A device for sand sampling through a water method includes a sampling cylinder and a triaxial sampler, where the sampling cylinder includes a cylinder, two ends of the cylinder being hermetically provided with an upper sealing cover and a lower sealing cover separately, one ends, facing inside of the cylinder, of the upper sealing cover and the lower sealing cover being provided with water-permeable stones, one end, facing outside of the cylinder, of the upper sealing cover being connected to a control valve, and the control valve being in communication with the inside of the cylinder; and the sampling cylinder is arranged in the triaxial sampler when sand sampling is performed through a water method, a lower end of the triaxial sampler is provided with a test operation table, and an upper end of the triaxial sampler is nested inside a restraint ring.

A device for sand sampling through a water method includes a sampling cylinder and a triaxial sampler, where the sampling cylinder includes a cylinder, two ends of the cylinder being hermetically provided with an upper sealing cover and a lower sealing cover separately, one ends, facing inside of the cylinder, of the upper sealing cover and the lower sealing cover being provided with water-permeable stones, one end, facing outside of the cylinder, of the upper sealing cover being connected to a control valve, and the control valve being in communication with the inside of the cylinder; and the sampling cylinder is arranged in the triaxial sampler when sand sampling is performed through a water method, a lower end of the triaxial sampler is provided with a test operation table, and an upper end of the triaxial sampler is nested inside a restraint ring.

The specification describes devices, methods, and kits for mincing biological tissue. The method includes conforming biological tissue to having about uniform cross-sectional area planes along its length, and cutting the biological tissue. The conforming and cutting is performed cooperatively to control the size of the minced biological tissue. The device is suitable for use with the method.

A disaggregation and homogenization device may be capable of photoactivation to improve heat resilience, photoactivation efficiency and simultaneous processing. Processes of disaggregation and homogenization may be handled in a simultaneous manner at will. A photoactivation means is also present such that rendering simultaneous utility of photoactivation and homogenization may be possible, and elimination of extra steps for preparation may be implemented. Protocols of the processes are registerable and adjustable in parameters i.e. rate of revolution and duration of process overall; and may be executed through an electronic control unit capable of storing and executing said protocols.

The present invention falls within the field of medical apparatuses. Disclosed are a method and a device for identifying platelet aggregation, and a flow cytometer, which are used for accurately giving an alarm about a platelet aggregation during blood cell analysis. The method comprises: detecting a pre-treated blood sample by using a flow cytometry technique so as to acquire scattered light signals and fluorescent light signals of the blood sample, wherein the scattered light signals are forward scattered light signals or side scattered light signals; differentiating between ghost particles and white blood cells by using a fluorescence-scattered light diagram generated by the scattered light signals and the fluorescent light signals of the blood sample; and counting a number of particles in a ghost characteristic region in the fluorescence-scattered light diagram of the blood sample and determining whether the number of particles exceeds a threshold value, and outputting a warning of platelet aggregation if the number of particles exceeds the threshold value.

The present invention falls within the field of medical apparatuses. Disclosed are a method and a device for identifying platelet aggregation, and a flow cytometer, which are used for accurately giving an alarm about a platelet aggregation during blood cell analysis. The method comprises: detecting a pre-treated blood sample by using a flow cytometry technique so as to acquire scattered light signals and fluorescent light signals of the blood sample, wherein the scattered light signals are forward scattered light signals or side scattered light signals; differentiating between ghost particles and white blood cells by using a fluorescence-scattered light diagram generated by the scattered light signals and the fluorescent light signals of the blood sample; and counting a number of particles in a ghost characteristic region in the fluorescence-scattered light diagram of the blood sample and determining whether the number of particles exceeds a threshold value, and outputting a warning of platelet aggregation if the number of particles exceeds the threshold value.

An experimentation method for a type I stress intensity factor test considering frost heaving force periodic changes, steps being 1: preparing a specimen, waterjet cutting on the specimen to simulate a non-penetrating rock mass fracture; step 2: vacuum saturating the specimen; step 3: affixing a strain gauge in a non-elastic area at a tip of the specimen; step 4: placing the specimen into a rock mass (1) fracture frost heaving experiment box (5), pressurizing by a pressurizing apparatus (4) balloons on either side of the frost heaving experiment box (5), shutting a valve and removing a pipe, placing the frost heaving experiment box (5) holding the specimen into a water tank, allowing water to immerse the specimen; and step 5: placing the water tank and the frost heaving experiment box (5) holding the specimen together into a high-low temperature alternating experiment box (7) to start a freeze-thaw cycle experiment.

A toilet for administering a product to a user is disclosed. The toilet includes a bowl, a mechanism for administering the product to the user, a storage structure for storing the product, a sensor that detects a property of the product, and a processor. The bowl is adapted to receiving excreta from the user. The processor compares the detected property with a range of values indicating the suitability of the product for being applied to a user. The processor generates an alert when the detected property falls outside the range of values.

A toilet for administering a product to a user is disclosed. The toilet includes a bowl, a mechanism for administering the product to the user, a storage structure for storing the product, a sensor that detects a property of the product, and a processor. The bowl is adapted to receiving excreta from the user. The processor compares the detected property with a range of values indicating the suitability of the product for being applied to a user. The processor generates an alert when the detected property falls outside the range of values.

The present disclosure also relates to systems and methods for quality control in histology systems. In some embodiments, a method is provided that includes receiving a tissue block comprising a tissue sample embedded in an embedding material, imaging the tissue block to create a first imaging data of the tissue sample in a tissue section on the tissue block, removing the tissue section from the tissue block, the tissue section comprising a part of the tissue sample, imaging the tissue section to create a second imaging data of the tissue sample in the tissue section, and comparing the first imaging data to the second imaging data to confirm correspondence in the tissue sample in the first imaging data and the second imaging data based on one or more quality control parameters.