34results about How to "Meet the needs of rapid analysis" patented technology

The invention provides a novel fast and non-destructive analysis method for the nutritional quality of cottonseed. The method comprises the following steps: 1) selecting whole cottonseeds of representative cotton varieties as experimental samples; 2) using a near-infrared spectrometer to collect near-infrared spectral data of whole cottonseeds, and the spectral scanning range is 800-2500nm; 3) using the national standard method Accurately analyze the nutritional quality of cottonseed; 4) Preprocess the near-infrared spectrum data; 5) Select spectral variables to eliminate non-informative variables; 6) Use the multivariate correction method to establish the near-infrared spectrum of whole cottonseed and the nutritional value of whole cottonseed 7) Performance evaluation of the calibration model; 8) Collect near-infrared spectral data of the whole cottonseed to be tested, and use the calibration model to predict its nutritional quality after preprocessing the spectral data. The invention has fast analysis speed, does not destroy samples, does not require sample pretreatment, has high detection accuracy, and can analyze various nutritional quality components in cotton seeds at the same time, and provides a convenient, fast and efficient analysis method for cotton breeding and cotton seed inspection.

The invention provides a method for detecting the water content and fat content in abalone through a low-field nuclear magnetic resonance technology. The method comprises the following first step of collecting samples, the second step of carrying out low-field nuclear magnetic analysis on the sample, the third step of measuring the samples, the fourth step of establishing a model, the fifth step of evaluating the model, and the sixth step of measuring the water content and the fat content of the samples to be detected. By means of the method, the water content and fat content in abalone can be measured at the same time, detection is rapid and accurate and free of the influence of the surface feature of abalone, and abalone is not damaged in the measuring process.

The invention discloses a low field nuclear magnetic resonance-applied frozen beef freshness nondestructive testing method. The low field nuclear magnetic resonance-applied frozen beef freshness nondestructive testing method comprises the following steps of (A) sample collection, (B) sample measurement, (C) sample low field nuclear magnetic analysis, (D) multiple freshness-related index measurement, (E) model establishment, (F) model assessment and (G) measurement of freshness of samples to be detected. By establishing a mathematical predication model reflecting fresh beef moisture content relaxation spectrum information and multiple indexes related to fresh beef freshness to accurately and reliably detect multiple indexes of an unknown fresh beef simultaneously such as thiobarbituric acidreactive substances (TBARS), volatile basic nitrogen (TVB-N) and pH, the low field nuclear magnetic resonance-applied frozen beef freshness nondestructive testing method can help predict the storagetime of the beef and achieve rapid and nondestructive detection and assessment of the freshness of the fresh beef. The low field nuclear magnetic resonance-applied frozen beef freshness nondestructivetesting method is rapid and accurate, avoids influence of beef surface properties, and during measurement, has no damage to the beef.

The invention discloses a method for detecting the content of rare earth in rock weathering crusts by using a visible light-near infrared reflection spectrometer and analyzing data. The content of therare earth in outcrops, surface soil and drilling samples of the rock weathering crusts is tested by using the handheld visible light-near infrared reflection spectrometer, through specific sample pretreatment and data processing means, the interference of water, organic matter, ferric oxides and other components in the samples with the testing accuracy of the content of the rear earth is eliminated, the accuracy and the sensitivity of testing the content of the rear earth in the rock weathering crusts are improved, and the requirements of weathering crust ion adsorption type rare earth deposit ore prospecting and exploration work for quick analysis of the samples are met.

The invention discloses a gene-sample analysis method. The gene-sample analysis method includes the steps that gene-sample selection instructions are received; a variation filter selection interface is displayed; meanwhile, according to selected gene samples, common variation information of all the selected gene samples is extracted, and to-be-analyzed sample data is formed and cached in a memory; filter-condition selection instructions are received; the to-be-analyzed sample data is called from the memory, and gene-sample variation analysis is completed according to filter conditions. The invention discloses an electronic device with the gene-sample analysis method. By means of the gene-sample analysis method and the electronic device, the response speed of gene-sample analysis can be increased.

The invention relates to a gridding-based point cloud data retrieval method. The method comprises the following steps: determining a boundary value of point cloud data; determining a boundary range and a reference point of the point cloud data according to the boundary value; dividing the point cloud data into point cloud grids according to the boundary range and a preset grid side length, and determining the number of the point cloud grids; determining index numbers of discrete points in the point cloud grids according to the reference points and the number of the point cloud grids; and retrieving the point cloud data according to a preset retrieval method and the index number. Through the steps, the point cloud data formed by a large number of discrete points are gridded, and retrieval is performed according to the adjacent clustering algorithm by taking the gridded point cloud grid as a unit in the point cloud data retrieval process, so that the problem of low efficiency caused by traversing the point cloud data in an existing mode is avoided, the data retrieval efficiency is improved, and the requirement on rapid analysis of the point cloud data is met.

The invention discloses an online dilution device, comprising a dilution device body and a control system, wherein the dilution device body comprises a fixed base and at least one proportional distributor; at least one liquid inlet pipeline and at least one liquid outlet pipeline are formed on the fixed base; an inlet of the proportional distributor is connected to a liquid inlet container througha pipeline, and an outlet of the proportional distributor is in communication with the liquid inlet pipeline of the fixed base; the liquid outlet pipeline is connected with a flow injection analyzer;the control system is connected to the proportional distributor by signals. The online dilution device can realize the online preparation of a standard curve based on the structure above, perform on-line dilution of high concentration samples with dilution ratio of 1 to 200 times, dilute and mix a sample and 12 kinds of reagents on line and work with the flow injection analyzer together without interference, has not only a high degree of automation, but also high work efficiency, and thus meets the needs of rapid analysis.

The invention discloses a method for quickly determining the content of barium in a nickel salt solution. In 0.12 mol/L of hydrochloric acid medium, tribromoarsenazo and barium can form a stable purple complex, and according to the spectrophotometric analysis principle, accurate determination of the content of the barium in a nickel chloride solution or a nickel nitrate solution is completed. Themethod comprises the specific steps that 5.0 mL of 0.6 mol/L hydrochloric acid solution and 2.0 mL of 50 g/L ascorbic acid solution are added into the pretreated nickel chloride or nickel nitrate solution in a 25 mL volumetric flask in sequence and mixed evenly, then 5.0 mL of 1g/L tribromoarsenazo solution is added, and the volume is metered; with the reagent blank as a reference, the absorbancyis measured at the wave length of 620 nm, and according to the absorbancy value, the content of the barium in the to-be-measured solution is obtained on a working curve. By means of the method, the content of the barium is within the range from 0 microgram/25 mL to 50 micrograms/25 mL and accords with the Beer's law, and the apparent molar absorption coefficient epsilon is 4.64*10<4>Lmol<-1>cm<-1>; the recycling rate is 95-103%, RSD is smaller than 10%, the method is stable, reliable, quick and simple, and requirements for quick analysis of the barium in the nickel chloride and nickel nitrateproduction process can be met.

The embodiment of the invention discloses a commodity object analysis method and electronic equipment, and the method comprises the steps: creating an analysis item according to received analysis demand information, and creating a target interface for the analysis item; the analysis demand information comprises basic information of a target commodity object and a plurality of to-be-analyzed feature description documents; selecting a target number of elements from the plurality of feature description copywrites for combination or arrangement to obtain a plurality of copywriting groups, and creating a plurality of analysis tasks; displaying the target interface to a plurality of first users for multiple times, and when the target interface is displayed to the first users, putting the basic information of the target commodity object and one analysis task into the target interface for display; and providing an analysis result according to the first user selection condition corresponding to the plurality of analysis tasks. According to the embodiment of the invention, the commodity object can be analyzed more effectively.

The invention relates to the field of preparation of SERS active substrates, and discloses a method for preparing an SERS active substrate based on a grating structure of an optical disc. The SERS active substrate is prepared by performing ink jet printing on the grating structure of the optical disc. The method of the invention has the beneficial effects that ink printing can be accurately carried out in a predefined area of the optical disc through an ink jet printing technology, the consumption of ink can be controlled, the ink waste can be reduced, and the SERS substrate with high repetition rate can also be produced.

The invention relates to a method for measuring the content of potassium chloride and sodium chloride in a potassium chloride and sodium chloride injection solution, and a method for determining whether the content of potassium chloride and sodium chloride in the potassium chloride and sodium chloride injection solution meets quality standards. The measuring method is carried out through an atomic absorption spectrometry method by an atomic absorption spectrophotometer.

The invention relates to a method for simultaneously and rapidly determining arsenic and antimony in sodium stannate by a vapor generation-atomic fluorescence spectrometry (VG-AFS). According to the method, a certain amount of citric acid and hydrochloric acid are used for dissolving sodium stannate, a standard addition method is adopted for determination, under the optimal concentration of citricacid and hydrochloric acid, matrix tin is not hydrolyzed, determination of arsenic and antimony by VG-AFS cannot be interfered, and simultaneous and rapid determination of arsenic and antimony in sodium stannate can be achieved. The method is high in sensitivity and accuracy, good in selectivity and low in detection limit, and the lower detection limit of arsenic and antimony is smaller than or equal to 0.00005%; and the method has the advantages of short analysis time, low cost, no matrix interference, safety, environmental protection and high efficiency, and can well satisfy the requirements of simultaneous rapid analysis of impurity elements arsenic and antimony in sodium stannate.

The invention relates to a portable disposable surface-enhanced Raman/colorimetric dual sensor as well as a preparation method, a detection method and application thereof. The sensor comprises a sample measuring tube and a sampling part. The sample measuring tube comprises a tube body, an opening end and a sealing end arranged at two ends of the tube body, a detection solution section arranged inthe tube body, and a closed section. The preparation method comprises the following steps: preparing an ion nanoparticle colloidal solution by adopting a sodium citrate reduction method, and injectingthe ion nanoparticle colloidal solution into the tube body in a vacuum state to obtain the sensor. The detection method comprises the following steps: wiping the surface of a to-be-detected object through a sampling part; breaking the closed section of the tube body to immerse a detection solution into the sampling part; and then performing colorimetric detection or in-situ SERS detection on a discoloration sampling part to obtain qualitative and quantitative analysis results. Compared with the prior art, the portable disposable surface-enhanced Raman/colorimetric dual sensor can meet the requirement for large-batch rapid analysis in a laboratory, is convenient to use at a time in pollution field detection to avoids cross contamination; and a novel portable device for fruit and vegetablepesticide residue detection, emergency analysis and judicial expertise can be provided.

The invention relates to a method for detecting microcystic toxins in water, which comprises the following steps: filtering a water sample through a 0.22 mu m MCE filter membrane, and then carrying out on-line solid-phase extraction and analytical determination on the filtered water sample through an on-line solid-phase extraction ultra-high performance liquid chromatography-tandem mass spectrometry method, wherein the online solid-phase extraction adopts a C8 solid-phase extraction column, the conditions of the ultra-high performance liquid chromatography are as follows: in a mobile phase, a solution A is a 0.1% formic acid acetonitrile solution, and a solution B is a 0.1% formic acid aqueous solution; the gradient elution procedure includes that in 0-4.6 min, and 98% of the solution B is used; in 4.6-10.0 min, 98% liquid B and 25% liquid B are used, and in 10.0-11.0 min, 25% liquid B and 100% liquid B are used; the flow rate is 0.4 mL/min; the column temperature is 35 DEG C, and the sample injection volume is 2mL. The method disclosed by the invention is a method which is high in sensitivity, high in accuracy, good in recovery rate and reproducibility, simple, convenient and rapid to operate and capable of simultaneously determining the eight MCs in the water body.

The invention discloses a two-dimensional liquid chromatography-mass spectrometry method for mass analysis of low-molecular-weight heparin, which comprises the following steps: 1) preparing and grading low-molecular-weight heparin as a raw material through medium-pressure column chromatography to obtain a plurality of low-molecular-weight heparin oligosaccharides with different polymerization degrees, and 2) qualitatively analyzing the low-molecular-weight heparin oligosaccharide by using a two-dimensional liquid phase on-line mass spectrometry, namely separating the low-molecular-weight heparin oligosaccharide with a single polymerization degree by using strong anion exchange chromatography in a first-dimensional liquid phase, cutting each SAX separation oligosaccharide peak into a second-dimensional molecular sieve chromatography, and finally, carrying out on-line mass spectrometry. And 3) comparing SAX standard maps of different samples under the same polymerization degree, and carrying out semi-quantitative analysis on oligosaccharides of each polymerization degree through peak areas. The method can be used for quickly and finely analyzing the structure and controlling the quality of the low-molecular-weight heparin, and has huge application potential.