María Dolores Gutiérrez-Álvarez
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
María Dolores Gutiérrez-Álvarez has a total of 101 co-authors. Here are the top co-authors by number of shared publications:
- Juan Jose Mangas Alonso
Area of Food Technology, SERIDA, Carretera de Oviedo S/N, 33300 Villaviciosa, Asturias, Spain
10 shared publications Domingo Blanco Gomis
Departamento de Quimica Fisica y Analitica, Universidad de Oviedo, Oviedo, Spain
8 shared publicationsEnrique Dapena de la Fuente
Servicio Regional de Investigacion y Desarrollo Agroalimentario (SERIDA), Carretera de Oviedo s/n, 33300, Villaviciosa, Spain
6 shared publications- Jaime González-Álvarez
Department of Physical and Analytical Chemistry, University of Oviedo, Julián Clavería 8, 33006 Oviedo, Spain
6 shared publications - Pilar Arias Abrodo
Department of Physical and Analytical Chemistry, University of Oviedo, Julián Clavería 8, 33006 Oviedo, Spain
6 shared publications Pilar Arias-Abrodo
Department of Physical and Analytical Chemistry, University of Oviedo, 33006 Oviedo, Spain
6 shared publications
Latest Publications
- Open Access
Polymeric Ionic Liquids Derived from L-Valine for the Preparation of Highly Selective Silica-Supported Stationary Phases in Gas Chromatography
A series of silica-supported polymeric ionic liquid (PIL)-based stationary phases derived from a vinylic L-valine ionic liquid monomer and divinylbenzene (DVB) as the crosslinking agent have been prepared and studied as gas chromatographic stationary phases. These coated gas chromatographic columns exhibited good thermal stabilities (230–300 °C) and high efficiencies (1700–2700 plates/m), and were characterized using a linear solvation parameter model in order to understand the effects of the amount of DVB on the features of the resulting composite systems. Their retention behavior and separation efficiencies were demonstrated using the Grob test. By tuning the crosslinking degree for the IL-derived stationary phase, the separation selectivity and resolution of different compounds were improved. The different retention behaviors observed for many analytes indicate that these stationary phases may be applicable as new types of GC stationary phases.
Open AccessPolymeric Ionic Liquids Derived from L-Valine for the Preparation of Highly Selective Silica-Supported Stationary Phases in Gas Chromatography
A series of silica-supported polymeric ionic liquid (PIL)-based stationary phases derived from a vinylic L-valine ionic liquid monomer and divinylbenzene (DVB) as the crosslinking agent have been prepared and studied as gas chromatographic stationary phases. These coated gas chromatographic columns exhibited good thermal stabilities (230–300 °C) and high efficiencies (1700–2700 plates/m), and were characterized using a linear solvation parameter model in order to understand the effects of the amount of DVB on the features of the resulting composite systems. Their retention behavior and separation efficiencies were demonstrated using the Grob test. By tuning the crosslinking degree for the IL-derived stationary phase, the separation selectivity and resolution of different compounds were improved. The different retention behaviors observed for many analytes indicate that these stationary phases may be applicable as new types of GC stationary phases.
- 1 March 2017
- Published by Springer Nature in Analytical and Bioanalytical Chemistry
- Vol. 409 (11) , 3033-3041
Determination of volatile compounds in cider apple juices using a covalently bonded ionic liquid coating as the stationary phase in gas chromatography
A chromatographic method for the separation of volatile compounds in Asturian cider apple juices has been developed. For this separation purpose, a monocationic imidazolium-based ionic liquid bearing a reactive terminal iodine atom was synthesized by a quaternization-anion exchange chemical sequence. Next, the gas chromatography (GC) stationary phase was prepared by covalently linking the imidazolium monolith to the reactive silanol groups of the inner capillary wall at 70 °C. This coated GC column exhibited good thermal stability (290 °C), as well as good efficiency (2000 plates/m) in the separation of volatile compounds from Asturian apple cider juices, and was characterized using the Abraham solvation parameter model. The intra-day and inter-day precision of the chromatographic method was evaluated, obtaining relative standard deviations from 3.7 to 12.9% and from 7.4 to 18.0%, respectively. Furthermore, recoveries from 82.5 to 122% were achieved. Covalent bonding of an ionic liquid to inner column wall led to a great improvement of the separation efficiencies of stationary phases in gas chromatography
- 1 March 2017
- Published by Springer Nature in Analytical and Bioanalytical Chemistry
- Vol. 409 (11) , 3033-3041
Determination of volatile compounds in cider apple juices using a covalently bonded ionic liquid coating as the stationary phase in gas chromatography
A chromatographic method for the separation of volatile compounds in Asturian cider apple juices has been developed. For this separation purpose, a monocationic imidazolium-based ionic liquid bearing a reactive terminal iodine atom was synthesized by a quaternization-anion exchange chemical sequence. Next, the gas chromatography (GC) stationary phase was prepared by covalently linking the imidazolium monolith to the reactive silanol groups of the inner capillary wall at 70 °C. This coated GC column exhibited good thermal stability (290 °C), as well as good efficiency (2000 plates/m) in the separation of volatile compounds from Asturian apple cider juices, and was characterized using the Abraham solvation parameter model. The intra-day and inter-day precision of the chromatographic method was evaluated, obtaining relative standard deviations from 3.7 to 12.9% and from 7.4 to 18.0%, respectively. Furthermore, recoveries from 82.5 to 122% were achieved. Covalent bonding of an ionic liquid to inner column wall led to a great improvement of the separation efficiencies of stationary phases in gas chromatography
- 24 May 2016
- Published by Springer Nature in Food Analytical Methods
- Vol. 9 (12) , 3492-3500
Characterization of Volatile Compounds in New Cider Apple Genotypes Using Multivariate Analysis
- 24 May 2016
- Published by Springer Nature in Food Analytical Methods
- Vol. 9 (12) , 3492-3500
Characterization of Volatile Compounds in New Cider Apple Genotypes Using Multivariate Analysis
- 25 August 2015
- Published by Royal Society of Chemistry (RSC) in New Journal of Chemistry
- Vol. 39 (11) , 8560-8568
Polymerized phosphonium-based ionic liquids as stationary phases in gas chromatography: performance improvements by addition of graphene oxide
The incorporation of graphene oxide sheets into phosphonium ionic liquid stationary phases led to a great improvement of their separation efficiencies.
- 25 August 2015
- Published by Royal Society of Chemistry (RSC) in New Journal of Chemistry
- Vol. 39 (11) , 8560-8568
Polymerized phosphonium-based ionic liquids as stationary phases in gas chromatography: performance improvements by addition of graphene oxide
The incorporation of graphene oxide sheets into phosphonium ionic liquid stationary phases led to a great improvement of their separation efficiencies.
- 30 March 2014
- Published by Springer Nature in Analytical and Bioanalytical Chemistry
- Vol. 406 (13) , 3149-3155
A chemometric approach to characterization of ionic liquids for gas chromatography
A chemometric study was carried out to characterize three ionic liquid types (ILs) with hexacationic imidazolium, polymeric imidazolium, and phosphonium cationic cores, using a range of contra-anions such as halogens, thiocyanate, boron anions, triflate, and bistriflimide. The solvation parameter model developed by Abraham et al., unsupervised techniques as cluster analysis (CA), and supervised techniques as linear discriminant analysis (LDA), step-LDA, quadratic discriminant analysis (QDA), and multivariate regression techniques as discriminant partial least squares (D-PLS), or multiple linear regression (MLR) were used to characterize the functionalized ILs above. CA established two main groups of phases, those with an acidic H-bond and those with basic ones. Once detected, the two natural groups, a linear and quadratic delimiters with good classification (>96 %) and prediction (>92 %) capacities were computed. The use of step-LDA technique allowed us to establish that a, b, and s solvation parameters were the most discriminant variables. These variables were used for modeling purposes, and a D-PLS and MLR models were constructed using a binary response. The explained variance of categorical variable by the model validated by cross-validation was 65 %, and 94.5 % of ILs were correctly predicted. IL characterization carried out would allow the appropriate selection of phases for gas chromatography (GC).
- 30 March 2014
- Published by Springer Nature in Analytical and Bioanalytical Chemistry
- Vol. 406 (13) , 3149-3155
A chemometric approach to characterization of ionic liquids for gas chromatography
A chemometric study was carried out to characterize three ionic liquid types (ILs) with hexacationic imidazolium, polymeric imidazolium, and phosphonium cationic cores, using a range of contra-anions such as halogens, thiocyanate, boron anions, triflate, and bistriflimide. The solvation parameter model developed by Abraham et al., unsupervised techniques as cluster analysis (CA), and supervised techniques as linear discriminant analysis (LDA), step-LDA, quadratic discriminant analysis (QDA), and multivariate regression techniques as discriminant partial least squares (D-PLS), or multiple linear regression (MLR) were used to characterize the functionalized ILs above. CA established two main groups of phases, those with an acidic H-bond and those with basic ones. Once detected, the two natural groups, a linear and quadratic delimiters with good classification (>96 %) and prediction (>92 %) capacities were computed. The use of step-LDA technique allowed us to establish that a, b, and s solvation parameters were the most discriminant variables. These variables were used for modeling purposes, and a D-PLS and MLR models were constructed using a binary response. The explained variance of categorical variable by the model validated by cross-validation was 65 %, and 94.5 % of ILs were correctly predicted. IL characterization carried out would allow the appropriate selection of phases for gas chromatography (GC).
- 1 November 2013
- Published by Elsevier in Sensors and Actuators B: Chemical
- Vol. 188, 837-846
Ionic liquids as modifiers for glass and SU-8 electrochemical microfluidic chips
- 1 November 2013
- Published by Elsevier in Sensors and Actuators B: Chemical
- Vol. 188, 837-846
Ionic liquids as modifiers for glass and SU-8 electrochemical microfluidic chips
- 19 September 2013
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 3 (44) , 21377-21380
Polymerized phosphonium-based ionic liquids as gas chromatography stationary phases
New phosphonium-based ionic liquids (ILs) were prepared and used as polymeric stationary phases in gas chromatography. The resulting columns exhibit exceptional thermal stability (250–360 °C) and unique selectivity for organic compounds, both polar and apolar (alkanes, alcohols, polycyclic aromatic hydrocarbons and pesticides). The excellent separation efficiencies obtained prove that the ILs do not lose the dual nature after polymerization. Incorporation of sheets of graphene oxide improved considerably the efficiency of the columns.
- 19 September 2013
- Published by Royal Society of Chemistry (RSC) in RSC Advances
- Vol. 3 (44) , 21377-21380
Polymerized phosphonium-based ionic liquids as gas chromatography stationary phases
New phosphonium-based ionic liquids (ILs) were prepared and used as polymeric stationary phases in gas chromatography. The resulting columns exhibit exceptional thermal stability (250–360 °C) and unique selectivity for organic compounds, both polar and apolar (alkanes, alcohols, polycyclic aromatic hydrocarbons and pesticides). The excellent separation efficiencies obtained prove that the ILs do not lose the dual nature after polymerization. Incorporation of sheets of graphene oxide improved considerably the efficiency of the columns.