CN 301-GEOENVIRONMENTAL ENGINEERING LECTURE 3 LEARNING OUTCOMES
Transcript of CN 301-GEOENVIRONMENTAL ENGINEERING LECTURE 3 LEARNING OUTCOMES
CN 301- GEOENVIRONMENTAL ENGINEERING
LECTURE 3
LEARNING OUTCOMES
1. Explain the soil characteristics related to geo-
environmental
2. Explain basic soil test
SOIL FORMATION
Soils are formed by the disintegration (or more precisely,
evolution) of rock material of the earth’s relatively deeper crust,
which itself is formed by the cooling of volcanic magma.
The stability of crystalline structure governs the rock formation.
As the temperature falls, new and often more stable minerals
are formed. For instance, one of the most abundant minerals in
soils known as quartz acquires a stable crystalline structure
when the temperature drops below 573°C.
The intermediate and less stable minerals (from which quartz
has evolved) lend themselves to easy disintegration during the
formation of soils.
The disintegration process of rocks leading to the formation of soils is called
weathering.
It is caused by natural agents; primarily wind and water (note that these are
the same agents that aid the evolution and life in other kingdoms).
The specific processes responsible for weathering of rocks are:
i. Erosion by the forces of wind, water, or glaciers, and alternate freezing and
thawing of the rock material.
ii. Chemical processes, often triggered by the presence of water. These
include:
Hydrolysis (reaction between H- and OH- ions of water and the ions of
the rock minerals),
Chelation (complexation and removal of metal ions),
Cation exchange between the rock mineral surface and the
surrounding medium
Oxidation and reduction reactions,
Carbonation of the mineral surface because of the presence of
atmospheric CO2.
iii. Biological processes which, through the presence of organic compounds,
affect the weathering process either directly or indirectly.
Once the rock material is weathered, the resultant soil
may either remain in place or may be transported by
the natural agencies of water, air, and glaciers.
In the former case, the soils are called residual soils.
Depending on the natural agent involved, the
transported soils are called alluvial or fluvial (water-
laid), aeolian (wind-laid), or glacial (ice-transported)
soils.
Several subdivisions are often made based on the
transportation and deposition conditions.
THE PROPERTIES OF THE SOIL DEPOSITS FORMED
DEPEND ON THE SOIL-FORMING FACTORS
Five independent variables may be viewed as governing soil formation:
Climate - Amount of moisture available, temperature,
chemical reaction speed and rate of plant growth
Organisms present - Organisms influence the soil's physical and
chemical properties and furnish organic matter to
soil
Topography - Angle: like Steep is poorly developed soils but flat
to undulating surface is the best. Orientation
(direction the slope is facing) - soil temperature and
Moisture
The nature of the
parent material
- Original mineral makeup and important in young
soils. Residual soil–from bedrock. Transported soil–
carried from elsewhere
Time - varies for soils in different climates, locations
MINERALOGY COMPOSITION IN SOIL
Five mains groups of mineral composition in soil (regular structure
elements and atomic elements) are :
i. CARBONATES - calcite and dolomite usually use in
cement
ii. OXIDES
iii. HYDROUS
OXIDES
– gibbsite and brucite minus OH’s sheet in
clay minerals
iv. PHOSPHATE – using for fertilizer
v. SILICATE – 90% of all soil
SILICATES
Silicates constitute well over 90% of the earth's
crust.
The fundamental unit of all silicate structures is
the SiO4 tetrahedron.
It consists of four O2- ions at the apices of a
regular tetrahedron coordinated to one Si4+ at
the center.
The individual tetrahedral are linked together
by sharing O2- ions to form more complex
structures.
Silica tetrahedron: The silica tetrahedron consists of four oxygen ions
and one silica ion.
The molecular arrangement is such that the four oxygen ions are
spaced at what would be the corners and tip of a three-dimensional,
three-sided pyramid, with the silicon located within the pyramid.
Oxygen ions at the base are shared by adjacent tetrahedrons, thus
combining and forming a sheet.
QUARTZ
Commonly found in soil and the mineral
composition SiO2.
The Quartz shape are in three dimensions and
each of quartz cannot absorb in acid and
cannot break easily.
There is no isomorphous substitution in
quartz, and each silica tetrahedronis firmly
and equally braced in all directions.
As a result, quartz has no planes of weakness
and is very hard and highly resistant to
mechanical and chemical weathering.
Quartz is not only the most common mineral
in sand and silt-sized particles of soils, but
quartz or amorphous silica is frequently
present in colloidal (1 to 100 nm) and
molecular (< 1 nm) dimensions.
FELDSPAR some of the silicon atoms are replaced by aluminum. This
results in a negative charge and in distortion of the crystal structure, because Al atoms are larger than Si atoms.
The negative charge is balanced by taking in cations such as K+, Na+, and Ca+ in orthoclase, albite, and anorthite feldspars, respectively. The distortion of the lattice and the inclusion of the cations cause cleavage planes that reduce the resistance of feldspars to mechanical and chemical weathering.
For these reasons, feldspars are not as common as quartz in the sand-, silt-, and claysized fractions of soils, even though feldspars are the most common constituent of the earth's crust.
MICACommon micas such as muscovite and biotite
are often present in the silt- and sand-sized
fractions of soils.
In a unit sheet of mica, which is 1 nm thick, two
tetrahedral layers are linked together with one
octahedral layer.
In muscovite, only two of every three octahedral
sites are occupied by aluminum cations,
whereas in biotite all sites are occupied by
magnesium.
In well-crystallized micas one fourth of the
tetrahedral Si+4 are replaced by A1+3.
The resulting negative charge in common micas
is balanced by intersheet potassiums. In a face-
to-face stacking of sheets to form mica plates,
the hexagonal holes on opposing tetrahedral
surfaces are matched to enclose the intersheet
potassiums.
ALUMINA OCTAHEDRONS:
The alumina octahedron consists of six-oxygen and one-aluminum.3
oxygen is in the top place of the octahedrons, and three are in the
bottom plane. The aluminum is within the oxygen grouping. It is possible
that the aluminum ion may be replaced with magnesium, iron, or other
neutral ions. The aluminum sheet is 5 x 10-7mm thick. Oxygen from the
tip of a silica tetrahedron can share an alumina sheet, thus layering
sheets. Different sheet arrangements are then combined to form the
different clay minerals. The composition and typical properties of the
more commonly occurring clay minerals are Kaolinite, Illite and
Montmorillonite
KAOLINITE
is a common mineral in soils and is the most common member of this
subgroup. A Kaolinite is the most prevalent clay mineral and is very stable,
with little tendencies for volume change when exposed to water. Kaolinite
layers are stack together to form relatively thick particle. Particles are plate
shaped. The composition is one-silica, one alumina sheet that is very
strongly bonded together. Kaolinites have very little isomorphous
substitution in either the tetrahedral or octahedral sheets and most
kaolinites are close to the ideal formula Al2Si2O5 (OH) 4.
ILLITE
Illite - has irregular plate shape, more plastic than kaolinites.
Its does not expand when exposed to water unless potassium deficiency
exists. This clay is most prevalent in marine deposits.
The composition is an alumina sheet sandwiched between two silica
sheets to form a layer. Potassium provides the bonds between the
layers.
MONTMORILLONITE
has irregular plate shapes or is fibrous because of the weak bond
between layers this clay readily absorbs water between layers.
This mineral has a great tendency for large volume change. The
composition is an alumina sheet sandwiched between two silica
sheets to form a layer.
Iron or magnesium may replace the alumina in the aluminum
sheet.
FUNDAMENTAL PROPERTIES OF SOILS
The soil type or category is based on particle size, however, where
the soil particle size is too small to be observed, an additional
physical property, known as plasticity is utilized as a criterion for
evaluation
Soil is all the material located above bedrock and can be grouped
into four major categories or types including gravel, sand, clay and
silt.
These four categories can be reduced to two groups termed coarse-
grained soil and fine-grained soil.
PARTICLE SIZE AND SHAPE
Particle size and shape affects the mechanical behavior of soils,
however, the effect of varies for coarse-grained and fine-grained soils.
The size and shape of the granular soil particles can increase or
decrease the tendency of particles to fracture, crush and degrade.
The grading of gravels and sands may be qualified in the field as well
graded (good representation of all particle sizes from largest to
smallest).
Poorly graded materials may be further divided into uniformly graded
(most particles about the same size) and gap graded (absence of one or
more intermediate sizes).
SOIL STRUCTURE
Soil structure is the shape that the soil takes based on its
physical and chemical properties; it is the geometric
arrangement of soil particles with respect to one another.
The process of sedimentation or rock weathering creates the
initial soil structure.
Among the many factors that effect soil structure is the shape,
size, and mineral composition of the soil particles, and the
nature and composition of soil water.
The basic terminology used to define the soil structure are
single-grained, honeycombed, flocculated and dispersed with
variations dependent upon the composition of the soil.
COHESIONLESS SOILS
The particle arrangement of cohesionless soils (gravel, sand
and silt) has been likened to arrangements attained by
stacking marbles, or “single-grained”.
In single grained structures soil particles are in a stable
position, with each particle in contact with the surrounding
ones.
For similar sized particles large variations in the void ratio are
related to the relative position of the particles.
COHESIVE SOILS
The term cohesive is used for clay soils, which have an inherent
strength, based on their particle structure which provides
considerable strength in an unconfined state.
The cohesiveness of a clay is due to its’ mineralogy and is a
controlling factor determining the shapes, sizes, and surface
characteristics of a particle in a soil.
It determines interaction with fluids.
Together, these factors determine plasticity, swelling,
compression, strength, and fluid conductivity behavior
IDENTIFICATION OF FUNDAMENTAL
CHARACTERISTIC SOILS
Fine grained soils are identified on the basis of some simple tests for :
i. Dry strength Dry strength is a qualitative measure of how hard it is to crush a dry
mass of fine grained soil between the fingers. Clays have very high dry
strength and silts have very low dry strength.
ii. Dilatancy Dilatancy is an indication of how quickly the moisture from a wet soil
can be brought to the surface by vibration. In silty soils, within a few
strikes water rises to the surface making it shine. In clays, it may
require considerable effort to make the surface shiny. In other words,
dilatancy is quick in silts and slow in clays.
iii. Toughness Toughness is a qualitative measure of how tough the soil is near its
plastic limit (where the soil crumbles when rolled to a 3 mm diameter
thread). Toughness increases with plasticity. Silty soils are soft and
friable (crumble easily) at Plastic Limits (PL), and clays are hard at PL.
The fines can also be identified by feeling a moist pat; clays feel sticky
and silts feel gritty. The stickiness is due to the cohesive properties of
the fines, which is also associated with the plasticity, and therefore
clays are called cohesive soils. Gravels, sands and silts are called
granular soils.
PARTICLE SIZE DISTRIBUTION OF SOILS
The grain size distribution of a coarse grained soil is generally determined
through sieve analysis, where the soil sample is passed through a stack of
sieves and the percentages passing different sizes of sieves are noted.
The grain size distribution of the fines are determined through hydrometer
analysis, where the fines are mixed with distilled water to make 1000 ml of
suspension and a hydrometer is used to measure the density of the soil-
water suspension at different times.
Three Limits Are in General Used to Characterize
The Clayey Soils:
Limit Description
i. Shrinkage limit which is the water content at which the
soil passes from solid to semisolid state
ii. Plastic limit which is the water content at which
transition from semisolid to plastic state
takes place
iii. Liquid limit which indicates the water content
required in order for the clayey soil to
begin exhibiting flow characteristics like
liquids
SOIL TEST
The BS 5930:1999 (Code of Practice for Site Investigations)
summarizes the purposes of laboratory testing to be to describe
and classify the samples, to investigate the fundamental behavior
of the soils in order to determine the most appropriate method to
be used in the analysis, and to obtain soil parameters relevant to
the technical objectives of the investigation.
The laboratory tests for soils commonly carried out include:
• Moisture content, which read in conjunction with liquid and
plastic limits gives an
• indication of undrained strength;
• Liquid and plastic limits to classify fine grained soil and the
fine fraction of mixed
• soils;
SOIL TEST
Particle size distribution to give the relative proportions of gravel, sand, silt
and clay;
Organic matter which may interfere with the hydration of Portland cement;
Mass loss of ignition which measures the organic content in soil, particularly
peat;
Sulfate content which assesses the aggressiveness of the soil or
groundwater to buried concrete;
pH value which is usually carried out in conjunction with sulfate contents
tests;
California bearing ration (CBR) used for the design of flexible pavements;
Soil strength tests such as Triaxial compression, unconfined compression
and vane shear;
Soil deformation tests;
Soil permeability tests.