pH is a measure of the concentration of the H3O+ ions in a solution, and buffers are solutions that resist changes in the pH when an acid or an alkali is added. The objective of this lab was to determine the ways in which a buffer could effect changes in pH of a solution. This was done through titrations of phosphate solutions, acidic HCl, and basic NaOH, with distilled water. The intent was to note the changes caused by the buffer by observing the buffering range and buffering capacity from the standard curved created from the pH readings. A buffering range is the pH range in which a buffer has effectively neutralized the acids and bases, while maintaining a constant pH. Buffering capacity, on the other hand is the measure of the efficiency of buffer in its resistance to pH change. Therefore, a good buffer with a high buffering capacity should be able to resist the changes in pH well. If the buffer solution is titrated with a strong acid, HCl, then the pH of the solution will decrease slowly, maintaining a constant pH value due to the presence of buffers (instead of the pH dropping in a linear line with huge values.) Likewise, if the mixture containing buffer solution, and water are titrated with a strong base, NaOH, then the pH of the solution will increase at a steady increments instead of the pH values shooting up in big numbers in a linear line.
In order to test this, method of serial dilution was first utilized to find the amount of buffer solution needed for the
The procedure of this lab is to determine if liver and potato cells contain natural buffers that resist large change in pH as 1. NaCl or 1. NaOH are added to the solution.
2. The different concentrations of ONPG solutions and buffer solutions were incubated in the water bath at 37°C for 5 minutes.
Procedure: I used a ruler, thermometer, and scale to take measurements. I used a graduated cylinder, short step pipet, scale, and ruler to determine volume and density. I used a volumetric flask, graduated pipet, pipet bulb, scale, and glass beaker to determine concentrations and densities of various dilutions.
10 microliters of the sample is then added and the assay absorption is measured at 340nm. If absorbance was above 1.5, samples were diluted.
To improve the results from the experiment buffer solutions that were not whole pHs could have been used e.g. pH 4.5, 5.5 etc. This would have provided more reliable results as a wider range of results would have been produced. Using pHs with decimals would also help to more accurately determine the optimum pH as the optimum may have been above or below the pH stated in the hypothesis; 8. In this experiment however the optimum is taken at 8 because the graph does not rise again.
In this experiment, a saturated calcium sulfate was already made and ready to use. 25.00 mL of this solution was then mixed with 10 mL of an ammonia buffer and 1 drop of
The pH of a solution is the measure of the concentration of charged Hydrogen ions in that given solution. A solution with a pH lower than seven is considered to be acidic. A solution with a higher pH is a base. It is very important for organisms to maintain a stable pH. Biological molecules such as proteins function only at a certain pH level and any changes in pH can result in them not functioning properly. To maintain these constant pH levels, buffer solutions are used. A buffer solution can resist change to small additions of acids or base’s. A good buffer will have components that act like a base, and components that act like an acid.
For this experiment, titrations on a weak acid, acetic acid, and a buffer were performed. Acetic acid was titrated with NaOH in order to observe the half-equivalence point as well as the equivalence point. Then, the buffer and the buffered acetic acid solution prepared faced additional titration with NaOH and HCl to evaluate the differing buffering effects following the addition of a strong acid and strong base. Finally, the buffer’s buffering capacity was calculated. If the experiment were to be repeated, it would be interesting to observe the buffering effects following a titration between a weak base and a buffer instead with greater concentrations. The change in the concentration following the preparation of buffer with a weak base and its conjugate acid would pose for an interesting experiment to observe an increase in the buffering capacity.
PH is the relative concentrations of hydrogen and hydroxide ions in a solution. The role of buffers in maintaining pH homeostasis in the body is that they prevent sharp changes in hydrogen ion concentration and maintain a relatively constant pH. They maintain stability in the pH of body fluids too. The body has to be kept at a close to neutral pH because if it goes above or below the normal range it can be harmful to the body, even fatal. Also body fluids are on the alkaline side of neutral and that is why body fluids are more on the alkaline
The titration curve of the unknown exhibited many characteristics, such as equivalence points, pKa of ionizable groups, isoelectric point, and buffer regions, that are particularly distinct to lysine. For unclear reasons, the pH during the titration did not reach the pH for pure 0.2 M NaOH nor 0.2 M HCl and normal equivalence points expected at two extreme ends of the titration curves for all amino acids were not observed. The titration of a phosphate buffer showed that the buffer capacity is directly proportional to the molarity of the buffer. However, our results showed that although the initial pH of the phosphate buffer was less than the pKa value, the measured buffer capacity was higher towards acid than base. The accuracy of the pH meter and calibration process was questioned under assumptions that the pH of the prepared phosphate buffer was actually above pKa.
The practical was carried out to investigate the effect of pH on the reaction of the enzyme acid phosphatase.
In this lab, the purpose was to determine the stability of a substance after adding an acid or a base. The results claim that liver and buffer are the most resistance to change in pH. Looking at figure 3, buffer and liver both maintain a stable pH even with the addition of an acid or base. However, potato and water have less buffer in them since their pHs did change. In figure 3, the potato acid’s pH level decreased by two, and the potato base’s pH level increased by two. The level of pH of a water acid decreased by 4, while the water base’s pH increased by 5. These results all tie to the fact that buffer is a substance that maintains a stable pH; the presence of buffer in organisms help maintain homeostasis by binding or releasing hydrogen
Phosphate buffer system; The major phosphates in Phosphate buffer system are monosodium (HPO42-) and disodium (H2PO4) phosphate. Disodium (H2PO4) is used as a weak acid and buffer for strong bases and monosodium (HPO42-) is used as a weak base and buffer for the H+ released by a strong
To make the buffer solution you need 0.2 mol dm-3 of Na2HPO4 and 0.1mol dm-3 of citric acid this will give 100cm3 of buffer. Here is how to get the different pH in the buffer solutions:
A pH system is located in all freshwater systems. A pH is a negative log oh hydrogen ion concentration in a water based solution. A biochemist Soren Peter Lauitz Sorensen discovered what pH means in 1909. He figured out that pH stands for “ power of hydrogen” where “ p” is short for the word “potenz” and the symbol “H” stands for the element of hydrogen.