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  • ....stanford.edu/jaic/articles/jaic19-01-003_1.html|title = Identification of dyes on old textiles|journal = J. Am. Inst. Conservation|volume = 19|issue = 1/3 ...sulfur]] and [[iodine]]. It readily mixes with other polar and non-polar [[solvent]]s such as water, [[chloroform]], and [[hexane]]. With higher alkanes (star
    41 KB (5,915 words) - 16:49, 27 September 2010
  • ...ed in many applications, from [[manufacturing]] pulp and paper, to setting dyes in textiles and fabric, to producing [[soap]]s, [[detergent]]s, and other b ...eader}}|Solubility of NaCl in various solvents<br/ >(g NaCl / 1&nbsp;kg of solvent at 25 °C)<ref>Burgess, J. ''Metal Ions in Solution'' (Ellis Horwood, New Y
    19 KB (2,579 words) - 16:51, 27 September 2010
  • ...-based and the first experimental use of these materials for separation of dyes was in 1949. However, the first protein imprinted polymer has been reported **[[Porogen]] ([[apolar]], [[non-protogenic]] [[solvent]])
    4 KB (446 words) - 10:09, 20 September 2010
  • ...ore, or as complex as increasing the selectivity of an [[adsorption]] or [[solvent extraction|extraction]] process. ...tion. While the droplets are in flight, a molten wall may be hardened or a solvent may be evaporated from the wall solution. Since most of the droplets are wi
    11 KB (1,664 words) - 10:10, 20 September 2010
  • ...er]]s can crystallize upon cooling from the melt, mechanical stretching or solvent evaporation. Crystallization affects optical, mechanical, thermal and chemi ...from the thermal mechanism, nucleation is strongly affected by impurities, dyes, plasticizers, fillers and other additives in the polymer. This is also ref
    18 KB (2,533 words) - 10:11, 20 September 2010
  • ...0.97 M <ref>[http://oru.edu/cccda/sl/solubility/ugidata.php?solute=aniline&solvent=methanol Solubility of aniline in methanol]</ref> | Solvent = [[methanol]]
    14 KB (2,008 words) - 13:10, 20 September 2010
  • ...ant]]s. It is also an intermediate for organic synthesis, and a civilian [[solvent dye]]. [[Category:Dyes]]
    3 KB (363 words) - 13:11, 20 September 2010
  • | Solvent = It readily forms [[diazo]] compounds and is used to make dyes and [[Sulfonamide (medicine)|sulpha drugs]]. <ref name="DOC"/>
    2 KB (272 words) - 13:11, 20 September 2010
  • ...sily and inexpensively with instruments called [[fluorometer]]s. Rhodamine dyes are used extensively in biotechnology applications such as [[Fluorescence m ...uitevis, "Effect of solvent polarity on nonradiative processes in xanthene dyes: Rhodamine B in normal alcohols," J. Phys. Chem., 92, 6590-6594, 1988</ref>
    4 KB (634 words) - 13:12, 20 September 2010
  • | ImageFile = Solvent Violet 13.png ...iolet 13''', also known as '''D&amp;C Violet No.2''', '''oil violet''', '''Solvent Blue 90''', '''Alizarine Violet 3B''', '''Alizurol Purple''', '''Duranol Br
    2 KB (264 words) - 13:12, 20 September 2010
  • ...sible]]. By moving into this [[hydrophobic]] environment and away from the solvent, the ethidium cation is forced to shed any water molecules that were associ ...9 |pmid=10029672 }}</ref>. Despite the performance advantage of using SYBR dyes instead of EtBr for staining purposes, many researchers still prefer EtBr s
    15 KB (1,980 words) - 13:13, 20 September 2010
  • ...<br /> Oil Yellow R <br /> Organol Yellow <br /> Organol Yellow 2A <br /> Solvent Yellow <br /> Somalia Yellow 2G <br /> Stearix Brown 4R <br /> Sudan Yellow ...d [[styrene]] [[resin]]s. It is also an intermediate in synthesis of other dyes, eg. [[chrysoidine]], [[indulines]], [[Solid Yellow]], and [[acid yellow|Ac
    3 KB (455 words) - 13:13, 20 September 2010
  • == Dyes and chemicals == ...[[isocyanate]]s, [[Bisphenol A]], [[diethylene triamine]], and others. The dyes in carbonless copy papers may cause [[contact dermatitis]] in sensitive per
    8 KB (1,154 words) - 21:30, 20 September 2010
  • ...] and [[textile]]s using a chemical [[solvent]] rather than [[water]]. The solvent used is typically [[tetrachloroethylene]] (perchloroethylene), abbreviated ...William Joseph Stoddard, a dry cleaner from Atlanta, to develop [[Stoddard solvent]] as a slightly less [[flammable]] alternative to gasoline-based solvents.
    22 KB (3,351 words) - 21:30, 20 September 2010
  • | Solvent = ...eaner product, the reaction is conducted in the gas phase or in an organic solvent.
    82 KB (11,709 words) - 21:31, 20 September 2010
  • ...ditive in [[gasoline]] is now limited, but it is an important industrial [[solvent]] and [[precursor]] in the production of [[medication|drugs]], [[plastic]]s ...) by [[Liquid-liquid extraction|extraction]] with any one of a number of [[solvent]]s, including [[diethylene glycol]] or [[sulfolane]], and benzene is then s
    45 KB (6,444 words) - 21:33, 20 September 2010
  • *as a [[solvent]], it is [[miscible]] with polar solvents and is used to solubilize [[prote
    9 KB (1,089 words) - 20:14, 21 September 2010
  • | Solvent = [[Category:Fluorescent dyes]]
    3 KB (410 words) - 20:15, 21 September 2010
  • ...tion solvents, or [[p-toluenesulfonic acid]] can be used with a non-acidic solvent. [[Lewis acid]]s such as [[boron trifluoride]] etherate and ytterbium trifl ...orphyrins, are used in commerce as dyes and catalysts. Synthetic porphyrin dyes that are incorporated in the design of solar cells are the subject of ongoi
    12 KB (1,605 words) - 20:15, 21 September 2010
  • | Solvent = [[THF]], [[ethanol]], [[methanol]]
    20 KB (2,855 words) - 20:16, 21 September 2010

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