Abstract: A basic ion optical system (2) in which the temporal focusing of ions is ensured includes a plurality of sector-shaped electrodes (11, 12, 13, and 14), an ion injection slit (15), and an ion ejection slit (16), which are placed on the same plane. A plurality of basic ion optical systems (2) are placed in such a manner as to be mutually separated at predetermined intervals in the direction approximately orthogonal to their planes. The ion ejection slit (16) of the lower-stage basic ion optical system (2) and the ion injection slit (15) of the next-stage basic ion optical system (2) are connected to each other via another basic ion optical system (3) in which the temporal focusing of the ions is ensured. Accordingly, the flight distance can be elongated while assuredly achieving the temporal focusing of the ions as an entire ion optical system (1), and a three-dimensional space can be efficiently utilized to compactify the ion optical system (1).

Abstract: The present invention provides hot dip plated high strength steel sheet for press forming use having a tensile strength of 380 MPa to less than 540 MPa, having a press formability able to be used for the automobile field, in particular fuel tank applications, and having superior secondary work embrittlement resistance and superior seam weld zone low temperature toughness and further superior plateability and a method of production of the same and provides hot dip plated high strength steel sheet for press forming use of the present invention having cold rolled steel sheet and a hot dip plated layer formed on the surface of said cold rolled steel sheet, characterized in that said cold rolled steel sheet contains, by mass %, C: 0.0005 to 0.0050%, Si: over 0.3 to 1.0%, Mn: 0.70 to 2.0%, P: 0.05% or less, Ti: 0.010 to 0.050%, Nb: 0.010 to 0.040%, B: 0.0005 to 0.0030%, S: 0.010% or less, Al: 0.01 to 0.30%, and N: 0.0010 to 0.

Abstract: It is an object to provide a honeycomb structure and a purifying apparatus that undergo relatively small decrease of capturing efficiency after a long period of capturing the diesel particulates. The honeycomb structure has a plurality of flow paths separated from each other by partition wall that extend from an input end face to an output end face, wherein the partition wall has a load length ratio (Rmr (c)) of 90% or less determined at a cutting level of 70% with a reference length of 0.8 mm.

Abstract: Based on the mass spectrum obtained by mass-analyzing a sample, the composition of the unknown substance is deduced, and after that, an MS/MS analysis is performed in which the unknown substance is set to be a precursor ion. Then, based on the peaks appearing on the MS/MS spectrum, the actually measured mass of each product ion is obtained (S1 through S4). On the other hand, the compositions of the product ion generated by the dissociation of the unknown substance are obtained by the combination, i.e. the condition, of the kind of the constituent element and the number of each element of the unknown substance's deduced component. Then, it is checked whether or not the theoretical mass in consistency with the actually measured mass of the product ion exists (S5). In the case where one which is consistent with a theoretical mass is not existent, it is possible to determine that the original deduction of the known substance's composition has been incorrect.

Abstract: When the analyzer provides the mass and composition formula of the product ion, which is probably produced in the process of a dissociation, through the input unit 8, based on known information, a composition formula list 62 is created in the database 6. When a product ion is obtained in an MSn analysis, the data processor 5 checks whether or not the ion's mass exists in the composition formula list 62, and in the case where it does, the composition formula corresponding to the mass is determined. Then, based the mass difference between the precursor ion and product ion or other factors, the precursor ion's composition formula is deduced, and if it is possible to ultimately narrow down the candidates for the target ion's composition formula, the analysis is terminated. Accordingly, if the composition formula list 62 is available, the refinement operation for the candidates for the composition formula can be omitted.

Abstract: A main peak list is created with the data obtained by an MSn analysis (S1), the difference between the mass-to-charge ratio of each product ion listed on this main peak list and that of the precursor ion is calculated (S2), and an auxiliary peak list for forming a virtual peak corresponding to the mass-to-charge ratio difference is created (S3). On the same graph, an MSn spectrum data is created so that each peak listed on the main peak list and each peak listed on the auxiliary peak list are drawn with different display colors (S4), and the MSn spectrum is displayed on the display screen (S5). Consequently, an MSn analysis result for a plurality of precursor ions with different mass-to-charge ratios becomes easy to be compared. In particular, it is possible to easily and visually determine whether or not a fragment having the same mass-to-charge ratio desorbed by a dissociation exists.

Abstract: A mass spectrometry system, in which a sample is introduced into each of a triple quadrupole-type mass spectrometry apparatus and another mass spectrometry apparatus, approximately concurrently in a parallel manner. The triple quadrupole-type mass spectrometry apparatus is operable to perform a neutral loss scan, and, when a specific ion is detected, a data processing section is operable to instruct a control section to initiate a mass spectrometric analysis in the other mass spectrometry apparatus. The control section is operable to control each device of the other mass spectrometry apparatus to allow the other mass spectrometry apparatus to perform a mass spectrometric analysis for the specific ion with a high degree of accuracy. A data integration processing section is operable to integrate respective analysis results obtained by data processing sections as if they are obtained from a single mass spectrometry apparatus.

Abstract: A laser light is linearly delivered onto the sample 4. The ions generated from the irradiated area are collected, mass-separated in the mass separator 27, and detected by the detector 28. A mass analysis is repeated while moving the sample stage 3 by a predetermined step width in the x-axis direction so that the one-dimensional mass spectrum information of the sample 4 at a certain rotational position is obtained. Additionally, while the sample 4 is rotated by a predetermined angle, the same measurement is repeated for the entire perimeter, so that the one-dimensional mass spectrum information at each rotational position is obtained. Based on the data obtained in this manner, a reconstruction computational processing is performed by the CT method to reconstruct the two-dimensional distribution image for a substance having a certain mass for example and the image is displayed on the display 35.

Abstract: In a mass analysis of a sample, candidate compositions Y of a fragment ion produced by a dissociating operation are deduced from the mass of that fragment ion (Steps S6 to S9). If the number of the candidates Y is larger than a predetermined value (“No” in Step S10), the repetition counter of the dissociating operation is increased by one and the mass analysis of the fragment ion is performed again. If the number of the candidates is equal to or smaller than the predetermined value, the difference between the masses of the fragment ions before and after each mass-analyzing stage is calculated (Step S11). From this mass difference, the candidates Z of the desorption ion at each stage is deduced (Step S12). These candidates Z and Y are used to narrow down the candidate composition formulae X deduced from the mass of the precursor ion (Step S13). If the number of the candidates has decreased to one or become equal to or smaller than a predetermined value, the result is displayed (Steps S14 and S15).

Abstract: The present invention provides a method and an apparatus for analyzing mass analysis data for selecting a component similar to a target component quickly and accurately, based on MSn analysis for each unknown component in the sample. First, MSn analysis is performed for each of the components in the mixed sample, and based on the obtained spectral data (measured data) and the spectral data of the target component (reference data), predetermined parameters are extracted (Step S11 to S13). Next, by multivariable analysis of the parameters, the similarity between the target component and each of the components in the mixed sample is evaluated (Step S14). Finally, based on the similarity value, components similar to the target component are selected (Step S16).

Abstract: When the target substance's composition formula is deduced by using a mass spectrometer capable of an MSn analysis, if the target substance's composition formula is deduced based on the MSn spectrum by the MS analysis and the candidates are found, a composition formula candidate list including all the composition formula candidates is created (S21), and the list is displayed in a list format. In addition, the composition formula candidates are narrowed down based on the MSn spectrum by an MS2 analysis or MS3 analysis (S22). In the case where there is a candidate to be excluded in the candidates previously lined up, the composition formula candidate list is updated (S23), and the excluded candidate is moved to the exclusion list (S24). Accompanying this, a composition formula candidate table is displayed in a list format on the display window.

Abstract: The present invention provides a single set of mass spectrometer capable of selectively performing the following two modes of analyses according to the purpose of analysis: the first mass spectrometry mode in which the analysis can be repeated at short intervals of time; and the second mass spectrometry mode in which the analysis can be performed with high mass resolution and high accuracy. In an embodiment of the present invention, ions ejected from an ion source 1 travel along a straight path B, on which gate electrodes 3 are provided. When a voltage is applied from an MS mode selection controller 7 to the gate electrodes 3, the ions are introduced into a loop orbit A. Located on the loop orbit A is a second ion detector 6, which is a nondestructive type of ion detector. Detection signals of the second ion detector 6 are sent to a data processor 9, which extracts flight time spectrum data from those signals and Fourier-transforms those data to convert the time axis to a frequency axis.

Abstract: In a combination of, for example, a rotor having eight magnetic poles and a stator having twelve slots and pulsating components of permeance, which generate a sinusoidal cogging torque having maxima of the same number as the number of poles of the rotor, pressurizing parts arranged in predetermined positions, applying a force at an outer periphery of the stator and directed inwardly cancels the pulsating components of the cogging torque.

Abstract: The invention provides a chromatograph mass analysis data processing apparatus in which operators can easily obtain information about plural compounds that characterize a difference between plural samples on the basis of the result of a multivariate analysis. A set of data collected by LC/MS analyses of plural samples is subjected to a multivariate analysis (principal component analysis) to create and display a loadings plot. On this loadings plot, the operator can specify a range A to select one or more characteristic data points that seem influential in the grouping of the plural samples. In response to this operation, one or more markings B indicating the peaks corresponding to the data points selected within the range A are displayed on an isointensity line graph whose two axes indicate the retention time and mass-to-charge ratio. These markings enable the operator to check, for example, that the compounds that are influential in the grouping of the samples belong to a specific compound series.

Abstract: A chromatograph mass spectrometer is provided for obtaining the information pertinent to a structural analysis, with a simple operation, on a compound series including a plurality of compounds whose structures and characters are similar. First, based on the data obtained by a normal LC/MS analysis, a two-dimensional isointensity line graph is created and displayed with a retention time and a mass-to-charge ratio on the two axes and with a signal intensity represented in contour (S1 and S2). When the operator specifies a desired range by a drag operation or the like by a mouse (S3), peaks included in the range specified are extracted and based on the peaks, precursor ions are selected (S4 through S6). Then a schedule is created so that an MS2 analysis is performed for the precursor ions selected in the course of an LC/MS analysis for the sample to be targeted (S7).

Abstract: A permanent magnet motor 1 includes a rotor in which permanent magnets 31 are fixed. In the rotor 20, the outer peripheral shape of rotor magnetic-pole portions 24 is formed so that, in the circumferentially central portion, the distance from the center of the rotor iron core 21 is longest, and, at the inter-polar space, the distance from the center of the rotor iron core is shortest, and so that the outermost surface of the rotor magnetic-pole portions 24 forms an arc, and given that sheath thickness tc formed by the outer-side surface of each permanent magnet 31 and the outermost surface of each rotor magnetic-pole portion 24 is practically constant, and letting the thickness of the permanent magnets be the magnet thickness tm, then the relation tc/tm?0.25 is satisfied.

Abstract: A chromatograph mass analysis data processing apparatus is provided for obtaining pertinent information, with a simple operation, on a compound series including a plurality of compounds whose structures and characters are similar. Based on the data obtained by a chromatograph mass analysis, a two-dimensional isointensity line graph is created and displayed with a retention time and a mass-to-charge ratio on the two axes and with a signal intensity represented with a contour (S1). When the operator specifies a desired range by a drag operation or the like through a mouse (S2), the data contained in the range specified are collected (S3), the signal intensities along the mass-to-charge ratio axis direction are summed up for every retention time to create a summed mass chromatogram based on the summed value (S4 and S5). Simultaneously, the signal intensities along the retention time axis direction are summed up for every mass-to-charge ratio to create a summed mass spectrum based on the summed value (S6 and S7).

Abstract: In a combination of, for example, a rotor having eight magnetic poles and a stator having twelve slots and pulsating components of permeance, which generate a sinusoidal cogging torque having maxima of the same number as the number of poles of the rotor, pressurizing parts arranged in predetermined positions applying a force at an outer periphery of the stator directed inwardly to cancel the pulsating components of the cogging torque.

Abstract: A mass spectrometer is provided in which ions are favorably introduced into a loop orbit or favorably led out from the loop orbit without affecting the motion of the ions flying along the loop orbit. An ion-introduction orbit 5 is set to correspond to the orbit (ejection orbit portion 4) of ions after being bent by the sector-shaped electric field E1 in the loop orbit 4. When ions are introduced, a voltage applied to the electrode unit 11 is put to zero to release the sector-shaped electric field E1. Then the ions emitted along the ion-introduction orbit 5 fly straight in the electrode unit 11. The direction and position of the ions coming out from the exit end of the electric field is the same as those ions flying along the loop orbit 4. Therefore, there is no need for placing a deflection electrode for introducing/leading-out ions on the loop orbit.

Abstract: An ion optical system to form a loop orbit is provided to sufficiently ensure required performance such as ion transmission efficiency while making it easy to design the system by alleviating a space-focusing condition. The loop orbit of the ion optical system is realized so as to satisfy (t|x)=(t|?)=(t|?)=0 as the time-focusing condition and to satisfy ?2<(x|x)+(?|?)<2, and ?2<(y|y)+(?|?)<2 as the space-focusing condition. (x|x) and other similar terms are constants determined by the elements indicated in the parenthesis in a general expression format of the ion optical system. The conditions are substantially alleviated as opposed to the conventional space-focusing condition where each of (x|x), (?|?), (y|y) and (?|?) needs to be ±1. Thus, the parameters to decide the shape of electrodes by which the ion optical system is configured have higher degree of freedom.