Related Experiment Video
Updated: Jan 15, 2026

Microwave-assisted Intramolecular Dehydrogenative Diels-Alder Reactions for the Synthesis of Functionalized Naphthalenes/Solvatochromic Dyes
Published on: April 1, 2013
The Role of TEMPO/NaBr/NaClO in Hemp Fiber Oxidation: Deciphering the Mechanism and Reaction Kinetics
Lingping Kong1,2, Peiyu Du1, Lizhou Pei3
1College of Light Industry and Textile, Qiqihar University, Qiqihar 161000, China.
Abstract:
In this study, the oxidation of industrial hemp staple fibers by the TEMPO/NaBr/NaClO system was explored by the real-time monitoring of the changes in reaction rate, selective oxidative conversion, and reaction time under different operating conditions such as TEMPO usage, NaBr usage, NaClO usage, reaction time, and reaction temperature. We propose a variable-speed competition mechanism between NaClO and TEMPO, which provides experimental support for the long-standing hypothesis that hypochlorite delays acid formation through modulation of the HOCl/OCl- and HOBr/OBr- equilibrium dynamics. The innovative use of combined analysis for several consecutive first-order reactions to investigate the rate-limiting reactions of TEMPO, TEMPO+, and TEMPOH over a range of concentrations revealed that the reaction that generates TEMPOH is the key rate-limiting reaction. We characterize the apparent oxidation kinetics of industrial hemp staple fiber in the TEMPO/NaBr/NaClO system using a pseudo-first-order kinetic model, revealing distinct apparent reaction rates across both primary and secondary bast fiber regions. This paper explained the difference in reaction rate between the two aspects of microfibril spatial structure and cellulose crystal structure. The single-factor analysis indicates that reaction time and temperature exert the most significant influence on the conversion rate of selective oxidation within this system.
More Related Videos
Related Concept Videos
E1 Reaction: Kinetics and Mechanism
E2 Reaction: Kinetics and Mechanism
Phase I Reactions: Oxidation of Aliphatic and Aromatic Carbon-Containing Systems
Oxidation reactions are fundamental in aromatic carbon-containing systems. An example is the hydroxylation of phenobarbital, a process that transforms it into...
¹H NMR of Conformationally Flexible Molecules: Temporal Resolution
Phase I Reactions: Oxidation of Carbon-Heteroatom and Miscellaneous Systems
In carbon-nitrogen systems, aliphatic and aromatic amines can undergo oxidative reactions. Secondary and tertiary amines, like those found in tricyclic antidepressants, can undergo N-dealkylation, a process that involves the oxidation of the alkyl group. In addition, oxidative...
SN2 Reaction: Kinetics
In a chemical reaction, a relationship exists between the concentration of reactants and the rate at which the reaction proceeds. The study to measure this relationship is known as the kinetics of a chemical reaction. Kinetic studies are used to deduce the rate law of a chemical reaction, which provides information about the species involved during the transition state of the rate-determining step. Thus, kinetic studies help to derive the mechanism of a...

