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Ascent Petrochem Holdings Co., Limited

Sulfato de éter Lauril de sódio 70

    • Nome do produto: Sulfato de éter Lauril de sódio 70
    • Site da Factroy: Condado de Yudu, Ganzhou, Jiangxi, China
    • Consulta de preço: sales10@ascent-chem.com
    • Fabricante: Ascent Petrochem Holdings Co., Limited
    • Contacte Agora
    Especificações
    Código SH 240437
    Nome Químico Sulfato de éter Lauril de sódio (SLES)
    Número Cas 9004-82-4
    Fórmula Molecular CH3(CH2)11(OCH2CH2)nOSO3Na (n normalmente 1-3)
    Aparência Líquido viscoso claro a ligeiramente nebuloso
    Conteúdo De Matéria Ativa 70% (normalmente 70 ± 2%)
    Ph Solução Aquosa A 1 6,5 - 8,5
    Cor Apha 20 máximos
    Viscosidade A 25 C 500 - 1500 mPa · s
    Conteúdo De Sulfato De Sódio 1,5% máximo
    Conteúdo De Matéria Não Sulfatada Máximo de 2,0%
    Teor De água Aproximadamente 30%
    Solubilidade Totalmente solúvel em água formando uma solução clara
    Classificação Química Surfactante aniônico

    Como fábrica acreditada de Sulfato de éter Lauril de sódio 70, aplicamos protocolos de qualidade rigorosos - cada lote é submetido a testes rigorosos para garantir padrões de eficácia e segurança consistentes.

    Embalagem e armazenamento
    Embalagem Sodium Lauryl Ether Sulfate 70 é embalado em tambores de 250 kg, sacos IBC de 1.100 kg ou tanques a granel.
    Carga de contêiner (20' FCL) 20′ FCL carregamento contêiner de Sodium Lauryl Ether Sulfate 70, segurando tambores /IBCs com adequada dunnage, rotulagem e ventilação para transporte seguro.
    Envio Sodium Lauryl Ether Sulfate 70 navios em tambores selados ou IBCs, rotulados como um produto químico. Transporte em recipientes secos e ventilados longe do calor ou frio extremos. Normalmente não perigoso para o transporte; no entanto, se os critérios de corrosividade forem cumpridos, classificar com o número ONU apropriado e rotulagem de perigo. Use EPI e contenção de derramamentos durante o carregamento e descarregamento.
    Armazenamento Armazenar Sodium Lauryl Ether Sulfate 70 em uma área fresca, seca e bem ventilada longe da luz solar direta e fontes de calor. Mantenha o recipiente bem fechado para evitar a absorção de umidade e contaminação. Evite congelamento e temperaturas extremas, que podem alterar o produto. Armazenar separadamente de oxidantes fortes e materiais incompatíveis.
    Prazo de validade O prazo de validade é tipicamente 1 ano a partir da fabricação quando armazenado selado, frio e seco, evitando temperaturas extremas.
    Aplicação de Sulfato de éter Lauril de sódio 70
    Cotação Grátis

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    Certificação e Conformidade
    • Sulfato de éter Lauril de sódio 70 É fabricado sob um sistema de qualidade ISO 9001 e está em conformidade com os requisitos regulamentares relevantes.
    • O COA, a SDS/MSDS e os certificados relacionados estão disponíveis mediante solicitação. Para pedidos de certificados ou dúvidas, entre em contato com: sales10@ascent-chem.com.
    Mais Introdução

    An aqueous concentrate containing nominally 70% w/w sodium lauryl ether sulfate (INCI: Sodium Laureth Sulfate, CAS 68891-38-3)—synthesized via sulfation of ethoxylated dodecyl alcohol followed by neutralization—is supplied as a clear, viscous liquid. The product typically carries a mean ethoxylation of 2 moles EO per mole fatty alcohol, yielding the predominant homologue C12H25(OCH2CH2)2OSO3Na. Industrial parlance frequently designates this material SLES-2 EO 70%, distinguishing it from higher-solids pastes and from narrow-range ethoxylates.

    How Does the Hydrotrope-Assisted Viscosity Profile Affect Metering Pump Selection?

    In raw form at 25 °C, SLES 70 exhibits a non-Newtonian, shear-thinning flow curve with typical viscosities spanning 5,000–25,000 mPa·s at low shear, dropping sharply under the shear rates encountered in positive-displacement transfer. This pseudoplasticity, governed by worm-like micellar entanglement, imposes specific constraints on diaphragm and progressive cavity pump sizing. Installation of a VFD-controlled pump with a suction-side pressure sensor prevents cavitation when ambient temperatures fall below 15 °C, where gel-phase domains can raise apparent viscosity beyond 50,000 mPa·s. Storage in 316L stainless steel jacketed vessels maintained at 30–35 °C, per supplier bulk handling guidelines, ensures consistent flow without exceeding the product’s thermal stability threshold of 50 °C, above which colour (Klett, <30 on 5% AM solution) begins to drift.

    Formulation chemists routinely exploit a hydrotrope-mediated viscosity dip: incorporation of 2–4% sodium xylene sulfonate (SXS) reduces the concentrate’s viscosity below 2,000 mPa·s, enabling direct metering through magnetic-drive gear pumps without heated lines. Published data for this specific configuration in a monodisperse ethoxylate distribution is limited; plant-scale trials typically calibrate pump stroke frequency against a Coriolis mass flow meter to compensate for day-to-day rheological drift.

    Representative Specification Ranges for SLES 70
    Parameter Typical Range Reference Method
    Active Matter (M.W. 382) 69.0–71.0% ISO 2271 (two-phase titration)
    Unsulfated Matter ≤ 2.0% ISO 894
    Sodium Sulfate ≤ 1.5% ISO 3262
    pH (2% aqueous) 7.0–9.0 ASTM D1172
    1,4-Dioxane ≤ 30 mg/kg Headspace GC-MS (EPA 8260C)
    Colour (Klett, 5% AM) ≤ 25 Klett-Summerson

    When the manufacturing environment requires AN (ammonium-neutralized) or MEA variants, the 70% sodium form serves as a benchmark for electrolyte tolerance. The divalent cation sensitivity—common to alkyl ether sulfates—dictates that process water hardness exceeding 120 mg/L CaCO₃ precipitates calcium lauryl ether sulfate, resulting in a dull haze that cannot be removed by downstream polishing filtration below 5 µm. Chelation with tetrasodium glutamate diacetate (GLDA) at a stoichiometric ratio of 1.2:1 relative to calcium concentration restores clarity without the nitrogen content of EDTA alternatives.

    What Differentiates SLES 70 from Unethoxylated SLS Pastes and Narrower EO Distributions?

    Comparison with sodium lauryl sulfate (SLS, SLS needles or SLS 30%) reveals the fundamental impact of the polyoxyethylene spacer. SLS denatures globular proteins aggressively; SLES-2 reduces ocular sting scores in Draize assessments by roughly 60–70% compared to SLS at equivalent active surface tension (28–32 mN/m at CMC), according to historical in-vivo data. The shift is attributed to a larger hydrated head group area, reducing monomer penetration into the stratum corneum. In shampoo formulation, the critical micelle concentration drops from 8.2 mM (SLS) to approximately 0.25 mM (SLES-2) in deionized water, allowing efficient micellization at lower surfactant mass.

    Measured against narrow-range ethoxylates (NRE), the conventional broad-ethoxamer SLES 70 exhibits a wider gel region upon dilution from concentrate to intermediate water contents. Phase diagram mapping at 25 °C identifies a hexagonal liquid crystalline phase between 35–50% active matter, where viscosity peaks above 1,000 Pa·s. Processing installations therefore inject the 70% concentrate directly into the vortex of a pre-filled batch with >60% free water to bypass this “gel band,” a handling step absent in cold-processable SLES-1 70% systems that exhibit no stiff mesophase at ambient temperature due to a different critical packing parameter.

    For structural foam applications in concrete admixtures, the ether sulfate’s 70% active matrix outperforms lower-solids grades (28% aqueous solutions) by eliminating unnecessary water freight and reducing the carbon footprint per kg transported surfactant by 38% (IPCC-derived transport emission factor for road freight). Field data from on-site foam generators operating at 3 bar compressed air pressure indicate that pre-dilution of SLES 70 to 30% active with chilled water (5–10 °C) suppresses pre-generated foam collapse caused by localised heating in the high-shear mixing head.

    Anionic Compatibility and Electrolyte-Induced Phase Behaviour in Finished Goods

    Formulation scientists must not treat anionic ether sulfates as mutually substitutable in multicomponent systems. SLES 70 interacts with amphoteric co-surfactants—cocamidopropyl betaine (CAPB) constitutes the canonical pairing—to form mixed micelles that maximise viscosity at a CAPB:SLES weight ratio near 1:3.5 on an active basis. The resulting peak viscosity of 8,000–15,000 mPa·s (Brookfield RV, Spindle 6, 20 rpm) in a 12–14% total active wash can be trimmed to 4,000 mPa·s by addition of 0.5% NaCl. Production sites operating continuous blending skids must control salt addition via a weigh cell and in-line static mixer to avoid over-thickening that triggers positive-displacement pump over-pressure trips set at 10 bar.

    Partial substitution of SLES 70 with sodium lauroyl sarcosinate at 5% of the total surfactant actives sharpens foam texture without destabilising the maltese-cross micellar structure verified under polarised light microscopy. In alkaline household cleaners (pH 10.5–11.0), the 70% ether sulfate resists hydrolysis significantly longer than the equivalent lauryl sulfate: half-life under pH 11 at 40 °C exceeds 90 days, whereas sodium lauryl sulfate monitors exhibit 15–20% sulfate cleavage within the same period, based on accelerated ageing data monitored by two-phase active titration.

    During the cold-fill production of pearlescent shampoos, ethylene glycol distearate crystal habit is sensitive to the ethoxamer distribution. The broad-distribution SLES 70 nucleates smaller, more uniform platelet clusters (5–10 µm) than narrow-range grades, resulting in a brighter pearl but occasionally retarding crystal settling rates in 500 kg holding tanks, risking stratification if batch holdup exceeds 4 hours.

    Where formulation requires extreme viscosity suppression for sprayable hand soaps, replacement of 30% of the SLES 70 active with sodium diethylhexyl sulfosuccinate (DOSS) shifts the packing parameter toward reverse micelles, lowering the system’s zero-shear viscosity below 200 mPa·s. However, this combination is incompatible with low-pH preservative systems (pH < 4.5) due to accelerated DOSS ester hydrolysis; citric acid buffer must maintain pH above 5.2.

    Key Differentiators: SLES 70 vs. Common Alternatives
    Attribute SLES-2 70% (Broad EO) SLS 30% SLES-1 70% Sodium Methyl 2-Sulfolaurate
    CMC in water (25 °C) ~0.25 mM ~8.2 mM ~0.18 mM ~0.04 mM
    Krafft Point <0 °C ~16 °C <0 °C <0 °C
    Gel Phase (25 °C) Present (35–50% AM) Present (35–60% AM) Absent Absent in typical ranges
    Ocular Irritation Potential Moderate-low High Moderate-low Very low
    Electrolyte Thickening Response Strong Strong Weaker Weak

    Regulatory Control of 1,4-Dioxane and Sulfate Ion Content in Cosmetic-Grade Material

    Global regulatory alignment imposes a bifurcation in SLES 70 quality: a high-conversion grade targeting <10 mg/kg 1,4-dioxane under REACH Annex XVII restrictions and the California Proposition 65 listing, versus a technical grade that may reach the 30 mg/kg ceiling acceptable for industrial I&I cleaners. Stripping columns operating under vacuum (50–80 mbar) post-neutralisation remove the bulk of dioxane, but subsequent storage in epoxy-lined drums at ambient temperature can regenerate trace amounts through acid-catalysed back-formation if the pH drifts below 6.5. Therefore, the product must be monitored quarterly using GC-MS per EPA 8260C, with a control limit of 20 mg/kg set at 3σ above process mean for batch release in personal-care supply chains.

    Residual sulfate ion, measured as sodium sulfate, directly impacts the freeze-thaw stability of finished shampoos. At sulfate levels above 1.8% in the concentrate, products stored at −5 °C develop needle-like sulfate crystals visible under 10x magnification, which do not redissolve upon warming to 25 °C—a failure criterion per internal cosmetics stability protocol based on ISO 18811:2018. Producers of SLES 70 for this sector therefore control the sulfation-to-neutralisation step with a post-reaction vacuum flash removing residual SO₂, keeping final sodium sulfate content within 0.8–1.2%.

    In compliance with the EU Ecolabel for rinse-off products (Commission Decision 2014/893/EU), the aerobic biodegradability of SLES 70 exceeds 90% within 28 days (OECD 301B, modified Sturm test), qualifying it as readily biodegradable. The ethoxylate chain is cleaved under standard activated sludge conditions without formation of stable polyethoxylate intermediates. No persistent, bioaccumulative or toxic (PBT) classification applies under REACH Annex XIII, although the concentrate is classified as Skin Irritant 2 (GHS07) and causes serious eye damage (Category 1, GHS05) in undiluted form, mandating secondary containment and splash protection during decanting.

    Automated drum decanting stations in continuous surfactant feeds often incorporate load cells with ±0.1% accuracy and a lance pump interlocked to a conductivity sensor in the drip tray to detect leaks. The material’s specific gravity of 1.05–1.07 g/mL at 40 °C permits a 1000 L IBC to be evacuated within 25 minutes using a 2-inch air-operated double diaphragm pump with a PTFE diaphragm specification, provided the discharge head does not exceed 12 m. Plant safety documentation must cover spill containment with inert absorbents such as vermiculite, noting that aqueous dilution generates abundant foam that interferes with floor scrubber vacuum recovery.