Experiment 1 (Simple and Fractional Distillation)

March 4, 2019 | Author: Cheng Bauzon | Category: Distillation, Vapor, Liquids, Transparent Materials, Gases
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Distillation is one of the oldest and still most common methods for both the purification and the identification of org...

Description

1

Simple and Fractional Distillation

 Adolfo, Angela Angela Nicole G.*, G.*, Alcaraz, Alcaraz, Frances Frances Jillian F.  Aliman, Stephanie Stephanie T., T., Astor, Astor, Jashmin D. Bazon, Franchesca D., !a"ral, Danica #ose G.

Department of Pharmacy, Faculty of Pharmacy University of Santo Tomas

ABSTRACT

Distillation is one of the oldest and still most common methods for "oth the prification and the identification of organic li$ids. %t is a ph&sical process sed to separate chemicals chemicals from a mi'tre "& the difference in ho( easil& the& )aporize. The e'periment sed the Simple Distillation ethod to separate the components of + malcohol )od/a0 and (ater. The distillate (as collected (ith the aid of a cali"rated test t"e . m-0 ntil it reaches the temperatre of 22 3!. Also, the first, second and last distillate (ere sed for testing the presence of alcohol. Throghot the process, there is a directl& proportional relationship "et(een "et(een the )olme and temperatre of the distillate. %n the flamma"ilit& test, the first and second distillate sho(s the presence of alcohol (hile the last one is not flamma"le at all. 4ith the records o"tained, a graph "et(een the )olme and temperatre of distillate (as plotted and the percentage of alcohol and percentage percentage loss (ere also compted. compted. Ths, simple distillation is not a so mch comple' process of e'traction and prif&ing li$ids. 5eating and )aporization are 6st the 7 ma6or  process sed to separate the components of alcohol )od/a0 and (ater.

mi'tr mi'tre e "& selec selecti) ti)e e cond conden ensat sation ion and and ITR!DUCTI!

e)aporation. %t is a process of prif&ing componds "& means of separating

Distil Distillat lation ion is sed sed to sepa separat rate e the comp compon onen entt s"s s"sta tanc nces es from from a li$ li$id id

more )olatile s"stance from non8)olatile or less )olatile )olatile s"stan s"stance. ce. There There are t(o t&pes t&pes of distilla distillation tion,, namel& namel& simple simple and

7

fractional.

Fractional

distillation

is

(hich the condensed )apor is collected.

essentiall& the same as simple distillation

These instrments (ere tightl&

e'cept that a fractionating colmn is

secred to pre)ent "rea/age of the

placed "et(een the "oiling flas/ and the

apparatses. First, in the distilling flas/

condenser. The fractionating colmn is

containing pieces of "oiling stones, a

sall& filled (ith glass or plastic "eads.

+m- of )od/a (as added. The flas/ (as heated (ith an alcohol lamp constantl&.

%n the e'periment, the simple

%deall&, the s"stance (ith the lo(est

distillation (as sed to separate the

"oiling

point

)aporizes

first

the

components s"stances of the )od/a.

temperatre remaining constant ntil that

The follo(ing are the o"6ecti)es to "e

s"stance has completel& distilled. The

achie)ed "& the grop9

)apor is led into the condenser (here, on "eing cooled, it re)erts to the li$id

1.0

To

"e

a"le

to

separate

the

condenses0 and rns off into a cali"rated

components of the alcoholic "e)erage

test t"e that ser)es as a recei)ing

)od/a0 "& distillation.

)essel. The one o"tained is called as the

7.0 To set p a distillation cr)e.

distillate and those s"stances ha)ing a

+.0 To calclate the percent ethanol

higher "oiling point remain in the flas/

present in the )od/a.

and constitte the reside.

:.0 To compare the simple and fractional distillation process; efficienc& in terms of  separating mi'tres of li$id.

 After (hich, the temperatre of the first drop in e)er& test t"e (as recorded ntil it reached the temperatre

"#T$!D!%!&'

of 22 3!. The first, second and last distillate (ere sed to test its flamma"ilit&

 A simple distillation apparats

in a (atch glass. The distilling flas/ (as

consists essentiall& of three parts9 a flas/

cooled and the )olme of the reside (as

e$ipped (ith a thermometer and (ith an

recorded.

otlet t"e from (hich the )apor is

temperatre then (as plotted in a graph

emitted< a condenser that consists of t(o

and the percentage of alcohol present in

t"es of placed one (ithin the other and

the distillates (ere compted. =n the

so arranged that the smaller in (hich the

contrar&, the percentage loss (as also

)apor is condensed0 is held in a stream of 

compted.

coolant in the larger< and a )essel in

The

)olme

and

the

+

Distillate First Second -ast

R#SU%TS AD DISCUSSI!

Flame Test   8

Ta(le )* >olme and Temperatre Ta"le 7 sho(s that a positi)e

of Distillate T#ST

+!%U"#

TUB#

m%. 1. 1. 7. 7. +. +. :. :. . . @. @. . . ?. ?. 2. 2. 1. 1. 11. 11. 17.

1 7 + :  @  ? 2 1 11 17 1+ 1: 1 1@ 1 1? 12 7 71 77 7+ 7:

T#"P#RATUR#

reslt in the flame test indicates the

.C-

presence of alcohol and a negati)e reslt

?+ ?: ?: ?: ?: ? ? ?? ?? ?2 2 21 27 27 2+ 2: 2 2 2@ 2@ 2 2? 2? 22

indicates that there is no alcohol. %n the first and second distillate, a "le (ith orange tip flames (as prodced (hile the last distillate did not prodce an& flame. %t sho(s that as the distillation contines, the amont of alcohol decreases.

Ta"le 1 sho(s that as the )olme of distillate increases, the temperatre also

increase

ntil

it

reaches

Fi0ure )* Simple Distillation Setp

the

temperatre of 22 3!. %t sho(s that the

Figre 1 sho(s the setp (here

)olme and temperatre are directl&

the distillation (as held. Since there is no

proportional.

fractionating colmn present, it is onl& 6st a Simple Distillation setp.

Ta(le /* Flamma"ilit& of Distillate

:

is sall& the atmospheric pressre. The )apor pressre is a )er& sensiti)e fnction of temperatre. %t does not increase linearl& "t in fact increases e'ponentiall& (ith temperatre, sho(ing that there the& are directl& proportional (ith each other. 4hen the )apor pressre of the li$id e$als the applied pressre, the li$id Fi0ure /* Graph of Temperatre and

"oils. Ths, the "oiling point of a li$id is

>olme of Distillate

the temperatre at (hich the )apor  pressre e$als the applied pressre.

Figre 7 sho(s that as the

The normal "oiling point of a li$id is the

mi'tre is heated, the temperatre rises

temperatre at (hich the )apor pressre

ntil it reaches the temperatre of the

of a li$id e$als atmospheric pressre

lo(est "oiling s"stance in the mi'tre.

1 atm0. The "oiling point of a li$id is a

The resltant hot )apor passes into a

measre of its )olatilit& and its prit&.

condenser and is con)erted to the li$id,

CA%CU%ATI!S

(hich is then collected in a recei)er flas/. The other components of the mi'tre

C)) alcohol E >f 8 >i ' 1

remain in their original phase ntil the

>s

most )olatile s"stance has all "oiled off. =nl& then does the temperatre of the

E 17. 8  ' 1

gas phase rises again ntil it reaches the

+

"oiling point of a second component in the mi'tre, and so on.

 E : C alcohol

This is the nderl&ing principle "ehind

distillation.

At

an&

gi)en

Closs E >s 8 >d  >r0 ' 1 >s

temperatre a li$id is in e$ili"rim (ith its )apor. This e$ili"rim is descri"ed "&

E + 8 17.  17.0 ' 1

the )apor pressre of the li$id. The

 +

)apor pressre is the pressre that the molecles at the srface of the li$id e'ert against the e'ternal pressre, (hich

 E 7 C loss



C!C%USI!

increases,

the

presence

of

alcohol

decreases and also ma/ing the mi'tre %n the

e'periment,

it (as fairl&

not flamma"le.

o"ser)ed the fact that the process of  distillation of simple and fractional are not

R#F#R#C#S

mch

5elmenstine, A. 71@0. nderstand the principles of distillation.  About education, 1-5.  #etrie)ed from http9chemistr&.a"ot.comcsf"ldi tillation.htm

different

e'cept

for

the

agmentation of the apparats of the fractional distillation. %t is /no(n as the fractionating colmn that is sall& filled (ith glass or plastic "eads. These "eads impro)e

the

separation "et(een

the

li$ids "eing distilled. The reason that fractional

distillation

gi)es

"etter 

separation "et(een the li$ids is "ecase the glass "eads in the fractionating

Natral %ngredient #esorce !enter. 71, a&0. Boiling points and distillation. #etrie)ed from http9natralingredient.org(p(p8con tentploadsDistillation.pdf  4in/le, . ). 12@0. ass Transfer Hrocesses. %n . ). !in/le, Distillation. Ne( Ior/9 cGra(85ill.

colmn pro)ide theoretical plates on (hich the refl'ing li$id can condense, re8e)aporate,

and

condense

again,

essentiall& distilling the compond o)er  and

o)er.

distillation

=ther is

a

than simple

that,

simple

process

of 

e'traction and prif&ing li$ids "& heating and )aporization of the components of  alcohol )od/a0 and (ater. Ths, "ased on the e'periment, as the temperatre D!CU"#TATI!

Ioder, !. 71@0. Distillation. Wired chemist. #etrie)ed from http9(((.(iredchemist.comchemist r&instrctionalla"orator&8ttorialsdis tillation

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