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Pharmaceutical Pressure Vessel

Pharmaceutical Pressure Vessel Specification

Application
Pharmaceutical Industry

Type
Vertical/Horizontal Pressure Vessel

Material
Stainless Steel (SS 316/304)

Capacity
50 to 10,000 Liters (customizable)

Weight
Variable as per capacity (approx. 100 to 2000 kg)

Dimension (L*W*H)
Customizable as per requirement

Condition
New

Testing
Hydro/Pneumatic tested

Mounting
Legs / Skid Mounted

Jacket Type
Single, Double or Limpet Jacket available

Nozzle Configuration
As per client specification

Design Pressure
Up to 10 bar (145 psi)

Surface Finish
Mirror/Matte Polished

Standards Complied
ASME, cGMP, FDA guidelines

Orientation
Vertical or Horizontal

Usage
Sterile liquids, WFI, buffer solutions, intermediate storage

Operating Temperature
-10C to +120C

Internal Finish
Ra 0.40.8 m (as per GMP requirement)

Gasket Material
PTFE, Silicon, EPDM

Accessories
Manhole, Inlet/Outlet Nozzles, Pressure Gauge, Safety Valve, Sight Glass, Vent, Drain Valve

Pharmaceutical Pressure Vessel Trade Information

Minimum Order Quantity
1 Piece

Supply Ability
100 Pieces Per Year

Delivery Time
1 Months

Packaging Details
as per standard

Main Domestic Market
All India

About Pharmaceutical Pressure Vessel

Vertical Design Type Pressure Vessels

Being a well-known Organization, we are presenting wide range ofVertical Design Type Pressure Vesselswith fully customized as per client specification and requirements.It is Vertical constructed designed to mount on Leg supports, Bracket Support, Skirt Support etc. at various location like on floor, on structure, on building etc.

Pressure vessels are containers designed to hold gases or liquids at a difference type of pressure and temperature. Manufacturing methods and materials of pressure vessels are depended on size of vessels, the contents, working pressure & Temperature and mounting locations etc. It is designed in many configurations depending upon customer requirement and design parameter.

Our Products meet requirements of nation & international standard and codes for design and fabrication.It manufactures by our trained professionals, who have expertise in manufacturing process & sequence, inspection and testing of products to ensure fill-full of client requirements.We prepare and submit Detailis manufacturing drawings to client base on client input design parameters, if required.

We have qualified WPS, PQR and WPQ in various type of materials, Thickness, Welding Process and other variable under witnessed and certified by reputed Third Party inspection (TPI) agencies. Welders can be qualified in presence of client representative or Third-Party inspection agencies, if client required.

Our products and their components pass through many quality parameters like vendor end inspection, material testing, in-coming and stage-wise inspection, Final Dimension & Visual inspection, NDT Examination, Leak Testing, Hardness, Positive material identification etc. in presence of client representative or Third-Party inspection agencies.

Technical Data:

Design& Manufacturing capability: -

Customized Design available.
Mechanical Strength Design Calculation as per ASME Section VIII, Division 1 on customer Request.
Prepare Detail manufacturing drawings base on client input design parameters.
Diameter of vessels up to 3000 mm & Length up to 10,000 mm (10 mtr.)
Plate thickness of Vessels up to 38 mm.

Material of Construction: -

SS 304 / SS 304L
SS 316 / SS 316L
SS 321
Duplex Steel (SS 2205)
Carbon Steel (SA 516 Gr 70)
Alloy Steel for low and High Temperature services

Welding Technology: -

SMAW (Shielded Metal Arc Welding)
GTAW (Gas Tungsten Arc Welding)

Applicable Destructive Testing: -

Chemical Analysis
Mechanical (Tensile) Testing
Bend Testing
Charpy Impact Testing

Applicable Non-Destructive Testing: -

Visual Inspection (VT)
Liquid Penetrant Testing (DPT)
Magnetic Particle Testing (MPT)
Ultrasonic Testing (UT)
Radiography Testing (RT)
Positive Material Identification (PMI)
Hardness Testing (HT)
Pneumatic Testing
Hydrostatic Testing

Applications:

Oil & Gas
Petrochemical
Refineries
Fertilizers
Chemical plants
Power-plant
Cement Plant
Process industries & any more

Engineered for Sterile Pharmaceutical Processes

Our pressure vessels provide superior hygiene for the storage and handling of sterile liquids, WFI, and buffer solutions. The high-grade stainless steel construction and finely controlled internal finish (Ra 0.4-0.8 m) ensure compliance with strict GMP and FDA guidelines, minimizing contamination risks while promoting process integrity.

Versatility in Design and Capacity

These vessels are customizable for vertical or horizontal installation, with capacities ranging from 50 to 10,000 liters. Adjustable nozzle configurations, jacket types (single, double, or limpet), and mounting styles (legs or skid) allow you to select specifications that seamlessly fit your process, facility size, and operation flow.

Safety, Compliance, and Ease of Use

Tested to stringent ASME standards and equipped with essential accessories-including manholes, safety valves, pressure gauges, and sight glasses-these vessels assure operational safety and simplify maintenance. Hydro and pneumatic testing are performed on each unit, ensuring reliable performance even under challenging conditions.

FAQ's of Pharmaceutical Pressure Vessel:

Q: How is the surface finish on the pharmaceutical pressure vessel achieved, and why is it important?

A: The vessel is available with a mirror or matte-polished surface, achieving an internal finish between Ra 0.4-0.8 m as required by GMP standards. This smooth finish minimizes the risk of microbial contamination and ensures easy cleaning and sterilization, which is vital for pharmaceutical applications.

Q: What materials and pressure ratings are supported by this pressure vessel?

A: The vessel is manufactured from stainless steel SS 316 or 304 and is designed for pressures up to 10 bar (145 psi). Material selection and pressure rating ensure compatibility with a range of pharmaceutical liquids and operational safety under stringent process conditions.

Q: When should a single, double, or limpet jacket be specified for a vessel?

A: The choice of jacket depends on your heating or cooling needs. A single jacket is suitable for basic temperature control, while a double or limpet jacket provides enhanced heat transfer for processes requiring faster or more precise temperature modulation.

Q: Where can these pressure vessels be installed in a pharmaceutical process?

A: The vessel can be integrated at various stages, such as in sterile liquid storage, WFI systems, buffer preparation, or as an intermediate storage container. Its customizable dimensions and mounting options (legs or skid) enable versatile placement within production facilities.

Q: What is the standard process of quality assurance for these vessels?

A: Each vessel undergoes hydro or pneumatic testing to ensure pressure integrity and is manufactured according to ASME, cGMP, and FDA guidelines. Full traceability of materials and rigorous inspection assure compliance with industry standards and client specifications.

Q: How is the vessel customized to match client requirements?

A: Nozzle configuration, orientation (vertical or horizontal), jacket type, gasket material (PTFE, Silicon, EPDM), and dimension (L*W*H) are all tailored according to each client's process specification and plant layout, guaranteeing seamless system integration.

Q: What are the key benefits of using this pharmaceutical pressure vessel for sterile liquids?

A: The vessel ensures maximum product purity, process safety, and regulatory compliance, thanks to its hygienic design, robust construction, and easy-clean features. Additionally, customizable options enhance operational flexibility across a range of pharmaceutical production and storage scenarios.