CN106497004A - A kind of capacitor encapsulant of stable performance and preparation method thereof - Google Patents
A kind of capacitor encapsulant of stable performance and preparation method thereof Download PDFInfo
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- CN106497004A CN106497004A CN201610946392.XA CN201610946392A CN106497004A CN 106497004 A CN106497004 A CN 106497004A CN 201610946392 A CN201610946392 A CN 201610946392A CN 106497004 A CN106497004 A CN 106497004A
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- capacitor
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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
- C08L71/00—Compositions of polyethers obtained by reactions forming an ether link in the main chain; Compositions of derivatives of such polymers
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- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08B—POLYSACCHARIDES; DERIVATIVES THEREOF
- C08B37/00—Preparation of polysaccharides not provided for in groups C08B1/00 - C08B35/00; Derivatives thereof
- C08B37/0006—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid
- C08B37/0024—Homoglycans, i.e. polysaccharides having a main chain consisting of one single sugar, e.g. colominic acid beta-D-Glucans; (beta-1,3)-D-Glucans, e.g. paramylon, coriolan, sclerotan, pachyman, callose, scleroglucan, schizophyllan, laminaran, lentinan or curdlan; (beta-1,6)-D-Glucans, e.g. pustulan; (beta-1,4)-D-Glucans; (beta-1,3)(beta-1,4)-D-Glucans, e.g. lichenan; Derivatives thereof
- C08B37/0027—2-Acetamido-2-deoxy-beta-glucans; Derivatives thereof
- C08B37/003—Chitin, i.e. 2-acetamido-2-deoxy-(beta-1,4)-D-glucan or N-acetyl-beta-1,4-D-glucosamine; Chitosan, i.e. deacetylated product of chitin or (beta-1,4)-D-glucosamine; Derivatives thereof
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- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K3/00—Materials not provided for elsewhere
- C09K3/10—Materials in mouldable or extrudable form for sealing or packing joints or covers
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- 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
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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
- C08L2201/00—Properties
- C08L2201/06—Biodegradable
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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
- C08L2203/00—Applications
- C08L2203/20—Applications use in electrical or conductive gadgets
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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
- C08L2205/03—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
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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
- C08L2205/04—Polymer mixtures characterised by other features containing interpenetrating networks
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- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
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- Life Sciences & Earth Sciences (AREA)
- Engineering & Computer Science (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- General Health & Medical Sciences (AREA)
- Molecular Biology (AREA)
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- Compositions Of Macromolecular Compounds (AREA)
Abstract
The invention belongs to capacitor technology field, and in particular to capacitor encapsulant of a kind of stable performance and preparation method thereof, it is made up of the raw material of following weight portion:Fir bark 10 13, pi-allyl epoxidized polyether 25 30 nitrify chitin 12, nanoflakes and cobalt hydroxide 12, distearyl acyl-oxygen isopropoxy plumbic acid ester 0.8 1.5, zinc naphthenate 0.6 0.8, Fischer-Tropsch wax 12, polydimethylsiloxane 0.2 0.3.The present invention has advantages below compared to existing technology:In the present invention, nitrification shitosan and fir bark aggregate into new network structure with reference to IPN under corresponding conditionses so as to good mechanical strength and elasticity, while raw material is more environmentally-friendly using rear easy degraded, reduce waste entrainment;There is stronger fatigue performance, wearability and oil resistivity, use time is long, low production cost.
Description
Technical field
The invention belongs to capacitor technology field, and in particular to a kind of capacitor encapsulant of stable performance and its preparation
Method.
Background technology
Capacitor is often referred to simply as electric capacity, is one of electronic component for being used in electronic equipment in a large number, is widely used in electricity
The aspects such as the separated by direct communication on road, coupling, bypass, filtering, resonant tank, energy conversion, control, capacitor is by housing, capacitance core
Son, end cap and binding post composition, capacitor casing are generally vegetable oil or mineral oil built with steeping medium, steeping medium,
The sealing position of capacitor is equipped with sealing gasket or sealing ring, as the working environment of capacitor varies, some capacitors
Need to work under rugged environment, capacitor encapsulant needs high temperature resistant, cold-resistant, acid and alkali-resistance, salt spray resistance etc. to have different wanting
Ask, need to ensure excellent wear-resisting, oil resistance and elasticity in corresponding environment, it is therefore desirable to which encapsulant is entered to advance
One step research.
Content of the invention
The purpose of the present invention is for existing problem, there is provided a kind of capacitor encapsulant of stable performance and its system
Preparation Method.
The present invention is achieved by the following technical solutions:A kind of capacitor encapsulant of stable performance, by following heavy
The raw material composition of amount part:Fir bark 10-13, pi-allyl epoxidized polyether 25-30, nitrify chitin 1-2, nanoflakes and cobalt hydroxide 1-
2, distearyl acyl-oxygen isopropoxy plumbic acid ester 0.8-1.5, zinc naphthenate 0.6-0.8, Fischer-Tropsch wax 1-2, polydimethylsiloxane 0.2-
0.3.
Used as further improvement of these options, the chitinous preparation method of the nitrification is:Chitin is added phase
When being that during mechanical agitation, Deca is equivalent to concentrated nitric acid weight in 60% salpeter solution in 100 times of mass fractions of its weight
The 2,4 toluene diisocyanate of amount 1/3rd, dripped off in 5 minutes, and after reaction 2-3 hours, terminating reaction obtains nitrifying first
Chitin.
A kind of preparation method of the capacitor encapsulant of stable performance, comprises the following steps:
(1)By fir bark humidity be 90-95%, temperature be 80-85 DEG C under conditions of process 2 hours after, rubbed with wire kneading machine
Broken, stirring and dissolving in pi-allyl epoxidized polyether is then added into, under conditions of 28-32 DEG C, makes which expanded standby;
(2)Nanoflakes and cobalt hydroxide, distearyl acyl-oxygen isopropoxy plumbic acid ester and Fischer-Tropsch wax is added in above-mentioned puffing material, and stirring is anti-
Answer 25-30 minutes;
(3)Zinc naphthenate and polydimethylsiloxane are added in above-mentioned compound, importing are stirred when having bubble to produce through pre-
In the mould of heat, baking oven is put into, solidifies 1.5-2 hours under conditions of 40-50 DEG C, obtain final product.
As further improvement of these options, the step(2)The temperature of middle stirring reaction is 32-36 DEG C.
The present invention has advantages below compared to existing technology:In the present invention, nitrification shitosan and fir bark are in corresponding conditionses
Lower combination IPN aggregates into new network structure so as to good mechanical strength and elasticity, while raw material is more environmentally-friendly making
With rear easy degraded, waste entrainment is reduced;There is stronger fatigue performance, wearability and oil resistivity, use time is long, production
Low cost.
Specific embodiment
Embodiment 1
A kind of capacitor encapsulant of stable performance, is made up of the raw material of following weight portion:Fir bark 10, pi-allyl epoxy
Polyethers 25, nitrifies chitin 2, nanoflakes and cobalt hydroxide 1, distearyl acyl-oxygen isopropoxy plumbic acid ester 0.8, zinc naphthenate 0.8, Fischer-Tropsch
Wax 1.6, polydimethylsiloxane 0.3.
Wherein, the chitinous preparation method of the nitrification is:Chitin is added equivalent to 100 times of mass fractions of its weight
In for 60% salpeter solution, 2,4- toluene two of the Deca equivalent to concentrated nitric acid weight 1/3rd during mechanical agitation
Isocyanates, dripped off in 5 minutes, and after reaction 2-3 hours, terminating reaction obtains nitrifying chitin.
A kind of preparation method of the capacitor encapsulant of stable performance, comprises the following steps:
(1)By fir bark humidity be 90-95%, temperature be 80-85 DEG C under conditions of process 2 hours after, rubbed with wire kneading machine
Broken, stirring and dissolving in pi-allyl epoxidized polyether is then added into, under conditions of 28-32 DEG C, makes which expanded standby;
(2)Nanoflakes and cobalt hydroxide, distearyl acyl-oxygen isopropoxy plumbic acid ester and Fischer-Tropsch wax is added in above-mentioned puffing material, and stirring is anti-
Answer 25-30 minutes;
(3)Zinc naphthenate and polydimethylsiloxane are added in above-mentioned compound, importing are stirred when having bubble to produce through pre-
In the mould of heat, baking oven is put into, solidifies 1.5-2 hours under conditions of 40-50 DEG C, obtain final product.
Wherein, the step(2)The temperature of middle stirring reaction is 32-36 DEG C.
Embodiment 2
A kind of capacitor encapsulant of stable performance, is made up of the raw material of following weight portion:Fir bark 12, pi-allyl epoxy
Polyethers 28, nitrifies chitin 2, nanoflakes and cobalt hydroxide 1, distearyl acyl-oxygen isopropoxy plumbic acid ester 1.2, zinc naphthenate 0.7, Fischer-Tropsch
Wax 1, polydimethylsiloxane 0.2.
Same as Example 1 in addition to above content.
Embodiment 3
A kind of capacitor encapsulant of stable performance, is made up of the raw material of following weight portion:Fir bark 13, pi-allyl epoxy
Polyethers 30, nitrification chitin 2, nanoflakes and cobalt hydroxide 1.5, distearyl acyl-oxygen isopropoxy plumbic acid ester 1.5, zinc naphthenate 0.6 takes
Support wax 1, polydimethylsiloxane 0.3.
Same as Example 1 in addition to above content.
Will be as follows for common to capacitor encapsulant in the present invention and matched group compound physical performance comparison:
Table 1
Encapsulant physical property in the present invention be can be seen that by data in table 1, better than common sizing material, to be applied to disliking
Capacitor sealing used in bad environment, good airproof performance are ageing-resistant.
Claims (4)
1. the capacitor encapsulant of a kind of stable performance, it is characterised in that be made up of the raw material of following weight portion:Fir bark
10-13, pi-allyl epoxidized polyether 25-30, nitrify chitin 1-2, nanoflakes and cobalt hydroxide 1-2, distearyl acyl-oxygen isopropoxy lead
Acid esters 0.8-1.5, zinc naphthenate 0.6-0.8, Fischer-Tropsch wax 1-2, polydimethylsiloxane 0.2-0.3.
2. the capacitor encapsulant of a kind of stable performance as claimed in claim 1, it is characterised in that the nitrification is chitinous
Preparation method is:It is in 60% salpeter solution, in mechanical agitation that chitin is added equivalent to 100 times of mass fractions of its weight
During Deca equivalent to the 2,4 toluene diisocyanate of concentrated nitric acid weight 1/3rd, drip off in 5 minutes, react 2-3
After hour, terminating reaction obtains nitrifying chitin.
3. a kind of preparation method of the capacitor encapsulant of stable performance as claimed in claim 2, it is characterised in that include with
Lower step:
(1)By fir bark humidity be 90-95%, temperature be 80-85 DEG C under conditions of process 2 hours after, rubbed with wire kneading machine
Broken, stirring and dissolving in pi-allyl epoxidized polyether is then added into, under conditions of 28-32 DEG C, makes which expanded standby;
(2)Nanoflakes and cobalt hydroxide, distearyl acyl-oxygen isopropoxy plumbic acid ester and Fischer-Tropsch wax is added in above-mentioned puffing material, and stirring is anti-
Answer 25-30 minutes;
(3)Zinc naphthenate and polydimethylsiloxane are added in above-mentioned compound, importing are stirred when having bubble to produce through pre-
In the mould of heat, baking oven is put into, solidifies 1.5-2 hours under conditions of 40-50 DEG C, obtain final product.
4. a kind of preparation method of the capacitor encapsulant of stable performance as claimed in claim 3, it is characterised in that the step
Suddenly(2)The temperature of middle stirring reaction is 32-36 DEG C.
Priority Applications (1)
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CN201610946392.XA CN106497004A (en) | 2016-10-26 | 2016-10-26 | A kind of capacitor encapsulant of stable performance and preparation method thereof |
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CN201610946392.XA CN106497004A (en) | 2016-10-26 | 2016-10-26 | A kind of capacitor encapsulant of stable performance and preparation method thereof |
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Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101906246A (en) * | 2010-07-30 | 2010-12-08 | 江苏中矿大正表面工程技术有限公司 | Single-component heat resistant type silane modified polyether sealant |
CN102731848A (en) * | 2012-05-30 | 2012-10-17 | 芜湖荣基密封系统有限公司 | Wear-resistant multiple-rubber-mixed rubber sealing ring |
CN104744735A (en) * | 2015-04-10 | 2015-07-01 | 合肥环照高分子材料厂 | Antibacterial type biodegradable plastic and preparation method thereof |
CN105131384A (en) * | 2015-07-27 | 2015-12-09 | 福建晟扬管道科技有限公司 | Abrasion-resistant composite tube material and production method of same |
CN105585751A (en) * | 2015-12-25 | 2016-05-18 | 林铭昭 | Rubber seal ring prepared from polished tile waste residues and preparation method of rubber seal ring |
-
2016
- 2016-10-26 CN CN201610946392.XA patent/CN106497004A/en active Pending
Patent Citations (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN101906246A (en) * | 2010-07-30 | 2010-12-08 | 江苏中矿大正表面工程技术有限公司 | Single-component heat resistant type silane modified polyether sealant |
CN102731848A (en) * | 2012-05-30 | 2012-10-17 | 芜湖荣基密封系统有限公司 | Wear-resistant multiple-rubber-mixed rubber sealing ring |
CN104744735A (en) * | 2015-04-10 | 2015-07-01 | 合肥环照高分子材料厂 | Antibacterial type biodegradable plastic and preparation method thereof |
CN105131384A (en) * | 2015-07-27 | 2015-12-09 | 福建晟扬管道科技有限公司 | Abrasion-resistant composite tube material and production method of same |
CN105585751A (en) * | 2015-12-25 | 2016-05-18 | 林铭昭 | Rubber seal ring prepared from polished tile waste residues and preparation method of rubber seal ring |
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Application publication date: 20170315 |
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