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Triethylene glycol

Triethylene glycol is a science topic covered in the lgStudy science library. This page brings together a partial reference excerpt, illustrations, worked examples, real-world applications and a short study plan, so you can understand Triethylene glycol rather than just read about it. In short: Triethylene glycol, TEG, or triglycol is a colorless odorless viscous liquid with molecular formula HOCH2CH2OCH2CH2OCH2CH2OH. It is used as a plasticizer for vinyl polymers.

Triethylene glycol — main illustration
Triethylene glycol — illustration

Key takeaways

  • Triethylene glycol belongs to science; place it in that map before memorising details.
  • Learn the definition first, then one example that makes the definition concrete.
  • Connect Triethylene glycol to a quantity you can measure, compute or draw — that is where exam questions come from.
  • Reproduce the core statement of Triethylene glycol from memory before moving on to harder problems.

Reference excerpt

Triethylene glycol, TEG, or triglycol is a colorless odorless viscous liquid with molecular formula HOCH2CH2OCH2CH2OCH2CH2OH. It is used as a plasticizer for vinyl polymers. It is also used in air sanitizer products, such as "Oust" or "Clean and Pure". When aerosolized it acts as a disinfectant. Glycols are also used as liquid desiccants for natural gas and in air conditioning systems. It is used as an additive for hydraulic fluids and brake fluids, and as a base for "smoke machine" fluid in the entertainment industry.

Properties Triethylene glycol is a member of a homologous series of polyethylene glycols. It is a colorless, odorless and stable liquid with high viscosity and a high boiling point. Apart from its use as a raw material in the manufacture and synthesis of other products, TEG is known for its hygroscopic quality and its ability to dehumidify fluids. This liquid is miscible with water, and at standard atmospheric pressure (101.325 kPa) has a boiling point of 286.5 °C and a freezing point of −7 °C. It is also soluble in ethanol, acetone, acetic acid, glycerine, pyridine, aldehydes; slightly soluble in diethyl ether; and insoluble in oil, fat and most hydrocarbons.

Preparation TEG is prepared commercially as a co-product of the oxidation of ethylene at high temperature in the presence of silver oxide catalyst, followed by hydration of ethylene oxide to yield mono(one)-, di(two)-, tri(three)- and tetraethylene glycols.

Applications TEG is used by the oil and gas industry to "dehydrate" natural gas. It may also be used to dehydrate other gases, including CO2, H2S, and other oxygenated gases. It is necessary to dry natural gas to a certain point, as humidity in natural gas can cause pipelines to freeze, and create other problems for end users of the natural gas. Triethylene glycol is placed into contact with natural gas, and strips the water out of the gas. Triethylene glycol is heated to a high temperature and put through a condensing system, which removes the water as waste and reclaims the TEG for continuous reuse within the system. The waste TEG produced by this process has been found to contain enough benzene to be classified as hazardous waste (benzene concentration greater than 0.5 mg/L). Triethylene glycol is well established as a relatively mild disinfectant toward a variety of bacteria, influenza A viruses and spores of Penicillium notatum fungi. However, its exceptionally low toxicity, broad materials compatibility, and low odor combined with its antimicrobial properties indicates that it approaches the ideal for air disinfection purposes in occupied spaces. Much of the scientific work with triethylene glycol was done in the 1940s and 1950s, however that work has ably demonstrated the antimicrobial activity against airborne, solution suspension, and surface bound microbes. The ability of triethylene glycol to inactivate Streptococcus pneumoniae (original citation: pneumococcus Type I), Streptococcus pyogenes (original citation: Beta hemolytic streptococcus group A) and Influenza A virus in the air was first reported in 1943. Since the first report the following microorganisms have been reported in the literature to be inactivated in the air: Penicillium notatum spores, Chlamydophila psittaci (original citation: meningopneumonitis virus strain Cal 10 and psittacosis virus strain 6BC), Group C streptococcus, type 1 pneumococcus, Staphylococcus albus, Escherichia coli, and Serratia marcescens Bizio (ATCC 274). Solutions of triethylene glycol are known to be antimicrobial toward suspensions of Penicillium notatum spores, Streptococcus pyogenes (original citation: Beta hemolytic streptococcus Group A), Streptococcus pneumoniae (original citation: pneumococcus Type I), Streptococcus viridans, and Mycobacterium bovis (original citation: tubercle bacilli Ravenel bovine-type). Further, the inactivation of H1N1 influenza A virus on surfaces has been demonstrated. The latter investigation suggests that triethylene glycol may prove to be a potent weapon against future influenza epidemics and pandemics. However, at least some viruses, including Pseudomonas phage phi6 become more infectious when treated with triethylene glycol.

Safety According to the European Chemicals Agency (ECHA), no hazards have been classified. https://echa.europa.eu/es/substance-information/-/substanceinfo/100.003.594

References

Worked examples

Example 1 — a first encounter with Triethylene glycol

Start with the simplest possible case. Write down what Triethylene glycol claims or describes in one sentence, then invent the smallest concrete situation in which that sentence is true. In science, the smallest case is usually a single object, a single equation or a single measurement. Check that every symbol or term in your sentence has a meaning in that case.

Example 2 — changing one variable

Take the situation from Example 1 and change exactly one quantity: double it, halve it, or set it to zero. Predict what should happen to Triethylene glycol before you calculate. Comparing your prediction with the result is the fastest way to find out whether you understand the idea or only the words.

Example 3 — an exam-style question

Typical questions about Triethylene glycol ask you to (a) state it precisely, (b) apply it to given data, and (c) explain a limitation. Practise writing all three answers in under five minutes; the third part is what separates a full-mark answer from an average one.

Applications of Triethylene glycol

In research
Triethylene glycol appears in science research whenever the underlying quantities have to be modelled precisely. Papers usually cite it as a starting assumption and then explore where it breaks down.
In technology and industry
Engineering practice reuses Triethylene glycol in design rules, simulations and safety margins. Knowing the idea lets you read a specification sheet and understand why the numbers look the way they do.
In the classroom
Triethylene glycol is common in secondary-school and first-year university syllabi. It links to neighbouring topics Diols, Glycol ethers, Solvents, so understanding it makes those chapters shorter.
In everyday life
Look for Triethylene glycol outside the textbook — in sport, cooking, traffic, electronics or the sky above you. An example you found yourself is remembered far longer than one you were given.
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How to study Triethylene glycol in 20 minutes

  1. Read the reference excerpt below once, without taking notes.
  2. Close the page and write down what Triethylene glycol means in your own words.
  3. Compare your version with the excerpt and mark what you missed.
  4. Work through the three examples above with pen and paper.
  5. Explain Triethylene glycol out loud to somebody else — or to Teacher Smith in the lgStudy chat.

Frequently asked questions

What is Triethylene glycol in simple terms?

Triethylene glycol, TEG, or triglycol is a colorless odorless viscous liquid with molecular formula HOCH2CH2OCH2CH2OCH2CH2OH. It is used as a plasticizer for vinyl polymers.

Why does Triethylene glycol matter?

Because it connects several science ideas at once: it gives you a definition you can apply, a quantity you can calculate, and a way to check whether a result is plausible.

How should I study Triethylene glycol?

Read the excerpt, restate it from memory, then work through the examples and applications listed on this page. The five-step study plan above takes about twenty minutes.

What does this page cover?

It gives you a compact reference excerpt plus original lgStudy explanations, examples, applications and study material on Triethylene glycol.

Tags

  • Diols
  • Glycol ethers
  • Solvents

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