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Additives forming

Addition of an excess of alkali displaces the equilibrium further and finally the hexahydroxoaluminate(III) ion [AllOH) ]- " is formed. Addition of causes the displacement of equilibrium... [Pg.151]

In each case the configuration around the boron changes from trigonal planar to tetrahedral on adduct formation. Because of this ability to form additional compounds, boron trifluoride is an important catalyst and is used in many organic reactions, notably polymerisation, esterification, and Friedel-Crafts acylation and alkylations. [Pg.154]

Carbon monoxide forms addition compounds. With chlorine in sunlight or in the presence of charcoal in the dark, carbonyl chloride... [Pg.179]

Hence, if chlorine is passed into a cold suspension (in hydrochloric acid) of lead(II) chloride, lead(IV) chloride is formed. Addition of ammonium chloride gives the complex salt ammonium hexachloro-plumbate(lV) as a yellow precipitate ... [Pg.200]

The product, commonly called calomel, is a white solid, insoluble in water in its reactions (as expected) it shows a tendency to produce mercury(II) and mercury. Thus under the action of light, the substance darkens because mercury is formed addition of aqueous ammonia produces the substance HjN—Hg—Hg—Cl, but this also darkens on standing, giving HjN—Hg—Cl and a black deposit of mercury. [Pg.437]

The student should note that ketones in class (1), t.c., those having the >CO group in the side chain, will form additive compounds with sodium bisulphite only if this >CO group is not directly joined to the benzene ring acetophenone therefore will not form such compounds, whereas benzyl methyl ketone, CaHsCHjCOCH, will do so. Many quinones, particularly ortho quinones such as phenanthraquinone, form additive compounds with sodium bisulphite. [Pg.257]

Aldehydes form addition products at the double bond of the carbonyl (>C 0) group, and hydrolysis gives secondary alcohols. Thus acetaldehyde gives isopropyl alcohol ... [Pg.282]

Because the individual elements of J are formed additively, but is not, it is straightforward to form eigenstates of... [Pg.623]

A 1 1 complex melting at 24.8°C is formed between PX and carbon tetrachloride (52). The other Cg aromatic compounds do not form these complexes. Carbon tetrabromide and chloral (CCl CHO) form addition compounds with PX. [Pg.414]

Physically or chemically modifying the surface of PET fiber is another route to diversified products. Hydrophilicity, moisture absorption, moisture transport, soil release, color depth, tactile aesthetics, and comfort all can be affected by surface modification. Examples iaclude coatiag the surface with multiple hydroxyl groups (40), creatiag surface pores and cavities by adding a gas or gas-forming additive to the polymer melt (41), roughening the surface... [Pg.325]

Reaction with Other Inorganic Halogen Compounds. Anhydrous HCl forms addition compounds at lower temperatures with halogen acids such as HBr and HI, and also with HCN. These compounds are stable at room temperature. [Pg.444]

The reaction can also be carried out with oleum, distilling the chlorosulfuric acid as it forms. Reaction with oxidizing oxyacids such as HNO Hberates chlorine. Anhydrous sulfates of the heavy metals form addition compounds with HCl that can be released by heating the complex to elevated temperatures. The complex CuSO 2HC1 has been used for storage and transport of HCl (23). [Pg.444]

Other Reactions of Phospholipids. The unsaturated fatty acid groups in soybean lecithin can be halogenated. Acetic anhydride combined with the amino group of phosphatidylethanolamine forms acetylated compounds. PhosphoHpids form addition compounds with salts of heavy metals. Phosphatidylethanolamine and phosphatidjhnositol have affinities for calcium and magnesium ions that are related to interaction with their polar groups. [Pg.99]

Anhydrous magnesium chloride is soluble in lower alcohols. In 100 g of methanol, its solubiUty is 15.5 g at 0°C and 20.4 g at 60°C. In ethanol, the solubihty is 3.61 g at 0°C and 15.89 g at 60°C. Upon cooling, anhydrous MgCl2 forms addition compounds with alcohols of crystallization such as magnesium chloride hexamethanolate [57467-93-0]andmagnesium chloride hexaethanolate [16693-00-8]Both of these alcoholates are deflquescent. [Pg.343]

Phosphoms haUdes and metals or metal salts form addition complexes. Some typical compounds are PCl iSbCl and PCl iAlCl. The trivalent complexes contain metal—phosphoms bonds. The pentavalent complexes involve rearrangements to produce assembles of tetrahedral PX cations and various anions. [Pg.366]

Aromatic amines form addition compounds and complexes with many inorganic substances, such as ziac chloride, copper chloride, uranium tetrachloride, or boron trifluoride. Various metals react with the amino group to form metal anilides and hydrochloric, sulfuric, or phosphoric acid salts of aniline are important intermediates in the dye industry. [Pg.229]

Unlike carbon, the silicon atom may utilise vacant orbitals to expand its valence beyond four, to five or six, forming additional bonds with electron donors. This is shown by isolated amine complexes. The stabiUty of the organosHane amine complexes varies over a wide range and depends on the nature of the donor and acceptor (2). [Pg.26]

Aldehydes form addition products with sulfamic acid salts. These are stable ia neutral or slightly alkaline solutions but are hydroly2ed ia acid and strongly alkaline solutions. With formaldehyde, the calcium salt of the methylol (hydroxymethyl) derivative [82770-57-8], Ca(02SNHCH20H)2, is obtained as a crystalline soHd. [Pg.62]

Vanadium (IV) Chloride. Vanadium(IV) chloride (vanadium tetrachloride, VCy is a red-brown hquid, is readily hydrolyzed, forms addition compounds with donor solvents such as pyridine, and is reduced by such molecules to trivalent vanadium compounds. Vanadium tetrachloride dissociates slowly at room temperature and rapidly at higher temperatures, yielding VCl and CI2. Decomposition also is induced catalyticahy and photochemically. This instabihty reflects the difficulty in storing and transporting it for industrial use. [Pg.391]

Zirconium tetrachloride forms additional compounds with phosphoms pentachloride ZtCl PCl and ZtCl 2PC1. However, the alleged... [Pg.435]

Zirconium tetraiodide is the least thermally stable zirconium tetrahaUde. At 1400°C, it disproportionates to Zr metal and iodine vapor. This behavior is utilized in the van Arkel-de Boer process to refine zirconium. As with the tetrachloride and tetrabromide, the tetraiodide forms additional adducts with gaseous ammonia which, upon heating, decompose through several steps ending with zirconium nitride. [Pg.436]

Zirconium monochloride reacts with sodium ethoxide to form additional adducts which hydrolyze in water. The monochloride does not react with benzene in a Friedel-Crafts reaction, and does not enter into intercalation reactions similar to those of zirconium disulfide. Both monohaUdes add hydrogen reversibly up to a limiting composition of ZrXH (131). [Pg.436]

Bismuth trichloride shows considerable tendency to form addition compounds. Reaction with ammonia yields the colodess, easily volatili2ed bismuth trichloride triammine [66172-89-2] BiCl ANH, as well as the red, thermally unstable bismuth trichloride hemiammine [66172-90-5] 2BiCl2 NH. Compounds of formula BiCl NO, BiCl 2N02, and BiCl NOCl may be isolated these are stable in dry air but are decomposed by moisture. Bismuth... [Pg.128]

Enzymes are specific, however. For example, starch is depolymerized using enzymes to D-glucose (dextrose). The solution of glucose is then treated with glucose isomerase [9055-00-9] to give D-fmctose in about 42% yield. No D-mannose is formed. Addition of isolated D-fmctose to this solution gives the common 55% high fmctose com symp (HFCS) so widely used in soft drinks in the United States. HFCS is about 1.5 times as sweet as sucrose. [Pg.482]

Forming additives or processing aids (2,33—37) are commonly used to render ceramic powders more processible. Binders and plasticizers (qv) are typically added to improve or aid dry powder and plastic forming, whereas deflocculants, surfactants (qv), and antifoams are commonly used in slurry processing. [Pg.307]

Liquids. Liquids (33) are common forming additives in plastic, paste, and slurry processing. In plastic forming operations, the Hquid aids forming and serves as the binder/plasticizer for the system. In pastes and slurries, other additives are also dissolved or dispersed in the Hquid/solvent. Water is a good, inexpensive solvent that can be recycled. Organic Hquids such as alcohols are used to process water-sensitive materials and to dissolve water-insoluble forming additives, however, at considerably more expense. [Pg.307]


See other pages where Additives forming is mentioned: [Pg.60]    [Pg.231]    [Pg.378]    [Pg.480]    [Pg.2765]    [Pg.370]    [Pg.269]    [Pg.399]    [Pg.445]    [Pg.393]    [Pg.301]    [Pg.341]    [Pg.352]    [Pg.516]    [Pg.29]    [Pg.228]    [Pg.332]    [Pg.332]    [Pg.478]    [Pg.480]    [Pg.389]    [Pg.130]    [Pg.454]    [Pg.408]    [Pg.307]   
See also in sourсe #XX -- [ Pg.2 , Pg.2 , Pg.3 , Pg.17 ]

See also in sourсe #XX -- [ Pg.2 , Pg.2 , Pg.3 , Pg.17 , Pg.18 ]




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Additive form

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