417 results about "Ion transfer" patented technology

A low or no pollution power generation system is provided. The system has an air separator to collect oxygen. A gas generator is provided with inputs for the oxygen and a hydrocarbon fuel. The fuel and oxygen are combusted within the gas generator, forming water and carbon dioxide. Water or other diluents are also delivered into the gas generator to control temperature of the combustion products. The combustion products are then expanded through at least one turbine or other expander to deliver output power. The combustion products are then passed through a separator where the steam is condensed. A portion of the water is discharged and the remainder is routed back to the gas generator as diluent. The carbon dioxide can be conditioned for sequestration. The system can be optimized by adding multiple expanders, reheaters and water diluent preheaters, and by preheating air for an ion transfer membrane oxygen separation.

The present invention relates generally to a multi-reflecting time-of-flight mass spectrometer (MR TOF MS). To improve mass resolving power of a planar MR TOF MS, a spatially isochronous and curved interface may be used for ion transfer in and out of the MR TOF analyzer. One embodiment comprises a planar grid-free MR TOF MS with periodic lenses in the field-free space, a linear ion trap for converting ion flow into pulses and a C-shaped isochronous interface made of electrostatic sectors. The interface allows transferring ions around the edges and fringing fields of the ion mirrors without introducing significant time spread. The interface may also provide energy filtering of ion packets. The non-correlated turn-around time of ion trap converter may be reduced by using a delayed ion extraction from the ion trap and excessive ion energy is filtered in the curved interface.

PCT No. PCT/EP95/02204 Sec. 371 Date Apr. 25, 1997 Sec. 102(e) Date Apr. 25, 1997 PCT Filed Jun. 7, 1995 PCT Pub. No. WO96/13721 PCT Pub. Date May 9, 1996Apparatus for carrying out patch clamp technique utilized in studying the effect of certain materials on ion transfer channels in biological tissue, and more particularly patch clamp apparatus utilizing an autosampler, such as those utilized with HPLC apparatus, to provide high throughput, is disclosed. The invention additionally includes novel microperfusion chamber assemblies capable of utilizing only small amounts of material to be tested and only small amounts of liquid carrier, thereby enabling many tests to be completed in a short period of time. The invention more broadly relates to a novel electrophysiology drug handling and application set up for screening of chemical substances while providing high throughput and requiring only low volume of solutions and samples to be tested. The invention also comprises several novel procedures for utilizing the apparatus of the invention.

The invention belongs to electrochemical technical field, in particular to a novel high performance water system lithium ion battery. The invention adopts an ion embedding in-out mechanism used by an organic system lithium ion battery in an energy storage element which uses a water solution as an electrolyte. The embedding-in reaction ion mainly includes lithium ion composite and sodium ion composite. In the invention, the positive pole adopts a material containing the positive ion embedding-in composite while the negative pole adopts a shell structure material of LiTi2(PO4)3; the electrolyte adopts a water system electrolyte of the positive ion. The electric charging and discharging process only relates to the ion transfer between the two electrodes, and the invention can still has the characteristic of a rocking-chair type organic system lithium ion battery; the invention is of long cycling service life, big power, safety, low cost and no pollution, and is particularly suitable to be used as an ideal power battery of electric vehicle.

The present invention is for an improved ionization source chamber and ion beam delivery system which includes a vacuum chamber and flange arrangement, for mounting the means for transferring sample ions from the port to a mass analyzer and for mounting the ion production means, respectively. The flange containing the ion production means may be attached to the vacuum chamber via a hinge such that the flange can open as a door to provide easy access to the ion transfer electrodes in the vacuum chamber. Further, a variety of different ion production means may be mounted on the flange of the ionization source chamber of the present invention. As a result, any ion production means may be used with the present invention by substituting a flange which includes the desired ion production means.

A multipole ion guide is configured to improve the transmission efficiency of ions which traverse the length of one ion guide and enter either another multipole ion guide such as a quadrupole mass analyzer or a three dimensional ion trap. The ion transfer multipole ion guide radial dimensions are reduced such that the pole assembly and an appropriately shaped exit lens can be positioned within a portion of the internal space defined by the larger radius second multipole ion guide poles. Ions exiting the first ion guide of reduced size find themselves inside the second ion guide close to the centerline. In this manner ions can be efficiently transferred from one ion guide to another, even for those ions with low kinetic energies. In a second embodiment of the invention, the exit region of a multipole ion guide is configured such that the multipole ion guide poles can be extended into a counterbore of a three dimensional ion trap end cap electrode. With this configuration, ions (including those with low kinetic energies) can be transferred into a three dimensional ion trap with increased trapping efficiency.

A rechargeable electrical storage device is disclosed, where one embodiment utilizes an anion (“A”) conducting electrolyte (18) and ion transfer between two electrodes (17, 19) where one electrode is preferably a metal electrode 19 that contains a mixture of metal and metal oxide, so that during operation, oxide-ions shuttle between the two electrodes (17, 19) in charging and discharging modes and the metal electrode (19) serves as a reservoir of species relevant to anion “A”.

An orthogonal ion injection apparatus and process are described in which ions are directly injected into an ion guide orthogonal to the ion guide axis through an inlet opening located on a side of the ion guide. The end of the heated capillary is placed inside the ion guide such that the ions are directly injected into DC and RF fields inside the ion guide, which efficiently confines ions inside the ion guide. Liquid droplets created by the ionization source that are carried through the capillary into the ion guide are removed from the ion guide by a strong directional gas flow through an inlet opening on the opposite side of the ion guide. Strong DC and RF fields divert ions into the ion guide. In-guide orthogonal injection yields a noise level that is a factor of 1.5 to 2 lower than conventional inline injection known in the art. Signal intensities for low m/z ions are greater compared to convention inline injection under the same processing conditions.

The invention relates to a method for design advanced materials with nano-scaled structure and techniques for preparing same. In particular, the invention relates to a carbon material capable of controllable laminated combination with the nano-holes of variable sizes and preparation and application thereof. The method comprises the steps of: preparing metal oxide sol in the alkali solution system, which is then mixed with an alcohol solution of an alcohol-soluble resin; the oxide sol being used as the template and water being the resin precipitation agent during the process to directly prepare resin/oxide sol composite system. After solvent removal, carbonization, activation and template removal processes, the carbon material with laminated nano-holes combination is prepared which is of controllable micro-holes proportion, controllable medium-holes aperture and proportion, controllable big-holes aperture and propotion and concentrated distribution of medium-holes and big-holes apertures. The carbon material capable of controllable laminated combination with the nano-holes of variable sizes prepared in the invention is characterized in laminated holes structure, excellent ion transfer performances and high electrochemical active specific surface area and the material is expected to be used as high energy density high power density electrochemical capacitor used electrode material.

An ion source includes an ion transfer tube having two segments for transporting a sample fluid containing ions between a first chamber and a second chamber maintained at a reduced pressure relative to the first chamber. A first segment may include a plurality of channels and heat conductive walls forming the plurality of channels. The plurality of channels and walls forming the channels promote efficient convective heat transfer to the sample fluid, thereby enabling operation at relatively high sample fluid flow rates, resulting in an increase in the number of ions that may be delivered to a mass analyzer. A second segment forms a single common channel that receives a plurality of sample streams and enables them to combine into a single ion stream that may be introduced as a single gas stream expansion into the second chamber.

A hybrid mass spectrometer has a branched ion path. A first ion path within the branched ion path operates as a triple quadrupole instrument having a mass selection device, collision cell, and first mass analyzer and provides information on a specific m/z ratio corresponding to ions of interest in a sample. A second ion path within the branched ion path includes a second mass analyzer in the form of an electrostatic trap or other ion trap device. A branched ion transfer device may provide the branched ion path and may include the collision cell. A controller actuates an ion path switch in the branched ion transfer device and diverts from the first ion path to the second ion path in response to a triggering event. Ions at or near the m/z ratio of interest are then analyzed in the trap to obtain more detailed information of a full spectrum.

Disclosed is use of a porous membrane and a composite membrane thereof in a redox flow batteries, and in particular the use thereof in a vanadium redox flow battery. The membrane can effectively realize the separation of ions with different valence states, and an ion transfer without any ion exchange group. The pore size and structure of the porous membrane can be controlled by filling an inorganic substance or grafting an ion exchange group in the pore, in order to improve the barrier properties of the porous membrane for vanadium ions and to increase proton conductivity.

An ionization method for use with mass spectrometry or ion mobility spectrometry is a small molecule compound(s) as a matrix into which is incorporated analyte. The matrix has attributes of sublimation or evaporation when placed in vacuum at or near room temperature and produces both positive and negative charges. Placing the sample into a region of sub-atmospheric pressure, the region being in fluid communication with the vacuum of the mass spectrometer or ion mobility spectrometer, produces gas-phase ions of the analyte for mass-to-charge or drift-time analysis without use of a laser, high voltage, particle bombardment, or a heated ion transfer region. This matrix and vacuum assisted ionization process can operate from atmosphere or vacuum and produces ions from large (e.g. proteins) and small molecules (e.g. drugs) with charge states similar to those observed in electrospray ionization.

A mass spectrometer capable of analyzing a wide mass range with high sensitivity and high mass accuracy. A mass spectrometer has an ionization source generating ions; an ion transfer optics transferring the ions; a first linear trap accumulating the ions and ejecting the ions in the specific mass range; a second linear trap having an end electrode disposed at the exit end ejecting the ions to change a DC potential gradient relative to a DC potential of the end electrode and trapping the ions ejected from the first linear trap to repeatedly eject them in pulse form; a time-of-flight mass spectrometer accelerating the ions ejected from the second linear trap in the orthogonal direction to detect them; and a controller changing the time duration of the ions in which the ions are ejected from the second linear trap or delay time from the completion of ejection to application of an accelerating voltage of the time-of-flight mass spectrometer according to the mass range of the ions ejected from the first linear trap to the second linear trap.