Polymers: Synthetic and Natural Polymers

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Description and Tags

Comprehensive vocabulary flashcards covering addition and condensation polymerization, plastic properties and cross-linking, industrial polymers (Teflon, Kevlar, Nylon-6,6, PET), and natural biological macromolecules.

36 Terms

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Polymer

A large chain compound composed of many repeating units called monomers, with no theoretical limit to length (most consist of 10001000 to 10 00010\,000 monomers).

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Monomer

The small molecular repeating unit that chemically links together to form a polymer chain.

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Homopolymer

A polymer composed of only one type of monomer unit (e.g., polyethylene synthesized from ethene).

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Copolymer

A polymer synthesized from two or more different monomers, characterized by alternating or mixed repeating sequences such as −A−B−A−B−-A-B-A-B- or (−A−B−)n(-A-B-)_n.

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Addition Polymer

A polymer formed by addition reactions where the starting monomers contain alkene double bonds that open up without producing by-products.

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Free Radical (R∗R^*)

A highly reactive species containing an unbonded electron (e−e^-) used to initiate addition polymerization by attacking and breaking the carbon-carbon double bond of a monomer.

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Polytetrafluoroethene (Teflon)

A synthetic addition polymer formed from tetrafluoroethene (CF2=CF2\text{CF}_2=\text{CF}_2) monomers, known for its low friction and use in non-stick cookware coatings.

<p>A synthetic addition polymer formed from tetrafluoroethene ($$\text{CF}_2=\text{CF}_2$$) monomers, known for its low friction and use in non-stick cookware coatings.</p>
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Polystyrene

An addition polymer formed from styrene monomers; its pure form is a hard plastic, and when air or N2\text{N}_2 is injected into it, it forms Styrofoam.

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Plastics

Synthetic polymers derived from petrochemicals (usually substituted ethene or vinyl monomers) that can be moulded into specific shapes under high heat and pressure.

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Biaxially Oriented Polypropylene (BOPP)

A durable polymer substrate used in currency notes that withstands high temperature ranges, resists counterfeiting, and lasts 2.52.5 times longer than paper bank notes.

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Low-Density Polyethene (LDPE)

A form of polyethene containing extensive branched chains that prevent polymer molecules from packing tightly together, producing flexible materials like plastic bags.

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High-Density Polyethene (HDPE)

A form of polyethene consisting predominantly of straight, unbranched chains that pack closely together, producing rigid materials like plastic bottles.

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Plasticizer

A substance (such as a phthalate) inserted between polymer chains to weaken intermolecular attractions and increase material flexibility.

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Polymer Cross-Linking

The creation of covalent bond bridges between adjacent polymer chains, often accomplished using diene monomers that react at two locations to increase strength and rigidity.

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Vulcanization

A chemical process that uses sulfur as an inorganic cross-linking agent to form disulfide (−S−S−-S-S-) cross-links between polymer chains, converting soft latex into hardened rubber.

<p>A chemical process that uses sulfur as an inorganic cross-linking agent to form disulfide ($$-S-S-$$) cross-links between polymer chains, converting soft latex into hardened rubber.</p>
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Thermoplastics

Plastics composed of linear polymer chains held by secondary forces that can be repeatedly melted, softened by heat, and remoulded (e.g., acrylic, PVC).

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Thermoset Polymers

Plastics containing extensive covalent cross-links that do not soften upon heating and cannot be reshaped or melted into moulds (e.g., vulcanized rubber, fiberglass, polyurethanes).

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Elastomers

Flexible, rubbery polymers that can be substantially stretched and automatically return to their original shape (e.g., silly putty).

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Condensation Polymers

Polymers formed by step-growth reactions between monomers with bifunctional groups, releasing a small by-product molecule such as H2O\text{H}_2\text{O} or HCl\text{HCl}.

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Polyesters

Condensation polymers formed through the reaction between dicarboxylic acids and dialcohols, creating repeating ester linkages (−COO−-\text{COO}-) along the polymer backbone.

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Polyethylene Terephthalate (PET / Dacron / Terylene)

A polyester synthesized from benzene-1,4-dicarboxylic acid (terephthalic acid) and ethane-1,2-diol (ethylene glycol) with the elimination of H2O\text{H}_2\text{O}, widely used in shrink-resistant clothing.

<p>A polyester synthesized from benzene-1,4-dicarboxylic acid (terephthalic acid) and ethane-1,2-diol (ethylene glycol) with the elimination of $$\text{H}_2\text{O}$$, widely used in shrink-resistant clothing.</p>
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Polyamides

Condensation polymers formed by reactions between carboxylic acids (or acyl chlorides) and amines, generating repeating amide linkages (−CONH−-\text{CONH}-) along the chain.

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Nomex

A synthetic aromatic polyamide (aramid) possessing high thermal stability and flame-resistant properties, used in protective gear for firefighters.

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Kevlar

A high-strength synthetic polyamide whose mechanical toughness arises from tangled polymer chains and extensive intermolecular hydrogen bonding between parallel aromatic chains.

<p>A high-strength synthetic polyamide whose mechanical toughness arises from tangled polymer chains and extensive intermolecular hydrogen bonding between parallel aromatic chains.</p>
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Nylon-6,6

A polyamide produced by reacting hexane-1,6-diamine and hexanedioyl dichloride (eliminating HCl\text{HCl}), where each '66' indicates the number of carbon atoms contributed by the diamine and dioic derivative, respectively.

<p>A polyamide produced by reacting hexane-1,6-diamine and hexanedioyl dichloride (eliminating $$\text{HCl}$$), where each '$$6$$' indicates the number of carbon atoms contributed by the diamine and dioic derivative, respectively.</p>
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Carbohydrates (Polysaccharides)

Natural polymers of monosaccharides (simple sugars) with the empirical formula Cx(H2O)y\text{C}_x(\text{H}_2\text{O})_y, serving as short-term energy stores, food sources, and structural materials.

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Starch

A natural glucose polymer that functions as the principal energy storage macromolecule in plants.

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Cellulose

A structural polymer composed of repeating glucose units that reinforces plant cell walls; recognized as the most abundant organic compound on Earth.

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Glycogen

A branched polymer of glucose that acts as the primary short-term energy reserve in animals.

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Proteins

Biological polymers composed of amino acid monomers joined in varying sequences by peptide bonds (amide linkages) to form functional polypeptides, enzymes, and structural components.

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Amino Acids

The 2020 natural organic monomers that build proteins, each containing a carboxylic acid group (−COOH-\text{COOH}) and an amino group (−NH2-\text{NH}_2) bonded to the same alpha-carbon atom.

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Peptide Bond

The covalent amide linkage formed by a condensation reaction between the amino group of one amino acid and the carboxyl group of another.

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Nucleic Acids

Biological macromolecules (DNA and RNA) formed by the polymerization of nucleotide monomers to store and transmit genetic information.

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Nucleotide

The repeating monomer unit of nucleic acids, consisting of a ribose sugar, an inorganic phosphate group, and one of four nitrogenous bases: adenine (A), thymine (T), cytosine (C), or guanine (G).

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Denaturation

The permanent structural alteration and loss of native biological function in a protein or macromolecule caused by elevated heat, pH extremes, radiation, or chemical mutations.

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Lipids

Non-polymeric biological macromolecules composed mainly of glycerol (propane-1,2,3-triol) and fatty acids (long-chain carboxylic acids), including fats, steroids, and cholesterol.