Direct miniaturized

Benson and Ponton (1993) and Ponton (1996) have speculated on the ultimate results of continuing efforts for process minimization. They envision a twenty-first century chemical industry totally revolutionized by technological innovation, automation, and miniaturization. Small, distributed manufacturing facilities would produce materials on demand, at the location where they are needed. Raw materials would be nonhazardous, and the manufacturing processes would be waste free and inherently safe. While their vision of future technology is speculative, we are beginning to see progress in this direction. 

The basic steps of the IM process produce unique structures in all molded products, whether they are miniature (micro) electronic components, compact discs, or large automotive bumpers. These structures have frequently been compared to plywood with several distinct layers, each with a different set of properties. In all IM products, a macroscopic skin-core structure results from the flow of melt into an empty cavity. Identifiable zones or regions within the skin are directly... 

Miniaturized catheter-type ISE sensors, such as the implantable probe shown in Figure 5-20 represent the preferred approach for routine clinical in-vivo monitoring of blood electrolytes. For these intravascular measurements the reference electrode is placed outside die artery (in die external arm of die catheter), tints obviating biocompatability and drift problems associated with its direct contact with the blood. 

Dream reactions can be performed using chemical micro process engineering, e.g., via direct routes from hazardous elements [18]. The direct fluorination starting from elemental fluorine was performed both on aromatics and aliphatics, avoiding the circuitous Anthraquinone process. While the direct fluorination needs hours in a laboratory bubble column, it is completed within seconds or even milliseconds when using a miniature bubble column. Conversions with the volatile and explosive diazomethane, commonly used for methylation, have been conducted safely as well with micro-reactors in a continuous mode. 

The current trend in analytical chemistry applied to evaluate food quality and safety leans toward user-friendly miniaturized instruments and laboratory-on-a-chip applications. The techniques applied to direct screening of colorants in a food matrix include chemical microscopy, a spatial representation of chemical information from complex aggregates inside tissue matrices, biosensor-based screening, and molec-ularly imprinted polymer-based methods that serve as chemical alternatives to the use of immunosensors. 

Atsuya I, Itoh K, Akatsuka K (1987) Development of direct analysis of powder samples by atomic absorption spectrometry using the inner miniature cup technique. Fresenius Z Anal Chem 328 338-341. 

Specifically for triazines in water, multi-residue methods incorporating SPE and LC/MS/MS will soon be available that are capable of measuring numerous parent compounds and all their relevant degradates (including the hydroxytriazines) in one analysis. Continued increases in liquid chromatography/atmospheric pressure ionization tandem mass spectrometry (LC/API-MS/MS) sensitivity will lead to methods requiring no aqueous sample preparation at all, and portions of water samples will be injected directly into the LC column. The use of SPE and GC or LC coupled with MS and MS/MS systems will also be applied routinely to the analysis of more complex sample matrices such as soil and crop and animal tissues. However, the analyte(s) must first be removed from the sample matrix, and additional research is needed to develop more efficient extraction procedures. Increased selectivity during extraction also simplifies the sample purification requirements prior to injection. Certainly, miniaturization of all aspects of the analysis (sample extraction, purification, and instrumentation) will continue, and some of this may involve SEE, subcritical and microwave extraction, sonication, others or even combinations of these techniques for the initial isolation of the analyte(s) from the bulk of the sample matrix. 

The electrolyte volume of the STM cells is usually very small (ofthe order of a 100 pi in the above-described case) and evaporation of the solution can create problems in long-term experiments. Miniature reference electrodes, mostly saturated calomel electrodes (SCE), have been described in the literature [25], although they are hardly used anymore in our laboratory for practical reasons Cleaning the glassware in caroic acid becomes cumbersome. For most studies, a simple Pt wire, immersed directly into solution, is a convenient, low-noise quasireference electrode. The Pt wire is readily cleaned by holding it into a Bunsen flame, and it provides a fairly constant reference potential of fcj>i — + 0.55 0.05 V versus SCE for 0.1 M sulfuric or perchloric acid solutions (+ 0.67 0.05 V for 0.1 M nitric acid), which has to be checked from time to time and for different solutions. 

The direction and flow rate of the test and hydraulic fluids are determined by nine three-way valves and six a1r-dr1ven hydraulic pumps that must be sequenced 1n the proper order. The position of the valves 1s determined by six air-driven actuators. Two of the pumps are miniaturized, air-driven, hydraulic pumps used for sample loading and pressurization. One of the remaining four pumps 1s a high-pressure, constant volume, positive displacement, piston metering pump to provide hydraulic pressure, and the other three are positive displacement syringe pumps for In-line addition of additives. 

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