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Effect of the Molecular Weight of a Substance on Its Rate of Diffusion

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Research paper for Bio 1 (General Biology 1). Revised (corrections after checking were noted in this copy) for future reference.
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The Effect of the Molecular Weight of a Substance on Its Rate of Diffusion 1 Mark Angelo A. Ordonio Group 4 Sec. Y – 5L August 22, 2012 1 A scientific paper submitted in partial fulfilment of the requirements in General Biology I Laboratory under Dr. Severina B. Exconde, 1 st semester 2012-2013.
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Page 1: Effect of the Molecular Weight of a Substance on Its Rate of Diffusion

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The Effect of the Molecular Weight of a Substance on Its Rate of Diffusion1

Mark Angelo A. Ordonio

Group 4 Sec. Y – 5L

August 22, 2012

1A scientific paper submitted in partial fulfilment of the requirements in General Biology I Laboratory under Dr. Severina B. Exconde, 1st semester 2012-2013.

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ABSTRACT

The effect of the molecular weight of a substance on its rate of diffusion was determined with two tests, each using a different medium. Using air as medium, ammonia (NH3) and hydrochloric acid (HCl) were made to react inside a glass tube to form ammonium chloride (NH4Cl). The distance travelled by the two reacting gases was measured, with HCl covering the shortest distance (dave = 18.125 cm); thus HCl travelled slower than NH3. Using gel as a medium, a drop each of potassium permanganate (KMnO4), potassium dichromate (K2Cr2O7), and methylene blue was placed on respective wells in an agar-water gel set-up. The diameter of each diffusion zone was measured at three-minute intervals for thirty minutes, with methylene blue having the shortest diameter of diffusion zone (dfinal = 9 mm); thus methylene blue diffused the slowest (rave = 0.199 mm/min). HCl has greater molecular weight compared to NH3 as well as with methylene blue compared with KMnO4 and K2Cr2O7, satisfying the premise that the higher the molecular weight, the slower the rate of diffusion is. In terms of time, the partial rate of diffusion is inversely proportional with the time elapsed.

INTRODUCTION

According to the molecular theory of matter, it states that all matter is

made up of tiny particles called molecules. In gases, the kinetic theory describes

a gas as a large number of molecules in constant, random motion, rapidly

moving and colliding with each other and with the walls of the container.

An assumption of the kinetic theory is that gas molecules travel in straight

lines. Since a molecule frequently collides with other molecules, its actual path is

a series of straight lines connected end to end in no particular pattern. However,

if the concentration of a particular substance is greater in one area of a container

than in another, its molecules will gradually spread out (Smoot, et al, 1990). The

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spread of molecules from a place where they are more abundant per unit of

volume (and, therefore, where collisions are more frequent) to places where they

are less abundant per unit of volume (where collisions are less frequent) is called

diffusion (BSCS, 1963). For example, releasing ammonia in one part of a room

will allow it to disperse it on the entire room, as noted by the odour. Adding a

coloured soluble solid in a water-filled beaker will also spread the colour on the

medium. Diffusion continues until the molecules are evenly distributed throughout

the space available; collisions and rebounds continue, with frequency equal from

one place with another, signifying no net change in the distribution of molecules.

In biology, the diffusion that concerns us the most is diffusion of

substances dissolved in water molecules and of water molecules themselves. All

active, non-dormant cells exist in a water environment; cells of the human body

are no exception. Thus, a living cell in is environment is a mixture of things in

water, separated by the cell membrane from another mixture of things in water

(BSCS, 1963).

Starr and Taggart (2004) pointed several factors that influence the rates of

movement down a concentration gradient: steepness, molecular size,

temperature, and electric or pressure gradients that may be present. The greater

the concentration of a substance in an area of a system entails that the

frequency of particles colliding with each other is higher, causing the particles to

collide at a faster rate. These collisions are due to the high molecular velocities

associated with the thermal energy “powering” the particles (Nave, 2008). At a

given temperature, a smaller particle is said to diffuse at a faster rate than a

larger one. This is because the larger the size of a particle, a greater amount of

force is said to be required to move the particle (Meyertholen, 2007). With the

same amount of energy, a smaller particle can be pushed faster than a larger

particle. Thus, the hypothesis of the study is that the rate of diffusion is inversely

proportional to the size of the particle. That is, a smaller particle will diffuse faster

than a larger one.

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To validate the hypothesis relating the molecular weight of a substance to

its rate of diffusion, two set-ups using different media were used. First, the glass

tube set-up using air as medium was used. Two cotton balls of identical sizes

were moistened with hydrochloric acid, HCl and ammonium hydroxide, NH4OH,

which were then placed concurrently in each end of the glass tubing. The

distance travelled by the two reacting gases (HCl and ammonia, NH3) was

measured – this will indicate the relationship between the molecular weight and

the rate of diffusion. On the other hand, the agar-water gel test, with water as

medium, was then used to assess and verify the effect of the molecular weight

on the rate of diffusion of different substances. A drop each of potassium

permanganate, KMnO4, potassium dichromate, K2Cr2O7, and methylene blue

was placed in three different wells on a petri dish with agar-water gel. Possessing

different colours, the substances are dyes which make them easily identifiable

and suitable for measurement of the diameter of the drops within a period of

thirty minutes.

This study intended to determine the effect the molecular weight of a

substance on its rate of diffusion using different media. The specific objectives

were

1. to identify the factors that could possibly affect the rate of diffusion of

substances; and

2. to explain the effect of molecular weight of a substance on its rate of

diffusion.

The study was conducted at Room C-107, Rafael B. Espino Wing

(Institute of Biological Sciences), Leopoldo B. Uichanco Hall (Biological Sciences

Building) of the College of Arts and Science, University of the Philippines Los

Baños Laguna on August 14, 2012.

Page 5: Effect of the Molecular Weight of a Substance on Its Rate of Diffusion

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MATERIALS AND METHODS

For the glass tube test, the set-up (Figure 4.1) was initially prepared. Two

equally-sized cotton balls each soaked in HCl and NH4OH were plugged

simultaneously at each end of the glass tube. The white smoke forming a ring

inside the tube was observed and marked. The distance (in cm) between the

cotton and at the marked position was then measured and recorded.

For the agar-water gel test, a petri dish containing water-agar gel with

three wells was initially prepared. A drop of the following coloured solutions,

substances which differed in their molecular weights was placed on their

respective wells: potassium permanganate (KMnO4), potassium dichromate

(K2Cr2O7), and methylene blue. The diameter (in mm) of each diffusion zone was

measured and recorded in regular three-minute intervals for thirty minutes. The

average rate of diffusion (in mm/min) was computed using the following formula:

푝푎푟푡푖푎푙푟푎푡푒 푟 = (1)

where di = diameter of diffusion zone at a given time

di-1 = diameter of diffusion zone immediately before di

ti = time when di was measured

ti-1 = time immediately before ti

All computed values were tabulated and the mean of the computed partial

rates as well as the average rate of diffusion of each substance was calculated.

Partial rates of each substance at a specific time were plotted for analysis.

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Figure 4.1. The glass tube set-up.

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RESULTS AND DISCUSSION

To be able to develop a hypothesis that relates the molecular weight of a

substance and its rate of diffusion, the glass tube test was utilized. It uses air as

medium of diffusion for the gases NH3 and HCl. The reaction involved, the

formation of NH4Cl, is described by the following mechanisms:

HCl(l) → HCl(g) (2)

NH4OH(l) → NH3 (g) + H2O(l) (3)

HCl(g) + NH3 (g) → NH4Cl(g) (4)

Table 4.1. Distances travelled by the diffusion of ammonia gas and hydrochloric acid gas and ratios of the distances to the total distance.

Trial

Distance (cm)

(d) Total

distance

(D)

Ratio

dHCl dNH3 dHCl

D dNH3

D NH3

HCl

1 25.0 15.5 40.5 0.6173 0.3827 0.6200

2 25.0 23.0 48.0 0.5258 0.4792 0.9201

3 24.0 17.0 41.0 0.5854 0.4146 0.7082

4 21.5 17.0 38.5 0.5584 0.4416 0.7908

Average 23.875 18.125 42.0 0.5717 0.4295 0.7598

The white smoke that formed inside the tube is ammonium chloride,

NH4Cl, the product of the reaction between HCl and NH3 by diffusion, as seen in

(4). Based on the presented data, we could deduce that the measured rates of

diffusion of a series of molecules are proportional to the molecular weights of

diffusing substances. As seen in Table 4.1, it shows that HCl travelled at a longer

distance (dave = 23.875 cm) as compared to NH3 (dave = 18.125 cm), which tells

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us that the site of the initial reaction occurred near NH3. Hydrochloric acid (MM =

36 g/mol) has a relatively larger molecular weight compared to ammonia (MM =

17 g/mol). Since HCl travelled faster, the hypothesis “the higher the molecular

weight, the faster the diffusion” is developed.

Gases do not diffuse at the same rate, with the assumption that the rate of

diffusion varies directly with the velocity of molecules. At constant temperature,

molecules of low mass diffuse faster than molecules of large mass because they

travel faster, which will also pass a small hole (effuse) more rapidly than the

molecules of higher mass. Given two substances in constant temperature, the

average kinetic energies must also be constant. From this, Graham’s Law was

derived,

= (5)

which shows that the relative rates of diffusion of two gases vary inversely as the

square root of their molecular masses (Smoot, et al, 1990).

Theoretically, since NH3 has a smaller molecular weight, it must also

diffuse at a higher rate; thus, NH3 must travel faster and must reach the other

end with a longer distance compared to HCl. However, the initial part of the

experiment showed the opposite.

Re-testing the hypothesis using the agar-water gel test was done. As the

difficulty arises from measuring unseen moving molecules in fluids (i.e. gases

and liquids), substances that can be seen to diffuse as well as a medium that

permits diffusion should be considered. Moving media affects the rate of

diffusion, so incorporating water into a gel still allows diffusion in the same

medium (water) but is not moving and will not influence the rate of diffusion. This

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(a)

(b)

Figure 4.2. (a) Initial and (b) final agar water-gel set-up with three wells, each

containing a drop of potassium permanganate (purple), potassium dichromate

(yellow), and methylene blue (dark blue).

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is because a gel is made up of a framework of solid particles (chains) which trap

water in their interstices, causing its immobilization.

The measured diameters in Table 4.2 show that KMnO4, after the thirty-

minute period, exhibited the largest diffusion zone among the three, while

methylene blue has the smallest. Comparing their molecular weights, KMnO4

(MM = 158 g/mol) has the least against K2Cr2O7 (MM = 294 g/mol) and

methylene blue (MM = 374 g/mol). Table 4.3 shows the average rate of diffusion,

with KMnO4 having the fastest rate of diffusion (rave = 0.465 mm/min) among the

three.

Table 4.2. Diameters of the diffusion zones made by drops of potassium permanganate, potassium dichromate, and methylene blue measured at three-minute intervals for thirty minutes.

Time

(min)

Diameter (mm)

Potassium

permanganate

Potassium

dichromate

Methylene

blue

0 5 5 3

3 11 8 7

6 12 9 7

9 14 10 7

12 15 10 7

15 16 11 7

18 17 11 8

21 17 12 9

24 18 12 9

27 18 12 9

30 19 12 9

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Table 4.3. Partial rates of diffusion of potassium permanganate, potassium dichromate, and methylene blue measured at three-minute intervals for thirty minutes.

Time

elapsed

(min)

Partial rates of diffusion (mm/min)

Potassium

permanganate

Potassium

dichromate

Methylene

blue

3 2.00 1.00 1.33

6 0.33 0.33 0.00

9 0.67 0.33 0.00

12 0.33 0.00 0.00

15 0.33 0.33 0.00

18 0.33 0.00 0.33

21 0.00 0.33 0.33

24 0.33 0.00 0.00

27 0.00 0.00 0.00

30 0.33 0.00 0.00

Average rate

of diffusion

(mm/min)

0.465 0.232 0.199

Figures 4.3 and 4.4 show graphs of the average rate of diffusion with

respect to the factors molecular weight and time, respectively, to further display

the trend and pattern with this phenomenon. From Figure 4.3, it can be observed

that potassium permanganate, being the lightest, had the largest diameter

covered after 30 minutes. Meanwhile, methylene blue, being the heaviest, had

the smallest diameter covered. The expansion of the diffusion zones measured

by the diameters show the diffusion of the substances. Graham’s law proves

these results; however, it does not support the hypothesis that the higher the

molecular weight, the faster the rate of diffusion, but support the theoretical claim

that the higher the molecular weight, the slower the rate of diffusion.

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Figure 4.3. Average rate of diffusion of three coloured solutions with respect to

molecular weight.

Figure 4.4 Partial rates of diffusion of various coloured solutions in an agar-water

gel with respect to time.

0

0.1

0.2

0.3

0.4

0.5

158 294 374

Aver

age

rate

of d

iffus

ion

(mm

/min

)

Molecular weight (g/mol)

0

0.5

1

1.5

2

3 6 9 12 15 18 21 24 27 30

Part

ial r

ate

of d

iffus

ion

(mm

/min

)

Time elapsed (min)

KMnO4

K2Cr2O7

methylene blue

Linear (KMnO4)

Linear (K2Cr2O7)

Linear (methylene blue)

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Figure 4.4 shows the relationship between the partial rates of diffusion

with respect to time elapsed. It indicates that as time proceeds, the rate of

diffusion tends to decrease, as suggested by the lines of best fit for each

coloured solution. The negative slope indicates that time is inversely proportional

to the rate of diffusion.

The inconsistency of the results shown in the first test with theoretical

basis is possibly caused by human errors. Non-spontaneity in plugging the cotton

balls can cause the gas on the first plugged cotton ball to diffuse first before the

other. For better results regarding the second experiment, the wells must be

equal in size and shape to provide better basis of comparison.

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SUMMARY AND CONCLUSION

The effect of molecular weight on the rate of diffusion was determined

using the glass tube set-up and the water-agar gel set-up. These set-ups differ in

the medium used: air on the glass tube set-up and water on the water-agar gel

set-up.

On the first experiment, results showed that HCl, the heavier substance

(MM= 36 g/mol; dave = 23.875 cm) diffused at a faster rate than NH3, the

substance with the lighter molecular weight value (MM= 17 g/mol; dave = 18.125

cm). Contrary to the previous results, the second experiment showed that

methylene blue (MM= 374 g/mol) the substance with heavier molecular value had

diffused the slowest (rave = 0.199 mm/min) than the other two substances.

However, since the first experiment was found to be inconsistent with theory, the

hypothesis was considered void, as verified by the second experiment.

Thus, the higher the molecular weight of a substance, the slower the rate

of diffusion. Also, as time proceeds, the rate of diffusion also decreases.

It is recommended that, to be able to arrive with results that can be easily

based with scientific claims, the experiment be strictly observed in terms of

handling and execution. Several factors such as irregularities in temperature and

concentration may affect the results.

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LITERATURE CITED

Biological Sciences Curriculum Study (BSCS). 1963. High School Biology. Chicago: Rand McNally & Company. p. 384-385.

Meyertholen, E. 2007. Diffusion. Retrieved Aug. 16, 2012 from http://www.austincc.edu/~emeyerth/diffuse1.htm

Nave, R. 2008. Diffusion. Retrieved Aug. 16, 2012 from http://hyperphysics.phyastr.gsu.edu/hbase/kinetic/diffus.html

Starr, C. and R. Taggart. 2004. Biology: The Unity and Diversity of Life. 10th ed. Belmont, California: Thomson Brooks/Cole. P. 87.

Smoot, R.C., R.G. Smith, and J. Price. 1990. Chemistry: A Modern Course. 2nd ed. Columbus, Ohio: Merrill Publishin Company. p. 365-366.


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