| HS Code | 912316 |
| Silver Content | ≥85 wt% |
| Solid Content | 90–95 wt% |
| Viscosity At 25 C | 50,000–150,000 mPa·s |
| Sintering Temperature Range | 200–350 °C |
| Sintering Atmosphere | Air or inert nitrogen |
| Bulk Resistivity After Sintering | ≤5 μΩ·cm |
| Sheet Resistance At 10 μm Sintered Thickness | ≤5 mΩ/sq |
| Adhesion Strength | ≥20 N/mm² |
| Thermal Conductivity After Sintering | ≥200 W/(m·K) |
| Average Silver Particle Size | 0.3–1.0 μm |
| Sintered Film Density | 7.5–8.5 g/cm³ |
| Storage Temperature | 5–10 °C |
| Shelf Life | 6 months |
As an accredited Pure Silver Full Sintering Silver Paste Electronic/EL Grade factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Pure Silver Full Sintering Silver Paste Electronic/EL Grade is packaged in sealed, moisture-proof jars, net weight 1 kg per container. |
| Container Loading (20′ FCL) | 20’ FCL of electronic-grade pure silver sintering paste, securely packed in sealed drums/pails, full container load, ready for shipment. |
| Shipping | This product ships via ground freight only, in sealed, moisture-resistant containers to preserve paste integrity. It is classified as non-hazardous for transport but requires careful handling and temperature-controlled storage. Ensure compliance with local regulations and avoid cold or extreme heat during transit to prevent material degradation. |
| Storage | Store in a tightly sealed, original container in a cool, dry, well-ventilated area, ideally between 2–8°C. Avoid exposure to light, moisture, and open flames. Keep away from incompatible materials and direct heat sources. Do not freeze. Ensure container remains upright to prevent leakage, and use within shelf life once opened. |
| Shelf Life | Shelf life is typically six months when stored unopened at 2–8°C in the original sealed container, protected from light. |
Screen-printed front-side metallization on p-type monocrystalline PERC cells is processed as a co-fired system in which the silver paste must sinter through an antireflective silicon nitride layer while forming ohmic contact to a phosphorus-doped emitter. Deposition on a high-speed screen printer with a front-side mesh count between 360 wires/inch and 430 wires/inch, a tensioned metal screen at 20 N to 30 N, and a snap-off distance of 0.0 mm to 0.3 mm produces finger widths below 40 µm. The as-deposited wet film is dried in a belt dryer at 200 °C to 300 °C with a residence time of 30 s to 60 s to remove volatile solvent before the wafer enters a multi-zone infrared firing furnace. Peak firing zone setpoints for p-type PERC typically fall between 760 °C and 830 °C; wafer peak temperature is profiled with a thermocouple-instrumented silicon wafer at least once per hour because belt loading and zone emissivity shift the true wafer temperature by 10 °C to 20 °C relative to setpoint. Overfiring produces excessive silver crystallite penetration into the emitter, which increases junction recombination and reduces open-circuit voltage under IEC 60904-1:2020 measurement conditions, while underfiring increases contact resistance and series resistance. The paste solids content after organic burn-off is normally between 88 wt% and 93 wt%; the glass frit fraction is adjusted to balance silicon nitride etching and contact resistance without excessive glass coverage at the emitter interface. Rheological control uses a Brookfield HBT viscometer at 10 rpm and 25 °C, with acceptable lot-release viscosity typically between 25 Pa·s and 45 Pa·s. A three-roll mill with 5 µm gap settings is used for final dispersion; fineness of grind is measured per ASTM D1210-05 to maintain a 4 to 6 Hegman fineness. Adhesion of fired fingers is evaluated after soldering with ASTM D3359-17 tape pull on witness strips and via electroluminescence-imaged cell sorters on production lines. Module-level qualification is covered by IEC 61215-1:2021, but front-side electrode stability under thermal cycling and damp heat is additionally monitored through fill factor loss below 5% after 1,000 h of exposure at 85 °C/85% RH in accordance with IEC 60068-2-78:2012; published data for paste-level degradation mechanisms at the silver-silicon interface under long-term potential-induced degradation is limited.
A thick-film hybrid microcircuit built on 96% alumina substrates is printed with a 200–325 mesh stainless-steel screen, a 60–80 Shore A squeegee, and a snap-off distance of 0.5 mm to 1.0 mm, then levelled and dried at 125 °C to 150 °C for 10–15 min before an eight-zone belt furnace fires the conductor at a peak temperature of 850 °C for 8–12 min above 800 °C. The fired film thickness after a single pass is normally 8–12 µm, measured with a stylus profilometer under ISO 25178-600:2019 or equivalent contact profilometry. Wire bondability is qualified with MIL-STD-883 Method 2011.9 destructive wire bond pull and MIL-STD-883 Method 2017.8 visual inspection; solderability is checked with IPC J-STD-002D test conditions for SMD terminations. Adhesion to the ceramic is verified by ASTM D3359-17 crosshatch pull from witness parts in each furnace lot, and surface insulation resistance is tested in accordance with IPC-TM-650 2.6.3.3 at 85 °C/85% RH under 50 V DC bias. Sodium contamination on the substrate must be controlled before printing; incoming alumina is ultrasonically cleaned in deionized water at 40 kHz to 60 kHz and followed by an alcohol rinse, because residual sodium from substrate sintering can reduce insulation resistance after fired thick-film resistors are trimmed. The paste cannot be used directly on substrates with tin-lead metallizations that undergo high-temperature rework, because molten tin penetration along sintered silver grain boundaries can occur above 260 °C. In high-frequency circuits, the conductor line width is verified by automated optical inspection at ±5 µm tolerance against artwork, and insertion loss is assessed by network analyzer measurements on stripline witness coupons per IPC-6018D where applicable.
Low-temperature co-fired ceramic tapes impose a coupled densification schedule on the conductor paste because the tape shrinks by 12–15% in the x–y plane and by 26–30% in the z-direction during the final co-firing ramp from 600 °C to 850 °C. Via fill paste formulated with pure silver full-sintering solids must reach high plug density before the surrounding tape closes, otherwise trapped organic residue forms carbon in the via and increases via resistance. The silver powder fraction is raised to 80–85 wt%, with median particle size controlled by laser diffraction under ISO 13320-1:2020 to a D50 between 1.0 µm and 3.0 µm. Rheology is adjusted for blind via diameters of 100 µm to 250 µm using a screen printer with a stencil thickness of 25 µm to 75 µm and multiple print-fill passes; shear viscosity is measured with a cone-and-plate rheometer under ISO 3219:1993 at a shear rate of 10 s-1. After printing, the panel is laminated in an isostatic press at 70 °C and 20.7 MPa to consolidate tape and via fill, then fired in a forced-air belt furnace with a peak dwell at 850 °C for 10–15 min. A processing conflict arises because the dielectric tape reaches maximum densification near 800 °C, while the pure silver conductor sinters at a different onset temperature; if the conductor begins densifying too early, it constrains tape shrinkage and induces camber or corner lift. Cross-section via fill is evaluated by scanning electron microscopy at 500x and 1,000x, with void area below 5% of via area accepted for production. Insulation resistance between buried conductors is tested per IPC-TM-650 2.6.3.3, and end-product microwave performance is assessed where applicable under IPC-6018D with insertion loss measured on a vector network analyzer from 10 MHz to 40 GHz. The paste is incompatible with low-softening-point glass tapes containing lead-borosilicate frits that begin to flow below 600 °C, because silver diffusion into the tape increases high-frequency loss tangent and can reduce breakdown voltage.
| Application segment | Primary standard | Test method | Process parameter verified |
|---|---|---|---|
| Photovoltaic front-side | IEC 61215-1:2021 | Thermal cycling / damp heat | Fill factor loss, electrode adhesion |
| Alumina hybrid microcircuit | MIL-PRF-38534H | MIL-STD-883 wire bond pull | Bond strength, visual bondability |
| LTCC multilayer circuit | IPC-6018D | Network analyzer S-parameter | Insertion loss, via resistance |
| Automotive glazing buss bar | ECE R43 | Four-wire grid resistance | Heating grid continuity, adhesion |
| MLCC internal electrode | IEC 60384-22:2015 | Capacitance, DF, IR | Electrode integrity, insulation resistance |
Lead zirconate titanate transducer wafers are metallized on opposing faces with pure silver full-sintering paste to provide low sheet resistance for poling and drive electrodes. The paste is applied through a 200–250 mesh screen after an ultrasonic clean in isopropanol, dried at 120 °C for 10 min, and fired in a belt furnace with a peak temperature maintained between 650 °C and 750 °C for 5–10 min, because prolonged firing above 750 °C causes measurable PbO loss from PZT-5A and PZT-5H ceramics. After cooling, poling is performed in silicone oil at 100–150 °C under a DC field of 1–3 kV/mm; the electrode must maintain continuity during polarization and subsequent operation under high electric fields. Volume resistivity of the fired layer is measured with a guarded electrode fixture according to ASTM D257-14, and adhesion is checked after poling by ASTM D3359-17 tape pull on witness wafers. Silver migration is a documented failure mode under DC bias and humidity; countermeasures include coating the electrode edges with a conformal barrier and limiting long-term operation above 85% RH unless electrically biased. The fired silver layer is not a true barrier against solder dissolution, so high-temperature soldering above 260 °C can remove the electrode unless a solderable overprint is used. Published data comparing fired silver adhesion on PZT-5A and PZT-5H compositions is limited, and incoming ceramic lot-to-lot surface roughness differences require adhesion witness pulls per furnace run rather than reliance on published nominal values.
Automotive float-glass bending lines require silver paste to be screen-printed on the concave surface of windshield defroster or antenna patterns before the glass is heated into the bending range, so the same thermal cycle that shapes the glazing also sinters the silver conductor into the glass surface. The paste is printed through a 195–235 mesh polyester or stainless-steel screen onto washed soda-lime glass, dried under forced air at 150–200 °C, and then enters a bending lehr where the glass temperature reaches 580–640 °C for a dwell of 60–180 s, depending on windshield thickness. The frit chemistry in the silver paste must fuse to the glass at this temperature without causing discoloration; lead-free frits are normally required for current production because of end-of-life vehicle recycling regulations, although the exact regional exemptions for automotive safety glazing must be checked against the applicable vehicle recycling directive. Electrical continuity of the heated grid is tested at the exit of the lehr with four-wire resistance measurement consistent with SAE J953-type methods, and optical transmittance and distortion are assessed under the requirements of ECE R43 or FMVSS 205 for safety glass. In high-humidity operation, sodium ion migration from the soda-lime substrate into the sintered silver buss bar can reduce adhesion and increase resistance; damp heat exposure at 85 °C/85% RH per IEC 60068-2-78:2012 is used to qualify the anti-migration overglaze. The paste must not be fired at temperatures above 650 °C because glass sag and optical distortion become unacceptable; below 560 °C the silver does not form sufficient interfacial bonding and grid peel occurs during wire termination. Line speed, lehr zone profiles, and paste open time in the print shop are adjusted together because the paste solvent package must evaporate before the glass reaches the frit transition temperature, failing which pinholes appear in the fired buss bar.
Multilayer ceramic capacitor manufacturing with pure silver internal electrodes is confined to low-firing ceramic dielectrics because silver melts at 961 °C. The paste is printed or slot-die coated onto barium titanate-based or other PME dielectric tape at a wet thickness of 2–5 µm, dried at 70–100 °C, then stacked and laminated in a heated press at 60–80 °C and 20–30 MPa for 10–20 min. The green chips are cut, debound in a nitrogen or air box furnace with a slow ramp between 200 °C and 400 °C, and sintered at a peak temperature below 900 °C with a dwell of 1–4 h; the actual peak depends on the dielectric densification curve. Capacitance, dissipation factor, and insulation resistance are measured on the completed chip by methods given in IEC 60384-1:2021 and the detailed specification IEC 60384-22:2015 for surface mount multilayer ceramic capacitors. The full-sintered silver electrode is incompatible with high-temperature X7R or C0G dielectric systems that densify above 1,150 °C, where palladium or base-metal electrodes are used instead. Pulse testing and bias aging require precautions because silver migration can occur at electrode edges under high DC fields; insulation resistance testing after 1,000 h at 85 °C/85% RH is used to verify the end-cap barrier system. The resulting component is not intended for high-current power capacitors because the pure silver electrode cross-section is limited by green tape thickness and lamination pressure; published data on electromigration in pure silver MLCC electrodes under high ripple current is limited.
Thick-film electroluminescent devices fabricated on alumina or other ceramic substrates use a screen-printed silver rear electrode that is sintered before the zinc sulfide phosphor and dielectric layers are deposited, because the Cu-doped or Mn-doped phosphor degrades if exposed to the temperatures used for full silver sintering. The rear electrode is printed with a 250–325 mesh screen, dried at 130–150 °C, and fired at a peak temperature between 500 °C and 600 °C when a high-temperature barrier dielectric is present; for bare alumina substrates the silver can be fired at up to 850 °C before the phosphor is applied, but this is not done after phosphor deposition. The configuration is used for aircraft cockpit displays, industrial annunciator lamps, and high-reliability backlights where moisture ingress into the phosphor layer is controlled by a hermetic overglaze. Adhesion of the rear electrode is evaluated after firing with ASTM D3359-17, and line resistance is measured with a four-point probe meeting the geometry limits of ASTM F84-93 or equivalent. Optical luminance after phosphor excitation is not a property of the paste itself but is strongly affected by rear electrode reflectivity; silver pastes with high sintered density produce higher reflectance than lower-density graphite counter electrodes. The paste cannot be processed with amine-based catalysts in the same wet process line because residual amine at the alumina–silver interface can reduce adhesion and increase via resistance. Published standard specifications specific to full-sintering silver in thick-film electroluminescent lamps are limited compared with photovoltaic and hybrid-microcircuit specifications, so incoming paste qualification is normally carried out with witness prints on the same ceramic batch used in the device.
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Pure Silver Full Sintering Silver Paste Electronic/EL Grade is supplied as a screen-printable thick-film conductor paste whose dried and fired deposit forms a continuous silver metal network by atomic diffusion rather than by polymer-chain entanglement or low-temperature additive sintering. The material is identified in procurement documents primarily by its metal loading, particle size class, and firing profile; no single ISO or IEC model designation governs this product category. Typical formulation windows for this class include 85–92 wt% silver solids, a metallic silver purity of ≥99.9%, a D50 particle size of 1.5–3.5 µm, and a Brookfield viscosity of 25–50 Pa·s at 25 °C and 10 rpm. The organic vehicle is composed of ethyl cellulose and high-boiling ester alcohol solvents, with burnout completed between 350 °C and 450 °C. A low-softening borosilicate glass frit is present at 2–6 wt% of solids to promote adhesion to alumina, glass, and silicon nitride substrates. The product is distinguished from polymer thick-film silver pastes by the requirement for a full sintering step at temperatures above 500 °C, which restricts its use to substrates that tolerate thermal exposure at these levels.
Incoming inspection of this product class typically includes laser diffraction particle size analysis according to ISO 13320:2020, thermogravimetric solids content according to ASTM E1131-08, and Brookfield viscosity according to ISO 2555:2018. The silver powder is held to a particle size distribution with D10 of 0.4–1.0 µm, D50 of 1.5–3.5 µm, and D90 of 6.0–10.0 µm; a broader distribution improves packing density, but a tail above 15 µm must be avoided to prevent screen clogging on 325 mesh screens. BET specific surface area of the silver phase is controlled between 0.8 m²/g and 2.5 m²/g because excessive surface area increases organic vehicle demand and raises the risk of agglomerate formation. Tap density of the silver powder is typically 3.5–5.5 g/cm³, while sintered film density after firing is expected to reach 7.4–9.2 g/cm³. Thermogravimetric analysis differentiates free solvent, binder decomposition, and residual ash; the ash content after burnout is 0.5–2.0 wt% above the silver solids and corresponds to the glass frit and inorganic additives.
Full sintering silver paste requires burnout of the organic vehicle followed by solid-state and liquid-phase transport of silver particles across particle contacts. During the temperature ramp from 350 °C to 450 °C, the ethyl cellulose decomposes and the solvent fraction volatilizes; the residual carbon must be removed before the glass frit softens at 480–560 °C. Above 580 °C, silver diffusion forms sinter necks that reduce grain-boundary scattering and produce a conductive path with typical sheet resistivity values of 2.0–6.0 mΩ/□/25 µm after firing at 600–650 °C for 10–15 min at peak temperature. By contrast, hybrid conductive adhesives rely on intimate contact between dispersed silver flakes within a cured epoxy or acrylic matrix; their volume resistivity is typically 1 × 10⁻³ Ω·cm to 1 × 10⁻⁴ Ω·cm, whereas a fully sintered silver film of this grade approaches 2.0–6.0 × 10⁻⁶ Ω·cm when measured by a four-point probe in accordance with ASTM F390-11. The full-sintering mechanism therefore produces metallic conduction with lower series resistance for high-brightness electroluminescent bus bars and hybrid circuit traces, but it cannot be processed on polyethylene terephthalate, polycarbonate, or paper substrates.
For thick-film electroluminescent devices, the paste is used as the rear electrode or as the bus-bar metallization on glass or ceramic substrates. AC drive frequencies in the range of 400–1000 Hz and peak voltages of 80–150 V are common in EL lamps; the low sheet resistance of the fired silver is required to maintain uniform luminance across large-area panels. A bus-bar resistance below 2 Ω/cm is maintained by printing a fired thickness of 8–12 µm and a width of 200–500 µm. Voltage drop is calculated from the rectangular trace dimensions and the measured sheet resistance according to IPC-2221 conductor sizing formulas.
Processing on a production belt furnace begins with screen printing through 200–325 mesh stainless-steel screens with emulsion thicknesses of 10–25 µm. A polyurethane squeegee with hardness 60–75 Shore A is operated at 40–80 mm/s, with snap-off distance controlled between 0.6 mm and 1.2 mm. The wet film is levelled for 5–10 min at ambient temperature and then dried at 120–150 °C for 5–10 min in an infrared or convection oven. The firing profile uses a three-zone belt furnace with a total cycle of 30–45 min: the first zone heats the substrate to 350–450 °C to complete binder burnout, the second zone ramps to 580–650 °C, and the third zone cools at a controlled rate below 100 °C/min to avoid thermal shock in glass substrates. The fired film thickness is typically 8–20 µm, and line widths down to 75–100 µm are achievable with optimized rheology and screen tension. For electroluminescent glass display electrodes, bus bars of 200–350 µm width are printed along panel edges to carry AC drive currents while minimizing voltage drop.
The paste is pseudoplastic and thixotropic. The thixotropic index, expressed as the ratio of viscosity at 0.5 rpm to viscosity at 5 rpm on a Brookfield RVDV-II+ viscometer at 25 °C, is typically 4.0–6.5; this value is selected to recover structure after screen passage and prevent line slumping. Solids content is held between 85% and 92% by weight. Below 85%, sag on vertical glass panels becomes significant, and above 92%, screen clogging and mesh skipping occur on 325 mesh screens. After full sintering, volume resistivity measured according to IPC-TM-650 method 2.5.17 typically falls between 2.0 × 10⁻⁶ Ω·cm and 6.0 × 10⁻⁶ Ω·cm; this range depends on peak firing temperature, glass frit volume fraction, and substrate surface roughness. Initial pull adhesion to 96% alumina substrates is substrate-dependent, and published data for this specific configuration is limited; supplier batch certificates should be requested when adhesion below 15 N/mm² is suspected. Electrical stability under high-humidity DC bias is limited by silver migration, and the material is therefore not recommended for closely spaced DC traces at field strengths above 10 V/mm in the presence of condensed moisture.
Production-scale failure modes observed on belt furnaces include pinhole formation from incomplete de-airing, mesh clogging from agglomerates above 15 µm, and slumping when the thixotropic index falls below 4.0. Pinholes in the wet film originate from air entrainment during high-speed screen release; use of a vacuum de-airing step at 10–20 kPa for 5–10 min reduces defect density. Blistering during firing occurs when the drying temperature exceeds 150 °C or when the solvent is trapped by a dense surface skin. Scavenging of the silver film by tin-lead solder is a known limitation; immersion at 230 °C for more than 5 s can partially dissolve the sintered silver, so soldering should be completed with fast dwell times or silver-bearing solder alloys.
Compliance documentation for this electronic/EL grade is supplied through X-ray fluorescence screening and wet digestion according to the IEC 62321 series. The lead-free glass frit is formulated to support RoHS 2011/65/EU and Commission Delegated Directive (EU) 2015/863. Antimony, arsenic, and cadmium are not intentionally added, and typical lot screening reports cadmium below 5 ppm, lead below 50 ppm, mercury below 2 ppm, and hexavalent chromium below 2 ppm. REACH Regulation (EC) No 1907/2006 requires disclosure if a substance of very high concern exceeds 0.1% w/w; this product is supplied with a statement that no SVHC on the current candidate list is present at or above that threshold. The manufacturing site operates under ISO 9001:2015 and ISO 14001:2015 certification, but this does not replace part-specific PPAP documentation for automotive or aerospace customers.
| Directive/regulation | Relevant restriction or requirement | Test or documentation method |
|---|---|---|
| RoHS 2011/65/EU and (EU) 2015/863 | Pb <1000 ppm, Cd <100 ppm, Hg <1000 ppm, Cr(VI) <1000 ppm, PBB/PBDE <1000 ppm | IEC 62321 series |
| REACH (EC) No 1907/2006 | SVHC disclosure threshold 0.1% w/w | Supplier SVHC statement; analytical screening by GC-MS/LC-MS |
| ISO 9001:2015 | Process control and traceability | Site certificate |
| ISO 14001:2015 | Environmental management | Site certificate |
During firing, process exhaust from the burnout zone should be scrubbed or vented because the organic vehicle generates carbon monoxide, carbon dioxide, and low-molecular-weight hydrocarbons between 150 °C and 450 °C. Occupational exposure to silver is evaluated against the EU indicative occupational exposure limit value of 0.1 mg/m³ as an 8-hour time-weighted average, and local jurisdictions may set lower limits. Silver migration testing for electronic/EL grade is performed under damp heat conditions at 40 °C and 93% relative humidity with a DC bias of 10 V across a 0.5 mm gap; the material is rated for AC electroluminescent use because migration is strongly suppressed under AC drive.
If the product is processed in a furnace with peak temperature below 450 °C, the ethyl cellulose binder does not fully oxidize and the borosilicate glass frit remains below its softening point. Carbonaceous residue raises the measured sheet resistivity and interferes with wire bonding and soldering. Incomplete sinter-neck formation leaves particle boundaries that increase the temperature coefficient of resistance and reduce adhesion to the substrate. This limitation separates the product from low-temperature nano-silver pastes, which are formulated with particle diameters below 100 nm and may be processed at 200–350 °C on polymer films. Those low-temperature materials achieve acceptable conductivity for flexible printed electronics but typically exhibit higher volume resistivity, lower film density, and greater sensitivity to humidity during storage than a fully sintered silver film. The full-sintering product should not be combined with amine-based low-temperature curing agents or acid-containing fluxes because amine residues can complex with silver at the firing surface and leave non-conductive residues.
Comparative selection among conductor pastes is governed by substrate thermal stability, sheet resistivity, adhesion, cost, and environmental testing. Silver-coated copper pastes contain a copper core with a silver surface layer; they reduce raw material cost but show oxidation at exposed edges after abrasion and are not suitable where edge corrosion is unacceptable. Carbon pastes are processed at low temperature but exhibit sheet resistivity in the range of 15–50 Ω/□/25 µm, several orders of magnitude higher than this silver paste. Polymer thick-film silver is printable on flexible polyester and polyimide, but contact resistance and long-term stability under AC electroluminescent drive conditions are inferior to a fully densified silver trace.
| Property | Full-sintering pure silver paste | Polymer thick-film silver | Silver-coated copper | Carbon paste |
|---|---|---|---|---|
| Firable substrate | Glass, alumina, silicon nitride | PET, PEN, polyimide | Glass, alumina | PET, polycarbonate |
| Peak process temperature | 580–650 °C | 80–150 °C | 450–650 °C in nitrogen | 80–150 °C |
| Sheet resistivity | 2.0–6.0 mΩ/□/25 µm | 20–60 mΩ/□/25 µm | 10–40 mΩ/□/25 µm | 15–50 Ω/□/25 µm |
| Oxidation resistance | High | Moderate | Moderate at exposed edges | High |
| Substrate suitability | Ceramic and glass only | Flexible films | Ceramic and glass with controlled atmosphere | Flexible films |
Unopened containers should be stored at 5–25 °C and 30–60% relative humidity. Shelf life under these conditions is typically 6 months from date of manufacture; after opening, the paste should be used within 24 h to avoid skinning and solvent evaporation. Before printing, the paste is stirred by hand or on a roll mill at 20–30 rpm for 3–5 min; solvent should not be added unless viscosity drift makes screen release impossible, and then only the supplier-designated thinner at 1–3 wt%. Freezing destroys the suspension and causes silver flocculation; material exposed to temperatures below 0 °C should be quarantined and not printed. Waste paste and contaminated solvents are classified according to local regulations for heavy-metal-containing waste.