Corrosion inhibitor for sulfur-containing wet gas pipeline and preparation method thereof
A technology for transportation pipelines and corrosion inhibitors, which is applied in the field of corrosion inhibitors and preparations for sulfur-containing wet gas transportation pipelines, can solve the problems of poor corrosion inhibition effects and limited protection effects, and achieve increased protection area, low cost, and long-term effect
- Summary
- Abstract
- Description
- Claims
- Application Information
AI Technical Summary
Problems solved by technology
Method used
Image
Examples
preparation example Construction
[0025] The preparation method of the intermediate product is as follows: add lauric acid and tetraethylenepentamine reaction materials into the reactor and react at 150±5°C for 3h, then raise the temperature to 230°C for 2h, then use sodium chloroacetate / alkali as a catalyst, and react at 180°C Stir at ±5°C for catalytic reaction for 1 to 1.5 hours, and cool to room temperature to obtain the intermediate product.
[0026] A preparation method for a corrosion inhibitor for a sulfur-containing wet gas pipeline, comprising the following steps:
[0027] Step 1: Add lauric acid and tetraethylenepentamine to the reactor according to the mass ratio of 1: (1~2), react at 150±5°C for 3h, then raise the temperature to 230°C for 2h, and then use sodium chloroacetate / alkali As a catalyst, stir the catalytic reaction at 180±5°C for 1-1.5 hours, then cool to room temperature to obtain the intermediate product;
[0028] Step 2: React 35-50 parts of intermediate product with 3.2-4.8 parts of...
Embodiment 1
[0032] On the three-neck flask equipped with water separator, reflux condenser and stirrer, add lauric acid and tetraethylenepentamine reaction materials into the reactor at a mass ratio of 1:1.05, and react at (150±5)°C for 3 hours. Rapidly raise the temperature to 230°C for 2 hours of reaction. During the reaction, water will continue to distill out. After dehydration at high temperature, use sodium chloroacetate / alkali as a catalyst, stir at 180±5°C for 1 hour of catalytic reaction, and cool to room temperature to obtain intermediate product.
[0033] The mass parts were 35 parts of intermediate product and 4.8 parts of thiourea were reacted at (150±5)°C for 3 hours, then 2.4 parts of triethanolamine phosphate and 1.2 parts of phosphorous acid were added for phosphating for 1 hour, and then the temperature was lowered to (50±5)°C and added Fully dissolved in 60 parts of water, cooled to normal temperature to obtain imidazolylphosphine corrosion inhibitor. Using n-octane to...
Embodiment 2
[0035] On the three-neck flask equipped with water separator, reflux condenser and stirrer, add lauric acid and tetraethylenepentamine reaction materials into the reactor at a mass ratio of 1:1.2, and react at (150±5)°C for 4 hours. Rapidly raise the temperature to 230°C for 2 hours of reaction. During the reaction, water will continue to distill out. After high temperature dehydration, use sodium chloroacetate / alkali as a catalyst, stir at 180±5°C for 1.5 hours, and cool to room temperature to obtain mid product.
[0036]The mass parts are 50 parts of the intermediate product and 3.2 parts of thiourea to react at (150±5)°C for 4 hours, then add 1.2 parts of triethanolamine phosphate and 2.4 parts of phosphorous acid for 2 hours, then cool down to (50±5)°C and add Fully dissolve 40 parts of water, cool down to (50±5)°C, add 50 parts of water to fully dissolve, cool to normal temperature to obtain imidazolylphos corrosion inhibitor. Using n-octane to simulate the influence of ...
PUM
Abstract
Description
Claims
Application Information
- R&D Engineer
- R&D Manager
- IP Professional
- Industry Leading Data Capabilities
- Powerful AI technology
- Patent DNA Extraction
Browse by: Latest US Patents, China's latest patents, Technical Efficacy Thesaurus, Application Domain, Technology Topic, Popular Technical Reports.
© 2024 PatSnap. All rights reserved.Legal|Privacy policy|Modern Slavery Act Transparency Statement|Sitemap|About US| Contact US: help@patsnap.com