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Film Stripping Solution Electronic/EL Grade

    • Product Name: Film Stripping Solution 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 253253
    Product Name Film Stripping Solution Electronic/EL Grade
    Appearance Clear colorless liquid
    Chemical Composition Proprietary blend of organic amines and polar solvents
    Active Content 98.0% minimum
    Specific Gravity At 20 C 0.850 - 0.950
    Ph 9.0 - 11.0
    Water Content ≤0.5%
    Chloride Content ≤1 ppm
    Trace Metals Each ≤0.1 ppm
    Non Volatile Residue ≤10 ppm
    Particulate Count At 0 2 µm ≤100 particles/mL
    Solubility In Water Soluble

    As an accredited Film Stripping Solution 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 a 4 L amber HDPE bottle with secure closure, labeled as Electronic/EL Grade Film Stripping Solution. Handle with care.
    Container Loading (20′ FCL) 20' FCL loaded with Film Stripping Solution (Electronic/EL Grade) — drums secured, labeled as chemical, ready for safe transport.
    Shipping Ship Film Stripping Solution (Electronic/EL Grade) as a hazardous chemical. Use UN-approved containers, isolate from incompatible materials, and follow strict temperature controls. Ensure proper labeling, documentation, and compliance with DOT/IATA regulations. Only trained personnel handle transport, with spill containment and emergency protocols readily available.
    Storage Store Film Stripping Solution Electronic/EL Grade in a tightly sealed original container in a cool, dry, well-ventilated area away from direct sunlight, heat, ignition sources, and incompatible materials such as strong oxidizers or acids. Keep container upright, protected from moisture and physical damage. Ensure proper labeling and segregation, with suitable spill containment and emergency access.
    Shelf Life Shelf life is typically 12 months from manufacture date when stored unopened in original container under recommended conditions.
    Application of Film Stripping Solution Electronic/EL Grade

    In front-end semiconductor lithography, high-dose ion implantation at doses above 1×1015 atoms/cm2 creates a cross-linked photoresist crust that conventional dry ashing cannot fully remove without leaving carbonaceous residues on silicon, poly-silicon, or shallow trench isolation structures. Electronic/EL grade film stripping solution is introduced in wet-bench or single-wafer spray tools immediately after ash; the solution operates at 65–85 °C with immersion times between 10 min and 30 min for batch immersion, or 45–90 s in single-wafer dispensing at flow rates of 1.0–1.5 L/min. Typical alkaline formulations contain 40–70 wt% of a polar aprotic solvent such as NMP or DMSO, 10–30 wt% of an alkanolamine such as monoethanolamine or 2-(2-aminoethoxy)ethanol, and 5–15 wt% ultrapure water, with tetramethylammonium hydroxide content below 5 wt% to accelerate cleavage of ester linkages in 193 nm photoresist polymers. EL-grade certification limits each alkali metal and transition metal to <10 ppb, as measured by inductively coupled plasma mass spectrometry in cleanroom-controlled samples, and liquid-borne particle counts are held below 50 particles/mL at 0.1 µm nominal sensitivity. Recirculation through 0.05 µm polytetrafluoroethylene cartridge filters at 10–15 L/min per 50 L bath maintains particulate cleanliness, while megasonic transducers operating at 780–950 kHz provide cavitation-assisted removal without damaging sub-30 nm gate structures. Fluid-contact polymer components are specified according to SEMI F57-0702, and cleanroom handling follows ISO 14644-1:2015 Class 5. The terminal devices are CMOS logic, DRAM, 3D NAND, and analog integrated circuits; the primary processing bottleneck observed in production is batch-to-batch variation in crust removal rate when the ash step overshoots by more than 10%, requiring extension of stripping time or elevated temperature.

    When Does EL-Grade Film Stripping Solution Replace NMP-Only Chemistries in Copper Dual-Damascene Post-Via Reveal?

    At the 14 nm node and below, post-ash residues on copper/low-k interconnects contain organometallic copper oxide complexes and fluorinated etch polymers that require selective solvation without increasing porous low-k dielectric surface roughness. An EL-grade aqueous alkaline stripper based on 30–50 wt% DMSO, 20–35 wt% monoethanolamine, 10–20 wt% water, and 0.5–2.0 wt% benzotriazole or 5-phenyltetrazole as copper corrosion inhibitor is dispensed in a single-wafer spin processor at 20–35 °C for 60–120 s. The low process temperature suppresses copper oxide growth below 0.5 nm equivalent thickness and maintains surface roughness change on carbon-doped oxide low-k films below 0.3 nm RMS as measured by atomic force microscopy on 1 µm × 1 µm scan areas. Dissolved oxygen is sparged with filtered nitrogen to below 50 ppb, measured with an optical oxygen probe in the chemical delivery line; the oxidation-reduction potential of the bath is maintained between -200 mV and -50 mV versus Ag/AgCl reference electrode. The stripper is recirculated through a 0.05 µm polytetrafluoroethylene membrane filter upstream of the dispense nozzle, and rinse is performed with ultrapure water having a resistivity of 18.2 MΩ·cm at 25 °C. Wafer-level purity limits for the EL-grade stripper are specified as <5 ppb for total copper and <1 ppb for chromium, nickel, and iron, verified by inductively coupled plasma mass spectrometry after 30 min acid digestion of a 100 mL sample. Where NMP is present, REACH Regulation (EC) No 1907/2006 Annex XVII entry 71 restricts its use unless specific derogations apply; many European fabs therefore specify NMP-free variants at this process step. The terminal product is a dual-damascene copper interconnect module; the main production failure mode is galvanic corrosion at the copper/barrier interface when the inhibitor is depleted below 0.4 wt% due to bath aging, which is monitored by cyclic voltammetric stripping analysis every 4 h.

    Array fabrication on Gen 8.5 and Gen 10.5 glass substrates requires removal of positive-tone photoresist after wet-etch patterning of molybdenum, aluminum, and indium tin oxide films without mobilizing alkali ions into the thin-film transistor channel. EL-grade film stripping solution is delivered through conveyorized shower or curtain-coater strip units at 40–55 °C with glass throughput between 4 m/min and 8 m/min, yielding contact times of 60–120 s before a 1.5 MPa air-knife drying zone. Formulations for display array stripping are typically diluted 1:5 to 1:10 with ultrapure water at point of use, reducing viscosity to below 2.0 mPa·s and enabling uniform coverage across 2.94 m × 3.37 m Gen 10.5 substrates. The critical ionic specification is sodium plus potassium below 5 ppb and total trace metals below 50 ppb, because mobile alkali contamination shifts threshold voltage by more than 0.1 V when surface concentration exceeds 1×1011 atoms/cm2 at the channel interface. Recirculating belt-type immersion tanks install 0.1 µm high-flow bag filters and in-line organic carbon analyzers; when total organic carbon exceeds 50 mg/L above fresh-bath baseline, the bath is replenished at a rate of 2–5 L per panel to maintain strip rate. Terminal products are amorphous silicon and oxide TFT backplanes for LCD televisions, as well as low-temperature polycrystalline silicon and organic light-emitting diode backplanes; final display modules must conform to RoHS Directive 2011/65/EU where applicable. Production-scale failure modes include photoresist redeposition in the rinse section if the intermediate rinse flow drops below 20 L/min per glass sheet width meter.

    If Molded Fan-Out Wafer-Level Packaging Uses Dry-Film Photoresist for Redistribution Layers

    If molded fan-out wafer-level packaging uses dry-film photoresist for redistribution layers, the stripping solution must remove acrylate-based dry film from copper pillars, epoxy mold compound, and cured polyimide without inducing delamination at the mold compound interface. The EL-grade stripper is typically formulated with 20–40 wt% NMP-free polar aprotic solvent, 15–25 wt% aminoethoxyethanol, 5–10 wt% potassium hydroxide or tetramethylammonium hydroxide, 1–3 wt% surfactant, and the balance ultrapure water. Processing occurs in batch immersion tools with wafer cassettes rotating at 20–30 rpm or in panel-level tools handling 600 mm × 600 mm molded frames; bath temperature is maintained at 55–70 °C and strip time is 5–15 min, depending on dry-film thickness of 15–40 µm. To prevent post-strip surface oxidation of electroplated copper traces, the bath is purged with nitrogen to keep dissolved oxygen below 100 ppb and a triazole inhibitor is held between 0.5 wt% and 1.5 wt%. The rinse sequence uses ultrapure water of 18.2 MΩ·cm at 25 °C for 10 min, followed by a 0.5 min fast-dump cascading rinse. Residual solvent on mold compound is controlled by thermal desorption-gas chromatography, with acceptance criterion below 1 µg/cm2 total organic residue on mold compound coupons. For REACH compliance, substances of very high concern are held below 0.1% by weight in the as-supplied stripper under Regulation (EC) No 1907/2006. Terminal products include application processors, power management integrated circuits, and radio-frequency modules in molded fan-out packages. The process bottleneck is wafer warpage caused by thermal expansion mismatch when bath temperature drifts above 70 °C; warpage is measured by shadow moiré at 25 °C and must remain below 2.0 mm across a 300 mm molded wafer.

    Comparative operating windows for EL-grade film stripping solution illustrate the asymmetric process demands across six downstream segments.

    Application sectorDominant residue classProcess temperatureContact timeFiltration ratingCritical control limit
    Front-end ion-implant photoresistCross-linked carbonaceous crust65–85 °C10–30 min batch / 45–90 s single-wafer0.05 µm PTFEStrip-rate batch drift < 10%
    Copper dual-damascene post-via revealCu-organic complexes, fluorinated etch polymer20–35 °C60–120 s0.05 µm PTFE membraneInhibitor > 0.4 wt%
    TFT-LCD/OLED array strippingPositive photoresist after wet etch40–55 °C60–120 s0.1 µm bag filterNa+K < 5 ppb
    Fan-out wafer/panel-level packagingDry-film acrylate residue55–70 °C5–15 min0.05 µm PTFEWarpage < 2.0 mm
    GaN LED metal lift-offMetal-clad resist edge bead45–60 °C20–45 min0.05 µm PESTotal aluminum < 500 ppb in bath
    HDI PCB and IC substrate solder mask removalAlkaline-strippable solder mask residue50–65 °C2–5 min0.1 µm bag filterIonic cleanliness < 1.56 µg/cm² NaCl equivalence

    Metal Lift-Off in GaN LED Fabrication Demands Low-Aluminum and Low-Silicon Stripper Speciation

    Metal lift-off in GaN LED fabrication demands stripper formulations with total aluminum below 1 ppb and total silicon below 10 ppb, because carryover onto p-GaN or indium tin oxide current-spreading layers creates point defects that reduce electroluminescence uniformity. After electron-beam evaporation of the p-contact metallization, the residual metal-clad photoresist is removed by immersion in EL-grade film stripping solution at 45–60 °C for 20–45 min in ultrasonic or megasonic tanks operating at 350–450 kHz with power density below 10 W/L to prevent delamination of the underlying sapphire. The solution consists of 45–60 wt% NMP or DMSO, 15–25 wt% amine solvent, 5–10 wt% water, and a low-sodium surfactant package, with sodium and potassium each controlled below 2 ppb. Bath recirculation through 0.05 µm polyethersulfone filters at 5–8 L/min for a 30 L tank removes detached metal flakes before they redeposit. The post-strip rinse uses overflow immersion in ultrapure water conforming to ASTM D5127-13 Type E-1 for 15 min until the rinse water reaches a resistivity of at least 1 MΩ·cm. Terminal products are indium gallium nitride multi-quantum well light-emitting diodes for display, horticultural lighting, and automotive forward lighting. A production-scale limitation is the accumulation of dissolved aluminum in the bath from metal lift-off; bath aluminum concentration is monitored every 8 h by ICP-MS and the bath is discarded when total aluminum exceeds 500 ppb.

    High-density IC substrate and flexible printed circuit manufacturing requires removal of alkaline-strippable solder mask or coverlay photoresist from microvia walls, embedded trace surfaces, and chip-attach pads without leaving ionic residues that compromise wire-bond pull strength or anisotropic conductive film adhesion. EL-grade film stripping solution in conveyorized spray equipment operates at 50–65 °C with nozzle pressure between 0.2 MPa and 0.4 MPa, contact time of 2–5 min, and an intermediate rinse stage at 15–20 L/min per 500 mm working width. The stripper is formulated as a high-water-content alkaline blend with 10–25 wt% polar aprotic solvent, 5–15 wt% amino alcohol, 2–5 wt% tetramethylammonium hydroxide, and 60–80 wt% ultrapure water, giving a working pH between 10.8 and 11.5. Ionic cleanliness after stripping is measured by resistivity of solvent extract according to IPC TM-650 2.3.25, with acceptance below 1.56 µg/cm² sodium chloride equivalence for Class 2 and Class 3 boards inspected to IPC-A-600. Surface energy after final rinse is checked with dyne pens or contact-angle goniometry, and must exceed 40 dyn/cm to support subsequent electroless copper or solder mask adhesion. Terminal products include high-density interconnect printed circuit boards, chip-scale package substrates, and flexible polyimide circuits. The dominant production failure mode is incomplete stripping inside blind microvias when conveyor speed exceeds 4 m/min; this is addressed by adding a 30 s ultrasonic immersion module downstream of the spray zone.

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    Certification & Compliance
    More Introduction

    Film Stripping Solution Electronic/EL Grade is supplied as a low-metal, low-particulate liquid formulation for the removal of positive-tone photoresist, ion-implanted resist, cured planarizing films, and light organic residues from semiconductor wafers, advanced packaging substrates, and flat-panel display mother glass. The product is filtered through 0.05 μm rated membrane in an ISO 14644-1:2015 classified cleanroom and is packaged in high-density polyethylene or fluoropolymer-lined containers after passivation. The typical metal ion budget is controlled below 10 ppb for sodium, potassium, iron, copper, calcium, and zinc by inductively coupled plasma mass spectrometry using ASTM D5673-16 protocols. The chemistry is intended for immersion and spray equipment operating below 80°C; it is not a vapor degreasing product.

    Product Definition and Electronic-Grade Certification Boundaries

    The product designation Electronic/EL Grade differentiates the material from laboratory and reagent-grade strippers on the basis of particle burden, extractable metals, and package cleanliness. The specification is built around three control families: trace cation content, submicrometre particle count, and low non-volatile residue. Cationic impurities are measured by ICP-MS after closed-vessel acid digestion; particle counts are determined with an optical particle counter calibrated under ISO 21501-4:2018 at a sensitivity of 0.1 μm. Non-volatile residue is determined gravimetrically after evaporation at 105°C for 2 h and is specified below 50 ppm. The product contains no intentionally added N-methyl-2-pyrrolidone, consistent with the restrictions described in EU REACH Annex XVII entry 71; it is supplied with a certificate of analysis listing individual metal values in ppb and particle counts in particles per millilitre. The product is assigned model ELS-EL-100 for undiluted use and ELS-EL-100D for dilution with deionized water meeting ASTM D5127-13 Type E-1.2 water quality. The product is not intended for food-contact, pharmaceutical, or consumer use.

    The transition-metal control is particularly relevant for copper and aluminum interconnects because trace levels of iron, copper, and nickel can catalyze decomposition reactions when the bath is accidentally exposed to oxygen or residual oxidizers, leading to localized pH excursions. For this reason, the product is handled through dedicated stainless steel or polymer fluid lines and should not be cross-contaminated with acidic process chemicals. The release specification profile is summarized in Table 1.

    Table 1. Release specification profile and test methods
    PropertyMethodSpecification
    Appearance, undilutedVisual after 0.45 μm filtrationClear, free of suspended solids
    ColorASTM D1209-00≤50 APHA
    Density at 20°CASTM D4052-181.02–1.08 g/cm³
    Viscosity at 25°CASTM D445-212.0–3.5 mPa·s
    pH as supplied at 25°CASTM E70-1911.5–12.5
    Flash pointASTM D93-20>93°C
    Water contentASTM E203-165–15 wt%
    Trace metals Na, K, Fe, Ca, Cu, ZnASTM D5673-16<10 ppb each
    Trace metals Li, Mg, Ni, CrASTM D5673-16<5 ppb each
    Particle count ≥0.1 μmISO 21501-4:2018 calibrated OPC<100 particles/mL
    Non-volatile residueGravimetric, 105°C, 2 h<50 ppm

    In single-wafer spray processors used for copper-pillar and solder-bump patterning, the product is dispensed through a heated manifold at 45–60°C. The spray tool wetted path consists of electropolished 316L stainless steel passivated to ASTM A967-17 and fluoropolymer diaphragm valves. Resist clearing is monitored by endpoint detection from broadband reflectance; the chemistry is compatible with static rinse and deionized water purge after dispense. Because the formulation contains an alkanolamine alkalinity reserve, bath life in recirculated immersion tanks is governed by water uptake, carbon dioxide absorption, and photoresist loading rather than a fixed calendar interval. A production-scale 200 L quartz-lined immersion bath operating at 70°C typically shows a drift of 0.2–0.5 pH units over 72 h when the bath is idle and not blanketed; nitrogen blanketing of the tank headspace extends this interval by reducing carbon dioxide absorption. Dynamic surface tension at 25°C, measured by maximum bubble pressure, is typically 32–38 mN/m; this range assists wetting of high-aspect-ratio through-silicon via structures without generating foam in high-pressure spray nozzles.

    Which Process Conditions Maximize Resist Removal Without Metal Attack?

    The operating window is constrained by the corrosion behavior of aluminum-copper metallization and the dissolution rate of cross-linked photoresist. The formulation is specified for immersion at 65–75°C, with lower-temperature 45–60°C spray operation. At bath temperatures above 80°C, the etch rate of exposed aluminum in high-pH media increases sharply; users should pre-screen patterned wafers by coupon immersion in accordance with a 15 min exposure at the maximum intended temperature. Agitation level is tool-specific. In immersion tanks, low-pressure recirculation of 1–3 L/min per 100 L of bath volume is typically sufficient to maintain concentration uniformity without generating damaging cavitation. If megasonic assistance is used, a power density of 0.8–1.2 W/cm² at 800–1000 kHz may reduce removal time on highly cross-linked films, but lower-frequency ultrasonic baths are not recommended for patterned wafers because acoustic transients can damage high-aspect-ratio structures. The concentration of dissolved photoresist should be kept below 20 g/L by partial bleed-and-feed replenishment; above this loading, particle redeposition increases and filtration skid pressure can rise above 2.0 bar differential across 0.1 μm polypropylene depth filters.

    For a 2 μm-thick positive-tone novolak resist, immersion removal rates at 70°C are typically 3–8 μm/min; in spray mode at 55°C, the rate falls to 0.5–2.0 μm/min for the same film. The difference is primarily mass-transport and thermal activation; therefore spray tools require longer dispense times or higher temperature within the allowed window. The product is not optimized for negative-tone chemically amplified resists after deep-UV cross-linking; published data for that specific configuration is limited, and plasma descum may be required before wet stripping. The effect of water content on resist dissolution is non-linear. Water is necessary for ionization of the alkanolamine and for hydration of dissolved resist fragments; however, water levels above 20 wt% lower the solvent power of the aprotic co-solvent and can cause precipitation of stripped polymers onto wafer edges. Process capability monitoring on 300 mm wafers indicates that maintaining water between 10–15 wt% yields stable endpoint times; outside this range, endpoint time variation increases by 10–20% lot-to-lot.

    When the EL Grade Replaces NMP-Based or Reagent-Grade Strippers

    Replacement scenarios can be grouped into three classes: replacement of N-methyl-2-pyrrolidone-based formulations for regulatory reasons, replacement of general-purpose reagent-grade strippers for metal ion control, and replacement of aggressive phenol/sulfonic acid strippers when metal etch is unacceptable. The product contains no N-methyl-2-pyrrolidone and is therefore outside the EU REACH Annex XVII entry 71 placement restrictions; the flash point above 93°C also reduces storage classification pressure relative to low-boiling solvent blends. The electronic-grade specification limits sodium and potassium to 10 ppb each and the combined lithium, magnesium, nickel, and chromium budget to 5 ppb each, whereas generic laboratory-grade alkalis may contain parts-per-million levels of alkali and transition metals. The product also omits hydroxylamine, which in concentrated form can decompose exothermically and is restricted in some semiconductor wet benches because of metal compatibility and safety concerns. A comparative profile is given in Table 2.

    Table 2. Comparative profile against common stripper classes
    ParameterFilm Stripping Solution Electronic/EL GradeReagent-grade solvent stripperNMP-based electronic stripper
    Trace metal control<10 ppb per specified elementOften 1–10 ppm without lot release0.1–1 ppm typical, dependent on supply
    Particle release certification<100/mL at ≥0.1 μmNot specifiedNot specified
    NMP contentNone detectedNone50–100 wt%
    Flash point>93°C40–70°C typical for acetone/methanol blends95°C for pure NMP
    Aluminum coupon etch at 70°C<2 nm/min on Al-0.5CuNot specified; may be high due to chloride contamination1–5 nm/min depending on inhibitor
    Main applicationPhotoresist removal in semiconductor packaging and wafer fabsLaboratory cleaning, not device-gradePhotoresist removal in older fabs, now substitution target

    Where the EL grade replaces a pure NMP-based stripper, the first production lot should include a dedicated compatibility coupon study in the target tool because the solvent blend has a different Hansen solubility parameter distribution and a different aluminum passivation behavior. Published data for this specific configuration is limited; therefore bath temperature should initially be maintained near the lower end of the immersion window until endpoint performance is confirmed.

    Rinse Compatibility, Bath Monitoring, and Failure Signatures

    After stripping, the wafers or substrates are rinsed with deionized water meeting ASTM D5127-13 Type E-1.2; the rinse step should be executed within 60 seconds of removal from the hot bath to prevent re-deposition of dissolved resist. The product is miscible with water and does not require an intermediate solvent rinse, but a 0.5–2.0 vol% isopropyl alcohol post-dip can reduce watermarks on aluminum bond pads. Bath monitoring is typically performed by refractive index, titratable alkalinity, and Karl Fischer water content. A water content above 20 wt% indicates dilution or excessive atmospheric moisture uptake and should trigger replenishment or tank charging. A pH drop below 11.2 or a titration value below 0.80 M alkalinity indicates carbon dioxide absorption or photoresist neutralization and requires corrective addition of the non-aqueous replenisher rather than inorganic alkali. Filtration skid differential pressure that exceeds 2.5 bar across 0.1 μm polypropylene depth filters indicates particulate loading from hardened resist crusts, and the filter stack should be changed before particle counts in the bath exceed 500 particles/mL at 0.1 μm. The product is not compatible with strong oxidizing acids or concentrated hydrogen peroxide; mixing with sulfuric acid or piranha-like solutions can generate heat and should be avoided in shared drain lines. It is also incompatible with polycarbonate, acrylic, and some epoxy tank liners; wetted materials should be limited to high-density polyethylene, polypropylene, fluoropolymers, quartz, or passivated 316L stainless steel.

    Because the stripper relies on a buffered alkanolamine/solvent system, adding inorganic hydroxide to a depleted bath alters the solvent-water balance and increases aluminum etch risk. Replenishment should be performed only with the non-aqueous replenisher matched to the bath. Peroxide, persulfate, and hypochlorite additions are incompatibilities. The formulation is also sensitive to chloride contamination; chloride should be below 1 ppm in the as-supplied product and below 50 ppb in the deionized water rinse to avoid aluminum pitting. These boundaries are checked by ion chromatography with conductivity detection using ASTM D4327-17. Unopened containers are specified for 12 months shelf life when stored at 10–30°C and protected from direct sunlight. Partially used containers should be blanketed with nitrogen at 0.2–0.5 bar gauge to limit water uptake and carbon dioxide exposure.

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