Inductively coupled plasma pressure

Plasma sources are also being iatroduced to produce plasmas at lower pressures and process temperatures. Inductively coupled plasma (ICP) and transformer-coupled plasma (TCP) are among the more commonly used sources, operating below 2.6 Pa (20 mTorr) (42). Low temperature RIE processiag operates between 26—67 Pa (200—500 mTorr). 

The intrinsic drawback of LIBS is a short duration (less than a few hundreds microseconds) and strongly non-stationary conditions of a laser plume. Much higher sensitivity has been realized by transport of the ablated material into secondary atomic reservoirs such as a microwave-induced plasma (MIP) or an inductively coupled plasma (ICP). Owing to the much longer residence time of ablated atoms and ions in a stationary MIP (typically several ms compared with at most a hundred microseconds in a laser plume) and because of additional excitation of the radiating upper levels in the low pressure plasma, the line intensities of atoms and ions are greatly enhanced. Because of these factors the DLs of LA-MIP have been improved by one to two orders of magnitude compared with LIBS. 

Inductively coupled plasma atomic emission spectrometry Electrothermal atomic absorption spectrometry High pressure liquid chromatography... 

Inductively coupled plasma Plasmas generated by application of radiofrequency power to a nonresonant inductive coil and maintained by an inductive electromagnetic field. Low-pressure ICP is a high-density plasma source. 

HPDSC High-pressure DSC ICP(I) Inductively coupled plasma... 

HPPLC (1) High-pressure planar liquid ICP-MS Inductively coupled plasma-mass... 

Analytes must be liberated from their associated solvent molecules as well as be ionized to allow mass separation. Several ionization methods enable ion production from the condensed phase and have been used for the coupling of CE to MS. Among them, atmospheric pressure ionization (API) methods, matrix-assisted laser desorption/ionization (MALDI), and inductively coupled plasma (ICP) ionization are mainly used. API techniques are undoubtedly the most widespread ionization sources and cover different analyte polarity ranges. 

A striking feature of the ILs is their low vapor pressure. This, on the other hand, is a factor hampering their investigation by MS. For example, a technique like electron impact (El) MS, based on thermal evaporation of the sample prior to ionization of the vaporized analyte by collision with an electron beam, has only rarely been applied for the analysis of this class of compounds. In contrast, nonthermal ionization methods, like fast atom bombardment (FAB), secondary ion mass spectrometry (SIMS), atmospheric pressure chemical ionization (APCI), ESI, and MALDI suit better for this purpose. Measurement on the atomic level after burning the sample in a hot plasma (up to 8000°C), as realized in inductively coupled plasma (ICP) MS, has up to now only rarely been applied in the field of IE (characterization of gold particles dissolved in IE [1]). This method will potentially attract more interest in the future, especially, when the coupling of this method with chromatographic separations becomes a routine method. 

Mass analysis is a relatively simple technique, with the number of ions detected being directly proportional to the number of ions introduced into the mass spectrometer from the ion source. In atomic mass spectrometry the ion source produces atomic ions (rather than the molecular ions formed for qualitative organic analysis) which are proportional to the concentration of the element in the original sample. It was Gray who first recognized that the inductively coupled plasma would make an ideal ion source for atomic mass spectrometry and, in parallel with Fassel and Honk, and Douglas and French developed the ion sampling interface necessary to couple an atmospheric pressure plasma with a mass spectrometer under vacuum. 

The introduction of inductively coupled plasma (ICP) in inorganic mass spectrometry means that there is an effective ion source operating at atmospheric pressure. Whereas solid mass spectrometric techniques allow direct analysis of solid samples in ICP-MS, the determination of trace impurities or isotope ratios in solid samples is often carried out after digestion and dissolution of the material. For the determination of trace impurities and isotope ratios in liquids, an additional nebulization... 

J. Moreda-Pineiro, E. Alonso-Rodriguez, P. Lopez-Mahia, S. Muniategui-Lorenzo, D. Prada-Rodriguez, A. Moreda-Pineiro and P. Bermejo-Barrera, Determination of major and trace elements in human scalp hair by pressurized-liquid extraction with acetic acid and inductively coupled plasma-optical-emission spectrometry. Anal. Bioanal. Chem., 388(2), 2007, 441 449. 

Data collected for each run included acid analysis using inductively coupled plasma (ICF) to determine cation concentration and titration to determine H concentration. Filtering characteristics were determined using solid and filtrate yield rates, as well as back pressures during the filtration cycle. The filter cake was characterized by moisture content and composition. Solid samples were analyzed with scanning electron microscopy (SEM) to determine changes in particle shape and size under various process conditions, and X-ray diffraction (XRD) was used to determine the solids composition. 

A very intense inductively coupled plasma (ICP) could be created, using a 13.56-MHz RF-source and coupling the power through a quartz tube into the plasma. Working pressure was 2 x 10-2 mbar and the substrate could be heated up to 800 °C [222]. The precursor was trimethylborazine ((HBN-CH3)3), which was transported in a nitrogen/argon carrier gas. Similar to other deposition processes, prior to the c-BN nucleation an oriented h-BN layer was formed [223]. 

Thompson and Zao [170] have described a solvent extraction-inductively coupled plasma atomic emission spectrometric method for the determination of down to 0.02 - 0.03 xg/g of molybdenum in soils. The soil sample is pressure-leached with 6 M hydrochloric acid and at 120 °C for 15 minutes. The digest is then extracted with heptan-2-one to separate molybdenum from potentially interfering elements such as iron, aluminium, calcium and magnesium. This organic extract is then directly sprayed into an inductively coupled plasma atomic emission spectrometer operated at 1.65 to 1.7 kW power. 

In this method the soil sample is dried overnight at 85 °C and ground into an homogeneous mixture. A 1 g soil sample is placed into a beaker and 10 ml of concentrated nitric acid added. The solution is heated to dryness and 5 ml of concentrated nitric acid is added. The uranium is redissolved in 5 ml of 8 N nitric acid and diluted to 25 ml with distilled water. The inductively coupled plasma mass spectrometry system used was an ELAN Model 250. The ion source consists of a modified plasma Thermal Model 2500 control box. The forward power was set at 1200 W with the plasma flow, auxiliary flow and nebuliser pressure set at 131/min, 1.0l/min and 0.27 MPa, respectively. The focusing lenses B, El, P and S2 are set at +5.3 V, -12.5 V, -18.0 V and -7.6 V, respectively. The m/z238 ion was monitored for two sec-... 

White, S., Catterick, T., Fairman, B. and Webb, K. (1998) Speciation of organo-tin compounds using liquid chromatography atmospheric pressure ionisation mass spectrometry and liquid chromatography inductively coupled plasma mass spectrometry as complementary techniques./. Chromatogr. A, 794, 211-218. 

The ionization methods reported for IMS included MALDI [41,76-80], Secondary Ion Mass Spectrometry (SIMS) [19, 81-86], Matrix-enhanced (ME)-SIMS [87, 88], Desorption Electrospray Ionization (DESI) [89-99], Nanostructure Initiator Mass Spectrometry (NIMS) [100-102], Atmospheric Pressure Infrared MALDI Mass Spectrometry (AP-IR-MALDI-MS) [103], Laser Ablation-inductively Coupled Plasma-Mass Spectrometry (LA-ICP-MS) [104-106], Laser Desorption Postionization (LDPI) [107], Laser Ablation Electrospray Ionization Mass Spectrometry (LAESI) [108, 109], and Surface-assisted Laser Desorption/ioniza-tion Mass Spectrometry (SALDI) [110-112], Another method was called probe electrospray ionization (PESI) that was used for both liquid solution and the direct sampling on wet samples. 

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