Mesoporous FCC Catalyst Using Sodium Silicate Matrix

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Solution Overview

Problem

Conventional mesoporous FCC catalysts are expensive to produce and can affect zeolite synthesis due to their acidic nature, leading to undesirable coke formation and reduced hydrocarbon product yields in fluidized catalytic cracking operations.

Innovation Solution

A catalytic cracking catalyst comprising an amorphous, porous matrix with specific pore distribution and a zeolite component, produced through a method involving a combination of molecular sieve, aluminum hydroxide, clay, urea, and alkaline silicate, followed by ion exchange and calcination, to minimize coke formation and enhance hydrocarbon production.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Productivity

If conventional mesoporous silica-alumina matrix is used in FCC catalyst, then feedstock conversion to high value hydrocarbon products is improved, but production cost increases and zeolite synthesis is adversely affected

Engineering Contradiction:
Improvefeedstock conversion to hydrocarbon productsVSAvoidcatalyst production cost
Core Design Contradiction:
ProductivityVSEase of manufacture

Solution Approach 1:

The patent replaces expensive conventional silica-alumina sols with inexpensive water glass (sodium silicate) as the matrix precursor. Water glass is a cheap, commercially available material that forms the desired mesoporous matrix structure without the high cost associated with traditional silica sol-based catalysts, directly addressing the production cost issue while maintaining catalytic performance

Inventive Principle:
Principle #27Cheap short-living objects (Disposable)

Solution Approach 2:

The patent changes the chemical composition parameters of the matrix by using water glass (sodium silicate) instead of conventional silica-alumina sols. This parameter change fundamentally alters the matrix chemistry to be less acidic and more compatible with zeolite synthesis, while still achieving the required mesoporous structure and catalytic activity through controlled formation processes

Inventive Principle:
Principle #35Parameter changes

2Shape

If conventional acidic silica sols are used to form mesoporous matrix, then mesoporous structure is achieved, but catalytic constituents such as zeolite are adversely affected

Engineering Contradiction:
Improvemesoporous matrix structureVSAvoidzeolite synthesis stability
Core Design Contradiction:
ShapeVSReliability

Solution Approach 1:

The patent substitutes expensive and problematic acidic silica-alumina sols with inexpensive water glass (sodium silicate). Water glass provides the necessary mesoporous matrix formation capabilities without the adverse acidic effects that damage zeolite structures, thereby protecting catalytic constituents while achieving the desired matrix morphology

Inventive Principle:
Principle #27Cheap short-living objects (Disposable)

Solution Approach 2:

The patent fundamentally changes the chemical parameters of the matrix precursor from acidic silica-alumina sols to alkaline/neutral water glass (sodium silicate). This parameter change eliminates the harmful acidity that adversely affects zeolite synthesis and stability, while still enabling mesoporous structure formation through alternative mechanisms such as evaporation-induced self-assembly or controlled precipitation

Inventive Principle:
Principle #35Parameter changes

3Reliability

If conventional FCC catalyst is used, then catalytic activity is maintained, but coke formation increases and hydrocarbon product yield decreases

Engineering Contradiction:
Improvecatalytic activityVSAvoidhydrocarbon product yield
Core Design Contradiction:
ReliabilityVSLoss of substance

Solution Approach 1:

The patent changes the chemical composition and acid-base properties of the catalyst matrix by using water glass instead of conventional silica-alumina sols. This parameter change modifies the catalyst's coke-forming tendency and product selectivity, leading to reduced coke formation and improved hydrocarbon product yields while maintaining necessary catalytic activity through optimized matrix structure and zeolite interactions

Inventive Principle:
Principle #35Parameter changes

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

The solution results in a catalyst that selectively produces more hydrocarbon products with lower coke yields, improved attrition resistance, and reduced production costs, while maintaining effective catalytic performance.

Implementation Method 1

a catalytic cracking catalyst comprising an amorphous, porous matrix with specific pore distribution

Methodology Applied
Scientific EffectAdsorption: Adsorption

Implementation Method 2

produced through a method involving a combination of molecular sieve, aluminum hydroxide, clay, urea, and alkaline silicate, followed by ion exchange and calcination

Methodology Applied
Scientific EffectIon exchange: Ion Exchange

Implementation Method 3

followed by ion exchange and calcination

Methodology Applied
Scientific EffectCalcination: Heat Treatment

Implementation Method 4

catalytic cracking catalyst comprising an amorphous, porous matrix with specific pore distribution and a zeolite component

Methodology Applied
Scientific EffectCatalysis: Catalysis

Data Source

PatentUS7504021B2FCC process using mesoporous catalyst
Publication Date: 2009.03.17 EXXONMOBIL TECHNOLOGY & ENGINEERING CO
  • US7504021B2 patent drawing
  • US7504021B2 patent drawing
  • US7504021B2 patent drawing

AI summary

This invention relates to a FCC process using a mesoporous catalytic cracking catalyst. The mesoporous fluidized catalytic cracking catalyst is selective for minimizing the production of coke and light gas. The catalyst comprises at least one amorphous, porous matrix, each matrix having pores ranging in diameter from about 1 Å to about 10 Å and pores ranging in diameter from about 40 Å to about 500 Å, wherein in the pore range from 50 Å to 250 Å, there is a single maximum in differential pore volume distribution over the 50 Å to 250 Å range.