| HS Code | 637145 |
| Productname | Silicone Gel RH-PG-4288 |
| Producttype | Two-component addition-cure silicone gel |
| Appearance | Colorless transparent liquid |
| Mixratio | 1:1 by weight |
| Viscosity | Approx. 1,000 mPa·s at 25°C |
| Density | Approx. 1.0 g/cm³ |
| Hardness | Low hardness, gel-like |
| Thermalconductivity | Approx. 0.2 W/(m·K) |
| Dielectricstrength | Approx. 20 kV/mm |
| Volumeresistivity | ≥1×10^13 Ω·cm |
| Tensilestrength | ≥1.0 MPa |
| Elongationatbreak | ≥100% |
| Operatingtemperaturerange | -50°C to +200°C |
| Curingconditions | Room temperature cure or heat accelerated |
| Shelflife | Approx. 6 months |
As an accredited Silicone Gel RH-PG-4288 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Silicone Gel RH-PG-4288 is supplied in 20 kg sealed plastic drums, clearly labeled with batch and safety information. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Silicone Gel RH-PG-4288 is packed and secured in a 20-foot full container load for shipment. |
| Shipping | Silicone Gel RH-PG-4288 is packaged in sealed, labeled containers and shipped upright, protected from heat, moisture, and direct sunlight. It is generally non-hazardous for transport, but final classification must follow the current SDS and applicable local/international regulations. Avoid freezing and handle with standard PPE. |
| Storage | Store Silicone Gel RH-PG-4288 in a cool, dry, well-ventilated area away from direct sunlight, heat, ignition sources, and incompatible materials such as strong oxidizers. Keep containers tightly closed, properly labeled, and upright to prevent leakage or contamination. Protect from moisture and freezing. Follow supplier SDS and local regulations; use oldest stock first. Do not store near food or drink. |
| Shelf Life | Shelf life: 12 months when stored unopened in a cool, dry, well-ventilated place, away from direct sunlight. |
In insulated-gate bipolar transistor (IGBT) power modules, SiC half-bridge assemblies, and high-density DC-DC converter blocks, Silicone Gel RH-PG-4288 is dispensed over wire-bonded dies and gate driver boards as a low-modulus encapsulant. The primary process objective is to eliminate air entrapment around wire bonds and metallized substrates without transmitting mechanical stress to bond loops during thermal excursions. Production-scale modules are typically filled under vacuum; the mixed material is first degassed at an absolute pressure of 1–5 kPa until bulk bubbles release, then dispensed through a piston or progressive cavity pump into the cavity with a static mixer of 18–30 mixing elements. Cavity fill volume is controlled by weight check within ±0.5% because pressure-time dispensing alone drifts when viscosity varies across batches. After dispensing, a second vacuum cycle at 0.5–2 kPa for 2–8 min collapses residual bubbles before cure. Addition-cure gel systems of this class can be accelerated at 80–120 °C for 30–90 min, but completion of cure should be verified by residual exotherm via differential scanning calorimetry per ISO 11357-2, because under-cured gel exhibits surface tack and reduced electrical performance. Dielectric acceptance on finished modules is commonly checked to ASTM D149-20 at a ramp of 500 V/s; volume resistivity is evaluated per ASTM D257-14 at 500 V DC with a one-minute electrification time. Tracking resistance under polluted conditions is assigned by IEC 60112:2020; power modules requiring Pollution Degree 2 or 3 per IEC 60664-1 should use a gel thickness that maintains creepage distances after gel shrinkage of 0.1–0.4%. A production-line failure mode is bubble pinning at the base of wire bonds where high pin count restricts flow; this is mitigated by reducing dispense needle speed to 5–20 mm/s and by orienting the module so gas rises away from adhesion shadow zones. Published data for gel-shrinkage interaction on SiC devices with operating junction temperatures above 175 °C is limited, so prototype qualification should include thermal cycling from −40 °C to +150 °C per IEC 60068-2-14:2009 test Nb for at least 500 cycles.
For high-voltage gel potting, representative production verification includes the following acceptance checks; actual values are to be confirmed against the supplier datasheet for the specific gel batch.
| Property | Method | Typical acceptance check |
|---|---|---|
| Dielectric breakdown strength | ASTM D149-20 | ≥ 15 kV/mm for a 1.0 mm cured sheet; report actual |
| Volume resistivity | ASTM D257-14 | ≥ 1.0 × 1014 Ω·cm at 500 V DC |
| Comparative tracking index | IEC 60112:2020 | ≥ 600 V for Pollution Degree 2 designs |
| Thermal cycling | IEC 60068-2-14:2009 test Nb | 500 cycles −40 °C / +150 °C, no delamination at wire bond interface |
Unlike rigid epoxy or hard polyurethane potting, cured silicone gel permits mechanical removal with hand tools or vacuum extraction, but complete residue removal from wire bonds and alumina substrates is difficult. Rework facilities operating under IPC 7711/7721 procedures may classify non-clean residues as an unacceptable risk when gel debris remains under deep gate driver connectors or between closely spaced pins. The low-modulus gel can be cut with a sharpened polyamide or PEEK probe, then lifted in sections; however, peeling cured gel from a failed wire bond can transmit enough localized force to fracture a degraded wire if the bond is already compromised by electromigration. After gel extraction, adhesion to the original cured gel surface is partial. Re-dispensing over partially removed gel builds an interface that can delaminate during thermal shock if surface contamination is present. Plasma activation with a low-pressure air or argon plasma at 13.56 MHz and a forward power of 50–150 W for 30–90 s may improve interlayer wetting, but plasma gas selection must avoid residual halide contamination that could promote corrosion. Solvent cleaning before re-dispensing is restricted; light aliphatic solvents that evaporate completely may be used to remove dust, whereas aromatic or ketone-based solvents can swell the silicone network and create void-forming decomposition products during subsequent cure. The rework process is therefore only viable when the failure analysis value justifies the cost of dry ice blasting or CO₂ snow cleaning after gel removal. If a manufacturer specifies no rework for RH-PG-4288-potted assemblies because long-term partial-discharge performance cannot be guaranteed across the gel-to-gel interface, that limitation should be written into the repair manual before field returns are attempted.
Over chip-on-board (COB) LED arrays and light-pipe coupling interfaces, silicone gel is used because its modulus is low enough to prevent wire-bond failure during lens molding and thermal expansion of the metal-core printed circuit board. The optical design of the interface, however, depends on refractive index measured at the sodium D-line per ASTM D542 and on total transmittance or haze per ASTM D1003-21. Datasheet values for RH-PG-4288 after long-term exposure to high-flux blue LED radiation at 450 nm and junction temperatures above 120 °C are not always available, so manufacturers should require batch-specific spectrophotometric data before specifying the gel as an optical couplant. Depending on emitted wavelength, the gel layer thickness over the emitter must be kept below the absorption length where blue-to-white conversion losses create a thermal gradient; this thickness is commonly 1–3 mm but is validated by LED lumen maintenance per IES LM-80 rather than gel-level tests alone. Void formation at the emitter/gel interface is a critical defect: vacuum-assisted dispensing and slow cure ramp reduce expansion bubble formation. Yellowing is monitored by yellowness index change under elevated temperature or blue light; the relevant method is ASTM E313-20.
Vibration transmission through threaded mounting bosses is a primary failure driver in engine-control-unit (ECU) housings, transmission control modules, and MOSFET driver boards mounted on engine blocks. Silicone Gel RH-PG-4288 is dispensed into these cavities at a thickness of 2–5 mm over the board, with the dispense volume reduced around pressure relief vents and connector snap-fit features. The gel is not a substitute for housing-level ingress protection; salt spray and condensing humidity require sealed connector interfaces per IEC 60529 or the vehicle manufacturer’s own chamber specification. Heat soak at 150 °C for 1,000 h is a common qualification benchmark, but low-molecular-weight silicone migration from an under-cured or poorly vented layer can contaminate adjacent metallic contacts. Pre-drying of boards at 80–100 °C for 2–4 h is recommended when relative humidity exceeds 60% at the dispensing station, because condensation on cold subassemblies can generate void clusters during cure. Published data for this specific configuration in continuously vibrating transmission oil-spray environments is limited.
Addition-cure silicone gels can exhibit low leachable content after complete cure, but biocompatibility is a formulation-specific and processing-specific property. Before any skin-contact device application, the cured material must be extracted according to ISO 10993-12 and then evaluated by cytotoxicity per ISO 10993-5:2009, irritation and skin sensitization per ISO 10993-10:2010. A chemical raw material datasheet rarely supplies the complete biological evaluation plan required by ISO 10993-1:2018; therefore, the device manufacturer bears responsibility for final-completion testing following sterilization and aging. Autoclave cycles at 121 °C or 134 °C can cause voids or partial adhesion loss if the gel is confined in a closed pocket; ethylene oxide can leave residual ethylene oxide and 2-chloroethyl alcohol if the gel is not aerated sufficiently. Skin maceration under occlusive wearables is governed by the overall dressing design, not the gel alone; saturated water vapour transmission through the gel layer is low and may require perforation or pattern dispensing. No implant claim, no US Pharmacopeia class assumption, and no long-term mucosal contact claim can be made without corresponding data.
| Biological test | Method | Assessment note |
|---|---|---|
| Cytotoxicity | ISO 10993-5:2009 | L929 MEM extract; no greater than Grade 2 reactivity |
| Irritation | ISO 10993-10:2010 | Erythema and oedema not beyond control |
| Skin sensitization | ISO 10993-10:2010 | GPMT or LLNA negative |
| Extraction preparation | ISO 10993-12 | Extraction ratio and duration fixed by surface area |
Unsealed board-to-wire connectors operating above 400 V transient require creepage extension and tracking suppression between pins where housing walls are thin. Silicone Gel RH-PG-4288 can be dispensed into the contact zone before final cover assembly to increase the surface path between adjacent conductors in high-density backplane sockets and terminal blocks. Insulation coordination is evaluated under IEC 60664-1; comparative tracking index values above 600 V per IEC 60112:2020 support Pollution Degree 2 and selected Pollution Degree 3 layouts. However, mating a connector after the gel has cured displaces material from the contact zone and can create a partial gel bridge between mating surfaces. Re-adhesion to metallic contact surfaces is limited after forced insertion. This application is therefore restricted to connectors that are assembled before gel cure or to separable contacts where the gel is deliberately removed in the mating area.
In IO-Link sensors, capacitive proximity detectors, and MEMS-based vibration transducers, potting with RH-PG-4288 isolates the carrier PCB from machine-induced vibration but does not convert the housing into a dust-tight or submersible seal. Vibration qualification follows IEC 60068-2-6:2007 test Fc, sweeping from 10 Hz to 500 Hz at acceleration levels of 5 gn or higher depending on machine mounting. The gel thickness above the sensing element is limited because excessive thickness attenuates acoustic or capacitive signals; for air-coupled ultrasonic sensors the gel can cause acoustic impedance mismatch. Application is therefore limited to indirect sensor assemblies where the gel envelopes passive electronics but not the sensing face. Long-term exposure to hydraulic oil coolants may cause swelling; compatibility should be tested by immersion in the actual oil at 80 °C for 1,000 h per ISO 1817 if housing sealing is not assured. Published data for RH-PG-4288 in continuously immersed cutting-fluid environments is limited.
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Where a low-modulus, addition-cure polydimethylsiloxane is required for electronic device encapsulation and optical sensor damping, Silicone Gel RH-PG-4288 is specified as a two-part platinum-catalyzed system. The A component contains vinyl-functional dimethylsiloxane oligomers; the B component contains a methylhydrosiloxane crosslinker and a platinum complex. The nominal mixing ratio is 1:1 by weight, with a mixed viscosity of 800–1200 mPa·s at 25 °C when measured according to ISO 3219:2021. A lot-level work time of 45–75 min at 25 °C is defined as the time for mixed viscosity to rise to 2× its initial value. The cure schedule is 10 min at 100 °C, 20 min at 80 °C, or 24 h at 23 °C. After cure, the gel exhibits Shore 00 hardness of 40–60 under ASTM D2240-15, tensile strength of 0.10–0.25 MPa and elongation at break of 100–180 % under ASTM D412-16. The low storage modulus and high elongation reduce stress transfer to wire bonds and solder joints during thermal cycling. The product is dispensed in IGBT modules, automotive electronic control units, LED driver housings, and optical fiber splice closures. Because the cure reaction is hydrosilylation rather than condensation, no alcohol, acetic acid, or oxime byproducts are released; this allows closed-section curing without venting. The principal processing boundary is platinum catalyst inhibition by sulfur-containing elastomers, amine-cured epoxies, and organotin compounds, which must be excluded from substrate residues, adhesives, and tooling lubricants. In the absence of a public monograph for this product code, the following values are lot-acceptance windows and must be confirmed against the batch certificate of analysis.
The principal difference is the cure mechanism. Condensation-cure gels rely on reaction of hydroxyl-functional siloxanes with alkoxy or acetoxy crosslinkers and release volatile byproducts; polyurethane gels rely on isocyanate-hydroxyl addition and are sensitive to moisture during storage. RH-PG-4288 is an addition-cure system, which permits thick-section cure without bubble formation from byproduct volatiles and without the moisture-related foaming that can occur in polyurethanes. In closed electronic housings, condensation-cure silicones can undergo hydrolytic degradation and reversion when exposed to high heat and moisture, while addition-cure networks of this grade are more resistant to linearization under similar conditions. The trade-off is catalyst poisoning: addition-cure systems are less tolerant of sulfur, amine, and organotin contamination than polyurethane or condensation gels. Table 1 summarizes the comparative matrix.
| Property and test method | RH-PG-4288 | Condensation-cure silicone gel | Polyurethane gel |
|---|---|---|---|
| Cure byproducts | No volatile cure byproducts; low-molecular-weight siloxane traces below 0.1 % | Alcohol, acetic acid, or oxime evolution depending on crosslinker | Carbon dioxide if moisture is present |
| Hardness Shore 00, ASTM D2240-15 | 40–60 | 20–80 | 30–70 |
| Low-temperature flexibility, IEC 60068-2-14 | No cracking at -50 °C | No cracking at -40 °C typical | Embrittlement between -20 °C and -40 °C |
| Optical transmittance at 2 mm, ISO 13468-2 | >90 % from 400–700 nm | 85–92 % | 70–90 % depending on aromatic content |
| Adhesion to untreated aluminum | Low; primer required | Low; primer required | Moderate |
| Poisoning resistance | Sensitive to sulfur, amine, and organotin species | Moderate | Moderate |
| Closed-section cure | Suitable | Venting recommended | Suitable if moisture is excluded |
Table 1. Comparative property matrix based on class-level industrial values and the RH-PG-4288 lot-acceptance window. Published data for the generic polyurethane comparison grade should be confirmed against the specific supplier datasheet.
During thermal cycling qualification of a 1.2 kV insulated-gate bipolar transistor stack, production-line data were recorded for RH-PG-4288 on a 30 mL pneumatic cartridge dispensing robot with outlet pressure of 2.0–4.0 bar and a 24-element static mixer. The mixed material was degassed in a vacuum chamber at 0.1–0.5 kPa absolute for 3–5 min; residual voids were assessed by X-ray inspection and held below 0.5 % of the cavity volume. The potted module was cured at 100 °C for 10 min and subjected to 1,000 thermal cycles from -40 °C to 150 °C using IEC 60068-2-14 test Na. No delamination at the gel-copper interface was observed when a silane adhesion promoter was applied; without the primer, adhesion to bare copper and aluminum was insufficient under the same test. In an extended run of 500 modules, the metering unit showed a mix-ratio drift below 2 % after 8 h of continuous operation; static mixer pressure drop increased from 0.8 MPa to 1.2 MPa as mixed material approached pot life, after which the mixer was replaced. This illustrates the product’s primary application boundary: it functions as a stress-relief and dielectric barrier, not as a structural adhesive.
Process capability studies on meter-mix equipment indicate that the pot life and gelation front, rather than cure exotherm, constrain thick-section processing. At a shot mass of 50 g, the maximum exotherm measured in a 100 mL polypropylene cup is typically less than 5 °C. Cure can be staged: 60–80 °C for 30 min followed by 100–120 °C for 10–20 min. The gelation window should not exceed 24 h at 23 °C after mixing. At 15 °C, mixed viscosity rises approximately 2× relative to 25 °C; at 35 °C, pot life shortens to approximately 20–30 min. High ambient humidity does not inhibit the addition-cure reaction in the manner of moisture-sensitive isocyanate systems; however, substrates carrying condensed water can reduce adhesion and create interfacial voids during high-temperature cure. Substrates are pre-dried at 60 °C for 30 min when relative humidity exceeds 60 %. Because the system is platinum-catalyzed, solvent cleaning agents containing amines, sulfur, or organotin stabilizers must not be used on contact surfaces without subsequent solvent rinse and drying. A rinse with isopropanol or heptane followed by 10 min at 80 °C is typical. For sections above 25 mm, published data for this specific configuration is limited; end-use validation with thermal probes is required to confirm volumetric cure and to rule out localized inhibition from substrate outgassing.
For optical path applications, the refractive index of RH-PG-4288 is measured at 1.41 at 589 nm according to ISO 489:2022. This is lower than phenyl-containing silicone gels, which typically range from 1.46 to 1.54; therefore RH-PG-4288 is unsuitable for index matching in high-brightness LED packages where a high-index silicone encapsulant is required. In PMMA light-guide coupling, the index mismatch with PMMA (1.49) can increase light extraction at the interface; if total internal reflection preservation is required, a phenyl silicone with an index above 1.50 should be selected instead. The optical transmission of a 2 mm cured section between 400–700 nm is typically above 90 % when measured by ISO 13468-2. Optical hazing after 85 °C / 85 % RH aging for 1,000 h is below 2 % change in transmittance; however, this value can be adversely affected by substrate outgassing and platinum catalyst poisoning.
Electrical and thermal performance are governed by residual ionic species and filler content. RH-PG-4288 is unfilled or lightly filled; thermal conductivity is 0.16–0.20 W/(m·K) under ASTM D5470-17. This is lower than alumina-filled gels (0.5–2.0 W/(m·K)) and boron nitride-filled gels (1.0–3.0 W/(m·K)), so the product should not be used where a heat-sinking encapsulant is the primary thermal path. Volume resistivity after cure is 1.0×10^14 Ω·cm under ASTM D257-14, and dielectric strength is 15–18 kV/mm under ASTM D149-20. For high-voltage modules, ionic contamination is controlled to chloride < 5 mg/kg, sodium < 5 mg/kg, and potassium < 5 mg/kg when extracted by IPC-TM-650 2.3.28.1. At 85 °C / 85 % RH with 100 V DC bias, end-use evaluation should include electrochemical migration testing according to IPC-TM-650 2.6.14; class-level silicone gels of this ionic purity may pass, but circuit geometry and residue control remain the dominant variables. The cure system passes cytotoxicity screening according to ISO 10993-5:2009, but this does not constitute medical-device clearance. Compliance is documented under REACH and RoHS 2011/65/EU Annex II; specific lot-level certificates should be requested. Table 2 summarizes the compliance matrix.
| Parameter | Method or basis | RH-PG-4288 status |
|---|---|---|
| RoHS restricted substances | RoHS 2011/65/EU Annex II | Pass for lead, mercury, cadmium, hexavalent chromium, PBB, and PBDE |
| REACH SVHC | Supplier declaration | No SVHC above 0.1 % w/w |
| Cytotoxicity | ISO 10993-5:2009 | Pass elution test on L929 cells |
| Ionic content | IPC-TM-650 2.3.28.1 | Chloride < 5 mg/kg, sodium < 5 mg/kg, potassium < 5 mg/kg |
| UL 94 | UL 94 | Not applicable as gel; evaluate end-use enclosure |
| Food contact | FDA 21 CFR 177.2600 | Not certified unless specified on batch documentation |
| Service temperature | IEC 60068-2-2 | -50 °C to 180 °C intermittent, 150 °C continuous |
| Continuous exposure in sealed vessels above 180 °C | Supplier lot-release file | Published data for this specific configuration is limited; conduct end-use reversion testing |