High Efficiency Nebulizer Research Articles

Investigation of calcium variations in single cells and the impact of Yoda1 on osteocytes by ICP-OES

BackgroundDetection of elements in individual cells by inductively coupled plasma (ICP) spectrometry has recently attracted significant interest in biological research, due to the unique ability of ICP spectrometry for trace element analysis. However, performing single-cell analysis using ICP optical emission spectrometry (ICP-OES) remains a challenge due to the small size and discrete nature of cells. This is while ICP-OES can serve as a cost-effective and label-free method for this purpose. Therefore, it is necessary to improve the current ICP-OES technique to facilitate the detection of elements in single cells, thereby unlocking novel applications. ResultsA new conical ICP torch, which has been illustrated to offer better analytical performance than the conventional ones, was applied to achieve the detection of calcium in single micro-sized cells. A new heated chamber was designed and coupled with a high-efficiency nebulizer as the sample introduction system. For the detection of single SiO2 particles, the number of particle events obtained by the new sample introduction system was found to be up to 9 times higher than that of the conventional system without sacrificing the signal intensity. Subsequently, calcium in human breast cancer cells (MDA-MB-231), mice breast cancer cells (Py8119), and mice osteocytes (MLO-Y4) was successfully detected using the new ICP-OES system. The cell detection efficiency turned out to be around 2%–3% which is much higher than that the reported values in previous single-cell ICP-OES research. Finally, as a new application, the effect of Yoda1, a recently identified activator of Piezo1 calcium channel, on osteocytes was investigated. The calcium content in Yoda1-treated MLO-Y4 cells was seen increase by 36% compared to the control sample. SignificanceThis research reveals the capability of ICP-OES in single-cell analysis for micro-sized cells which was made possible by the new conical ICP torch and the new sample introduction system. The ability to detect calcium in single mammalian cells enables the first ever application of this technique to assess the impact of the Yoda1 activator on the calcium level in osteocytes.

ICP-OES as a Viable Alternative to ICP-MS for Trace Analysis: Meeting the Detection Limits Challenge

This month’s column focuses on the applicability of inductively coupled plasma–optical emission spectroscopy (ICP-OES) fitted with a high efficiency nebulizer as a real-world alternative to ICP–mass spectrometry (ICP-MS) for certain applications. It is well-recognized that ICP-MS is the most widely used and recommended technique for ultra trace element analysis because it offers extremely high sensitivity. However, if the necessary sensitivity is achieved, an ICP-OES instrument can be a viable option because it is simpler to operate and less costly to maintain than an ICP-MS instrument. In this study, the sensitivity of ICP-OES was significantly enhanced by using a highly efficient yet robust sample introduction system. The increased efficiency was accomplished by employing an external impact surface positioned close to the nebulizer gas orifice at an optimized angle. The robustness by a non-concentric design was achieved by separating the gas and sample channels throughout the entire body of the nebulizer. The results of applying this approach to the ICP-OES analysis of a select group of sample matrices and meeting the required challenging detection limits are demonstrated.

Chip-based microfluidics on-line with inductively coupled plasma - mass spectrometry for standard dilution analysis

Microfluidics coupled on-line with ICP-MS detection can be combined with powerful quantitation procedures that take advantage of internal standardization and standard additions, such as the recently introduced Standard Dilution Analysis (SDA). Although so far used at mL min−1 flow rates, here we demonstrate that SDA can be conveniently employed with a microfluidic chip-based ICP-MS system to improve determination accuracy for various sample types, including water, biological and cell digest samples, analyzed at μL min−1 flow rates. The efficient coupling of a microfluidic chip to ICP-MS was accomplished using a combination of commercially available components, including a pneumatic high-efficiency nebulizer and a spray chamber designed to allow for the addition of a laminar flow makeup gas. The addition of the makeup gas was crucial in order to avoid detrimental suction effects that can disrupt the operation of the microfluidic chip and cause signal instability, while it still allowed for the highly sensitive detection of metal isotopes by using ICP-MS. All mixing and dilution operations of the sample with the two calibration solutions required for SDA were performed in an automated and highly reproducible fashion on the microfluidic chip with the assistance of an external distributor valve. High average recoveries (97.4–100.1%) and low average relative standard deviations (2.9–4.8%) were achieved for the determined elements (Cd, Co, Pb, Cr) across several spiked matrices and certified reference materials, whereas only 140 μL of sample is required for SDA in triplicate or 40 μL for a single analysis. Hence, accuracy, precision, limited sample consumption, and the elimination of the need for manual sample dilution and mixing manipulations are some of the advantages of this newly developed chip-based microfluidic SDA ICP-MS technique.

Detection of nanoparticles by single-particle ICP-MS with complete transport efficiency through direct nebulization at few-microlitres-per-minute uptake rates.

Measurement of nanoparticle (NP) concentration and size by single-particle inductively coupled plasma mass spectrometry (spICP-MS) usually requires the use of a NP reference material to determine the loss of NPs and/or ions during their transport from the sample solution to the detection system. The determination of this loss, qualified as nebulization efficiency (ηNebulization) and/or transport efficiency (ηTransport), is time-consuming, costly and lacks reliability. Nebulization of the NPs directly into the plasma (without a spray chamber) results in ηNebulization = 100% and is thus a promising strategy to avoid these calibration steps. In this work, we used the μ-dDIHEN introduction system: a demountable direct injection high-efficiency nebulizer (dDIHEN) hyphenated to a flow-injection valve and a gas displacement pump. For the first time with a continuous flow nebulizer, complete transport efficiency was reached (i.e. ηTransport = 100%). Operated at a very low uptake rate (as low as 8μLmin-1), the μ-dDIHEN accurately and reproducibly determined average diameters of Au-, Ag- and Pt-NPs, in full agreement with their reference values. It was also successfully tested for Au-NPs in complex matrices, such as surface waters. spICP-MS analyses with the μ-dDIHEN sample introduction system only require a dissolved standard calibration to determine NP average diameter (dNPs in nm) and number concentration (NNPs) from the simplified set of equations: [Formula: see text] and [Formula: see text]Graphical abstract.

Improved bioavailability of cromolyn sodium using inhaled PA101 delivered via eFlow® nebulizer

ABSTRACT In 1960s, cromolyn sodium (CS) has been introduced as the first non-steroidal anti-inflammatory drug for the treatment of allergic and mast-cell driven diseases. Its applicability has been limited due to a poor bioavailability. Here we present pharmacokinetic data of a novel high concentration formulation of CS (PA101) delivered via a high-efficiency nebulizer (eFlow®) in healthy volunteers (HVs), allergic asthmatics and patients with indolent systemic mastocytosis (ISM). In HVs, PA101 40 mg and 80 mg (30 L) and PA101 40 mg (40 L), IntalTM (via LC® Plus) 20 mg and Nalcrom® (oral suspension) 200 mg showed maximum measured plasma concentration (Cmax) of 156, 236, 88.6, 17.8 and 5.23 ng/mL, respectively, with respective areas under the plasma time-concentration curve (AUC) of 338, 526, 212, 40.6 and 33.3 h·ng/mL. Systemic exposure (AUC) to CS with PA101 40 mg was approximately 8-fold and 11-fold higher compared to IntalTM and Nalcrom® in HVs, respectively. PA101 via eFlow® yielded comparable PK profiles in HVs and patients. Systemic bioavailability of PA101 was approximately 25% compared to approximately 1% for Nalcrom® and approximately 10% for IntalTM, respectively. These data warrant further research on the therapeutic potential of PA101 (via eFlow®) in allergic and mast-cell driven diseases.

Quantitative Analysis of Transferrin Receptor 1 (TfR1) in Individual Breast Cancer Cells by Means of Labeled Antibodies and Elemental (ICP-MS) Detection.

Cells are able to precisely control the amount of iron they acquire in the form of transferrin (TF)-bound iron by modulating the synthesis of transferrin receptor 1 (TfR1). In tumor cells, elevated TfR1 seems to be related to poorer outcome for patients. Thus, the direct measurement of this biomarker in breast cancer tissues and cells might serve as a prognosis biomarker. In this work, we have used Nd-labeled antibodies to tag the TfR1 present on the cell surface of two cell models of breast cancer with different malignancy (MCF7 and MDA-MB 231). For this aim, monoclonal antibody anti-TfR1 is first labeled with a polymeric chelator (MAXPAR) with the subsequent incorporation of several isotopic 143Nd atoms. The characterization of the labeled antibody revealed a stoichiometry of 21 Nd atoms per antibody molecule that can be used for further quantification experiments. This antibody is used for cell tagging followed by single-cell analysis using inductively coupled plasma mass spectrometry (ICP-MS) detection. In this case, cell introduction is conducted using a high-efficiency nebulizer and spray chamber to achieve transport efficiencies of up to 55% for cells. Quantitative results revealed a number of receptors per cell significantly higher in the case of the most malignant phenotype (MDA-MB-231). Absolute and relative TfR1 concentration values are obtained in individual cells for the first time using the proposed system.

Piloted Liquid Spray Flames: A Numerical and Experimental Study

ABSTRACT Liquid-fuel spray flames are the primary mode of energy conversion in many high-power-density practical combustion devices. As compared to gaseous fuels, the phase change in liquid-fuel spray flames complicates the environment for laser-based combustion diagnostics and formulating predictive computational models. In this work, we present in-situ, non-intrusive measurement strategies and predictive models for combustion and carbon monoxide (CO) formation in piloted liquid-methanol spray flames. Resolving CO is essential to understand the incomplete oxidation of liquid hydrocarbon fuels and subsequent soot formation. A modified, flat-flame McKenna burner fitted with a direct-injection high-efficiency nebulizer (DIHEN) is used to produce piloted liquid-methanol spray flames. Hydroxyl (OH) planar laser-induced fluorescence (PLIF) is used for characterizing the reaction zones and temperature profiles of liquid-spray flames and two-dimensional (2D) images of CO are obtained via two-photon laser-induced fluorescence (TPLIF) using ultrashort, femtosecond-duration (fs) laser pulses. A three-dimensional (3D) computational model comprised of compressible continuous gas phase using unsteady Reynolds-averaged Navier-Stokes (URANS) in conjunction with two-way coupled Eulerian-Lagrangian spray modeling approach and partially-stirred reactor combustion model has been adapted to the modified McKenna burner. The computational model predicts the general trends of OH, temperature and CO profiles well at certain heights above the burner surface. Limitations of experimental measurements and strategies for improved model predictions pertaining to distributions of droplet sizes, pilot flame temperature, and the coflow temperature are discussed.

CO Imaging in piloted liquid-spray flames using femtosecond two-photon LIF

Abstract Liquid-spray flames are encountered in many practical combustion devices such as gasoline direct injection and diesel engines, gas turbine combustors as well as industrial furnaces. As opposed to gaseous fuels, additional phase-change steps present in liquid sprays not only complicate the overall combustion process, but also make in-situ, laser-based combustion diagnostics challenging. In particular, the formation of carbon monoxide (CO) due to incomplete fuel-air mixing and partial oxidation becomes a major challenge. In this study, we apply femtosecond, two-photon laser-induced fluorescence (fs-TPLIF) to measure CO concentration in piloted liquid-spray flames, taking into account possible signal interferences in the 230.1-nm, B1Σ+←X1Σ+ excitation scheme. A modified, flat-flame McKenna burner fitted with a direct-injection high-efficiency nebulizer (DIHEN) was used to produce piloted liquid-methanol spray flames. Although single-laser-shot OH-PLIF images show the presence of strong turbulent interactions in the core region, shot-averaged OH-PLIF images indicate that near the nozzle-exit region, the primary reaction takes place in an annular region around the droplet cloud, in general. A detailed spectroscopic study reveals that the signal interference at 460 nm originating from the second-order scattering of the excitation laser, which becomes approximately an order of magnitude stronger than CO fluorescence spectral lines near the nozzle exit region. The specific spectral filtering scheme introduced in our recent work is proved to be capable of suppressing interferences primarily originating from C2 Swan-band emissions. Two-dimensional CO maps along with OH-PLIF flame structure data provide key insights into the CO formation in piloted liquid-spray flames, while providing critical validation datasets for advanced computational models.

Method for Ultratrace Level (241)Am Determination in Large Soil Samples by Sector Field-Inductively Coupled Plasma Mass Spectrometry: With Emphasis on the Removal of Spectral Interferences and Matrix Effect.

A new method using sector field-inductively coupled plasma mass spectrometry (SF-ICPMS) was developed for the determination of (241)Am in large soil samples to provide realistic soil-plant transfer parameter data for dose assessment of nuclear waste disposal plans. We investigated four subjects: extraction behaviors of interfering elements (Bi, Tl, Hg, Pb, Hf, and Pt) on DGA resin (normal type, abbreviated as DGA-N); soil matrix element removal (Mg, Fe, Al, K, Na) using Fe(OH)3, CaF2, and CaC2O4 coprecipitations; Am and rare earth elements (REEs) separation on DGA-N and TEVA resins; and optimization of SF-ICPMS (equipped with a high efficiency nebulizer (HEN)) for Am determination. Our method utilized concentrated HNO3 to leach Am from 2 to 20 g soil samples. The CaC2O4 coprecipitation was used to remove major metals in soil and followed by Am/interfering elements separation using the proposed UTEVA + DGA-N procedure. After a further separation of REEs on TEVA resin, (241)Am was determined by HEN-SF-ICPMS. This method eliminated the matrix effect in ICPMS (241)Am measurement for large soil samples. The high decontamination factors (DFs) of interfering elements enable their thorough removal, and in particular, the DF of Pu (7 × 10(5)) was the highest ever reported in (241)Am studies; thus, this method is capable of analyzing (241)Pu-contaminated Fukushima Daiichi Nuclear Power Plant (FDNPP) sourced soil samples. A low detection limit of 0.012 mBq g(-1) for (241)Am was achieved. The chemical recovery of Am (76-82%) was stable for soil samples. This method can be employed for the low level (241)Am determination in large size soil samples that are contaminated with (241)Pu.

Efficacy and safety of nebulized glycopyrrolate for administration using a high efficiency nebulizer in patients with chronic obstructive pulmonary disease.

AimsTo establish the dose−response for pharmacodynamics (bronchodilatation), safety and pharmacokinetics for a nebulized formulation of the long acting muscarinic antagonist glycopyrrolate (EP-101) with a high efficiency nebulizer in patients with chronic obstructive pulmonary disease (COPD).MethodsPatients with moderate to severe COPD (GOLD II/III), with reversible lung function, were enrolled into this randomized, double-blind, placebo-controlled, six period crossover study (n = 42). Patients received single doses of EP-101 (12.5–400 μg) and placebo via a high efficiency nebulizer (eFlow® PARI nebulizer), with washout between treatments. Plasma pharmacokinetics were assessed in a subset of patients (n = 11).ResultsAll treatments were well tolerated with similar adverse event rates reported with placebo and at all doses. There were no clinically relevant changes in heart rate, systolic and diastolic blood pressure or in ECG parameters including QTc interval. Following treatment with EP-101 at all doses there was a rapid bronchodilator response within 5 min. Significant improvements in mean change from baseline FEV1 at 24 h were reported at doses ≥50 μg compared with placebo, with a clear dose−response relationship. Mean changes in FEV1 were 0.10 l (95% CI 0.06, 0.14) and 0.12 l (95% CI 0.08, 0.16) for 100 μg and 200 μg, respectively.ConclusionSingle doses of EP-101 ranging from 12.5 μg to 400 μg were well tolerated. EP-101 delivered by high efficiency nebulizer device produced a rapid onset of bronchodilatation with clinically meaningful improvements in lung function maintained over a 24 h period at all doses >50 μg.

Metal Determination in Tea, Wheat, and Wheat Flour Using Diluted Nitric Acid, High-Efficiency Nebulizer, and Axially Viewed ICP OES

This study deals with the determination of Cu, Al, Cd, Mo, Pb, V, Sr, Ni, Cr, Co, Zn, Mn, and Fe in tea, wheat grain, and wheat flour by inductively coupled plasma optical emission spectrometry (ICP OES) with axially viewed plasma. Ultrasonic nebulization (USN) or pneumatic nebulization with aerosol desolvation (PN/DES) is used to introduce the sample solution into the ICP. Solutions of nitric acid (HNO3) with different concentrations of the acid (4.6 to 9.1 mol L−1) and hydrogen peroxide (H2O2) were investigated for sample decomposition in closed vessel (made of TFM-polytetrafluoroethylene (PTFE)) under microwave irradiation. Certified reference materials of tea, wheat flour, or bush branches and leaves were analyzed (0.5 g of sample in the presence of 2 mL H2O2 + 3 mL HNO3 + 2 mL H2O). Element concentrations found were in accordance with those certified in most cases, excepting for Al and V. Plasma-related matrix effects were not observed as denoted by the signal of the Ar 420.069-nm emission line. The analyte recoveries in spiked chamomile tea and wheat flour samples ranged from 87 to 107 %. By using USN, the limits of quantification (LOQs) of Cu, Al, Cd, Mo, Pb, V, Sr, Ni, Cr, Co, Zn, Mn, and Fe were 0.033, 0.006, 0.023, 0.33, 2.0, 0.33, 0.001, 0.33, 0.07, 0.033, 0.07, 0.001, and 0.02 μg g−1, respectively. Quite similar LOQs were obtained for both nebulizers employed, with the exception of Pb; the LOQ of Pb was three times lower by using PN/DES. Commercialized tea, wheat grain, and wheat flour were analyzed, and the concentrations found were reported.

Determination of 234U/238U, 235U/238U and 236U/238U isotope ratios in urine using sector field inductively coupled plasma mass spectrometry

Quantification of the isotopic composition of uranium in urine at low levels of concentration is important for assessing both military and civilian populations' exposures to uranium. However, until now there has been no convenient, precise method established for rapid determination of multiple uranium isotope ratios. Here, the authors report a new method to measure (234)U/(238)U, (235)U/(238)U and (236)U/(238)U. It uses solid-phase chelation extraction (via TRU columns) of actinides from the urine matrix, followed by measurement using a magnetic sector field inductively coupled plasma mass spectrometer (SF-ICP-MS-Thermo Element XR) equipped with a high-efficiency nebulizer (Apex PFA microflow) and coupled with a membrane desolvating nebulizer system (Aridus II™). This method provides rapid and reliable results and has been used successfully to analyse Certified Reference Materials.

Preparation of a high-efficiency nebulizer of betamethasone dipropionate by high pressure microfluidization

Preparation of a high-efficiency nebulizer of betamethasone dipropionate by high pressure microfluidization

A Low-cost Demountable Direct Injection High-Efficiency Nebulizer for Inductively Coupled Plasma Mass Spectrometry

We developed a low-cost,demountable direct injection high-efficiency nebulizer(DIHEN) for inductively coupled plasma mass spectrometry(ICP-MS).It consisted of an enlarged microconcentric nebulizer based body,a tapered capillary(0.25 mm i.d.and 0.37 mm o.d.,30 μm i.d.and 40 μm o.d.at the tip),a hollow stainless steel tubing(0.5 mm i.d.and 2.0 mm o.d.) and two adapters made from polytetrafluoroethylene(PTFE),which were assembled by epoxy resin.The tapered capillary was reproducibly fabricated according to a flame-heated two-step drawing method.After immerging into boiling water,the epoxy resin became soft and the components could be taken apart simply.Then the broken or blocked sample capillary was replaced by a new tapered capillary with the same dimensions and then they were assembled again.The optimal sensitivity was obtained when the gas flow rate was 0.27 L/min with a sample uptake rate of 50 μL/min and a forward power of 1500 W.The sensitivities,detection limits and precisions of the homemade DIHEN under optimal operating conditions are similar,or better than those obtained with the MicroMist nebulizer,to some extent,though the polymeric ion levels of the former are higher than those of the latter.The utility of the homemade DIHEN for the analysis of small-volume samples was demonstrated by microscale flow injection analysis of Pt in serum samples.Then the homemade DIHEN was further utilized to couple microchip electrophoresis to ICP-MS for iodine speciation.The cost of the homebuilt DIHEN is about 1% price of the commercial Meinhard DIHEN,and the demountable construction permits that the blocked or broken sample capillary could be conveniently renewed with the same capillary in dimensions,obtaining low cost and easy maintenance.

Nebulized live-attenuated influenza vaccine provides protection in ferrets at a reduced dose

Live-attenuated influenza vaccine (LAIV) is delivered to vaccine recipients using a nasal spray syringe. LAIV delivered by this method is immunogenic at current doses; however, improvements in nasal delivery might allow for significant dose reduction. We investigated LAIV vaccination in ferrets using a high efficiency nebulizer designed for nasal delivery. LAIV nasal aerosol elicited high levels of serum neutralizing antibodies and protected ferrets from homologous virus challenge at conventional (107TCID50) and significantly reduced (103TCID50) doses. Aerosol LAIV also provided a significant level of subtype-specific cross-protection. These results demonstrate the dose-sparing potential of nebulizer-based nasal aerosol LAIV delivery.

Interfacing a microchip-based capillary electrophoresis system with a microwave induced plasma spectrometry for copper speciation

Abstract A microchip-based capillary electrophoresis (µCE) system was interfaced with a microwave induced plasma optical emission spectrometry (MIP-OES) to provide copper species separation capabilities. This system uses an extremely low flow demountable direct injection high efficiency nebulizer (D-DIHEN) sited directly at the liquid exit of the chip. A supplementary flow of buffer solution at the channel exit was used to improve nebulization efficiency. A small evaporation chamber has been incorporated into the interface in order to prevent the losses associated with traditional spray chambers, allowing the entire aerosol sample to enter the plasma. Syringe pumps were used to manipulate the flow rate and flow direction of the sample, buffer, and supplementary buffer solution. Sample volumes of 25 nL can be analyzed. With application of an electric field up to 500 V cm−1, species such as Cu(II) and Cu(EDTA)2− were separated in acidic solution within 90 s using a 26 mm long separation channel etched in a glass base. Resolution of the Cu(II) and Cu(EDTA)2− peaks was 1.1 using the chip-based µCE-MIP-OES system.

MC‐ICP‐MS Isotope Measurements with Direct Injection Nebulisation (d‐DIHEN): Optimisation and Application to Boron in Seawater and Carbonate Samples

We report here an optimisation of the demountable direct injection high efficiency nebuliser (d‐DIHEN) for isotopic measurements with a Neptune (ThermoFisher Scientific, Bremen, Germany) multi‐collector inductively coupled plasma‐mass spectrometer (MC‐ICP‐MS) and describe a method for boron isotopic ratio determination. With direct injection nebulisation 100% of the analyte was introduced into the ICP‐MS plasma and wash times were drastically reduced for elements such as boron and thorium. Compared to the classical stable introduction system (SIS: double Scott/cyclonic spray chamber), sensitivity for boron was 2–5 times higher with d‐DIHEN and wash times up to ten times shorter. Repeatability of 11B/10B sample‐calibrator bracketing measurements reached 0.25‰ (2s) for seawater and coral samples. Method accuracy and reproducibility were tested on mixed reference solutions having δ11B values in the ranges −90 to +40‰ and −2 to +2.5‰, demonstrating our ability to distinguish δ11B values with differences of only 0.25‰. The international seawater reference material NRCC NASS‐5 (National Research Council, Ottawa, Canada), analysed in different sessions over a 10‐month period, yielded an average δ11B value of +39.89 ± 0.25‰, in the upper range of previously published seawater values. A comparison between δ11B determined by d‐DIHEN MC‐ICP‐MS and positive‐TIMS (P‐TIMS) for four modern corals showed an excellent agreement (with bias of less than 0.4‰).

Fast determination of arsenosugars in algal extracts by narrow bore high-performance liquid chromatography–inductively coupled plasma mass spectrometry

The potential of narrow bore high-performance liquid chromatography (HPLC) with detection by inductively coupled plasma mass spectrometry (ICP-MS) for fast determination of arsenosugars in algal extracts was explored. The retention behavior of four naturally occurring dimethylarsinoylribosides on an anion-exchange microbore column was investigated, with the mobile phase flow rate ranging from 60 to 200 μL min −1. A low sample consumption system consisting of a micronebulizer and a low inner volume cyclonic spray chamber was used as the interface between the micro-column and the ICP mass spectrometer. Both the high efficiency nebulizer, HEN, and the PFA micronebulizer were tested, with the former providing 20–50% greater sensitivity than PFA (depending on the liquid flow rate), but comparable limits of detection and slightly lower chromatographic resolution. With the setup employed and under the optimal conditions, a satisfactory separation of the arsenosugars was achieved in less than 5 min. The instrumental limit of detection was 0.20 μg As L −1 and the precision was better than 3% (RSD%, n = 5). The accuracy of the determination was verified by the analysis of a reference algal extract, obtaining values in good agreement with the reference ones.

Effect of solvent dilution on the ICP-AES based silicon sensitivity, the aerosol characteristics and the resulting organic solution properties in the analysis of petroleum products

The effects of the solvent dilution factor on the physical properties of the resulting organic solutions, the aerosol characteristics and the silicon sensitivity were studied in ICP-AES for four different petroleum products by using near total sample consumption systems. The four samples were two gasoline products having very different volatilities along with a kerosene and a diesel sample. Petroleum product samples were diluted with xylene using four sample dilutions; 1:2, 1:5, 1:10 and 1:50. The sample introduction systems were a single pass spray chamber associated with a micronebulizer and a demountable Direct Injection High Efficiency Nebulizer (d-DIHEN). A cyclonic spray chamber also associated with a micronebulizer was taken as the reference system. Silicon was used as the test element, because it has been previously demonstrated that the ICP-AES Si sensitivity was significantly modified according to its chemical form. Silicon was spiked in each diluted solution with the same concentration to test sensitivity. When considering the dilution factor as the key variable, it was found that for the two gasoline samples and the kerosene one, the higher this variable, the lower the sensitivity. This result was explained in terms of changes in the solution volatility and/or in the aerosol characteristics. It was also observed that the total sample consumption systems were less sensitive to changes in the properties of the resulting organic solutions than the system based on the cyclonic spray chamber. However, for the latter chamber, the properties of the resulting organic solution had a marked influence on the extent of the effect of the silicon chemical form on the sensitivity. This fact demonstrated the appearance of an undefined interaction between the analyte and the organic solution during the aerosol transport step. However, both the single pass spray chamber and the d-DIHEN mitigated this effect for all the samples.

Original use of a direct injection high efficiency nebulizer for the standardization of liquid fuels spray flames

It is of practical importance to lead laboratory-scale experiments allowing a better understanding of the impact of commercial fuels composition on the formation of combustion residues such as soot particles. To this end, a hybrid burner has been designed recently to burn high-speed sprays of small liquid fuel droplets. It consists of a Holthuis (previously McKenna) burner originally equipped with a direct injection high efficiency nebulizer for the atomization of liquid hydrocarbons. A detailed description of this original setup is given in this paper. A priori estimations of atomization and evaporation times and length scales are then proposed and compared with experimental data. Droplet-size distribution measurements obtained in nonreacting conditions using a Malvern Spraytec particle sizer are presented and compared with values estimated by calculation. Cold sprays contours and liquid jet lengths in flames determined by Mie scattering at 532 and 1064 nm, respectively, are also presented. The results discussed in this work indicate that the hydrodynamic characteristics of the sprays generated with our system are relatively independent of the physical properties of fuels leading to comparable flames with identical liquid jet lengths, dimensions, and global structure. This feature facilitates an accurate comparison of flames burning various liquid hydrocarbons, which is of interest to emphasize differences in pollutants emissions and to highlight chemical effects for soot formation analysis.