非晶聚合物二噻嗪apDTZ固体污染:三嗪基硫化氢缓解的关键回顾、分析和解决方案

G. Taylor, J. Wylde, W. Samaniego, K. Sorbie
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引用次数: 1

摘要

尽管试图抑制或避免使用MEA三嗪形成污垢沉积物(聚合无定形二噻嗪或简称apDTZ),但这仍然是一个主要的操作问题,并限制了这种最流行和普遍存在的硫化氢(H2S)清除剂的使用。本文(a)回顾和总结了前人的工作,(b)对反应产物和形成机理有了新的认识,(c)提出了一种有效的去除方法,(d)提出了apDTZ的一些消化机制。讨论了apDTZ的形成机理,并从多个角度对mea -三嗪与H2S的反应机理进行了推理。这些包括碱度和亲核取代的考虑,空间性质和电子密度的理论计算。通过深入研究和实验验证,提出了与这种固体污垢发生化学反应并破坏这种固体污垢的新方法。对化学破坏apDTZ的药剂进行了综述,发现过氧乙酸是一种非常有效的解决方案,它比以前建议的过氧化物更强大和有效。重点介绍了非晶态聚合物二噻嗪的结构,并分析了其不能被1,3,5-三硫烷污染的原因。因此,这项工作通过提供对反应途径中两个主要悖论的见解,克服了当前行业的误解;即i)为什么从未观察到三羟乙基三嗪(MEA三嗪)的噻嗪反应产物,ii)为什么在所有情况下,二嗪都从未进展到三硫烷(第三硫分子取代)?后一个问题可能是工业界和文献中关于三嗪和H2S反应的最大误解。提出了许多原因,并驳斥了“过量使用”三嗪的常见误解。发现了一种非常有效的化学反应,产生可溶的副产物,抵消了这种顽固性聚合物产生的问题,并提出了它们的组成并进行了实验验证。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Amorphous Polymeric Dithiazine apDTZ Solid Fouling: Critical Review, Analysis and Solution of an Ongoing Challenge in Triazine-Based Hydrogen Sulphide Mitigation
Despite attempts to inhibit or avoid the formation of fouling deposits (polymeric amorphous dithiazine or apDTZ for short) from the use of MEA triazine, this remains a major operational problem and limits the use of this most popular and ubiquitous hydrogen sulphide (H2S) scavenger. This paper (a) reviews and summarizes previous work, (b) provides fresh insights into the reaction product and mechanism of formation, (c) proposes an effective method of removal, and (d) proposes some mechanisms of apDTZ digestion. The mechanism of apDTZ formation is discussed and reasoning is provided from a variety of perspectives as to the mechanism of MEA-triazine reaction with H2S. These include basicity and nucleophilic substitution considerations, steric properties and theoretical calculations for electron density. Novel procedures to chemically react with and destroy this solid fouling are presented with an in-depth study and experimental verification of the underlying chemistry of this digestion process. A review of agents to chemically destroy apDTZ is undertaken and a very effective solution has been found in peroxyacetic acid, which is much more powerful and effective than previously suggested peroxides. The structure of amorphous polymeric dithiazine is emphasized and the reason why this fouling cannot be 1,3,5-trithiane is stressed. This work therefore overcomes a current industry misconception by providing insight on two major paradoxes in the reaction pathway; namely i) why the thiadiazine reaction product from tris hydroxyethyl triazine (MEA triazine) is never observed and ii) why does the dithiazine in all cases never progress to the trithiane (3rd sulphur molecule substitution)? The latter issue is probably the biggest misconception in the industry and literature regarding triazine and H2S reactions. Many reasons for this are put forward and the common misconception of "overspent" triazine is refuted. A very effective chemical reaction that results in soluble by-products, counteracting the problems produced by this intractable polymer is found and their composition is proposed and experimentally verified.
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