The methods used for determining heavy metal concentrations (Cr, Cu, Ni, Pb, Cd, Zn, Co, and Hg), arsenic, mineral oil hydrocarbons, and PAHs have been previously described in detail [20 (link)]. The concentration of Mo was determined in the same way as the heavy metals. For PCB detection, the oven-dried samples (5 g) were transferred to a Soxhlet apparatus and extracted with 100 mL of n-hexane. The extracts were evaporated on a rotary evaporator (Rotavapor R-210 with Heating Bath B-491, Vacuum Pump V-700, and Vacuum Controller V-850, Büchi) and concentrated in a stream of nitrogen gas. They were then transferred into a centrifuge tube and cleaned up with concentrated sulphuric acid (min. 96%). If the samples were highly contaminated repeated acid clean-up was employed. PCBs were quantified by a gas chromatography with a 63Ni Electron capture detector (GC-17A-ECD, Shimadzu) according to EPA 8082 [21 ] standard method.
Vacuum controller v 850
The Vacuum Controller V-850 is a compact and versatile instrument designed to precisely monitor and control vacuum levels in laboratory applications. It features a digital display for real-time vacuum pressure readings and intuitive controls for setting and adjusting the desired vacuum levels.
Lab products found in correlation
3 protocols using vacuum controller v 850
Sediment Pollution Analysis in WWTP Effluent
The methods used for determining heavy metal concentrations (Cr, Cu, Ni, Pb, Cd, Zn, Co, and Hg), arsenic, mineral oil hydrocarbons, and PAHs have been previously described in detail [20 (link)]. The concentration of Mo was determined in the same way as the heavy metals. For PCB detection, the oven-dried samples (5 g) were transferred to a Soxhlet apparatus and extracted with 100 mL of n-hexane. The extracts were evaporated on a rotary evaporator (Rotavapor R-210 with Heating Bath B-491, Vacuum Pump V-700, and Vacuum Controller V-850, Büchi) and concentrated in a stream of nitrogen gas. They were then transferred into a centrifuge tube and cleaned up with concentrated sulphuric acid (min. 96%). If the samples were highly contaminated repeated acid clean-up was employed. PCBs were quantified by a gas chromatography with a 63Ni Electron capture detector (GC-17A-ECD, Shimadzu) according to EPA 8082 [21 ] standard method.
Preparation of Coated Calcium Carbonate Nanoparticles
EXAMPLE 4
260 g calcium carbonate nano particles (; American Elements 97.5%) with 13 g of octadecyltrimethoxysilane (C18H37Si(OMe)3; abcr chemicals 97%) were mixed in 260 g of DMAC and run once through a ball mill (WAB Dyno®-Mill Multi Lab at 10 rpm pumping rate and 3800 U/min milling rotation with 1 mm zirconium dioxide milling beads). The particles were dried on a rotary evaporator (Buchi Rotavapor R-210 with a Vacuum Controller V-850) to receive the coated particles. 700 g of polymer mixture was hand-mixed with 273 g C18 Sin-CaCO3. Further mixing was conducted in a ball mill (WAB Dyno®-Mill Multi Lab at 10 rpm pumping rate and 3800 U/min milling rotation with 1 mm zirconium dioxide milling beads) by running the mixture 4 times through the mill to receive the final dispersion to be degassed in vacuum.
Quantitative Phenolic and Carotenoid Analysis
The estimation of Total Phenolic Content (TPC) and Total Tannin Content (TTC) was implemented using an Infinite® 200 PRO microplate reader (Tecan Group Ltd., San Jose, CA, USA) and the estimation of Total Carotenoid Content (TCC) was performed using an x-ma 100 spectrophotometer (Human Corporation, Seoul, Republic of Korea).
An Accela Ultra High-Performance Liquid Chromatography system equipped with an autosampler and coupled with a TSQ Quantum Access triple-quadrupole mass spectrometer (Thermo Fisher Scientific, Inc., Waltham, MA, USA) was used for the determination of the phenolic and carotenoid compounds qualitative and quantitative content.
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