CN1037798A - Tantalum powder mixed aluminide for capacitor stage - Google Patents

Tantalum powder mixed aluminide for capacitor stage Download PDF

Info

Publication number
CN1037798A
CN1037798A CN88102739A CN88102739A CN1037798A CN 1037798 A CN1037798 A CN 1037798A CN 88102739 A CN88102739 A CN 88102739A CN 88102739 A CN88102739 A CN 88102739A CN 1037798 A CN1037798 A CN 1037798A
Authority
CN
China
Prior art keywords
water
doping
powder
soluble
phosphate
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Withdrawn
Application number
CN88102739A
Other languages
Chinese (zh)
Other versions
CN1014847B (en
Inventor
王向东
宋显申
佟世昌
毛襄苹
晏志凡
阚素荣
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.)
Beijing General Research Institute for Non Ferrous Metals
Original Assignee
Beijing General Research Institute for Non Ferrous Metals
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 Beijing General Research Institute for Non Ferrous Metals filed Critical Beijing General Research Institute for Non Ferrous Metals
Priority to CN88102739A priority Critical patent/CN1014847B/en
Publication of CN1037798A publication Critical patent/CN1037798A/en
Publication of CN1014847B publication Critical patent/CN1014847B/en
Expired legal-status Critical Current

Links

Landscapes

  • Powder Metallurgy (AREA)
  • Manufacture Of Metal Powder And Suspensions Thereof (AREA)

Abstract

A kind of doping process method of producing the capacitor level ta powder, be characterized in adding simultaneously dopant water-soluble aluminum salt and water-soluble phosphate, the water-soluble aluminum salt that is added is 3000ppm following (in a metallic element aluminium), and the amount that adds water-soluble phosphate is 5-100ppm (in an element phosphor).Because the mixing and doping of water-soluble aluminum salt and water-soluble phosphate can improve specific volume and puncture voltage simultaneously.

Description

Tantalum powder mixed aluminide for capacitor stage
The present invention relates to the production technology of Ta powder used in capacitor, be used for making the process of the doping that tantalum powder that electrolytic capacitor anode uses produces more precisely.
The anodic oxide of tantalum surface is one deck densification, amorphous tantalum pentoxide film, and its stable chemical performance, corrosion-resistant, dielectric constant is big.So the tantalum powder is an ideal material of making electrolytic capacitor, and tantalum electrolytic capacitor is the ideal element in the modern electronic product.
One of approach that improves tantalum powder specific volume is to mix in a certain operation of powder process.Usually claim preceding doping with the doping before the sodium reduction of potassium floutaramite, then claim the back to mix thereafter.
American documentation literature US4,009,007 has introduced the process of producing the back doping of Ta powder used in capacitor, in middle pressure tantalum powder, add phosphate, its doping is that 5-400ppm(is in element phosphor), the advantage of this technology is that its specific volume is increased to some extent, and shortcoming is that leakage current increases, and puncture voltage generally descends.
British patent document GB2126253A has introduced the back doping process method of another kind of production Ta powder used in capacitor.This technology is blended metal oxide in the tantalum powder, the amount of its doping up to 5000ppm(in amount of metal), the metal oxide of adding is silicon dioxide, alundum (Al, titanium dioxide.Its advantage is that breakdown potential is pressed with bigger raising, but specific volume and leakage current are constant substantially, and because what mixed is the metal oxide powder, the proportion of metal oxide powder and ta powder differs bigger, be difficult for mixing, and make alloy skewness in the tantalum powder, and influence product quality, and bring difficulty for industrial production in the future.
Purpose of the present invention just is to improve the process of the back doping of above-mentioned production Ta powder used in capacitor, work out under the constant substantially condition of leakage current, make the dopant that puncture voltage and specific volume increase simultaneously, and make dopant and ta powder be easy to mix, be convenient to industrial large-scale production.
The present invention is a kind of process of producing the doping of capacitor level ta powder, ta powder raw material and dopant water-soluble inorganic salt are added water fully to be mixed well, make it be pulpous state, oven dry, the cohesion degassing under the condition of high vacuum high temperature, broken, levigate, said water-soluble inorganic salt is an aluminium salt, and its doping is 3000ppm following (in a metallic element aluminium).
In order to make Ta powder used in capacitor under the constant substantially situation of leakage current, when puncture voltage increases, its specific volume is also increased, when adding aluminium salt, it is good adding the dopant water-soluble phosphate again, and the specific volume of the Ta powder used in capacitor of producing and puncture voltage are all increased to some extent.
The water-soluble aluminum salt that is added is wherein a kind of in the aluminium salt such as meta-aluminate, aluminum sulfate, aluminum nitrate, is good with sodium metaaluminate, and the amount that is added is 3000ppm following (in a metallic element aluminium, down with), again with 50-1000ppm for better.If the amount of its adding increases the oxygen content in the product greater than 1000ppm, and the crisp phenomenon of silk easily takes place, and less than 50ppm, the added value of puncture voltage is less; The water-soluble phosphate that is added is wherein a kind of of diammonium hydrogen phosphate, ammonium dihydrogen phosphate, sodium hydrogen phosphate, sodium dihydrogen phosphate, dipotassium hydrogen phosphate, potassium dihydrogen phosphate, sodium phosphate, potassium phosphate, but with ammonium dihydrogen phosphate is good, because the adding ammonium dihydrogen phosphate, the ammonia volatilization is removed when aggegation outgases.
The amount that adds ammonium dihydrogen phosphate simultaneously with sodium metaaluminate in 50-100ppm(with element phosphor) for well.
Tantalum powder and dopant water-soluble aluminum salt and water-soluble phosphate mix, and add water and fully mix well, and make it be pulpous state, and used water is distilled water, and deionized water is to avoid bringing into harmful impurity.
The temperature of the mixed slurry oven dry of tantalum powder raw material and dopant is controlled between 50 °-80 ℃ is advisable, less than 50 ℃ of drying times use oversize, have oxidative phenomena to take place greater than 80 ℃ of tantalum powder, the time of oven dry generally was controlled at more than 5 hours.
The vacuum degree that the cohesion degassing is controlled in the tantalum degasification furnace should be less than 5 * 10 -5Holder generally is controlled at 5 * 10 -5-1 * 10 -7Between the holder, if vacuum degree is lower, greater than 5 * 10 -5Holder makes product be easy to take place oxidation, increases the oxygen content of product; The temperature that the cohesion degassing is controlled with between 1300 °-1500 ℃ for well, surpass 1500 ℃ the product specific volume reduced, outgas in cohesion below 1300 ℃, make the mobile variation of product.
After the cohesion degassing, carry out fragmentation, levigate, the granularity that makes product forms doping tantalum powder all by 60 mesh sieves.
Employed tantalum powder raw material is that potassium floutaramite is produced through sodium reduction, produces in this way to read anxious and fearful Ji  play and hold location Feng and drag Zheng location, abundant approve street gather ∮ 0 order, and when 1900 ℃ of sintering, specific volume is about 4000 μ Fv/g.Fine powder is less than 320 orders, and when 1500 ℃ of sintering, specific volume is about 18000 μ Fv/g.
Advantage of the present invention is to have improved the process of the back doping of producing Ta powder used in capacitor, adds two kinds of dopants simultaneously, makes puncture voltage and the specific volume to increase simultaneously and leakage current remains unchanged substantially.Thereby, or the operating voltage of raising electrolytic capacitor; Or reduce sintering temperature and anodic oxidation voltage is constant, thereby improved capacitance.This all will reduce the powder amount of using, and reduce the cost of tantalum capacitor.Because used dopant is water-soluble aluminium salt and phosphate, easy and tantalum powder raw material mixes, and is convenient to industrial large-scale production.
More specifically describe the present invention with following non-limiting examples, protection scope of the present invention is not subjected to the qualification of these embodiment.
Embodiment 1
Used raw material is the fine powder (Guangxi chestnut tin mineral) of potassium floutaramite through sodium reduction.Accurately take by weighing tantalum powder and dopant sodium metaaluminate (NaAlO 2Commercially available analysis is pure) a certain amount of, mix, fully mix well with deionized water, be pulpous state.Paste mixture is placed baking oven, dried 6 hours for 75 ℃, in tantalum piece degasification furnace (being a vacuum degassing furnace, is heater with the tantalum piece, Shanghai Vaccum Pump Factory's outlet), control vacuum degree 5 * 10 then -6Holder, 1400 ℃ of degassings one hour with its fragmentation, levigate to by 60 sieve meshes, and are made doping tantalum powder after coming out of the stove.
Take by weighing doping tantalum powder 0.5 gram, with the mould of diameter 4.5mm, pressed density is 4.5g/cm 3, place stove sheet sintering furnace then, generally control vacuum degree less than 5 * 10 -5Holder is controlled at 3 * 10 in the present embodiment -5Holder.Fine powder is generally 1500-1600 ℃ of sintering 30 minutes, in the present embodiment in 1560 ℃ of sintering 30 minutes.
Tantalum piece electrical property condition determination is, with sintering tantalum piece in 90 ° 0.01%.In the phosphoric acid solution of (percetage by weight), anodic oxidation under the constant current of 35mA/g, be oxidized to 70v after, constant voltage 2 hours makes the electric current free damping, and makes the tantalum anode piece.With CE-I type electrolytic capacitor leakage current tester, in the 0.01%(percetage by weight) phosphoric acid solution in, stablize 3 minutes readings after the charging of tantalum anode piece, record tantalum anode piece leakage current value, use the MO-230A volumeter, in the 38%(percetage by weight) sulfuric acid solution in measure the capacitance of tantalum anode piece.Measure puncture voltage with puncture voltage tester (Beijing Non-Ferrous Metal Research General Academy's product), in airtight container, in 90 ℃ 0.01%(percetage by weight) phosphoric acid solution in, anodic oxidation under the constant current of 35mA/g is till oxide-film is breakdown.Measuring the results are shown in Table one.
From the visible doping phosphoric acid ammonium dihydrogen of table one specific volume is risen, but puncture voltage descends, during the doping sodium metaaluminate, specific volume is constant substantially, and makes the puncture voltage 15v that risen.
Embodiment 2~7
Process that doping tantalum powder is produced and relevant method of testing are substantially with embodiment 1, and only used tantalum powder raw material is a meal, and the temperature of oven dry is controlled at 78 ℃, dries by the fire 5 hours; The vacuum degree of controlling during the degassing is 5 * 10 -6Holder, the temperature of degassing control is 1500 ℃, outgases 1 hour; Pressed density 5.6g/cm 3, 1900 ℃ of sintering 30 minutes, the tantalum agglomerate is oxidized to 200v, constant voltage 2 hours.Its measuring the results are shown in Table two.
Figure 881027391_IMG2
During from the visible doping sodium metaaluminate of table two, specific volume and k value are constant substantially, and puncture voltage then increases with the increase of doping.
Embodiment 8~9
The manufacturing technique method of doping tantalum powder and relevant method of testing thereof are substantially with embodiment 1, and only used tantalum powder raw material is a meal, and bake out temperature is controlled at 80 ℃, dry by the fire control vacuum degree 8 * 10 during the degassing 5 hours -7Holder, the temperature of degassing control is 1490 ℃, outgases pressed density 5.6g/cm 1 hour 3, 1900 ℃ of sintering 30 minutes, the tantalum agglomerate was oxidized to the 200v constant voltage 2 hours, and its measuring the results are shown in Table three.
Figure 881027391_IMG3
From table three sodium metaaluminate and monoammonium phosphate mixing and doping as can be known, can improve specific volume and puncture voltage simultaneously.
Embodiment 10
The manufacturing technique method of doping tantalum powder and relevant method of testing thereof are substantially with embodiment 1, and only used tantalum powder raw material is a meal, and bake out temperature is controlled at 80 ℃, dry by the fire control vacuum degree 5 * 10 during the degassing 5 hours -6Holder outgased pressed density 5.6g/cm 1 hour 3, 1900 ℃ of sintering 30 minutes, the tantalum agglomerate was oxidized to the 200v constant voltage 2 hours, and its measuring the results are shown in Table four.
Figure 881027391_IMG4
Embodiment 11~13
The manufacturing technique method of doping tantalum powder and relevant method of testing thereof are substantially with embodiment 1, and only used tantalum powder raw material is a meal, and bake out temperature is controlled at 80 ℃, dry control vacuum degree 5 * 10 during the degassing 5 hours -6Holder, the temperature of degassing control is 1450 ℃, outgases pressed density 5.6g/cm 1 hour 3, 1900 ℃ of sintering 30 minutes, the tantalum agglomerate was oxidized to the 200v constant voltage 2 hours, and its measuring the results are shown in Table five.
Figure 881027391_IMG5

Claims (4)

1, a kind of process of producing the doping of capacitor level ta powder, ta powder and dopant water-soluble inorganic salt are added water fully to be mixed well, be pulpous state, oven dry, the cohesion degassing under high vacuum high temperature, broken, levigate, feature of the present invention is, said water-soluble inorganic salt is an aluminium salt, and its doping is 3000ppm following (in a metallic element aluminium).
2, according to a kind of doping process method of claim 1, it is characterized in that, add water-soluble phosphate when adding aluminium salt.
According to a kind of doping process method of claim 2, it is characterized in that 3, water-soluble aluminum salt is a sodium metaaluminate, water-soluble phosphate is a monoammonium phosphate.
According to a kind of doping process method of claim 3, it is characterized in that 4, the amount that adds sodium metaaluminate is that 50-1000ppm(is in metallic element aluminium), the amount that adds ammonium dihydrogen phosphate is that 5-100ppm(is in element phosphor).
CN88102739A 1988-05-20 1988-05-20 Tantalum powder mixed aluminide for capacitor stage Expired CN1014847B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN88102739A CN1014847B (en) 1988-05-20 1988-05-20 Tantalum powder mixed aluminide for capacitor stage

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN88102739A CN1014847B (en) 1988-05-20 1988-05-20 Tantalum powder mixed aluminide for capacitor stage

Publications (2)

Publication Number Publication Date
CN1037798A true CN1037798A (en) 1989-12-06
CN1014847B CN1014847B (en) 1991-11-20

Family

ID=4832283

Family Applications (1)

Application Number Title Priority Date Filing Date
CN88102739A Expired CN1014847B (en) 1988-05-20 1988-05-20 Tantalum powder mixed aluminide for capacitor stage

Country Status (1)

Country Link
CN (1) CN1014847B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1311091C (en) * 2005-05-24 2007-04-18 长沙南方钽铌有限责任公司 Method of making tantalum material from tantalum powder-yttrium nitrate liquid-slid adulterant

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1311091C (en) * 2005-05-24 2007-04-18 长沙南方钽铌有限责任公司 Method of making tantalum material from tantalum powder-yttrium nitrate liquid-slid adulterant

Also Published As

Publication number Publication date
CN1014847B (en) 1991-11-20

Similar Documents

Publication Publication Date Title
CN1046878C (en) A process for making an improved tantalum powder and high capacitance low leakage electrode made therefrom
DE3309891A1 (en) METHOD FOR PRODUCING VALVE METAL ANLANDS FOR ELECTROLYTE CAPACITORS
KR100901283B1 (en) Tin oxide material with improved electrical properties for glass melting
EP3184205B1 (en) Preparation method for composite tantalum powder
DE60037753T2 (en) SPUTTERTARGET, METHOD FOR THE PRODUCTION THEREOF AND METHOD FOR MAKING A FILM
US4365011A (en) Process for preparing pieces composed of solid electrolyte based on stabilized zircon and to pieces obtained by this process
CN1196552C (en) Method for manufacturing tantalum sintered object for electrolytic capacitor
US4885073A (en) Activated carbon anode including lithium
US6824586B2 (en) Powder for capacitor, sintered body thereof and capacitor using the sintered body
CN85108080A (en) Contacts for vacuum-break switches
US6663687B2 (en) Niobium powder for capacitor, sintered body thereof and capacitor using the sintered body
CN1037798A (en) Tantalum powder mixed aluminide for capacitor stage
US9607770B2 (en) Method for producing capacitor
CN100338702C (en) Niobium powder for capacitor, sintered body thereof and capacitor using the sintered body
KR20020079800A (en) Niobium powder for capacitor, sintered body thereof and capacitor using the sintered body
JPH07192754A (en) Solid electrolyte for sodium- sulfur battery and its preparation
JP3030913B2 (en) Manufacturing method of ITO sintered body
CN1212910C (en) Niobiam powder, and solid electrolytic capacitor
JP2004076063A (en) Niobium alloy powder, anode for solid electrolytic capacitor, and solid electrolytic capacitor
RU2446499C1 (en) Method to manufacture anodes of volume-porous electrolytic capacitors
CN1675725A (en) Niobium capacitor and method for manufacturing same
JPH05275293A (en) Manufacture of solid electrolytic capacitor
CN106392060A (en) Mixed tantalum powder and preparation method thereof
JPH07220982A (en) Manufacture of solid electrolytic capacitor
CN102992763B (en) Potassium sodium niobate-titanium zinc bismuth-bismuth aluminate ternary lead-free high-temperature capacitor dielectric material and preparation method thereof

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C13 Decision
GR02 Examined patent application
C14 Grant of patent or utility model
GR01 Patent grant
C19 Lapse of patent right due to non-payment of the annual fee
CF01 Termination of patent right due to non-payment of annual fee