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Characteristic elimination mass

Table 2. Characteristic elimination masses observed in product ion spectra. (Reproduced from reference 16, with permission from the Australian Society of Viticulture and Oenology)... Table 2. Characteristic elimination masses observed in product ion spectra. (Reproduced from reference 16, with permission from the Australian Society of Viticulture and Oenology)...
The advantage of suspension processes over mass processes is the excellent temperature control that can be obtained through the suspending medium, water. This allows for rapid heat removal and shorter polymerization times. It reduces or eliminates hot spots or heat-kicks characteristic of mass reactors. It also allows the polymerization to be driven very close to completion so that no devolatilization step is normally required. [Pg.87]

To eliminate mass transfer influence in practice, the characteristic transfer time should be roughly one order of magnitude smaller than the characteristic reaction time. Because the mass transfer times in MSRs are up to two orders of magnitude smaller than in conventional reactors,... [Pg.55]

To eliminate mass transfer resistances in practice, the characteristic transfer time should be roughly one order of magnitude smaller than the characteristic reaction time. As the mass andheat transfer performance ina microstructured reactor (MSR) is up to two orders of magnitude higher than in conventional tubular reactors, the reactor performance can be considerably increased, leading to the desired intensification of the process. In addition, consecutive reactions can be efficiently suppressed due to strict control of the residence time and a narrow residence time distribution (RTD). Therefore, fast reactions carried out in a M SR show higher product selectivity and yield. [Pg.398]

The reasonable stable products are characterized by an ir-absorption near 1615 cm". The 4-protons resonate near 6.2 ppm in the H NMR spectrum (23). NMR spectra exhibit a carbonyl atom signal near 173 ppm, whereas C-4 resonates near 8 108 these positions are characteristic of other mesoionic ring carbon atoms (24). In the mass spectra, decomposition with loss of CO, rupture of the 1,5 and 2.3 bonds with elimination of R NC2R 0 and cleavage of the 1,2 and 3,4 bonds with elimination of C2R 0S is observed (11)... [Pg.9]

In GC-MS effluent from the column is introduced directly into the mass spectrometer s ionization chamber in a manner that eliminates the majority of the carrier gas. In the ionization chamber all molecules (remaining carrier gas, solvent, and solutes) are ionized, and the ions are separated by their mass-to-charge ratio. Because each solute undergoes a characteristic fragmentation into smaller ions, its mass spectrum of ion intensity as a function of mass-to-charge ratio provides qualitative information that can be used to identify the solute. [Pg.571]

The electron impact mass spectrometric fragmentations of (E)-3- and ( )-4-styryl-pyridazines show that the intensity ratio of the M and (M -1)" ions, the general degree of fragmentation and the elimination pathways of nitrogen are the most characteristic features distinguishing between the two isomeric compounds (81JHC255). [Pg.8]

As can be seen from Fig, 3.7, the pinch decomposes the synthesis problem into two regions a rich end and a lean end. The rich end comprises all streams or parts of streams richer than the pinch composition. Similarly, the lean end includes all the streams or parts of streams leaner than the pinch composition. Above the pinch, exchange between the rich and the lean process streams takes place. External MSAs are not required. Using an external MSA above the pinch will incur a penalty of eliminating an equivalent amount of process lean streams from service. On the other hand, below the pinch, both the process and the external lean streams should be used. Furthermore, Fig. 3.7 indicates that if any mass is transferred across the pinch, the composite lean stream will move upward and, consequently, external MSAs in excess of the minimum requirement will be used. Therefore, to minimize the cost of external MSAs, mass should not be transferred across the pinch. It is worth pointing out that these observations are valid only for the class of MEN problems covered in this chapter. When the assumptions employed in this chapter are relaxed, more general conclusions can be made. For instance, it will be shown later that the pinch analysis can still be undertaken even when there are no process MSAs in the plant. The pinch characteristics will be generalized in Chapters Five and Six. [Pg.53]

It is possible to take advantage of the differing characteristics of the periphery and the interior to promote chemical reactions. For example, a dendrimer having a non-polar aliphatic periphery with highly polar inner branches can be used to catalyse unimolecular elimination reactions in tertiary alkyl halides in a non-polar aliphatic solvent. This works because the alkyl halide has some polarity, so become relatively concentrated within the polar branches of the dendrimer. This polar medium favours the formation of polar transition states and intermediates, and allows some free alkene to be formed. This, being nonpolar, is expelled from the polar region, and moves out of the dendrimer and into the non-polar solvent. This is a highly efficient process, and the elimination reaction can be driven to completion with only 0.01 % by mass of a dendrimer in the reaction mixture in the presence of an auxiliary base such as potassium carbonate. [Pg.144]

Mass spectra of compounds 11 are characterized by the presence of fission products of the molecule tricyclic moiety (m/e of fragments depending on alkaloid type) and ergolene moiety with m/e 448 and after SO2 elimination m/e 384 = 448 -SO2. The characteristic IH-NMR is the absence of signal for C - 2 proton and a new multiplet at region 7-7.5 ppm for aromatic protons from saccharin moiety. [Pg.87]

An unfortunate characteristic of early zinc polycarboxylate cements was the early development of elastomeric characteristics- cobwebbing -in the cement pastes as they aged, thus shortening working time (McLean, 1972). Improvements in cement formulation, the addition of stannous fluoride to the oxide powder (Foster Dovey, 1974, 1976) and modifications in the polyacid have eliminated this defect. However, the cements have to be mixed at quite a low powder/liquid ratio, 1 -5 1 0 by mass, when used for luting. [Pg.107]

The MAB ion source offers several advantages over El for PyMS. By eliminating excessive fragmentation, characteristic of electron ionisation, and by producing highly reproducible mass spectra MAB (Kr) greatly simplifies the analysis of pyrolysis data. Furthermore, MAB ionisation, when combined to MS/MS, provides a useful tool for structural elucidation of pyrolysis products. The ability for selective ionisation can be very useful to reduce the background combination in techniques such as GC-MS, LC-MS or SFC-MS. [Pg.367]

Principles and Characteristics Extraction or dissolution methods are usually followed by a separation technique prior to subsequent analysis or detection. While coupling of a sample preparation and a chromatographic separation technique is well established (Section 7.1), hyphenation to spectroscopic analysis is more novel and limited. By elimination of the chromatographic column from the sequence precol-umn-column-postcolumn, essentially a chemical sensor remains which ensures short total analysis times (1-2 min). Examples are headspace analysis via a sampling valve or direct injection of vapours into a mass spectrometer (TD-MS see also Section 6.4). In... [Pg.449]

Principles and Characteristics The most commonly used and widely known technique coupled to gas chromatography is mass spectroscopy. In early couplings, with packed GC columns being the major problem encountered, elimination of the carrier gas at relatively high flow-rates (25mLmin 1), resulted in a significant loss of sensitivity. With the advent of open tubular devices, the column flow could be passed directly into the mass spectrometer. GC-MS is typically... [Pg.459]

As the vast majority of LC separations are carried out by means of gradient-elution RPLC, solvent-elimination RPLC-FUR interfaces suitable for the elimination of aqueous eluent contents are of considerable use. RPLC-FTTR systems based on TSP, PB and ultrasonic nebulisa-tion can handle relatively high flows of aqueous eluents (0.3-1 ml.min 1) and allow the use of conventional-size LC. However, due to diffuse spray characteristics and poor efficiency of analyte transfer to the substrate, their applicability is limited, with moderate (100 ng) to unfavourable (l-10pg) identification limits (mass injected). Better results (0.5-5 ng injected) are obtained with pneumatic and electrospray nebulisers, especially in combination with ZnSe substrates. Pneumatic LC-FI1R interfaces combine rapid solvent elimination with a relatively narrow spray. This allows deposition of analytes in narrow spots, so that FUR transmission microscopy achieves mass sensitivities in the low- or even sub-ng range. The flow-rates that can be handled directly by these systems are 2-50 pLmin-1, which means that micro- or narrow-bore LC (i.d. 0.2-1 mm) has to be applied. [Pg.492]


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Characteristic mass

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