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These digital transcripts are meant to share information on process safety practices in order to help improve process safety performance and awareness throughout industry. The goal is to capture and share knowledge that could be used by other companies or sites when developing new process safety practices or improving existing ones. The documents being shared have been used by an industry member, but this does not mean it should be used or that it will produce similar results at any other site. Rather, it is an option to consider when implementing or adjusting programs and practices at a site. ​

BY THEMSELVES, THESE DIGITAL TRANSCRIPTS ARE NOT STANDARDS OR RECOMMENDED PRACTICES. THEY ARE NOT INTENDED TO REPLACE SOUND ENGINEERING JUDGMENT. THEY DO NOT PRECLUDE THE USE OF ALTERNATIVE METHODS THAT COMPLY WITH LEGAL REQUIREMENTS. A SUBJECT MATTER EXPERT SHOULD BE CONSULTED PRIOR TO DETERMINING WHETHER A PRACTICE CAN BE USED IN ANY SPECIFIC SITUATION. 

​

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(2016) Question 8: Do you have experience starting up an isomerization unit (an alumina chloride catalyst type) without first acidizing the reactor loop? What was the impact on catalyst activity?

Honeywell UOP strongly recommends that acidizing of the reactor circuit should be included in the commissioning and startup of a new grassroots or revamped Penex™ or of Butamer™ units (isomerization units with chlorided alumina catalyst). If not, the consequence can be a significant amount of catalyst deactivation, as well as possible corrosion in the reactor section of the unit. A recent experience in which the customer elected to NOT complete the dry out and acidizing of a new reactor section resulted in an estimated deactivation of 60 to 85% of the new catalyst load.
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(2016) Question 9: Describe your experience and application of advanced separation techniques, such as DWCs (dividing-wall columns), to reduce capital investment and operating expense.

At Valero, we actually have several dividing-wall column applications. We have four in aromatics recovery service and one in a sat(saturated)gas plant service. The towers in aromatic service have been in operation between three and six years, and the tower in the sat gas service has been in operation since early 2016. All towers are meeting their design expectations. The dividing -wall towers have several advantages relative to the traditional sequential column designs.
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(2016) Question 11: What is your acceptable limit for organic chloride concentration in a naphtha hydrotreater feed? What are the possible consequences if this limit is exceeded?

Chloride in naphtha hydrotreater feed can often lead to fouling and/or corrosion issues in the naphtha hydrotreater heat exchange equipment. Recommendations to keep chloride levels under 0.5 ppm in the feed are typical.
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(2016) Question 12: What operating strategies do you employ to successfully regenerate catalyst in a continuous catalyst regeneration (CCR) unit with a carbon content in excess of 10 wt%?

The burn zone in a Honeywell UOP Platforming™ CCR Regenerator is designed for operation at 5 wt.% carbon on catalyst or about 5.25 wt.% coke at the design catalyst circulation rate. We find that most units can operate normally at coke levels 40% above the design (about 7.4 wt.% coke) and some at even higher levels of coke.
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(2016) Question 13: When the regenerator in a CCR unit is shut down for an extended periodof time, how do you predict coke on catalyst with no catalyst circulation?

There are two broad scenarios which might result in the catalyst circulation of a CCR Platforming™ unit being stopped for an extended period of time. The first is that there is maintenance being performed that requires the regenerator to be taken off-line for several days.
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(2016) Question 14: Do you have experience with CCR heel catalyst contaminating the circulating inventory during operation? How can this contamination be prevented?

The most common situation that results in the contamination of a catalyst load with heel catalyst occurs during a turnaround as a result of accidentally reloading drums of used catalyst that contain heel catalyst back into the reactors. This type of contamination occurs in one or two units every year.
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(2016) Question 15: How do you remove the CCR heel catalyst from the unit during an outage and underwhat atmospheric conditions?

Catalyst unloading from a CCR Platforming™ reactor stack is done under nitrogen atmosphere using the normal catalyst transfer line under the catalyst collector. Typically, the last 10 to 15% of the catalyst unloaded will be contaminated with heel catalyst. This percentage may be higher if there has been damage to internals or blockage of catalyst transfer lines.
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(2016) Question 16: What is your Best Practice for inspecting and preventing erosion in CCR lift lines?

In CCR Platforming™ units, the movement of catalyst through the lift pipe results in contact between the catalyst pills and the inner surface of the lift pipe.
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(2016) Question 42: What are your typical H2S (hydrogen sulfide) detection and monitoring methods used on heavy oil fractions being transported via truck, rail, or barge? What are the mitigation options you employ?

We see typically dragger tube testing and head space H2S monitors being used. Mitigation is still done, for the most part, with chemical additives. The most commonly used additives are from the triazine family. As a result of the concerns that refiners have with some of the existing triazine and non-triazine (e.g., glyoxal) being used with respect to the impact on downstream equipment, Nalco Champion has developed both non-triazine, non-acidic (non-glyoxal), and low nitrogen alternative H2S scavengers.
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(2016) Question 43: Have you experienced high corrosion rates in carbon steel piping in resid service operating below 500°F? Please comment on corrosion mechanisms.

High corrosion rates have been experienced in heavier streams, like RCO (reduced crude oil) and vacuum residue operating at a temperature of 450 to 600°F. The role of naphthenic acid corrosion is difficult to determine in such streams with respect to the TAN (total acid number) distribution, temperature and velocity. The key precursor is sulfur species which causes “sulfidic corrosion” in such residue streams.
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