CN107090144A - A kind of preparation method of the special sound-absorbing material of interior decoration - Google Patents
A kind of preparation method of the special sound-absorbing material of interior decoration Download PDFInfo
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- CN107090144A CN107090144A CN201710345977.0A CN201710345977A CN107090144A CN 107090144 A CN107090144 A CN 107090144A CN 201710345977 A CN201710345977 A CN 201710345977A CN 107090144 A CN107090144 A CN 107090144A
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/04—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08L27/06—Homopolymers or copolymers of vinyl chloride
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J9/00—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof
- C08J9/04—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent
- C08J9/06—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a chemical blowing agent
- C08J9/10—Working-up of macromolecular substances to porous or cellular articles or materials; After-treatment thereof using blowing gases generated by a previously added blowing agent by a chemical blowing agent developing nitrogen, the blowing agent being a compound containing a nitrogen-to-nitrogen bond
- C08J9/102—Azo-compounds
- C08J9/103—Azodicarbonamide
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F1/00—General methods for the manufacture of artificial filaments or the like
- D01F1/02—Addition of substances to the spinning solution or to the melt
- D01F1/10—Other agents for modifying properties
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F11/00—Chemical after-treatment of artificial filaments or the like during manufacture
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F11/00—Chemical after-treatment of artificial filaments or the like during manufacture
- D01F11/02—Chemical after-treatment of artificial filaments or the like during manufacture of cellulose, cellulose derivatives, or proteins
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
- D01F8/02—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from cellulose, cellulose derivatives, or proteins
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- D—TEXTILES; PAPER
- D01—NATURAL OR MAN-MADE THREADS OR FIBRES; SPINNING
- D01F—CHEMICAL FEATURES IN THE MANUFACTURE OF ARTIFICIAL FILAMENTS, THREADS, FIBRES, BRISTLES OR RIBBONS; APPARATUS SPECIALLY ADAPTED FOR THE MANUFACTURE OF CARBON FILAMENTS
- D01F8/00—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof
- D01F8/18—Conjugated, i.e. bi- or multicomponent, artificial filaments or the like; Manufacture thereof from other substances
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2327/00—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers
- C08J2327/02—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment
- C08J2327/04—Characterised by the use of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08J2327/06—Homopolymers or copolymers of vinyl chloride
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08J—WORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G or C08H
- C08J2401/00—Characterised by the use of cellulose, modified cellulose or cellulose derivatives
- C08J2401/08—Cellulose derivatives
- C08J2401/26—Cellulose ethers
- C08J2401/28—Alkyl ethers
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L2205/00—Polymer mixtures characterised by other features
- C08L2205/14—Polymer mixtures characterised by other features containing polymeric additives characterised by shape
- C08L2205/16—Fibres; Fibrils
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Abstract
The invention discloses a kind of preparation method of the special sound-absorbing material of interior decoration, belong to building and ornament materials preparing technical field.The present invention first mixes the peach gum slurries after fermentation and carboxymethyl cellulose and agar etc., spinning solution is made, composite fibre is made through high-voltage electrostatic spinning again, composite fibre is set to occur dehydration and oxidation operation decomposition by slowly heating up again, form hollow shell supporting construction, continuing thereafter with heating makes the hollow shell breakage of fiber form crackle, and spread to form helical structure along by the face of shear stress, to discharge stress, again by the hollow screw fiber being made and polyvinyl chloride resin mixed foaming, the special sound-absorbing material of interior decoration is made.The present invention reaches the absorption to wideband sound, and material therefor safety and environmental protection using the pore structure of hollow screw fiber and the diffuse reflection effect of helical structure, and it is poor to efficiently solve traditional sound-absorbing material feature of environmental protection, the problem of sound-absorbing frequency range is narrower.
Description
Technical field
The invention discloses a kind of preparation method of the special sound-absorbing material of interior decoration, belong to building and ornament materials and prepare skill
Art field.
Background technology
In today's society, noise pollution have become after after water pollution, atmosphere pollution by of interest main of world wide
One of problem of environmental pollution.In recent years, with the continuous improvement and the increasingly enhancing of environmental consciousness of people's quality of the life, people couple
The requirement of living environment is also stepped up, and the control problem of noise has caused people's most attention.
The conventional means that sound insulation noise reduction is improvement noise pollution is carried out using sound-absorbing acoustic material.Therefore, various sound absorbers
Material is widely used in Noise measarement, and with the continuous growth of sound-absorbing material consumption, people it is also proposed higher to its performance
It is required that, from realizing single sound absorbing capabilities to having the performance transitions such as high acoustic absorption, dicoration, economy and the feature of environmental protection concurrently.
Acoustic material is used to suppress sound transmission, and sound-absorbing material is then used to reduce sound reflection.According to the structure of material
Difference, sound-absorbing material can be divided into porous, resonance, the class of special construction 3.Current porous sound absorbing materials application is the most extensive, main bag
4 classes such as organic fiber, inorfil, inorganic foamed and foamed plastics are included, its surface is mutually passed through rich in pore between hole and hole
It is logical, and it is deep into internal layer.But although traditional sound-absorbing material can possess certain sound-absorbing effect, the frequency range of sound-absorbing compared with
Narrow, only centering high-frequency sound has good assimilation effect, poor to low frequency sound absorption effect, and the feature of environmental protection is not good, easily
Cause pruitus and respiratory tract anaphylaxis, be hazardous to the human body, unsuitable interior is used, limit using and pushing away for sound-absorbing material
Extensively.Therefore, a kind of special sound-absorbing material of interior decoration with wide sound-absorbing frequency range is researched and developed to have important practical significance.
The content of the invention
Present invention mainly solves technical problem:It is narrower for the frequency range of traditional sound-absorbing material sound-absorbing, only to medium-high frequency sound
Sound has good assimilation effect, and there is provided a kind of special sound-absorbing of interior decoration the problem of poor to low frequency sound absorption effect
The preparation method of material.
In order to solve the above-mentioned technical problem, the technical solution adopted in the present invention is:
(1)200~300g peach gums are weighed, are poured into the beaker for filling 500~800mL water, stood after stirring mixing and be swelled 12~
16h, then the peach gum after being swelled in beaker is poured into fermentation tank, constant-temperature enclosed fermentation is treated fermentation ends, through autoclaving, obtained
Modified peach gum slurries;
(2)The above-mentioned gained of 400~500g is weighed successively is modified peach gum slurries, 60~80g carboxymethyl celluloses, 30~50g agar,
Pour into the beaker for filling 100~150mL water, then beaker be placed in digital display and test the speed in constant temperature blender with magnetic force, in temperature be 55
~65 DEG C, under the conditions of rotating speed is 500~700r/min, constant temperature stirring 80~120min of mixing, derived from spinning solution processed, then by gained
Self-control spinning solution is transferred to high-voltage electrostatic spinning machine, will make spinning solution electrostatic spinning by oneself, after being solidified through coagulating bath, obtains composite fibre;
(3)The above-mentioned gained composite fibres of 100~120g are weighed, pours into and fills 500~600mL mass fractions for 70~80% ethanol
In the three-necked flask of solution, after 10~15min of ultrasonic disperse, three-necked flask is moved into digital display and tested the speed constant temperature blender with magnetic force
In, in temperature be 40~45 DEG C, rotating speed be 300~500r/min under the conditions of, 40 are added dropwise into three-necked flask by dropping funel
~50mL tetraethyl orthosilicates, control is dripped off in 15~20min, treats completion of dropping, continues constant temperature 20~30min of stirring reaction,
Material in three-necked flask is poured into beaker again, stood after 8~10h, filters, dry to constant weight, then is calcined through slow heating, is obtained
Hollow screw composite fibre;
(4)Count by weight, 60~80 parts of hollow screw composite fibres, 100~120 parts of PVC are sequentially added in batch mixer
Resin, 4~6 parts of azodicarbonamides are 75~80 DEG C in temperature, rotating speed is under the conditions of 600~800r/min, constant temperature stirring is mixed
Close 45~60min, then material in batch mixer be transferred to twin-roll plastic mixing mill, in temperature be plasticate 6 under the conditions of 100~110 DEG C~
8min, then material in plasticator is transferred to single screw extrusion machine continuously extruded, extrusion molding after-drawing cooling produces interior
Decorate special sound-absorbing material.
Step(1)Described constant-temperature enclosed fermentation condition is:32~35 DEG C of fermentation temperature, fermentation tank speed of agitator is 200
~300r/min, fermentation time is 4~6h.
Step(1)It is described be swelled after peach gum in, 0.3~0.5g sodium sulfites can also be added.
Step(2)In described constant temperature stirring mixed process, 20~40g wheat gluten flours can also be added into beaker.
Step(2)Described electrostatic spinning process parameter is:Spinning voltage is 20~22kV, and spinning temperature is 40~42
DEG C, fltting speed is 0.6~0.8mm/s, and it is 8~10cm to receive distance.
Step(2)Described coagulating bath be by 100~120g mass fractions be 98% sulfuric acid, 280~300g sodium sulphate, 10
~15g zinc sulfate, is mixed with 1200~1500mL deionized waters.
Step(3)Described slow heating calcination condition is:400 are warming up to 0.2~0.4 DEG C/min rate programs~
420 DEG C, it is incubated after 6~9h, continues to be warming up to 700~850 DEG C with 0.3~0.5 DEG C/min rate programs, 2~4h is incubated, with stove
It is cooled to room temperature.
The beneficial effects of the invention are as follows:
(1)Peach gum is swelled rear sealed fermenting by the present invention first, and adds sodium sulfite during the fermentation, is reduced in fermentation tank
Dissolved oxygen, makes yeasting be in reproducibility environment, improves fermentation efficiency, during the fermentation, macromolecular is organic in peach gum
Matter is degraded to small molecule, increases active group in peach gum, and has part small-molecule substance to be further degraded to ethanol, is easy to
Next step and carboxymethyl cellulose etc. are sufficiently mixed uniformly, while by being aided with wheat gluten flour, improving electrostatic spinning process institute
Obtain the ductility and toughness of composite fibre;
(2)The present invention because in initial breakdown, peach gum after peach gum premenstruum (premenstrua) saccharomycetes to make fermentation active group increase so that compound fibre
Tie up surface active groups increasing number, and the active group of composite fiber surface be added dropwise Hydrolysis of Ethyl Silicate in, can
The silica absorption produced will be hydrolyzed, then in slowly heating calcination process, relatively low heating rate sends out composite fibre
Raw dehydration and oxidation operation are decomposed, and form hollow shell supporting construction, in subsequently heating contraction process, the fibre being relatively large in diameter
Denapon amount of contraction and thermal stress are larger, and supporting construction is difficult to maintain, and make the hollow shell of fiber damaged and form crackle, and along receipts
Spread to shear stress face and form helical structure, to discharge stress, after the hollow screw fiber of formation is added in product, profit
With the pore structure and the diffuse reflection effect of helical structure of hollow screw fiber, the good absorption to high, medium and low frequency sound is reached
And shielding.
Embodiment
200~300g peach gums are weighed first, are poured into the beaker for filling 500~800mL water, with glass bar stirring mixing 3
After~5min, standing is swelled 12~16h, then the peach gum after being swelled in beaker is poured into fermentation tank, and sequentially adds 5~10g
Dry ferment, 0.3~0.5g sodium sulfites, in temperature be 32~35 DEG C, rotating speed be 200~300r/min under the conditions of, it is constant-temperature enclosed
Ferment 4~6h, treats fermentation ends, material in fermentation tank is transferred in high-pressure sterilizing pot, under the conditions of temperature is 120 DEG C, sterilizing
15~20min is handled, modified peach gum slurries are obtained, modified peach gum slurries, 60~80g carboxymethyls obtained by 400~500g are weighed successively
Cellulose, 30~50g agar, 20~40g wheat gluten flours are poured into the beaker for filling 100~150mL water, then beaker is put
It it is 55~65 DEG C in temperature, rotating speed is under the conditions of 500~700r/min, constant temperature stirs in digital display tests the speed constant temperature blender with magnetic force
80~120min of mixing is mixed, high-voltage electrostatic spinning machine is transferred to derived from spinning solution processed, then by gained self-control spinning solution, in spinning voltage
For 20~22kV, temperature is 40~42 DEG C, and fltting speed is 0.6~0.8mm/s, is received under the conditions of distance is 8~10cm, will be from
Spinning solution spinning processed, after being solidified through coagulating bath, obtains composite fibre;Described coagulating bath be by 100~120g mass fractions be 98%
Sulfuric acid, 280~300g sodium sulphate, 10~15g zinc sulfate is mixed with 1200~1500mL deionized waters;Weigh 100 again~
120g composite fibres, pour into and fill in the three-necked flask that 500~600mL mass fractions are 70~80% ethanol solutions, then by three mouthfuls
Flask is placed in sonic oscillation instrument, disperses 10~15min with 40~45kHz frequency ultrasounds, then three-necked flask is moved into digital display to survey
In fast constant temperature blender with magnetic force, in temperature be 40~45 DEG C, rotating speed be 300~500r/min under the conditions of, by dropping funel to
40~50mL tetraethyl orthosilicates are added dropwise in three-necked flask, control is dripped off in 15~20min, treats completion of dropping, continue constant temperature and stir
20~30min of reaction is mixed, question response terminates, material in three-necked flask is poured into beaker, under room temperature condition, stand 8~
10h, then by material filtering in beaker, filter cake is obtained, then filter cake is transferred in baking oven, dried under the conditions of temperature is 105~110 DEG C
It is transferred to constant weight, then by dried filter cake in Muffle furnace, 400~420 DEG C is warming up to 0.2~0.4 DEG C/min rate programs,
It is incubated after 6~9h, continues to be warming up to 700~850 DEG C with 0.3~0.5 DEG C/min rate programs, be incubated 2~4h, cool to the furnace
Room temperature, discharging, obtain hollow screw composite fibre, finally count by weight, sequentially added in batch mixer 60~80 parts it is hollow
Spiral composite fibre, 100~120 parts of polyvinyl chloride resins, 4~6 parts of azodicarbonamides are 75~80 DEG C in temperature, rotating speed is 600
Under the conditions of~800r/min, constant temperature stirring 45~60min of mixing, then material in batch mixer is transferred to twin-roll plastic mixing mill, in temperature
For the 6~8min that plasticated under the conditions of 100~110 DEG C, then material in plasticator is transferred to single screw extrusion machine continuously extruded, squeezed
Go out to be molded after-drawing cooling, produce the special sound-absorbing material of interior decoration.
Example 1
200g peach gums are weighed first, are poured into the beaker for filling 500mL water, and after glass bar stirring mixing 3min, standing is swelled
12h, then the peach gum after being swelled in beaker is poured into fermentation tank, and 5g dry ferments are sequentially added, it is 32 DEG C in temperature, rotating speed is
Under the conditions of 200r/min, constant-temperature enclosed fermentation 4h treats fermentation ends, material in fermentation tank is transferred in high-pressure sterilizing pot, Yu Wen
Spend under the conditions of 120 DEG C, sterilization treatment 15min obtains modified peach gum slurries, modified peach gum slurries, 60g obtained by 400g are weighed successively
Carboxymethyl cellulose, 30g agar, 20g wheat gluten flours are poured into the beaker for filling 100mL water, then beaker is placed in into digital display survey
It it is 55 DEG C in temperature, rotating speed is under the conditions of 500r/min, constant temperature stirring mixes 80min, derived from system in fast constant temperature blender with magnetic force
Spinning solution, then gained self-control spinning solution is transferred to high-voltage electrostatic spinning machine, it is 20kV in spinning voltage, temperature is 40 DEG C, is promoted
Speed is 0.6mm/s, receives distance under the conditions of 8cm, to make spinning solution spinning by oneself, and after solidifying through coagulating bath, obtain composite fibre;
It by 100g mass fractions is 98% sulfuric acid that described coagulating bath, which is, and 280g sodium sulphate, 10g zinc sulfate is mixed with 1200mL deionized waters
Conjunction is formed;100g composite fibres are weighed again, are poured into and are filled in the three-necked flask that 500mL mass fractions are 70% ethanol solution, then will
Three-necked flask is placed in sonic oscillation instrument, disperses 10min with 40kHz frequency ultrasounds, then three-necked flask is moved into digital display to test the speed perseverance
In warm magnetic stirring apparatus, in temperature be 40 DEG C, rotating speed be 300r/min under the conditions of, be added dropwise by dropping funel into three-necked flask
40mL tetraethyl orthosilicates, control is dripped off in 15min, treats completion of dropping, continues constant temperature stirring reaction 20min, and question response terminates,
Material in three-necked flask is poured into beaker, under room temperature condition, 8h is stood, then by material filtering in beaker, obtains filter cake, then will
Filter cake is transferred in baking oven, and drying is transferred in Muffle furnace to constant weight, then by dried filter cake under the conditions of temperature is 105 DEG C, with
0.2 DEG C/min rate programs are warming up to after 400 DEG C, insulation 6h, continue to be warming up to 700 DEG C, insulation with 0.3 DEG C/min rate programs
2h, cools to room temperature with the furnace, discharging, obtains hollow screw composite fibre, finally counts by weight, is sequentially added in batch mixer
60 parts of hollow screw composite fibres, 100 parts of polyvinyl chloride resins, 4 parts of azodicarbonamides are 75 DEG C in temperature, rotating speed is 600r/min
Under the conditions of, constant temperature stirring mixing 45min, then material in batch mixer is transferred to twin-roll plastic mixing mill, moulded under the conditions of temperature is 100 DEG C
6min is refined, then material in plasticator is transferred to single screw extrusion machine and is continuously extruded, extrusion molding after-drawing cooling produces room
The special sound-absorbing material of interior trim.
Example 2
250g peach gums are weighed first, are poured into the beaker for filling 650mL water, and after glass bar stirring mixing 4min, standing is swelled
14h, then the peach gum after being swelled in beaker is poured into fermentation tank, and 8g dry ferments are sequentially added, it is 34 DEG C in temperature, rotating speed is
Under the conditions of 250r/min, constant-temperature enclosed fermentation 5h treats fermentation ends, material in fermentation tank is transferred in high-pressure sterilizing pot, Yu Wen
Spend under the conditions of 120 DEG C, sterilization treatment 18min obtains modified peach gum slurries, modified peach gum slurries, 70g obtained by 450g are weighed successively
Carboxymethyl cellulose, 40g agar, 30g wheat gluten flours are poured into the beaker for filling 125mL water, then beaker is placed in into digital display survey
It it is 60 DEG C in temperature, rotating speed is under the conditions of 600r/min, constant temperature stirring mixing 100min derives from fast constant temperature blender with magnetic force
Spinning solution processed, then gained self-control spinning solution is transferred to high-voltage electrostatic spinning machine, it is 21kV in spinning voltage, temperature is 41 DEG C, is pushed away
Enter speed for 0.7mm/s, receive distance under the conditions of 9cm, spinning solution spinning will be made by oneself, after solidifying through coagulating bath, fibre must be combined
Dimension;Described coagulating bath be by 110g mass fractions be 98% sulfuric acid, 290g sodium sulphate, 13g zinc sulfate, with 1350mL deionizations
Water is mixed;110g composite fibres are weighed again, pour into three mouthfuls of burnings for filling that 500~600mL mass fractions are 75% ethanol solution
In bottle, then three-necked flask is placed in sonic oscillation instrument, 13min disperseed with 43kHz frequency ultrasounds, then three-necked flask is moved into number
In the aobvious constant temperature blender with magnetic force that tests the speed, it is 43 DEG C in temperature, under the conditions of rotating speed is 400r/min, is burnt by dropping funel to three mouthfuls
45mL tetraethyl orthosilicates are added dropwise in bottle, control is dripped off in 18min, treats completion of dropping, is continued constant temperature stirring reaction 25min, is treated
Reaction terminates, and material in three-necked flask is poured into beaker, under room temperature condition, stands 9h, then by material filtering in beaker, obtain
Filter cake, then filter cake is transferred in baking oven, dried under the conditions of temperature is 108 DEG C and be transferred to horse to constant weight, then by dried filter cake
Not in stove, it is warming up to 0.3 DEG C/min rate programs after 410 DEG C, insulation 8h, continuation is warming up to 0.4 DEG C/min rate programs
775 DEG C, 3h is incubated, room temperature is cooled to the furnace, discharged, obtain hollow screw composite fibre, finally count by weight, in batch mixer
In sequentially add 70 parts of hollow screw composite fibres, 110 parts of polyvinyl chloride resins, 5 parts of azodicarbonamides, in temperature be 78 DEG C, rotating speed
Under the conditions of 700r/min, material in batch mixer then is transferred to twin-roll plastic mixing mill by constant temperature stirring mixing 53min, in temperature be 105
Plasticate 7min under the conditions of DEG C, then material in plasticator is transferred into single screw extrusion machine continuously extruded, extrusion molding after-drawing
Cooling, produces the special sound-absorbing material of interior decoration.
Example 3
300g peach gums are weighed first, are poured into the beaker for filling 800mL water, and after glass bar stirring mixing 5min, standing is swelled
16h, then the peach gum after being swelled in beaker is poured into fermentation tank, and sequentially add 10g dry ferments, 0.5g sodium sulfites, Yu Wen
Spend for 35 DEG C, rotating speed is under the conditions of 300r/min, constant-temperature enclosed fermentation 6h treats fermentation ends, material in fermentation tank is transferred into height
Press in autoclave, under the conditions of temperature is 120 DEG C, sterilization treatment 20min obtains modified peach gum slurries, weighs successively obtained by 500g
Modified peach gum slurries, 80g carboxymethyl celluloses, 50g agar, 40g wheat gluten flours are poured into the beaker for filling 150mL water, then
Beaker is placed in into digital display to test the speed in constant temperature blender with magnetic force, in temperature be 65 DEG C, under the conditions of rotating speed is 700r/min, constant temperature stirring
120min is mixed, high-voltage electrostatic spinning machine is transferred to derived from spinning solution processed, then by gained self-control spinning solution, is in spinning voltage
22kV, temperature is 42 DEG C, and fltting speed is 0.8mm/s, receives distance under the conditions of 10cm, spinning solution spinning will be made by oneself, through solidifying
Gu after bath solidification, obtain composite fibre;Described coagulating bath be by 120g mass fractions be 98% sulfuric acid, 300g sodium sulphate, 15g sulphur
Sour zinc, is mixed with 1500mL deionized waters;120g composite fibres are weighed again, are poured into and are filled 600mL mass fractions for 80% second
In the three-necked flask of alcoholic solution, then three-necked flask is placed in sonic oscillation instrument, 15min is disperseed with 45kHz frequency ultrasounds, then will
Three-necked flask moves to digital display and tested the speed in constant temperature blender with magnetic force, is 45 DEG C in temperature, under the conditions of rotating speed is 500r/min, passes through drop
50mL tetraethyl orthosilicates are added dropwise into three-necked flask for liquid funnel, and control is dripped off in 20min, treats completion of dropping, are continued constant temperature and are stirred
Reaction 30min is mixed, question response terminates, material in three-necked flask is poured into beaker, under room temperature condition, standing 10h, then will burnt
Wine material is filtered, and obtains filter cake, then filter cake is transferred in baking oven, is to dry to constant weight under the conditions of 110 DEG C in temperature, then by drying
Filter cake afterwards is transferred in Muffle furnace, is warming up to after 420 DEG C, insulation 9h, continued with 0.5 DEG C/min with 0.4 DEG C/min rate programs
Rate program is warming up to 850 DEG C, is incubated 4h, cools to room temperature with the furnace, discharges, obtains hollow screw composite fibre, by weight finally
Number meter, sequentially adds 80 parts of hollow screw composite fibres in batch mixer, 120 parts of polyvinyl chloride resins, 6 parts of azodicarbonamides, in
Temperature is 80 DEG C, and rotating speed is under the conditions of 800r/min, constant temperature stirring mixes 60min, then material in batch mixer is transferred into double roller modeling
Mill, is to plasticate 8min under the conditions of 110 DEG C in temperature, then material in plasticator is transferred into single screw extrusion machine continuously to be squeezed
Go out, extrusion molding after-drawing cooling produces the special sound-absorbing material of interior decoration.
The performance of the interior decoration special sound-absorbing material made to example 1~3 and common commercially available interior decoration sound-absorbing material
Tested, test result is as follows:
Above-described embodiment is not limited for the present invention preferably embodiment, but embodiments of the present invention by above-described embodiment
System, other any Spirit Essences without departing from the present invention and the change made under principle, modification, replacement, combine, simplification,
Equivalent substitute mode is should be, is included within protection scope of the present invention.
Claims (7)
1. a kind of preparation method of the special sound-absorbing material of interior decoration, it is characterised in that specifically preparation process is:
(1)200~300g peach gums are weighed, are poured into the beaker for filling 500~800mL water, stood after stirring mixing and be swelled 12~
16h, then the peach gum after being swelled in beaker is poured into fermentation tank, constant-temperature enclosed fermentation is treated fermentation ends, through autoclaving, obtained
Modified peach gum slurries;
(2)The above-mentioned gained of 400~500g is weighed successively is modified peach gum slurries, 60~80g carboxymethyl celluloses, 30~50g agar,
Pour into the beaker for filling 100~150mL water, then beaker be placed in digital display and test the speed in constant temperature blender with magnetic force, in temperature be 55
~65 DEG C, under the conditions of rotating speed is 500~700r/min, constant temperature stirring 80~120min of mixing, derived from spinning solution processed, then by gained
Self-control spinning solution is transferred to high-voltage electrostatic spinning machine, will make spinning solution electrostatic spinning by oneself, after being solidified through coagulating bath, obtains composite fibre;
(3)The above-mentioned gained composite fibres of 100~120g are weighed, pours into and fills 500~600mL mass fractions for 70~80% ethanol
In the three-necked flask of solution, after 10~15min of ultrasonic disperse, three-necked flask is moved into digital display and tested the speed constant temperature blender with magnetic force
In, in temperature be 40~45 DEG C, rotating speed be 300~500r/min under the conditions of, 40 are added dropwise into three-necked flask by dropping funel
~50mL tetraethyl orthosilicates, control is dripped off in 15~20min, treats completion of dropping, continues constant temperature 20~30min of stirring reaction,
Material in three-necked flask is poured into beaker again, stood after 8~10h, filters, dry to constant weight, then is calcined through slow heating, is obtained
Hollow screw composite fibre;
(4)Count by weight, 60~80 parts of hollow screw composite fibres, 100~120 parts of PVC are sequentially added in batch mixer
Resin, 4~6 parts of azodicarbonamides are 75~80 DEG C in temperature, rotating speed is under the conditions of 600~800r/min, constant temperature stirring is mixed
Close 45~60min, then material in batch mixer be transferred to twin-roll plastic mixing mill, in temperature be plasticate 6 under the conditions of 100~110 DEG C~
8min, then material in plasticator is transferred to single screw extrusion machine continuously extruded, extrusion molding after-drawing cooling produces interior
Decorate special sound-absorbing material.
2. a kind of preparation method of special sound-absorbing material of environment-friendly type interior decoration according to claim 1, it is characterised in that:
Step(1)Described constant-temperature enclosed fermentation condition is:32~35 DEG C of fermentation temperature, fermentation tank speed of agitator is 200~300r/
Min, fermentation time is 4~6h.
3. a kind of preparation method of special sound-absorbing material of environment-friendly type interior decoration according to claim 1, it is characterised in that:
Step(1)It is described be swelled after peach gum in, 0.3~0.5g sodium sulfites can also be added.
4. a kind of preparation method of special sound-absorbing material of environment-friendly type interior decoration according to claim 1, it is characterised in that:
Step(2)In described constant temperature stirring mixed process, 20~40g wheat gluten flours can also be added into beaker.
5. a kind of preparation method of special sound-absorbing material of environment-friendly type interior decoration according to claim 1, it is characterised in that:
Step(2)Described electrostatic spinning process parameter is:Spinning voltage is 20~22kV, and spinning temperature is 40~42 DEG C, promotes speed
Spend for 0.6~0.8mm/s, it is 8~10cm to receive distance.
6. a kind of preparation method of special sound-absorbing material of environment-friendly type interior decoration according to claim 1, it is characterised in that:
Step(2)Described coagulating bath be by 100~120g mass fractions be 98% sulfuric acid, 280~300g sodium sulphate, 10~15g sulfuric acid
Zinc, is mixed with 1200~1500mL deionized waters.
7. a kind of preparation method of special sound-absorbing material of environment-friendly type interior decoration according to claim 1, it is characterised in that:
Step(3)Described slow heating calcination condition is:400~420 DEG C, insulation are warming up to 0.2~0.4 DEG C/min rate programs
After 6~9h, continue to be warming up to 700~850 DEG C with 0.3~0.5 DEG C/min rate programs, be incubated 2~4h, cool to room with the furnace
Temperature.
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JPH10150930A (en) * | 1996-11-21 | 1998-06-09 | Japan Organo Co Ltd | Method for refining peach resin and peach resin |
CN102517661A (en) * | 2011-12-22 | 2012-06-27 | 福建鑫华股份有限公司 | Preparation method of triangular hollow dacron short fiber and spinneret plate for preparing triangular hollow dacron short fiber |
CN103696132A (en) * | 2013-11-25 | 2014-04-02 | 芜湖跃飞新型吸音材料股份有限公司 | Active carbon noise-absorbing cotton and preparation method thereof |
CN105544276A (en) * | 2015-12-03 | 2016-05-04 | 高大元 | Non-woven self-cleaning flame retardation sound-absorbing wallpaper preparation method |
CN106117661A (en) * | 2016-06-28 | 2016-11-16 | 郭舒洋 | A kind of preparation method of lightweight broad-band sound-absorbing material |
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2017
- 2017-05-17 CN CN201710345977.0A patent/CN107090144A/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
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JPH10150930A (en) * | 1996-11-21 | 1998-06-09 | Japan Organo Co Ltd | Method for refining peach resin and peach resin |
CN102517661A (en) * | 2011-12-22 | 2012-06-27 | 福建鑫华股份有限公司 | Preparation method of triangular hollow dacron short fiber and spinneret plate for preparing triangular hollow dacron short fiber |
CN103696132A (en) * | 2013-11-25 | 2014-04-02 | 芜湖跃飞新型吸音材料股份有限公司 | Active carbon noise-absorbing cotton and preparation method thereof |
CN105544276A (en) * | 2015-12-03 | 2016-05-04 | 高大元 | Non-woven self-cleaning flame retardation sound-absorbing wallpaper preparation method |
CN106117661A (en) * | 2016-06-28 | 2016-11-16 | 郭舒洋 | A kind of preparation method of lightweight broad-band sound-absorbing material |
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