Chapter 8. Sampling, Standardization, and Calibration Flashcards

1
Q

uses only a small fraction of the available sample, the
process of sampling is a very important operation.

A

chemical analysis

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2
Q

used to aid in the selection of a representative
sample.

A

statistical methods

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3
Q

are traditionally classified as
gravimetric methods,
volumetric methods, and
instrumental methods.

A

quantitative methods

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4
Q

are those present in the range of 1 to 100% by mass.

A

major constituents

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5
Q

Species present in the range of 0.01 to 1%

A

minor constituents

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6
Q

Those present in amounts between 100 ppm (0.01%) and 1 ppb

A

trace constituents

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7
Q

Components present in amounts lower than 1 ppb

A

ultratrace constituents

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8
Q

A general problem in trace procedures is that the reliability of results usually decreases
dramatically with a decrease in analyte level.

A
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9
Q

The relative standard deviation between laboratories increases as the level of analyte
decreases.

A
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10
Q

If the interferences are caused by extraneous species in the matrix, they are often called

A

matrix effects

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11
Q

Samples are analyzed, but constituents or concentrations are determined.

A
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12
Q

read on sampling uncertainties

A
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13
Q

a miniature replica of the entire mass of material to be
analyzed. It is the collection of individual sampling units. It must be representative of the
whole in composition and in particle-size distribution.

A

gross sample

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14
Q

Well-mixed solutions of liquids and gases require only a very small sample because
they are homogeneous down to the molecular level. Gases can be sampled by several
methods.

A
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15
Q

Samples of metals and alloys are obtained by sawing, milling, or drilling

A
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16
Q

copy formulas in 1/8

A
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17
Q

can lead to higher throughout (more analyses per
unit time), higher reliability, and lower costs than manual sample handling.

A

automated sample handling

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18
Q

These often mimic the operations that would be performed manually.
Some discrete sample processors automate only the measurement step of the
procedure or a few chemical steps and the measurement step.

A

discrete (batch) methods

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19
Q

The sample is inserted into a flowing stream where a number of operations can
be performed prior to transporting it to a flow-through detector.
These methods can perform not only sample processing operations but also the
final measurement step.

A

continuous flow methods

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20
Q

a band-spreading or mixing
phenomenon that results from the
coupling of fluid flow with molecular
diffusion.

A

dispersion

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21
Q

mass transport due to a
concentration gradient.

A

diffusion

22
Q

determines the relationship between the analytical
response and the analyte concentration, which is usually determined by
the use of chemical standards prepared from purified reagents.

A

calibration

23
Q

interferences from other constituents in the sample matrix,

A

concomitants

24
Q

one of the most accurate of all analytical procedures.

A

titration

25
Q

calibration curve or working curve

A
26
Q

A series of standard solutions is prepared separately from the sample.

A

external standard calibration

27
Q

is a rough measure of the
magnitude of a typical deviation from the regression line.

A

standard deviation about regression

standard error of the estimate

standard error

28
Q

measures the variation in the observed
values of the dependent variable (y values) that are not explained by the presumed linear
relationship between x and y

A

sum of the squares of the residuals

29
Q

is one in which the variation in the y
values due to the presumed linear relationship is large
compared to that due to error (residuals).

A

significant regression

30
Q

The F value gives us an indication of the significance of the
regression. When the regression is significant, a large value of
F occurs.

A
31
Q

gives best estimates of the transformed variables,
but these may not be optimal when transformed back to obtain
estimates of the original parameters.

A

linear least squares

32
Q

involves adding the interfering species to all the
samples, standards, and blanks so that the interference effect becomes
independent of the original concentration of the interfering species in the
sample.

A

saturation method

33
Q

is a species, not itself an interfering species, added to
samples, standards, and blanks in sufficient amounts to make the analytical
response independent of the concentration of the interfering species.

A

matrix modifier

34
Q

is added that reacts selectively with the
interfering species to form a complex that does not interfere.

A

masking agent

35
Q

can sometimes be used if the interfering species
produces no significant effect below a certain concentration level.

A

dilution method

36
Q

attempts to duplicate the sample matrix
by adding the major matrix constituents to the standard and blank
solutions.

A

matrix-matching method

37
Q

Errors in procedures can be minimized by saturating with interfering
species, by adding matrix modifiers or masking agents, by diluting the
sample, or by matching the matrix of the sample.

A
38
Q

is a reference species, chemically and physically
similar to the analyte, that is added to samples, standards, and blanks.

A

internal standard

39
Q

The ratio of the response of the analyte to that of the internal standard
is plotted versus the concentration of analyte

A
40
Q

The response signal is then not the analyte signal itself but the ratio of
the analyte signal to the reference species signal.

A
41
Q

is used when it is difficult or
impossible to duplicate the sample matrix.

A

method of standard additions

42
Q

read on chapter 8 in case u missed something

A
43
Q

the change in
the response signal per unit change in analyte concentration

A

calibration sensitivity

44
Q

is the ratio of the
calibration curve slope to the standard
deviation of the analytical signal at a given
analyte concentration. The analytical
sensitivity is usually a strong function of
concentration

A

analytical sensitivity

45
Q

is the smallest
concentration that can be reported with a
certain level of confidence.

A

detection limit, DL

46
Q

The calibration sensitivity is thus the slope of the calibration curve.

A
47
Q

most often refers to the
concentration range over which the analyte can be determined using a linear calibration
curve .

A

linear dynamic range of an analytical method

48
Q

is generally considered to be the detection limit

A

lower limit

49
Q

is usually taken as the concentration at which the analytical signal or
the slope of the calibration curve deviates by a specified amount

A

upper end

50
Q

is a sequential plot of some quality characteristic that is important in
quality assurance

A

control chart

51
Q

determines the suitability of an analysis for providing the sought-for
information and can apply to samples, to methodologies, and to data

is often done by the analyst, but it can also be done by supervisory personnel

A

validation