Abstract: A heat exchanger processing method, in which a heat exchanger includes a plurality of micro-channel flat tubes, and the heat exchanger processing method includes: providing a plurality of micro-channel flat tubes, in which each micro-channel flat tube includes a plurality of channels extending in a length direction of the micro-channel flat tube, and the plurality of micro-channel flat tubes are spaced in a first direction; moving a collection assembly starting from an initial position along the first direction to collect specific information of one or more micro-channel flat tubes one by one, and transmitting the specific information to a control assembly; comparing, by the control assembly, the specific information with pre-stored information and generating, based on a comparison result, feedback information; generating, by an instruction assembly based on the feedback information, instruction information; and adjusting a position of a corresponding micro-channel flat tube based on the instruction informati

Abstract: A heat exchanger processing method, in which a heat exchanger includes a plurality of micro-channel flat tubes, and the heat exchanger processing method includes: providing a plurality of micro-channel flat tubes, in which each micro-channel flat tube includes a plurality of channels extending in a length direction of the micro-channel flat tube, and the plurality of micro-channel flat tubes are spaced in a first direction; moving a collection assembly starting from an initial position along the first direction to collect specific information of one or more micro-channel flat tubes one by one, and transmitting the specific information to a control assembly; comparing, by the control assembly, the specific information with pre-stored information and generating, based on a comparison result, feedback information; generating, by an instruction assembly based on the feedback information, instruction information; and adjusting a position of a corresponding micro-channel flat tube based on the instruction informati

Abstract: The present invention provides a method for preparing renal podocytes by discontinuous differentiation. Induced pluripotent stem cells are differentiated into the renal podocytes by using a discontinuous method. According to the method, pluripotent stem cells can be subjected to targeted induction of differentiation to obtain renal progenitor cells; renal progenitor cells with a high degree of differentiation are identified and cryopreserved, and then are thawed and subjected to targeted induction of differentiation into podocytes after large-scale preparation. The podocytes obtained by this method have high differentiation efficiency, high consistency, and a high survival rate.

Abstract: Disclosed is an alumina membrane, its preparation method and application. The preparation method comprises the following steps: carrying out constant voltage anodizing treatment on a surface on one side of an aluminum sheet to obtain an alumina membrane with a porous structure on the surface on one side; removing pure aluminum on an other side of the alumina membrane by a physical processing method, and carrying out pore-enlarging treatment to obtain a membrane with interconnected pores on both sides; and depositing a silicon coating on the surface of the membrane on the side that has been physically processed to obtain the alumina membrane. According to the disclosure, the pure aluminum on the other side is etched by physical processing method after the aluminum on one side is oxidized, so as to avoid an absorbability of an alumina crystal form formed by chemical reagent corrosion on a platelet membrane protein.

Abstract: Provided are a biological assembly method for Faraday wave multi-wavelength synthesis and an application. The present method has advantages that the system is easy to build, manipulation is simple, patterns are dynamically adjustable, biocompatibility is good, etc. The present method is different from a cell manipulation principle under a single wavelength condition in an existing acoustic biological assembly method; sine or cosine signals having different wavelengths are synthesized, so that a single-wavelength assembly mode in a conventional Faraday wave frequency domain is improved into a multi-wavelength assembly mode, complex and arbitrary pattern arrangement of liquid-bottom multi-scale cells is achieved, and thus the method is more suitable for the requirement for complex arrangement of cells in tissue engineering and biological manufacturing, and has huge application prospects and commercial value.

Abstract: An exemplary printable composition comprises a liquid or gel suspension of a plurality of metallic nanofibers or nanowires; a first solvent; and a viscosity modifier, resin, or binder. In various embodiments, the metallic nanofibers are between about 10 microns to about 100 microns in length, are between about 10 nm to about 120 nm in diameter, and are typically functionalized with a coating or partial coating of polyvinyl pyrrolidone or a similar compound. An exemplary metallic nanofiber ink which can be printed to produce a substantially transparent conductor comprises a plurality of metallic nanofibers; one or more solvents such as 1-butanol, ethanol, 1-pentanol, n-methylpyrrolidone, cyclohexanone, cyclopentanone, 1-hexanol, acetic acid, cyclohexanol, or mixtures thereof; and a viscosity modifier, resin, or binder such as polyvinyl pyrrolidone or a polyimide, for example.

Abstract: An exemplary printable composition comprises a liquid or gel suspension of a plurality of metallic nanofibers or nanowires; a first solvent; and a viscosity modifier, resin, or binder. In various embodiments, the metallic nanofibers are between about 10 microns to about 100 microns in length, are between about 10 nm to about 120 nm in diameter, and are typically functionalized with a coating or partial coating of polyvinyl pyrrolidone or a similar compound. An exemplary metallic nanofiber ink which can be printed to produce a substantially transparent conductor comprises a plurality of metallic nanofibers; one or more solvents such as 1-butanol, ethanol, 1-pentanol, n-methylpyrrolidone, cyclohexanone, cyclopentanone, 1-hexanol, acetic acid, cyclohexanol, or mixtures thereof; and a viscosity modifier, resin, or binder such as polyvinyl pyrrolidone or a polyimide, for example.

Abstract: An exemplary printable composition comprises a liquid or gel suspension of a plurality of metallic nanofibers or nanowires; a first solvent; and a viscosity modifier, resin, or binder. In various embodiments, the metallic nanofibers are between about 10 microns to about 100 microns in length, are between about 10 nm to about 120 nm in diameter, and are typically functionalized with a coating or partial coating of polyvinyl pyrrolidone or a similar compound. An exemplary metallic nanofiber ink which can be printed to produce a substantially transparent conductor comprises a plurality of metallic nanofibers; one or more solvents such as 1-butanol, ethanol, 1-pentanol, n-methylpyrrolidone, cyclohexanone, cyclopentanone, 1-hexanol, acetic acid, cyclohexanol, or mixtures thereof; and a viscosity modifier, resin, or binder such as polyvinyl pyrrolidone or a polyimide, for example.

Abstract: Disclosed is a protein comprising no more than three human autoantigenic proteins, wherein a first human autoantigenic protein comprises a truncated myelin oligodendrocyte glycoprotein (MOG) amino acid sequence, a second human autoantigenic protein comprises a myelin basic protein (MBP) amino acid sequence, and a third human autoantigenic protein comprises a truncated proteolipid protein (PLP) amino acid sequence. Also disclosed are related nucleic acids, pharmaceutical compositions, methods of treating a demyelinating disease, and methods of producing the proteins.

Abstract: Disclosed is a protein comprising no more than three human autoantigenic proteins, wherein a first human autoantigenic protein comprises a truncated myelin oligodendrocyte glycoprotein (MOG) amino acid sequence, a second human autoantigenic protein comprises a myelin basic protein (MBP) amino acid sequence, and a third human autoantigenic protein comprises a truncated proteolipid protein (PLP) amino acid sequence. Also disclosed are related nucleic acids, pharmaceutical compositions, methods of treating a demyelinating disease, and methods of producing the proteins.

Abstract: An exemplary printable composition comprises a liquid or gel suspension of a plurality of metallic nanofibers or nanowires; a first solvent; and a viscosity modifier, resin, or binder. In various embodiments, the metallic nanofibers are between about 10 microns to about 100 microns in length, are between about 10 nm to about 120 nm in diameter, and are typically functionalized with a coating or partial coating of polyvinyl pyrrolidone or a similar compound. An exemplary metallic nanofiber ink which can be printed to produce a substantially transparent conductor comprises a plurality of metallic nanofibers; one or more solvents such as 1-butanol, ethanol, 1-pentanol, n-methylpyrrolidone, cyclohexanone, cyclopentanone, 1-hexanol, acetic acid, cyclohexanol, or mixtures thereof; and a viscosity modifier, resin, or binder such as polyvinyl pyrrolidone or a polyimide, for example.

Abstract: Active LEDs have a control transistor in series with an LED and have a top electrode, a bottom electrode, and a control electrode. The active LEDs are microscopic and dispersed in an ink. A substrate has column lines, and the active LEDs are printed at various pixel locations so the bottom electrodes contact the column lines. A hydrophobic mask defines the pixel locations. Due to the printing process, there are different numbers of active LEDs in the various pixel locations. Row lines and control lines contact the top and control electrodes so that the active LEDs in each single pixel location are connected in parallel. If the LEDs emit blue light, red and green phosphors are printed over various pixel locations to create an ultra-thin color display. Any active LED may be addressed using row and column addressing, and the brightness may be controlled using the control lines.

Abstract: An exemplary printable composition comprises a liquid or gel suspension of a plurality of metallic nanofibers or nanowires; a first solvent; and a viscosity modifier, resin, or binder. In various embodiments, the metallic nanofibers are between about 10 microns to about 100 microns in length, are between about 10 nm to about 120 nm in diameter, and are typically functionalized with a coating or partial coating of polyvinyl pyrrolidone or a similar compound. An exemplary metallic nanofiber ink which can be printed to produce a substantially transparent conductor comprises a plurality of metallic nanofibers; one or more solvents such as 1-butanol, ethanol, 1-pentanol, n-methylpyrrolidone, cyclohexanone, cyclopentanone, 1-hexanol, acetic acid, cyclohexanol, or mixtures thereof; and a viscosity modifier, resin, or binder such as polyvinyl pyrrolidone or a polyimide, for example.

Abstract: An improved erasable tattoo ink and a method and apparatus for removing tattoos using an energy transfer photodisruptive mechanism whereby efficiency of the transfer of energy from a low energy light source to a higher energy donor and then to a tattoo pigment molecule for photodecomposition of the ink color pigmentation is optimized.

Abstract: Active LEDs have a control transistor in series with an LED and have a top electrode, a bottom electrode, and a control electrode. The active LEDs are microscopic and dispersed in an ink. A substrate has column lines, and the active LEDs are printed at various pixel locations so the bottom electrodes contact the column lines. A hydrophobic mask defines the pixel locations. Due to the printing process, there are different numbers of active LEDs in the various pixel locations. Row lines and control lines contact the top and control electrodes so that the active LEDs in each single pixel location are connected in parallel. If the LEDs emit blue light, red and green phosphors are printed over various pixel locations to create an ultra-thin color display. Any active LED may be addressed using row and column addressing, and the brightness may be controlled using the control lines.

Abstract: Disclosed is a protein comprising no more than three human autoantigenic proteins, wherein a first human autoantigenic protein comprises a truncated myelin oligodendrocyte glycoprotein (MOG) amino acid sequence, a second human autoantigenic protein comprises a myelin basic protein (MBP) amino acid sequence, and a third human autoantigenic protein comprises a truncated proteolipid protein (PLP) amino acid sequence. Also disclosed are related nucleic acids, pharmaceutical compositions, methods of treating a demyelinating disease, and methods of producing the proteins.

Abstract: A PV panel is manufactured using a monolayer of small silicon sphere diodes (10-300 microns in diameter) connected in parallel. The spheres are embedded in an uncured aluminum-containing layer on an aluminum foil substrate in a roll-to-roll process, and the aluminum-containing layer is heated to anneal the aluminum-containing layer as well as p-dope the bottom surface of the spheres. The diffusion of the p-type dopants also creates a back surface field in the spheres to improve efficiency. A dielectric layer is formed, and a phosphorus-containing layer is deposited over the spheres to dope the top surface n-type, forming a pn junction. The phosphorus layer is then removed. A conductor is deposited to contact the top surface. Conformal, index-graded lenses are then formed over each of the spheres to form a thin and flexible PV panel.

Abstract: An improved erasable tattoo ink and a method and apparatus for removing tattoos using an energy transfer photodisruptive mechanism whereby efficiency of the transfer of energy from a low energy light source to a higher energy donor and then to a tattoo pigment molecule for photodecomposition of the ink color pigmentation is optimized.

Abstract: A flexible light sheet includes a bottom conductor layer overlying a flexible substrate. An array of vertical light emitting diodes (VLEDs) is printed as an ink over the bottom conductor layer so that bottom electrodes of the VLEDs electrically contact the bottom conductor layer. A top electrode of the VLEDs is formed of a first transparent conductor layer, and a temporary hydrophobic layer is formed over the first transparent conductor layer. A dielectric material is deposited between the VLEDs but is automatically de-wetted off the hydrophobic layer. The hydrophobic layer is then removed, and a second transparent conductor layer is deposited to electrically contact the top electrode of the VLEDs. The VLEDs can be made less than 10 microns in diameter since no top metal bump electrode is used. The VLEDs are illuminated by a voltage differential between the bottom conductor layer and the second transparent conductor layer.

Abstract: An improved system for energy transfer photopolymerization which optimizes the transfer efficiency of energy from a low energy light source to a higher energy donor and then to a polymerization initiator for the polymerization of a monomer material. The energy transfer efficiency is optimized by introducing stably miscible surface treated upconverting nanocrystal donors into a monomer matrix for near infrared to blue and ultraviolet upconversion and resonantly coupling the energy stored in the donor to the initiator via Förster Resonance Energy Transfer (FRET).