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Eurostar

Manufactured by IKA Group
Sourced in Germany

The Eurostar is a laboratory equipment product offered by IKA Group. It is a stirrer that is designed to mix and homogenize liquids and suspensions in various laboratory applications.

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Lab products found in correlation

3 protocols using eurostar

1

Fiber Coating and Treatment Protocol

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Example 5

The entire process was performed inside a fume-hood. A desired length of fiber (5-10 m) of desired diameter (i.e. 500 micrometers, 200 micrometers) was wound on a customized reel with minimum surface contact. The reel was attached to a digital mixer (Eurostar, IKA Labortechnik) and then lowered in a narrow neck beaker filled with 800 mL of treatment solution (480 mL TFE, 320 mL deionized H2O and 16 g tin oxalate, 40 mL Disperbyk 187 (Byk Chemie)). In cases where fibers are dyed pink/red, 1 g of Rhodamine 6G was added to the solution prior to fiber addition. The beaker was suspended in a temperature-controlled water bath on a programmable hot plate with an external temperature probe. The solution was agitated with a digital mixer (Eurostar, IKA Labortechnik), driving the reel at 350 RPM for 24 h at 37° C. The entire apparatus was sealed using saran wrap to prevent evaporation of TFE. After 24 h, the reel containing wound fibers was removed and allowed to air dry inside a fume hood for 1 h at which time the fiber was unwound from the reel and wound on spindles for later use.

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2

Fiber Dyeing and Coating Protocol

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Example 5

The entire process was performed inside a fume-hood. A desired length of fiber (5-10 m) of desired diameter (i.e. 500 micrometers, 200 micrometers) was wound on a customized reel with minimum surface contact. The reel was attached to a digital mixer (Eurostar, IKA Labodechnik) and then lowered in a narrow neck beaker filled with 800 mL of treatment solution (480 mL TFE, 320 mL deionized H2O and 16 g tin oxalate, 40 mL Disperbyk 187 (Byk Chemie)). In cases where fibers are dyed pink/red, 1 g of Rhodamine 6G was added to the solution prior to fiber addition. The beaker was suspended in a temperature-controlled water bath on a programmable hot plate with an external temperature probe. The solution was agitated with a digital mixer (Eurostar, IKA Labortechnik), driving the reel at 350 RPM for 24 h at 37° C. The entire apparatus was sealed using saran wrap to prevent evaporation of TFE. After 24 h, the reel containing wound fibers was removed and allowed to air dry inside a fume hood for 1 h at which time the fiber was unwound from the reel and wound on spindles for later use.

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3

Hydroxyapatite Nanoparticle Synthesis

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HApN were prepared via wet precipitation.19 (link),20 (link) Precursor solutions of CaCl2 and Na2HPO4 were prepared in deionized water with a molar Ca:P ratio of 1.67, as per standard HAp stoichiometry,20 (link) and pH was adjusted to 10±0.5. HApN chemical precipitation progressed by the dropwise addition of PO43– ion solution to Ca2+ ion solution under magnetic stirring (Eurostar; IKA Labortechnik, Staufen im Breisgau, Germany). Precipitation proceeded at 50°C while maintaining pH at 11–12 for higher-purity HAp.21 (link) This was followed by aging of the prepared particles. Afterward, the mixture was centrifuged (3K-30; Sigma, Osterode, Germany) at 15,000 rpm, 4°C for 15 minutes to separate the formed pellet, which was washed three times with water, then absolute ethanol.
For optimization of HApN and elaboration of the impact of different process parameters on surface-area properties, a two-level (23) factorial design was employed. HApN formulations were prepared by varying precursor concentrations, aging time, and aging temperature. Design-Expert (version 9.0.6.1; Stat-Ease, Minneapolis, MN, USA) was used for establishing the design model and further data analysis.
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