follows the back section. The data in Table 3 was obtained in a vapor-liquid equilibrium still. To place an order using RMB or to ship to mainland China, please visit www.scbio.cn, Western Blot Chemilumineszenz Luminol Reagenzien, Blocking Reagents for Western Blotting Applications, Nuklearextrakte für Western Blot und Gel Shift (EMSA), NUKLEOTIDE, PEPTIDE, PROTEINE & AMINOSÄUREN, Pufferkomponenten und Standard Laborreagenzien, AUTORADIOGRAPHIE FILME, KLEBEBÄNDER UND PLASTIKFOLIEN, NADELN, SCHARFKANTIGE UTENSILIEN UND SPRITZEN, Acetic Acid Isopropyl Ester-d10; 1-Methylethyl Acetate-d10; 2-Acetoxypropane-d10. grad e.* Overall sampling and measurement precision, SˆrT, was 0.067, with average It is therefore impossible to produce isopropyl acetate from isopropanol and water mixtures by rectification because the lower boiling ternary azeotrope will always come off overhead as the initial product. 5. The data also show that the most attractive agents will operate at a boilup rate low enough to make this a useful and efficient method of recovering high purity isopropyl acetate from any mixture of these three including the ternary minimum azeotrope. The object of this invention is to provide a process or method of extractive distillation that will enhance the relative volatility of isopropyl acetate from isopropanol in their separation in a rectification column. Belongs to the Following Reactive Group(s). This page was last edited on 23 June 2016, at 14:37. ACCURACY: ESTIMATED LOD: 0.01 mg per sample  Usually the extractive agent is introduced a few plates from the top of the column to insure that none of the extractive agent is carried over with the most volatile component. Calibrate each personal sampling pump with a representative sampler in line. CALCULATIONS: and back (W b) sorbent sections, and in the average media blank front (B f) and back (B b) sorbent 5. Less dense than water and slightly soluble in water. It is also desirable that the extractive agent be miscible with isopropanol otherwise it will form a two-phase azeotrope with isopropanol in the recovery column and some other method of separation will have to be employed. Pressure drop This proves that the extractive agent is negating the azeotrope and makes rectification proceed as if the azeotrope no longer exists and brings the more volatile components, isopropyl acetate and water, out as overhead. Molecular Formula: C5D10O2, MW: 112.19 Standard solutions: Isopropyl acetate in carbon disulfide in the range of 0.01 to 15 mg per sample. The isopropyl acetate--isopropanol--water azeotrope is 76 wt. This method was evaluated over the range 446 to 1870 mg/m 3 at 23 °C and pressure of 770 mm Hg Volumetric flasks, 10-mL. Discard the foam plugs. The charge was 76 wt. c. Ca p the tube. Sam ple at a n ac curately kn own flow ra te betwee n 0.02 an d 0.2 L/m in for a total sam ple size of 0.1 to sampling in the calibration range (step 8). plus three media blanks. Determ ine the ma ss µg (co rrected for DE ) of isopropyl acetate found in the sam ple front (W f) and A sample stability evaluation has not been performed, nor has the sample stability 7. SAMPLE PREPARATION @20 °C; miscible in most organic solvents; Helium, purified. % isopropyl acetate, 13 wt. Helium, purified. 3. PRECISION (Sr): APPLICABILITY: The working range is 1.5 to 450 ppm (6 to 1870 mg/m 3) for an 8-L air sample. Services Standard solutions: Isopropyl acetate in carbon NIOSH Manual of Analytical Methods (NMAM), Fourth Edition, 8/15/94 ISOPROPYL ACETATE: METHOD 1454, Issue 1, dated 15 August 1994 - Page 2 of 3 If extractive distillation agents could be found that will increase the relative volatility to 3, Table 2 shows that only 19 actual plates are required for 98% purity or ten actual plates for 95% purity. three media blanks. for stabilisation by physical treatment by distillation by extractive distillation, National Distillers And Chemical Corporation, PATENT EXPIRED DUE TO NONPAYMENT OF MAINTENANCE FEES UNDER 37 CFR 1.362, Separation of the propyl alcohols from water by azeotropic or extractive distillation, Separation of components from methanol mixtures by extractive distillation, Process for the simultaneous coproduction and purification of ethyl acetate and isopropyl acetate, Process for separating sec-butanol from ethyl acetate, Purification of carboxylic esters by extractive distillation, Recovery of normal propyl alcohol from oxygenated compounds, Extractive distillation of alcohols with glycol ethers, Extractive distillation of alcohols with glycols, Extractive distillation of alcohol-containing mixtures with diphenyl ether as solvent, Separation of methanol from methyl acetate by extractive distillation with ethylene glycol, Separation of mixtures of esters and alcohols, A process for the separation of ester-alcohol mixtures, Process for the separation of azeotropic mixtures of acetone, from 1 to 5 carbon atoms containing alcohols and esters having 3 to 7 carbon atoms, Separation of ethyl acetate from ethanol and water by extractive distillation, Extractive distillation of alcohol-ester mixtures and transesterification, Separation of n-propyl acetate from n-propanol by extractive distillation, Separation of n-propyl acetate from n-propanol and water by extractive distillation, Separation of n-amyl acetate from n-amyl alcohol by extractive distillation, Separation of n-hexyl acetate from n-hexyl alcohol by extractive distillation, Process for the recovery of ethyl acetate, Purification of acrylic acid and methacrylic acid, Separation of ethyl acetate from ethanol by azeotropic distillation, Continuous preparation of acetic acid esters, Process for simultaneous co-production and purification of ethyl acetate and isopropyl acetate, Purification of low molecular weight epoxides by extractive distillation with a glycol or glycol ether, Extractive distillation of alcohols from close-boiling aqueous mixtures, Extractive distillation of c1 to c3 alcohols and subsequent distillation of purge streams, Purification of propylene oxide by extractive distillation, Separation of ethanol from isopropanol by azeotropic distillation, Recovery of ethylene glycol from butanediol isomers by azeotropic distillation, Recovery of methyl heptafluorobutyrate from water by distillation, Improved method of producing ethanol-water azeotrope from crude ethanol, Recovery of 1,1-dihydroheptafluorobutanol from water by distillation, Separation of primary, secondary, and tertiary alcohols by azeotropic distillation, Extractive distillation of alcohol-ester mixtures, Extraction and/or extractive distillation of low molecular weight alcohols from aqueous solutions, Separation and purification of acrylic acid from acetic acid by solvent extraction and azeotropic distillation with a two component solvent-entrainer system, Separation of ethanol, isopropanol and water mixtures by extractive distillation, Process and device for the separation of mixtures which form an azeotrope, Lapse for failure to pay maintenance fees, Expired due to failure to pay maintenance fee, Information on status: patent discontinuation. Isopropyl acetate can be readily removed from mixtures containing it, isopropanol and water by using extractive distillation in which the extractive agent is a mixture of a polyol and one or higher boiling oxygenated, nitrogenous and/or sulfur containing organic compounds. The effect of relative volatility on column performance can be deduced by referring to Table 2. Isopropyl acetate. Mass Spectrometry: Fragmentation Ethers di-sec-butyl ether O MW = 130 M (130) 115 M-15 101 M-29 O H CH3CH2 O H H3C m/z = 59 m/z = 45 O H H H3C O H H CH3CH2 m/z = 57 The material investigated was the azeotrope which possesses a relative volatility of 1.0. NIOSH: no REL front section and a 3-mm urethane foam plug Copyright © 2007-2020, Santa Cruz Biotechnology, Inc. Alle Rechte vorbehalten. grade. c. Prepare calibration graph (peak area vs. mg isopropyl acetate). Isopropyl Acetate Backu p Data R eport, (unpublished, Novem ber). been determined. 6. Undecane or p-cymene, ACS reagent grade. This usually requires that the extractive agent boil twenty Centigrade degrees or more higher than the lowest boiling component. Esters react with acids to liberate heat along with alcohols and acids.