| HS Code | 260378 |
| Product Name | SuA-101 |
| Appearance | Silver gray viscous paste |
| Silver Content | 80-85 wt% |
| Viscosity | 30-50 Pa·s (Brookfield, 25°C) |
| Specific Gravity | 2.5-3.0 g/cm³ |
| Volume Resistivity | ≤1.0×10⁻⁴ Ω·cm |
| Sheet Resistance | ≤0.05 Ω/sq at 25 μm thickness |
| Curing Temperature | 150-180°C |
| Curing Time | 30-60 minutes |
| Adhesion Strength | ≥5 MPa (on glass) |
| Thixotropic Index | ≥2.0 |
| Storage Temperature | 5-10°C |
| Shelf Life | 6 months from production date |
| Particle Size | ≤10 μm |
As an accredited Conductive Silver Paste (SuA-101) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Conductive Silver Paste SuA-101 is packaged in a sealed 100g jar with secure lid, safety labeling, and usage instructions. |
| Container Loading (20′ FCL) | 20′ FCL: palletized drums of Conductive Silver Paste, securely braced, ventilated, labeled, with spill containment. |
| Shipping | Conductive Silver Paste (SuA-101) must ship as a hazardous/UN-classified material, in sealed, grounded containers to prevent spills and static discharge. Avoid extreme heat, moisture, and impact. Use authorized couriers for flammable/industrial chemicals, with proper labels, SDS, and temperature-controlled transport if required. |
| Storage | Store Conductive Silver Paste (SuA-101) in a tightly sealed, original container in a cool, dry, well-ventilated area. Keep away from heat, sparks, open flames, and incompatible materials such as strong oxidizers. Protect from direct sunlight and freezing. Ensure container is properly closed after each use to prevent solvent evaporation and maintain paste consistency. |
| Shelf Life | Shelf life: 6 months from manufacture date when stored unopened in original container at recommended cool, dry conditions. |
Conductive Silver Paste (SuA-101) is a silver flake-loaded, screen-printable thick-film paste supplied for downstream bonding, metallization, and circuit-patterning operations where cured or fired films must maintain volumetric resistivity below 1.5 × 10−5 Ω·cm at 25 °C. The application zones in this section are limited to industrial segments with established deposition windows, published reliability test methods, and production-scale equipment records. Performance data are reported with the associated measurement standard, process range, or equipment configuration; statements without such anchors are excluded.
| Application zone | Primary compliance anchors | Wet deposition / loading | Peak thermal condition | Terminal product classes |
|---|---|---|---|---|
| Heterojunction photovoltaic metallization | IEC 61215-1:2021, IEC 61730-1:2023, RoHS 2011/65/EU, REACH SVHC | Ag 88–92 wt%, dry film 15–25 µm | Cure 200 °C, 25 min | HJT modules, BIPV, vehicle-integrated PV |
| Automotive glass heating circuits | ECE R43, FMVSS 205, RoHS 2011/65/EU | Ag 80–85 wt%, wet film 18–22 µm | Fire 620–700 °C, 3–5 min | Heated rear windows, camera heaters, wiper rest heaters |
| Thick-film hybrid microelectronics | MIL-PRF-38534, IPC-A-600J, ASTM D257-14 | Ag 88–92 wt%, wet film 15–20 µm | Fire 850 °C, 10 min | Military radar modules, downhole sensors, hermetic telemetry circuits |
| RFID antenna printing on PET | RoHS 2011/65/EU, REACH, ISO/IEC 18000-6C | Ag 75–80 wt%, wet film 12–16 µm | Cure 125–135 °C, 15–20 min | UHF RFID inlets, smart packaging, anti-theft labels |
| Electrochemical biosensor electrodes | ISO 13485:2016, FDA 21 CFR 820.30, ISO 10993-5:2009 | Ag 80–85 wt%, wet film 8–12 µm | Cure 120 °C, 15 min | Glucose test strips, lactate biosensors, point-of-care diagnostics |
| Die-attach and power package bonding | AEC-Q200 Rev E, MIL-STD-883 Method 2019.7, JEDEC J-STD-020 | Ag 80–86 wt%, bond-line 25–45 µm | Step cure 100 °C 30 min + 150 °C 60 min | LED packages, high-power sensor packages, MEMS attachment |
For silicon heterojunction (HJT) front-side metallization, the paste is printed onto indium tin oxide (ITO) or indium zinc oxide (IZO) transparent conductive oxide layers that cannot tolerate firing above 200 °C without passivation degradation. The formulation addition ratio for this process is constrained to 88–92 wt% silver flake, 1–3 wt% glass frit, and 6–9 wt% organic vehicle; thinning is permitted only with butyl carbitol acetate at 0.5–1.5 wt% when spindle viscosity at 25 °C exceeds 220 Pa·s, and any addition above this range creates line slumping and finger width drift from 25–35 µm to above 40 µm. Compliance anchors for the finished module are IEC 61215-1:2021 thermal cycling, humidity-freeze, and damp-heat sequences, IEC 61730-1:2023 insulation and reverse-current safety requirements, plus RoHS 2011/65/EU and REACH SVHC restrictions; paste adhesion is monitored after damp-heat exposure at 85 °C/85% RH for 1000 h, with peel force above 8 N/mm. Downstream production uses a screen printer with mesh count 360, wire diameter 14 µm, emulsion over mesh 10–12 µm, squeegee hardness 70–75 Shore A, pressure 0.25–0.35 MPa, and print speed 200–250 mm/s; the film is dried at 120 °C for 10 min and cured in a convection oven at 200 °C for 25 min with temperature uniformity better than ±3 °C. The allowable thermal budget is a hard process boundary: excursions to 210 °C for longer than 2 min increase series resistance and reduce fill factor by more than 1.5% absolute. Terminal product types include HJT photovoltaic modules, bifacial HJT panels, building-integrated photovoltaics, and vehicle-integrated PV laminates where low-temperature interconnection is mandatory.
Screen-printed silver busbars for automotive glazing are applied to soda-lime float glass before the bending and tempering operation. The formulation addition ratio for this glass-fire grade is 80–85 wt% silver flake, 3–6 wt% bismuth borosilicate glass frit, and 8–12 wt% pine-oil-based vehicle; wet film deposit is held at 18–22 µm through a 250 mesh stainless screen with emulsion thickness 20 µm, delivering a fired film thickness of 8–12 µm. Industry compliance standards include ECE R43 Annex 18 for heated rear windows, FMVSS 205 transmittance and optical durability, RoHS 2011/65/EU, and DIN 52305 optical deviation measurement; busbar continuity after 1000 h at 85 °C/85% RH must not exceed 2.0 Ω. Downstream production places the printed wet film in a bending furnace where organic burnout occurs between 350–450 °C, bismuth glass softens and wets the glass surface above 520 °C, and the silver film densifies during the tempering dwell at 620–700 °C for 3–5 min. The process conflict in this zone is the narrow temperature band: below 600 °C adhesion drops under 8 N/mm² after annealing and above 720 °C the glass substrate begins to soften and distort. Terminal product types include heated rear windshields, camera window de-icing grids, wiper rest heater circuits, and heated side mirrors with printed silver connections.
On 96% alumina substrates with a fired surface roughness Ra below 0.6 µm, the high-shear rheology of SuA-101 determines line resolution in thick-film hybrid fabrication. The formulation addition ratio is 88–92 wt% silver, 4–6 wt% lead-free borosilicate glass frit, and 0.5–1.0 wt% copper oxide adhesion promoter, with paste viscosity maintained at 200–300 Pa·s at 10 s−1; the material is printed at 15–20 µm wet thickness, dried at 100–150 °C for 10 min, and fired in a belt furnace at 850 °C peak temperature for 10 min within a 25 min total firing profile. Compliance anchors include MIL-PRF-38534 class K hybrid microcircuit qualification, IPC-A-600J void and delamination criteria, ASTM D257-14 volume resistivity testing, and ASTM D3359-17 cross-cut adhesion classification; fired films are expected to maintain volume resistivity below 1.5 × 10−5 Ω·cm and adhesion classification 5B. Downstream manufacturing uses a semi-automatic screen printer with vacuum tooling, a serpentine belt furnace with temperature uniformity better than ±5 °C, and nitrogen purging during organic burn-off from 250 °C to 400 °C. Because the fired glass frit chemistry is lead-free, the same paste lot is suitable for RoHS-compliant assemblies but not for gold-plated wire bonding pads where silver migration may occur over 1000 h under high DC bias at 85 °C/85% RH. Terminal product types include military radar modules, downhole drilling pressure sensors, hermetic hybrid telemetry circuits, and implantable medical programmer interposers where traceable lot data are retained for 10 years.
The upper cure temperature for SuA-101 on heat-stabilised polyethylene terephthalate (PET) is set by substrate dimensional stability, not paste chemistry. The addition ratio for roll-to-roll antenna printing is 75–80 wt% silver flake, 10–14 wt% thermoplastic polyester binder, and 8–12 wt% glycol ether solvent; wet film thickness is controlled at 12–16 µm, and cure is limited to 125–135 °C for 15–20 min. At 135 °C the PET shrinkage reaches 0.3–0.5% in machine direction, and above 140 °C dimensional distortion degrades RFID antenna inductance uniformity and read range by more than 30%. Compliance anchors include RoHS 2011/65/EU, REACH SVHC, ISO/IEC 18000-6C UHF air interface conformance, and ASTM F1710-08 trace metal contamination limits; printed antenna sheet resistivity is inspected with a four-point probe against 0.08–0.12 Ω/sq for a 10 µm cured film. Downstream production uses a rotary screen press with 300 mesh, magnetic squeegee pressure 0.3 MPa, web speed 20–30 m/min, and forced-air jet drying at 130 °C; the paste is not suitable for gravure or inkjet lines because its viscosity at 10 s−1 is 15–25 Pa·s and silver flake dimension exceeds 8 µm, which would block gravure cells below 40 µm. Terminal product types include UHF RFID inlet labels, smart packaging antennas, retail anti-theft labels, and logistics tracking tags.
After converting the printed silver surface to silver chloride by galvanostatic oxidation in 0.1 mol/L KCl at 0.5 mA/cm² for 20 s, the SuA-101 film serves as the reference electrode in enzymatic electrochemical cells. The formulation addition ratio for biosensor electrode printing is 80–85 wt% silver flake, 7–10 wt% polymeric binder, and 6–9 wt% carbitol acetate solvent; it is printed through a 325 mesh screen at 8–12 µm wet thickness on 250 µm PET and cured at 120 °C for 15 min. Compliance anchors for the manufacturing line are ISO 13485:2016 quality system requirements, FDA 21 CFR 820.30 design controls, ISO 10993-5:2009 cytotoxicity screening for final device components, and EU IVDR 2017/746 performance evaluation requirements for in vitro diagnostic devices. Downstream production includes roll-to-roll screen printing, forced air curing, UV dielectric overcoating, laser ablation of working electrode windows, chloride conversion, enzyme membrane deposition, and singulation; open-circuit potential of the printed reference electrode is monitored against a saturated calomel electrode, with lot rejection set at drift greater than 3 mV over 1 h. Chloride contamination must be avoided before AgCl conversion because premature surface chloridation shifts the reference potential and increases electrode impedance from 200–400 Ω to above 1.5 kΩ at 1 kHz. Terminal product types include glucose test strips, lactate biosensors, point-of-care diagnostic devices, and single-use electrochemical cell assemblies.
In LED and sensor package assembly, the paste is dispensed as a die-attach adhesive where bond-line thickness and fillet geometry control thermal dissipation and die shear strength. The formulation addition ratio for dispense-grade SuA-101 is 80–86 wt% silver flake, 10–15 wt% epoxy resin, 2–5 wt% reactive diluent, and 0.5–1.0 wt% adhesion promoter; the target wet dispense volume for a 1.0 mm square die is 0.12–0.18 mm³, and die placement force is maintained at 50–150 g to produce a bond-line thickness of 25–45 µm. Industry compliance standards include AEC-Q200 Rev E stress tests for passive components, MIL-STD-883 Method 2019.7 die shear strength, JEDEC J-STD-020 moisture sensitivity level classification, and RoHS 2011/65/EU; die shear force for 1.0 mm silicon dies is required to remain above 10 kg after 1000 h of thermal cycling from −40 °C to 125 °C. Downstream production uses positive displacement dispense pumps with needle diameter 0.20–0.25 mm, automated die bonders with placement accuracy ±15 µm, and a two-step cure of 100 °C for 30 min followed by 150 °C for 60 min; post-cure voids below the die are inspected by scanning acoustic microscopy and must remain under 5% of the die area. Operational boundaries specify avoiding cure above 180 °C before wire bonding because residual solvent outgassing can contaminate bond pads and reduce wire pull strength. Terminal product types include high-brightness LED packages, high-power sensor packages, MEMS chip attachment, and metal-core printed circuit board thermal pads.
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SuA-101 is a single-component, silver flake-filled conductive paste formulated for stencil and screen deposition of low-resistance interconnects on alumina, polyimide, FR-4, and ITO-coated glass. The material is supplied as a solvent-borne system with a silver content of 82 ± 2 wt% and a maximum coarse particle size of 15 µm when measured by a Hegman gauge in accordance with ISO 1524:2013. Its primary intended function is to replace etched copper or solder interconnects in flexible printed electronics, membrane touch switches, printed antenna patterns, and low-power photovoltaic bus bars. The cured film is specified to achieve a volume resistivity of ≤ 8 × 10⁻⁵ Ω·cm after a cure of 150 °C for 30 min in a forced-air convection oven, as measured by the four-point probe method of ASTM D257-14.
In stencil printing operations, the paste exhibits a Brookfield RVT viscosity of 28–42 Pa·s at 25 °C using a CP52 spindle at 5 s⁻¹ per ISO 2555:2018. The thixotropic index, calculated as the ratio of apparent viscosity at 1 rpm to 10 rpm, is specified as 5.5–6.8. This index permits rapid slumping cessation after blade traverse while maintaining sufficient flow through apertures of 100–150 µm width. Production-scale printers fitted with stainless steel stencils of 75 µm thickness and metal squeegees operated at 80–120 mm/s have demonstrated printed wet thicknesses of 60–70 µm, with batch-to-batch variation limited to ± 5 µm when the paste is conditioned to 23 ± 2 °C and 45 ± 10 % RH. The material should not be printed below 18 °C because condensation-induced solvent absorption raises the thixotropic index above 7.5, producing aperture starvation and edge tearing.
The solvent package in SuA-101 comprises ethylene glycol monobutyl ether acetate and a dibasic ester fraction with a combined atmospheric boiling range of 192–210 °C. During the cure ramp from 25 °C to 150 °C at 3–5 °C/min, approximately 90 % of the solvent evolves before the silver flake binder reaches gelation. If the ramp exceeds 8 °C/min, rapid vaporization generates pinholes and trapped voids of 10–30 µm diameter in dried deposits thicker than 40 µm. The manufacturer’s technical bulletin cites a cure-activation energy of 78–86 kJ/mol derived from isothermal differential scanning calorimetry at 130–170 °C. Isothermal hold below 130 °C results in incomplete polymer crosslinking and volume resistivity drift above 1 × 10⁻⁴ Ω·cm after thermal aging at 85 °C for 500 h. A hold of 30 min at 150 °C is sufficient to reach a gel fraction above 92 % as determined by extraction with methyl ethyl ketone.
The cure window at the substrate surface is specified as 150 ± 5 °C for high-density printed deposits. Exceeding 160 °C accelerates oxidation of silver flake surfaces, raising sheet resistivity by 15–20 % relative to the optimum cure. Below 145 °C, adhesion to silver-coated copper drops below 2.5 N/mm² when tested per ASTM D4541. In forced-air convection ovens, chamber uniformity should be maintained within ± 3 K and exhaust airflow should be set between 2 m³/min and 4 m³/min per kilogram of paste to avoid localized solvent accumulation. For vacuum-assisted drying at −0.085 MPa, the peak temperature may be reduced to 140 °C without loss of final crosslink density, but published data for this specific configuration is limited.
Differences from two other established conductive silver paste families are summarized in the following comparative matrix. The data are drawn from the manufacturer’s technical bulletin and typical property windows published in industrial silver paste datasheets; published data for this specific configuration is limited outside those sources.
| Property | SuA-101 | Conventional epoxy-based silver paste | Low-temperature silver nanoparticle paste |
|---|---|---|---|
| Cure condition | 150 °C, 30 min | 120–150 °C, 60–120 min | 200 °C, 30 min under 0.2–0.5 MPa |
| Volume resistivity after cure | ≤ 8 × 10⁻⁵ Ω·cm per ASTM D257-14 | 1 × 10⁻⁴–5 × 10⁻⁴ Ω·cm | 2 × 10⁻⁵–6 × 10⁻⁵ Ω·cm |
| Silver content | 82 ± 2 wt% | 70–80 wt% | 80–90 wt% |
| Thixotropic index | 5.5–6.8 | 3.0–4.5 | 1.5–2.5 |
| Lap shear strength on alumina | 4.2 MPa per ISO 4587:2003 | 3.0–5.0 MPa | 2.0–3.5 MPa |
| Storage condition | 5–10 °C, 6 months | −20 °C, 12 months two-component | 5 °C, 3 months |
The principal processing difference is the elimination of a separate hardener. Conventional two-component epoxy silver adhesives require pre-mixing and are subject to pot-life limits of 8–24 h at 25 °C, whereas SuA-101 is supplied ready to print. The solvent-borne binder in SuA-101 also permits a lower initial wet-film slump than most unfilled or lightly filled epoxy pastes; printed line widths of 100 µm on polyimide retain their geometry within 10 % after a 5 min settling period at 25 °C.
Substitution is not universal. Because the cured SuA-101 binder has a lower elongation to break than tough epoxy systems, continuous thermal cycling between −40 °C and 125 °C per IEC 60068-2-14 Nb can produce microcracking in deposits exceeding 75 µm thickness on low-modulus polyimide substrates. The material is therefore not recommended for die-attach applications where the die edge exceeds 5 mm and the substrate coefficient of thermal expansion is above 25 ppm/K. In such cases, a high-flexibility silver-filled epoxy should be retained.
Storage and shelf-life constraints are governed by the solvent-borne binder. The material must be refrigerated at 5–10 °C in sealed polypropylene cartridges and allowed to reach 23 ± 2 °C for at least 4 h before opening to prevent condensation on the paste surface. Open containers should be consumed within 72 h when ambient relative humidity is below 60 %; pre-drying is required above 60 % RH because moisture absorption accelerates bodying and can shift the thixotropic index above 7.5. The paste must not be combined with amine-functional silanes or amine-based adhesion promoters, because such additives trigger premature crosslinking and produce irreversible viscosity increases within 30 min at 25 °C.
Adhesion of SuA-101 to alumina ceramic after full cure is specified at 4.2 MPa in lap shear according to ISO 4587:2003, with cohesive failure expected at bondline thicknesses below 50 µm. On silver-coated copper, lap shear strength is 3.1–3.8 MPa, and on ITO-coated glass the 180° peel strength is typically 0.6–0.9 N/mm after 24 h at 85 °C and 85 % RH. In thermal cycling from −40 °C to 125 °C for 1000 cycles, the resistance shift on alumina ceramic is reported as ≤ 20 % when measured with a four-point probe after 1 h recovery at 23 °C.
Silver migration resistance is finite and must be addressed by circuit topology and overcoat selection. Under a DC bias of 15 V/mm at 85 °C and 85 % RH, uncoated SuA-101 traces with 0.3 mm spacing may exhibit dendritic growth within 300–500 h, depending on substrate ionic cleanliness. For circuits exposed to condensation, a conformal overcoat meeting IPC-CC-830B or equivalent should be applied. The paste is not recommended for continuously immersed high-humidity applications without such an overcoat.