monomer styrene first has to be purified before it can be used. The purification is performed in order to remove inhibitors and impurities‚ which can have a detrimental effect on the reaction. Styrene is purified by passing the monomer through a column of activated basic aluminum oxide and by this treatment the inhibitors and impurities are adsorbed. The styrene used in this laboratory experiment has already been purified in this way‚ and has then been kept in a refrigerator to prevent thermal
Premium Polymer Monomer
SCHOOL OF BIOTECHNOLOGY VIGNAN UNIVERSITY: Vadlamudi B .Tech- BIOTECHNOLOGY STUDENTS FORMAT –FORSUBMITTION OF PROJECT REPORT (MINI PROJECT) 1. Title/Component of the Project 2. Introduction about the topic 3. Previous studies 4. Objective 5. Methodology/ Material & Methods 6. Process 7. Results and Discussions 8. Bibliography/ References STUDIES ON AFLATOXIN PRESENT IN CHILLES A Mini Project Report Submitted in partial fulfillment of the requirement for the
Premium Aflatoxin
C5-C30 n-alkanes were used to made retention indices (RI) and 2‚4‚6-trimethylpyridine (TMP‚ purity 99 %‚ I.S.) was used to internal standard which were purchased from Sigma-Aldrich Trading Co.‚ Ltd (Shanghai‚ China). Mono Trap (MT) (Diameter 2.9 mm ×Length 5 mm‚ Hole Diameter 1 mm) (ODS‚ silica gel and activated carbon) was used for headspace MMSE was obtained from GL Science (Shinjuku‚ Tokyo‚ Japan). Extraction of volatile compounds Fish sauce samples were extracted volatile compounds by Monolithic
Premium Chemistry Solvent Ethanol
Barnidipine hydrochloride is ([3S]-l-benzyl-3-pyrrolidinyl methyl [4S]-2‚6-dimethyl-4-[m-nitrophenyl]-l‚4-dihydropyridine-3‚5-dicarboxylate hydrochloride) has been synthesized and developed as an antihypertensive drug by Yamanouchi Pharmaceutical Co Ltd. (Tokyo‚ Japan). Physicochemically‚ Barnidipine hydrochloride differs from other dihydropyridines‚ such as nifedipine or nisoldipine‚ in its water solubility. The solubility of Barnidipine at room temperature is 2.89 mg/ml [1]. Literature review reveals
Premium Solvent Chemical reaction Chemistry
In IC‚ the analyte is injected into the eluent‚ which then passes through a column and separates ions between a stationary and mobile phase (Harris & Lucy‚ chap. 26). Depending on how well the anions stick to the column will determine the retention order of the element. Since the anions that are smaller in size and have higher negative charges will stick to the stationary phase the best‚ the first
Premium Analytical chemistry Chemistry
Residual solvents Identification and control of the residual solvents (USP 32(467)‚ page 181 Determination by gas chromatography with mass detector and headspace sampler Conditions of the chromatograph Agilent 7890A (LCTG CGMS): * Column DB-624 30m 0.25 mm 1.4µ (CG-2) * Injector temperatura: 160ºC * Flux: 1.0 ml/min * Split: 5:1 * Carrier gas: Helium * Time per test: 30.6 min Conditions of the detector 5975C inert MSD * Data adquisition mode: Scan/SIM * Mass:
Premium Gas chromatography Thermodynamics Chromatography
Food Chemistry journal homepage: www.elsevier.com/locate/foodchem Analytical Methods Determination of volatile N-nitrosamines in meat products by microwave-assisted extraction coupled with dispersive micro solid-phase extraction and gas chromatography – Chemical ionisation mass spectrometry Man-Chun Huang‚ Hsin-Chang Chen‚ Ssu-Chieh Fu‚ Wang-Hsien Ding ⇑ Department of Chemistry‚ National Central University‚ Chung-Li 320‚ Taiwan a r t i c l e i n f o Article history: Received 21
Premium Analytical chemistry Pork Sodium hydroxide
CLINICAL CHEMISTRY – defined as the study of biochemical processes associated with health & dse & the measurement of constituents in body fluids or tissues to facilitate dx of dse - dual nature since it’s both a basic and applied science thus clin chem. technologists & technicians should have an understanding of the physiologic & biochemical processes occurring in the body‚ as well as technical skills to perform the various tests - chemistry in connection with the management
Premium Concentration Blood Chemistry
They then hybridized these cDNA fragments to a td deletion mutant and submitted it to HAP chromatography to eliminate the hybridized dsDNA‚ resulting in the isolation of the transforming (sarc) gene. The isolated cDNAsarc was found to be 1600 nucleotides in length‚ which was deemed an adequate length to code for a protein with the ability to transform
Premium Infectious disease DNA Vaccine
2a: Infrared Spectroscopy and Analgesic Drug Identification Abstract: To be able to understand how organic soluble compounds could be isolated from non-organic components‚ a chromatographic separation process was used. The objective of the analgesic drug identification is to isolate the organic compounds/ active ingredients in an unknown drug. The identity of the drug was determined through melting point‚ percent recover‚ and Rf values. The comparable data for acetaminophen from the manufacturer
Premium Paracetamol Solvent Acetic acid