Selective fixed-bed fractionation of stilbene subfamilies from grape cane waste using a pyridine-amide adsorbent

The selective separation of structurally analogous polyphenols from complex plant matrices remains a longstanding challenge in bioseparation engineering. This study introduces a custom-designed adsorbent, poly(2,6-bis(acrylamido)pyridine) (poly(BAAPy)), tailored for subfamily-level resolution of stilbenes obtained from crude grape cane extracts. Leveraging dual amide and pyridine functionalities, poly(BAAPy) achieves selective retention of oligomeric stilbenes (e.g., trans-ε-viniferin, miyabenol C) via multivalent hydrogen bonding and π-π stacking interactions. Comparative breakthrough experiments against commercial poly(4-vinylpyridine) (poly(4VP)) demonstrate superior oligomer retention across both ethanol-water and acetonitrile systems. In dynamic closed-loop adsorption mode, poly(BAAPy) enabled polarity-driven elution and achieved up to a 3.4-fold enrichment of stilbene oligomers, with their recovery in fractions containing ≥ 90% oligomeric content in a single desorption cycle. Uptake profiles and adsorption selectivity coefficients confirmed poly(BAAPy)’s preference for oligomers under both ethanol-water and acetonitrile conditions. The total stilbene recovery was 75%. Breakthrough data were fitted using both empirical (Clark, Thomas) and mechanistic models, revealing distinct adsorption dynamics for poly(BAAPy) versus a commercial poly(4VP) resin. This work demonstrates a sustainable valorisation route for grape cane waste, converting viticultural residues into a high-value source of bioactive compounds. The use of green solvents and fixed-bed adsorption aligns with circular economy principles and environmentally conscious separation processes. • A novel poly(2,6-bis(acrylamido)pyridine) adsorbent was developed for stilbene purification. • Subfamily-selective retention and fractionation of oligomeric stilbenes was demonstrated • Multivalent hydrogen bonding and π–π stacking interactions ground the adsorbent performance • Total stilbene recovery of 75%, subfamily purities ≥ 90%, and enrichment factors exceeding 3.4 achieved in a single desorption cycle • Sustainable valorization route for viticultural residues into a high-value source of bioactive compounds is demonstrated

Authors

Institutions

Publication Details

Journal
Journal of environmental chemical engineering
Published
2026-02-12
DOI
https://doi.org/10.1016/j.jece.2026.121773
Primary Topic
Enzyme Catalysis and Immobilization
Type
article
Field-Weighted Citation Impact
0.00
Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Selective fixed-bed fractionation of stilbene subfamilies from grape cane waste using a pyridine-amide adsorbent

Amir Bzainia, Erik Keller, Mário Rui P.F.N. Costa, André Heeres et al.
Journal of environmental chemical engineering
Enzyme Catalysis and Immobilization
article

Selective fixed-bed fractionation of stilbene subfamilies from grape cane waste using a pyridine-amide adsorbent

Amir Bzainia, Erik Keller, Mário Rui P.F.N. Costa, André Heeres, Rolando C.S. Dias
article en

Abstract

The selective separation of structurally analogous polyphenols from complex plant matrices remains a longstanding challenge in bioseparation engineering. This study introduces a custom-designed adsorbent, poly(2,6-bis(acrylamido)pyridine) (poly(BAAPy)), tailored for subfamily-level resolution of stilbenes obtained from crude grape cane extracts. Leveraging dual amide and pyridine functionalities, poly(BAAPy) achieves selective retention of oligomeric stilbenes (e.g., trans-ε-viniferin, miyabenol C) via multivalent hydrogen bonding and π-π stacking interactions. Comparative breakthrough experiments against commercial poly(4-vinylpyridine) (poly(4VP)) demonstrate superior oligomer retention across both ethanol-water and acetonitrile systems. In dynamic closed-loop adsorption mode, poly(BAAPy) enabled polarity-driven elution and achieved up to a 3.4-fold enrichment of stilbene oligomers, with their recovery in fractions containing ≥ 90% oligomeric content in a single desorption cycle. Uptake profiles and adsorption selectivity coefficients confirmed poly(BAAPy)’s preference for oligomers under both ethanol-water and acetonitrile conditions. The total stilbene recovery was 75%. Breakthrough data were fitted using both empirical (Clark, Thomas) and mechanistic models, revealing distinct adsorption dynamics for poly(BAAPy) versus a commercial poly(4VP) resin. This work demonstrates a sustainable valorisation route for grape cane waste, converting viticultural residues into a high-value source of bioactive compounds. The use of green solvents and fixed-bed adsorption aligns with circular economy principles and environmentally conscious separation processes. • A novel poly(2,6-bis(acrylamido)pyridine) adsorbent was developed for stilbene purification. • Subfamily-selective retention and fractionation of oligomeric stilbenes was demonstrated • Multivalent hydrogen bonding and π–π stacking interactions ground the adsorbent performance • Total stilbene recovery of 75%, subfamily purities ≥ 90%, and enrichment factors exceeding 3.4 achieved in a single desorption cycle • Sustainable valorization route for viticultural residues into a high-value source of bioactive compounds is demonstrated

Journal of environmental chemical engineeringVol. 14(2)
Hanze University of Applied Sciences (NL), Universidade do Porto (PT), Universidade Politécnica de Bragança (PT)
Responsible consumption and production
Openalex Percentile: Top 59%
Enzyme Catalysis and Immobilization
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.