Shungite is an incredible stone with some pretty mindblowing potential and proven abilites! What makes Shungite so special is the FULLERENES in its internal structure. What are Fullerenes? And what exactly do they do? Read on to find out!
Estimated reading time: 9 minutes
Table of contents
- Shungite is an incredible stone with some pretty mindblowing potential and proven abilites! What makes Shungite so special is the FULLERENES in its internal structure. What are Fullerenes? And what exactly do they do? Read on to find out!
- SHUNGITE HEALING PROPERTIES
- ELITE NOBLE VS CLASSIC SHUNGITE
- WHAT ARE FULLERENES?
- OK, BUT… BUCKYBALLS?
- WHEN WERE FULLERENES DISCOVERED?
- THE ORIGIN OF SHUNGITE & FULLERENES
- WHAT CAN FULLERENES DO?
What makes Shungite so unique, and such an exciting find, is in its atomic arrangement. This is the third article on Shungite in our series. This article is taking a deep dive into Fullerenes and will get a bit technical.
SHUNGITE HEALING PROPERTIES
Article one will give you all the highlights on Shungite.
ELITE NOBLE VS CLASSIC SHUNGITE
Article two will explain how Shungite is graded, and what the difference is.
Carbon is the primary content of Shungite. It’s also the building material for our planet – and the basis of all living organisms on Earth. It has the most Allotropes (i.e. modifications or different arrangements of atoms) of all the elements.
Examples of Carbon Allotropes include Diamond, Graphite, Carbyne and the special Fullerenes in Shungite.
WHAT ARE FULLERENES?
Fullerenes are 3D spherical molecules (resembling soccer balls). They’re made of 60, 70 or more carbon atoms (known as C60, C70 or Cn) bound in linear chains forming a lattice.
This formation has also been referred to as a type of carbon nanostructure (CNS).
The C60 fullerene is often referred to as “buckyballs”.
OK, BUT… BUCKYBALLS?
The most famous fullerene is the C60, also known as the “Buckminsterfullerene”. It consists of 60 carbon atoms.
The C60 fullerene garnered the nickname “buckyballs” after the famous American architect and futurist Richard Buckminster “Bucky” Fuller.
Fuller designed the geodesic dome, whose shape resembles the structure of the C60 molecule.
The molecule is formed by twenty hexagons and twelve pentagons. A carbon atom is at each vertex of each polygon and there is a bond along each polygon edge.
The C60 formation is the most symmetrical molecule a carbon atom can take.
WHEN WERE FULLERENES DISCOVERED?
Originally, this CNS fullerene structure was just a hypothesis – and one that science didn’t take much heed in at that! Then, in the 80s, scientists accidentally created them in a lab as a byproduct of another experiment. This accidental discovery led to a Nobel Prize award in 1996 jointly to the scientists involved (Professor Robert F. Curl, Harold W. Kroto and Richard E. Smalley). Finally, Fullerenes were found existing in nature in 1992 – in Shungite. This was the first time natural fullerenes had been found, and not artificially made in a lab!
“Nature, it turns out, made a molecule long before people did… Carbon-based molecules shaped like soccer balls have fascinated chemists since the first one was synthesized seven years ago. Now for the first time these molecules, fullerenes, have been found in nature, lodged in rock that seems to date from the dawn of life on our planet. The discovery, reported in today’s issue of the journal Science, has mystified scientists, who cannot explain the origin of the natural fullerene molecules or even of the enigmatic mineral in which they were found.”New York Times, 1992
K.S.Misra of the Geological Survey of India (GSI) was the first to report fullerene-bearing shungitic rocks from the volcano-sedimentary Proterozoic formations. Both C60 and C70 forms of fullerene were identified by laser desorption/ionization spectrometry in black carbonaceous shales (now called shungitic rocks) having an organic carbon content of 5-13%. The associated rocks include grey shales, dolomites and quartzites.
“We report on the occurrence of fullerenes in Proterozoic shungite (∼2 Ga) from the shungite mine, Kondopoga, Karelia, Russia (62.12°N 34.17°E). The presence of fullerenes has been confirmed by mass spectrometry, with peaks at 360 and 720 amu (atomic mass unit), powder X-ray diffraction showing ten diffraction peaks corresponding to the fullerite structure with a = 1.4201(5) nm, and 13C nuclear magnetic resonance (NMR) spectroscopic studies, showing a peak at 143.2 ppm. In the Kondopoga shungite mine, fullerenes occur in silty shales that have experienced greenshist facies metamorphism.”G. Parthasarathy, et al- “Occurrence of natural fullerenes in low grade metamorphosed Proterozoic shungite from Karelia, Russia”, Geochimica et Cosmochimica Acta, Volume 62, Issues 21–22, 1998
THE ORIGIN OF SHUNGITE & FULLERENES
AS discussed in article 1, Shungite’s origins were initially shrouded in mystery. It’s currently accepted by most scientists that Shungite was most likely formed from emerging fungi / microorganisms. However, some still believe that the fullerenes were in fact brought here on a meteoroid from space.
In the 2012 paper “Fullerenes and The Origin of Life“, scientists hypothesise further on this theory:
“We hypothesize that by virtue of the unique properties of fullerene, this hollow, ultra-robust, large, purely carbon molecule was the earliest progenitor of life. It acted as a stable universal biologic template on which small molecules spontaneously assembled and then formed, by further assembly, a surface mantle (here termed rosasome) of larger molecules. We submit that this process, by its inherent flexibility, initiated evolution, allowing the emergence of parallel diverse rosasome lines responding selectively to varying spatial environments.“Goodman G, et al. Fullerene and the origin of life. Isr Med Assoc J. 2012 Oct;14(10):602-6. PMID: 23193780.
WHAT CAN FULLERENES DO?
Fullerene’s unique carbon cage structure coupled with its immense scope for derivatization make them incredibly interesting as a potential therapeutic agent. Some say their usefulness could be infinite.
Fullerenes, specificaly C60, have anti-viral and anti-oxidant activity – with strong implications in the treatment of HIV.
They are also being studied as treatment for antibiotic-resistant bacteria (by binding specific antibiotics to the structure to target the resistant bacteria) – and even target certain cancer cells.
Fullerenes light-activated anti-microbial agent properties are also under study.
“The fullerene family, and especially C60, has appealing photo, electrochemical and physical properties, which can be exploited in various medical fields. Fullerene is able to fit inside the hydrophobic cavity of HIV proteases, inhibiting the access of substrates to the catalytic site of enzyme. It can be used as radical scavenger and antioxidant. At the same time, if exposed to light, fullerene can produce singlet oxygen in high quantum yields. This action, together with direct electron transfer from excited state of fullerene and DNA bases, can be used to cleave DNA. In addition, fullerenes have been used as a carrier for gene and drug delivery systems. Also they are used for serum protein profiling as MELDI material for biomarker discovery.“Bakry, R., et al. (2007). Medicinal applications of fullerenes. International journal of nanomedicine, 2(4), 639–649.
In the 1970s, shungite was exploited in the production of an insulating material, known as shungisite. Shungisite is prepared by heating rocks with low shungite concentrations to 1090–1130 °C and is used as a low density filler.
FULLERENE USES INCLUDE:
- Antiviral agents
- Gene and drug delivery
- Photosensitizers in photodynamic therapy
- Commercial technologies including nanosphere powders, protective eye wear and solar cells
- Chemical technologies including hydrogen storage and lubrication
- Endless biomedicine exploration, from Cartilage degeneration treatment and Osteoporosis therapy to HIV, cancer, Alzheimer’s & Parkinson’s disease treatment
- “Technical Physics Letters” Vol. 26 No 8, 9, and 15 doi:10.1134/1.1307814. S2CID 5199911
- “A Giant Paleoproterozoic Deposit of Shungite in NW Russia: Genesis & Practical Applications” – Melezhik, V.A.; Filippov M.M.; Romashkin A.E
- Ore Geology Reviews – Elsevier
- “Organic & Mineral Matter in a Precambrian Shungite from Karelia, Russia” – Mastarlez, M.; Glikson M.; Stankiewicz B.A.; Volkova I.B.; Bustin R.M.
- “Organic Matter & Mineralisation: Thermal Alteration, Hydrocarbon Generation, and Role in Metallogenesis” – Springer
- “Pigment Compendium: A Dictionary & Optical Microscopy of Historic Pigments” – Easthaugh, N.; Walsh V.; Chaplin T.; Siddall R. Routledge.
- “Water Treatment with a Shungite Sorbent & Biosorbents on its Base” – Efremova, S.V. Russian Journal of Applied Chemistry
- “Medical Geology in Russia and NIS” – Volfson, I.F.; Farrakhov E.G.; Pronin A.P.; Beiseyev O.B.; Beiseyev A.O.; Bogdasarov M.A.; Oderova A.V.; Pechenkin I.G.; Khitrov A.E.; Pikhur O.L.; Plotkina J.V.; Frank-Kamanetskya O.V.; Rosseeva E.V.; Denisova O.A.; Chernogoryuk G.E.; Baranovskya N.; Rikhvanov L.P.; Petrov I.M.; Saghatelyan A.K.; Sahakyan L.V.; Menchinskaya O.V.; Zangiyeva T.D; Kajtukov M.Z.; Uzdenova Z.H.; Dorozhko A.L.
- “Medical Geology in Russia and NIS” – Selinus O.; Finkelman R.B.; Centeno J.A.
- “Medical Geology: A Regional Synthesis” – Springer
- Augustyniak-Jabłokow, M.A., V. Yablokov, Y.V., Andrzejewski, B., Kempiński, W., Łoś, S., Tadyszak, K., Yablokov, M.Y., Zhikharev, V.A. (2010) EPR and magnetism of the nanostructured natural carbonaceous material shungite. Physics and Chemistry of Minerals: 37: 237-247.
- Mosin, O. & Ignatov, I. (2013) The structure and composition of natural carbonaceous fullerene containing mineral shungite. International Journal of Advanced Scientific and Technical Research, 6 (3), 9-21.
- Melezhik, V.A.; Filippov M.M.; Romashkin A.E. (2004). “A giant Paleoproterozoic deposit of shungite in NW Russia: genesis and practical applications”. Ore Geology Reviews. Elsevier. 24 (1–2): 135–154. doi:10.1016/j.oregeorev.2003.08.003
- Tegos, G. P.; Demidova, T. N.; Arcila-Lopez, D.; Lee, H.; Wharton, T.; Gali, H.; Hamblin, M. R. (2005). “Cationic Fullerenes Are Effective and Selective Antimicrobial Photosensitizers”. Chemistry & Biology. 12 (10): 1127–1135. doi:10.1016/j.chembiol.2005.08.014. PMC 3071678. PMID 16242655