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There is significant contamination of our water resources and an accelerating accumulation of hazardous species in the aquatic biosphere. Whether for instance mercury as a contaminant constantly released from a multitude of industrial processes or chemical warfare agents (CWAs) such as Tabun (GA), Sarin (GB) or Soman (GD) as highly toxic remnants of World War II, released from dumped containers upon their progressive corrosion, are concerned such hazards can cause serious problems to human health even at low concentration and monitoring them becomes increasingly essential. Conclusively, it is necessary to develop sensors for such hazards that combine high sensitivity, good selectivity, fast responses and can dispense with complex instrumentation.
Here, we present SBA-15-type mesoporous silica materials containing boron–dipyrromethene (BODIPY) probes in their pore systems that allow for the sensitive and selective detection of the two target analytes CWAs and Hg2+ in natural waters via a change in the optical properties. In case of Hg2+, the BODIPY dye is directly adsorbed on the (inner and outer) surface of the highly porous material and coordinates the metal ion, leading to an enhancement of fluorescence with a limit of detection (LOD) of 15 ppt. Using the same silica material but incorporating a covalently attached BODIPY dye, the CWAs GA, GD and GB can be detected via fluorescence quenching induced by an intraannular cyclization. The obtained LOD in natural waters is in the pM range and hence below the Maximum Permissible Concentrations for CWAs in drinking water. Aspects of system design as well as application in water and food analysis (fish extracts) will be presented.
There is significant contamination of our water resources and an accelerating accumulation of hazardous species in the aquatic biosphere. Whether for instance mercury as a contaminant constantly released from a multitude of industrial processes or chemical warfare agents (CWAs) such as Tabun (GA), Sarin (GB) or Soman (GD) as highly toxic remnants of World War II, released from dumped containers upon their progressive corrosion, are concerned such hazards can cause serious problems to human health even at low concentration and monitoring them becomes increasingly essential. Conclusively, it is necessary to develop sensors for such hazards that combine high sensitivity, good selectivity, fast responses and can dispense with complex instrumentation.
Here, we present SBA-15-type mesoporous silica materials containing boron–dipyrromethene (BODIPY) probes in their pore systems that allow for the sensitive and selective detection of the two target analytes CWAs and Hg2+ in natural waters via a change in the optical properties. In case of Hg2+, the BODIPY dye is directly adsorbed on the (inner and outer) surface of the highly porous material and coordinates the metal ion, leading to an enhancement of fluorescence with a limit of detection (LOD) of 15 ppt. Using the same silica material but incorporating a covalently attached BODIPY dye, the CWAs GA, GD and GB can be detected via fluorescence quenching induced by an intraannular cyclization. The obtained LOD in natural waters is in the pM range and hence below the Maximum Permissible Concentrations for CWAs in drinking water. Aspects of system design as well as application in water and food analysis (fish extracts) will be presented.
The need for rapid and high-throughput screening in analytical laboratories has led to significant growth in interest in suspension array technologies (SATs), especially with regard to cytometric assays targeting a low to medium number of analytes. Such SAT or bead-based assays rely on spherical objects that constitute the analytical platform. Usually, functionalized polymer or silica (SiO2) microbeads are used which each have distinct advantages and drawbacks. In this paper, we present a straightforward synthetic route to highly monodisperse SiO2-coated polystyrene core−shell (CS) beads for SAT with controllable architectures from smooth to raspberry- and multilayer-like shells by varying the molecular weight of poly(vinylpyrrolidone) (PVP), which was used as the stabilizer of the cores. The combination of both organic polymer core and a structurally controlled inorganic SiO2 shell in one hybrid particle holds great promises for flexible next-generation design of the spherical platform. The particles were characterized by electron microscopy (SEM, T-SEM, and TEM), thermogravimetry, flow cytometry, and nitrogen adsorption/desorption, offering comprehensive information on the composition, size, structure, and surface area. All particles show ideal cytometric detection patterns and facile handling due to the hybrid structure. The beads are endowed with straightforward modification possibilities through the defined SiO2 shells. We successfully implemented the particles in fluorometric SAT model assays, illustrating the benefits of tailored surface area which is readily available for small-molecule anchoring. Very promising assay performance was shown for DNA hybridization assays with quantification limits down to 8 fmol.
Ammonia and its conversion product ammonium have a strong negative impact on human health and ecosystems. Most ammonia measurements in ambient air are performed in the molar fraction range (0.5 to 500) nmol/mol. There is a need for reliable traceable ammonia gas standards as well as in situ analytical procedures for the monitoring of ammonia in ambient air.
The permeation method is an effective tool for dynamically generating precise gas standards with a low uncertainty in the concentration range of a few nmol/mol to several µmol/mol in an inert carrier gas, e. g. pure nitrogen or purified ambient air. Here, we present our ammonia gas standard generator as well as results of the characterisation of its individual components supporting the uncertainty assessment according to GUM for stable gas concentrations in this range.
In order to detect ammonia in the nmol/mol-range, a suitable sensor has to be developed. In this contribution, we therefore additionally present first approaches on the development of such a sensor using optical fluorescence as transduction mechanism due to its intrinsically high sensitivity and high spatial resolution. Incorporation of a fluorescent dye, which shows fluorescence enhancement in the presence of ammonia, into a polymer matrix allows to reversibly recognize low amounts of ammonia. It can be concluded that fluorescence sensor is a robust tool for measurements of ammonia; however it needs calibration for the planed use.
Test strips that in combination with a portable fluorescence reader or digital camera can rapidly and selectively detect chemical warfare agents (CWAs) such as Tabun (GA), Sarin (GB), and Soman (GD) and their simulants in the gas phase have been developed. The strips contain spots of a hybrid indicator material consisting of a fluorescent BODIPY indicator covalently anchored into the channels of mesoporous SBA silica microparticles. The fluorescence quenching response allows the sensitive detection of CWAs in the μg m−3 range in a few seconds.
A universal fast and easy access at room temperature to transparent sols of nanoscopic Eu3+ and Tb3+ doped CaF2, SrF2 and BaF2 particles via the fluorolytic sol–gel synthesis route is presented. Monodisperse quasi-spherical nanoparticles with sizes of 3–20 nm are obtained with up to 40% rare earth doping showing red or green luminescence. In the beginning luminescence quenching effects are only observed for the highest content, which demonstrates the unique and outstanding properties of these materials. From CaF2:Eu10 via SrF2:Eu10 to BaF2:Eu10 a steady increase of the luminescence intensity and lifetime occurs by a factor of ≈2; the photoluminescence quantum yield increases by 29 to 35% due to the lower phonon energy of the matrix. The fast formation process of the particles within fractions of seconds is clearly visualized by exploiting appropriate luminescence processes during the synthesis. Multiply doped particles are also available by this method. Fine tuning of the luminescence properties is achieved by variation of the Ca-to-Sr ratio. Co-doping with Ce3+ and Tb3+ results in a huge increase (>50 times) of the green luminescence intensity due to energy transfer Ce3+ → Tb3+. In this case, the luminescence intensity is higher for CaF2 than for SrF2, due to a lower spatial distance of the rare earth ions.
An ideal sensor system is a combination of a selective receptor, an effective transducer, and a sensitive detector. To utilize molecularly imprinted polymers (MIPs) as responsive recognition phases in sensors, the employment of fluorescent molecules or nanoparticles (NPs) that show prominent changes in their spectroscopic properties after binding of the target molecule in the MIP’s cavity is particularly attractive. Such fluorescent MIPs (fMIPs) act through target-induced quenching, enhancement, or spectral shifts of the fluorescence. This contribution introduces different strategies of incorporation of fluorescent dyes, probes, and NPs into fMIPs. In addition, various sensing mechanisms are reviewed, and depending on the application of the sensor, the different deployable formats, their advantages, drawbacks, and impact will be presented and discussed.
Pollution through emission of toxic gases is an increasing problem for the environment. It affects similarly agricultural, industrial and urban areas. In future, environmental emissions in ambient air must be monitored at even lower concentrations as nowadays. One environmental relevant compound is ammonia and its conversion product ammonium that have strong negative impact on human health and ecosystems. Most ammonia measurements in ambient air are performed in the range below 1000 nmol·mol-1 and thus there is a need for reliable traceable ammonia gas standards and in addition in situ analytical procedures for monitoring (in ambient air to avoid that thresholds are exceeded). Therefore, the use of reference materials is necessary for development accompanying test or for calibration, e. g. of structure-integrated sensors and mobile multi-gas sensors.
The developed gas standard generator produces gas mixtures that comply with the metrological traceability for ammonia gas standards in the desired environmentally relevant measurement range. The method is based on the permeation of ammonia through a membrane at constant temperature and pressure. The resulting ammonia penetrant gas flow is then mixed with a carrier gas flow to generate a gas standard flow of known concentration. The dynamic rage is enlarged by using a two dilution steps. Depending on the permeation rate, generable molar fractions are possible in the range nmol·mol-1 to a few µmol·mol-1. We present the design of an ammonia gas standard generator and first results of the characterisation of its individual components supporting the uncertainty assessment according to GUM for stable gas concentrations in this range. The relative uncertainty of the generated ammonia gas standard is smaller than 4 % (k = 2).
Pollution through emission of toxic gases is of utmost environmental concern, raising the interest in developing reliable gas sensors. Exemplarily, ammonia and its conversion products can provoke considerable damage on human health and ecosystems. Hence, there is a need for reliable and reversible sensor materials to monitor traces of gaseous ammonia in ambient air, which at best can be used on-site for field measurements. Although various types of sensors such as potentiometric, amperometric, and biological sensors are available for detecting trace amounts of gases, fluorescent sensors have gained importance due to several advantages such as high sensitivity, possible miniaturization, as well as potential multiplexing. Herein, we present the development of a sensor material for gaseous ammonia in the lower ppm or even ppb range using optical fluorescence as transduction mechanism due to its intrinsically high sensitivity and high spatial resolution.[1] Therefore, a fluorescent dye, which shows reversible fluorescence enhancement in the presence of the analyte was incorporated into a polymer matrix, the latter to ensure the accumulation of ammonia. To calibrate the designed optical sensor system a gas standard generator was used, producing standard gas mixtures, which comply with the metrological traceability for ammonia gas standards in the desired environmentally relevant measurement range.[2] Beside the development of a highly sensitive, selective, and reversible sensor, the integration of such systems into mobile sensor devices is addressed. Therefore, a prototype of a miniaturized hand-held instrument was developed enabling a straightforward and long-term read-out of the measurement signal.
Because ammonia and its reaction products can cause considerable damage to human health and ecosystems, there is a need for reliably operating and reversibly interacting sensor materials to monitor traces of gaseous ammonia in ambient air, which at best can be used on-site for in-the-field measurements. Herein, the development of a sensor material for gaseous ammonia in the lower ppm to ppb range using optical fluorescence as transduction mechanism is presented. A fluorescent dye, which shows reversible fluorescence enhancement in the presence of ammonia is incorporated into a polymer matrix, the latter to ensure the accumulation of ammonia. The sensor material is integrated into a prototype of a miniaturized sensor device, facilitating long-term operation. To calibrate the optical sensor system a gas standard generator, producing standard gas mixtures, is used, leading to a sensitivity down to lower ppm concentrations of ammonia.