Medical injection-molded products, directly related to human health and safety, require significantly higher dimensional accuracy, structural stability, and surface quality than ordinary industrial products. However, warping and deformation remain critical factors limiting the pass rate of medical injection-molded parts. This article systematically analyzes the causes of warping and deformation in medical injection-molded products from four dimensions: material properties, mold design, molding processes, and post-processing, and proposes targeted solutions.
Case Study: A TV base bracket (PBT+30%GF) suffered from corner uplifting due to uneven wall thickness. By optimizing the gate position (from the center of the long side to the short side) and simplifying the melt flow path, the glass fiber orientation was unified, significantly reducing warping deformation.
Optimization Strategies:
Adopt multi-point gate layouts to shorten melt flow paths.
Adjust gate positions to the short sides of products to reduce flow ratios (L/t).
Use fan gates for circular products to balance shrinkage.
Imbalanced Cooling Systems: Excessive temperature differences between mold cavities and cores can cause rapid cooling of melt layers adjacent to cold mold surfaces, while hotter inner layers continue to shrink, creating bending moments. For example, flat products (e.g., mobile phone battery cases) with cavity-core temperature differences exceeding 5°C exhibit significantly higher warping deformation rates.
Optimization Strategies:
Arrange dense cooling water channels to ensure cavity-core temperature differences ≤3°C.
Use straight-through water channels instead of S-shaped loops to reduce cooling medium temperature rise.
Add cooling circuits in deformed areas of long, rectangular products.
Defective Ejection System Design: Uneven ejection forces or small ejector pin cross-sectional areas can cause localized overstressing and deformation. For example, deep-cavity thin-wall products (e.g., TPU materials) using only mechanical ejection are prone to puncturing or folding due to high demolding resistance.
Optimization Strategies:
Optimization Strategies:
Reduce injection pressure to the lowest feasible value.
Adopt multi-stage injection speeds (slow-fast-slow) to minimize shear stress.
Increase material temperature (per manufacturer recommendations) to promote stress relaxation.
Insufficient Packing and Cooling Times: Excessive packing pressure can leave residual compressive stress, while insufficient packing time may cause backflow through unsolidified gates, generating residual shear stress. Inadequate cooling time results in premature ejection of partially solidified products, leading to deformation due to uneven shrinkage.
Optimization Strategies:
Use two-stage packing: high pressure at distant gates and low pressure at nearby gates.
Extend cooling time until the product is fully solidified (typically 50%–70% of the cycle time).
Determine optimal packing time and pressure combinations through CAE simulations.
Improper Mold Temperature Control: High mold temperatures increase residual shear stress, while low mold temperatures may cause rapid cooling and stress concentration. For example, PP products with mold temperatures below 60°C exhibit significantly higher warping deformation rates.
Optimization Strategies:
Annealing Treatment: For highly stressed products (e.g., glass fiber-reinforced resins), annealing eliminates residual stress. Annealing temperatures are typically 10–20°C below the material's glass transition temperature, with durations adjusted based on product thickness (usually 2–4 hours).
Stress-Relief Design: During mold design, structures such as fillets and ribs can reduce stress concentration. For example, adding ribs at the ends of long, rectangular products significantly reduces bending deformation.
Resolving warping and deformation issues in medical injection-molded products requires systematic optimization across four areas: material selection, mold design, molding processes, and post-processing.
By predicting deformation trends via CAE simulations (e.g., C-MOLD) and adjusting parameters through practical mold trials, the pass rate of medical injection-molded products can be significantly improved to meet stringent medical industry standards.