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Anatase
1.
2. OUTLINES
1. INTRODUCTION OF ANATASE
2. OCCURRENCE
3. CHEMICAL FORMULA
4. CRYSTALLOGRAPHY STRUCTURE
5. TRANSFORMATION STRUCTURE
6. SYNTHESIS AND GENESIS
7. LOCATION IN PAKISTAN
9. STRENGTH
10. USES
11. AGRICULTURE USE
12. INDUTRIAL USE
13. PRACTICAL USE
14. CEC
15. AEC
8. ORIGIN
3. INTRODUCTION
ANATASE (Titanium dioxide ) also known as titanium oxide is the certainly arising oxide of
titanium, having the chemical formula TiO2
Once used as a pigment, it is known as titanium white, Pigment White 6 Normally, it is traced
from limonite, rutile, and Anastase . World invention in 2014 surpassed 9 million tones. It has
been expected that titanium dioxide is used in two-thirds of all pigments, and pigments built on
the oxide have been priced at $13.2 billion. Anastase is a metastable mineral form OF
ANATASE. The mineral in likely forms is mostly faced as a black solid, granting the pure
material is dull or white. Two other as expected occurring mineral forms of TiO2 are well-
known, bookie and rutile. Anastasia is always found as small, isolated and sharply settled
crystals, and like the thermodynamically stable rutile, it crystallizes in the tetragonal system.
Anastasia is metastable at all temperatures and pressures, with rutile being the symmetry
polymorph. However, anatase is often the first titanium dioxide phase to form in many processes,
due to its lower surface energy, with a conversion to rutile taking place at elevated temperatures.
While the degree of balance is the same for both anatine and rutile stages, there is no relative
between the interfacial angles of the two minerals, excluding in the prism zone of 45° and 90°.
The common pyramid of anatine, parallel to the faces of which there are perfect cleavages, the
parallel angle of rutile being 56°52½'. Additional important differences exist between the
physical types of anatine and rutile: the former is less rigid and dense ,specific gravity about
3.9. ANATASE is optically negative whereas rutile is progressive and its polish is more toughly
metallic-adamantine than that of rutile.
https://en.wikipedia.org/wiki/Anatase
4. OCCURRENCE
Derived from other titanium bearing minerals. In alpine veins, derived from the surrounding
gneisses or schist’s by hydrothermal way out. In the igneous and metamorphic mountains, in
Pegmatite’s, from a carbonate a mutual detrital mineral
Place of protection of form material
National history museum, Paris, France
Geological location of form materials
Alpine veins, originate from the enfolding gneisses or schist’s by hydrothermal farm
Titanium dioxide arises in natural surroundings as the minerals Rutile and Anatase. Furthermore
two demanding forms are well-known minerals: a Monoclinic Baddeleyite alike form known as
Akaogiite, and the other is an orthorhombic α-PbO2 like as Brookite, both can initiate at the
Rise crater in Bavaria. It is obtained from Ilmenite ore. This is common form of titanium
dioxide having ore around the world. Rutile is succeeding most rich and having around 98%
titanium dioxide in the ore. The metastable anatase and brookite cycle change indirectly to
symmetry rutile cycle upon heating overhead temperatures in array 600–800 °C. Titanium
dioxide has eight modifications in addition to rutile, Anatase, akaogiite, and brookite, three
metastable phases can be formed unnaturally, and five high-pressure forms also occur
CHEMICAL FORMULA
Chemical formula of ANATASE is Tio2 O2Ti, stands for TATNIUM dioxide which belongs to
category oxide minerals having crystal system is tetragonal and crystal class is ditetragonal
dipyramidal (4/mmm) and formula mass is 79.88 g/moll
CHEMICAL COMPOSITION
The structural properties and chemical composition of ANATASE were study using X ray
diffraction, S E M, and x ray photoelectron spectroscopy. The X RAY POWDER
DIFFRACTION method confirm that the particle are only composed of ANATASE phase with
preferential orientation along direction. Physical parameters such as stress, strain and energy
density were investigating by assuming UD Model (uniform deformation method) UDEDM
5. (uniform deformation energy density model). W H analysis show strain in ANATASE.
SCANNING ELECTRON MICROSCOPE show particle size of ANATASE is range from 60 to
80 nm. X ray spectroscopy show complete amount of titanium react to ANATASE
CRYSTALLOGRAPHIC STRUCTURE
Crystal System Tetragonal
Class 4/mmm Di tetragonal Di pyramidal
Cell Parameters a = 3.7845 Å, c = 9.5143 Å
Ratio 1: 2.514
Unit Cell (Voltage) 136.27 ų (Calculated from Unit Cell)
Atomic number 04
Morphology Crystals typically acute Di pyramidal, often highly modified; obtuse pyramidal or
tabular
https://en.wikipedia.org/wiki/Anatase
6. TRANSFORMATION STRUCTURE
Process about the founding of TiO2 acceptable units by Gas‐ Phase Reaction of TiCl4 and O2 are
deliberate by Aerosol Reactors. Biochemical reaction of TiCl4, sintering of spots, reactants will
blend, and completely alteration from ANATASE to RUTILE are appreciated as the system
issues of the recreation model submitted. The crystallite dimension in the collection of 55–65 nm
is estimated by a model which suppose the highest fusible particle size, 15 nm the mark
concentration in TiO2 crystallites hardly mix transformation rate, and ANATASE particles
produced at 1,173 K are altered to Rutile readily than those created. The conversion is imaginary
quantitatively by model with manages for interfered time, particle size and rutile proportion. The
model know how to truthful to some particle production cycle as collected, sintering and crystal
remodeling probably. NANOMETRIC elements of spotless BROOKITE TiO2 were produced by
modified THERMOLYSIS of reactant mixture that have TITANIA powder, H C l, and urea.
Unique flower like BROOKITE agglomerates by a simple diameter of 400 to 450 nm calm of
single BROOKITE NANOCRYSTALS of 4 to 5 nm were present. The BROOKITE; rutile
transformation has measured and TiO2 solution with bendable amount of ANATASE,
BROOKITE and RUTILE polymorphs at different temperatures were originate. Main drive
spread electron microscopy, electron diffraction pattern used to check cycle collection, crystallite
unpackaged and pore volume of pure phase BROOKITE and TiO2 mixes. In order to check
metastable stable TiO2 cycle transformation X-ray precipitate diffraction was implemented. The
Photo activity of pure BROOKITE and TiO2 powders with different arrangements of the
BROOKITE,-ANATASE -RUTILE AND ANATASE–RUTILE polymorphs got in the
alterations was tested by photo catalyzed humiliation of 4 Chloro phenols in liquid solution
7. TITANIA section consuming the maximum catalytic action was got at 500 °C, contained 3.2%
BROOKITE, 42.9% ANATASE and 53.9% RUTILE.
SYNTHESIS AND GENESIS
1. Production of TiO2 by sol gel method
TiO2 colloidal mixture created by hydrolysis of titanium tetra isopropoxide. In a typical
process, 1M of titanium tetra isopropoxide motley organized with 4 M of acetic acid.
The subsequent mixture mixed with 10M of dual purified liquid and the mixture shake
energetically for 1 hour to get clear mixture. After an advance period of 24 hour, the
mixture kept in oven at 70°C for 12 hour to get Ti(OH)4 mixture. Then the achieved
mixture was dehydrated at 100 °C to obtain TiO2 crystals. Then crumpled hooked on
fine powders with grout and pounder. Lastly the well powders were hardened at
dissimilar heats i.e. 280 and 580 °C for 1 hour. For comparison as-equipped samples
were also characterized.
2. Synthesis of TiO2 through hydrothermal method
For organizing TiO2 by hydrothermal method, the overhead mentioned method used firstly.
After old for 24 hour, the mixture moved to stainless steel autoclave and positioned in to oven at
180 °C for 12 hour. Then the autoclave was air-conditioned down to possibility temperature. The
mixture was dehydrated at 100 °C to obtain TiO2 crystals. Then crumpled into fine powders
with filling and grinder. Lastly the fine powders hardened at 580 °C for 1 h before description in
all prepared TiO2 the top positions and their comparative intensities are reliable with the
standard dust diffraction patterns of anatase-TiO2. It has a main highest at 25.2° corresponding
8. to the plane. The uttermost position at 37.7, 47.8, 54.1, 62.5 and 69.4 are in agreement with the
TiO2 ANATASE cycle. The lattice parameter of the pure TiO2 are also in according with the
reported value. For the TiO2 bits able by sol gel method the high intensity of ANATASE phase
increases with the claimed temperature. Aimed at the hydrothermally prepared samples, we can
observe very high peak intensity than any other samples. This specifies the detail that the sample
preserved with the hydrothermal method knowledgeable higher crystallinity. Also the peak
expansion designates that the unit size of the hydrothermally factory-made particle is fewer than
the models ready by sol-gel technique importantly it is well-known that the prepared models by
both sol-gel and hydrothermal methods displays clean form of ANATASE cycle
ANALYSIS
The microstructure of the TiO2 synthesized by sol gel and hydrothermal method in the current
study was experiential by FESEM .As in the morphologies of TiO2, the sol-gel sample shows
particle with countless combination. The size of the particle is about 50 nm. The structure of the
particle is not even and it appearances like sphere-shaped in shape. The microstructure of the
sol-gel mixture claimed at 300 °C shows reduction in the accumulation. The formed
nanoparticles are noticeable clearly. Here also the figure of the particle was experiential almost
sphere like morphology with different size. Additional increasing the calcinations temperature to
580 °C also not showed much difference in the morphology of the product. But the visibility of
the distinct nanoparticles is bigger. Also the size circulation is almost uniform likened to other
particles. But for the samples treated with hydrothermally displays much difference compared to
sol-gel method. The delivery of the particle is very uniform and the size of the particle is nearly
same. It is observed that the particle possess clear round shape
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9. Figure 1 TiO2 SYNTHESIS BY SOL GEL METHOD
Figure 2TiO2 SYNTHESIS BY HYDRO THERMAL METHOD
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10. LOCATION IN PAKISTAN
IN PAKISTAN
BALOCHISTAN REGION
DALBADIN
TAFTAN
KHARAN DISTRICT
CHAR KOHAN
NAUSHERWANI MINE
RAS KOH MOUNTAINS
ZARD MTN
NAUSHERWANI MINE
GIGIT BALTISTAN
GIGIT DISTIRCTS
SKARDU DISTRICT
HARAMOSH MTS
TORMIQ VALLEY
KHYBER PAKHTUNKHWA
PROVINCE
SOUTHWAZIRISTAN DISTRICT
WANA
TOLE
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11. ORIGIN
ANATASE, RUTILE and BROOKITE are 3 logically arising isomorphic shapes of TiO2.
ANATASE shapes see-through crystals wavering in shade from black to reddish brown,
yellowish brown, dark blue or gray. Pledges have been originate in the Alps, Brazil, and the Ural
hills, it is also shaped by the enduring of TITANITE and ILMENITE. Mineral ANATASE is not
a major component of artists' materials; however, it has been reported as a minor constituent in
white paints on ancient artifacts from diverse sites, as a mineral impurity in white clay-based
pigments.
ANATASE was produced synthetically in the early 20th century for use as a white paint pigment
with remarkable hiding power. The most successful processes were based on extraction from
crushed and roasted limonite through sulfuric acid. The main glitches in creating a white
ANATASE pigment were to eradicate iron, a chief element in the ILMENITE starting material,
and towards prevent the creation of rutile throughout the final calcination phase the initial
investigational pigments classically not cheerful white, contained scums i.e. remaining iron along
with some rutile. In place of at least an era from about 1908 forward, laboratory research into
likely purification besides production methods led in Europe and the United States. While the
first profitable ANATASE invention less than pure pigment shaped in Norway, almost directly
substituted by a complex pigment having calcium phosphate and barium sulfate in 1919, the
early amalgams explained. In the United States, pure pigment was only fashioned in small
tentative sets until 1926, and the pigments that commercially obtainable from 1916 until 1925
were mixtures with barium sulphate. The Americans ultimately accepted the Norwegian
12. knowledge and the two companies amalgamated in 1920. In France, the BLUMENFELD
procedure was exposed in 1920 to permit manufacture of pure ANATASE titanium dioxide
pigment ,but only in 1923 did manufacture of 96-99% titanium dioxide pigment begin the pure
ANATASE had knowingly greater walloping power than composites. Pigment cleanliness
sustained to be a tricky, however, and even by 1927 the pure ANATASE shaped at THANN in
France was labelled as somewhat yellow. Since rutile had beneficial withstanding properties and
higher hiding power, research to improve experimental rutile-based pigments that were patented
in 1931 concluded in commercial production in Europe and in the United States in 1937. While
rutile products now dominate the market, ANATASE-based pigments continue to be shaped. The
possibility has been elevated that at least one performer, who was a friend of Rossi, was given
some experimental pigment to try in a performer claim. Until the profitable production of
complexes in 1916, these pigments comprised small lots of a few pounds only, and while it is
possible that this limited distribution could have been occurring as early as about 1912, it is
extremely doubtful that more than a few performers remained involved, and they would have
been linked with the investigators in some way The possibility has been raised that at least one
artist , who was a friend of Rossi ( early researchers in the United States), was given some
starting experimental pigment to try in an artistic application. Until the commercial production
of composites in 1916, these pigments comprised small batches of a few pounds only, and
although it is possible that this limited distribution could have been occurring as early as about
1912, it is extremely unlikely that more than a few artists were involved, and they would have
been connected with the researchers in some way
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13. STRENGTH /PHYSICAL PROPERTIES
The smacking command is measured through its aptitude to incomprehensible a contextual of
opposing color. White pigments throw event noticeable light at altogether wavelengths while
tinted pigments engross incident noticeable light at typical wavelengths. Beating power is related
to titanium dioxide's tall refractive key and enhanced particle scope. To attain its occupied
beating power possible in coatings, titanium dioxide necessity be well discrete originally and
evade particle re-agglomeration through the covering lifetime, even earlier claim. TiO2 marks
are intended to facilitate easy dispersal and to be well-matched with other covering
mechanisms that power persuade re-agglomeration of the TiO2 particles. The comparing the
hiding ability and tint strength of TiO2 Select TS-6300 versus 3 general grades in extremely
crowded shade systems, TS-6300 visibly gives the highest whacking power and perkiest colored
paint. This outstanding smacking power gives two benefits to coating follows
Better presentation at the same flat of pigment stocking
Charge decline by using less color while still gaining a good level of walloping power by using
less dye while still gaining a decent level of hiding
Molar mass 79.8658 g/ mol-1
Refractive index 2.55
Hardness 5.5-6
Capacitance ratio 114
Thermal Conductivity: 1.809 - 10.3
Particle size 0.2 ~ 0.3
Solubility: It is inexplicable in frail alkali, dilute acid, but soluble in hot focused sulfuric acid,
hydrochloric acid, nitric acid. The solubility of titanium dioxide is connected to solutes.
14. The relative thickness: In the usually used white pigment, the proportional thickness of titanium dioxide
is less. Of the similar dominance white pigment, titanium dioxide surface area is the chief and pigment
capacity is the all-out.
USES
ANATASE TITANIUM DIOXIDE has a respectable photo catalytic result and is extensively
recycled in photo catalysts and air filter. it is due to high specific surface has been approximately
used in solar cells ,conservational decontamination ,photo catalysts, catalyst broadcasting ,gas
sensor ,and lithium batteries .it is far used in plastics ,ink, papers, rubber ,chemical ,ceramics,
pharmaceutical, food ,and selected extra commerce. Titanium dioxide used as a bleaching and
agreeing agent in porcelain enamels, charitable them illumination, hardness, and acid surrender.
In current times it is used in cosmetics, for example in peel care goods and sunblock lotions, with
entitlements that titanium dioxide guards the skin from ultraviolet radiation since of its things to
absorb ultraviolet bright The photo catalytic action of titanium dioxide consequences in thin
coatings showing self-cleaning and disinfecting belongings below expert Elsevier Bovine to
ultraviolet radiation. Amalgams are branded by existence lightweight and that have very
extraordinary tensile strength , high corrosion confrontation, and an skill to endure extreme
temperatures and therefore are used mainly in flying machine, piping for power plants, protective
covering plating, naval ships, spacecraft, and missiles Because of its single properties, titanium
dioxide is extensively used and is well known in Nano science and nanotechnology.
. Many ornamental companies’ custom titanium dioxide nanoparticles. For of its bright
whiteness, it is used in products such as dyes, coatings, papers, toners, toothpaste, expression
powder, and food coloring Even nevertheless it is one of the greatest produced chemicals, the
http//:www.elsevier.com.pk
15. real and potential benefits of titanium dioxide are not without disagreements. Powder gulp may
cause breathing difficulties. Titanium dioxide has been confidential by the International Agency
aimed at Research on Cancer as a chemical, a “possible carcinogen to humans,” based on studies
of rats that gasped the substance
AGRICULTURE USES
The distinctive physiochemical possessions of small silicon atoms have valuable requests in
diverse parts, with talented requests in the agricultural section. The exclusive properties of TiO2
permit them to manage with agrarian injury that through climate alteration and abiotic stress. The
submission of Si- well as the impacts of chemical and organic fertilizers, for crop improvement.
Nanometer-sized titanium dioxide is an ecologically welcoming visual semiconductor physical.
It has wide submission price in many arenas due to its exceptional structural, optical, and
biochemical possessions. The photo catalytic procedure of -TiO2 changes light energy into
chemical energy under mild conditions. In current years, the application of TiO2 in the
agricultural segment gradually involved care. The TiO2 applications of debasing insecticides,
plant propagation and growth, plants illness control, water purification, pest scum discovery, etc.
are better forecasts. This appraisal labels all of these uses and the research status and
development, including the fundamental values, properties, comprehensive applications, useful
modification, and possible future instructions, for TiO2 in agriculture Soils are fronting new
ecological stress, i.e. titanium dioxide Nano particles . Though these developing contaminants
are progressively unconfined into most bionetworks, with agricultural sectors, their beneficiary
influences on soil and its purpose continue to be observe. The report the response of the
microbial environment of an agricultural soil open over 90 days to TiO2-NPs. To degree their
effect on soil purpose, we absorbed on the nitrogen cycle and slow nitrification and de
nitrification enzymatic actions and by counting explicit illustrative genes Advance, diversity
changes were inspected in bacteria, and the ammonia-oxidizing clades of every area. With
powerful opposite effect on nitrification enzyme actions and the profusions of ammonia-
oxidizing microorganism, TiO2 activated flowing negative belongings on DE nitrification
enzyme action and a profound alteration of the bacterial envoi mental construction after just
ninety days of contact to even the lowest, realistic concentration of NPs. These consequences
16. appeal further research to evaluate how these developing pollutants adapt the soil fitness and
wider ecology purpose .Nanoparticles ACTIVITY is below unfathomable study. In this , the
antioxidant reply to TiO2-NP TRITIUM AESTIVUM was gritty. Enzymatic and the non-
enzymatic antioxidants were assessed in plants bare to the P25 ANATASE: rutile material calm
of TiO2-NP and beneath ecologically realistic doses. Sprout but not root growing stood reduced.
In leaves, thiol metabolism and acrobat buildup were the favored route while in roots the
ALREADY PRESENT antioxidant capacity was specially used. Both leaves and roots presented
augmented glutathione reductive and de hydroascorbate reductive actions and reduced acrobat
peroxidase action. Roots, however, offered higher enzymatic basal stages than leaves. On the
other SIDE, when probing non-enzymatic antioxidants, the proportion of reduced-to-oxidized
glutathione bigger in leaves and reduced in roots. Unprotected leaves likewise obtainable higher
whole acrobat buildup likened to roots. TiO2-NP experience down regulated, with more fame in
roots, antioxidant enzyme genes programming catalase, acrobat peroxidase, and
dehydroascorbate reductive. In leaves, superoxide dismutase gene expression was augmented.
All data locate to TiO2-NP toxicity overhead 5 mg/L, with airborne shares being more
vulnerable, which draws concerns on the safety doses for the use of these NPs in agricultural
performs.
https://www.avensonline.org/blog/application-agriculture
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http//:Wikipedia.com .pk. ANATASE
17. INDUSTRIAL USE
Titanium dioxide consumes extraordinary optical possessions, with a very tall refractive index
near to diamond. It is also a very stable compound and can be excited to over 2000 K before
melting. These possessions that motivate its most significant uses. Titanium dioxide is a
solitary crystalline system in the superficial science of metal oxides. The superficial science of
Titanium dioxide is now liking a rapid development of interest from investigators and
scientists. Titanium dioxide is used as a varied catalysis, photo catalyst and also discoveries its
requests in solar cells. Other application includes usage as gas devices and as white pigments
in paint trades. Titanium dioxide act as a corrosive defensive covering which can again be
secondhand as an optical coating and in electronic devices. The fresh use of it IS in
biocompatibility of bone grafts and an INSULATOR in MOSEFETS. It can also use in a Nano
planned form in Li founded batteries and electro chromic devices. TiO2 is a constituent used in
titanic catalysts for discerning oxidation reactions. Though TiO2 is not appropriate to be
additional as a structural sustenance the strong bonding among titanium and oxygen stretches
countless thermal steadiness, melting at 2100 K. It is thus used as a ceramic material. It is also
used to increase the acid confrontation of vitreous coatings material but by doing small additions
of titanic the metallic based catalysts can be adapted in a very profound way. Titanium dioxide
used for many years in a vast variety of industrial and consumer goods i.e. dyes, coatings, rag
and paperboard, plastics and rubber, letterpress inks, and textiles, catalyst systems, ceramics,
floor coat, roof materials, and pharmaceuticals, water treatment agents, food pigments and in
automotive foodstuffs. Exteriors then items that are white in color comprise ANATASE.
Numerous materials in our house contain titanium dioxide much smaller amounts of titanium
dioxide are secondhand as a semi-conductor and to catalyze the photo arrangement of water into
18. H and O2, ceramics, floor coat, roof materials, and pharmaceuticals, water treatment agents, food
pigments and in automotive foodstuffs. Exteriors then items that are white in color comprise
ANATASE. Numerous materials in our house contain titanium dioxide much smaller amounts of
titanium dioxide are secondhand as a semi-conductor and to catalyze the photo arrangement of
water into H and O2.
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19. PRACTICAL USE
The Communication Of Water With Tio2 Is Vital To Many Of Its Practical Applications,
Counting Photo Catalytic Water Partial. Next the First Protest Of This Marvel Forty Years Ago
There Plentiful Educations of the Rutile Solitary Crystal Tio2 Border with Water. This Has
Providing An Atomic Level Sympathetic Of The Water–Tio2 Communication. However, Closely
All Of The Earlier Studies Of Water Boundaries Include H2o In The Vapors Cycle. Discover
The Interfacial Construction Between Liquid Water And A Rutile Tio2 Shallow Pre-Considered
At The Atomic Level. Scanning Tunneling Microscopy And Superficial X-Ray Diffraction Are
Cast-Off To Control Construction, Which Is Included Of A Well-Ordered Collection Of
Hydroxyl Molecules With H2o In The 2nd Layer. The Quantitative Structural Properties
Derived Here Provide A Basis With Which To Explore The Atomistic Properties And Hence
Mechanisms Complicated In Tio2 Photo catalysis Titanium Dioxide Is By Distant The Most
Used Semiconductor Material For Photo catalytic Claims. Still, It Is Transparent To Visible
Light. Recently, It Has Been Proved Alignment For The Rutile Anastasia Mix Would Recover
Noticeable Light Absorption It Is Recycled To Crop Dyes And Coverings Counting Glazes And
Enamels. An efficient photo catalyst converts solar energy into chemical energy which can be
used for environmental and energy applications such as water treatment, air purification, self-
cleaning surfaces, and hydrogen production by water cleavage and CO2 conversion to
hydrocarbon fuel water. It befits very critical so to find maintainable ways to mitigate
contamination in order to deliver a clean and safe environment for humans.
20. CEC
CEC is said in m e q/100 g that is equal to cent moles of charge /kg of exchanger. CEC having
range from 0 - 2 m e q 1100g at about 1s 6 he clay mineral and organic matter components of
soil -VE charged place on their area which adsorb and grip +VE charged ions through
electrostatic strength. This electrical charge is serious to the source of nutrients to plants because
many nutrients happen as cat ions (e.g. magnesium, and calcium etc.). In over-all terms, soils
with large extents of -vet charge are more productive because they retain extra cat ions however,
creative crops and fallows can mature on low CEC soils. The main ions related with CEC in
soils are the exchangeable Ca2+, Mg2+, Na+ and K+ , and are normally mentioned to as the base
cat ions. In most cases, resulting the examined base cat ions stretches a passable measure of
CEC
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21. . Though, as soils become additional acidic these cat ions are substituted by H+, Al3+ and Mn2+,
and common means will yield CEC ideals much higher than what occurs in the field). This
exchange acidity desires to be encompassed when summing the base cat ions and this dimension
is mentioned to as effective CEC The CEC of soils differs execution the clay %, the kind of
clay, soil pH and sum of organic matter. Unadulterated sand has an actual low CEC, less than 2
m e q/100 g, and the CEC of the sand and silt extent fractions (2 µm/2 mm) of most soils is
negligible. Claying sandy soils for managing water repellence increases the CEC of the surface
coatings by a small amount liable on type and quantity of clay further. Normally CEC is
increased via less than 1 m e q/100 g.
The utmost frequently happening clay in Western Australian soils, kaolinite, has a CEC of about
10 m e q/100 g. Supplementary clays such as ILLITE and SMECTITE have CECs fluctuating
from 25 - 100 m e q/100 g. Organic matter has a very high CEC reaching from 250 - 400 m e
q/100 g . Because a higher CEC usually designates more clay and organic stuff is present in the
soil, high CEC soils normally have superior water field capacity than low CEC soils
AEC
Anion Exchange Capacity Is Defined As Number Of Anion Negative Charges Retained By 100
Grams Of Soil.
AEC Represents the Positive Charge Available to attracts The Anions in the Solution
Ranges From 0 To 2 m e q 1100g At AEC Expressed As The m e q Per 100 Grams Of Soil (
Or Of Other Adsorbing Materials , Such As Clay) sum total of exchangeable anions that a soil
can adsorb. In addition to predominantly negative charge sites which attract soil captions, all soil
22. clays and organic substance instantaneously have comparatively small number of +V charge sites
which retain anions in dynamic equilibrium with the soil solution. The ANION EXCHANGE
CAPACITY of a soil, -VE charge VOLUME of the soil particles at given pH value necessity be
known a priori in order to evaluate the mean free binding energy of cat ions and anions to the
soil. To regulate this -VE charge density, the clay -size PROPORTION of soil particles of
breadth IS ABOUT< 2 μ m was detached by sedimentation, dehydrated, and ground. The
positive and negative charge densities of the clay fractions of the soils at different pH values
were resolute, yielding plots of the +VE and -VE charge densities versus pH standards. Constant-
charge soil particles convey no important +VE charge, which is a precondition for the proposed
method of characterizing their interactions with captions, and their negative charge densities are
pH dependent
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