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58 results about "Common logarithm" patented technology

In mathematics, the common logarithm is the logarithm with base 10. It is also known as the decadic logarithm and as the decimal logarithm, named after its base, or Briggsian logarithm, after Henry Briggs, an English mathematician who pioneered its use, as well as standard logarithm. Historically, it was known as logarithmus decimalis or logarithmus decadis. It is indicated by log₁₀(x), or sometimes Log(x) with a capital L (however, this notation is ambiguous since it can also mean the complex natural logarithmic multi-valued function). On calculators, it is usually "log", but mathematicians usually mean natural logarithm (logarithm with base e ≈ 2.71828) rather than common logarithm when they write "log". To mitigate this ambiguity, the ISO 80000 specification recommends that log₁₀(x) should be written lg(x) and logₑ(x) should be ln(x).

Non-Magnetic Toner

An object of the present invention is to provide a toner excellent in fixing ability and developing ability. Provided is a non-magnetic toner including: toner particles each containing at least a binder resin, a colorant, and a wax component; and an inorganic fine powder, wherein: the toner has a specific storage elastic modulus at each of 110 C and 150 C; when a temperature at which a differential curve of a temperature and the common logarithm LogG′ of a storage elastic modulus G′ shows the minimum value in the temperature region of 60 to 130 C is denoted by T0, a straight line having the largest gradient out of straight lines each connecting points on the differential curve at temperatures of T0+a and (T0+a)+1 (C) [where a represents an integer of 0 to 9] is denoted by A, a straight line having the smallest gradient out of straight lines each connecting points on the differential curve at temperatures of T0+b (C) and (T0+b)+10 (C) [where b represents an integer of 0 or more] is denoted by B, and a straight line having the largest gradient out of straight lines each connecting points on the differential curve at temperatures of T0+c and (T0+c)+10 (C) [where c represents an integer larger than “a value b when a straight line B is given”] is denoted by C, the relationship of 1C ? ¢TA (from T0 to the point of intersection of the straight lines A and B) ? 20 C and the relationship of 100 C ? TBC (the point of intersection of the straight lines B and C) ? 120 C are established.
Owner:CANON KK

Method for detecting SPA FC fragment bound mammalian blood serum total IgG by dolloidal gold marker protein A

A method for detecting total IgG combined with Fc fragment of Staphylococci protein A (SPA) in mammalian serum with colloidal gold-labeled protein A comprises the following steps of: 1) construction of a standard curve and calculation of regression equation for each batch of colloidal gold-labeled probe and micro-reaction by (1) setting 8 standard holes, adding 50MuL 0.01M TBS solution (pH 7.4, containing 0.1% calf serum) to each hole; (2) adding 50MuL standard IgG solution from the first hole to the sixth hole by doubling dilution, sucking out 50MuL TBS solution from the seventh hole, adding 50MuL standard IgG solution, and leaving the eighth hole as a blank control; (3) adding 50MuL colloidal gold-labeled probe diluted by 2-6 times in the reaction holes; (4) completely mixing the reaction plate, and reacting at room temperature for 20-40min; (5) detecting absorbance at 620nm with a microplate-reader for ELISA; and (6) calculating common logarithm of the absorbance associated with the standard IgG; and 2) sample detection by (1) adding 50MuL sample solution in the sample holes; (2) adding 50MuL diluted colloidal gold-labeled probe in the sample holes; (3) completely mixing the reaction plate, and reacting at room temperature for 20-40min; and (4) detecting absorbance of each hole at 620nm with the microplate-reader for ELISA, and calculating corresponding IgG values according to the regression equation of the standard curve.
Owner:HENAN AGRICULTURAL UNIVERSITY

Method for detection of maltopentaose by ultra-high performance liquid chromatography-mass spectrometry

ActiveCN108732291ASuitable for analytical testingQualitatively accurateComponent separationMass numberGradient elution
The invention discloses a method for detection of maltopentaose by ultra-high performance liquid chromatography-mass spectrometry. The method includes the steps of: (1) taking an appropriate amount ofmaltopentaose, adding water for dissolving to prepare a test solution of certain solution; (2) performing sample introduction, and conducting detection according to the following chromatographic andmass spectrometric conditions that: according to the chromatographic conditions: Waters Xbridge BEH Amide 2.1*100mm is adopted as the chromatographic column, acetonitrile-water is used as the mobile phase for gradient elution, 87% acetonitrile can be maintained in 0-15min, and in 15-20min, 87% acetonitrile gradually decreases to 15% acetonitrile, and in 20-30min, 15% acetonitrile is maintained; according to the mass spectrometric conditions: an ESI source is taken, a selected ion monitoring (SIM) mode is used, the fragmentor is 130v, the sheath gas flow is 12L / min, the caplliary voltage is 4000v, the accurate mass number [M-H]<->827.4 is extracted, and the common logarithm of concentration and peak area is utilized for linear quantitation. The method has the characteristics of accurate qualitative analysis, high sensitivity, high precision, good linearity and simple operation, and is suitable for analysis and detection of maltopentose.
Owner:SHANGHAI BAINIAN SHIDANDE INSPECTION TECH +2
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