Classifications

• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
  • C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
  • C09K11/08—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials
  • C09K11/61—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing fluorine, chlorine, bromine, iodine or unspecified halogen elements
  • C09K11/617—Silicates
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
  • C01G17/00—Compounds of germanium
  • C01G17/006—Compounds containing germanium, with or without oxygen or hydrogen, and containing two or more other elements
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
  • C01G19/00—Compounds of tin
  • C01G19/006—Compounds containing tin, with or without oxygen or hydrogen, and containing two or more other elements
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
  • C01G23/00—Compounds of titanium
  • C01G23/002—Compounds containing titanium, with or without oxygen or hydrogen, and containing two or more other elements
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
  • C01G25/00—Compounds of zirconium
  • C01G25/006—Compounds containing zirconium, with or without oxygen or hydrogen, and containing two or more other elements
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01G—COMPOUNDS CONTAINING METALS NOT COVERED BY SUBCLASSES C01D OR C01F
  • C01G27/00—Compounds of hafnium
  • C01G27/006—Compounds containing hafnium, with or without oxygen or hydrogen, and containing two or more other elements
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
  • C09K11/00—Luminescent, e.g. electroluminescent, chemiluminescent materials
  • C09K11/08—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials
  • C09K11/67—Luminescent, e.g. electroluminescent, chemiluminescent materials containing inorganic luminescent materials containing refractory metals
  • C09K11/674—Halogenides
  • C09K11/675—Halogenides with alkali or alkaline earth metals
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
  • C01P2002/00—Crystal-structural characteristics
  • C01P2002/50—Solid solutions
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
  • C01P2002/00—Crystal-structural characteristics
  • C01P2002/50—Solid solutions
  • C01P2002/52—Solid solutions containing elements as dopants
  • C01P2002/54—Solid solutions containing elements as dopants one element only
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
  • C01P2002/00—Crystal-structural characteristics
  • C01P2002/80—Crystal-structural characteristics defined by measured data other than those specified in group C01P2002/70
  • C01P2002/84—Crystal-structural characteristics defined by measured data other than those specified in group C01P2002/70 by UV- or VIS- data
• • C—CHEMISTRY; METALLURGY
  • C01—INORGANIC CHEMISTRY
  • C01P—INDEXING SCHEME RELATING TO STRUCTURAL AND PHYSICAL ASPECTS OF SOLID INORGANIC COMPOUNDS
  • C01P2004/00—Particle morphology
  • C01P2004/60—Particles characterised by their size
  • C01P2004/61—Micrometer sized, i.e. from 1-100 micrometer

Definitions

• the present invention relates to a formula A 2 MF 6 : Mn useful as a red fluoride phosphor for a blue LED (wherein M is one or more selected from Si, Ti, Zr, Hf, Ge and Sn 4
• M is one or more selected from Si, Ti, Zr, Hf, Ge and Sn 4
• the valence element, A is selected from Li, Na, K, Rb and Cs and is at least one or two or more alkali metals containing Na and / or K.
• the present invention relates to a phosphor (double fluoride phosphor) and a method for producing the same.
• Patent Document 1 discloses a double footing represented by a formula such as A 2 MF 6 (A is Na, K, Rb, etc., M is Si, Ge, Ti, etc.). It is described that a compound obtained by adding Mn to a compound (double fluoride phosphor) is useful.
• Patent Document 1 discloses a method (evaporation concentration method) in which a hydrofluoric acid solution in which all constituent elements are dissolved or dispersed is evaporated and precipitated (evaporation concentration method).
• Patent Document 2 As another manufacturing method, in US Pat. No. 3,576,756 (Patent Document 2), after mixing a hydrofluoric acid solution in which each constituent element is dissolved, acetone, which is a water-soluble organic solvent, is added to lower the solubility. A method of precipitation by adding (a poor solvent addition method) is disclosed.
• Patent Document 3 Japanese Patent No. 4582259
• Patent Document 3 Japanese Patent Application Laid-Open No.
• Patent Document 4 disclose solutions containing hydrofluoric acid in which the element M and the element A in the above formulas are separate from each other.
• a method mixed deposition method is disclosed in which a phosphor is precipitated by dissolving a solution in which Mn has been added and mixing again.
• the purity of the product is not sufficient in the above-mentioned evaporation concentration method, and fine particles with poor crystallinity are likely to be generated in the poor solvent addition method. It didn't be said.
• the mixed precipitation method can be said to be a more improved method, but detailed conditions are still under investigation, and in particular, depending on the concentration and composition of the reaction solution, those with sufficient characteristics cannot be obtained, or the solubility relationship In some cases, precipitation does not occur.
• the present invention has been made in view of the above circumstances, and is a double fluoride phosphor having excellent light emission characteristics and good light emission characteristics even at high temperatures, and double fluoride fluorescence capable of stably producing such a phosphor with high yield. It aims at providing the manufacturing method of a body.
• the present inventors have intensively studied the conditions for producing the phosphor by the above mixed precipitation method, particularly the composition and concentration of the reaction solution, and have made the present invention. That is, the present invention provides the following method for producing a double fluoride phosphor.
• a 2 MF 6 Mn (I) (In the formula, A is one or more alkali metals selected from Li, Na, K, Rb and Cs and containing at least Na and / or K, and M is Si, Ti, Zr, Hf, (One or more tetravalent elements selected from Ge and Sn.) And a first hydrofluoric acid solution containing M and a second hydrofluoric acid solution containing A, and Mn.
• a 2 MF 6 Mn (I) (In the formula, A is one or more alkali metals selected from Li, Na, K, Rb and Cs and containing at least Na and / or K, and M is Si, Ti, Zr, Hf, (One or more tetravalent elements selected from Ge and Sn.)
• a phosphor of double fluoride characterized in that the emission intensity at 130 ° C. is 90% or more of the emission intensity at 20 ° C.
• M is Si.
• the method for producing a double fluoride according to the present invention comprises the following formula (I): A 2 MF 6 : Mn (I) Wherein M is one or more tetravalent elements selected from Si, Ti, Zr, Hf, Ge and Sn, A is selected from Li, Na, K, Rb and Cs, and at least Na and And / or one or more alkali metals containing K.)
• M is preferably Si, Ti or Ge, particularly Si or Ti, and A is preferably Na or K.
• a first hydrogen fluoride containing a tetravalent element M (M is one or more tetravalent elements selected from Si, Ti, Zr, Hf, Ge, and Sn).
• M is one or more tetravalent elements selected from Si, Ti, Zr, Hf, Ge, and Sn).
• the first solution is prepared by dissolving a compound containing M, such as a fluoride, oxide, hydroxide, or carbonate of M, in an aqueous solution containing hydrofluoric acid.
• hydrofluoric acid is used in excess of the amount necessary for dissolution.
• the concentration of hydrofluoric acid is preferably 10 to 60% by mass, more preferably 20 to 50% by mass.
• examples of the M source in this case include SiO 2 and TiO 2 .
• the aqueous solution substantially contains the polyfluoro acid salt of element M.
• a solution of a polyfluoro acid salt such as H 2 SiF 6 can also be obtained and used.
• an aqueous solution of these polyfluoro acid salts is mixed with an aqueous hydrofluoric acid solution.
• a second hydrofluoric acid solution containing alkali metal A (A is one or more selected from Li, Na, K, Rb and Cs, preferably Na and / or K) is prepared.
• the second solution consists of fluoride AF, hydrogen fluoride AHF 2 , nitrate ANO 3 , sulfate A 2 SO 4 , hydrogen sulfate AHSO 4 , carbonate A 2 CO 3 , bicarbonate AHCO 3 and hydroxide. It can be prepared by dissolving a compound of A selected from AOH and the like in an aqueous hydrofluoric acid solution.
• hydrogen fluoride salt hydrogen fluoride HF elutes at the time of dissolution even if it is dissolved only in water.
• the concentration of hydrofluoric acid is preferably 5 to 60% by mass, particularly 10 to 50% by mass.
• Manganese the luminescent center element
• Manganese can be added to either the first or second solution, or added separately when mixing the first and second solutions, or can be added by either method. Preferred is a method of adding to the first solution before mixing with the second solution.
• M is 0.1 mol / liter or more and 0.5 mol / liter or less. Even if it is less than 0.1 mol / liter or more than 0.5 mol / liter, there is a possibility that the emission characteristics of the phosphor obtained are not sufficient. Further, when the amount is less than 0.1 mol / liter, the yield of the phosphor is deteriorated, and when the amount exceeds 0.5 mol / liter, the viscosity of the liquid in a state where precipitation occurs is excessively increased and the reaction operation is difficult. is there. More preferred is 0.12 to 0.4 mol / liter, and particularly preferred is 0.13 to 0.35 mol / liter.
• the amounts of the first solution and the second solution are also related, but the concentration of M in the first solution is 0.1 to 1.5 mol / It is preferably liters.
• the amount of A in the state where all are mixed needs to be 2.5 or more in molar ratio with respect to the total of M and Mn. If it is less than 2.5, the solubility of the double fluoride is large, and the yield may be lowered or precipitation may not be obtained. Preferably they are 2.7-5, Especially preferably, they are 2.8-4. There is no essential upper limit to A / (M + Mn), but there is no advantage if it is increased beyond 5.
• the ratio of Mn in M + Mn is preferably 0.1 to 20 mol%, particularly 0.3 to 10 mol%.
• the amounts of the first solution and the second solution are also related, but the concentration of A in the second solution is 0.25 to 10 mol. / Liter is preferred.
• the concentration of hydrogen fluoride is preferably 20% by mass or more and 60% by mass or less. More preferably, it is 25 to 50% by mass. If the hydrogen fluoride is less than 20% by mass, hydrolysis and reduction of the manganese complex ion may occur, resulting in the possibility that the luminescent properties may be deteriorated, and exceeding 60% by mass is not preferable from the viewpoint of safety.
• the temperature of the first solution, the second solution, and the solution after mixing may be any temperature in the range of ⁇ 10 ° C. to 100 ° C. Particularly preferred is 0 to 40 ° C.
• heating may be performed, or cooling may be performed in anticipation of an increase in temperature due to heat generation during liquid preparation or mixing of the first and second solutions.
• one liquid is poured into the place where the other liquid is stirred with a stirrer, and the other liquid is circulating and flowing.
• any method such as combining the other liquid, mixing both liquids while flowing them simultaneously, and the like.
• the reaction apparatus is simple and easy to implement, and satisfactory in terms of product performance is a method in which the second solution is poured into the stirring of the first solution.
• the reaction time in this mixing step is usually 10 seconds to 1 hour. Preferably, it is 20 seconds to 20 minutes.
• the phosphor obtained as a precipitate by the reaction can be separated and solid-liquid separated by a method such as filtration, centrifugation, or decantation. After solid-liquid separation, treatments such as washing and solvent replacement can be performed as necessary, and drying can be performed by vacuum drying or the like.
• the phosphor obtained by the production method of the present invention is a bifluoride phosphor having an emission center of Mn, and emits red light when excited by blue (400 to 480 nm, for example, 450 nm) light.
• An emission spectrum having the strongest peak around 630 nm and consisting of several sharp linewidth peaks is shown.
• the absorbance for 450 nm light is 0.6 or more, preferably 0.63 to 0.85, and the internal quantum efficiency is 0.8 or more, preferably 0.83. 0.93, which is suitable as a red phosphor for a white LED using a blue LED as an excitation source.
• a double fluoride phosphor having an emission intensity at 130 ° C. of 90% or more of the emission intensity at 20 ° C., particularly 95 ° C. or more can be obtained.
• the emission intensity characteristics at such a high temperature are excellent.
• the measurement of emission intensity is as described in Experimental Example 2 described later.
• Examples 1 and 2 are examples of K 2 SiF 6 : Mn
• Example 3 is an example of K 2 TiF 6 : Mn.
• a hydrofluoric acid aqueous solution in which manganese (II) was dissolved was placed on the anode side of the reaction tank, and a hydrofluoric acid aqueous solution was placed on the cathode side. Both electrodes were connected to a power source, and electrolysis was performed at a voltage of 3 V and a current of 0.75 A. After the electrolysis, an excessive solution of potassium fluoride saturated with an aqueous hydrofluoric acid solution was added to the reaction solution on the anode side. The produced yellow solid product was separated by filtration and collected to obtain K 2 MnF 6 .
• Example 1 First, 234 cm 3 of 40 mass% hydrofluoric acid (H 2 SiF 6 ) aqueous solution (Morita Chemical Industry Co., Ltd.), 50 mass% hydrofluoric acid (HF) (SA-X, manufactured by Stella Chemifa Corporation) ) Mixed with 2,660 cm 3 . To this, 13.32 g of K 2 MnF 6 powder prepared in advance by the method of Reference Example was added and dissolved by stirring (first solution: Si—F—Mn).
• H 2 SiF 6 aqueous solution
• HF hydrofluoric acid
• Example 2 50 wt% HF in amounts 1,110Cm 3 for creating a second solution, in addition to that the amount of water in 910 cm 3 was prepared weighed each raw material in the same manner as in Example 1. Both the first solution and the second solution were placed in a plastic container with a screw-type lid, and the container was placed in a cold water bath and cooled to 7 ° C. From here, the reaction was carried out in the same manner as in Example 1. The second solution was poured over 1 minute 30 seconds while stirring the first solution. The temperature of the liquid became 14 ° C., and a pale orange precipitate was formed. After further stirring for 10 minutes, the precipitate was filtered off with a Buchner funnel and drained as much as possible.
• Example 3 First, 436 cm 3 of a 40% by mass titanium hydrofluoric acid (H 2 TiF 6 ) aqueous solution (Morita Chemical Co., Ltd.) was mixed with 50% by mass HF 2,458 cm 3 . To this, 14.8 g of the same pre-K 2 MnF 6 powder as in Example 1 was added and dissolved by stirring (first solution: Ti—F—Mn). Separately, 468.6 g of KHF 2 was mixed with 1,910 cm 3 of pure water and dissolved (second solution: KHF). Both solutions were put in a cold water bath together with the container in the same manner as in Example 2 and cooled to 10 ° C.
• H 2 TiF 6 40% by mass titanium hydrofluoric acid
• Comparative Example 1A 800 cm 3 of acetone (special grade reagent manufactured by Wako Pure Chemical Industries, Ltd.) 800 cm 3 was added to the mixed solution with no precipitation as a result of Comparative Example 1 over 5 minutes while stirring. Precipitation occurred and finally the liquid was at 28 ° C. The precipitate was filtered off, washed with acetone and vacuum dried to obtain 13.88 g of a powder product.
• Example 1 The emission characteristics, emission spectrum and absorption rate, and quantum efficiency of the phosphors obtained in Examples and Comparative Examples were measured with a quantum efficiency measurement device QE1100 (manufactured by Otsuka Electronics Co., Ltd.). Table 1 shows the absorptance and quantum efficiency at an excitation wavelength of 450 nm.

Landscapes

• Chemical & Material Sciences (AREA)
• Organic Chemistry (AREA)
• Inorganic Chemistry (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Life Sciences & Earth Sciences (AREA)
• Environmental & Geological Engineering (AREA)
• General Life Sciences & Earth Sciences (AREA)
• Geology (AREA)
• Luminescent Compositions (AREA)

Priority Applications (1)

Applications Claiming Priority (4)

Publications (1)

Family

ID=53756772

Family Applications (1)

Country Status (4)

Cited By (4)

Families Citing this family (6)

Citations (6)

Family Cites Families (5)

• 2014
  • 2014-11-14 JP JP2014231476A patent/JP6394307B2/ja active Active
• 2015
  • 2015-01-15 WO PCT/JP2015/050929 patent/WO2015115195A1/ja not_active Ceased
  • 2015-01-15 US US15/115,326 patent/US10294418B2/en active Active
  • 2015-01-29 TW TW104103051A patent/TWI638773B/zh active

Patent Citations (6)

Also Published As

Similar Documents

Legal Events