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Model 600

Manufactured by Memmert
Sourced in Germany

The Memmert Model 600 is a compact incubator designed for various laboratory applications. It features a temperature range of 5°C above ambient to 80°C and a volume of 53 liters. The unit has a forced air circulation system to ensure uniform temperature distribution throughout the interior.

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8 protocols using model 600

1

Preparation and Sterilization of Zirconia Discs

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Commercially available zirconia blocks (Ivoclar IPS e.max® ZirCAD MT A2, Lot:VM9002) of 98.5 mm in diameter and 14 mm in thickness were cut into discs of 25 mm in diameter and 1.2 mm in thickness by a high-speed linear precision saw (Isomet® 5000, BUEHLER, USA) with a diamond blade under running water. The samples were then polished with SiC abrasive papers of 1000-grit and 2000-grit in sequence on a polishing machine, and reached a surface roughness value of 0.5 µm. The polished zirconia blocks were sintered following the manufacturer’s protocol. The size of the sintered samples turned into 20.0 ± 0.5 mm in diameter and 1.0 mm in thickness due to the phase transformation during sintering. After the above treatments, the samples were ultrasonically cleaned with a 70% ethanol solution for 15 min, rinsed with double deionized water, and dried in clean ambient air for four hours before the samples were blown with clean high-pressure gas to remove any possible residue on the surface. The samples were finally sterilized with a dry heat method in 160 °C for two hours in a heating and drying oven (Model 600, MEMMERT, Germany).
A total of 24 cylindrical zirconia samples were randomly divided into six groups. A control group of four specimens was taken without any further treatment.
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2

Optimizing Hop Leaf Drying Techniques

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Humulus lupulus leaves from five hop genotypes (Table 1) grown under organic farming conditions were collected at harvest at the farm I Vizi del Luppolo (Cori, Italy; 41°63′46″ N-12°87′18″ E) and cold-transported to the Food Chemistry and Biotechnology laboratory at CREA Research Centre for Olive, Fruit and Citrus Crops (Rome, Italy). An aliquot of leaves (300 g) of each genotype was subjected to oven drying (OD) at 45 °C (air velocity: 0.6 ms−1, relative humidity < 0.5%, system power: 1.4 kW/h; model 600, Memmert GmbH + Co.KG, Schwabach, Germany). This type of drying and the temperature were chosen considering the possibility of exploiting the drying systems for hop cones that are generally present in these farms. The remaining part (300 g) was freeze-dried at −54 °C and 0.075 mbar (model Modulyo 4 K, Edwards, UK). Sample dehydration using all of the methods mentioned above was continued until about 8–10% final moisture content was reached. At the end of each drying treatment, samples were finely milled (sieve 0.5 mm), stored under vacuum and kept protected from light and moisture until analysis. Four replicates for each treatment were carried out.
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3

Sour Cherry Pomace Drying Methods

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Single-cultivar pomaces (2.5 kg each one), from the juice processing of two different sour cherry varieties (a local "Morello or visciola" sour cherry selection recovered by Bianchi in Offagna AN, Italy, and Montmorency, namely BO and MM, respectively) grown under organic farming, were kindly provided by Italia Selvatica SRL Agricola Offagna, Italy. Pits, stems and other foreign materials were manually removed from pomaces, which were then stored at -20°C in low-density polyethylene bags until use. An aliquot of pomace (100g) was directly analysed and considered as control samples (CTRs) whereas (400g) of each variety was subjected to oven drying (OD) at 60° C for 24 h (air velocity: 0.6 ms -1 , relative humidity < 0.5%, system power: 1.4 kW/h); model 600, Memmert GmbH + Co.KG, Schwabach, Germany), and the remaining part (400g) was freeze-dried (FD) at -54°C and 0.075 mbar for 72h (model Modulyo 4K, Edwards, United Kingdom). Sample dehydration using all the methods mentioned above was continued up to 9% final moisture content was reached. At the end of each drying treatment, pomaces were finely milled (sieve 0.5 mm) and kept protected from light and humidity until analysis. Three replicates for each treatment were carried on.
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4

Pulp and Seed Proximate Analysis

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The pulp and seed proximate composition was determined using the methods of AOAC (1984). Moisture content was obtained by difference weighing of 2 g of the sample before and after oven‐drying (model 600; Memmert, Schwabach, Germany) at 105°C for 12 hr. Crude protein was estimated using the macro‐Kjeldahl method, then calculated by multiplying the measured nitrogen by a factor of 6.25. Ash was determined by incinerating the dried sample (2 g) in a muffle furnace (Gallenkamp, England) at 550°C for 6 hr. A sample (10 g) was used to determine crude fat by extracting with n‐hexane (40–60°C) in a Soxhlet apparatus. The crude fiber was determined by digesting the defatted sample (2 g) in 1.25% HCl and 1.25% NaOH. Carbohydrate levels were calculated by subtracting the total sum of moisture, crude protein, crude fat, and ash from 100%.
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5

Particle Size Analysis of Samples

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The particle size analysis was determined using the method described by Wolf et al. [21 (link)]. The sample, weighing about 30–40 g, was placed into a container with one L of distilled water and mixed for 10 s. After 1 h of soaking, the suspension was then added to a sieve tower consisting of eight analysis sieves (mesh sizes: 3.15, 2.0, 1.4, 1.0, 0.8, 0.56, 0.4, and 0.2 mm, respectively). Ten L of distilled water were used to rinse the sieve tower and put overnight in the drying oven at 103 °C (model 600, Memmert GmbH & Co. KG, Schwabach, Germany) until constant weight was achieved. According to Wolf et al. [21 (link)], the individual sieves were then weighed, and a percentage of the total amount of weighed DM was calculated.
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6

Physical Stability Assessment of Acrylic Denture Spray

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The denture spray was subjected to physical stability studies, including centrifugation test and temperature cycling test. A centrifuge test was performed at 3000 round per minute (rpm) for 30 min to assess the stability of the acrylic denture spray (Centrifuge Z 206 A, Hermle Labortechnik GmbH, Wehingen, Germany). The temperature cycling test was carried out on the Memmert drying oven (Model 600, Memmert GmbH + Co. KG, Schwabach, Germany) by holding the tested samples at 50 ± 2 °C for 24 h before switching to 42 ± 2 °C for another 24 h. This procedure was repeated six times (i.e., 12 days). Color, odor, clarity, homogeneity, and pH (measured with Mettler Toledo S220 pH meter, Mettler Toledo, Ohio, USA) were used to assess the stability of the product before and after temperature cycling [22 ].
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7

Medicinal Plant Preparation Protocol

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The parts of medicinal plants in Table 1 were carefully washed with sterilized distilled water to eliminate any dirt before being utilized in the experiment. After that, the two-step drying procedure was carried out. In the first step, the samples were shade dried at a moderate temperature (21–30°C) for two weeks by spreading them out on paper and rolling them back and forth to let the most moisture evaporate. In the second step, the shed-dried plants were dehydrated in an oven (Model-600, Memmert, Germany) at 45°C for three hours to remove any remaining moisture. A dry mill (Kenwood Multi-Mill, Havant, UK) was used to grind plant samples into a fine powder which was then passed through a screen (mesh size 30) to ensure an equal pulverization of the plants. The samples were stored in sterilized, sealed plastic bags at room temperature until use (38 ).
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8

Fourier Transform Infrared Spectroscopy of Algal Biomass

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The algal sample was dried in an oven (Memmert: Model: 600, GmbH Co, Ltd) at 70 °C overnight. The dried biomass was ground to fine powder. The powder mixture was transferred to compression dye under high pressure to form a pellet. The pellet was kept in sample cuvette and analyzed according to standard FTIR (Perkin Elmer) test method ASTM: 1252-98 with light source in middle range infrared (4000–600cm−1). The technique was employed for the determination of chemical composition of sample based on functional groups.
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