Mineralogy Flashcards

1
Q
  • What is the definition of a mineral?

Minerals 1

A

Mineral: a crystalline, homogenous, inorganic solid with a defined chemical composition that occurs naturally.

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2
Q
  • Define “crystalline” in minerals:

Minerals 1

A

Minerals have a crystal structure:
* Their building blocks (atoms, ions, molecules) are arranged in an ordered and repeated pattern.
* The unit cell is the smallest unit that still has the full symmetry of the crystal structure of a material.
* Repeating this unit cell over and over again forms a crystal.

  • The ordered atomic network within a crystal can be simple or fairly complex.
  • However: some minerals are not (fully crystalline).
    • These are sometimes called a mineraloid (e.g, Opal [SiO2nH2O] can be microcrystalline or completely without any crystal structure)
  • Others include:
    • pearl,
    • jet,
    • obsidian.
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3
Q
  • Define “homogenous” in minerals:

Minerals 1

A

Following from the indefinitely repeatable unit cell of the crystal structure, minerals should by definition be homogenous
- (minerals with uniform chemical composition and internal structure throughout)
- However:
- Zonations (i.e., “Watermelon” tourmaline)
- Crystal defects.

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4
Q
  • Define “inorganic” in minerals:

Minerals 1

A

Minerals are inorganic substances:
- Inorganic being defined as “not organic”

Organic substances typically involve:
1. carbon-carbon and/or carbon-hydrogen bonds
1. molecules of C ± H, O, N (and P)
2. no carbon chains in mineralogy (except alcohol in beer/gin)
2. sugars, fats, oils, proteins and plastic

Instead, minerals typically are a COMBINATION OF SEVERAL OTHER ELEMENTS.

However:
1. Biominerals are formed by a living organism usually inorganic in composition but may contain organic material.
2. Amber is fossilised tree resin with an organic composition (gemstone)

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5
Q
  • Define “solids” in minerals:

Minerals 1

A

Minerals are (crystalline) solids at Earth surface conditions:

However:
1. Mercury is liquid (melting point: -39C)
2. Ice is crystalline (melting point: 0C)

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6
Q
  • Define “defined chemical composition” in minerals:

Minerals 1

A

In many minerals, one element can easily be substituted with another, and their relative proportions vary:
- The mineral is then referred to as a solid solution of/between two endmembers

However:
Same composition does not require same crystal structure:
- Polymorphs are minerals with the same composition, but different chemical structure.
- (i.e., graphite and diamond)

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7
Q
  • Define “naturally” in minerals:

Minerals 1

A

Minerals typically form in natural processes, when atoms arrange themselves into a crystal structure by:
1. crystallisation of a magma due to cooling (effectively the same as freezing)
1. Magma cools below its liquidus, and starts to crystallise minerals. The mix of melt + minerals keeps on crystallising until it “hits” the solidus, now all melt has solidified.
2. precipitation from a solution, by evaporation, other change in solubility, or aided by an organism.
3. (solid state) rearrangement of elements due to changes in pressure and temperature

However:
There are synthetic minerals:
1. Diamond (C)
2. Ruby (Al2O3 (w/ traces of Cr2O3)

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8
Q
  • What is the smallest building block?

Minerals 1

A

** *Atoms are the building blocks of matter.
* They have a dense core (or nucleus) of positively-charged protons and neutral neutrons.
* The core is surrounded by a cloud of negatively-charged electrons
* The number of electrons is equal to the number of protons, so their charges are balanced.

  • Ions are atoms or molecules with a number of electrons that does not match with number of protons.
    * They have a positive or negative charge.
    * An ion with a negative charge (e- > p+) is called anion.
    * An ion with a positive charge (e- < p+) is called cation.
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9
Q
  • How do we bind atoms together?

Minerals 2

A
  1. Metallic bonds:
    are a type of chemical bonds where there is an electrostatic attractive force between delocalised electrons and positively charged metal ions (in the form of sharing free electrons among a structure of cations)
    • In pure metals, the electrons are free to roam across the metal.
  2. Covalent bonds:
    are a type of chemical bonds where two atoms share one or more of their electrons to form a stable molecule.
    • The covalent bonds don’t have to be between atoms of the same elements
    • Covalent bonds are very strong, especially between atoms of the same element.
      - All carbon in diamond is covalently bonded.
  3. Electronegativity:
    Atoms of different elements have different strengths in attracting electrons: this is measured as electronegativity.
    • It is a function of the number of protons (→ size of the core) and how far the outermost electrons are from the core.
  4. Ionic bonds:
    are a type of chemical bonds where two atoms with sharply contrasting electronegativities form an electrostatic attraction that occur between a metal (gives the electron) and a non-metal (takes away the electron) to form a cation and anion.
    • A typical example for an ionic bond is halite (NaCl), or table salt.
      - Sodium is a metal that readily can lose an electron to a non-metal like chlorine.
  5. Other weaker bonds:
    Not all bonds involve sharing or the transfer of electrons.
    • Intermolecular bonds can occur when a molecule has a slightly asymmetric charge.
  6. Mix the bonds:
    Often, bonds are not purely ionic or covalent, but of ionic or covalent “character” (many minerals haave more than one type of bond)
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10
Q
  • What are the definitions of coorddination and site?

Minerals 2

A
  1. Coordination: the number of direct neighbours that an atom/ion is bonded to in a crystal structure. Typically we talk about cations and their surrounding ion-neighbours.
  2. Site: a space in a crystal lattice that can be occupied by an atom/ion. It is typically named by its coordination.
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11
Q
  • What are some examples of coordination?

Minerals 2

A
  • Tetrahedral: or 4-fold coordination (Si by 4 O in quartz)
  • Octahedral: or 8-fold coordiantion (Na by CI in halite)
  • Cubic: or 8-fold coordination (Ca by F in fluorite)
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12
Q
  • What are some examples of sites?

Minerals 2

A
  • A crystal lattice made up of CI- (chloride ion) anions has gaps/holes that are surrounded by 6 CI-
  • These octahedral sites can be occupied by cations:
    • In halite, sodium chloride, they are occupied by Na+ (sodium)
    • In slyvite, potassium chloride, they are occupied by K+ (potassium)
  • In more complicated crystal lattices, it is not necessarily the case that all ions have the same coordination.
  • Sites in a crystal structure have a certain size. Simply put, the size is determined by the ideal crystal sturcture of a mineral.
    - The coordination also affects the site size:
    - Bond distances are smaller when shared with less atoms (less sharing, stronger pull):
    1. site size goes up, as coordination goes up.
    2. tetrahedral is smaller than octahedral and so on.
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13
Q
  • What is atomic/ionic radius?

Minerals 2

A

The atomic radius of a chemical element is a measure for the size of its atoms (and ions).

On the periodic table, atomic radii:
- decrease along a group (=row) because the charge increases (the core pulls more strongly on the electrons)
- increase within a group (=column) because of the number of protons and electrons (and electron shells) increases.

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14
Q
  • What is compatibility?

Minerals 2

A

Since sites in a crystal lattice has a given size:
- Atoms/ions in a crystal lattice can be substituted by other elements, as long as their radius is similar.
- Ideally, their charge would also be same!
- If an element fits readily into a crystal structure, it is called compatible.

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15
Q
  • What is an example of compatibility?

Minerals 2

A

Minerals that have Mg2+ (magnesium cation) in a certain site, can often also accommodate Fe2+ in the same site as an alternative, because their radius and charge is very similar.

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16
Q

What are sites?

Minerals 2

A

A space in a crystal lattice that can be occupied by an atom/ion. It is typically named by its coordination.
* A crystal lattice made up of CI- anions has gaps/holes that are surrounded by 6 CI-.
* These octahedral sites can be occupied by cations.
* In halite, sodium chloride, they are occupied by Na+.
* In sylvite, potassium chloride, they are occupied by K+.

Sites in a crystal structure have a certain size. Simply put, the size is determined by the ideal crystal structure of a mineral.
1. The coordination also affects the site size.
2. Bond distances are smaller when shared with less atoms (less sharing, stronger pull).
3. Site size goes up, as coordination goes up.
4. Tetrahedral is smaller than octahedral and so on.

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17
Q

What are atomic/ionic radius?

Minerals 2

A

The atomic radius of a chemical element is a measure for the size of its atoms (and ions).

On the periodic table, atomic radii:
- decrease along a period (=row) because the charge increases (the core pulls more strongly on the electrons)
- increase within a group (=column) because the number of protons and electrons (and electron shells) increases.

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18
Q

What is the (Nickel-) Strunz classification?

Minerals 2

A

Karl Hugo Strunz developed a classification scheme for minerals based on their anions:
- These anions can be:
- single ions: Cl- , S2-…
- polyatomic ions: [CO3] 2-, [SiO4] 4

Strunz mineral classes:
1. elements
2. sulfides and sulfosalts
3. halides
4. oxides, hydroxides and arsenites
5. carbonates and nitrates
6. borates
7. sulfates, chromates, molybdates and tungstates
8. phosphates, arsenates and vanadates
9. silicates and germanates
10. organic compounds

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19
Q

What is the elements classification? (Strunz)

Minerals 2

A

Pure elements, metals which are often called “native”.
- These are usually bound by metallic (in metals) or covalent bonds.

Examples:
1. Native gold (Au)
2. Diamond (C)
3. Sulphur (S)

20
Q

What are sulfides and sulfosalts (Strunz)?

Minerals 2

A

Minerals that have sulphur as an anion.

Examples:
1. Pyrite (FeS2)
2. Galena (PbS)
3. Realgar (AsS)

21
Q

What are halides (Strunz)?

Minerals 2

A

Minerals with halogens (F, Cl, Br, I) as an anion.

Examples:
1. Halite (NaCl — table salt)
2. Fluorite (CaF2)
3. Atatcamite (Cu2Cl(OH)3)

22
Q

What are oxides, hydroxides and arsenites? (Strunz)

Minerals 2

A

Minerals with oxygen and/or OH as anion

Examples:
1. Spinel
2. Hematite
3. Goethite

23
Q

What are carbonates and nitrates (Strunz)?

Minerals 2

A

Minerals with the carbonate ion (CO3) 2- as anion

Examples:
1. Calcite (CaCo3)
2. Azurite (Cu3(CO3)2(OH)2
3. Malachite (Cu3(CO3)2(OH)2

24
Q

What are borates (Strunz)?

Minerals 2

A

Minerals with the borate ion (BO3) as anion

Examples:
1. Ulexite
2. Borax

25
Q

What are sulfates, chromates, molybdates, and tungstates? (Strunz)

Minerals 2

A

Minerals with the sulphate ion (SO4)2- as anion

Examples:
1. Anhydrite
2. Gypsu
3. Baryate

26
Q

What are phosphates, arsenates and vanadates? (Strunz)

Minerals 2

A

Carbonates with the phosphate ion (PO4)3- as anion

Examples:
1. Apatite
2. Turquoise

27
Q

What are silicates and germanates?

Minerals 2

A

Silicates are by far the most common mineral group:
* They form about 90% of the Earth’s crust.
* They all contain a combination of Si and O as their anions

The building block of all silicates:
* SiO4 tetrahedron:
* One Si-atom is surrounded by 4 O-atoms:
Si4+ + 4 O2- makes [SiO4]4-
* SiO4-tetrahedron is a quadruply negative molecule-ion.

28
Q

What are neosilicates?

Minerals 2

A

Nesosilicates = island silicates

Island silicates:
- Consist of isolated “islands” of [SiO4]4- tetrahedrons.
- Since a mineral cannot be charged, we have to balance the quadruply-negative charge.
- A charge balance can be achieved by throwing cations in the mix.

  1. Olivine: achieves charge balance by adding two divalent cations per [SiO4]4- island. It can be either Mg2+ or Fe2+.
    ⟶ (Mg,Fe)2SiO4
  2. Garnet: has a more complicated structure and achieves charge balance by adding three divalent cations and two trivalent cations per three [SiO4]4- islands.
    ⟶ X3Y2[SiO4]3
  3. Aluminosilicates (Ai2siO5):
    • Andalusite,
    • kyanite,
    • sillimanite
      Polymorph = same chemical composition, but different crystal structure ⟶ coordination of Al.
29
Q

What are sorosilicates?

Minerals 2

A
  1. Group silicates:
    Two SiO4-tetrahedrons can share one oxygen and form a group:
    ⟶ 2 Si4+ + 7 O2- makes [Si2O7] 6
    Examples: zoisite (Ca2Al3 [(O/OH)/SiO4 /Si2O7 ])
30
Q

What are cyclosilicates?

Minerals 2

A
  1. Ring silicates:
    When a SiO4-tetrahedron shares two of its oxygen corners, we can form rings.
    • Depending on the number of rings, we get different molecular anions, with different charges…
    • But always a multiple of:
      ⟶ Si4+ + 3 O2- → [SiO3 ] 2-

Examples:
1. Tourmaline:
2. Elbaite
3. Beryl:

31
Q

What are inosilicates?

Minerals 2

A
  1. Chain silicates:
    Like an unclosed ring, sharing two oxygen corners creates chains
    ⟶ 2 Si4+ + 6 O2- → [Si2O6] 4-
  2. Pyroxenes:
    Two slightly different cation-sites in their lattice:
    ⟶ M2M1[Si2O6]
    • M2 (larger cation site): Ca, Na, Mn, Fe, Mg
    • M1 (smaller cation site): Mg, Fe, Al, Mn, Cr, Ti, Li…
      • e.g. Augite (Ca,Mg,Fe)2Si2O6
  3. Double chains:
    Every other SiO4-tetrahedron must share three instead of just two of it’s corners
    ⟶ SiO3 + SiO2.5 = Si2O5.5 or 4 Si4+ + 11 O2- → [Si4O11] 6-
  4. Amphiboles:
    are complicated and have a lot of cation-sites, but are a common mineral.
32
Q

What are phyllosilicates?

Minerals 2

A

Phyllosilicates = sheet silicates

  1. Sheet silicates:
    Every SiO4 tetrahedron shares three of its corner oxygens:
  2. Micas:
33
Q

What are tectosilicates?

Minerals 2

A

Tectosilicates = framework silicates

  1. Framework silicates:
    Every SiO4 tetrahedron shares all four of its corner oxygens
  2. Feldspars:
    Framework structure is not charged, no cations needed
    • Need to alter to create a charge (so we can use some cations)
    • Coupled substitution: change something that requires another change
    • Three endmembers exist:
      1. KAISi3O8 = K-feldspar (typically: Orthoclase)
      2. NaAISi3)8 = albite
      3. CaAI2Si208 = anorthite
    • Two different solid solutions series (with two endmembers)
      • alkali-feldspare (orthoclase - albite)
        • often pink or white simple twinning
      • plagioclase (albite - anorthite)
        • typically milky white multiple twinning

(No mixing of orthoclase with anorthite!)
Feldspars are the most abundant mineral in the crust

34
Q

What is density (in mineraology)?

Minerals 3

A

Density = mass per volume

Therefore:
density of minerals depend on two things:
1. composition (how heavy are the building blocks?)
- heavy elements made a dense mineral
2. packing (how much volume does a number of blocks occupy?)
- if the same atoms are packed more tightly, more will fit into a cm3
- tightly packed atoms make a dense mineral

Density is not easy to measure on samples because not all our samples are 1cm3.
- Therefore we use a relative estimate: “does this feel heavy or light for its size?

35
Q

What are some chemical and physical properties specific to certain minerals?

A

There are some chemical and physical properties that are specific to only one or two certain minerals.
1. Double refraction:
1. Technically the majority of transparent and translucent minerals double-refract light:
2. Calcite (CaCO3) double-refracts so strongly that it is visible in hand samples.

  1. (Photo- ) Luminescence:
    1. In some minerals, absorbing (high-energy) light results in the emission of (visible) light.
      1. Fluorescence: the light emission stops when the high-energy light stops.
      2. Phosphorescence: the light emission can continue for some time after the excitation stops
  2. Magnetism:
    1. The mineral magnetite (Fe3O4) is magnetic.
  3. Reaction with acid:
    1. A few carbonate minerals, especially calcite, react with dilute hydrochloric acid (10% Hcl)
    2. Dolomite also reacts with dilute HCI
      1. Dolomite reacts less vigorous than calcite (bubbles may only be visible if the dolomite is powdered)
  4. Taste:
    1.Halite (NaCl) and sylvite (KCI) can look alike.
    1. The way to tell them apart is to lick them:
      1. Halite taste salty
      2. Sylvite tastes salty, too, but has a bitter aftertaste.
36
Q

What is twinning?

Minerals 3

A

Twinning:
- the intergrowth of two (or more) crystals of the same mineral through a slight change in orientation of the crystal lattice

Twinning as a diagnostic feature in feldspars (twins will reflect light at a slightly different angle)

37
Q

What is lustre?

A

Lustre:
- how a mineral reflects

There are lots more words:
1. vitreous (glassy),
2. metallic,
3. dull,
4. resinous,
5. submetallic,
6. pearly,
7. adamantine,
8. fatty,
9. greasy,
10. waxy,
11. silky.

38
Q

What is transparency?

Minerals 3

A

Transparency:
- describes whether a material allows light to pass through

Levels of transparency:
1. Transparent (light can pass more or less freely)
2. Translucent (some light can pass, but some scattering occurs, making it blurry)
3. Opaque (no light can pass)

Some minerals can appear opaque, but are translucent when thin enough. This is often the case for dark minerals.

39
Q

What is colour?

Minerals 3

A

Absorption colour:
- colour as a result of interaction with (sun)light

Sunlight = white light (contains all wavelengths of the visible spectrum)

  • Minerals have a colour when they absorb some wavelengths of the (natural) light. The colour is defined by the remaining, scattered wavelengths.
    • Quartz (SiO2) does not absorb any colours in the visible spectrum of light. It is colourless (or white when it scatters)
    • Olivine (Mg,Fe)2SiO4 absorbs light in the blues and reds. The remaining light makes it green,.

Warning: small changes in a crystal can change the way it interacts with light (colour can not be relied on for mineral ID)
- Same mineral (SiO2, same crystal structure), but different colour!

Streak colour: Is the colour the same for mineral powder?
- We can “powder” a mineral by grinding it against a hard and rough surface, like an unglazed ceramic tile (leaving a “streak”)
- In most cases, the answer is more or less, yes. We already learned that the same mineral can have different appearance/colour.
- For some minerals, streak colour can be diagnostic, even if the crystals can have different appearances.

40
Q

What are the key features to determine the value of gems?

Minerals 5

A
  1. Clarity:
    • should be free from inclusions
    • only 20% of mined diamond is good enough for gems, but inclusions can be interesting for earth scientists as probes of the deep interior.
  2. Colour:
    • Generally, the most popular is colourless.
    • However, blue, pink and green diamonds are very rare and hence more valuable.
  3. Cut:
    • The shape and the quality (i.e, does the cut promote total internal reflection)
  4. Carat:
    The weight/size of 1 carat = 0.2g
    • From carob seeds, where people used to think every seed would weigh exactly 0.2g
  5. The 5th C — Certification:
    Blood diamonds = diamond mined in war zones; trade finances further war activities.
    • Certification of “good” diamond as an attempt to fright blood diamond trade (“cleanwashing”)
    • Issues include:
      • forced and child labour,
      • environmental pollution,
      • health and safety

How could an earth scientist help?
Provenancing
- finding a way to link a material, such as a gemstone to a location; by comparing to materials of known origin
- This helps to identify gems of “good” and “bad” origin blood diamonds, but also many other gemstones (premium for certain provenance — e.g. Scottish gold)
- By using geochemistry:
- Distinguishing between natural, synthetic and treated gems:
- synthetic/created/cultured gems come with less potential for ethical burden, but they sell for less money

41
Q

What is a gemstone?

Minerals 5

A

Gemstone is not well defined, but it is usually a hard and rare mineral that is cut and/or polished and gets used in jewellery or other ornamental items.
- Exceptions to this include amber (fossil tree resin), jet (lignite) pearls, and lapis lazuli (actually a rock)

42
Q

What are inference colours?

Minerals 5

A

Interference colours depend on two things:
- thickness of the mineral/thin section (affecting the travel time for both rays)
- birefringence of a mineral (=double refraction) (how much are the two rays separated = path difference)

Minerals of the cubic crystal system do not doubly-refract at all (no birefringence)
→ no two light rays → no interference

43
Q

How does retardation work?

Minerals 5

A

The retardation causes a shift amongst the different waves peaks and the peaks and troughs of both waves interfere with each other.
- This affects wavelengths and hence colour (we are able to observe interference colours)

44
Q

How do minerals polarise light?

Minerals 5

A

Minerals polarise the light again in other directions, which then get filtered down to one direction by the second polariser

Minerals double-refraction (also called birefringence) splits the light into two rays.
Light travels at a different speed in minerals compared to air.
- One of the two rays covers more distance in the mineral.
- It is slowed down longer and comes out “retarded”.

45
Q

What is doubly-polarised light microscopy?

Minerals 5

A

A petrographic microscope can use two polarisers, which are arranged at 90° to each other.
- But then no light passes through the microscope: you see a dark/black view.

46
Q

What is polarised light microscopy?

Minerals 5

A

Light swings in all directions.
- We can use a polariser to filter out all but one direction.

47
Q

How do we see rocks through the microscopes?

A

Rocks need to be made into thin sections:

Looking at a thin section of rock, even small minerals can be identified.
- Dark minerals reveal their colour
- Cleavage can be observed.

By using doubly-polarised light microscopy: