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chemistry

Polyol

Polyol is a chemistry 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 Polyol rather than just read about it. In short: In organic chemistry, a polyol is an organic compound containing multiple hydroxyl groups (−OH). The term "polyol" can have slightly different meanings depending on whether it is used in food science or polymer chemistry.

Polyol — main illustration
Polyol — illustration

Key takeaways

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

Reference excerpt

In organic chemistry, a polyol is an organic compound containing multiple hydroxyl groups (−OH). The term "polyol" can have slightly different meanings depending on whether it is used in food science or polymer chemistry. Polyols containing two, three and four hydroxyl groups are diols, triols, and tetrols, respectively.

Classification Polyols may be classified according to their chemistry. Some of these chemistries are polyether, polyester, polycarbonate and also acrylic polyols. Polyether polyols may be further subdivided and classified as polyethylene oxide or polyethylene glycol (PEG), polypropylene glycol (PPG) and polytetrahydrofuran or PTMEG. These have 2, 3 and 4 carbon atoms respectively per oxygen atom in the repeat unit. Polycaprolactone polyols are also commercially available. There is also an increasing trend to use biobased (and hence renewable) polyols.

Uses Polyether polyols have numerous uses. As an example, polyurethane foam is a big user of polyether polyols. Polyester polyols can be used to produce rigid foam. They are available in both aromatic and aliphatic versions. They are also available in mixed aliphatic-aromatic versions often made from recycled raw materials, typically polyethylene terephthalate (PET). Acrylic polyols are generally used in higher performance applications where stability to ultraviolet light is required and also lower VOC coatings. Other uses include direct to metal coatings. As they are used where good UV resistance is required, such as automotive coatings, the isocyanate component also tends to be UV resistant and hence isocyanate oligomers or prepolymers based on Isophorone diisocyanate are generally used. Caprolactone-based polyols produce polyurethanes with enhanced hydrolysis resistance. Polycarbonate polyols are more expensive than other polyols and are thus used in more demanding applications. They have been used to make an isophorone diisocyanate based prepolymer which is then used in glass coatings. They may be used in reactive hotmelt adhesives. All polyols may be used to produce polyurethane prepolymers. These then find use in coatings, adhesives, sealants and elastomers.

Low molecular weight polyols

Low molecular weight polyols are widely used in polymer chemistry where they function as crosslinking agents and chain extenders. Alkyd resins for example, use polyols in their synthesis and are used in paints and in molds for casting. They are the dominant resin or "binder" in most commercial "oil-based" coatings. Approximately 200,000 tons of alkyd resins are produced each year. They are based on linking reactive monomers through ester formation. Polyols used in the production of commercial alkyd resins are glycerol, trimethylolpropane, and pentaerythritol. In polyurethane prepolymer production, a low molecular weight polyol-diol such as 1,4-butanediol may be used as a chain extender to further increase molecular weight though it does increase viscosity because more hydrogen bonding is introduced.

Sugar alcohols Sugar alcohols, a class of low molecular weight polyols, are commonly obtained by hydrogenation of sugars. They have the formula (CHOH)nH2, where n = 4–6. Sugar alcohols are added to foods because of their lower caloric content than sugars; however, they are also, in general, less sweet, and are often combined with high-intensity sweeteners. They are also added to chewing gum because they are not broken down by bacteria in the mouth or metabolized to acids, and thus do not contribute to tooth decay. Maltitol, sorbitol, xylitol, erythritol, and isomalt are common sugar alcohols. Sugar alcohols, such as myoinositol, pinitol, and mannitol, have roles in maintaining cellular water balance and responding to drought or low temperature stress.

Polymeric polyols

The term polyol is used for various chemistries of the molecular backbone. Polyols may be reacted with diisocyanates or polyisocyanates to produce polyurethanes. MDI finds considerable use in PU foam production. Polyurethanes are used to make flexible foam for mattresses and seating, rigid foam insulation for refrigerators and freezers, elastomeric shoe soles, fibers (e.g. Spandex), coatings, sealants and adhesives. The term polyol is also attributed to other molecules containing hydroxyl groups. For instance, polyvinyl alcohol is (CH2CHOH)n with n hydroxyl groups where n can be in the thousands. Cellulose is a polymer with many hydroxyl groups, but it is not referred to as a polyol.

Polyols from recycled or renewable sources There are polyols based on renewable sources such as plant-based materials including neem oil, castor oil, and cottonseed oil. Vegetable oils and biomass are also potential renewable polyol raw materials. Seed oil can even be used to produce polyester polyols.

Properties Since the generic term polyol is only derived from chemical nomenclature and just indicates the presence of several hydroxyl groups, no common properties can be assigned to all polyols. However, polyols are usually viscous at room temperature due to hydrogen bonding.

See also Cyclitol Oligomer Polyurethane

References

External links Media related to Polyols at Wikimedia Commons

Illustrations

Polyol illustration
Polyol illustration
Polyol illustration

Worked examples

Example 1 — a first encounter with Polyol

Start with the simplest possible case. Write down what Polyol claims or describes in one sentence, then invent the smallest concrete situation in which that sentence is true. In chemistry, 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 Polyol 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 Polyol 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 Polyol

In research
Polyol appears in chemistry 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 Polyol 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
Polyol is common in secondary-school and first-year university syllabi. It links to neighbouring topics Commodity chemicals, Organic polymers, Polymer chemistry, so understanding it makes those chapters shorter.
In everyday life
Look for Polyol 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 Polyol in 20 minutes

  1. Read the reference excerpt below once, without taking notes.
  2. Close the page and write down what Polyol 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 Polyol out loud to somebody else — or to Teacher Smith in the lgStudy chat.

Frequently asked questions

What is Polyol in simple terms?

In organic chemistry, a polyol is an organic compound containing multiple hydroxyl groups (−OH). The term "polyol" can have slightly different meanings depending on whether it is used in food science or polymer chemistry.

Why does Polyol matter?

Because it connects several chemistry 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 Polyol?

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 Polyol.

Tags

  • Commodity chemicals
  • Organic polymers
  • Polymer chemistry
  • Polyols
  • Polyurethanes
  • Sugar substitutes
  • Synthetic resins

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