Products

High-Purity Hydrocarbon Resin for PCB Manufacturing - Nippon Soda

    • Product Name: High-Purity Hydrocarbon Resin for PCB Manufacturing - Nippon Soda
    • Factroy Site: Yudu County, Ganzhou, Jiangxi, China
    • Price Inquiry: admin@ascent-chem.com
    • Manufacturer: Ascent Petrochem Holdings Co., Limited
    • CONTACT NOW
    Specifications
    HS Code 244218
    Product Name High-Purity Hydrocarbon Resin for PCB Manufacturing - Nippon Soda
    Appearance Pale yellow flakes or beads
    Softening Point 85-120°C
    Color Gardner Scale ≤2
    Acid Value <0.1 mg KOH/g
    Bromine Value <5 g Br2/100g
    Number Average Molecular Weight 400-800 g/mol
    Glass Transition Temperature 40-70°C
    Thermal Decomposition Temperature >250°C
    Dielectric Constant 1 Mhz 2.2-2.5
    Dissipation Factor 1 Mhz <0.001
    Moisture Absorption <0.05%
    Halogen Content Chlorine <10 ppm, Bromine <10 ppm
    Solubility Soluble in aromatic and aliphatic hydrocarbons
    Purity ≥99%

    As an accredited High-Purity Hydrocarbon Resin for PCB Manufacturing - Nippon Soda factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Supplied in sealed 25 kg polyethylene-lined fiber drums, ensuring high-purity hydrocarbon resin stays contamination-free and moisture-protected for PCB manufacturing.
    Container Loading (20′ FCL) 20′ FCL: High-purity hydrocarbon resin sealed in drums/pallets, containerized for safe, moisture-free transport to PCB manufacturing facilities.
    Shipping High-Purity Hydrocarbon Resin for PCB Manufacturing (Nippon Soda) ships in sealed, moisture-proof containers to preserve purity. Store away from heat, sparks, and incompatible oxidizers. Standard ground freight is typical; avoid extreme temperatures. Ensure proper labeling and documentation per hazardous/non-hazardous chemical regulations. Handle with PPE and adequate ventilation.
    Storage Store in a cool, dry, well-ventilated area away from direct sunlight, heat sources, and open flames. Keep the container tightly sealed to prevent moisture contamination and oxidation. Avoid contact with strong oxidizers. Maintain temperatures below 40°C (104°F) and protect from physical damage. Use appropriate ventilation and ensure proper labeling for safe handling.
    Shelf Life Shelf life is typically 12 months when stored unopened in a cool, dry place away from direct sunlight and heat.
    Application of High-Purity Hydrocarbon Resin for PCB Manufacturing - Nippon Soda

    In multilayer inner-layer dry film processing, the most exacting purity demand is placed on the hydrocarbon resin because residual chloride, sodium, or iron ions released from a lower-purity tackifier at the copper-resist interface are measurable as electrochemical contamination in downstream cupric chloride etching and electrolytic copper deposition. In published starting-point dry film photoresist formulations for low-profile copper and mSAP processing, Nippon Soda high-purity hydrocarbon resin is incorporated at 3–8 wt% of total solids, replacing an equivalent mass of the acrylic binder phase. The lower addition boundary is not cosmetic: below 3 wt%, tape adhesion after 50 °C cupric chloride etching falls below the IPC-TM-650 2.4.1 pass criterion on 1/2 oz low-profile copper, and tenting over 0.30 mm drilled holes fails during cupric chloride etching after development in 1.0 wt% Na₂CO₃ at 30 °C. The upper boundary at 8 wt% is set by aqueous development kinetics: the thermoplastic hydrocarbon phase reduces the developer solubility of the acrylate binder, and at loadings above 8 wt% residues remain in 50 µm line openings after 45 s of spray development at 1.2 kg/cm². The dry film itself is produced by dissolving the acrylic binder, polyfunctional acrylic monomers, photoinitiator, and hydrocarbon resin in a solvent blend, filtering through 10 µm absolute cartridge filters, slot-die coating onto 25 µm polyester carrier film, and drying in a multi-zone oven with heated air at 70–90 °C. On the lamination line, the dry film is applied at 110–120 °C, 3.5–4.5 kg/cm², and 1.5–2.5 m/min; boards above RH 60% require preconditioning at 45–55% RH for 24 h to prevent moisture-induced tenting failure. Exposure uses 365 nm collimated UV at 40–80 mJ/cm², followed by development in 1.0 wt% Na₂CO₃ at 30 °C, acid cupric chloride etching, and dry film stripping in 3% NaOH at 50 °C. Compliance for inner-layer production is aligned to IPC-6012E Class 3, IPC-TM-650 2.4.1, RoHS Directive 2011/65/EU, and REACH Regulation (EC) No 1907/2006. Terminal product types include multilayer PCB inner layers for data-communication boards, IC substrates using modified semi-additive processing, and high-density interconnect boards with line width/space below 40/40 µm. Published data for the exact Nippon Soda grade in a specific dry film acrylic matrix is limited outside supplier-published purity specifications, but the above loading window is consistent with publicly documented hydrocarbon-resin-modified photoresist systems.

    The most significant production-scale failure mode is not adhesive loss during etching but microgel formation during slot-die coating when the hydrocarbon resin is blended at low shear and then subjected to high shear in the coating pump. If the resin is not pre-dissolved in the solvent phase, undissolved gel particles above 20 µm produce streaking and coating weight variation across the web width. Slot-die coaters with closed-loop gravimetric feed and 10 µm absolute filtration upstream of the die are required; production-scale coating can require a speed reduction of up to 15% when gel particle counts exceed 50 particles/mL in the filtered solution. This operational boundary, rather than the resin chemistry itself, often determines the upper addition ratio in production.

    When Alkali-Developable Solder Mask Must Withstand 260°C Reflow Without Cracking or Blistering

    Because alkali-developable solder mask on rigid FR-4 boards must survive multiple 260 °C reflow cycles without cracking, blistering, or adhesion loss, the formulation uses the hydrocarbon resin as a co-binder at 5–12 wt% of total resin solids in published starting-point formulations. Grade-specific loading for the Nippon Soda resin must be confirmed by response-surface testing because the tertiary amine content of the photoinitiator package shifts the apparent acid value of the carboxylated acrylic resin. The lower boundary of 5 wt% is set by the need to maintain wetting on bare copper, OSP, and ENIG surfaces during screen printing, while the upper boundary of 12 wt% is limited by sodium carbonate developability after UV exposure and by cured-network hardness. At loadings above 12 wt%, the saturated alicyclic resin acts as a plasticizer in the final crosslinked matrix, reducing pendulum hardness below the value required for IPC-SM-840E Class T cure acceptance and increasing the risk of blistering when the board is floated at 288 °C for 10 s per IPC-TM-650 2.6.3.2. The resin should not be combined with amine-based latent hardeners above 0.5 wt% in this system because amine-initiated epoxy homopolymerization raises viscosity during the 30 min screen-print working window and produces pinhole formation after pre-cure at 75 °C for 30 min.

    The production process follows a three-roll mill route in which the carboxylated acrylic binder, epoxy acrylate oligomer, photoinitiator, filler, pigment, and hydrocarbon resin are dispersed to a final grind below 10 µm Hegman. Resin addition is made as a pre-dissolved solution to avoid dry-particle agglomeration, and the mill is water-cooled to keep paste temperature below 45 °C. Printing uses 43T polyester mesh with a solvent-resistant squeegee at 20–40 m/min, followed by pre-cure at 75 °C for 30 min, collimated UV exposure at 400–800 mJ/cm², developing in 1.0 wt% Na₂CO₃ at 30 °C, and final thermal cure at 150 °C for 60 min. Volume resistivity after cure is evaluated by ASTM D257-14 and should remain above 1×10¹² Ω·cm at 25 °C; flame retardance is verified by UL 94 V-0; restricted substance compliance is assessed against RoHS Directive 2011/65/EU and REACH Regulation (EC) No 1907/2006. Terminal products include double-sided and multilayer rigid PCB for communication infrastructure, flexible circuits where solder mask replaces coverlay in selected areas, and rigid-flex boards for industrial and automotive modules.

    Standard or test methodScenarioMeasured or controlled propertyAcceptance condition used in application screening
    IPC-SM-840E Class TUV solder maskCure, adhesion, chemical resistancePass after 260 °C reflow and 288 °C float
    IPC-TM-650 2.4.1Dry film, plating resist, legend inkTape adhesion to copperNo resist removal beyond 10% area
    IPC-TM-650 2.6.3.2UV solder maskChemical resistanceNo blistering after 10 s float at 288 °C
    ASTM D257-14Solder mask and via fillVolume resistivity> 1×10¹² Ω·cm at 25 °C
    UL 94 V-0Solder mask and via fillFlammabilitySelf-extinguishing after 10 s
    ASTM D3418-15Via plugging pasteGlass transition temperatureCured Tg at least 15 °C below cure plateau
    IPC-4761Via pluggingVia protection designNo air entrapment or meniscus collapse
    RoHS Directive 2011/65/EUAll applicationsRestricted substance complianceBelow Annex II maximum concentration values
    REACH Regulation (EC) No 1907/2006All applicationsSVHC candidate listNo restricted substance above threshold

    For panel plating and pattern plating of multilayer boards, temporary resist integrity during electrolytic copper deposition at 2.0–3.5 A/dm² is the primary selection criterion. High-purity hydrocarbon resin is compounded into the plating resist at 4–10 wt% of total formulation as an adhesion promoter and plating-solution barrier. Below 4 wt%, the cured resist edge lifts during the plating cycle, allowing copper creep under the resist and producing shorting at 50 µm pitch; above 10 wt%, the stripping time in 3% NaOH at 50 °C extends beyond 60 s and leaves hydrophobic residues on the copper surface that degrade subsequent electroless copper deposition. The resist is applied by screen printing or curtain coating, then pre-cured at 70–80 °C for 20–30 min, UV-cured at 300–600 mJ/cm², and thermal-cured at 120–130 °C for 20–30 min before plating. After electrolytic copper deposition, the resist is stripped in 3% NaOH at 50 °C, and the exposed board proceeds to solder mask or surface finish. Compliance is assessed by IPC-6012E Class 3 for conductor width and spacing, IPC-TM-650 2.4.1 tape adhesion, RoHS Directive 2011/65/EU, and REACH Regulation (EC) No 1907/2006. Terminal product types include multilayer PCB plated through-holes, HDI boards with plated microvias, and power electronics boards with thick copper tracks. Published data for the Nippon Soda grade in this specific plating resist configuration is limited; the addition range reflects publicly documented hydrocarbon-resin-containing plating resist formulations and should be validated on the target plating line.

    What Limits Resin Flow into 0.20 mm Laser-Drilled Blind Vias during Vacuum Plugging?

    Vacuum plugging pastes for HDI blind-via and through-hole fill use high-purity hydrocarbon resin at 10–20 wt% of total formulation as a thermoplastic binder that lowers high-shear viscosity during screen printing while providing post-cure dimensional stability. The critical process boundary is the relationship between resin glass transition temperature and the plateau temperature of the final cure. If the resin Tg is too close to the cure plateau, meniscus collapse occurs after the vacuum release cycle, leaving recessed vias that fail IPC-4761 via protection requirements and produce entrapped air in subsequent solder mask application. Formulation work therefore specifies a cured paste glass transition temperature measured by ASTM D3418-15 at least 15 °C below the final cure plateau, and a coefficient of thermal expansion below 60 ppm/°C from 50 °C to 150 °C. The paste is printed on a vacuum screen printer capable of holding −0.08 MPa panel vacuum with a metal squeegee pressure of 1.5–2.5 kg/cm², then planarised and cured at 150 °C for 60 min. Processing difficulty scales with via aspect ratio: 0.20 mm blind vias at 80 µm dielectric thickness fill reliably at 10–15 wt% resin loading, while 0.10 mm blind vias often require the resin loading to move toward 15–20 wt% to maintain penetration under vacuum. Filled panels are evaluated for void content by cross-section and for flammability by UL 94 V-0; restricted substance compliance is assessed against RoHS Directive 2011/65/EU and REACH Regulation (EC) No 1907/2006. Terminal product types include high-density interconnect smartphone mainboards, automotive radar boards requiring zero voiding under wire-bond pads, and IC substrates with filled blind vias beneath fine-feature signal layers.

    ApplicationPublished starting-point addition ratioLower-boundary failure modeUpper-boundary failure mode
    Dry film photoresist3–8 wt% of total solidsTape adhesion loss after cupric chloride etchingDeveloper residue in 50 µm lines
    UV-curable solder mask5–12 wt% of resin solidsWetting failure on OSP/ENIGReduced hardness and blistering at 288 °C
    Plating resist4–10 wt% of total formulationResist edge lift and copper creepStrip residue in 3% NaOH
    Via plugging paste10–20 wt% of total formulationHigh-shear viscosity too high for penetrationTg too close to cure plateau and meniscus collapse
    Legend ink2–6 wt% of total formulationCharacter spread below 0.15 mmYellowing after three reflows at 260 °C

    Legend Ink Colour Stability and Capillary Flow on 0.15 mm Character Height

    To maintain 0.15 mm character height without ink spread after reflow, legend formulations use high-purity hydrocarbon resin at 2–6 wt% of total formulation as a rheology modifier and adhesion promoter on bare copper, OSP, ENIG, and solder mask surfaces. At loadings below 2 wt%, viscosity at 25 °C falls below the range required to maintain character edge definition; at loadings above 6 wt%, yellowing index after three reflow cycles at 260 °C exceeds the visual acceptance threshold of IPC-A-600K for component designation legibility. The ink is prepared by three-roll milling the binder, pigment, filler, and resin to a 10 µm Hegman grind, printed through 120T polyester mesh at 20–30 m/min, and thermally cured at 150 °C for 30 min. Adhesion is checked by IPC-TM-650 2.4.1 tape pull after 260 °C reflow; marking legibility is inspected per IPC-A-600K; restricted substance compliance is assessed against RoHS Directive 2011/65/EU and REACH Regulation (EC) No 1907/2006. Terminal product types include assembled PCBs for consumer electronics, LED boards requiring high-contrast white legends, and automotive modules where post-reflow legibility is a customer audit criterion.

    Free Quote

    Competitive High-Purity Hydrocarbon Resin for PCB Manufacturing - Nippon Soda prices that fit your budget—flexible terms and customized quotes for every order.

    For samples, pricing, or more information, please contact us at +8618136850665 or mail to admin@ascent-chem.com.

    We will respond to you as soon as possible.

    Tel: +8618136850665

    Email: admin@ascent-chem.com

    Inquiry

    Get Free Quote of Ascent Petrochem Holdings Co., Limited

    Flexible payment, competitive price, premium service - Inquire now!

    Certification & Compliance
    More Introduction

    Nippon Soda’s electronic-grade high-purity hydrocarbon resin, distributed under the NISSO-PB designation and specified as B-3000 for higher-viscosity build-up applications, is a vinyl-rich liquid polybutadiene intended for dielectric build-up films, solder resist binders, and adhesion-promoting layers in printed circuit board manufacturing. The manufacturer’s technical bulletin reports a number-average molecular weight of 3,200 g/mol, a 1,2-vinyl content of ≥90%, a dynamic viscosity at 45 °C of 80 Pa·s, an iodine value of 420 g I₂/100 g, and an ash content below 0.05 wt%. The anionic polymerisation route used for this grade avoids the metal chloride catalysts and halogenated solvent residues typical of C5/C9 aliphatic-aromatic hydrocarbon tackifiers. Consequently, the cured matrix exhibits lower extractable ion load and reduced risk of electrochemical migration under high-humidity bias testing.

    What limits conventional hydrocarbon resins in high-frequency PCB dielectrics?

    Conventional C5/C9 resins retain variable hydrolyzable chloride from Friedel-Crafts catalysis, with bulk concentrations reported from 50 ppm to 500 ppm depending on downstream neutralisation. Under 85 °C and 85% RH bias, these mobile ions contribute to conductive anodic filament formation when evaluated by IPC-TM-650 2.6.25. An electronic-grade polybutadiene such as B-3000 is produced by anionic polymerisation, leaving no catalyst-derived halogen residue and reducing the ionic conductivity of the unfilled cured film. Dielectric measurements at 1 MHz by ASTM D150 indicate a dielectric constant of approximately 2.5 and a dissipation factor below 0.001 for the unfilled cured resin. A standard DGEBA epoxy laminate measured under the same conditions typically exhibits a dielectric constant near 3.8 and a dissipation factor near 0.020. The difference is attributable to the absence of polar hydroxyl groups in the cured hydrocarbon network and to the restricted mobility of the vinyl-rich crosslink segments. For high-frequency PCB substrates, the lower dissipation factor reduces signal attenuation, but the hydrocarbon resin alone lacks the dimensional stability and copper adhesion of epoxy; it is therefore used as a co-binder at 20–50 wt% of the organic matrix rather than as a neat dielectric.

    When the resin is incorporated into semi-additive process build-up films, the formulation is typically laminated in a vacuum press at 100–120 °C and cured at 170–200 °C for 60–120 min. The B-3000 grade contributes a viscosity plateau that limits resin squeeze-out during lamination while retaining enough flow to fill variable copper circuit topography. High-shear dispersion of silica or alumina filler into the hydrocarbon matrix is performed on a co-rotating twin-screw extruder with L/D 40:1, with barrel zones held between 80 °C and 120 °C and screw speed from 300 min⁻¹ to 500 min⁻¹. In laser via formation, a 355 nm UV laser or 9.3 µm CO₂ laser processes the cured film; the low aromatic content of polybutadiene reduces carbonaceous residue in the via base after alkaline permanganate desmear at 70–80 °C. Swelling of the cured hydrocarbon network in the desmear bath is typically below 5%, whereas epoxy-rich build-up films can swell more than 20% during the same step, increasing via blind-hole void formation. This swelling differential is a primary processing advantage when the resin is used as a replacement for a portion of the epoxy in via-opening layers.

    When the resin is blended into halogen-free build-up dielectric pastes, processing latitude shifts toward lower peroxide levels

    Cure response of the B-3000/triallyl isocyanurate system is monitored by dynamic differential scanning calorimetry according to ASTM E2160. At a heating rate of 10 K/min, the cure exotherm onset is observed at 135–145 °C, with peak exotherm at 165–175 °C. Increasing dicumyl peroxide from 1.0 wt% to 3.0 wt% shortens gel time at 170 °C from approximately 90 s to 35 s, but the faster crosslinking reaction raises the risk of microvoid entrapment during vacuum lamination because matrix viscosity rises before complete air removal. Production-scale vacuum laminators therefore operate with a compounded paste viscosity of 5–20 Pa·s at 100 °C; the neat B-3000 viscosity of 80 Pa·s at 45 °C is reduced by dilution with B-1000 or a low-molecular-weight styrenic monomer. Halogen-free flame retardance is obtained by addition of phosphorus-based synergists rather than brominated additives. The resin itself contributes negligible halogen content, but compliance of the finished laminate is verified by IEC 61249-2-21 extraction and combustion methods rather than by resin composition alone.

    Moisture absorption of the cured unfilled polybutadiene network is below 0.1 wt% after 24 h immersion per ASTM D570; this is lower than the 0.5–1.0 wt% moisture uptake typical of cured bisphenol A epoxy under the same procedure. In stacked via structures exposed to 288 °C solder float, the low moisture absorption reduces the vapour-pressure-driven delamination that occurs when absorbed water flashes at reflow temperature. The hydrocarbon network, however, exhibits lower polar interaction with copper oxide than an epoxy matrix, so adhesion to copper foil must be supplemented with an interfacial primer or a silane-functional coupling agent. Peel strength testing according to IPC-TM-650 2.4.8 on a 35 µm low-profile copper foil requires the user to establish a process-specific baseline; published data for this specific resin-foil configuration is limited. Comparative evaluations generally show that a hydrocarbon-epoxy interpenetrating network retains a higher fraction of its initial peel strength after 288 °C solder float than the hydrocarbon resin alone, while the hydrocarbon component reduces the moisture uptake of the epoxy matrix.

    Copper foil adhesion and desmear processing windows

    Adhesion in a build-up dielectric is controlled not only by resin chemistry but also by the conversion of the copper surface after brown oxide or silane treatment. A resin with high vinyl content can undergo free-radical addition at the copper surface only after the oxide layer is reduced; therefore, typical adhesion promoters for B-3000 include methacrylate-functional silanes applied to the copper at 0.1–0.5 wt% of the formulation. In desmear lines, the permanganate bath temperature is held at 70–80 °C with sodium hydroxide concentration of 40–60 g/L; the nonpolar hydrocarbon matrix swells less than epoxy, so desmear residence time can be extended from 3 min to 8 min without severe via enlargement. This wider desmear window is operationally significant on continuous lines where upstream laser output variation changes smear thickness across a panel. Lot-to-lot variation in the resin’s iodine value is controlled within ±10 g I₂/100 g, and the manufacturer’s certificate of analysis should be checked for any drift in 1,2-vinyl content because a drop below 88% reduces crosslink density and raises the cured network’s coefficient of thermal expansion.

    PropertyTest methodNISSO-PB B-3000Conventional C5/C9 resinDGEBA epoxy baseline
    Number-average molecular weightISO 16014-13,200 g/mol500–1,500 g/mol340–380 g/mol
    1,2-vinyl contentFT-IR internal method≥90%not applicablenot applicable
    Ash contentASTM D5630<0.05 wt%0.1–0.5 wt%<0.05 wt%
    Dielectric constant, 1 MHzASTM D1502.52.4–2.63.8
    Dissipation factor, 1 MHzASTM D150<0.0010.005–0.0100.020
    Moisture uptake, 24 h immersionASTM D570<0.1 wt%<0.1 wt%0.5–1.0 wt%

    The comparative table identifies the differentiation of the electronic-grade hydrocarbon resin not principally in zero-shear viscosity but in ionic purity, dielectric loss, and moisture resistance. Finished laminate dielectric validation according to IPC-TM-650 2.5.5.2 is required because resin-only measurements do not capture the influence of glass fabric, copper roughness, or residual solvent on the final buried capacitance signal integrity.

    Regulation or standardScopeApplicable threshold
    RoHS Directive 2011/65/EU Annex IIPb, Cd, Hg, Cr(VI), PBB, PBDE< 0.1 wt% homogeneous material; Cd < 0.01 wt%
    REACH 1907/2006 Candidate ListSVHC content< 0.1 wt% per item
    IEC 61249-2-21Halogen-free laminate definitionCl < 900 ppm, Br < 900 ppm, total < 1,500 ppm

    Storage and handling of the B-3000 grade require sealed steel drums under nitrogen blanket to limit oxidative viscosity drift. The material is supplied with moisture content below 0.1 wt%; pre-drying is not normally required when drums are stored below 30 °C. If a drum is opened in an environment above 60% RH, the headspace should be purged with dry nitrogen before re-sealing because prolonged exposure increases peroxide demand during subsequent cure. Production lot release includes iodine value, viscosity at 45 °C, 1,2-vinyl content, ash content, and moisture content, with the certificate of analysis issued against the manufacturer’s internal specification for electronic-grade resin.

    Top