MINERALS and Their LOCALITIES
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Dr. Öğr. Üyesi Fatma Tuğçe (Şenberber) Dumanli
DR. ÖĞR. ÜYESİ FATMA TUĞÇE (ŞENBERBER) DUMANLI ÖZGEÇMİŞ VE ESERLER LİSTESİ ÖZGEÇMİŞ 1. Adı Soyadı : FATMA TUĞÇE (ŞENBERBER) DUMANLI İletişim Bilgileri Adres : Cevizlik Mah. Kırmızı Şebboy Sok. Ebru Ap. A Blok 11/14 Bakırköy- İSTANBUL Telefon : 0554 3021265 Mail : [email protected] 2. Doğum Tarihi : 10/03/1988 3. Unvanı: DOKTOR ÖĞRETİM ÜYESİ 4. Öğrenim Durumu: Derece Alan Üniversite Yıl Lisans Kimya Mühendisliği ABD YTU, Fen Bilimleri Enstitüsü 2006-2010 Y. Lisans Kimya Mühendisliği ABD YTU, Fen Bilimleri Enstitüsü 2010-2012 Doktora Kimya Mühendisliği ABD YTU, Fen Bilimleri Enstitüsü 2012-2016 Yüksek Lisans Tez Başlığı ve Tez Danışmanı: “Magnezyum Oksit ve Borik Asit Kaynaklarından Magnezyum Boratların Üretimi, Karakterizasyonu ve Üretimi Etkileyen Faktörlerin İncelenmesi” YTÜ Fen Bilimleri Enstitüsü, Kimya Mühendisliği Anabilim Dalı, 2012. Tez Danışmanı: Yrd.Doç. Dr. Emek Möröydor Derun Doktora Tez Başlığı ve Tez Danışmanı: “Elektrik İletkenliğe Sahip Yeni Nesil Boyanın Isıl İletkenlik Özelliklerinin Belirlenmesi” YTÜ Fen Bilimleri Enstitüsü, Kimya Mühendisliği Anabilim Dalı, 2016. Tez Danışmanı: Prof. Dr. Sabriye Pişkin 1 5. Akademik Unvanlar Akademik Görev Görev Ünvanı Görev Yeri Yıl Dr.Öğr.Üyesi Nişantaşı Üniversitesi, Mühendislik ve Mimarlık Fakültesi, 2018-… İnşaat Mühendisliği Bölümü Öğr. Gör. Dr. Ataşehir Adıgüzel Meslek Yüksekokulu, İş Sağlığı ve 2016-2018 Güvenliği Programı 6. Yayınlar 6.1. Uluslararası hakemli dergilerde yayımlanan makaleler: 6.1.1. SCI/SCI-exp 1. Senberber, F.T., Kipcak, A.S., Vardar, D.S., Tugrul, N. (2020). Ultrasonic-Assisted Synthesis of Zinc Borates: Effect of Boron Sources, Journal of Chemical Society of Pakistan, Volume 42, Issue 6, pp. 839 – 845. 2. Senberber, F.T., Dere Ozdemir, O. (2020). Effect of Synthesis Parameters on the Color Performance of Blue CoAl2O4 Ceramic Pigment, Russian Journal of Inorganic Chemistry, Volume 65, Issue 14, pp. -
Mineral Processing
Mineral Processing Foundations of theory and practice of minerallurgy 1st English edition JAN DRZYMALA, C. Eng., Ph.D., D.Sc. Member of the Polish Mineral Processing Society Wroclaw University of Technology 2007 Translation: J. Drzymala, A. Swatek Reviewer: A. Luszczkiewicz Published as supplied by the author ©Copyright by Jan Drzymala, Wroclaw 2007 Computer typesetting: Danuta Szyszka Cover design: Danuta Szyszka Cover photo: Sebastian Bożek Oficyna Wydawnicza Politechniki Wrocławskiej Wybrzeze Wyspianskiego 27 50-370 Wroclaw Any part of this publication can be used in any form by any means provided that the usage is acknowledged by the citation: Drzymala, J., Mineral Processing, Foundations of theory and practice of minerallurgy, Oficyna Wydawnicza PWr., 2007, www.ig.pwr.wroc.pl/minproc ISBN 978-83-7493-362-9 Contents Introduction ....................................................................................................................9 Part I Introduction to mineral processing .....................................................................13 1. From the Big Bang to mineral processing................................................................14 1.1. The formation of matter ...................................................................................14 1.2. Elementary particles.........................................................................................16 1.3. Molecules .........................................................................................................18 1.4. Solids................................................................................................................19 -
Molecular Biogeochemistry, Lecture 8
12.158 Lecture Pigment-derived Biomarkers (1) Colour, structure, distribution and function (2) Biosynthesis (3) Nomenclature (4) Aromatic carotenoids ● Biomarkers for phototrophic sulfur bacteria ● Alternative biological sources (5) Porphyrins and maleimides Many of the figures in this lecture were kindly provided by Jochen Brocks, RSES ANU 1 Carotenoid pigments ● Carotenoids are usually yellow, orange or red coloured pigments lutein β-carotene 17 18 19 2' 2 4 6 8 3 7 9 16 1 5 lycopenelycopene 2 Structural diversity ● More than 600 different natural structures are known, ● They are derived from the C40 carotenoid lycopene by varied hydrogenation, dehydrogenation, cyclization and oxidation reaction 17 18 19 2' 2 4 6 8 3 7 9 16 1 5 lycopene neurosporene α-carotene γ -carotene spirilloxanthin siphonaxanthin canthaxanthin spheroidenone 3 Structural diversity Purple non-sulfur bacteria peridinin 7,8-didehydroastaxanthin okenone fucoxanthin Biological distribution ● Carotenoids are biosynthesized de novo by all phototrophic bacteria, eukaryotes and halophilic archaea ● They are additionally synthesized by a large variety of non-phototrophs ● Vertebrates and invertebrates have to incorporate carotenoids through the diet, but have often the capacity to structurally modifiy them 4 Carotenoid function (1) Accessory pigments in Light Harvesting Complex (LHC) (annual production by marine phytoplancton alone: 4 million tons) e.g. LH-II Red and blue: protein complex Green: chlorophyll Yellow: lycopene (2) Photoprotection (3) photoreceptors for phototropism -
Infrared and Raman Spectroscopic Characterization of the Carbonate Bear- Ing Silicate Mineral Aerinite - Implications for the Molecular Structure
This may be the author’s version of a work that was submitted/accepted for publication in the following source: Frost, Ray, Scholz, Ricardo, & Lopez Toro, Andres (2015) Infrared and Raman spectroscopic characterization of the carbonate bear- ing silicate mineral aerinite - Implications for the molecular structure. Journal of Molecular Structure, 1097, pp. 1-5. This file was downloaded from: https://eprints.qut.edu.au/84503/ c Consult author(s) regarding copyright matters This work is covered by copyright. Unless the document is being made available under a Creative Commons Licence, you must assume that re-use is limited to personal use and that permission from the copyright owner must be obtained for all other uses. If the docu- ment is available under a Creative Commons License (or other specified license) then refer to the Licence for details of permitted re-use. It is a condition of access that users recog- nise and abide by the legal requirements associated with these rights. If you believe that this work infringes copyright please provide details by email to [email protected] License: Creative Commons: Attribution-Noncommercial-No Derivative Works 2.5 Notice: Please note that this document may not be the Version of Record (i.e. published version) of the work. Author manuscript versions (as Sub- mitted for peer review or as Accepted for publication after peer review) can be identified by an absence of publisher branding and/or typeset appear- ance. If there is any doubt, please refer to the published source. https://doi.org/10.1016/j.molstruc.2015.05.008 Infrared and Raman spectroscopic characterization of the carbonate bearing silicate mineral aerinite – implications for the molecular structure Ray L. -
Thirty-Fourth List of New Mineral Names
MINERALOGICAL MAGAZINE, DECEMBER 1986, VOL. 50, PP. 741-61 Thirty-fourth list of new mineral names E. E. FEJER Department of Mineralogy, British Museum (Natural History), Cromwell Road, London SW7 5BD THE present list contains 181 entries. Of these 148 are Alacranite. V. I. Popova, V. A. Popov, A. Clark, valid species, most of which have been approved by the V. O. Polyakov, and S. E. Borisovskii, 1986. Zap. IMA Commission on New Minerals and Mineral Names, 115, 360. First found at Alacran, Pampa Larga, 17 are misspellings or erroneous transliterations, 9 are Chile by A. H. Clark in 1970 (rejected by IMA names published without IMA approval, 4 are variety because of insufficient data), then in 1980 at the names, 2 are spelling corrections, and one is a name applied to gem material. As in previous lists, contractions caldera of Uzon volcano, Kamchatka, USSR, as are used for the names of frequently cited journals and yellowish orange equant crystals up to 0.5 ram, other publications are abbreviated in italic. sometimes flattened on {100} with {100}, {111}, {ill}, and {110} faces, adamantine to greasy Abhurite. J. J. Matzko, H. T. Evans Jr., M. E. Mrose, lustre, poor {100} cleavage, brittle, H 1 Mono- and P. Aruscavage, 1985. C.M. 23, 233. At a clinic, P2/c, a 9.89(2), b 9.73(2), c 9.13(1) A, depth c.35 m, in an arm of the Red Sea, known as fl 101.84(5) ~ Z = 2; Dobs. 3.43(5), D~alr 3.43; Sharm Abhur, c.30 km north of Jiddah, Saudi reflectances and microhardness given. -
Yuksporite (K; Ba)(Na; Sr)Ca2(Si; Ti)4O11(F; OH) ² H2O C 2001 Mineral Data Publishing, Version 1.2 ° Crystal Data: Orthorhombic
Yuksporite (K; Ba)(Na; Sr)Ca2(Si; Ti)4O11(F; OH) ² H2O c 2001 Mineral Data Publishing, version 1.2 ° Crystal Data: Orthorhombic. Point Group: n.d. Fibrous, scaly, or lamellar; in irregular aggregates, to 10 cm. Physical Properties: Hardness = 5 D(meas.) = 3.05(3) D(calc.) = [2.98] Optical Properties: Semitransparent. Color: Rose-red to straw-yellow. Optical Class: Biaxial (+). Pleochroism: Marked; X = pale rose-yellow; Y = Z = rose-yellow. ® = 1.644(2) ¯ = n.d. ° = 1.660(2) 2V(meas.) = 46±{76± Cell Data: Space Group: n.d. a = 24.869(8) b = 16.756(6) c = 7.057(3) Z = 10 X-ray Powder Pattern: Khibiny massif, Russia. 2.778 (10), 3.00 (9), 1.786 (9), 3.10 (8), 3.05 (8), 1.888 (7), 2.92 (6) Chemistry: (1) (2) (1) (2) SiO2 40.92 38.40 BaO 8.60 TiO2 11.00 Na2O 7.94 3.84 Al2O3 0.07 K2O 12.57 6.15 Fe2O3 9.10 0.75 F 3.05 MnO 0.91 0.29 Cl 0.80 + MgO 0.42 H2O 2.20 CaO 20.56 18.90 H2O 8.52 SrO 5.87 O = (F; Cl) 1.46 ¡ 2 Total 100.94 [98.46] (1) Khibiny massif, Russia. (2) Murun massif, Russia; original total given as 99.07%, 3+ corresponds to (K0:70Ba0:30)§=1:00(Na0:66Sr0:30)§=0:96(Ca1:80Ti0:19Fe0:06Mn0:02)§=2:07 (Si3:42Ti0:57Al0:01)§=4:00O11[F0:86Cl0:12(OH)0:02]§=1:00 ² 0:6H2O: Occurrence: In veins in nepheline syenite in a di®erentiated alkalic massif (Khibiny massif, Russia). -
Paleomineralogy of the Hadean Eon: What Minerals Were Present at Life’S Origins?
Paleomineralogy of the Hadean Eon: What Minerals Were Present at Life’s Origins? Robert M. Hazen—Geophysical Lab 1st ELSI International Symposium Tokyo Institute of Technology March 30, 2013 CONCLUSIONS As many as 90% of the 4700 known mineral species were not present on Earth prior to the origins of life before ~4.0 billion years ago. Origins-of-life models that rely on minerals for catalysis, selection, concentration, protection, or other processes must employ plausible prebiotic mineral species. List of 420 Mineral Species R. M. Hazen (2013) “Paleomineralogy of the Hadean Eon: A Preliminary List” American Journal of Science, in press. What Is Mineral Evolution? A change over time in: • The diversity of mineral species • The relative abundances of minerals • The compositional ranges of minerals • The grain sizes and morphologies of minerals “Ur”-Mineralogy Pre-solar grains contain about a dozen micro- and nano-mineral phases: • Diamond/Lonsdaleite • Graphite (C) • Moissanite (SiC) • Osbornite (TiN) • Nierite (Si3N4) • Rutile (TiO2) • Corundum (Al O ) 2 3 • Spinel (MgAl2O4) • Hibbonite (CaAl12O19) • Forsterite (Mg2SiO4) • Nano-particles of TiC, ZrC, MoC, FeC, Fe-Ni metal within graphite. • GEMS (silicate glass with embedded metal and sulfide). Mineral Evolution: How did we get from a dozen minerals to >4700 on Earth today? What minerals were not present at the origin of life (~4.0 Ga), and why? Mineral Evolution What Drives Mineral Evolution? Deterministic and stochastic processes that occur on any terrestrial body: 1. The progressive separation and concentration of chemical elements from their original uniform distribution. What Drives Mineral Evolution? Deterministic and stochastic processes that occur on any terrestrial body: 1. -
L'leve~Th List of New Mineral Na~Es. ~
556 L'leve~th list of new mineral na~es. ~ By L. J. SPENCER, M.A., Sc.D., F.R.S. Keeper of Minerals ia the British Museum (Natural History). [Communicated June 12~ 1928.] Ajkaite. (L. Zeehmeister, Math. Termdszettud. ~:rtesitS, Badapest, 1926, vol. 43, p. 332 (ajkait); L. Zechmeister and V. Vrab~ly, Per. Deutsch. Chem. Gesell., 1926, vol. 59, Abt. B, p. 1426). The same as ajkite (Bull. Soc. Min. France, 1878, vol. 1, p. 126 ; abstract from... ?). A fossil resin containing 1-5 ~ sulphur and no succinic acid, from Ajka, com. Veszpr~m, Hungary. [M.A. 3-362.] Albiclase. A. N. Winchell, 1925. Journ. Geol. Chicago, vol. 83, p. 726 ; Elements of optical mineralogy, 2nd edit., 1927, pt. 2, p. 319. P. Niggli, Lehrbuch Min., 1926, vol. 2, p. 536 (Albiklas). A contrac- tion of albite-oligoclase for felspars of the plagioclase series ranging in composition from Ab~Anlo to AbsoAn~o. Allite. tL Harrassowitz, 1926. Laterit, Material und Versuch erdgesehichtlicher Auswertung, Berlin 1926, p. 255 (Allit, plur. Allite). A rock-name to include both bauxite and laterite. Later (Metall und Erz, Halle, ]927, vol. 24, p. 589) bauxite with A1208. H~O is distinguished as monohydrallite (Monohydrallit) and laterite with Al~0s.3H20 as trihydrallite (Trihydrallit). These, although suggestive of mineral- names (and given so i~ error in Chem. Zentr., 1926, vol. 1, p. 671), are proposed as rock-names ; from aluminium and M~o~. Similarly, siallites (1926, p. 252, Siallit, from Si, A1, M0o~), to include kaolinite and allo- phanite, are rocks composed of the aluminium silicates kaolin and allophane. -
New Mineral Names*
American Mineralogist, Volume 73, pages 1492-1499. 1988 NEW MINERAL NAMES* JOHN L. JAMBOR CANMET, 555 Booth Street, Ottawa, Ontario KIA OGI, Canada ERNST A. J. BURKE lnstituut voor Aardwetenschappen, Vrije Universitiete, De Boelelaan 1085, 1081 HV, Amsterdam, Netherlands T. SCOTT ERCIT, JOEL D. GRICE National Museum of Natural Sciences, Ottawa, Ontario KIA OM8, Canada Acuminite* prismatic to acicular crystals that are up to 10 mm long and 0.5 H. Pauly, O.Y. Petersen (1987) Acuminite, a new Sr-fluoride mm in diameter, elongate and striated [001], rhombic to hex- from Ivigtut, South Greenland. Neues Jahrb. Mineral. Mon., agonal in cross section, showing {l00} and {l10}. Perfect {100} 502-514. cleavage, conchoidal fracture, vitreous luster, H = 4, Dm'.. = 2.40(5) glcm3 (pycnometer), Dcale= 2.380 glcm3 for the ideal Wet-chemical analysis gave Li 0.0026, Ca 0.0185, Sr 37.04, formula, and Z = 4. Optically biaxial positive, a = 1.5328(4), (3 Al 11.86, F 33.52, OH (calc. from anion deficit) 6.82, H20 (calc. = 1.5340(4), 1.5378(4), 2 Vmoa,= 57(2)°, 2 Vcale= 59°; weak assuming 1 H20 in the formula) 7.80, sum 97.06 wt%, corre- 'Y = dispersion, r < v; Z = b, Y A c = -10°. X-ray structural study sponding to Sro98AIl.o2F.o7(OH)o.93H20. The mineral occurs as indicated monoclinic symmetry, space group C21c, a = 18.830(2), aggregates of crystals shaped like spear points and about I mm b= I 1.517(2), c= 5.190(I)A,{3 = 100.86(1)°. A Guinierpowder long. -
Carbon Mineral Ecology: Predicting the Undiscovered Minerals of Carbon
American Mineralogist, Volume 101, pages 889–906, 2016 Carbon mineral ecology: Predicting the undiscovered minerals of carbon ROBERT M. HAZEN1,*, DANIEL R. HUMMER1, GRETHE HYSTAD2, ROBERT T. DOWNS3, AND JOSHUA J. GOLDEN3 1Geophysical Laboratory, Carnegie Institution, 5251 Broad Branch Road NW, Washington, D.C. 20015, U.S.A. 2Department of Mathematics, Computer Science, and Statistics, Purdue University Calumet, Hammond, Indiana 46323, U.S.A. 3Department of Geosciences, University of Arizona, 1040 East 4th Street, Tucson, Arizona 85721-0077, U.S.A. ABSTRACT Studies in mineral ecology exploit mineralogical databases to document diversity-distribution rela- tionships of minerals—relationships that are integral to characterizing “Earth-like” planets. As carbon is the most crucial element to life on Earth, as well as one of the defining constituents of a planet’s near-surface mineralogy, we focus here on the diversity and distribution of carbon-bearing minerals. We applied a Large Number of Rare Events (LNRE) model to the 403 known minerals of carbon, using 82 922 mineral species/locality data tabulated in http://mindat.org (as of 1 January 2015). We find that all carbon-bearing minerals, as well as subsets containing C with O, H, Ca, or Na, conform to LNRE distributions. Our model predicts that at least 548 C minerals exist on Earth today, indicating that at least 145 carbon-bearing mineral species have yet to be discovered. Furthermore, by analyzing subsets of the most common additional elements in carbon-bearing minerals (i.e., 378 C + O species; 282 C + H species; 133 C + Ca species; and 100 C + Na species), we predict that approximately 129 of these missing carbon minerals contain oxygen, 118 contain hydrogen, 52 contain calcium, and more than 60 contain sodium. -
Environmental Speciation and Monitoring Needs for Trace Metal -Contai Ni Ng Substances from Energy-Related Processes
STAND NATL iNST OF AU107 1=17^05 NBS 1>l PUBLICATIONS z CO NBS SPECIAL PUBLICATION * / Of U.S. DEPARTMENT OF COMMERCE / National Bureau of Standards -QC 100 .U57 NO. 618 1981 c. 2 NATIONAL BUREAU QF STANDARDS The National Bureau of Standards' was established by an act of Congress on March 3, 1901. The Bureau's overall goal is to strengthen and advance the Nation's science and technology and facilitate their effective application for public benefit. To this end, the Bureau conducts research and provides: (1) a basis for the Nation's physical measurement system, (2) scientific and technological services for industry and government, (3) a technical basis for equity in trade, and (4) technical services to promote public safety. The Bureau's technical work is per- formed by the National Measurement Laboratory, the National Engineering Laboratory, and the Institute for Computer Sciences and Technology. THE NATIONAL MEASUREMENT LABORATORY provides the national system of physical and chemical and materials measurement; coordinates the system with measurement systems of other nations and furnishes essential services leading to accurate and uniform physical and chemical measurement throughout the Nation's scientific community, industry, and commerce; conducts materials research leading to improved methods of measurement, standards, and data on the properties of materials needed by industry, commerce, educational institutions, and Government; provides advisory and research services to other Government agencies; develops, produces, and distributes -
The Effect of Solution Density on the Synthesis of Magnesium Borate from Boron-Gypsum
World Academy of Science, Engineering and Technology International Journal of Chemical and Molecular Engineering Vol:8, No:10, 2014 The Effect of Solution Density on the Synthesis of Magnesium Borate from Boron-Gypsum N. Tugrul, E. Sariburun, F. T. Senberber, A. S. Kipcak, E. Moroydor Derun, S. Piskin reaction mixture to up to a size large enough to be filtered out Abstract—Boron-gypsum is a waste which occurs in the boric of the solution. acid production process. In this study, the boron content of this waste Gypsum crystallization reaction is given in (2): is evaluated for the use in synthesis of magnesium borates and such evaluation of this kind of waste is useful more than storage or Ca 2+ 2SO2- + H O (l) CaSO 2H O(s) (2) disposal. Magnesium borates, which are a sub-class of boron 4 2 4 2 minerals, are useful additive materials for the industries due to their remarkable thermal and mechanical properties. Magnesium borates Boron-Gypsum which is waste product of boric acid were obtained hydrothermally at different temperatures. Novelty of production process consist gypsum, B2O3 and some impurities this study is the search of the solution density effects to magnesium that causes various environmental and storage problems. The borate synthesis process for the increasing the possibility of boron- content of B2O3 in boron-gypsum obtained during the boric gypsum usage as a raw material. After the synthesis process, products acid production increases up to 7%. It is a valuable industrial are subjected to XRD and FT-IR to identify and characterize their crystal structure, respectively.