WO2013033153A1 - Preparation of inorganic samples by fusion - Google Patents
Preparation of inorganic samples by fusion Download PDFInfo
- Publication number
- WO2013033153A1 WO2013033153A1 PCT/US2012/052783 US2012052783W WO2013033153A1 WO 2013033153 A1 WO2013033153 A1 WO 2013033153A1 US 2012052783 W US2012052783 W US 2012052783W WO 2013033153 A1 WO2013033153 A1 WO 2013033153A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- mold
- sample
- mix
- crucible
- inert gas
- Prior art date
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
- B22D21/00—Casting non-ferrous metals or metallic compounds so far as their metallurgical properties are of importance for the casting procedure; Selection of compositions therefor
- B22D21/02—Casting exceedingly oxidisable non-ferrous metals, e.g. in inert atmosphere
- B22D21/025—Casting heavy metals with high melting point, i.e. 1000 - 1600 degrees C, e.g. Co 1490 degrees C, Ni 1450 degrees C, Mn 1240 degrees C, Cu 1083 degrees C
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
- B22D23/00—Casting processes not provided for in groups B22D1/00 - B22D21/00
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B22—CASTING; POWDER METALLURGY
- B22D—CASTING OF METALS; CASTING OF OTHER SUBSTANCES BY THE SAME PROCESSES OR DEVICES
- B22D25/00—Special casting characterised by the nature of the product
- B22D25/02—Special casting characterised by the nature of the product by its peculiarity of shape; of works of art
Definitions
- the present invention relates generally to the preparation of inorganic samples by fusion and, more particularly, concerns an improved method and system for the preparation of inorganic samples by fusion.
- the sample (geological, mineralogical or some inorganic material) in powdered form is mixed with a powdered reagent called a flux.
- a powdered reagent called a flux.
- the mixture is placed in a platinum-gold alloy crucible, and heated to a temperature slightly above 1000°C. At such temperatures, the flux will melt in a few minutes and dissolve the oxides present in the sample, producing a homogenous mix.
- This molten mix is then poured into a mold made of the same alloy as the crucible. Upon cooling, the material in the mold will solidify, resulting in a glassy disk that can be analyzed.
- melt stickiness can also cause fast mold degradation
- the method and system should be convenient and reliable in use, and preferably should realize cost savings in comparison with the existing process.
- a smooth receiving surface for the mix is ensured and the amount of surface re-polishing minimized by pouring the homogenous mix on an inert, molten metal surface, such as liquid gold.
- the speed of the process is improved by pre-melting the flux in a heating chamber and mixing it with the sample in a liquid state. It is also contemplated that the speed of the process can be increased by cooling the glassy disk with a fluid that has a substantially higher thermal capacity than air, which is normally used for cooling.
- Preferred fluids include water and liquefied gases, which are very cold when depressurized from their stored form to atmospheric pressure.
- savings can be realized by eliminating crucibles made of precious metals (e.g. a platinum-gold alloy, hereafter also referred to as “platinumware”) and replacing them with crucibles made of a glassy graphite (hereafter also referred to as “graphiteware").
- precious metals e.g. a platinum-gold alloy, hereafter also referred to as “platinumware”
- graphiteware glassy graphite
- the process must be performed in an inert gas ambient atmosphere, preferably one containing nitrogen, argon, or neon, or combinations thereof.
- the preparation of inorganic samples by fusion in accordance with the present invention involves the heating of a crucible containing a mixture of lithium borate flux and the sample itself, finely ground. Very often, laboratory personnel performing the process will also add a halogen chemical compound to facilitate the removal of the end-product.
- the lithium borate dissolves the sample, and this dissolution can be enhanced by the agitation of the crucible. After complete reaction, the resulting hot solution is poured into a plate-shaped mold and cooled, to produce a glassy disk that can then be used conveniently in an elemental analyzer.
- FIG. 1 is a schematic diagram of a system 10 for the preparation inorganic samples by fusion which embodies the present invention. All processes are performed within a main enclosure 12 which is preferably airtight. Enclosure 12 is continuously filled from below with an inert gas, such as nitrogen, argon or neon, the gas being selected to inhibit oxidation and other reactions, even at very high temperatures. The primary purpose of the gas is to prevent oxidation of the components inside the enclosure, such as a crucible 14 and mold 16, discussed further below.
- an inert gas such as nitrogen, argon or neon
- Fresh inert gas is piped into an input sash 18 and an output sash 20, which are used, respectively, to insert samples into and withdraw completed samples from enclosure 12.
- sashes 18 and 20 are designed with doors that allow gas flow into the main enclosure 12, but not out of it. Any excess gas that accumulates in main enclosure 12 exits via an exhaust 22 at the top of enclosure 12, preferably into an existing fume hood piping system (not shown).
- a sample is fed into enclosure 12 through the input sash 18 and retained in crucible 14, which is made of graphite.
- Crucibles for this type of process are most often made of a platinum-gold alloy, which is quite expensive, and the use of a graphite crucible realizes considerable savings.
- the use of an inert gas atmosphere makes a graphite crucible an effective replacement by avoiding the deterioration of the crucible which would occur inside enclosure 12 in the presence of oxygen, since process temperatures exceed 1000° C.
- Crucible 14 is heated by means of a heater 24, and it sits directly on a mechanical support 26, which, in turn, sits upon an electronic scale (and system controller) 28, which is located outside enclosure 12, to ensure temperature measurement stability. Scale 28 senses the mass of the sample and the system controller calculates the mass of flux to be added.
- Powdered flux 30 is stored in a hopper 33 above the enclosure 12.
- a heater 31 in the lower portion of hopper 33 melts the flux to a liquid state.
- the addition of molten flux to crucible 14 is regulated by means of a servo valve 35, which is controlled by controller 28.
- controller 28 controls the addition of molten flux to crucible 14 to a precisely correct amount of flux to the sample within the crucible. Dissolution of the sample into the flux occurs in the presence of heat provided by heater 24.
- the mold assembly 16 comprises a rigid case containing a re-meltable material 32, such as gold.
- a re-meltable material 32 such as gold.
- This material must be denser than molten flux, must be inert to the material, must have a melting point below 1200° C, and must not adhere to flux.
- the gold is melted while the sample is still in the crucible, thus forming a smooth receiving surface. Upon pouring, the flux floats upon the molten gold. Mold 16 is then cooled by operating a valve 34 to inject inert gas under mold 16, forming a glassy disk on top of the gold.
- the base of mold 16 is a plain, polished surface, while its upper portion is hollowed out with a conical wall to allow easy removal of the disk.
- the lower portion of mold 16 contains an undercut groove portion 36 to retain the gold inside the mold. That is, when the glassy disk is removed, the solidified gold is held in place at the bottom of the crucible by the solidified gold forming toward the bottom of the crucible as shown, which holds the gold in place and allows only the glassy disk to be removed.
Abstract
Description
Claims
Priority Applications (5)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
KR1020147008556A KR20140091518A (en) | 2011-08-30 | 2012-08-29 | Preparation of inorganic samples by fusion |
ES12828170T ES2725789T3 (en) | 2011-08-30 | 2012-08-29 | Preparation of inorganic samples by fusion |
EP12828170.6A EP2750849B1 (en) | 2011-08-30 | 2012-08-29 | Preparation of inorganic samples by fusion |
CN201280051961.4A CN103930250B (en) | 2011-08-30 | 2012-08-29 | Inorganic samples is prepared by fusion |
AU2012302126A AU2012302126B2 (en) | 2011-08-30 | 2012-08-29 | Preparation of inorganic samples by fusion |
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US13/220,904 US8403025B2 (en) | 2011-08-30 | 2011-08-30 | Preparation of inorganic samples by fusion |
US13/220,904 | 2011-08-30 |
Publications (1)
Publication Number | Publication Date |
---|---|
WO2013033153A1 true WO2013033153A1 (en) | 2013-03-07 |
Family
ID=47742501
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
PCT/US2012/052783 WO2013033153A1 (en) | 2011-08-30 | 2012-08-29 | Preparation of inorganic samples by fusion |
Country Status (7)
Country | Link |
---|---|
US (1) | US8403025B2 (en) |
EP (1) | EP2750849B1 (en) |
KR (1) | KR20140091518A (en) |
CN (1) | CN103930250B (en) |
AU (1) | AU2012302126B2 (en) |
ES (1) | ES2725789T3 (en) |
WO (1) | WO2013033153A1 (en) |
Families Citing this family (5)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US20160003720A1 (en) * | 2014-07-07 | 2016-01-07 | Spex Sample Prep Llc | Apparatus Comprising an Increased-Capacity Platinumware Holder and Method Therefor |
AU2015318537B2 (en) * | 2014-09-15 | 2021-02-25 | Materiaux Nieka Inc. | Method and apparatus for preparing an analytical sample by fusion |
CN104197008A (en) * | 2014-09-28 | 2014-12-10 | 无锡市新颖密封材料厂 | Production technology for graphite gasket |
US10814388B2 (en) | 2018-01-24 | 2020-10-27 | General Electric Company | Heated gas circulation system for an additive manufacturing machine |
US10814395B2 (en) | 2018-01-24 | 2020-10-27 | General Electric Company | Heated gas circulation system for an additive manufacturing machine |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB1357003A (en) * | 1971-02-04 | 1974-06-19 | British Aircraft Corp Ltd | Production of foamed synthetic resin materials |
FR2381303A1 (en) * | 1977-02-21 | 1978-09-15 | Siderurgie Fse Inst Rech | APPARATUS FOR THE AUTOMATIC PREPARATION OF SAMPLES INTENDED FOR X-FLUORESCENCE ANALYSIS |
JPS6027847A (en) * | 1983-07-26 | 1985-02-12 | Nippon Steel Corp | Preparation of specimen for fluorescent x-ray analysis |
FR2556095B1 (en) * | 1983-12-02 | 1986-09-05 | Philips Ind Commerciale | AUTOMATIC SAMPLE DOSING PROCESS AND AUTOMATIC MACHINE FOR DOSING AND ANALYZING |
US4865784A (en) * | 1989-02-21 | 1989-09-12 | Hill Francis U | Method of making porous inorganic particle filled polyimide foam insulation products |
US5269827A (en) * | 1991-03-01 | 1993-12-14 | Leco Corporation | Analytical sample preparation system |
JPH1164186A (en) * | 1997-08-18 | 1999-03-05 | Daido Steel Co Ltd | Preparing method for specimen for fluorescent x-ray analysis |
DE10361525B4 (en) * | 2003-12-23 | 2005-11-17 | Umicore Ag & Co. Kg | Process for the preparation of orodispersible tablets for the determination of the content of ceramic powders on platinum group metals by means of RFA |
US20090295013A1 (en) * | 2005-12-16 | 2009-12-03 | Bin Luo | Method and apparatus for manufacturing plastic products |
AU2007202703B2 (en) * | 2007-05-04 | 2009-01-15 | X-Ray Flux Pty Ltd | X-ray flux composition |
AU2010249195B1 (en) * | 2010-12-07 | 2011-06-30 | X-Ray Flux Pty Ltd | Lithium X-Ray flux composition |
-
2011
- 2011-08-30 US US13/220,904 patent/US8403025B2/en active Active
-
2012
- 2012-08-29 EP EP12828170.6A patent/EP2750849B1/en active Active
- 2012-08-29 KR KR1020147008556A patent/KR20140091518A/en not_active Application Discontinuation
- 2012-08-29 WO PCT/US2012/052783 patent/WO2013033153A1/en active Application Filing
- 2012-08-29 AU AU2012302126A patent/AU2012302126B2/en not_active Ceased
- 2012-08-29 ES ES12828170T patent/ES2725789T3/en active Active
- 2012-08-29 CN CN201280051961.4A patent/CN103930250B/en not_active Expired - Fee Related
Non-Patent Citations (1)
Title |
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No relevant documents disclosed * |
Also Published As
Publication number | Publication date |
---|---|
AU2012302126A1 (en) | 2014-04-17 |
CN103930250A (en) | 2014-07-16 |
ES2725789T3 (en) | 2019-09-27 |
CN103930250B (en) | 2016-10-19 |
EP2750849A4 (en) | 2015-08-26 |
US8403025B2 (en) | 2013-03-26 |
KR20140091518A (en) | 2014-07-21 |
EP2750849A1 (en) | 2014-07-09 |
US20130049247A1 (en) | 2013-02-28 |
EP2750849B1 (en) | 2019-02-20 |
AU2012302126B2 (en) | 2017-01-12 |
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