CN109574624A - Novel super nano ceramics film - Google Patents

Novel super nano ceramics film Download PDF

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Publication number
CN109574624A
CN109574624A CN201811576232.6A CN201811576232A CN109574624A CN 109574624 A CN109574624 A CN 109574624A CN 201811576232 A CN201811576232 A CN 201811576232A CN 109574624 A CN109574624 A CN 109574624A
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nano ceramics
embryo
novel super
ceramics film
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CN109574624B (en
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魏东林
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Guangdong Ivy Environment Technology Co Ltd
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Guangdong Ivy Environment Technology Co Ltd
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Abstract

The present invention relates to nano ceramics technical field of membrane, for the general problem of the effect of filter sewage, provide a kind of novel super nano ceramics film, the technical solution is as follows: novel super nano ceramics film is in a tubular form and both ends open, several micropores are provided on the tube wall of novel super nano ceramics film, the aperture of micropore is 50-60nm;Novel super nano ceramics film includes the component of following mass fraction: 40-55 parts of kaolin;10-15 parts of feldspar;22-30 parts of zircon;45-60 parts of starch;5-10 parts of fumed silica;1.5-1.8 parts of black mud;1.2-1.6 parts of dolomite;0.9-1.2 parts of water-reducing agent.It is that 50-60nm makes most harmful substances in sewage can not be by the tube wall of novel super nano ceramics film to completely cut off in the pipe shaft of novel super nano ceramics film, so that filter effect is preferable by micropore size.

Description

Novel super nano ceramics film
Technical field
The present invention relates to nano ceramics technical field of membrane, more particularly, to a kind of novel super nano ceramics film.
Background technique
Nano ceramics film can play the filter effect of very strength because of the presence of its nanometer micropore in sewage treatment.
General ceramic material has stronger compactness, and micropore to be generated then needs the foaming in sintering, but common hair For infusion in foaming, gas flowing is mixed and disorderly unordered after bubble generates, and often will appear the gas that multiple foaming agents generate and converges It is poly- and the case where generate the biggish micropore in aperture, while being difficult to control micropore and being used through ceramic material thickness direction with forming filtering Micropore, therefore the nanometer micropore aperture on general nano ceramics film is larger so that the effect of filter sewage is general, therefore, There are also improve space.
Summary of the invention
In view of the deficiencies of the prior art, the present invention intends to provide a kind of novel super nano ceramics film, tool Have the advantages that the effect of filter sewage is preferable.
To achieve the above object, the present invention provides the following technical scheme that
A kind of novel super nano ceramics film, the novel super nano ceramics film are in a tubular form and both ends open, described new Several micropores are provided on the tube wall of the super nano ceramics film of type, the aperture of the micropore is 50-60nm;
The novel super nano ceramics film includes the component of following mass fraction:
40-55 parts of kaolin;
10-15 parts of feldspar;
22-30 parts of zircon;
45-60 parts of starch;
5-10 parts of fumed silica;
1.5-1.8 parts of black mud;
1.2-1.6 parts of dolomite;
0.9-1.2 parts of water-reducing agent.
The present invention is further arranged to: the novel super nano ceramics film includes the component of following mass fraction:
45-50 parts of kaolin;
10-12 parts of feldspar;
28-30 parts of zircon;
55-60 parts of starch;
5-6 parts of fumed silica;
1.5-1.8 parts of black mud;
1.2-1.6 parts of dolomite;
0.9-1.2 parts of water-reducing agent.
By using above-mentioned technical proposal, in a tubular form and both ends open by novel super nano ceramics film, filter sewage When, will novel super nano ceramics film one end block after from open end inject sewage, by the water purification after micro porous filtration from novel The tube wall exudation of super nano ceramics film is that 50-60nm makes in sewage by micropore size to complete sewage water filtration purification Most harmful substances can not be completely cut off by the tube wall of novel super nano ceramics film in novel super nano ceramics film In pipe shaft, so that filter effect is preferable;By the way that starch is added using as thickener, when increasing the film preparation of novel super nano ceramics The consistency of slurry condition reduces mobility, and then is easy to embryo processed, and idiosome is made to be not easy deformation, and stability is preferable;High temperature is burnt When knot, starch carbonizing is to form a large amount of carbons and then generate carbon with the silicon dioxde reaction in fumed silica and zircon SiClx, so that the structural strength of novel super nano ceramics film is preferable;By the way that fumed silica is added using as thixotroping Agent so that improving the mobility of mud when wearing into mud, and generates hydrogen bond by fumed silica after embryo processed to be formed Network structure forms constraint in turn, so that idiosome is unlikely to deform, further increases the stability of idiosome.
The present invention is further arranged to: the preparation method of the novel super nano ceramics film the following steps are included:
(1) slurrying, specific as follows:
By kaolin, feldspar, zircon, starch, fumed silica, black mud, dolomite, thickener, water-reducing agent and water It is added in ball mill and is milled into mud;
(2) slurry dewatering, specific as follows:
By filters pressing moisture is discharged to form filter residue;
(3) embryo processed, specific as follows:
Filter residue is put into compression moulding in mold to form the raw embryo of tubulose;
(4) dry idiosome, specific as follows:
Natural air drying forms dry embryo after raw embryo demoulding;
(5) dry embryo Tu Fu You slurry;
(6) fiber is planted, specific as follows:
The polyacrylonitrile fibre that diameter is 40-50nm is radially planted on dry embryo along dry embryo, the polyacrylonitrile fibre Length is greater than the pipe thickness of dry embryo, the polyacrylonitrile fibre through dry embryo tube wall and both ends stretch out the tube wall of dry embryo Outside;
(7) it is sintered, specific as follows:
It is sintered by electric arc furnaces, 2800-3000 DEG C of sintering temperature.
By using above-mentioned technical proposal, by polyacrylonitrile fibre being planted on the tube wall of dry embryo to pass through in calcining High temperature thermally decomposes polyacrylonitrile fibre, so that dry indusium polyacrylonitrile fibre through part forms micropore, so that The novel super nano ceramics film that sintering is formed forms micropore, since the diameter of polyacrylonitrile fibre is 40-50nm, in polypropylene Nitrile fiber can generate portion gas when thermally decomposing, will so that on dry embryo by the perforative micropore of polyacrylonitrile fibre by gas strut with Reaming is stretched out due to polyacrylonitrile fibre both ends outside the tube wall of dry embryo, ensure that the micropore and the external world on the tube wall of dry embryo connect It is logical, so that the gas that polyacrylonitrile is decomposed and generated can smoothly be discharged along micropore, so that reaming effect is lower, avoid The case where reaming excessively causes micropore size to increase, so that sintered novel super nano ceramics film forms the micro- of 50-60nm Hole, far below the micropore size that common nano ceramics film 100nm is acted on, so that the filtering of novel super nano ceramics film is dirty The effect of water is preferable;By on dry embryo plant polyacrylonitrile fibre with utilize dry embryo with certain structural strength characteristic, It avoids causing idiosome to crumble when plantation;By the thixotropy of fumed silica, so that the stabilization constrained by fumed silica Molding dry embryo, because of external force, has interrupted the hydrogen of fumed silica when polyacrylonitrile fibre runs through the tube wall of dry embryo Key so that the decline of local restriction power even disappears so that dry embryo had both been able to maintain good shape stability, at the same be easy to by Polyacrylonitrile fibre runs through, easy for construction;It is sintered by electric arc furnaces so that the carbon formed after starch carbonizing restores zircon In zirconium dioxide form zirconium carbide, and carbon and the silica in fumed silica and zircon are anti-at high temperature Silicon carbide should be formed, so that the high temperature resistance and physical property of novel super nano ceramics film greatly improve;Pass through starch It is carbonized and starch is used as thickener before sintering and provides carbon in sintering to form carbon, make full use of original Material reduces cost while reducing impurity to reduce additive.
The present invention is further arranged to: in the step (2), filter residue moisture content is 30-33%.
By using above-mentioned technical proposal, enabling has preferable structural stability when filter residue compression moulding, reduce because Situations such as filter residue water content causes greatly very much raw embryo to be collapsed, deformation, while guaranteeing enough moisture content so that filter residue is easy to moulding, Convenient for construction.
The present invention is further arranged to: natural air drying 24-48 hours in the cool in the step (4).
By using above-mentioned technical proposal, by natural air drying to further increase green structure intensity, while passing through foot The enough long time is so that each raw material directly preferably combines, and avoids high temperature drying that dry embryo is caused to harden and then influence subsequent The case where planting fiber.
The present invention is further arranged to: in the step (6), polyacrylonitrile fibre length is the pipe wall thickness of dry embryo 120%.
By using above-mentioned technical proposal, guarantee the tube wall that polypropylene fibre has enough length to stretch out dry embryo with both ends Outside.
The present invention is further arranged to: in the step (6), driving polyacrylonitrile fibre through dry by high-voltage electrostatic field The tube wall of embryo.
By using above-mentioned technical proposal, so that plantation fiber operation is convenient, high-efficient, verticality is higher when plantation, matter Amount is preferable.
The present invention is further arranged to: in the step (6), positive pole pipe being axially inserted into dry embryo along dry embryo, will be adhered to There is the cathode tube of polyacrylonitrile fibre along dry plumular axis to covering outside dry embryo, electrostatic field is generated so that polyacrylonitrile fibre by high pressure It circles in the air with negative electrical charge and towards positive pole pipe and then through dry embryo.
By using above-mentioned technical proposal, cooperated by positive pole pipe and cathode tube to reduce the case where losing dry embryo, and So that electrostatic field distance is shorter, electrostatic adsorption force is larger, so that the acceleration that polyacrylonitrile fibre is generated by electrostatic field It is larger, to guarantee that polyacrylonitrile fibre runs through the effect of dry embryonic tube wall with stronger penetration power.
In conclusion the invention has the following advantages:
1. being that 50-60nm makes most harmful substances in sewage that can not receive by novel super by micropore size The tube wall of rice ceramic membrane is to completely cut off in the pipe shaft of novel super nano ceramics film, so that filter effect is preferable;
2. by the way that starch is added so that as thickener, slurry condition is thick when increasing the film preparation of novel super nano ceramics Degree, and then is easy to embryo processed, when high temperature sintering, starch carbonizing with formed a large amount of carbons so that with fumed silica and zircon In silicon dioxde reaction generate silicon carbide so that the structural strength of novel super nano ceramics film is preferable;
3. being sintered by electric arc furnaces so that the zirconium dioxide in the carbon reduction zircon formed after starch carbonizing is formed Zirconium carbide, and the silicon dioxde reaction in carbon and fumed silica and zircon forms silicon carbide at high temperature, makes The high temperature resistance and physical property for obtaining novel super nano ceramics film greatly improve.
Specific embodiment
With reference to embodiments, invention is further described in detail.
In following embodiment, water-reducing agent uses the polycarboxylate water-reducer of Guangzhou Gongshi chemical materials Co., Ltd.
Embodiment 1
A kind of novel super nano ceramics film, novel super nano ceramics film is in a tubular form and both ends open, novel super are received Several micropores are provided on the tube wall of rice ceramic membrane, the aperture of micropore is 50-60nm, pipe thickness 0.5cm, length 20cm, Interior caliber is 1cm.
The preparation method of novel super nano ceramics film the following steps are included:
(1) slurrying, specific as follows:
By kaolin 40kg, feldspar 10kg, zircon 22kg, starch 45kg, fumed silica 5kg, black mud 1.5kg, white Marble 1.2kg, water-reducing agent 0.9kg and water 125.6kg, which are added in ball mill, to be ground and forms mud;
Mud is added in stirred tank and is heated to 60 DEG C and constant temperature stirring 5min so that Starch formation paste, it is thick to increase mud Degree.
(2) slurry dewatering, specific as follows:
By plate and frame filter press press mud, to form filter residue, filters pressing pressure 0.35Mpa is controlled, it is aqueous to control filter residue Rate is 30%.
(3) embryo processed, specific as follows:
Filter residue is put into mold, after molding, applies 1Mpa pressure to be press-formed, constant pressure keeps 1h, forms tubulose Raw embryo, the pipe thickness of raw embryo are 0.5cm, and length 20cm, interior caliber is 1cm.
(4) dry idiosome, specific as follows:
Raw embryo demoulding, place in the cool natural air drying for 24 hours, to form dry embryo.
(5) dry embryo Tu Fu You slurry, specific as follows:
You is starched on the outer wall and inner wall for being sprayed on dry embryo, standing and drying 6h.
(6) fiber is planted, specific as follows:
Dry embryo is placed on insulator foot vertically;
Positive pole pipe is axially inserted into dry embryo along dry embryo, the outer diameter of positive pole pipe is 0.5cm;
By cathode tube along dry plumular axis to covering outside dry embryo, the internal diameter of cathode tube is 5cm;
The positive axis of pole pipe and the axis of cathode tube are overlapped with dry plumular axis line;
Positive pole pipe is connected to positive pole, and cathode tube is connected to power cathode, and cathode tube is first powered to generate negative electrical charge, by poly- third It after alkene nitrile fiber uniform adsorption is on cathode inside pipe wall, then covers outside dry embryo, and cathode tube is kept to be in energized state;
After packaging cathode tube, positive pole pipe is powered to generate positive charge, and then forms electrostatic field, and due to polyacrylonitrile fibre A large amount of negative electrical charges will be had when being adsorbed on cathode inside pipe wall, so that polyacrylonitrile fibre is under the action of electrostatic field, court It goes at express speed to positive pole pipe, and then extends radially through the tube wall of dry embryo along dry embryo;
Controlling the voltage being applied on positive pole pipe and cathode tube is 120KV, and overtension is avoided to cause polyacrylonitrile fine Dimension can not rest on the situation on dry embryo after the tube wall of dry embryo.
Polyacrylonitrile fibre diameter is 40-50nm, and the length of polyacrylonitrile fibre is 0.6cm.
(7) it is sintered, specific as follows:
The dry embryo for having planted fiber is placed in electric arc furnaces and is sintered, sintering temperature control is 2800 DEG C, sintering time 132min obtains the novel super nano ceramics film of tubulose after cooling.
Embodiment 2
A kind of novel super nano ceramics film, novel super nano ceramics film is in a tubular form and both ends open, novel super are received Several micropores are provided on the tube wall of rice ceramic membrane, the aperture of micropore is 50-60nm, pipe thickness 0.5cm, length 20cm, Interior caliber is 1cm.
The preparation method of novel super nano ceramics film the following steps are included:
(1) slurrying, specific as follows:
By kaolin 45kg, feldspar 12kg, zircon 24kg, starch 50kg, fumed silica 6kg, black mud 1.6kg, white Marble 1.4kg, water-reducing agent 1kg and water 141kg, which are added in ball mill, to be ground and forms mud;
Mud is added in stirred tank and is heated to 60 DEG C and constant temperature stirring 5min so that Starch formation paste, it is thick to increase mud Degree.
(2) slurry dewatering, specific as follows:
By plate and frame filter press press mud, to form filter residue, filters pressing pressure 0.35Mpa is controlled, it is aqueous to control filter residue Rate is 30%.
(3) embryo processed, specific as follows:
Filter residue is put into mold, after molding, applies 1Mpa pressure to be press-formed, constant pressure keeps 1h, forms tubulose Raw embryo, the pipe thickness of raw embryo are 0.5cm, and length 20cm, interior caliber is 1cm.
(4) dry idiosome, specific as follows:
Raw embryo demoulding, place in the cool natural air drying for 24 hours, to form dry embryo.
(5) dry embryo Tu Fu You slurry, specific as follows:
You is starched on the outer wall and inner wall for being sprayed on dry embryo, standing and drying 6h.
(6) fiber is planted, specific as follows:
Dry embryo is placed on insulator foot vertically;
Positive pole pipe is axially inserted into dry embryo along dry embryo, the outer diameter of positive pole pipe is 0.5cm;
By cathode tube along dry plumular axis to covering outside dry embryo, the internal diameter of cathode tube is 5cm;
The positive axis of pole pipe and the axis of cathode tube are overlapped with dry plumular axis line;
Positive pole pipe is connected to positive pole, and cathode tube is connected to power cathode, and cathode tube is first powered to generate negative electrical charge, by poly- third It after alkene nitrile fiber uniform adsorption is on cathode inside pipe wall, then covers outside dry embryo, and cathode tube is kept to be in energized state;
After packaging cathode tube, positive pole pipe is powered to generate positive charge, and then forms electrostatic field, and due to polyacrylonitrile fibre A large amount of negative electrical charges will be had when being adsorbed on cathode inside pipe wall, so that polyacrylonitrile fibre is under the action of electrostatic field, court It goes at express speed to positive pole pipe, and then extends radially through the tube wall of dry embryo along dry embryo;
Controlling the voltage being applied on positive pole pipe and cathode tube is 120KV, and overtension is avoided to cause polyacrylonitrile fine Dimension can not rest on the situation on dry embryo after the tube wall of dry embryo.
Polyacrylonitrile fibre diameter is 40-50nm, and the length of polyacrylonitrile fibre is 0.6cm.
(7) it is sintered, specific as follows:
The dry embryo for having planted fiber is placed in electric arc furnaces and is sintered, sintering temperature control is 2800 DEG C, sintering time 132min obtains the novel super nano ceramics film of tubulose after cooling.
Embodiment 3
A kind of novel super nano ceramics film, novel super nano ceramics film is in a tubular form and both ends open, novel super are received Several micropores are provided on the tube wall of rice ceramic membrane, the aperture of micropore is 50-60nm, pipe thickness 0.5cm, length 20cm, Interior caliber is 1cm.
The preparation method of novel super nano ceramics film the following steps are included:
(1) slurrying, specific as follows:
By kaolin 50kg, feldspar 14kg, zircon 28kg, starch 55kg, fumed silica 8kg, black mud 1.7kg, white Marble 1.5kg, water-reducing agent 1.1kg and water 159.3kg, which are added in ball mill, to be ground and forms mud;
Mud is added in stirred tank and is heated to 60 DEG C and constant temperature stirring 5min so that Starch formation paste, it is thick to increase mud Degree.
(2) slurry dewatering, specific as follows:
By plate and frame filter press press mud, to form filter residue, filters pressing pressure 0.35Mpa is controlled, it is aqueous to control filter residue Rate is 30%.
(3) embryo processed, specific as follows:
Filter residue is put into mold, after molding, applies 1Mpa pressure to be press-formed, constant pressure keeps 1h, forms tubulose Raw embryo, the pipe thickness of raw embryo are 0.5cm, and length 20cm, interior caliber is 1cm.
(4) dry idiosome, specific as follows:
Raw embryo demoulding, place in the cool natural air drying for 24 hours, to form dry embryo.
(5) dry embryo Tu Fu You slurry, specific as follows:
You is starched on the outer wall and inner wall for being sprayed on dry embryo, standing and drying 6h.
(6) fiber is planted, specific as follows:
Dry embryo is placed on insulator foot vertically;
Positive pole pipe is axially inserted into dry embryo along dry embryo, the outer diameter of positive pole pipe is 0.5cm;
By cathode tube along dry plumular axis to covering outside dry embryo, the internal diameter of cathode tube is 5cm;
The positive axis of pole pipe and the axis of cathode tube are overlapped with dry plumular axis line;
Positive pole pipe is connected to positive pole, and cathode tube is connected to power cathode, and cathode tube is first powered to generate negative electrical charge, by poly- third It after alkene nitrile fiber uniform adsorption is on cathode inside pipe wall, then covers outside dry embryo, and cathode tube is kept to be in energized state;
After packaging cathode tube, positive pole pipe is powered to generate positive charge, and then forms electrostatic field, and due to polyacrylonitrile fibre A large amount of negative electrical charges will be had when being adsorbed on cathode inside pipe wall, so that polyacrylonitrile fibre is under the action of electrostatic field, court It goes at express speed to positive pole pipe, and then extends radially through the tube wall of dry embryo along dry embryo;
Controlling the voltage being applied on positive pole pipe and cathode tube is 120KV, and overtension is avoided to cause polyacrylonitrile fine Dimension can not rest on the situation on dry embryo after the tube wall of dry embryo.
Polyacrylonitrile fibre diameter is 40-50nm, and the length of polyacrylonitrile fibre is 0.6cm.
(7) it is sintered, specific as follows:
The dry embryo for having planted fiber is placed in electric arc furnaces and is sintered, sintering temperature control is 2800 DEG C, sintering time 132min obtains the novel super nano ceramics film of tubulose after cooling.
Embodiment 4
A kind of novel super nano ceramics film, novel super nano ceramics film is in a tubular form and both ends open, novel super are received Several micropores are provided on the tube wall of rice ceramic membrane, the aperture of micropore is 50-60nm, pipe thickness 0.5cm, length 20cm, Interior caliber is 1cm.
The preparation method of novel super nano ceramics film the following steps are included:
(1) slurrying, specific as follows:
By kaolin 55kg, feldspar 15kg, zircon 30kg, starch 60kg, fumed silica 10kg, black mud 1.8kg, white Marble 1.6kg, water-reducing agent 1.2kg and water 174.6kg, which are added in ball mill, to be ground and forms mud;
Mud is added in stirred tank and is heated to 60 DEG C and constant temperature stirring 5min so that Starch formation paste, it is thick to increase mud Degree.
(2) slurry dewatering, specific as follows:
By plate and frame filter press press mud, to form filter residue, filters pressing pressure 0.35Mpa is controlled, it is aqueous to control filter residue Rate is 30%.
(3) embryo processed, specific as follows:
Filter residue is put into mold, after molding, applies 1Mpa pressure to be press-formed, constant pressure keeps 1h, forms tubulose Raw embryo, the pipe thickness of raw embryo are 0.5cm, and length 20cm, interior caliber is 1cm.
(4) dry idiosome, specific as follows:
Raw embryo demoulding, place in the cool natural air drying for 24 hours, to form dry embryo.
(5) dry embryo Tu Fu You slurry, specific as follows:
You is starched on the outer wall and inner wall for being sprayed on dry embryo, standing and drying 6h.
(6) fiber is planted, specific as follows:
Dry embryo is placed on insulator foot vertically;
Positive pole pipe is axially inserted into dry embryo along dry embryo, the outer diameter of positive pole pipe is 0.5cm;
By cathode tube along dry plumular axis to covering outside dry embryo, the internal diameter of cathode tube is 5cm;
The positive axis of pole pipe and the axis of cathode tube are overlapped with dry plumular axis line;
Positive pole pipe is connected to positive pole, and cathode tube is connected to power cathode, and cathode tube is first powered to generate negative electrical charge, by poly- third It after alkene nitrile fiber uniform adsorption is on cathode inside pipe wall, then covers outside dry embryo, and cathode tube is kept to be in energized state;
After packaging cathode tube, positive pole pipe is powered to generate positive charge, and then forms electrostatic field, and due to polyacrylonitrile fibre A large amount of negative electrical charges will be had when being adsorbed on cathode inside pipe wall, so that polyacrylonitrile fibre is under the action of electrostatic field, court It goes at express speed to positive pole pipe, and then extends radially through the tube wall of dry embryo along dry embryo;
Controlling the voltage being applied on positive pole pipe and cathode tube is 120KV, and overtension is avoided to cause polyacrylonitrile fine Dimension can not rest on the situation on dry embryo after the tube wall of dry embryo.
Polyacrylonitrile fibre diameter is 40-50nm, and the length of polyacrylonitrile fibre is 0.6cm.
(7) it is sintered, specific as follows:
The dry embryo for having planted fiber is placed in electric arc furnaces and is sintered, sintering temperature control is 2800 DEG C, sintering time 132min obtains the novel super nano ceramics film of tubulose after cooling.
Embodiment 5
A kind of novel super nano ceramics film, novel super nano ceramics film is in a tubular form and both ends open, novel super are received Several micropores are provided on the tube wall of rice ceramic membrane, the aperture of micropore is 50-60nm, pipe thickness 0.5cm, length 20cm, Interior caliber is 1cm.
The preparation method of novel super nano ceramics film the following steps are included:
(1) slurrying, specific as follows:
By kaolin 55kg, feldspar 15kg, zircon 30kg, starch 60kg, fumed silica 10kg, black mud 1.8kg, white Marble 1.6kg, water-reducing agent 1.2kg and water 174.6kg, which are added in ball mill, to be ground and forms mud;
Mud is added in stirred tank and is heated to 60 DEG C and constant temperature stirring 5min so that Starch formation paste, it is thick to increase mud Degree.
(2) slurry dewatering, specific as follows:
By plate and frame filter press press mud, to form filter residue, filters pressing pressure 0.32Mpa is controlled, it is aqueous to control filter residue Rate is 33%.
(3) embryo processed, specific as follows:
Filter residue is put into mold, after molding, applies 1Mpa pressure to be press-formed, constant pressure keeps 1h, forms tubulose Raw embryo, the pipe thickness of raw embryo are 0.5cm, and length 20cm, interior caliber is 1cm.
(4) dry idiosome, specific as follows:
Raw embryo demoulding, places natural air drying 48h in the cool, to form dry embryo.
(5) dry embryo Tu Fu You slurry, specific as follows:
You is starched on the outer wall and inner wall for being sprayed on dry embryo, standing and drying 6h.
(6) fiber is planted, specific as follows:
Dry embryo is placed on insulator foot vertically;
Positive pole pipe is axially inserted into dry embryo along dry embryo, the outer diameter of positive pole pipe is 0.5cm;
By cathode tube along dry plumular axis to covering outside dry embryo, the internal diameter of cathode tube is 5cm;
The positive axis of pole pipe and the axis of cathode tube are overlapped with dry plumular axis line;
Positive pole pipe is connected to positive pole, and cathode tube is connected to power cathode, and cathode tube is first powered to generate negative electrical charge, by poly- third It after alkene nitrile fiber uniform adsorption is on cathode inside pipe wall, then covers outside dry embryo, and cathode tube is kept to be in energized state;
After packaging cathode tube, positive pole pipe is powered to generate positive charge, and then forms electrostatic field, and due to polyacrylonitrile fibre A large amount of negative electrical charges will be had when being adsorbed on cathode inside pipe wall, so that polyacrylonitrile fibre is under the action of electrostatic field, court It goes at express speed to positive pole pipe, and then extends radially through the tube wall of dry embryo along dry embryo;
Controlling the voltage being applied on positive pole pipe and cathode tube is 120KV, and overtension is avoided to cause polyacrylonitrile fine Dimension can not rest on the situation on dry embryo after the tube wall of dry embryo.
Polyacrylonitrile fibre diameter is 40-50nm, and the length of polyacrylonitrile fibre is 0.6cm.
(7) it is sintered, specific as follows:
The dry embryo for having planted fiber is placed in electric arc furnaces and is sintered, sintering temperature control is 3000 DEG C, sintering time 122min obtains the novel super nano ceramics film of tubulose after cooling.
Comparative example 1
A kind of novel super nano ceramics film, novel super nano ceramics film is in a tubular form and both ends open, novel super are received Several micropores are provided on the tube wall of rice ceramic membrane, the aperture of micropore is 50-60nm, pipe thickness 0.5cm, length 20cm, Interior caliber is 1cm.
The preparation method of novel super nano ceramics film the following steps are included:
(1) slurrying, specific as follows:
By kaolin 55kg, feldspar 15kg, zirconium carbide 20kg, silicon carbide 10kg, starch 60kg, fumed silica 10kg, black mud 1.8kg, dolomite 1.6kg, water-reducing agent 1.2kg and water 174.6kg, which are added in ball mill, to be ground and forms mud Slurry;
Mud is added in stirred tank and is heated to 60 DEG C and constant temperature stirring 5min so that Starch formation paste, it is thick to increase mud Degree.
(2) slurry dewatering, specific as follows:
By plate and frame filter press press mud, to form filter residue, filters pressing pressure 0.32Mpa is controlled, it is aqueous to control filter residue Rate is 33%.
(3) embryo processed, specific as follows:
Filter residue is put into mold, after molding, applies 1Mpa pressure to be press-formed, constant pressure keeps 1h, forms tubulose Raw embryo, the pipe thickness of raw embryo are 0.5cm, and length 20cm, interior caliber is 1cm.
(4) dry idiosome, specific as follows:
Raw embryo demoulding, places natural air drying 48h in the cool, to form dry embryo.
(5) dry embryo Tu Fu You slurry, specific as follows:
You is starched on the outer wall and inner wall for being sprayed on dry embryo, standing and drying 6h.
(6) fiber is planted, specific as follows:
Dry embryo is placed on insulator foot vertically;
Positive pole pipe is axially inserted into dry embryo along dry embryo, the outer diameter of positive pole pipe is 0.5cm;
By cathode tube along dry plumular axis to covering outside dry embryo, the internal diameter of cathode tube is 5cm;
The positive axis of pole pipe and the axis of cathode tube are overlapped with dry plumular axis line;
Positive pole pipe is connected to positive pole, and cathode tube is connected to power cathode, and cathode tube is first powered to generate negative electrical charge, by poly- third It after alkene nitrile fiber uniform adsorption is on cathode inside pipe wall, then covers outside dry embryo, and cathode tube is kept to be in energized state;
After packaging cathode tube, positive pole pipe is powered to generate positive charge, and then forms electrostatic field, and due to polyacrylonitrile fibre A large amount of negative electrical charges will be had when being adsorbed on cathode inside pipe wall, so that polyacrylonitrile fibre is under the action of electrostatic field, court It goes at express speed to positive pole pipe, and then extends radially through the tube wall of dry embryo along dry embryo;
Controlling the voltage being applied on positive pole pipe and cathode tube is 120KV, and overtension is avoided to cause polyacrylonitrile fine Dimension can not rest on the situation on dry embryo after the tube wall of dry embryo.
Polyacrylonitrile fibre diameter is 40-50nm, and the length of polyacrylonitrile fibre is 0.6cm.
(7) it is sintered, specific as follows:
The dry embryo for having planted fiber is placed in electric arc furnaces and is sintered, sintering temperature control is 3000 DEG C, sintering time 122min obtains the novel super nano ceramics film of tubulose after cooling.
Experiment 1
Each Examples and Comparative Examples preparation is detected according to GB/T4740-1999 " ceramic material compressive strength test method " The compression strength of novel super nano ceramics film.
Experiment 2
Each Examples and Comparative Examples preparation is detected according to GB/T4741-1999 " ceramic material anti-reflecting bending strength test method " The bending strength of novel super nano ceramics film.
Experiment 3
Each Examples and Comparative Examples preparation is detected according to GB/T4742-1984 " domestic ceramics impact toughness test method " The impact flexibility of novel super nano ceramics film.
Experiment 4
After novel super nano ceramics film prepared by each Examples and Comparative Examples is amplified 10,000 times by electron microscope It observes and measures micropore size.
Specific experiment data are shown in Table 1
Table 1
It can be obtained according to table 1, in the physical property and comparative example of the novel super nano ceramics film of embodiment 1-5 preparation directly The physical property that novel super nano ceramics film prepared by silicon carbide and zirconium carbide is added is close, so that starch is as thickener After can make full use of, reduce waste of material, save the cost.
The micropore size of embodiment 1-5 is that 50-60nm makes the filter effect of novel super nano ceramics film preferable.
The embodiment of present embodiment is presently preferred embodiments of the present invention, not limits protection of the invention according to this Range, therefore: the equivalence changes that all structures under this invention, shape, principle are done, should all be covered by protection scope of the present invention it It is interior.

Claims (8)

1. a kind of novel super nano ceramics film, it is characterized in that: the novel super nano ceramics film is in a tubular form and both ends open, Several micropores are provided on the tube wall of the novel super nano ceramics film, the aperture of the micropore is 50-60nm;
The novel super nano ceramics film includes the component of following mass fraction:
40-55 parts of kaolin;
10-15 parts of feldspar;
22-30 parts of zircon;
45-60 parts of starch;
5-10 parts of fumed silica;
1.5-1.8 parts of black mud;
1.2-1.6 parts of dolomite;
0.9-1.2 parts of water-reducing agent.
2. novel super nano ceramics film according to claim 1, it is characterized in that: the novel super nano ceramics film packet Include the component of following mass fraction:
45-50 parts of kaolin;
10-12 parts of feldspar;
28-30 parts of zircon;
55-60 parts of starch;
5-6 parts of fumed silica;
1.5-1.8 parts of black mud;
1.2-1.6 parts of dolomite;
0.9-1.2 parts of water-reducing agent.
3. novel super nano ceramics film according to claim 2, it is characterized in that: the novel super nano ceramics film Preparation method the following steps are included:
(1) slurrying, specific as follows:
Kaolin, feldspar, zircon, starch, fumed silica, black mud, dolomite, thickener, water-reducing agent and water are added Mud is milled into ball mill;
(2) slurry dewatering, specific as follows:
By filters pressing moisture is discharged to form filter residue;
(3) embryo processed, specific as follows:
Filter residue is put into compression moulding in mold to form the raw embryo of tubulose;
(4) dry idiosome, specific as follows:
Natural air drying forms dry embryo after raw embryo demoulding;
(5) dry embryo Tu Fu You slurry;
(6) fiber is planted, specific as follows:
The polyacrylonitrile fibre that diameter is 40-50nm is radially planted on dry embryo along dry embryo, the polyacrylonitrile fibre length Greater than the pipe thickness of dry embryo, the polyacrylonitrile fibre runs through the tube wall of dry embryo and both ends are stretched out outside the tube wall of dry embryo;
(7) it is sintered, specific as follows:
It is sintered by electric arc furnaces, 2800-3000 DEG C of sintering temperature.
4. novel super nano ceramics film according to claim 3, it is characterized in that: in the step (2), filter residue moisture content For 30-33%.
5. novel super nano ceramics film according to claim 3, it is characterized in that: in the step (4) in the cool certainly So air-dry 24-48 hours.
6. novel super nano ceramics film according to claim 3, it is characterized in that: polyacrylonitrile is fine in the step (6) Tie up the 120% of the pipe wall thickness that length is dry embryo.
7. novel super nano ceramics film according to claim 3, it is characterized in that: in the step (6), it is quiet by high pressure Electric field driven polyacrylonitrile fibre runs through the tube wall of dry embryo.
8. novel super nano ceramics film according to claim 7, it is characterized in that: in the step (6), by positive pole pipe edge Dry embryo is axially inserted into dry embryo, and the cathode tube for being stained with polyacrylonitrile fibre is passed through high pressure to covering outside dry embryo along dry plumular axis Electrostatic field is generated so that polyacrylonitrile fibre circles in the air with negative electrical charge and towards positive pole pipe and then through dry embryo.
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Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114538893A (en) * 2022-02-10 2022-05-27 深圳瑞新达新能源科技有限公司 Nano ceramic membrane and preparation method thereof

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1287048A (en) * 2000-06-30 2001-03-14 隋贤栋 Gradient ceramic-film tube and its preparation
CN1629099A (en) * 2003-12-18 2005-06-22 山东理工大学 Process for preparing ceramic filter element with desulfuration function
CN101830729A (en) * 2010-06-21 2010-09-15 中国建筑股份有限公司 Porous ceramic filter and preparation method thereof
CN102884022A (en) * 2010-03-05 2013-01-16 (株)庆东One Thermal insulator using closed cell expanded perlite
CN104671788A (en) * 2014-07-28 2015-06-03 上海柯瑞冶金炉料有限公司 Method for sintering silicon carbide ceramic by in-situ synthetic nano SiC particle reinforcement reaction
CN104803604A (en) * 2015-03-20 2015-07-29 天津市中一高科技有限公司 Wear-resistant and high-hardness ceramic formula and production technology of ceramic
CN107500731A (en) * 2017-09-22 2017-12-22 苏州瓷气时代净化设备有限公司 A kind of micropore ceramic filter scavenging material

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1287048A (en) * 2000-06-30 2001-03-14 隋贤栋 Gradient ceramic-film tube and its preparation
CN1629099A (en) * 2003-12-18 2005-06-22 山东理工大学 Process for preparing ceramic filter element with desulfuration function
CN102884022A (en) * 2010-03-05 2013-01-16 (株)庆东One Thermal insulator using closed cell expanded perlite
CN101830729A (en) * 2010-06-21 2010-09-15 中国建筑股份有限公司 Porous ceramic filter and preparation method thereof
CN104671788A (en) * 2014-07-28 2015-06-03 上海柯瑞冶金炉料有限公司 Method for sintering silicon carbide ceramic by in-situ synthetic nano SiC particle reinforcement reaction
CN104803604A (en) * 2015-03-20 2015-07-29 天津市中一高科技有限公司 Wear-resistant and high-hardness ceramic formula and production technology of ceramic
CN107500731A (en) * 2017-09-22 2017-12-22 苏州瓷气时代净化设备有限公司 A kind of micropore ceramic filter scavenging material

Non-Patent Citations (1)

* Cited by examiner, † Cited by third party
Title
杨乐芳等: "《纺织材料与检测》", 28 February 2018, 上海:东华大学出版社 *

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN114538893A (en) * 2022-02-10 2022-05-27 深圳瑞新达新能源科技有限公司 Nano ceramic membrane and preparation method thereof

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