Abstract: A method for measuring drop time of a control rod cluster integrated with a rod position measurement device is provided, wherein the method is used to measure the drop time of each control rod cluster, and includes: Si, monitoring a voltage Ua of coils in Group A to capture a rod cluster drop signal; S2, searching a point (tmax, Vmax) with a maximum drop speed or with a local maximum drop speed; S3, retroactively calculating, from tmax, an end of a time period T4 when the control rod cluster starts to drop; S4, retroactively searching, from a minimum value point of a drop reference signal DROPref, a start of the time period T4 when the drop reference signal DROPref drops from a maximum value to 33% thereof; and S5, determining, from tmax forward, a time point t6 when a drop speed of the control rod cluster is lower than 0.

Abstract: A droplet preparation and size control device based on electrowetting step emulsification is provided, including a syringe pump, a metal pipeline, a micro-channel, two electrode plates, a continuous phase container and a direct-current power supply, wherein: the syringe pump, the metal pipeline and the micro-channel are successively connected; an outlet of the micro-channel is clamped and sealed between the two electrode plates; each electrode plate consists of four layers, respectively a base layer, a conducting layer, an insulating layer and a hydrophobic layer; a cathode of the direct-current power supply is connected with the metal pipeline, and an anode of the direct-current power supply is connected with the conducting layer of each electrode plate; the syringe pump is filled with dispersed phase fluid; continuous phase fluid is injected into the continuous phase container and immerses the electrode plates.

Abstract: A droplet preparation and size control device based on electrowetting step emulsification is provided, including a syringe pump, a metal pipeline, a micro-channel, two electrode plates, a continuous phase container and a direct-current power supply, wherein: the syringe pump, the metal pipeline and the micro-channel are successively connected; an outlet of the micro-channel is clamped and sealed between the two electrode plates; each electrode plate consists of four layers, respectively a base layer, a conducting layer, an insulating layer and a hydrophobic layer; a cathode of the direct-current power supply is connected with the metal pipeline, and an anode of the direct-current power supply is connected with the conducting layer of each electrode plate; the syringe pump is filled with dispersed phase fluid; continuous phase fluid is injected into the continuous phase container and immerses the electrode plates.

Abstract: Provided herein are fluorescent bioprobes comprising fluorogens that exhibit aggregation-induced emission (AIE) labeled on biomolecules. The present subject matter relates to a fluorescent bioprobe comprising one or more fluorogen labeled on chitosan. The present subject matter is also directed to methods of preparing the fluorescent bioprobes, methods of labeling and detecting DNA and/or proteins with the fluorescent bioprobe, and methods of cell imaging including live cell tracking.