To test the shear bond strength (SBS) of the experimental composites to dentin through an adhesive system, the occlusal surfaces of extracted, caries-free, human molars were removed and their roots embedded in polycarbonate holders with chemical curing poly(methyl methacrylate) tray resin (Bosworth Fastray Powder and Liquid, Bosworth Company, Skokie, IL, USA). The exposed dentin surfaces were ground flat perpendicular to the longitudinal axis of the teeth with 320 grit silicon carbide paper (Fig. 1a ). The bonding protocol included the following steps. Ground dentin surfaces were first dried, then etched for 15 s with phosphoric acid gel (mass fraction H3PO4 38 %; Etch-Rite®, Pulpdent Corporation, Watertown, MA, USA). The acid was rinsed away with distilled water for 10 s, and a moistened paper towel (Kimwipes®; Kimberly-Clark Global Sales, Inc., Roswell, GA, USA) was used to blot the surface to a near-dry condition. Two protocols were used to prime the moist dentin surfaces. In the ACP base-lining composite series, dentin surfaces were sequentially primed first with N-phenylglycine (NPG; mass fraction 5 %) solution in acetone for 30 s, and then with five consecutive coats of pyromellitic glycerol dimethacrylate (PMGDMA; mass fraction 20 %) in acetone solution and camphorquinone (CQ; mass fraction 0.028 %) as photo-activator. In the ACP orthodontic composite series, only one coating of PMGDMA-acetone primer (DenTASTIC UNO, Pulpdent Corporation, Watertown, MA, USA) was applied. Following the application of NPG and PMGDMA, or PMGDMA alone, the surfaces were air-dried for 10 s to remove acetone and visible-light cured for 10 s (Spectrum Curing Light, Dentsply Caulk Limited, Milford, DE USA). A poly(tetrafluoroethylene) (PTFE)-coated iris (4 mm in diameter and 1.5 mm thick) that defined the bonding area was positioned on the tooth surface, filled by the experimental composite and light-cured for 20 s for the experimental base-liner composites and 60 s for the orthodontic composites. ACP base-liner specimens were completed by applying a commercial resin-based composite (TPH, Dentsply Caulk, Milford, DE, USA), which was cured for an additional 60 s. The assemblies were then exposed to air for 5 min to allow further dry-curing at room temperature, after which they were immersed at 37 °C in either distilled water (ACP base-liner series) or a saliva-like solution [10 ] (orthodontic ACP series) for up to 6 months.
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Chemicals & Drugs
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Hazardous or Poisonous Substance
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Tetrafluoroethylene
Tetrafluoroethylene
Tetrafluoroethylene is a colorless, flammable gas with a faint ethereal odor.
It is used in the manufacture of fluoropolymers, such as polytetrafluoroethylene (PTFE), which have a wide range of applications due to their unique chemical and physical properties.
Tetrafluoroethylene is an important industrial chemical with numerous applications, including in the production of non-stick coatings, electrical insulation, and chemical-resistant materials.
Researchers can optimize their Tetrafluoroethylene studies using the PubCompare.ai platform, which provides access to accurate and reproducible protocols from literature, preprints, and patents, as well as data-driven insights to improve the reliability of their experiments.
It is used in the manufacture of fluoropolymers, such as polytetrafluoroethylene (PTFE), which have a wide range of applications due to their unique chemical and physical properties.
Tetrafluoroethylene is an important industrial chemical with numerous applications, including in the production of non-stick coatings, electrical insulation, and chemical-resistant materials.
Researchers can optimize their Tetrafluoroethylene studies using the PubCompare.ai platform, which provides access to accurate and reproducible protocols from literature, preprints, and patents, as well as data-driven insights to improve the reliability of their experiments.
Most cited protocols related to «Tetrafluoroethylene»
Acetone
Acids
camphorquinone
Composite Resins
Dental Caries
Dental Cavity Liner
Dentastic
Dentin
Dentsply
Epistropheus
Fastray
Glycerin
Homo sapiens
Iris
Light
Light, Visible
Molar
Oligonucleotide Primers
phosphoric acid
Plant Roots
Poly A
polycarbonate
Polymethyl Methacrylate
Polytetrafluoroethylene
Powder
Pulpdent
Resins, Plant
Saliva
Shear Strength
tetrafluoroethylene
Tooth
Bieleski buffer (60% methanol, 25% CHCl3, 10% HCOOH and 5% H2O) was used as extraction solvent (50 μl per sample). Tritium-labelled (105 dpm) or unlabelled (1 pmol) cytokinin standards were added to the sample extracts during the method optimization to determine the recoveries of the StageTip purification procedure. To validate the quantification of the endogenous cytokinin levels in A. thaliana seedlings, roots and shoots, the following stable isotope-labelled cytokinin internal standards (IS) were added as internal tracers at a concentration 0.5 pmol of each compound per 50 μl of Bieleski buffer: [13C5]cZ, [13C5]tZ, [2H5]tZR, [2H5]tZ7G, [2H5]tZ9G, [2H5]tZOG, [2H5]tZROG, [2H5]tZMP, [2H3]DHZ, [2H3]DHZR, [2H3]DHZ9G, [2H7]DHZOG, [2H3]DHZMP, [2H6]iP, [2H6]iPR, [2H6]iP7G, [2H6]iP9G, [2H6]iPMP. The plant material was placed in 2.0 ml microcentrifuge tubes and extracted in Bieleski solvent using a MM 301 vibration mill (Retsch GmbH & Co. KG, Haan, Germany) at a frequency of 27 Hz for 3 min after adding 3 mm tungsten carbide beads (Retsch GmbH & Co. KG, Haan, Germany) to increase the extraction efficiency. The tube content was ultrasonicated for 3 min and then stirred for 30 min at 4°C. After centrifugation (10 min, 15,000 rpm, 4°C) the supernatants (50 μl aliquots) were immediately transferred onto StageTips and purified according to the following protocol.
The PT-SPE was performed in self-packed StageTips by placing a very small disk of matrix in an ordinary pipette tip. Commercially available matrix of poly-tetrafluoroethylene containing reversed-phase octadecyl-bonded silica phase (C18) or poly(styrene-divinylbenzene) (SDB) copolymer modified with sulfonic acid groups to make it more hydrophilic (SDB-RPS Disk) was normally used. Alternatively, ion-exchange sorbent including sulfonic acid as cation exchanger (Cation-SR Disk) was also employed. The procedure shown in Additional file5 was described by Rappsilber et al. [23 (link),26 (link)]. Small disks (approximately 1.0 mm diameter, 0.5 mm thickness) were cut out manually from the EmporeTM High Performance Extraction Disk placed on a clean surface (Petri dish) using a hollow tool cutter (blunt-ended syringe needle). The cutter was gently pressed into the Empore disk and the material penetrated to the inside of the needle. Subsequently, the cutter was placed inside a pipette tip (disposable GELoader® Tip, 100 μl, from Eppendorf). The small disk was then released using a plunger (rod) that fitted into the needle (both parts from Hamilton) and pressed gently repeatedly into place using the weight of the plunger. After removing the cutter and plunger, the single-StageTip was finished. Additional disks were added the same way to produce combined multi-StageTips.
The Empore sorbents were tested individually (C18, SDB-RPS, and Cation-SR) or in combination (C18/SDB-RPS, C18/Cation-SR, C18/SDB-RPS/Cation-SR). All solutions were loaded from the top of the tip in a volume of 50–100 μl using a pipette. The prepared StageTip was inserted into a hole at the centre of the lid of the microcentrifuge tube (1.5 ml) and placed in a centrifuge after solvent pipetting (Figure2 ). Prior to loading the sample the StageTip sorbents were activated with 50 μl acetone (by centrifugation at 1,500 rpm, 15 min, 4°C), 50 μl water (1,500 rpm, 15 min, 4°C), 50 μl methanol (1,500 rpm, 15 min, 4°C), 50 μl water (1,500 rpm, 15 min, 4°C), equilibrated with 50 μl 50% (v/v) nitric acid (1,000 rpm, 20 min, 4°C), 50 μl water (1,500 rpm, 15 min, 4°C) and 50 μl Bieleski solvent (1,500 rpm, 15 min, 4°C). Afterwards, the samples were loaded in extraction buffer (500 rpm, 45 min, 4°C). The tips were washed using 50 μl methanol (1,500 rpm, 15 min, 4°C) and elution of samples was performed with 50 μl of 0.5 M NH4OH in 60% MeOH (500 rpm, 45 min, 4°C). Eluates were collected into new clean microcentrifuge tubes and directly mixed with scintillation buffer prior to measurement of radioactivity or evaporated to dryness in a Speed-Vac concentrator RC1010 (Jouan, Winchester, UK) and dissolved in 20 μl of mobile phase prior to UHPLC-MS/MS analyses.
The PT-SPE was performed in self-packed StageTips by placing a very small disk of matrix in an ordinary pipette tip. Commercially available matrix of poly-tetrafluoroethylene containing reversed-phase octadecyl-bonded silica phase (C18) or poly(styrene-divinylbenzene) (SDB) copolymer modified with sulfonic acid groups to make it more hydrophilic (SDB-RPS Disk) was normally used. Alternatively, ion-exchange sorbent including sulfonic acid as cation exchanger (Cation-SR Disk) was also employed. The procedure shown in Additional file
The Empore sorbents were tested individually (C18, SDB-RPS, and Cation-SR) or in combination (C18/SDB-RPS, C18/Cation-SR, C18/SDB-RPS/Cation-SR). All solutions were loaded from the top of the tip in a volume of 50–100 μl using a pipette. The prepared StageTip was inserted into a hole at the centre of the lid of the microcentrifuge tube (1.5 ml) and placed in a centrifuge after solvent pipetting (Figure
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ammonium bicarbonate
Biological Assay
Buffers
Capillaries
Cell Lines
Cells
Colon Adenocarcinomas
Enzymes
Fetal Bovine Serum
Homo sapiens
Ions
Pellets, Drug
Penicillins
Peptides
Phosphates
phosphine
Proteins
Radionuclide Imaging
Saline Solution
Serum
Streptomycin
Tandem Mass Spectrometry
tetrafluoroethylene
tris(2-carboxyethyl)phosphine
Tromethamine
Trypsin
A 4 wt% PLGA solution was prepared from poly(lactic-co-glycolic acid) granules (PLGA, 85/15, Corbion Purac, Amsterdam, The Netherlands) in hexafluoroisopropanol ((CF3)2CHOH, P&M Invest, Moscow, Russia) and a 5 wt% VDF-TeFE solution was prepared from vinylidene fluoride-tetrafluoroethylene granules (VDF-TeFE, Galopolymer, Moscow, Russia) in acetone (C3H6O, Ekos-1, Moscow, Russia). After electrospinning, all fabricated scaffolds were stored separately for one week in a dark, dry place at room temperature in order to let the solvents evaporate gradually from the samples. The polymer scaffolds were fabricated by the electrospinning method on a NANON-01A setup (MECC Co., Fukuoka, Japan), equipped with a cylindrical collector with a length of 200 mm and a diameter of 100 mm, which rotated at a speed of 200 rpm. For the fabrication of PLGA scaffolds, the following electrospinning parameters were applied: voltage: 22 kV, distance between the nozzle and the collector: 150 mm, solution flow rate: 4 mL/h, syringe volume: 10 mL, spinneret width: 200 mm, spinneret speed: 10 mm/s, a 20 G needle. The VDF-TeFE scaffolds were fabricated under the following electrospinning parameters: voltage: 20 kV, distance between nozzle and collector: 150 mm, solution flow rate: 6 mL/h, syringe volume: 10 mL, spinneret width: 200 mm, spinneret speed: 10 mm/s, a 22 G needle. The morphology of the scaffolds fabricated differs significantly since the used parameters of electrospinning cause these differences for polymers, and mechanically stable VDF-TeFE and PLGA scaffolds can be fabricated with these parameters. To remove the excess solvent, the electrospun scaffold samples were dried for 48 h in a drying oven at room temperature and a pressure of 0.5 Pa.
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1,1-difluoroethylene
Acetone
Chromatography, Micellar Electrokinetic Capillary
Cytoplasmic Granules
Glycols
hexafluoroisopropanol
Needles
poly(lactic acid)
Polylactic Acid-Polyglycolic Acid Copolymer
Polymers
Pressure
Solvents
Syringes
tetrafluoroethylene
Most recents protocols related to «Tetrafluoroethylene»
The vinylidene fluoride copolymer with tetrafluoroethylene P (VDF-TFE) was investigated. The microstructure of its chains was studied with the 19F NMR method, employing the 19F type of fluorine isotope with a number of protons equal to 19. The spectra of solutions in acetone-d6 were recorded with H-decoupling at 303 K using the Bruker Avance II spectrometer (Bruker Corporation, Karlsruhe, Germany) operating at the fluorine frequency of 282.48 MHz. The 19F NMR chemical shifts were referenced externally to CFCl3 (0 ppm).
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Synthesis of purple CQDs (p-CQDs): 2,7-naphthalenediol (0.04 g) and urea (0.02 g) were dissolved in 10 mL of toluene, the mixture solution was transferred into a poly(tetrafluoroethylene) (Teflon)-lined autoclave in an oven after ultra-sounding for 5 min. Then the reaction was performed with a ramp rate of 8 °C/min at 180 °C for 12 h.
Synthesis of blue CQDs (b-CQDs): 2,7-naphthalenediol (0.04 g) and EDA (170 μL) were added in 10 mL of H 2 O, the mixture solution was transferred into a poly(tetrafluoroethylene) (Teflon)-lined autoclave in an oven after ultra-sounding for 5 min. Then the reaction was performed with a ramp rate of 7 °C/min at 200 °C for 11 h.
Synthesis of cyan CQDs (c-CQDs): 2,7-naphthalenediol (0.08 g) and urea (0.1 g) were dissolved in 4 mL of H 2 O, the mixture solution was transferred into a poly(tetrafluoroethylene) (Teflon)-lined autoclave in an oven after ultra-sounding for 5 min. Then the reaction was performed with a ramp rate of 8 °C/min at 160 °C for 4 h.
Synthesis of darkcyan CQDs (dc-CQDs): 2,7-naphthalenediol (0.06 g) and urea (0.06 g) were dissolved in 10 mL of H 2 O, the mixture solution was transferred into a poly(tetrafluoroethylene) (Teflon)-lined autoclave in an oven after ultra-sounding for 5 min. Then the reaction was performed with a ramp rate of 8 °C/min at 220 °C for 12 h.
Synthesis of green CQDs (g-CQDs): 2,7-naphthalenediol (0.02 g) and urea (0.06 g) were dissolved in 10 mL of ethanol, the mixture solution was transferred into a poly(tetrafluoroethylene) (Teflon)-lined autoclave in an oven after ultra-sounding for 5 min. Then the reaction was performed with a ramp rate of 8 °C/min at 160 °C for 12 h.
Synthesis of yellow green CQDs (yg-CQDs): 2,7-naphthalenediol (0.06 g) and EDA (940 μL) were added in 10 mL of DMF, the mixture solution was transferred into a poly(tetrafluoroethylene) (Teflon)-lined autoclave in an oven after ultra-sounding for 5 min. Then the reaction was performed with a ramp rate of 8 °C/min at 80 °C for 7 h.
Synthesis of yellow CQDs (y-CQDs): 2,7-naphthalenediol (0.02 g) and H 2 SO 4 (500 μL) were added in 7 mL of ethanol, the mixture solution was transferred into a poly(tetrafluoroethylene) (Teflon)-lined autoclave in an oven after ultra-sounding for 5 min. Then the reaction was performed with a ramp rate of 3 °C/min at 220 °C for 7 h.
Synthesis of orange CQDs (o-CQDs): 2,7-naphthalenediol (0.06 g) and acetic acid (260 μL) were added in 10 mL of ethanol, the mixture solution was transferred into a poly(tetrafluoroethylene) (Teflon)-lined autoclave in an oven after ultra-sounding for 5 min. Then the reaction was performed with a ramp rate of 6 °C/min at 200 °C for 12 h.
Synthesis of orange red CQDs (or-CQDs): 2,7-naphthalenediol (0.04 g) and urea (0.02 g) were dissolved in 10 mL of ethanol, the mixture solution was transferred into a poly(tetrafluoroethylene) (Teflon)-lined autoclave in an oven after ultra-sounding for 5 min. Then the reaction was performed with a ramp rate of 6 °C/min at 200 °C for 12 h. Synthesis of red CQDs (r-CQDs): 2,7-naphthalenediol (0.05 g) and EDA (26 µL) were added in 10 mL of ethanol, the mixture solution was transferred into a poly(tetrafluoroethylene) (Teflon)-lined autoclave in an oven after ultra-sounding for 5 min. Then the reaction was performed with a ramp rate of 5 °C/min at 200 °C for 12 h. All the CQDs solution were filtered with a 0.22 μm microporous membrane under the reaction cooled down to room temperature. Subsequently, the CQDs were removed solvent with a rotary evaporator, and dialyzed against a dialysis bag (MW: 3500 Da) for one week. The CQDs powders were further vacuum drying at 80 o C after dialyzing.
Synthesis of blue CQDs (b-CQDs): 2,7-naphthalenediol (0.04 g) and EDA (170 μL) were added in 10 mL of H 2 O, the mixture solution was transferred into a poly(tetrafluoroethylene) (Teflon)-lined autoclave in an oven after ultra-sounding for 5 min. Then the reaction was performed with a ramp rate of 7 °C/min at 200 °C for 11 h.
Synthesis of cyan CQDs (c-CQDs): 2,7-naphthalenediol (0.08 g) and urea (0.1 g) were dissolved in 4 mL of H 2 O, the mixture solution was transferred into a poly(tetrafluoroethylene) (Teflon)-lined autoclave in an oven after ultra-sounding for 5 min. Then the reaction was performed with a ramp rate of 8 °C/min at 160 °C for 4 h.
Synthesis of darkcyan CQDs (dc-CQDs): 2,7-naphthalenediol (0.06 g) and urea (0.06 g) were dissolved in 10 mL of H 2 O, the mixture solution was transferred into a poly(tetrafluoroethylene) (Teflon)-lined autoclave in an oven after ultra-sounding for 5 min. Then the reaction was performed with a ramp rate of 8 °C/min at 220 °C for 12 h.
Synthesis of green CQDs (g-CQDs): 2,7-naphthalenediol (0.02 g) and urea (0.06 g) were dissolved in 10 mL of ethanol, the mixture solution was transferred into a poly(tetrafluoroethylene) (Teflon)-lined autoclave in an oven after ultra-sounding for 5 min. Then the reaction was performed with a ramp rate of 8 °C/min at 160 °C for 12 h.
Synthesis of yellow green CQDs (yg-CQDs): 2,7-naphthalenediol (0.06 g) and EDA (940 μL) were added in 10 mL of DMF, the mixture solution was transferred into a poly(tetrafluoroethylene) (Teflon)-lined autoclave in an oven after ultra-sounding for 5 min. Then the reaction was performed with a ramp rate of 8 °C/min at 80 °C for 7 h.
Synthesis of yellow CQDs (y-CQDs): 2,7-naphthalenediol (0.02 g) and H 2 SO 4 (500 μL) were added in 7 mL of ethanol, the mixture solution was transferred into a poly(tetrafluoroethylene) (Teflon)-lined autoclave in an oven after ultra-sounding for 5 min. Then the reaction was performed with a ramp rate of 3 °C/min at 220 °C for 7 h.
Synthesis of orange CQDs (o-CQDs): 2,7-naphthalenediol (0.06 g) and acetic acid (260 μL) were added in 10 mL of ethanol, the mixture solution was transferred into a poly(tetrafluoroethylene) (Teflon)-lined autoclave in an oven after ultra-sounding for 5 min. Then the reaction was performed with a ramp rate of 6 °C/min at 200 °C for 12 h.
Synthesis of orange red CQDs (or-CQDs): 2,7-naphthalenediol (0.04 g) and urea (0.02 g) were dissolved in 10 mL of ethanol, the mixture solution was transferred into a poly(tetrafluoroethylene) (Teflon)-lined autoclave in an oven after ultra-sounding for 5 min. Then the reaction was performed with a ramp rate of 6 °C/min at 200 °C for 12 h. Synthesis of red CQDs (r-CQDs): 2,7-naphthalenediol (0.05 g) and EDA (26 µL) were added in 10 mL of ethanol, the mixture solution was transferred into a poly(tetrafluoroethylene) (Teflon)-lined autoclave in an oven after ultra-sounding for 5 min. Then the reaction was performed with a ramp rate of 5 °C/min at 200 °C for 12 h. All the CQDs solution were filtered with a 0.22 μm microporous membrane under the reaction cooled down to room temperature. Subsequently, the CQDs were removed solvent with a rotary evaporator, and dialyzed against a dialysis bag (MW: 3500 Da) for one week. The CQDs powders were further vacuum drying at 80 o C after dialyzing.
Both PMA and CNC-g-PMA samples were processed
into 250 μm films by hot-pressing
at 100 °C at 1 ton of pressure for 2 min between poly(tetrafluoroethylene)
sheets. Control of the thickness was done by using 250 μm thick
poly(tetrafluoroethylene) as a spacer. For PMMA, PMA-b-PMMA, and CNC-g-PMA-b-PMMA, samples were processed into 250 μm films by hot-pressing
at 140 °C at 2 tons of pressure for 2 min between Kapton sheets.
Control of the thickness was done by using 250 μm thick aluminum
sheets as spacers. The samples were kept in a desiccator to remain
dry until mechanical and thermal testing.
into 250 μm films by hot-pressing
at 100 °C at 1 ton of pressure for 2 min between poly(tetrafluoroethylene)
sheets. Control of the thickness was done by using 250 μm thick
poly(tetrafluoroethylene) as a spacer. For PMMA, PMA-b-PMMA, and CNC-g-PMA-b-PMMA, samples were processed into 250 μm films by hot-pressing
at 140 °C at 2 tons of pressure for 2 min between Kapton sheets.
Control of the thickness was done by using 250 μm thick aluminum
sheets as spacers. The samples were kept in a desiccator to remain
dry until mechanical and thermal testing.
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The concentrations of the 35 amino acid-PSTD peptide and LFcinB11 in 20 mM phosphate buffer (pH 6.7) with 25% tetrafluoroethylene (TFE) were 8.0 μM and 400 μM, respectively. The methods used to measure and record the CD spectra were the same as those described in previous articles [23 (link),30 (link)].
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The recyclability
of photocatalytic fabrics was tested by three consecutive RhB photodegradation
experiments. Between each cycle, the tested fabrics were thoroughly
washed with distilled water for 30 min. After the photodegradation
test, photocatalyst particles and fabrics were separated from the
RhB solution by the filter (0.22 μm poly(tetrafluoroethylene)
membrane), and the leaked Fe3+ and Ag+ concentrations
were measured by ICP-MS.
of photocatalytic fabrics was tested by three consecutive RhB photodegradation
experiments. Between each cycle, the tested fabrics were thoroughly
washed with distilled water for 30 min. After the photodegradation
test, photocatalyst particles and fabrics were separated from the
RhB solution by the filter (0.22 μm poly(tetrafluoroethylene)
membrane), and the leaked Fe3+ and Ag+ concentrations
were measured by ICP-MS.
Top products related to «Tetrafluoroethylene»
Sourced in United States, China, Germany
Nafion solution is a clear, colorless, and highly conductive liquid. It is a perfluorinated ion-exchange polymer solution primarily composed of a copolymer of tetrafluoroethylene and a perfluorinated vinyl ether containing sulfonic acid groups. The core function of Nafion solution is to provide a highly proton-conductive medium for various electrochemical applications.
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Ethanol is a clear, colorless liquid chemical compound commonly used in laboratory settings. It is a key component in various scientific applications, serving as a solvent, disinfectant, and fuel source. Ethanol has a molecular formula of C2H6O and a range of industrial and research uses.
Sourced in India, Germany, United States
Acetylene black is a type of carbon black material produced through the thermal decomposition of acetylene gas. It is a fine, powdery substance with a high surface area and electrical conductivity. Acetylene black is commonly used as a conductive additive in various applications, such as batteries, conductive coatings, and rubber compounds.
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Bovine serum albumin (BSA) is a common laboratory reagent derived from bovine blood plasma. It is a protein that serves as a stabilizer and blocking agent in various biochemical and immunological applications. BSA is widely used to maintain the activity and solubility of enzymes, proteins, and other biomolecules in experimental settings.
Sourced in United States, Germany, United Kingdom, Switzerland, France, Belgium, Spain
The Agilent 1200 series is a line of high-performance liquid chromatography (HPLC) instruments designed for analytical and preparative applications. The core function of the 1200 series is to provide precise and reliable separation, detection, and quantification of chemical compounds in complex mixtures.
Sourced in Germany, United States, United Kingdom, Switzerland, Japan, France, Italy, China
The Vertex 70 is a Fourier Transform Infrared (FTIR) spectrometer manufactured by Bruker. It is designed to perform high-resolution infrared spectroscopy analysis of various samples. The Vertex 70 provides accurate measurements of the absorption, emission, or reflectance properties of materials across the infrared spectrum.
Sourced in United States
Polyvinyl butyral (PVB) is a thermoplastic polymer that is commonly used in the manufacturing of various lab equipment. It has a high degree of toughness, flexibility, and optical clarity, making it a suitable material for numerous applications in the laboratory setting. PVB is primarily used as an interlayer in safety glass, but it can also be found in other lab-related products, such as specialty coatings and adhesives.
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Sodium hydroxide is a chemical compound with the formula NaOH. It is a white, odorless, crystalline solid that is highly soluble in water and is a strong base. It is commonly used in various laboratory applications as a reagent.
PTFE powder is a fine, white, particulate material made from polytetrafluoroethylene (PTFE). It exhibits excellent chemical resistance, low coefficient of friction, and high thermal stability. The powder can be used as a raw material for various industrial applications.
Sourced in Switzerland, United States, Malaysia
Polytetrafluoroethylene (PTFE) is a synthetic fluoropolymer commonly used in laboratory equipment. It is a chemically inert, non-stick, and thermally stable material that can withstand high temperatures and corrosive environments. PTFE is often used in the construction of laboratory equipment, such as tubing, valves, and gaskets, due to its unique properties.
More about "Tetrafluoroethylene"
tetrafluoroethylene, TFE, fluoropolymers, PTFE, non-stick coatings, electrical insulation, chemical-resistant materials, PubCompare.ai, Nafion solution, Ethanol, Acetylene black, Bovine serum albumin, 1200 series, Vertex 70, Polyvinyl butyral (PVB), Sodium hydroxide, PTFE powder, Polytetrafluoroethylene (PTFE)