크로마토그래피: 상 상호작용을 통한 혼합물 분리

### 크로마토그래피: 이동상 및 고정상을 이용한 혼합물 분리
* 🖋 종이에 검은색 잉크가 물에 번지면 잉크가 다양한 색상으로 분리되는 것을 볼 수 있는데, 이는 **검은색 염료가 다양한 염료와 성분**으로 구성되어 있기 때문에 종이 크로마토그래피의 기본적인 예시를 보여줍니다.
* 📝 크로마토그래피는 이동상과 고정상을 사용하여 혼합물을 분리하는 기술로 **종이 크로마토그래피, 박층 크로마토그래피(TLC), 컬럼 크로마토그래피, 크기 배제 크로마토그래피, 이온 교환 크로마토그래피, 친화성 크로마토그래피, 고성능 액체 크로마토그래피(HPLC), 기체 크로마토그래피 등 다양한 종류**가 있습니다.
* 📄 종이 크로마토그래피에서 고정상은 종이이고 이동상은 **모세관 작용을 통해 종이 위로 이동하여 혼합물의 성분을 함께 운반하는 용매**입니다.
* 📏 시간이 지남에 따라 극성에 따라 성분이 분리되는데, **극성이 강한 성분은 이동상에 끌리게** 되고 **극성이 약한 성분은 고정상에 끌리게** 됩니다.
* 박층 크로마토그래피(TLC)는 종이 크로마토그래피와 유사하지만 **실리카겔 층으로 코팅된 유리 슬라이드**를 고정상으로 사용합니다.
* 🗂 컬럼 크로마토그래피는 고정상(예: 실리카겔 비드)으로 채워진 컬럼에 이동상이 추가될 때 **극성에 따라 화합물을 분리**하는 방식입니다.
* 이온 교환 크로마토그래피에서 고정상은 하전기를 포함하고 있으므로 **같은 전하를 가진 화합물은 서로 밀어내고 더 빠르게 이동**합니다.
* 🔬 기체 크로마토그래피는 **액체 고정상과 운반 기체를 이동상**으로 사용하여 휘발성의 차이에 따라 화합물을 분리합니다.

크로마토그래피는 이동상 또는 고정상에 대한 성분의 인력에 따라 혼합물을 분리하며 종이, TLC, 컬럼, 크기 교환, 이온 교환, 친밀도, HPLC 및 가스 방법을 사용할 수 있습니다.

Have you ever scribbled something down with a black pen on a piece of paper, then accidentally smudged the paper with water? What do you remember seeing? Well, what happens is that you might see the black ink start to smudge and start to see some colors that aren't black at all, maybe some dark blues and some darker purples. But why is this? This is because black dye is actually made out of a bunch of different other dyes and different components. And what you've just witnessed is a basic example of paper chromatography. Chromatography involves taking some kind of mixture and using either solid or liquid to separate it out into its different parts. There are many different kinds of chromatography, but they all rely on having a mobile phase and a stationary phase. Let's go over how paper chromatography works, since this is the simplest kind.

In paper chromatography, the stationary phase is the paper. So here's your piece of paper. You can draw a little line at the bottom and draw a spot for where you're putting on your dot of your sample. Next, you'll want to prep a beaker, or actually, any kind of container will do. But in this, you'll be putting in your mobile phase. And your mobile phase can be some kind of solvent. It could be water, or it could be any organic solvent you want. Now that you have this, you pour a small amount of solvent. Again, not too much, because you don't want this to already be above the level of your spot, or else it will just all bleed. And now when you put in your paper into this container, what you'll get is something that looks like this, with the spot being around here. And what you'll observe over time

is that through
capillary action, this pink solvent will
travel up the piece of paper. And as it does that, it'll
actually take some of the dyes from that green spot with it. And let's see what happens at
a few different time points. At the first time
point, you might see that it separated
into two spots. This implies that it's composed
of two different components. However, if this were
a very complex mixture, you could even see five,
six, or a lot of other spots. If you wait even longer,
this is what you'll see next. You'll see that the spots will
continue traveling even farther up the plate, and the
separation between them, that distance will
increase even more. So ultimately what
you've shown here is that whatever was in
the green spot originally wasn't just one compound. It was two compounds. And why do they
separate in this manner?

Well, the blue spot
traveled farther. That means that it was pretty
attracted to that pink solvent that was traveling along. Whereas, the yellow spot
didn't move quite as much, which means it
was more attracted to the paper for the
stationary phase. This competition between
the stationary phase and the mobile phase
pulling at the components is what drives the
separation that occurs in all different
kinds of chromatography. So, let's try to lay this
information out in a table. We've talked about how
for paper chromatography, the stationary phase is
a solid; the mobile phase is some kind of
solvent, so a liquid; and they're separating
it based on polarity, meaning how attracted it is to
the paper versus the solvent, depending on its
chemical properties. The next kind of
chromatography that's almost identical to
paper chromatography is known as thin-layer
chromatography.

or TLC for short. We'll see that all the
spots on this table are pretty much the same. The main difference
is that instead of having a piece of paper,
you have a glass slide that is coated with a
layer of silica gel. This is a great preparative
tool that is commonly used in the organic
chemistry lab. To remind you that these two are
related, what I've drawn here is a little beaker with a
small either plate or piece of paper inside. And the arrow shows that
the solvent is traveling up the plate through
capillary action. The next kinds of chromatography
we'll be going over are column chromatography. And in this case,
you have a column that I've drawn right
here on the left. And you fill it with some
kind of packing material and dump in some
solvent as well. You can lower your sample
that you want to separate out, and what you'll
find is that as you

keep dumping in
more solvent. This can separate into bands that
represent different compounds, and they will travel
down the column. So in basic column
chromatography, you're usually using
something like silica gel as your stationary phase. Your mobile phase is
typically an organic solvent, and again, you're separating
based on polarity. In size-exchange chromatography,
your stationary phase is composed of beads. However, these
little beads actually have some holes in the middle. And because of that, with
size-exchange chromatography, these beads completely
fill the column, and tiny compounds can
get through that center of the hole, like so. But really big
compounds kind of have to go around and go
between the beads. So what happens here is
that really small compounds travel pretty far, pretty fast,
whereas large compounds take a longer time to
come out the bottom. In ion-exchange
chromatography, the beads that are filling this column
have some kind of group on them.

that is charged. Compounds that have
the same charge will be repelled by
the column, meaning they'll travel pretty quickly. But compounds that
have an opposite charge will bind tightly to
the column and will be more reluctant to come
out since they are so attracted to the
stationary phase. Affinity chromatography
is also pretty similar, but this usually relies upon
very specific interactions, such as between an
enzyme and a substrate, and really relies on
this binding affinity. Things that will bind
tightly to the enzyme will probably just be
primarily the substrate, and everything else will
just get washed right off the column. Later on, what you
can do is wash out the compound of interest
that was previously bound to the column, using something
that that molecule is even more attracted to. With HPLC, HPLC stands for
high-performance liquid chromatography,
formerly known as high-pressure liquid
chromatography.

This is essentially the same as the basic column chromatography that you see there in yellow. However, with HPLC, it's a more advanced technique in that you're working with very, very small quantities, and the detector in the machine is much more sensitive. The last kind of chromatography is gas chromatography. Now, this looks pretty different compared to the others. And in this case, your stationary phase is a liquid, while your mobile phase is some kind of carrier gas that's passing over the liquid. So what happens is, you inject your sample, and it travels in a coil tube into that box known as the gas chromatograph. That's a fancy name for the equipment used to run gas chromatography. Inside the chromatograph is a heated chamber through which an inert gas flows. Here, the sample vaporizes and enters the gas flow onto the column. The things that are the most volatile,

meaning have a
lower boiling point, are able to travel faster,
whereas things with a higher boiling point take
longer to come out. And so this is a
separation method that's great when you have
differences in boiling point. So we've gone over all
these different kinds of chromatography, but
you could certainly go into each of these
in much more detail.

Basics of chromatography | Chemical processes | MCAT | Khan Academy

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종이 크로마토그래피는 고정상(종이)과 이동상(용매)을 사용하여 혼합물을 여러 성분으로 분리하는 방법입니다.

검은색 잉크가 번지면서 다른 색을 드러내는 것이 이 과정의 기본적인 예입니다.

종이 크로마토그래피에서는 시료를 종이 위에 점을 찍고 용매가 종이를 통과하면서 이동상과 고정상에 대한 서로 다른 친화도에 따라 혼합물의 성분이 분리됩니다.

크로마토그래피는 용매가 종이 위로 이동하여 용매와 고정상에 대한 인력을 바탕으로 성분을 분리하는 과정입니다.

분리 결과 여러 개의 반점이 나타나며, 이는 서로 다른 화합물의 존재를 나타냅니다.

이 기술은 고정상과 이동상 간의 경쟁에 의존하여 화학적 특성과 극성에 따라 성분 분리를 유도합니다.

다양한 크로마토그래피 기술 개요

박층 크로마토그래피(TLC)는 실리카겔로 코팅된 유리 슬라이드를 사용하여 모세관 작용을 통해 화합물을 분리합니다.

컬럼 크로마토그래피는 실리카겔과 같은 고정상을 사용하여 화합물이 극성에 따라 밴드로 분리되어 컬럼을 따라 이동합니다.

크기 배제 크로마토그래피는 비드를 사용하여 크기에 따라 화합물을 분리하며, 작은 화합물은 구멍을 통과하여 더 빨리 용출됩니다.

이온 교환 크로마토그래피는 그룹을 가진 비드를 사용하여 전하를 기준으로 화합물을 분리할 수 있습니다.

크로마토그래피의 다양한 유형과 그 메커니즘

이온 교환 크로마토그래피는 같은 전하가 빠르게 이동하고 반대 전하가 컬럼에 결합하는 등 전하를 기준으로 화합물을 분리합니다.

친화성 크로마토그래피는 효소와 기질 사이의 특정 상호 작용에 의존하며, 기질은 효소에 단단히 결합합니다.

HPLC는 고감도 검출기를 사용하여 소량으로 작업하는 고급 기술인 반면, 기체 크로마토그래피는 액체 고정상과 운반 기체 이동상을 사용하여 휘발성에 따라 화합물을 분리합니다.

크로마토그래피에서 끓는점의 중요성

크로마토그래피는 끓는점의 차이에 기반한 분리 방법입니다.

끓는점이 낮은 물질은 더 빨리 이동할 수 있는 반면 끓는점이 높은 물질은 용출하는 데 시간이 오래 걸림니다.

이 기술은 다양한 형태로 제공되며, 각각 고유한 응용 분야와 세부 사항이 있습니다.