Nitric Acid Tail Gas Pre-heating for N2O Abatement

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Solution Overview

Problem

Existing methods for tertiary and quaternary abatement of NOx and N2O from nitric acid process tail gases are ineffective at temperatures below 400°C due to low catalytic activity of iron-loaded zeolite catalysts, resulting in substantial N2O and NOx emissions exceeding regulatory limits.

Innovation Solution

A process that pre-heats the tail gas to temperatures above 400°C using indirect heat exchange with conditioned gas from exothermic abatement stages, enhancing the catalytic activity of iron-loaded zeolite catalysts for significant N2O decomposition and NOx reduction, with optional use of vanadium or copper zeolite catalysts for NOx reduction, and configuring deN2O and deNOx stages in separate or combined catalytic beds for optimal performance.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Temperature

If iron-loaded zeolite catalyst is used for N2O decomposition at temperatures below 400°C, then the process can operate at lower temperatures, but the catalytic activity is too low to achieve substantial N2O abatement

Engineering Contradiction:
Improveoperating temperatureVSAvoidN2O decomposition rate
Core Design Contradiction:
TemperatureVSProductivity

Solution Approach 1:

The invention applies preliminary heating of the tail gas to at least 400°C using a heat exchanger before the gas enters the catalytic bed. This pre-heating action ensures that the catalyst operates at its optimal temperature range for N2O decomposition, achieving over 90% abatement efficiency. The heat exchanger recovers heat from the hot conditioned gas downstream to pre-heat the incoming tail gas, eliminating the need for external energy input.

Inventive Principle:
Principle #10Preliminary action

2Device complexity

If deN2O and deNOx stages are performed without intermediate heat exchange, then the process is simpler, but the iron-loaded zeolite catalyst cannot achieve substantial N2O abatement due to low catalytic activity

Engineering Contradiction:
Improveprocess complexityVSAvoidN2O decomposition efficiency
Core Design Contradiction:
Device complexityVSProductivity

Solution Approach 1:

The invention merges the deN2O and deNOx stages into a single integrated process where both catalytic reactions occur in sequence within the same system. The tail gas passes through a catalytic bed containing both N2O decomposition catalyst (iron-loaded zeolite) and NOx reduction catalyst (copper-loaded zeolite or vanadium-based catalyst). This combined approach allows efficient abatement of both N2O and NOx while recovering heat from the exothermic reactions to maintain catalyst temperature.

Inventive Principle:
Principle #5Merging (Combining)

3Loss of energy

If tail gas is expanded before abatement, then energy recovery is optimized, but abatement must be performed at lower temperatures where catalysts are less effective

Engineering Contradiction:
Improveenergy recovery efficiencyVSAvoidabatement temperature
Core Design Contradiction:
Loss of energyVSTemperature

Solution Approach 1:

The invention performs preliminary heating of the tail gas to at least 400°C before it enters the catalytic abatement stage. This ensures that even after expansion which reduces temperature, the gas maintains sufficient temperature for effective catalytic activity. The heat exchanger recovers heat from the hot conditioned gas to pre-heat the incoming expanded tail gas, ensuring optimal catalytic conditions are achieved without requiring additional external energy input.

Inventive Principle:
Principle #10Preliminary action

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

Achieves substantial decomposition of N2O and NOx, meeting stringent emission limits without external energy input, reducing residual ammonia levels, and allowing for efficient energy recovery through heat exchange, thereby modernizing nitric acid plants to comply with environmental regulations.

Implementation Method 1

catalytic decomposition of N2O over an iron-loaded zeolite

Methodology Applied
Scientific EffectCatalysis: Catalysis

Implementation Method 2

catalytic reduction of NOx with a suitable reducing agent, typically ammonia

Methodology Applied
Scientific EffectCatalytic reduction: Catalysis

Implementation Method 3

pre-heated to a temperature of at least 400° C. by indirect heat exchange with at least a portion of said conditioned gas

Methodology Applied
Scientific EffectHeat exchange: Heat Exchanger

Implementation Method 4

indirect heat exchange with at least a portion of said conditioned gas

Methodology Applied
Scientific EffectExothermic reaction: Exothermic Reaction

Data Source

PatentUS11925900B2Process for reducing the content of NOx and N2O from a tail gas of a nitric acid process
Publication Date: 2024.03.12 CASALE SA
  • US11925900B2 patent drawing

AI summary

Process for reducing the content of NOx and N2O from an input tail gas of a nitric acid process, said input tail gas having a temperature lower than 400° C., the process comprising an abatement stage at least including a deN2O stage and deNOx stage and providing a conditioned tail gas having a temperature greater than the input tail gas, wherein, prior to submission to said abatement stage, said input tail gas is pre-heated to a temperature of at least 400° C. by indirect heat exchange with at least a portion of said conditioned gas.