Abstract: A photovoltaic module, which includes a module, a module frame, a mounting piece, and a power converter. The module covers the module frame. The module frame includes a plurality of frame sides. Each frame side extends in a direction away from the module. The plurality of frame sides are sequentially connected to enclose accommodation space of the module frame. Both the mounting piece and the power converter are located in the accommodation space. The mounting piece includes a fastening portion and a support plate that are connected to each other. The fastening portion is connected to a side wall that is of one frame side and that faces the accommodation space. The support plate extends toward an inside of the accommodation space in a direction away from the fastening portion. The power converter is detachably connected to the support plate.

Abstract: A multi-gantry asynchronous precision laser cutting machine, comprising a horizontally arranged lathe bed, a longitudinal beam and a number of gantry cutting mechanisms; the gantry cutting mechanism comprises a crossbeam, a lifting mechanism and a laser cutting head; a first guide rail is arranged at the top of each of the two longitudinal beams; a first linear motor is arranged at the top of the one longitudinal beam; connecting bases are arranged at the bottom of each end of the crossbeam; the connecting base is connected to a slider of the first guide rail and an actuator component of the first linear motor; a second guide rail is arranged on the side of the crossbeam; a second linear motor is arranged at the top of the crossbeam; the lifting mechanism is connected to a slider of the second guide rail and an actuator component of the second linear motor through a first sliding base; the lifting mechanism comprises a servomotor and a second sliding base; and the laser cutting head is fixed to the second sli

Abstract: The present invention discloses a hollow spherical catalyst for a fixed bed with internal fluidization of particles and a method for preparing the same. The preparation method used in the present invention is characterized in: fully mixing precious metal nanopowder with an organic oil phase to form an internal oil phase; preparing a gel ball of an oil-in-water structure by taking an aluminum oxide molding solution as an outer aqueous phase using an independently researched and developed coaxial dual-dropper forming apparatus; and then preparing a hollow aluminum oxide catalyst containing precious metal powder from the gel ball through processes of aging, calcination, and reduction. The resulting catalyst is expressed as X@Al2O3, where the precious metal nanopowder X is wrapped inside hollow Al2O3, and the catalyst has an outer diameter of 1.5-5.0 mm, a shell pore diameter (aluminum oxide) of 10-50 nm, and the precious metal nanopowder sized 200-500 nm.

Abstract: Cuy/MMgOx interfacial catalyst for selective alkyne hydrogenation and its preparation method are disclosed. The preparation method of the catalyst includes: the mixture of salt and alkali solution is nucleated momentarily by nucleation/crystallization isolation method, preparing the composite metal hydroxide CuyMMg4-LDHs as precursor, which has typical hexagonal morphology of the double hydroxide; the precursor is topologically transformed by heat treatment to produce unsaturated oxide; the catalyst with Cuy-MMgOx interface structure is prepared by separating and electronically modifying Cu particles. By adjusting the ratio of Cu2+/M3+ in LDHs, the electronic and geometric structure of Cuy-MMgOx interface can be flexibly controlled, thus enhancing the reaction activity, product selectivity and stability. The catalyst can be used in the selective hydrogenation of various alkynes in the fields of petrochemical and fine chemical industry, with the outstanding catalytic activity and C?C double bond selectivity.

Abstract: The present invention discloses a catalyst for in-situ CO2 capture and coupling reduction with biomass oxidation, a preparation method therefor and an application thereof. The catalyst is applied to the coupling reaction of photocatalytic CO2 reduction and biomass oxidation. The preparation of the catalyst is to synthesize layered double hydroxides (LDHs) containing CO32? between layers by using coprecipitation method, hydrothermal method, sol-gel method and the like, wherein the chemical formula is [M1-x2+Mx3+(OH)2]x+(An?)x/n·mH2O, which has a thickness of 20-30 nm and an average particle diameter of 60-90 nm. Then metal ion vacancy defects are produced on LDHs laminate by using a NaOH/KOH selective etching to obtain the corresponding catalyst.

Abstract: Cuy/MMgOx interfacial catalyst for selective alkyne hydrogenation and its preparation method are disclosed. The preparation method of the catalyst includes: the mixture of salt and alkali solution is nucleated momentarily by nucleation/crystallization isolation method, preparing the composite metal hydroxide CuyMMg4-LDHs as precursor, which has typical hexagonal morphology of the double hydroxide; the precursor is topologically transformed by heat treatment to produce unsaturated oxide; the catalyst with Cuy-MMgOx interface structure is prepared by separating and electronically modifying Cu particles. By adjusting the ratio of Cu2+/M3+ in LDHs, the electronic and geometric structure of Cuy-MMgOx interface can be flexibly controlled, thus enhancing the reaction activity, product selectivity and stability. The catalyst can be used in the selective hydrogenation of various alkynes in the fields of petrochemical and fine chemical industry, with the outstanding catalytic activity and C?C double bond selectivity.

Abstract: The purpose of the invention is to provide a supported bimetallic core-shell structure catalyst and its preparation method. Supporter, metal salt and reducing agent solution are mixed to synthesize the catalyst M@PdM/ZT by using a one-step synthesis method, wherein the active metal particle M@PdM as core-shell structure, M Is the core representing one of the Ag, Pt, Au and Ir. ZT is the supporter, representing one of hydrotalcite (Mg2Al-LDH), alumina (Al2O3) and silica (SiO2). By changing the temperature and the reaction time to control the kinetic behavior of the reduction of two kinds of metal ions to realize the construction of core-shell structure. Active metal particle composition and shell thickness are regulated by controlling metal ion concentration. The bimetallic core-shell catalyst prepared by this method showed excellent selectivity and stability in acetylene selective hydrogenation and anthraquinone hydrogenation.

Abstract: The purpose of the invention is to provide a supported bimetallic core-shell structure catalyst and its preparation method. Supporter, metal salt and reducing agent solution are mixed to synthesize the catalyst M@PdM/ZT by using a one-step synthesis method, wherein the active metal particle M@PdM as core-shell structure, M Is the core representing one of the Ag, Pt, Au and Ir. ZT is the supporter, representing one of hydrotalcite (Mg2Al-LDH), alumina (Al2O3) and silica (SiO2). By changing the temperature and the reaction time to control the kinetic behavior of the reduction of two kinds of metal ions to realize the construction of core-shell structure. Active metal particle composition and shell thickness are regulated by controlling metal ion concentration. The bimetallic core-shell catalyst prepared by this method showed excellent selectivity and stability in acetylene selective hydrogenation and anthraquinone hydrogenation.