Amit K. Jha , Daniella V. Martinez , Jay E. Salinas , Estevan J. Martinez , Ryan D. Davis , Alberto Rodriguez , Hemant Choudhary , Michael S. Kent , Oleg Davydovich
{"title":"通过 COOH 功能化和芬顿化学解构碳-碳键聚合物以进行生物转化","authors":"Amit K. Jha , Daniella V. Martinez , Jay E. Salinas , Estevan J. Martinez , Ryan D. Davis , Alberto Rodriguez , Hemant Choudhary , Michael S. Kent , Oleg Davydovich","doi":"10.1016/j.polymdegradstab.2024.111081","DOIUrl":null,"url":null,"abstract":"<div><div>For carbonaceous waste materials that cannot be readily recycled, upcycling through deconstruction and subsequent biological conversion of the breakdown products to fuels, chemicals, or intermediates is a promising strategy. However, deconstructing certain important types of waste plastics such as polyolefins and polystyrene, and also lignin, requires cleaving carbon-carbon bonds. We show that carbon-carbon backbone bonds can be cleaved efficiently by a Fenton reaction in polymers that contain carboxylic acid (COOH) groups. For polyacrylic acid, a model water-soluble polymer, decrease in molecular weight from M<sub>p</sub> = 28,000 g/mol to M<sub>p</sub> < 700 g/mol occurred with H<sub>2</sub>O<sub>2</sub> loading of only 2 molar equivalents to monomer at pH 4. This method was then applied to partially deconstruct two commercial oxidized polyethylene (oxPE) wax samples with much lower density of COOH groups. A modification of the method, in which dihydroxybenzene was included for a chelator-mediated Fenton (CMF) reaction, greatly increased the deconstruction efficiency. For a sample with acid number of 35 (or ∼ 1 COOH per 114 C atoms), 9.5 % +/- 0.6 % of the carbon was recovered as water-soluble species and an additional 13 % was recovered with subsequent acetone extraction. Mass spectrometry analysis of the water-soluble compounds revealed that most of the low molecular weight fragments form three series, where the members of each series differ by the number of CH<sub>2</sub> units. The series contains carboxylic acid and alcohol groups. A panel of microorganisms was tested for growth on this substrate as sole carbon source and several organisms showed promising growth as measured by optical density of cultures at 600 nm. <em>Rhodococcus ruber</em> and <em>Brevundimonas vesicularis</em> grew well on the PE breakdown products with no further carbon or nitrogen sources added whereas <em>Bacillus megaterium, Yarrowia lipolytica</em> MYA 2613<em>, Sphingopyxis witflariensis</em>, and <em>Sphingomonas</em> PWE1 along with <em>Rhodococcus ruber</em> and <em>Brevundimonas vesicularis</em> grew well on the PE breakdown products in the presence of tryptone. Several ideas are discussed to improve the overall conversion with this approach.</div></div>","PeriodicalId":406,"journal":{"name":"Polymer Degradation and Stability","volume":"231 ","pages":"Article 111081"},"PeriodicalIF":6.3000,"publicationDate":"2024-11-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Deconstruction of carbon-carbon bonded polymers for biological conversion through COOH-functionalization and Fenton chemistry\",\"authors\":\"Amit K. Jha , Daniella V. Martinez , Jay E. Salinas , Estevan J. Martinez , Ryan D. Davis , Alberto Rodriguez , Hemant Choudhary , Michael S. Kent , Oleg Davydovich\",\"doi\":\"10.1016/j.polymdegradstab.2024.111081\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>For carbonaceous waste materials that cannot be readily recycled, upcycling through deconstruction and subsequent biological conversion of the breakdown products to fuels, chemicals, or intermediates is a promising strategy. However, deconstructing certain important types of waste plastics such as polyolefins and polystyrene, and also lignin, requires cleaving carbon-carbon bonds. We show that carbon-carbon backbone bonds can be cleaved efficiently by a Fenton reaction in polymers that contain carboxylic acid (COOH) groups. For polyacrylic acid, a model water-soluble polymer, decrease in molecular weight from M<sub>p</sub> = 28,000 g/mol to M<sub>p</sub> < 700 g/mol occurred with H<sub>2</sub>O<sub>2</sub> loading of only 2 molar equivalents to monomer at pH 4. This method was then applied to partially deconstruct two commercial oxidized polyethylene (oxPE) wax samples with much lower density of COOH groups. A modification of the method, in which dihydroxybenzene was included for a chelator-mediated Fenton (CMF) reaction, greatly increased the deconstruction efficiency. For a sample with acid number of 35 (or ∼ 1 COOH per 114 C atoms), 9.5 % +/- 0.6 % of the carbon was recovered as water-soluble species and an additional 13 % was recovered with subsequent acetone extraction. Mass spectrometry analysis of the water-soluble compounds revealed that most of the low molecular weight fragments form three series, where the members of each series differ by the number of CH<sub>2</sub> units. The series contains carboxylic acid and alcohol groups. A panel of microorganisms was tested for growth on this substrate as sole carbon source and several organisms showed promising growth as measured by optical density of cultures at 600 nm. <em>Rhodococcus ruber</em> and <em>Brevundimonas vesicularis</em> grew well on the PE breakdown products with no further carbon or nitrogen sources added whereas <em>Bacillus megaterium, Yarrowia lipolytica</em> MYA 2613<em>, Sphingopyxis witflariensis</em>, and <em>Sphingomonas</em> PWE1 along with <em>Rhodococcus ruber</em> and <em>Brevundimonas vesicularis</em> grew well on the PE breakdown products in the presence of tryptone. 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Deconstruction of carbon-carbon bonded polymers for biological conversion through COOH-functionalization and Fenton chemistry
For carbonaceous waste materials that cannot be readily recycled, upcycling through deconstruction and subsequent biological conversion of the breakdown products to fuels, chemicals, or intermediates is a promising strategy. However, deconstructing certain important types of waste plastics such as polyolefins and polystyrene, and also lignin, requires cleaving carbon-carbon bonds. We show that carbon-carbon backbone bonds can be cleaved efficiently by a Fenton reaction in polymers that contain carboxylic acid (COOH) groups. For polyacrylic acid, a model water-soluble polymer, decrease in molecular weight from Mp = 28,000 g/mol to Mp < 700 g/mol occurred with H2O2 loading of only 2 molar equivalents to monomer at pH 4. This method was then applied to partially deconstruct two commercial oxidized polyethylene (oxPE) wax samples with much lower density of COOH groups. A modification of the method, in which dihydroxybenzene was included for a chelator-mediated Fenton (CMF) reaction, greatly increased the deconstruction efficiency. For a sample with acid number of 35 (or ∼ 1 COOH per 114 C atoms), 9.5 % +/- 0.6 % of the carbon was recovered as water-soluble species and an additional 13 % was recovered with subsequent acetone extraction. Mass spectrometry analysis of the water-soluble compounds revealed that most of the low molecular weight fragments form three series, where the members of each series differ by the number of CH2 units. The series contains carboxylic acid and alcohol groups. A panel of microorganisms was tested for growth on this substrate as sole carbon source and several organisms showed promising growth as measured by optical density of cultures at 600 nm. Rhodococcus ruber and Brevundimonas vesicularis grew well on the PE breakdown products with no further carbon or nitrogen sources added whereas Bacillus megaterium, Yarrowia lipolytica MYA 2613, Sphingopyxis witflariensis, and Sphingomonas PWE1 along with Rhodococcus ruber and Brevundimonas vesicularis grew well on the PE breakdown products in the presence of tryptone. Several ideas are discussed to improve the overall conversion with this approach.
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.