CN106785937A - A kind of lightning rod for transformer station - Google Patents

A kind of lightning rod for transformer station Download PDF

Info

Publication number
CN106785937A
CN106785937A CN201710101072.9A CN201710101072A CN106785937A CN 106785937 A CN106785937 A CN 106785937A CN 201710101072 A CN201710101072 A CN 201710101072A CN 106785937 A CN106785937 A CN 106785937A
Authority
CN
China
Prior art keywords
substrate
lightning rod
solution
corrosion
coating
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.)
Granted
Application number
CN201710101072.9A
Other languages
Chinese (zh)
Other versions
CN106785937B (en
Inventor
不公告发明人
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
NINGXIA CN-SC LIGHTING PROTECTION CO., LTD.
Original Assignee
Shanghai Sail Automation Technology Co Ltd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Shanghai Sail Automation Technology Co Ltd filed Critical Shanghai Sail Automation Technology Co Ltd
Priority to CN201710101072.9A priority Critical patent/CN106785937B/en
Publication of CN106785937A publication Critical patent/CN106785937A/en
Application granted granted Critical
Publication of CN106785937B publication Critical patent/CN106785937B/en
Active legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • HELECTRICITY
    • H01ELECTRIC ELEMENTS
    • H01TSPARK GAPS; OVERVOLTAGE ARRESTERS USING SPARK GAPS; SPARKING PLUGS; CORONA DEVICES; GENERATING IONS TO BE INTRODUCED INTO NON-ENCLOSED GASES
    • H01T19/00Devices providing for corona discharge
    • H01T19/04Devices providing for corona discharge having pointed electrodes
    • HELECTRICITY
    • H02GENERATION; CONVERSION OR DISTRIBUTION OF ELECTRIC POWER
    • H02GINSTALLATION OF ELECTRIC CABLES OR LINES, OR OF COMBINED OPTICAL AND ELECTRIC CABLES OR LINES
    • H02G13/00Installations of lightning conductors; Fastening thereof to supporting structure

Landscapes

  • Physics & Mathematics (AREA)
  • Engineering & Computer Science (AREA)
  • Plasma & Fusion (AREA)
  • Paints Or Removers (AREA)

Abstract

The application is related to a kind of lightning rod for transformer station, including substrate, and some mounting rods are fixed on the substrate, boom end fixed tuft shape lightning rod is installed, stabiliser bar is provided between adjacent tufted lightning rod, stabiliser bar two ends are separately fixed on the tufted lightning rod, forms stable triangle.The present invention is coated with corrosion resistant coating in the substrate surface of the lightning rod, and its electric conductivity is good, can prevent the corrosion of lightning rod, and can intelligently repair, cryoprotective effects it is good, with good use value.

Description

A kind of lightning rod for transformer station
Technical field
The application is related to lightning rod field, more particularly to a kind of lightning rod for transformer station.
Background technology
Lightning rod is a kind of electric installation, with the connect setting, the arrester of lightning rod such as building, beacon, electric power facility It is set to tip-shape so that its surrounding electric field intensity is very big, and air is ionized between thunder and lightning and arrester, and arrester can just connect By the electric current of thunder and lightning, and conducted to greatly by electric installation, it is to avoid thunder and lightning is to building, beacon, electric power facility etc. Infringement.
If however, building, beacon, electric power facility etc. be mounted with arrester but be not grounded or earthing effect not If good, instead bigger infringement can be caused to building etc. in arrester.Because arrester is connected by metal with the earth, Metal easily causes resistance excessive due to reasons such as corrosion, and electric conductivity declines, so as to cause very big potential safety hazard.
The content of the invention
To overcome problem present in above-mentioned background technology, the application to provide a kind of lightning rod for transformer station.
The present invention is achieved by the following technical programs:
A kind of lightning rod for transformer station, including substrate, are installed with some mounting rods, mounting rod on the substrate Distal portion be fixed with tufted lightning rod, be provided with stabiliser bar between the adjacent tufted lightning rod, the two ends point of stabiliser bar It is not fixed on the tufted lightning rod, forms the triangle structure of stabilization.
Wherein, the substrate is connected with transformer station by wire, and the substrate is electrolysis copper base.
Wherein, the substrate surface coating corrosion-resistant layer.
Wherein, ZnO nano particle, isopropanol and hollow mesoporous silicon oxide CNT are contained in the corrosion resistant coating Microballoon.
Wherein, the substrate is processed by following processing mode:Will be during electrolysis copper base impregnated in the HCl solution of 0.1M 2h, then with the mesh of sand paper 16,80 mesh and 800 mesh successively to be electrolysed copper base surface polish, be then soaked in 60% Then 2h in KOH solution, the electrolysis copper base after immersion is rushed using 60~90 DEG C of hot water injection 5min with 5~10 DEG C of water 5min is washed, is dried up using 50 DEG C of hair dryers standby.
Wherein, the preparation method of the corrosion resistant coating layer is as follows:
S1, the preparation of hollow mesoporous silica microsphere:
1. styrene monomer first is washed with the KOH solution that mass fraction is 10%, polymerization inhibitor is removed with separatory funnel point liquid, It is repeated 5 times, then with ultrapure water to pH=6.8~7.5;
2. 0.25g trimethyl ammonium chlorides are weighed to be dissolved in 80mL ultra-pure waters, reflux condensation mode system is loaded onto, leads to nitrogen, by Drop is added dropwise the styrene after 1. 10g is processed through step, and 30~45 DEG C of magnetic agitation 1h add 5wt% azo diisobutyl amidine salt The aqueous solution 20ml of hydrochlorate, is subsequently placed in 5min in vacuum drying chamber, and the temperature of drying box is adjusted to 50 DEG C, magnetic force is continued after taking-up Heating stirring, heating-up temperature is for 50 DEG C and is placed in polymerisation 24h under nitrogen environment, obtains polystyrene microsphere solution;
3. 1.0g cetyl trimethylammonium bromides are weighed to be dissolved in 49mL deionized waters, 10g ethanol, 1.0mL is added Concentrated ammonia liquor, is placed on magnetic stirring apparatus and stirs, and rotating speed is 1000rpm/min;Then 10g polystyrene microsphere emulsions are dropwise dripped Plus in stating cetyl trimethylammonium bromide mixed liquor, ultrasonic disperse 30min is finally added dropwise over 4.0g tetraethyl orthosilicates, Magnetic stirring apparatus temperature is risen to 40~50 DEG C, 10h is persistently stirred;
4. the emulsion centrifugal sedimentation of gained will be 3. processed through step, centrifugal speed is 10000rpm/min, and centrifuging temperature is 5 DEG C, after precipitation is washed using ethanol, repeated centrifugation is washed 5 times, vacuum drying chamber 50KPa, 40 DEG C dry 3.5h, desciccate in 1500 DEG C of calcining 5h in Muffle furnace;
S2, CNT-corrosion inhibitor solution is prepared:
1. the 500mg hollow mesoporous silica microspheres as obtained in step S1 are weighed and is dissolved in L-Histidine saturated aqueous solution In, ultrasonic disperse 15min;
2. weigh 50mg CNTs to be dissolved in 10ml ultra-pure waters, ultrasonic disperse 15min, then by carbon nano-tube solution Add to containing hollow mesoporous silica microsphere the L-Histidine aqueous solution in, then in 25 ± 5 DEG C of vacuum drying chamber in 400~500KPa negative reaction 24h, vacuum cooled high speed centrifugation, centrifuging temperature be 0~5 DEG C, centrifugal speed be 8000~ 1000rpm/min, centrifugation gained is dried overnight in being deposited in 70~100 DEG C of vacuum tanks, obtains final product and has adsorbed the hollow of L-Histidine Mesopore silicon oxide CNT microballoon;
S3, prepares substrate coating liquid:
1. 20ml methyl alcohol is added in 80ml ultra-pure waters, is placed on magnetic stirring apparatus, 40 DEG C of heating, 100rpm/min stirrings 5min, glycidyl ether oxygen propyl-methoxy silane is slowly added in above-mentioned solution, and 0.1M HCl regulations pH to 6.1~ 6.8,10min is stirred at room temperature, obtain solution a;
2. then 1.0mg ZnO nano particles are weighed to be added in 35ml isopropanols, under 50 DEG C for the treatment of of water-bath, stirring 30min, is well mixed it, and isopropanol then is added into above-mentioned solution a, obtains substrate coating liquid;
S4, prepares microsphere suspensions:To be dissolved in 100ml ultra-pure waters through microballoon 100mg obtained in step S2, be stirred at room temperature 10min, forms transparent solution, and 30mg novolak resin precursor liquid solutions are then added dropwise in solution, stirs 10min, obtains micro- Ball suspension;
S5, the solution that will be prepared in S4 is dropwise added dropwise on through treated substrate by the way of glue is dripped, and drips the speed of glue It is 1000rpm/s to spend, and the drop glue time is 5s, and spin coating speed is 1000rpm/s, spin coating 30s, repeats drop glue and spin coating 3 times;Will drop The substrate of good glue is placed in after being dried overnight in 90 DEG C of baking oven and forms film;
S6, the solution configured in step S3 is coated on the substrate processed by step S5 by the way of Best-Effort request On, 120~150 DEG C of heating in baking oven are placed the substrate in, the heat time is 5~10min, forms transparent with substrate surface Film.
Wherein, the thickness of the substrate surface coating corrosion-resistant layer is 50~100nm.
Relative to prior art, the beneficial effect of the application:
The present invention is coated with corrosion resistant coating in the substrate surface of the lightning rod, and its electric conductivity is good, can prevent The corrosion of lightning rod, and can intelligently repair, cryoprotective effects it is good, with good use value.
The substrate surface of lightning rod described herein forms mat surface by polishing, then again by HCl, sand paper and alkali The surface of the substrate of lightning rod is showed rough surface by dipping, further increases the degree of roughness on the surface of substrate, is increased The substrate of big lightning rod and the contact area of coating, and then extend the out-of-service time of coating so that it is described herein to keep away Thunder pin decay resistance is strengthened.
The surface of the substrate of lightning rod described herein is coated with protective coating layer, and the superficial layer of the coating is using hollow Mesoporous silicon dioxide micro-sphere absorption amino acid and CNT as the surface of lightning rod protective coating, in the base of lightning rod Piece surface forms pH responsive thin films, and when the substrate surface of lightning rod is corroded, the pH responsive thin films can be sensed to be kept away The change of the H+ or OH-ion concentration of the substrate surface of thunder pin, and then the L-Histidine corrosion inhibiter and carbon nanometer adsorbed in microballoon Pipe voluntarily excites the place for flowing out and being subject to corrode on the substrate for repairing lightning rod.
The surface of the substrate of lightning rod described herein is also coated with the film containing ZnO nano particle, because ZnO receives Rice grain has antibacterium and antiviral effect, therefore is received with hollow mesoporous silica microsphere absorption amino acid and carbon Mitron film is combined, and on the one hand realizes the intelligence reparation of air terminal surface, and the substrate that on the other hand increased lightning rod makes With life-span and anti-bacteria and anti-virus performance.
Isopropanol is added with the film coated on the substrate of lightning rod described herein, isopropanol makes as antifreeze With, it is ensured that lightning rod keeps its good mechanical performance in the relatively low environment of temperature.
, relative to the lightning rod of same type, the cost of its production and the cost of reparation are significantly for lightning rod described herein Reduce, and then, substantial amounts of labour and material resources cost are saved, with very strong potential use value.
The film of the substrate surface coating of the pretreatment mode and lightning rod of the substrate of lightning rod described herein is used Reagent there is the performance of environmental protection, the secondary pollution of environment is not resulted in its product withdraw to environment, hence in so that root The lightning rod being molded according to the preparation method of the film provided herein has the performance of environmental protection.
The aspect and advantage that the application is added will be set forth in part in the description, and will partly become from the following description Substantially, or recognized by the practice of the application.It should be appreciated that the general description of the above and detailed description hereinafter are only It is exemplary and explanatory, the application can not be limited.
Brief description of the drawings
Accompanying drawing herein is merged in specification and constitutes the part of this specification, shows and meets implementation of the invention Example, and be used to explain principle of the invention together with specification.
Fig. 1 is the structural representation of the application lightning rod.
Wherein:Substrate 1, mounting rod 2, tufted lightning rod 3, stabiliser bar 4.
Specific embodiment
Here exemplary embodiment will be illustrated in detail, its example is illustrated in the accompanying drawings.Following description is related to During accompanying drawing, unless otherwise indicated, the same numbers in different accompanying drawings represent same or analogous key element.Following exemplary embodiment Described in implementation method do not represent and the consistent all implementation methods of the present invention.Conversely, they be only with it is such as appended The example of the consistent apparatus and method of some aspects being described in detail in claims, of the invention.
In the description of the present application, it is necessary to explanation, unless otherwise prescribed and limit, term " installation ", " connected ", " connection " should be interpreted broadly, for example, it may be mechanically connect or electrical connection, or two connections of element internal, can Being to be joined directly together, it is also possible to be indirectly connected to by intermediary, for the ordinary skill in the art, can basis Concrete condition understands the concrete meaning of above-mentioned term.
Fig. 1 shows a kind of lightning rod for transformer station that embodiments herein is related to, as shown in figure 1, including base Piece 1, fixes some mounting rods 2 on the substrate 1, tufted lightning rod 3 is fixed in the end of mounting rod 2, between adjacent tufted lightning rod 3 Be provided with stabiliser bar 4, the two ends of stabiliser bar 4 are separately fixed on the tufted lightning rod 3, formed stable triangle, the substrate 1 with Transformer station is connected by wire, and the substrate 1 is electrolysis copper base, the surface coating corrosion-resistant layer of the substrate 1.Pass through Corrosion resistant coating is coated with the surface of the substrate of lightning rod, its electric conductivity is good, can prevent the corrosion of lightning rod, and Can intelligently repair, cryoprotective effects it is good.
Further, ZnO nano particle, isopropanol and hollow mesoporous silicon oxide are contained in the corrosion resistant coating layer CNT microballoon.
Further, in the present embodiment, the treatment of the preparation method including substrate of corrosion resistant coating layer and corrosion-resistant The preparation of dope layer, it is specific as follows:
S1, metal pretreated substrate will be electrolysed copper base and impregnated in 2h in the HCl solution of 0.1M, then with the mesh of sand paper 16, The surface of 80 mesh and 800 mesh successively to being electrolysed copper base is polished, and 2h in 60% KOH solution is then soaked in, after immersion Electrolysis copper base using 60~90 DEG C of hot water injection 5min, then with 5~10 DEG C of water flushing 5min, use 50 DEG C of electricity Blowing drying is standby;
1. S2, the preparation of hollow mesoporous silica microsphere first washs styrene with the KOH solution that mass fraction is 10% Monomer, polymerization inhibitor is removed with separatory funnel point liquid, is repeated 5 times, then with ultrapure water to pH=6.8~7.5;2. weigh 0.25g trimethyl ammonium chlorides are dissolved in 80mL ultra-pure waters, load onto reflux condensation mode system, lead to nitrogen, and 10g is dropwise added dropwise through step 1. the styrene after processing, 30~45 DEG C of magnetic agitation 1h add the aqueous solution of 5wt% azo diisobutyl amidine hydrochlorides 20ml, is subsequently placed in 5min in vacuum drying chamber, and the temperature of drying box is adjusted to 50 DEG C, and magnetic force heating stirring is continued after taking-up, plus Hot temperature is for 50 DEG C and is placed in polymerisation 24h under nitrogen environment, obtains polystyrene microsphere solution;3. 1.0g hexadecanes are weighed Base trimethylammonium bromide is dissolved in 49mL deionized waters, adds 10g ethanol, and 1.0mL concentrated ammonia liquors are placed on magnetic stirring apparatus and stir Mix, rotating speed is 1000rpm/min;Then 10g polystyrene microspheres emulsion is dropwise added dropwise above-mentioned cetyl trimethyl bromination In ammonium mixed liquor, ultrasonic disperse 30min is finally added dropwise over 4.0g tetraethyl orthosilicates, and magnetic stirring apparatus temperature is risen into 40 ~50 DEG C, persistently stir 10h;4. the emulsion centrifugal sedimentation of gained will be 3. processed through step, centrifugal speed is 10000rpm/min, Centrifuging temperature is 5 DEG C, and after precipitation is washed using ethanol, repeated centrifugation is washed 5 times, vacuum drying chamber 50KPa, 40 DEG C of dryings 3.5h, desciccate 1500 DEG C of calcining 5h in Muffle furnace;
S3, CNT-corrosion inhibitor solution is prepared, and weighs the hollow mesoporous silicon oxides of the 500mg as obtained in step S2 micro- Ball is dissolved in L-Histidine saturated aqueous solution, ultrasonic disperse 15min;50mg CNTs are weighed to be dissolved in 10ml ultra-pure waters, Ultrasonic disperse 15min, then adds to the L-Histidine aqueous solution containing hollow mesoporous silica microsphere carbon nano-tube solution In, then in 400~500KPa negative reaction 24h, vacuum cooled high speed centrifugation, centrifugation in 25 ± 5 DEG C of vacuum drying chamber Temperature is 0~5 DEG C, and centrifugal speed is 8000~1000rpm/min, and centrifugation gained is dried in being deposited in 70~100 DEG C of vacuum tanks Overnight, the hollow mesopore silicon oxide CNT microballoon for having adsorbed L-Histidine is obtained final product;
S4, prepares substrate coating liquid, in 80ml ultra-pure waters add 20ml methyl alcohol, be placed on magnetic stirring apparatus, 40 DEG C heating, 100rpm/min stirs 5min, and glycidyl ether oxygen propyl-methoxy silane is slowly added in above-mentioned solution, and 0.1M HCl are adjusted Section pH is stirred at room temperature 10min to 6.1~6.8, obtains solution a;Then 1.0mg ZnO nano particles are weighed and is added to 35ml isopropyls In alcohol, under 50 DEG C for the treatment of of water-bath, 30min is stirred, be well mixed it, isopropanol is then added into above-mentioned solution a, obtain base Piece coating liquid;
S5, prepares microsphere suspensions, will be dissolved in 100ml ultra-pure waters through microballoon 100mg obtained in step S3, is stirred at room temperature 10min, forms transparent solution, and 30mg novolak resin precursor liquid solutions are then added dropwise in solution, stirs 10min, obtains micro- Ball suspension;
S6, the solution that will be prepared in S5 is dropwise added dropwise on the substrate treated through step S1 by the way of glue is dripped, drop The speed of glue is 1000rpm/s, and the drop glue time is 5s, and spin coating speed is 1000rpm/s, spin coating 30s, repeats drop glue and spin coating 3 It is secondary;To drip glue substrate be placed in be dried overnight in 90 DEG C of baking oven after form film;
S7, the solution configured in step S4 is coated on the substrate processed by step S6 by the way of Best-Effort request On, 120~150 DEG C of heating in baking oven are placed the substrate in, the heat time is 5~10min, forms transparent with substrate surface Film.
Corrosion Protection to the lightning rod carries out experimental test:Using the lightning rod of the uncoated corrosion prevention film of substrate as sky White control, the lightning rod that corrosion prevention film is coated on blank lightning rod and substrate is placed in 1.0M NaCl solutions and is soaked, and is passed through After different time corrosion test, two kinds of electrochemical parameters of lightning rod are as shown in Table 1 and Table 2.
Corrosion potentials value (the unit of 1 two kinds of lightning rods of table:mv)
1h 12h 24h 48h 72h
Blank -989.00 -1053.32 -1500.10 -2015.26 -2089.56
The present invention -356.12 -370.21 -389.56 -500.78 -600.89
Corrosion electric current density value (the unit of 2 two kinds of lightning rods of table:nA/cm2)
1h 12h 24h 48h 72h
Blank 5600.00 6800.22 7856.32 8900.56 9000.78
The present invention 15.20 15.30 18.20 20.21 50.26
The corrosion electric current density as the lightning rod of blank is can be seen that with corrosion electricity from the end value of Tables 1 and 2 The increase of pressure and be increased dramatically, illustrate that blank is substantial in NaCl solution.And corrosion prevention film is scribbled on substrate Lightning rod provided herein compared with blank, with the increase of corrosion potentials, the lightning rod that the application is provided Corrosion electric current density increasess slowly, and illustrates in the range of the regular hour, and the corrosion reaction of lightning rod provided by the present invention is not Occur.
The anti-microbial property test of the lightning rod:Using absorbance method, the lightning-arrest of corrosion resistant coating is coated with detection substrate The lightning rod of coating is not coated with pin and substrate fungistatic effect to Escherichia coli is compareed as empty table.Result is as shown in table 3.
The antibacterial absorbance of the lightning rod of table 3 and blank to Escherichia coli
Experiment shows that the lightning rod for being coated with coating is compared with the lightning rod of uncoated coating, because prepared by coating Journey with the addition of ZnO nano particle so that lightning rod of the invention has good fungistatic effect.Then check experiment is used, it is right Than be added with isopropanol antifreeze and without addition antifreeze isopropanol coating, it is at -10 DEG C, and anti-corrosion effects difference is bright It is aobvious.
It should be appreciated that the invention is not limited in the precision architecture being described above and be shown in the drawings, and And can without departing from the scope carry out various modifications and changes.The scope of the present invention is only limited by appended claim.

Claims (7)

1. a kind of lightning rod for transformer station, including substrate, it is characterised in that some installations are installed with the substrate Bar, the distal portion of mounting rod is fixed with tufted lightning rod, and stabiliser bar, stabiliser bar are provided between the adjacent tufted lightning rod Two ends be separately fixed on the tufted lightning rod, formed stabilization triangle structure.
2. lightning rod according to claim 1, it is characterised in that the substrate is connected with transformer station by wire, described Substrate is electrolysis copper base.
3. lightning rod according to claim 2, it is characterised in that the substrate surface coating corrosion-resistant layer.
4. lightning rod according to claim 3, it is characterised in that containing ZnO nano particle, different in the corrosion resistant coating Propyl alcohol and hollow mesoporous silicon oxide CNT microballoon.
5. according to any described lightning rod of claim 1~2, it is characterised in that the substrate by following processing mode at Reason:Electrolysis copper base impregnated in 2h in the HCl solution of 0.1M, then with the mesh of sand paper 16,80 mesh and 800 mesh successively to cathode copper The surface of substrate is polished, and is then soaked in 2h in 60% KOH solution, and the electrolysis copper base after immersion uses 60~90 DEG C Hot water injection 5min, then rinse 5min with 5~10 DEG C of water, dried up using 50 DEG C of hair dryers standby.
6. the lightning rod described in a claim 3, it is characterised in that the preparation method of the corrosion resistant coating layer is as follows:
S1, the preparation of hollow mesoporous silica microsphere:
1. styrene monomer first is washed with the KOH solution that mass fraction is 10%, polymerization inhibitor is removed with separatory funnel point liquid, repeated 5 times, then with ultrapure water to pH=6.8~7.5;
2. 0.25g trimethyl ammonium chlorides are weighed to be dissolved in 80mL ultra-pure waters, reflux condensation mode system is loaded onto, leads to nitrogen, dropwise dripped Plus 10g 1. processed through step after styrene, 30~45 DEG C of magnetic agitation 1h, add 5wt% azo diisobutyl amidine hydrochlorides Aqueous solution 20ml, be subsequently placed in 5min in vacuum drying chamber, the temperature of drying box is adjusted to 50 DEG C, after taking-up continue magnetic force heating Stirring, heating-up temperature is for 50 DEG C and is placed in polymerisation 24h under nitrogen environment, obtains polystyrene microsphere solution;
3. 1.0g cetyl trimethylammonium bromides are weighed to be dissolved in 49mL deionized waters, 10g ethanol, the dense ammonia of 1.0mL is added Water, is placed on magnetic stirring apparatus and stirs, and rotating speed is 1000rpm/min;Then 10g polystyrene microspheres emulsion is dropwise added dropwise State in cetyl trimethylammonium bromide mixed liquor, ultrasonic disperse 30min is finally added dropwise over 4.0g tetraethyl orthosilicates, by magnetic Power agitator temperature rises to 40~50 DEG C, persistently stirs 10h;
4. the emulsion centrifugal sedimentation of gained will be 3. processed through step, centrifugal speed is 10000rpm/min, and centrifuging temperature is 5 DEG C, Precipitation using ethanol wash after, repeated centrifugation wash 5 times, vacuum drying chamber 50KPa, 40 DEG C dry 3.5h, desciccate is in horse Not in stove 1500 DEG C calcining 5h;
S2, CNT-corrosion inhibitor solution is prepared:
1. the 500mg hollow mesoporous silica microspheres as obtained in step S1 are weighed to be dissolved in L-Histidine saturated aqueous solution, is surpassed Sound disperses 15min;
2. weigh 50mg CNTs to be dissolved in 10ml ultra-pure waters, then ultrasonic disperse 15min adds carbon nano-tube solution Into the L-Histidine aqueous solution containing hollow mesoporous silica microsphere, then in 25 ± 5 DEG C of vacuum drying chamber in 400~ 500KPa negative reaction 24h, vacuum cooled high speed centrifugation, centrifuging temperature is 0~5 DEG C, and centrifugal speed is 8000~1000rpm/ Min, centrifugation gained is dried overnight in being deposited in 70~100 DEG C of vacuum tanks, obtains final product the hollow mesoporous oxidation for having adsorbed L-Histidine Silicon-carbon nanotube microballoon;
S3, prepares substrate coating liquid:
1. 20ml methyl alcohol is added in 80ml ultra-pure waters, is placed on magnetic stirring apparatus, 40 DEG C of heating, 100rpm/min stirring 5min, Glycidyl ether oxygen propyl-methoxy silane is slowly added in above-mentioned solution, 0.1M HCl regulation pH to 6.1~6.8, room temperature Stirring 10min, obtains solution a;
2. 1.0mg ZnO nano particles then are weighed to be added in 35ml isopropanols, under 50 DEG C for the treatment of of water-bath, stir 30min, It is well mixed, isopropanol is then added into above-mentioned solution a, obtain substrate coating liquid;
S4, prepares microsphere suspensions:To be dissolved in 100ml ultra-pure waters through microballoon 100mg obtained in step S2, be stirred at room temperature 10min, forms transparent solution, and 30mg novolak resin precursor liquid solutions are then added dropwise in solution, stirs 10min, obtains micro- Ball suspension;
S5, the solution that will be prepared in S4 is dropwise added dropwise on through treated substrate by the way of glue is dripped, and the speed for dripping glue is 1000rpm/s, the drop glue time is 5s, and spin coating speed is 1000rpm/s, spin coating 30s, repeats drop glue and spin coating 3 times;Glue will be dripped Substrate be placed in be dried overnight in 90 DEG C of baking oven after form film;
S6, the solution configured in step S3 is coated on the substrate processed by step S5 by the way of Best-Effort request, will Substrate is placed in 120~150 DEG C of heating in baking oven, and the heat time is 5~10min, and transparent film is formed with substrate surface.
7. the lightning rod described in a claim 3, it is characterised in that the thickness of the substrate surface coating corrosion-resistant layer is 50~100nm.
CN201710101072.9A 2017-02-23 2017-02-23 A kind of lightning rod for substation Active CN106785937B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201710101072.9A CN106785937B (en) 2017-02-23 2017-02-23 A kind of lightning rod for substation

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201710101072.9A CN106785937B (en) 2017-02-23 2017-02-23 A kind of lightning rod for substation

Publications (2)

Publication Number Publication Date
CN106785937A true CN106785937A (en) 2017-05-31
CN106785937B CN106785937B (en) 2018-05-25

Family

ID=58960109

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201710101072.9A Active CN106785937B (en) 2017-02-23 2017-02-23 A kind of lightning rod for substation

Country Status (1)

Country Link
CN (1) CN106785937B (en)

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108598875A (en) * 2018-07-25 2018-09-28 方流生 A kind of lightning arrester
CN114994981A (en) * 2022-06-14 2022-09-02 江苏弘德光电材料科技有限公司 Polarizing brightening adhesive film for liquid crystal display backlight module and preparation method thereof
CN115710417A (en) * 2022-11-28 2023-02-24 江西省萍乡市轩品塑胶制品有限公司 Biodegradable sheet lunch box master batch and preparation method thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN203871659U (en) * 2014-04-02 2014-10-08 国家电网公司 Lightning arrester
RU146246U1 (en) * 2013-12-26 2014-10-10 Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Уфимский государственный нефтяной технический университет" DEVICE FOR PROTECTING PIPELINES FROM CORROSION DESTRUCTION UNDER THE INFLUENCE OF LIGHTNING CURRENTS
CN104927583A (en) * 2015-07-06 2015-09-23 江苏固格澜栅防护设施有限公司 Preparation method and application of intelligent anti-corrosion coating capable of being automatically repaired
CN106099648A (en) * 2016-06-16 2016-11-09 江西省雷电监测预警与防护技术中心 One connects sudden strain of a muscle bar

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
RU146246U1 (en) * 2013-12-26 2014-10-10 Федеральное государственное бюджетное образовательное учреждение высшего профессионального образования "Уфимский государственный нефтяной технический университет" DEVICE FOR PROTECTING PIPELINES FROM CORROSION DESTRUCTION UNDER THE INFLUENCE OF LIGHTNING CURRENTS
CN203871659U (en) * 2014-04-02 2014-10-08 国家电网公司 Lightning arrester
CN104927583A (en) * 2015-07-06 2015-09-23 江苏固格澜栅防护设施有限公司 Preparation method and application of intelligent anti-corrosion coating capable of being automatically repaired
CN106099648A (en) * 2016-06-16 2016-11-09 江西省雷电监测预警与防护技术中心 One connects sudden strain of a muscle bar

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN108598875A (en) * 2018-07-25 2018-09-28 方流生 A kind of lightning arrester
CN114994981A (en) * 2022-06-14 2022-09-02 江苏弘德光电材料科技有限公司 Polarizing brightening adhesive film for liquid crystal display backlight module and preparation method thereof
CN115710417A (en) * 2022-11-28 2023-02-24 江西省萍乡市轩品塑胶制品有限公司 Biodegradable sheet lunch box master batch and preparation method thereof

Also Published As

Publication number Publication date
CN106785937B (en) 2018-05-25

Similar Documents

Publication Publication Date Title
CN106785937B (en) A kind of lightning rod for substation
EP3000931B1 (en) Heat insulation sheet and method of producing the same
CN103456928B (en) composite anode material for lithium ion battery and preparation method thereof
CN103305122B (en) A kind of polynite-silicon-dioxide super-hydrophobic coat and preparation method thereof
CN104892935B (en) A kind of method of synthesized polyaniline nanotube
CN109251345A (en) A kind of super hydrophilic or super-hydrophobic frosting of durability and preparation method thereof
CN104497870A (en) Preparation method of vinyltrimethoxysilane/zinc oxide superhydrophobic composite coating
CN103146147A (en) Toughened epoxy resin/glass fiber prepreg and preparation method
CN102632031A (en) Method for preparing superhydrophobic surface
CN110449094B (en) Preparation method of self-repairing microcapsule and application of self-repairing microcapsule in super-hydrophobic coating
CN109745876A (en) A kind of method of modifying super hydrophobicity electromagnetic shielding composite material
CN105405657A (en) Electrolytic capacitor manufacturing method and product thereby
CN109336545A (en) A kind of silicon dioxide silica aerogel composite material, preparation method and application
CN106883463A (en) A kind of preparation method of pattern and size tunable type starch nanometer granule
CN105413626A (en) Preparation method of blocky hybrid aerogel
CN113088162B (en) Wear-resistant epoxy resin coating and preparation method thereof
CN108767113A (en) A kind of TiO2Nano-pillar-Au Nanocomposites array, preparation method and applications
CN105887492A (en) Nano-organosilicon waterproof stain-resistant finishing method for polyester fabrics
CN105400141A (en) Preparation method of carbon nano tube doped TiO<2>/ epoxy hybridization fiberglass composite
CN111057442A (en) Preparation method of hollow mesoporous silica \ APS \ graphene oxide nano container
CN114106416B (en) Preparation method and application of double-response halloysite nano container
CN111235559A (en) Surface treatment method of stainless steel, hydrophobic stainless steel and application thereof
CN115193666A (en) Preparation method of super-hydrophobic surface with micro-nano scale step structure for anti-icing
CN102321976A (en) Preparation and use methods of carbon fiber surface modifier
CN109626954A (en) A kind of heatproof damp-proof silicon dioxide silica aerogel composite material and its preparation method and application

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
CB03 Change of inventor or designer information

Inventor after: Ran Danting

Inventor after: Gao Panliang

Inventor after: Dong Na

Inventor before: The inventor has waived the right to be mentioned

CB03 Change of inventor or designer information
TA01 Transfer of patent application right

Effective date of registration: 20180425

Address after: 750000 Yinchuan, the Ningxia Hui Autonomous Region, Jinfeng District, Ning'an Street 490, Yinchuan IBI breeding center two phase 6 Building 1401 room.

Applicant after: NINGXIA CN-SC LIGHTING PROTECTION CO., LTD.

Address before: 200000 Shanghai Songjiang District Songjiang District Mun Road No. 1

Applicant before: Shanghai sail Automation Technology Co., Ltd.

TA01 Transfer of patent application right
GR01 Patent grant
GR01 Patent grant