>> Part a).
>> Pearlite :- Pearlite is a two-phased, lamellar (or layered) structure composed of alternating
layers of ferrite (88 wt%) and cementite (12 wt%) that occurs in some steels and cast irons. In
fact, the lamellar appearance is misleading since the individual lamellae within a colony are
connected in three dimensions; a single colony is therefore an interpenetrating bicrystal of ferrite
and cementite. In an iron-carbon alloy, during slow cooling pearlite forms by a eutectoid reaction
as austenite cools below 727 °C (1,341 °F) (the eutectoid temperature). Pearlite is a
microstructure occurring in many common grades of steels.
>> Cementite :- Cementite, also known as iron carbide, is an interstitial compound of iron and
carbon, more precisely an intermediate transition metal carbide with the formula Fe3C. By
weight, it is 6.67% carbon and 93.3% iron. It has an orthorhombic crystal structure. It is a hard,
brittle material, normally classified as a ceramic in its pure form, though it is more important in
ferrous metallurgy. While iron carbide is present in most steels and cast irons, it is produced as a
raw material in the Iron Carbide process, which belongs to the family of alternative ironmaking
technologies.
>> Austenite :- Austenite, also known as gamma-phase iron (-Fe), is a metallic, non-magnetic
allotrope of iron or a solid solution of iron, with analloying element. In plain-carbon steel,
austenite exists above the critical eutectoid temperature of 1,000 K (1,340 °F; 730 °C); other
alloys of steel have different eutectoid temperatures. It is Face Centred Cubic Configuration
(FCC).
>> Eutectoid Phase :- When the solution above the transformation point is solid, rather than
liquid, an analogous eutectoid transformation can occur. For instance, in the iron-carbon system,
the austenite phase can undergo a eutectoidtransformation to produce ferrite and cementite, often
in lamellar structures such as pearlite and bainite.
>> Proeutectoid :- When a hot steel with carbon content very close to 0.8%, is cooled down
slowly, there is a temperature (723 deg C) at which a constant-temperature transformation takes
place. This is called eutectoid transformation. And this results in formation of alternate layers of
Ferrite and Iron-Carbide (Fe3C).
But if the carbon content in this hot steel is much less than 0.8%, and it is cooled down slowly,
then till the temperature reduces to 723 deg C, a part of Austenite (also called gamma iron) gets
transformed to Ferrite by rejecting carbon from the solution. This is not a constant-temperature
process and occurs over a range of temperature. The ferrite so formed is called Proeutectoid...At
723 deg C, all the remaining Austenite get converted to Pearlite at this constant temperature -
which is nothing but alternate layers of Ferrite and cementite
>> Martensite :- Martensite, most commonly refers to a very hard form of steel crystalline
structure, but it can also refer to any crystal structure that is form.
Mumbai University.
Mechanical Engineering
SEM III
Material Technology
MOdule 2.2
Theory of Alloys& Alloys Diagrams :
Significance of alloying, Definition, Classification and properties of different types of alloys, Solidification of pure metal, Different types of phase diagrams (Isomorphous, Eutectic,
08
University of Mumbai, B. E. (Mechanical Engineering), Rev 2016 19
Peritectic, Eutectoid, Peritectoid) and their analysis, Importance of Iron as engineering material, Allotropic forms of Iron, Influence of carbon in Iron- Carbon alloying Iron-Iron carbide diagram and its analysis
Mumbai University.
Mechanical Engineering
SEM III
Material Technology
MOdule 2.2
Theory of Alloys& Alloys Diagrams :
Significance of alloying, Definition, Classification and properties of different types of alloys, Solidification of pure metal, Different types of phase diagrams (Isomorphous, Eutectic,
08
University of Mumbai, B. E. (Mechanical Engineering), Rev 2016 19
Peritectic, Eutectoid, Peritectoid) and their analysis, Importance of Iron as engineering material, Allotropic forms of Iron, Influence of carbon in Iron- Carbon alloying Iron-Iron carbide diagram and its analysis
The term Lewis acid refers to a definition of aci.pdfannaelctronics
The term Lewis acid refers to a definition of acid published by Gilbert N. Lewis in
1923, specifically: An acid substance is one which can employ an electron lone pair from another
molecule in completing the stable group of one of its own atoms.[1] Thus, H+ is a Lewis acid,
since it can accept a lone pair, completing its stable form, which requires two electrons. The
modern-day definition of Lewis acid, as given by IUPAC is a molecular entity (and the
corresponding chemical species) that is an electron-pair acceptor and therefore able to react with
a Lewis base to form a Lewis adduct, by sharing the electron pair furnished by the Lewis
base.[2] This definition is both more general and more specific—the electron pair need not be a
lone pair (it could be the pair of electrons in a p bond, for example), but the reaction should give
an adduct (and not just be a displacement reaction). Crystal field theory (CFT) is a model that
describes the breaking of degeneracies of electronic orbital states, usually d or f orbitals, due to a
static electric field produced by a surrounding charge distribution (anion neighbors). This theory
has been used to describe various spectroscopies of transition metal coordination complexes, in
particular optical spectra (colours). CFT successfully accounts for some magnetic properties,
colours, hydration enthalpies, and spinel structures of transition metal complexes, but it does not
attempt to describe bonding. CFT was developed by physicists Hans Bethe and John Hasbrouck
van Vleck[1] in the 1930s. CFT was subsequently combined with molecular orbital theory to
form the more realistic and complex ligand field theory (LFT), which delivers insight into the
process of chemical bonding in transition metal complexes. In chemistry, valence bond (VB)
theory is one of two basic theories, along with molecular orbital (MO) theory, that were
developed to use the methods of quantum mechanics to explain chemical bonding. It focuses on
how the atomic orbitals of the dissociated atoms combine to give individual chemical bonds
when a molecule is formed. In contrast, molecular orbital theory has orbitals that cover the whole
molecule.
Solution
The term Lewis acid refers to a definition of acid published by Gilbert N. Lewis in
1923, specifically: An acid substance is one which can employ an electron lone pair from another
molecule in completing the stable group of one of its own atoms.[1] Thus, H+ is a Lewis acid,
since it can accept a lone pair, completing its stable form, which requires two electrons. The
modern-day definition of Lewis acid, as given by IUPAC is a molecular entity (and the
corresponding chemical species) that is an electron-pair acceptor and therefore able to react with
a Lewis base to form a Lewis adduct, by sharing the electron pair furnished by the Lewis
base.[2] This definition is both more general and more specific—the electron pair need not be a
lone pair (it could be the pair of electrons in a p bond, for example.
MnO2 may act as a catalyst.in the other reaction .pdfannaelctronics
MnO2 may act as a catalyst.in the other reaction of KBrO3 and Sulfuric acid.
ANSWER
Solution
MnO2 may act as a catalyst.in the other reaction of KBrO3 and Sulfuric acid.
ANSWER.
Intermolecular attractions are attractions betwee.pdfannaelctronics
Intermolecular attractions are attractions between one molecule and a neighbouring
molecule. The forces of attraction which hold an individual molecule together (for example, the
covalent bonds) are known as intramolecular attractions. These two words are so confusingly
similar that it is safer to abandon one of them and never use it. The term \"intramolecular\" won\'t
be used again on this site. All molecules experience intermolecular attractions, although in some
cases those attractions are very weak. Even in a gas like hydrogen, H2, if you slow the molecules
down by cooling the gas, the attractions are large enough for the molecules to stick together
eventually to form a liquid and then a solid. In hydrogen\'s case the attractions are so weak that
the molecules have to be cooled to 21 K (-252°C) before the attractions are enough to condense
the hydrogen as a liquid. Helium\'s intermolecular attractions are even weaker - the molecules
won\'t stick together to form a liquid until the temperature drops to 4 K (-269°C). van der Waals
forces: dispersion forces Dispersion forces (one of the two types of van der Waals force we are
dealing with on this page) are also known as \"London forces\" (named after Fritz London who
first suggested how they might arise). The origin of van der Waals dispersion forces Temporary
fluctuating dipoles Attractions are electrical in nature. In a symmetrical molecule like hydrogen,
however, there doesn\'t seem to be any electrical distortion to produce positive or negative parts.
But that\'s only true on average. The lozenge-shaped diagram represents a small symmetrical
molecule - H2, perhaps, or Br2. The even shading shows that on average there is no electrical
distortion. But the electrons are mobile, and at any one instant they might find themselves
towards one end of the molecule, making that end -. The other end will be temporarily short of
electrons and so becomes +. Note: (read as \"delta\") means \"slightly\" - so + means \"slightly
positive\". An instant later the electrons may well have moved up to the other end, reversing
the polarity of the molecule. This constant \"sloshing around\" of the electrons in the molecule
causes rapidly fluctuating dipoles even in the most symmetrical molecule. It even happens in
monatomic molecules - molecules of noble gases, like helium, which consist of a single atom. If
both the helium electrons happen to be on one side of the atom at the same time, the nucleus is
no longer properly covered by electrons for that instant. How temporary dipoles give rise to
intermolecular attractions I\'m going to use the same lozenge-shaped diagram now to represent
any molecule which could, in fact, be a much more complicated shape. Shape does matter (see
below), but keeping the shape simple makes it a lot easier to both draw the diagrams and
understand what is going on. Imagine a molecule which has a temporary polarity being
approached by one which happens to be entirely non-polar just at .
Xenodiagnosis is the method used to document presesnce of a microorg.pdfannaelctronics
Xenodiagnosis is the method used to document presesnce of a microorganism by exposing the
infected tissue to a vector and than examining the vector for the presence of microorganisms.
Uninfected vectors and detection of pathogen DNA in host cell will be required for
xenodiagnosis.
Solution
Xenodiagnosis is the method used to document presesnce of a microorganism by exposing the
infected tissue to a vector and than examining the vector for the presence of microorganisms.
Uninfected vectors and detection of pathogen DNA in host cell will be required for
xenodiagnosis..
There are many more conditions than just the norms of the culture th.pdfannaelctronics
There are many more conditions than just the norms of the culture that affect and assert the
statement
Solution
There are many more conditions than just the norms of the culture that affect and assert the
statement.
The three layers of smooth muscle that includes mucosa. innermost tu.pdfannaelctronics
The three layers of smooth muscle that includes mucosa. innermost tunic of a ureter; formed by
transitional epithelium that is both stretchable and impermeable to the passage of urine; external
to the transitional epithelium is the lamina propria, composed of dense irregular connective tissue
The correct answer is 2
Solution
The three layers of smooth muscle that includes mucosa. innermost tunic of a ureter; formed by
transitional epithelium that is both stretchable and impermeable to the passage of urine; external
to the transitional epithelium is the lamina propria, composed of dense irregular connective tissue
The correct answer is 2.
The independent variable is the one which changes in each plant. Thi.pdfannaelctronics
The independent variable is the one which changes in each plant. This is the concentration of the
salt solution in each case.Based on the independent variable the changes seen give us the
dependent variable. This is the height of the plants. The heights of the plants[dependent variable]
may be influenced by the salt solutions[independent variable].
Solution
The independent variable is the one which changes in each plant. This is the concentration of the
salt solution in each case.Based on the independent variable the changes seen give us the
dependent variable. This is the height of the plants. The heights of the plants[dependent variable]
may be influenced by the salt solutions[independent variable]..
Species diversity is more in near island as rate of immigration is m.pdfannaelctronics
Species diversity is more in near island as rate of immigration is more.
Also it is more in large islands as more resources are available there and rate kf extinction is low.
Solution
Species diversity is more in near island as rate of immigration is more.
Also it is more in large islands as more resources are available there and rate kf extinction is low..
Solution Flies do not have teeth for chewing food.So,like human f.pdfannaelctronics
Solution
:
Flies do not have teeth for chewing food.So,like human flies have some acid in their stomach for
digestion of food.But digestion of food in flies not occur in the stomach.It is occur outside of the
body.Flies vomit acids present in their stomach on solid food and convert it into liquid form.Flies
can intake food in liquid form only.After converting it into liquid form it is consume by the flies..
Program To change this license header, choose License Heade.pdfannaelctronics
Program:
/*
* To change this license header, choose License Headers in Project Properties.
* To change this template file, choose Tools | Templates
* and open the template in the editor.
*/
package chegg;
// A Java program for Dijkstra\'s single source shortest path algorithm.
// The program is for adjacency matrix representation of the graph
import java.util.*;
import java.lang.*;
import java.io.*;
class DijkstraAlgorithem
{
// A utility function to find the vertex with minimum distance value,
// from the set of vertices not yet included in shortest path tree
static final int V=6;
int minDistance(int dist[], Boolean sptSet[])
{
// Initialize min value
int min = Integer.MAX_VALUE, min_index=-1;
for (int v = 0; v < V; v++)
if (sptSet[v] == false && dist[v] <= min)
{
min = dist[v];
min_index = v;
}
return min_index;
}
// A utility function to print the constructed distance array
void print
Solution
(int dist[], int n,int src)
{
System.out.println( \" Here Infinite=\"+Integer.MAX_VALUE);
System.out.println(\" Source Vertex:\"+(src+1));
System.out.println(\"Vertex Distance from Source\");
for (int i = 0; i < V; i++)
System.out.println((i+1)+\" \\t\\t \"+dist[i]);
}
// Funtion that implements Dijkstra\'s single source shortest path
// algorithm for a graph represented using adjacency matrix
// representation
void dijkstra(int graph[][], int src)
{
int dist[] = new int[V]; // The output array. dist[i] will hold
// the shortest distance from src to i
// sptSet[i] will true if vertex i is included in shortest
// path tree or shortest distance from src to i is finalized
Boolean sptSet[] = new Boolean[V];
// Initialize all distances as INFINITE and stpSet[] as false
for (int i = 0; i < V; i++)
{
dist[i] = Integer.MAX_VALUE;
sptSet[i] = false;
}
// Distance of source vertex from itself is always 0
dist[src] = 0;
// Find shortest path for all vertices
for (int count = 0; count < V-1; count++)
{
// Pick the minimum distance vertex from the set of vertices
// not yet processed. u is always equal to src in first
// iteration.
int u = minDistance(dist, sptSet);
// Mark the picked vertex as processed
sptSet[u] = true;
// Update dist value of the adjacent vertices of the
// picked vertex.
for (int v = 0; v < V; v++)
// Update dist[v] only if is not in sptSet, there is an
// edge from u to v, and total weight of path from src to
// v through u is smaller than current value of dist[v]
if (!sptSet[v] && graph[u][v]!=0 &&
dist[u] != Integer.MAX_VALUE &&
dist[u]+graph[u][v] < dist[v])
dist[v] = dist[u] + graph[u][v];
}
// print the constructed distance array
print.
plexusFormed from anterioe rani o these spinal nervesMajor nerve.pdfannaelctronics
plexus
Formed from anterioe rani o these spinal nerves
Major nerves formed from the plexus
Cervical
The cervical plexus is a plexus of the front rami of the initial four cervical spinal nerves which
are situated from C1 to C4 cervical fragment in the neck.
They are found along the side to the transverse procedures between prevertebral muscles from
the average side and vertebral (m. scalenus, m. levator scapulae, m. splenius cervicis) from
horizontal side. There is anastomosis with extra nerve, hypoglossal nerve and thoughtful trun
The cervical plexus has two sorts of branches: cutaneous and strong.
Cutaneous (4 branches):
Incredible auricular nerve - innervates skin close concha auricle (external ear) and outer acoustic
meatus (ear waterway) (C2&C3)
Transverse cervical nerve - innervates front locale of neck (C2&C3)
Lesser occipital - innervates the skin and the scalp posterosuperior to the auricle (C2)
Supraclavicular nerves - innervate the skin above and underneath the clavicle (C3,C4)
Muscular:
Ansa cervicalis (circle framed from C1-C3), and so forth (geniohyoid (C1 just), thyrohyoid (C1
just), sternothyroid, sternohyoid, omohyoid)
Phrenic (C3-C5 (fundamentally C4))- innervates stomach and the pericardium
Segmental branches (C1-C4)- innervates front and center scalenes
Brachial
The brachial plexus is a system of nerves shaped by the foremost rami of the lower four cervical
nerves and first thoracic nerve (C5, C6, C7, C8, and T1). This plexus stretches out from the
spinal line, through the cervicoaxillary trench in the neck, over the primary rib, and into the
armpit. It supplies afferent and efferent nerve strands to the mid-section, shoulder, arm and hand.
The Brachial Plexus
1 Roots.
2 Trunks.
3 Divisions.
4 Cords.
5 Major Branches. 5.1 Musculocutaneous Nerve. 5.2 Axillary Nerve. 5.3 Median Nerve. 5.4
Radial Nerve. 5.5 Ulnar Nerve. 5.6 Practical Relevance: Dissecting the Brachial Plexus.
6 Minor Branches.
lumbosacral
The anterior divisions of the lumbar nerves, sacral nerves, and coccygeal nerve form the
lumbosacral plexus, the first lumbar nerve being frequently joined by a branch from the twelfth
thoracic. For descriptive purposes this plexus is usually divided into three parts:
lumbar plexus
sacral plexus
pudendal plexus
lumbar plexus
sacral plexus
pudendal plexus
plexus
Formed from anterioe rani o these spinal nerves
Major nerves formed from the plexus
Cervical
The cervical plexus is a plexus of the front rami of the initial four cervical spinal nerves which
are situated from C1 to C4 cervical fragment in the neck.
They are found along the side to the transverse procedures between prevertebral muscles from
the average side and vertebral (m. scalenus, m. levator scapulae, m. splenius cervicis) from
horizontal side. There is anastomosis with extra nerve, hypoglossal nerve and thoughtful trun
The cervical plexus has two sorts of branches: cutaneous and strong.
Cutaneous (4 branches):
Incredible auricular nerve - innervates skin close con.
Ok, so the number of double bond equivalents in the compound is [C4H.pdfannaelctronics
Ok, so the number of double bond equivalents in the compound is [C4H10)-(C4H8)]/2 = 1 DBE
1) IR
so the large trough from 3400cm-1 to 2400cm-1 as well as the peak at ~1700cm-1 indicates an
acid. That accounts for 1 carbon, both oxygens, and one hydrogen. That also accounts for the one
double bond equivalent.
That leaves 3 carbons and 7 hydrogens.
2) NMR
Methyl groups usually give proton peaks around 0.9ppm and shift further downfield when
adding electron withdrawing groups nearby. It\'s a pretty good guess that the triplet at ~1.1ppm is
a methyl group. The fact that it\'s a triplet indicates the carbon next to it has two protons attached
to it.
That gives a CH3-CH2- (as well as the -COOH group)
all that\'s left now is one carbon and two hydrogens (CH2)
Looking at the other two proton peaks in the nmr ... there\'s one triplet and one sextet.
The triplet would be a CH2 group that is next to another CH2 group (and not anything else), so it
must be a CH2 next to the COOH
Now you would have two pieces:
CH3-CH2- and -CH2-COOH
put them together and check the coupling of the protons...
you should end up with two triplets (proton split by two others), one sextet (proton split by 5
others), and a small peak somewhere around 9-13ppm. (that\'s the peak indicated by the offset of
2.0ppm on the spectrum)
So the structure would be:
CH3-CH2-CH2-COOH (C4H8O2)
Solution
Ok, so the number of double bond equivalents in the compound is [C4H10)-(C4H8)]/2 = 1 DBE
1) IR
so the large trough from 3400cm-1 to 2400cm-1 as well as the peak at ~1700cm-1 indicates an
acid. That accounts for 1 carbon, both oxygens, and one hydrogen. That also accounts for the one
double bond equivalent.
That leaves 3 carbons and 7 hydrogens.
2) NMR
Methyl groups usually give proton peaks around 0.9ppm and shift further downfield when
adding electron withdrawing groups nearby. It\'s a pretty good guess that the triplet at ~1.1ppm is
a methyl group. The fact that it\'s a triplet indicates the carbon next to it has two protons attached
to it.
That gives a CH3-CH2- (as well as the -COOH group)
all that\'s left now is one carbon and two hydrogens (CH2)
Looking at the other two proton peaks in the nmr ... there\'s one triplet and one sextet.
The triplet would be a CH2 group that is next to another CH2 group (and not anything else), so it
must be a CH2 next to the COOH
Now you would have two pieces:
CH3-CH2- and -CH2-COOH
put them together and check the coupling of the protons...
you should end up with two triplets (proton split by two others), one sextet (proton split by 5
others), and a small peak somewhere around 9-13ppm. (that\'s the peak indicated by the offset of
2.0ppm on the spectrum)
So the structure would be:
CH3-CH2-CH2-COOH (C4H8O2).
order of overlap of atomic orbitals from highest extent of overlap t.pdfannaelctronics
order of overlap of atomic orbitals from highest extent of overlap to lowest is,
I2 > IBr > ICl > IF
Because,
I2-is homo diatomic molecule and having good overlapping between the atomic orbitals of two
iodine atoms.
IBr-is a hetero di-atomic molecule and having almost good overlapping between the atomic
orbitals of iodine and bromine atoms even though these two atoms belongs to different periods.
ICl-is a hetero di-atomic molecule and having moderate overlapping between the atomic orbitals
of iodine and chlorine atoms.Because, these two atoms belongs to different periods and size
different is more.
IF-is a hetero di-atomic molecule and having poor overlapping between the atomic orbitals of
iodine and fluorine atoms.Because, these two atoms belongs to different periods and size
different is too more.
Solution
order of overlap of atomic orbitals from highest extent of overlap to lowest is,
I2 > IBr > ICl > IF
Because,
I2-is homo diatomic molecule and having good overlapping between the atomic orbitals of two
iodine atoms.
IBr-is a hetero di-atomic molecule and having almost good overlapping between the atomic
orbitals of iodine and bromine atoms even though these two atoms belongs to different periods.
ICl-is a hetero di-atomic molecule and having moderate overlapping between the atomic orbitals
of iodine and chlorine atoms.Because, these two atoms belongs to different periods and size
different is more.
IF-is a hetero di-atomic molecule and having poor overlapping between the atomic orbitals of
iodine and fluorine atoms.Because, these two atoms belongs to different periods and size
different is too more..
Unit 8 - Information and Communication Technology (Paper I).pdfThiyagu K
This slides describes the basic concepts of ICT, basics of Email, Emerging Technology and Digital Initiatives in Education. This presentations aligns with the UGC Paper I syllabus.
Biological screening of herbal drugs: Introduction and Need for
Phyto-Pharmacological Screening, New Strategies for evaluating
Natural Products, In vitro evaluation techniques for Antioxidants, Antimicrobial and Anticancer drugs. In vivo evaluation techniques
for Anti-inflammatory, Antiulcer, Anticancer, Wound healing, Antidiabetic, Hepatoprotective, Cardio protective, Diuretics and
Antifertility, Toxicity studies as per OECD guidelines
Welcome to TechSoup New Member Orientation and Q&A (May 2024).pdfTechSoup
In this webinar you will learn how your organization can access TechSoup's wide variety of product discount and donation programs. From hardware to software, we'll give you a tour of the tools available to help your nonprofit with productivity, collaboration, financial management, donor tracking, security, and more.
Read| The latest issue of The Challenger is here! We are thrilled to announce that our school paper has qualified for the NATIONAL SCHOOLS PRESS CONFERENCE (NSPC) 2024. Thank you for your unwavering support and trust. Dive into the stories that made us stand out!
Francesca Gottschalk - How can education support child empowerment.pptxEduSkills OECD
Francesca Gottschalk from the OECD’s Centre for Educational Research and Innovation presents at the Ask an Expert Webinar: How can education support child empowerment?
Synthetic Fiber Construction in lab .pptxPavel ( NSTU)
Synthetic fiber production is a fascinating and complex field that blends chemistry, engineering, and environmental science. By understanding these aspects, students can gain a comprehensive view of synthetic fiber production, its impact on society and the environment, and the potential for future innovations. Synthetic fibers play a crucial role in modern society, impacting various aspects of daily life, industry, and the environment. ynthetic fibers are integral to modern life, offering a range of benefits from cost-effectiveness and versatility to innovative applications and performance characteristics. While they pose environmental challenges, ongoing research and development aim to create more sustainable and eco-friendly alternatives. Understanding the importance of synthetic fibers helps in appreciating their role in the economy, industry, and daily life, while also emphasizing the need for sustainable practices and innovation.
2024.06.01 Introducing a competency framework for languag learning materials ...Sandy Millin
http://sandymillin.wordpress.com/iateflwebinar2024
Published classroom materials form the basis of syllabuses, drive teacher professional development, and have a potentially huge influence on learners, teachers and education systems. All teachers also create their own materials, whether a few sentences on a blackboard, a highly-structured fully-realised online course, or anything in between. Despite this, the knowledge and skills needed to create effective language learning materials are rarely part of teacher training, and are mostly learnt by trial and error.
Knowledge and skills frameworks, generally called competency frameworks, for ELT teachers, trainers and managers have existed for a few years now. However, until I created one for my MA dissertation, there wasn’t one drawing together what we need to know and do to be able to effectively produce language learning materials.
This webinar will introduce you to my framework, highlighting the key competencies I identified from my research. It will also show how anybody involved in language teaching (any language, not just English!), teacher training, managing schools or developing language learning materials can benefit from using the framework.
Acetabularia Information For Class 9 .docxvaibhavrinwa19
Acetabularia acetabulum is a single-celled green alga that in its vegetative state is morphologically differentiated into a basal rhizoid and an axially elongated stalk, which bears whorls of branching hairs. The single diploid nucleus resides in the rhizoid.
How to Make a Field invisible in Odoo 17Celine George
It is possible to hide or invisible some fields in odoo. Commonly using “invisible” attribute in the field definition to invisible the fields. This slide will show how to make a field invisible in odoo 17.
Chapter 3 - Islamic Banking Products and Services.pptx
Part a). Pearlite - Pearlite is a two-phased, lamellar (or l.pdf
1. >> Part a).
>> Pearlite :- Pearlite is a two-phased, lamellar (or layered) structure composed of alternating
layers of ferrite (88 wt%) and cementite (12 wt%) that occurs in some steels and cast irons. In
fact, the lamellar appearance is misleading since the individual lamellae within a colony are
connected in three dimensions; a single colony is therefore an interpenetrating bicrystal of ferrite
and cementite. In an iron-carbon alloy, during slow cooling pearlite forms by a eutectoid reaction
as austenite cools below 727 °C (1,341 °F) (the eutectoid temperature). Pearlite is a
microstructure occurring in many common grades of steels.
>> Cementite :- Cementite, also known as iron carbide, is an interstitial compound of iron and
carbon, more precisely an intermediate transition metal carbide with the formula Fe3C. By
weight, it is 6.67% carbon and 93.3% iron. It has an orthorhombic crystal structure. It is a hard,
brittle material, normally classified as a ceramic in its pure form, though it is more important in
ferrous metallurgy. While iron carbide is present in most steels and cast irons, it is produced as a
raw material in the Iron Carbide process, which belongs to the family of alternative ironmaking
technologies.
>> Austenite :- Austenite, also known as gamma-phase iron (-Fe), is a metallic, non-magnetic
allotrope of iron or a solid solution of iron, with analloying element. In plain-carbon steel,
austenite exists above the critical eutectoid temperature of 1,000 K (1,340 °F; 730 °C); other
alloys of steel have different eutectoid temperatures. It is Face Centred Cubic Configuration
(FCC).
>> Eutectoid Phase :- When the solution above the transformation point is solid, rather than
liquid, an analogous eutectoid transformation can occur. For instance, in the iron-carbon system,
the austenite phase can undergo a eutectoidtransformation to produce ferrite and cementite, often
in lamellar structures such as pearlite and bainite.
>> Proeutectoid :- When a hot steel with carbon content very close to 0.8%, is cooled down
slowly, there is a temperature (723 deg C) at which a constant-temperature transformation takes
place. This is called eutectoid transformation. And this results in formation of alternate layers of
Ferrite and Iron-Carbide (Fe3C).
But if the carbon content in this hot steel is much less than 0.8%, and it is cooled down slowly,
then till the temperature reduces to 723 deg C, a part of Austenite (also called gamma iron) gets
transformed to Ferrite by rejecting carbon from the solution. This is not a constant-temperature
process and occurs over a range of temperature. The ferrite so formed is called Proeutectoid...At
723 deg C, all the remaining Austenite get converted to Pearlite at this constant temperature -
which is nothing but alternate layers of Ferrite and cementite
2. >> Martensite :- Martensite, most commonly refers to a very hard form of steel crystalline
structure, but it can also refer to any crystal structure that is formed by diffusionless
transformation. It includes a class of hard minerals occurring as lath- or plate-shaped crystal
grains. When viewed in cross section, the lenticular (lens-shaped) crystal grains are sometimes
incorrectly described as acicular (needle-shaped)
>> Bainite :-
Bainite is a plate-like microstructure or phase morphology (not an equilibrium phase) that forms
in steels at temperatures of 250–550 °C (depending on alloy content). It is one of the
decomposition products that may form when austenite (the face centered cubic crystal structure
of iron) is cooled past a critical temperature. This critical temperature is 1000K (727 °C, 1340
°F) in plain carbon steels. Davenport and Bain originally described the microstructure as being
similar in appearance to tempered martensite.
A fine non-lamellar structure, bainite commonly consists of cementite and dislocation-rich
ferrite. The high concentration of dislocations in the ferrite present in bainite makes this ferrite
harder than it normally would be.
Part b). Two major differences are:
1) atomic diffusion is necessary for the pearlitic transformation, whereas the martensitic
transformation is diffusionless; and
2) relative to transformation rate, the martensitic transformation is virtually instantaneous, while
the pearlitic transformation is time-dependent.
>> Part c).
A proeutectoid phase (ferrite or cementite) always forms along austenite grain boundaries
because associated with grain boundaries is an interfacial energy (i.e., grain boundary energy). A
lower net interfacial energy increase results when a proeutectoid phase forms along existing
austenite grain boundaries than when the proeutectoid phase forms within the interior of the
grains.
>>The main difference between martensite and bainite is how they form. When heated austenite
tends to cool, then in first case, if it make to cool at a particular rate, then diffusion of carbon
inside its gets lowerd and carbon granules just lie inside the cementite matrix. This is known as
Bainite.
Now, if cooling rate is too high, then it will be just hardened. Its strength will be too high . This
is martensite.
>> Now, as said above, Martensite is too hard to be used. So, to make it useful, martensite is
heated for a particular time to induce some softness into it. The product formed is known as
Tempered Martensite
3. Solution
>> Part a).
>> Pearlite :- Pearlite is a two-phased, lamellar (or layered) structure composed of alternating
layers of ferrite (88 wt%) and cementite (12 wt%) that occurs in some steels and cast irons. In
fact, the lamellar appearance is misleading since the individual lamellae within a colony are
connected in three dimensions; a single colony is therefore an interpenetrating bicrystal of ferrite
and cementite. In an iron-carbon alloy, during slow cooling pearlite forms by a eutectoid reaction
as austenite cools below 727 °C (1,341 °F) (the eutectoid temperature). Pearlite is a
microstructure occurring in many common grades of steels.
>> Cementite :- Cementite, also known as iron carbide, is an interstitial compound of iron and
carbon, more precisely an intermediate transition metal carbide with the formula Fe3C. By
weight, it is 6.67% carbon and 93.3% iron. It has an orthorhombic crystal structure. It is a hard,
brittle material, normally classified as a ceramic in its pure form, though it is more important in
ferrous metallurgy. While iron carbide is present in most steels and cast irons, it is produced as a
raw material in the Iron Carbide process, which belongs to the family of alternative ironmaking
technologies.
>> Austenite :- Austenite, also known as gamma-phase iron (-Fe), is a metallic, non-magnetic
allotrope of iron or a solid solution of iron, with analloying element. In plain-carbon steel,
austenite exists above the critical eutectoid temperature of 1,000 K (1,340 °F; 730 °C); other
alloys of steel have different eutectoid temperatures. It is Face Centred Cubic Configuration
(FCC).
>> Eutectoid Phase :- When the solution above the transformation point is solid, rather than
liquid, an analogous eutectoid transformation can occur. For instance, in the iron-carbon system,
the austenite phase can undergo a eutectoidtransformation to produce ferrite and cementite, often
in lamellar structures such as pearlite and bainite.
>> Proeutectoid :- When a hot steel with carbon content very close to 0.8%, is cooled down
slowly, there is a temperature (723 deg C) at which a constant-temperature transformation takes
place. This is called eutectoid transformation. And this results in formation of alternate layers of
Ferrite and Iron-Carbide (Fe3C).
But if the carbon content in this hot steel is much less than 0.8%, and it is cooled down slowly,
then till the temperature reduces to 723 deg C, a part of Austenite (also called gamma iron) gets
transformed to Ferrite by rejecting carbon from the solution. This is not a constant-temperature
process and occurs over a range of temperature. The ferrite so formed is called Proeutectoid...At
723 deg C, all the remaining Austenite get converted to Pearlite at this constant temperature -
4. which is nothing but alternate layers of Ferrite and cementite
>> Martensite :- Martensite, most commonly refers to a very hard form of steel crystalline
structure, but it can also refer to any crystal structure that is formed by diffusionless
transformation. It includes a class of hard minerals occurring as lath- or plate-shaped crystal
grains. When viewed in cross section, the lenticular (lens-shaped) crystal grains are sometimes
incorrectly described as acicular (needle-shaped)
>> Bainite :-
Bainite is a plate-like microstructure or phase morphology (not an equilibrium phase) that forms
in steels at temperatures of 250–550 °C (depending on alloy content). It is one of the
decomposition products that may form when austenite (the face centered cubic crystal structure
of iron) is cooled past a critical temperature. This critical temperature is 1000K (727 °C, 1340
°F) in plain carbon steels. Davenport and Bain originally described the microstructure as being
similar in appearance to tempered martensite.
A fine non-lamellar structure, bainite commonly consists of cementite and dislocation-rich
ferrite. The high concentration of dislocations in the ferrite present in bainite makes this ferrite
harder than it normally would be.
Part b). Two major differences are:
1) atomic diffusion is necessary for the pearlitic transformation, whereas the martensitic
transformation is diffusionless; and
2) relative to transformation rate, the martensitic transformation is virtually instantaneous, while
the pearlitic transformation is time-dependent.
>> Part c).
A proeutectoid phase (ferrite or cementite) always forms along austenite grain boundaries
because associated with grain boundaries is an interfacial energy (i.e., grain boundary energy). A
lower net interfacial energy increase results when a proeutectoid phase forms along existing
austenite grain boundaries than when the proeutectoid phase forms within the interior of the
grains.
>>The main difference between martensite and bainite is how they form. When heated austenite
tends to cool, then in first case, if it make to cool at a particular rate, then diffusion of carbon
inside its gets lowerd and carbon granules just lie inside the cementite matrix. This is known as
Bainite.
Now, if cooling rate is too high, then it will be just hardened. Its strength will be too high . This
is martensite.
>> Now, as said above, Martensite is too hard to be used. So, to make it useful, martensite is
heated for a particular time to induce some softness into it. The product formed is known as
Tempered Martensite