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A novel miniaturized sample extraction capillary was developed to provide a simple and sensitive method for analyzing gaseous formaldehyde (FA) using conventional high-performance liquid chromatography (HPLC). The extraction capillary was prepared by packing silica gel particles in a stainless steel capillary with a 1.6-mm o.d. Before the gaseous samples were collected, the silica gel particles were impregnated with a derivatizing reagent 2,4-dinitrophenylhydrazine (DNPH) by passing a solution of DNPH through the extraction capillary. FA was derivatized to form the corresponding hydrazone during the active sampling of a gaseous sample, and the derivative was sorbed by the silica gel. The capillary was then directly connected to a six-port valve, and desorption from the capillary and injection into the HPLC were achieved simultaneously by passing a solvent through the capillary. The run-to-run and device-to-device variabilities, as relative standard deviations, were both less than 6.9 %. The limit of detection for FA was 2.5 ng/L using a sampling volume of 100 mL, and a sample collection time of 2 min. Acetaldehyde and acetone in a gaseous sample could also be simultaneously extracted and determined using this method. The applicability of the developed method for determining FA in real indoor air samples was confirmed by comparing the results obtained using the proposed method and a conventional sample preparation method. The developed method enables the rapid and simple sample preparation of gaseous FA and gives a good level of sensitivity. [ABSTRACT FROM AUTHOR]

A miniaturized sample preparation technique that uses a fine-fiber-packed needle as the extraction medium is reviewed, especially in relation to its application to the analysis of volatile organic compounds by gas chromatography. When the needle was packed longitudinally with a bundle of fine filaments (12 µm o.d.) which were also surface-coated with polymeric materials, successful sample preconcentration was obtained. Improved sensitivity was also established by introducing simultaneous derivatization reactions into the extraction process in the fiber-packed needle. The storage performance of the needle clearly demonstrated the potential of the technique for typical on-site sampling during environmental analysis. In this short review, the fiber-packed extraction needle developed by the authors is summarized along with applications that use the fiber-packed needle as a miniaturized extraction device. [ABSTRACT FROM AUTHOR]

A novel in-needle sample preparation device has been developed for the determination of volatile aldehydes in gaseous samples. The needle device is designed for the gas chromatographic (GC) analysis of aldehydes and ketones commonly found in typical in-house environments. In order to prepare the extraction device, a bundle of polymer-coated filaments was longitudinally packed into a specially designed needle. Derivatization reactions were prompted by 2,4-dinitrophenylhydrazine (NDPH) included in the needle, and so the aldehydes and ketones were derivatized to the corresponding hydrazones and extracted with the extraction needle. A reproducible extraction needle preparation process was established, along with a repeatable derivatization/extraction process that ensures the successful determination of aldehydes. The storage performance of the extraction needle was also evaluated at room temperature for three days. The results demonstrate the successful application of the fiber-packed extraction device to the preparation of a gaseous sample of aldehydes, and the future possibility of applying the extraction device to the analysis of in-house environments. [ABSTRACT FROM AUTHOR]

A fiber-packed needle was developed as a novel extraction device for gas-chromatographic analysis of trace organic compounds in aqueous samples. In the extraction device, a bundle of the polymer-coated filaments as the sorbent material was longitudinally packed into a specially designed needle. The extraction was made by pumping the aqueous sample solution into the needle extraction device, and the subsequent desorption process was carried out with a flow of desorption solvent through the needle in a heated gas chromatograph injector. The needle device showed an excellent thermal stability for repeated use without any deterioration of extraction performance, and no carryover effect was observed after the optimization of the desorption conditions. Additionally, the extraction efficiency of the fiber-packed needle could be enhanced by optimizing the number of packed filaments. The selectivity for various compounds could be also tuned using an appropriate combination of the fibrous medium and the coating polymer. The relative standard deviation for run to run was from 3.88 to 4.55% ( n = 5), and that for needle to needle was 7.21% ( n = 3), clearly suggesting a good repeatability of the needle extraction technique developed. Upon successful optimization of the extraction conditions, a rapid extraction of trace organic compounds from an aqueous sample matrix was successfully demonstrated, where each extraction process was completed within 10 min. [ABSTRACT FROM AUTHOR]

“F-free” CeOBiS 2 single crystals have successfully grown, thoroughly eliminating a concern about F-contamination by using a high-purity CsCl flux. The obtained crystals have a plate-like shape with a size of 1.0–3.0 mm in the well-developed plane. Single crystal X-ray structural analysis clearly revealed that the CeOBiS 2 crystallizes with a space group P 4/ nmm (with lattice parameters of a = 4.0189 (6) Å, c = 13.573 (2) Å). The bond valence sum estimation and X-ray photoelectron spectroscopy analysis showed that the chemical state of Ce was in the mixed valence of Ce 3+ and Ce 4+ . The single crystals show superconductivity with zero resistivity at ∼1.3 K. This is the first conclusive evidence of superconductivity driven by Ce valence fluctuation in surely non-doped CeOBiS 2 . The superconducting transition temperature was enhanced up to ∼3.8 K by applying hydrostatic pressure. [ABSTRACT FROM AUTHOR]