Abstract: A detection device includes a frame, a transport mechanism, detection mechanisms, and a grasping mechanism. The transport mechanism includes a feeding line, a first flow line, and a second flow line arranged in parallel on the frame. The detection mechanisms are arranged on the frame and located on two sides of the transport mechanism. The grasping mechanism is arranged on the frame and used to transport workpieces on the feeding line to the detection mechanisms, transport qualified workpieces to the first flow line, and transport unqualified workpieces to the second flow line.

Abstract: A battery pack, a vehicle, and an energy storage device are provided. The battery pack includes a cell array and a support member, where the cell array includes a plurality of cells, the cell has a first dimension, and the first dimension is a maximum spacing between two imaginary parallel planes sandwiching the cell; and at least one of the cells 600 mm?first dimension?2500 mm the at least one cell includes a casing and a core located inside the casing, a supporting region is formed on the casing, and the cell is connected to the support member through the supporting region and is supported by the support member. The support member is connected to the supporting region to support the cell.

Abstract: A power battery pack includes: a pack body; a plurality of cells, disposed in the pack body; the cell having a length L0, a width H0, and a thickness D0, where at least one cell meets: L0>H0?D0, a length direction of the cell is arranged along a width direction of a vehicle body of the electric vehicle, and in the width direction of the electric vehicle, the length L0 of the cell and a size W of the vehicle body of the electric vehicle in the width direction meet: 46%?L0/W?76%; or at least one cell meets: L0>H0?D0, a length direction of the cell is arranged along a length direction of a vehicle body of the electric vehicle, and in the length direction of the electric vehicle, the length L0 of the cell and a size X of the vehicle body of the electric vehicle in the length direction meet: 40%?L0/W?76%.

Abstract: A transmission power allocation method is provided. The transmission power allocation method is applied in user equipment (UE). The transmission power allocation method includes the following steps. The UE calculates the target power. The UE calculates the path loss of each antenna of the UE. The UE adjusts the transmission power of each antenna, except for a first antenna which corresponds to the maximum path loss, based on the maximum path loss.

Abstract: A battery pack for optimizing the structure of the battery pack includes a case, a battery module and a blocking member. The case includes an accommodating cavity and a drain hole in communication with the accommodating cavity. The battery module is contained inside the accommodating cavity. The blocking member is mounted to the case, and located between the drain hole and the battery module to block a binder for fixing the battery module from entering the drain hole. In the above-described technical solution, the blocking member can produce the effect of reducing or even avoiding binder for fixing the battery module from clogging in the drain hole.

Abstract: A novel aryl ether substituted heterocyclic compound has GLP1R agonist activity. A GLP1R agonist is represented by formula (I), or a pharmaceutically acceptable salt, solvate, hydrate, isotope substituent or isomer thereof.

Abstract: The present invention relates to the technical field of automobile fittings, and discloses a foldable and flexible vent for an air conditioner, comprising a base, a hose and an air guide cylinder, wherein one end of the base communicates with the vent for the air conditioner, and the other end communicates with the hose; the air guide cylinder is arranged at one end of the hose away from the base; the vent further comprises an air damper and a rotating mechanism. The plurality of air dampers are distributed in a circular array in the air guide cylinder with the axis thereof as the center, and then adjusted by the synchronous angle of the rotating mechanism, so that the wind direction of the hose flowing into the air guide cylinder is uniformly discharged in a spiral manner, achieving the effect of simple, convenient and efficient uniform venting.

Abstract: The present invention relates to a modified polyurethane prepolymer, a two-component polyurethane adhesive and the preparation method thereof. The modified polyurethane prepolymer is prepared from the raw materials comprising the following components: polyurethane prepolymer and graphene oxide; wherein, the polyurethane prepolymer is prepared from the raw materials comprising the following components: copolymer containing ureidopyrimidinone groups and aliphatic isocyanate; wherein, the copolymer containing ureidopyrimidinone groups is formed by copolymerization of the raw materials comprising the following components: alkyl acrylate ureidopyrimidinone, and hydroxyethyl alkyl acrylate; wherein, the alkyl acrylate ureidopyrimidinone has the structure shown in Formula (I); and the hydroxyethyl alkyl acrylate has the structure shown in Formula (II). The two-component polyurethane adhesive containing the modified polyurethane prepolymer has excellent mechanical properties and aging resistance simultaneously.

Abstract: Systems and method for versatile multiplexed spinning/rotating bioassays are provided. This bioassay platform can take the advantage of the high-speed spinning motion, which naturally provides on-the-fly cellular imaging at the rate that cannot be reached by the conventional cameras or laser-scanning techniques, but ultrafast imaging modalities. More importantly, the functionalized solid substrates derived from the disk substrate can be compatible with adherent cell culture as well as biochemically-specific cell-capture, which can now be assayed with ultrafast imaging modalities at an ultra-high-speed line-scan rate of >10 MHz. Large-format spinning high-throughput imaging assay could thus be a potent tool for scaling both the assay throughput as well as content/multiplexity as demanded in many applications, e.g. drug discovery, and rare cancer cell screening.

Abstract: A quick screening method for microbial strains includes the steps of: feeding a carrier worm with Styrofoam for a plurality of days; and sampling a digestive system of the carrier worm and placing the sampled digestive system of the carrier worm into a culture medium. The digestive system of the carrier worm includes at least one Styrofoam degrading microbial strain. The culture medium includes an emulsion formed by dissolving the Styrofoam with chloroform and adding a surfactant to the dissolved Styrofoam. A culture medium for fast culturing of the at least one microbial strain is also provided.

Abstract: Systems and method for high-speed single-pixel quantitative phase contrast optical imaging are provided. This imaging technique can bypass the use of conventional image sensors and their associated speed limitations. The quantitative phase images can be acquired much faster than conventional quantitative phase imaging by a chirped-wavelength-encoding mechanism via wavelength-swept laser sources or optical time-stretch based on optical fibers, without the need for interferometric approaches.

Abstract: A lithium hydrogen titanate Li—H—Ti—O material includes Li, H, Ti, and O elements, wherein a mass percentage of Li is in a range from about 3% to about 12%, a mass percentage of H is in a range from about 0.1% to about 8%, a mass percentage of Ti is in a range from about 46% to about 56%, and a mass percentage of O is in a range from about 28% to about 50%. A lithium ion battery and a method for making the lithium hydrogen titanate Li—H—Ti—O material are also disclosed.

Abstract: A quick screening method for microbial strains includes the steps of: feeding a carrier worm with Styrofoam for a plurality of days; and sampling a digestive system of the carrier worm and placing the sampled digestive system of the carrier worm into a culture medium. The digestive system of the carrier worm includes at least one Styrofoam degrading microbial strain. The culture medium includes an emulsion formed by dissolving the Styrofoam with chloroform and adding a surfactant to the dissolved Styrofoam. A culture medium for fast culturing of the at least one microbial strain is also provided.

Abstract: A lithium hydrogen titanate Li—H—Ti—O material includes Li, H, Ti, and O elements, wherein a mass percentage of Li is in a range from about 3% to about 12%, a mass percentage of H is in a range from about 0.1% to about 8%, a mass percentage of Ti is in a range from about 46% to about 56%, and a mass percentage of O is in a range from about 28% to about 50%. A lithium ion battery and a method for making the lithium hydrogen titanate Li—H—Ti—O material are also disclosed.

Abstract: Systems and method for high-speed single-pixel quantitative phase contrast optical imaging are provided. This imaging technique can bypass the use of conventional image sensors and their associated speed limitations. The quantitative phase images can be acquired much faster than conventional quantitative phase imaging by a chirped-wavelength-encoding mechanism via wavelength-swept laser sources or optical time-stretch based on optical fibers, without the need for interferometric approaches.

Abstract: A method for preparing temsirolimus, the method including: using a substituted aromatic aldehyde to protect 2,2-dimethylol propionic acid to produce intermediate II; carrying out reaction between the intermediate II and 2,4,6-trichlorobenzoyl chloride; carrying out condensation reaction between a resulting product and rapamycin to produce intermediate III; and finally using sulfuric acid to remove a protecting group from the intermediate III to yield temsirolimus.

Abstract: A method for synthesizing temsirolimus, the method including: using a substituted boric acid to protect 2,2-dimethylol propionic acid to produce intermediate II; carrying out a reaction between the intermediate II and 2,4,6-trichlorobenzoyl chloride; carrying out condensation reaction between a resulting product and rapamycin to produce intermediate III; and finally using a diol to remove a protecting group from the intermediate III to yield temsirolimus.

Abstract: A method for synthesizing temsirolimus, the method including: using a substituted boric acid to protect 2,2-dimethylol propionic acid to produce intermediate II; carrying out a reaction between the intermediate II and 2,4,6-trichlorobenzoyl chloride; carrying out condensation reaction between a resulting product and rapamycin to produce intermediate III; and finally using a diol to remove a protecting group from the intermediate III to yield temsirolimus.

Abstract: A method for preparing temsirolimus, the method including: using a substituted aromatic aldehyde to protect 2,2-dimethylol propionic acid to produce intermediate II; carrying out reaction between the intermediate II and 2,4,6-trichlorobenzoyl chloride; carrying out condensation reaction between a resulting product and rapamycin to produce intermediate III; and finally using sulfuric acid to remove a protecting group from the intermediate III to yield temsirolimus.