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Process interfering

The most striking characteristic of an electrolytic action is that it occurs in two places— at the anode and at the cathode. This peculiarity can be made less marked by bringing the electrodes nearer and nearer together. When the distance between them vanishes, we have a chemical reaotion in the ordinary sense of the word and not an electrochemical reaction. Any chemical reaction, therefore, which can be made to take place electrolytically, must consist of an anode and a oathode process. Considering the matter in this light, we see that there is a possibility of the anode and cathode processes interfering and of one perhaps masking the other. [Pg.593]

Thermal emission and other processes interfering with the Raman spectrum... [Pg.156]

While geometric isomerization without any ligand substitution processes interfering is well known, it is not unusual to observe substitution reactions also occurring along with geometrical isomerization. An example is given in Equation (5.52). [Pg.159]

Experimentally we can introduce synthetic double-stranded RNA into cells. This processed interfering RNA (RNAi) catalyzes the destruction of endogenous mRNAs of the same sequence, so it is possible to observe the effect of down-regulating the expression of a particular protein in a cell. [Pg.225]

In the quantitative determination of lindane and PCP from the matrix blood, the sample preparation process is an essential step for ensuring that the results will be of good quality. In this process, interfering substances contained in the matrix are removed, and the substances to be determined are converted into a chemical form that enables them to be measured by GCZMS. [Pg.174]

In the presence of cyanides the samples should be mineralized due to the complex bonding of Ni(CN)z i2-. In this process interfering organic impurities are simultaneously eliminated. Evaporate the samples (30 - 1000 ml) under a fume hood with 2 ml of concentrated sulphuric acid and 2 - 3 ml of concentrated nitric acid until SO3 vapour appears. If the solution is still... [Pg.381]

One of the most widely used techniques for preventing an interference is to bind the interferent as a soluble complex, preventing it from interfering in the analyte s determination. This process is known as masking. Technically, masking is not a separation... [Pg.207]

Therefore, if a large quantity of sample is introduced into the flame over a short period of time, the flame temperature will fall, thus interfering with the basic processes leading to the formation and operation of the plasma. Consequently introduction of samples into a plasma flame needs to be controlled, and there is a need for special sample-introduction techniques to deal with different kinds of samples. The major problem with introducing material other than argon into the plasma flame is that the additives can interfere with the process of electron formation, a basic factor in keeping the flame self-sustaining. If electrons are removed from the plasma by... [Pg.97]

Second-generation juvenoids incorporate more substantial stmctural departures from neotenin and are more resistant to metaboHc and environmental degradation. Epiphenonane, 2-ethyl-3-[3-ethyl-5-(4-ethylphenoxy)-pent-3-en-yl] 2-methyloxirane (131), has a rat oral LD q of 4000 mg/kg. It and similar juvenoids are used in China and Japan to prolong the last larval instar of the silkworm so that silk production is increased 10—15%. Fenoxycarb, ethyl [2-(4-phenoxyphenoxy)ethyl] carbamate (132) (mp 53°C, vp 0.0078 mPa at 20°C), is soluble in water to 6 mg/L. The rat oral LD q is >16,800 mg/kg. Fenoxycarb has a wide spectmm of activity, interfering with the developmental processes of fleas, cockroaches, and ants. [Pg.294]

Pecrystallisation of a copolymer having 15 wt % VC has been found to be nucleated by material that survives the melting process plus new nuclei (74). The maximum crystallisation rate occurred at 373 K the maximum nucleation rate at 283 K. Attempts to melt all the polymer led to degradation that interfered with recrystallisation. [Pg.432]

Eor example, beryUium occurs at the bottom of a displacement series with NTA allowing this metal to be recovered as the hydroxide by pH adjustment of an ore processing solution all of the interfering metals remain sequestered by chelation (14). Additionally, because other metals present caimot displace iron in an iron—EHPG chelate, the chelate can be used in highly calcareous soils to supply iron as a trace nutrient in agriculture (15). [Pg.386]

Selectivity for a single metal of a group is the basis of a solvent extraction process for the recovery of copper (qv) from low concentration ore leach solutions containing high levels of iron (qv) and other interfering metals (16). [Pg.386]

WTiile his cxpcrilnciits yielded acceptable gasolines, serious problems arose as Burton attempted to scale up his process. The short cycles forced on producers by extensive coking worked against continuous operations. The carbon buildup interfered with heat transfer from the furnace to the petroleum and resulted in the formation of hot spots and in turn damage to the vessel. Pressure control was also a problem. [Pg.989]

The presupposition is that parallel electrochemical reactions (i.e., ion or electron transfer) occur across the phase boundary, if the measured ions and interfering ions are both present in the solution. A redox process in which electrons pass the phase boundary is also considered an interfering electrochemical reaction. [Pg.240]

The reduction of K2TaF7 can also be performed using sodium vapors [584]. This process is conducted at an Na pressure as low as 0.1 torr, which enables the removal of interferring gases such as N, O and H20. The interaction begins at 350°C. The temperature further increases up to 800°C to prevent the condensation of sodium and the formation of colloidal tantalum powder. The product of the interaction is removed from the reactor after cooling and treated with boiled HC1 and HF solutions. The method enables the production of coarse grain tantalum powder with 99.5% purity. [Pg.330]

With flame emission spectroscopy, there is greater likelihood of spectral interferences when the line emission of the element to be determined and those due to interfering substances are of similar wavelength, than with atomic absorption spectroscopy. Obviously some of such interferences may be eliminated by improved resolution of the instrument, e.g. by use of a prism rather than a filter, but in certain cases it may be necessary to select other, non-interfering, lines for the determination. In some cases it may even be necessary to separate the element to be determined from interfering elements by a separation process such as ion exchange or solvent extraction (see Chapters 6, 7). [Pg.792]

Occasionally, separation, e.g. by solvent extraction or by an ion exchange process, may be necessary to remove an interfering element such separations are most frequently necessary when dealing with flame emission spectroscopy. [Pg.794]


See other pages where Process interfering is mentioned: [Pg.476]    [Pg.103]    [Pg.54]    [Pg.476]    [Pg.103]    [Pg.54]    [Pg.251]    [Pg.109]    [Pg.334]    [Pg.295]    [Pg.384]    [Pg.80]    [Pg.379]    [Pg.259]    [Pg.296]    [Pg.388]    [Pg.455]    [Pg.241]    [Pg.303]    [Pg.428]    [Pg.112]    [Pg.40]    [Pg.49]    [Pg.228]    [Pg.242]    [Pg.546]    [Pg.134]    [Pg.518]    [Pg.149]    [Pg.21]    [Pg.460]    [Pg.411]    [Pg.1235]    [Pg.239]    [Pg.603]   
See also in sourсe #XX -- [ Pg.19 ]




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