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Copper-Nickel Alloy Paste Electronic/EL Grade

    • Product Name: Copper-Nickel Alloy Paste 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 476195
    Product Name Copper-Nickel Alloy Paste Electronic/EL Grade
    Composition Copper-Nickel alloy powder in organic binder/solvent system
    Particle Size D50 ≤ 5 µm
    Viscosity 8,000–20,000 mPa·s (Brookfield, 25°C)
    Solid Content 75–85 wt%
    Volume Resistivity ≤ 5×10⁻⁵ Ω·cm
    Sheet Resistance ≤ 50 mΩ/sq at 25.4 µm (1 mil) cured film
    Adhesion 100/100 cross-cut (5B) on ITO/PET and glass
    Curing Conditions 130–150°C for 20–30 minutes
    Shelf Life 6 months in sealed container at 5–25°C
    Storage Temperature 2–10°C away from sunlight and moisture

    As an accredited Copper-Nickel Alloy Paste Electronic/EL Grade factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.

    Packing & Storage
    Packing Copper-Nickel Alloy Paste (Electronic/EL Grade) packaged in a sealed 25 g container, ensuring purity and stability for electronic applications.
    Container Loading (20′ FCL) Copper-nickel alloy paste, electronic/EL grade, loaded in 20' FCL as palletized, sealed drums, safely secured with proper hazard labeling.
    Shipping Ship Copper-Nickel Alloy Paste (Electronic/EL Grade) in sealed, anti-contamination containers to preserve purity and performance. Keep upright, avoid extreme temperatures and moisture. No special hazard classification for general transport, but ensure compliance with local regulations. Use proper grounding to prevent static discharge during handling.
    Storage Store Copper-Nickel Alloy Paste (Electronic/EL Grade) in a tightly sealed original container, in a cool, dry, well-ventilated area away from direct sunlight, heat, and ignition sources. Maintain a stable temperature between 5–25°C. Avoid moisture and condensation. Keep upright, close immediately after use, and observe the specified shelf life before re-dispersing.
    Shelf Life Shelf life is typically 6 months from manufacture date when stored sealed at room temperature, away from moisture.
    Application of Copper-Nickel Alloy Paste Electronic/EL Grade

    On 96% alumina substrates for engine-control hybrid modules, the copper-nickel alloy paste, electronic/EL grade, is pre-conditioned at 22 ± 2 °C for 8 h to erase thixotropic shear history before screen printing. The metal fraction consists of gas-atomized Cu-Ni flake with a mass ratio of 80:20, D50 of 1.5–2.0 µm, and tap density of 3.8–4.2 g/cm³. The inorganic binder is a 6.0–7.0 wt% lead-free bismuth silicate glass with softening point 565 °C; the organic vehicle is terpineol, ethyl cellulose, and dibutyl phthalate at 10:3:1 by mass. Once dispersed on a three-roll mill with back pressure 0.4–0.6 MPa, the paste reaches a fineness of grind below 12 µm on a Hegman gauge and a viscosity of 180–220 Pa·s at 10 s⁻¹ and 25 °C. The paste is not specified for pure air firing above 600 °C, because copper oxide enrichment raises sheet resistivity beyond acceptable limits for wire-bonded hybrid layouts.

    Screen printing uses 280-mesh stainless steel fabric with 25 µm emulsion thickness, a 45° polyurethane squeegee, and snap-off of 0.8 mm; wet film thickness is 35–40 µm, and line resolution remains within ±15 µm after drying at 150 °C for 10–12 min. The belt furnace profile ramps at 30 °C/min to a peak of 850 ± 5 °C, holds for 10 min, and cools at 40 °C/min; the atmosphere is nitrogen with residual oxygen held between 3 ppm and 10 ppm. Residual oxygen above 20 ppm produces a copper-rich oxide skin that raises sheet resistivity by 12–18% and lowers wire bond pull strength by approximately 15%.

    Ni:Cu mass ratioD50 (µm)Bismuth silicate frit (wt%)Fired sheet resistivity at 25 µm (mΩ/square)Adhesion per ASTM F2675-19 (N/mm²)
    90:102.0–2.55.0–6.020–2620–24
    80:201.5–2.06.0–7.025–3318–22
    70:301.0–1.57.0–8.030–3816–20

    After firing, film thickness is 14–16 µm and sheet resistivity is 25–33 mΩ/square at 25 µm normalized thickness per ASTM B193-20. Pull adhesion on 96% alumina is 18–22 N/mm² when tested per ASTM F2675-19; solderability after 8 h steam aging meets IPC J-STD-002D category 2. The resulting conductor is used as die-attach and wire-bond pads for silicon power transistors in automotive ignition modules. RoHS 2011/65/EU Annex II limits are met for the finished conductor; REACH EC 1907/2006 SVHC screening reports no candidate substances above 0.1 wt%. The paste is not specified for direct immersion soldering above 260 °C for more than 10 s, because glass frit dissolution at the solder interface reduces pull adhesion below 15 N/mm².

    What Limits Silver Migration in Screen-Printed Wearable Electrodes?

    Replacing silver-loaded paste in single-use electrocardiogram monitoring patches, the Cu-Ni alloy paste suppresses dendritic growth under 85 %RH and 37 °C bias. The alloy flake loading is 55–65 wt% in a solvent-borne vinyl copolymer resin; D50 is 1.2–1.6 µm, and the Ni:Cu ratio is 85:15. Butyl carbitol acetate and cyclohexanone at 4:1 by mass dilute the paste to a viscosity of 22–28 Pa·s at 10 s⁻¹ for 200-mesh polyester screens. Wet film deposits at 25–30 µm on 75 µm thermoplastic polyurethane film. No sintering occurs during cure, so the paste remains compatible with low-glass-transition polymer substrates.

    Cure is performed in forced-convection ovens at 125 °C for 25 min; volume resistivity remains 2.5–4.0 × 10⁻⁴ Ω·cm measured by four-point probe per IEC 60468. Sheet resistance is 80–120 mΩ/square/mil. Mandrel bend testing at 2 mm radius per ASTM D522/D522M-17 shows less than 10% resistance increase after 10,000 cycles. Cytotoxicity is evaluated per ISO 10993-5:2009 using L929 cells; extraction from cured electrodes reports cell viability above 90%. Because the alloy is not selectively leached in chloride-containing gel, no dendrite formation is observed during 24 h electrochemical migration testing at 5 V and 85% RH per IPC-TM-650 Method 2.6.14.1. Prolonged immersion in isopropyl alcohol beyond 10 min causes resin swelling and more than 15% resistance drift; the paste is therefore not specified for solvent-cleaning processes without immediate drying. The finished electrode assembly is integrated into flexible printed biosensor patches for continuous cardiac monitoring. REACH EC 1907/2006 and RoHS 2011/65/EU Article 4 apply; the paste contains no elemental mercury, lead, cadmium, hexavalent chromium, PBB, or PBDE.

    Diluted to a viscosity of 45–55 Pa·s at 10 s⁻¹, the paste is dispensed with a pneumatic auger valve at 0.25 MPa nozzle pressure and 22 G needle diameter. The trace width is 0.6 mm with 0.3 mm height after two passes; the alloy loading is 70–75 wt% Cu-Ni flake with D50 2.0–2.5 µm in an epoxy-silicone hybrid resin. Thermal cure at 140 °C for 30 min yields volume resistivity 1.8–2.5 × 10⁻⁴ Ω·cm and Shore A hardness 68–72. Shielding effectiveness of the cured trace, measured per ASTM D4935-18 from 100 MHz to 1.5 GHz, is 55–62 dB; at 22–28 GHz using flange-type waveguides, average attenuation is 42–48 dB. The paste is applied over a 5 µm nickel-phosphorus adhesion layer on the LCP surface; without this layer, cross-cut adhesion per ISO 2409:2020 falls from class 0 to class 3. The terminal product is a module-level shield for beamforming antenna arrays, where the Cu-Ni alloy replaces silver-coated copper to reduce galvanic mismatch with nickel-plated aluminium housings. Repeated reflow cycles above 260 °C at module level reduce shielding effectiveness by 6–8 dB due to alloy oxidation at the trace surface. REACH Annex XVII nickel release restrictions are out of scope for this sealed module; UL 94 V-0 flame classification is obtained for the cured resin system.

    Zinc Oxide Varistor Silver-Palladium Replacement in Nitrogen-Fired Terminations

    For zinc oxide multilayer varistor bodies sintered at 1,150–1,200 °C, the termination paste consists of 68–72 wt% Cu-Ni alloy powder with Ni:Cu ratio 75:25, D50 1.0–1.5 µm, and 4–6 wt% zinc-bismuth-borosilicate frit. The vehicle is pine oil and polyvinyl butyral at 8:1 mass ratio. Screen printing with 250-mesh stainless steel screens across the ceramic end faces deposits 20–25 µm dry film. The parts are fired at 800 ± 10 °C for 15 min in a nitrogen tunnel with 2–8 ppm oxygen. The fused termination forms ohmic contact with ZnO grains; contact resistance is below 5 mΩ·cm² per IEC 61051-1:2019.

    After solder dip at 260 °C for 5 s, adhesion force exceeds 25 N on 1206 package varistors. The replacement of silver-palladium terminations removes Ag+ migration paths under 85 °C/85% RH load; no insulation resistance loss is measured after 1,000 h, whereas Ag-Pd terminations typically lose two decades of insulation resistance under the same bias. Oxygen above 10 ppm during firing leads to copper-oxide segregation at the ZnO interface and increases contact resistance to 12–18 mΩ·cm². The terminal varistor assemblies are used in automotive 12 V and 24 V load-dump suppression modules. Compliance with AEC-Q200 Table 9 and RoHS 2011/65/EU is specified on the product data sheet.

    When Co-Firing Temperature Exceeds 900 °C in LTCC Constraint Sintering

    To achieve hermetic inner conductor continuity in Ca-Al-B-Si-O glass-ceramic tapes, the paste is blended at 70–74 wt% alloy solids with an Ni:Cu ratio of 70:30, D50 1.5–2.0 µm, and 3–5 wt% crystalline quartz filler. The organic system is terpineol and butyl stearate at 9:1 mass ratio. Vias of 150 µm diameter are filled by stencil printing, and traces are patterned by 325-mesh screens. Co-firing with the tape is performed at 900 ± 5 °C for 20 min in nitrogen with 5–15 ppm oxygen; constraint plates maintain x-y shrinkage at 0.2–0.4%, while z shrinkage is 36–40%. The fired conductor exhibits sheet resistivity 12–18 mΩ/square at 10 µm thickness and tape adhesion of 12–16 N/mm² by peel test per IPC-TM-650 Method 2.4.8.

    After co-firing, the conductor is electrically continuous across 300 µm via strands with resistance below 30 mΩ per via stack. The low copper oxidation in the constrained nitrogen atmosphere avoids blistering observed in pure copper paste when oxygen surpasses 20 ppm. Residual oxygen above 15 ppm causes copper oxidation at the via wall and increases via resistance by 25–40%. The resulting multilayer packages are used in RF filters and baluns for automotive keyless entry modules at 434 MHz. The conductor meets the inner-layer resistance requirements of IPC-6012F Class 3 after co-firing. Published data for exact Cu-Ni alloy behaviour in other glass-ceramic tape chemistries is limited.

    After a 70 µm dielectric isolation layer is screen-printed and cured on 0.8 mm 430 stainless steel plate, the Cu-Ni alloy paste is screen-printed as serpentine traces with 0.5 mm line width and 0.3 mm spacing. The paste contains 62–68 wt% alloy flake with Ni:Cu ratio 80:20, D50 1.0–1.5 µm, and 8–10 wt% alkali-resistant barium-zinc-borosilicate frit. The vehicle is a rosin-free ester alcohol system. Wet film thickness is 40–45 µm. Firing on the insulated steel substrate is performed in a nitrogen tunnel at 820 ± 5 °C for 12 min, with oxygen limited to 4–10 ppm.

    The heater trace develops sheet resistivity 18–24 mΩ/square at 15 µm fired thickness. Temperature coefficient of resistance is 180–220 ppm/K over -40 °C to 150 °C. Thermal cycling from -40 °C to 150 °C for 2,000 cycles per IEC 60068-2-14 Test Na changes resistance by less than 5%. The completed thick-film heater is used in electric vehicle battery thermal management plates for cold-start preheating. Dielectric withstand is tested at 1,500 VAC for 60 s per IEC 60664-1. Operation beyond 150 °C under 85% RH leads to alkali-assisted glass frit leaching and heater resistance drift exceeding 10%. The printed heater assembly is supplied as a UL 94 V-0 recognized component with operating temperature class 150 °C.

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    Certification & Compliance
    More Introduction

    Copper-Nickel Alloy Paste Electronic/EL Grade, product designation CNP-EL-702, is a screen-printable thick-film conductor formulated for nitrogen-fired ceramic termination and electrode-layer deposition. The metallic phase is a spherical copper-nickel alloy with a nominal Cu:Ni ratio of 70:30 by weight. The product family includes three controlled-rheology variants identified as CNP-EL-702A, CNP-EL-702B, and CNP-EL-702C. The vehicle is an ethyl cellulose/terpineol system with a non-halogenated thixotrope; the paste is not formulated for air firing and must be processed in a controlled nitrogen atmosphere with oxygen below 10 ppm in the burnout and peak-temperature zones. The designation Electronic/EL Grade covers MLCC inner electrodes, hybrid thick-film circuits, chip resistor terminations, and electroluminescent lamp bus electrodes.

    Representative target values for the 702A variant are listed in Table 1. Viscosity is determined at 25.0 ± 0.5 °C with a Brookfield RVDV-II+ cone/plate viscometer using an CP52 spindle at 10 rpm; the specified range is 130–160 Pa·s. Solids content by mass is 89.0 ± 0.5% according to a gravimetric method based on ISO 3251:2019, with dry residue measured after 60 min at 150 °C. Particle size distribution by laser diffraction following ISO 13320:2020 gives D50 1.2 μm, D90 3.0 μm, and D100 not exceeding 8.0 μm. Fired film thickness after screen printing and drying is 25–40 μm. Sintered sheet resistance at 850 °C peak temperature in nitrogen with ≤ 10 ppm O₂ is 30–60 mΩ/□ at 25 μm fired thickness, measured by four-point probe in accordance with ASTM F390-11.

    PropertyCNP-EL-702ACNP-EL-702BCNP-EL-702C
    Solids content (wt%)89.0 ± 0.590.5 ± 0.587.5 ± 0.5
    Viscosity at 25°C, CP52 10 rpm (Pa·s)130–16080–120180–220
    D50 (μm) per ISO 13320:20201.20.81.8
    D90 (μm) per ISO 13320:20203.02.24.5
    Sheet resistance at 25 μm fired film (mΩ/□)30–6030–6040–70

    What Distinguishes the 702A from 702B and 702C Variants?

    The three variants differ primarily in metallic particle size distribution and vehicle solvent release profile. CNP-EL-702A is the standard electrode-layer product for MLCC inner electrode printing where a 30 μm wet film is required after a single squeegee pass at 70 durometer and 45° attack angle. CNP-EL-702B has a D50 of 0.8 μm and a viscosity range of 80–120 Pa·s; it is designated for fine-line electroluminescent lamp bus electrodes where line width is 150 μm or less. CNP-EL-702C uses a coarse D50 of 1.8 μm and viscosity 180–220 Pa·s to build edge thickness on chip resistor terminations without flow-out. Switching between variants on the same production line requires recalibration of the printing gap; observed batch-to-batch variation on a 150 mm flatbed printer with a 70-durometer polyurethane squeegee is controlled within ±5 μm of wet film thickness when paste temperature is held at 22–25 °C and ambient RH is below 55%.

    On a production-scale 200 mm three-roll mill with water-cooled chrome rolls at 2.0 MPa nip pressure, the paste is premixed for 20 min and then sheared at 50–80 rpm to reduce air entrainment. A 30-min vacuum de-airing step at 0.08 MPa is recommended before printing. The product is applied through screens with photosensitive emulsions of 20–30 μm thickness; mesh counts between 250 and 325 per inch give the specified wet film. For MLCC inner electrodes, green ceramic layers are printed at 30 μm wet thickness and dried in an IR conveyor oven with a peak surface temperature of 120 °C for 3–5 min. For EL lamps, CNP-EL-702B is printed as a bus electrode onto ITO-coated PET; drying must remain below 90 °C to avoid PET deformation. Metal-mesh screens are used instead of polyester mesh to reduce paste drag and improve line straightness on 150 μm pitch features.

    Nitrogen-Firing Process Window and Oxygen Limits

    The binder burnout and sintering of CNP-EL-702 require a reducing nitrogen atmosphere. A tube furnace fitted with a 99.999% N₂ source and zirconia oxygen sensor is used. The burnout segment runs from room temperature to 450 °C at 3–5 °C/min with O₂ maintained at 8–10 ppm; rapid outgassing above 450 °C increases carbon residue. Peak sintering at 780–850 °C for 10 min is used on 96% Al₂O₃ and BaTiO₃ substrates; extended dwell beyond 30 min causes nickel diffusion from the alloy into adjacent silver-palladium layers. Oxygen excursions above 15 ppm during cooling produce visible oxidation: the fired film shifts from a metallic rose-grey to a dull green-black and sheet resistance increases by more than . On a 250 mm belt furnace, the recommended cooling rate is 20–30 °C/min to below 100 °C.

    Thermogravimetric analysis in N₂ at 10 °C/min shows 93–95 wt% vehicle removal by 450 °C; residual carbon after sintering is 0.05–0.15 wt%. If peak temperature is reached before carbon removal is complete, CO bubbles from the Boudouard reaction create blisters in the fired film. The use of 99.999% N₂ is insufficient if the furnace is not leak-tested to 10⁻³ mbar·L/s. The oxygen partial pressure must remain below 10 ppm because the equilibrium oxidation partial pressure for Cu₂O at 800 °C is near 10⁻⁶ atm; nickel forms a passivating NiO skin, but excess oxygen leads to CuO formation and loss of solderability.

    Under steady shear at 25 °C, the paste exhibits a shear-thinning index n of 0.65–0.75 over the shear rate range 0.1–100 s⁻¹. Yield stress at rest is 120–180 Pa, measured by a controlled-stress rheometer with 40 mm parallel plate geometry and a 500 μm gap. After screen printing, viscosity recovery to 70% of the initial yield stress occurs within 30 s, enabling line resolution of ±10 μm on 250-mesh screens. High-speed printing lines require a thixotropic index between 1.5 and 2.5, calculated as the ratio of viscosity at 1 rpm to viscosity at 10 rpm on a Brookfield viscometer. If the paste is over-rolled for more than 90 min, chain breakdown of the thixotrope reduces recovery to 40–50%, producing edge slump on 150 μm line features.

    Documented production failure modes include edge oxidation when carrier boats are not preheated before entering the belt furnace, and carbon blisters from incomplete burnout when oxygen remains below 3 ppm during the 300–450 °C segment. Carbon residues not only reduce adhesion; they create solder voids in plated terminations. In one high-volume MLCC line, sulfur contamination at 0.2 wt% from elastomer seals raised sintered sheet resistance from 45 mΩ/□ to 110 mΩ/□ due to Cu₂S formation at grain boundaries. Therefore, all wetted parts use peroxide-cured EPDM or silicone seals with sulfur content below 0.1 wt%.

    When Palladium-Free Formulations Must Meet Silver-Migration Resistance

    Compared with air-fired silver thick-film conductors, CNP-EL-702 has higher sheet resistance but substantially reduced electrochemical migration under humid bias. In surface insulation resistance testing at 85 °C/85% RH with 12 V DC bias, silver conductors typically fail by dendritic bridging within 500–1000 h under IPC TM-650 2.6.3.2, whereas copper-nickel alloy terminations have been shown to maintain >10⁸ Ω in the same test configuration. The trade-off is atmosphere cost and throughput: nitrogen firing adds 0.02–0.05 kWh per 100 g of paste in a 250 mm belt furnace, and peak zone length must increase by 15–20% relative to air-fired silver. Against silver-palladium 85/15 systems, CNP-EL-702 eliminates palladium supply-chain exposure; it cannot be fired in air and is not recommended for high-frequency circuits above 3 GHz due to magnetic permeability contributions from nickel. Against pure copper conductor paste, the nickel addition improves oxidation resistance and permits a wider oxygen window in the furnace; however, it raises sheet resistance and requires a higher peak sintering temperature for densification.

    AttributeCNP-EL-702ASilver conductorAg/Pd 85/15Copper conductor
    Firing atmosphereN₂, O₂ ≤ 10 ppmAirAirN₂, O₂ ≤ 5 ppm
    Sheet resistance (mΩ/□/25 μm)30–603–515–2010–15
    85°C/85% RH, 12 V DC migration behaviour per IPC TM-650 2.6.3.2>10⁸ Ω, 1000 hdendritic failure <500 hmoderate resistancehigh resistance

    Under REACH Regulation (EC) No 1907/2006 and RoHS Directive 2015/863/EU, the product contains no intentionally added Pb, Cd, Hg, hexavalent chromium, PBBs, or PBDEs. Certificate of analysis reports Fe ≤ 50 ppm, Zn ≤ 30 ppm, Pb ≤ 5 ppm, Cd ≤ 2 ppm, S ≤ 10 ppm by ICP-OES after microwave-assisted digestion per ISO 11885:2007. The product meets halogen-free criteria for chlorine and bromine below 900 ppm combined when measured by EN 14582:2016.

    CNP-EL-702 has a shelf life of 6 months at 5–10 °C in sealed opaque jars. Storage above 30 °C accelerates solvent separation and increases yield stress; material reclaimed from the jar must be conditioned at 22–25 °C for at least 12 h before opening to prevent moisture condensation. If ambient RH exceeds 60%, unopened jars must be pre-dried in a desiccated cabinet at 25 °C for 24 h before printing. The paste is incompatible with lead-containing frits and bismuth oxide additives above 2 wt% because low-melting bismuth phases reduce termination adhesion. For Pb-free solderability, fired CuNi terminations require a nickel electroplating barrier and tin plating to meet ANSI/J-STD-002B; direct soldering to bare CuNi alloy can fail wetting balance after steam aging.

    CNP-EL-702B can be used in nitrogen-filled glovebox dispensing for fine-line electrode repair. A 22-gauge stainless steel needle with 0.41 mm inner diameter and dispense pressure of 0.08–0.12 MPa yields a 0.5–0.7 mm wide line at 5 mm/s. The paste shows no stringing when the needle retract distance is set to 0.5 mm and the needle temperature is held at 23 °C. Clean room class ISO 7 is recommended; particulate contamination above 20 μm must be filtered at final filling.

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