| HS Code | 675210 |
| Product Name | Hainan Yisheng Petrochemical PTA |
| Chemical Name | Purified Terephthalic Acid |
| Manufacturer | Hainan Yisheng Petrochemical Co., Ltd. |
| Plant Location | Yangpu Economic Development Zone, Hainan, China |
| Cas Number | 100-21-0 |
| Einecs Number | 202-830-0 |
| Chemical Formula | C8H6O4 |
| Molecular Weight | 166.13 g/mol |
| Appearance | White crystalline powder |
| Odor | Odorless |
| Purity | ≥99.9% |
| Moisture Content | ≤0.2% |
| Ash Content | ≤0.001% |
| 4 Carboxybenzaldehyde 4 Cba | ≤25 ppm |
| P Toluic Acid | ≤150 ppm |
| Iron Content | ≤1 ppm |
| Total Heavy Metals | ≤5 ppm |
| Melting Point | >300 °C (sublimes) |
| Sublimation Point | ~402 °C |
| Density | 1.51 g/cm³ |
| Bulk Density | 0.8–1.0 g/cm³ |
| Particle Size | D50 100–200 μm |
| Solubility | Slightly soluble in water; soluble in dimethyl sulfoxide |
| Acid Value | ~675 mg KOH/g |
| Flash Point | >300 °C |
| Storage Conditions | Cool, dry, ventilated area away from moisture and incompatible materials |
As an accredited Hainan Yisheng Petrochemical PTA factory, we enforce strict quality protocols—every batch undergoes rigorous testing to ensure consistent efficacy and safety standards.
| Packing | Hainan Yisheng Petrochemical PTA is packaged in 1,100 kg jumbo bags with inner polyethylene liners for safe bulk transport. |
| Container Loading (20′ FCL) | Container Loading (20′ FCL): Hainan Yisheng Petrochemical PTA, palletized jumbo bags, moisture-protected, evenly distributed, and secured for safe sea transport. |
| Shipping | Hainan Yisheng Petrochemical PTA (purified terephthalic acid) ships as a non-hazardous, white crystalline powder in 25 kg bags, 1,000 kg jumbo bags, or bulk. Transport by sea, rail, or truck in clean, dry containers; keep dry, ventilated, and away from moisture, heat, and oxidizers. |
| Storage | Hainan Yisheng Petrochemical PTA (purified terephthalic acid) should be stored in a cool, dry, well-ventilated warehouse away from direct sunlight, moisture, heat, and ignition sources. Keep containers tightly closed, palletized, and labeled. Store in original packaging under dry conditions. Separate from strong oxidizers, alkalis, and acids. Prevent dust generation; use grounding and appropriate PPE. Maintain clean, dry storage areas. |
| Shelf Life | Hainan Yisheng Petrochemical PTA has a 24-month shelf life when stored dry, cool, and sealed in its original packaging. |
In direct melt-to-yarn conversion of PTA-based polyester, Hainan Yisheng Petrochemical purified terephthalic acid is specified by non-fibre contaminants that survive continuous oxidation and transfer into melt colour, carboxyl end-group balance, and spinneret pack life. Textile filament lines maintain the ethylene glycol-to-PTA molar feed ratio between 1.10:1 and 1.15:1. The excess glycol compensates for distillation losses during esterification while limiting diethylene glycol formation to 1.0–1.5 wt%. The first esterification reactor operates at 265–270 °C under 0.10–0.30 MPa absolute, and the second-stage reactor reduces carboxyl end-groups to below 25 mmol/kg before polycondensation. Antimony trioxide catalyst is metered at 200–300 ppm Sb on polymer mass, and 0.30 wt% TiO₂ is dispersed when semi-dull fibre is required. Polycondensation proceeds at 285–290 °C and 0.2–0.5 kPa absolute until intrinsic viscosity reaches 0.62–0.68 dL/g by ISO 1628-5 or ASTM D4603. Esterification conversion must exceed 97 % before vacuum application because residual carboxyl end-groups above 30 mmol/kg accelerate hydrolytic chain scission during chip drying and melt conveying. The filtered melt passes through 20–40 µm sintered metal candles before reaching spin beams. In high-speed partially oriented yarn winding at 2,800–3,200 m/min, a CIE b* colour below 1.5 and consistent melt viscosity are required to avoid winding tension variation and downstream dye uptake shifts. Terminal products include drawn textured yarn, fully drawn filament, and staple fibre for cotton-blend spun yarn. Textile processing compliance is assessed through OEKO-TEX Standard 100 and ZDHC MRSL, while the polymer itself is registered under REACH.
For bottle-grade production, PTA is esterified with monoethylene glycol and purified isophthalic acid. The isophthalic acid is metered at 1.5–3.0 mol% of total acid to slow spontaneous crystallisation during preform cooling. Diethylene glycol is targeted at 1.2–1.4 wt%. Levels below this window produce stiff preforms with poor stretch uniformity, whereas higher levels depress glass transition and increase acetaldehyde precursor. Melt polycondensation is stopped at an intrinsic viscosity of 0.60–0.65 dL/g, after which the amorphous chip enters a solid-state polycondensation vessel operating at 210–220 °C under 0.10–0.50 kPa absolute or with heated nitrogen at 0.5–1.0 m/s superficial velocity. SSP increases intrinsic viscosity to 0.80–0.84 dL/g over 12–20 h and strips acetaldehyde, but injection moulding at 270–290 °C regenerates acetaldehyde by thermal oxidation and ester interchain reactions. Headspace acetaldehyde in preforms for carbonated soft drinks is measured by ASTM F2013 and must remain below 4 µg/L, requiring low residual acetaldehyde precursor, controlled injection barrel temperatures, and short residence time. The reciprocating screw compression ratio is held near 2.5:1, and hot-runner temperatures are kept below 280 °C to avoid local degradation. Preforms are reheat-stretch-blow moulded at 90–110 °C surface temperature with longitudinal stretch 2.8–3.2× and hoop stretch 2.5–3.0×. Food-contact compliance is established under FDA 21 CFR 177.1630 and Commission Regulation (EU) No 10/2011. Migration testing follows EN 1186. Oxygen barrier is measured by ASTM D3985 for barrier-grade containers. Terminal products include carbonated soft drink bottles, still water bottles, and hot-fill containers for pasteurised beverages.
Biaxially oriented polyester film conversion places tighter ceilings on cyclic trimer content than bottle or fibre production because oligomers sublimate from the cast sheet and condense on cooler stenter clip assemblies. Film-grade PTA is esterified with ethylene glycol at a molar ratio of 1.12:1 to 1.18:1, and polycondensation is stopped at an intrinsic viscosity of 0.62–0.66 dL/g. Diethylene glycol is held at 0.8–1.5 wt% and carboxyl end-groups below 30 mmol/kg to limit hydrolysis during extrusion. The melt is extruded through a slot die at 275–285 °C onto a polished chill roll maintained at 20–30 °C. Electrostatic pinning at 7–10 kV prevents air entrapment. The cast sheet enters a sequential linear motor stenter where machine-direction draw is 3.0–4.0× at 85–95 °C, transverse-direction draw is 3.5–4.5× at 100–120 °C, and heat-setting is applied at 220–230 °C with 2–5 % relaxation. Cyclic trimer, predominantly cyclic tri(ethylene terephthalate), is present at 1.5–2.5 wt% in amorphous cast film and blooms to the surface during orientation and heat-setting. Deposits on stenter clips, chain rails, and exhaust ducting increase transverse drag force and can release back onto film edges as specks unless removed by hot ethylene glycol or aqueous alkaline wash every 150–250 h of line operation. Operators monitor oligomer deposition via differential pressure across exhaust filters and stenter chain current. Mechanical properties are tested by ASTM D882, and oxygen permeability by ASTM D3985 at 23 °C and 50 % RH. Compliance for food packaging is assessed under EU Regulation No 10/2011 and FDA 21 CFR 177.1630. Terminal products include printed flexible packaging laminates, capacitor dielectric films, and photovoltaic backsheet base films where oligomer haze below 0.5 % is required.
Polybutylene terephthalate is produced from PTA and 1,4-butanediol by molten esterification at 220–250 °C with tetrabutyl titanate at 50–150 ppm Ti. The butanediol-to-PTA molar ratio is held between 1.20:1 and 1.30:1 because excess butanediol promotes tetrahydrofuran formation. Tetrahydrofuran is recovered from the overhead stream and monitored by gas chromatography. Elevated THF concentration indicates over-temperature excursions in the esterifier. Polycondensation proceeds at 250–260 °C under 0.1–0.5 kPa vacuum until intrinsic viscosity reaches 0.85–1.20 dL/g as determined by ASTM D4603 in phenol/tetrachloroethane 60/40. PBT pellets are dried to 0.02 % moisture or below at 120 °C for 3–4 h in desiccant dryers before compounding. Glass fibre reinforcement at 30 wt% is fed downstream in a co-rotating twin-screw extruder with L/D 40:1. The fibres are side-fed after the melt seal, and melt temperature is kept below 270 °C to avoid polymer degradation. Flame-retarded PBT compounds for connectors are formulated with brominated flame retardant and antimony trioxide to achieve UL 94 V-0 at 0.8 mm. Comparative tracking index is measured by IEC 60112 and is typically above 400 V for unfilled grades but can drop to 250–300 V when glass and flame retardant packages are added. Injection moulding uses barrel temperatures of 245–265 °C, mould temperatures of 60–90 °C, and anisotropic shrinkage of 0.8–1.2 % in flow direction and 1.0–1.5 % transverse. Terminal parts include automotive sensor housings, relay sockets, lamp sockets, and electrical connectors where heat deflection temperature is validated by ISO 75-2 method A at 1.80 MPa. Published data for specific Hainan Yisheng PTA-derived PBT molecular weight distribution are limited. Compounders use PTA with low p-toluic acid because monofunctional impurities cap chain ends and reduce impact strength measured by ISO 179-1/1eA.
Because CHDM suppresses spherulitic crystallisation, PTA-based amorphous sheet is produced with a glycol mixture in which 1,4-cyclohexanedimethanol comprises 30–50 mol% of total glycol. At the lower bound, haze and impact still resemble crystalline PET behaviour, while at the upper bound melt strength drops and calendering becomes difficult. Esterification is carried out at 230–250 °C with a glycol-to-acid molar ratio of 1.05:1 to 1.15:1, and polycondensation is stopped at an intrinsic viscosity of 0.70–0.80 dL/g. The amorphous pellets require closed-loop desiccant drying at 65–70 °C for 4–6 h to below 0.01 % moisture because hydrolytic degradation in the extruder increases yellowness and extrudate thickness variation. Sheet extrusion uses a single-screw extruder with a barrier screw and a polished three-roll stack at 220–250 °C. Die lip opening is set to 1.2–1.5× final sheet thickness to accommodate die swell and roll draw. Coextruded cap layers with higher CHDM content are used for chemical resistance and gloss. Thermoforming is performed on plug-assisted formers at 90–110 °C surface temperature. Food-contact suitability is assessed under EU Regulation No 10/2011, and medical packaging is evaluated by ISO 10993-5 for cytotoxicity after gamma or ethylene oxide sterilisation. Terminal products include clear medical device trays, retail display clamshells, and printed card overlays. The absence of a sharp melting endotherm is confirmed by ISO 11357-1 differential scanning calorimetry.
Aromatic polyester polyols for rigid polyurethane and polyisocyanurate foam are synthesized by transesterifying PTA with diethylene glycol. PTA loads of 20–35 wt% of the total polyol charge are typical because higher levels raise viscosity beyond pumpable handling at ambient temperature. The reaction is run at 200–220 °C with overhead water removal until the acid value drops below 2 mg KOH/g. Titanium-based catalysts are used at 20–60 ppm Ti, and vacuum is applied only in the final stage to avoid excessive DEG loss. The hydroxyl number is targeted between 250 mg KOH/g and 350 mg KOH/g as measured by ASTM D4274. Brookfield viscosity at 25 °C is controlled between 5,000 mPa·s and 20,000 mPa·s by ASTM D2196. This aromatic polyester polyol is blended with blowing agent, surfactants, and polymeric MDI in a high-pressure foam machine. In rigid polyisocyanurate panel lamination, higher terephthalate content increases char yield and reduces smoke release in ASTM E84 Steiner tunnel testing, but published data for Hainan Yisheng PTA in this specific polyol formulation are limited. The main operational boundary is storage stability of low-viscosity formulations: free diethylene glycol above 12 wt% causes phase separation and viscosity drift at 15 °C. Terminal products include metal-faced sandwich panels for cold-storage enclosures, continuous-line insulation board, and pour-in-place foam for pipe supports. Compressive strength is measured by ASTM D1621 at 10 % deformation, and density by ASTM D1622.
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Purified terephthalic acid manufactured by Hainan Yisheng Petrochemical Co., Ltd. at the Yangpu, Hainan petrochemical complex is a single polyester-grade aromatic dicarboxylic acid stream supplied without model sub-designations. The material carries CAS 100-21-0, has the condensed formula C8H6O4, and has a molecular weight of 166.13 g/mol. It is produced by continuous liquid-phase oxidation of para-xylene in acetic acid under a cobalt/manganese/bromine catalytic system, followed by hydrogenation of the crude oxidation product, crystallization, and drying. The output is a white crystalline powder intended for melt-phase polyethylene terephthalate polymerization, with secondary application in polybutylene terephthalate and certain copolyester systems.
The product is typically released against SH/T 1612.1-2005 and/or GB/T 32685-2016 polyester-grade PTA specifications. Because the powder is sensitive to moisture and forms wall scale in dense-phase conveying when relative humidity exceeds 60%, receiving silos are maintained under dried air at dew point below -20 °C. Contact surfaces should be stainless steel or aluminum; copper-alloy lines are avoided because residual acetic acid vapors and wet product can create local corrosion and metal contamination. The absence of sub-model designations means that differentiation from other PTA products is based on certificate-of-analysis impurity data and particle-size behavior rather than product identifiers.
The primary specification values are given in Table 1. These values are polyester-grade release windows reported for hydrogenation-refined PTA of this class; the producer’s certificate of analysis should be used for final acceptance. The most sensitive value is 4-carboxybenzaldehyde, which functions as a chain-stopping impurity and chromophore precursor during downstream molten polymerization.
| Property | Test basis | Release limit or typical window |
|---|---|---|
| Appearance | SH/T 1612.1-2005 visual inspection | White crystalline powder |
| 4-Carboxybenzaldehyde | High-performance liquid chromatography | ≤ 20 mg/kg |
| p-Toluic acid | High-performance liquid chromatography | ≤ 130 mg/kg |
| Ash | Sulfated ash, GB/T 7531-1987 | ≤ 8 mg/kg |
| Total heavy metals | Inductively coupled plasma optical emission spectrometry | ≤ 10 mg/kg |
| Iron | Inductively coupled plasma optical emission spectrometry | ≤ 1.0 mg/kg |
| Moisture | Karl Fischer coulometry, GB/T 6284-2006 | ≤ 0.2% mass fraction |
| CIE b* color | Reflectance spectrophotometer | ≤ 1.0 |
| Median particle size | Laser diffraction, ISO 13320:2020 | 100–150 µm |
| Acid value | Aqueous titration | 675 ± 3 mg KOH/g |
On a 600 t/day continuous PET melt-phase line producing bottle-grade chip, the PTA is mixed with ethylene glycol as a high-solids paste. Esterification is operated between 255 °C and 270 °C at 0.15–0.30 MPa; the oligomer is then forwarded to a finisher at 278–288 °C under vacuum below 1 mbar. In this operating window, a 4-CBA value near 20 mg/kg can raise oligomer color only modestly if antimony trioxide catalyst is held at 140–190 mg Sb/kg PET, but higher 4-CBA concentrations increase the risk of conjugated aldehyde end groups and b* drift. The particle-size window is operationally significant: fines below 45 µm can bridge hoppers and produce dust, while particles above 250 µm may reduce esterification mass transfer and raise screen-pack pressure. Plants with high-shear slurry mixers typically monitor the 45–250 µm mass fraction and the laser diffraction span rather than relying on a single D50 value.
The acid value of 675 mg KOH/g is derived from the two carboxylic acid functions of terephthalic acid. A significantly lower value indicates partial esterification or contamination, while a higher value may reflect residual acidic synthesis impurities. Because PTA is a weak organic acid, wet powder in prolonged contact with carbon steel can produce iron contamination; this is why stainless steel or aluminum contact surfaces are specified for storage and conveying equipment. Sampling from bulk tankers and silos should be performed under dry-air protection to avoid moisture condensation on the product surface.
The hydrogenation purification step distinguishes this product from unrefined crude terephthalic acid and older oxidation-only PTA streams. In the hydrogenation circuit, 4-carboxybenzaldehyde is reduced to p-toluic acid over a supported palladium catalyst in aqueous solution. The reduction lowers 4-CBA by one to two orders of magnitude relative to crude oxidation cake. The p-toluic acid that remains is monofunctional and less chromophoric, but it still must be controlled because high p-toluic acid can modify terminal acid end groups and oligomerization kinetics. For converter operations, the low 4-CBA value translates into a narrower melt-color trajectory during finisher residence times above 90 min and a more predictable carboxyl end-group response in solid-state PET.
Residual cobalt, manganese, and bromine values are not zero in refined PTA; they are reduced to low milligrams-per-kilogram levels but can still influence downstream catalyst selection. Antimony-based polycondensation catalysts tolerate moderate traces of these metals without major kinetic shift. Titanium-based polyester catalysts, particularly hydrolytically sensitive organotitanates, may require a tighter incoming metal profile because iron and cobalt can promote hydrolysis and yellowing in the presence of residual oxygen. Users switching to titanium catalyst packages should compare certificate-of-analysis total heavy metals and iron values against the catalyst supplier’s upper metal tolerance. When published data for Hainan Yisheng PTA in a specific titanium formulation is limited, the formulation should be qualified by a pilot esterification run followed by ASTM D4603 intrinsic viscosity and ASTM D6290 color measurements.
Secondary use in polybutylene terephthalate relies on direct esterification with 1,4-butanediol at 150–170 °C, followed by polycondensation at 250–260 °C under vacuum, typically with a titanium tetrabutoxide catalyst. In this application, ash control is more critical than in PET because titanium butoxide is hydrolytically active and metal residues can shift melt viscosity and hydrolytic stability. The product’s low iron and total heavy metal windows reduce the risk of excessive catalytic side reactions. Copolyester manufacture using isophthalic acid, cyclohexanedimethanol, or diethylene glycol also benefits from controlled 4-CBA because these copolymers are more sensitive to color shift at high finisher temperatures.
For bottle-grade resins that are further polymerized in the solid state, the PTA specification intersects with final pellet quality in three process zones. First, melt-phase prepolymer exiting the finisher is pelletized and then heated under nitrogen at 205–215 °C; residual aldehyde and acid impurities can form acetaldehyde and free carboxyls during this heating. Second, any moisture ingress from PTA above 0.2% feed moisture can alter the esterification water balance and produce oligomer with irregular end groups, which later affects solid-state reactivity. Third, the final intrinsic viscosity target of 0.80–0.85 dL/g under ASTM D4603 requires stable stoichiometry and limited side reactions from residual impurities. The refinery-controlled 4-CBA, ash, and moisture window makes the product suitable for this application class, but actual solid-state response must be established with the site’s pellet geometry, crystallizer temperature, and nitrogen dew point.
Table 2 provides representative published ranges for impurity phenotypes across three PTA-like materials. The values are not a substitute for the certificate of analysis but are useful for understanding why a hydrogenation-refined product behaves differently from unrefined CTA or mechanically recovered material.
| Parameter | Hydrogenation-refined PTA, Hainan Yisheng type | Non-hydrogenated crude terephthalic acid | Mechanically recovered PTA |
|---|---|---|---|
| 4-CBA | ≤ 20 mg/kg | 200–3500 mg/kg | 10–80 mg/kg |
| p-Toluic acid | ≤ 130 mg/kg | 250–1000 mg/kg | 20–200 mg/kg |
| Ash | ≤ 8 mg/kg | 15–60 mg/kg | 5–30 mg/kg |
| CIE b* | ≤ 1.0 | 2–5 | 1–3 |
In a direct comparison, the ≤20 mg/kg 4-CBA window is the primary specification differentiator. Unrefined CTA containing 200–3500 mg/kg 4-CBA cannot be used directly in high-clarity PET because the aldehyde groups introduce chromophoric structures and chain termination during finisher operation. Mechanically recovered PTA can be blended with virgin PTA only when 4-CBA and metal contamination are measured lot-by-lot; otherwise spinneret pressure increases and sheet color variation may occur. Hainan Yisheng PTA therefore enters the supply chain as a direct-replacement polyester-grade intermediate rather than a blend stock, subject to the user’s incoming-particle-size and moisture checks.
The product is transported in bulk road tankers, railcars, and marine containers. The Hainan coastal location makes moisture protection during marine transit a key receiving requirement; packaging is not used for typical large-scale polyester operations. Receiving silos should be purged with dried air at a dew point below -20 °C and vented through filters that prevent dust release. Dense-phase conveying should use oil-free air or nitrogen, and line velocities should be kept below the saltation velocity for fine fractions to reduce pipe wear. The material should be segregated from strong bases, volatile amines, and sources of polyethylene or polypropylene fines; amine bases can form terephthalate salts, while polymer fines may reduce melt purity and create black specks.
PTA dust clouds present a combustible dust hazard. Housekeeping, bonding, and grounding should follow NFPA 652 and, where applicable, IEC 60079-10-2. The product should be stored away from direct sunlight and high-temperature surfaces to prevent localized sintering of fines. If exposed to moisture and then compressed in a hopper, the powder can form crusts that release unevenly into the slurry mixer. These crusts are removed mechanically and should not be forced through pneumatic lines, because the resulting surge can alter esterification feed ratio and downstream melt viscosity.
Safety and compliance documentation should include the product safety data sheet, REACH registration or equivalent regional chemical inventory status, and food-contact clearance of the final polyester article. In the United States, PET resins made from this monomer are normally evaluated under 21 CFR 177.1630; in the European Union, the finished plastic is assessed under EU Regulation (EC) No 1935/2004 and the specific migration limits of EU 10/2011. These clearances apply to the final article rather than the PTA intermediate. Users selecting PTA for food-grade PET should perform migration testing on the finished container or film according to GB 4806.6-2016 or GB 31604.1-2015 where Chinese food-contact requirements apply.
Because Hainan Yisheng Petrochemical PTA is released as a single polyester-grade stream, supplier qualification is controlled by the certificate of analysis, not by a model number. The operational comparators are 4-CBA, p-toluic acid, ash, moisture, particle-size distribution, and the trace metal signature. A change of supplier to this product, or from this product to another PTA, should be executed under a measured transition protocol on the downstream line, with attention to esterification pressure, slurry mixer power, finisher vacuum, and the 45–250 µm coarse-laden fraction. That measured transition is the only reliable basis for confirming interchangeability.