Ioulia Valla

Dr. Ioulia Valla

Chemical and Biomolecular Engineering, University of Connecticut, Storrs, CT 06269-3222, USA

Research Focus & Metrics

Academic Career Length

24Years (2003-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
5 September 2013 in ChemCatChem
Verified
Journal Article
Closed access
PDF file
KLKunhao Li
Kunhao Li
Ioulia VallaIoulia Valla
Ioulia Valla
JGJavier Garcia‐Martinez
Javier Garcia‐Martinez

11 January 2012 in Catalysis Science & Technology
Verified
Journal Article
Closed access
PDF file
JGJavier García-Martínez
Javier García-Martínez
MJMarvin Johnson
Marvin Johnson
Ioulia VallaIoulia Valla
Ioulia Valla
KLKunhao Li
Kunhao Li
Jackie Y. YingJackie Y. Ying
Jackie Y. Ying
Controlled mesoporosity is successfully introduced into zeolite Y crystals through a surfactant templating approach. The mesoporous zeolite shows superb hydrothermal stability in the resulting mesostructure, while retaining strong acidity. Fluid catalytic cracking catalysts made from the mesostructured Y zeolites demonstrate significant improvement in product selectivity as a result of reduced limitation in reactant and product diffusion.

1 February 2017 in Applied Catalysis B: Environment and Energy
Verified
Journal Article
Closed access
KLKevin X. Lee
Kevin X. Lee
Ioulia VallaIoulia Valla
Ioulia Valla

13 September 2013 in Green Chemistry
Verified
Journal Article
Closed access
PDF file
SDShoucheng Du
Shoucheng Du
Ioulia VallaIoulia Valla
Ioulia Valla
George M. BollasGeorge M. Bollas
George M. Bollas
Char and coke from biomass catalytic pyrolysis have different origins. They cannot be lumped as one since they occupy different locations on the catalyst surface and, thus, contribute differently to catalyst deactivation. In this study, catalyst (ZSM-5) deactivation in the perspective of comparison of char and coke from pyrolysis of different biomass types is investigated. Pine sawdust, glucose, and cellulose are used as feedstocks in the pyrolysis experiments. Biomass char and coke samples produced via slow and fast, thermal and catalytic pyrolysis are characterized with respect to their overall content, oxidation reactivity, catalyst surface area, pore size distribution changes, bonding groups and their effect on catalyst performance. In particular, it is shown that char forms as an external layer on the catalyst surface and in its macropores, whereas coke forms inside the zeolite micropores via hydrogen transfer and addition reactions. The catalyst effect on glucose and pine slow catalytic pyrolysis is minor compared with that on cellulose slow catalytic pyrolysis, due to macropore blocking by char formation. In fast catalytic pyrolysis, catalyst deactivation is mainly attributed to micropore blocking by coke formation. Char and coke are shown to coexist on the catalyst surface after fast catalytic experiments, with the char content after glucose fast catalytic pyrolysis being 30 wt% of the total solid residue. The origins of char and coke in the cellulose, hemicellulose and lignin components of pine are identified and mechanisms for their formation are proposed.

8 July 2019 in Reaction Chemistry & Engineering
Verified
Journal Article
Closed access
PDF file
KLKevin X. Lee
Kevin X. Lee
Ioulia VallaIoulia Valla
Ioulia Valla
Adsorptive desulfurization using modified Y zeolite is an efficient process for the removal of sulfur from transportation fuels.

1 March 2016 in Applied Catalysis A: General
Verified
Journal Article
Closed access
SDShoucheng Du
Shoucheng Du
DGDavid P. Gamliel
David P. Gamliel
MGMarcus V. Giotto
Marcus V. Giotto
Ioulia VallaIoulia Valla
Ioulia Valla
GBGeorge M. Bollas
George M. Bollas