Chemistry

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Recent Veritasium video on per- and polyfluoroalkyl substances.

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cross-posted from: https://mander.xyz/post/31227704

This weekend I did some experiments with turmeric powder. Here are some images of the results, and the description of how to create these microscopic chemical landscapes is given below.

Turmeric powder is a fantastic material to play with. The powder has a high concentration of colored and fluorescent curcuminoids and volatile turmerone oils.

When you use a polar solvent to extract these compounds, what you get is a kind of fluorescent oily resin called a turmeric 'oleoresin'.

The curcuminoids are yellow at acidic and neutral pH, but they become bright red at high pH due to keto-enol tautomerization. There is a lot of cool things you can do with the curcuminoids in terms of photo/electrochemistry.

I have been playing with very simple chemistry under the microscope, and I have noticed that you can create some cool-looking micro-landscapes. During this process you can also see different types of physico-chemical processes happening in real time.

Procedure to do this:

  • Place a few grams of turmeric powder into a glass container
  • Add enough isopropanol to cover the material, and a bit more
  • Mix
  • Wait for the solids to settle
  • Collect a bit of the isopropanol liquid from the top and place on a glass coverslip
  • Wait for the isopropanol to evaporate.

At this time, you can see under the microscope that golden oil droplets have been deposited, and that the surroundings are also yellow. The drops are oleoresins, which consist of curcuminoids suspended in turmerones and other oily compounds. Thin curcuminoid films might also be forming in between these droplets.

  • Add a sprinkle of baking soda crystals (sodium bicarbonate) on top of the coverslip. You can blow on the coverslip if you accidentally add too much.

  • Add a small drop of water, and wait a bit.

At this time you can see that the crystals are dissolving under the microscope, but the colors are not changing. The water and oils are not mixing, and so you get this film of alkaline water surrounding the oil droplets, but nothing is yet really changing.

  • After waiting a few minutes, add a drop of isopropanol.

Now the isopropanol will re-dissolve the oleoresin and mix with the alkaline water. The carbonate ions are now able to react with the curcuminoids, and when they do, they go into the ketone form and instantly turn red. Under the microscope you can see quite dramatic movements of yellow and rad streaking as well as turbulent movements of the baking soda crystals.

  • Wait some time for the liquids to evaporate again

  • You will end up with a landscape that combines yellow resins, red resins, sodium bicarbonate crystals, and several different patterns.


You can vary the parameters - the amount of sodium bicarbonate, the position and size of the drops, you can pre-mix the water and isopropanol, etc. Small changes can drastically affect the resulting landscape.

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From the description:

We're at GSI in Germany where rare samples of enriched isotopes are fashioned into targets for their epic accelerator.

Featuring Sir Martyn Poliakoff speaking with Dr Bettina Lommel in the Target Lab.

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Dr Thomas de Prinse undertakes the third step of his large-scale cubane synthesis, the bromination of the ethylene ketal of cyclopentanone to its tribromocyclopentanone derivative.

Previous episode

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A humorous look at FOOF by the inimitable Derek Lowe

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This is not some sort of fancy new development, but it's such a classical experiment that it's always worth sharing IMO. Plus it's fun.

When you initially mix both solutions, nothing seems to happen. But once you wait a wee bit, the colour suddenly changes, from transparent to a dark blue.

There are a bunch of variations of this reaction, but they all boil down to the same things:

  • iodide - at the start of the reaction, it'll flip back and forth between iodide (I⁻) and triiodide ([I₃]⁻)
  • starch - it forms a complex with triiodide, with the dark blue colour you see in the video. But only with triiodide; iodide is left alone. So it's effectively an indicator for the triiodide here.
  • some reducing agent - NileRed used vitamin C (aka ascorbic acid; C₆H₈O₆), but it could be something like thiosulphate (S₂O₃²⁻) instead. The job of the reducing agent is to oxidise the triiodide back to iodide.
  • some oxidiser - here it's the hydrogen peroxide (H₂O₂) but it could be something like chlorate (ClO₃⁻) instead. Its main job is to oxidise the iodide to triiodide. You need more than enough oxidiser to be able to fully oxidise the reducing agent, plus a leftover.

"Wait a minute, why are there a reducing agent and an oxidiser, doing opposite things? They should cancel each other out!" - well, yes! However this does not happen instantaneously. And eventually the reducing agent will run dry (as long as there's enough oxidiser), the triiodide will pile up, react with the starch and you'll get the blue colour.

Here are simplified versions of the main reactions:

  1. 3I⁻ + H₂O₂ → [I₃]⁻ + 2OH⁻
  2. [I₃]⁻ + C₆H₈O₆ + 2H₂O → 3I⁻ + C₆H₆O₆ + 2H₃O⁺

(C₆H₆O₆ = dehydroascorbic acid) Eventually #2 stops happening because all vitamin C was consumed, so the triiodide piles up, reacts with the starch, and suddenly blue:

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Dr Thomas de Prinse makes yttrium oxide doped with erbium and ytterbium.

Upconversion: Material absorbs two infrared photons, emits one visible photon.

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A chemist told me rust does not spread. The top of my refrigerator gives me some doubt. It’s covered in these spots. The center of every spot is a small break in the paint, but the rust all around those spots is on top of the paint.

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cross-posted from: https://lemmy.ca/post/39143995

The authors of the academic study, published in the Journal of the American Chemical Society on Thursday, had to get the smell from inside the sarcophagus without interfering with the mummy inside.

The researchers, from UCL and the University of Ljubljana in Slovenia, did so by inserting a tiny tube so they were able measure the scent without taking any physical samples.

If you want to smell the smell too

They say recreating the composition of the smells chemically will allow others to experience a mummy's whiff - and help to tell when the bodies inside may be starting to rot.

"We want to share the experience we had smelling the mummified bodies, so we're reconstructing the smell to be presented in the Egyptian Museum in Cairo," Cecilia Bembibre, one of the researchers, told BBC Radio 4's Today programme.

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It's not really "professional" but you can look at the process, see the results and come to your own conclusion about it's viability.

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[Maurycyz] points out right up front: several of the reagents used are very corrosive and can produce toxic gasses. We weren’t sure if they were trying to dissuade us not to replicate it or encourage us to do so. The project in question is making strontium aluminate which, by the way, glows in the dark.

The material grows strongly for hours and, despite the dangers of making it, it doesn’t require anything very exotic. As [Maurycyz] points out, oxygen and aluminum are everywhere. Strontium sounds uncommon, but apparently, it is used in ceramics.

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Scott usually focuses on spaceflight and aviation topics, but there is some nice chemistry overlap in this video.

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submitted 4 months ago* (last edited 4 months ago) by [email protected] to c/[email protected]
 
 

Dr Thomas de Prinse undertakes the first two steps of his large-scale cubane synthesis in his shed.

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Another fantastic video from the OG YouTube Chemist.

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Dr Thomas de Prinse announces his intentions to repeat his cubane synthesis on a larger scale.

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I put an aluminum wok lid in the dishwasher and it came out with black marks on it. I’ve also seen other aluminum cookware come out with some kind of white powder specs on it.

So apparently aluminum is dishwasher unsafe. But obviously it’s not the water that’s the problem. It must be the detergent. So the question is, what can a lazy motherfucker like myself do? Why don’t I see aluminum-safe dishwasher detergents on the shelf?

Possibly related: Bailey’s creme liquor turns black underneath an aluminum cap. Is that a chemical reaction or spoilage, or something else?

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Thought u guys might find this useful

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AbstractCotton fiber fabric with practicability and functionality attracts much attention and plays an important role in many occasions. However, its surface contains many hydroxyl groups to show a hydrophilicity, leading to easy adhesion to stains to limit the application. In this work, polyglycidyl methacrylate (PGMA) was used as an oily and flexible matrix and graphene oxide (GO) particles were used as a filler. PGMA/GO composite modified fabrics with hydrophobicity, self-cleaning feature and wear resistance were prepared by constructing surface coatings. Compared with original fabric, PGMA/GO composite modified fabric has a surface hydrophobicity attributed to organic oily characteristic of PGMA, and high surface roughness from GO surface enrichment. The reasonable GO content (1 wt%) in composite coating makes the modified fabric exhibit the best overall performance (surface water contact angle of ~ 151.7°; chromatism of ~ 2.4; large water contact angle of ~ 140.2° after 200 surface wear cycles). This work provides an effective method for an industrial production of high-performance waterproof cotton garment fabrics.

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