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Manual hydraulic press

Manufactured by Specac
Sourced in United Kingdom

The Manual Hydraulic Press is a lab equipment product designed for controlled compaction and pelletization of samples. It utilizes a hydraulic system to apply pressure to a sample, enabling the creation of uniform pellets for various analytical applications. The core function of this press is to provide a reliable and consistent means of sample preparation.

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12 protocols using manual hydraulic press

1

Bone Elemental Analysis by XRF

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For each bone, a few grams were taken with a polyester tool (Retsch GmbH, Germany). Due to the poor preservation state of some bones, the use of a mortar and pestle was enough to reduce them to powder. For the more intact bones the samples were powdered in a polyester mill (Retsch GmbH, Germany). In both cases the resulting bone powder was pressed into pellets 15 mm in diameter, by a 10 t manual hydraulic press from Specac. There was no further chemical treatment or additive to the samples.
For each bone n¼9 pellets were made to minimize effects of inhomogeneity. Each pellet, with a thickness of about 1 mm, was glued (heptane mixture) on a Mylar film, fixed into a slide mount and placed on the sample holder (50 mm x 50 mm) in front of the X-ray beam for the element determination.
The remains of two burial shrouds were also analyzed by this instrument but no further treatment was needed, a small piece was placed in front of the beam and the X-ray spectrum was obtained. For the bones of interest transversal sections, around 1 mm thick, were obtained using a microtome equipped with a diamond saw (Buehler Isomet 1000, USA). The resulting sample slice would then be placed inside the XRF chamber on a table attached to a XY translatable stage and directly exposed to the X-ray microbeam to perform the elemental mappings. For each bone of interest one map was acquired.
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2

Fourier Transform Infrared Spectroscopy of Glass System

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Fourier transform infrared spectroscopy (FT-IR) was performed in order to identify the correlation between absorption wavelengths and the chemical structure of the samples. The analysis was performed on powder samples for xCuO (100 − x)(CaF2∙3P2O5∙CaO) glass system with 0 ≤ x ≤ 16 mol%). In this regard, 0.005 g of vitreous oxide powders were homogenized with 0.2 g of potassium bromide (KBr), which were subsequently pressed in the form of pellets with a Manual Hydraulic Press (Specac Ltd, Orpington, UK) for 3 min/10 tons. The spectra were recorded using the Jasco FT-IR 4100 spectrometer with a spectral resolution of 4 cm−1, in the range of 350–4000 cm−1 wave numbers, with 256 scans/sample.
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3

Compacts of α-Indomethacin for Dissolution

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Compacts composed of α indomethacin were prepared by manual
hydraulic compression (Manual Hydraulic Press, Specac Ltd., Orpington,
U.K.) for 30 s with 1 ton and were further used as a reference for
intrinsic dissolution testing.
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4

Characterizing Calcite by FTIR Spectroscopy

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Calcite was collected as described by Mahamid et al., with some modifications (Mahamid et al., 2008 (link)): agar samples were slightly bleached with 6% sodium hypochlorite for 1 min to remove organic matter, washed with Milli-Q water twice and dehydrated in acetone.
FTIR spectra of the bleached samples were acquired in KBr pellets by using a NICOLET iS5 spectrometer (Thermo Scientific, Pittsburgh, PA, USA). The samples were homogenized in an agate mortar and pestle with about 40 mg of KBr, and pressed into a 7 mm pellet using a manual hydraulic press (Specac, Orpington, UK). Infrared spectra were obtained at 4 cm−1 resolution for 32 scans.
The infrared calcite spectrum has three characteristic peaks, designated v2, v3, and v4. Calcium carbonate ν3 peak is expected at 1425 cm−1 for calcite, 1490 cm−1 for vaterite and 1475 cm-1 for aragonite. The calcium carbonate ν2 peak is expected at 875 cm−1 for calcite, 850 cm−1 for vaterite and 855 cm−1 for aragonite. Finally, the calcium carbonate ν4 peak is expected at 713 cm−1 for calcite, 750 cm−1 for vaterite and 715 cm−1 for aragonite (Politi et al., 2004 (link)).
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5

FTIR Characterization of Produced Crystals

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FTIR spectra of the produced crystals were acquired in KBr pellets by using a NICOLET iS5 spectrometer (Thermo Scientific, Pittsburgh, PA, USA). A few milligrams of sample were homogenised and powdered in an agate mortar and pestle. About 0.3 mg were left in the mortar and mixed with about 40 mg of KBr and pressed into a 7 mm pellet using a manual hydraulic press (Specac, Orpington, UK ). Each sample was measured repeatedly, either by repetitive grinding of the same KBr pellet. Typically, a few seconds of regrinding were applied. Infrared spectra were obtained at 4 cm−1 resolution for 32 scans using a Nicolet 380 instrument (Thermo, Instruments LLC, Madison, WI, USA). The baselines for the height measurements of the v2, v3 and v4 peaks were determined as done previously.64 The v2, v3 and v4 heights were normalised to a v3 height of 1,000, corresponding to 1.0 a.u.65 The X-ray diffraction was performed as done previously.66
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6

XRF Analysis of Plant Biomass

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XRF measurements were performed as previously described [47 (link)], using a commercial Portable XRF instrument (Niton XL3t900 Analyzer, Thermo Scientific, Hemel Hempstead,
Hertfordshire, UK) equipped with an X-ray tube and a silicon drift detector. All measurements were carried out in a helium atmosphere with a helium flow rate of 70 centiliters min-1, and the samples were exposed to X-rays for 30 s (instrument settings: main range: 5 s, 6.2 kV, 100 uA, filter blank (no physical filter in the primary beam); low range: 25 s, 6.2 kV, 100 uA, filter blank). XRF experiments were performed on the raw powder biomasses, previously dried at 60°C for 24 h, and silica powder (Fisher Scientific, Loughborough, UK; product number S/0680/53) was used as standard to the calibration curve generation. To obtain a repeatable photon flux from the sample to the XRF detector, sample pellets were prepared using approximately 0.7 g of ground plant material, submitted to 11 tons for 2 s using a manual hydraulic press (Specac, Orpington, UK). Cylindrical pellets of around 5 mm thickness and 12 mm diameter were obtained and measured on both surface sides.
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7

Direct Compression of Orally Disintegrating Tablets

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Orally disintegrating tablets were prepared using the direct compression method. All ingredients were passed through mesh No. 60 separately, then, the ingredients were weighed and mixed in geometrical order and compressed into tablets of 200 mg using 9 mm round flat punches on a manual hydraulic press (Specac Limited, Kent, UK). The mixing time was 10 min and the amplitude was 40 mm. A batch of 100 tablets was prepared for each of the designed formulations.
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8

Cylindrical Tablets for Tetracycline Delivery

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Cylindrical tablets of LIG and MCC with a diameter of 13 mm, a mass of approximately 500 mg and thicknesses of 2.56–2.85 mm were produced by using a manual hydraulic press (Specac Limited, England, UK) and by applying two different compression forces (2 or 5 tonnes) for 1 min, for each tablet formulation. Prior to compression the different excipients and the tetracycline were properly mixed in a 50 mL Falcon tube using a vortex mixer. For each tablet, tetracycline represented 50% of the total mass (250 mg), while the remaining 50% consisted of different proportions of the other constituents. Subsequently, the die was filled manually.
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9

Electrical Conductivity Measurement of Ceramic Pellet

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Electrical conductivity
measurement was acquired in the temperature range from 25 to 850 °C
under H2/N2 (5%/95%) flow using the dc four-probe
method under a dc current applied between 0.01 and 0.5 A. A bar-shaped
pellet (∼2 mm × 3 mm × 9 mm) was prepared by uniaxial
pressing using 0.3 g of powder with a Specac Manual Hydraulic Press,
subsequently annealed at 1050 °C for 12 h under a H2/N2 (5%/95%) atmosphere. A Potentiostat-Galvanostat AUTOLAB
PGSTAT302 from ECO CHEMIE was used to measure the electrical conductivity
of the samples collected every 50 °C.
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10

Thermal Treatment of UiO-66 Powder Samples

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UiO-66 powder samples were heat-treated in a Micromeritics SmartVac at specified temperatures for 16 hours under vacuum (~10 -7 ). The temperatures of choice were as follows: 80, 110, 140, 170, 200, 230, 260, 290, and 320 o C in order to obtain fully hydroxylated, partially dehydroxylated and fully dehydroxylated UiO-66 samples. For each of the heat-treated powder samples, a 400 mg portion was compacted at ~700 MPa using a Specac Manual Hydraulic Press and held at that pressure for 5 minutes.
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