CN110067127A - A kind of preparation method of impregnation aramid fiber short fibre - Google Patents
A kind of preparation method of impregnation aramid fiber short fibre Download PDFInfo
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- CN110067127A CN110067127A CN201910212407.3A CN201910212407A CN110067127A CN 110067127 A CN110067127 A CN 110067127A CN 201910212407 A CN201910212407 A CN 201910212407A CN 110067127 A CN110067127 A CN 110067127A
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- C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
- C08G8/00—Condensation polymers of aldehydes or ketones with phenols only
- C08G8/04—Condensation polymers of aldehydes or ketones with phenols only of aldehydes
- C08G8/08—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ
- C08G8/20—Condensation polymers of aldehydes or ketones with phenols only of aldehydes of formaldehyde, e.g. of formaldehyde formed in situ with polyhydric phenols
- C08G8/22—Resorcinol
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- C08J5/00—Manufacture of articles or shaped materials containing macromolecular substances
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- C08J5/06—Reinforcing macromolecular compounds with loose or coherent fibrous material using pretreated fibrous materials
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- D06B21/00—Successive treatments of textile materials by liquids, gases or vapours
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- D06B3/00—Passing of textile materials through liquids, gases or vapours to effect treatment, e.g. washing, dyeing, bleaching, sizing, impregnating
- D06B3/10—Passing of textile materials through liquids, gases or vapours to effect treatment, e.g. washing, dyeing, bleaching, sizing, impregnating of fabrics
- D06B3/18—Passing of textile materials through liquids, gases or vapours to effect treatment, e.g. washing, dyeing, bleaching, sizing, impregnating of fabrics combined with squeezing, e.g. in padding machines
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- D06M13/00—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment
- D06M13/322—Treating fibres, threads, yarns, fabrics or fibrous goods made from such materials, with non-macromolecular organic compounds; Such treatment combined with mechanical treatment with compounds containing nitrogen
- D06M13/395—Isocyanates
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- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M15/39—Aldehyde resins; Ketone resins; Polyacetals
- D06M15/41—Phenol-aldehyde or phenol-ketone resins
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- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/19—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
- D06M15/37—Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
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- D06M15/00—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
- D06M15/693—Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with natural or synthetic rubber, or derivatives thereof
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- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2307/00—Characterised by the use of natural rubber
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- C08J2477/00—Characterised by the use of polyamides obtained by reactions forming a carboxylic amide link in the main chain; Derivatives of such polymers
- C08J2477/10—Polyamides derived from aromatically bound amino and carboxyl groups of amino carboxylic acids or of polyamines and polycarboxylic acids
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- C08K13/02—Organic and inorganic ingredients
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- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
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- C08K5/00—Use of organic ingredients
- C08K5/04—Oxygen-containing compounds
- C08K5/09—Carboxylic acids; Metal salts thereof; Anhydrides thereof
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- D06M2101/00—Chemical constitution of the fibres, threads, yarns, fabrics or fibrous goods made from such materials, to be treated
- D06M2101/16—Synthetic fibres, other than mineral fibres
- D06M2101/30—Synthetic polymers consisting of macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
- D06M2101/34—Polyamides
- D06M2101/36—Aromatic polyamides
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Abstract
The present invention provides a kind of preparation method of impregnation aramid fiber short fibre comprising following processing step: A: one bath is carried out to aramid fiber precursor；B: it dries for the first time；C: two baths；D: secondary drying；E: winding；F: cutting；Wherein: pre- impregnation being carried out using the isocyanates that the high activity of aqueous solution type is reacted in the step A；It is impregnated in step C using RFL maceration extract.The present invention is using the two-bath process impregnation technology for first activating again RFL thickening, not only improved in the fiber surface activating pretreatment technology of a bath, innovation transformation more is carried out in the RFL tackified finish formula and process aspect of the second bath, the bonding enhancing that can meet different matrix requires.The present invention one bathes maceration extract, two bath RF resins, the proportion of RFL maceration extract and the technological parameter of impregnation and have passed through and test repeatedly, it is determined that specific parameter has reached optimum efficiency.
Description
Technical field
The present invention relates to aramid fiber preparation technical field, specially a kind of preparation method of impregnation aramid fiber short fibre.
Background technique
Impregnation aramid fiber short fibre is distributed in rubber components as a kind of framework material, solves aramid fiber short fibre in rubber
Disperse bad problem in glue, while improving all performances.Including lower tension mould originally is greatly improved
Amount, while wear-resistant, being folded without breaking and tensile capacity have also all obtained huge raising, in addition, dynamic fatigue degree, energy loss
A small amount of raising has also been obtained with compact strength.The necessary addition component of impregnation aramid fiber short fibre seldom in other fiber products, because
This decreases adverse effect, such as capillarity and osmosis.Impregnation aramid fiber short fibre uses RFL impregnation mode, solves rubber
Bonding between glue and aramid fiber, product includes 1mm, 2mm, 3mm and 6mm.Suitable for rubber, epoxy resin, thermoplastic
The enhancing of the composite materials such as property polyurethane, nylon, polyethylene (PE), polyphenylene sulfide (PPS), syndiotactic polytyrene (SPS)
But due to aramid fiber its with the very high degree of orientation and cleanliness, and there is no amorphous region, and molecule
There are a large amount of phenyl ring in segment, steric hindrance is larger, therefore amide group is more difficult chemically reacts with other atoms or group, so
It is relatively difficult that bonding impregnation is carried out for aramid fiber surface.Based on this domestic and international experts and scholars to the table of aramid fiber
Face is adhesion-modified to be had conducted extensive research and tests, and company produced and develops in polyester fibre surface pretreatment by many years
On the basis of, using the two-bath process impregnation technology for first activating again RFL thickening, not only in the fiber surface pre-activated of first bath
It is improved on processing technique, has more carried out innovation transformation in the RFL tackified finish formula and process aspect of the second bath, can expire
The bonding requirement of foot difference rubber matrix.Enter aramid fiber/rubber composite material aramid fiber table of industrial applications at present
Surface treatment achieves one frequently with the surface treatment method for using coupling agent after latex, plasma, phosphoric acid corrosion fiber surface
Fixed effect, but mainly improve the interfacial bonding of base rubber material and aramid fiber in a manner of physics, therefore interfacial adhesion strength
There is the space further increased.The dispersion of fiber is then the another technical problem of industry, excessive if making fiber be uniformly dispersed
Be kneaded, will lead to fibre length excessively reduces, molecular weight rubber decline, deteriorate performance；If fibre length is long but dispersion is uneven
It equally also cannot get the composite material of function admirable.Inventor is by pre-processing production and exploitation in polyester fibre surface for many years
On the basis of, fiber surface activating pretreatment is technically improved, the enhancing requirement of different rubber matrixs can be met.
Summary of the invention
The purpose of the present invention is to provide a kind of preparation methods of impregnation aramid fiber short fibre, to solve above-mentioned background technique
The problem of middle proposition.
To achieve the above object, the invention provides the following technical scheme:
A kind of preparation method of impregnation aramid fiber short fibre comprising following processing step is carried out to aramid fiber precursor:
A: one bath；
B: it dries for the first time；
C: two baths；
D: secondary drying；
E: winding；
F: cutting；
Wherein:
Pre- impregnation is carried out using the isocyanates that the high activity of aqueous solution type is reacted in the step A；
It is impregnated in step C using RFL maceration extract, the formula of the RFL maceration extract is:
RF resin: 420.6 parts of parts by weight；
Soft water: 95.2 parts of parts by weight；
VP latex 40%: 484.2 parts of parts by weight；
The wherein formula of RF resin are as follows:
Soft water: 425.6 parts of parts by weight；
Sodium hydroxide 7%: 16 parts of parts by weight；
Resorcinol solid: 22 parts of parts by weight；
Formaldehyde 38%: 13 parts of parts by weight；
Its specific work step includes:
S1: it by the smooth releasing of aramid fiber precursor pay off rack, keeps not loose, not upper and twists；
S2: being combed by separated time and reach first group of drawing-off rod, is entered the first glue groove by deflector roll and is carried out a bath；
S3: entering first layer baking oven and dry, and drying temperature is 105 DEG C, and drying time is 3 hours；
S4: enter second layer baking oven by second group of draw roll and carry out 230 DEG C of hot settings；
S5: and then enter the second glue groove by third group draw roll and carry out two baths；With RFL dipping solution obtained at 19 DEG C
At a temperature of impregnate aramid fiber 3.2 hours；
S6: it is dried by third layer；Drying temperature be 85 DEG C, the time be 2.5 hours；
S7: up- coiler molding is sent to by the 4th group of draw roll after the 4th layer of pyroreaction of progress and is made into semi-finished product；
S8: finished product is made into after semi-finished product are cut off using fibre cutting machine.
Wherein, in the step S2, the closed polyisocyanates of phenol is selected in a bath, specifically
Step 1: being impregnated aramid fiber 1~3 hour at a temperature of 50~15 DEG C with isocyanates, cleans drying；
Step 2: the acetone soln for the epoxy resin for being again 6~18% with mass percent concentration impregnates virtue at normal temperature
It synthetic fibre fiber 2.5~4 hours, is completed after drying modified to the surface of aramid fiber.
Further, specific as follows in the step S5:
One, prepare 420.6 parts of parts by weight of RF resin liquid, 95.2 parts of parts by weight of soft water and 484.2 parts of parts by weight of VP
Latex 40%, total weight parts 1000；
Two, soft water and VP latex are put into blend tank；
Three, RF resin liquid is transplanted in blend tank, and continues to stir, transfer RF resin liquid is completed in 10 minutes, RF
Resin liquid uses the transfer mode of fountain, and blend tank, which is adopted, is water-cooled jacket heat-preservation, keeps the glue temperature 20 in blend tank
DEG C, pH value is adjusted between 8-9；
Four, since the transfer of RF resin, after curing in 27 hours, obtained RFL maceration extract is sent into subsequent cement dipping machine
It uses.
The preparation method of RF resin liquid therein, comprising the following steps:
(1) prepare the formaldehyde 38% of soft water, 22 parts of parts by weight of resorcinol solid and parts by weight 13；
(2) soft water is put into reactor tank, water temperature is controlled at 23 DEG C；
(3) sodium hydroxide is dissolved in soft water, is launched after being configured to the sodium hydrate aqueous solution that concentration is 7% to anti-
It answers in tank, sodium hydrate aqueous solution parts by weight are 16 parts, and are stirred 10 minutes；
(4) resorcinol solid is dissolved in soft water, is launched after being configured to the resorcinol solution of concentration 10~20%
Into reactor tank, and it is stirred 20 minutes；
(5) formaldehyde 38% is launched into soft water and is mixed, the formalin that concentration is 5~20% is configured to, by formaldehyde
Aqueous solution is slowly added in reactor tank, and continues stirred tank；
(6) with 10 DEG C of temperature of the cooling reactor tank of cooling water, control reaction temperature is 20 DEG C, and the reaction time is 12.5 small
When, obtain RF resin liquid.
In conclusion the invention has the following advantages:
1, inventor is increased for many years on the basis of polyester fibre surface pre-processes production and exploitation using RFL is first activated again
Viscous two-bath process impregnation technology not only improves in the fiber surface activating pretreatment technology of a bath, more second
The RFL tackified finish formula and process aspect of bath have carried out innovation transformation, and the bonding enhancing that can meet different matrix requires.
2, the present invention one bathes maceration extract, two bath RF resins, the proportion of RFL maceration extract and the technological parameter of impregnation
It has passed through and test repeatedly, it is determined that specific parameter has reached optimum efficiency.
Specific embodiment
Below in conjunction with the embodiment of the present invention, technical solution in the embodiment of the present invention is clearly and completely retouched
It states, it is clear that described embodiments are only a part of the embodiments of the present invention, instead of all the embodiments.Based on the present invention
In embodiment, every other implementation obtained by those of ordinary skill in the art without making creative efforts
Example, shall fall within the protection scope of the present invention.
A kind of preparation method of impregnation aramid fiber short fibre comprising carry out following processing step to aramid fiber precursor: A: one
Bath；B: it dries for the first time；C: two baths；D: secondary drying；E: winding；F: cutting；Wherein: using aqueous solution type in the step A
The isocyanates of high activity reaction carries out pre- impregnation；It is impregnated in step C using RFL maceration extract, the RFL maceration extract
Formula is: RF resin: 420.6 parts of parts by weight；Soft water: 95.2 parts of parts by weight；VP latex 40%: 484.2 parts of parts by weight；Wherein
The formula of RF resin are as follows: soft water: 425.6 parts of parts by weight；Sodium hydroxide 7%: 16 parts of parts by weight；Resorcinol solid: parts by weight
22 parts；Formaldehyde 38%: 13 parts of parts by weight；
Its specific work step includes:
S1: it by the smooth releasing of aramid fiber precursor pay off rack, keeps not loose, not upper and twists；
S2: being combed by separated time and reach first group of drawing-off rod, is entered the first glue groove by deflector roll and is carried out a bath；One bath is selected
The closed polyisocyanates of phenol, specifically includes step 1: aramid fiber 1 is impregnated at a temperature of 50~15 DEG C with isocyanates
~3 hours, clean drying；Step 2: the acetone soln for the epoxy resin for being again 6~18% with mass percent concentration is normal
It temperature lower dipping aramid fiber 2.5~4 hours, is completed after drying modified to the surface of aramid fiber.
S3: entering first layer baking oven and dry, and drying temperature is 105 DEG C, and drying time is 3 hours；
S4: enter second layer baking oven by second group of draw roll and carry out 230 DEG C of hot settings；
S5: and then enter the second glue groove by third group draw roll and carry out two baths；With RFL dipping solution obtained at 19 DEG C
At a temperature of impregnate aramid fiber 3.2 hours；
S6: it is dried by third layer；Drying temperature be 85 DEG C, the time be 2.5 hours；
S7: up- coiler molding is sent to by the 4th group of draw roll after the 4th layer of pyroreaction of progress and is made into semi-finished product；
S8: finished product is made into after semi-finished product are cut off using fibre cutting machine.
The allotment of embodiment 1:RF resin liquid；
(1) prepare the formaldehyde 38% of soft water, 22 parts of parts by weight of resorcinol solid and parts by weight 13；
(2) soft water is put into reactor tank, water temperature is controlled at 23 DEG C；
(3) sodium hydroxide is dissolved in soft water, is launched after being configured to the sodium hydrate aqueous solution that concentration is 7% to anti-
It answers in tank, sodium hydrate aqueous solution parts by weight are 16 parts, and are stirred 10 minutes；
(4) resorcinol solid is dissolved in soft water, is launched after being configured to the resorcinol solution of concentration 10~20%
Into reactor tank, and it is stirred 20 minutes；
(5) formaldehyde 38% is launched into soft water and is mixed, the formalin that concentration is 5~20% is configured to, by formaldehyde
Aqueous solution is slowly added in reactor tank, and continues stirred tank；
(6) with 10 DEG C of temperature of the cooling reactor tank of cooling water, control reaction temperature is 20 DEG C, and the reaction time is 12.5 small
When, obtain RF resin liquid.
The allotment of embodiment 2:RFL maceration extract；
One, prepare 420.6 parts of parts by weight of RF resin liquid, 95.2 parts of parts by weight of soft water and 484.2 parts of parts by weight of VP
Latex 40%, total weight parts 1000；
Two, soft water and VP latex are put into blend tank；
Three, RF resin liquid is transplanted in blend tank, and continues to stir, transfer RF resin liquid is completed in 10 minutes, RF
Resin liquid uses the transfer mode of fountain, and blend tank, which is adopted, is water-cooled jacket heat-preservation, keeps the glue temperature 20 in blend tank
DEG C, pH value is adjusted between 8-9；
Four, since the transfer of RF resin, after curing in 27 hours, obtained RFL maceration extract is sent into subsequent cement dipping machine
It uses.
Experimental example 1:
Aramid filament (trade mark: AF-1000,1500 denier, ALKEX company, South Korea) is cut into 20mm sections, it is clear with acetone ultrasound
It is dried after washing aramid fiber 1 hour, removes the organic coating of its surface attachment；
S1: it by the smooth releasing of aramid fiber precursor pay off rack, keeps not loose, not upper and twists；
S2: being combed by separated time and reach first group of drawing-off rod, is entered the first glue groove by deflector roll and is carried out a bath；One bath is selected
The closed polyisocyanates of phenol, specifically includes step 1: aramid fiber 1 is impregnated at a temperature of 50~15 DEG C with isocyanates
~3 hours, clean drying；Step 2: the acetone soln for the epoxy resin for being again 6~18% with mass percent concentration is normal
It temperature lower dipping aramid fiber 2.5~4 hours, is completed after drying modified to the surface of aramid fiber.
S3: entering first layer baking oven and dry, and drying temperature is 105 DEG C, and drying time is 3 hours；
S4: enter second layer baking oven by second group of draw roll and carry out 230 DEG C of hot settings；
S5: and then enter the second glue groove by third group draw roll and carry out two baths；Made from embodiment 1 and embodiment 2
RFL dipping solution impregnates aramid fiber 3.2 hours at a temperature of 19 DEG C；
S6: it is dried by third layer；Drying temperature be 85 DEG C, the time be 2.5 hours；
S7: up- coiler molding is sent to by the 4th group of draw roll after the 4th layer of pyroreaction of progress and is made into semi-finished product；
S8: finished product aramid fiber short fibre is made into after semi-finished product are cut off using fibre cutting machine.
Experimental example 2:
Under same experimental conditions, the step S1-S8 of comparative experiments example 1, step is changed to produce using Changzhou Shuguang Chemical Factory
" Vulkabond E " RP mono bath impregnation, it is a kind of parachlorophenol being dissolved in ammonium hydroxide, formaldehyde and resorcinol
Condensation polymer impregnates at a temperature of 19 DEG C aramid fiber 3.2 hours, then carries out baking and curing at 240 DEG C of temperature and handle to obtain virtue
Synthetic fibre fiber filament.
Experimental example 3:
Under same experimental conditions, the step S1-S8 of comparative experiments example 1 does not carry out any processing.
Comparative experiments:
40 grams of aramid fiber short fibre are weighed obtained in experimental example 1,2,3 respectively, are equipped with 1000 grams of natural rubbers, 17 grams of sulphur
Sulphur vulcanizing agent and 10 grams of compounding agents；Compounding agent includes 30 grams of zinc oxide, 20 grams of stearic acid, 17.1 grams of captaxes, 14.7 grams of rush
Into agent DM, 5 grams of diphenylguanidines, 3.2 grams of Vulcanization accelerator TMTDs and 10 grams of antioxidant SP-C.
They are kneaded 10 minutes in mixer at 120 DEG C, revolving speed 80r/min, then the double roller at 60 DEG C is opened
It is kneaded in mill, 17g sulfur vulcanizing agent and 100g compounding agent is added, Bao Tong 4 times, obtains rubber compound；By rubber compound at 145 DEG C
Under according to vulcameter measurement sulfurizing time tc90 vulcanize, prepare modifying aramid fiber and sulfurized natural rubber composite material.
Table 1 is by two-bath process of the present invention, mono bath dipping process, the native rubber composite material performance pair for not being modified processing
Than
Show the mechanical property of the aramid fiber enhancing rubber composite material of the technology of the present invention preparation according to the test result of table 1
It is better than mono bath dipping process and is not modified the rubber composite material of processing, the aramid fiber of the technology of the present invention preparation enhances rubber
Glue composite material has a clear superiority.
It is obvious to a person skilled in the art that invention is not limited to the details of the above exemplary embodiments, Er Qie
In the case where without departing substantially from spirit or essential attributes of the invention, the present invention can be realized in other specific forms.Therefore, nothing
By from the point of view of which point, the present embodiments are to be considered as illustrative and not restrictive, and the scope of the present invention is by institute
Attached claim rather than above description limit, it is intended that will fall within the meaning and scope of the equivalent elements of the claims
All changes be included within the present invention.Any label in claim should not be construed as limiting the claims involved.
Claims (4)
1. a kind of preparation method of impregnation aramid fiber short fibre, which is characterized in that it includes carrying out following processing to aramid fiber precursor
Step:
A: one bath；
B: it dries for the first time；
C: two baths；
D: secondary drying；
E: winding；
F: cutting；
Wherein:
Pre- impregnation is carried out using the isocyanates that the high activity of aqueous solution type is reacted in the step A；
It is impregnated in step C using RFL maceration extract, the formula of the RFL maceration extract is:
RF resin: 420.6 parts of parts by weight；
Soft water: 95.2 parts of parts by weight；
VP latex 40%: 484.2 parts of parts by weight；
The wherein formula of RF resin are as follows:
Soft water: 425.6 parts of parts by weight；
Sodium hydroxide 7%: 16 parts of parts by weight；
Resorcinol solid: 22 parts of parts by weight；
Formaldehyde 38%: 13 parts of parts by weight；
Its specific work step includes:
S1: it by the smooth releasing of aramid fiber precursor pay off rack, keeps not loose, not upper and twists；
S2: being combed by separated time and reach first group of drawing-off rod, is entered the first glue groove by deflector roll and is carried out a bath；
S3: entering first layer baking oven and dry, and drying temperature is 105 DEG C, and drying time is 3 hours；
S4: enter second layer baking oven by second group of draw roll and carry out 230 DEG C of hot settings；
S5: and then enter the second glue groove by third group draw roll and carry out two baths；With RFL dipping solution obtained in 19 DEG C of temperature
Lower dipping aramid fiber 3.2 hours；
S6: it is dried by third layer；Drying temperature be 85 DEG C, the time be 2.5 hours；
S7: up- coiler molding is sent to by the 4th group of draw roll after the 4th layer of pyroreaction of progress and is made into semi-finished product；
S8: finished product is made into after semi-finished product are cut off using fibre cutting machine.
2. a kind of preparation method of impregnation aramid fiber short fibre according to claim 1, it is characterised in that: the step S2
In, the closed polyisocyanates of phenol is selected in a bath, specifically
Step 1: being impregnated aramid fiber 1~3 hour at a temperature of 50~15 DEG C with isocyanates, cleans drying；
Step 2: the acetone soln for the epoxy resin for being again 6~18% with mass percent concentration impregnates aramid fiber at normal temperature
It 2.5~4 hours, is completed after drying modified to the surface of aramid fiber.
3. a kind of preparation method of impregnation aramid fiber short fibre according to claim 1, it is characterised in that: the step S5
In, it is specific as follows:
One, prepare 420.6 parts of parts by weight of RF resin liquid, 95.2 parts of parts by weight of soft water and 484.2 parts of parts by weight of VP latex
40%, total weight parts 1000；
Two, soft water and VP latex are put into blend tank；
Three, RF resin liquid is transplanted in blend tank, and continues to stir, transfer RF resin liquid is completed in 10 minutes, RF resin
Liquid uses the transfer mode of fountain, and blend tank, which is adopted, is water-cooled jacket heat-preservation, keeps 20 DEG C of glue temperature in blend tank, PH
Value is adjusted between 8-9；
Four, since the transfer of RF resin, after curing in 27 hours, obtained RFL maceration extract is sent into subsequent cement dipping machine and is used.
4. a kind of preparation method of impregnation aramid fiber short fibre as claimed in claim 3, it is characterized in that the RF resin liquid
Preparation method, comprising the following steps:
(1) prepare the formaldehyde 38% of soft water, 22 parts of parts by weight of resorcinol solid and parts by weight 13；
(2) soft water is put into reactor tank, water temperature is controlled at 23 DEG C；
(3) sodium hydroxide is dissolved in soft water, is launched after being configured to the sodium hydrate aqueous solution that concentration is 7% to reactor tank
Interior, sodium hydrate aqueous solution parts by weight are 16 parts, and are stirred 10 minutes；
(4) resorcinol solid is dissolved in soft water, is launched after being configured to the resorcinol solution of concentration 10~20% to anti-
It answers in tank, and is stirred 20 minutes；
(5) formaldehyde 38% is launched into soft water and is mixed, be configured to the formalin that concentration is 5~20%, formaldehyde is water-soluble
Liquid is slowly added in reactor tank, and continues stirred tank；
(6) with 10 DEG C of temperature of the cooling reactor tank of cooling water, control reaction temperature is 20 DEG C, and the reaction time is 12.5 hours, is obtained
To RF resin liquid.
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| CN111021068A (en) * | 2019-12-26 | 2020-04-17 | 青岛天邦线业有限公司 | Impregnation treatment technology for impregnated aramid fiber ropes for polyurethane synchronous belt |
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| CN112442816A (en) * | 2020-11-26 | 2021-03-05 | 浙江尤夫高新纤维股份有限公司 | Heat setting method for high-strength hard wire rope impregnation process |
| CN112853761A (en) * | 2020-12-30 | 2021-05-28 | 青岛天邦线业有限公司 | Pretreatment liquid for dipping aramid fiber flexible cord and aramid fiber flexible cord dipping method |
| CN114438792A (en) * | 2022-02-18 | 2022-05-06 | 河南省亚安绝缘材料厂有限公司 | Organosilicon impregnated flame-retardant non-woven fabric |
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| CN112442816A (en) * | 2020-11-26 | 2021-03-05 | 浙江尤夫高新纤维股份有限公司 | Heat setting method for high-strength hard wire rope impregnation process |
| CN112853761A (en) * | 2020-12-30 | 2021-05-28 | 青岛天邦线业有限公司 | Pretreatment liquid for dipping aramid fiber flexible cord and aramid fiber flexible cord dipping method |
| CN114438792A (en) * | 2022-02-18 | 2022-05-06 | 河南省亚安绝缘材料厂有限公司 | Organosilicon impregnated flame-retardant non-woven fabric |
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