Dialysis configurations

Figure 6 shows typical online dialysis configurations. A continuously working dialysis cell can be coupled directly to the valve IV (Figure 6A) injecting the prepurified and conditioned sample solution into a nonsegmented carrier flow stream, e.g., of liquid column chromatography. The analytes are separated... 

When classifying chemical products, Seider et al. [3] identify three categories (1) basic chemicals (commodity and specialty chemicals, bio-materials, and polymeric materials) (2) industrial chemicals (films, fibers, paper,. ..) and (3) configured consumer products (dialysis devices, post-it notes, transparencies, drug delivery patches,. ..). In the manufacture of epitaxial silicon wafers, a thin film of crystalline silicon is often deposited on a polished crystalline silicon... 

Notwithstanding the excellent analytical features inherent in molecular phosphorimetric measurements, their use has been impeded by the need for cumbersome cryogenic temperature techniques. The ability to stabilize the "triplet state" at room temperature by immobilization of the phosphor on a solid support [69,70] or in a liquid solution using an "ordered medium" [71] has opened new avenues for phosphorescence studies and analytical phosphorimetry. Room-temperature phosphorescence (RTF) has so far been used for the determination of trace amounts of many organic compounds of biochemical interest [69,72]. Retention of the phosphorescent species on a solid support housed in a flow-cell is an excellent way of "anchoring" it in order to avoid radiationless deactivation. A configuration such as that shown in Fig. 2.13.4 was used to implement a sensor based on this principle in order to determine aluminium in clinical samples (dialysis fluids and concen-... 

Sensors based on integrated dialysis, reaction and detection differ from those described in Section 4.3.1 in the fact that a (bio)chemical reaction takes place after separation (simultaneously with detection). They thus fit the generic configuration depicted in Fig. 5.1. A. Some of the ingredients of such a reaction may be immobilized at the sensing microzone, even though the reaction may also take place in the solution passed through it. 

Membranes are used to separate gaseous mixtures or liquid mixtures. Membrane modules can be tubular, spiral-wound, or plate and frame configurations. Membrane materials are usually proprietary plastic films, ceramic or metal tubes, or gels with hole size, thickness, chemical properties, ion potential, and so on appropriate for the separation. Examples of the kinds of separation that can be accomplished are separation of one gas from a gas mixture, separation of proteins from a solution, dialysis of blood of patients with kidney disease, and separation of electrolytes from non electrolytes. 

Selectivity parameters, needed for the BOHLM or BAHLM module design and their determination techniques, are analyzed. Selectivity can be controlled by adjusting the concentration, volume, and flow rate of the LM phase. Such control of the selectivity is one of the advantages of the bulk liquid membrane systems in comparison with other liquid membranes configurations and Donnan dialysis techniques. The idea of dynamic selectivity and determination techniques are presented and discussed. 

In an externally buffered enzyme electrode (Fig. 45), substrate-free buffer is continuously pumped between the dialysis membrane and the enzyme layer (Cleland and Enfors, 1984), i.e., the sample is diluted before it reaches the enzyme. The intensity of the buffer flow may be used to adjust the measuring range and sensitivity. The configuration of the sensor permits it to be sterilized. While the membrane is protected by continuously flowing buffer, the rest of the sensor can be sterilized for 1 h in a solution of 95% ethanol and 5% H2SO4. 

As early as 1955, Kolff and Balzer" described a device patterned after an early renal dialysis unit (the Inouye artificial kidney) wherein polyethylene tubing was used in a coil configuration. While the concept was sound, the membrane material choices available at that time were limited. 

The basic configuration of a FI manifold for on-line dialysis with volume-based sampling is shown in Fig. 6.1. The manifold differs from gas-diffiision manifolds in that usually no reagents are added to the donor stream while most applications involve merging of a reagent to the acceptor stream to transform the dialysate into a detectable species. 

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