On April 16, 2020, Wylde, J. J.; Taylor, G. N.; Sorbie, K. S.; Samaniego, W. N. published an article.Safety of 2,2′,2”-(1,3,5-Triazinane-1,3,5-triyl)triethanol The title of the article was Synthesis and Reaction Byproduct Characterization and Mechanistic Understanding of Hemiformal Based Hydrogen Sulfide Scavengers. And the article contained the following:
When hydrogen sulfide (H2S) gas is produced from oil reservoirs, it leads to a number of well-known problems relating to both metal corrosion and health and safety. Up to a certain concentration (~1000s of ppm in the gas phase) the H2S can be removed by adding a chem. “scavenger” to the system, which reacts with H2S to form less harmful byproducts. A range of different chem. species have been applied as H2S scavengers in petroleum production systems, operating through either oxidative or nonoxidative mechanisms; the former group includes such species as alk. sodium nitrite and hydrogen peroxide, and in the latter group triazine type scavengers have been very prominent. Although triazine based H2S scavengers have been hugely successful in practical and com. terms, there have been associated issues with the related byproducts from the scavenging reaction (discussed in this work). An alternative non-triazine chem. range of H2S scavengers that has emerged in recent years has been based on hemiacetal chemistries, where a hemiacetal is produced by the reaction of an alc. with an aldehyde. Where the aldehyde is formaldehyde, the resulting species are known as hemiformals. In this work, the synthetic chem. reaction pathway for hemiformals based on ethylene glycol and glycerol were studied. This work is novel in four major respects: (i) first, we examine hemiformal production via acid, base, and neutral catalysis systems; (ii) we perform detailed structural determinations of the oligomeric series thus produced (which are different) by analyzing the products by derivatized gas chromatog. mass spectrometry and making subsequent structural assignments; (iii) we then assess the effectiveness of these species as H2S scavenging using an industry standard multiphase test methodol. and make some correlation between their structure and performance; and (iv) finally, we studied the structures of product and byproducts of the scavenging reaction both before and after the scavenging reaction with H2S. This latter part of the study examines issues of byproduct structure early in the development of these newer products in order to address any problems that may be encountered “up front”. This greatly facilitates our application of using hemiformals as fully optimized non-triazine based scavengers by addressing byproduct chem. anal. of these relatively new H2S scavenger systems. The experimental process involved the reaction of 2,2′,2”-(1,3,5-Triazinane-1,3,5-triyl)triethanol(cas: 4719-04-4).Safety of 2,2′,2”-(1,3,5-Triazinane-1,3,5-triyl)triethanol
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