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Investigating The Rate Of Reaction Between Sodium

Thiosulphate And Hydrochloric Acid Essay, Research Paper


Investigating the rate of reaction between Sodium


Thiosulphate and Hydrochloric Acid Diagram


Aim : We did 4 experiments to find out how


the rate of reaction changes with differing concentrations of Sodium


Thiosulphate, Hydrochloric Acid and water. As an inert and stable liquid, water


was used to alter concentration of Sodium Thiosulphate without changing the end


amount of solution. All the atoms in a water molecule have a full outer shell,


so they would not react with the other chemicals.Equipment ???? Beakers, ??????????????????????? Measuring cylinders Clamp stand and Clamps ??????????????????????? Black paper tube ??????????????????????? Light probe and Blue box ??????????????????????? Datalogger ??????????????????????? Lamp ??????????????????????? Total of 30cm3 H 0,


50cm3 Na S O , 12cm3 HClMethod : We wanted to change the concentration


of Sodium Thiosulphate and Hydrochloric Acid, but without changing the overall


quantities. To do this, the Sodium Thiosulphate and water were mixed at


different ratios, with always a constant amount of acid. The table below shows


the 4 different experiments, and what each solution composed of. The ?Graph?


column relates to the graphs taken from the Datalogger for that experiment,


which are included at the back of this piece. Sodium


Thio-sulphate (cm3) Water


(cm3) Hydrochloric


Acid (cm3) Graph


number 20 0 3 DPPAS_02 15 5 3 DPPAS_03 10 10 3 DPPAS_04 5 15 3 DPPAS_05 ? ??????????? We did not do the experiment in


which 0cm3 Sodium Thiosulphate and 20cm3 water were used, as there would have


been no reaction. In total, there were always 20cm3 of water and Sodium


Thiosulphate, with 3cm3 Hydrochloric Acid, giving a total solution of 23cm3 ??????????? The black tube was put around and


below the beaker to help prevent any unwanted light from entering the light


probe, as this would have impaired our results. The reason we used a Datalogger and light


probe instead of the old ?cross? method, is threefold. First, human error. The


cross would not just disappear ? it would fade. There would be no specific


point at which the cross would disappear, and the results of your experiment


would be based entirely on a person?s eyesight. Second, this method will only


tell you (albeit inaccurately) when the cross disappeared, i.e. how long it


took for the reaction to get to a certain point of cloudiness. It would not


tell you the varying rates of the reaction. You would not be able to tell if


the reaction speeded up, slowed down, went steady all the way e.t.c. Lastly,


what would you do if the reaction never got as far as making the cross


disappear? Or what if the reaction took a number of hours to get that far? This


traditional method is about as accurate as taking the temperature from a beaker


of water with your finger. To do the experiment, we set up the


apparatus as explained above. We put the various amounts of chemicals into the


beaker, and used the Datalogger and blue box to record the first 3 minutes of


the experiment, and then used the computer to draw up a graph. The blue box was


set to SLOW


and 10k lux.Prediction : I predict that the rate of reaction


will increase (and get more cloudy, more quickly) when the solution of Sodium


Thiosulphate and Hydrochloric Acid are strongest, and there is no water. The


reason for this is that it will be easier for the Sodium Thiosulphate to react


with the Hydrochloric Acid, as they are the only two chemicals in the beaker,


and there is not water to hinder the rate of the reaction. There will also be more Sodium Thiosulphate to react with


the Hydrochloric Acid, regardless of how much water there is.Results : The graphs from the Datalogger are


included in this project. The filename of each graph correspond to the


filenames (DPPAS_xx) listed in the table above. The table below shows the


amount of time that each graph took to level out, i.e. how long the experiment


took to finish. To work out the rate of reaction over the whole reaction (up to


>

the point where the reaction levelled), I divided the light depreciation (k


lux) by the time taken (minutes) to give a rate of k lux/min. Light


depreciation is k lux at start minus k lux at end of reaction. Here are the


results: Graph Reaction


Finished in k lux at start k lux at end k lux dep./s DPPAS_02 70s 8.9 2.1 .097 DPPAS_03 80s 8.9 2.7 .078 DPPAS_04 100s 8.4 3.2 .052 DPPAS_05 N/A 8.3 N/A N/A ??????????? Analysis


/ Conclusion : Our


results show that, as predicted, the more concentrated solutions reacted more


quickly than the weaker ones. As the concentration got weaker, the reaction was


slower. I would expect the same pattern of you swapped Sodium Thiosulphate and


Hydrochloric Acid for two other chemicals, which are not affected by water, but


will react with each other. There were a few anomalies at the beginning of two of


our graphs, but the end results were all in proportion. The experiment shown in


DPPAS_02 twice as concentrated as the experiment in DPPAS_04. In theory, this


means that the light depreciation was twice as much. 0.052 times two is 0.104,


which is very close to the result we got of 0.097. This is assuming that the


result of 0.052 was correct. Giving leeway for inaccuracies, this was as good a


correlation as we could have expected ? only 0.008 k lux inaccurate. Also, as


you can see from the k lux/sec depreciation rate, I was not able to write up


figures for the last experiment. This was because, in the time we recorded the


experiment for, the chemicals never stopped reacting. As with most of the


graphs we never, for some reason, recorded a full 3m (all our graphs finished


at between 2m45s and 2m55s). This didn?t really matter, as all the other graphs


levelled out within the time recorded. But we stopped recording DPPAS_05 before


the reaction stopped, and as a result were not able to work out a finishing


time, and thus an overall rate of reaction. For this reason, I did not think it


fair to put in the results we got from the partial experiment into the main


table above. We can still however work out a rate for the amount of the


experiment that we did. Start light of 8.3, minus finish light of 4.6 is 3.7,


divided by time, which is 165, equals 0.022 k lux dep./s. Assuming this is the rate of reaction throughout the experiment, we


could times this number by four (as DPPAS_05 was four times weaker than


DPPAS_02), and end up with 0.088, which is only 0.009 k lux dep./s out. So by


correlation these three rates of reaction against concentration, we can see


that the results are related, and that the experiment worked well.? Evaluation : In all, our experiment worked quite


well. We did come across a few problems with accuracy though. One of the most


significant one was that the Dataloggers are not 100% accurate, and do not give


very detailed readings So when you take results into account, you have to give


some leeway for the inaccuracy of the Datalogger. ??????????? On DPPAS_05, we had a huge anomaly,


of nearly 4 k lux. This appeared about 20s into our experiment (according to


our graph). We have no idea how or why this happened. My best guess is that


somebody knocked the experiment and/or the Datalogger whilst it was recording. ??????????? I would do many things to improve


the experiment if I did it again in the future. Firstly, I would leave the


experiment for a long time (at least an hour) so that all the experiments would


finish. Second, I would do the experiment in a darkroom, and make the tube


extend upwards as well so that it covered the lamp, and all the light coming


out of the lamp would go through the beaker. If I could, I would also use a


more expensive and better quality Datalogger that could record the light more


precisely and accurately, but this would prove impractical for just one


experiment. ??????????? One thing I would be hard pushed to


overcome would be the light that passes down through the glass sides of the


beaker, via TIR. This is however not that important, as any light entering the


light sensor via this route would remain constant.

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