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Introduction:
Passive transport is when particles move from high concentration to low concentration across the
cell membrane, it requires no extra energy or ATP, and moves with the concentration gradient.
To be selectively permeable means that the membrane will only let certain things pass in and out
in certain quantitates. Osmosis is the movement of water from a high to low concentration. There
are three different osmosis environments: hypotonic, hypertonic, and isotonic. A hypotonic
solution is when there is a higher concentration of solute inside the cell causing water to flow
inside the cell (McGraw-Hill companies , 2012). A hypertonic environment is when there is a
higher concentration of solutes outside the cell, causing the water inside to flow outside of the
cell (McGraw-Hill companies , 2012). An isotonic environment is when there is an equal amount
of water and solutes inside and outside the cell (McGraw-Hill companies , 2012). It is important
to know the importance of osmosis and its environments because if we drink too much or too
little we could be putting our cells into dangerous environments like hypotonic or hypertonic. If
our cells are in a hypotonic environment they could burst, and if they are in a hypertonic
environment they could shrivel up. Dialysis tubing is made up of selectively permeable cellulose
tubing perforated with microscopic pores. (Flinn Scientific 201) The dialysis tubing acts as a
selectively permeable membrane in the lab for the water. One purpose for this lab was to
compare the effects of diffusion using the dialysis tubing in different solutions of water. Another
purpose was to determine if specific substances are capable of passing in or out of the cell.
Finally, another purpose is to see if the dialysis tubing would react differently in the
environments it was placed in. Beaker one represents a simulated cell in an isotonic environment.
Beaker two represents a simulated cell in a hypotonic environment. Beaker three represents a cell
in a simulated cell also in a hypotonic environment. Beaker four represents a simulated cell in a
O’Hara The Average Mass of Dialysis Tubing During Osmosis 3
hypertonic environment. Beaker five had two simulated cells in it, one represented a hypertonic
environment, and the other represented a cell in a hypotonic environment. The dependent
variable for part 1 was the mass of the bags after they were in the beakers of solutions, the
independent variable was the solutions. For part two the dependent variable was the dialysis
tubing and what it is permeable to, and the independent variable was the iodine. The constants
for part one was the beakers, the amount of water, and the dialysis tubing. The experimental
groups were the groups with the different solutions and the control group was the beaker filled
with pure water and the tubing with pure water. The constants in part two was the dialysis tubing
and the amount of water and iodine. Since there was only one beaker filled with iodine that is the
experimental group. If you place a dialysis tubing filled with 5 mL of water into 200 mL of
water, then the mass will stay around the same. If you place a dialysis tubing filled with 5 mL of
20% glucose solution in 200 mL of water, then the tubing will gain mass. If you place a dialysis
tubing filled with 40% glucose solution into 200 mL of water, then the tubing will gain mass. If
you place a dialysis tubing filled with 5 mL of 60% glucose solution into 200 mL of water, then
the tubing will gain mass. If you place a dialysis tubing filled with 5 mL of water into 200 mL of
60% glucose solution, then the tubing will lose mass. If you place a dialysis tubing filled with 5
mL of 80% glucose solution into 200 mL of 60% glucose solution, then the mass will stay about
the same. For part two, if the iodine is placed in the beaker, then the iodine will get in the bag as
Materials:
String
Scale
Timer
1 Dialysis Tubing
String
Spoonful of Starch
20 Drops of Iodine
Procedures:
2. Fold over the top of the dialysis tubing, and then fold it sideways, and then fold over
again. Pinch the middle of the folds and tie a knot around it with the string. Fold over
11. Weigh all of the dialysis tubing and record down their mass in grams.
14. At the same time put the dialysis tubing with the water in one of the beakers with water,
the tubing with 20% glucose in water, the tubing with 40% glucose in water, and the
tubing with 60% glucose in the last beaker of water. Put the tubing of 80% glucose and
15. Keep the different tubing in the beakers for 3 minutes and then take them all out at the
same time.
16. Weigh all of the different tubing and mark down the mass in ounces.
17. Put all of the tubing back in their beakers at the same time and start the timer.
18. Take them all out after 3 minutes and weigh them.
19. Put them all back in their beakers for 3 minutes again, and then weigh them.
20. Find the difference of the masses between each time interval and mark it down to find
results.
Part Two:
2. Put a spoonful of starch and water in the dialysis tubing and tie it like the tubing in part
one.
3. Put the simulated cell in the beaker and drop 20 drops of iodine in the beaker of water.
4. This will make the water turn yellow and will see if the dialysis tubing is permeable to
Results:
1.50
1.00
Mass in Ounces
0.50
0.00
-0.50
-1.00
0.00 3.00 6.00 9.00
Time in Minutes
Part One:
In part one six different dialysis tubing were placed into six different environments. The dialysis
tubing represented a simulated cell and was tested to see how the environments would affect the
dialysis tubing after certain time intervals. All of the tubing started out at time zero and had an
average change of mass at zero. After three minutes the dialysis tubing was taken out of the
beakers and was weighed. For the tubing that was filled with 5 mL of water and placed in a
beaker of 200 mL of water the average change in mass was 0.21 ounces after three minutes. In
O’Hara The Average Mass of Dialysis Tubing During Osmosis 8
the dialysis tubing that had 5 mL of 20% glucose in it and placed into 200 mL of water the
average change in mass was 0.32 ounces after three minutes. In the dialysis tubing that had 5 mL
of 40% glucose and placed into 200 mL of water had an average weight change of 0.41 ounces
after three minutes. The tubing that had 5 mL of 60% glucose solution and was placed into 200
mL of water had an average weight change of 0.57 ounces after three minutes. The tubing that
had 5 mL of water and was placed into 200 mL of 60% glucose had an average change in weight
of -0.15 ounces. Lastly, the tubing that had 5 mL of 80% glucose and was placed into 200 mL of
60% glucose had an average change in mass of 0.24 ounces. The second time the bags were
weighed was three minutes after they got put into the beakers again, at six minutes in total. The
first tubing filled with water and placed in water had an average mass change of 0.29 ounces at
six minutes. The second tubing filled with 20% glucose and placed in water had an average mass
change of 0.53 ounces at six minutes. The third tubing filled with 40% glucose and placed in
water had an average mass change of 0.80 ounces at six minutes. The fourth tubing filled with
60% glucose and placed in water had an average mass change of 1.01 ounces at six minutes. The
fifth tubing filled with water and placed in 60% glucose had an average mass change of -0.53
ounces after six minutes. The sixth tubing filled with 80% glucose and placed in 60% glucose
had an average mass change of 0.32 ounces after six minutes. Once again, the tubing is placed
back in their beakers for another three minutes and taken out at a total time of nine minutes. The
first tubing had an average mass change of 0.25 ounces after nine minutes. The second tubing
had an average mass change of 0.70 ounces after nine minutes. The third tubing had an average
mass change of 0.80 ounces after nine minutes. The fourth tubing had an average mass change of
nine minutes. Finally, the sixth tubing had an average mass change of 0.40 ounces in nine
minutes. Table One and Figure One both show the data described above.
O’Hara The Average Mass of Dialysis Tubing During Osmosis 9
Part Two:
In part two it was tested to see what the dialysis tubing, the simulated cell in this experiment, was
permeable to. Starch was put into the tubing and then placed into water that had 20 drops of
iodine in it. It was left to sit and soon the water started turning yellow with the iodine in it. Later,
the bag started turning purple, showing that iodine got in the bag. However, the starch was not
Discussion:
Certain bags were able to gain mass or lose mass in part one of the lab based on what
environment they were in. For example, bag number three, that had 40% glucose in water gained
mass because the tubing was placed in a hypotonic environment. The water was coming into the
cell because the water goes from a high to low concentration during osmosis. But in bag number
five, the water placed into 60% glucose, the bag lost mass because it was placed into a
hypertonic environment. The water was going out of the cell, from the high to low concentration,
causing the cell to lose weight. As the simulated cell gets closer to equilibrium the rate of
osmosis slows down. The higher the concentration gradient, the faster the rate of osmosis. When
the concentration gradient gets slower, it means that the cell is getting closer to equilibrium. The
tubing filled with 80% glucose and was placed in 60% glucose did not gain as much weight as
the 20% glucose in water because it had a higher solute concentration. In the tubing with the
20% in the water, there was all pure water on the outside, so the concentration gradient was
higher making the rate of osmosis faster. But, in the tubing with the 80% placed in 60% glucose,
they were closer to equilibrium, making the rate of osmosis slower, not making it gain as much
mass. In part two, the inside of the dialysis tubing turned blue because the iodine was permeable
to the membrane of the simulated cell, that was the dialysis tubing. This shows that iodine is
O’Hara The Average Mass of Dialysis Tubing During Osmosis 10
permeable to the membrane, however starch is not since it was not able to get to the outside of
the tubing. In the experiment, four sources of error could have been that the groups mixed up
their bags, they measured their mass in different measurements, or they didn’t put the right
amount of substances in the bags or beakers. The biggest source of error however, is that the
groups did not leave their bags in long enough due to time circumstances. If a change could be
made to this lab, it would be to experiment more with the different environments and leave the
tubing in the beakers longer to see how they would react. For example, seeing if the tubing
placed in the hypotonic environment would actually burst eventually, or if the cell in the
References: