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Ultrathin Membranes Promise Energy Savings in Hydrocarbon Processing

🌍 Phys.org Materials3D PrintingThu, 18 Jun 2026 18:40:08 GMT· edited
Ultrathin Membranes Promise Energy Savings in Hydrocarbon Processing

International researchers have developed novel ultrathin polymer membranes capable of efficiently separating complex hydrocarbon mixtures, potentially revolutionizing crude oil refining and significantly reducing energy consumption.

A team of international researchers has engineered a new class of ultrathin polymer membranes designed to rapidly and selectively separate complex hydrocarbon mixtures. This development holds the potential to transform crude oil refining and the processing of refinery streams, offering substantial energy savings for one of the world's most energy-intensive industrial processes.

The breakthrough, detailed in the study "Ultrathin polymer membranes with locked intrinsic microporosity for hydrocarbon fractionation," introduces a novel method for creating the separating layers within polymer membranes. The key innovation lies in the controlled addition of a cross-linking agent to the polymer during membrane fabrication, resulting in a scalable technology that achieves unprecedented efficiency in separating organic mixtures into valuable fractions. These membranes uniquely combine high molecular selectivity with rapid liquid transport, a long-sought goal in the field.

Conventional crude oil refining primarily uses thermal distillation, a process known for its high energy demands and significant contribution to global energy use. While membrane technologies have been explored as a more energy-efficient alternative, their widespread industrial adoption has been hindered by material limitations. This new membrane technology addresses these challenges by stabilizing the nanoscale pores of polymers of intrinsic microporosity (PLIMs) when exposed to hydrocarbons. Typically, these polymers swell in hydrocarbons, causing pore expansion and loss of selectivity. The researchers' in-situ cross-linking approach effectively "locks" the pores in their optimal configuration, preserving their separation capabilities while facilitating fast flow.

Utilizing quasi-elastic neutron scattering to study polymer chain dynamics, the team confirmed the molecular mechanisms behind this pore stabilization. When tested with synthetic crude oil, the PLIM membranes demonstrated up to a tenfold increase in permeance compared to current leading membranes, while maintaining high selectivity and the ability to differentiate between hydrocarbon molecules with minimal size differences. Similar high performance was observed with real Arabian Extra Light crude oil and refinery streams like virgin naphtha, efficiently separating lighter hydrocarbons from heavier fractions.

Crucially, the researchers have demonstrated the scalability of this membrane technology, producing sheets over a meter wide using roll-to-roll processing and integrating them into standard industrial membrane modules. Long-term testing over 30 days of continuous operation confirmed stable performance, indicating strong potential for industrial deployment. This advancement could lead to significant energy reductions in refining processes, even as the global energy system transitions towards lower-carbon alternatives.

Editor's Analysis — through the multi-planetary lens

This development represents a significant leap in membrane separation technology for hydrocarbon processing. By overcoming the traditional trade-off between selectivity and flux, and enabling scalable production, these PLIM membranes offer a viable, energy-efficient alternative to thermal distillation. This aligns with the broader additive manufacturing push towards high-performance materials and processes that reduce energy intensity and improve efficiency in critical industrial sectors.

Original headline: Ultrathin membranes could transform hydrocarbon processing by slashing energy use
Read the full story at Phys.org Materials →

Edited by the news editor with AI from the original report — please refer to the original source.

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