Measurement of monomers and oligomers (≤20mer) as intermediates using LC–Orbitrap MS from marine biodegradation of poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) in laboratory
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引用次数: 0
Abstract
Degraded intermediates in the marine biodegradation of poly(3-hydroxybutyrate-co-3-hydroxyhexanoate) (PHBH), a microbial polyester, were detected and quantified using LCOrbitrap MS. Intermediates were extracted from a biofilm (BF) attached to the biodegraded film using solvent extraction. Monomers and oligomers up to 11mer were identified on the surface of a marine biodegraded PHBH film and in the associated BF. The biodegradability and intermediate amounts of three films (ca. 90 mg) on day 9 were 13 % and 9.2 μg in the first test, 30 % and 13 μg in the second test, and 52 % and 19 μg in the third test, respectively. Differences in biodegradability and intermediate amounts between the biodegradation tests suggest that variation in the microbial community and quantity in seawater affect enzymatic degradation and mineralization rates. The amounts of 3-hydroxybutyric acid (3HB) monomer, 3-hydroxyhexanoate (3HH) monomer, and oligomers (3HB equivalent) were 67:5:28 (9.2 μg) in the first test, 69:5:26 (13 μg) in the second test, and 79:7:14 (19 μg) in the third test, respectively. The substantial occupancy of monomers in the intermediates suggests that the oligomers are rapidly enzymatically degraded into monomers, which are slowly mineralized and metabolized. Monomers were the only species identified in the pore water (free water within the BF), and the concentrations of intermediates in seawater were below the detection limit. The monomer composition (3HB:3HH) in the intermediate was consistent with the copolymer composition, indicating no selective accumulation of specific monomers.
期刊介绍:
Polymer Degradation and Stability deals with the degradation reactions and their control which are a major preoccupation of practitioners of the many and diverse aspects of modern polymer technology.
Deteriorative reactions occur during processing, when polymers are subjected to heat, oxygen and mechanical stress, and during the useful life of the materials when oxygen and sunlight are the most important degradative agencies. In more specialised applications, degradation may be induced by high energy radiation, ozone, atmospheric pollutants, mechanical stress, biological action, hydrolysis and many other influences. The mechanisms of these reactions and stabilisation processes must be understood if the technology and application of polymers are to continue to advance. The reporting of investigations of this kind is therefore a major function of this journal.
However there are also new developments in polymer technology in which degradation processes find positive applications. For example, photodegradable plastics are now available, the recycling of polymeric products will become increasingly important, degradation and combustion studies are involved in the definition of the fire hazards which are associated with polymeric materials and the microelectronics industry is vitally dependent upon polymer degradation in the manufacture of its circuitry. Polymer properties may also be improved by processes like curing and grafting, the chemistry of which can be closely related to that which causes physical deterioration in other circumstances.