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Cellulose mixed ester filter membranes

Manufactured by Merck Group

Cellulose mixed ester (CME) filter membranes are a type of laboratory equipment used for filtration purposes. These membranes are made from a combination of cellulose esters and provide a selective barrier to the passage of particles, molecules, or other materials in a solution or suspension. The core function of CME filter membranes is to facilitate the separation and purification of various substances during laboratory processes.

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3 protocols using cellulose mixed ester filter membranes

1

Phytolith Extraction and Germanium Analysis

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Prior to the phytolith extraction nickel crucibles (99.6% Ni) were cleaned with 10% HCl and 10% H 2 O 2 for 1 h and subsequently heated up to 500 °C in a muffle furnace for one hour. Dried leaves of each of the three grasses (reference plants without artificial Ge treatment and plants treated with 50 lmol L -1 Ge) were placed inside the crucible and were calcined at 500 °C for 4 h. After cooling down the ash was transferred into sample tubes by adding 10 ml of 1% HNO 3 . The sample tubes were slowly shaken for one hour. The solutions were subsequently filtered through 200 nm cellulose mixed ester (CME) filter membranes (MERCK MILLIPORE). Each filter was washed three times with deionized water. A blank filter without ash was processed as reference. The membrane filters with the adhering phytoliths were dried at 60 °C for 48 h and weighed. After cooling, the filters of three out of four replicates were placed into microwave digestion tubes (Ethos plus 2, MLS) and totally dissolved by using a mixture of HNO 3 , H 2 O 2 and HF (Wiche et al. 2016) . The last remaining filter with adhering phytoliths was later used for microscopy and EDX measurements. Concentrations of Si and Ge in the resulting solutions and the filtrates were measured by ICP-MS using 10 lg l -1 rhodium and rhenium as internal standards.
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2

Phytolith Extraction and Germanium Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Prior to the phytolith extraction nickel crucibles (99.6% Ni) were cleaned with 10% HCl and 10% H 2 O 2 for 1 h and subsequently heated up to 500 °C in a muffle furnace for one hour. Dried leaves of each of the three grasses (reference plants without artificial Ge treatment and plants treated with 50 lmol L -1 Ge) were placed inside the crucible and were calcined at 500 °C for 4 h. After cooling down the ash was transferred into sample tubes by adding 10 ml of 1% HNO 3 . The sample tubes were slowly shaken for one hour. The solutions were subsequently filtered through 200 nm cellulose mixed ester (CME) filter membranes (MERCK MILLIPORE). Each filter was washed three times with deionized water. A blank filter without ash was processed as reference. The membrane filters with the adhering phytoliths were dried at 60 °C for 48 h and weighed. After cooling, the filters of three out of four replicates were placed into microwave digestion tubes (Ethos plus 2, MLS) and totally dissolved by using a mixture of HNO 3 , H 2 O 2 and HF (Wiche et al. 2016) . The last remaining filter with adhering phytoliths was later used for microscopy and EDX measurements. Concentrations of Si and Ge in the resulting solutions and the filtrates were measured by ICP-MS using 10 lg l -1 rhodium and rhenium as internal standards.
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3

Phytolith Extraction and Germanium Analysis

Check if the same lab product or an alternative is used in the 5 most similar protocols
Prior to the phytolith extraction nickel crucibles (99.6% Ni) were cleaned with 10% HCl and 10% H 2 O 2 for 1 h and subsequently heated up to 500 °C in a muffle furnace for one hour. Dried leaves of each of the three grasses (reference plants without artificial Ge treatment and plants treated with 50 lmol L -1 Ge) were placed inside the crucible and were calcined at 500 °C for 4 h. After cooling down the ash was transferred into sample tubes by adding 10 ml of 1% HNO 3 . The sample tubes were slowly shaken for one hour. The solutions were subsequently filtered through 200 nm cellulose mixed ester (CME) filter membranes (MERCK MILLIPORE). Each filter was washed three times with deionized water. A blank filter without ash was processed as reference. The membrane filters with the adhering phytoliths were dried at 60 °C for 48 h and weighed. After cooling, the filters of three out of four replicates were placed into microwave digestion tubes (Ethos plus 2, MLS) and totally dissolved by using a mixture of HNO 3 , H 2 O 2 and HF (Wiche et al. 2016) . The last remaining filter with adhering phytoliths was later used for microscopy and EDX measurements. Concentrations of Si and Ge in the resulting solutions and the filtrates were measured by ICP-MS using 10 lg l -1 rhodium and rhenium as internal standards.
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