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Oil preparation

JajmiD oil prepared from liie pomade has Ihe following characters —... [Pg.277]

Sweet orangr oil, prepared in a simiJai manner to It-iiiun oil, has tlie following oharadiirs... [Pg.426]

A niimber of Mandarin orang oils prepared In Japan have h, cn esaminedfi hnt as ihev appear usually lo he prepared hv dislillation they do not always agree in physical characters with Italian oils, nor are they, as a rnlc, nearly so fragrant. These samples had the following characters... [Pg.427]

A typical polyalphaolefin oil prepared from 1-decene and BF3t -C4H9OH catalyst at 30 °C contains predominantly trimer (C30 hydrocarbons) with much smaller amounts of dimer, tetramer, pentamer, and hexamer. While 1-decene is the most common starting material, other alphaolefins can be used, depending on the needs of the product oil. [Pg.259]

Polyalphaolefin Hydraulic Fluids. Polyalphaolefms are made by oligomerizing alphaolefins such as 1-decene in the presence of a catalyst (Newton 1989 Shubkin 1993 Wills 1980). The crude reaction mixture is quenched with water, hydrogenated, and distilled. The number of monomer units present in the product polyalphaolefin oil depends on a number of reaction parameters including the type of catalyst, reaction temperature, reaction time, and pressure (Shubkin 1993). The exact combination of reaction parameters used by a manufacturer is tailored to fit the end-use of the resulting polyalphaolefin oil. A typical polyalphaolefin oil prepared from 1-decene and BF3- -C4H9OH catalyst at 30 °C contains predominantly trimer (C30 hydrocarbons) with much smaller amounts of dimer, tetramer, pentamer, and hexamer. While 1-decene is the most common starting material, other alphaolefins can be used, depending on the needs of the product oil. [Pg.286]

The oil prepared at —20°C explodes while warming to ambient temperature. [Pg.733]

Fat-emulgated preparations for parenteral administration have been elaborated for clinical applications. Since these are administered to the patients intravenously, the size of fat emulsion particles should not exceed the size of the largest naturally occurring lipoproteins-chylomicrons, i.e. about I fiin. Fat emulsions on the basis of com oil (preparation lipomaize), cottonseed oil (lipofundin, lipomol). [Pg.213]

The fatty acid modification was used in operating plants at Kolwezi, Koumbore and Kakanda. The fatty acid used was hydrolysed palm oil prepared as a mixture consisting of 75% hydrolysed palm oil/21% gas oil/4% Unitol. [Pg.56]

Uses Antiseptic and disinfectant pharmaceuticals dyes indicators slimicide phenolic resins epoxy resins (bisphenol-A) nylon-6 (caprolactum) 2,4-D solvent for refining lubricating oils preparation of adipic acid, salicylic acid, phenolphthalein, pentachlorophenol, acetophenetidin, picric acid, anisole, phenoxyacetic acid, phenyl benzoate, 2-phenolsulfonic acid, 4-phenolsulfonic acid, 2-nitrophenol, 4-nitrophenol, 2,4,6-tribromophenol, 4-bromophenol, 4-/ert-butylphenol, salicylaldehyde, and many other organic compounds germicidal paints laboratory reagent. [Pg.955]

The pure chemical (100% diazinon) is a colorless and practically odorless oil. Preparations used in agriculture and by exterminators contain 85-90% diazinon and appear as a pale to dark-brown liquid. This form of diazinon is diluted with other chemicals before use. The diazinon available for home and garden use contains 1-5% diazinon in a liquid or as solid granules. These preparations have a slight chemical odor but cannot be identified by smell. Most of the diazinon used is in liquid form, but it is possible to be exposed to the chemical in a solid form. Diazinon does not bum easily and does not dissolve easily in water. It will dissolve in alcohol or other organic solvents such as petroleum products. Its basic physical and chemical properties are summarized in Chapter 3 for more information on its production and use, see Chapter 4. [Pg.14]

Figure D1.2.3 Sample GC chromatogram of the FAME of fish oil (menhaden oil) prepared using the boron trifluoride method (see Basic Protocol 1). Equipment DB-23 fused silica capillary column, 30 m x 0.32 mm i.d., 0.25 pm film thickness, FID detector. Temperature, injector 225°C detector 250°C. Column (oven) temperature program 140°C initial, hold 2 min, ramp to 198°C at 1.5°C/min, hold 20 min. Total run time was 60 min. Split injection. Figure D1.2.3 Sample GC chromatogram of the FAME of fish oil (menhaden oil) prepared using the boron trifluoride method (see Basic Protocol 1). Equipment DB-23 fused silica capillary column, 30 m x 0.32 mm i.d., 0.25 pm film thickness, FID detector. Temperature, injector 225°C detector 250°C. Column (oven) temperature program 140°C initial, hold 2 min, ramp to 198°C at 1.5°C/min, hold 20 min. Total run time was 60 min. Split injection.
Belluzzi A, Brignola C, Campieri M, Pera A, Boschi S, Miglioli M. Effect of an enteric-coated fish-oil preparation on relapses in Crohn s disease. N Engl J Med 1996 334(24) 1557-60. [Pg.543]

The yield of fuel oil prepared from the blended dewaxed residuum was 21.5 volume-percent of the in situ crude. The total of this, plus the 51.6 volume-percent of diesel fuels, amounted to 73.1 volume-percent of the in situ crude that could be used as low-sulfur diesel fuels or Nos. 1 through 4 burner fuels. [Pg.114]

Evening primrose oil is rich in the essential fatty acid linoleic acid and its metabolite, y-linolenic acid. In the U.K., evening primrose oil preparations have received approval as medicines for the relief of atopic eczema and for the symptomatic treatment of breast pain. [Pg.61]

Composition of ginger oil prepared from fresh ginger rhizomes was determined by gas chromatography (GC) and GC-MS techniques. The main sesquiterpene hydrocarbons identified were a-zingiberene (27-30%), a-curcumene... [Pg.79]

The phase relationships of two-phase polymer systems also have been of considerable interest in recent years. In an important series of papers, Molau and co-workers (19-24) studied systems, which were denoted POO emulsions (polymeric oil-in-oil), prepared by dissolving a given polymer in monomer and then polymerizing the monomer. During polymerizations of this type the composition of the respective phases reverses, and a phase inversion process was proposed to explain this. A similar process has been suggested as the mechanism by which poly-butadiene forms the dispersed phase in the manufacture of high-impact polystyrenes (22,25). Recently, Kruse has pointed out that this phase-inversion point may correspond to that point on a ternary phase diagram at which the reaction line bisects a tie line (26), and we have advanced a similar point of view in our earlier reports (17,18, 27). [Pg.376]

An enzymatic process cannot be adopted for industrial production of BDF, if immobilized lipase cannot be used for long period. Studies on the stability of immobilized C. antarctica lipase revealed that it was the most stable when the reaction was conducted with 5 to 8 mol MeOH for total FAs in acid oil prepared from soapstock (Watanabe et al., 2007). The phenomenon, that there is the optimum region of MeOH concentration, may be explained as follows ... [Pg.68]

Method H (Animal Fats and Vegetable and Marine Oils) Prepare a solvent mixture consisting of equal parts, by volume, of isopropyl alcohol and toluene. Add 2 mL of a 1% solution of phenolphthalein in isopropyl alcohol to 125 mL of the mixture, and neutralize with alkali to a faint but permanent pink color. Weigh accurately the appropriate amount of well-mixed liquid sample indicated in the table below, dissolve it in the neutralized solvent mixture, warming if necessary, and shake vigorously while titrating with 0.1 TV potassium hydroxide to the first permanent pink color of the same intensity as that of the neutralized solvent before mixing with the sample. Calculate the acid value by the formula... [Pg.934]

Steam-Volatile Oil Proceed as directed for Volatile Oil Content under Essential Oils and Flavors, Appendix VI, using 25.0 mL of the oil prepared as directed in the Assay. [Pg.32]

Essential oil preparations from a variety of plants have found industrial applications relating to taste (liqueurs and flavour additives) and odour (perfumes, liqueurs, agents for masking unpleasant odours and pleasant-smelling phenolic antiseptics). Many... [Pg.398]


See other pages where Oil preparation is mentioned: [Pg.262]    [Pg.116]    [Pg.157]    [Pg.277]    [Pg.426]    [Pg.463]    [Pg.326]    [Pg.327]    [Pg.34]    [Pg.197]    [Pg.316]    [Pg.332]    [Pg.178]    [Pg.120]    [Pg.336]    [Pg.116]    [Pg.35]    [Pg.286]    [Pg.217]    [Pg.28]    [Pg.76]    [Pg.77]    [Pg.68]    [Pg.1340]    [Pg.249]    [Pg.32]    [Pg.612]   
See also in sourсe #XX -- [ Pg.40 , Pg.41 , Pg.43 ]




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Preparation, of essential oils

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