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      Functionalized Superparamagnetic Iron Oxide Nanoparticles as a Sustainable Approach for Gas Hydrate Control

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      ACS Omega
      American Chemical Society

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          Abstract

          Gas hydrate blockage in multiphase flow lines is a critical issue in upstream operations. One method to prevent this from happening is by the use of kinetic hydrate inhibitors (KHIs). KHIs are polymers containing tailored amphiphilic groups. These polymers often have limited marine biodegradability, and their recovery and recycling to reduce operational costs remain a challenge. A novel approach involves attaching KHIs to magnetic nanoparticles, enabling recovery and recycling without environmental discharge. We have developed superparamagnetic iron oxide nanoparticles (SPIONs) reacted first with vinyltrimethoxysilane (VTMS) and then coated with N-vinylpyrrolidone/ N-vinyl caprolactam (VP/VCap) copolymer chains using radical polymerization of the VP and VCap monomers (SPIONs-VTMS-VPVCap). These nanoparticles are stable in aqueous solutions with a particle size of 10 nm and a dispersion size of 205 nm. High-pressure tests demonstrated that SPIONs-VTMS-VPVCap performed comparably to the free VP/VCap copolymer, achieving a hydrate formation onset temperature ( T o) of 12.9 °C at 5000 ppm. Significantly, the magnetic KHIs were successfully recovered and reused multiple times without performance loss. The solution exhibited a high cloud point (80 °C) and compatibility with n-butyl glycol ether (BGE), enhancing the performance. Adding 5000 ppm of BGE lowered the hydrate formation T o to 7.3 °C, a 9.7 °C improvement compared to no additive. These results establish a proof of concept for recyclable magnetic KHIs, offering a sustainable solution to eliminate chemical discharge in marine environments while maintaining effective hydrate inhibition.

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          Spreading of nanofluids on solids.

          Suspensions of nanometre-sized particles (nanofluids) are used in a variety of technological contexts. For example, their spreading and adhesion behaviour on solid surfaces can yield materials with desirable structural and optical properties. Similarly, the spreading behaviour of nanofluids containing surfactant micelles has implications for soil remediation, oily soil removal, lubrication and enhanced oil recovery. But the well-established concepts of spreading and adhesion of simple liquids do not apply to nanofluids. Theoretical investigations have suggested that a solid-like ordering of suspended spheres will occur in the confined three-phase contact region at the edge of the spreading fluid, becoming more disordered and fluid-like towards the bulk phase. Calculations have also suggested that the pressure arising from such colloidal ordering in the confined region will enhance the spreading behaviour of nanofluids. Here we use video microscopy to demonstrate both the two-dimensional crystal-like ordering of charged nanometre-sized polystyrene spheres in water, and the enhanced spreading dynamics of a micellar fluid, at the three-phase contact region. Our findings suggest a new mechanism for oily soil removal--detergency.
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            History of the Development of Low Dosage Hydrate Inhibitors

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              • Book Chapter: not found

              1. The power of databases: The RRUFF project

                Author and article information

                Journal
                ACS Omega
                ACS Omega
                ao
                acsodf
                ACS Omega
                American Chemical Society
                2470-1343
                22 May 2025
                03 June 2025
                : 10
                : 21
                : 21951-21962
                Affiliations
                [] deptDepartment of Chemistry, Bioscience and Environmental Engineering, Faculty of Science and Technology , Ringgold source:pplus56627, University of Stavanger; , Stavanger N-4036, Norway
                [] deptDepartment of Chemistry and Earth Sciences, College of Arts and Sciences , Ringgold source:pplus61780, Qatar University; , 2713 Doha, Qatar
                Author notes
                Author information
                https://orcid.org/0000-0002-1711-5862
                https://orcid.org/0000-0003-2295-5804
                https://orcid.org/0000-0002-4636-0066
                Article
                10.1021/acsomega.5c01960
                12138677
                a9ec619c-faca-4277-b00e-08730ff65228
                © 2025 The Authors. Published by American Chemical Society

                This article is licensed under CC-BY 4.0

                History
                : 03 March 2025
                : 19 May 2025
                : 15 May 2025
                : 22 May 2025
                Funding
                Funded by: Norges Forskningsr?d, doi open-funder-registry10.13039/open_funder_registry10.13039/501100005416;
                Award ID: 300754
                Categories
                Article
                Custom metadata
                ao5c01960
                ao5c01960
                3
                acs-titles
                dates-used-rcd-rvd-acc
                fe0160b152ceecaa5b5311ef3536ecbbacc79225ab9130ee3de602da2ba1c522

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