Many types of hydrocarbon processing operations are carried out under relatively harsh operating conditions, including high temperatures and / or pressures and within various harsh chemical environments.
This and other specialty austenitic stainless steels have been used in these applications but are susceptible to high temperature H2S, sulfur, and chloride-SCC corrosion and high temperature hydrogen attack issues that are present in these processes.
Many metals, including austenitic stainless steels, can be subject to a highly localized form of corrosion known as stress-corrosion cracking (SCC).
SCC often takes the form of branching cracks in apparently ductile material and can occur with little or no advance warning.
In low pressure vessels, the first sign of stress corrosion cracking is usually a leak, but there have been instances of catastrophic failures of high pressure vessels due to stress corrosion cracking.
Stress corrosion cracking occurs when the surface of the material exposed to a corroding medium is under tensile stress (applied or residual) and the corroding medium specifically causes stress corrosion cracking of the metal.
One particularly harsh environment in which austenitic stainless steels are typically observed to undergo stress corrosion cracking is an environment containing halides, usually in the form of inorganic chlorides.
The presence of chlorides along with an aqueous phase and tensile stresses can result in chloride stress corrosion cracking (“chloride-SCC”) of austenitic stainless steels.
In addition, while high temperatures may reduce the amount of time required for a particular chloride concentration to result in chloride-SCC, lower temperatures can cause chlorides to condense on surfaces, thereby increasing the concentration of the chlorides on the surfaces.
Thus, chloride-SCC can be problematic at many temperature ranges.
One particularly problematic area of chloride-SCC is in condensers where chloride condenses and concentrates on surfaces of the vessel.
The precipitation of chromium depletes the chromium content adjacent to the grain boundaries, forming chromium depleted zones and drastically reducing the corrosion and / or cracking resistance in corrosive environments in these zones.
The PTA can attack the chromium depleted zones formed by sensitization, causing corrosion and ultimately polythionic acid stress corrosion cracking (PTA-SCC) where the vessel is put under tensile stresses either by being pressurized or by having residual stresses from, for example, welding during fabrication.
Each of these processes is time consuming and impractical during the operation of an oil refinery complex because it requires additional materials and additional downtime of the particular equipment to perform the purge or neutralization steps.
Moreover, the catalyst in the reactor can be poisoned if trace levels of the chemicals remain, which is often the case.
However, such austenitic stainless steels are also susceptible to PTA-SCC as a result of exposure to polythionic acid, since the operating conditions of many hydrocarbon treatment processes fall within the time at temperature at which sensitization occurs.
Similarly, these materials are still susceptible to chloride-SCC through exposure to chlorides, oxygen, water, and stress at sufficient times and temperatures.
The need for special procedures during shutdown and startup of a refinery complex affects not only costs, but also production time since they take a certain amount of time to carry out.
However, even with these precautions, chloride corrosion of welded plate heat exchangers is often observed when liquid water is present in the feed leading to chloride pitting, chloride pitting due to under-deposit corrosion, and when a water dew-point occurs during regeneration of a fixed bed reforming unit leading to chloride pitting, and chloride-SCC due to the presence of chlorides, oxygen, and water.
Any failure due to corrosion or cracking will reduce product quality by contaminating the product stream with the feed stream.
In addition, some welded plate heat exchangers are damaged by thermal stress which can cause mechanical damage to the heat exchanger.
This type of mechanical damage accounts for the majority of all damage that causes bundle cross leakage.
Flow mal-distributions can occur when there is a fouling of the bundle, when there is a sudden plugging of the bundle, when there is plugging of a distributor, or when there are low velocities resulting in poor liquid flow up in the bundle.
Thermal stress damage that causes bundle cross leaking is costly to the end user because it results in cross-leakage of the higher pressure stream into the lower pressure stream resulting in a reduction in heat transfer efficiency, as well as potentially contaminating a product stream with a feed stream.
This damage can result in reduced throughput, reduced product quality, and eventually may require shutdown to repair or replace the heat exchanger.
In corrosion and SCC cases, the bundles cannot be repaired because the damage typically occurs to most of or all the plate channels, requiring replacement of the bundle or the entire heat exchanger.
However, when 10-20% or more of the channels are plugged, the resulting increase in pressure-drop can significantly reduce throughput.
Furthermore, repaired bundles can be more susceptible to further damage by thermal stresses.