Bleaching Mechanism
Chemical decolorisation of greige cellulosic substrates through aqueous alkaline perhydroxyl ion reactions removes natural seed-coat fragments and polyphenolic pigments. During preparation, hydrogen peroxide oxidation transforms light-absorbing conjugated double bonds within cotton impurities into colorless, water-soluble carboxylated fragments. The oxidative potential is governed strictly by liquor pH, where sodium hydroxide activates peroxide to generate perhydroxyl anions at processing temperatures between 95 and 100 degrees Celsius.
In the absence of strict pH regulation, unmoderated decomposition shifts the reaction pathway toward violent molecular oxygen generation, degrading bleaching efficacy and increasing bath instability.
Radical Decomposition
Uncontrolled metal contamination catalyses destructive homolytic cleavage of the oxygen-oxygen single bond. Minute trace concentrations of iron, copper or manganese within mill water generate transient hydroxyl radicals and superoxide radicals through Fenton-type reactions. These non-selective radicals attack the cellulose polymer chain directly, randomly cleaving 1,4-beta-glucosidic bonds and generating oxycellulose.
Viscosity testing of cupriethylenediamine solutions confirms chain fragmentation, showing depressed average degree of polymerization values that correspond to unacceptable drops in burst strength. Mill chemists counteract this hazard by incorporating organic phosphonates or sodium silicate stabilizers that sequester polyvalent cations before continuous steaming.
Alkaline Checkpoint
Industrial bleaching lines enforce continuous chemical metering within the saturator trough to maintain peroxide concentrations between three and six grams per litre. Titration against standardized potassium permanganate or sodium thiosulfate solutions verifies bath strength at thirty-minute intervals during bulk production. Spectrophotometric measurement of fabric whiteness via the Berger or CIE index, alongside fluid capillary rise assessments, serves as the final inspection benchmark for lot acceptance.
Cellulosic Damage
Excessive peroxide concentration or unchecked thermal exposure oxidizes cellulose hydroxyl groups into carbonyl and carboxyl functional groups. These alterations provoke severe fabric tenderising that presents commercially as reduced fabric burst strength and unlevel reactive dyeing. In severe production incidents, pinpoint fabric pinholing emerges where discrete iron particles settle on the fabric face and foster hyper-localised radical degradation.
Routine testing balances whiteness targets against acceptable tensile reduction thresholds on bleached lots destined for piece dyeing.