124results about How to "Fast corrosion" patented technology

The invention relates to a nickel-chromium alloy metallographic corrosion solution and a corrosion method. The corrosion solution is a mixed solution of concentrated nitric acid, concentrated hydrochloric acid, glacial acetic acid and water in a volume ratio of 1:1:1:1. The concrete steps include: (1) preparing the corrosion solution, firstly adding water into a container, then adding concentrated nitric acid, concentrated hydrochloric acid and glacial acetic acid respectively, conducting stirring and then performing standing for 10-20min; (2) dripping the corrosion solution on the corrosion surface of a ground and polished nickel-chromium alloy metallographic sample, immersing the sample into the corrosion solution to a depth of 1-2mm, and controlling the corrosion time at 10s-10min; (3) flushing the sample surface with distilled water for more than 2min; and (4) flushing the sample surface with alcohol, and then wiping the sample surface with alcohol-carrying absorbent cotton. According to the invention, the corroded metallographic sample has obvious grain contrast and clear grain boundary line, and at the same time, the defects of under-corrosion and over-corrosion can be avoided. The corrosion solution can rapidly and efficiently corrode the metallographic structure of the sample.

A corrosion sensor includes an insulating substrate, a thin film of a first metallic material formed on the substrate; and an array of areas what includes a second metallic material provided at the surface of the thin film. A method for manufacturing such a sensor is also disclosed. An exemplary embodiment is disclosed in which the thin film is patterned to define a number of tracks, the resistance of which can be monitored in order to determine the degree to which the thin film has corroded.

The invention provides a preparation method of a material-on-insulator. The method comprises the following steps: (S1) a substrate is provided; (S2) a first material layer, a boron-doped first material layer and a second material layer sequentially extend on the surface of the substrate; (S3) the step (S2) is repeated at least once; (S4) ion implantation is carried out, so that the ions are injected into the first material layer which is the furthest to the substrate; (S5) a base plate formed with an insulating layer on the surface is provided; and the insulating layer and the second material layer on the top layer are bonded to form a bonding wafer; and (S6) annealing treatment is carried out on the bonding wafer; and the boron-doped first material layer on an ion implantation layer absorbs the ions to form microcracks for stripping, so as to obtain the material-on-insulator. According to the preparation method, the substrate can be repeatedly utilized, so that the cost of the production material is reduced; the technological process is simplified; the ion implantation dosage is relatively low; improvement of the crystal quality is facilitated; the implantation cost is reduced; and the obtained material-on-insulator is very smooth in surface and does not need to be polished.

The invention belongs to the technical field of bearing detection. The invention relates to a rapid metallographic determination method for of grain size of a GCr15 steel bearing assembly. The rapid metallographic determination method comprises the following steps of 1), preparing an etching solution; 2), etching a sample of the bearing assembly; 3), determining the grain size: shooting a metallograph of a grain boundary profile by using an optical microscope, then determining the grain size of the metallograph by using image analysis software and in reference to steel size determination standards of an average grain size of the steel by an intercept method. The clear grain boundary profile can be obtained by using a rapid and easily operational chemical etching method; and efficient and accurate determination for the GCr15 steel bearing assembly can be realized by combining the metallographic determination method for the grain size.

The invention provides an electro-catalyst Pt/amTiO2/rGO and a preparation method, and belongs to the technical field of fuel-cell catalysts. The preparation method comprises the following steps: firstly, an improved sol-gel method is adopted to prepare TiO2-GO (graphene oxide) sol, the sol is volatilized naturally in water bath at the temperature of 25 DEG C, and a GO complex amTiO2/GO uniformly modified by amorphous TiO2 is obtained; and then chloroplatinic acid is taken as a platinum source, ethylene glycol is taken as a solvent and a reducing agent, Pt nanoparticles are loaded on amTiO2/GO with an impregnation reduction method, meanwhile, GO is reduced to reduced GO rGO, and the electro-catalyst Pt/amTiO2/rGO is obtained. For the catalyst, an amTiO2 modifier is uniformly dispersed on the surface of rGO, one function of the amTiO2 modifier is to solve the corrosion problem of rGO, another function is to increase the dispersion degree of the loaded Pt nanoparticles, meanwhile, the electrical conductivity of amTiO2 is improved by rGO, so that performance advantages of rGO and amTiO2 can be played sufficiently, the electrocatalytic activity and stability of the catalyst are improved, and the precious metal Pt is used efficiently. The electro-catalyst Pt/amTiO2/rGO and the preparation method have the advantages of simple technology, easiness in operation and environmental protection.

Methods of providing fire barrier protection comprise installing a fire barrier system comprising a flexible graphitized polymer sheet in a structure. Additionally, the fire barrier system installed in a structure is described.

The invention discloses a saline solution corrosion method for a flocked ZnO-base thin film. A flocked structure is formed by corroding an intrinsic or doped ZnO, ZnMgO, ZnCdO, ZnBeO or ZnCaO thin film by adopting ammonium sulphate, ammonium nitrate or ammonium phosphate solution. The saline solution corrosion method has proper corrosion speed and is easy to operate; the texture process can be controlled well; and the prepared flocked ZnO-base thin film has high optical and electric characteristics and a remarkable light trapping effect.

The invention discloses an absorbable iron-based alloy stent, comprising an iron-based alloy substrate and a degradable polyester in contact with the surface of the substrate, in which the degradable polyester has a weight average molecular weight of between 20,000 and 1,000,000 and a polydispersity index of between 1.2 and 30. With the degradable polyester, the iron-based alloy is capable of corroding rapidly and controllably within a predetermined period. Following implantation into the human body, the degradable stent serves as a mechanical support at early stage, then gradually degrading and being metabolized and absorbed by the human body. During the process of degradation, minimal or no solid product is produced. Ultimately, the configuration of the lumen with an implanted stent as well as the systolic and diastolic functions thereof return to their natural states.

The present invention discloses an apparatus and method for preparing a metal probe tip and controlling the curvature radius of the metal probe tip. The method includes the steps as follows: 1) a magnetic metal wire to be prepared is provided; 2) one end of the metal wire to be prepared is immersed under the electrolyte level of an electrochemical cell, and the other end of the metal wire to be prepared is connected with a positive electrode side of a control circuit; 3) a switch is closed, the constant current or constant voltage of the apparatus is maintained by a constant current and constant voltage source of the control circuit, and the electrochemical cell performs reaction until the metal wire to be prepared forms the metal probe tip under the electrolyte level. The method for preparing the magnetic probe tip has fast preparing speed and high efficiency, and can control the probe tip shape. The curvature radius of the probe tip is small, the probe tip surface is smooth, and the probe tip has stable quality. Additionally, the curvature radius of the probe tip can be controlled by the adjustment of the outputted constant current value and the concentration ratio of electrolyte. The prepared magnetic probe tip can realize spinning resolution in magnetic sample measurement.

The invention relates to a semi-submerged etching laser plate making method. The method comprises the following steps: performing skim coating or spraying on the surface of a copper-plated plate base to form a surface protection glue layer on the surface; then engraving patterns on the glue layer through a laser engraving machine; putting the copper-plated plate base with the patterns into a cleaning tank to perform pre-etching; after pre-etching, putting the copper-plated plate base on a wheel of an etching groove, and turning on a rotating switch to ensure that the copper-plated plate base starts rotating; and then pressing a direction switch to ensure that one third of the surface of the copper-plated plate base is submerged into etching liquid to start etching, and finally obtaining a copper plated plate with required patterns. Compared with the prior art, the semi-submerged etching laser plate making method disclosed by the invention solves the problems that a laser plate has inconsistent mesh points and is non-uniform in etching, dappled etching of the plate surface is too deep or too shallow, and the like.

The invention provides a method for preparing light calcium carbonate from carbide slag as a raw material. The method comprises following steps: (1), performing slurrying to remove toxins and foul smell; (2), performing filtration and dissolution separation; (3), performing spraying carbonization; (4), performing drying and powder grinding, or performing washing, drying and powder grinding or performing spray drying to obtain the product. The method is simple to operate, free of secondary pollution, easy to implement and low in energy consumption, main raw materials only comprise industrial residue carbide slag and CO2 captured in carbon capture and emission reduction projects, the cost is low, and the method has market competitiveness; a large quantity of limestone resources can be savedindirectly, and therefore, environmental protection and blue sky and green water social engineering construction are facilitated.

A method for minimizing corrosion and the build-up of deposits on surfaces of a flue-gas system exposed to moist substances and elevated temperatures, and which includes a desulfurizer and heat transfer means communicating with the desulfurizer, said method involving adding to the system at the heat transfer means a readily water soluble alkaline substance such as sodium hydroxide in amounts sufficient to produce with said flue-gas in said heat transfer means a minimum pH of about 5, preferably 7 or higher.

A process for preparing pinholes, pattern, or holes on the surface of Ti-alloy by chemical etching includes such steps as washing the Ti-alloy workpiece for removing oil, spraying a plastic protecting layer, carving pinholes, preparing the etching liquid from nitric acid and hydrofluoric acid through proportional mixing, chemical etching to form the pinholes, and removing said plastic protecting layer.

The invention relates to an absorbable implantable device comprising an absorbable metal matrix and a degradable polyester layer at least partially covering the surface of the absorbable metal matrix.The contact angle of the degradable polyester layer is more than or equal to 150 degrees. The degradable polyester layer has superhydrophobicity, and can form a hydrophobic barrier in body fluid to isolate the absorbable metal matrix from the body fluid, so as to protect the absorbable metal matrix from slow corrosion or even non-corrosion at the early stage of implantation; moreover, due to thesuperhydrophobicity of the degradable polyester layer, degradation of the degradable polyester layer in the aqueous body fluid environment can be delayed, and delaying or avoiding of the formation ofa local acidic environment at the early stage of implantation is facilitated. Therefore, adequate mechanical support can be provided in the repair period of lesion sites after implantation; while after the repair of the lesion sites is completed, the local micro-acid environment is produced by the degradation of the degradable polyester itself, and the absorbable metal matrix is allowed to be rapidly corroded.

The invention relates to dendritic crystal corrosive liquid for precipitated reinforced martensitic stainless steel and a use method thereof, and belongs to the technical field of continuous casting steel metallographic analysis. According to the formula, the dendritic crystal corrosive liquid comprises 2 to 4 g of sodium metabisulfite, 5 to 8 ml of hydrochloric acid, 2 to 4 ml of nitric acid, and75 ml of distilled water; the sodium metabisulfite, the distilled water, the hydrochloric acid, and the nitric acid are sequentially added into a container, and are evenly stirred; during use, a detection sample polishing face is immersed in the corrosive liquid upwards, standing is carried out, and after the dendritic structure is displayed out, the corroded precipitatted reinforced martensiticstainless steel detection face is subjected to detection observation through an optical microscope or scanning electron microscope. The corrosive liquid can simply, conveniently and rapidly corrode out the clear dendritic structure of the precipitated reinforced martensitic stainless steel, the dendritic structure can be directly observed, the dendrite spacing is measured, and the corrosive liquidis used for evaluating the casting state structure quality of the precipitated reinforced martensitic stainless steel and assisting in evaluating the removing effect of homogenization heat treatmenton the dendritic segregation.