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Carboxylated SBR Latex (XSBR)
- Product Name: Carboxylated SBR Latex (XSBR)
- Factroy Site: Yudu County, Ganzhou, Jiangxi, China
- Price Inquiry: sales3@ascent-chem.com
- Manufacturer: Ascent Petrochem Holdings Co., Limited
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- Carboxylated SBR Latex (XSBR) is a carboxylated styrene-butadiene copolymer in aqueous dispersion, commonly used in the construction and adhesives industries, where high adhesion and mechanical stability are required.
| HS Code | 461722 |
| Appearance | Milky white liquid |
| Chemical Composition | Styrene-butadiene copolymer with carboxyl functional groups |
| Solids Content | 45-55% |
| Ph | 7.0-9.0 |
| Viscosity | 20-500 mPa·s |
| Particle Size | 100-200 nm |
| Glass Transition Temperature | -10 to +10 °C |
| Minimum Film Formation Temperature | 0-20 °C |
| Surface Tension | 30-45 mN/m |
| Density | Approximately 1.0 g/cm³ |
| Mechanical Stability | Good |
| Chemical Stability | Resistant to dilute acids and alkalis |
| Storage Stability | 6-12 months at 5-35 °C |
| Tensile Strength Of Film | 1-10 MPa |
| Elongation At Break | 100-600% |
As an accredited Carboxylated SBR Latex (XSBR) factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Carboxylated SBR Latex (XSBR) is packaged in 200 kg drums or 1,000 kg IBC totes, sealed to prevent contamination. |
| Container Loading (20′ FCL) | Carboxylated SBR Latex loaded in 20′ FCL: drums or IBCs on pallets, secured, sealed, with proper ventilation and spill containment. |
| Shipping | Carboxylated SBR Latex (XSBR) ships as a water-based dispersion in lined drums, IBC totes, or iso-tanks. Protect from freezing and excessive heat; store between 5–35°C. Ensure secure, leak-proof containment, adequate ventilation, and avoid prolonged exposure to air to prevent skinning. Non-hazardous, but handle with standard PPE. |
| Storage | Store Carboxylated SBR Latex (XSBR) in sealed, corrosion-resistant containers, preferably with mild agitation. Keep at 5–35°C; avoid freezing and excessive heat. Store in a dry, well-ventilated area away from direct sunlight, oxidizers, and contamination. Use within the manufacturer’s shelf-life period, and stir gently before use to maintain uniform dispersion. |
| Shelf Life | Shelf life: 6–12 months when stored sealed, cool, and frost-free; avoid freezing, overheating, and prolonged agitation. |
In tufted carpet manufacturing, carboxylated SBR latex is compounded into a pre-coat liquor with ground calcium carbonate at filler loadings from 150 phr to 350 phr on dry latex solids. A 20% aqueous sodium polyacrylate dispersant is added at 0.1–0.4 dry phr and an alkali-swellable associative thickener raises Brookfield RV viscosity to 8,000–14,000 mPa·s at 20 rpm. The compound is applied by puddle applicator or lick roller at 700–1,000 g/m² wet add-on to the back of a 1/10-gauge tufted nylon or polypropylene cut-pile cover before the assembly enters a gas-fired impingement oven at 130–150 °C for 2.5–5.0 min. Carboxylic acid groups on the butadiene backbone provide calcium ion tolerance and allow post-applied zinc oxide crosslinking at 0.5–2.0 dry phr; zinc-free systems for antimony trioxide-free carpet tile formulations may instead use ammonium zirconium carbonate at 1.0–2.5 dry phr. Production-scale failure modes include tuft bind loss when filler exceeds 350 phr because binder continuity is interrupted at the yarn base, and edge curling when the pre-coat film is over-dried beyond 160 °C. Tuft bind is assessed on a tensile testing machine according to ASTM D1335-21, while secondary backing delamination is tested per ASTM D3936-17. Terminal goods include broadloom carpet, carpet tiles, and modular carpet for contract interiors.
What Limits Binder Penetration in High-Loft Nonwoven Wipes?
Binder penetration in high-loft nonwoven wipes is constrained by latex surface tension, web density, and drying airflow. Carboxylated SBR latex with solids at 48–52%, pH 7.0–8.0, and Tg between -25 °C and -15 °C is diluted with deionized water to 8–20% solids before foam bonding or spray application to carded viscose/polyester webs at 20–60 g/m² basis weight. A through-air oven set at 150–170 °C with residence time 60–120 s removes water and initiates crosslinking. Crosslinker choice is limited by formaldehyde release: melamine-formaldehyde at 3.0–5.0 dry phr with ammonium chloride catalyst at 0.1–0.3 dry phr provides wet strength, while blocked aliphatic polyisocyanate at 1.0–3.0 dry phr is used for low-formaldehyde grades. Surface tension should be maintained at 38–42 mN/m because lower values drive binder migration to the web surface and produce a stiff, boardy handle. For skin-contact wipes, formulations are screened against Oeko-Tex Standard 100 class II limits for formaldehyde and residual monomers. Wet strip tensile strength is measured according to ISO 9073-3:2022, and absorbency is measured per ISO 9073-6:2001. Fluids with pH below 4.0 must be avoided during clean-up because acid shock coagulates the carboxylated latex on cellulosic fibers. Terminal products include spunlace floor wipes, kitchen cleaning sheets, and high-loft hygiene acquisition layers.
In coated paper and board manufacture, carboxylated SBR latex is blended with enzyme-converted starch at pigment binder ratios that prevent blistering during heat-set web offset printing. A typical coating color contains 100 parts pigment at a kaolin/ground calcium carbonate ratio from 50:50 to 20:80, 4–12 dry parts XSBR latex, 2–6 dry parts starch, 0.2–0.5 parts carboxymethyl cellulose, and 0.5–1.0 parts calcium stearate, with final solids of 60–68% and pH 8.2–9.0. Application on a high-speed blade coater running at 1,200–1,600 m/min uses a preheated web at 70–85 °C and hot-air drying at 150–200 °C, followed by supercalendering at 80–120 °C and 200–500 kN/m line load. Carboxylated SBR latex with gel content 40–70% and bound styrene 25–45% contributes wet pick resistance and porosity retention, while calcium ion tolerance prevents grit formation when coarse ground calcium carbonate is present. Surface strength is evaluated on an IGT printability tester according to ISO 3783:2006; gloss is measured per ISO 8254-1:2009; opacity is measured per ISO 2471:2008. Food-contact paper and board uses latex compliant with FDA 21 CFR 176.170 and EU 1935/2004, with formulation records maintained under the BfR XXXVI recommendation. A process limit at high shear: latex with aqueous phase conductivity above 1,500 µS/cm may show blade coater streaking due to colloidal destabilization. Terminal products include coated art paper, label stock, and folding boxboard for food packaging.
DMF-Free Synthetic Leather Base Web Impregnation with XSBR
For polyurethane synthetic leather, the needlepunched nonwoven base web is impregnated with carboxylated SBR latex before polyurethane coating to control fullness and delamination resistance. A padder with squeeze rolls set to an expression ratio of 70–90% applies a formulation containing 100 dry parts XSBR latex, 3–6 dry phr aliphatic polyisocyanate crosslinker, 0.5–1.0 wet phr fatty acid ester defoamer, and ammonium hydroxide to pH 8.0–8.8. The resin add-on is maintained at 15–30% on base web mass. Pre-drying at 100–120 °C is followed by curing at 145–160 °C for 1.5–3.0 min. Because N,N-dimethylformamide is not used, the impregnated base meets DMF-free criteria under REACH Annex XVII restrictions and the ZDHC MRSL v3.1. Tensile strength is tested by ISO 3376:2020, tongue tear by ISO 3377-1:2011, and coating adhesion by ISO 11339:2010 T-peel after 24 h at 23 °C and 50% RH. Production-scale limitations include residual anionic surfactant accumulation on the padder rolls, which reduces wetting of hydrophobic bicomponent PET/PA fibers if the latex surface tension exceeds 45 mN/m. A pre-wash with 40–60 °C deionized water is required when the base web contains spin finish above 0.3% by mass. Terminal products include automotive seat side bolsters, shoe tongue liners, and furniture upholstery bases.
| Application | Key control range | Cited method or regulation | Production boundary |
|---|---|---|---|
| Carpet pre-coat | 150–350 phr CaCO3; 130–150 °C | ASTM D1335-21, ASTM D3936-17 | Filler above 350 phr reduces tuft bind |
| Nonwoven wipes | 8–20% solids; 150–170 °C | ISO 9073-3:2022, ISO 9073-6:2001 | Surface tension below 38 mN/m induces surface migration |
| Paper coating | 4–12 dry parts latex; 60–68% solids | ISO 3783:2006, FDA 21 CFR 176.170 | Conductivity above 1,500 µS/cm correlates with blade streaking |
| Synthetic leather base | 15–30% add-on; 145–160 °C cure | ISO 3376:2020, ISO 3377-1:2011, REACH Annex XVII | Base web spin finish above 0.3% requires pre-wash |
| Cementitious waterproofing | 0.35:1–0.50:1 liquid:powder; 5–35 °C application | EN 14891:2017, EN 1542:1999, GB/T 23445-2009 | Below 5 °C film formation ceases |
| Abrasive pads | 15–25% binder add-on; 140–160 °C | ISO 9073-3:2022, ISO 9073-4:2021 | Free formaldehyde limited to ≤30 mg/kg |
| Flocking adhesive | 20,000–60,000 mPa·s; 150–160 °C cure | ISO 105-X12:2016, ISO 105-C06:2010, ISO 11339:2010 | Cure above 170 °C embrittles adhesive |
Two-component cementitious waterproofing slurries require careful control of polymer-cement ratio, mixing shear, and curing temperature. A liquid component containing carboxylated SBR latex at 50–80 parts (approximately 25–40 dry parts), mineral oil defoamer at 0.2–0.5 parts, and water at 20–50 parts is mixed with a powder component composed of CEM I 42.5 R cement 100 parts, 0.1–0.3 mm quartz sand 150–250 parts, and polycarboxylate superplasticizer 0.5–1.0 parts. The mixing ratio is fixed at 0.35:1 to 0.50:1 liquid-to-powder by weight, yielding a dry polymer-cement ratio of approximately 0.20–0.40. High-shear mixing at 600–900 rpm for 3 min disperses the latex into the cement paste without phase inversion; material temperature above 35 °C during mixing shortens pot life below 45 min. The slurry is applied by notch trowel or airless spray in two coats to a total dry film thickness of 0.8–1.5 mm. After 24 h at 23 °C, light foot traffic is possible, and full test loading is performed after 28 days at 23 °C and 50% RH. Testing follows EN 14891:2017 for liquid-applied water impermeable products and EN 1542:1999 for pull-off adhesion to concrete. In the PRC market, GB/T 23445-2009 type II requirements apply to flexible polymer-modified cementitious waterproofing coatings. Application below 5 °C is prohibited because film formation ceases and cement hydration is retarded; rain exposure within the first 24 h causes latex washout and pinholing. Terminal products include balcony waterproofing membranes, shower floor tanking, and roof repair slurries.
Abrasive Fiber Bonding and Scour Pad Resin Systems
Nonwoven abrasive pad production uses carboxylated SBR latex to bond 6–15 denier nylon or polyester fibers before abrasive grain addition. The binder bath contains 100 dry parts latex, 4.0–8.0 dry phr methylated melamine-formaldehyde crosslinker, 0.3–0.6 dry phr p-toluenesulfonic acid catalyst, and 0.2–0.5 dry phr silicone-polyether defoamer. Spray or dip-squeeze application targets 15–25% dry binder add-on on fiber mass. Fused aluminium oxide abrasive grain is then sprinkled onto the wet web at 10–30% of final pad mass before forced-air curing at 140–160 °C for 5–10 min. Residual free formaldehyde in the cured pad is limited by the customer specification to ≤ 30 mg/kg for consumer scourers, which requires precise melamine-formaldehyde stoichiometry and post-cure forced ventilation. The cured nonwoven is tested for strip tensile strength per ISO 9073-3:2022 and trapezoid tear per ISO 9073-4:2021. Delamination or abrasive grain shedding is evaluated by a 1,000-cycle Taber abrasion pass against ASTM D3884-22 using H-18 wheels at 500 g load, although published data for carboxylated SBR latex in this specific configuration is limited. Terminal products include maroon floor maintenance pads, green hand scouring pads, and industrial deburring discs.
When Textile Flocking Adhesives Require Controlled Rheology and Fast Cure
Textile flocking adhesives formulated with carboxylated SBR latex are adjusted to a pseudoplastic viscosity of 20,000–60,000 mPa·s at 20 rpm and pH 8.0–9.0. The compound contains 100 dry parts latex, 0.3–1.2 dry phr alkali-swellable polyacrylate thickener, 10–20 dry phr ground calcium carbonate, 2.0–5.0 dry phr blocked aliphatic polyisocyanate, and 0.1–0.3 wet phr nonionic wetting agent. Rotary screen printing or engraved roller application deposits 80–150 g/m² wet adhesive onto woven or knitted cotton, polyester, or nylon substrates. Electrostatic flocking at 40–70 kV with an electrode distance of 150–250 mm drives 0.5–1.0 mm polyamide or viscose flock fibers into the wet layer. Gelation at 120–140 °C for 60–90 s prevents fiber collapse before cure at 150–160 °C for 2–3 min. Dry crock resistance is assessed per ISO 105-X12:2016, domestic wash fastness per ISO 105-C06:2010, and adhesive peel strength per ISO 11339:2010. Skin-contact flocked apparel must meet Oeko-Tex Standard 100 class II limits for formaldehyde and extractable heavy metals. A production hazard occurs above 170 °C: excessive crosslinking embrittles the adhesive layer and reduces crock fastness while yellowing white flock. Terminal products include flocked automotive window channels, apparel logos, and decorative packaging inserts.
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- Carboxylated SBR Latex (XSBR) is manufactured under an ISO 9001 quality system and complies with relevant regulatory requirements.
- COA, SDS/MSDS, and related certificates are available upon request. For certificate requests or inquiries, contact: sales3@ascent-chem.com.
Aqueous carboxylated styrene-butadiene copolymer dispersions, designated carboxylated SBR latex (XSBR), are produced by emulsion copolymerization of styrene, butadiene, and one or more carboxylic acid monomers, commonly acrylic acid, methacrylic acid, or itaconic acid. Commercial XSBR is supplied at total solids of 50 ± 1 wt% when measured in accordance with ISO 3251:2019, with pH 7.5–9.0 by ISO 976:2013 and Brookfield RVT viscosity 50–500 mPa·s at 25 °C, spindle 2, 20 rev min⁻¹, as specified by ISO 2555:2018. Density is 1.00–1.03 g cm⁻³ using ISO 2811-1:2016. Bound carboxylic acid content is typically 1–10 wt% of dry polymer, while glass transition temperature, determined by differential scanning calorimetry under ISO 11357-2:2020, is adjusted between −20 °C and +20 °C by varying the styrene-to-butadiene mass ratio. Particle size measured by dynamic light scattering is generally 100–200 nm, with reference to ISO 22412:2017. Residual monomer concentrations are commonly specified below 1000 ppm, with reduced-VOC grades below 500 ppm. Model identifiers are supplier-specific and commonly encode nominal bound styrene content, carboxylation level, emulsifier type, or coagulant sensitivity; no harmonized industry model code exists. Grade selection therefore rests on bound styrene, carboxylation level, ion tolerance, and film flexibility rather than on a model designation alone.
How Does Carboxylation Alter Film Formation, Adhesion, and Crosslinking Response?
The presence of carboxylate groups on the SBR backbone shifts colloidal stabilization toward higher electrosteric repulsion, which raises mechanical stability and permits filler loading up to 200–400 phr calcium carbonate in carpet compounds without coagulum formation. Compared with non-carboxylated SBR of equivalent bound styrene, XSBR develops stronger wet adhesion to polar substrates such as wood, concrete, aluminum, and polyester through polar and coordinate interfacial interactions; however, film water sensitivity increases unless the acid groups are neutralized with alkali or converted into crosslinks. Crosslinking agents used industrially include zinc oxide, melamine-formaldehyde resins, polyfunctional aziridines, epoxy silanes, and blocked isocyanates. Zinc oxide reacts with carboxyl groups to form ionic clusters, increasing tensile strength and reducing elongation at break; this is measured under ASTM D412 as an increase in modulus at 300% elongation. Melamine-formaldehyde addition is typically 1–5 wt% on dry polymer and requires cure at 130–150 °C for 1–3 min. The curing window is narrow: below 130 °C crosslink density remains incomplete, while above 160 °C discoloration and embrittlement may occur. Formulation pH is maintained at 8.0–9.5; acidification below pH 6.5 promotes viscosity build and possible coagulation.
| Comparative property | XSBR | Non-carboxylated SBR | Acrylic latex |
|---|---|---|---|
| Total solids | 50 ± 1 wt% | 48–52 wt% | 45–55 wt% |
| Glass transition temperature | −20 °C to +20 °C | −30 °C to +20 °C | −30 °C to +30 °C |
| Film tensile strength, ASTM D412 | 8–18 MPa | 5–12 MPa | 5–12 MPa |
| Elongation at break, ASTM D412 | 400–800% | 500–900% | 200–600% |
| Wet adhesion to polar substrates | High | Moderate | High |
| UV weathering resistance, ASTM G154 | Moderate | Moderate | Higher |
| Filler tolerance at equal viscosity | High | Moderate | Moderate |
In carpet precoat and secondary backing formulations, XSBR is compounded with ground calcium carbonate at 200–400 phr and thickened with alkali-swellable associative or polyacrylate thickeners to Brookfield RVT viscosity of 3000–6000 mPa·s before application. Froth density is adjusted to 200–500 g L⁻¹ by air injection in a foam mixer; the compound is applied by knife-over-roll or air knife at gap settings of 0.2–0.5 mm and dried in multizone ovens with zone temperatures of 90 °C, 120 °C, and 140 °C for 2–5 min total residence time. The dried coating is evaluated for dry and wet tuft bind strength according to ISO 4919 or ASTM D1335; acceptance values in residential carpet technical specifications frequently fall above 30 N dry and 20 N wet. XSBR provides higher filler tolerance and lower compound cost than acrylic binders, but storage of compounded formulation beyond 24 h requires pH monitoring because bacterial growth and ammonia loss shift rheology.
Paper coating formulations use XSBR as the synthetic latex portion at 6–14 parts per 100 parts pigment, co-bound with oxidized starch or polyvinyl alcohol. Blade coater solids are held at 48–52 wt%, with viscosity 300–1200 mPa·s at 100 s⁻¹. The carboxylated surface improves pigment binding and wet pick resistance measured by IGT or Prüfbau printability testers; thermal yellowing must be controlled with antioxidants when high drying temperatures are used.
When XSBR Replaces Acrylic Latex in Nonwoven Saturation
Nonwoven saturation with XSBR is selected when cost-to-tensile performance and solvent resistance are prioritized over exterior UV stability. In wet-laid or dry-laid nonwovens, binder add-on is controlled at 15–30 wt% of final fabric mass, and the saturated web is dried at 110–130 °C for 2–4 min. Tensile strength measured by ISO 9073-3 or ASTM D5035 for a 40 g m⁻² polyester web typically increases from 8–12 N 50 mm⁻¹ before bonding to 35–60 N 50 mm⁻¹ after XSBR saturation. The carboxylic acid groups provide polar adhesion to polyester fibers, but the unsaturated SBR backbone remains susceptible to photo-oxidative embrittlement; outdoor applications require compounded antioxidants or topcoating. Comparative exposure under ASTM G154 generally shows earlier tensile loss for XSBR than for acrylic or vinyl acetate-ethylene binders after 500 h. When formaldehyde-free crosslinking is required, polyfunctional aziridine or zinc oxide systems replace melamine-formaldehyde, but pot life shortens to 4–12 h and viscosity drift must be recorded by ISO 2555:2018.
Modification of cementitious tile adhesives with XSBR is constrained by a narrow polymer-cement ratio window. The latex is dosed at 5–15 wt% polymer solids on cement, with the water phase of the latex subtracted from the mix water to maintain total water-cement ratio at 0.35–0.45. Flexural strength measured by ASTM C348 commonly improves from 5–7 MPa for unmodified mortar to 8–11 MPa at 10 wt% polymer solids on cement. Above a polymer-cement ratio of 0.15, compressive strength under ASTM C349 can decline by 10–20%, which may move the mortar below structural load-bearing requirements. The processing boundary is also mixing-related: high-shear dispersers above 1500 rev min⁻¹ entrain air bubbles and reduce tensile adhesion strength under EN 1348; low-speed forced-action mixers at 100–300 rev min⁻¹ with 0.1–0.3 wt% defoamer based on latex solids are specified. Curing is staged: 24 h wet cure followed by 27 days at 23 °C and 50% relative humidity before adhesion and mechanical testing. Freeze-thaw exposure of the cured mortar is assessed under ASTM C666, where high-carboxylation grades may absorb water and lose adhesion unless crosslinked or coformulated with silane coupling agents.
Compliance Profile and Documented Operational Boundaries
| Property or requirement | Test method or standard | Representative specification |
|---|---|---|
| Nonvolatile content | ISO 3251:2019 | 50 ± 1 wt% |
| pH | ISO 976:2013 | 7.5–9.0 |
| Brookfield viscosity | ISO 2555:2018 | 50–500 mPa·s |
| Glass transition temperature | ISO 11357-2:2020 | −20 °C to +20 °C |
| Film tensile strength | ASTM D412 | 8–18 MPa |
| Food-contact paper components | FDA 21 CFR 176.170, 176.180 | Grade-specific extraction verification |
| Toy migration limits | EN 71-3, ASTM F963 | Grade-specific |
Selected XSBR grades are supplied with documentation supporting use under FDA 21 CFR 176.170 and FDA 21 CFR 176.180 for paper and paperboard components; extraction testing is batch-specific and must be verified against the end-use food type. REACH registration is maintained on the constituent monomers by suppliers; the polymer itself is exempt from registration but requires safety data sheet classification for residual monomers and ammonia. Heavy metals are controlled to packaging and toy limits when requested, with analytical confirmation by EN 71-3 or ASTM F963. Storage requires sealed containers at 5–35 °C; the product is not freeze-thaw stable and must not be stored below 0 °C, because coagulation is irreversible. Shelf life in unopened containers is generally 6–12 months, after which pH, viscosity, and screen residue are retested. The dispersion is coagulated by strong acids below pH 6.5, by concentrated polyvalent cations such as calcium or aluminum salts, and by water-miscible organic solvents above 10–20 vol%; compatibility with amine-functional additives is formulation-specific because high pH shifts can reduce colloidal stability. Corrosion-resistant equipment of stainless steel 304 or 316 is specified for handling, because zinc-containing galvanized surfaces may introduce metal ions that promote localized coagulation.
