Hi. It's Mr. Andersen and this is chemistry essentials video 9. It's on mass
spectrometry which is a way that we can separate atoms, isotopes and even fragments of molecules
based on their mass. And so it's an incredibly effective machine. But before we get to the
specifics of that I want to talk a little bit about John Dalton. John Dalton was one
of the pioneers of modern chemistry. And he was presenting at a conference in 1803 when
he put forward his Dalton's atomic theory. And so let me go through that. And what I
want you to think about is which of these have we changed over the last 200 plus years?
He believed number 1 that elements are made of extremely small particles called atoms.
He believed that atoms of a given element are identical in size, mass and other properties.
Atoms of different elements differ in size, mass and other properties. He believed that
atoms cannot be subdivided, created or destroyed. He believed that atoms of different elements
combine in simple whole number ratios to form chemical compounds. Then number 5, in chemical
reactions, atoms are combined, separated or rearranged. And so over the last 200 plus
years, if we were to look at those five things he put forward, there's really only two errors
that I can find. Number 1, are all elements or all atoms of the same element going to
have the same exact mass? No. Remember there are going to be isotopes. Those are going
to be the same atom, excuse me, the same element, but they're going to vary in the number of
neutrons that they have. And then the other one is that we can subdivide atoms, so when
we're looking at fusion or fission. But those really lay outside of normal chemistry. And
so he did an incredible job. And what we're really going to focus on in this video is
number two. Identification of isotopes. And so mass spectrometry is a way that we can
modify Dalton's atomic theory. And we did that through the identification of isotopes.
And that's around the early part of the 1900s. Isotopes remember are going to be the same
element but they're going to have a different mass. And that's based on the number of neutrons
that they have. And what we can do from that is we can eventually calculate the average
atomic mass. And that's going to be on the periodic table. Sometimes referred to as the
atomic weight. Now also mass spectrometry can be used to look at individual atoms. Elements
in a sample. And we can even break apart big macromolecules and look at the fragments that
are found within that. Or molecules within it. And so if we look at a basic mass spectroscope,
what we're going to see are three parts. We're going to have a ionizer. A mass analyzer.
And then a detector. And so let's look inside the ionizer. What are we going to find? Well
the first thing we're going to find is it's a total vacuum. In other words this doesn't
work unless we remove all of the gas particles that are found inside the mass spec. The next
thing we're going to do is we're going to insert our sample in. That could be a solid.
It could be a liquid. It could be a gas. But we're going to inject it into this ionizing
tube. And then we're going to hit it with electrons. And so we're going to move electrons
through the sample. And so there's a little cathode ray tube. It produces all of these
electrons. What it's going to do is it's going to pull electrons away from the sample. And
then as it does that it's going to create a number of positive ions. And so we're going
to ionize that sample inside here. Remember it's still the sample, it's just ionized.
It's lost its electrons. And so now we move to the mass analyzer. That's really only going
to have two parts in it. It's going to have an electrical field. You can see that's negative
because we want to move the ions into the mass analyzer. And then we're going to have
a magnet. And what that magnet is going to do is it's going to bend the path of the ions.
And so as we're bending the path of the ions, it's just like driving around a corner. If
you're really heavy it's harder for you to make a corner, let's say if you're in a big
semi truck. But if you're in a little motorcycle, it's easier to make it. And so this is where
we're going to figure out the difference between the mass of those ions. And then finally we
have a detector. That detector is going to be made up of two things. We're going to have
an electron multiplier which is essentially a plate. As an electron hits it, it spawns
more electrons which hit the next plate, which spawns more electrons. And so we can really
have a small amount of ions or anything hitting that plate and we're going to get a signal.
Now that signal has to be amplified, but eventually we can send that into a computer. And we can
look at the spectrum coming from those different masses. And so the first thing you have to
do is you have to calibrate the machine. What does that mean? You're going to start sending
ions through. Okay. So that ion didn't hit the detector. Why is that? It's because the
magnet is turned up too high. And so we're going to have to lower the strength of that
electromagnet. We run another ion. Okay. Now the magnet's not quite strong enough. And
so now we run another ion. Another ion. Another ion. Okay. So we've calibrated it. And so
it seems like it's working well. Which of these would be heavier? Well the ones that
are heavier are going to be the ones that can't quite make the corner. And so they're
going to end up out here. And then the light ions are going to end up right here. Now let's
actually get to some sampling. And so this is what it's going to look like when we create
a spectrum. We're going to have the different weights across the bottom. And then we're
going to have the intensity. And so wherever the intensity is high, we're going to have
peaks. That means we have a lot of ions that are with that specific atomic weight. And
let's try chlorine. So we're going to put chlorine through here. Chlorine really only
has two stable isotopes. It's going to have chlorine 35 and 37. And so let's watch and
see what happens as we send this chlorine through the mass spec. Okay. So what did we
find? Well there's really only two types of ions. And so we're having two peaks. Which
one is going to be the chlorine 37, which one is going to be the heavier ion? Well that's
going to be this one right here, because it wasn't bent as much using that magnet. And
if we look back at that, let's look at those ions flow again. So you can see that chlorine
37 doesn't quite make it around the corner. And which do we have more of? Well we're going
to have more of that atomic, those with an atomic mass of 35. Okay. So once we've got
that we can really figure out this average atomic mass. And so how do we figure that
out? Well I'm using values right here that I grabbed from wikipedia. So here are going
to be the two stable isotopes that we have of chlorine. Here's going to be their mass.
Their actual mass. So that's based on the number of protons, neutrons and electrons
inside it. And then this is going to be their abundance. In other words it's around 75 percent
of chlorine 35. And around 25 percent of chlorine 37. And that's why this peak is going to be
three times the height of this peak, if you're looking at a spectrum. So how do we figure
that out? Well that average atomic mass, sometimes referred to as the atomic weight, is simply
going to be the mass times the abundance. Plus the mass times the abundance. And so
in this case since we only have two isotopes, we're just going to only have two values here.
But if we had a lot of isotopes we're just going to have more mass times abundance, mass
times abundance. We just add on like that. So let's throw in the values here. So we've
got mass A which is going to be 34.97. And we're going to take that times it's abundance
which is around 75%. We then take the other isotope which is chlorine 37. And times its
abundance. And what we get is 35.45. And that's what's going to be on the periodic table.
And so when you're looking at those values on the periodic table, what you're looking
at is the average atomic mass. And they've figured that out by looking at the natural
abundance. Okay. Now what's important is a mass spec that can be used for other things.
Not only for atoms and isotopes within individual or isotopes within an individual element,
but we could look at atoms within a molecule. And we can even look at fragments within macromolecules.
And this right here is myoglobin, which is a massive protein. And what we can do is we
can send it through a mass spec. And what we can figure out is all the amino acids that
are found within it. And so remember wherever the peaks are going to be little bit higher,
then we're going to have more of that amino acid. And so usually what they measure this
in is m to z, which is a mass to charge ratio. And so did you learn this? How to use data
from a mass spectrometry to identify elements? And mass of individuals atoms in an element?
Remember it all ends up on that curve. And if you can make the curve or not is going
to be based on your mass. We can look at a spectrum from that to figure out their abundance.
And I hope that was helpful.