CN107245157A - A kind of preparation method of snap joint sealing ring - Google Patents
A kind of preparation method of snap joint sealing ring Download PDFInfo
- Publication number
- CN107245157A CN107245157A CN201710538953.7A CN201710538953A CN107245157A CN 107245157 A CN107245157 A CN 107245157A CN 201710538953 A CN201710538953 A CN 201710538953A CN 107245157 A CN107245157 A CN 107245157A
- Authority
- CN
- China
- Prior art keywords
- parts
- sealing ring
- water
- added
- minutes
- 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.)
- Withdrawn
Links
Classifications
-
- 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
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
- C08J7/04—Coating
- C08J7/0427—Coating with only one layer of a composition containing a polymer binder
-
- 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
- C08J7/00—Chemical treatment or coating of shaped articles made of macromolecular substances
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L1/00—Compositions of cellulose, modified cellulose or cellulose derivatives
- C08L1/08—Cellulose derivatives
- C08L1/26—Cellulose ethers
- C08L1/28—Alkyl ethers
- C08L1/284—Alkyl ethers with hydroxylated hydrocarbon radicals
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L7/00—Compositions of natural rubber
- C08L7/02—Latex
-
- 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
- C08J2307/00—Characterised by the use of natural rubber
- C08J2307/02—Latex
-
- 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
- C08J2491/00—Characterised by the use of oils, fats or waxes; Derivatives thereof
- C08J2491/06—Waxes
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K3/00—Use of inorganic substances as compounding ingredients
- C08K3/18—Oxygen-containing compounds, e.g. metal carbonyls
- C08K3/20—Oxides; Hydroxides
- C08K3/22—Oxides; Hydroxides of metals
- C08K2003/2296—Oxides; Hydroxides of metals of zinc
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
- C08K2201/00—Specific properties of additives
- C08K2201/011—Nanostructured additives
-
- 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
- C08L2205/02—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group
- C08L2205/025—Polymer mixtures characterised by other features containing two or more polymers of the same C08L -group containing two or more polymers of the same hierarchy C08L, and differing only in parameters such as density, comonomer content, molecular weight, structure
-
- 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
- C08L2205/03—Polymer mixtures characterised by other features containing three or more polymers in a blend
- C08L2205/035—Polymer mixtures characterised by other features containing three or more polymers in a blend containing four or more polymers in a blend
-
- 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
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
- Sealing Material Composition (AREA)
Abstract
A kind of method that utilization natural plant gum prepares sealing ring, first prepares plant gum powder, is 1 by gained plant gum powder and Heveatex ratio:3, it is well mixed that rubber cement is made;Cotton sail cloth impregnation 20~40 minutes in rubber cement will be dried, (roller speed is than being 1 through two roll calender:1, roll spacing is 3mm) extruding even uniform after be dried to obtain adhesive plaster;Adhesive plaster is paved into after 2~3 layers by specification with 45° angle severing, compacting is rolled to be put into sealing ring mould, die inside wall scribbles wear-resisting glue, vulcanizes 30~45 minutes under conditions of 145~155 DEG C, 8~10 MPa, by the sealing ring of shaping, it is put into 35 portions of hardening agents and soaks 2 hours, bubble in low pressure removing system, after drying, coating of wax is smeared using cotton sail cloth, it can be fully cured after being heat-treated 4h at 100 DEG C, you can.This law sealing ring performance is stable, is difficult to be swelled in media as well, thermal pinch is small, while enhancing tensile strength, elongation and tearing toughness.
Description
Technical field:
The present invention relates to a kind of sealing ring, and in particular to a kind of preparation method method of snap joint sealing ring.
Background technology:
The circular cowling that sealing ring is made up of one or several parts, be fixed on a lasso of bearing or packing ring and with it is another
One lasso or washer contacts form narrow labyrinth clearance, prevent lubricating oil from spilling and foreign object intrusion.Sealing ring is a kind of section
For circular rubber ring, because its section is O-shaped, therefore O-ring seal is called.
Existing sealing ring has a rubber seal and metal o-ring, and metal o-ring has very strong characteristic, without appointing
What rubber constituent, and rubber seal is generally rubber chemistry composition composition, preparation process influences very big to staff, while dirty
Contaminate environment.
The content of the invention:
The technical problems to be solved by the invention are to overcome the defect of prior art, and there is provided a kind of snap joint sealing ring
Preparation method.
The technical problems to be solved by the invention are realized using following technical scheme.
A kind of preparation method of snap joint sealing ring, it is characterised in that:
100-120 parts of soybean protein is taken, protein isolate 8%-20%, urea 15%-17%, polyphosphoric acids from soybean
Sodium 1%-10%, urea is dispersed in water, and is mixed and made into urea liquid, adds albumen and mixture, 1-2 is stirred at normal temperatures
Hour, 5-7 parts of coupling agent is added, continues to stir 2-3 hours, it is high finally by the 15-20 parts of additions of 50% sodium hydrate aqueous solution
Temperature stirring 20 minutes, temperature control is at 90-95 DEG C;
30-40 parts of toughener and 2-5 parts of epoxy organosilicon, 0~80 DEG C of temperature are slowly added under stirring and/or ultrasonication
The lower reaction of degree 0.1~12 hour, after reaction terminates, is dehydrated by vaporizing extract process, by eluting, granulating repeatedly, dried;
Grain will be dried to mix for 15-20 part with ethyl cyanoacetate, beaten, 15-20 parts of 50% sodium hydrate aqueous solution of addition with
100-130 parts of water mixing, heating adds 30-50 parts of cornstarch after being added 2 hours after 20 minutes, refines 2 hours, obtain glue
Liquid;
30-140 parts of water intaking, 10-40 parts of hydrophilic chemicals, 2-30 parts of urea, inorganic or 2-30 parts of organic acid, are utilized
More than 50 DEG C of hot water or steam is mixed with glue, inorganic base and is incubated 30 minutes to 1 hour more than 50 DEG C, makes glue
Abundant water swelling, so that its close molecular structure be pulled open and become bulk, then adds required hydrophilic chemistries thing
Matter and inorganic or organic acid, are 0.5-4 hours in reaction at 50-100 DEG C, produce the aqueous chemical modification plant for 20-60%
Film, after extrusion, drying, crushing, produce it is aqueous be less than 10% quick-dissolving chemically modified vegetable gum powder;
It is 1 by gained plant gum powder and Heveatex ratio:3, it is well mixed that rubber cement is made;Will dry cotton sail cloth in
Impregnation 20~40 minutes in rubber cement, through two roll calender, (roller speed is than being 1:1, roll spacing is 3mm) it is dry after extruding even uniform
To adhesive plaster;Adhesive plaster is paved into after 2~3 layers by specification with 45° angle severing, compacting is rolled and is put into sealing ring mould, die inside
Wall scribbles wear-resisting glue, vulcanizes 30~45- minutes under conditions of 145~155 DEG C, 8~10-MPa, by the sealing of shaping
Circle, is put into 35 portions of hardening agents and soaks 2 hours, the bubble in low pressure removing system, after drying, and one is smeared using cotton sail cloth
Layer wax, can be fully cured after being heat-treated 4h at 100 DEG C, you can.
Described wear-resisting glue is prepared from including following components:N330-23-25 parts of carbon black, dioctyl adipate DOA-
15-17 parts, 6-8 parts of zinc oxide, 7-9 parts of stearic acid, 10-13 parts of age resistor, DCP-4-6 parts of vulcanizing agent, vulcanization aid TAIC-5-
8 parts, 12-18 parts of hydroxypropyl cellulose, 7-15 parts of pulullan polysaccharide, 13-16 parts of nano silicon.
Described wear-resisting glue, which comprises the following steps, to be prepared from:
Dioctyl adipate DOA is dissolved by heating in 70 DEG C of hot bath, the stirring of stearic acid mixing and emulsifying is then added
Uniformly, carbon black is taken into container, is added zinc oxide, is mixed evenly;Mixture is used into emulsification in 60~80 DEG C of water-baths
Device stirs, regulation emulsification stirring speed to 6000r/min, turns down rotating speed to 3000r/min after 5min, continues to stir
30min, when temperature is down to 8 DEG C, adds 2 age resistor, then adds vulcanizing agent DCP, vulcanization aid, is dehydrated 15min, centrifugation point
From, hydroxypropyl cellulose is added, drying at room temperature obtains solid powder, by pulullan polysaccharide, nano silicon, ultrasound
After vibration dispersion is uniform, centrifuges and remove big particulate, drying at room temperature obtains particle, in the water that particle is added to 2 times, mix
Close, 200 DEG C of heating 30min obtain wear-resisting glue.
Described hardening agent is prepared from including following components:Including 30 parts of intensity modifying agents:30%-40% acrylic acid fourths
Ester, 30-40% ethyl acetate, remaining is water;
5 parts of form retention agents:Ethyl acetate 15-25%, pentaerythrite 30-35%, 15%-20% parts of paraffin, remaining is
Water.
Described hardening agent, which comprises the following steps, to be prepared from:Butyl acrylate, ethyl acetate and water are sequentially added, machinery
It is uniformly mixed, 1 obtains form retention agent;
Paraffin and ethyl acetate is taken to heat mixing, vaccum dewatering 5 minutes;Pentaerythrite is added, low pressure after being well mixed
Bubble in removing system, can be fully cured after being heat-treated 4h at 100 DEG C;Solidfied material is mixed with 60 DEG C of temperature water,
Stirring 1 hour, as form retention agent;
Form retention agent is mixed with intensity modifying agent, 60 DEG C are heated 1 hour, and 30 DEG C cool down 1 hour, and 90 DEG C add 5 points
Clock, you can.
Described wax is that 90% paraffin and 10% age resistor are mixed.
Beneficial effects of the present invention:Using vegetable rubber made from the formula, lightweight, quality is good, cheap, anti-
Ageing properties are good, durable in use, and performance is stable, is difficult to be swelled in media as well, thermal pinch (Joule effect) is small, strengthen simultaneously
Tensile strength, elongation and tearing toughness.This kind of elastomeric material intensity is high simultaneously, good toughness, it is not easy to be damaged easily,
, can be good with product hermeticity made from this kind of elastomeric material and its anti-wear performance is splendid, market uses wide, natural plant gum dirt
Dye is small, and great role is played to environmental protection, deep to be favored by vast chemical enterprise.
Embodiment:
In order that the technical means, the inventive features, the objects and the advantages of the present invention are easy to understand, tie below
Specific embodiment is closed, the present invention is expanded on further.
Embodiment 1:A kind of preparation method of snap joint sealing ring,
100 parts of soybean protein is taken, protein isolate 8%-20%, urea 15%-17%, sodium polyphosphate from soybean
1%-10%, urea is dispersed in water, and is mixed and made into urea liquid, adds albumen and mixture, 1-2 is stirred at normal temperatures small
When, 5 parts of coupling agent is added, continues to stir 2-3 hours, finally by 50% sodium hydrate aqueous solution, 15 parts of additions, high-temperature stirring
20 minutes, temperature control was at 90-95 DEG C;
It is slowly added under stirring and/or ultrasonication at a temperature of 2 parts, 0~80 DEG C of 30 parts of toughener and epoxy organosilicon
Reaction 0.1~12 hour, after reaction terminates, is dehydrated by vaporizing extract process, by eluting, granulating repeatedly, is dried;
Grain will be dried to mix for 15 parts with ethyl cyanoacetate, beat, add 50% sodium hydrate aqueous solution, 15 parts and 100 parts water
Mixing, heating adds 30 parts of cornstarch after being added 2 hours after 20 minutes, refines 2 hours, obtain glue;
30 parts of water intaking, 10 parts of hydrophilic chemicals, 2 parts of urea, inorganic or 2 parts of organic acid, utilize more than 50 DEG C heat
Water or steam are mixed with glue, inorganic base and are incubated 30 minutes to 1 hour more than 50 DEG C, glue is fully absorbed water swollen
It is swollen, so that its close molecular structure be pulled open and become bulk, hydrophilic chemicals needed for then adding and it is inorganic or
Organic acid, is 0.5-4 hours in reaction at 50-100 DEG C, the aqueous chemically modified vegetable gum piece for 20-60% is produced, through extruding
It is expanded, dry, crush after, produce it is aqueous be less than 10% quick-dissolving chemically modified vegetable gum powder;
It is 1 by gained plant gum powder and Heveatex ratio:3, it is well mixed that rubber cement is made;Will dry cotton sail cloth in
Impregnation 20~40 minutes in rubber cement, through two roll calender, (roller speed is than being 1:1, roll spacing is 3mm) it is dry after extruding even uniform
To adhesive plaster;Adhesive plaster is paved into after 2~3 layers by specification with 45° angle severing, compacting is rolled and is put into sealing ring mould, die inside
Wall scribbles wear-resisting glue, vulcanizes 30~45- minutes under conditions of 145~155 DEG C, 8~10-MPa, by the sealing of shaping
Circle, is put into 35 portions of hardening agents and soaks 2 hours, the bubble in low pressure removing system, after drying, and one is smeared using cotton sail cloth
Layer wax, can be fully cured after being heat-treated 4h at 100 DEG C, you can.
Wear-resisting glue is prepared from including following components:N330-23 parts of carbon black, DOA-15 parts of dioctyl adipate, oxidation
It is 6 parts of zinc, 7 parts of stearic acid, 10 parts of age resistor, DCP-4 parts of vulcanizing agent, TAIC-5 parts of vulcanization aid, 12 parts of hydroxypropyl cellulose, general
Shandong orchid 7 parts of polysaccharide, 13 parts of nano silicon,.
Wear-resisting glue, which comprises the following steps, to be prepared from:
Dioctyl adipate DOA is dissolved by heating in 70 DEG C of hot bath, the stirring of stearic acid mixing and emulsifying is then added
Uniformly, carbon black is taken into container, is added zinc oxide, is mixed evenly;Mixture is used into emulsification in 60~80 DEG C of water-baths
Device stirs, regulation emulsification stirring speed to 6000r/min, turns down rotating speed to 3000r/min after 5min, continues to stir
30min, when temperature is down to 8 DEG C, adds 2 age resistor, then adds vulcanizing agent DCP, vulcanization aid, is dehydrated 15min, centrifugation point
From, hydroxypropyl cellulose is added, drying at room temperature obtains solid powder, by pulullan polysaccharide, nano silicon, ultrasound
After vibration dispersion is uniform, centrifuges and remove big particulate, drying at room temperature obtains particle, in the water that particle is added to 2 times, mix
Close, 200 DEG C of heating 30min obtain wear-resisting glue.
Hardening agent is prepared from including following components:Including 30 parts of intensity modifying agents:30% butyl acrylate, 30% acetic acid
Ethyl ester, remaining is water;
5 parts of form retention agents:Ethyl acetate 15%, pentaerythrite 30%, 15% part of paraffin, remaining is water.
Hardening agent, which comprises the following steps, to be prepared from:Butyl acrylate, ethyl acetate and water are sequentially added, mechanical agitation is mixed
Close uniform, 1 obtains form retention agent;
Paraffin and ethyl acetate is taken to heat mixing, vaccum dewatering 5 minutes;Pentaerythrite is added, low pressure after being well mixed
Bubble in removing system, can be fully cured after being heat-treated 4h at 100 DEG C;Solidfied material is mixed with 60 DEG C of temperature water,
Stirring 1 hour, as form retention agent;
Form retention agent is mixed with intensity modifying agent, 60 DEG C are heated 1 hour, and 30 DEG C cool down 1 hour, and 90 DEG C add 5 points
Clock, you can.
Wax is that 90% paraffin and 10% age resistor are mixed.
Through experiment, sealing ring prepared by this law is contrasted with existing sealing ring:
Existing sealing ring:Product hardness:HS85 ± 2 ° A operating temperatures:TPU:- 40~+80 DEG C of CPU:- 40~+120 DEG C of works
Make pressure:≤32Mpa;
This law sealing ring:Product hardness:HS110 ± 2 ° A operating temperatures:TPU:- 49~+86 DEG C of CPU:- 40~+120 DEG C
Operating pressure:≤36Mpa.
This law sealing ring performance is stable, is difficult to be swelled in media as well, thermal pinch (Joule effect) is small, enhances simultaneously
Tensile strength, elongation and tearing toughness.
Embodiment 2:A kind of preparation method of snap joint sealing ring,
120 parts of soybean protein is taken, protein isolate 8%-20%, urea 15%-17%, sodium polyphosphate from soybean
1%-10%, urea is dispersed in water, and is mixed and made into urea liquid, adds albumen and mixture, 1-2 is stirred at normal temperatures small
When, 7 parts of coupling agent is added, continues to stir 2-3 hours, finally by 50% sodium hydrate aqueous solution, 20 parts of additions, high-temperature stirring
20 minutes, temperature control was at 90-95 DEG C;
It is slowly added under stirring and/or ultrasonication at a temperature of 5 parts, 0~80 DEG C of 40 parts of toughener and epoxy organosilicon
Reaction 0.1~12 hour, after reaction terminates, is dehydrated by vaporizing extract process, by eluting, granulating repeatedly, is dried;
Grain will be dried to mix for 20 parts with ethyl cyanoacetate, beat, add 50% sodium hydrate aqueous solution, 20 parts and 130 parts water
Mixing, heating adds 50 parts of cornstarch after being added 2 hours after 20 minutes, refines 2 hours, obtain glue;
140 parts of water intaking, 40 parts of hydrophilic chemicals, 30 parts of urea, inorganic or 30 parts of organic acid, utilize more than 50 DEG C
Hot water or steam are mixed with glue, inorganic base and are incubated 30 minutes to 1 hour more than 50 DEG C, glue is fully absorbed water swollen
It is swollen, so that its close molecular structure be pulled open and become bulk, hydrophilic chemicals needed for then adding and it is inorganic or
Organic acid, is 0.5-4 hours in reaction at 50-100 DEG C, the aqueous chemically modified vegetable gum piece for 20-60% is produced, through extruding
It is expanded, dry, crush after, produce it is aqueous be less than 10% quick-dissolving chemically modified vegetable gum powder;
It is 1 by gained plant gum powder and Heveatex ratio:3, it is well mixed that rubber cement is made;Will dry cotton sail cloth in
Impregnation 20~40 minutes in rubber cement, through two roll calender, (roller speed is than being 1:1, roll spacing is 3mm) it is dry after extruding even uniform
To adhesive plaster;Adhesive plaster is paved into after 2~3 layers by specification with 45° angle severing, compacting is rolled and is put into sealing ring mould, die inside
Wall scribbles wear-resisting glue, vulcanizes 30~45- minutes under conditions of 145~155 DEG C, 8~10-MPa, by the sealing of shaping
Circle, is put into 35 portions of hardening agents and soaks 2 hours, the bubble in low pressure removing system, after drying, and one is smeared using cotton sail cloth
Layer wax, can be fully cured after being heat-treated 4h at 100 DEG C, you can.
Wear-resisting glue is prepared from including following components:N330-25 parts of carbon black, DOA-17 parts of dioctyl adipate, oxidation
It is 8 parts of zinc, 9 parts of stearic acid, 13 parts of age resistor, DCP-6 parts of vulcanizing agent, TAIC-8 parts of vulcanization aid, 18 parts of hydroxypropyl cellulose, general
Shandong orchid 15 parts of polysaccharide, 16 parts of nano silicon,.
Wear-resisting glue, which comprises the following steps, to be prepared from:
Dioctyl adipate DOA is dissolved by heating in 70 DEG C of hot bath, the stirring of stearic acid mixing and emulsifying is then added
Uniformly, carbon black is taken into container, is added zinc oxide, is mixed evenly;Mixture is used into emulsification in 60~80 DEG C of water-baths
Device stirs, regulation emulsification stirring speed to 6000r/min, turns down rotating speed to 3000r/min after 5min, continues to stir
30min, when temperature is down to 8 DEG C, adds 2 age resistor, then adds vulcanizing agent DCP, vulcanization aid, is dehydrated 15min, centrifugation point
From, hydroxypropyl cellulose is added, drying at room temperature obtains solid powder, by pulullan polysaccharide, nano silicon, ultrasound
After vibration dispersion is uniform, centrifuges and remove big particulate, drying at room temperature obtains particle, in the water that particle is added to 2 times, mix
Close, 200 DEG C of heating 30min obtain wear-resisting glue.
Hardening agent is prepared from including following components:Including 30 parts of intensity modifying agents:40% butyl acrylate, 40% acetic acid
Ethyl ester, remaining is water;
5 parts of form retention agents:Ethyl acetate 25%, pentaerythrite 35%, 20% part of paraffin, remaining is water.
Hardening agent, which comprises the following steps, to be prepared from:Butyl acrylate, ethyl acetate and water are sequentially added, mechanical agitation is mixed
Close uniform, 1 obtains form retention agent;
Paraffin and ethyl acetate is taken to heat mixing, vaccum dewatering 5 minutes;Pentaerythrite is added, low pressure after being well mixed
Bubble in removing system, can be fully cured after being heat-treated 4h at 100 DEG C;Solidfied material is mixed with 60 DEG C of temperature water,
Stirring 1 hour, as form retention agent;
Form retention agent is mixed with intensity modifying agent, 60 DEG C are heated 1 hour, and 30 DEG C cool down 1 hour, and 90 DEG C add 5 points
Clock, you can.
Wax is that 90% paraffin and 10% age resistor are mixed.
Existing sealing ring:Product hardness:HS85 ± 2 ° A operating temperatures:TPU:- 40~+80 DEG C of CPU:- 40~+120 DEG C of works
Make pressure:≤32Mpa;
This law sealing ring:Product hardness:HS96 ± 2 ° A operating temperatures:TPU:- 50~+90 DEG C of CPU:- 43~+120 DEG C of works
Make pressure:≤51Mpa.
This law sealing ring performance is stable, is difficult to be swelled in media as well, thermal pinch (Joule effect) is small, enhances simultaneously
Tensile strength, elongation and tearing toughness.
General principle, principal character and the advantages of the present invention of the present invention has been shown and described above.The technology of the industry
Personnel are it should be appreciated that the present invention is not limited to the above embodiments, and the simply explanation described in above-described embodiment and specification is originally
The principle of invention, without departing from the spirit and scope of the present invention, various changes and modifications of the present invention are possible, these changes
Change and improvement all fall within the protetion scope of the claimed invention.The claimed scope of the invention by appended claims and its
Equivalent thereof.
Claims (6)
1. a kind of method that utilization natural plant gum prepares sealing ring, it is characterised in that:
100-120 parts of soybean protein is taken, protein isolate 8%-20%, urea 15%-17%, sodium polyphosphate from soybean
1%-10%, urea is dispersed in water, and is mixed and made into urea liquid, adds albumen and mixture, 1-2 is stirred at normal temperatures small
When, 5-7 parts of coupling agent is added, continues to stir 2-3 hours, finally by the 15-20 parts of additions of 50% sodium hydrate aqueous solution, high temperature
Stirring 20 minutes, temperature control is at 90-95 DEG C;
It is slowly added under stirring and/or ultrasonication at a temperature of 2-5 parts, 0~80 DEG C of 30-40 parts of toughener and epoxy organosilicon
Reaction 0.1~12 hour, after reaction terminates, is dehydrated by vaporizing extract process, by eluting, granulating repeatedly, is dried;
Grain will be dried to mix for 15-20 parts with ethyl cyanoacetate, beat, add 15-20 parts of 50% sodium hydrate aqueous solution and 100-
130 parts of water mixing, heating adds 30-50 parts of cornstarch after being added 2 hours after 20 minutes, refines 2 hours, obtain glue;
30-140 parts of water intaking, 10-40 parts of hydrophilic chemicals, 2-30 parts of urea, inorganic or 2-30 parts of organic acid, utilize 50 DEG C
Hot water or steam above is mixed with glue, inorganic base and is incubated 30 minutes to 1 hour more than 50 DEG C, makes glue abundant
Water swelling, so that its close molecular structure be pulled open and become bulk, hydrophilic chemicals needed for then adding and
Inorganic or organic acid, is 0.5-4 hours in reaction at 50-100 DEG C, produces the aqueous chemically modified vegetable gum piece for 20-60%,
After extrusion, drying, crushing, produce it is aqueous be less than 10% quick-dissolving chemically modified vegetable gum powder;
It is 1 by gained plant gum powder and Heveatex ratio:3, it is well mixed that rubber cement is made;Cotton sail cloth will be dried in rubber cement
Middle impregnation 20~40 minutes, through two roll calender, (roller speed is than being 1:1, roll spacing is 3mm) extruding even uniform after be dried to obtain glue
Cloth;Adhesive plaster is paved into after 2~3 layers by specification with 45° angle severing, compacting is rolled and is put into sealing ring mould, die inside wall is applied
There is wear-resisting glue, vulcanize 30~45- minutes under conditions of 145~155 DEG C, 8~10-MPa, by the sealing ring of shaping, put
Enter in 35 portions of hardening agents and soak 2 hours, after drying, coating of wax is smeared using cotton sail cloth for the bubble in low pressure removing system,
It can be fully cured after being heat-treated 4h at 100 DEG C, you can.
2. the method that a kind of utilization natural plant gum according to claim 1 prepares sealing ring, it is characterised in that:Described is resistance to
Mill glue is prepared from including following components:N330-23-25 parts of carbon black, DOA-15-17 parts of dioctyl adipate, zinc oxide 6-8
Part, 7-9 parts of stearic acid, 10-13 parts of age resistor, DCP-4-6 parts of vulcanizing agent, TAIC-5-8 parts of vulcanization aid, hydroxypropyl cellulose
12-18 parts, 7-15 parts of pulullan polysaccharide, 13-16 parts of nano silicon.
3. the method that a kind of utilization natural plant gum according to claim 1 prepares sealing ring, it is characterised in that:Described is resistance to
Mill glue, which comprises the following steps, to be prepared from:
Dioctyl adipate DOA is dissolved by heating in 70 DEG C of hot bath, stearic acid mixing and emulsifying is then added and stirs,
Carbon black is taken into container, zinc oxide is added, is mixed evenly;Mixture is stirred in 60~80 DEG C of water-baths with emulsifier
Uniformly, regulation emulsification stirring speed is turned down rotating speed to 3000r/min after 5min to 6000r/min, continues to stir 30min, treats
When temperature is down to 8 DEG C, 2 age resistor are added, vulcanizing agent DCP, vulcanization aid is then added, 15min is dehydrated, centrifuged, then are added
Enter hydroxypropyl cellulose, drying at room temperature obtains solid powder, by pulullan polysaccharide, nano silicon, ultrasonic vibration disperses
After uniform, centrifuge and remove big particulate, drying at room temperature obtains particle, in the water that particle is added to 2 times, mixing, 200 DEG C
30min is heated, wear-resisting glue is obtained.
4. the method that a kind of utilization natural plant gum according to claim 1 prepares sealing ring, it is characterised in that:Described is strong
Agent is prepared from including following components:Including 30 parts of intensity modifying agents:30%-40% butyl acrylates, 30-40% acetic acid second
Ester, remaining is water;
5 parts of form retention agents:Ethyl acetate 15-25%, pentaerythrite 30-35%, 15%-20% parts of paraffin, remaining is water.
5. the method that a kind of utilization natural plant gum according to claim 1 prepares sealing ring, it is characterised in that:Described is strong
Agent, which comprises the following steps, to be prepared from:Butyl acrylate, ethyl acetate and water are sequentially added, mechanical agitation is well mixed, 1
To form retention agent;
Paraffin and ethyl acetate is taken to heat mixing, vaccum dewatering 5 minutes;Pentaerythrite is added, low pressure is removed after being well mixed
Bubble in system, can be fully cured after being heat-treated 4h at 100 DEG C;Solidfied material is mixed with 60 DEG C of temperature water, stirring 1
Hour, as form retention agent;
Form retention agent is mixed with intensity modifying agent, 60 DEG C heat 1 hour, 30 DEG C cool down 1 hour, 90 DEG C add 5 minutes, i.e.,
Can.
6. the method that a kind of utilization natural plant gum according to claim 1 prepares sealing ring, it is characterised in that:Described wax
Paraffin and 10% age resistor for 90% are mixed.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201710538953.7A CN107245157A (en) | 2017-07-04 | 2017-07-04 | A kind of preparation method of snap joint sealing ring |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN201710538953.7A CN107245157A (en) | 2017-07-04 | 2017-07-04 | A kind of preparation method of snap joint sealing ring |
Publications (1)
Publication Number | Publication Date |
---|---|
CN107245157A true CN107245157A (en) | 2017-10-13 |
Family
ID=60014924
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN201710538953.7A Withdrawn CN107245157A (en) | 2017-07-04 | 2017-07-04 | A kind of preparation method of snap joint sealing ring |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN107245157A (en) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0945498A1 (en) * | 1998-03-23 | 1999-09-29 | Firma Carl Freudenberg | A seal assembly with new resin stabilized adhesive composition to bond an insert member to the elastomeric seal material |
CN1935848A (en) * | 2006-08-25 | 2007-03-28 | 甘肃省庆阳长庆井下化工厂 | Method for preparing quick-dissolving chemically modified vegetable gum |
CN104194699A (en) * | 2014-08-26 | 2014-12-10 | 安徽神舟飞船胶业有限公司 | Formula and preparation process of epoxy resin-soybean protein glue environment-friendly copolymer adhesive |
CN106626468A (en) * | 2016-12-21 | 2017-05-10 | 齐齐哈尔大学 | Preparation method of fabric-mixed seal ring employing cement-dipping method |
-
2017
- 2017-07-04 CN CN201710538953.7A patent/CN107245157A/en not_active Withdrawn
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
EP0945498A1 (en) * | 1998-03-23 | 1999-09-29 | Firma Carl Freudenberg | A seal assembly with new resin stabilized adhesive composition to bond an insert member to the elastomeric seal material |
CN1935848A (en) * | 2006-08-25 | 2007-03-28 | 甘肃省庆阳长庆井下化工厂 | Method for preparing quick-dissolving chemically modified vegetable gum |
CN104194699A (en) * | 2014-08-26 | 2014-12-10 | 安徽神舟飞船胶业有限公司 | Formula and preparation process of epoxy resin-soybean protein glue environment-friendly copolymer adhesive |
CN106626468A (en) * | 2016-12-21 | 2017-05-10 | 齐齐哈尔大学 | Preparation method of fabric-mixed seal ring employing cement-dipping method |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN103203810B (en) | Rubber masterbatch and rubber prepared by the method for continuously producing and the method for rubber masterbatch | |
CN102239202B (en) | Spherical composite particles and manufacturing method therefor | |
CN102775654A (en) | Preparation method for liquid phase stirring and mixing of white carbon black and natural rubber | |
JP2018111768A (en) | Fiber material and method for producing fiber material, and composite material and method for producing composite material | |
CN108424563B (en) | High-performance rubber composite material containing Kevlar nanofibers and preparation method thereof | |
CN107250241B (en) | Thermal expansivity micro-capsule complex, its manufacturing method, the rubber composition for being combined with the complex and the pneumatic tire for having used the composition | |
Kim et al. | Self-healing starch-based ‘green’thermoset resin | |
CN104910426A (en) | Full-degradable plastic film taking surface hydrophobically modified starch as base material and preparation method thereof | |
CN113789124A (en) | Special non-cured rubber asphalt waterproof coating and preparation method thereof | |
KR20040023816A (en) | Process for regeneration of rubber from scrap | |
CN106554528B (en) | Butadiene-styrene rubber/white carbon black/lignocellulosic/montmorillonite rubber composite material and preparation method thereof | |
CN107216475A (en) | A kind of preparation method of the double-layer seal cushion rubber of the outer glue of interior metal | |
CN107245157A (en) | A kind of preparation method of snap joint sealing ring | |
CN107325342A (en) | A kind of method that utilization natural plant gum prepares sealing ring | |
JP2018111769A (en) | Swollen fiber material and method for producing swollen fiber material, and composite material and method for producing composite material | |
CN107339430A (en) | A kind of anti abrasive snap joint sealing coil preparation method | |
CN107189094A (en) | A kind of snap joint compared with high resilience seals coil preparation method | |
JP2018111770A (en) | Gelatinous body, manufacturing method of gelatinous body, composite material and manufacturing method of composite material | |
CN101481472B (en) | Preparation of single-shell sulfur microcapsule | |
CN106800785B (en) | A kind of environment-friendly rubber flowing dispersing agent and preparation method thereof | |
CN105862165B (en) | A kind of protein modified acrylic fiber spinning solution with phase-changing and temperature-regulating function and preparation method thereof | |
CN101824126A (en) | Hydrophilic carbon black | |
CN104961106B (en) | A kind of method for improving dispersity of insoluble sulfur | |
CN111978570A (en) | Method for vulcanizing and packaging graphene modified natural latex | |
CN105623051A (en) | Special color master batch for floor heating tube and preparation method of special color master batch |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
PB01 | Publication | ||
PB01 | Publication | ||
SE01 | Entry into force of request for substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
WW01 | Invention patent application withdrawn after publication |
Application publication date: 20171013 |
|
WW01 | Invention patent application withdrawn after publication |