Abstract

The reaction process of gaseous 1,3-butadiene following ultraviolet irradiation at the temperature range from 298 to 323 K under nitrogen atmosphere was monitored by UV–vis spectrophotometry. A gaseous mini-reactor was used as a reaction vessel and could be directly monitored in a UV–vis spectrophotometer. We investigated the reactivity and kinetics of 1,3-butadiene under non-UV and UV irradiation to evaluate its photochemical stability. A second-order kinetic model with 50.48 kJ·mol–1 activation energy fitted the reaction data for non-UV irradiation, whereas a first-order kinetic model was appropriate in the case of UV irradiation with activation energies of 19.92–43.65 kJ mol–1. This indicates that ultraviolet light could accelerate the photolysis reaction rate of 1,3-butadiene. In addition, the reaction products were determined using gas chromatography-mass spectrometry (GC–MS), and the reaction pathways were identified. The photolysis of 1,3-butadiene gave rise to various volatile products by cleavage and rearrangement of single C–C bonds. The differences between dimerization and dissociation of 1,3-butadiene under ultraviolet irradiation were elucidated by combining experimental and theoretical methods. The present findings provide fundamental insight into the photochemistry of 1,3-butadiene compounds.

Highlights

  • As an important organic precursor, 1,3-butadiene is widely used in the production of polybutadiene and other copolymers, such as cis-polybutadiene rubber [1, 2], neoprene, and styrene-butadiene polymers [3,4,5]

  • Quantitative analysis of 1,3‐butadiene by UV–vis spectrophotometry UV–vis spectrophotometry is widely employed for the quantitative determination of the concentration of liquids [21, 22]; it has rarely been applied to the analysis of other states of matter, such as gas

  • In this study we aimed to fill this gap by using UV–vis spectrophotometry for the quantitative analysis of gaseous 1,3-butadiene

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Summary

Introduction

As an important organic precursor, 1,3-butadiene is widely used in the production of polybutadiene and other copolymers, such as cis-polybutadiene rubber [1, 2], neoprene, and styrene-butadiene polymers [3,4,5]. Owing to conjugation effects [6], 1,3-butadiene is prone to polymerize to form polymers and polyperoxides upon contact with light, heat, and oxygen in air [7], resulting in reduced performance and limiting its applications. Polyperoxides were reported to be impact-sensitive and thermally unstable, and slow deposition over some time can lead to highly hazardous conditions in 1,3-butadiene plants [8]. Many serious explosion accidents have occurred during the production of 1,3-butadiene [9,10,11,12]. In addition to thermal polymerization, the UV-based photopolymerization processes of 1,3-butadiene have been extensively studied in the past decades.

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