A two-stage hydrogenation route removes residual hydrogen from aromatic fractions while limiting monocyclic aromatic loss and downstream cavitation issues.
Substituted stilbene ligands stabilize Ni(0) complexes in air, enabling open-flask handling and strong catalytic activity across organic reactions.
Quinone methides and phenylene diamines help high-temperature ethylene fractionation trains suppress polymerization, gum formation, and fouling.
Bio-based triglycerides are converted into linear alkylbenzenes through selective cracking and catalytic upgrading to maximize C9-C14 yield and biodegradability.
A sub-100 μm fouling inhibitor changes polymer morphology in oligomerizing reactors, reducing deposition and downtime while supporting linear alpha olefin yield.
Natural oils become linear alkylbenzenes through hydrogen recycling and heat integration, reducing energy use and fossil feedstock reliance.
Series-connected reactors divide chlorination stages, controlling gas velocity and removing hydrogen chloride to prevent foaming and preserve reactivity.