Injection port

Caffeine is extracted from beverages by a solid-phase microextraction using an uncoated fused silica fiber. The fiber is suspended in the sample for 5 min and the sample stirred to assist the mass transfer of analyte to the fiber. Immediately after removing the fiber from the sample it is transferred to the gas chromatograph s injection port where the analyte is thermally desorbed. Quantitation is accomplished by using a C3 caffeine solution as an internal standard. 

Programmed-temperature vaporizers are flexible sample-introduction devices offering a variety of modes of operation such as spHt/sphtless, cool-sample introduction, and solvent elimination. Usually the sample is introduced onto a cool injection port liner so that no sample discrimination occurs as in hot injections. After injection, the temperature is increased to vaporize the sample. 

Operabihty (ie, pellet formation and avoidance of agglomeration and adhesion) during kiln pyrolysis of urea can be improved by low heat rates and peripheral speeds (105), sufficiently high wall temperatures (105,106), radiant heating (107), multiple urea injection ports (106), use of heat transfer fluids (106), recycling 60—90% of the cmde CA to the urea feed to the kilns (105), and prior formation of urea cyanurate (108). 

The purity of a dicyclopentadiene stream may be expressed in terms of DCPD itself or in terms of available CPD monomer. Both analyses are deterrnined by gas chromatography (gc). The first analysis is capillary gc on a nonpolar column. The data from the analysis can be used to calculate the available CPD, assuming that all the DCPD and CPD codimers crack completely. In the second analysis the sample is charged to the gc equipment under temperature conditions (injection port 400°C) that cause essentially complete reaction of the dimers to monomers. 

Another dynamic measurement is the LCEC technique which can be thought of, simpHsticaHy, as EIA using a chromatographic column positioned between the sample injection port and the detector. Bioanalytical systems (BAS) of West Lafayette, Indiana, specializes in instmmentation for LCEC. Their catalogs come with extensive bibhographies covering a variety of appHcations. 

If the hub removal is necessary, such as required on compressor with non-split seals, a tapered hub fit on the shaft should be used. The removable hubs should have tapped puller holes. The shaft should be keyless with the preferred method of installation and removal by use of hydraulic dilation. Two injection ports 180° apart should be used whether injection is through the shaft or through the hub. Shrink fits should be 2 to 2.5 mil/in. of diameter. API 671 rcL ommends 1,5 mil/in. minimum, but experience indicates the heavier shrink may be required. For the juncture rating calculation, a f ra lion value of. 12 is recommended. 

Technology Description Fluidized bed incinerators utilize a very turbulent bed of inert granular material (usually sand) to improve the transfer of heat to the waste streams to be incinerated. Air is blown through the granular bed materials until they are "suspended" and able to move and mix in a manner similar to a fluid, i.e., they are "fluidized".In this manner, the heated bed particles come in intimate contact with the wastes being burned. The process requires that the waste be fed into multiple injection ports for successful treatment. Advantages... 

An on-line supercritical fluid chromatography-capillary gas chromatography (SFC-GC) technique has been demonstrated for the direct transfer of SFC fractions from a packed column SFC system to a GC system. This technique has been applied in the analysis of industrial samples such as aviation fuel (24). This type of coupled technique is sometimes more advantageous than the traditional LC-GC coupled technique since SFC is compatible with GC, because most supercritical fluids decompress into gases at GC conditions and are not detected by flame-ionization detection. The use of solvent evaporation techniques are not necessary. SFC, in the same way as LC, can be used to preseparate a sample into classes of compounds where the individual components can then be analyzed and quantified by GC. The supercritical fluid sample effluent is decompressed through a restrictor directly into a capillary GC injection port. In addition, this technique allows selective or multi-step heart-cutting of various sample peaks as they elute from the supercritical fluid... 

Figure 13.3 Schematic diagram of the parallel cryogenic trap MDGC-IR-MS system A, splitless injection port B, RC-5 non-polar first-stage separation column C, HP 5970B MSD D, HP 5965B IRD E, four-poit two-way valve (300 °C maximum temperature) F, external auxiliary earner gas G, six-poit selection valve (300 °C maximum temperature) H, stainless-steel cryogenic caps I, tliree-poit two- way valve (300 °C maximum temperature) ...

In continuous mixing, the numerous thermocouple wells on the barrel may be used as injection ports for the introduction of separate additive streams (crosslinker, curing agent, etc.) on-line. Figure 19 shows the cross-section of a hollow flighted-screw shaft together with a... 

Figure 19 Cross-section of split barrel showing a series of injection ports.

The rearrangement of 3-acetyl-2-piperidino-3/f-azepine to 3-acetyl-2-piperidinopyridine in the injection port during GC analysis of the 3/7-azepine has been noted.124... 

Clean or change injection port liners frequently because nonvolatile materials in extracts from body fluids can accumulate in the injection port and/or head of the GC column and cause separation problems. 

If the injection port temperature is too high, the sample will partially decompose but the GC peak for the intact material will be sharp and rK will not be affected. However, if the sample decomposes on the column the tR will vary and the observed peak will be broad. For normal stable samples, the injection port temperatures should be in the range of 150-280°. 

The purge activation time (or the sample transfer time) depends on the sample solvent and carrier gas flow relative to the volume of the injection port liner and the boiling points of the sample components. For most applications, a purge activation time of 50-120 sec is better than 25-50 sec. Early activation results in the loss of sample, while late activation results in peak tailing. A more accurate method of determining purge activation time is to divide the volume of the injector liner by the flow rate (F) of the carrier gas and multiply this value by 1.5 or 2.0. (Do not use a packed liner.)... 

Sample components adsorb in the injection port, in the transfer line, or on the column. 

Mold construction FRP spray metal, cast aluminum gusket seal, air vents, self-sealing injection port FRP FRP, spray metal, cast aluminum, pinch (land) Metal, shear edge High grade steel shear edge... 

To determine secondary alkanesulfonates in sewage wastewaters, solid phase extraction (SPE) and a single-step procedure which combines elution and injection port derivatization for analysis with GC-MS were developed [36]. Again a tetrabutylammonium ion pair reagent was employed both to elute the secondary alkanesulfonates as their ion pairs from CI8-bonded silica disks and to derivatize sulfonate ion pairs under GC injection port conditions. Secondary alkanesulfonates were effectively recovered from samples of raw sewage (>92%) and from primary (>98%) and secondary (>85%) effluents. No... 

One field study on the mass flow of secondary alkanesulfonates was conducted in the Zurich-Glatt municipal wastewater treatment plant [37]. The concentration of alkanesulfonates in samples of raw sewage and primary and secondary effluents was analyzed using the above-described SPE with C18 Empore disks and injection port derivatization with GC-MS detection. The con-... 

Injection 5 pi of petroleum ether solution Injection port temperature 250°C Detector temperature ... 

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