High Temperature Corrosion By Catalytically Formed Hydrogen Sulfide

CORROSION ◽  
1962 ◽  
Vol 18 (8) ◽  
pp. 291t-298t ◽  
Author(s):  
A. S. COUPER ◽  
ANDREW DRAVNIEKS

Abstract Organic sulfur compounds are known to be a major cause of high-temperature corrosion in refining processes. Chromium steels are widely used in such environments. The required chromium content for adequate resistance depends upon the chemical form of sulfur encountered. Surfaces of corroding metals can act as catalysts in forming hydrogen sulfide, either from hydrogen and sulfur or by decomposition of organic sulfur compounds. Catalytically formed H2S is more corrosive than the same concentration of other H2S and can be corn-batted by adding chromium to the steel. Because corrosion is proportional to the concentration of H2S, a surface concentration of H2S is postulated as proportional to the catalytic activity of the surface. Laboratory tests on sulfur vapor mixed with hydrogen and on amyl mercaptan mixed with nitrogen or hydrogen indicate that corrosion is proportional to the yield of catalytically formed H2S. Chromium additions to the steel, oxide scales on the metal surfaces, additions of chlorides to the stream, and increased velocity decreased both H2S yields and corrosion, whereas increased temperatures and addition of oxidizing agents caused increases. Further work should be done to develop practical methods to reduce the catalytic activity of corroding steel surfaces, thereby improving corrosion resistance to certain high-temperature streams that contain sulfur compounds. 3.4.2, 4.4.9, 3.5.9, 3.7.2, 8.4.3

1974 ◽  
Vol 22 (6) ◽  
pp. 1071-1076 ◽  
Author(s):  
Mans. Boelens ◽  
Leendert M. Van der Linde ◽  
Pieter J. De Valois ◽  
Hans M. Van Dort ◽  
Henk J. Takken

Energies ◽  
2020 ◽  
Vol 13 (20) ◽  
pp. 5286
Author(s):  
Valery Meshalkin ◽  
Elena Shinkar ◽  
Nadezhda Berberova ◽  
Nadezhda Pivovarova ◽  
Foat Ismagilov ◽  
...  

A logical-informational model of energy resource-efficient chemical technology for the utilization of hydrogen sulfide and low molecular alkanethiols, which are toxic and difficult to remove sulfur components of residual fuel (fuel oil), is proposed. Based on the IDEF1 methodology and existing knowledge about the technological processes of the demercaptanization of various hydrocarbon raw materials (oils, gas condensates), a scheme for the production of organic sulfur compounds from sulfur waste extracted from fuel oil has been modeled. For a sufficiently complete removal of hydrogen sulfide and low molecular weight alkanethiols, energy- and resource-saving stages of the technological process have been developed, which are implemented by ultrasonic and/or magnetic treatment of fuel oil. It is proposed to use the combined action of two alternative methods of processing fuel oil to increase the efficiency of cleaning fuel oil from sulfur components. For the first time, an approach has been developed to utilize unwanted sulfuric impurities contained in fuel oil by involving electric and microwave synthesis in green technological processes, to obtain practically useful organic sulfur compounds with biological activity. It is shown that the use of one-electron oxidant thiols and hydrogen sulfide in organic media leads to the synthesis of organic disulfides and elemental sulfur. Indirect (with the use of mediators) electrosynthesis contributes to the cyclic conduct of the technological process, an increase in efficiency and a decrease in energy consumption compared to the direct (on electrodes) initiation of sulfur components.


2017 ◽  
Vol 70 (1) ◽  
pp. 9 ◽  
Author(s):  
Lotfi Shiri ◽  
Arash Ghorbani-Choghamarani ◽  
Mosstafa Kazemi

Compounds containing sulfur–sulfur bonds (often called disulfides or more specifically disulfanes) are arguably one of the most valuable functional groups in organic synthetic chemistry. They exist extensively in nature, in which they exhibit important biological activities. Furthermore, a diverse range of natural and synthetic disulfides have been discovered that have many applications as pharmaceutical and agriculture chemicals as well as synthetic intermediates. Since thiols are commercially accessible or easily synthesizable materials and their choice as starting materials is widely reported for the synthesis of organic sulfur compounds, unsurprisingly the oxidative coupling of thiols is the best and simplest route for the preparation of disulfides. In recent times, nanocatalysts have shown excellent catalytic activity and reusability in the oxidation of thiols to disulfides. Herein, we summarize the recently reported breakthroughs in the use of nanocatalysts for the oxidative coupling of thiols to their corresponding disulfides, with the goal of stimulating further progress in this field.


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