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1.
Larreta J Vallejo A Bilbao U Usobiaga A Arana G Zuloaga O 《Journal of separation science》2007,30(14):2293-2304
Odorous organic compounds from liquid and gas samples of animal wastes were studied by headspace (HS)-solid-phase microextraction (SPME)-GC-MS. 1-Pirenyldiazomethane (PDAM) was adsorbed/absorbed on the SPME fibre in order to obtain the corresponding ester derivatives during the preconcentration step. The SPME fibre was immersed into a PDAM solution. Then, the SPME fibre was withdrawn and exposed to the HS of the liquid cow slurry. This way derivatisation of VFAs took place in the SPME fibre together with the preconcentration of the rest of the analytes of interest. The analytes were desorbed in the hot injection port (300 degrees C) of a GC-MS for 3 min. Four different fibre types and different immersion periods of the fibre in the PDAM solution were studied in order to obtain the best sensitivity with the selected fibre. Accuracy, precision and the LODs were calculated using spiked liquid and gas samples. The possibility of storing liquid samples after sampling by preconcentration on the fibre was also considered. Storage time and temperature were studied. The optimised method was applied to the determination of the analytes in liquid and gas samples from cow slurries from an intensive production farm. 相似文献
2.
Zabaljauregui M Delgado A Usobiaga A Zuloaga O de Diego A Madariaga JM 《Journal of chromatography. A》2007,1148(1):78-85
A simple, fast, and accurate method for the simultaneous determination of methylmercury (MeHg(+)), monobutyltin (MBT), dibutyltin (DBT) and tributyltin (TBT) in seafood is proposed. The method makes use of relatively cheap instrumentation and allows simultaneous analysis of those four species in a routine basis. The sample is treated with methanolic potassium hydroxide in an ultrasound bath, derivatised with sodium tetraethylborate (NaBEt(4)), preconcentrated into n-hexane and analysed by gas chromatography with atomic emission detection (GC-MIP/AES). The soft extraction conditions provided by ultrasound energy prevent chemical decomposition of the analytes and allow fast and efficient recovery of the species considered. Both the extraction and the derivatisation/preconcentration steps were optimised. Detection limits of 34, 3, 6 and 8 ng g(-1) (dry mass) were obtained for MeHg(+), MBT, DBT and TBT, respectively, using the best experimental conditions found. The uncertainty of the analysis ranged from 11% (MeHg(+)) to 15% (MBT). The accuracy of the method was checked by the analysis of several certified reference materials, e.g., BCR 477 (mussel tissue, MBT, DBT and TBT), DOLT-2 (dogfish liver, MeHg(+)), BCR 463 (tuna fish, MeHg(+)) and NIST 2976 (mussel tissue, MeHg(+)) with satisfactory results. Several oyster samples collected in the estuary of the Oka River (Urdaibai, Unesco Reserve of the Biosphere, Basque Country) during four sampling campaigns in 2003-2004 were processed following the proposed procedure. Concentrations ranging from 65 to 149 ng g(-1) (MeHg(+)), 相似文献
3.
A modification of the Falkenhagen equation is proposed, which fits correctly data of 29 different 1:1 aqueous electrolyte solutions up to very high concentrations. The concept of activity is used to account for deviations from ideality appearing at higher concentrations. A discussion about trends in the value of the ‘distance of closest approach between two ions’, a, and novel conductivity data for several concentrated electrolyte solutions estimated by the proposed model are also provided. 相似文献
4.
Jone Omar Asier Vallejo Maitane Olivares Aresatz Usobiaga Olatz Zuloaga Nestor Etxebarria 《Journal of Chemometrics》2015,29(4):237-244
The interest in the analysis of alkylphenols (APs) has widely increased in the last decades because of the endocrine disrupting features of these phenol derivatives. However, the isolation and identification of many of the multiple chemical structures of all APs is a very challenging task because of their similar physicochemical properties. In this work, the co‐elution of the isomers present in technical mixtures and using comprehensive two‐dimensional gas chromatography coupled to quadrupole mass spectrometry was resolved using multivariate curve resolution‐alternating least squares algorithm. The mass spectrum of each resolved compound was compared with the theoretical mass spectrum obtained from the literature, in order to assign the appropriate identification of each isomer. Two commercial mixtures were studied; in one of them, 34 compounds were resolved, and in the second mixture, 40 compounds were resolved. The relative abundances of the compounds were also calculated in both mixtures. Copyright © 2015 John Wiley & Sons, Ltd. 相似文献
5.
Joana Larreta Urdax Bilbao Asier Vallejo Aresatz Usobiaga Gorka Arana Olatz Zuloaga 《Chromatographia》2008,67(1-2):93-99
In this work the simultaneous purge-and-trap (P&;T) preconcentration of volatile fatty acids (acetic acid, propanoic acid, butanoic acid, iso-butanoic acid, pentanoic acid, iso-pentanoic acid, hexanoic acid and heptanoic acid), phenols (phenol, 4-methylphenol and 4-ethylphenol) and indoles (indole and 3-methylindole) from cow slurries was carried out in order to quantify them by gas chromatography flame ionisation detection (GC–FID). The optimisation of the preconcentration was performed using spiked cow slurries and the variables studied were the nature of the trap, the purge and heating time and the amount of inert salt (NaCl) added. Other parameters such as purge flow, sample volume, desorption time and temperature and baking time and temperature were kept constant. The first variable studied was the nature of the preconcentration trap. Four different commercially available traps (Vocarb 4000, Vocarb 3000, BTEXTRAP and Tenax/silica gel/carbon) were studied and Vocarb 3000 gave best results. Once the optimum trap was chosen, appearance of possible memory peaks were studied and significant signals were observed for 4-methylphenol, 4-ethylphenol, indole and 3-methylindole. In order to improve the blanks after each analysis the following actions were taken: (1) the needle sparger was located in the headspace of the sample and (2) all the replaceable parts of the P&;T (sample tube, needle sparger, Teflon ferrules, nuts, etc.) were washed, sonicated in acetone for 15 min and dried in an oven at 350 °C. Once the blank problems were minimised, the remaining variables (purge and heating time and the amount of NaCl) were optimised using the MultiSimplex® program, which enabled the study of several variables and responses simultaneously. Optimum conditions for the simultaneous preconcentration were obtained after 24 experiments and the final optimised preconcentration conditions were as follows: 0.4 g of NaCl were added to 10 mL sample which was heated at 80 °C for 10 min and purged for 20 min while the Vocarb 3000 trap remained at room temperature. Once the purge step was over, the trap was desorbed at 250 °C for 6 min and baked at 260 °C for 10 min. After the optimisation of the P&;T based preconcentration, the precision (within and among days), accuracy and detection limits of the method were studied. 相似文献
6.
Prieto A Zuloaga O Usobiaga A Etxebarria N Fernández LA 《Analytical and bioanalytical chemistry》2008,390(2):739-748
A method for the determination of polybrominated diphenyl ethers (PBDEs) and polybrominated biphenyls (PBBs) in water samples
is proposed. The method involving stir bar sorptive extraction (SBSE) and thermal desorption followed by gas chromatography
coupled with mass spectrometry was optimised using statistical design of experiments. In the first place, the influence of
different polydimethylsiloxane stir bars was studied. A Plackett–Burman design was chosen to estimate the influence of five
factors on the efficiency of the SBSE process: desorption time (5–10 min), desorption temperature (250–300 °C), desorption
flow (50–100 mL min−1), cryofocusing temperature (-130 to 40 °C) and vent pressure (0–12.8 psi). Afterwards, two central composite designs were
used to find the optimal process settings that were applied to the optimisation of both desorption and extraction efficiency.
In the case of the desorption parameters, long desorption times (10 min) and desorption flows lower than 70 mL min-1 yielded the best signals for the majority of compounds. However, different behaviour among the analytes was observed for
the vent pressure and we decided to fix it at an intermediate value (7 psi). In the case of extraction parameters, the sample
volume and the addition of NaCl did not have a significant effect, while the addition of methanol yielded better extraction
responses. Remarkable recovery (82–106%) and repeatability (less than 18%) were attained. Furthermore, excellent regression
coefficients (r
2 = 0.991–0.999) and low detection limits (1.1–6.0 ng L−1) were also achieved for the congeners studied. The proposed method was applied to the analyses of PBDEs and PBBs in waters
from the Basque Country, Spain. 相似文献
7.
Martínez-Arkarazo I Sarmiento A Usobiaga A Angulo M Etxebarria N Madariaga JM 《Talanta》2008,75(2):511-516
Thermodynamic and Raman spectroscopic speciation was used to define the operating conditions for an innovative cleaning treatment of the decayed carbonate-based stones using ion exchange technology. The conditioning process of the Lewatit OC1071 anion exchanger with EDTA (Y) was monitored by ionic chromatography. Characterisation of the initial (R-Cl) and the final (R2-H2Y) forms of the ion exchanger was carried out by dispersive Raman microprobe spectroscopy. The subtraction spectrum obtained between the chloride and the EDTA forms of the ion exchanger shows Raman bands at 1403, 1324, 1223, 1122, 932, 908, 591, 431 and 350 cm(-1), which agree with bands showed in the spectrum of the standard solution of the H2Y(2-) species. Therefore, this seems to be the EDTA species which takes part in the cleaning treatment performed by using resin poultices on black crusted limestone samples from an historical building. 相似文献
8.
Vallejo A Fernández LA Olivares M Prieto A Etxebarria N Usobiaga A Zuloaga O 《Journal of chromatography. A》2010,1217(52):8327-8333
Large volume injection-programmable temperature vaporization-gas chromatography-mass spectrometry (LVI-PTV-GC-MS) was optimized for the determination of estrone (E1), 17β-estradiol (E2), 17α-ethynyl estradiol (EE2), mestranol (MeEE2) and estriol (E3) for their determination in environmental samples (estuarine water, wastewater, fish bile and fish homogenate) after derivatization with 25 μL (BSTFA+1% TMCS) and 125 μL of pyridine. Experimental designs such as Plackett-Burman (PBD) and central composite designs (CCDs) were used to optimize the LVI-PTV variables (cryo-focusing temperature, vent time, vent flow, vent pressure, injection volume, purge flow to split vent, splitless time and injection speed). Optimized conditions were as follows: 45 μL of n-hexane extract are injected at 60°C and 6 μL/s with a vent flow and a vent pressure of 50 mL/min and 7.7 psi, respectively, during 5 min; then the split valve is closed for 1.5 min and afterwards the injector is cleaned at 100 mL/min before the next injection. The method was applied to the determination of estrogenic compounds in environmental samples such as estuarine water, wastewater, and fish homogenate and bile. Limits of detection (0.04-0.15 ng/L for water samples, 0.04-0.67 ng/g for fish bile and 0.1-7.5 ng for fish homogenate) obtained were approx. ten times lower than those obtained by means of a common split/splitless inlet. 相似文献
9.
Asier Vallejo Aresatz Usobiaga Irantzu Martinez‐Arkarazo Ailette Prieto Nestor Etxebarria Olatz Zuloaga Luis A. Fernández 《Journal of separation science》2010,33(1):104-111
Cup horn boosters are miniaturized ultrasound baths that maximize efficiency and precision. The optimization of an ultrasonic‐assisted derivatization step by means of a cup horn booster and the determination of estrone, 17β‐estradiol, estriol, 17α‐ethynyl estradiol and mestranol was developed by GC‐MS. Different derivatization reagents and solvents were studied for maximizing the di‐derivatization of 17α‐ethynyl estradiol under ultrasound energy. Only N,O‐bis(trimethylsilyl)trifluoroacetamide with 1% of trimethylchlorosilane in pyridine gave satisfactory results and this mixture was further used in the optimization of the ultrasound assisted derivatization. The experiment designs included sonication time (1–10 min), sonication power (20–80%), sonication cycles (1–9), derivatization reagent volume (25–125 μL) and solvent volume (25–125 μL). Once the optimum conditions were fixed, the effect of organic matter and the frequency of the water bath change were studied. Finally, the validation of the analytical method was carried out using spiked natural and synthetic waters. Recoveries (natural (138–70%) and synthetic (112–89%)), the LODs (0.35–1.66 ng/L), and LOQs (1.16–5.52 ng/L) and the precision (0.2–5.3%) of the method were studied. This is the first work in the literature where a cup horn booster is used with the aim of minimizing derivatization time during the determination of estrogenic compounds. 相似文献
10.
Vallejo A Olivares M Fernández LA Etxebarria N Arrasate S Anakabe E Usobiaga A Zuloaga O 《Journal of chromatography. A》2011,1218(20):3064-3069
In the present work, the separation of complex nonylphenol technical mixtures has been optimized using comprehensive two-dimensional gas chromatography coupled with a flame ionization detector and quadrupole mass spectrometer (GC×GC-qMS), using valve-based modulator. The optimization of GC×GC-qMS has been carried out using experimental designs and the optimal separation was obtained at the following conditions: 1st column flow: 1mL/min; 2nd column flow: 17.75 mL/min, oven temperature ramp: 1°C/min, modulation period: 1.5s and discharge time: 0.12s. These values have been used to determinate the previously synthesized 22OP, 33OP, 363NP and 22NP isomers in two different nonylphenol technical mixtures. Percentages obtained were as follows: 4.86% and 0.59% for 22OP, 4.91% and 2.82% for 33OP, 11.79% and 7.71% for 363NP and 2.28% and 1.98% for 22NP, in Fluka and Aldrich mixtures, respectively. The values obtained for NP isomers are in good agreement with the literature. 相似文献