Apparatus for pressurized planar electrochromatography in a completely closed system

Pressurized planar electrochromatography (PPEC) is the mode which offers much higher separation efficiency in comparison to conventional planar chromatography, including both higher performance and much higher speed of separation. In this paper, we present a new device for performing PPEC in which the whole area of the chromatographic plate is pressurized. Both electrodes (anode and cathode) are washed with the mobile phase during the experiment, which prevents gas bubbles from collection in the region of the electrodes. This device enables directly controlling the flow rate of the mobile phase during the electrochromatography process. Mobile phase control offers the possibility of researching the influence of various properties of the PPEC system on separation efficiency. One important relationship to investigate is plate height vs mobile phase flow rate. This relationship helps to choose the optimal value of the mobile phase flow rate during the separation process. Considerable difference in shape of this relationship is demonstrated for conventional planar chromatography plates and high performance planar chromatography plates. Examples of the influence of some properties of the separating system on flow rate of the mobile phase are demonstrated, such as the buffer concentration in the mobile phase, the pH value of the buffer solution of the mobile phase, the type of chromatographic plate, and the voltage applied to the electrodes.     

Results with an apparatus for pressurized planar electrochromatography

Pressurized planar electrochromatography (PPEC) is a fast and efficient planar chromatographic technique. The mobile phase is driven by electroosmotic flow, while the system is pressurized in a manner that allows heat to flow between the sorbent layer and the pressurizing medium. The reproducibility of solute retention was not satisfactory in the initial report describing PPEC. In the current report, this reproducibility is improved by better control of several experimental variables. The pressure at which PPEC is performed is now free of drift, and the temperature at which the layer is preconditioned is maintained to within +/-1 degrees C. The best reproducibility of retention is obtained when the plate is soaked in the mobile phase for a defined time before each run. In the original prototype, the temperature of the sorbent layer was not controlled. In the present apparatus, water, at a constant temperature between 3 and 60 degrees C, is circulated through channels in the two die blocks that pressurize the layer. The highest efficiency is obtained at an intermediate temperature. This behavior is ascribed to high resistance to mass transfer at the lower temperatures and increased diffusion at higher temperatures. Efficiency, as measured by the number of theoretical plates, increases with increasing migration distance. The height equivalent of a theoretical plate diminishes with increasing migration distance, and values as low as 0.0106 mm are obtained under appropriate conditions. This extrapolates to 94 000 plates/m. Manual spotting was used in this report. Evidence is presented that substantially better efficiency would be obtained if the initial spot size were smaller. The efficiency of PPEC in its current form is illustrated by a chromatogram showing the separation of nine solutes in 2 min. PPEC was also performed with TLC plates in a back-to-back configuration, and this doubles the number of samples that can be simultaneously separated.     

雌激素的加压毛细管电色谱分析研究

论文基于苯乙烯基功能整体柱,建立了五种环境雌激素的加压毛细管电色谱分析方法,并应用于鱼肉样品分析。实验考察了有机溶剂浓度、酸度、分离电压、盐浓度、流速等条件对五种雌激素分离的影响。在最优条件下,五种环境雌激素在18 min内实现了基线分离,在4.0×10-7-8.0×10-5g/mL范围内线性良好,检测限在0.8×10-7-5×10-7g/mL范围内。该方法应用于鱼肉实际样的测定,获得回收率范围是78.0%-88.5%。效果良好。     

Influence of pressure upon coupling pressurized capillary electrochromatography with nuclear magnetic resonance spectroscopy

In this work, the influence of supplementary pressure on the separation efficiency of pressurized capillary electrochromatography (pCEC) was examined. At low pressures of up to 30 bar, which is more than sufficient to prevent bubble formation, no significant loss in separation efficiency is observed. Even at 100 bar, the efficiency of pCEC is still significantly better than without application of an electric field. In addition, analysis times are drastically reduced compared to both capillary electrochromatography (CEC) and capillary HPLC. On the basis of these results, an improved interface for capillary NMR coupling is described and used for the separation and identification of a mixture of unsaturated fatty acid methyl esters. Under these conditions, the analysis time could be shortened by up to a factor of 10 when pCEC is coupled to NMR spectroscopy.     

On-column coaxial flow chemiluminescence detection for underivatized amino acids by pressurized capillary electrochromatography using a monolithic column

A new method for pressurized capillary electrochromatography (pCEC) coupling with chemiluminescence (CL) detection using a modified on-column coaxial flow detection interface was developed. To evaluate the feasibility and reliability of the experimental setup, the typical CL compounds luminol and isoluminol were separated and detected by using this pCEC-CL system. A detailed investigation of CL detection interface and postcolumn CL reagent flow rate parameters was described. The excellent resolution and detection sensitivity was achieved by using 3-microm ODS-C18 packed column with 30% ACN (v/v), 5 mmol/L phosphate buffer (pH 8.0). Moreover, with the presence of Co(II) (1.0 x 10(-4) mol/L) in the mobile phase, the linear range of the concentration for luminol was 2.0 x 10(-9)-2.0 x 10(-6) mol/L with a detection limit (S/N = 3) of 2.0 x 10(-10) mol/L, and 2.5 x 10(4) theoretical plates was achieved. In addition, separation and detection of the underivatized amino acids (l-threonine and l-tyrosine) were accomplished by using a polymerized monolithic column based on the principle of the luminol-H2O2-Cu(II)-amino acid CL system. Under the optimum conditions, the mixture of amino acids was efficiently separated with satisfactory results.     

Nanoinjector for capillary electrophoresis and capillary electrochromatography

A rotary valve nanoinjector was devised for use in capillary electrophoresis (CE) and capillary electrochromatography (CEC). A fused-silica capillary tip was inserted in a small through-hole in the rotor. The narrow and short capillary tip, with an inner volume of 6-24 nL, was embedded in the hole using epoxy resin. The injection volume was confirmed chromatographically by comparing the peak areas obtained with the nanoinjector to those of a conventional injector. In addition, both the rotor and stator of the injector were made of a nonconducting material, polyimide resin, to be utilized for CE and CEC. The application of the nanoinjector for CE was demonstrated.     

Photopolymerized sol-gel monoliths for capillary electrochromatography

A solution of methacryloxypropyltrimethoxysilane in the presence of an acid catalyst, water, toluene, and a photoinitiator was irradiated at 365 nm for 5 min in a 75-microm i.d. capillary to prepare a porous monolithic sol-gel column by a one-step, in situ, process. The photopolymerized sol-gel (PSG) column shows reversed-phase behavior. Using this column, a variety of low-molecular-weight neutral compounds, including polycyclic aromatic hydrocarbons, alkyl benzenes, alkyl phenyl ketones, and steroids are separated from mixtures. Various different operational parameters, such as buffer composition, field strength, and column temperature, were varied to assess their influence on column performance. Use of PSG as a stationary phase for a pressure-driven separation is also demonstrated.     

Macroporous photopolymer frits for capillary electrochromatography

Macroporous polymer frits have been fabricated in fused-silica capillaries by the UV photopolymerization of a solution of glycidyl methacrylate and trimethylopropane trimethacrylate. This in situ preparation is a simple, rapid, and reproducible process. The frit can be placed at any desired position along the column. Photopolymer frits can withstand the short exposure to a high pressure (over 6000 psi). Bubble formation is no observed to occur with these frits under our experimental conditions. By choice of porogens, it is possible to control the porous properties. The use of such frits in capillaries to retain particles of chromatographic packing has been demonstrated to be stable and robust with continuous operation over 3 days.     

Magnetically immobilized beds for capillary electrochromatography

Fritless packed beds comprised of magnetically responsive octadecylsilane bonded silica particles have been constructed for reversed-phase electrochromatography. The magnetic particles were immobilized in the capillary by applying an external magnetic field transverse to the direction of electroosmotic flow. Being subjected to the interplay of fluid dragging and magnetic forces, the initial loosely packed particle assembly was compacted into a uniform packing structure. The magnetically immobilized beds obtained were used as stationary phases for separation of neutral compounds, with retention behavior and column efficiency similar to those of slurry-packed columns. The results suggest that the magnetic attraction approach to fritless column packing may be used for construction of advanced chip-based chromatography, especially in complex architectures comprising curved and intersecting channels.     

Single-particle fritting technology for capillary electrochromatography

Large perfusive silica beads (particle size 110 microm, through pore approximately 2 microm) held in place by the keystone effect were used as single-particle frits for the manufacture of particulate packed capillary columns. High-quality capillary electrochromatographic separations of a standard test mixture of alkylbenzenes were obtained over the full voltage range of 5-30 kV, with no requirement for pressurization. Excellent robustness was demonstrated by the reproducibility of migration times, peak efficiencies, and resolution during 100 consecutive runs at the highest voltage (30 kV) without thermostating and pressurization. Superior performance relative to traditional sinter-fritted columns is ascribed to the heat-free fritting process and short frit length of approximately 110 microm.     

Some results on the geometrically exact equations of pressurized,axisymmetric membranes

Summary The geometrically exact, axisymmetric equations for elastic membranes are examined in the case of constant internal pressure. Particular attention is paid to the scenario wherein both the reference configuration and the current configuration are spherical caps. Hookean and non-Hookean materials are considered. For Hookean and neo-Hookean materials, it is shown that there is a maximum allowable pressure and two solutions (spheres) exist for each pressure less than the maximum, while for Mooney materials there is a unique solution for all pressures. The material properties that account for this dichotomy are identified in the Conclusion.With 4 FiguresThis work was supported by an Internal Research Grant at Southwest Research Institute.     

Use of a mixed-mode packing and voltage tuning for peptide mixture separation in pressurized capillary electrochromatography with an ion trap storage/reflectron time-of-flight mass spectrometer detector.

A mixed-mode (reversed-phase/anion-exchange) stationary phase has been used as the capillary column packing for investigation of the separation of peptide mixtures in pressurized capillary electrochromatography (pCEC). This stationary phase contains both octadecylsilanes and dialkylamines. The amine groups of the stationary phase determine the charge density on the surface of the packing and can produce a strong and constant electroosmotic flow (EOF) at low pH. A comparison was made in terms of the capability of separating tryptic digests between the mixed-mode phase and C18 reversed phase. In addition, the constant EOF enabled the tuning of the retention and the selectivity of the separation by adjusting the mobile phase pH from 2 to 5. Furthermore, the magnitude and the polarity of the electric voltage were demonstrated to greatly influence the elution profiles of the peptides in pCEC. An ion trap storage/reflectron time-of-flight mass spectrometer was used as an on-line detector in these experiments due to its ability to provide rapid and accurate mass detection of the sample components eluting from the separation column.     

Calculation of initial stage of heating a planar body with variable properties

A method is presented for calculation of upper and lower limits of the temperature field of a planar body with temperature-dependent thermophysical properties.Translated from Inzhenerno-Fizicheskii Zhurnal, Vol 41, No. 3, pp. 532–535, September, 1981.     

Ensemble tracking for 2D vector velocity measurement: Experimental and initial clinical results

We describe a new method, called ensemble tracking, for estimating two-dimensional velocities with ultrasound. Compared to previous speckle tracking techniques, ensemble tracking measures motion over smaller times and distances, increasing maximum velocities and reducing errors due to echo decorrelation. Ensemble tracking uses parallel receive processing, 2D pattern matching, and interpolation of the resulting tracking grid to estimate sub-pixel speckle translations between successive ultrasonic acquisitions. In this study, small translations of a tissue mimicking phantom were quantified at transducer angles of 0 degrees , 45 degrees , and 90 degrees . Measurements over three parallel beam spacings and all transducer angles had mean errors from -4% to +11%, when parallel beam amplitudes were normalized. Such amplitude normalization substantially improved results at 45 degrees and 90 degrees . The amplitude, spacing, and correlation between the parallel beams were quantified, and their effects on the accuracy and precision of estimates are discussed. Finally, initial clinical results demonstrate the ability to track and display blood flow in the carotid artery.     

Cloud physics lidar: instrument description and initial measurement results

The new Cloud Physics Lidar (CPL) has been built for use on the NASA ER-2 high-altitude aircraft. The purpose of the CPL is to provide multiwavelength measurements of cirrus, subvisual cirrus, and aerosols with high temporal and spatial resolution. The CPL utilizes state-of-the-art technology with a high repetition rate, a low-pulse-energy laser, and photon-counting detection. The first deployment for the CPL was the Southern African Regional Science Initiative's 2000 field campaign during August and September 2000. We provide here an overview of the instrument and initial data results to illustrate the measurement capability of the CPL.     

非甾体类抗炎药的毛细管电色谱分析研究

论文应用氰基键合毛细管开管柱,建立了非甾体类抗炎药(舒林酸、芬布芬、布洛芬、萘普生、酮洛芬、氟比洛芬和双氯芬酸钠)的开管毛细管电色谱分析模式。在最优分离条件下,七种非甾体类抗炎药在18分钟内实现良好分离,其线性范围均为1.5×10~(-5)mol/L-4.0×10~(-4)mol/L,检测限在3.5×10~(-6)mol/L-1.0×10~(-5)mol/L之间。应用于猪肝样品分析,平均回收率在85.0%-92.6%之间。该方法为非甾体类抗炎药的分离测定提供了新的技术。     

Gold nanoparticle-modified etched capillaries for open-tubular capillary electrochromatography

The use of gold nanoparticles in conjunction with etched capillary-based open-tubular capillary electrochromatography (OTCEC) to improve the efficiency of separation and the selectivity between selected solutes is described. The fused-silica capillaries (50-microm i.d.) were etched with ammonium hydrogen difluoride, followed by prederivatization of the new surface with (3-mercaptopropyl)trimethoxysilane (MPTMS) for the immobilization of dodecanethiol gold nanoparticles, for OTCEC. The electrochromatography of a "reversed-phase" test mixture and of selected polycylic aromatic hydrocarbons was investigated, and efficient separations and high theoretical plate numbers per meter were obtained. The electroosmotic flow characteristics of the etched gold nanoparticle capillary, unetched gold nanoparticle capillary, bare capillary, and etched bare capillary were studied by varying the percentage of organic modifier in buffer, buffer pH, and separation voltage. Optical microscopy and scanning electron microscopy were used to examine the process of etching and modification and the surface features of the etched gold nanoparticle capillary. The results confirm that dodecanethiol gold nanoparticles bonded on the etched inner wall of the fused-silica capillary can provide sufficient solute-bonded phase interactions to obtain OTCEC separations with reproducible retention, as well as characteristic reversed-phase behavior, even with the inner diameter of the capillary of 50 microm.