Textile Finishing: Easy Care, Wrinkle-Free, and Durable Press Finishes

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Comprehensive vocabulary flashcards covering cellulose structure, cross-linking chemistry, aminoplasts, cellulose reactants (DMEU, DMDHEU, DMeDHEU), formaldehyde release standards, and finishing application processes based on the TE-452 lecture notes.

Last updated 9:32 AM on 9/26/26
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20 Terms

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<p>Cellulose</p>

Cellulose

A linear polysaccharide polymer composed of glucose monosaccharide units joined by beta-acetal linkages, forming a highly crystalline, oriented, and rigid molecular structure in plant cell walls.

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Anhydroglucose

The repeating monosaccharide unit of cellulose, containing three hydroxyl groups: one primary hydroxyl group on C-6 and two secondary hydroxyl groups on C-2 and C-3.

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<p>Cross-linking</p>

Cross-linking

The joining of polymer chains with covalent bonds to restrict molecular chain movement in amorphous regions, improving crease recovery, imparting durable press properties, and reducing shrinkage.

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Crease Recovery Angle (CRA)

The total sum of the crease recovery angles of a fabric measured in both warp and weft directions, which increases from approximately 150o150^\text{o} to 300o300^\text{o} following easy-care finishing.

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Aminoplasts

A class of cellulose cross-linkers, such as urea-formaldehyde and melamine-formaldehyde compounds, that self-polymerise into resinous three-dimensional polymers as well as cross-link with cellulose.

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Cellulose Reactants

N-methylol cross-linking compounds (such as DMEU and DMDHEU) that predominantly cross-link with cellulose hydroxyl groups without forming three-dimensional self-condensation polymers.

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Dimethylol Urea (DMU)

A bifunctional aminoplast prepared from 1 mole of urea and 2 moles of formaldehyde, characterized by short shelf life, high formaldehyde release (approx. 2000 ppm\text{approx. } 2000\text{ ppm}), and poor durability to laundering due to hydrolysis.

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Melamine/Formaldehyde Resins

Aminoplast condensates formed by reacting melamine with up to 6 moles of formaldehyde (such as TMM and HMM) that offer improved laundering durability, act as nitrogen synergists with phosphorus flame retardants, and reduce wool shrinkage.

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<p>Ethylene Urea</p>

Ethylene Urea

A 5-membered heterocyclic nitrogen compound containing two -NH groups that acts as a formaldehyde scavenger and chemical building block for DMEU.

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Dimethylolethylene Urea (DMEU)

A cellulose reactant synthesized from ethylene urea and formaldehyde that cures at 90 to 100oC90\text{ to } 100^\text{o}\text{C} and provides high efficiency, but exhibits poor hydrolysis and chlorine resistance.

<p>A cellulose reactant synthesized from ethylene urea and formaldehyde that cures at $$90\text{ to } 100^\text{o}\text{C}$$ and provides high efficiency, but exhibits poor hydrolysis and chlorine resistance.</p>
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Dimethylol-4,5-Dihydroxyethylene Urea (DMDHEU)

Also known as Glyoxal resin, it is the primary durable press cross-linker accounting for over 85% of crease-resistant chemicals consumed, requiring curing temperatures exceeding 130oC130^\text{o}\text{C}.

<p>Also known as Glyoxal resin, it is the primary durable press cross-linker accounting for over 85% of crease-resistant chemicals consumed, requiring curing temperatures exceeding $$130^\text{o}\text{C}$$.</p>
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Oeko-Tex Standard 100

A European labelling standard setting maximum formaldehyde limits in fabrics: 300 ppm300\text{ ppm} for non-skin contact furnishings, 75 ppm75\text{ ppm} for adult direct skin contact clothing, and 20 ppm20\text{ ppm} for children's items.

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Free Formaldehyde

Uncombined monomeric formaldehyde present in a finish bath, caused by stoichiometric excess of formaldehyde in resin manufacturing or uncured resin containing pendent N-methylol groups.

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Methylated DMDHEU

A modified low-formaldehyde (LF) reactant formed by alkylating DMDHEU with methanol to convert hydroxyl groups to −OCH3-OCH_3, reducing released formaldehyde to approximately 300 to 500 ppm300\text{ to } 500\text{ ppm}.

<p>A modified low-formaldehyde (LF) reactant formed by alkylating DMDHEU with methanol to convert hydroxyl groups to $$-OCH_3$$, reducing released formaldehyde to approximately $$300\text{ to } 500\text{ ppm}$$.</p>
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Glycolated DMDHEU

An ultra-low formaldehyde (ULF) resin prepared by reacting 1 mole of DMDHEU with 2 moles of diethylene glycol, lowering fabric formaldehyde release to below 50 ppm50\text{ ppm} while maintaining high durable press performance.

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Formaldehyde Scavengers

Chemical additives (such as urea, ethylene urea, or high-boiling alcohols) added directly to finish formulations to bind monomeric formaldehyde.

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Pad-Dry-Cure Procedure

The standard dry pre-cure application method where fabric is dipped in a chemical bath, passed through squeeze rolls for wet pick-up, dried, and subsequently heat-cured.

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Wet Fixation Process

A post-cure method where fabric padded with finish chemicals is wrapped in plastic film and batched in an oven to allow internal fiber penetration and polymerization prior to washing, drying, and final curing.

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Dimethyl-4,5-Dihydroxyethylene Urea (DMeDHEU)

A non-formaldehyde finish produced from dimethyl urea and glyoxal that cross-links cellulose via ring hydroxyl groups but requires stronger catalysts and higher thermal energy to cure.

<p>A non-formaldehyde finish produced from dimethyl urea and glyoxal that cross-links cellulose via ring hydroxyl groups but requires stronger catalysts and higher thermal energy to cure.</p>
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Magnesium Chloride

The most widely used mild metal salt catalyst for dry cross-linking, which functions effectively at high temperatures, is non-corrosive, and minimizes side reaction issues such as fiber damage and shade changes.