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VISCOSITY MEASUREMENT 
Ubbelohde Viscometer, for measuring 
viscocity of dilute solution 
upper and lower level 
(measure the flow time t, of 
solution, drop from upper level 
to lower level) 
h = krt 
k = viscometer constant 
r = density of solution 
t = flow time 
If, t = time for solution 
to = time for solvent 
r = ro  dilute solution 
ro = solvent density
Dilute Solution Viscosity Designationsa 
Common name IUPAC name Definition 
= = t 
h 
h h 
rel t 
o o 
t t 
- 
= rel 
= - 1 
- 
= 
o 
o 
h h 
o 
o 
sp t 
h 
h 
h 
h h 
sp rel 
C C 
red 
-1 
= = 
h 
C 
rel 
inh 
h 
h ln = 
ö 
æ 
= 
sp h 
0 ) ( ] [ = = ÷ ÷ø 
ç çè 
= 
C 
C inh 
c o 
h 
h 
Relative viscosity Viscosity ratio 
Specific viscosity - 
Reduced viscosity Viscosity number 
Inherent viscosity Logarithmic viscosity 
number 
Intrinsic viscosity Limiting viscosity 
number 
aConcentrations (most commonly expressed in 
grams per 100 mL of solvent) of about 0.5 g/dL
All Dilute Solution Viscosity Designations can be 
obtained for dilute polymer solution using 
viscometer by measuring the flow time between 
the two level for dilute polymer solution and the 
solvent. 
c co c1 c2 c3 c4 c5 
t to t1 t2 t3 t4 t5 
hsp / c 
{ln hr}/ c
Huggins (a ) & Kramer (b) Equations 
(a)h/ c = [h] + k[h]2C 
sp 1 (b){ln hr}/ c = [h] + k[h]2 
C 
2 Graph,: 
k1 + k2 = 1/2 
[h] 
(a) 
(b) 
x 
x x 
x 
x 
xx 
x 
x x 
hsp / c 
or 
{ln hr}/ c 
C 
Concentration C x 10-2 (g cm-3)
Intrinssic visscosity is the most useful of the various 
Viscosity designations because it can be related to 
molecular weight by the Mark-Houwink-Sakurada equation: 
a 
- 
K M v 
[h] = 
where , v M - 
is the viscosity average molecular weight, defined as 
a 
- + 
M N M 
1 1/ 
i i 
a 
i i 
S 
v N M 
ö 
÷ ÷ø 
ç çè æ 
S 
= 
Log [ ŋ ] = log K + a log Mv
Log K and a are the intercept and slope, respectively, 
of a plot of log [h] versus log Mv 
Log [ ŋ ] = log K + a log Mv 
Value of K between 0.001 – 0.5 and a between 0.5 – 0.8 
…………. Mv can be calculated (approximation value) 
Measurement of [ ŋ ], just for estimation, can also be conducted from a 
value of one solution concentration using Schulz dan Blaschke Equation 
Value of [ ŋ ] can be calculated using the following 
equation 
Ŋsp / C 
[ ŋ ] = 
1 + kn Ŋsp 
For most of polymer solvent system, 
kn = 0.28
During measurement: 
 Viscometer: Vertical 
 no dirt or suspension 
 Temperature. Should be constant 
Importance of Molecular Weight, why? 
Properties of polymers are closely 
related to their molecular weight 
Hard, soft, impact resistance, 
tensile strenght etc.

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Viscosity measurement

  • 1. VISCOSITY MEASUREMENT Ubbelohde Viscometer, for measuring viscocity of dilute solution upper and lower level (measure the flow time t, of solution, drop from upper level to lower level) h = krt k = viscometer constant r = density of solution t = flow time If, t = time for solution to = time for solvent r = ro dilute solution ro = solvent density
  • 2. Dilute Solution Viscosity Designationsa Common name IUPAC name Definition = = t h h h rel t o o t t - = rel = - 1 - = o o h h o o sp t h h h h h sp rel C C red -1 = = h C rel inh h h ln = ö æ = sp h 0 ) ( ] [ = = ÷ ÷ø ç çè = C C inh c o h h Relative viscosity Viscosity ratio Specific viscosity - Reduced viscosity Viscosity number Inherent viscosity Logarithmic viscosity number Intrinsic viscosity Limiting viscosity number aConcentrations (most commonly expressed in grams per 100 mL of solvent) of about 0.5 g/dL
  • 3. All Dilute Solution Viscosity Designations can be obtained for dilute polymer solution using viscometer by measuring the flow time between the two level for dilute polymer solution and the solvent. c co c1 c2 c3 c4 c5 t to t1 t2 t3 t4 t5 hsp / c {ln hr}/ c
  • 4. Huggins (a ) & Kramer (b) Equations (a)h/ c = [h] + k[h]2C sp 1 (b){ln hr}/ c = [h] + k[h]2 C 2 Graph,: k1 + k2 = 1/2 [h] (a) (b) x x x x x xx x x x hsp / c or {ln hr}/ c C Concentration C x 10-2 (g cm-3)
  • 5. Intrinssic visscosity is the most useful of the various Viscosity designations because it can be related to molecular weight by the Mark-Houwink-Sakurada equation: a - K M v [h] = where , v M - is the viscosity average molecular weight, defined as a - + M N M 1 1/ i i a i i S v N M ö ÷ ÷ø ç çè æ S = Log [ ŋ ] = log K + a log Mv
  • 6. Log K and a are the intercept and slope, respectively, of a plot of log [h] versus log Mv Log [ ŋ ] = log K + a log Mv Value of K between 0.001 – 0.5 and a between 0.5 – 0.8 …………. Mv can be calculated (approximation value) Measurement of [ ŋ ], just for estimation, can also be conducted from a value of one solution concentration using Schulz dan Blaschke Equation Value of [ ŋ ] can be calculated using the following equation Ŋsp / C [ ŋ ] = 1 + kn Ŋsp For most of polymer solvent system, kn = 0.28
  • 7. During measurement:  Viscometer: Vertical  no dirt or suspension  Temperature. Should be constant Importance of Molecular Weight, why? Properties of polymers are closely related to their molecular weight Hard, soft, impact resistance, tensile strenght etc.