{"title":"烷基铝/尿素杂化助催化剂及其在铁催化乙烯齐聚中的应用","authors":"Ying Zhang, Jian Ye, Yinzhi Jiang, Shuqin Jiang, Wei Xiao, Dongchu Wei","doi":"10.1002/mren.202300013","DOIUrl":null,"url":null,"abstract":"<p>The bis(imino)pyridyl iron-based ethylene oligomerization catalysts have the advantages of mild reaction conditions, high activity and high selectivity to linear <i>α</i>-olefins. However, barriers, such as high polymer content in the product mixture and large methylaluminoxane (MAO) dosage, are still limitations for the development of these systems at the industrial scale. In this study, new cocatalysts are prepared by the reaction of alkylaluminums with urea and its derivatives, and successfully used to activate iron-based catalysts. It is found that the type and molar ratio of alkylaluminum and urea have significant influence on the performance of the cocatalysts. The activity of the preferred triisobutylaluminum/urea activated systems reaches more than 3.0 × 10<sup>8</sup> g (mol-Fe)<sup>−1</sup> h<sup>−1</sup>, and the polymer content can be controlled to be less than 2 wt.%. Notably, the catalytic system exhibits good high temperature stability, the activity can still reach 1.0 × 10<sup>8</sup> g (mol-Fe)<sup>−1</sup> h<sup>−1</sup> even at 120 °C. Further <sup>1</sup>H NMR studies show that alkylaluminum can react with the N<span></span>H moieties of urea, forming complex alkylaluminum clusters, even aluminoxane-like structures. This study offers a promising family of cocatalysts, making it possible to simultaneously improve their performance and reduce their cost.</p>","PeriodicalId":18052,"journal":{"name":"Macromolecular Reaction Engineering","volume":"17 3","pages":""},"PeriodicalIF":1.8000,"publicationDate":"2023-03-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Alkylaluminum/Urea Hybrid Cocatalysts and Their Use in Iron-Catalyzed Oligomerization of Ethylene\",\"authors\":\"Ying Zhang, Jian Ye, Yinzhi Jiang, Shuqin Jiang, Wei Xiao, Dongchu Wei\",\"doi\":\"10.1002/mren.202300013\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The bis(imino)pyridyl iron-based ethylene oligomerization catalysts have the advantages of mild reaction conditions, high activity and high selectivity to linear <i>α</i>-olefins. However, barriers, such as high polymer content in the product mixture and large methylaluminoxane (MAO) dosage, are still limitations for the development of these systems at the industrial scale. In this study, new cocatalysts are prepared by the reaction of alkylaluminums with urea and its derivatives, and successfully used to activate iron-based catalysts. It is found that the type and molar ratio of alkylaluminum and urea have significant influence on the performance of the cocatalysts. The activity of the preferred triisobutylaluminum/urea activated systems reaches more than 3.0 × 10<sup>8</sup> g (mol-Fe)<sup>−1</sup> h<sup>−1</sup>, and the polymer content can be controlled to be less than 2 wt.%. Notably, the catalytic system exhibits good high temperature stability, the activity can still reach 1.0 × 10<sup>8</sup> g (mol-Fe)<sup>−1</sup> h<sup>−1</sup> even at 120 °C. Further <sup>1</sup>H NMR studies show that alkylaluminum can react with the N<span></span>H moieties of urea, forming complex alkylaluminum clusters, even aluminoxane-like structures. This study offers a promising family of cocatalysts, making it possible to simultaneously improve their performance and reduce their cost.</p>\",\"PeriodicalId\":18052,\"journal\":{\"name\":\"Macromolecular Reaction Engineering\",\"volume\":\"17 3\",\"pages\":\"\"},\"PeriodicalIF\":1.8000,\"publicationDate\":\"2023-03-28\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Macromolecular Reaction Engineering\",\"FirstCategoryId\":\"5\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1002/mren.202300013\",\"RegionNum\":4,\"RegionCategory\":\"工程技术\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"ENGINEERING, CHEMICAL\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Macromolecular Reaction Engineering","FirstCategoryId":"5","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1002/mren.202300013","RegionNum":4,"RegionCategory":"工程技术","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"ENGINEERING, CHEMICAL","Score":null,"Total":0}
引用次数: 0
摘要
双(亚胺)吡啶基铁基乙烯低聚催化剂具有反应条件温和、活性高、对线型α-烯烃选择性高的优点。本研究通过烷基铝与尿素及其衍生物的反应制备了新的助催化剂,并成功地用于激活铁基催化剂。结果表明,烷基铝和尿素的种类和摩尔比对助催化剂的性能有显著影响。优选的三异丁基铝/尿素活化体系活性可达3.0 × 108 g (mol-Fe)−1 h−1以上,聚合物含量可控制在2 wt.%以下。值得注意的是,该催化体系表现出良好的高温稳定性,即使在120℃时,活性仍可达到1.0 × 108 g (mol-Fe)−1 h−1。进一步的1H NMR研究表明,烷基铝可以与尿素的N - H基团反应,形成复杂的烷基铝团簇,甚至形成类似铝氧烷的结构。本研究提供了一个很有前途的共催化剂家族,使其性能的提高和成本的降低成为可能。
Alkylaluminum/Urea Hybrid Cocatalysts and Their Use in Iron-Catalyzed Oligomerization of Ethylene
The bis(imino)pyridyl iron-based ethylene oligomerization catalysts have the advantages of mild reaction conditions, high activity and high selectivity to linear α-olefins. However, barriers, such as high polymer content in the product mixture and large methylaluminoxane (MAO) dosage, are still limitations for the development of these systems at the industrial scale. In this study, new cocatalysts are prepared by the reaction of alkylaluminums with urea and its derivatives, and successfully used to activate iron-based catalysts. It is found that the type and molar ratio of alkylaluminum and urea have significant influence on the performance of the cocatalysts. The activity of the preferred triisobutylaluminum/urea activated systems reaches more than 3.0 × 108 g (mol-Fe)−1 h−1, and the polymer content can be controlled to be less than 2 wt.%. Notably, the catalytic system exhibits good high temperature stability, the activity can still reach 1.0 × 108 g (mol-Fe)−1 h−1 even at 120 °C. Further 1H NMR studies show that alkylaluminum can react with the NH moieties of urea, forming complex alkylaluminum clusters, even aluminoxane-like structures. This study offers a promising family of cocatalysts, making it possible to simultaneously improve their performance and reduce their cost.
期刊介绍:
Macromolecular Reaction Engineering is the established high-quality journal dedicated exclusively to academic and industrial research in the field of polymer reaction engineering.