TheVerneuil method(orVerneuil processorVerneuil technique), also calledflame fusion,was the first commercially successful method of manufacturing syntheticgemstones,developed in the late 1883[1]by theFrenchchemistAuguste Verneuil.It is primarily used to produce theruby,sapphireandpadparadschavarieties ofcorundum,as well as thediamond simulantsrutile,strontium titanateand spinel. The principle of the process involves melting a finely powdered substance using anoxyhydrogenflame, and crystallising the melted droplets into aboule.The process is considered to be the founding step of modern industrialcrystal growthtechnology, and remains in wide use to this day.[2][3]

Crystallization
Fundamentals
Concepts
Methods and technology

History

edit
A sketch of an early furnace used by Verneuil to synthesise rubies using the Verneuil process.

Since the study ofalchemybegan, there have been attempts to synthetically produce precious stones, andruby,being one of the prizedcardinal gems,has long been a prime candidate. In the 19th century, significant advances were achieved, with the first ruby formed by melting two smaller rubies together in 1817, and the first microscopic crystals created from alumina (aluminium oxide) in a laboratory in 1837. By 1877, chemistEdmond Frémyhad devised an effective method for commercial ruby manufacture by using molten baths of alumina, yielding the first gemstone-quality synthetic stones. TheParisianchemist Auguste Verneuil collaborated with Frémy on developing the method, but soon went on to independently develop the flame fusion process, which would eventually come to bear his name.

One of Verneuil's sources of inspiration for developing his own method was the appearance of synthetic rubies sold by an unknownGenevanmerchant in 1880. These "Geneva rubies" were dismissed as artificial at the time, but are now believed to be the first rubies produced by flame fusion, predating Verneuil's work on the process by 20 years. After examining the "Geneva rubies", Verneuil came to the conclusion that it was possible to recrystallise finely ground aluminium oxide into a large gemstone. This realisation, along with the availability of the recently developed oxyhydrogen torch and growing demand for synthetic rubies, led him to design the Verneuil furnace, where finely ground purified alumina andchromium oxidewere melted by a flame of at least 2,000 °C (3,630 °F), and recrystallised on a support below the flame, creating a large crystal. He announced his work in 1902, publishing details outlining the process in 1904.

By 1910, Verneuil's laboratory had expanded into a 30-furnace production facility, with annual gemstone production by the Verneuil process having reached 1,000 kg (2,200 lb) in 1907. By 1912, production reached 3,200 kg (7,100 lb), and would go on to reach 200,000 kg (440,000 lb) in 1980 and 250,000 kg (550,000 lb) in 2000, led byHrand Djevahird gian's factory inMonthey,Switzerland,founded in 1914. The most notable improvements in the process were made in 1932, byS. K. Popov,who helped establish the capability for producing high-quality sapphires in theSoviet Unionthrough the next 20 years. A large production capability was also established in theUnited StatesduringWorld War II,when European sources were not available, andjewelswere in high demand for their military applications such as for timepieces.

The process was designed primarily for the synthesis of rubies, which became the first gemstone to be produced on an industrial scale. However, the Verneuil process could also be used for the production of other stones, includingblue sapphire,which required oxides ofironandtitaniumto be used in place of chromium oxide, as well as more elaborate ones, such asstar sapphires,where titania (titanium dioxide) was added and the boule was kept in the heat longer, allowing needles ofrutileto crystallise within it. In 1947, theLinde Air Productsdivision ofUnion Carbidepioneered the use of the Verneuil process for creating such star sapphires, until production was discontinued in 1974 owing to overseas competition.

Despite some improvements in the method, the Verneuil process remains virtually unchanged to this day, while maintaining a leading position in the manufacture of synthetic corundum andspinelgemstones. Its most significant setback came in 1917, whenJan Czochralskiintroduced theCzochralski process,which has found numerous applications in thesemiconductor industry,where a much higher quality of crystals is required than the Verneuil process can produce. Other alternatives to the process emerged in 1957, whenBell Labsintroduced thehydrothermal process,and in 1958, whenCarroll Chathamintroduced theflux method.In 1989 Larry P Kelley of ICT, Inc. also developed a variant of the Czochralski process where natural ruby is used as the 'feed' material.

Process

edit
A simplified diagram of the Verneuil process
A small ruby boule, still attached to the rod, produced by the Verneuil process

One of the most crucial factors in successfully crystallising an artificial gemstone is obtaining highly pure starting material, with at least 99.9995% purity.[4]In the case of manufacturing rubies, sapphires orpadparadscha,this material is alumina. The presence ofsodiumimpurities is especially undesirable, as it makes the crystalopaque.[4]But because thebauxitefrom which alumina is obtained is most likely by way of theBayer process(the first stage of which introducescaustic sodain order to separate the Al2O3) particular attention must be paid to the feedstock.[5]

Depending on the desired colouration of the crystal, small quantities of variousoxidesare added, such as chromium oxide for a red ruby, or ferric oxide and titania for a blue sapphire. Other starting materials include titania for producing rutile, or titanyl doubleoxalatefor producing strontium titanate. Alternatively, small, valueless crystals of the desired product can be used.

This starting material is finely powdered, and placed in a container within a Verneuil furnace, with an opening at the bottom through which the powder can escape when the container is vibrated. While the powder is being released,oxygenis supplied into the furnace, and travels with the powder down a narrow tube. This tube is located within a larger tube, into whichhydrogenis supplied. At the point where the narrow tube opens into the larger one,combustionoccurs, with a flame of at least 2,000 °C (3,630 °F) at its core. As the powder passes through the flame, it melts into small droplets, which fall onto an earthen support rod placed below. The droplets gradually form asintercone on the rod, the tip of which is close enough to the core to remain liquid. It is at that tip that theseed crystaleventually forms. As more droplets fall onto the tip, asingle crystal,called aboule,starts to form, and the support is slowly moved downward, allowing the base of the boule to crystallise, while its cap always remains liquid. The boule is formed in the shape of a tapered cylinder, with a diameter broadening away from the base and eventually remaining more or less constant. With a constant supply of powder and withdrawal of the support, very long cylindrical boules can be obtained. Once removed from the furnace and allowed to cool, the boule is split along its vertical axis to relieve internal pressure, otherwise the crystal will be prone to fracture when the stalk is broken due to a verticalparting plane.[6]

When initially outlining the process, Verneuil specified a number of conditions crucial for good results. These include: a flame temperature that is not higher than necessary for fusion; always keeping the melted product in the same part of the oxyhydrogen flame; and reducing the point of contact between the melted product and support to as small an area as possible. The average commercially produced boule using the process is 13 mm (0.51 in) in diameter and 25 to 50 mm (0.98 to 1.97 in) long, weighing about 125 carats (25.0 g). The process can also be performed with a custom-oriented seed crystal to achieve a specific desiredcrystallographic orientation.

Synthetic Corundum

Crystals produced by the Verneuil process are chemically and physically equivalent to their naturally occurring counterparts, and strong magnification is usually required to distinguish between the two. A telltale characteristic is the Verneuil crystal is curved growth lines (curved striae) form, as the cylindrical boule grows upwards in an environment with a highthermal gradient,while the equivalent lines in natural crystals are straight. Another distinguishing feature is the common presence of microscopic gas bubbles formed due to an excess of oxygen in the furnace; imperfections in natural crystals are usually solid impurities.[6]

See also

edit

References

edit
  1. ^Verneuil, Auguste (20 February 1891)."The Chemical News and Journal of Physical Science"[translated from the FrenchRevue Générale des Sciences Pures et Appliquéesvol 2, number 1, 15 January 1891]: 96.{{cite journal}}:Cite journal requires|journal=(help)
  2. ^Dobrovinskaya, Elena R.; Lytvynov, Leonid A.; Pishchik, Valerian (2009).Sapphire: Material, Manufacturing, Applications.Springer Science & Business Media.ISBN9780387856957.
  3. ^Pelleg, Joshua (2016). "Diffusion in Alumina Single Crystals".Diffusion in Ceramics(PDF).Solid Mechanics and Its Applications. Vol. 221. Springer Science & Business Media. pp. 113–177.doi:10.1007/978-3-319-18437-1_11.ISBN978-3-319-18436-4.
  4. ^abBhat, H.L. (2014).Introduction to Crystal Growth: Principles and Practice.CRC Press. p. 173.ISBN9781439883303.
  5. ^Kelly, James Leslie (1962)."A Study of the Influences of Bayer Process Impurities on the Crystallization of Alumina Trihydrate".LSU Historical Dissertations and Theses.A Dissertation Submitted to the Graduate Facility of the Louisiana State University and Agricultural and Mechanical College In partial fulfillment of the requirements for the degree of Doctor of Philosophy in The Department of Chemical Engineering: Louisiana State University and Agricultural & Mechanical College.doi:10.31390/gradschool_disstheses.761.S2CID103735465.
  6. ^ab"Verneuil / Flame-Fusion Method".Gemstone Buzz. Archived fromthe originalon 21 November 2008.