跪求英文高手帮小弟翻译几段话~老师催~救命了
AbstractX2Y Yt(R8TGh/`)R—The approximation of titration curves by logarithmic functions was described for the titration of a9e O\9U5k'|]*~m
mixture of two monobasic acids. It was demonstrated with the titration of a mixture of CHCl2COOH,CH2ClCOOH, C6H5COOH, and H3BO3
that this method can be used for the precise determination of equivalence
points. The relative error in the determination of titration end-points depends on the values of the corresponding
jumps and, to some extent, on the choice of a weight function and lies in the range from 0.1 to 1%.#d@3F9Z:{%NVoq
At present, two groups of computer-assisted methods
are used for the determination of equivalencet^k-vX H7U
points in potentiometric titration.
Methods [1–3] based on the approximation of a
titration curve by polynomials and followed by the
determination of their inflection points comprise the
first group. The polynomial approximation has no`P@7m.r-rSg[7Qe
physical meaning and is undesirable for use in the`c tF4lu
determination of titration end-points in the case when
inflection points in the jump region do not coincide
with equivalence points. In spite of this, the simplicity%?JFh!N7q'r/[
and versatility of this approximate approach requiring
a minimum of calculations make it an attractive tool for
processing titration curves of different nature.
The second group includes a greater number of
methods (see, for example, [4–9]). The use of materialu6SU}~a8_-j
balance equations and the law of mass action for processing
the data of potentiometric titration not only
solves the main problem of titrimetry, highly precise+q6|d7nr ^{)@
determination of titration end-points, but also providesYl-SO4] pU$c4D;\
the calculation of equilibrium constants for titrationI{r#g-c%H
reactions in many cases. Depending on specific conditions,
the the disadvantages of these methods may be as