Selective Hydrogenation Reactor for Naphtha Octane Preservation

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Solution Overview

Problem

The existing hydrodesulfurization processes face challenges in selectively hydrogenating di-alkenes and alkynes without saturating mono-alkenes, leading to octane loss and equipment issues due to polymerization and catalyst deactivation, especially at higher temperatures.

Innovation Solution

A selective hydrogenation reactor system is implemented with a fractionation column to separate naphtha streams, where a heavier olefinic naphtha stream is hydrogenated upstream and a lighter stream is hydrogenated downstream, using a catalyst with specific properties to minimize mono-alkene saturation and polymerization, while maintaining the octane rating of the product stream.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If high temperature processing is used to remove di-alkenes and alkynes, then conversion efficiency improves, but mono-alkenes saturation increases leading to octane loss

Engineering Contradiction:
Improveconversion efficiency of di-alkenes and alkynesVSAvoidoctane rating
Core Design Contradiction:
ProductivityVSManufacturing precision

Solution Approach 1:

The naphtha stream is divided into two separate streams based on boiling point ranges: a lighter stream (C5-C7) and a heavier stream (C7+). Each stream is selectively hydrogenated in separate reaction zones, allowing optimized conditions for each fraction and preventing excessive mono-alkene saturation while maintaining high di-alkene conversion efficiency.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

Different hydrogenation conditions are applied to different portions of the naphtha stream. The lighter stream receives milder hydrogenation conditions while the heavier stream receives more intensive treatment, creating local optimization that preserves octane rating in the lighter fraction while effectively removing di-alkenes and alkynes from the heavier fraction.

Inventive Principle:
Principle #3Local quality

2Productivity

If high temperature processing is used to remove di-alkenes and alkynes, then conversion efficiency improves, but polymerization and gum formation increase deactivating catalyst

Engineering Contradiction:
Improveconversion efficiency of di-alkenes and alkynesVSAvoidcatalyst life
Core Design Contradiction:
ProductivityVSReliability

Solution Approach 1:

The feed stream is segmented into lighter and heavier portions, with the heavier stream (rich in di-alkenes and alkynes) directed to the primary hydrogenation zone where intensive treatment occurs. The lighter stream bypasses this zone, avoiding conditions that would cause polymerization and catalyst deactivation, thereby extending catalyst life while maintaining high conversion efficiency for the problematic components.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The heavier naphtha stream containing the majority of di-alkenes and alkynes is extracted and directed to the hydrogenation reaction zone for selective treatment. By separating and treating only the problematic fraction, the system achieves high conversion efficiency while minimizing exposure of the lighter, more stable components to conditions that cause polymerization and catalyst deactivation.

Inventive Principle:
Principle #2Taking out (Extraction)

3Manufacturing precision

If selective hydrogenation is performed to preserve mono-alkenes, then octane rating is maintained, but di-alkene and alkyne removal efficiency decreases

Engineering Contradiction:
Improveoctane ratingVSAvoiddi-alkene and alkyne removal efficiency
Core Design Contradiction:
Manufacturing precisionVSProductivity

Solution Approach 1:

The naphtha feed is segmented into lighter (C5-C7) and heavier (C7+) streams. The heavier stream, which contains the majority of di-alkenes and alkynes, is directed to the hydrogenation reaction zone for intensive treatment. This segmentation allows aggressive hydrogenation conditions to be applied where needed (heavier stream) while preserving mono-alkenes in the lighter stream, thereby maintaining both high di-alkene removal efficiency and octane rating.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

Intensive hydrogenation conditions are applied locally to the heavier naphtha stream in the reaction zone, while the lighter stream receives milder conditions or bypasses the zone entirely. This local quality approach ensures high di-alkene and alkyne removal efficiency in the heavier fraction without causing excessive mono-alkene saturation, thus maintaining overall octane rating while achieving effective contaminant removal.

Inventive Principle:
Principle #3Local quality

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

This approach effectively reduces di-alkene conversion to mono-alkenes, preserving the octane rating and extending catalyst life by minimizing polymerization and saturation, thereby producing a high-grade fuel that meets stringent sulfur and nitrogen limits.

Implementation Method 1

a fractionation column for producing a lighter naphtha stream at a lighter outlet and a heavy naphtha stream at a second outlet at a location in the column below the lighter outlet

Methodology Applied
Scientific EffectFractionation: Fractionation

Implementation Method 2

A selective hydrogenation reactor is typically provided upstream of a hydrodesulfurization reactor to remove di-alkenes and alkynes

Methodology Applied
Scientific EffectCatalysis: Catalysis

Implementation Method 3

selective hydrogenation of di-alkenes and alkynes without saturating mono-alkenes

Methodology Applied
Scientific EffectHydrogenation: Hydrogenation

Data Source

PatentUS9393538B2Process and apparatus for selectively hydrogenating naphtha
Publication Date: 2016.07.19 UOP LLC
  • US9393538B2 patent drawing
  • US9393538B2 patent drawing
  • US9393538B2 patent drawing

AI summary

The process and apparatus of the present invention selectively hydrogenates a heavier olefinic naphtha stream in an upstream catalyst bed and the hydrogenated effluent and a lighter olefinic naphtha stream in a downstream catalyst bed. The heavier di-alkenes are less re-active and are contacted with more hydrogenation catalyst than the lighter di-alkenes which are more re-active.