Liquid sample introduction direct

Solid foods in powder form can be analyzed directly by means of LA- or ETV-ICP-MS to eliminate time-consuming sample dissolution procedures (see Table 8.2). However, this requires the preparation of homogeneous powdered samples and the subsequent analytical determination is not as straightforward as the one based on liquid sample introduction. Another way to perform direct analysis of solid foods is to grind and suspend them into slurries. The viability of slurry nebulization relies on the ability to prepare samples of fine particle size in a reproducible manner and on the adoption of suitable (e.g., high-solids) nebulizers. Otherwise, slurries can be analyzed by ETV-ICP-MS resorting to the ultrasonic slurry sampling technique [72-74]. 

The liquid sample introduction system most commonly used on an ICP-MS is very similar to that used on a flame Atomic Absorption Spectrometer or an ICP-OES. Liquid samples can be directly injected using a pneumatic nebulizer and a spray chamber. 

Westphal, C.S. McLean, J.A. Aeon, B.W. AUen, L.A. Montaser, A. Axial Inductively Coupled Plasma TOF-MS Using Direct Liquid Sample Introduction. J. Anal. Atom. Spectrom. 2002, 17, 669-675. 

Todoli j. L. and Mermet J. M. (2001) Evaluation of a direct injection nebulizer (DIHEN) by comparison with a high efficiency nebulizer (HEN) coupled to a cyclonic spray chamber as a liquid sample introduction system for ICP-AES, J. Anal. At. Spectrom. 16 514-520. 

More recently, Montaser and co-workers have developed a new low cost DIN called the direct injection high etficiency nebuliser (DIHEN). The DIHEN is entirely made of glass and is similar in construction to a HEN, but it is longer. The main advantages provided by the DIHEN with respect to other conventional liquid sample introduction systems for ICP-MS are higher sensitivities, better signal stability and lower limits of detection. The dead volume of the DIHEN can be made lower than 10 nL, which significantly reduces the wash-out times for elements such as iodine, mercury and boron. As a result, this nebuliser has also proven to be suitable as an interface between separation techniques and ICP-MS. " Note that in these later studies, with a modified low dead volume DIHEN, the liquid flow rate can be lowered down to 0.5 pL/min. 

Westphal, C. S., McLean, J. A., Aeon, B. W., Allen, L. A., and Montaser, A. (2002) Axial inductively coupled plasma time-of-flight mass spectrometry using direct liquid sample introduction. J. Anal. At. Spectom., 17, 669-75. 

W. E. Petit and G. Horlick. Spect. Acta. 41B, 699, 1986. Describes an automated system for direct sample-insertion introduction of 10-pL liquid samples or small amounts (10 mg) of powder samples. 

Ionisation in an API source can take place in a variety of ways depending on the type of applications, namely by gas-phase ionisation, liquid- and plasma-based ionisation. At present, there are three major application areas of API-MS air or gas analysis (industrial emissions), on-line LC-MS (largest commercial application), and ICP-MS. A wide variety of sample introduction devices are available for gas analysis by API-MS. For use in ICP-MS, ions are sampled directly from the inductively... 

In ICP-AES and ICP-MS, sample mineralisation is the Achilles heel. Sample introduction systems for ICP-AES are numerous gas-phase introduction, pneumatic nebulisation (PN), direct-injection nebulisation (DIN), thermal spray, ultrasonic nebulisation (USN), electrothermal vaporisation (ETV) (furnace, cup, filament), hydride generation, electroerosion, laser ablation and direct sample insertion. Atomisation is an essential process in many fields where a dispersion of liquid particles in a gas is required. Pneumatic nebulisation is most commonly used in conjunction with a spray chamber that serves as a droplet separator, allowing droplets with average diameters of typically <10 xm to pass and enter the ICP. Spray chambers, which reduce solvent load and deal with coarse aerosols, should be as small as possible (micro-nebulisation [177]). Direct injection in the plasma torch is feasible [178]. Ultrasonic atomisers are designed to specifically operate from a vibrational energy source [179]. 

For the purpose of sample introduction, any sample introduction system (also sample inlet system or inlet) suitable for the respective compound can be employed. Hence, direct probes, reservoir inlets, gas chromatographs and even liquid chromatographs can be attached to an El ion source. Which of these inlet systems is to be preferred depends on the type of sample going to be analyzed. Whatever type the inlet system may be, it has to manage the same basic task, i.e., the transfer of the analyte from atmospheric conditions into the high vacuum of the El ion source Table 5.1 provides an overview. 

Brauers, F. von Btinau, G. Mass Spectrometry of Solutions a New Simple Interface for the Direct Introduction of Liquid Samples. Int. J. Mass Spectrom. Ion Proc. 1990, 99,249-262. 

Mass spectrometry is a sensitive analytical technique which is able to quantify known analytes and to identify unknown molecules at the picomoles or femto-moles level. A fundamental requirement is that atoms or molecules are ionized and analyzed as gas phase ions which are characterized by their mass (m) and charge (z). A mass spectrometer is an instrument which measures precisely the abundance of molecules which have been converted to ions. In a mass spectrum m/z is used as the dimensionless quantity that is an independent variable. There is still some ambiguity how the x-axis of the mass spectrum should be defined. Mass to charge ratio should not lo longer be used because the quantity measured is not the quotient of the ion s mass to its electric charge. Also, the use of the Thomson unit (Th) is considered obsolete [15, 16]. Typically, a mass spectrometer is formed by the following components (i) a sample introduction device (direct probe inlet, liquid interface), (ii) a source to produce ions, (iii) one or several mass analyzers, (iv) a detector to measure the abundance of ions, (v) a computerized system for data treatment (Fig. 1.1). 

Elements such as As, Se and Te can be determined by AFS with hydride sample introduction into a flame or heated cell followed by atomization of the hydride. Mercury has been determined by cold-vapour AFS. A non-dispersive system for the determination of Hg in liquid and gas samples using AFS has been developed commercially (Fig. 6.4). Mercury ions in an aqueous solution are reduced to mercury using tin(II) chloride solution. The mercury vapour is continuously swept out of the solution by a carrier gas and fed to the fluorescence detector, where the fluorescence radiation is measured at 253.7 nm after excitation of the mercury vapour with a high-intensity mercury lamp (detection limit 0.9 ng I l). Gaseous mercury in gas samples (e.g. air) can be measured directly or after preconcentration on an absorber consisting of, for example, gold-coated sand. By heating the absorber, mercury is desorbed and transferred to the fluorescence detector. 

Most flame spectrometers use a premix burner, such as that in Figure 21-5, in which fuel, oxidant, and sample are mixed before introduction into the flame. Sample solution is drawn into the pneumatic nebulizer by the rapid flow of oxidant (usually air) past the tip of the sample capillary. Liquid breaks into a fine mist as it leaves the capillary. The spray is directed against a glass bead, upon which the droplets break into smaller particles. The formation of small droplets is termed nebulization. A fine suspension of liquid (or solid) particles in a gas is called an aerosol. The nebulizer creates an aerosol from the liquid sample. The mist, oxi-... 

Another powerful means of sample introduction is direct, on-line supercritical fluid extraction. A small amount of solid (or liquid) sample can be placed in an extraction vessel, followed by the introduction of the supercritical fluid. The material can be... 

As noted earlier, the development of the dual cell (37), tandem quadrupole-FTMS (46, 47) and external ionization cell (48, 49) has facilitated the coupling of FTMS and chromatographic methods. Advances in interfacing separation techniques with FTMS will be important in the analysis of mixtures, especially where high mass resolution is required. For example, liquid chromatographic introduction of mixtures isolated from biological systems directly into an FTMS for analysis would eliminate the need for laborious sample clean up. 

Jinno, K., Nakanishi, S. and Fujimoto, C. (1985) Direct sample introduction system for inductively coupled plasma emission spectrometric detection in microcolumn liquid chromatography. Anal. Chem., 57, 2229-2235. 

Sample introduction is a major hardware problem for SFC. The sample solvent composition and the injection pressure and temperature can all affect sample introduction. The high solute diffusion and lower viscosity which favor supercritical fluids over liquid mobile phases can cause problems in injection. Back-diffusion can occur, causing broad solvent peaks and poor solute peak shape. There can also be a complex phase behavior as well as a solubility phenomenon taking place due to the fact that one may have combinations of supercritical fluid (neat or mixed with sample solvent), a subcritical liquified gas, sample solvents, and solute present simultaneously in the injector and column head [2]. All of these can contribute individually to reproducibility problems in SFC. Both dynamic and timed split modes are used for sample introduction in capillary SFC. Dynamic split injectors have a microvalve and splitter assembly. The amount of injection is based on the size of a fused silica restrictor. In the timed split mode, the SFC column is directly connected to the injection valve. Highspeed pneumatics and electronics are used along with a standard injection valve and actuator. Rapid actuation of the valve from the load to the inject position and back occurs in milliseconds. In this mode, one can program the time of injection on a computer and thus control the amount of injection. In packed-column SFC, an injector similar to HPLC is used and whole loop is injected on the column. The valve is switched either manually or automatically through a remote injector port. The injection is done under pressure. 

From the late 1960s onwards, a number of research groups around the world began to investigate alternatives to pneumatic nebulization for sample introduction, in an attempt to overcome transport efficiency limitations. The most successful approaches were those which involved heating small, discrete liquid samples, and sometimes even solid samples, directly on a metal filament, boat, or cup which could be positioned reproducibly into a flame. However, since the temperature of the metal would be lower than that of the flame itself, the techniques were confined to the determination of relatively easily atomized elements such as arsenic, bismuth, cadmium, copper, mercury, lead, selenium, silver, tellurium, thallium, and zinc. 

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