Chong Yang Du
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Chong Yang Du has a total of 15 co-authors. Here are the top co-authors by number of shared publications:
- Milan Marić
Department of Chemical Engineering, McGill University, Montréal, QC H3A 0C5, Canada
5 shared publications - Phillip Servio
Department of Chemical Engineering, McGill University, Montréal, QC H3A 0C5, Canada
5 shared publications - Adam McElligott
Department of Mechanical Engineering and Maritime Studies, University of Western Norway, Inndalsveien 28, 5063 Bergen, Norway
4 shared publications - André Guerra
Department of Chemical Engineering, McGill University, Montréal, QC H3A 0C5, Canada
4 shared publications Alejandro Rey
Department of Chemical Engineering, McGill University, Montreal H3A 0C5, Quebec, Canada
2 shared publicationsAlejandro D. Rey
Department of Chemical Engineering, McGill University, Montreal, QuebecH3A 0C5, Canada
1 shared publication
Latest Publications
- Open Access
Evaluation of Acrylamide/α-Lipoic Acid Statistical Copolymers as Degradable Water-Soluble Kinetic Gas Hydrate Inhibitors
Readily degradable low-dose hydrate inhibitors are of great significance for flow assurance in the petroleum industry. Recently, α-lipoic acid (LA) was shown to undergo ring-opening reaction via reversible addition–fragmentation chain-transfer copolymerization with acrylamides to introduce labile disulfide bonds into the stable vinyl polymer backbone. Here, LA was copolymerized with acryloyl morpholine (AM) to evaluate their performance as kinetic hydrate inhibitors. Degradability was confirmed for the copolymers with 20 mol.% LA (AM/LA20, Mn = 19 → 9 kDa) after disulfide reduction. Thermogravimetric analysis also indicated faster thermal degradation of AM/LA due to the incorporation of weaker S-S and S-C linkages. Increasing LA content reduced hydrophilicity, and the copolymers were treated with NaOH to ensure water solubility. However, at 700 ppm, poly(AM) homopolymer reduced methane consumption during hydrate growth to 54% with respect to the uninhibited system, while gas consumption for the carboxylate AM/LA20 reached 78%. An advantageous feature of LA is its carboxylic acid, allowing desired functionalities to be grafted onto the degradable copolymer. Isopropyl amine (IPAm) was coupled with LA to form an amide known to be effective during hydrate inhibition (LA(IPAm)). The copolymer AM/LA(IPAm)20 demonstrated better water solubility compared to the original AM/LA20. Furthermore, the desirable IPAm functionality allowed the hydrate inhibition to be re-established at 54%, nearly recovering the performance of the poly(AM) homopolymer. This article assesses the application of LA and LA derivatives as building blocks for degradable amide-based kinetic hydrate inhibitors by validating their degradability with material characterizations and their inhibition performance during structure I hydrate growth.
Open AccessEvaluation of Acrylamide/α-Lipoic Acid Statistical Copolymers as Degradable Water-Soluble Kinetic Gas Hydrate Inhibitors
Readily degradable low-dose hydrate inhibitors are of great significance for flow assurance in the petroleum industry. Recently, α-lipoic acid (LA) was shown to undergo ring-opening reaction via reversible addition–fragmentation chain-transfer copolymerization with acrylamides to introduce labile disulfide bonds into the stable vinyl polymer backbone. Here, LA was copolymerized with acryloyl morpholine (AM) to evaluate their performance as kinetic hydrate inhibitors. Degradability was confirmed for the copolymers with 20 mol.% LA (AM/LA20, Mn = 19 → 9 kDa) after disulfide reduction. Thermogravimetric analysis also indicated faster thermal degradation of AM/LA due to the incorporation of weaker S-S and S-C linkages. Increasing LA content reduced hydrophilicity, and the copolymers were treated with NaOH to ensure water solubility. However, at 700 ppm, poly(AM) homopolymer reduced methane consumption during hydrate growth to 54% with respect to the uninhibited system, while gas consumption for the carboxylate AM/LA20 reached 78%. An advantageous feature of LA is its carboxylic acid, allowing desired functionalities to be grafted onto the degradable copolymer. Isopropyl amine (IPAm) was coupled with LA to form an amide known to be effective during hydrate inhibition (LA(IPAm)). The copolymer AM/LA(IPAm)20 demonstrated better water solubility compared to the original AM/LA20. Furthermore, the desirable IPAm functionality allowed the hydrate inhibition to be re-established at 54%, nearly recovering the performance of the poly(AM) homopolymer. This article assesses the application of LA and LA derivatives as building blocks for degradable amide-based kinetic hydrate inhibitors by validating their degradability with material characterizations and their inhibition performance during structure I hydrate growth.
- Open Access
- 12 May 2025
- Published by Elsevier in Chemical Engineering Journal Advances
- Vol. 23
Acryloyl piperidine/pyrrolidine statistical and block copolymers as hydrate inhibitors: effects of cloud point temperature and copolymer microstructure
- 12 May 2025
- Published by Elsevier in Chemical Engineering Journal Advances
- Vol. 23
Open AccessAcryloyl piperidine/pyrrolidine statistical and block copolymers as hydrate inhibitors: effects of cloud point temperature and copolymer microstructure
- 13 November 2023
- Published by Elsevier in Journal of Molecular Liquids
- Vol. 393
Non-Einsteinian viscosity reduction in boron nitride nanotube nanofluids
- 13 November 2023
- Published by Elsevier in Journal of Molecular Liquids
- Vol. 393
Non-Einsteinian viscosity reduction in boron nitride nanotube nanofluids
- 20 July 2023
- Published by American Chemical Society (ACS) in Industrial & Engineering Chemistry Research
- Vol. 62 (30) , 11795-11804
Effects of Poly(styrene/Pentafluorostyrene-block-vinylpyrrolidone) Amphiphilic Kinetic Hydrate Inhibitors on the Dynamic Viscosity of Methane Hydrate Systems at High-Pressure Driving Forces
- 20 July 2023
- Published by American Chemical Society (ACS) in Industrial & Engineering Chemistry Research
- Vol. 62 (30) , 11795-11804
Effects of Poly(styrene/Pentafluorostyrene-block-vinylpyrrolidone) Amphiphilic Kinetic Hydrate Inhibitors on the Dynamic Viscosity of Methane Hydrate Systems at High-Pressure Driving Forces
- 17 November 2022
- Published by American Chemical Society (ACS) in Energy & Fuels
- Vol. 36 (23) , 14163-14173
Effects of Poly(vinylpyrrolidone) on the Dynamic Viscosity of Methane Hydrate Systems at High-Pressure Driving Forces: Investigation of Concentration, Molecular Weight, and Shear Rate
- 17 November 2022
- Published by American Chemical Society (ACS) in Energy & Fuels
- Vol. 36 (23) , 14163-14173
Effects of Poly(vinylpyrrolidone) on the Dynamic Viscosity of Methane Hydrate Systems at High-Pressure Driving Forces: Investigation of Concentration, Molecular Weight, and Shear Rate
- 10 October 2022
- Published by American Chemical Society (ACS) in ACS Applied Energy Materials
- Vol. 5 (10) , 12977-12990
Non-Einsteinian Viscosity Behavior in Plasma-Functionalized Graphene Nanoflake Nanofluids and Their Effect on the Dynamic Viscosity of Methane Hydrate Systems
- 10 October 2022
- Published by American Chemical Society (ACS) in ACS Applied Energy Materials
- Vol. 5 (10) , 12977-12990
Non-Einsteinian Viscosity Behavior in Plasma-Functionalized Graphene Nanoflake Nanofluids and Their Effect on the Dynamic Viscosity of Methane Hydrate Systems
- 26 April 2012
- Published by SPIE-Intl Soc Optical Eng
- Vol. 8345, 83452X-83452X-8
The connection technology based on high temperature silica fiber optic sensor
The connection technology between silica Fiber Bragg Grating sensors (FBGs) and ultra-high temperature ceramic composites (UHTCs) is solved to measure the temperature and strain at the same time when the structural temperature higher than 500°C in this paper. A series experiments were carried out to compare the connection properties, and then the best adhesive was selected. A lot of attempts have been made to choose the best curing process. The experiments were carried out at 500°C, and results shown that the response wavelength and the heated temperature have positive linear relationship. The wavelength will increase 0.0096nm with the temperature rise 1°C, and 1με changes will induce the response wavelength increase 0.002nm. A feasible method for high temperature measuring based fiber Bragg grating was given in this study, and the results of this study can be used as an important reference data for hot structure the thermal protection systems designing.
- 26 April 2012
- Published by SPIE-Intl Soc Optical Eng
- Vol. 8345, 83452X-83452X-8
The connection technology based on high temperature silica fiber optic sensor
The connection technology between silica Fiber Bragg Grating sensors (FBGs) and ultra-high temperature ceramic composites (UHTCs) is solved to measure the temperature and strain at the same time when the structural temperature higher than 500°C in this paper. A series experiments were carried out to compare the connection properties, and then the best adhesive was selected. A lot of attempts have been made to choose the best curing process. The experiments were carried out at 500°C, and results shown that the response wavelength and the heated temperature have positive linear relationship. The wavelength will increase 0.0096nm with the temperature rise 1°C, and 1με changes will induce the response wavelength increase 0.002nm. A feasible method for high temperature measuring based fiber Bragg grating was given in this study, and the results of this study can be used as an important reference data for hot structure the thermal protection systems designing.