Preconcentration step

Eeed should be close to saturation limit before cooling to maximize potential recovery (consider preconcentration step to remove excess solvent). [Pg.452]

Generally best when crystallising component is large percentage of feed (consider preconcentration step if dilute). [Pg.452]

Because a preconcentration step is probably needed to make the final sequence more economical, it is logical to start with the opportunistic separation. This separation produces one of the products, pure water, as the underflow and a concentrated distillate appropriate for feed into either strategic separation. Arbitrarily choosing pervaporation first, the retentate has a composition on the 2-propanol-rich side of the azeotrope, whereas the permeate is pure water. No further strategic separations are required. [Pg.454]

First procedure consists of several stages. 11-molybdo-bismuthphosphate (MBP) is formed and extracted with butyl acetate, stripped with ammonia or acetate buffer solution and determined in aqueous solution using reaction of MBP with Astro Floxine (AF) or other polymethine dyes. Full separation from molybdate excess is not necessary in this procedure as spectiaim of lA differs considerable from dye spectiaim. Therefore sepai ation is simplified and used only as preconcentration step. Concentration factor 50 and good reproducibility make possible determination of low P(V) concentrations at 10 mol/1 level and lower. [Pg.125]

In recent decades the development of preconcentration steps to be implemented prior to analytical determinations of trace level compounds has been explored in considerable depth. With a view to eliminating or at least minimising the use of organic solvents used in conventional liquid-liquid extraction, other methodologies have been developed, such as membrane extraction, solid-phase extraction, solid-phase microextraction, etc. [Pg.422]

Sodium dodecylsulphate was selected as an anionic surfactant Factors affecting acid-induced cloud point extraction including surfactant, hydrochloric acid, PAHs, and electrolyte concentration, centrifugation have been examined. Finally, we applied the optimized acid-induced CPE system for combination of the extraction and preconcentration steps with fluorimetric determination of some representatives of PAHs. Suggested means was used for PAHs determination in tap water. [Pg.422]

Shipping analysis is an extremely sensitive electrochemical technique for measuring trace metals (19,20). Its remarkable sensitivity is attributed to the combination of an effective preconcentration step with advanced measurement procedures that generate an extremely favorable signal-to-background ratio. Since the metals are preconcentrated into the electrode by factors of 100 to 1000, detection limits are lowered by 2 to 3 orders of magnitude compared to solution-phase voltammetric measurements. Hence, four to six metals can be measured simultaneously in various matrices at concentration levels down to 10 10 i. utilizing relatively inexpensive... [Pg.75]

Potential of zero charge, 20, 23, 25, 66 Potential scanning detector, 92 Potential step, 7, 42, 60 Potential window, 107, 108 Potentiometry, 2, 140 Potentiometric stripping analysis, 79 Potentiostat, 104, 105 Preconcentrating surfaces, 121 Preconcentration step, 121 Pretreatment, 110, 116 Pulsed amperometric detection, 92 Pulse voltammetry, 67... [Pg.208]

The presence of redox catalysts in the electrode coatings is not essential in the c s cited alx)ve because the entrapped redox species are of sufficient quantity to provide redox conductivity. However, the presence of an additional redox catalyst may be useful to support redox conductivity or when specific chemical redox catalysis is used. An excellent example of the latter is an analytical electrode for the low level detection of alkylating agents using a vitamin 8,2 epoxy polymer on basal plane pyrolytic graphite The preconcentration step involves irreversible oxidative addition of R-X to the Co complex (see Scheme 8, Sect. 4.4). The detection by reductive voltammetry, in a two electron step, releases R that can be protonated in the medium. Simultaneously the original Co complex is restored and the electrode can be re-used. Reproducible relations between preconcentration times as well as R-X concentrations in the test solutions and voltammetric peak currents were established. The detection limit for methyl iodide is in the submicromolar range. [Pg.76]

Analytical procedures for the determination of cobalt in seawater generally use graphite furnace absorption spectrometry after a preconcentration step... [Pg.166]

One of the advantages of the isotope dilution technique is that the quantitative recovery of the analytes is not required. Since it is only their isotope ratios that are being measured, it is necessary only to recover sufficient analyte to make an adequate measurement. Therefore, when this technique is used in conjunction with graphite furnace atomic absorption spectrometry, it is possible to determine the efficiency of the preconcentration step. This is particularly important in the analysis of seawater, where the recovery is very difficult to determine by other techniques, since the concentration of the unrecovered analyte is so low. In using this technique, one must assume that isotopic equilibrium has been achieved with the analyte, regardless of the species in which it may exist. [Pg.286]

The benefits imparted by preconcentration to improved sensitivity are illustrated in the example of lead preconcentration on Chelex 100 resin [871,872], followed by analysis by ICP-AES. Without preconcentration the best detection bmit achievable is 60 ng/1, via direct nebubsation. When the Chelex 100 preconcentration step is included, the detection limit improves to 0.6 ng/1, i.e., 100 times better, which is a very important improvement achieved in the analysis of seawaters. Examinaton of Table 5.12 reveals that the following metals can be determined with detection limits in the 1 -10 ng/1 range beryllium (0.6 ng/1),... [Pg.304]

Enzymic methods are usually very specific and sensitive. Unfortunately the only methods in the literature for carbohydrates are all for glucose. Hicks and Carey [163] reported such a method, with a fluorometric final measurement, which was down to 3 x 10 8 M. Andrews and Williams [ 164] used a preconcentration step, sorption onto charcoal, elution, and a final determination with glucose oxidase. [Pg.398]

Aniline, methyl aniline, 1-naphthylamine, and diphenylamine at trace levels were determined using this technique and electrochemical detection. Two electrochemical detectors (a thin-layer, dual glassy-carbon electrode cell and a dual porous electrode system) were compared. The electrochemical behavior of the compounds was investigated using hydrodynamic and cyclic voltammetry. Detection limits of 15 and 1.5nmol/l were achieved using colourimetric and amperometric cells, respectively, when using an in-line preconcentration step. [Pg.412]

A method for the determination of organotin compounds by anodic stripping polarography has been published [121]. It has yet to be applied to seawater. Since the sensitivity permits the measurement of 0.01 ppm of the tin compounds, it is likely to be not quite sensitive enough for seawater and would require a preconcentration step. [Pg.475]

Determination of Pb(II) ion by classical or reversed FIA consists of a preconcentration step either on columns packed with a chelating sorbent (PC-FIA) or on a mercury film, followed by spectrophotometric determination of the complex with 4-(2-pyridylazo)resorcinol (11, kmax 518 nm) in borate buffer solution RSD 3-6% at 0.01-1 pM. End analysis by ASV was also applied99. [Pg.439]

Due to the predicted and previously detected low concentrations of pesticides in environmental samples (usually around the nanogram per liter level), a preconcentration step of the water samples is necessary prior to measurement. In this way, a preconcentration factor of several orders of magnitude (200-1,000-fold) is mandatory to reach the low detection limits necessary for the identification of pesticides, especially in complex wastewater samples. Also, the use of surrogate standards (e.g., triphenyl phosphate) added before the extraction step is a common practice in order to account for possible errors during the extraction process and for quantitative purposes. The commonly used extraction methods for polar compounds from water matrices involve isolation using liquid-liquid extraction (LLE) and solid-phase extraction (SPE), which are commented on below. Other methods such as semipermeable membrane devices (SPMD) are also mentioned. [Pg.54]

Prior to the quantitative determination of surfactants from aqueous environmental samples, a preconcentration step is needed to enrich low amounts of target analytes and to remove interfering matrix components. [Pg.425]

The iron-based redox cycle depicted in Figure 18.9 provides an effective preconcentrating step for phosphorus by trapping remineralized phosphate in oxic sediments. The conversion of phosphorus from POM to Fe(lll)OOH to CFA is referred to as sink switching. Overall this process acts to convert phosphorus from unstable particulate phases (POM to Fe(lll)OOH) into a stable particulate phase (CFA) that acts to permanently remove bioavailable phosphorus from the ocean. This is pretty important because most of the particulate phosphate delivered to the seafloor is reminer-alized. Without a trapping mechanism, the remineralized phosphate would diffuse back into the bottom waters of the ocean, greatly reducing the burial efficiency of phosphorus. [Pg.464]

Most existing methods are based on instrumental analysis involving exhaustive sample pretreatment and preconcentration steps, followed by purification and fractionation before final chromatographic separation and detection. For fat and oil samples, dissolving the lipids in an appropriate solvent is usually the first treatment. This has been achieved by melting the fat at 90°C followed by LLE or direct solid liquid extraction (SEE) with an apolar solvent [37], column extraction with a mixture of apolar solvents after drying of the sample with anhydrous Na2S04, Soxhlet extraction and/or sonication with apolar solvents. Typically, sample intake is between 0.5 g and 1 g and quantitative recoveries >60% have been reported. [Pg.21]

The development of multiclass methods for the detection of antibacterials and coccidiostats in food samples has shown a growing interest during the last years since the regulations concerning the presence of such chemicals in animal-derived foodstuffs is becoming more and more stringent. The challenges that these types of analyses pose to the analysts mainly have to do with the complexity of the matrix and the different physicochemical properties of the antibacterial families. Therefore, very often, a purification and preconcentration step is required prior to analysis in order to minimize matrix effects and reach the desired sensitivities [192, 193]. [Pg.30]

The measurement of very low levels of environmental pollutants is becoming increasingly important. The determination of lead, a cumulative toxin, is a good example. The current maximum allowable concentration of lead in British drinking water, before it enters the distribution network, is SO ng ml [29]. Although electrothermal atomization atomic-absorption spectrometry (AAS) can be used to measure this and lower concentrations, it is slow and requires considerable effort to ensure accurate results. Flames can provide simple and effective atom sources, but, if samples are aspirated directly, do not provide sufficient sensitivity. Thus, if a flame is to be used as the atom source, a preconcentration step is required. [Pg.151]

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