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In order to calibrate our spectrometer we used a mercury vapor tube (S-68755-30-K). To start, the mercury tube was placed inside the spectrum tube power supply (Model SP200) and warmed for about five to ten minutes. Meanwhile, the spectrometer was adjusted such that the cross-hairs were brought into focus by adjusting the ocular to suit our vision. The slit was then brought into focus using the large ring near the center of the viewing telescope, turning the screw only in one direction to ensure that "gear backlash" can be avoided. This setup can be seen in '''Figure 3'''.
In order to calibrate our spectrometer we used a mercury vapor tube (S-68755-30-K). To start, the mercury tube was placed inside the spectrum tube power supply (Model SP200) and warmed for about five to ten minutes. Meanwhile, the spectrometer was adjusted such that the cross-hairs were brought into focus by adjusting the ocular to suit our vision. The slit was then brought into focus using the large ring near the center of the viewing telescope, turning the screw only in one direction to ensure that "gear backlash" can be avoided. This setup can be seen in '''Figure 3'''.


[[Image:3aa.JPG|thumb|center|'''Figure 4. Slit Width.''' This is the slit width from the spectrometer. It was adjusted using the large knob to the right of the slit. In order to find the various spectral lines, a wide slit was used, whereas the more focused thin slit was used to focus in on the wavelength for each spectral line.]]


Using the spectrometer with a wide slit as seen in '''Figure 4''', a line of the mercury spectrum could be distinguished and then, with a narrowed slit, the line was brought into focus until it was quite narrow and sharp. Noting the orientation and value of the spectrometer dial, as seen in '''Figure 5''', the corresponding wavelengths of light were applied as given in '''Table 1''' '''[3]''':
Using the spectrometer with a wide slit as seen in '''Figure 4''', a line of the mercury spectrum could be distinguished and then, with a narrowed slit, the line was brought into focus until it was quite narrow and sharp. Noting the orientation and value of the spectrometer dial, as seen in '''Figure 5''', the corresponding wavelengths of light were applied as given in '''Table 1''' '''[3]''':

Revision as of 03:58, 14 December 2009

The Balmer Series of Hydrogen and Deuterium in Atomic Physics

Author: Anastasia A. Ierides

Experimentalists: Anastasia A. Ierides, Alexandra S. Andrego

University of New Mexico, Department of Physics and Astronomy, Albuquerque NM, 87131

Physics 307L Junior Lab: December 14, 2009

aierides@nm.edu

Abstract

The importance of the Balmer series lies in the prediction of absorption/emission lines of hydrogen in the visible spectrum. The Balmer series led to the ensuing discoveries of the Lyman, Paschen, and Brackett series. These series predict the spectral lines of hydrogen in the non-visible parts of the spectrum. In order to detect the Balmer Series, of first Hydrogen and then Deuterium, we used a Constant-Deviation Spectrometer (which was calibrated using a Mercury Vapor bulb), in an environment with limited light, to measure the wavelength of the emission spectra of each. The excitation of the electrons in the atoms of each gas through electrical stimulation allows a release of photons at specific wavelengths corresponding to the Balmer series (the excitation of electrons from the first ionized state, [math]\displaystyle{ n = 2 }[/math], to the second, [math]\displaystyle{ n = 3 }[/math]). Then using a generalized form of the Balmer formula, the Rydberg formula, we used our measured wavelength to compute Rydberg's constant and to verify whether or not a deviation between the Hydrogen spectra and the Deuterium spectra could be found. Our calculated value of Rydberg's constant for each Hydrogen [math]\displaystyle{ (1.0972781 \pm 0.0025) \times10^7 }[/math] per meter and Deuterium [math]\displaystyle{ (1.0983221 \pm 0.0007) \times10^7 }[/math] per meter is in close proximity with the accepted value of [math]\displaystyle{ 1.0967758 \times10^7 }[/math] per meter.

Introduction

The Balmer series a series of predicted and confirmed wavelengths of photons emitted from hydrogen spectrum belonging to the visible spectrum. It is the culmination of the excitation

of electrons from the n=2 state to the n=3,4,5, and 6 states in an atom causing a release of photons of corresponding energies [5]. These wavelengths compose the visible part of the hydrogen spectrum and are hence called the Balmer series.

Balmer Series of the Hydrogen Spectrum [9]
The prediction of these spectral lines comes from the Balmer formula, written as:
[math]\displaystyle{ \frac{1}{\lambda }=R(\frac{1}{2^2}-\frac{1}{n^2}) }[/math]
[math]\displaystyle{ n=3,4,5,...\,\! }[/math]

where [math]\displaystyle{ \lambda }[/math] is the wavelength to be predicted for each transition, [math]\displaystyle{ n }[/math] is the principle quantum number of the electron, and [math]\displaystyle{ R }[/math] is a constant called Rydberg's constant, derived as seen in the Appendix below [3]. This constant however is a variant one when it comes to dealing with various elements due to the reduced mass of the subatomic particles involvement in the calculation.

The theory behind this constant and the above equation is that for every element, there is some value R for which the wavelength of each photon emitted by each transition can be

predicted. The discrepancy between the "R" values of hydrogen and deuterium is ever so slight due to the mass change of deuterium from its extra neutron, which in turn may or should cause a shift in the spectral lines [7]. To test this hypothesis, a "constant-deviation" spectrometer is used within an allowed precision to experimentally attain data to support this hypothesis [3].

During our experiment we found that slight discrepancy in our values could be due to some oversight when using the 'scope'. There might have gear back lash from not turning the knob

all the way back before remeasuring spectra for each trial, even though we took great care in doing so. Also, the lab lasted over two days, with a week interval and during that interval another group had used the same device used for our experiment, so re-calibration for our set of data was necessary during the second day.

Background

Before 1885, the year that the Balmer formula was founded by a Swiss school teacher Johann Jakob Balmer, physicists, although aware of atomic emissions, lacked the tools to

predict the location of each spectral line [5]. The Balmer equation is used in the prediction of each of the four visible emission/absorption lines of hydrogen with high precision. This had inspired the Rydberg equation, invented by a Swedish physicist Johannes Robert Rydberg [6]. This new equation was a generalization of the Balmer formula, which in turn "led to the finding of the Lyman, Paschen, and Brackett series used in predicting the absorption/emission lines of hydrogen found outside the visible spectrum" [5].

According to the Rutherford Bohr model (devised by Neils Bohr in 1913 from the amelioration of a model created by Ernest Rutherford in 1911) of the Hydrogen atom, an electron

transition that occurs between the second energy level or first excited state in the atom (corresponding to n=2) and any other higher energy level results in the Balmer lines [8].

The Balmer series has been helpful in astronomical and physical use for years due to the abundance of hydrogen in the universe. It has been used for several means such as

spectral classification, the measure radial velocities of objects in space due to doppler shifting, and the distances to those objects.

The Balmer series is one of six series in which the spectral line emissions of hydrogen are designated. There are four different emission wavelengths of visible light by which the

hydrogen spectrum is defined. These wavelengths can be calculated using the Balmer formula (found by Johann Balmer, 1885) written above in the "Purpose" and reflect emissions of photons by transitions of electrons between principal quantum number levels from [math]\displaystyle{ n\geq3 }[/math] to [math]\displaystyle{ n = 2 \,\! }[/math] [5].

Compared to the Hydrogen atom, which contains one proton in the nucleus, the Deuterium atom, contains a proton and a neutron in its nucleus. Thus the Deuterium atom is heavier

than the regular Hydrogen atom. By observing and classifying spectra lines of the hydrogen and deuterium atoms the Balmer series can be determined [7]. By using electrical stimulation to excite the atoms to higher energy levels we can measure the emitted photons of wavelengths equivalent to the energy of our excited electrons.


Materials and Methods

Apparatus: Constant-Deviation Spectrometer

Figure 1 A Pellin-Broca constant-deviation prism [10] has a wavelength dependent index of refraction which makes it act as a spectrometer [3].

A constant-deviation spectrometer (SER. #12610) in use during this lab consists of a Pellin-Broca constant-deviation prism whose incident and exit angles are fixed with an appropriate rotation of the prism. The only requirement in this setting consists of keeping a the incident light ray and the axis of the analyzing telescope perpendicular [3].

Figure 2 The actual prism inside the constant-deviation spectrometer separating the spectral lines. This prism is adjusted in order to calibrate the spectrometer [11]

Calibration of the Spectrometer

Figure 3. Constant-Deviation Spectrometer and Power Supply [11]. Here the spectrometer is set up in front of the bulb to begin calibration. Books were necessary to be placed underneath the power supply in order to achieve the best resolution possible through the spectrometer.
Figure 4. Slit Width. This is the slit width from the spectrometer. It was adjusted using the large knob to the right of the slit. In order to find the various spectral lines, a wide slit was used, whereas the more focused thin slit was used to focus in on the wavelength for each spectral line.

In order to calibrate our spectrometer we used a mercury vapor tube (S-68755-30-K). To start, the mercury tube was placed inside the spectrum tube power supply (Model SP200) and warmed for about five to ten minutes. Meanwhile, the spectrometer was adjusted such that the cross-hairs were brought into focus by adjusting the ocular to suit our vision. The slit was then brought into focus using the large ring near the center of the viewing telescope, turning the screw only in one direction to ensure that "gear backlash" can be avoided. This setup can be seen in Figure 3.


Using the spectrometer with a wide slit as seen in Figure 4, a line of the mercury spectrum could be distinguished and then, with a narrowed slit, the line was brought into focus until it was quite narrow and sharp. Noting the orientation and value of the spectrometer dial, as seen in Figure 5, the corresponding wavelengths of light were applied as given in Table 1 [3]:

Figure 5 The open prism apparatus and measuring gear are visible here. The spectrometer dial was used to orient the correct wavelength to the corresponding spectral line.


TABLE 1

Color Wavelength (nm)
Deep Violet (very hard to see) 404.7
Violet 435.8
Very Weak Blue-Green skip this one
Green 546.1
Yellow 1 577.0
Yellow 2 579.0
Red 690.75


The calibration of the spectrometer was then completed and the compilation of data was commenced.

Measurement of the Hydrogen and Deuterium Spectrum

Figure 6. Full Spectrometer and Hydrogen Bulb. Here the apparatus can be seen with the hydrogen bulb placed inside of the power supply and the spectrometer pointing towards it.

After turning off the power supply and replacing the mercury spectrum tube with the hydrogen spectrum tube (S-68755-30-G), we allowed the hydrogen tube to warm up for approximately five minutes, as seen in Figure 6. Then we began to take measurements making sure not to dislodge the prism from its calibrated state. We began measuring the hydrogen spectrum by finding each spectral line, focusing it in the cross hairs, while turning the dial to the appropriate wavelength, and adjusting the slit width. This process was repeated for a few more trials and then the bulb was replaced by the deuterium spectrum tube (S-68755-30-E) and the entire process used for the hydrogen spectral line measurements was repeated for the deuterium spectrum lines.

Results and Analysis

FIGURE 4: The HYDROGEN linear fit data of 1/Lambda vs the Quantum Transition Term . Here you can see the linear relationship between the inverse of the wavelength of the spectrum light and the quantum transition term that was calculated for each spectral line from the Balmer-Rydberg equation described in the formal report. The resulting slope of this graph is the experimental mean value for the Rydberg constant of the Hydrogen Balmer series.
FIGURE 5: The DEUTERIUM linear fit data of 1/Lambda vs the Quantum Transition Term. Here you can again see the linear relationship between the inverse of the wavelength of the spectrum light and the quantum transition term. Through comparision with this graph and the one seen in FIGURE 4 of the Hydrogen case, we can see very little difference between the resulting slope of the graphs and the experimental mean values for the Rydberg constants.


Our results from this experiment can be seen in TABLE 2 below. The transition column refers to the structure of the Balmer series and the Balmer-Rydberg equation discussed earlier in this paper. All error margins included in the data table are the results of the standard error of mean calculation performed by excel. The excel spreadsheet with these calculations can be refered to in our Primary Lab Notebook under the Analysis section [6].


{{#widget:Google Spreadsheet

|key=t_1tTZFJkNFGN2kIa2cLLfg |width=832 |height=150

}}


From the values listed in TABLE 2, a Rydberg's constant was calculated from the Balmer-Rydberg equation as follows:
[math]\displaystyle{ \frac{1}{\lambda }=R(\frac{1}{2^2}-\frac{1}{n^2}), n=3,4,5,6\,\! }[/math]
[math]\displaystyle{ \frac{1}{\lambda }=R(\frac{n^2-4}{4n^2})\,\! }[/math]
[math]\displaystyle{ R=\frac{4n^2}{\lambda(n^2-4)}\,\! }[/math]
Where the relationship between [math]\displaystyle{ \frac{1}{\lambda }\,\! }[/math] and the term [math]\displaystyle{ \frac{n^2-4}{4n^2}\,\! }[/math] were graphed using excel and the resulting slope for both the Hydrogen and Deuterium cases was the average experimental value of the Rydberg Constant (see FIGURE 4 for the Hydrogen Linear Fitting and FIGURE 5 for the Deuterium Linear Fitting). Excel was used for the creation of theses graphs and for the linear fit seen on both figures. For any and all excel spreadsheets please refer to our Primary Lab Notebook [6].
The average values for the measured Rydberg's constants are:
[math]\displaystyle{ R_{Hydrogen,average}\approx1.0973\pm 0.0025\times10^7 m^{-1}\,\! }[/math]
[math]\displaystyle{ R_{Deuterium,average}\approx1.0983\pm 0.0007\times10^7 m^{-1}\,\! }[/math]


We discovered that our experimental Rydberg constant for the Hydrogen Spectrum was approximately off by a small magnitude of the fifth order, and henceforth our experiment proved to be successful in estimating an appropriate value for the Rydberg constant for the Hydrogen Spectrum Balmer Series. However,our experimental mean value for the Deuterium Balmer Series was not as successful. Our uncertainty in our experimental Rydberg constant for the Deuterium spectrum does not put the accepted value in our attained range. This goes to show that our experiement set-up on day two of our data trials (Deuterium data was only taken on the second day of trials and had a different calibration), falls short in statistically minimizing both our random and systematic error. The accepted value of the Rydberg constant, for which we have based all comparisons, is [5]:
[math]\displaystyle{ R_{accepted}=1.0973731568525\times10^7 m^{-1}\,\! }[/math]

Discussion/Conclusion

In order to fully comprehend the results above, it is beneficial to compare the experimental results with the accepted values. Through such a comparison it is evident that the measured values attained through this experiment were sufficiently close to the accepted value given above. It is evident from results such as these that the systematic error was not completely minimized for this experiment. As stated above, I believe that some of this systematic error could be the result of the two different calibrations for the data taken on the hydrogen spectrum tube versus the data taken for the deuterium spectrum tube. This systematic error could be reduced by retaking data without a second calibration. We did try to achieve this in an extra lab session, but we proved to be unsuccessful in appropriately calibrating our spectrometer. Therefore the extra data was determined to be insufficient in minimizing the systematic error, and was thrown out. In our first two data taking sessions we did not see the need to throw out any of our taken data. When we compared the results from the hydrogen bulb and the deuterium bulb, we noticed that both results had insignificantly different true means for each wavelength of the spectrum and the calculated Rydberg constant. Because our error cannot be said to be minimized any noticeable difference between the true means cannot be said to be purposeful, and hence from our data we cannot discern any difference between the values obtained for hydrogen and deuterium based on their masses. According to the theory behind the Balmer series and Rydberg constant, there should exist a true mean value difference due to the difference in mass that exists between the two atoms, as described above. This should therefore be true for all atoms of varying mass, but was not evident in this experiment.

Conclusions

SJK 00:42, 30 November 2009 (EST)

00:42, 30 November 2009 (EST)
I think you are on the right track for conclusions, but more can be included: "In conclusion, we were able to precisely measure the Rydberg constant for both hydrogen and deuterium. The accepted value for the Rydberg constant for Hydrogen was statistically significantly different from our measurement (___ SEMs discrepancy), indicating some systematic error. Our measurements for H and D were statistically signficantly different, although theoretically their difference should be too small for us to discern with this instrument. Possible reasons for these results are ... and can be investigated further by ...

According to our data, although the Deuterium spectral lines varied from the Hydrogen lines in wavelength, as seen by the percentage error in the Rydberg Constant of each, the variance is slight. The largest value by which the wavelengths varied was designated in the red wavelength measurement as seen in our data tables. But also according to our data, the wavelength measurements of each color seemed to be shifted from the Hydrogen in the Deuterium spectrum.

Acknowledgements

Please note that Alexandra S. Andrego was my lab partner for this lab. I thank her for her collaboration in the acquisition of data and helpful analysis.
Thanks to Professor Gold for using his lab manual [3] as a guide for the calibration process as well as a guide for data collection
Also thanks to the many authors of Wikipedia for the useful open-access articles discussing the Balmer series [5], Rydberg's constant [6], and Deuterium [7].
Finally, I extend my gratitude to Professor Steven Koch as well as his teaching assistant, Pranav Rathi, for their extensive feedback as well as guidance throughout this lab.

References

[1] "Hydrogen energies and spectrum." Test Page for Apache Installation. N.p., n.d. Web. 13 Dec. 2009. http://hyperphysics.phy-astr.gsu.edu/Hbase/hyde.html#c4

[2] "Hydrogen spectrum." Test Page for Apache Installation. N.p., n.d. Web. 13 Dec. 2009. http://hyperphysics.phy-astr.gsu.edu/hbase/Tables/hydspec.html

[3] "The University of New Mexico Dept. of Physics and Astronomy." PHYSICS 307L: 'Junior Laboratory Manual Fall 2006'. Professor Michael Gold. http://www-hep.phys.unm.edu/~gold/phys307L/manual.pdf

[4] "User:Anastasia A. Ierides/Notebook/Physics 307L/2009/09/28 - OpenWetWare." Main Page - OpenWetWare. N.p., n.d. Web. 13 Dec. 2009. http://openwetware.org/wiki/User:Anastasia_A._Ierides/Notebook/Physics_307L/2009/09/28

[5] "Balmer series - Wikipedia, the free encyclopedia." Wikipedia, the free encyclopedia. N.p., n.d. Web. 14 Dec. 2009. http://en.wikipedia.org/wiki/Balmer_series

[6] "Rydberg constant - Wikipedia, the free encyclopedia." Wikipedia, the free encyclopedia. N.p., n.d. Web. 14 Dec. 2009. http://en.wikipedia.org/wiki/Rydberg_constant

[7] "Deuterium - Wikipedia, the free encyclopedia." Wikipedia, the free encyclopedia. N.p., n.d. Web. 14 Dec. 2009. http://en.wikipedia.org/wiki/Deuterium

[8] "Bohr model - Wikipedia, the free encyclopedia." Wikipedia, the free encyclopedia. N.p., n.d. Web. 14 Dec. 2009. http://en.wikipedia.org/wiki/Bohr_model

[9] "Balmer series." Department of Mathematics, Texas A&M University. N.p., n.d. Web. 14 Dec. 2009. http://www.math.tamu.edu/~comech/balmer/balmer.html

[10] "Pellin-Broca prism - Wikipedia, the free encyclopedia." Wikipedia, the free encyclopedia. N.p., n.d. Web. 14 Dec. 2009. http://en.wikipedia.org/wiki/Pellin-Broca_prism

[11] "Physics307L F07:People/Rivera/Notebook/Formal Report - OpenWetWare." Main Page - OpenWetWare. N.p., n.d. Web. 14 Dec. 2009. http://openwetware.org/wiki/Physics307L_F07:People/Rivera/Notebook/Formal_Report

Appendix

Derivation of the Rydberg Equation [5]


We can start from the equation of total energy of an electron in the nth energy state derived from the Bohr model:

[math]\displaystyle{ E_\mathrm{total} = - \frac{m_e e^4}{8 \epsilon_0^2 h^2}. \frac{1}{n^2} \ }[/math]

The change in energy of an electron transitioning from one energy state with a value [math]\displaystyle{ n }[/math] to another is:

[math]\displaystyle{ \Delta E = \frac{ m_e e^4}{8 \epsilon_0^2 h^2} \left( \frac{1}{n_\mathrm{initial}^2} - \frac{1}{n_\mathrm{final}^2} \right) \ }[/math]

Using [math]\displaystyle{ \frac{1}{ \lambda} = \frac {E}{hc} \rightarrow \Delta{E} = hc \Delta \frac{1}{\lambda}\,\! }[/math] to change the units to wavelength, we get

[math]\displaystyle{ \Delta \left( \frac{1}{ \lambda}\right) = \frac{ m_e e^4}{8 \epsilon_0^2 h^3 c} \left( \frac{1}{n_\mathrm{initial}^2} - \frac{1}{n_\mathrm{final}^2} \right) \ }[/math]

where

[math]\displaystyle{ h \ }[/math] is Planck's constant,
[math]\displaystyle{ m_e \ }[/math] is the rest mass of the electron,
[math]\displaystyle{ e \ }[/math] is the elementary charge,
[math]\displaystyle{ c \ }[/math] is the speed of light in vacuum, and
[math]\displaystyle{ \epsilon_0 \ }[/math] is the permittivity of free space.

And the Rydberg constant for Hydrogen is found as:

[math]\displaystyle{ R_H=\frac{m_e e^4}{8 \epsilon_0^2 h^2}\,\! }[/math]

List of Used Constants

[math]\displaystyle{ \mu\,\! }[/math] is the reduced mass of an atom
[math]\displaystyle{ e=1.602\times10^{-19} C\,\! }[/math]
[math]\displaystyle{ \epsilon_0=8.854\times10^{-12} F\cdot m^{-1}\,\! }[/math]
[math]\displaystyle{ c=2.998\times10^8 m\cdot s^{-1}\,\! }[/math]
[math]\displaystyle{ h=6.626\times10^{-34}J\cdot s\,\! }[/math]
Rydberg's constant for hydrogen is calculated to be approximately:
[math]\displaystyle{ R\simeq1.0967758\times10^7m^{-1}\,\! }[/math]