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 materials, e.g. electroluminescent or chemiluminescent
  • C09K11/08—Luminescent materials, e.g. electroluminescent or chemiluminescent containing inorganic luminescent materials
  • C09K11/77—Luminescent materials, e.g. electroluminescent or chemiluminescent containing inorganic luminescent materials containing rare earth metals
  • C09K11/7766—Luminescent materials, e.g. electroluminescent or chemiluminescent containing inorganic luminescent materials containing rare earth metals containing two or more rare earth metals
  • C09K11/7777—Phosphates
• • H—ELECTRICITY
  • H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
  • H10H—INORGANIC LIGHT-EMITTING SEMICONDUCTOR DEVICES HAVING POTENTIAL BARRIERS
  • H10H20/00—Individual inorganic light-emitting semiconductor devices having potential barriers, e.g. light-emitting diodes [LED]
  • H10H20/80—Constructional details
  • H10H20/85—Packages
  • H10H20/851—Wavelength conversion means
  • H10H20/8511—Wavelength conversion means characterised by their material, e.g. binder
  • H10H20/8512—Wavelength conversion materials

Definitions

• the present invention relates to the use as a phosphor in a plasma or X-ray system, of a lanthanum phosphate-based compound comprising thulium.
• Plasma systems (screens and lamps) are among the new visualization and lighting techniques that are being developed. A concrete example is that of replacing current television screens with flat screens, lighter and larger, a replacement which is about to be resolved by the use of plasma panels.
• a gas introduced into an enclosure is ionized under the effect of an electric discharge. During this process, high energy electromagnetic radiation is emitted. The photons are directed towards a luminescent material.
• this material must be a phosphor absorbing in the emission range of plasma or X-rays, and emitting in the appropriate spectral range with the highest possible efficiency.
• the object of the invention is to provide such a phosphor material.
• a phosphor in a plasma or X-ray system a compound based on a lanthanum phosphate comprising thulium is used.
• the invention also relates to a plasma or X-ray system, characterized in that it comprises the above-mentioned compound as a phosphor.
• the invention also covers a lanthanum phosphate which is characterized in that it comprises thulium and in that it consists of particles of average size between 1 and 20 ⁇ m with a dispersion index of less than 0.6.
• the invention relates to a phosphor having the same characteristics as those given above for phosphate. Other characteristics, details and advantages of the invention will appear even more completely on reading the description which follows, as well as various concrete but nonlimiting examples intended to illustrate it.
• the invention is based on the discovery of the luminescence properties of certain phosphates with respect to plasma or X radiation.
• the invention therefore relates first of all to the use of the compound described above as a phosphor under conditions which are those plasma systems.
• a gas emitting after ionization a radiation corresponding at least to wavelengths situated between 10 and 200 nm, more particularly between 140 and 200 nm, ie the distant ultraviolet domain.
• Examples of such systems include plasma screens and lamps.
• the phosphor of the invention can also be used in systems implementing X-ray radiation.
• X-rays here and for the present description, mean photons whose energy is between 10 and 10OKev.
• imaging systems in particular medical imaging.
• the phosphor of the invention is a compound comprising a matrix of the LaPO ⁇ type.
• This phosphate further comprises, as dopant, thulium. Thulium is present in phosphate in a trivalent form.
• This phosphate excited by plasma or X type radiation, emits in blue.
• This phosphate can also comprise, as co-dopant, gadolinium.
• the thulium content is between 0.1 and 10, more particularly between 0.5 and 5.
• the gadolinium content expressed in atomic% relative to lanthanum, can vary between 10 and 40%.
• a lanthanum phosphate which consists of particles of average size between 1 and 20 ⁇ m with a dispersion index of less than 0.6.
• the particle size can more particularly be between 2 and 6 ⁇ m.
• the dispersion index can more particularly be at most 0.5.
• the size and particle size characteristics are measured by a sedimentation technique using a particle size analyzer of the Sedigraph type.
• the measurement is carried out in a conventional manner on an aqueous dispersion of the product with ultrasonic deagglomeration treatment (5 minutes, 120Watt).
• dispersion index is meant the ratio: in which :
• 6 is the particle diameter for which 16% of the particles have a diameter less than d ⁇ 6 ;
• the invention also relates to plasma or X-ray systems or devices which comprise a phosphor compound as described above. All the characteristics which have been given above with regard to the phosphor compound and phosphate also apply here to the description of the systems or devices. These characteristics will therefore not be repeated here.
• the invention also relates to the use of the phosphor compound in the manufacture of these same systems or devices.
• This implementation is done according to well known techniques, for example by deposition by screen printing, electrophoresis or sedimentation.
• the invention also relates, as a new product particularly suitable for use as a phosphor described above, a specific lanthanum phosphate and its preparation process.
• the preparation process will first be described. This process consists in carrying out direct precipitation and at controlled pH by reacting a first solution containing soluble salts of rare earths (lanthanum, thulium and, where appropriate, gadolinium salts), these elements then being present in stoichiometric proportions. required to obtain the product of the desired formula, with a second solution containing phosphate ions.
• the solution of soluble rare earth salts is introduced into the solution containing the phosphate ions. This is generally done by gradually and continuously introducing the salt solution into the phosphate ion solution.
• the initial pH of the solution containing the phosphate ions is less than 3, and preferably between 1 and 3.
• the pH of the precipitation medium is then controlled at a pH value less than 2, and preferably between 1 and 2 If the initial pH of the solution containing the phosphate ions is greater than 3, the introduction of the solution of rare earth salts leads to a lowering of the pH value of the reaction medium formed by mixing this solution with the initial solution phosphate ions. In this case, the pH value is allowed to fall to a value less than 2 and it is once the desired pH value is reached that this value is checked.
• controlled pH is meant maintaining the pH of the precipitation medium at a certain value, constant or substantially constant, by addition of compounds or buffer solutions, in the solution containing the phosphate ions, and this simultaneously with the introduction into the latter of the solution containing the soluble salts of rare earths.
• the pH of the medium will thus vary by at most 0.5 pH unit around the set target value, and more preferably by at most 0.1 pH unit around this value.
• This pH control is advantageously carried out by adding a basic compound as will be explained below.
• the precipitation is preferably carried out in an aqueous medium at a temperature which is not critical and which is advantageously between room temperature (15 ° C - 25 ° C) and 100 ° C. This precipitation takes place with stirring of the reaction medium.
• the concentrations of the rare earth salts in the first solution can vary within wide limits.
• the total concentration of rare earths can be between 0.01 mol / liter and 3 mol / liter.
• the suitable rare earth salts are in particular the salts soluble in an aqueous medium, such as, for example, nitrates, chlorides, acetates, carboxylates, or a mixture of these.
• the preferred salts according to the invention are nitrates.
• the phosphate ions intended to react with the solution of the rare earth salts can be provided by pure compounds or in solution, such as for example phosphoric acid, alkaline phosphates or other metallic elements giving with the anions associated with rare earths a soluble compound.
• the phosphate ions are added in the form of ammonium phosphates because the ammonium cation will decompose during subsequent calcination, thus making it possible to obtain a lanthanum phosphate of high purity.
• ammonium phosphates diammonium or monoammonic phosphate are the preferred compounds for the implementation of the invention.
• the phosphate ions are present in an amount such that there is, between the two solutions, a PO4 / rare earth molar ratio greater than 1, and advantageously between 1.05 and 3.
• the solution containing the phosphate ions must initially present (that is to say before the start of the introduction of the solution of rare earth salts) a pH lower than 3, and preferably ranging between 1 and 3.
• suitable basic compound there may be mentioned, by way of example, metal hydroxides (NaOH, KOH, Ca (OH) 2) or ammonium hydroxide, or any other basic compound whose constituent species will not form any precipitated during their addition to the reaction medium, by combination with one of the species also contained in this medium, and allowing control of the pH of the precipitation medium.
• metal hydroxides NaOH, KOH, Ca (OH) 2
• ammonium hydroxide or any other basic compound whose constituent species will not form any precipitated during their addition to the reaction medium, by combination with one of the species also contained in this medium, and allowing control of the pH of the precipitation medium.
• a phosphate precipitate is directly obtained which can be recovered by any means known per se, in particular by simple filtration.
• the recovered product can then be washed, for example with water, in order to rid it of any impurities, in particular nitrates and / or ammonium groups adsorbed.
• It can finally be heat treated, and this under various conditions chosen essentially according to the degree of transformation desired for the final product (nature of the crystalline phase, degree of hydration, purity, level of luminescence and the like), as will be explained in more detail below. With or without the use of subsequent heat treatments, it will be noted that the method according to the invention always leads to products having a fine and extremely tight particle size.
• This LaPO phosphate which comprises thulium as a dopant consists of particles of average size between 1 and 20 ⁇ m with a dispersion index of less than 0.6.
• the particle size can more particularly be between 2 and 6 ⁇ m.
• the dispersion index can more particularly be at most 0.5.
• This phosphate can also comprise, as co-dopant, gadolinium.
• the contents of thulium and, optionally, gadolinium are those given above.
• This lanthanum orthophosphate doped with thulium can be in a crystalline form of either hexagonal or monoclinic type, and this essentially as a function of the temperature undergone by the product during its preparation.
• the hexagonal form corresponds to the phosphate either having not undergone any subsequent heat treatment or having undergone a heat treatment but at a temperature generally not exceeding 600 ° C.
• the monoclinic form corresponds to the phosphate which is obtained after a thorough heat treatment carried out at a temperature at least above 600 ° C, advantageously between 700 and 1000 ° C, with the aim of carrying out the transformation of the hexagonal crystalline phase into a pure monoclinic phase.
• a non-heat treated product is generally hydrated; however, simple drying, operated for example between 60 and 100 ° C, is sufficient to remove most of this residual water, the minor amounts of remaining water being removed by calcinations conducted at higher and higher temperatures. at around 400 ° C.
• the thulium-doped lanthanum phosphate of the invention has specific surfaces which vary according to the calcination temperatures to which it has been brought, these decreasing regularly with the latter.
• the thulium-doped lanthanum phosphate of the invention has specific surfaces which vary according to the calcination temperatures to which it has been brought, these decreasing regularly with the latter.
• the thulium-doped lanthanum phosphate of the invention has specific surfaces which vary according to the calcination temperatures to which it has been brought, these decreasing regularly with the latter.
• the thulium-doped lanthanum phosphate of the invention has specific surfaces which vary according to the calcination temperatures to which it has been brought, these decreasing regularly with the latter.
• after heat treatment at a temperature below 600 ° C. it has a specific surface greater than or equal to 30 m2 / g; after calcination at 800 ° C, this surface is of the order of about ten m2 / g approximately
• the specific surface is measured by the B.E.T. which is determined by nitrogen adsorption in accordance with standard ASTM D3663-78 established from the BRUNAUER-EMMETT-TELLER method described in the periodical "The Journal of the American Society", 60.309 (1938).
• the thulium-doped lanthanum phosphate of the invention also has the particularly remarkable and advantageous property of not clumping during calcination, that is to say that the particles constituting them are not, or do not tend to be, agglomerated and therefore end up in a final form of large granules of size from 0.1 to several mm for example; it is thus not necessary to carry out a prior grinding of the powders before carrying out the conventional treatments thereon intended to obtain the final phosphor.
• the lanthanum phosphate according to the invention has luminescence properties, after having undergone heat treatment at a temperature generally above 600 ° C., and advantageously between 700 and 1000 ° C., it may prove necessary to '' further improve these luminescence properties by carrying out post-treatments on the product, in order to obtain a real phosphor directly usable as such in the desired application.
• the border between a simple lanthanum phosphate and a real phosphor remains, after all, quite arbitrary, and depends on the only luminescence threshold from which it is considered that a product can be directly implemented in an acceptable manner by a user.
• the thulium-doped lanthanum phosphate of the invention can be subjected to a heat treatment in the presence of a flux. It will be noted that such a treatment is in itself already well known in itself and is conventionally used in the processes for developing the main phosphors, in particular to adapt them to the desired application (surface finish, gloss, for example).
• the flux is mixed with the phosphate to be treated, then the mixture is brought to a temperature of at least 1000 ° C, generally between 1000 ° C and 1200 ° C, and this under a necessarily reducing atmosphere. After treatment, the product is washed and then rinsed, so as to obtain the purest luminophore possible and in a deagglomerated state.
• This phosphor has a monoclinic type crystal structure.
• the contents of thulium and, optionally gadolinium, are those given above for phosphate.
• This example relates to the preparation of phosphates and phosphors according to the invention at different levels of thulium.
• a phosphate of formula is prepared P0 4- On a stirred tank bottom, consisting of 1.341 of a 1.1 M / 1 phosphoric acid solution, preneutralized to a pH of 1.6 with an ammonia solution and heated to 60 ° C, 0.551 rare earth nitrates at 2.2M / I are added over 1 hour, while maintaining the temperature of the mixture as well as its pH by adding ammonia.
• the precipitate is filtered and then washed with cold demineralized water.
• the cake obtained is then calcined at 900 ° C for 2 hours.
• the powder obtained has a monoclinic crystallographic structure and an average diameter of 5 ⁇ m with a dispersion index of 0.4.
• LiF 1% by mass
• the precursor is transformed into a phosphor by a heat treatment at 1000 ° C.
• Phosphates and phosphors with the thulium content indicated in Table 1 below are prepared in the same way by adding the amounts stoichiometric of nitrates.
• the products obtained have the same particle size and crystallographic characteristics as the preceding phosphate.
• the intensity of the emission peak of Tm3 + located at 450 nm in the blue under X excitation of the phosphors prepared in Example 1 is measured as a function of the thulium content. The results are given below.
• the 0.5 atomic% thulium product was evaluated on a plasma screen test cell containing a xenon-neon gas. A blue light emission characteristic of trivalent thulium was observed.

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• Chemical & Material Sciences (AREA)
• Inorganic Chemistry (AREA)
• Engineering & Computer Science (AREA)
• Materials Engineering (AREA)
• Organic Chemistry (AREA)
• Luminescent Compositions (AREA)
• Conversion Of X-Rays Into Visible Images (AREA)

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• 1997
  • 1997-10-24 FR FR9713367A patent/FR2770223B1/fr not_active Expired - Fee Related
• 1998
  • 1998-10-23 US US09/530,090 patent/US6419852B1/en not_active Expired - Fee Related
  • 1998-10-23 EP EP98951544A patent/EP1027401A1/de not_active Withdrawn
  • 1998-10-23 KR KR1020007004396A patent/KR20010015788A/ko not_active Ceased
  • 1998-10-23 CA CA002307132A patent/CA2307132A1/fr not_active Abandoned
  • 1998-10-23 WO PCT/FR1998/002275 patent/WO1999021938A1/fr not_active Ceased
  • 1998-10-23 JP JP2000518032A patent/JP2001521055A/ja active Pending
  • 1998-10-23 CN CN98811135A patent/CN1278855A/zh active Pending

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