1077-56-1 Purity
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Specification
Optical cellulose fibers for water sensing were prepared using Cellulose Acetate. The core of the fiber was prepared from cellulose dissolved in [EMIM]OAc, which was then wet-spun into water. The cladding on the cellulose core was produced by applying a layer of cellulose acetate dissolved in acetone using a filament coater. The chemical and optical properties of regenerated cellulose and cellulose acetate in cast films were investigated using UV-visible spectroscopy and Fourier transform infrared spectroscopy measurements. The regenerated cellulose film was observed to absorb UV light, passing visible wavelengths. The tensile strength of the fiber was 120 MPa. The prepared optical fiber guided light in the range of 500-1400 nm. The attenuation constant of the cellulose fiber was observed to be 6.3 dB/cm at 1300 nm. The use of the prepared optical cellulose fiber in water sensor applications was demonstrated. When the optical fiber was placed in water, a significant attenuation of the light intensity was observed. The investigated optical fiber can be used in sensor applications, where easy modification and high heat resistance are advantageous properties.
The core filaments were prepared from the cellulose spinning solution using a laboratory-scale wet-jet spinning apparatus equipped with a spinning nozzle. The dissolved cellulose was filled into a 10 ml plastic syringe and then passed through a nozzle (diameter and length of 0.41 lm and 31.75 mm, respectively) into a water coagulation bath. A constant rotation rate of 0.5 ml/min was used. After spinning, the filaments were placed in water for at least two hours and then dried under tension at room temperature and ambient humidity. The coating layer was prepared on the core filament using a homemade coater. 25 g of cellulose acetate was dissolved in 25 g of acetone using a laboratory mixer. The dissolved CA was placed in the coater and the pre-made filaments were pulled out through the homemade filament coater. The acetone was evaporated from the coated filaments at room temperature. The thickness of the cellulose acetate layer was determined by the diameter of the output hole.
Three solvents, acetone, acetic acid, and dimethylacetamide (DMAc), with certain solubility parameters, surface tensions, viscosities, and boiling temperatures were used to generate mixtures for electrospinning cellulose acetate (CA). While none of these solvents formed fibers continuously on their own, mixing DMAc with acetone or acetic acid produced a suitable solvent system. The 2:1 acetone:DMAc mixture was the most versatile mixture as it allowed for continuous electrospinning of fibrous membranes from 12.5-20% CA concentrations. These CA solutions, with 1.2 to 10.2 poise and approximately 26 dynes/cm, produced smooth fibers with diameters ranging from 100 nm to 1 m. Fiber size generally decreased with decreasing CA concentration. The nature of the collector affected the morphology and packing of the fibers. Fibers collected on paper had more uniform size, smooth surfaces, and fewer defects, whereas fibers collected in water had greater size variation. The pores in the membranes collected on aluminum foil and paper were better interconnected in the planar direction than those in the membranes collected on water. There is evidence that electrospinning can induce fiber ordering. Deacetylation of CA membranes in NaOH/ethanol was more efficient and complete than in aqueous NaOH, producing DS values between 0.15 and 2.33 without altering the fiber surface, packing, or organization. Fully regenerated cellulose membranes had similar hydrophilicity to commercial cellulose fiber substrates but absorbed nearly 10 times more water than commercial cellulose fiber substrates.
CA was dissolved in acetone, acetic acid, DMAc, and their mixtures under constant stirring at room temperature. For electrospinning, each polymer solution was placed in a glass capillary and a stainless steel electrode was immersed in the solution and connected to a power supply. A grounded counter electrode was connected to a collector consisting of paper, aluminum foil, copper mesh, and water. At a critical voltage, the electrostatic force acting on the cone surface overcomes the surface tension of the solution and the jet is ejected and accelerated toward the grounded collector by the electric field generated between the electrode and the counter electrode. While traveling, electrostatic instabilities caused the jet to split into many smaller filaments, which were placed on the collector in a random manner to form an interconnected fibrous membrane. As the solvent evaporated, the polymer filaments solidified on the collector. The obtained CA membrane was separated from the collector and dried under vacuum at 80 °C for 10 h.
Efficient Isolation of RBC-EVs using Cellulose Acetate Syringe Filters
As a researcher in the science field, I have been using Cellulose Acetate syringe filters from Alfa Chemistry for the isolation of RBC-EVs in my experiments. I must say, I have been extremely impressed with the performance and efficiency of these filters.
Exceptional Cellulose Acetate Filter for Precise Cell Sorting
I recently had the opportunity to work with the cellulose acetate filter from Alfa Chemistry during a cellular sorting experiment. The filter provided exceptional quality and precision, allowing for accurate separation of EYFP+/ABCB1+ cells during flow cytometry analysis.
The PubChem CID of cellulose acetate is 57469.
The molecular formula of cellulose acetate is C14H16N4.
The molecular weight of cellulose acetate is 240.30 g/mol.
The IUPAC name of cellulose acetate is 1-(2-methylpropyl)imidazo[4,5-c]quinolin-4-amine.
The InChIKey of cellulose acetate is DOUYETYNHWVLEO-UHFFFAOYSA-N.
Some synonyms of cellulose acetate include IMIQUIMOD, Aldara, and Zyclara.
The CAS number of cellulose acetate is 99011-02-6.
The ChEMBL ID of cellulose acetate is CHEMBL1282.
The UNII of cellulose acetate is P1QW714R7M.
The Wikipedia page for cellulose acetate is "Imiquimod".