| HS Code | 903403 |
| Product Name | Fluffy Silicone Oil RH-NB-8438 |
| Product Model | RH-NB-8438 |
| Product Type | Fluffy silicone oil textile finishing agent |
| Chemical Composition | Silicone polymer emulsion |
| Appearance | Milky white to light yellow liquid |
| Ionicity | Weak cationic |
| Ph Value | 5.0-7.0 (1% aqueous solution) |
| Solid Content | Approximately 30% |
| Solubility | Easily dispersible or soluble in water |
| Application | Cotton, polyester, nylon and their blended fabrics |
| Hand Feel | Fluffy, soft and smooth |
| Emulsion Stability | Good emulsion stability |
| Yellowing Tendency | Low yellowing |
| Storage | Store in a cool, dry place and avoid freezing |
| Shelf Life | 6 months in unopened original packaging |
| Packaging | 125 kg plastic drum |
As an accredited Fluffy Silicone Oil RH-NB-8438 factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Fluffy Silicone Oil RH-NB-8438 is supplied in 200 kg net-weight sealed plastic drums for industrial transport and storage. |
| Container Loading (20′ FCL) | Fluffy Silicone Oil RH-NB-8438 is securely packed and loaded into a sealed 20′ FCL container for safe chemical transport. |
| Shipping | Fluffy Silicone Oil RH-NB-8438 is typically shipped in sealed, clearly labeled drums or IBCs. Keep containers closed, upright, and protected from moisture, freezing, and contamination. Transport in cool, dry, ventilated conditions away from oxidizers, following the SDS and all applicable local, national, and international shipping regulations. |
| Storage | Store Fluffy Silicone Oil RH-NB-8438 in a cool, dry, well-ventilated area away from direct sunlight, heat sources, sparks, and open flames. Keep containers tightly closed, properly labeled, and upright to prevent leakage. Avoid contact with strong oxidizers, acids, and alkalis. Protect from freezing and moisture, and follow local regulations and the supplier’s SDS. |
| Shelf Life | Shelf life is typically six months when stored in original sealed packaging in a cool, dry place, away from direct sunlight. |
Reactive-dyed cotton single jersey knitted from ring-spun yarns in the range 19.7–24.6 tex is wetted and then passed through a horizontal two-bowl pneumatic pad mangle fitted with bowls of 70–75 Shore A hardness and a working pressure of 2.0–3.5 bar. RH-NB-8438 is diluted in cold deionized water at 20–40 g/L and the pad liquor is adjusted to pH 5.0–6.0 with acetic acid 60% before the fabric is immersed for 4–6 s. The liquor pickup is held at 65–80%; higher pickup shifts the dried film thicker and produces surface chroma loss on dark shades because the silicone layer alters reflectance at the fabric surface. The padded fabric is dried on a multi-pass stenter with the first zone at 110–120 °C and the curing zone at 150–160 °C for 60–90 s. The process conflict is that cure energy must be sufficient to fix the silicone film and prevent migration to the fabric surface during subsequent garment washing, but excessive residence time causes aminofunctional yellowing on white and pastel goods. Dimensional stability is verified according to AATCC TM 135 after three home launderings at 40 °C; fabric width reduction above 5% indicates insufficient overfeed or an excessive softener film that permits yarn slippage. Pilling resistance under ISO 12945-2:2020 should be assessed after finishing because the lubricating film can lower inter-fiber cohesion and allow staple protrusion. Terminal goods include underwear, T-shirts and sleepwear assembled on flatseaming lines where seam pucker remains a primary rejection criterion.
The bath must not contain anionic optical brighteners, anionic wetting agents or residual reactive dye hydrolyzates above 0.5% owf because the resulting coacervation produces oily spot deposits on fabric edges. The pad concentrate is prepared with a high-shear mixer at 1000–1500 rpm for 10–15 min, then filtered through a 200-mesh filter before entering the machine tank. In production, batch-to-batch variation is controlled by measuring the pad liquor turbidity with a nephelometer; a change greater than 20 NTU from the control batch indicates incompatibility or hard water precipitation. Water hardness above 150 ppm CaCO₃ requires a sequestering agent that is compatible with weak cationic emulsions, otherwise localized gelation forms on the stenter clips. The surface pH of the finished fabric is measured with an agar plate electrode according to ISO 3071:2020 and should remain below 7.0 to avoid skin irritation complaints in direct-wear categories.
Terry towel pile in 100% cotton and cotton-bamboo blends is processed in soft flow dyeing machines at a liquor ratio of 1:6–1:8 with transport speed 200–350 m/min and nozzle pressure 0.4–0.8 bar. RH-NB-8438 is added at 0.5–1.5% owf to the exhausted bath after the reactive dye has been hydrolyzed and rinsed; the bath is adjusted to pH 5.0–5.5 with acetic acid and held at 40–50 °C for 20–30 min. The silicone deposits preferentially on the pile tip when the liquor circulation is high, reducing the uniform distribution between pile base and pile tip. This migration is controlled by lowering rope rotation speed to 180–250 m/min during the final 10 min and adding a nonionic penetrating agent at 0.2–0.5 g/L. If the bath temperature exceeds 60 °C, the emulsion can destabilize and produce a dull, harsh pile surface that is detected as a reduction in compression recovery. Drying on a stenter at 110–130 °C with overfeed 3–5% and a contact drum temperature below 120 °C preserves the pile loft; pile collapse is measured as thickness loss under ISO 5084 before and after one wash at 40 °C. Absorbency is checked by the AATCC TM 79 drop test; a wetting time above 5 s on the pile surface indicates excessive silicone deposition or incomplete drying.
The exhaustion process is more sensitive than pad application to residual salts, because sodium sulfate above 5 g/L in the retained liquor reduces emulsion stability and produces a rigid handle. Therefore the softener exhaustion is separated from the neutralization step; reactive dye hydrolyzate is drained and the fabric is rinsed until the conductivity of the drain bath falls below 300 µS/cm. When RH-NB-8438 is combined with cationic softeners, the bath often requires higher energy input to prevent localized gel formation; a mixing test at 500 rpm for 15 min in the factory laboratory is performed before bulk addition. Bulk density of the towel after finishing is taken with a thickness gauge at 0.5 kPa pressure and compared with an unfinished control; a deviation above 8% triggers a rinse cycle. Terminal products include bath towels, bathrobes and beach ponchos where color fastness to washing under ISO 105-C06:2010, test A1S must remain at least grade 4.
In high-loft polyester staple fiber processing for quilted wadding and pillow fill, RH-NB-8438 is applied from an aqueous emulsion in the spin finish line after crimping and heat-setting. The fiber is a semi-dull PET staple with linear density 0.9–3.3 dtex and cut length 32–64 mm. The finish mixture is applied by metering pumps onto the fiber surface at 0.08–0.25% oil-on-fiber active content, then distributed by a series of kiss rollers before the fiber enters the dryer at 60–80 °C. In this application the silicone modifies the fiber-to-fiber friction coefficient; too low friction reduces card web cohesion and increases the number of cylinder wrap defects on a nonwoven card operating at 120–180 m/min cylinder speed. The finished fiber is evaluated for static half-life under ISO 18080-1:2015 or an equivalent static propensity protocol, and for compressibility and recovery using ISO 9073-2:2018 thickness measurement at 0.1 kPa and 2.0 kPa. A typical acceptance limit is a thickness recovery of at least 85% after compression; published data for this specific RH-NB-8438 configuration is limited, so mill trials are required to fix the exact oil-on-fiber level. The process conflict arises when the lubricant film is too thick: the card clothing loads, the doffer transfer efficiency falls below 80%, and the web breaks at the cross-lapper. The dilution water should be below 50 ppm CaCO₃ hardness and free of heavy-metal coagulants. Terminal goods include high-loft between-fill wadding, quilting batts and thermal insulating liners for outerwear.
At the point of conversion, the wadding is thermobonded or needle-punched; the silicone oil must not generate volatile condensates above 0.1% at 180 °C because deposition on the calendar rollers creates a surface film that transfers to the nonwoven and impairs downstream lamination. The standard method for volatile content is ISO 1817:2015 or an internal thermogravimetric procedure under nitrogen. In needle-punch lines running at 800–1200 strokes/min, the silicone-treated fiber requires a slightly higher needle penetration density because the reduced friction allows fiber slippage; this is measured by air permeability change under ISO 9073-15:2008. The anti-static package is selected for compatibility with the silicone emulsion, because many quaternary ammonium antistats precipitate in the presence of anionic emulsifiers. The final wadding is die-cut and enclosed in cotton or microfiber shell fabrics; seam slip resistance after garment filling is tested under ASTM D1683 on the shell fabric, not on the wadding itself.
Indigo-dyed denim garments are rinsed in front-loading industrial washing machines with a capacity of 100–300 kg, inner drum speed 30–40 rpm, and a bath ratio of 1:8–1:10. The garment load is softened after desizing and enzyme washing, when the bath is drained and refilled with clean water at 35–45 °C. RH-NB-8438 is added at 0.5–2.0% on weight of goods, and the bath pH is maintained at 5.5–6.5 with a non-neutralized acetic acid solution. The drum runs for 15–20 min, followed by a cold rinse at 20–25 °C. The operational boundary is that the silicone emulsion must not contact the garment before the residual cellulase enzyme is fully deactivated, because residual enzyme can hydrolyze the cotton surface and produce shade unevenness that is amplified by the lubricating film. Deactivation is carried out at 80 °C for 10 min with a nonionic detergent before the softener cycle. The finished denim is extracted at 600–800 rpm and dried in a rotary tumble dryer at 65–75 °C to retain a soft, bulky hand; the final garment is evaluated for seam puckering and crease retention after ISO 6330:2021 home laundering. Color retention is tested under ISO 105-C06:2010, test A2S, and the oily film must not cause staining of the white pocket lining above a grey scale rating of 4–5. The replacement of conventional amino-functional silicone is justified only where the production line records a higher rate of yellowing on light denim areas under AATCC TM 114 chlorine retention or where the final dresser demands a less mushy hand.
The key process conflict in denim rinsing is that the silicone can reduce the abrasive effect of pumice stones or synthetic stones if the addition is made before destoning. Therefore softening is always sequenced after the abrasion stage. The foam generated by the silicone in the washing machine must be controlled with a defoamer that does not contain silicone, otherwise the additive changes the surface tension and causes uneven deposition on the seams and belt loops. The wash water hardness is kept below 120 ppm CaCO₃; higher hardness causes the emulsion to separate and form white spots on the indigo surface. The spots are identified under UV light as silicone migration and differentiated from enzyme streaks by their failure to re-dye in a cold pad batch repair. Terminal products include raw-denim jeans, jackets and workwear with a final garment pH below 7.5 measured by ISO 3071:2020.
For pigment-printed polyester/cotton sheeting, the finishing route follows a pad–dry–cure sequence on an open-width stenter. The base fabric is a 30/1 Ne ring-spun P/C blend with a warp density of 110–130 ends/inch and weft density of 70–90 picks/inch. RH-NB-8438 is introduced into the finishing liquor at 15–30 g/L together with a crosslinking agent and a nonionic polyethylene wax, but only after a compatibility trial in a 1000 mL beaker with the specific catalyst. The pad liquor is adjusted to pH 4.5–5.5 using acetic acid; below 4.0 the silicone emulsion may split under the pressure of the pad mangle and produce a non-uniform film on the fabric edges. The wet pickup is limited to 60–70% because the low-molecular-weight fraction of the silicone can migrate during the pre-dry step and create a denser film at the fabric surface. Drying is performed at 100–120 °C on a multi-pass stenter, followed by curing at 160–170 °C for 45–60 s. The treated fabric is tested for tensile strength retention under ISO 13934-1:2013; the target is at least 70% of the unfinished control because acid-catalyzed crosslinking weakens the cellulosic component. Tear strength is measured under ISO 13937-2:2000 with an Elmendorf apparatus, and the silicone film can reduce tear propagation only up to a certain film thickness; beyond that, the fabric becomes stiff and the tear strength drops. The handle is quantified with a PhabrOmeter or Kawabata system, reporting bending stiffness and surface friction; the fluffy characteristic is reflected in a lower bending rigidity and higher compressional recovery compared with a standard amino silicone. Terminal products include hotel bed sheets, duvet covers and pillowcases where dimensional stability under ISO 6330:2021 after five home launderings must be within ±3%.
In high-speed cutting and sewing of the finished sheeting, excessive surface lubrication can produce seam slippage and puckering; the fabric is therefore subjected to a seam slippage test according to ISO 13936-2:2004. The silicone application must not reduce the wetting of the fabric below a drop absorption time of 10 s when the sheeting is marketed as absorbent bed linen; this is measured by AATCC TM 79. Residual free formaldehyde from the crosslinking agent is monitored under ISO 14184-1:2011, and the silicone component does not remove formaldehyde but can shield the surface from extraction if the film is too thick, so the cure must be complete before the analytical extraction. Batches that fail the formaldehyde requirement are re-dried at 120 °C for 5 min and re-tested; this is a common mill correction, not a product-specific property.
Synthetic sewing thread in nylon 6,6, polyester filament, or core-spun cotton/polyester constructions is wound on high-speed bobbin winding machines at 800–1200 m/min. The thread must possess a controlled surface friction to prevent ballooning instability and thread breakage, while retaining enough cohesion for uniform package density. RH-NB-8438 is applied as a final coning oil or in a combined dye-bath application at 0.5–1.5% on thread weight; the finish is heated to 40–50 °C and applied by a single- or double-disc oiler with a ceramic metering pump. The friction coefficient is measured by a thread-to-thread friction meter with an input tension of 20 cN and a test speed of 100 m/min; the finished thread should achieve a dynamic friction coefficient between 0.15 and 0.30, depending on the package build and downstream sewing speed. The thread is conditioned for 24 h at 65 ± 2% relative humidity and 20 ± 2 °C according to ISO 139:2005 before testing. The silicone oil must not soften the package so much that the thread layers slip; this is detected as a decrease in Shore A hardness of the package below 80 on a durometer or as a package diameter collapse after compression. On multi-head embroidery machines running at 1200 st/min, the oil film reduces needle heat generation and thread breakage; the needle temperature is measured with an infrared sensor and should remain below 180 °C for polyester thread. Terminal products include all-purpose sewing thread, core-spun thread for high-stretch seams, and embroidery threads for computerized flatbed and cap embroidery.
The process conflict is that a thicker oil film reduces thread-to-thread friction but contaminates the needle eye and tension discs, increasing downtime for cleaning. The amount of finish is therefore controlled gravimetrically by extracting the finish from the thread with petroleum ether using a validated mill extraction method; published standard reproducibility for finish content in this specific thread configuration is limited, so the laboratory must calibrate against control thread packages. The softener is not recommended for threads that will be dyed after finishing, because the silicone film can act as a barrier to dye uptake and produce the visual defect known as finish barré. After winding, the packages are tested for unwinding tension at 600 m/min with a tensiometer; tension spikes above 5 cN from the mean indicate uneven lubrication or package build variation. The final thread is certified under OEKO-TEX Standard 100 if intended for apparel and home textile use; the certificate holder must include RH-NB-8438 in the relevant product class and submit the oil to a laboratory for volatile organic compound testing according to VDA 278 or ISO 12219-2 if the thread enters automotive interior applications.
| Downstream segment | Test method designation | Reported parameter | Typical acceptance band |
|---|---|---|---|
| Knitted cotton garments | AATCC TM 135 | Dimensional change after three launderings | length −5% to +2%; width −5% to +3% |
| Terry toweling | ISO 5084 | Thickness change after one wash | ≤ 8% loss |
| Polyester wadding | ISO 9073-2:2018 | Compression recovery | ≥ 85% |
| Denim garments | ISO 105-C06:2010 A2S | Staining of white pocketing | grey scale 4–5 |
| P/C sheeting | ISO 13934-1:2013 | Tensile strength retention | ≥ 70% |
| Sewing thread | OEKO-TEX Standard 100 | Certificate class | Apparel / home textile class |
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Fluffy Silicone Oil RH-NB-8438 is supplied as a phenylmethyl silicone fluid whose batch certificate typically lists viscosity, refractive index, volatile matter, flash point, and platinum-catalyzed addition-cure compatibility. Publicly available data for this specific grade is limited; the following specification ranges are derived from the phenylmethyl silicone fluid class and must be confirmed against the batch certificate of analysis. The product is distinguished from conventional polydimethylsiloxane fluids by a controlled phenyl substitution on the dimethylsiloxane backbone. This substitution raises the refractive index at 25 °C from approximately 1.403 for a comparable-viscosity dimethyl fluid to 1.540 ± 0.005 when measured under ASTM D1218-12(2020). The resulting optical, thermal, and solubility characteristics are the primary basis for selecting RH-NB-8438 over dimethyl, amino-functional, or polyether-modified silicone oils.
In high-temperature lubricant and optical interlayer applications, the replacement of dimethyl silicone oil with RH-NB-8438 changes three measurable parameters. The phenyl groups increase the refractive index and density of the fluid while reducing the thermal coefficient of viscosity. Under ASTM D2270-10(2016), the viscosity index of phenylmethyl silicone fluids in this range is commonly reported between 200 and 300, compared with values below 180 for some low-phenyl dimethyl fluids. The phenyl groups also shift the compatibility envelope: RH-NB-8438 is more compatible with aromatic ester plasticizers, bisphenol-A epoxy resins, and some aromatic urethane prepolymers than unmodified polydimethylsiloxane, but it is not water-dilutable and cannot be emulsified by simple high-shear addition of water without an external emulsifier. Amino-functional silicone fluids, by contrast, offer greater substantivity on metal oxide surfaces but introduce primary amine sites that can yellow in the presence of aldehydes or undergo acid-base reaction with acidic release agents. RH-NB-8438 does not contain primary or secondary amine functionality and therefore avoids the yellowing mechanism associated with those groups.
Compared with polyether-modified silicones, RH-NB-8438 exhibits slower orientation at air-water interfaces and has no inverse solubility cloud point. This limits its use in water-based mold-release sprays but improves its retention in hydrophobic films. Compared with fluorosilicone oils, RH-NB-8438 has lower resistance to aggressive solvents such as toluene and methyl ethyl ketone, but higher optical transmission in the visible range and simpler re-equilibration in silicone polymer networks. These differences are engineering trade-offs, not absolute superiorities; the selection depends on the continuous service temperature, solvent exposure, and required refractive index.
Thermal degradation of dimethyl silicone oils at continuous exposure near 180 °C proceeds through radical oxidation of methyl groups, leading to gel formation, acid number increase, and volatile cyclic siloxane release. The phenyl substitution in RH-NB-8438 reduces the concentration of abstractable methyl hydrogens and raises the onset temperature of oxidative mass loss. Under thermogravimetric analysis at 10 °C/min in nitrogen, phenylmethyl silicone fluids of this refractive index class typically exhibit 5% mass loss above 350 °C according to ASTM E2550-21; in air, the onset is lower and depends on airflow rate and surface-to-volume ratio. Volatile matter after 3 h at 150 °C is specified below 0.5 wt% using ASTM D4559-19. The flash point measured by Cleveland open cup is usually above 290 °C under ASTM D92-18. Published data for continuous 1,000 h exposure of RH-NB-8438 in a confined oxidation cell is limited; qualification should include accelerated aging at the intended service temperature with periodic measurement of viscosity, acid number, and gel content.
At service temperatures above 200 °C, the phenylmethyl silicone fluid may still undergo Si–C bond cleavage and liberate low-molecular-weight aromatic silanes. Local exhaust ventilation is required during open-bath processing above this temperature. The fluid is not suitable for use in closed systems where evolved volatiles can condense and form flammable films on internal surfaces unless the system is designed for continuous venting and collection. Batch stability at 180 °C is strongly influenced by trace iron and copper residues; contact with brass, bronze, or uncoated copper heating coils should be avoided because these metals accelerate oxidative gelation.
When RH-NB-8438 is dispersed into a platinum-catalyzed addition-cure silicone encapsulant, the mixing sequence must account for its higher viscosity and aromatic content. A planetary mixer with a 10–20 L working capacity and a maximum blade tip speed of 3–5 m/s is commonly used. The fluid is often blended with a vinyl-terminated phenyl silicone prepolymer at a mass ratio between 70:30 and 50:50 to achieve a mixed viscosity of 3,000–5,000 mPa·s at 25 °C. Vacuum degassing at 5–10 kPa for 15–20 min removes air bubbles and trace moisture. The addition of amine-based adhesion promoters, sulfur-containing mold-release additives, or certain tin catalysts can inhibit platinum cure; activity testing should be performed before scaling to production. In high-shear environments above 500 s⁻¹, viscous heating can raise the batch temperature; jacket cooling is recommended to keep the batch below 40 °C.
For semiconductor-grade optical coupling, filtration is performed through a 0.45 µm absolute-rated membrane after compounding. The phenyl fluid has a higher density than dimethyl silicone oil, which increases particle transport efficiency during filtration but also raises the energy input per unit volume. Batch logs from production-scale planetary mixers indicate that incorporation time increases by approximately 15–20% relative to dimethyl fluids of the same viscosity when the same blade geometry is maintained. This processing delay is offset by a reduction in post-cure optical haze in 1 mm thick encapsulant specimens measured according to ASTM D1003-13.
Solventless release coating formulations receive RH-NB-8438 at addition levels between 1.0 wt% and 5.0 wt%. The phenyl groups reduce migration of the fluid to the film surface, but they also increase the internal refractive index and can slightly raise the coefficient of friction relative to a dimethyl fluid. Coating trials on a pilot-scale reverse-roll coater at a wet film gauge of 50 µm require corona-treated polyethylene terephthalate film with surface energy above 42 mN/m for wetting. Substrates below this surface energy require the addition of a reactive wetting agent; solvent dilution with toluene is an alternative but changes the flash point and VOC loading of the bath. Batch-to-batch variation in phenyl content can shift the refractive index by ±0.005 and the viscosity by ±10%; incoming inspection by ASTM D1218 and ASTM D445 is recommended for critical optical applications.
The following table summarizes typical specification ranges for RH-NB-8438 and a comparable dimethyl silicone oil. The dimethyl fluid values are included for reference only and correspond to a 1000 mm²/s grade commonly used in release agents.
| Property | RH-NB-8438 typical range | Dimethyl silicone oil 1000 mm²/s | Test method |
|---|---|---|---|
| Kinematic viscosity at 25 °C | 5000 ± 500 mm²/s | 1000 ± 50 mm²/s | ASTM D445-21 |
| Refractive index nD25 | 1.540 ± 0.005 | 1.403 ± 0.002 | ASTM D1218-12(2020) |
| Volatile content after 3 h at 150 °C | ≤0.5 wt% | ≤1.0 wt% | ASTM D4559-19 |
| Flash point Cleveland open cup | ≥290 °C | ≥260 °C | ASTM D92-18 |
| Pour point | ≤−45 °C | ≤−50 °C | ASTM D97-17b |
| Density at 25 °C | 1.10 ± 0.02 g/cm³ | 0.97 ± 0.01 g/cm³ | ASTM D4052-20 |
The batch-to-batch consistency of phenylmethyl silicone fluids is influenced by the phenyl monomer purity, the equilibrium polymerization catalyst neutralization step, and stripping efficiency for low-molecular-weight cyclic siloxanes. A poorly neutralized batch can exhibit drift in viscosity during storage and can liberate cyclic siloxanes that exceed the volatile specification. Incoming inspection should therefore include Karl Fischer water content under ASTM D6304-16e1, acid number under ASTM D664-18e2, and color under ASTM D1209-05(2019) in addition to the primary optical and rheological tests. The product is supplied in sealed steel or fluorinated high-density polyethylene containers; once opened, it should be blanketed with dry nitrogen and stored below 30 °C to minimize moisture uptake and dust contamination.
For food-contact and pharmaceutical adjacent uses, the end user is responsible for verifying that the specific batch of RH-NB-8438 meets the relevant migration limit under FDA 21 CFR 178.3570 for incidental contact lubricants or EU 10/2011 for plastic food-contact materials. Phenylmethyl silicone fluids may not automatically satisfy the same food-contact listings as dimethyl silicone oils; the aromatic substitution can change migration behavior and toxicological profile. Documentation should be requested from the manufacturer, including REACH registration and SVHC screening under Regulation (EC) No 1907/2006, and RoHS recast 2011/65/EU for electrical and electronic applications. The fluid may not be classified as hazardous under the GHS criteria at typical supply conditions, but thermal decomposition above 300 °C can release benzene and low-molecular-weight aromatic silanes; local exhaust ventilation is required during high-temperature processing. Avoid contact with strong Lewis acids such as aluminum chloride or iron(III) chloride at elevated temperature, because these can catalyze siloxane bond cleavage and gel formation.