György Tibor Balogh

Dr. György Tibor Balogh

1. Department of Chemical and Environmental Process Engineering, Budapest University of Technology and Economics, Műegyetem Quay 3, H-1111 Budapest, Hungary
+1

Research Focus & Metrics

Academic Career Length

28Years (1999-Present)

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

Representative Publications

View All Publications
1 April 2012 in European Journal of Pharmaceutical Sciences
Verified
Journal Article
Closed access
BSBálint Sinkó
Bálint Sinkó
TGTeresa M Garrigues
Teresa M Garrigues
György Tibor BaloghGyörgy Tibor Balogh
György Tibor Balogh
ZNZsombor K. Nagy
Zsombor K. Nagy
OTOksana Tsinman
Oksana Tsinman
KTKrisztina Takács-Novák
Krisztina Takács-Novák

16 August 2017 in ChemSusChem
Verified
Journal Article
Open access
PDF file
TFTamas Fodi
Tamas Fodi
CDChristos Didaskalou
Christos Didaskalou
Jozsef KupaiJozsef Kupai
Jozsef Kupai
György Tibor BaloghGyörgy Tibor Balogh
György Tibor Balogh
Peter HuszthyPeter Huszthy
Peter Huszthy
G SG S
G S
Solvent usage in the pharmaceutical sector accounts for as much as 90 % of the overall mass during manufacturing processes. Consequently, solvent consumption poses significant costs and environmental burdens. Continuous processing, in particular continuous‐flow reactors, have great potential for the sustainable production of pharmaceuticals but subsequent downstream processing remains challenging. Separation processes for concentrating and purifying chemicals can account for as much as 80 % of the total manufacturing costs. In this work, a nanofiltration unit was coupled to a continuous‐flow rector for in situ solvent and reagent recycling. The nanofiltration unit is straightforward to implement and simple to control during continuous operation. The hybrid process operated continuously over six weeks, recycling about 90 % of the solvent and reagent. Consequently, the E‐factor and the carbon footprint were reduced by 91 % and 19 %, respectively. Moreover, the nanofiltration unit led to a solution of the product eleven times more concentrated than the reaction mixture and increased the purity from 52.4 % to 91.5 %. The boundaries for process conditions were investigated to facilitate implementation of the methodology by the pharmaceutical sector.

27 September 2016 in Molecular Pharmaceutics
Verified
Journal Article
Closed access
EBEnikő Borbás
Enikő Borbás
BSBálint Sinkó
Bálint Sinkó
OTOksana Tsinman
Oksana Tsinman
KTKonstantin Tsinman
Konstantin Tsinman
ÉKÉva Kiserdei
Éva Kiserdei
ZNZsombor Kristóf Nagy
Zsombor Kristóf Nagy

1 August 2015 in International Journal of Pharmaceutics
Verified
Journal Article
Closed access
EBEnikő Borbás
Enikő Borbás
ABAttila Balogh
Attila Balogh
KBKatalin Bocz
Katalin Bocz
JMJudit Müller
Judit Müller
ÉKÉva Kiserdei
Éva Kiserdei
ZNZsombor Kristóf Nagy
Zsombor Kristóf Nagy

1 February 2003 in Archives of Biochemistry and Biophysics
Verified
Journal Article
Closed access
György Tibor BaloghGyörgy Tibor Balogh
György Tibor Balogh
JIJános Illés
János Illés
ZSZsuzsanna Székely
Zsuzsanna Székely
EFErika Forrai
Erika Forrai
AGAnikó Gere
Anikó Gere

8 April 2013 in Journal of Natural Products
Verified
Journal Article
Closed access
ÁKÁrpád Könczöl
Árpád Könczöl
JMJudit Müller
Judit Müller
EFEmília Földes
Emília Földes
ZBZoltán Béni
Zoltán Béni
KVKrisztina Végh
Krisztina Végh
György Tibor BaloghGyörgy Tibor Balogh
György Tibor Balogh