Recent Posts
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Meet TYM at K 2025 -The World’ s No.1 Trade Fair for Plastics and Rubber
Welcome to the World’s No.1 Trade Fair for Plastics and Rubber -K 2025, taking place from October 8–15, 2025 at Messe Düsseldorf, Germany. As a professional LSR injection molding machine, mold, and robot solution provider, TYM Technology Co., Ltd. is proud to present our latest innovations at Booth 16E77.
09/23/2025
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ISO 9001, CE, CCC: What These Certifications Actually Mean for Your Equipment Purchase
When you're evaluating LSR injection molding machines from an overseas supplier, certification logos on a company website can start to blur together. ISO 9001, CE, CCC — they all sound reassuring, but they don't all mean the same thing, and they don't all matter for the same reasons. Understanding what each certification actually covers will help you ask better questions during due diligence and avoid assuming a certificate guarantees something it doesn't.
07/17/2026
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Turnkey LSR Injection Molding Solutions
Launching a liquid silicone rubber (LSR) injection molding operation involves far more than simply purchasing a machine. From material selection and mold design to automation integration and staff training, the journey from concept to full-scale production presents numerous challenges—each with the potential to delay your time-to-market and inflate your budget.
07/14/2026
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Industrial Silicone Seals & Waterproof Parts: LSR Guide
This guide helps product and sourcing engineers who need reliable industrial sealing components-gaskets, O-rings, grommets, and enclosure seals-understand why LSR injection molding is the preferred process for waterproof parts at volume, and how to specify them.
07/10/2026
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LSR Prototype to Production: Timeline & Process
A typical liquid silicone rubber (LSR) part moves from prototype to mass production in about 10-18 weeks, spanning design/DFM, prototyping, production mold fabrication, T1 sampling and validation, and pilot-to-ramp - with mold build and validation being the longest stages.
07/07/2026
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LSR Injection Molding Machine Parameters Explained
An LSR injection molding machine spec sheet lists dozens of numbers, but only a handful decide whether your silicone parts cure fully, stay flash-free and cost little to run. This 2026 guide explains the parameters that matter most, so engineers and buyers can compare machines on the specs that actually affect part quality, not marketing figures.
07/02/2026
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Automatic vs Semi-Automatic Silicone Molding Lines
This guide is for production and procurement decision-makers sizing a new LSR line—comparing the two configurations across throughput, quality, cost, and payback so you can match the investment to real demand.
07/01/2026
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LSR Cold Runner Systems: Cut Waste & Cost
LSR cold runner system is the single fastest way to cut material waste and labor out of liquid silicone rubber molding. By keeping the silicone liquid until it reaches the cavity, it eliminates cured runners and trimming entirely. This guide helps process engineers and buyers decide when a cold runner pays for itself.
06/30/2026
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How to Select LSR Injection Molding Machine Tonnage
Choosing the right clamping force is the single most consequential spec decision when buying a liquid silicone rubber (LSR) injection molding machine. Pick too little and you fight flash on every shot; pick too much and you pay for energy and floor space you never use.
06/29/2026
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Liquid Silicone Rubber Market 2026: Size, Growth & Demand Drivers
The global liquid silicone rubber (LSR) market is valued at roughly USD 3.4-3.8 billion in 2026 and growing about 7-9% annually, led by medical-grade demand (~44% of revenue) and rising EV production. Asia-Pacific dominates manufacturing capacity.
06/26/2026
Quality Control Standards in LSR Injection Molding Production
Quality control standards in LSR injection molding production adhere to internationally recognized frameworks rigorously. ISO 9001 certification validates our commitment to consistent quality management systematically. Good Manufacturing Practice (GMP) guidelines govern production environments ensuring sterility where applicable. Material certifications verify composition meeting pharmaceutical or food-grade requirements stringently. In-process inspections monitor critical dimensions preventing nonconformities proactively. Statistical Process Control (SPC) methods identify variations quickly enabling corrective actions promptly. These comprehensive standards ensure customer satisfaction through reliable product delivery consistently.
Incoming material qualification procedures scrutinize supplier credentials thoroughly. Certificates of Analysis confirm chemical compositions match specifications exactly. Physical property tests validate viscosity, cure rate, and mechanical characteristics adequately. Storage conditions are monitored maintaining material integrity properly. Lot traceability systems track materials from receipt through final shipment comprehensively. Quarantine protocols isolate suspect materials preventing contamination effectively. Approved vendor lists ensure sourcing from reputable suppliers exclusively. Stringent incoming inspection prevents substandard materials entering production confidently.
In-process quality checks occur at strategic points throughout manufacturing cycles continuously. Dimensional measurements verify conformance to tolerances using calibrated instruments accurately. Visual inspections detect surface defects like burns, voids, or flash promptly. Weight monitoring ensures consistent material usage per part reliably. Cycle time tracking identifies efficiency opportunities proactively. Machine parameter logging maintains process consistency historically. Operator polling checklists standardize routine verification tasks systematically. Immediate feedback loops enable rapid correction of deviations effectively.
Final product testing encompasses extensive evaluation ensuring compliance fully. Mechanical property assessments measure tensile strength, elongation, and tear resistance accurately. Chemical resistance tests expose samples to relevant media verifying compatibility adequately. Biocompatibility evaluations follow ISO 10993 standards where applicable medically. Sterilization validations confirm effectiveness against specified microorganisms thoroughly. Packaging integrity checks ensure protection during shipping and storage adequately. Certificate of Conformance documentation accompanies each shipment verifying compliance comprehensively. Robust final testing guarantees customer satisfaction with every delivery reliably.

