# US 2014/0152984 A1 · Method of evaluating dispersion degrees of mixed epoxy resins > Agents: this data is available as JSON from the patentgrep API and MCP server — see https://patentgrep.com/llms.txt - Number: US 2014/0152984 A1 - Document ID: US20140152984A1 - Status: Published application - Kind: A1 - Application number: 14/093,672 - Filed: 2013-12-02 - Published: 2014-06-05 - Earliest claimed: 2012-12-04 - Assignees: Honda Motor Co., Ltd. - Applicants: Honda Motor Co., Ltd. - Inventors: Shuichiro Yoshida - Web page: https://patentgrep.com/patent/US20140152984A1 ## CPC - G01J 3/42: Absorption spectrometry; Double beam spectrometry; Flicker spectrometry; Reflection spectrometry (beam switching arrangements G01J3/08) - C08L 63/00: Compositions of epoxy resins; Compositions of derivatives of epoxy resins - G01N 21/314: {with comparison of measurements at specific and non-specific wavelengths (dual wavelength spectrometry G01J3/427)} - G01N 21/35: using infrared light (G01N21/39 takes precedence) - G01N 2021/3595: {using FTIR} - G01J: MEASUREMENT OF INTENSITY, VELOCITY, SPECTRAL CONTENT, POLARISATION, PHASE OR PULSE CHARACTERISTICS OF INFRARED, VISIBLE OR ULTRAVIOLET LIGHT; COLORIMETRY; RADIATION PYROMETRY (light sources F21, H01J, H01K, H05B; investigating properties of materials by optical means G01N) - C08L: COMPOSITIONS OF MACROMOLECULAR COMPOUNDS (compositions based on polymerisable monomers C08F, C08G; artificial filaments or fibres D01F; textile treating compositions D06) - G01N: INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES (measuring or testing apparatus or processes other than immunoassay, involving enzymes or microorganisms C12M, C12Q) ## Abstract A method of evaluating dispersion degrees of mixed epoxy resins includes, first, obtaining a resin mixture by mixing a plurality of aromatic epoxy resins, and taking a plurality of measurement samples from a plurality of sites of the resin mixture. The measurement samples are spectroscopically analyzed to obtain the spectra, and a plurality of common functional group peaks in the spectra are selected. The absorbances of the selected peaks are standardized to obtain absorbance ratios, based on the absorbance of a standard peak, in each of the spectra. Then, the standard deviations of the absorbance ratios of the selected peaks are calculated between the measurement samples. The maximum value of the obtained standard deviations is compared with a predetermined threshold value to evaluate the dispersion degrees of the aromatic epoxy resins. ## Claims ### Claim 1 A method of evaluating dispersion degrees of a plurality of aromatic epoxy resins in a resin mixture obtained by mixing the aromatic epoxy resins, the method comprising the steps of: taking a plurality of measurement samples from a plurality of sites of the resin mixture, spectroscopically analyzing the measurement samples to obtain spectra, selecting a plurality of common functional group peaks in the spectra of the measurement samples, standardizing absorbances of the selected peaks to obtain absorbance ratios, based on an absorbance of a standard peak, in each of the spectra, calculating standard deviations of the absorbance ratios of the selected peaks between the measurement samples, and comparing a maximum value of the standard deviations with a predetermined threshold value to evaluate the dispersion degrees of the aromatic epoxy resins. ### Claim 2 (depends on 1) The method according to claim 1, wherein the resin mixture contains at least two of a polyfunctional glycidylamine-type epoxy resin represented by a following structural formula (1), a p-aminophenol-type liquid epoxy resin represented by a following structural formula (2), and a bisphenol A-type liquid epoxy resin or a bisphenol A-type solid epoxy resin represented by a following structural formula (3): wherein n is a number of repeating units in the structural formula (3). ### Claim 3 (depends on 2) The method according to claim 2, wherein the resin mixture is obtained by mixing 30 to 52 phr of the polyfunctional glycidylamine-type epoxy resin and 70 to 48 phr of at least one of the p-aminophenol-type liquid epoxy resin, the bisphenol A-type liquid epoxy resin, and the bisphenol A-type solid epoxy resin. ### Claim 4 (depends on 3) The method according to claim 3, wherein the resin mixture is obtained by mixing 30 to 52 phr of the polyfunctional glycidylamine-type epoxy resin, 23 to 50 phr of the p-aminophenol-type liquid epoxy resin, 10 to 30 phr of the bisphenol A-type liquid epoxy resin, and 10 to 30 phr of the bisphenol A-type solid epoxy resin. ### Claim 5 (depends on 2) The method according to claim 2, wherein the resin mixture contains 100 parts by weight of the aromatic epoxy resins and 26 to 60 parts by weight of a hardener. ### Claim 6 (depends on 1) The method according to claim 1, wherein the threshold value is 0.01 to 0.11. ### Claim 7 (depends on 1) The method according to claim 1, wherein the measurement samples are spectroscopically analyzed by a Fourier transform infrared spectroscopy, and the absorbances of the selected peaks are standardized to obtain the absorbance ratios based on an absorbance of a benzene ring at 1593 cm−1. ### Claim 8 (depends on 7) The method according to claim 7, wherein peaks at 1610, 1504, 1288, 1103, 904, 826 and 548 cm−1 are selected from the peaks in each of the spectra obtained by spectroscopically analyzing the measurement samples, and the absorbances of the selected peaks obtained respectively from heights of the selected peaks are standardized to obtain the absorbance ratios based on the absorbance of the benzene ring at 1593 cm−1.