465 results about "Photometer" patented technology

A self-calibrating hybrid spectrophotometer comprises a receptacle for receiving the cuvette, first and second optodes that are configured to permit light to enter the cuvette, third and fourth optodes that are configured to permit light to leave the cuvette, and a controller that is configured to control delivery of light to one of the first and second optodes. Light entering one of the first and second optodes is received at the third and fourth optodes after having interacted with the turbid sample along different paths having different lengths. Measurements made at the third and fourth optodes in response to having illuminated both the first and second source optodes provide two slopes of optical transmittance as a function of path length. The spectrophotometer uses these slopes to identify a slope that is indicative of the absorption coefficient and the reduced scattering coefficient of the sample.

The invention discloses a ground photometer aerosol parameter inversion algorithm based on integrated machine learning. According to the method, a training data set for training an integrated machine learning model is obtained by adopting a forward radiation transmission simulation model, and the training data set is independent of an aerosol product of an existing algorithm and observation interfered by noise; the algorithm has good generalization ability and is excellent in performance after being used for real observation of a photometer, and inverted aerosol parameters have the ability of representing aerosol types; an aerosol inversion algorithm based on an integrated machine learning model is developed aiming at observation of a ground photometer, and the time for completing aerosol inversion for one time is at a millisecond level; the multi-band and multi-angle radiance observation can be utilized at the same time to invert aerosol parameters of multiple bands at a time; any prior hypothesis and smooth constraint are not needed during aerosol parameter inversion, inversion result loss caused by non-convergence of gradient descent in a numerical inversion algorithm is avoided to a certain extent, and waste of effective observation is reduced.

The invention provides a detection device for a density gradient centrifugal sample, and belongs to the technical field of detection devices. The device comprises a sample suction platform mechanism which is used for sucking layered samples to be detected in a centrifugal tube layer by layer and conveying the layered samples to a sample detection chamber of an optical detector mechanism; the optical detector mechanism is provided with a xenon lamp light source and a beam shrinking light path system and supports 200-1100 nm full-wavelength detection; and the automatic collecting platform mechanism is used for sub-packaging the samples detected by the optical detector mechanism. According to the invention, a separation system and a collection system are integrated into a continuous process, so that man-made interference is reduced, and the resolution ratio and efficiency are improved. The xenon lamp light source and the beam shrinking light path system are adopted, the detection precision and stability are improved based on the spectrophotometer principle, the detection wavelength can be freely selected, and the limitation of traditional dual wavelengths is broken through.

The invention discloses a method for detecting the purity of a phosphorus-containing flame retardant, and belongs to the technical field of flame retardant detection. The specific test method comprises the test steps of selecting a solvent, preparing a to-be-tested solution, determining the maximum absorption wavelength, determining absorbance, calculating the purity of a sample and the like, and analyzing and processing an experimental result. The solvent is filtered through a 600-mesh screen, the influence of impurities in the solvent on an experimental result is eliminated, and the scientificity of the experimental result is ensured by parallelly determining the average value recorded for three times; the testing method has the advantages of low cost, simplicity and convenience in operation, short detection period and the like, and can realize rapid detection of a plurality of samples based on multiple stations of an ultraviolet-spectrophotometer, so that the working efficiency is improved; meanwhile, the method for detecting the purity of the phosphorus-containing flame retardant provided by the invention can be used for comparing the quality of products from different manufacturers and the batch stability of the products at the same time, and is beneficial for enterprises to control the quality of the products.

A photometric process measurement arrangement and a photometric measurement method The invention refers to a photometric process measurement arrangement (10) comprising a photometric immersion probe (20) comprising a photometer flashlight source (61) for providing photometric light impulses, a photometric detector arrangement (70) comprising a separate wavelength-selective detection element (71, 72, 73), and a photometer control (80) controlling the photometer flashlight source (61) and the detector arrangement (70), The photometer control (80) comprises: An impulse signal integrator (819, 829, 839) for integrating the electric impulses having the impulse intensity (Ui) generated by the detection element (71, 72, 73) of one impulse integration cycle (204; 221; 264), a measurement cycle control (90) for adapting the total number of 20 integrated cycle impulses of an impulse integration cycle (204;221;264) to the impulse intensity (Ui) of the single electric impulses, an A / D-converter (81, 82, 83) for converting the voltage of the impulse signal integrator (819, 829, 839) in an optional compulsory A / D conversion interval (100) after the impulse integration cycle (204;221;264), and an A / D-conversion management module (150) for balancing the total number of A / D conversion intervals (100-111) within a time frame (F), whereas the number of supplementary A / D conversion intervals (101-111) after the compulsory A / D conversion interval (100) depends on the length of the corresponding impulse integration cycle (204; 221; 264).

An embodiment of a spectrophotometric device for measuring blood oxygen saturation includes a light source, a detector for detecting a light signal reflected by a subject's tissue, an electronic data processing unit to calculate blood oxygen saturation based on the light signal, and a motion sensor for detecting a motion signal indicative of motion of the light source and / or the light detector. The electronic data processing unit may discard a light signal measured by the detector if the motion signal detected by the motion sensor exceeds a predetermined threshold value. An embodiment of a method for measuring blood oxygen saturation includes emitting a light signal into a subject's tissue, detecting the light signal reflected by the tissue, calculating blood oxygen saturation using the light signal measured by the detector, and detecting a contact signal indicative of contact between a subject's skin and the light source and / or the detector.

The invention relates to a diatomic catalyst for detecting carbosulfan pesticide residue and a preparation method, and belongs to the technical field of food safety detection. According to the invention, a reducing sulfide generated by breaking a nitrogen-sulfur (N-S) bond of carbosulfan under an acidic condition is used as a specific substance. The reductive sulfide not only can prevent bimetal active sites in the diatomic catalyst, but also consumes hydroxyl radicals generated by catalyzing hydrogen peroxide (H2O2), and the sensing switch enzyme formed by a dual enzyme inhibition mechanism causes the enzyme substrate 3, 4-dihydroxyl-3, 4-dione to be converted into the diatomic catalyst, so that the catalytic activity of the diatomic catalyst is improved. The blue color of the 3, 3 ', 5, 5'-tetramethyl benzidine (TMB) gradually becomes light along with the increase of the concentration of carbosulfan, sensitive visual detection is implemented, and after a blue product is read by using an ultraviolet spectrophotometer, the absorbance value generated by an ultraviolet absorption spectrum at 654 nm is linearly dependent on carbosulfan. The prepared diatomic catalyst effectively improves the detection sensitivity of the carbosulfan pesticide residue, and has good popularization and application prospects.

The invention refers to a photometric process measurement arrangement (10) with a photometric immersion probe (20). The photometric immersion probe (20) comprises a photometer flashlight source (61) for providing photometric light impulses, a photometric detector arrangement (70) comprising at least two separate wavelength-selective detection elements (71, 72, 73), and a photometer control (80) controlling the photometer flashlight source (61) and the detector arrangement (70). The photometer control (80) comprises several impulse signal integrators (819, 829, 839) for integrating the electric impulses generated by the detection elements (71, 72, 73), several A / D-converters (81, 82, 83) for converting the voltages of the impulse signal integrators (819, 829, 839) when high-precision-converting trigger ports (H) of the A / D-converters (81, 82, 83) are triggered, and a measuring cycle control (90) with an integration target memory (94) memorizing an integration target voltage value (Ut). The photometer control (80) is provided with a high-precision-request port (93) for synchronously triggering the high-precision-converting trigger ports (H) of all A / D-converters (81, 82, 83) after the voltage of the first of all impulse signal integrators (819, 829, 839) has exceeded the memorized integration target voltage value (Ut).

The invention provides pathological tissue section dyeing equipment and method. The method comprises the following steps: dividing a to-be-dyed lymphatic tissue section into a plurality of dyeing partitions according to the structural characteristics of lymphocyte tissues in the to-be-dyed lymphatic tissue section; dyeing agents with different concentrations are applied to different dyeing partitions according to the reference light transmittance of the lymphocyte tissue to obtain color gradient vectors of the lymphocyte tissue slices, light absorption characteristics of the dyeing partitions are measured through a photometer, and dyeing characteristics are determined based on the light absorption characteristics and the color gradient vectors; obtaining a dyeing image after dyeing the lymph tissue section, extracting deep features of the dyeing partitions from the dyeing image, and determining a dyeing loss value when dyeing the dyeing partitions based on the deep features and the dyeing features; and based on the dyeing loss value, carrying out self-adaptive adjustment on the dyeing agent concentration of each dyeing zone. By adopting the scheme provided by the invention, optimal adjustment on the concentration of the coloring agent in the sample dyeing process can be realized based on the characteristic difference of the cell tissues at different parts.

The invention relates to the technical field of photovoltaic film detection, in particular to photovoltaic film performance detection equipment which comprises a spectrophotometer with an integrating sphere accessory, the integrating sphere accessory is mounted in a sample bin of the spectrophotometer, and a mounting mechanism and a wrinkle generator are further mounted in the sample bin. The wrinkle generator comprises a jacking head for applying local mechanical pressure to the photovoltaic film and an L-shaped jacking rod for applying non-uniform mechanical tension, the wrinkle generator further comprises a transmission part, and the jacking head and the L-shaped jacking rod alternately extend out in the front-back direction under the transmission action of the transmission part so that different wrinkles can be generated on the surface of the photovoltaic film; the light transmittance of the photovoltaic film with different inclination degrees and different wrinkle conditions is detected through the spectrophotometer with the integrating sphere accessory, the method is more suitable for the actual use state of the photovoltaic film, the detection result is more accurate, and more reliable basis is provided for performance evaluation of the photovoltaic film.

The invention discloses an organic-inorganic hybrid zero-dimensional halide perovskite single crystal material and a preparation method thereof. The chemical formula of the organic-inorganic hybrid zero-dimensional halide perovskite single crystal material is PMA4InCl7.H2O, and the chemical formula of the antimony-doped single crystal material is PMA4InCl7.H2O: Sb, the corresponding single crystal material is obtained through the steps of raw material adding, cooling crystallization, suction filtration, drying and the like. The optical band gap of the PMA4InCl7. H2O is determined to be 4-5 eV through an ultraviolet-visible spectrophotometer, and when the PMA4InCl7. H2O is irradiated by a 365 nm portable ultraviolet lamp, the PMA4InCl7. H2O shows light blue; the optical band gap of the PMA4InCl7. H2O: Sb is determined to be 3-4 eV through an ultraviolet-visible spectrophotometer, and when the PMA4InCl7. H2O: Sb is irradiated by a 365 nm portable ultraviolet lamp, the PMA4InCl7. H2O: Sb shows bright yellow. The maximum quantum yield measured by an absolute fluorescence quantum yield spectrometer can reach 72%.

An UPLC can offer the advantages of improved resolution, shorter analysis time, reduced solvent consumption, and easy connectivity to a mass spectrometer. One of our unique approaches is to use four small linear pumps to achieve gradient elution. We use four binary pumps to achieve continuous gradient elution. We designed an on-line degassing to greatly reduce interference from gas bubbles, thereby maintaining stable pressure. The range of flow speed is controlled from 300 nl / min to 100 ul / min. This portable UPLC can withstand pressures of 15,000 psi or higher. Its size is 30 cm×30 cm×30 cm, and it weighs less than 20 kg. This portable UPLC is equipped with an LED detector, which reduces both cost and system size and has higher sensitivity than a spectrophotometer. We also have the option to easily switch to a conventional detector with a discharge light source and a grating spectrophotometer.

The present disclosure relates to a chemiluminescence analyzer, comprising: a sample preparation device configured to pre-dilute a blood sample under test by using a diluent, and mix the pre-diluted blood sample under test and a reaction reagent in a reaction vessel to obtain a sample liquid under test; a substrate providing device configured to provide a luminescent substrate into the reaction vessel containing the sample liquid under test so as to carry out a chemiluminescence reaction; a photometric device, at least comprising a photometer; and a data processing device configured to obtain a test result of human chorionic gonadotropin (HCG) in the blood sample under test on the basis of a luminescent signal and a preset calibration model. A first linear test range of the photometer is [A1, A2] photon count / second, and in the first linear test range, the intensity of the luminescent signal generated in the chemiluminescence reaction is linearly related to the photon count output by the photometer, wherein A1 is less than or equal to 2000 and A2 is greater than or equal to 108. Therefore, the testing efficiency and accuracy of HCG can be improved without increasing the costs.

Provided is a phosphor powder in which the balance of suitability, brightness, and excitation light blocking properties of a complex obtained from the phosphor powder with respect to a small-sized light-emitting device is improved. A phosphor powder containing SCASN phosphor particles, the phosphor powder having a volume-based median diameter (D50) of 0.1 [mu] m to 5.0 [mu] m (inclusive) as determined by a laser diffraction scattering method, and a peak wavelength of a fluorescence spectrum measured by a spectrophotometer when the phosphor powder is irradiated with light having a wavelength of 455 nm of 590.0 nm to 630.0 nm (inclusive), the absorption rate when the phosphor powder is irradiated with light having a wavelength of 455 nm is 80.0% or more.

The embodiment of the invention provides a preparation method of octahedral Ag2O nano-enzyme and a method for detecting H2O2 through a colorimetric method, and relates to the technical field of H2O2 detection. The method for detecting H2O2 by using the colorimetric method comprises the following steps: step S11, taking a plurality of centrifugal tubes, adding quantitative Ag2O solution and H2O2 with different concentrations into each centrifugal tube, and uniformly mixing; step S12, adding a NaAc-Hac buffer solution and a TMB (Tetramethylbenzidine) solution into each centrifugal tube treated in the step S11 to form an Ag2O-TMB-H2O2 reaction system, heating the Ag2O-TMB-H2O2 reaction system in each centrifugal tube in a water bath for a preset time, and observing the color change of the solution in each centrifugal tube; and step S13, determining a light absorption value of the Ag2O-TMB-H2O2 reaction system at a preset wavelength through an ultraviolet photometer, and recording data. The method for detecting H2O2 through the colorimetric method has the advantages of being simple in operation process, accurate in detection, visual in result and the like.

To provide a molecule capable of recognizing a cytosine-cytosine mismatch in DNA.SOLUTION: A solution of FcDANP represented by the chemical formula below, and three solutions each obtained by mixing FcDANP with one of three DNAs having different base sequences, are measured using an ultraviolet-visible spectrophotometer. In the wavelength range of approximately 375-400 nm, the sample containing FcDANP and the DNA having a C-C mismatch exhibits a significantly higher absorption intensity than the other samples.SELECTED DRAWING: Figure 1

The invention provides a novel back contact photovoltaic cell film color sorting method, and relates to the technical field of back contact photovoltaic cell film color sorting.The novel back contact photovoltaic cell film color sorting method comprises a test table top, a back contact photovoltaic cell is arranged on the upper surface of the test table top, and a first test positioning device is arranged at the upper left corner of the test table top; the upper right corner of the test table board is provided with a second test point, the lower left corner of the test table board is provided with a third test point, the lower right corner of the test table board is provided with a fourth test point, and the center of the test table board is provided with a fifth test point. According to the method, the lightness value (L), the red-green chroma value (a) and the yellow-green chroma value (b) of the battery piece are tested by the spectrum luminosity tester through the Lab color model and are compared with the film color standard value to calculate the color difference value, whether the battery piece has color difference or not can be accurately determined through the HSV color model and the lab color model, operation is easy, production line application is convenient, the situation that color difference pieces are mixed into bulk goods can be eradicated, and the production efficiency is improved. And the product quality is improved.

The application discloses a kind of copper azide content trace detection method, the detection method includes: detecting copper azide content: taking the sample to be measured and inorganic acid mixed dissolution, then sequentially adding NaOH solution, buffer solution and copper nitrate solution, using ultraviolet visible spectrophotometer to measure absorbance and calculate corresponding azide radical concentration, determine the content of copper azide and cuprous azide in the sample to be measured by azide radical and copper azide content relationship model;Detect copper azide and cuprous azide: on the basis of measuring copper azide content, determine the content of copper azide and cuprous azide in the sample to be measured by azide radical and copper azide / cuprous azide content relationship model.The copper azide content trace detection method needs simple device of the application, low requirement to equipment, does not need organic solvent or color developing agent, and environmental pollution is small, and sub-milligram level copper azide used in MEMS fuze can be detected.

An anti-reflection film (1) is provided with a transparent base film (2), an anti-reflection layer (3), and an antifouling layer (4) in this order toward one side in the thickness direction. The transparent substrate film (2) is provided with a transparent resin film (21). The anti-reflection layer (3) is an alternating laminate comprising at least one niobium oxide layer (31) and at least one silicon oxide layer (32), and the layer of the anti-reflection layer (3) closest to the antifouling layer (4) is the silicon oxide layer (32). Furthermore, in a difference spectrum calculated from Fourier transform infrared spectrophotometer analysis (FT-IR analysis), when the maximum absorption peak intensity originating from Si-O-Si symmetric scaling near 1050 cm <-1 > is standardized to 1 and the absorption peak intensity originating from Si-O-Si asymmetric scaling at 1200 cm <-1 > is defined as X, 1 / X is 5.0 or more.

The invention discloses an in-situ ultraviolet and visible spectrophotometer with high measurement precision, and relates to the technical field of ultraviolet and visible spectrophotometers, the in-situ ultraviolet and visible spectrophotometer comprises a bottom shell, an optical unit is arranged on the inner wall of the bottom of the bottom shell, and a light source module and a monochromator are arranged in the optical unit; the top of the optical unit is fixedly connected with an operation platform through a supporting rod, the top of the operation platform is provided with a motor mounting frame, the top of the motor mounting frame is provided with a linear motor, the output end of the linear motor is connected with a lifting fixing plate, and the lifting fixing plate is of a Z-shaped structure. The end, away from the linear motor, of the lifting fixing plate is connected with a light shield, and the top of the light shield is provided with an optical fiber clamping frame. According to the method, result deviation caused by dilution multiple estimation errors in a traditional method is avoided, the dilution frequency of the high-concentration sample is reduced, reagent consumption and waste liquid generation are reduced, and the method conforms to the green analytical chemistry concept.

The invention discloses preparation and visual detection application of an Ag / {001} Bi2Fe4O9 nanosheet, relates to the technical field of visual ultra-sensitive detection of 2, 4-dichlorophenol, and aims to realize an in-situ and ultra-sensitive visual detection method for the 2, 4-dichlorophenol. The method comprises the following steps: uniformly mixing a xanthene dye fluorescein aqueous solution, an Ag / {001} Bi2Fe4O9 nanosheet suspension and a 2, 4-dichlorophenol aqueous solution to obtain a solution to be detected; the method comprises the following steps: putting a solution to be detected into a Pomfiley multi-channel photocatalytic reactor, carrying out dark adsorption by stirring without illumination, then starting visible light, carrying out sufficient illumination, filtering by adopting a 22-micron water-phase filtering membrane, and finally testing by adopting an ultraviolet and visible spectrophotometer, thereby completing photosensitization detection of 2, 4-dichlorophenol. According to the invention, the Ag / {001} Bi2Fe4O9 nanosheet can be prepared and applied to visual detection.

The utility model discloses a precision photometer with a fine tuning structure, which relates to the technical field of precision photometers, and is characterized in that a moving mechanism comprises a fixed block fixed at the bottom of a support plate, a screw rod penetrates through the fixed block, two ends of the screw rod are rotatably connected with a photometer body, and moving blocks are arranged on two sides of the bottom of the support plate; the supporting plate can be driven to move by arranging the rotating mechanism, meanwhile, the diameter of a main gear is larger than that of a secondary gear, and therefore the rotating speed of a lead screw is lower than that of a rotating rod, and fine adjustment of the position of the supporting plate is achieved; and the placing frames can be conveniently and rapidly disassembled and assembled according to the number of the needed placing frames, and the practicability is improved.

The invention discloses an offshore salt mist aerosol monitoring system and method based on a drifting buoy, and relates to the technical field of marine atmospheric environment monitoring, and the method comprises the steps: transmitting the position and time information received by a GNSS receiver to a main control module, and carrying out the resolving of the main control module, and obtaining a preliminary direction; transmitting the data of the attitude measuring instrument to the main control module; the main control module corrects the initial azimuth angle and the elevation angle according to the attitude data, and adjusts the accurate direction of the sun photometer according to the correction result; calculating the optical thickness of the aerosol according to radiation data measured by the sun photometer; the aerosol particle spectrum distribution is inversed according to the aerosol optical thickness; and the main control module performs information interaction on the inverted aerosol particle spectrum distribution and the land through the wireless communication module. The defects of a traditional mode are effectively overcome, and the optical parameters and the dynamic change process of the salt mist aerosol are captured more accurately.

The invention provides a rapid pollutant detection method based on spectral feature analysis, and relates to the technical field of environmental pollutant spectral detection, and the method comprises the following steps: obtaining an original absorption spectrum of a sample, and preprocessing and reconstructing an intrinsic spectral signal; extracting three types of features of morphology, frequency domain energy distribution and phase disturbance, and splicing to obtain a multi-dimensional joint feature tensor; pollutant classification and confidence judgment are completed through an improved CNN, and concentration is predicted through a linear regression model synchronously; in combination with a Mahalanobis distance verification result, deep residual network secondary feature mining is triggered for a low-confidence sample, a final type is determined according to a fusion result, and the concentration is corrected; and generating a detection report and dynamically updating the spectral feature intrinsic library. The method is adaptive to a portable ultraviolet-visible spectrophotometer, the single sample detection time consumption is less than 10min, the classification accuracy is greater than or equal to 90%, the unknown pollutant judgment accuracy is greater than or equal to 89%, and the method is suitable for on-site rapid detection.

The utility model discloses a micro-arc oxidation device and a semiconductor film preparation system, and the micro-arc oxidation device comprises an electrolytic tank, a pulse power supply, a monitoring module and a controller. The electrolytic tank is provided with a stirrer and an ultrasonic generator, and a constant-temperature cooling module is mounted on the side wall of the electrolytic tank; the pulsed power supply is mounted on one side of the electrolytic tank; the cathode of the pulsed power supply is connected with the electrolytic tank; the monitoring module comprises a conductivity probe, a photometer probe, a conductivity meter and an ultraviolet spectrometer; the controller is electrically connected with the constant-temperature cooling module and the monitoring module. The change of solute in the electrolyte is monitored through the ultraviolet spectrograph and the conductivity meter, accurate control over the concentration of the electrolyte and the nano-particles in the electrolyte is achieved, reaction conditions and reaction parameters can be automatically detected and regulated, accurate regulation and doping of the nano-particles in the semiconductor film growth process are achieved, and the yield of the semiconductor film is improved. The operation is simple and convenient, the controllability is strong, and the yield is high.

A light therapy system is comprised of a pressure cuff system having a cuff positionable on or near a body part of a user and receiving pressurized air to selectively pressurize and depressurize the cuff, and a light emitting system configured to emit light to the cuff. The light emitting system has a support structure and a light emitter positioned on the support structure, the light emitter being controllably powered. The support structure is positionable on the inner surface of the cuff such that the light emitter may direct light onto the body part. The light therapy system may also include a controller capable of controllably providing power to the light emitter, where the controller may adjust an intensity or duration of light directed onto the body part in response to an input or measurement relating to a state of the body part. A photometer may be provided individually or integrally to measure the state of a body part. A method of providing light therapy is also provided.

The embodiment of the invention discloses a concentration detection device. The concentration detection device comprises a micro-fluidic chip, an optical fiber photometer and a data processing system, the micro-fluidic chip comprises an extraction channel, and an inlet and an outlet are formed in the two ends of the extraction channel respectively. An organic extraction agent and a sample solution enter the extraction channel through the inlet, and the organic extraction agent is used for extracting Pu (IV) in the sample solution and forming an organic phase containing Pu (IV) and a water phase containing Pu (III). The optical fiber photometer comprises a liquid core waveguide capillary pool, an optical fiber, a light source and a spectrograph. The liquid core waveguide capillary pool is communicated with the outlet, and a water phase enters the liquid core waveguide capillary pool through the outlet. The light source and the spectrograph are connected with the liquid core waveguide capillary pool through optical fibers. The light transmitted by the optical fiber is totally reflected in the liquid core waveguide capillary pool, so that the light with sample information is transmitted to a spectrograph through the optical fiber for detection. And the data processing system is connected with the spectrograph.

The invention discloses a rapid detection method for AN content in a polymer solution, and belongs to the technical field of rapid detection of the AN content in the polymer solution. Based on the principle of a spectrophotometer, the light absorption value of a sample is calculated according to the absorption condition of acrylonitrile under light with the specific wavelength of 220nm, the relation between the absorbance and the acrylonitrile concentration is established according to the Beer law, and a standard curve is fitted; compared with a traditional method, the method has the advantages that the sensitivity is higher, the detection limit is lower, meanwhile, the influence of interference factors is reduced, and the reliability of a measurement result is improved. In addition, the ultraviolet spectrophotometer has the advantages of being high in instrument universality, convenient to operate, low in professional requirement for detection personnel and the like.

The present invention provides excellent visibility of a printed part formed by laser marking. This liquid compression molding material comprises (A) an epoxy resin, (B) a curing agent, (C) an inorganic filler, and (D) a coloring material, wherein the absorbance measured under the following absorbance measurement conditions using a photometer is 3.5 or more. (Absorbance measurement conditions) Measurement sample: a cured product obtained by curing the liquid compression molding material through a heat treatment at 150°C for 60 minutes. Thickness of measurement sample: 260 μm Measurement wavelength: 1064 nm