Chapter 3: Atoms, Elements, Minerals, Rocks: Earth s Building Materials. Introduction : What Is A Mineral? Introduction : What Is A Mineral?

Chapter 3: Atoms, Elements, Minerals, Rocks: Earth’s Building Materials Introduction : What Is A Mineral? ƒ The four components of our planet: ƒ Atom...
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Chapter 3: Atoms, Elements, Minerals, Rocks: Earth’s Building Materials

Introduction : What Is A Mineral? ƒ The four components of our planet: ƒ Atom - The smallest individual particle that retains the distinctive properties of a chemical element.

ƒ Element - Any of the 92 naturally occurring fundamental substances into which matter can be broken down chemically (for example, hydrogen, oxygen, carbon, silicon, lead).

Introduction : What Is A Mineral? (2) ƒ Mineral - Naturally formed, inorganic, solid material with a specific chemical composition and a characteristic crystalline structure. ƒ Rock - Naturally formed, coherent mass of one or more minerals, sometimes including organic debris.

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Mineraloids ƒ Mineraloid ƒ Some naturally occurring solid compounds do not meet the definition of a mineral because they lack: - a definite composition, or - a characteristic crystal structure, or - both.

Key Characteristics of Minerals ƒ Minerals have two key characteristics. ƒ Composition: - The chemical elements that compose a mineral, and their proportions.

ƒ Crystal structure: - The organized way in which the atoms of the elements are packed together in a mineral.

Composition of Minerals ƒ A few minerals are composed of a single element (examples are diamond, graphite, gold, copper, and sulfur). ƒ Most minerals are compounds, containing more than one element. ƒ Chemical elements are the most fundamental substances into which matter can be separated by chemical means.

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SALT: Mineral or Element? ƒ Salt (NaCl) is not an element, because it can be separated into sodium and chlorine.

ƒ Sodium (Na) and chlorine (Cl) cannot be broken down further chemically, so each is an element.

ƒ Each element is identified by a symbol.

Atoms: Elementary Structure ƒ Protons and neutrons are dense, and form the nucleus (core) of an atom. ƒ Protons have positive electric charges. ƒ Neutrons have no charge. ƒ The nuclei of atoms always have a positive charge. ƒ Electrons, which have negative electrical charges that balance exactly the positive charges of protons, move in orbitals around the nucleus.

Figure 3.1

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Atomic Number ƒ The number of protons in the nucleus gives each atom its special chemical characteristics.

ƒ Elements are catalogued by atomic number. ƒ Uranium, with 92 protons in its nucleus, has the highest atomic number of the naturally occurring elements. ƒ Ununquadium,the heaviest synthesized element, reported early in 1999, has an atomic number of 114.

Isotopes ƒ Mass number: the sum of the numbers of neutrons and protons in an atom.

ƒ Isotopes: atoms with the same atomic number but different mass numbers (for example, carbon-12, carbon-13, and carbon-14 all have six protons per atom, and thus have the same atomic number).

Energy-Level Shells ƒ Electrons move around the nucleus of an atom in complex three-dimensional patterns called orbitals. ƒ Groupings of orbitals are called energy-level shells. ƒ Electrons require different amounts of energy to orbit in different energy-level shells.

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Ions ƒ Ions: Atoms that have lost or gained an electron. ƒ Cation: An atom that has lost an electron and thus has a positive charge.

ƒ Anion: An atom that has gained an electron and thus has a negative charge.

Compounds ƒ Chemical compounds form when atoms of different elements combine in a specific ratio.

ƒ Properties of compounds are quite different from the properties of their constituent elements.

Figure 3.2

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Bonding ƒ A molecule is the smallest unit that has the

distinctive chemical properties of a compound.

ƒ A molecular compound always consists of two or more kinds of atoms held together.

ƒ The force that holds the atoms together in a compound is called bonding.

ƒ Bonding determines the physical and chemical properties of a compound.

Four Types of Bonding (1) There are four important kinds of bonds: ƒ Ionic bonding: electron transfers between atoms produce cations and anions. ƒ Covalent bonding: some atoms share electrons rather than transferring them, creating a strong bond. - Elements and compounds with covalent bonding tend to be strong and hard. - The sparkle that makes diamonds attractive gems is due to covalent bonding.

Four Types of Bonding (2) ƒ Metallic bonding: closely packed atoms share electrons in higher energy-level shells among several atoms.

- Because the electrons are loosely held, they can drift from one atom to another.

ƒ Van der Waals bonding: weak secondary attraction between certain molecules formed by transferring electrons.

- Much weaker than ionic, covalent,or metallic bonding. - Graphite and talc.

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Figure 3.3 A

Figure 3.3 B

Figure 3.4

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Figure 3.5

Complex Ions ƒ Two or more kinds of ions form such strong covalent bonds that the combined atoms act as if they were a single entity. ƒ Such a strongly bonded unit is called a complex ion. ƒ Calcite (CaCO3) ƒ Gypsum (CaSO42H2O)

Periodic Table of Chemical Elements (1) ƒ Dmitri Mendeleev (1834-1907) developed the Periodic Table.

ƒ Within rows, elements increase in atomic number from left to right. ƒ Elements within each column have the same number of electrons in their outermost energylevel shell.

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Periodic Table of Chemical Elements (2) ƒ All elements in the first column easily give up the lone outer-shell electron to form cations (H+, Li+,etc.). ƒ The farthest columns to the right contains the six elements that have full energy-level shells. ƒ These are called noble gases because they have no tendency to gain or lose electrons and thus no tendency to form compounds.

Figure 3.6

Crystal Structure of Minerals ƒ The atoms in most solids are organized in

regular, geometric patterns, called the crystal structure. ƒ Solids that have a crystal structure are said to be crystalline. ƒ Ice in a glacier meets the definition of a mineral. ƒ Solids that lack crystal structures are amorphous. ƒ glass and amber.

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Ionic Substitution ƒ Ionic substitution is the substitution of one ion for another in a compound.

ƒ The bonding in most common minerals is ionic. ƒ Ionic substitution depends upon: ƒ Crystal structure; ƒ Ion size; - commonly expressed as ionic radius (distance from the center of the nucleus to the outermost shell of orbital electrons);

ƒ Ion electrical charge.

Figure 3.7

Figure 3.8

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Figure B3.1

Figure B3.2

Crystal Form ƒ Crystal form ƒ Crystal: any solid body that grows with planar surfaces. ƒ The interfacial angle in any crystalline structure remains constant.

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Figure 3.10

Figure 3.12

Growth Habit and Polymorphism ƒ Growth habit: - The characteristic crystal form of each mineral.

ƒ Polymorphism: - Some elements and compounds form two or more different minerals: - C Graphite, Diamond - CaCO3 Calcite, Aragonite Pyrite, Marcasite - FeS2 - SiO2 Quartz, Cristobalite

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Cleavage ƒ Cleavage is the tendency to break in preferred directions along bright, reflective planar surfaces. ƒ A cleavage surface is a breakage surface, whereas a crystal face is a growth surface. ƒ The planar directions along which cleavage occurs are governed by the crystal structure. ƒ They are planes along which the bonding between atoms is relatively weak.

Figure 3.13

Luster ƒ Luster is the quality and intensity of light reflected from a mineral.

ƒ The most important lusters are: ƒ ƒ ƒ ƒ ƒ

Metallic (polished metal surface). Vitreous (glass). Resinous (resin): the look of dried glue or amber. Pearly (pearl): the iridescent look of a pearl. Greasy (as if the surface were covered by a film of oil).

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Color and Streak ƒ Color is determined by several factors, but its main cause is chemical composition. ƒ Unreliable for identification.

ƒ Streak is the thin layer of powdered material left when a specimen is rubbed on an unglazed ceramic plate. ƒ Much more reliable than color for identification.

Hardness and the Mohs Scale ƒ Hardness is a mineral’s relative resistance to scratching.

ƒ The Mohs relative hardness scale uses ten minerals, each with its distinctive hardness: ƒ scale indicate relative hardness.

Figure 3.16 A

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Figure 3.16 B

Figure 3.16 C

Figure 3.18

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Hardness and the Mohs Scale (2) ƒ We test relative hardness by using common objects: ƒ copper penny,equivalent to fluorite’s hardness of 4. ƒ steel knife blade, equivalent to feldspar’s hardness of 6.

Density and Specific Gravity ƒ Density is mass per unit volume. ƒ Minerals with a high density, such as gold,

contain atoms with high mass numbers that are closely packed. ƒ Minerals with a low density, such as ice have loosely packed atoms. ƒ The unit of density is gram per cubic centimeter (g/cm3).

Specific Gravity ƒ Density is easily measured using the property called specific gravity.

ƒ Specific gravity is the weight of a substance in air divided by the weight of an equal volume of pure water. ƒ Specific gravity is a ratio of weight.

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Mineral Properties and Bond Types ƒ Minerals properties depend strongly on the kinds of bonds present.

ƒ Ionic and covalent bonds are strong, making minerals hard and strong.

ƒ Metallic and van der Waals bonds are much weaker.

Common Minerals in Earth’s Crust ƒ Only 12 elements occur in the continental crust in amounts greater than 0.1 percent by weight.

ƒ These 12 elements make up 99.23 percent of the crustal mass.

ƒ The crust, therefore, is constructed mostly of a limited number of minerals. ƒ Approximately 4,000 minerals have been identified, but only about 30 are commonly encountered.

Figure 3.19

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Three Mineral Groups ƒ Silicate minerals (SiO4)4-, the most abundant in Earth’s crust.

ƒ Carbonate (CO3)2-, phosphate (PO4)3-, and sulfate (SO4)2- minerals. ƒ Ore minerals, sulfides (S2-) and oxides (O2-) that contain valuable metals.

Silicates: The Largest Mineral Group ƒ Two elements, oxygen and silicon, make up more than 70 percent of the weight of the continental crust. ƒ Polymerization is the creation of compounds by accepting or sharing electrons. ƒ Linking silicate tetrahedra by oxygen sharing results in huge anions. ƒ It produces endless chains.

Figure 3.20

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Figure 3.21

Figure 3.22

Olivines and Garnets ƒ Two very important rock-forming mineral

groups, the olivines and the garnets, have crystal structures in which the silicate tetrahedra are isolated. ƒ Olivine is among Earth’s most abundant mineral groups, a very common constituent of igneous rocks in oceanic crust and the upper part of the mantle.

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Figure 3. 23 A

Olivines and Garnets (2) ƒ Olivine occurs in such flawless and beautiful crystals that is used as a gem, peridot.

Chains: Pyroxenes and Amphiboles ƒ One of the most important mineral groups, the pyroxenes, contains single-chain linkages. ƒ The most common pyroxene is called augite.

ƒ A very common and important family of minerals, the amphiboles, contains double chains. ƒ The most common of the amphiboles is called hornblende.

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Chains: Pyroxenes and Amphiboles ƒ The pyroxenes and the amphiboles are hard to tell apart. ƒ The cleavages in pyroxene are right angles (90o). ƒ The cleavages in amphibole are at 120o.

Figure 3.23

Sheets: Clays, Micas, Chlorites, and Serpentines ƒ Kaolinite, Al4Si4O10(OH)8, is one of the most common clays.

ƒ Muscovite, KAl2(Si3Al)O10(OH)2, is a common mica. ƒ Chlorite, which contains Mg2+ and Fe2+ cations, is usually greenish in color.

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Figure 3. 25

Sheets: Clays, Micas, Chlorites, and Serpentines (2) ƒ The serpentine group consists of three polymorphs with the formula Mg6Si4O10(OH)8. ƒ Chrysotile is the white asbestos of commerce.

Figure 3.24

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Quartz ƒ Quartz is pure SiO2. ƒ Forms six-sided crystals. ƒ Found in many colors. ƒ The colors come from minute amounts of iron, aluminum,titanium, and other elements present by ionic substitution. ƒ Fine grain forms of quartz are called chalcedony: - Agate - Flint (gray) - Jasper (red)

The Feldspar Group — Most Common Minerals in Earth’s Crust ƒ Feldspar: ƒ The most common mineral group in Earth’s crust. ƒ Accounts for about 60 percent of all minerals in the continental crust. ƒ Feldspar and quartz constitute 75 percent of the volume of the continental crust. ƒ Feldspar has a structure formed by polymerization.

Figure 3. 26

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Figure 3. 28

The Carbonates Group ƒ Carbonates: ƒ The carbonate anion, (CO3)2-, forms three common minerals: - Calcite. - Aragonite. - Dolomite.

ƒ Calcite reacts vigorously to HCl.

Figure 3.29

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The Phosphate and Sulfate Mineral Groups ƒ Phosphates: ƒ Apatite is the most important phosphate mineral. - Contains the complex anion ((PO4)3-. - Common mineral in many varieties of igneous and sedimentary rocks. - Main source of the phosphorus used for making phosphate fertilizers.

The Phosphate and Sulfate Mineral Groups (2) ƒ Sulfates: ƒ All sulfate minerals contain the sulfate anion, (SO4)2ƒ Only two are common: - Anhydrite(CaSO4); - Gypsum (CaSO4.2H2O). Gypsum is the raw material used for making plaster.

The Ore Mineral Group—Our Source for Metals ƒ Sulfides: ƒ Pyrite (FeS2) and pyrrhotite (FeS) are the most common. ƒ Galena (PbS), sphalerite (ZnS), chalcopyrite (CuFeS2). ƒ Familiar metals extracted from sulfide ore minerals are cobalt, mercury, molybdenum, and silver.

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Oxides ƒ Oxides; ƒ The iron oxides, magnetite (Fe3O4) and hematite (Fe2O3), are the two most common oxide minerals. - Hematite is red when powdered.

ƒ Other oxide ore minerals are: - Rutile (TiO2), the principal source of titanium; - Cassiterite (SnO2), the main ore mineral for tin; - Uraninite (U3O8), the main source of uranium.

Oxides (2) ƒ Other metals extracted from oxide ore minerals are chromium, manganese, niobium, and tantalum.

Minerals Give Clues To Their Environment Of Formation (1) ƒ Scientists are able to determine the temperature and pressures at which carbon will form a diamond or form graphite, its polymorph. ƒ Diamonds were at one time subjected to pressures and temperatures equivalent to those in the mantle at least 150 km below Earth’s surface.

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Figure 3.31

Minerals Give Clues to Their Environment of Formation (2) ƒ Clues to climate: - Regolith is the blanket of loose rock particles that covers Earth. - Some minerals form in regolith during the weathering process. - We can decipher past climates from the kinds of minerals preserved in sedimentary rocks.

ƒ Clues to seawater composition: - The content of past seawater can be determined from minerals formed when the seawater evaporated and deposited its salts.

Rocks: Mixtures of Minerals ƒ Igneous rocks ƒ Formed by solidification of magma.

ƒ Sedimentary rocks ƒ Formed by sedimentation of materials transported in solution or suspension.

ƒ Metamorphic rocks ƒ Formed by the alteration of preexisting sedimentary or igneous rocks in response to increased pressure and temperature.

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Distinguishing The Three Rock Types The differences among rock types are identified by two features. ƒ Texture: - The overall appearance of a rock due to the size, shape, and arrangement of its constituent mineral grain.

ƒ Mineral assemblage: - The type and abundance of the minerals making up a rock.

Texture and Mineral Assemblage ƒ A systematic description of a rock includes both texture and mineral assemblage. ƒ Megascopic textural features of rocks are those that we can see with the unaided eye. ƒ Microscopic textural features of rocks are those that require high magnification to be viewed.

Figure 3.32 A

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Figure 3.32 B

Figure 3.32 C

Figure 3.32 D

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Mineral Concentration ƒ The two most common processes of concentration of a mineral are: ƒ Vapors are released by a cooling body of magma. ƒ A hot saline solution, such as heated seawater, reacts with and alters a rock, and in the process extracts the scarce metals. - As such a solution cools the metals are deposited in veins.

Figure 3.33

Figure 3.34

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