How to choose a suitable jet mill based on powder characteristics?

With the development of industrial technology, micro-nano powders have special volume effects and surface effects, and their optical, magnetic, acoustic, electrical and mechanical properties are very different from normal conditions, and are used as the key to many new functional materials. Based on the basic raw materials, the corresponding micro-nano powder processing technology has also achieved unprecedented development. Jet mills (jet mills) use high-speed airflow to cause materials to collide, impact, and shear with impact components. They can not only produce fine particles with narrow distribution, but also have clean and smooth particle surfaces, regular particle shapes, good dispersion, and high activity. of micro-nano powder, and the entire crushing system adopts a closed crushing mode to reduce dust pollution and at the same time, the degree of contamination of the crushed materials is small.

However, since there are many types of airflow pulverizers with different working principles and different crushing effects for various materials, it is necessary to choose a suitable airflow pulverizer according to different materials. At present, according to the different structures or working methods of jet mills, they can usually be divided into: collision type, flat type, fluidized bed type, circulating tube type and target type, etc. On this basis, it can also be classified according to the material characteristics. , adopting methods such as low-temperature cryogenic airflow crushing and inert gas protection to further optimize the crushing effect of the airflow grinder.

Collision airflow crusher
Opposing jet mills are also called opposing jet mills and reverse jet mills. When the equipment is working, two accelerated materials and high-speed airflow meet at a certain point on the horizontal straight line and collide to complete the crushing process. The crushed fine particles enter the external classifier with the airflow under the action of the classification rotor, and pass through the airflow. solid separation and become a product. The coarse particles remain at the edge of the classification chamber and return to the crushing chamber for further crushing until they meet the particle size requirements and enter the external classifier.

Spiral jet pulverizer
Spiral jet mill, also known as horizontal disc jet mill, It is the earliest and most widely used jet mill in industry. The main component of a conventional flat airflow mill is a disc crushing chamber, around which are arranged several (6 to 24) high-pressure working fluid nozzles, Venturi tube feeders, finished product collectors, etc. at a certain angle. The material to be crushed enters the venturi tube driven by the gas. Using the special structure of the venturi tube, the material is accelerated to supersonic speed and then enters the crushing chamber. In the crushing chamber, the materials move in a circular motion driven by high-speed swirling flow. The particles, particles and the inner wall of the machine impact, collide, and rub against each other to be crushed. The coarse particles are thrown towards the peripheral wall of the crushing chamber due to centrifugal force for circulation and crushing, while the fine particles enter the cyclone separator and are collected under the action of centrifugal airflow.

Fluidized bed jet pulverizer
Fluidized bed airflow mill is currently the leading model of airflow pulverizer. It mainly combines the principle of counter-jet with the expanding gas jet flow in the fluidized bed. It is commonly used in the production of chemical raw materials, medicines, cosmetics, advanced ceramics, magnetic powder and other materials. . When the equipment is working, air is sprayed into the crushing area through several reverse nozzles, and the materials to be crushed are accelerated by the high-pressure airflow in the crushing chamber to form a fluidized state. Then the accelerated materials collide and rub with each other at the intersection of each nozzle to be crushed. The crushed fine materials are carried by the upward airflow to the ultra-fine classifier for classification. The fine materials that meet the product requirements are then collected by the cyclone separator, and the coarse materials are After settling back to the crushing area under the action of gravity, crushing continues.


5 types of commonly used surface modifiers for kaolin clay

After surface modification, kaolin powder can be hydrophobic, reduce surface energy, improve its dispersion and compatibility with polymer base materials, so as to improve the comprehensive performance of polymer base composite materials such as plastics and rubber.

At present, the main modification method of kaolin is surface chemical modification. Commonly used surface modifiers mainly include silane coupling agents, organic silicon (oil) or silicone resin, surfactants and organic acids.

1. Commonly used surface modifiers for kaolin clay

(1) Silane coupling agent
Silane coupling agent is the most commonly used and effective surface modifier for kaolin fillers. Since R of the silane coupling agent is an organophilic group, calcined kaolin can be compatible with organic matrices such as rubber and plastics after surface modification. . When modified kaolin is used as a filler in rubber, the R group will react with the rubber macromolecules during the vulcanization process, so that the kaolin molecules are completely dispersed and integrated into the rubber matrix molecules.

The treatment process using silane coupling agent is relatively simple. Generally, kaolin powder and prepared silane coupling agent are added into the modification machine for surface coating treatment. The process can be carried out continuously or in batches.

The factors that affect the final treatment effect are mainly the particle size, specific surface area and surface characteristics (surface functional groups and activity) of kaolin powder, the type, dosage and usage of silane coupling agent, the performance of modification equipment and the time and temperature of surface modification treatment. wait.

(2) Silicone oil
In addition to silane coupling agents, kaolin used as fillers for wires and cables (such as polyvinyl chloride) is often surface modified with 1%-3% silicone oil. The modification process and equipment are similar to those using silane coupling agents.

Calcined kaolin powder treated with silicone oil is used as a filler for wires and cables. It can not only improve the mechanical and physical properties of the cable, but also improve or enhance the electrical insulation and hydrophobic properties of the cable, and the electrical insulation properties in humid and cold environments. Significant improvement.

(3) Unsaturated organic acids
Unsaturated organic acids, such as oxalic acid, sebacic acid, dicarboxylic acid, etc., can also be used to modify the surface of aminated kaolin powder. This modified kaolin can be used as filler for nylon 66, etc.

(4) Cationic surfactant
For example, octadecylamine can also be used for surface modification of kaolin powder. Its polar groups interact with the surface of kaolin particles through chemical adsorption and physical adsorption. The surface hydrophobicity of kaolin modified by organic amines is enhanced.

(5) Inorganic surface modifier
Titanium dioxide, calcium carbonate, calcium sulfate, etc. can also be used for surface modification of calcined kaolin. The modification method is a surface precipitation reaction in an aqueous solution. After the modified product is washed, filtered and dried, calcined kaolin with a titanium dioxide coating on the surface is obtained.

2. Selection principles of kaolin surface modifiers

The type, dosage and method of use of surface modifiers directly affect the effect of surface modification. Different uses require different types and formulas of surface modifiers.

If we only consider it from the perspective of the interaction between surface modifier molecules and the surface of inorganic powder, of course the stronger the interaction between the two, the better. However, in actual operation, the cost and cost of the modified product must also be considered comprehensively. Application purpose and other factors.

For example, when calcined kaolin is modified and used as a filler for cable insulation rubber and plastics, the dielectric properties and volume resistivity of the surface modifier need to be considered;

If modified kaolin is used as a reinforcing filler for rubber, when selecting a modifier, not only the bonding strength between the modifier and kaolin must be considered, but also the bonding strength between the modifier molecules and the rubber macromolecules. , only when both of them are optimized can the surface modifier have the best modification effect.

For specific application purposes, it is sometimes necessary to use two coupling agents for mixed modification. Utilizing their synergistic effect for modification will achieve unexpected good results. However, attention should be paid to the use method and order of addition of the two modifiers. .


Recycling of ceramic waste materials

The production and consumption of ceramics is increasing year by year, followed by tens of millions of tons of ceramic waste. At the same time, the harm caused by ceramic waste has also been widely criticized. With the widespread spread of concepts such as green development and sustainable development, it is particularly important to convert ceramic waste into recyclable resources.

At present, there are two main ways to reuse ceramic waste resources. One is direct processing to recombine various waste ceramic materials into decorations; the other is to recycle them as raw materials to make different products. Specific applications are as follows:

(1) Recycled handicrafts

Using ceramic waste and other waste generated during the production process as the main raw materials, various ceramic decorative arts are prepared through personalized design and recombination. The texture, pattern, color of the ceramic itself and the irregular patterns produced after the ceramic is broken have unique aesthetic value. These ceramic waste products are combined and processed through aesthetic design to produce handicrafts that can not only protect the environment, but also protect the environment. Unique beauty, it is a good green decorative material. This recycling method has relatively low utilization cost, simple production process, and can be designed to meet people's individual needs, so it has extensive promotion value.

(2) As raw materials for processing

building materials

The main components of ceramic solid waste are silicates, so ceramic waste has certain activity. After treatment, its performance can meet the requirements of active mixed materials and can be used as cement mixed materials. In addition, ceramic solid waste can also be added as aggregate into concrete materials. The use of ceramic waste residue can not only save cement and reduce costs, but also reduce the internal temperature of concrete, enhance later strength, and improve corrosion resistance. Ceramic waste has become an indispensable and important component in the production of high-performance concrete.

Recycle heavy metals

Ceramic waste contains a variety of precious metals, especially silver and palladium, which are highly valuable for recycling. At present, the main methods for extracting precious metals from ceramic waste include liquid-liquid extraction, nitric acid dissolution-sodium carbonate reduction, etc. Recycling precious metals from waste materials to produce high-grade renewable resources not only disposes of waste materials, but also generates considerable economic benefits.

Recycled ceramic tiles

Ceramic waste can also be reused in the production of ceramics itself. For example, waste mud and water can be added to the ingredients of ceramic tiles after being recycled and iron removed. The unglazed green body can also be slurried and reused. The glazed green body waste can be mixed with mud and reused without affecting the glaze firing quality. The waste materials fired at high temperatures can be crushed and reused to recreate ceramics. At present, recycled ceramics from ceramic waste are mainly used to produce ceramic bricks, permeable bricks, antique bricks, porous ceramic plates, etc.

Other uses

Ceramic waste can be used to make fireproof and heat-insulating materials, and can also be used to make new ceramic building materials, such as sound-absorbing materials, shock-absorbing materials, water storage materials, etc. Piezoelectric ceramic waste can be mixed into damping and vibration-damping materials such as asphalt and rubber to improve the material's vibration-damping performance.


What are the requirements for alumina powder in high value-added applications?

Alumina high-density particles for sapphire crystal growth

In fact, sapphire is an alumina single crystal. Its growth uses high-purity alumina powder with a purity of >99.995% (commonly called 5N alumina) as a raw material. However, due to the small packing density of micronized alumina particles, it is generally Less than 1g/cm3, the charging amount of a single furnace is small, which affects the production efficiency. Generally, the alumina is densified into high-density particles through appropriate treatment before charging to grow crystals.

 

Nano-alumina abrasives for CMP polishing abrasives

Currently, the commonly used CMP polishing fluids include silica sol polishing fluid, cerium oxide polishing fluid and alumina polishing fluid. The first two have small abrasive grain hardness and cannot be used for polishing high-hardness materials. Therefore, the oxide polishing fluid with Mohs hardness of 9 Aluminum is widely used in the precision polishing of sapphire fairings and flat windows, crystallized glass substrates, YAG polycrystalline ceramics, optical lenses, high-end chips and other components.

The size, shape, and particle size distribution of abrasive particles all affect the polishing effect. Therefore, alumina particles used as chemical mechanical polishing abrasives should meet the following requirements:

1. In order to achieve angstrom-level flatness, the alumina particle size must be at least 100nm and the distribution must be narrow;

2. In order to ensure hardness, complete α-phase crystallization is required. However, to take into account the above particle size requirements, sintering needs to be completed at a lower temperature to avoid complete α-phase transformation while the grains grow.

3. Since the polishing of wafers has extremely high purity requirements, Na, Ca, and magnetic ions need to be strictly controlled, up to ppm level, while radioactive elements U and Th need to be controlled at ppb level.

4. Polishing fluids containing Al2O3 have low selectivity, poor dispersion stability, and easy agglomeration, which can easily cause serious scratches on the polishing surface. Generally, modifications are required to improve its dispersion in the polishing fluid to obtain good polished surface

Low-alpha emissive spherical alumina for semiconductor packaging

In order to ensure the reliability of semiconductor devices and enhance the core competitiveness of products, it is often required to use Low-α ray spherical alumina as packaging material. On the one hand, it can prevent the operation failure of memory devices caused by α rays, and on the other hand, it can utilize its high heat The conductivity provides good heat dissipation performance for the device.

 

Alumina transparent ceramic

First of all, in order to prevent impurities in Al2O3 powder from easily forming different phases and increasing the scattering center of light, resulting in a reduction in the intensity of the projected light in the incident direction, thereby reducing the transparency of the product, the purity of Al2O3 powder is required to be no less than 99.9%, and It should be α-Al2O3 with a stable structure. Secondly, in order to weaken its own birefringence effect, its grain size should also be reduced as much as possible. Therefore, the particle size of the powder used to prepare alumina transparent ceramics should also be less than 0.3 μm and have high sintering activity. In addition, in order to avoid agglomeration into large particles and losing the advantages of the original small particles, the powder should also meet the requirements of high dispersion.

 

High frequency communication alumina ceramic substrate

High-purity alumina ceramics are currently the most ideal and most widely used packaging substrate material due to their good dielectric properties, rigid load-bearing capacity, and resistance to environmental erosion. However, the main performance of alumina substrates increases with the increase in alumina content. In order to meet the needs of high-frequency communications, the purity of alumina ceramic substrates is required to reach 99.5% or even 99.9%.


Sintered NdFeB manufacturing process-jet mill

Jet mill (JM) powder making is a new type of powder making method that uses high-pressure airflow (usually high-purity nitrogen) to accelerate powder particles to supersonic speed in the airflow grinding chamber, causing the powder particles to collide with each other and break.

The specific process is: mix the crushed hydrogen flakes (SC) with a certain proportion of antioxidant, then add it to the airflow mill feeding bin, add it to the airflow grinding chamber according to the quantitative amount, and high-pressure nitrogen (7kg) is sprayed from the four nozzles of the grinding chamber. , accelerate the material to supersonic speed to form a fluidized bed, and the particles collide with each other and break. The diameter of the broken particles is distributed between 1-8 μm.

Depending on the performance and distribution of the materials, the average airflow milling powder size SMD is between 2.5-4μm. The powder produced by airflow milling is uneven and requires three-dimensional mixing. Before mixing, a certain proportion of lubricant and antioxidants are added to the material tank according to the process to control the oxygen content and improve the molding orientation performance.


The “core strength” of semiconductor equipment—silicon carbide components

Silicon carbide (SiC) is a structural ceramic material with excellent properties. Silicon carbide parts, that is, equipment parts made of silicon carbide and its composite materials as the main materials, have the characteristics of high density, high thermal conductivity, high bending strength, large elastic modulus, etc., and can be adapted to wafer epitaxy, etching, etc. Due to the highly corrosive and ultra-high temperature harsh reaction environment in the manufacturing process, it is widely used in major semiconductor equipment such as epitaxial growth equipment, etching equipment, and oxidation/diffusion/annealing equipment.

According to the crystal structure, there are many crystal forms of silicon carbide. Currently, the common SiC are mainly 3C, 4H and 6H types. Different crystal forms of SiC have different uses. Among them, 3C-SiC is also often called β-SiC. An important use of β-SiC is as a film and coating material. Therefore, β-SiC is currently the main material for graphite base coating.

According to the preparation process, silicon carbide parts can be divided into chemical vapor deposition silicon carbide (CVD SiC), reaction sintered silicon carbide, recrystallization sintered silicon carbide, atmospheric pressure sintered silicon carbide, hot pressing sintered silicon carbide, hot isostatic pressing sintering and carbonization Silicon etc.

Silicon carbide parts

1. CVD silicon carbide parts

CVD silicon carbide components are widely used in etching equipment, MOCVD equipment, SiC epitaxial equipment, rapid heat treatment equipment and other fields.

Etching equipment: The largest market segment for CVD silicon carbide components is etching equipment. CVD silicon carbide components in etching equipment include focusing rings, gas shower heads, trays, edge rings, etc. Due to the low reactivity and conductivity of CVD silicon carbide to chlorine- and fluorine-containing etching gases, it becomes a plasma Ideal material for components such as focus rings in etching equipment.

Graphite base coating: Low-pressure chemical vapor deposition (CVD) is currently the most effective process for preparing dense SiC coatings. The thickness of CVD-SiC coatings is controllable and has the advantages of uniformity. SiC-coated graphite bases are commonly used in metal-organic chemical vapor deposition (MOCVD) equipment to support and heat single crystal substrates. They are the core and key components of MOCVD equipment.

2. Reaction sintered silicon carbide parts

For reaction-sintered (reactive infiltration or reaction bonding) SiC materials, the sintering line shrinkage can be controlled below 1%, and the sintering temperature is relatively low, which greatly reduces the requirements for deformation control and sintering equipment. Therefore, this technology has the advantage of easily achieving large-scale components and has been widely used in the fields of optical and precision structure manufacturing.


12 Modification Methods of Bentonite

The modification of bentonite usually uses physical, chemical, mechanical and other methods to treat the surface and purposefully change the physical and chemical properties of the mineral surface according to application needs.

1. Sodium modification

Since montmorillonite has a stronger adsorption capacity for Ca2+ than Na+, the bentonite found in nature is generally calcium-based soil. However, in practical applications, it is found that the exchange capacity of Ca2+ in calcium-based soil is much lower than that of Na+. Therefore, calcium-based soil is often sodiumified before being put into the market.

2. Lithium modification

Lithium bentonite has excellent swelling, thickening and suspending properties in water, lower alcohols and lower ketones, so it is widely used in architectural coatings, latex paints, casting coatings and other products to replace various organic cellulose suspending agents. There are very few natural lithium bentonite resources. Therefore, artificial lithiation is one of the main methods for preparing lithium bentonite.

3. Acid leaching modification

The acid modification method mainly uses acids of different types and concentrations to soak bentonite. On the one hand, the acid solution can dissolve the interlayer metal cations and replace them with H+ with smaller volume and lower valence, thereby reducing the interlayer van der Waals force. The interlayer spacing increases; on the other hand, impurities in the channel can be removed, thereby expanding the specific surface area.

4. Roasting activation modification

The bentonite roasting modification method is to calcine bentonite at different temperatures. When bentonite is calcined at high temperature, it will successively lose surface water, bound water in the skeleton structure, and organic pollutants in the pores, causing the porosity to increase and the structure to become more complex.

5. Organic modification

The basic principle of the organic modification method is to organicize bentonite, using organic functional groups or organic matter to replace the bentonite layers to exchange cations or structural water, thereby forming an organic composite bonded by covalent bonds, ionic bonds, coupling bonds or van der Waals forces. Bentonite.

6. Inorganic pillar modification

Inorganic modification is to expand the interlayer spacing by forming an inorganic columnar structure between the bentonite layers, increase the specific surface area, and form a two-dimensional hole network structure between the layers. It also prevents the bentonite from collapsing in high temperature environments and improves its thermal stability.

7. Inorganic/organic composite modification

The inorganic/organic composite modification method takes advantage of the large interlayer gaps and cation exchangeability of bentonite. It mainly uses inorganic polymers to open up the interlayer domains, and then uses activators to change the surface properties of bentonite. method.

8. Microwave modification

The principle of microwave modification is to use microwaves with a frequency range between 300Hz and 300GHz to process bentonite and activate it. Microwave treatment has the advantages of strong penetration, uniform heating, safe and simple operation, low energy consumption, and high efficiency. It has better results when combined with traditional acidification and roasting methods.

9. Ultrasonic modification

Ultrasonic modified bentonite can improve its adsorption performance. Short-term ultrasound can increase the interlayer spacing and loosen the structure, making it easier for metal ions to enter; long-term ultrasound can change the Si-O-Si bonds on the surface of the crystal lamellae in bentonite, adding some metal ions to the bentonite.

10. Inorganic salt modification

Inorganic salt modification is to immerse bentonite in salt solution (NaCl, MgCl2, AlCl3, CaCl2, Cu(NO3)2, Zn(NO3)2, etc.). The adsorption capacity of bentonite modified by salt solution is even better than that of the original soil. has seen an increase.

11. Rare earth metal doping modification

Commonly used rare earth modifiers are lanthanum salts and their oxides. After doping bentonite with the rare earth metal lanthanum, a certain amount of metal oxides and hydroxides are introduced on its surface or between layers, thus weakening the montmorillonite in the bentonite. of interlayer bond energy.

12. Metal-loaded modification

Metal-loaded modified bentonite uses bentonite as a carrier and uses sol-gel method, direct precipitation method, impregnation method and other processes to highly disperse the metal active components on the carrier, using the carrier to have good pore size structure and other characteristics The active components can exert a better catalytic effect in the catalytic reaction.


What methods can help surface modification of ultrafine powders?

Ultrafine powder, also known as nanopowder, refers to a type of powder whose particle size is in the nanometer range (1~100nm). Ultrafine powder can usually be prepared by ball milling, mechanical crushing, spraying, explosion, chemical deposition and other methods.

Nanopowders have attracted people's attention due to their special properties in terms of magnetism, catalysis, light absorption, thermal resistance and melting point due to their volume effect and surface effect. However, due to their small size and high surface energy, nanoparticles have a tendency to spontaneously agglomerate. The existence of agglomeration will affect the performance of nanopowder materials. In order to improve the dispersion and stability of the powder and make the application range of the material wider, it is necessary to modify the surface of the powder.

There are many methods of surface modification, which can generally be divided into: surface coating modification, surface chemical modification, mechanochemical modification, capsule modification, high-energy modification, and precipitation reaction modification.

 

Surface coating modification

Surface coating modification means that there is no chemical reaction between the surface modifier and the particle surface. The coating and the particles are connected by physical methods or van der Waals forces. This method is suitable for the surface modification of almost all types of inorganic particles. This method mainly uses inorganic compounds or organic compounds to coat the surface of the particles to weaken the agglomeration of the particles. Moreover, the steric repulsion generated by the coating makes it very difficult for the particles to reunite. Modifiers used for coating modification include surfactants, hyperdispersants, inorganic substances, etc.

Applicable powders: kaolin, graphite, mica, hydrotalcite, vermiculite, rectorite, metal oxides and layered silicates, etc.

 

Surface chemical modification

Surface chemical modification uses the adsorption or chemical reaction of functional groups in organic molecules on the surface of inorganic powder to modify the particle surface. In addition to surface functional group modification, this method also includes surface modification using free radical reaction, chelation reaction, sol adsorption, etc.

Applicable powders: quartz sand, silica powder, calcium carbonate, kaolin, talc, bentonite, barite, wollastonite, mica, diatomaceous earth, brucite, barium sulfate, dolomite, titanium dioxide, aluminum hydroxide, Various powders such as magnesium hydroxide and aluminum oxide.

 

Mechanochemical modification

Mechanochemical modification refers to the change of mineral lattice structure, crystal form, etc. through mechanical methods such as crushing, grinding, and friction. The energy in the system increases and the temperature rises, which promotes particle dissolution, thermal decomposition, and free generation. A modification method that uses radicals or ions to enhance the surface activity of minerals and promote the reaction or attachment of minerals and other substances to achieve the purpose of surface modification.

Applicable powders: kaolin, talc, mica, wollastonite, titanium dioxide and other types of powders.

 

Capsule modification

Capsule modification is a surface modification method that covers the surface of powder particles with a uniform and certain thickness film.

High energy modification method

High-energy modification method is a method that uses plasma or radiation treatment to initiate polymerization reaction to achieve modification.

 

Precipitation reaction modification

The precipitation reaction method is to add a precipitant to a solution containing powder particles, or add a substance that can trigger the generation of the precipitant in the reaction system, so that the modified ions undergo a precipitation reaction and precipitate on the surface of the particles, thereby coating the particles. Precipitation methods can be mainly divided into direct precipitation methods, uniform precipitation methods, non-uniform nucleation methods, co-precipitation methods, hydrolysis methods, etc.

Applicable powders: titanium dioxide, pearlescent mica, alumina and other inorganic pigments.


Application of jet mill in anticorrosive coatings

Fly ash, also called fly ash, is a powdery waste formed by calcining in boilers.
Fly ash is typically captured from the flue gas by an electrostatic precipitator or other particle filtering device before the flue gas reaches the chimney.

Fly ash is composed of crystals, glass bodies, and residual carbon. It is gray or gray-black and irregular in shape. Most of the particles are microspherical, with a particle size of 0.1 to 300.0 μm, a density of about 2 g/cm3, and a bulk density of 1.0 to 300.0 μm. 1.8 g/cm3, it has a large specific surface area and strong adsorption activity.

Anti-corrosion performance mechanism of fly ash enhanced coatings

Fly ash contains a large number of microbeads and sponge vitreous structures. Moreover, after the microbeads are crushed, that is, after the surface is destroyed, more pore structures and sponge vitreous structures will be exposed, which can increase the specific surface area of the powder. Utilizing these characteristics, it can be used as a filler in other products, thereby making it a better functional filler for coatings. Research shows that ultrafine fly ash, as a paint filler, can combine covering, leveling and wear resistance.

The corrosion resistance of the coating is closely related to the porosity of the coating. Fly ash is added as a filler in the coating. Due to the pozzolanic effect of fly ash, it can fill the pores of the coating to prevent corrosive media from penetrating into the interior of the coating through the anti-corrosion coating.
Fly ash has good mechanical properties. The fly ash/resin composite coating can increase the durability of the coating, prevent local pores due to wear and loss of protection, and greatly extend the service life of the coating.
The addition of conductive polymer not only improves the water-blocking performance of the coating, but also reduces the oxidation rate of the metal. By adding zinc powder or aluminum powder to the anti-corrosion coating, the active material becomes the anode of the corrosion reaction and protects the metal matrix as the cathode.

Application of jet mill in anticorrosive coatings
Different from the traditional mechanical crushing principle, under the action of high-speed airflow, the material is crushed through the impact between its own particles, the impact and shearing effect of the airflow on the material, and the impact, friction and shearing of the material and other parts. In addition to impact force, the crushing force also includes friction and shearing forces. Friction is caused by the friction and grinding motion between the material particles and the inner wall. Of course, this friction and grinding process also occurs between particles. Because the two crushing methods of impact and grinding are mainly suitable for fine crushing of brittle materials, they are especially suitable.

Jet crushing has some special characteristics because it is different from ordinary crushers in terms of crushing methods and principles:

The fineness of the product is uniform. For the airflow crusher, during the crushing process, due to the centrifugal force of the airflow rotation, the coarse and fine particles can be automatically classified.
The average particle size of the crushed materials is fine and can be crushed to sub-micron level;
The production process is continuous, the production capacity is large, and the degree of self-control and automation is high.


Calcite ultrafine powder preparation process flow

Calcite ultrafine powder, as a commonly used non-metallic mineral material, has a wide range of applications in industry and technology. Its preparation process and quality directly affect the performance and market competitiveness of the product. In this article, we will introduce you to the preparation process of calcite ultrafine powder and its price, hoping to provide you with valuable information.

Calcite ultrafine powder preparation process flow

The preparation of calcite ultrafine powder mainly involves the grinding process. The following is the general process flow:
1. Raw material selection

Selecting high-quality calcite ore as raw material is the first step in preparing ultra-fine powder. The quality of raw materials is directly related to the purity and performance of the final product.
2. smash

The selected calcite ore is crushed, usually using jaw crusher, cone crusher and other equipment to crush the original ore into smaller particles.
3. Grinding

After crushing, the particles are further ground using ultra-fine grinding equipment to obtain the required ultra-fine powder. The selection of ultrafine grinding equipment and the adjustment of process parameters have an important impact on the fineness and particle distribution of the product.
4. Grading

The ground calcite powder may have certain particle inhomogeneity. The ultra-fine powder is screened and classified through classification equipment to obtain the required fineness.
5. Packaging

The finally obtained calcite ultrafine powder is packaged through packaging equipment to ensure product quality and facilitate storage, transportation and sales.

Calcite ultrafine powder is an important non-metallic mineral material, and its preparation process and price are crucial to related industries and application fields.