CN101880480B - Preparation method of calcinated argil - Google Patents
Preparation method of calcinated argil Download PDFInfo
- Publication number
- CN101880480B CN101880480B CN 201010169726 CN201010169726A CN101880480B CN 101880480 B CN101880480 B CN 101880480B CN 201010169726 CN201010169726 CN 201010169726 CN 201010169726 A CN201010169726 A CN 201010169726A CN 101880480 B CN101880480 B CN 101880480B
- Authority
- CN
- China
- Prior art keywords
- gains
- potter
- clay
- calcining
- weight
- 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.)
- Expired - Fee Related
Links
Abstract
The invention discloses a preparation method of calcined argil, comprising the following process steps of: selecting kaoline containing silicon dioxide not less than 4.8%, aluminium oxide not more than 36% and ferrum not less than 0.5% as raw materials and then calcinating the kaoline as the raw material 3-6 hours at constant temperature, wherein the calcinating temperature is 1000-1100 DEG C; smashing products obtained by calcinating and cooling the kaoline; adding 1-1.5 wt% of silane coupling agents in the smashed products, and then uniformly stirring and mixing under a heating condition to obtain the calcinated argil. The calcinated argil prepared with the method can be used as fillers for manufacturing wires and cables.
Description
Technical field
The present invention relates to chemical industry filler manufacturing technology field, especially a kind of process of preparing that is used as the calcinated argil of Ethylene Propylene Terpolymer electric wire loading material of rubber.
Background technology
The calcinated argil stable chemical nature, have as loading material of rubber and to extrude or the calendered goods smooth in appearance, have the good characteristics of resistance to acids and bases, thermotolerance and electrical insulating property, can give the good insulativity of terpolymer EP rubber, ventilation property, anti-Jie's property, therefore, calcinated argil obtains to widely apply in terpolymer EP rubber is made.At present the terpolymer EP rubber filler mainly depends on the imported product of the U.S., Britain with calcinated argil, and China is in for this class inorganic non-metallic chief of a pit the phase only sells the raw ore state, and does not still appear in the newspapers for the processing method of making calcinated argil.
Summary of the invention
Problem to be solved by this invention provides a kind of loading material of rubber with the preparation method of calcinated argil, adopts the calcinated argil of this method acquisition can reach the technical requirements that electric wire is used rubber as filler for the manufacture of terpolymer EP rubber.
In order to address the above problem, the preparation method of this calcinated argil is by following processing step:
(1), with through after the magnetic separation bleaching, the weight in wet base percentage is that 7% kaolin is raw material, wherein: SiO
248%, Al
2O
336.5%, Fe 0.4%, crystal water content 13.2%, and halloysite crystal habit weight accounts for 60%, whiteness 84%;
(2), making particle diameter with tablets press is 10 millimeters the particle without solid shape;
(3), the kaolin particle after the moulding is placed in the tunnel furnace calcining 3 hours, calcining temperature is 1020 ℃ ± 20 ℃;
(4), adopt supper micron mill to carry out grinding and processing and reach diameter less than 45 microns calcining cooled gains, screenings≤0.03%, fineness reaches more than 2500 orders;
(5), to pulverize in the gains by weight 1% add the A-172 silane coupling agent, under 110 ℃ of heating conditions, mix 25 minutes, make silane coupling agent be wrapped in well the potter's clay surface, adopt the potter's clay after efficient cyclone sieve effects on surface is processed to sieve to cooled gains, make potter's clay product 200 order all-pass mistakes, namely get the calcinated argil finished product.
The preparation method of this calcinated argil can be by following processing step:
(1), with through after the magnetic separation bleaching, the weight in wet base percentage is that 10% kaolin is raw material, wherein SiO
246.5%, Al
2O
338.2%, Fe
2O
30.4%, crystal water content 14%, halloysite crystal habit weight accounts for 70%, whiteness 86%;
(2), making particle diameter with tablets press is 20 millimeters the particle without solid shape;
(3), the kaolin particle after the moulding is placed in the tunnel furnace calcining 6 hours, calcining temperature is 1080 ℃ ± 20 ℃;
(4), adopt supper micron mill to carry out grinding and processing and reach diameter less than 45 microns calcining cooled gains, screenings≤0.03%, fineness reaches more than 2500 orders;
(5), to pulverize in the gains by weight 1.5% add the A-172 silane coupling agent, under 120 ℃ of heating conditions, mix 30 minutes, make silane coupling agent be wrapped in well the potter's clay surface, adopt the potter's clay after efficient cyclone sieve effects on surface is processed to sieve to cooled gains, make potter's clay product 200 order all-pass mistakes, namely get the calcinated argil finished product.
The preparation method of this calcinated argil can be by following processing step:
(1), with through after the magnetic separation bleaching, the weight in wet base percentage is that 4% kaolin is raw material, wherein SiO
247.8%, Al
2O
337.2%, Fe
2O
30.4%, crystal water content 13.5%, whiteness 85%, halloysite crystal habit weight accounts for 70%, whiteness 85%;
(2), making particle diameter with tablets press is 20 millimeters the particle without solid shape;
(3), the kaolin particle after the moulding is placed in the tunnel furnace calcining 5 hours, calcining temperature is 1070 ℃ ± 20 ℃;
(4), adopt supper micron mill to carry out grinding and processing and reach diameter less than 45 microns calcining cooled gains, screenings≤0.03%, fineness reaches more than 2500 orders;
(5), to pulverize in the gains by weight 1.5% add the A-172 silane coupling agent, under 120 ℃ of heating conditions, mix 20 minutes, make silane coupling agent be wrapped in well the potter's clay surface, adopt the potter's clay after efficient cyclone sieve effects on surface is processed to sieve to cooled gains, make potter's clay product 200 order all-pass mistakes, namely get the calcinated argil finished product.
Because the beneficial effect that has adopted aforesaid method, the present invention to obtain is as follows:
Prepared cable rubber is through cable research institution check, and its properties all reaches and meets GB/T12706.3-2002 " voltage rating 1KV (Um=1.2KV) is to 35KV (Um=40.5KV) extrusion insulating power cable and annex " the 3rd part: " voltage rating 35KV(Um=40.5KV) cable " standard-required.
Embodiment
Below in conjunction with specific embodiment present method is described in further detail:
Embodiment 1:
1, with through after the magnetic separation bleaching, the weight in wet base percentage is that China's Period In Maoming Area kaolin of 7% is raw material, and wherein: SiO2 48%, and Al2O3 36.5%, and Fe 0.4%, crystal water content 13.2%, and halloysite crystal habit weight accounts for 60%, whiteness 84%;
2, making particle diameter with tablets press is 10 millimeters the particle without solid shape;
3, the kaolin particle after the moulding is placed in the tunnel furnace calcining 3 hours, calcining temperature is 1020 ℃ ± 20 ℃;
4, adopt supper micron mill to carry out grinding and processing and reach diameter less than 45 microns calcining cooled gains, screenings≤0.03%, fineness reaches more than 2500 orders;
5, to pulverize in the gains by weight 1% add the A-172 silane coupling agent, under 110 ℃ of heating conditions, mix 25 minutes, make silane coupling agent be wrapped in well the potter's clay surface, adopt the potter's clay after efficient cyclone sieve effects on surface is processed to sieve to cooled gains, make potter's clay product 200 order all-pass get the calcinated argil final product after namely.
The physical and chemical index of the obtained calcinated argil final product of present embodiment is as follows: SiO
254.5%, Al
2O
341.5%, Fe
2O
30.5%, whiteness 90.5%, 325 mesh sieve surplus 0.022%, fineness 2500 orders, turbidity 5.
With the Ethylene Propylene Terpolymer cable rubber experiment that rubber 100, vulcanizing agent 3, anti-aging agent 2, calcinated argil 60 proportionings are made, the technical indicator of the cable rubber that obtains is as follows:
1, the tensile strength of cable rubber: 15.2MPa;
2, the elongation at break of cable rubber: 260%;
3, thermal ageing test (135 ℃ * 168h):
(1) the maximum velocity of variation of the tensile strength of cable rubber :+3;
(2) the maximum velocity of variation of the extension at break of cable rubber:--14;
4, volume specific resistance during 20 ℃ of cable rubber: 1.4 * 10
14Ω m;
5, the specific inductivity of cable rubber: 2.51;
6, the dielectric loss angle tangent of cable rubber: 2.6 * 10
-3
7, dielectric strength: 28MV/m during 20 ℃ of cable rubber.
Embodiment 2:
1, with through after the magnetic separation bleaching, the weight in wet base percentage is that China's Period In Maoming Area kaolin of 10% is raw material, wherein SiO
246.5%, Al
2O
338.2%, Fe
2O
30.4%, halloysite crystal habit weight accounts for 70%, crystal water content 14%, whiteness 86;
2, making particle diameter with tablets press is 20 millimeters the particle without solid shape;
3, the kaolin particle after the moulding is placed in the tunnel furnace calcining 6 hours, calcining temperature is 1080 ℃ ± 20 ℃;
4, adopt supper micron mill to carry out grinding and processing and reach diameter less than 45 microns calcining cooled gains, screenings≤0.03%, fineness reaches more than 2500 orders;
5, to pulverize in the gains by weight 1.5% add the A-172 silane coupling agent, under 120 ℃ of heating conditions, mix 30 minutes, make silane coupling agent be wrapped in well the potter's clay surface, adopt the potter's clay after efficient cyclone sieve effects on surface is processed to sieve to cooled gains, make potter's clay product 200 order all-pass get the calcinated argil final product after namely.
The physical and chemical index of the obtained calcinated argil final product of present embodiment is as follows: SiO
252.6%, Al
2O
343.2%, Fe
2O
30.5%, whiteness 91.6%,, 325 mesh sieve surpluses 0.02%, fineness 2500 orders, turbidity 2;
The Ethylene Propylene Terpolymer cable rubber of making take rubber 100, vulcanizing agent 3, anti-aging agent 2, calcinated argil 60 proportionings is as example, and the technical indicator of the cable rubber that obtains is as follows:
1, the tensile strength of cable rubber: 16.2MPa;
2, the elongation at break of cable rubber: 290;
3, thermal ageing test (135 ℃ * 168h):
(1) the maximum velocity of variation of the tensile strength of cable rubber :+2;
(2) the maximum velocity of variation of the extension at break of cable rubber:--10;
4, volume specific resistance during 20 ℃ of cable rubber: 2.5 * 10
14Ω m;
5, the specific inductivity of cable rubber: 2.54;
6, the dielectric loss angle tangent of cable rubber: 2.5 * 10
-3
7, dielectric strength: 35MV/m during 20 ℃ of cable rubber.
Embodiment 3:
1, with through after the magnetic separation bleaching, the weight in wet base percentage is that China's Period In Maoming Area kaolin of 4% is raw material, wherein SiO
247.8%, Al
2O
337.2%, Fe
2O
30.4%, crystal water content 13.5%, whiteness 85%, halloysite crystal habit weight accounts for 70%, whiteness 85;
2, making particle diameter with tablets press is 20 millimeters the particle without solid shape;
3, the kaolin particle after the moulding is placed in the tunnel furnace calcining 5 hours, calcining temperature is 1070 ℃ ± 20 ℃;
4, adopt supper micron mill to carry out grinding and processing and reach diameter less than 45 microns calcining cooled gains, screenings≤0.03%, fineness reaches more than 2500 orders;
5, to pulverize in the gains by weight 1.5% add the A-172 silane coupling agent, under 120 ℃ of heating conditions, mix 20 minutes, make silane coupling agent be wrapped in well the potter's clay surface, adopt the potter's clay after efficient cyclone sieve effects on surface is processed to sieve to cooled gains, make potter's clay product 200 order all-pass get the calcinated argil final product after namely.
The physical and chemical index of the obtained calcinated argil final product of present embodiment is as follows: SiO
253.8%, Al
2O
342.6%, Fe
2O
30.5%, whiteness 91%, 325 mesh sieve surplus 0.023%, fineness 2500 orders, turbidity 3.
The Ethylene Propylene Terpolymer cable rubber of making take rubber 100, vulcanizing agent 3, anti-aging agent 2, calcinated argil 60 proportionings is as example, and the technical indicator of the cable rubber that obtains is as follows:
1, the tensile strength of cable rubber: 15.6MPa;
2, the elongation at break of cable rubber: 260;
3, thermal ageing test (135 ℃ * 168h):
(1) the maximum velocity of variation of the tensile strength of cable rubber :+5;
(2) the maximum velocity of variation of the extension at break of cable rubber:--12;
4, volume specific resistance during 20 ℃ of cable rubber: 1.6 * 10
14Ω m;
5, the specific inductivity of cable rubber: 2.5;
6, the dielectric loss angle tangent of cable rubber: 2.6 * 10
-3
7, dielectric strength: 30MV/m during 20 ℃ of cable rubber.
Claims (3)
1. the preparation method of a calcinated argil is characterized in that each processing step is as follows:
(1), with through after the magnetic separation bleaching, the weight in wet base percentage is that 7% kaolin is raw material, wherein: SiO
248%, Al
2O
336.5%, Fe 0.4%, crystal water content 13.2%, and halloysite crystal habit weight accounts for 60%, whiteness 84%;
(2), making particle diameter with tablets press is 10 millimeters the particle without solid shape;
(3), the kaolin particle after the moulding is placed in the tunnel furnace calcining 3 hours, calcining temperature is 1020 ℃ ± 20 ℃;
(4), adopt supper micron mill to carry out grinding and processing and reach diameter less than 45 microns calcining cooled gains, screenings≤0.03%, fineness reaches more than 2500 orders;
(5), to pulverize in the gains by weight 1% add the A-172 silane coupling agent, under 110 ℃ of heating conditions, mix 25 minutes, make silane coupling agent be wrapped in well the potter's clay surface, adopt the potter's clay after efficient cyclone sieve effects on surface is processed to sieve to cooled gains, make potter's clay product 200 order all-pass mistakes, namely get the calcinated argil finished product.
2. the preparation method of a calcinated argil is characterized in that each processing step is as follows:
(1), with through after the magnetic separation bleaching, the weight in wet base percentage is that 10% kaolin is raw material, wherein SiO2 46.5%, Al
2O
338.2%, Fe
2O
30.4%, crystal water content 14%, halloysite crystal habit weight accounts for 70%, whiteness 86%;
(2), making particle diameter with tablets press is 20 millimeters the particle without solid shape;
(3), the kaolin particle after the moulding is placed in the tunnel furnace calcining 6 hours, calcining temperature is 1080 ℃ ± 20 ℃;
(4), adopt supper micron mill to carry out grinding and processing and reach diameter less than 45 microns calcining cooled gains, screenings≤0.03%, fineness reaches more than 2500 orders;
(5), to pulverize in the gains by weight 1.5% add the A-172 silane coupling agent, under 120 ℃ of heating conditions, mix 30 minutes, make silane coupling agent be wrapped in well the potter's clay surface, adopt the potter's clay after efficient cyclone sieve effects on surface is processed to sieve to cooled gains, make potter's clay product 200 order all-pass mistakes, namely get the calcinated argil finished product.
3. the preparation method of a calcinated argil is characterized in that each processing step is as follows:
(1), with through after the magnetic separation bleaching, the weight in wet base percentage is that 4% kaolin is raw material, wherein SiO
247.8%, Al
2O
337.2%, Fe
2O
30.4%, crystal water content 13.5%, whiteness 85%, halloysite crystal habit weight accounts for 70%, whiteness 85%;
(2), making particle diameter with tablets press is 20 millimeters the particle without solid shape;
(3), the kaolin particle after the moulding is placed in the tunnel furnace calcining 5 hours, calcining temperature is 1070 ℃ ± 20 ℃;
(4), adopt supper micron mill to carry out grinding and processing and reach diameter less than 45 microns calcining cooled gains, screenings≤0.03%, fineness reaches more than 2500 orders;
(5), to pulverize in the gains by weight 1.5% add the A-172 silane coupling agent, under 120 ℃ of heating conditions, mix 20 minutes, make silane coupling agent be wrapped in well the potter's clay surface, adopt the potter's clay after efficient cyclone sieve effects on surface is processed to sieve to cooled gains, make potter's clay product 200 order all-pass mistakes, namely get the calcinated argil finished product.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN 201010169726 CN101880480B (en) | 2010-05-12 | 2010-05-12 | Preparation method of calcinated argil |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
CN 201010169726 CN101880480B (en) | 2010-05-12 | 2010-05-12 | Preparation method of calcinated argil |
Publications (2)
Publication Number | Publication Date |
---|---|
CN101880480A CN101880480A (en) | 2010-11-10 |
CN101880480B true CN101880480B (en) | 2013-03-27 |
Family
ID=43052630
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
CN 201010169726 Expired - Fee Related CN101880480B (en) | 2010-05-12 | 2010-05-12 | Preparation method of calcinated argil |
Country Status (1)
Country | Link |
---|---|
CN (1) | CN101880480B (en) |
Families Citing this family (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN102702624B (en) * | 2011-12-31 | 2015-08-12 | 深圳市罗庚电气有限公司 | A kind of Ethylene Propylene Terpolymer insulation compound for 35KV HV cable accessories and preparation method thereof |
CN103332926B (en) * | 2013-05-28 | 2014-06-25 | 西南石油大学 | Chlorine oxygen magnesium silicon clay material for inner layers of molds, preparation technology and evaluation method thereof |
CN108298993B (en) * | 2018-03-12 | 2021-11-09 | 天津城建大学 | Dry granulation method for ceramic material in rotary kiln |
CN112125580B (en) * | 2020-08-15 | 2022-01-04 | 上海理迪道具有限公司 | Interior trimming panel, and preparation method and mold of interior trimming panel |
Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4950628A (en) * | 1989-04-19 | 1990-08-21 | Corning Incorporated | Material and process to produce low thermal expansion cordierite structures |
US6290771B1 (en) * | 1997-09-08 | 2001-09-18 | Moon Han Kim | Activated koalin powder compound for mixing with cement and method of preparing the same |
CN1653133A (en) * | 2002-03-26 | 2005-08-10 | 拜尔材料科学股份公司 | Impact-modified polycarbonate compositions with calcined talc |
Family Cites Families (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JP2000063182A (en) * | 1998-08-11 | 2000-02-29 | Maruwa Ceramic:Kk | Production of ceramic raw material capable of being sintered at low temperature |
CN1250654C (en) * | 2002-12-24 | 2006-04-12 | 中国矿业大学(北京校区) | Nanometer kaolinite powder and preparing method thereof |
ATE416151T1 (en) * | 2004-07-02 | 2008-12-15 | Basf Catalysts Llc | USE OF CALCINATED KAOLIN WITH HIGH MULLITE INDEX |
CN101372558B (en) * | 2008-08-15 | 2011-11-16 | 芜湖同达新材料科技有限公司 | Superfine composite modified kaoline powder, preparation and use thereof |
-
2010
- 2010-05-12 CN CN 201010169726 patent/CN101880480B/en not_active Expired - Fee Related
Patent Citations (3)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US4950628A (en) * | 1989-04-19 | 1990-08-21 | Corning Incorporated | Material and process to produce low thermal expansion cordierite structures |
US6290771B1 (en) * | 1997-09-08 | 2001-09-18 | Moon Han Kim | Activated koalin powder compound for mixing with cement and method of preparing the same |
CN1653133A (en) * | 2002-03-26 | 2005-08-10 | 拜尔材料科学股份公司 | Impact-modified polycarbonate compositions with calcined talc |
Non-Patent Citations (1)
Title |
---|
JP特开2000-63182A 2000.02.29 |
Also Published As
Publication number | Publication date |
---|---|
CN101880480A (en) | 2010-11-10 |
Similar Documents
Publication | Publication Date | Title |
---|---|---|
CN101880480B (en) | Preparation method of calcinated argil | |
CN103555005B (en) | Preparation method of modified kaolin used as rubber reinforcing agent | |
CN100402462C (en) | Superhigh intensity electric ceramic formulation | |
CN101550254B (en) | Preparation technique of high temperature resistant, anti-corona high-resistance ethylene propylene terpolymer | |
CN101824223B (en) | Blended rubber of silicon rubber and high density polyethylene and preparation method thereof | |
CN106782824A (en) | A kind of insulated electric conductor | |
CN102674814A (en) | 1100KV rod post porcelain insulator | |
CN107034738A (en) | A kind of high-temperature resistance insulation paper | |
CN105174972A (en) | Preparation method of glass/ceramic nano composite material | |
CN110950633A (en) | Electric porcelain insulator and preparation method thereof | |
CN101774594A (en) | Method for preparing modified acicular wollastonite | |
CN102515855B (en) | Raw material formula of wire-post type sand-coating glaze | |
CN104250428B (en) | One kind is used for dry-type transformer high strength high insulation material and preparation method thereof | |
CN106116518A (en) | The toughness reinforcing porcelain insulator of the above high-performance of 420KN grade and manufacture method thereof | |
CN113443892A (en) | High-toughness conical suspension type porcelain insulator and preparation method thereof | |
CN105860339A (en) | Insulated cable material and preparation method thereof | |
CN104592733A (en) | Insulation material for electrical engineering | |
CN103408949B (en) | Ultrahigh hardness rubber unvulcanizate and preparation method thereof | |
CN106916452A (en) | A kind of non-aging insulation material and its preparation technology | |
CN107936342A (en) | It is a kind of that there is the CABLE MATERIALS of antimildew and antibacterial | |
CN103410044A (en) | Preparation method of polyacrylamide composite mica paper | |
CN103937114A (en) | Low-cost high-performance insulating rubber material | |
CN103489540B (en) | A kind of electrification railway contact net insulator | |
CN107057365A (en) | Flame retardant type fire-resisting cable is with can porcelain SiClx rubber and preparation method thereof | |
CN104327364A (en) | Mould-proof, moisture-proof and anti-bacterial cable material |
Legal Events
Date | Code | Title | Description |
---|---|---|---|
C06 | Publication | ||
PB01 | Publication | ||
C10 | Entry into substantive examination | ||
SE01 | Entry into force of request for substantive examination | ||
C14 | Grant of patent or utility model | ||
GR01 | Patent grant | ||
CF01 | Termination of patent right due to non-payment of annual fee |
Granted publication date: 20130327 Termination date: 20160512 |
|
CF01 | Termination of patent right due to non-payment of annual fee |