Physics307L:People/Knockel/Notebook/071024: Difference between revisions

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<math>R=</math>.
<math>R=</math>.


Perhaps the best idea would be to say that <math>R=R_6</math>, since this has the smallest uncertainty.  This method gives
Perhaps the best idea would be to say that <math>R=R_6</math>, since <math>R_6</math> has the smallest uncertainty.  This method gives


<math>R=</math>.
<math>R=</math>.

Revision as of 12:51, 5 November 2007

Balmer Series

Experimentalists: 2 of the greatest

Goal

We want to see if we can measure the wavelengths of the emission spectra (EM radiation produced from electron transitions) of hydrogen and deuterium. We also want to calculate Rydberg's constant for hydrogen and deuterium. Basically, we are studying emission spectra of atoms with 1 outer electron, which is something that quantum mechanics can explain very easily to be quantized.

For hydrogen, the Balmer series, which is the series that results when electrons transition from a high principle quantum number to the second principle quantum number, produces visible light that can be observed through a spectroscope. The wavelengths produced from these transitions are predicted to be given by

[math]\displaystyle{ \frac{1}{\lambda}=R\left(\frac{1}{2^2}-\frac{1}{n^2}\right) }[/math],

where [math]\displaystyle{ n }[/math] is an integer greater than 2 that represents the initial principle quantum number of the electron before it transitions to the second principle quantum number, [math]\displaystyle{ \lambda }[/math] is the wavelength, and [math]\displaystyle{ R }[/math] is some constant called the Rydberg constant.

We hope to observe the Balmer series for hydrogen, which contains the following wavelengths:

Hydrogen's actual wavelenghts
[math]\displaystyle{ n\, }[/math] 3 4 5 6
[math]\displaystyle{ \lambda\, }[/math] (nm) 656.3 486.1 434.1 410.2

And we hope to find that the Rydberg constant for hydrogen is [math]\displaystyle{ R }[/math]=1.097758x107 1/m.

For deuterium, we expect the Rydberg constant to be very slightly larger because, for a larger nucleus, the nucleus wiggles less as the electron moves, which causes slightly smaller wavelengths.

Equipment

The current generator is on the left and the two shiny scopes (at a right angle with each other) are parts of the spectroscope.
  • Something to send current through samples to excite the electrons
  • Mercury, hydrogen, deuterium, and sodium samples
  • Constant-deviation spectrometer (ours was made at and for UNM)

Setup

We plugged in the electric current source, and calibrated the spectrometer using mercury by rotating the prism inside of it. We knew the wavelengths mercury produces, so we simply had to make sure the spectrometer was measuring the wavelengths at what we knew them to be.

The most difficult obstacle was that the spectrometer (made at UNM) had a loose knob for rotating the prism and changing the wavelength to be observed. This knob was supposed to give us precise readings, but, since it was loose, we did not know which data to take. This problem would have been easy to fix if the looseness did not vary as the knob was turned to different wavelengths. At low wavelengths, the looseness vanished, and this is where we calibrated. We noticed that, for higher wavelengths, the knob's looseness was causing error that had little to no bias towards too high or too low (ie, the knob's wiggling is basically centered on the correct value).

Procedure

For both helium and deuterium, we put current through the samples and used the spectroscope to measure the strongest wavelengths produced. When taking a measurement, we took the value from the rightmost part of the band of light since the adjustable slit that lets light into the spectrometer only changes the left side (we calibrated on the rightmost part of the band also).

We took each measurement twice. One measurement was by turning the wavelength-selecting knob to increasing wavelengths, and the other was by turning the knob to decreasing wavelengths. We did this because the looseness of the knob made these values different. We only needed these two numbers instead of repeating over and over and getting a Gaussian, because the systematic uncertainty of the knob far outweighed any random error.

Data

The decreasing wavelength is when the knob is being turned as to only decrease the wavelength, and vice versa.

I am providing as many significant digits as our spectroscope can allow us to give.

Also, I would like to point out that low wavelength means high energy and high frequency, so, as the wavelength decreases, the color is changing from red to purple.

Hydrogen Data
[math]\displaystyle{ n\, }[/math] 3 4 5 6
[math]\displaystyle{ \lambda\, }[/math] (nm) decreasing 656.0 485.6 434.0 410.3
[math]\displaystyle{ \lambda\, }[/math] (nm) increasing 658.0 485.9 434.2 410.4


Deuterium Data
[math]\displaystyle{ n\, }[/math] 3 4 5 6
[math]\displaystyle{ \lambda\, }[/math] (nm) decreasing 654.9 485.5 433.8 409.8
[math]\displaystyle{ \lambda\, }[/math] (nm) increasing 658.0 486.2 434.3 410.2


Calculating Rydberg constant for helium and deuterium

For a given substance such as hydrogen, there are four different Rydberg constants for the four wavelengths of the Balmer series that we measured, where

[math]\displaystyle{ R_n=\frac{1}{\lambda\left(\frac{1}{2^2}-\frac{1}{n^2}\right)} }[/math],

which will produce [math]\displaystyle{ R_3 }[/math], [math]\displaystyle{ R_4 }[/math], [math]\displaystyle{ R_5 }[/math], and [math]\displaystyle{ R_6 }[/math].

To calculate the Rydberg constant for a substance, I will use the average:

[math]\displaystyle{ R=\frac{R_3+R_4+R_5+R_6}{4} }[/math].

Before I can do this, I must first determine the wavelengths I will use and the uncertainty of those wavelengths. The uncertainty will be dominated by the systematic error of the looseness of the knob, and I will simply use the difference between the "increasing wavelength" and "decreasing wavelength" values as the uncertainty. The wavelengths and the uncertainty are as follows...

Hydrogen Wavelengths
[math]\displaystyle{ n\, }[/math] 3 4 5 6
[math]\displaystyle{ \lambda\, }[/math] (nm) 657.00 [math]\displaystyle{ \pm }[/math] 2.00 485.75 [math]\displaystyle{ \pm }[/math] 0.30 434.10 [math]\displaystyle{ \pm }[/math] 0.20 410.35 [math]\displaystyle{ \pm }[/math] 0.10


Deuterium Wavelengths
[math]\displaystyle{ n\, }[/math] 3 4 5 6
[math]\displaystyle{ \lambda\, }[/math] (nm) 656.45 [math]\displaystyle{ \pm }[/math] 3.10 485.85 [math]\displaystyle{ \pm }[/math] 0.70 434.05 [math]\displaystyle{ \pm }[/math] 0.50 410.00 [math]\displaystyle{ \pm }[/math] 0.40


Using the above formula for R and propagating the uncertainty, we get

[math]\displaystyle{ R= }[/math].

Perhaps the best idea would be to say that [math]\displaystyle{ R=R_6 }[/math], since [math]\displaystyle{ R_6 }[/math] has the smallest uncertainty. This method gives

[math]\displaystyle{ R= }[/math].

Error and conclusions

Also...

There was an unknown sample of gas that we tried to identify. Koch recognized the orange color as that of neon from neon lights, and, after comparing the spectrum of the unknown sample with the internet and with the neon sample we had and noticing the spectra were identical, we concluded that the unknown sample was indeed neon. Since neon has many electrons, there were many more observable wavelengths than there was for hydrogen and deuterium.