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Free fusion

Scheme 8.1 Three key methods of the synthesis of lanthanide(lll) bis(phthalocyanine) complexes. Homoleptic complexes symmetrical (A, B) and unsymmetrical (C1 and C2, D1). Thereby, the thermal fusion group A can be subdivided into (A1) solvent free fusion (A2) refluxing in the mixture of protic solvents in the presence of organic base - DBU and (A3) MW assisted fusion. Scheme 8.1 Three key methods of the synthesis of lanthanide(lll) bis(phthalocyanine) complexes. Homoleptic complexes symmetrical (A, B) and unsymmetrical (C1 and C2, D1). Thereby, the thermal fusion group A can be subdivided into (A1) solvent free fusion (A2) refluxing in the mixture of protic solvents in the presence of organic base - DBU and (A3) MW assisted fusion.
To facilitate leak-free fusion bonding of chips consisting of metal electrodes, the metal layers were deposited in pre-etched recesses on chips [141,276-280,747,1127],... [Pg.49]

Reid,J. E., Horn, I., Longerich, H. R, Forsythe, L., and Jenner, G.A. (1999). Determination of Zr and Hf in a flux-free fusion of whole rock samples using laser ablation inductively coupled plasma-mass spectrometry (LA-ICP-MS) with isotope dilution calibration. Geostand, Newsl. 23(2), 149. [Pg.259]

Figure 2 Conjugation of peptide fusions with TBMB. (a) Molecular spectrometry of the GCGSGCGSGCG-D1-D2 (disulfide-free) fusion protein before and after reaction with 10 jiM TBMB, as in the Methods. The mass difference corresponds to the mesitylene core, (b) Titers (transducing units) of phage treated with various concentrations of TBMB as in the Methods. Figure 2 Conjugation of peptide fusions with TBMB. (a) Molecular spectrometry of the GCGSGCGSGCG-D1-D2 (disulfide-free) fusion protein before and after reaction with 10 jiM TBMB, as in the Methods. The mass difference corresponds to the mesitylene core, (b) Titers (transducing units) of phage treated with various concentrations of TBMB as in the Methods.
Lassaigne s test is obviously a test also for carbon in the presence of nitrogen. It can be used therefore to detect nitrogen in carbon-free inorganic compounds, e.g., complex nitrites, amino-sulphonic acid derivatives, etc., but such compounds must before fusion with sodium be mixed with some non-volatile nitrogen-free organic compound such as starch... [Pg.323]

To determine which halogen is present, take 1-2 ml. of the filtrate from the sodium fusion, and add dilute sulphuric acid until just acid to litmus. Add about 1 ml. of benzene and then about 1 ml. of chlorine water and shake. A yellowish-brown colour in the benzene indicates bromine, and a violet colour iodine. If neither colour appears, the halogen is chlorine. The result may be confirmed by testing the solubility of the silver halide (free from cyanide) in dilute ammonia solution silver chloride is readily soluble, whereas the bromide dissolves with difficulty, and the iodide not at all. [Pg.325]

The fusion of hydrogen into helium provides the energy of the hydrogen bomb. The helium content of the atmosphere is about 1 part in 200,000. While it is present in various radioactive minerals as a decay product, the bulk of the Free World s supply is obtained from wells in Texas, Oklahoma, and Kansas. The only known helium extraction plants, outside the United States, in 1984 were in Eastern Europe (Poland), the USSR, and a few in India. [Pg.6]

This relationship is sketched in Fig. 4.7a, which emphasizes that P, must vary linearly with 6 and that P, ° must be available, at least by extrapolation. The heat of fusion is an example of a property of the crystalline phase that can be used this way. It could be difficult to show that the value of AH is constant per unit mass at all percentages of crystallinity and to obtain a value for AHj° for a crystal free from defects. Therefore, while conceptually simple, the actual utilization of Eq. (4.37) in precise work may not be easy. [Pg.228]

The most popular device for fluoride analysis is the ion-selective electrode (see Electro analytical techniques). Analysis usiag the electrode is rapid and this is especially useful for dilute solutions and water analysis. Because the electrode responds only to free fluoride ion, care must be taken to convert complexed fluoride ions to free fluoride to obtain the total fluoride value (8). The fluoride electrode also can be used as an end poiat detector ia titration of fluoride usiag lanthanum nitrate [10099-59-9]. Often volumetric analysis by titration with thorium nitrate [13823-29-5] or lanthanum nitrate is the method of choice. The fluoride is preferably steam distilled from perchloric or sulfuric acid to prevent iaterference (9,10). Fusion with a sodium carbonate—sodium hydroxide mixture or sodium maybe required if the samples are covalent or iasoluble. [Pg.138]

Niobic Acid. Niobic acid, Nb20 XH2O, includes all hydrated forms of niobium pentoxide, where the degree of hydration depends on the method of preparation, age, etc. It is a white insoluble precipitate formed by acid hydrolysis of niobates that are prepared by alkaH pyrosulfate, carbonate, or hydroxide fusion base hydrolysis of niobium fluoride solutions or aqueous hydrolysis of chlorides or bromides. When it is formed in the presence of tannin, a volurninous red complex forms. Freshly precipitated niobic acid usually is coUoidal and is peptized by water washing, thus it is difficult to free from traces of electrolyte. Its properties vary with age and reactivity is noticeably diminished on standing for even a few days. It is soluble in concentrated hydrochloric and sulfuric acids but is reprecipitated on dilution and boiling and can be complexed when it is freshly made with oxaHc or tartaric acid. It is soluble in hydrofluoric acid of any concentration. [Pg.28]

Quantitatively, sulfur in a free or combined state is generally determined by oxidizing it to a soluble sulfate, by fusion with an alkaH carbonate if necessary, and precipitating it as insoluble barium sulfate. Oxidation can be effected with such agents as concentrated or fuming nitric acid, bromine, sodium peroxide, potassium nitrate, or potassium chlorate. Free sulfur is normally determined by solution in carbon disulfide, the latter being distilled from the extract. This method is not useful if the sample contains polymeric sulfur. [Pg.124]

PVC Fusion (Gelation). The PVC piimaiy particle flow units (biUion molecule bundles) can partially melt, freeing some molecules of PVC... [Pg.498]

Random copolymers of vinyl chloride and other monomers are important commercially. Most of these materials are produced by suspension or emulsion polymerization using free-radical initiators. Important producers for vinyl chloride—vinyUdene chloride copolymers include Borden, Inc. and Dow. These copolymers are used in specialized coatings appHcations because of their enhanced solubiUty and as extender resins in plastisols where rapid fusion is required (72). Another important class of materials are the vinyl chloride—vinyl acetate copolymers. Principal producers include Borden Chemicals Plastics, B. F. Goodrich Chemical, and Union Carbide. The copolymerization of vinyl chloride with vinyl acetate yields a material with improved processabihty compared with vinyl chloride homopolymer. However, the physical and chemical properties of the copolymers are different from those of the homopolymer PVC. Generally, as the vinyl acetate content increases, the resin solubiUty in ketone and ester solvents and its susceptibiUty to chemical attack increase, the resin viscosity and heat distortion temperature decrease, and the tensile strength and flexibiUty increase slightly. [Pg.185]

Fluxes. Fluxes, composed mostly of salts or oxides of metals, serve to protect underlying metal from the air. This prevents the formation of surface oxides that impede fusion and the formation of a strong solder joint. Fluxes may also act to selectively leach elements from the surface of the underlying metal. The result is a surface free of obstacles to fusion, and of a composition readily wetted by the solder. [Pg.487]

In recent years, proprietary catalysts for advancement have been incorporated in precataly2ed Hquid resins. Thus only the addition of bisphenol A is needed to produce soHd epoxy resins. Use of the catalysts is claimed to provide resins free from branching which can occur in conventional fusion processes (10). Additionally, use of the catalysts results in rapid chain-extension reactions because of the high amount of heat generated in the processing. [Pg.367]

Unless stated otlieiwse, tlie values have been taken from the compilations by K. K. Kelley on Heats of Fusion of Inorganic Compounds, U.S. Bur. Mines Bull. 393 (1936), and The Free Energies of V aporization and V apor Pressures of Inorganic Siibstances, U.S. Bur. Mines Bull. 383 (1935). [Pg.195]

Fig. 5-9 Effect of KOH concentration on disbonding depth steel pipe with PE coating on fusion adhesive, free corrosion, 10 days, 25°C, defect 1 cm diameter. Fig. 5-9 Effect of KOH concentration on disbonding depth steel pipe with PE coating on fusion adhesive, free corrosion, 10 days, 25°C, defect 1 cm diameter.
Further information on the effect of polymer structure on melting points has been obtained by considering the heats and entropies of fusion. The relationship between free energy change AF with change in heat content A// and entropy change A5 at constant temperature is given by the equation... [Pg.72]

As pointed out by Flory [16], the principle of equal reactivity, according to which the opportunity for reaction (fusion or scission) is independent of the size of the participating polymers, implies an exponential decay of the number of polymers of size / as a function of /. Indeed, at the level of mean-field approximation in the absence of closed rings, one can write the free energy for a system of linear chains [11] as... [Pg.520]


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