I. Characteristics and Advantages of Polyacrylate (PAA) Binders

1. Minimal Swelling in Electrolyte Solvents: Exhibits low swelling, maintaining structural integrity of electrode sheets during charge/discharge cycles.
2. High Proportion of Carboxyl Groups: The high density of polar carboxyl groups forms strong hydrogen bonds with hydroxyl-containing active materials, enhancing dispersion stability.
3. Continuous Film Formation: Creates a uniform film on material surfaces, improving contact between active materials and current collectors.
4. Excellent Mechanical Stability: Facilitates ease of processing during electrode manufacturing.
5. Enhanced SEI Formation and Cycling Performance: The high concentration of polar functional groups promotes hydrogen bonding with silicon material surfaces and aids in forming a stable Solid Electrolyte Interphase (SEI) layer, resulting in superior cycle life.

II. Development Challenges

Conventional PAA (Polyacrylic Acid) binder systems for electrodes typically utilize cross-linked PAA polymers as the anode binder. As a high-molecular-weight polymer, PAA offers excellent adhesion, dispersion stability, and corrosion inhibition. It stabilizes the network structure within the anode slurry, ensures uniform dispersion of active materials, and extends electrode sheet lifespan.

• However, the polar functional groups facilitate hydrogen bonding within the long molecular chains of PAA. This restricts free rotation of the chains, increasing their rigidity. Consequently, PAA-based electrode sheets generally exhibit poor toughness. This compromises their ability to withstand stresses induced by the volume expansion of active materials during cycling, hinders cell winding processes, and ultimately limits improvements in battery electrochemical performance.

III. Research Practices in Practical Applications of Battery-Grade PAA

1. Sodium-Ion Battery Hard Carbon Anodes

Manufacturers of hard carbon anodes for Sodium-Ion Batteries (SIBs) impose stringent requirements on PAA binders. A high-quality, highly flexible PAA binder is crucial for protecting the structural integrity of hard carbon anodes.

• In the current SIB hard carbon anode market, using substandard PAA binders significantly increases the risk of elevated internal resistance, negatively impacting battery efficiency and reliability. Conversely, a premium, highly flexible PAA binder effectively mitigates these issues.
• The electrochemical performance, conductivity, environmental adaptability, and corrosion resistance of the flexible PAA binder are also critical factors, directly influencing the quality of the final hard carbon anode product.
• Beyond inherent characteristics, practical application focuses heavily on performance parameters such as binder characteristics, solid content, adhesion strength, and pH level. These parameters directly correlate with the operational efficiency of the hard carbon anode.

2. Silicon-Based Anodes

Silicon-based lithium-ion battery anodes offer a specific capacity an order of magnitude higher than conventional graphite. However, forming stable silicon anodes is challenging due to significant volume changes during the electrochemical alloying/dealloying of silicon with lithium. Binder selection and optimization are vital for improving silicon anode stability. Most research utilizes Carboxymethyl Cellulose (CMC) and Polyvinylidene Fluoride (PVDF) binders.

• A significant body of experimental research indicates that pure PAA possesses mechanical properties comparable to CMC but contains a higher concentration of carboxyl functional groups. This enables PAA to act as a binder for Si anodes, delivering superior performance.
• Research further demonstrates the positive impact of carbon coating on anode stability. Carbon-coated Si nanopowder anodes (tested between 0.01 and 1 V vs. Li/Li+), incorporating PAA at levels as low as 15 wt%, exhibit exceptional stability over the first 100 cycles. These findings open new avenues for exploring novel binders like the Polyvinyl Alcohol (PVA) series.
• Crosslinking PAA with other materials represents a new development direction, including AA-CMC cross-linked binders, PAA-PVA cross-linked binders, PAA-PANI (Polyaniline) cross-linked binders, and EDTA-PAA binders.

3. PVA-g-PAA (PVA-grafted-PAA)

A novel water-soluble binder, PVA-g-PAA, is synthesized by grafting PAA onto the side chains of highly flexible PVA (Polyvinyl Alcohol). This functional group modification enhances the flexibility of the PAA binder system while leveraging PVA's excellent adhesion properties.

• This free-radical grafting polymerization introduces elasticity, compensating for the structural limitations of pure PAA binders.
• During electrode sheet fabrication, rolling compaction is performed continuously using varying roller pressures across defined length segments of the sheet. This process enhances sheet toughness, minimizing deformation, increasing electrode specific capacity, improving rate capability, and extending battery cycle life.

4. PAA Prelithiation (LiPAA)

The application of silicon-carbon (Si-C) materials imposes higher demands on anode binder and conductive agent systems. Traditional rigid PVDF binders are unsuitable for Si anodes. Acrylic PAA binders contain numerous carboxyl groups capable of forming hydrogen bonds with functional groups on Si surfaces, promoting SEI formation and significantly improving the cycle life of Si anodes. Thus, PAA binders are highly effective for Si anodes.

• Studies indicate that Lithium Polyacrylate (LiPAA) outperforms PAA itself, although the underlying reasons were unclear. Extensive research has been conducted to elucidate the mechanism behind LiPAA's superior performance.
• Electrodes composed of 15% nano-Si, 73% artificial graphite, 2% carbon black, and 10% binder (either PAA or LiPAA) were studied. After initial drying, a secondary drying step at 100-200°C was performed to remove residual moisture completely. Coin cell testing revealed capacities of ~790 mAh/g for LiPAA-based anodes versus ~610 mAh/g for PAA-based anodes.

Cycle performance curves of full cells using NMC532 cathodes

• Figure A: Cells with LiPAA binder show no significant correlation between cycle performance and secondary drying temperature. The NMC532 cathode delivered an initial capacity of 127 mAh/g at C/3, declining to ~91 mAh/g after 90 cycles.
• Figure B: Cells with PAA binder exhibit a clear dependence on secondary drying temperature (120°C red, 140°C gold, 160°C green, 180°C blue). While the 160°C dried PAA cell showed the highest initial capacity and the 120°C dried cell the lowest, the 160°C dried cell degraded fastest, reaching ~62 mAh/g after 90 cycles. The 140°C dried cell degraded slower, maintaining ~71 mAh/g.
• First-cycle Coulombic Efficiency (CE): LiPAA cells achieved ~84% (only the 200°C LiPAA cell was slightly lower at ~82%). Their Coulombic efficiency rapidly increased to ~99.6% within the first 5 cycles. PAA cells achieved ~80% first-cycle CE (only the 180°C PAA cell was significantly lower at ~75%), requiring ~40 cycles to reach 99.6% CE – markedly slower than LiPAA cells.
• Pulse discharge tests at 50% Depth of Discharge (DOD) revealed significantly lower internal resistance in LiPAA cells compared to PAA cells [Referenced Figure Below], with no apparent link to secondary drying temperature for LiPAA. In contrast, PAA cell resistance increased noticeably with higher secondary drying temperatures.

• Thermogravimetric Analysis (TGA) by Kevin A. Hays [Referenced Figure Below] on LiPAA and PAA anodes identified two main dehydration steps: 1) Free water removal (~40°C), 2) Adsorbed water removal (LiPAA ~75°C, PAA ~125°C). Additional weight loss peaks occurred for PAA between 140-208°C and LiPAA between 85-190°C, attributed to polymerization of some carboxyl groups releasing water [Referenced Reaction Below]. This reaction is less pronounced in LiPAA, where Li replaces H in ~80% of carboxyl groups.

• High-temperature polymerization of PAA carboxyl groups may weaken the interaction between PAA and Si, potentially explaining the poor cycle performance of high-temperature dried PAA anodes. However, peel strength tests showed that while PAA adhesion decreased with higher drying temperatures, it remained higher than LiPAA overall, suggesting other factors contribute to LiPAA's superior cycling.

Ⅳ. Conclusion

This study identifies poor electrochemical stability as a key factor limiting PAA's cycle performance. At low potentials, PAA undergoes partial conversion to LiPAA, generating hydrogen gas:

PAA + ... -> LiPAA + H₂

This reaction explains the lower first-cycle CE of PAA cells (~80%) compared to LiPAA cells (~84%), and the significantly longer time (~40 cycles vs. <5 cycles) required for PAA cells to achieve high Coulombic efficiency (99.6%).

TOB NEW ENERGY - Your Professional Partner in Battery Materials, Equipment, and Production Line Solutions.

In lithium-ion battery manufacturing, the fineness of the slurry (mainly referring to the electrode slurry) is a key parameter affecting electrode performance (such as capacity, rate capability, cycle life, safety) and process stability. Different battery types have significantly different fineness requirements for the slurry (usually measured by particle size distribution indicators such as D50, D90, Dmax), due to the intrinsic characteristics of their positive/negative electrode active materials (such as crystal structure, ionic/electronic conductivity, specific surface area, mechanical strength, reactivity) and different requirements for electrode microstructure.

The following is a detailed analysis of slurry fineness requirements for major battery types:

I. Lithium Cobalt Oxide (LCO) Batteries

1. Material Characteristics:

Layered structure (R-3m), high theoretical capacity (~274 mAh/g), high compaction density, but relatively poor structural stability (especially at high voltages), moderate cycle life and thermal stability, high cost.

2. Fineness Requirements):

High fineness is required. Typically requires D50 in the range of 5-8 μm, D90 < 15 μm, maximum particle size Dmax < 20-25 μm.

3. Reasons:

• High rate performance: Finer particles shorten the lithium-ion diffusion path within the particles, facilitating high-rate charging and discharging.
• High compaction density: Fine particles can pack more tightly, increasing the electrode's compaction density and volumetric energy density.
• Reducing side reactions/Improving cycling: Small and uniform particles help form a more uniform solid electrolyte interphase (SEI) film, reducing cracks caused by localized stress concentration in large particles and side reactions with the electrolyte, improving cycle stability (especially at high voltages).
• Reducing polarization: Reducing particle size can lower charge transfer resistance and concentration polarization.

II. Lithium Iron Phosphate (LFP) Batteries

1. Material Characteristics:

Olivine structure (Pnma), extremely stable structure (strong P-O bonds), long cycle life, excellent thermal safety, low cost. However, both electronic conductivity and ionic conductivity are low, compaction density and voltage plateau are low.

2. Fineness Requirements:

Very high fineness is required. Typically requires D50 in the range of 0.2-1.0 μm (200-1000 nm), D90 < 2-3 μm. This is the highest fineness requirement among all mainstream lithium-ion battery cathode materials.

3. Reasons:

• Overcoming intrinsic low conductivity: This is the core reason. LFP's extremely low electronic and ionic conductivity is the main bottleneck for its performance. Nanosizing it (D50<1μm) is a key strategy to improve rate capability, significantly shortening the transport paths of electrons and lithium ions.
• Improving rate performance: Nanoparticles enable high-rate charge/discharge capability.
• Improving tap/compaction density: Although nanoparticles themselves have low tap density, through reasonable particle morphology (such as spheroidization) and slurry/electrode processes, fine primary particles can fill better, improving electrode compaction density (though still lower than LCO/NCM).
• Fully utilizing capacity: Ensures all particles can fully participate in the electrochemical reaction, avoiding unreactive "dead zones" inside large particles.

III. NCM Batteries (LiNiₓCoᵧMn₂O₂)

1. Material Characteristics:

Layered structure (R-3m), combines the high capacity/high voltage of lithium cobalt oxide, the high capacity of lithium nickelate, and the stability/low cost of lithium manganate. Performance (energy density, rate capability, cycle life, safety, cost) depends on the specific ratio (e.g., NCM111, 523, 622, 811). Higher nickel content leads to higher capacity and energy density, but greater challenges in structural stability and safety.

2. Fineness Requirements:

High fineness is required, but specific requirements become stricter with increasing nickel content.

• Medium/Low Nickel (e.g., NCM523 and below): D50 typically 6-10 μm, D90 < 18-22 μm.
• High Nickel (e.g., NCM622, 811, NCA): D50 requires finer particles, typically 3-8 μm (especially 811/NCA tends to be finer), D90 < 12-15 μm, strict control of Dmax < 20 μm.

3. Reasons:

• High energy density/rate performance: Fine particles help increase compaction density and rate performance (shortening Li⁺ diffusion path).
• Improving structural stability of high-nickel materials: High-nickel materials (high reactivity) are more prone to structural degradation (e.g., phase transition, microcracks) during cycling.
• Fine and monodisperse particles can: Reduce stress concentration within particles and crack initiation/propagation.
• Form a more uniform and stable CEI film, reducing electrolyte consumption and transition metal ion dissolution.
• Mitigate particle pulverization during cycling, improving cycle life.
• Reduce interfacial impedance/polarization: Similar to LCO.
• Safety considerations: Finer particles have relatively better heat dissipation and more stable structure, helping to improve safety (especially for high-nickel materials).

IV. NCA Batteries (LiNiₓCoᵧAl₂O₂)

1. Material Characteristics:  Very similar to high-nickel NCM (high capacity, high energy density). Aluminum doping aims to improve structural stability and cycle performance, but processing challenges (e.g., sensitivity to humidity) and safety challenges remain.

2. Fineness Requirements:

Very high fineness is required, close to or equivalent to high-nickel NCM (e.g., 811). D50 typically 3-7 μm, D90 < 12-15 μm, strict control of Dmax.

3. Reasons:

Identical to high-nickel NCM. The core lies in maximizing structural stability, cycle life, and safety through nano-sizing/fine particles while pursuing high energy density.

V. Lithium Titanate (LTO) Batteries)

1. Material Characteristics:

Spinel structure (Fd-3m), used as anode. Has "zero-strain" characteristic (minimal volume change), ultra-long cycle life (over 10,000 cycles), excellent rate capability and low-temperature performance, extremely high safety. However, high operating voltage (~1.55V vs Li+/Li) leads to low full-cell voltage and low energy density.

2. Fineness Requirements:

Medium to fine fineness is required. D50 typically in the range of 1-5 μm, D90 < 10-15 μm. Coarser than LFP, possibly slightly finer or comparable to some NCM/LCO.

3. Reasons:

• High-rate performance: LTO itself has good conductivity, but fine particle size is still an effective means to improve ultra-high-rate performance (e.g., fast charging), shortening the Li⁺ solid-phase diffusion path.
• Increasing compaction density: Although LTO is "zero-strain", increasing compaction density still helps improve volumetric energy density (despite its low absolute value).
• Reducing electrode impedance: Fine particles facilitate the formation of a tighter conductive network.
• Balancing processability and performance: Excessively fine LTO nanoparticles have a huge specific surface area, which significantly increases slurry viscosity, reduces solid content, increases binder/conductive agent usage, and exacerbates side reactions with the electrolyte (although LTO is stable, nano-sizing increases surface activity). Therefore, the fineness requirement is a balance between high-rate performance and processability/cost.

VI. Solid-State Batteries (SSBs)

1. Important Note:

"Solid-state batteries" cover various technical routes (polymer, oxide, sulfide electrolytes), and the choice of positive/negative electrode materials is also diverse (can be any of the above materials or new materials such as lithium-rich manganese-based, lithium metal anode). The requirements for slurry fineness are extremely complex and highly dependent on the specific system, but there are some common trends.

2. Core Challenge:

Solid-solid interfacial contact. In liquid batteries, the electrolyte can wet and fill pores, while the solid electrolyte is rigid particles, and point contact with active materials leads to huge interfacial impedance. This is one of the core challenges of solid-state batteries.

3. Fineness Requirement Trends:

• Generally higher fineness is required: Both active material and solid electrolyte particles usually require finer particle size (D50 often in the sub-micron to micron range).
• Reasons:

(1) Increasing solid-solid contact area: Fine particles provide a larger contact interface, reducing interfacial impedance.

(2) Shortening ion transport path: Fine particles can shorten the Li⁺ transport distance within the active material and solid electrolyte, and at the interface between them.

(3) Achieving more uniform composite: When preparing composite electrodes (active material + solid electrolyte + conductive agent + binder), the particle size and morphology matching of each component is crucial. Usually, all components need to achieve comparable fineness levels to mix uniformly and form effective ionic/electronic conductive networks.

4. Specific System Differences:

• Sulfide solid-state batteries: Highest fineness requirements. Sulfide electrolytes (e.g., LPS) usually need to be made into sub-micron or even nano-sized particles (D50 < 1 μm), active materials also often need to be nano-sized, and extremely uniform mixing (often using high-energy ball milling) is required to form a good ion-percolating network. Maximum particle size control is very strict.
• Oxide solid-state batteries: Electrolytes (e.g., LLZO) are usually hard and have larger particle sizes (micron level). To improve contact, active materials (especially the cathode) also tend to use smaller particles (e.g., D50 1-5 μm), and may require the introduction of a small amount of polymer binder or liquid wetting agent (quasi-solid). High requirements for mixing uniformity.
• Polymer solid-state batteries: The process is relatively close to traditional liquid batteries. Polymer electrolytes have a certain fluidity after heating. The fineness requirements for active materials are similar to or slightly higher than the corresponding liquid systems (e.g., using LFP, NCM), mainly for better interfacial contact and ion transport. The fineness of the polymer electrolyte itself (e.g., PEO particles) also needs to be controlled.
• Anode (e.g., lithium metal, silicon-based): If lithium metal foil is used, there is no slurry fineness requirement. If composite anodes are used (e.g., pre-lithiated silicon/graphite mixed with solid electrolyte), the fineness and mixing uniformity requirements for silicon particles and solid electrolyte particles are extremely high.

VII. Summary and Key Points:

1. Most Stringent Requirements:

Lithium iron phosphate requires the highest fineness (nanoscale) due to its intrinsic low conductivity. High-nickel ternary (NCM811/NCA) and active materials/electrolytes in sulfide solid-state batteries also require very high fineness (sub-micron to microns).

2. High Fineness Requirements:

Lithium cobalt oxide, medium/low-nickel ternary, and active materials in oxide/polymer solid-state batteries usually require high fineness (D50 several microns) to improve energy density, rate performance, and stability.

3. Moderate Fineness Requirements:

Lithium titanate requires medium to fine fineness (D50 1-5 μm), balancing rate performance and processability.

4. Core Driving Factors:

• Overcoming material intrinsic defects: The low conductivity of LFP is the most typical example requiring ultrafine particles.
• Improving kinetic performance (rate capability): Almost all materials need to reduce particle size to shorten ion diffusion paths.
• Increasing energy density (compaction density): Fine particles facilitate tight packing (especially for LCO, NCM).
• Improving structural stability and cycle life: Particularly important for layered materials (LCO, NCM, NCA). Fine particles can reduce stress cracks and side reactions. This is the key reason why high-nickel materials pursue finer particles.
• Optimizing solid-solid interface (solid-state batteries): This is the core requirement distinguishing solid-state batteries from liquid batteries, universally driving the demand for finer particles and more uniform mixing.

5. Trade-off Considerations:

Fineness is not always finer the better. Excessively fine particles can cause:

• Dramatically increased specific surface area -> High slurry viscosity, difficult dispersion, low solid content, increased binder/conductive agent usage -> Increased cost, greater process difficulty, potential reduction in energy density.
• High surface activity -> Aggravated side reactions (consuming electrolyte/lithium source, gas generation), cycle performance may instead decrease (especially for highly reactive materials like high-nickel).
• Severe particle agglomeration -> Affects uniformity and performance

Therefore, the optimal slurry fineness for each battery material is the result of meticulous trade-offs and optimization between its material characteristics, performance targets (energy, power, lifespan, safety), and process feasibility/cost. Manufacturers usually determine the most appropriate fineness control range based on specific material suppliers, formulation design, process equipment, and product positioning.

At TOB NEW ENERGY, we are committed to being your strategic partner in advancing energy storage technologies. We empower next-generation lithium battery production through precision battery mixing systems, electrode preparation systems, battery assembly line, intelligent battery production lines, and high-performance battery materials.  Our offerings extend to cutting-edge battery manufacturing equipment and battery tester, ensuring seamless integration across every stage of battery production. With a focus on quality, sustainability, and collaborative innovation, we deliver solutions that adapt to evolving industry demands. Whether you’re optimizing existing designs or pioneering next-generation batteries, our team is here to support your goals with technical expertise and responsive service. Let’s build the future of energy storage together. Contact us today to explore how our integrated solutions can accelerate your success.

In lithium battery manufacturing, the often-overlooked A/B-side coating misalignment issue during the coating process significantly affects battery capacity, safety, and cycle life. Misalignment refers to inconsistencies in the positional alignment or thickness distribution of coatings on the front and back sides of electrodes, which can lead to risks such as localized lithium plating and mechanical damage to the electrodes.

This article analyzes the root causes of misalignment from perspectives including equipment precision, process parameter settings, and material properties, while proposing targeted optimization strategies to help enterprises enhance product consistency and stability.

Ⅰ. Causes of A/B-Side Misalignment

1. Equipment Factors

Insufficient roll system assembly accuracy: Horizontal or coaxial deviations during the installation of backing rolls and coating rolls may cause positional shifts.

Coating head positioning errors: Low-resolution encoders/grating rulers or sensor feedback drift result in deviations between actual and preset coating positions.

Tension fluctuations: Unstable unwinding/winding tension causes substrate stretching or wrinkling, reducing coating precision.

2. Substrate (Foil) Issues

Non-uniform ductility: Inconsistent foil plasticity complicates gap control during coating.

Poor surface quality: Residual oxide layers weaken slurry adhesion, leading to partial coating or misalignment.

3. Slurry Properties

High viscosity impairing leveling: Poor slurry flowability causes uneven accumulation.

Large surface tension differences: Uneven edge shrinkage due to tension disparities between front/back coatings.

4. Process Settings

Inconsistent coating speeds: Speed differences between sides disrupt slurry spreading.

Drying condition variations: Temperature differences induce uneven thermal shrinkage, causing misalignment.

Ⅱ. Proposed Solutions

1. Equipment Precision Optimization

Regularly inspect roll coaxiality/flatness to control installation errors.

Upgrade coating head positioning components (e.g., high-resolution encoders) to limit deviations within ±0.1 mm.

Implement closed-loop tension control (e.g., PID adjustment) to maintain tension fluctuations below ±3%.

2. Substrate Consistency Control

Select high-uniformity copper/aluminum foils with stable elongation properties.

Adopt advanced surface treatments (e.g., low-temperature plasma cleaning) to enhance slurry adhesion uniformity.

3. Slurry Performance Adjustment

Optimize viscosity (anode: 10–12 Pa·s; cathode: 4–5 Pa·s) for better leveling.

Add surfactants (e.g., PVP, SDS) to balance surface tension between sides.

4. Process Parameter Refinement

Maintain identical coating speeds for both sides (error <0.5 m/min).

Apply segmented temperature control: Low-temperature pre-drying for stress relief and high-temperature curing, with overall temperature differences <5°C.

Ⅲ. Diagnosis and Monitoring Mechanisms

1. Equipment Diagnosis

Use laser interferometers to verify roll parallelism (error <0.02 mm/m).

Inspect motor/sensor signal stability to prevent drift exceeding 0.5% of the range.

2. Substrate Evaluation

Test elongation at break (deviation <±5%).

Analyze surface microstructure/oxide layers via SEM (thickness <50 nm).

3. Slurry Testing

Measure viscosity and thixotropy via rheometers (thixotropic area difference <5%).

Ensure surface tension difference <2 mN/m using tensiometers.

4. On-Line Process Control

Monitor coating thickness with laser sensors (CV <1%).

Post-drying X-ray inspection for coating density uniformity (lateral deviation <2%).

Conclusion

Through precise equipment calibration, material screening, slurry optimization, and systematic process management, A/B-side misalignment can be controlled within ≤0.5 mm. This effectively enhances battery consistency, safety, and cycle life.

At TOB NEW ENERGY, we are committed to being your strategic partner in advancing energy storage technologies. We empower next-generation lithium battery production through precision battery coating systems, intelligent battery production lines, and high-performance materials.  Our offerings extend to cutting-edge battery manufacturing equipment and battery tester, ensuring seamless integration across every stage of battery production. With a focus on quality, sustainability, and collaborative innovation, we deliver solutions that adapt to evolving industry demands. Whether you’re optimizing existing designs or pioneering next-generation batteries, our team is here to support your goals with technical expertise and responsive service.

This article analyzes the available pump types for specific media to help you make a faster and more effective selection, and also provides some data for your reference.

1.Working condition characteristics analysis

Medium characteristics

Strong acidity: pH=2 is a strong acid environment, and the acid corrosion resistance of the material needs to be considered

Oxidation: The medium has oxidizing properties, and the material's antioxidant capacity needs to be evaluated

Containing solid particles: The presence of small sand particles will cause wear problems (it is recommended to confirm the particle size distribution and concentration)

2.Material selection

2.1 It is recommended to use PTFE (polytetrafluoroethylene) or F46 lined pump body, which has the following features:

✓ Strong acid resistance (applicable to the full range of pH 0-14)

✓ Excellent oxidation resistance

✓ Smooth surface and not easy to scale

2.2 Mechanical seals are recommended to use SiC/SiC pairing, which is more resistant to particle wear than graphite

2.3 Key selection parameters

Required notes Speed ≤ 2900rpm: reduce particle erosion and wear

Impeller type semi-open/open impeller: avoid blockage of closed impeller flow channel

Gap design is 0.3-0.5mm larger than standard pump to accommodate particle passage

Shaft seal type: double-end mechanical seal + flushing water (Plan53B external flushing solution is recommended)

3. Special design points

Wear-resistant structure

The impeller front cover is thickened by 2-3mm

A replaceable wear-resistant plate is set at the volute of the pump body

The surface of the flow-through parts can be hardened

4. Operation suggestions

It is recommended to install a Y-type filter at the inlet (the mesh size is determined by the particle size)

The minimum flow rate should be >30% Qn to prevent solid deposition

The flow channel should be flushed in time when the machine is shut down

5. Recommended typical models

Domestic: IHF80-65-160 fluoroplastic centrifugal pump (with wear-resistant modification kit)

Imported: CPK80-200F (with impeller for granular media)

If the budget is li mited, you can consider: FSB80-50-200 (need to confirm the actual particle parameters)

If you have better ideas, please leave a message. We are happy to learn new knowledge and provide better service.

Attached is the performance curve of our IHF chemical pump：

With the continuous development of industrial production, the demand for cooling equipment is also increasing. As an efficient and energy-saving cooling solution, air cooled screw chillers have been widely used and recognized.

The air cooled screw chiller uses advanced air-cooling technology to quickly and effectively discharge the generated heat through cold water circulation and fan heat dissipation, thereby achieving cooling purposes. Compared with traditional water cooling methods, air-cooled screw chillers have the following significant advantages.

First of all, air cooled screw chillers perform well in terms of energy saving. The traditional water cooling method requires additional cooling water systems and water pumps for circulation, which not only consumes energy, but also requires a lot of maintenance and management. The air-cooled screw chiller dissipates heat through fans and does not require an additional water cooling system, which greatly reduces energy consumption and operating costs, achieving high efficiency and energy saving.

Secondly, air cooled screw chillers have a smaller footprint. The traditional water cooling system requires the establishment of a special computer room and the installation of water pumps, cooling towers and other equipment, which takes up a lot of space resources. The air-cooled screw chiller has a compact structure and can be placed directly next to the production line or in the corner of the factory, saving valuable space and improving production efficiency.

In addition, the air cooled screw chiller has good flexibility and stability. It can be adjusted according to production needs to achieve matching cooling capacity. At the same time, the air-cooled screw chiller uses reliable screw compressor technology, which has a low failure rate and stable operation. This means that it can maintain a stable cooling effect under various working conditions and ensure continuous production.

After the above summary, it can be seen that air cooled screw chiller, as an efficient and energy-saving cooling solution, has become the first choice of many enterprises. It can not only meet the needs of industrial production for cooling equipment, but also save energy, reduce floor space, improve production efficiency, and contribute to the sustainable development of enterprises. As a supplier of air cooled screw chillers, we aim to provide the best services to more companies.

As the plastics industry continues to develop, the demand for cooling equipment is getting higher and higher. As a professional industrial chiller manufacturer, we are very proud to launch a customized stainless steel screw chiller, which is committed to providing excellent cooling solutions for the plastics industry. As an advanced cooling equipment, the customized stainless steel screw air-cooled chiller is becoming the first choice of more and more plastic factories, bringing them many advantages and conveniences. This article will focus on the advantages of 304 stainless steel sheet metal screw air-cooled chillers to help you understand why you choose this product.

Strong corrosion resistance: 304 stainless steel sheet metal screw air-cooled chillers are made of high-quality 304 stainless steel materials and have good corrosion resistance. This means that in harsh working environments, it can operate stably for a long time without being affected by corrosion, ensuring that your production line always runs smoothly.

Efficient cooling performance: This screw air-cooled chiller uses advanced screw compressor technology and has excellent cooling performance. It can quickly reduce the temperature of the extruder, ensure that plastic products are cooled quickly, and achieve the ideal curing effect. With its efficient cooling capacity, you can significantly improve production efficiency, shorten production cycles, and achieve higher output.

If you have any questions about the customized stainless steel screw air-cooled chiller or want to know more details, please feel free to contact us. We will wholeheartedly provide you with professional solutions and quality services

Water cooled chillers

are an essential component in various industrial and commercial applications that require efficient cooling solutions. As a manufacturer of water-cooled chillers, it is important showcase the advantages of our products compared to similar offerings in the market. In this article, we will explore the unique and benefits that set our water-cooled chillers apart, resulting in enhanced performance, energy efficiency, and environmental sustainability.



Water cooled chillers are known for their superior cooling efficiency compared to air cooled alternatives. By utilizing water as a cooling medium, our chiller systems offer a higher heat absorption capacity and faster cooling rates. This results in improved process stability, reduced downtime, and enhanced productivity for our customers.



Our water cooled chillers are designed with a focus on energy efficiency, resulting in significant cost savings for our customers. Unlike air-cooled chillers, which rely on ambient air temperatures for heat dissipation, water-cooled systems can operate at lower condensing temperatures. This allows for more efficient heat transfer, reducing electricity consumption and minimizing overall operating costs.



We pride ourselves on offering water cooled chillers that feature a compact design without compromising on performance. This enables our customers to optimize space utilization, especially in environments where space is limited. Additionally, the flexibility in installation options ensures easy integration into existing infrastructure, making our chillers an ideal choice for retrofit projects.



In many applications, noise levels can be a critical consideration. Our water cooled chillers are designed with noise reduction in mind, employing advanced acoustic insulation materials and sound-dampening features. This ensures a quieter operating environment, maintaining workplace comfort and adhering to regulatory guidelines where noise restrictions are in place.



Our water cooled chillers offer excellent scalability, allowing customers to expand their cooling capacity as their needs grow. By implementing modular design principles, our chillers can be easily integrated into existing systems and expanded by adding additional units. Moreover, our chiller control systems provide advanced load management capabilities, optimizing energy consumption based on real-time cooling demands.



Water cooled chillers excel in terms of environmental sustainability compared to air cooled counterparts. By utilizing water as the primary cooling medium, our chillers reduce the reliance on refrigerants, which often have a high global warming potential. Furthermore, our systems enable the efficient recovery and reuse of waste heat, contributing to energy conservation and reduced carbon emissions.



As a manufacturer of water-cooled chillers, we offer a range of unique advantages that set our products apart from other similar offerings on the market. With superior cooling efficiency, energy efficiency, compact design, noise reduction, scalability, and environmental sustainability, our water-cooled chillers ensure optimal performance, cost savings, and reduced environmental impact for our customers. Investing in our water cooled chillers will not only enhance your cooling capabilities but also contribute to a more sustainable future.

In today's competitive manufacturing market, efficient cooling solutions have become the goal pursued by industrial manufacturing companies in all walks of life. As a leading supplier, OUMAL Refrigeration Machinery Co.,Ltd . has developed water chiller cooling system and 30 ton air cooled screw chiller to meet customer needs, bringing a new turn to the manufacturing industry.

The water chiller cooling system is an excellent process cooling solution that provides efficient and reliable cooling effects by utilizing the sensible heat transfer characteristics of water. The water cooling system mainly uses advanced technology and sophisticated control devices to provide accurate and stable process temperature control for manufacturing processes in different industries. Whether it is injection molding, thermoforming, blown film or plastic extrusion, compound mixing and other processes, our water cooling system can effectively improve product quality and shorten manufacturing time.

On the other hand, our 30 ton air cooled screw chiller is an innovative product that has attracted much attention in the industry. The equipment enjoys a high reputation for its excellent cooling effect and high energy-efficient operation. Using air-cooling technology, the chiller eliminates the reliance on external water sources, providing manufacturers with greater flexibility and convenience. Whether it is a large-scale production environment or an application scenario with special requirements, the 30 ton air cooled screw chiller can give full play to its advantages, ensuring efficient cooling and energy-saving operation.

With years of industry experience and expertise, OUMAL Refrigeration Machinery Co.,Ltd .continues to improve the performance and reliability of our water chiller cooling system and 30 ton air cooled screw chiller. At the same time, we also focus on user experience, simplify the operating interface, and make installation and maintenance more convenient. Whether it is a new project or upgrading existing equipment, we are committed to meeting customer needs and providing reliable solutions.

Choose OUMAL Refrigeration Machinery Co.,Ltd , you will get excellent products and quality services.

In modern industrial production, industrial cooling water chillers are indispensable key equipment, providing efficient cooling solutions for various industries. Take the 50 ton water cooled chiller as an example. It integrates advanced technology and reliability and has become a highly respected choice in the industry.

The first key feature of the industrial cooling water chiller is high efficiency and energy saving. With advanced refrigeration technology and efficient cooling system, the 50 ton water cooled chiller can quickly reduce the temperature of the working environment and provide a stable cooling effect. More importantly, it can minimize energy consumption and save energy costs through intelligent control and optimized operation mode.

Secondly, the 50 ton water cooled chiller has excellent stability and reliability. During long-term operation, it can maintain a stable cooling effect and has good temperature control capabilities. Whether in hot summer or other harsh environments, it can maintain reliable operation and will not affect production efficiency due to changes in external conditions.

Finally, industrial cooling water chillers are widely used in various industrial fields. It can provide stable cooling effects for production and processing equipment, machine tools, injection molding machines, laser equipment, etc. to ensure the normal operation of the equipment. Especially in large-scale industrial production, the high cooling capacity and stable performance of the 50 ton water cooled chiller can meet the demand for large amounts of cooling water in the production process.

In addition to the characteristics of high efficiency, energy saving, stability and reliability, industrial cooling water chillers also have a variety of advanced functions and advantages. For example, the intelligent control system can realize remote monitoring and operation, which improves the convenience of equipment management. In addition, the compact design structure and advanced noise reduction technology enable it to generate lower noise and vibration during operation, reducing interference with the working environment.

Industrial cooling water chillers are an indispensable and important equipment in modern industrial production. The 50 ton water cooled chiller has become the first choice of many companies due to its high efficiency, energy saving, stability and reliability. With the continuous development and innovation of advanced technology, industrial cooling water chillers will continue to provide more efficient and reliable cooling solutions, injecting new impetus into the industrial manufacturing industry.

In the process of producing stretch film, the cooling system is very important, which directly affects the quality and output of stretch film. In general, we recommend choosing a chiller model with a cooling capacity slightly larger than the flow rate required for cooling, so as to ensure that the temperature and water flow rate can be kept within the required range under long-term stable operation.

When choosing a water chiller system for your stretch film machine and film blowing machine, there are several factors to consider:

Cooling Capacity: Determine the cooling capacity required for your machines based on their heat load. Consider factors such as the machine size, material type, production rate, and ambient temperature.

Temperature Control: Assess the temperature control requirements of your machines. Depending on the application, you may need precise temperature control to achieve optimal production conditions.

Chiller Type: Select a chiller type that suits your specific needs. Water-cooled chillers offer more efficient cooling but require a water source, while air-cooled chillers are easier to install and maintain but may be less efficient in certain environments. Oumal Chiller will provide professional suggestion of water cooling system for your stretch film machine. Below is the picture of our air cooled screw chiller in a plastic factory cooling the film stretch machine.

Chiller Size: Ensure that the chiller's physical dimensions and capacity fit the space and power constraints of your facility. Consider factors such as the available floor space, electrical capacity, and accessibility for service and maintenance.

Energy Efficiency: Look for chiller systems that are energy-efficient to help reduce operational costs. Consider features such as variable-speed drives, heat recovery options, and high-efficiency components.

Reliability and Maintenance: Choose a chiller system from a reputable manufacturer known for reliability and ease of maintenance. Look for features like easy access to components, built-in diagnostics, and reliable service support.

Water Quality: Consider the quality and availability of the water source needed for the chiller system. Assess the water's temperature, pressure, and the presence of any impurities that may affect the chiller's performance.

Cost Considerations: Evaluate the initial investment cost, operating costs, and long-term maintenance requirements of the chiller system. Consider the overall value and return on investment that the system can provide.

It is recommended to consult with chiller manufacturers or suppliers who specialize in industrial cooling solutions. They can assess your specific requirements and suggest the most suitable chiller system for your stretch film machine and film blowing machine applications. Oumal Chiller specializing in industrial cooling systems for over 15 years. Provide reliable industrial water chiller system for your stretch film machines. Also can provide Cooling air chiller for blowing the stretch film. Welcome to contact.