The Temperature Dependence of the Rate of Crosslinking with Formaldehyde and of the Hydrolysis of Cotton Cellulose

1976 ◽  
Vol 46 (12) ◽  
pp. 880-886 ◽  
Author(s):  
U. Meyer ◽  
K. Müller ◽  
H. Zollinger

The kinetics of the crosslinking of cotton fabrics in aqueous solution with formaldehyde using hydrochloric acid as catalyst, and the acid degradation (hydrolysis) of cotton were measured simultaneously at 67.4°C, 77.6°C, and 87.0°C. Some related kinetic measurements of these two reactions were also carried out with the pad-dry-cure process, catalyzed by MgCl2, at 140°C, 160°C, and 180°C. The apparent activation energies of crosslinking and hydrolysis were calculated. They are discussed with reference to the improvement in the dry crease-recovery angle/tensile strength relation at lower reaction temperatures. For the reaction in aqueous solution the rate of degradation of the accessible as well as the highly-ordered fractions of cellulose were determined. Finally, the apparent reaction enthalpy of the crosslinking reaction was estimated.

2013 ◽  
Vol 67 (4) ◽  
Author(s):  
Ahmad Mohamad ◽  
Mohamed Adam

AbstractThree ligands of 2-pyridinylmethylene-8-quinolinyl (L1), methyl-2-pyridinylmethylene-8-quinolinyl (L2), and phenyl-2-pyridinylmethylene-8-quinolinyl (L3), Schiff bases were synthesised by direct condensation of 8-aminoquinoline with 2-pyridinecarboxaldehyde, 2-acetylpyridine, or 2-benzoylpyridine. They coordinated to Fe(II) ion in a 1: 2 mole ratio followed by treatment with iodide ions affording complexes with a general formula [Fe(L)2]I2·2H2O, (L = L1, L2, or L3). Spectrophotometric evaluation of the kinetics of base catalysed hydrolysis of these complex cations was carried out with an aqueous solution of NaOH in different ratios of water/methanol binary mixtures. Kinetics of the hydrolysis followed the rate law (k 2[OH−] + k 3[OH−]2)[complex]. Reactivity trends and their rate constants were compared and discussed in terms of ligand structure and solvation parameters. The methanol ratio affects the hydrolysis as a co-solvent which was analysed into initial and transition state components. The increase in the rate constant of the base hydrolysis of Fe(II) complexes, as the ratio of methanol increases, is predominantly caused by the strong effect of the organic co-solvent on the transition states.


1968 ◽  
Vol 21 (7) ◽  
pp. 1727
Author(s):  
RA Fredlein ◽  
I Lauder

The kinetics of the acid-catalysed hydrolysis of a-methylallyl acetate in aqueous solution have been studied over the range 30-100�. Oxygen-18 tracer experiments reveal the mechanism to be solely Aac2 and the Arrhenius parameters are consistent with this conclusion. Crotyl alcohol is observed in the reaction products. The formation of rearranged alcohol is explained by allylic isomerization of the α-methylallyl alcohol produced by the hydrolysis.


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