based MOF2-Ti3C2Tx composite photocatalyst and application thereof | |
CN1760124A (en) | Method for reactivating and regenerating waste silicon powder | |
CN101285494A (en) | Fastening piece and its manufacturing technique | |
CN101817552A (en) | Titanium dioxide micron tube material and preparation method thereof | |
CN110819176A (en) | Preparation method of anticorrosive and antiscale coating | |
JP2000516904A (en) | Corrosion resistant composites useful in chemical reactors | |
CN110318251B (en) | Method for growing one-dimensional zinc oxide nanowire on surface of carbon fiber | |
CN201815185U (en) | Basalt fiber high-temperature filter material | |
CN1948224A (en) | Preparation method of C/C composite material conductive threaded rod | |
CN204891404U (en) | High temperature resistant filter material containing carbon fiber acupuncture layer | |
CN112726018A (en) | Preparation method of oil-water separation material based on PP non-woven fabric | |
CN1749251A (en) | Process for preparing cyanuric acid | |
CN107059418A (en) | Dirty corrosion resistant environmentally friendly filtering material of anti-static oil-resistance and preparation method thereof | |
CN109457323B (en) | The method being carbonized using gallium | |
CN1269875C (en) | Process for purification refine of macromolecular weight poly benzene thioether resin | |
CN1087650C (en) | Corrugated plate regular packing of glass fibre reinforced plastics and its preparing process |
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 | ||
C17 | Cessation of patent right | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20101110 Termination date: 20110615 |