摘要:
A technique for measuring concentration of ions in the parts per trillion range (10.sup.-5 to 10.sup.-6 milligram per liter) uses a new interconnection of ordinary components in a four step technique. In the first two steps, standard solutions of known, but widely different, concentrations are measured to determine a calibration factor (C) which is then applied in the second two steps to determine the very weak unknown concentration of the sample. The process can be automated and is useful in applications such as nuclear power plants where the presence of even very small concentrations of certain ions is undesirable because of the extreme conditions prevailing, and such as the semiconductor industry where extreme purity is required.
摘要:
A suppressor for use in ion chromatography including at least an effluent flow channel separated by a charged membrane from a suppressor flow channel. A screen of the same charge as the membrane is placed in at least the effluent flow channel. Preferably, a similar screen is placed in the regenerant flow channel. The screen increases the dynamic capacity of the membrane suppressor.
摘要:
A stable baseline is achieved in a gradient ion chromatographic analysis by adding a nonionic modifier to the electrolytic eluent. The addition of the modifier may occur at any point upstream of the detector. The nonionic modifier has the effect of shifting the equilibrium of unsuppressed effluent electrolyte towards it nonionic form. For example, the addition of the nonionic modifier shifts both bicarbonate and carbonate towards the nonionic, nonconductive carbonic acid form.
摘要:
A method of ion chromatography in which the sample passes through a chromatographic column, a suppressor, and a conductivity detector, using a gradient electrolyte eluent. A non-ionic polyhydroxy compound is added with the eluent to the chromatographic column at a concentration inversely related to the concentration of the electrolyte which increases with time. The effluent is passed through a membrane suppressor for the conductivity of the electrolyte. The regenerant stream in the suppressor includes a complexing agent (boric acid) which passes through the membrane into the effluent to form highly ionized complex which counterbalances the increased background conductivity of the electrolyte to stabilize the background conductivity in the conductor.
摘要:
In chromatographic analysis by the steps of adding a sample solution to a flow of an eluant, passing the eluant flow through a separation column thereby converting the eluant flow into an eluate flow containing component ions of the eluant flow in separate zones, passing the eluate flow through an ion-exchange membrane tube thereby allowing the eluate to come into contact with an aqueous solution of an H.sup.+ form or OH.sup.- form electrolyte outside the tube through the wall of the membrane tube, substituting those of the component ions contained in the eluate flow which have the same type of electric charge as H.sup.+ or OH.sup.- with said H.sup.+ or OH.sup.- thereby giving rise to a deionized solution flow, and passing the deionized solution flow through a detection cell thereby causing the component ions which have survived the substitution to be detected as separated into distinct zones, improvements are obtained by causing the aqueous solution of H.sup.+ or OH.sup.- form electrolyte to be contacted with an insoluble ion exchanger of the same H.sup.+ or OH.sup.- type as said electrolyte to the aqueous solution. Use of a high molecular weight electrolyte having a molecular weight of 500 or more permits detecting anion or cation present in a very low concentration with ample sensitivity and high reproducibility without provision of forwarding means.
摘要:
In chromatographic analysis by the steps of adding a sample solution to a flow of an eluant, passing the eluant flow through a separation column thereby converting the eluant flow into an eluate flow containing component ions of the eluant flow in separate zones, passing the eluate flow through an ion-exchange membrane tube thereby allowing the eluate to come into contact with an aqueous solution of an H.sup.+ form or OH.sup.- form electrolyte outside the tube through the wall of the membrane tube, substituting those of the component ions contained in the eluate flow which have the same type of electric charge as H.sup.+ or OH.sup.- with said H.sup.+ or OH.sup.- thereby giving rise to a deionized solution flow, and passing the deionized solution flow through a detection cell thereby causing the component ions which have survived the substitution to be detected as separated into distinct zones, improvements are obtained by causing the aqueous solutions of H.sup.+ or OH.sup.- form electrolyte to be contacted with an insoluble ion exchanger of the same H.sup.+ or OH.sup.- type as said electrolyte to the aqueous solution. Use of a high molecular weight electrolyte having a molecular weight of 500 or more permits detecting anion or cation present in a very low concentration with ample sensitivity and high reproducibility without provision of forwarding means.
摘要:
An oxygen concentration sensing device for sensing an oxygen concentration in a gaseous body includes a pair of solid electrolyte members having oxygen ion permeability which are arranged to face each other forming a predetermined gap portion between them. Each of the solid electrolyte members is provided with a pair of electrodes and one of the solid electrolyte members is operative as an oxygen pump element when a drive current is supplied across the electrodes thereof and the other one of the solid electrolyte members is operative as a sensor cell element for producing a sensor output signal. The sensing device is provided with a current supply circuit for supplying the drive current of the oxygen pump element and a delay control circuit for delaying the increase of the magnitude of drive current of the oxygen pump element at a start time, so as to prevent an overcurrent to the oxygen pump element which otherwise is generated by the current supply circuit and causes the so called blackening phenomenon of the solid electrolyte members.
摘要:
An ion-chromatography system for analyzing one or more ionic species of a given polarity in solution, the system comprising an ion-exchange material reactive with such species, an eluant fluid, means for adding the eluant fluid and ionic species to the separation column, a stripper column and a detector. The eluant fluid includes at least a pair of electrically neutral molecular species reactive with one another to provide ionic constituents, the molecular species being in substantial equilibrium with the ionic constituents. The stripper column is positioned at the outlet of the separation column to receive the eluant fluid from the latter and reduce the concentration of the ionic constituents in the eluant fluid. The stripper column includes a conduit relatively permeable to the neutral molecular species in the eluant and relatively impermeable to the ionic constituents. Means are also provided for removing any of the neutral species that permeate the conduit, whereby a concentration gradient is established across the conduit. The detector is provided to quantitatively measure the chromatographically separated ionic species in the eluant discharged from the stripper column.
摘要:
A versatile and highly sensitive procedure of indirect photometric chromatography in which a variable capacity pH dependent weakly basic or weakly acidic ion exchange medium is used in the chromatographic column to effect ion separations. Adjusting eluent pH allows increased detection limits without extended analysis time, reduced column efficiency, or the need for a battery of conventional strongly basic/acidic ion exchange columns.
摘要:
An improved technique and apparatus for the independent measurement of anions and cations in solution, wherein the sample ions are chromatographically displaced in a plurality of ion exchange columns by an eluting ion which is or is made light-absorbing and wherein the sample ions are detectable from decrements in absorbance of the eluting ions as revealed by photometric monitoring; and the sample ions, cations and anions, are further detected independently by means for monitoring eluting anion and cation absorbance differences calibrated according to characteristic absorbance ratios of the selected eluting ion species at a plurality of wavelengths.