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1

THERMODYNAMICS & RESERVOIR


FLUID PROPERTIES

Mohamed.hassan@port.ac.uk

Dr Hassan
Who is your Course Instructor
What is this course about
How will we conduct the course
Assessments
Home work
Come to class. Par?cipate, ask ques?ons don't be
afraid, KNOWLEDGE is acquired, is not hereditary.
Study your lessons and chapter guides

Mohamed.hassan@port.ac.uk

The Book to have For TB 1

Chapter1: Components of Naturally


Occurring Petroleum Fluids (p.1-45)
Chapter 2: Phase Behavior: Pure
Substances (p.46-61)
C h a p t e r 2 : P h a s e B e h a v i o r : 2
component systems (p.63-75)
Chapter 3: Equa?ons of State (Gas):
Ideal Gases (p.90-102)
Chapter 3: Equa?ons of State (Gas):
Mixtures of Ideal Gases (p.102-112)
Chapter 4: Equa?ons of State for Real
Gases (p. 129-146)
Chapter 5: Five Reservoir Fluids: Black
and Vola?le Oils (p.147-158)
Chapter 5: Five Reservoir Fluids:
Retrograde, Wet & Dry Gases (p.
154-158)
Mohamed.hassan@port.ac.uk

Technical Requirements for


4
HOMEWORK and REPORTS
ability to properly analyze and solve problems will
Your demonstrated
determine your grade in this course. There are three objec?ves which you
must sa?sfy for full credit on each problem: (The three C's).

1. Is it CLEAR? The deni?on of the problem, the methods and procedures
you apply, and your results should be clearly presented so that anyone who
is unfamiliar with the problem could easily follow what you have done by
looking at your paper (report). If I can't tell what you did, it must be wrong.

2. Is it COMPLETE All given data and unknowns, all symbols, all equa?ons
represen?ng the principles you use, all calcula?ons with units, and all results
should be iden?ed and presented in a logical, complete and
comprehensive form.

3. Is it CORRECT? The right answer is important. You may get par?al credit
for wrong answers in school, but there is no par?al credit for wrong answers
in the real world.

Mohamed.hassan@port.ac.uk

Achieve These Objec?ves

1. Draw a diagram (beger than 1000 words). This needs not to be a


"work of art", but it is usually a graph or a block diagram which
represents the process you are analyzing, with appropriate lines
represen?ng "paths", and "outputs" to the problem, and all
reference points are properly iden?ed.
2. Label the Diagram. Symbols represen?ng all variables and
parameters of signicance in the problem should be placed at
appropriate points on the diagram. Values of quan??es which
are given or known should be indicated, and those quan??es
which are to be found should be iden?ed. The symbols used to
represent the physical quan??es should be obvious, or clearly
dened.
3. State your Assump?ons. Major assump?ons as to the nature of
the system, uid proper?es, pressure and temperature
condi?ons, etc. which limit or restrict the range of applica?on of
your solu?on should be stated explicitly.
Mohamed.hassan@port.ac.uk

6
4. Write Equa?ons. All general principles which are applied to
problem solu?ons that should be expressed in equa?on form.
These general equa?ons can then be reduced to a form
consistent with your assump?ons, and should be wrigen using
the symbols which you have used to label the diagram.
5. Solve Equa?ons. The equa?ons should be solved for the
unknown quan??es in terms of the known quan??es. The
solu?on should be carried out in terms of the symbols
represen?ng the variables, whenever possible, before
introducing an numbers or data. This procedure ojen saves a lot
of ?me doing unnecessary calcula?ons. Some?mes, for complex
problems, doing some intermediate calcula?ons will simplify the
solu?on, but otherwise save the "number crunching" un?l last.
6. Calculate Answers. Introduce known quan??es and appropriate
data with units in consistent form (including conversion factors
where needed) into the equa?ons and calculate the answer. All
answers should be clearly iden?ed, and expressed in a number
of signicant digits consistent with given data.
Mohamed.hassan@port.ac.uk

Exam Rules & Format


1.
2.
3.
4.

Be able to derive equa?ons from given Informa?on


Bring your own calculator, ruler, pencil, and eraser
Cell phones must not be used or be on your person
Write down clearly and show all intermediate
work or NO CREDIT
5. Highlight / box nal answers

Mohamed.hassan@port.ac.uk

Moodle

Lectures
Addi?onal Reading Material (papers)
Some Solved exercises
Syllabus, Study Guide
Mock exam papers

Mohamed.hassan@port.ac.uk

Read

Chapters 1 from McCain's book.

Assignment # 1 Fluids
Solve Exercise Problems from W.D. McCain, Chapter 1
(pages 42-44):
1.3 (Table 10-2 in on page 270)
1.5
1.12
1.13
1.14
Mohamed.hassan@port.ac.uk

10

Organic Naming Rules

For complete Rules go to:


hgp://www.acdlabs.com/iupac/nomenclature/
Mohamed.hassan@port.ac.uk

Organic Compounds
Consist of mainly four
elements

Carbon
Hydrogen
Oxygen
Nitrogen
Mohamed.hassan@port.ac.uk

11

Numbers and Types of Bonds for 12


Common Elements in Organic Compounds
Applica'on of the octet rule indicates that these elements
should bond as shown below:

Mohamed.hassan@port.ac.uk

Section 14.1

Iden?fying Valid & Incorrect


14 | 13
Structural Formulas

13

An Example

Two structural formulas are shown above. Which on


does not represent a real compound?
In structure (a) each H and halogen has one bond,
each C has four bonds, and each O has two bonds.
This is a valid structure.
Mohamed.hassan@port.ac.uk

Section 14.1

Iden?fying Valid & Incorrect


14 | 14
Structural Formulas

14

An Example

As we examine (b), we note that each H has one


bond, each C has four bonds, the N has three
bonds, BUT the O has three bonds.
The O should only have two bonds.
Therefore (b) is not a valid structure.
Mohamed.hassan@port.ac.uk

Section 14.1

15
Iden?fying Incorrect Structural
F
ormulas
14 | 15

Condence Exercise

The structural formula above appears in a recent


chemistry book. Check the number of bonds to
each atom and determine whether any bonding
rules are violated.

Mohamed.hassan@port.ac.uk

Section 14.1

16

Iden?fying
I
ncorrect
S
tructural
O should have two
Each C should have
bonds, C should have 4
4 bonds
Formulas

bonds
Condence Exercise

This is not a valid


structure for caffeine!
Mohamed.hassan@port.ac.uk

Each N should have


3 bonds
Section 14.1

Hydrocarbons

17

14 | 17

Hydrocarbons are the most simple organic


compounds.
Hydrocarbons contain only carbon (C) and
hydrogen. (H)
For classica?on purposes, all other organic
compounds are considered deriva?ves of
hydrocarbons.
Hydrocarbons can be divided into aroma?c and
alipha?c hydrocarbons.

Mohamed.hassan@port.ac.uk

Section 14.2

18

Why Do We Need a Separate Set of


Rules?
Examine some typical organic compounds
CH4 Carbon tetrahydride
C2H6 Dicarbon hexahydride
Name these using typical covalent rules

Mohamed.hassan@port.ac.uk

19

So?
That wasnt so bad, right?
How about these:
Tetracarbon decahydride
C4H10
C5H12
Pentacarbon ??? hydride
See my point?

Mohamed.hassan@port.ac.uk

20

Isomers
If thats not enough, how about this one:
H

Formula?

C4H10
Mohamed.hassan@port.ac.uk

Dierent
Structure

Same
Formula

H
H

H
H

Formula?

C4H10

Overall Problems
Memorizing too many prexes for large numbers
Dierent chemicals having the same formulas
Keep in mind that thus far weve only dealt with
TWO dierent elements!

Mohamed.hassan@port.ac.uk

21

22

So what to do?
Number of hydrogens is going to be the same,
regardless of isomerism
H

C5H12
Mohamed.hassan@port.ac.uk

H
H

C
H

H
H
C
H

C
C

H
H
C

H H

C5H12

H
H

H
H

H
H

H
C H
H

C5H12

Solu?on

23

Since number of hydrogens dont change with isomerism,


why bother naming them?
Name the molecule simply based on number of CARBONS
We can always add prexes or suxes later for
dieren?a?on

Mohamed.hassan@port.ac.uk

24

Name based on number of Carbons

Mohamed.hassan@port.ac.uk

1
2
3
4
5
6
7
8
9
10

Methane
Ethane
Propane
Butane
Pentane
Hexane
Heptane
Octane
Nonane
Decane

Did that Really Help?


H
H

CH4

Carbon tetrahydride becomes:

25

Methane

C2H6

Dicarbon hexahydride becomes:

Mohamed.hassan@port.ac.uk

Ethane

C8H18

Octacarbon ???hydride becomes:


Octane

Branches
Straight-chain alkanes (Just C & H with single
bonds) are now easy
H H H H
H

C4H10 Butane

But how do we deal with branches?


H

H
H

H
H

H H H
Mohamed.hassan@port.ac.uk

C4H10 ????

26

Rules pt. 2

27

Iden?fy the longest unbranched chain of carbons


Name it as normal
Iden?fy the branch
Name it but give it a yl sux
Put the names of all branches rst, then put name of longest
chain

Mohamed.hassan@port.ac.uk

28

Example
methyl

Branch is one long


H
Longest unbranched chain of
carbons is three long

H
H

H
H

propane

Methyl Propane

Mohamed.hassan@port.ac.uk

29

H
H

Prac?ce
Methyl butane

H
C H
H

H
H

H
H

H
Mohamed.hassan@port.ac.uk

Ethyl pentane

30

One More Prac?ce

It doesnt mager
which way you go!

(Provided you correctly pick


the longest unbranched
chain)

Mohamed.hassan@port.ac.uk

Methyl Butane

31

Be Careful
H

This is your longest


uninterrupted chain

H
H

Methyl

Hexane

Methyl Hexane

Mohamed.hassan@port.ac.uk

32

A Small Wrinkle
H

Methyl Pentane

Methyl Pentane

H
H

These are dierent molecules, though!!!


Mohamed.hassan@port.ac.uk

So Now What?
Since two dierent molecules cant have the same
name, we must dieren?ate
If we look closely, though, the only dierence
between them is the posi?on of the methyl group

Mohamed.hassan@port.ac.uk

33

34

Posi?oning
2- Methyl Pentane 3- Methyl Pentane
H

H
H

Here the methyl group is on


the second carbon from the
end

Here the methyl group is on


the third carbon from the end

So
Mohamed.hassan@port.ac.uk

Rules pt. 3

35

Iden?fy the longest unbranched chain of carbons


Name it as normal
Iden?fy the branch
Name it but give it a yl sux
Put the names of all branches rst, then put name of longest
chain
Put the number of the carbon the branch is on (start
numbering from the closest single end)

Mohamed.hassan@port.ac.uk

36

H
H

H
H

Prac?ce
C
2-methyl
heptane
H

4-methyl octane

H
H
H

C C C

H
H

Mohamed.hassan@port.ac.uk

2-methyl hexane

Mul?ple Branches

So far weve only had one branch


What happens when there are multple branches?
Just add a prex to indicate the number of a
par?cular type of branch

Mohamed.hassan@port.ac.uk

37

Prac?ce
2- methyl

H
H

H
H

H
H

38

heptane

2- methyl

2-methyl, 2-methyl
heptane

2,2 dimethyl

Mohamed.hassan@port.ac.uk

Sounds
redundant

More Prac?ce

39

H
H

H
H

2, 6-dimethyl
octane

H
H

C
H

H
H

Mohamed.hassan@port.ac.uk

3 ethyl-2,4-
dimethyl pentane

Shorthand nota?on
H
H

40

Keep in mind that we have been ignoring the


hydrogens for a long ?me.

Our names have been based en?rely on the


posi?oning of the carbons.

So lets now ignore the hydrogens

completely!
Mohamed.hassan@port.ac.uk

41

H
H

Is it that easy?
H

H
H

H
H

C
H

Mohamed.hassan@port.ac.uk

42

One More

Shorthand nota?on?

H
H

C
H

H
H

3-ethyl-2,4 dimethyl hexane


Name?
Mohamed.hassan@port.ac.uk

Rings
Thus far we have dealt with chains that are
straight or branched.
If hydrocarbons are long enough, one end can
wrap around and link up with itself!
We call these cyclic hydrocarbons.

Mohamed.hassan@port.ac.uk

43

Cyclic Hydrocarbons

44

Name the molecule as normal


Add the prex cyclo- to the front of the name of the
longest chain
Start numbering from the most important branch
in the ring

Cyclohexane
Cyclooctane
Mohamed.hassan@port.ac.uk

45

More Examples
Methyl cyclopentane

1,2 dimethyl
cyclohexane
Mohamed.hassan@port.ac.uk

46

Try These
1 ethyl, 3 methyl
cyclobutane
3 methyl, 1 propyl
cylclohexane
Mohamed.hassan@port.ac.uk

Mul?ple Bonds
So far, even with the cyclic structures we have
dealt only with single bonds
Carbon can make mul?ple bonds to another
carbon
This changes the name
Why?

Mohamed.hassan@port.ac.uk

47

48

Examine Structures
H

C2H6

Ethane- no?ce that each carbon has


four bonds

What will happen to the structure if we double bond the two carbons?

C2H4

Mohamed.hassan@port.ac.uk

Each carbon s?ll has four bonds BUT


now the hydrogens have changed!!

Naming molecules with mul?ple


bonds
Name the molecule as
normal
Change the sux of the
longest chain name
Double bonds = ene
Triple bonds = yne
Use numbering and
prexes for posi?oning
and mul?ple mul?ple
bonds.
Mohamed.hassan@port.ac.uk

49

50

So.
H

C2H6

C2H4

C2H2

ethane

ethene

ethyne

Mohamed.hassan@port.ac.uk

51

H
H

Prac?ce

2-heptene

1-butene

H
H

H
H

Mohamed.hassan@port.ac.uk

3 methyl-1-pentene

52

How about in Shorthand?

No?ce the two lines


means the double
bond is there!

Mohamed.hassan@port.ac.uk

2 pentene

53

Prac?ce!
Methyl propene
2,4-dimethyl-2-
pentene

Mohamed.hassan@port.ac.uk

3-ethyl-2,4,4-trimethyl-1-
pentene

54

Tough Ones
2 methyl 1,3 butadiene

1,2 dimethyl-1,4 cyclohexadiene


Mohamed.hassan@port.ac.uk

55

Triples?
3, 3-dimethyl-1-butyne

1,4 cyclohexadiyne
Mohamed.hassan@port.ac.uk

Func?onal Groups
Nature has done us a favor.
There are many common groups that we can
organized or le into dierent categories.
Then we can name them based on these
categories.
A group of atoms that, when added to a
hydrocarbon chain, alter the chemical proper?es
of the chain.
Just a few dierent func?onal groups to know
Mohamed.hassan@port.ac.uk

56

57

Func?onal Groups
Halogens
Alcohols
Ethers
Aldehydes
Ketones
Carboxylic Acids
Esters
Amines

Mohamed.hassan@port.ac.uk

R-F, R-Cl, R-Br, R-I


R-OH
R-O-R
R-COH
R-CO-R
R-COOH
R-COO-R
R-NH2

Halides

58

Fluorides, Chlorides, Bromides, and Iodides


Simply name the molecule as normal but add the
prex Fluoro, Chloro, Bromo, or Iodo as necessary
Cl

2, 3 dichlorohexane
I

Cl

3, 3 diiodo-1-pentene
I
Mohamed.hassan@port.ac.uk

Alcohols
OH

R-OH
Name like normal
except add an ol
sux

2 propanol
H

Mohamed.hassan@port.ac.uk

59

OH

1cyclobutenol
OH

ethanol

Ethers

60

R-O-R
Name two R groups with yl endings
End name in ether

O
Mohamed.hassan@port.ac.uk

Dimethyl ether
Ethyl methyl ether

Aldehyde

R-COH
This is a carbon to oxygen double bond with a
hydrogen at the end.
Name as normal except use a -al sux

Cl

Cl

Mohamed.hassan@port.ac.uk

61

butanal

3,3 dichloropentanal

Ketones
R-CO-R
This is a carbon to oxygen double bond but in the
center of a hydrocarbon chain rather than the end
Name as normal but give it a -one sux

propanone

O H

C
H

Mohamed.hassan@port.ac.uk

2 hexanone

62

Carboxylic Acids

63

R-COOH or R-CO2H
This is a carbon to oxygn double bond with the same
carbon single-bonded to an OH group.
Name as normal except give it the sux -anoic acid.
H

HO

OH

H H
Mohamed.hassan@port.ac.uk

Butanoic acid

3-Fluoropropanoic acid

Esters

64

R-COO-R
This is a carbon to oxygen double bond with a carbon to oxygen
single bonded to another single bonded carbon
Name by given secondary branch -yl sux and main branch
-anoate sux.

Secondary
Methyl Pentanoate Branch

Main Branch

pentanoate
Mohamed.hassan@port.ac.uk

H
O

methyl

65

H
H

C
H

Esters

O H

Mohamed.hassan@port.ac.uk

Butyl propanoate

Methyl
hexanoate

Amines

66

R-NH2
Name the R group or groups with -yl endings
Add the word amine
H
H

Methyl amine

C
H

N
C

H
H
Mohamed.hassan@port.ac.uk

Dimethyl amine

67

Summary
Cl

OH
R C
Carboxylic Acid

O
R

O
C
Ester

Mohamed.hassan@port.ac.uk

Ketone

Aldehyde

O
Ether

O
C

Alcohol

Halide

OH

NH2

Amine

68

Summary

Alkanes
Alkenes
Alkynes
Halides
Alcohols
Ethers
Aldehydes
Ketones
Carboxylic Acids
Esters
Amines
Mohamed.hassan@port.ac.uk

-
=

R-X
R-OH
R-O-R
R-COH
R-CO-R
R-COOH
R-COO-R
R-NH2

-ane
-ene
-yne
-o
-ol
-yl ether
-al
-one
-anoic acid
-yl -anoate
-yl amine

69

Classica?on of Hydrocarbons

Mohamed.hassan@port.ac.uk

Can You Do This?

Mohamed.hassan@port.ac.uk

YES!
It takes:
Memoriza?on
Prac?ce
Prac?ce
Prac?ce
Prac?ce
And, oh yes
Prac?ce!

70

Read

71

Chapters 1 from McCain's book.

Assignment # 1 Fluids
Solve Exercise Problems from W.D. McCain, Chapter 1
(pages 42-44):
1.3 (Table 10-2 in on page 270)
1.5
1.12
1.13
1.14
Mohamed.hassan@port.ac.uk

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