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Avery Polak
Period 4 Honors Biology
North Catholic High School
16 April 2019
2
Osmosis and Diffusion through Cell Membrane Lab
Introduction:
Diffusion is a type of passive transport, and this means the cells do not lose energy when
diffusion takes place (Bailey, 2019). Passive transport also means the cells do not need protein
channels to cross the permeable membrane (Ngyuyen, 2017). Diffusion can occur across a
which mean the membrane allows certain substances to pass through it. The rate of diffusion
(Bailey, 2019). Osmosis is similar to diffusion, however osmosis involves a solvent, water, to
move through a membrane (The Cell Membrane). Osmosis is the movement of water across a
transport (The Cell Membrane). The osmotic flow of water molecules into a cell cause osmosis
pressure. If there is a high osmotic pressure inside the cell, the cell will expand. If there is a high
osmotic pressure outside the cell, the cell size will decrease. Also, if there is a larger
concentration of water molecules on the inside of the cell, the water molecules will move to the
outside where there is a lower concentration, and vice versus. This occurs so the cell can achieve
equilibrium. There are three types of osmotic environments. Each of these environments explain
the osmotic state that is around the cell, and not in the cell (Ngyuyen, 2017). The first is
hypertonic, and these conditions lead the water to diffuse out of the cell, which causes the cell to
shrink. The second environment is hypotonic, and these conditions make the water to go into the
cell, which makes the cell’s size increase. The last one is an isotonic environment, and in this
situation the water moves in and out of the cell equally, which causes no increase or decrease in
balance and control the osmotic pressure and concentration of solute on each side of the
permeable membrane of the cell. During osmosis, the cells receive nutrients and waste is
transported out of the cell (Shukla, 2018). So, without osmosis, cells would not be able to excrete
their waste and keep the bloodstream clean. Also, plants would not exist either without osmosis
because plant cells use osmosis to absorb moisture and nutrients from the soil (Shukla, 2018).
This means if plants did not exist, all life would cease to exist because plants are an important
base of the food chain. So, osmosis is keeping mostly everything on earth alive.
In this lab, the different types of osmotic environments in cells will be demonstrated. The
purposes of this lab are to observe how osmosis and diffusion take place through a semi-
permeable membrane, determine and watch the concentration gradient effects on the rate of
osmosis, and figure out how permeable dialysis tubing is. Dialysis tubing will act as the
It helps facilitate the movement of smaller particles through the membrane and blocks large
The set of for Part I of this lab includes six beakers and six filled dialysis tubes. Each
beaker and bag represent a type of osmotic environment. Beaker one and bag one are both filled
with tap water (Diffusion through Cell Membranes, 2019). This represents a cell in an isotonic
environment. Beaker two is filled with tap water and bag two is filled with 20% starch solution.
This represents a cell in hypotonic environment. Beaker three is filled with tap water and bag
three is filled with 40% starch solution. This represents a cell in a hypotonic environment
(Diffusion through Cell Membranes, 2019). Beaker four is filled with tap water and bag four is
filled with 60% starch solution. This represents a cell in a hypotonic environment. Beaker five is
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Osmosis and Diffusion through Cell Membrane Lab
filled with 60% glucose solution and bag five is filled with tap water. This represents a cell in a
hypertonic environment. Beaker six is filled with 60% glucose solution and bag six is filled with
80% starch solution. This represents a cell in a hypotonic environment (Diffusion through Cell
Membranes, 2019). In this part, the dependent variable is the mass of the dialysis tubing and the
independent variable is the percent of concentration of solution in each dialysis tubing. The
constants are the size of the beaker, the size of the dialysis tubing, and the amount of solution in
each bag. The control group is bag one because it is an isotonic environment. Because bag one is
being placed into an isotonic environment, there will be no mass change because the particles are
moving in and out of the semi-permeable membrane at an equal rate (Biology, 2012). The
experimental groups are bags two, three, four, five, and six because they are hypertonic and
hypotonic. These bags will have a mass change because they are in hypertonic and hypotonic
environments which means the particles will be trying to move from a high concentration to
where there is low concentration (Biology, 2012). If the environment is hypertonic and
hypotonic there will be a mass change, whereas if the environment in isotonic there will be no
mass change.
The set up for Part II of this lab involves one beaker filled with iodine water and one
dialysis tubing bag filled with starch solution (Diffusion through Cell Membranes, 2019). In this
part, the dialysis bag continues to represent a selectively permeable cell membrane. The
dependent variable was the color the bag and water turned, and the independent variable is the
amount of time the bag is in the beaker. The constants are the beaker, the amount of time,
amount of iodine, and length of dialysis tubing. There is no control group, but there is one
experimental group which is the one beaker with the one dialysis tubing bag. If the iodine is able
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Osmosis and Diffusion through Cell Membrane Lab
to pass though the semi-permeable dialysis tubing, then a color change will occur within the
dialysis tubing.
Materials:
Part I:
2. Fold down approximately one inch of the tubing and tie one end with string. Make sure to
closed and secured. Also be sure to not stretch the dialysis tubing.
6. Place each bag onto a numbered paper towel after finished tying it to avoid confusion.
7. Use the scale to measure the starting mass of each bag and then record the weight on a
chart on paper.
8. Place each dialysis tube into the correct beaker at the same time using the diagram as
follows:
1 2 3 4 5 6
9. At the five minute mark, remove each bag at the same time and place them on the paper
towel. Then weigh each dialysis tubing in grams using the scale. Record on the chart.
10. Then place all the bags back in the beakers at the same time.
11. Repeat steps 9 and 10 at the 10, 15, and 20 minute mark, and make sure to record the
12. Fill Table 1 of the lab packet in with the class averages (Diffusion through Cell
Membranes, 2019).
Part II:
1. Take one piece of pre-soaked dialysis tubing and fold down approximately one inch of
the tubing and tie one end with string. Make sure to tie tightly and cut the excess string.
3. Using a spoon full of starch, add it to the water inside the bag.
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Osmosis and Diffusion through Cell Membrane Lab
4. Tie the end of the nag tightly using the same process as in step one.
5. Rinse the bag off with water to avoid cross contamination and dry the tubing off.
7. Add 20 drops of iodine into the same beaker filled with water.
9. Hand the beaker to the teacher and record the data in Table 2 of the Diffusion through
Results:
Part I:
Description: Table 1 shows the mass change of the dialysis tubing from the class averages. The
table starts with the initial mass at 0 minutes and then the mass for every five minutes after is
recorded. Each dialysis tubing bag had an initial starting weight of five grams.
Description: Figure 1 illustrates the data information from Table 1. The table and graph exhibit
the mass changes of each bag through the 20 minute time period. Bag 1 became equalized from
0-10 minutes and then the mass of the bag rose slightly at a steady rate from 10-20 minutes. Bag
2’s mass increased at a steady rate from 0-10 minutes, then from 10-15 minutes the mass had an
abrupt increase, and then started to level out from 12-20 minutes. Bag 3 had an extreme increase
from 0-5 minutes and then continued to increase at a fast but steady pace from 5-15. From 15-20
minutes the slope decreased and began to equalize. Bag 4 had a slight increase from 0-5 minutes
and then suddenly rose from 10-20 minutes, but eventually started to level out. Bag 5 rose from
0-5 minutes but after 5 minutes the mass decreased at a large but steady rate. Bag 5 did not equal
out, and the slope remained constant. Bag 6 had an abrupt increase almost identical to bag 3 from
0-5 minutes. For bag 6 there was a slight decrease in mass from 5-10 minutes, however there was
also a slight increase from 10-15 minutes. From 15-20 minutes, bag 6 had a sudden increase.
Part II:
Discussion: Table 2 displays the color of solution in the dialysis bag and the color of the solution
in the beaker. The table shows the color before and after a day of the bag sitting in the beaker.
The initial color of the solution in the dialysis bag was pale white color. The final color of the
dialysis bag after one day is purple. The initial color of the solution in the beaker was an orange-
yellow mix. There was no color in the beaker after one day.
Discussion:
In part one of this lab, the results differed from the predicted outcome. Beaker one and
bag one should have had an isotonic environment because each were filled with water (Biology,
2012). However, there was an unusual slight rise in mass from 0-5 minutes. This was most likely
due to human error and cross contamination between the pipets used because this would change
it from isotonic to hypertonic or hypotonic. For set up number two, the environment was
hypotonic which meant that the mass and weight should have an increase, and it did from 0-15
minutes. Then the mass started to equal out which is because the environment was almost at
equilibrium. This means the rate of osmosis and concentration gradient was decreasing (Biology,
2012). In the third setup, the environment was also hypotonic, and the actual data follows the
predicted results. The dialysis tubing bag’s mass increased at a steady rate and then began to
equal off as predicted. Beaker four and bag four were a hypertonic environment, and the
predicted results and the actual data were a match. The fifth setup was a hypertonic environment,
and the bag’s mass had an increase from 0-5 minutes. Then there was a sudden sharp but steady
increase from 5-20 minutes. This was unusual for a hypertonic environment so it could have
been caused by human error. An example is someone not tying the dialysis tubing knot tight
enough or cross contamination. Setup six was a hypertonic environment. This set up did not
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Osmosis and Diffusion through Cell Membrane Lab
match the predicted results and expectations. There was a rapid increase from 0-5 minutes which
was continued by the equaling off from 5-15 minutes. Then there was a sudden sharp increase
from 15-20 minutes. This was also probably a human error caused from cross contamination
with glucose (Biology, 2012). Once the bags started to level off, they have begun to reach
equilibrium, and this was shown through the results. This is due to the fact that osmosis is
particles moving from a high concentration to a low concentration with the end goal of reaching
equilibrium within each side of the semi-permeable membrane (Biology, 2012). The higher the
rate of osmosis, the higher the concentration gradient, and same as the lower the rate of osmosis,
the lower the concentration gradient. This is because the solution and tubing are each trying to
reach equilibrium as fast as they can (Biology, 2012). For part two of this lab, the iodine moved
into the dialysis tubing’s semi-permeable membrane, causing the dialysis tubing to turn a blue
color. This color change took place because the iodine passed though the membrane and can into
contact with the starch. There could have been errors such as cross contamination with the
pipets, mixing up the amount of iodine, not tying the dialysis tubing bags tight enough, or wrong
measurements. If this lab were to be revised, there should be practice beforehand to eliminate the
amount of cross contamination between pipets and solutions. This would help ensure more
Conclusion:
The hypothesis of part one of this lab was shown to be accurate because the different
changing osmotic environments did change the concentration gradient and the rate of osmosis.
This was demonstrated through the mass changes of the dialysis tubing bags. The osmotic
environments changed the mass, and this was shown through the results and discussion of data.
The hypothesis for part two of this lab was also shown to be accurate because the iodine was able
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Osmosis and Diffusion through Cell Membrane Lab
to pass through the dialysis tubing’s semi-permeable membrane. This creates a color change
within the dialysis tubing causing the color to go from white to purple. The importance of this
lab is to comprehend and understand how osmosis and diffusion work and how osmosis affects
References:
https://www.thoughtco.com/what-is-diffusion-3967439
Nguyen, D. H. (2017, November 21). What Are the Two Main Types of Diffusion & Osmosis?
Shukla, I. C. (2018, March 19). Bet You Didn't Know the Importance of Osmosis Living in
living-
organisms
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Osmosis and Diffusion through Cell Membrane Lab
The Cell Membrane: Diffusion, Osmosis, and Active Transport. (n.d.). Retrieved from
https://www.dummies.com/education/science/anatomy/the-cell-membrane-diffusion-
osmosis-and-active-transport/