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When I view most glass from the side it's green which I've found out is due to impurities in the glass specifically from iron oxide. Why is it when I view the larger face from an oblique angle, it isn't nearly as green?

I cannot personally notice any different on the piece I have next to me even when I hold it at an angle that would be almost looking at the edge of the glass. It is pretty small (about 2.5" x 5" x .0625" or about 61mm x 127mm x 2mm, l x w x h) but I feel like it's big enough that I'd be looking through enough glass to get the green.

Cobertos
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  • Please provide data. I think you will find that all that matters is the amount of a glass you look through. If you have a block of glass that doesn't look green perhaps it's a different type of glass? Without solid information (i.e. an experiment with a control) you have nothing to go on. – Brandon Enright Mar 29 '14 at 23:04
  • I mean, the glass I have looks green at the edges (confirming it has the impurity) but when looking at it the front/larger face at an angle, I don't see nearly as much if not any green. I guess I could draw some pictures to show like the distances and stuff I am observing the light at but it seems my question was already answered. – Cobertos Mar 30 '14 at 00:51

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This might be surprising to some viewers. Feel free to down vote me, but please let me know if anything is wrong except the fact that I'm not relating the color of glass to impurities.

A "pure" piece of glass (without the iron impurity) can also appear green. This is not because of the color of metal ions. This can be explained by the classical drude model.


Here is a rather concise derivation. I use the steps from the material cited with the link. The Drude model assumes that the electrons in a material is locally bounded by a "spring" force. The response (spatial displacement $\vec{r}$) of individual electrons to an external electric field $\vec{E}$ can be described by the force equation $$ m \frac{\partial ^2 \vec{r}}{\partial t^2} + m \Gamma \frac{\partial \vec{r}}{\partial t} + m \omega_0^2 \vec{r} = -q \vec{E} $$

Take the Fourier transform and get $$ \left ( -m \omega^2 - j\omega m \Gamma + m \omega_0^2 \right )\vec{r}\left ( \omega \right )= -q \vec{E}\left ( \omega \right ) $$

The dipole moment under field $\vec{E}$ is $$ \vec{\mu}\left ( \omega \right ) = -q\vec{r} = \left[ \frac{q^2}{m} \frac{1}{\omega_0^2 - \omega^2 - j\omega\Gamma} \right] \vec{E}\left ( \omega \right ) $$

The polarization of the material (containing $N$ dipoles per volume) is the sum of all dipoles $$ \vec{P}\left ( \omega \right ) = N \left< \vec{\mu}\left ( \omega \right ) \right> $$

We also define the susceptibility $\chi_e$ of the material as $$ \vec{P} \left ( \omega \right ) = \varepsilon_0 \chi_e\left ( \omega \right ) \vec{E}\left ( \omega \right ) $$

Therefore $$ \chi_e\left ( \omega \right ) = \frac{Nq^2}{\varepsilon_0 m}\frac{1}{\omega_0^2 - \omega^2 - j \omega \Gamma} $$

The complex dielectric constant (or truly, function vs frequency) is $$ \tilde{\varepsilon_r} \left ( \omega \right ) = 1+\chi_e\left ( \omega \right ) = {\varepsilon_r}'\left ( \omega \right ) + j{\varepsilon_r}''\left ( \omega \right ) $$

Now introduce the complex refractive index $$ \tilde{n}\left ( \omega \right ) = n\left ( \omega \right ) + jk\left ( \omega \right ) = \sqrt{\tilde{\varepsilon_r}} $$

What does this mean? For a planar wave incident on the glass, we have transmission, absorption and reflection. Particularly, the absorption is characterized by the imaginary part of the refractive index, $k$.

The transmission, absorption and reflection are dependent on the wave (light) frequency. Without showing the full expression of $k$ here, one can imagine there are absorption peaks at certain frequencies when the electrons resonant with the incident wave, so the wave attenuates when it travels through the glass.

So far I haven't stated whether or not the glass contains impurity iron oxide. The frequency response of the material is a first-principle model derived from classical physics. It predicts that, no matter if a piece of glass has impurity or not, it will have a frequency-dependent absorption!


How does it compare to reality? Here is some data for soda-lime glass.

  1. A rather unreliable source.
  2. A reported research work.

Source #2 contains full-range data in terms of wavelength. It has both "clear" glass (with iron impurity) and "low-iron" glass (which I assume does not contain as much iron as the other one). I plotted a portion of their data. I mapped the wavelength to RGB color using this formula. You may also check this table for wavelength-color relationship as well.

enter image description here

Apparently, the "clear" glass with iron impurity has an absorption peak for red light. Other than that, both the "clear" glass and "low-iron" glass have similar trends in absorption vs wavelength. The longer the wavelength, the more the absorption. Although the deviation is tiny, it can still make a difference.

Since the glass absorbs a slightly larger portion of the red light, the "color" or what's left in the transmitted light seems to have a hint of green.

Also I suspect that the reason it looks "green" rather than "cyan" (missing red) is because human eyes are more sensitive to green lights. But I don't have reference here, so don't quote me on this.

The Drude model can also explain that glass is about 4% reflective. Think of the rear-view mirror in a car.


To answer OP's question, when you look at a piece of glass from an oblique angle, the length of the path a beam of light has to travel through the glass before reaching your eyes becomes longer. According to general electromagnetic wave theory, in a lossy dielectric material, the longer the distance, the higher the exponential decay.

Edit: A more thorough but lengthy explanation of the electromagnetic wave decay in glass is here.

This also answers the question "The same happens for a thick glass block too. Why?"


All references, including those used in the text and additional ones:

$$ k = \frac{1}{\sqrt{2}} \sqrt{ -{\varepsilon_r}' + \sqrt{{\varepsilon_r}'^2 + {\varepsilon_r}''^2} } \\ {\varepsilon_r}' = 1 + \frac{\omega_p^2 \left ( \omega_0^2 - \omega^2 \right )}{\left ( \omega_0^2 - \omega^2 \right )^2 + \left ( \omega \Gamma \right )^2} \\ {\varepsilon_r}'' = \frac{\omega_p^2 \omega \Gamma }{\left ( \omega_0^2 - \omega^2 \right )^2 + \left ( \omega \Gamma \right )^2} \\ \omega_p^2 = \frac{Nq^2}{\varepsilon_0 m} $$

Yvon
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As you stated, the degree of green is directly dependent on the thickness of glass you stare at (Beer-Lambert law). It actually comes from the absorption of the other wavelengths by the glass.

Due to refraction, even when you look at the glass from a grazing angle in the air, the light rays bend to a higher angle in the glass which makes the light path through the glass shorter (figure 2).

On the contrary, when you stare at the glass from the edge, total internal reflection makes the light rays travel through the whole length of the glass to your eye (figure 3).

enter image description here

Anael
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  • If you find a room with two mirrors on either side, you will also find that the repeated reflections oftentimes eventually take a greenish tint, presumably because the reflected light travels through enough of the glass in front of the reflective mirror surface. – aquirdturtle May 28 '18 at 04:56
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Even when held at a glancing angle, the light within the glass follows a relatively short path. As light crosses the boundary between the air an the glass its angle changes (refraction). Light that leaves the glass at a glancing angle and enters your eye was traveling much closer to perpendicular to the surface when it was within the glass. It hasn't passed through a thick layer, hasn't encountered many impurities, and hence hasn't had its color changed much.

garyp
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  • So you're saying that, this is what's happening http://imgur.com/iQOIcFy (albeit probably at a less dramatic angle)? This makes a lot of sense. Thanks – Cobertos Mar 30 '14 at 00:56