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Atlas evacuable pellet die

Manufactured by Specac
Sourced in United Kingdom

The Atlas Evacuable Pellet Die is a laboratory equipment designed for the compression of powder samples into pellets. It allows for the creation of uniform, high-quality pellets through the application of controlled pressure and the ability to evacuate air from the die cavity.

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Lab products found in correlation

3 protocols using atlas evacuable pellet die

1

Uniform Propranolol-HPMC Tablet Formulation

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A mixture of HPMC (30% w/w) and propranolol (70% w/w) was prepared by blending the powders in a tubular mixer (Artisan Technology Group®) at 50 rpm for 15 min. Content uniformity tests carried out using ultraviolet spectroscopy confirmed uniform mixing. A Testometric™ M500 – 50 CT (Testometric™ Company Ltd., United Kingdom) apparatus directly connected to a computer was used to compress 300 mg of the powder mixture with a 50 kN load cell equipped with a 13.00 mm Atlas Evacuable Pellet Die (Specac® Limited, UK). Polished flat-faced punches were used, where the lower punch was held stationary while the upper punch moved at a speed of 3 mm min−1 during loading and 1 mm min−1 on unloading. The compacts or tablets were produced at an applied pressure of 150 MPa. After the tablets were ejected, they were stored in an air-tight container over silica gel for 24 h to allow for elastic recovery before further investigation. Relative humidity and temperature during compaction work were in the range of 20 to 35% RH and 25 to 27 °C, respectively.
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2

Preparation of Stainless Steel-Encapsulated Au(SR) Solids

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50 mg of the powdery a-[Au(SR)]n solids were deposited between two 13 mm highly polished stainless steel disks and inserted in a Specac™ Atlas™ Evacuable Pellet Die, usually used for KBr pellet production for FTIR analysis samples. The pressure applied with the pressing system was 10 tons for 60 s at room temperature and under ambient atmosphere. Pellets with 100 mg of powder were also prepared under the same conditions. All the characterizations of the glasses, except for transmittance, were carried out on the ones fabricated with 50 mg of amorphous powder.
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3

Propranolol Tablet Formulation and Characterization

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A pharmaceutical tablet formulation (model sample material) was prepared as described by Nirwan et al., 2019 [3 (link)]. Briefly, a powder mixture of HPMC (30% w/w) and propranolol (70% w/w) was prepared using a tubular mixer (Artisan Technology Group®, Kansas City, MO, USA) at 50 rpm for 15 min, followed by content uniformity testing of the mixture using ultraviolet spectroscopy which confirmed uniform mixing. Tablets of 300 mg of the powder mixture were prepared using a Testometric™ M500–50 CT (Testometric™ Company Ltd., Rochdale, U.K.) apparatus directly connected to a computer with a 50 kN load cell equipped with a 13.00 mm Atlas Evacuable Pellet Die (Specac® Limited, Orpington, U.K.). Polished flat-faced punches were used, where the lower punch was held stationary while the upper punch moved at a speed of 3 mm min−1 during loading and 1 mm min−1 on unloading and an applied pressure of 150 MPa was used. Following ejection of the tablets, they were stored in an air-tight container over silica gel for 24 h to allow for elastic recovery before further investigation. All compaction work was conducted at a relative humidity and temperature in the range of 20% to 35% RH and 25 °C to 27 °C, respectively.
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