对聚乙烯脱聚合和上循环中的产品和速率进行定量分析
Yu-Hsuan Lee1, Jiakai Sun1, Susannah L Scott2
1Department of Chemistry and Biochemistry, University of California, Santa Barbara, Santa Barbara, CA 93106, USA.
STAR protocols
|September 20, 2023
概括
本研究介绍了分析聚乙烯脱聚合产品的方法. 这些技术可以定量测量反应速率和塑料上循环的产品选择性.
科学领域:
- 聚合物化学 聚合物化学
- 材料科学 材料科学 材料科学
- 化学工程是化学工程的重要组成部分.
背景情况:
- 塑料废物管理是一个全球性的挑战.
- 脱聚合和上循环为聚烯提供了可持续的解决方案.
- 脱聚合产品的定量分析是复杂和具有挑战性的.
研究的目的:
- 开发和详细技术的回收和分析产品从聚乙烯脱聚合.
- 为了使反应速率和产品选择性的定量测量.
- 提供适用于其他塑料和复杂产品混合物的协议.
主要方法:
- 聚乙烯的批量去聚合.
- 产品回收技术产品回收技术.
- 对反应产物的定量分析方法.
主要成果:
- 成功实施聚乙烯脱聚合产品回收和分析技术.
- 获得的关于反应速度和产品选择性的定量数据.
- 该协议对其他塑料和长链烯混合物的证明适用性.
结论:
- 开发的协议解决了聚烯脱聚合分析中的关键挑战.
- 能够准确评估反应动力学和选择性.
- 促进塑料上循环技术的发展.
相关概念视频
Types of Step-Growth Polymers: Polyesters
2.3K
The introduction of polyesters has brought major development to the textile industry. The wrinkle-free behavior of polyester blends has eliminated the need for starching and ironing clothes.
Polyesters are commonly prepared from terephthalic acid and ethylene glycol; the crude product is known as poly(ethylene terephthalate) or PET. However, polyesters are synthesized industrially by transesterification of dimethyl terephthalate with ethylene glycol at 150 °C. The two reactants and the...
Polyesters are commonly prepared from terephthalic acid and ethylene glycol; the crude product is known as poly(ethylene terephthalate) or PET. However, polyesters are synthesized industrially by transesterification of dimethyl terephthalate with ethylene glycol at 150 °C. The two reactants and the...
2.3K
Free-Radical Chain Reaction and Polymerization of Alkenes
7.9K
The conversion of alkenes to macromolecules called polymers is a reaction of high commercial importance. The structure of the polymer is defined by a repeating unit, while the terminal groups are considered insignificant. The average degree of polymerization represents the number of repeating units in the polymer molecule and is denoted by the subscript n.
7.9K
Radical Chain-Growth Polymerization: Chain Branching
2.0K
The skeletal structure of polymers synthesized via radical polymerization is always branched. For example, the polymerization of ethylene by radical polymerization results in a low-density grade of polyethylene with a heavily branched skeletal structure. Here, the radical site abstracts hydrogen from the growing chain, and the radical site shifts from the end (a primary carbon center) to anywhere within the growing chain (a secondary carbon center). Consequently, the part of the chain from the...
2.0K
Polymer Classification: Architecture
2.8K
Polymers are classified as linear or branched on the basis of their chain architecture. The polymer chains in linear polymers have a long chain-like structure with minimal to no branching at all. Even if a polymer features large substituent groups on the monomer, which appear as branches to the skeleton, it is not considered a branched polymer. A branched polymer contains secondary polymer chains that arise from the main polymer chain. The branching occurs when the polymer growth shifts from...
2.8K
Olefin Metathesis Polymerization: Acyclic Diene Metathesis (ADMET)
1.9K
Acyclic diene metathesis polymerization or ADMET polymerization involves cross-metathesis of terminal dienes, such as 1,8-nonadiene, to give linear unsaturated polymer and ethylene. As ADMET is a reversible process, the formed ethylene gas must be removed from the reaction mixture to complete the polymerization process.
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
Similar to cross-metathesis, ADMET also involves the formation of metallacyclobutane intermediate by [2+2] cycloaddition of one of the double bonds of a terminal diene with...
1.9K
Polymer Classification: Stereospecificity
2.5K
Polymerization generates chiral centers along the entire backbone of a polymer chain. Accordingly, the stereochemistry of the substituent group has a significant effect on polymer properties. Polymers formed from monosubstituted alkene monomers feature chiral carbons at every alternate position in the polymer backbone. Relative to the predominant orientation of substituents at the adjacent chiral carbons, the polymer can exist in three different configurations: isotactic, syndiotactic, and...
2.5K


