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Underfill Adhesive (High Fluidity) Electronic/EL Grade

    • Product Name: Underfill Adhesive (High Fluidity) Electronic/EL Grade
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
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    Specifications
    HS Code 898759
    Viscosity At 25 C 400-700 mPa·s
    Glass Transition Temperature Tg 130-145°C
    Cure Temperature 150°C
    Cure Time 5-10 minutes
    Shelf Life 6 months
    Storage Temperature -10°C to 5°C
    Filler Content 60-70 wt% silica
    Coefficient Of Thermal Expansion Below Tg 20-25 ppm/°C
    Dielectric Constant 1 Mhz 3.5-4.0
    Volume Resistivity ≥1 x 10^15 ohm·cm
    Moisture Absorption ≤0.3%

    As an accredited Underfill Adhesive (High Fluidity) Electronic/EL Grade factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Packaged in 10 mL sealed syringes with dispensing tips; high-fluidity Electronic/EL Grade underfill adhesive for precise, contamination-free application.
    Container Loading (20′ FCL) 20′ FCL: secure drums/pails, protect from moisture and heat, proper labeling, no mixing with incompatible goods.
    Shipping Underfill Adhesive (High Fluidity, Electronic/EL Grade) ships in sealed, contamination-free containers. Transport complies with IATA/IMDG/ADR regulations for chemical adhesives. Keep away from heat, moisture, and sunlight. Ensure proper labeling, and avoid skin contact during handling and transit.
    Storage Store Underfill Adhesive (High Fluidity Electronic/EL Grade) in its original tightly sealed container in a cool, dry, refrigerated environment at 2–8°C. Protect from moisture, direct light, and heat sources. Avoid freezing. Allow product to reach room temperature before opening to prevent condensation. Follow manufacturer’s expiry and rotation guidelines.
    Shelf Life Shelf life is typically six months when stored unopened at -40°C, protected from light and moisture.
    Application of Underfill Adhesive (High Fluidity) Electronic/EL Grade

    What Determines Capillary Flow Completion in High-Density WLCSP Flip-Chip Assembly?

    The capillary underfill process for 0.4 mm pitch WLCSP devices mounted on organic substrates is governed by the interrelationship between filler particle size distribution, resin viscosity at the dispense temperature, and die standoff height. Industry compliance for this application segment is established through IPC-A-610H Class 3 workmanship requirements, IPC/JEDEC J-STD-020E moisture sensitivity classification at MSL 3, and RoHS Directive 2011/65/EU as amended by Commission Delegated Directive (EU) 2015/863. The material is applied as a single-component liquid without solvent addition. The formulation addition ratio commonly used in high-fluidity electronic/EL grade underfill places fused silica filler content between 50 wt% and 65 wt%, with a viscosity of 0.8 Pa·s to 8.0 Pa·s at 25 °C when measured by ASTM D2196-20 using a Brookfield spindle SC4-14 at 10 rpm. For a 5.0 mm × 5.0 mm die with a standoff of 45 µm to 55 µm, the metered dispense mass is calculated as V = k·A·h, where A is the die area, h is the standoff, and k is a fillet factor between 1.3 and 1.8; this yields a typical per-die dispense mass of 2.0 mg to 3.5 mg. The downstream production sequence begins with substrate prebaking at 125 °C for 4 h to remove absorbed moisture, followed by argon/oxygen plasma cleaning at 200 W to 300 W to raise surface energy on solder mask and die passivation. The underfill is dispensed with a positive displacement auger valve through a 0.10 mm to 0.20 mm stainless steel needle along one or two edges of the die. The substrate stage is held at 80 °C to 95 °C to reduce transient viscosity and accelerate capillary flow; flow completion for a 5 mm die is typically specified at less than 30 s. Void content is inspected after cure by scanning acoustic microscopy at 30 MHz to 100 MHz; voids greater than 0.3 mm² or occupying more than 2% of die area are rejected under Class 3 criteria. Curing is performed in a forced convection tunnel or batch oven at 150 °C for 30 min, with ramp rates limited to 3 °C/min to avoid fillet cracking. Terminal finished product types include smartphone mainboards, tablet logic boards, wearable modules, and other high-density organic substrate assemblies where WLCSP components require mechanical stress relief under repeated thermal cycling.

    ParameterTest methodTypical industrial acceptance band
    Viscosity at 25 °CASTM D2196-20, Brookfield SC4-14, 10 rpm0.8–8.0 Pa·s
    Fused silica filler contentISO 3451-1:2019 ashing at 600 °C50–65 wt%
    CTE below glass transitionASTM E831-19, TMA22–35 ppm/°C
    Glass transition temperatureASTM D3418-15, DSC at 10 °C/min120–155 °C

    Within RF front-end module assembly on low-temperature co-fired ceramic (LTCC) substrates, the underfill is applied after lead-free reflow and dispense is performed on the component side at a stage temperature of 70 °C to 85 °C. Industry compliance for this downstream segment follows J-STD-020E MSL 3 for moisture sensitivity, JEDEC JESD22-A104E Condition G thermal cycling for package-level qualification, and RoHS Directive 2011/65/EU with Delegated Directive (EU) 2015/863 for restricted substances. The formulation addition ratio for LTCC modules is typically a fused silica filler loading of 55 wt% to 65 wt%, adjusted downward from high-reliability ceramic grades to maintain flow under a 3.0 mm × 3.0 mm flip-chip die with 40 µm to 60 µm standoff. The dispense mass for this die size is between 1.0 mg and 2.5 mg, calculated from the same fillet-volume factor used in WLCSP work. Plasma cleaning with argon at 150 W to 200 W is performed prior to underfill to remove flux residues from the solder joints, because residual flux can inhibit capillary wetting and produce selective delamination at the solder mask/LTCC boundary. After dispense, the assembly is held at 80 °C for 60 s to allow complete flow, then cured in a batch oven at 150 °C for 60 min. Terminal finished product types include 5G RF front-end modules, antenna-in-package modules, and narrowband IoT transceiver boards where the thermal expansion mismatch between gallium arsenide or silicon germanium die and LTCC requires controlled underfill coverage without bridging adjacent passives.

    Automotive Camera Module Flip-Chip Reliability Limits

    Adhesive selection for automotive flip-chip image sensor packages is constrained by the requirement to survive temperature cycling from -40 °C to 125 °C without delamination at the silicon dioxide passivation interface. Package-level compliance is tested according to JEDEC JESD22-A104E Condition G, 1000 cycles, and component qualification follows AEC-Q100 Grade 2 for forward-looking camera modules; Grade 1 may be required when the module is located in an engine bay or high-ambient environment. The adhesive must also meet RoHS Directive 2011/65/EU and REACH Regulation (EC) No 1907/2006 for EU-bound automotive supply chains. The formulation addition ratio in this segment is typically shifted toward a higher fused silica filler loading of 60 wt% to 70 wt%, accepting a trade-off in capillary flow to achieve a CTE below 28 ppm/°C measured by ASTM E831-19. For an 8.0 mm × 8.0 mm sensor die with 60 µm standoff, the single-side dispense mass is commonly 8.5 mg to 10.5 mg. The downstream process includes substrate prebake at 125 °C for 8 h, followed by vacuum-assisted underfill dispense at 5 mbar to 10 mbar to reduce trapped air under low-clearance solder joints. Cure is performed at 150 °C for 60 min, and the module is subjected to post-cure outgassing evaluation because condensed volatiles on the image sensor cover glass cause dark-current drift. Ionic purity is controlled because mobile chloride and sodium ions accelerate electrochemical migration at the fine-pitch peripheral pad geometry. Terminal finished product types include ADAS forward-looking cameras, surround-view cameras, and LiDAR receiver modules where thermomechanical reliability and low outgassing are co-dominant requirements.

    After solder ball collapse in a package-on-package stack, the underfilled interface between the bottom application processor package and the top LPDDR memory package is filled by capillary action along the exposed joint perimeter. Industry compliance for this PoP segment includes IPC-A-610H Class 3 for mobile high-reliability assemblies, IPC/JEDEC J-STD-020E MSL 3, and RoHS Directive 2011/65/EU as amended by Commission Delegated Directive (EU) 2015/863. The addition ratio is maintained at 55 wt% to 65 wt% fused silica, with a dispense viscosity below 4.5 Pa·s at 25 °C to ensure penetration across a 14.0 mm × 14.0 mm PoP gap of 80 µm to 120 µm without edge-only fillet starvation. The metered dispense mass for this geometry is 25 mg to 40 mg, applied along two adjacent package edges using a jet dispensing system with 0.20 mm to 0.30 mm nozzle diameter. Process order matters in this segment: underfill is applied only after reflow joint formation because dispense before reflow can cause component shift during solder melting. After dispense, the assembly is held at 85 °C for 90 s to complete fillet formation under the top package, then cured at 150 °C for 30 min with a 2 °C/min ramp rate to limit warpage on the thin core substrate. Void inspection is performed by scanning acoustic microscopy at 50 MHz, with rejection criteria set at 1.5% of the total PoP interface area. Terminal finished product types include smartphone application processor and LPDDR4/LPDDR5 stacks, tablet PoP assemblies, and compact edge computing modules where repeated drop and thermal loads are transferred directly through the underfilled joint.

    When a 40 µm Interposer Gap Restricts Capillary Flow in HBM and 2.5D Package Assembly

    Capillary underfill penetration below a 50 µm standoff is governed by the Washburn equation, where flow length scales with the square root of time and inversely with viscosity; in 2.5D packaging, the interposer gap of 35 µm to 45 µm creates a process threshold at which filler particle size distribution rather than bulk viscosity becomes the dominant yield loss mechanism. Compliance for this segment is anchored to IPC/JEDEC J-STD-020E MSL 2 or MSL 3, JEDEC JESD22-A104E Condition G thermal cycling, and RoHS Directive 2011/65/EU; for AI accelerator modules destined for data center use, JEDEC JESD22-A113E preconditioning may be specified before temperature cycling. The formulation addition ratio for high-fluidity interposer underfill is typically set at 40 wt% to 55 wt% filler loading, with a maximum individual particle diameter below 0.7 µm and D99 below 3.0 µm to pass through 25 µm40 µm gaps without particle bridging. The dispensed mass for a 1100 mm² silicon interposer area with 40 µm gap is calculated as 80 mg to 110 mg including a fillet factor of 1.2 to 1.6. The lower filler loading in this configuration reduces viscosity but also raises the CTE toward 35 ppm/°C to 40 ppm/°C, which is acceptable only when the interposer and mold compound provide secondary mechanical constraint. Dispensing is performed from two adjacent edges of the bonded HBM stack with the stage held at 90 °C to 100 °C, and a vacuum chamber at 3 mbar to 5 mbar is applied for 5 min to prevent void formation in the sub-50 µm gap. Cure uses a stepped profile of 100 °C for 30 min followed by 150 °C for 60 min; dynamic warpage is measured by thermal shadow moiré before and after cure. Terminal finished product types include high-bandwidth memory stacks on silicon interposers, 2.5D packages for AI training and inference accelerators, and high-performance computing modules where die-level stress from CTE mismatch must be reduced without sacrificing package-level electrical continuity through the silicon interposer.

    MCM-C Ceramic Hermetic Module Underfill in MIL-STD-883 Class K Applications

    Hermetic multichip modules built on alumina substrates require underfill only when flip-chip devices are present without hermetic cavity sealing; the underfill must not compromise outgassing limits and must withstand high-temperature storage at 150 °C. Industry compliance is defined by MIL-STD-883E Method 5011 for polymeric materials, JEDEC JESD22-A104E Condition G for temperature cycling, and, for export-controlled defense modules, MIL-PRF-38534 or MIL-PRF-38535 as applicable to the hybrid assembly. The filler loading in this application segment is 60 wt% to 70 wt% fused silica to achieve CTE matching to alumina, and the underfill is dispensed at 1.5 mg to 3.0 mg per 4.0 mm × 4.0 mm flip-chip device. Published data for high-fluidity underfill in Class K ceramic hybrids is limited; qualification campaigns therefore rely on internal material characterization according to ASTM E595-15 outgassing, ASTM E831-19 CTE, and ASTM D3418-15 glass transition measurement rather than vendor-supplied nominal values. The downstream process includes ceramic substrate prebake at 150 °C for 12 h, argon plasma activation, manual or automated needle dispense at 0.10 mm needle diameter, vacuum-assisted flow at 10 mbar for 3 min, and cure at 150 °C for 60 min under nitrogen. After cure, the module is subjected to gross leak testing and ionic contamination testing in accordance with MIL-STD-883E Method 5011. Terminal finished product types include aerospace transponder multichip ceramic modules, military radar MMIC modules, and high-reliability hybrid modules where the underfill must function not as a cosmetic fillet but as a structural agent preventing passivation cracks in extreme thermal-shock environments.

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    Certification & Compliance
    More Introduction

    The product designated UFH-EL-4100 is a single-component, high-fluidity capillary underfill adhesive supplied in frozen syringe and cartridge formats for electronic/EL-grade assembly. The resin matrix is a low-chloride bisphenol F epoxy with a cycloaliphatic anhydride hardener and a submicronic fused-silica filler. The filler median particle size is controlled below 0.5 µm because fine-pitch gap channels can be blocked by a small population of oversize particles. The electronic/EL designation is confirmed by limits on extractable chloride, sodium, and potassium; by a cured volume resistivity above 1.0 × 10¹² Ω·cm; and by low outgassing values measured under vacuum. The material is intended for post-reflow capillary flow between the silicon die and organic substrate in flip-chip, chip-scale package, and ball-grid-array assemblies with standoff heights below 50 µm. It is not a no-flow underfill; it is dispensed after solder joint formation and is not designed to be trapped in the solder joint during reflow.

    Which Acceptance Criteria Define the Electronic/EL Grade Material?

    Because high-fluidity capillary underfill is used in high-impedance and long-life electronic packages, the acceptance window is established by rheological, thermal, electrical, and cleanliness tests. The low-shear viscosity is 2.5 Pa·s at 25 °C by ASTM D2196-20, with a thixotropic index of 1.1 measured by the same method. Filler loading is controlled at 55 wt% by ASTM E1131-20 thermogravimetric analysis; this loading is selected to reduce the coefficient of thermal expansion without raising the viscosity above capillary-fill limits. The cured glass transition temperature is 135 °C by ISO 11357-2:2020 differential scanning calorimetry. The coefficient of thermal expansion below Tg is 28 ppm/K and above Tg is 85 ppm/K by ISO 11359-2:1999. Electrical acceptance values include a volume resistivity of 1.0 × 10¹² Ω·cm after 168 h at 85 °C/85% RH by ASTM D257-14, a dielectric constant of 3.4 at 1 MHz by ASTM D150-18, and outgassing total mass loss of 0.05% with collected volatile condensable material of 0.01% by ASTM E595-15. The cleanliness requirement is particularly stringent for electronic/EL grade: extractable chloride, sodium, and potassium are each held below 5 ppm when tested by the ion chromatography procedure of IPC-TM-650 2.3.28.

    PropertyAcceptance CriterionTest Method
    Low-shear viscosity at 25 °C2.5 Pa·sASTM D2196-20
    Filler loading55 wt%ASTM E1131-20
    Glass transition temperature135 °CISO 11357-2:2020
    CTE below Tg / above Tg28 ppm/K / 85 ppm/KISO 11359-2:1999
    Extractable Cl⁻, Na⁺, K⁺<5 ppm eachIPC-TM-650 2.3.28
    Volume resistivity after 168 h at 85 °C/85% RH1.0 × 10¹² Ω·cmASTM D257-14
    Dielectric constant at 1 MHz3.4ASTM D150-18
    Outgassing TML / CVCM0.05% / 0.01%ASTM E595-15

    Because the filler is a fused silica with median particle size below 0.5 µm and a maximum particle size controlled by a sieve residue test, the suspension exhibits moderate shear-thinning behaviour at elevated dispense rates. The yield stress is below 0.5 Pa, which allows the material to flow under capillary pressure alone at a preheat temperature of 80 °C to 110 °C. The particle size distribution is bimodal to increase filler packing without increasing low-shear viscosity; an excess of particles below 100 nm can raise the yield stress and reduce the capillary fill front velocity. The silica surface is treated with an epoxy-silane coupling agent to improve adhesion to silicon nitride and solder mask and to reduce moisture adsorption at the filler-matrix interface. This surface treatment is important for electronic/EL grade because interfacial moisture can raise the dissipation factor and reduce insulation resistance after biased humidity testing.

    Capillary dispensing occurs after reflow and after flux residue removal or verification. The substrate is preheated between 80 °C and 110 °C to reduce the resin viscosity and to raise the surface energy of the solder mask and silicon nitride passivation. The fill front advances according to the Washburn relationship; fill time is directly proportional to viscosity and the square of the fill length, and inversely proportional to surface tension, contact-angle cosine, and gap height. For a die length of 10 mm and a standoff of 25 µm, a resin with viscosity below 3 Pa·s at the preheat temperature typically completes edge-to-edge fill in less than 60 s; the value is not universal and must be confirmed on the actual die and substrate pad geometry. On production lines using positive-displacement dispensing equipment, the material is applied as one or two continuous beads along adjacent die edges. A tapered stainless-steel needle with an internal diameter above 10 µm reduces shear heating and avoids bridging of oversize filler particles. Needle idle time is a critical process variable: at 25 °C and 60% RH, a static exposed meniscus can skin in approximately 20 s, and that skinned layer can interrupt the next dispense pulse or become a void nucleus at the fillet edge. Jetting valves are acceptable only if the fluid path has no recirculation dead zone and the valve run-down confirms that the thixotropic index remains below 1.2 after 8 h of intermittent operation.

    The dispense pattern determines whether the fillet remains continuous around the die perimeter. A single L-shaped pass along two adjacent edges often produces a more uniform fill front than a U-shaped pass because air exits at the opposite corner. The fillet height should be below the die top surface unless the design specifically requires a fillet climb. Excess fillet can wick onto the die backside and alter the thermal interface material contact area. The cured fillet width is controlled by the dispensed volume, needle speed, and surface tension; a fillet width of 0.3–0.8 mm is representative for a 5 mm die. This practical process window should be established with shadow moiré or laser profilometry on the first production build.

    Mechanical Property Evolution During Snap Cure and Post-Cure Drift

    The one-part epoxy-anhydride system is cured by an autocatalytic mechanism after an initial thermal trigger. A typical in-line cure profile is 150 °C for 30 min or 165 °C for 10 min; the shorter profile is valid only when thermocouple data from the package die area demonstrate that the adhesive has reached the specified temperature. The final reaction conversion is sensitive to oven exit cooling rate. A cured glass transition temperature below 125 °C indicates undercure, moisture contamination, or incomplete thawing of the frozen cartridge. The flexural modulus after full cure is 8.5 GPa by ISO 178:2019. Adhesion to silicon nitride and solder mask is specified as a die shear value greater than 25 MPa after 260 °C reflow preconditioning. The cured network retains a measurable post-cure drift in the first 48 h after cool-down; assemblies should not proceed to accelerated reliability testing until this post-cure period has elapsed. Filler settling during frozen storage and thawing can create a viscosity gradient in the syringe; cartridges are thawed upright and gently rolled by hand, not shaken or placed on a mechanical mixer. High-volume manufacturing lines using progressive-cavity pumps have observed that air entrapment at cartridge changeover is the most common cause of intermittent fill voids, followed by needle tip skinning.

    When the Interconnect Pitch Falls Below 40 µm, Capillary Underfill Must Displace Flux Residue Without Vapor Entrapment

    At pitches below 40 µm, the gap height can fall below 20 µm, and the capillary pressure required to move the fill front approaches the pressure required to displace a thin no-clean flux film. If the viscosity at the preheat temperature is too high, the resin can flow around flux residues rather than displacing them, leaving trapped pockets that become crack-initiation sites during thermal cycling. The high-fluidity grade is formulated with a non-amine wetting additive that lowers the advancing contact angle on solder mask to below 20° without increasing extractable ionic content. For a gap of 15 µm, the corresponding capillary pressure exceeds 50 kPa. The user must verify compatibility with the specific no-clean flux because acidic residues can protonate the latent accelerator and alter cure kinetics at the interface. Underfill voiding is best detected by C-mode scanning acoustic microscopy after cure; acceptance limits for void area are process-specific and should be tied to thermal-cycle failure data, not to a universal threshold. Published data for this specific configuration is limited, so a design of experiments on the production substrate stack is required before setting a pass/fail criterion.

    In addition to extractable chloride and alkali metal limits, the resin is controlled for ammonium and sulfate ions. The total extractable conductivity of the cured material after 7 days in deionized water at 85 °C is below 20 µS/cm by the extraction procedure of IPC-TM-650 2.3.25. This is relevant for high-impedance circuits where ionic migration can reduce surface insulation resistance. The product is formulated without intentionally added boron, antimony, or halogenated flame retardants, which supports a RoHS-compliant bill of materials under Directive 2011/65/EU Annex II. Users must verify final article compliance because the printed circuit board and solder mask also contribute extractable ions.

    Storage, Thawing, and Pot Life Are Controlled by Moisture Uptake and Shear History

    Frozen storage at -40 °C or below is required. The sealed syringe or cartridge must equilibrate to 23 ± 2 °C before opening; opening a cold container causes condensation that introduces water into the anhydride cure system. A 10 mL syringe requires approximately 4 h of static thaw, and a 30 mL cartridge can require 8 h to 12 h. The working pot life of opened material is 72 h at 25 °C when protected from moisture; at 60% RH the useful life is reduced to approximately 24 h because water hydrolyses anhydride groups and shifts the cure exotherm. Do not add amine-based accelerators or adhesion promoters; free amines cause room-temperature crosslinking and can raise the resin viscosity beyond the dispensing window in a matter of minutes. Ultrasonic mixing is not permitted after thaw because cavitation can fracture or re-agglomerate the filler and shift the maximum particle size above the needle-passing limit. The material is not compatible with condensed moisture on the substrate; substrate preheat should be maintained above the dew point of the assembly area to prevent water films at the flow front.

    Comparative Process Windows for Capillary, No-Flow, and Perimeter Adhesive Routes

    High-fluidity capillary underfill is post-reflow and fills the complete die-to-substrate gap. No-flow underfill is dispensed before die placement and is compressed during reflow; it removes the post-reflow dispense step but can interfere with solder joint collapse if the filler content is too high. Edge-bond and corner-bond materials are applied only along the die perimeter after reflow; they reinforce the die edge but do not fill the bump array. The electronic/EL grade is selected when the assembly requires complete bump coverage, low void content, a CTE between that of the die and substrate, and controlled ionic purity for high-impedance circuits. The comparative process envelope is summarised in Table 2.

    AttributeHigh-fluidity capillary underfillNo-flow underfillEdge-bond/corner-bond
    Application timingPost-reflowPre-reflowPost-reflow
    Full die-to-substrate gap fillYesYesNo
    Practical minimum standoff15 µm30 µmNot gap-limited
    Filler loading55 wt%35–50 wt%0–20 wt%
    Primary limitationCapillary flow time and void controlSolder joint collapse interferenceNo protection of interior bumps

    Reliability qualification of underfilled assemblies is commonly conducted under JEDEC JESD22-A104 thermal cycling from -55 °C to 125 °C for consumer electronics or from -40 °C to 85 °C for telecommunications infrastructure. The underfill is not a structural adhesive in the conventional sense; its function is to redistribute shear strain from the solder bump array to the die and substrate. The silicon die CTE is approximately 2.6 ppm/K, and the organic substrate CTE is generally 12–18 ppm/K; this mismatch creates recurring shear deformation in thermal cycling. The specified CTE values of the underfill are 28 ppm/K below Tg and 85 ppm/K above Tg. The above-Tg value is intentionally higher because a low CTE above Tg would raise the high-temperature modulus and transfer excessive stress to the die backside. Thermal-cycle life is strongly dependent on die size, substrate construction, and void population; a cycle-count prediction for a given package cannot be transferred from one supplier data sheet to another. Qualification data for this specific configuration is limited, and the user should generate finite-element model validation and thermal-cycle failure data on the actual assembly stack before setting a reliability target. The product has not been evaluated for direct contact with unbuffered acidic flux residues or for immersion in liquid water at operating temperature.

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