45 research outputs found
Simultaneous detection of ammonium and nitrate in environmental samples using on ion-selective electrode and comparison with portable colorimetric assays
Simple, robust, and low-cost nitrate-and ammonium-selective electrodes were made using substrate prepared from household materials. We explored phosphonium-based ILs and poly (methyl methacrylate)/poly(decyl methacrylate)(MMA-DMA) copolymer as matrix materials alternative to classical PVC-based membranes. IL-based membranes showed suitability only for nitrate-selective electrode exhibiting linear concentration range between 5.0 × 10−6 and 2.5 × 10−3 M with a detection limit of 5.5 × 10−7 M. On the other hand, MMA-DMA—based membranes showed suitability for both ammonium-and nitrate-selective electrodes, and were successfully applied to detect NO3− and NH4+ in water and soil samples. The proposed ISEs exhibited near-Nernstian potentiometric responses to NO3− and NH4+ with the linear range concentration between 5.0 × 10−5 and 5.0 × 10−2 M (LOD = 11.3 µM) and 5.0 × 10−6 and 1.0 × 10−3 M (LOD = 1.2 µM), respectively. The power of ISEs to detect NO3− and NH4+ in water and soils was tested by comparison with traditional, portable colorimetric techniques. Procedures required for analysis by each technique from the perspective of a non-trained person (e.g., farmer) and the convenience of the use on the field are compared and contrasted
Simultaneous detection of ammonium and nitrate in environmental samples using on ion-selective electrode and comparison with portable colorimetric assays
Simple, robust, and low-cost nitrate-and ammonium-selective electrodes were made using substrate prepared from household materials. We explored phosphonium-based ILs and poly (methyl methacrylate)/poly(decyl methacrylate)(MMA-DMA) copolymer as matrix materials alternative to classical PVC-based membranes. IL-based membranes showed suitability only for nitrate-selective electrode exhibiting linear concentration range between 5.0 × 10−6 and 2.5 × 10−3 M with a detection limit of 5.5 × 10−7 M. On the other hand, MMA-DMA—based membranes showed suitability for both ammonium-and nitrate-selective electrodes, and were successfully applied to detect NO3− and NH4+ in water and soil samples. The proposed ISEs exhibited near-Nernstian potentiometric responses to NO3− and NH4+ with the linear range concentration between 5.0 × 10−5 and 5.0 × 10−2 M (LOD = 11.3 µM) and 5.0 × 10−6 and 1.0 × 10−3 M (LOD = 1.2 µM), respectively. The power of ISEs to detect NO3− and NH4+ in water and soils was tested by comparison with traditional, portable colorimetric techniques. Procedures required for analysis by each technique from the perspective of a non-trained person (e.g., farmer) and the convenience of the use on the field are compared and contrasted
Effect of applied currents to growth in oil palm (Elaeis guineensis Jacq.) tissue cultures
External currents of ± 2 μA were applied to the calluses of oil palm in three different culture medium recipes containing different growth substances and the effects of the current were investigated. The three media were medium for callus growth, embryogenetic medium, and organogenetic medium. The stimulation of callus growth was found for both directions of current in one unit of experiments where the embryogenetic culture medium contained NAA. In other cases the use of current seemed to have no significant stimulation effect. The mechanism by which the current may cause the alignment of the cells to promote polar transport of NAA which then increase growth and the relationship of these findings to earlier reports of the stimulation of growth in tobacco callus cultures is discussed
Ionic currents in sunflower (Helianthus annuus) roots = กระแสไฟฟ้าไอออนในรากทานตะวัน (Helianthus annuus)
Sol-gel based sensor for selective formaldehyde determination
We report the development of transparent sol–gels with entrapped sensitive and
selective reagents for the detection of formaldehyde. The sampling method is
based on the adsorption of formaldehyde from the air and reaction with β-
diketones (for example acetylacetone) in a sol–gel matrix to produce a yellow
product, lutidine, which was detected directly. The proposed method does not
require preparation of samples prior to analysis and allows both screening by
visual detection and quantitative measurement by simple spectrophotometry. The
detection limit of 0.03 ppmv formaldehyde is reported which is lower than the
maximum exposure concentrations recommended by both the World Health
Organisation (WHO) and the Occupational Safety and Health Administration (OSHA).
This sampling method was found to give good reproducibility, the relative
standard deviation at 0.2 and 1 ppmv being 6.3% and 4.6%, respectively. Other
carbonyl compounds i.e. acetaldehyde, benzaldehyde, acetone and butanone do not
interfere with this analytical approach. Results are provided for the
determination of formaldehyde in indoo
A Novel Microfluidic-Based OMC-PEDOT-PSS Composite Electrochemical Sensor for Continuous Dopamine Monitoring
Fast and precise analysis techniques using small sample volumes are required for next-generation clinical monitoring at the patient’s bedside, so as to provide the clinician with relevant chemical data in real-time. The integration of an electrochemical sensor into a microfluidic chip allows for the achievement of real-time chemical monitoring due to the low consumption of analytes, short analysis time, low cost, and compact size. In this work, dopamine, used as a model, is an important neurotransmitter responsible for controlling various vital life functions. The aim is to develop a novel serpentine microfluidic-based electrochemical sensor, using a screen-printed electrode for continuous dopamine detection. The developed sensor employed the composite of ordered mesoporous carbon (OMC) and poly (3,4 ethylenedioxythiophene)-poly (styrene sulfonate) (PEDOT-PSS). The performance of a microfluidic, integrated with the sensor, was amperometrically evaluated using a computer-controlled microfluidic platform. The microfluidic-based dopamine sensor exhibited a sensitivity of 20.2 ± 0.6 μA μmol L−1, and a detection limit (LOD) of 21.6 ± 0.002 nmol L−1, with high selectivity. This microfluidic-based electrochemical sensor was successfully employed to determine dopamine continuously, which could overcome the problem of sensor fouling with more than 90% stability for over 24 h. This novel microfluidic sensor platform provides a powerful tool for the development of a continuous dopamine detection system for human clinical application
Fritless Xterra Particles Encapsulated Within a Poly(butylmethacrylate) Based Monolith for Use in CEC
Capacitive immunosensor for the detection of host cell proteins.
A new analysis for monitoring host cell proteins in preparations of transgenically produced protein pharmaceuticals is described. A capacitive biosensor with a very high sensitivity is used to monitor trace amounts of host cell proteins. The sensor consists of a gold electrode, the surface of which is well insulated and on which a preparation of a population of polyclonal antibodies raised against the complete protein set-up of the host cell. Host cell proteins are present at very low concentrations during the production of a transgenic protein. The system studied here is a mode system with an enzyme expressed in Escherichia coli (E. coli). Due to the high sensitivity, it may even be possible to dilute the samples to be analyzed, thereby reducing negative influence from non-specific binding to the sensor surface
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