Volumetric Solutions 2

Preparation
pubs.acs.org/doi/book/10.1021/acsreagents
.
es
ng
ha
EXPIRED
Volumetric Solutions
c
of
Part 3, Solutions and Mixtures Used in Tests
ry
eISBN: 9780841230460
ma
Tom Tyner Chair, ACS Committee on Analytical Reagents
James Francis Secretary, ACS Committee on Analytical Reagents
um
Portions of this monograph have been updated. Please visit the current version for a summary of changes
s
and links to other versions. http://pubs.acs.org/doi/full/10.1021/acsreagents.3003.
nd
na
ABSTRACT
sio
Publication Date (Web): February 28, 2017 | doi: 10.1021/acsreagents.3003.20160601
er
Throughout the monographs in this book, the term “volumetric solution” is used to designate a solution prepared and
tv
standardized as described in this section.
Downloaded by RICE UNIV on May 26, 2018 | https://pubs.acs.org
n
re
Two background references that the analyst may find helpful are ASTM E20008(2008) and the section on Volumetric
ur
Solutions in United States Pharmacopeia (see the bibliographies on Analytical Chemistry [Part 6: List of Bibliographies;
oc
Analytical Chemistry], and on Physical Properties [Part 6: List of Bibliographies; Physical Properties]). Various textbooks
on chemical analysis also deal with volumetric solutions and volumetric analysis on both a theoretical and a practical
basis.
kt
lin
SUPPLEMENTS & UPDATES

or
e rf
ad
Published Authoritative Expired Type Summary Other Versions

he
28 Feb 2017 01 Jun 2016 12 Sep 2017 Original First on-line publication, based on 11th ed.
ee
GENERAL INFORMATION
S
d.
ge
The concentrations of volumetric solutions usually are expressed as N, normality (number of gram-equivalent weights in each
liter of solution), although concentration sometimes is expressed as M, molarity (number of gram-molecular weights in each
n
ha
liter of solution).
ec
The accuracy of many analytical procedures is dependent on the manner in which such solutions are prepared, standardized,
and stored. The directions that follow describe the preparation of these solutions and their standardization against primary
av
standards or against already-standardized solutions. Alternatively, in cases where suitable primary standard chemicals are
hh
available, volumetric solutions may be prepared by dissolving accurately weighed portions of these substances to make an
accurately known volume of solution. All volumetric solutions, of course, must be thoroughly mixed as part of their
ap
preparation. Stronger or weaker solutions than those described are prepared and standardized in the same general manner,
gr
using proportional amounts of reagents and standards. Lower strengths frequently may be prepared by accurately diluting a
no
stronger solution. However, when necessary because of the accuracy requirements of the analysis being performed, volumetric
solutions prepared in this manner should be standardized before use against a primary standard or by comparison with an
mo
appropriate volumetric solution of known strength.

s
Certain reagents, such as arsenic trioxide, reductometric standard, are designated as standards in this book. Certified
thi
standards of a number of chemical compounds are available as standard reference materials (SRMs) from NIST.
of
It is desirable to standardize a solution in such a way that the end point is observed at the same pH value (or
ns
oxidation–reduction potential) anticipated during subsequent use.

rtio
For example, a sodium hydroxide solution found to be 0.1000 N when standardized against potassium hydrogen phthalate to
Po
phenolphthalein (pH 8.5) may behave like 0.1002 N when used for titrating a strong acid to methyl red (pH 5). Only a small part
of this difference is due to the NaOH required to bring pure water from pH 5 to 8.5. In this case, the error can be avoided by
titrating the strong acid to phenolphthalein (pH 8.5), the same indicator that was used in standardizing the sodium hydroxide.
DOI:10.1021/acsreagents.3003
© 2017 American Chemical Society A ACS Reagent Chemicals, Part 3
ACS Reagent Chemicals

ACS Reagent Chemicals; American Chemical Society: Washington, DC, 2017.
ACS Reagent Chemicals Preparation
.
es
Storage
ng
ha
Glass containers are suitable for the storage of most volumetric solutions. However, polyolefin containers are recommended
for alkaline solutions. Volumetric solutions are stable for varying lengths of time, depending on their chemical nature and
c
their concentration. Dilute solutions are likely to be less stable than those that are 0.1 N or stronger. If there is any doubt
of
about the reliability of a solution, it should be restandardized at the time of use. Volumetric solutions should be stored
ry
appropriately to avoid environmental interaction that may adversely affect the stability of the assigned normality or
ma
molarity. Opaque containers and carbon dioxide or oxygen traps may be appropriate under certain conditions.
um
Temperature Considerations
s
nd
If possible, volumetric solutions should be prepared, standardized, and used at 25 °C. If a titration is carried out at a
temperature different from that at which the solution was standardized, a temperature correction may be needed,
na
depending on the accuracy requirement of the analysis being performed. If the temperature of use is higher than the
o
temperature of standardization, the correction is to be subtracted from the standardization value; if the temperature of
rsi
use is lower than the temperature of standardization, the correction is to be added. For guidance with respect to
ve
temperature corrections, consider that a 5 °C temperature change will alter the normalities of solutions approximately as
follows: For aqueous solutions 0.1 N or less, by 1 part in 1000; 0.5 N, by 1.2 parts in 1000; and 1 N, by 1.4 parts in 1000. For
nt
nonaqueous solutions, based on the expansion coefficients of the solvents, by 5.4 parts in 1000 for glacial acetic acid; 5.5
rre
parts in 1000 for dioxane; and 6.2 parts in 1000 for methanol.
cu
Errors caused by temperature differences, as well as by improper drainage of burettes or pipettes, can be avoided if
measurements are made on a weight basis. With a sensitive direct-reading balance and the use of squeeze bottles,
titrations by weight have become very practical and precise. to
nk
li
Correction Factors
or
rf
It is not necessary that volumetric solutions have the identical normalities (or molarities) indicated in this section or as
de
specified in many of the standardization and assay calculations in this book. It is necessary, however, that the exact value be
ea
known because if it is different from the nominal value specified, a correction factor will have to be applied. Thus, if a
calculation is based on an exactly 0.1 N volumetric solution and the solution actually used is 0.1008 N, its volume must be
eh
multiplied by a factor of 1.008 to obtain the corrected volume of 0.1 N solution to use in the calculation. Similarly, if the
actual normality is 0.0984 N, the factor is 0.984.
. Se
ed
Replication
ng
Because the results obtained by titrations depend on the reliability of the volumetric solutions used, it is imperative that
ha
the latter be standardized at least in triplicate with particular care and preferably by experienced analysts. Triplicate
ec
standardizations for solutions from 0.1 N to 1 N should agree at least to within 2 parts in 1000. Triplicates for 0.05 N
solutions may differ by as much as 10 parts in 1000. If deviations are greater than indicated, the determinations should be
av
repeated until the criteria are met.

hh
SOLUTIONS
ap
gr
no
mo
Note: When “measure accurately” is specified in this section, the volumetric ware used shall conform to the
tolerance accepted by NIST (see the bibliography on Measurement Techniques [Part 6: List of Bibliographies;
Measurement Techniques]).
s
thi
of
Acetic Acid, 1 N
ns
rtio
Add 61 g (58.1 mL) of glacial acetic acid to a 1 L volumetric flask, dilute to volume with water, and mix thoroughly.
Standardize as follows: Measure accurately 40 mL of the solution into a 250 mL conical flask, add 0.10 mL of
Po
© 2017 American Chemical Society B ACS Reagent Chemicals, Part 3

.
es
phenolphthalein indicator solution, and titrate with freshly standardized 1 N sodium hydroxide volumetric solution to a
ng
permanent pink color.
c ha
of
ry
ma
Ammonium Thiocyanate, 0.1 N
s um
Dissolve 7.61 g of ammonium thiocyanate in 100 mL of water. Transfer to a 1 L volumetric flask, dilute to volume with water,
nd
and mix thoroughly. Standardize as follows: Measure accurately 40 mL of freshly standardized 0.1 N silver nitrate
volumetric solution into a 250 mL conical flask containing 50 mL of water. Add 2 mL of nitric acid and 2 mL of ferric
na
ammonium sulfate indicator solution. While stirring, titrate with ammonium thiocyanate solution to the first appearance of
o
a red-brown color.
rsi
ve
nt
rre
cu
Bromine, 0.1 N, Solution I
to
nk
(Prepared from bromine.) In a well-ventilated hood, pipette 2.6 mL of bromine into a 1 L glass-stoppered volumetric flask
li
containing 25 g of potassium bromide and 5 mL of hydrochloric acid dissolved in 500 mL of water. Stopper and swirl until the
or
bromine is dissolved, dilute to volume with water, and mix thoroughly. Standardize as follows: Measure accurately 40 mL of
rf
the solution into a 250 mL iodine flask containing 100 mL of water. Add 3 g of potassium iodide and titrate the liberated
iodine with freshly standardized 0.1 N sodium thiosulfate volumetric solution. Add 3 mL of starch indicator solution near the
de
end of the titration and continue to the absence of the blue starch–iodine complex.
ea
eh
. Se
ed
ng
Bromine, 0.1 N, Solution II

ha
ec
(Prepared as a potassium bromate–potassium bromide mixture.) Transfer 2.8 g of potassium bromate plus 15 g of potassium
bromide to a 1 L volumetric flask, dilute to volume with water, and mix thoroughly. Standardize as follows: Measure
av
accurately 40 mL of the solution into a 250 mL iodine flask and dilute with 100 mL of water. Add 3 g of potassium iodide,
hh
stopper the flask, and swirl the contents carefully. Then add 3 mL of hydrochloric acid, stopper the flask again, swirl
vigorously, and allow to stand in the dark for 5 min. Titrate the liberated iodine with freshly standardized 0.1 N sodium
ap
thiosulfate volumetric solution. Add 3 mL of starch indicator solution near the end of the titration and continue to the
absence of the blue starch–iodine complex.
gr
no
smo
thi
of
Ceric Ammonium Sulfate, 0.1 N

ns
rtio
Place 63.26 g of ceric ammonium sulfate dihydrate in a 1500 mL beaker and slowly add 30 mL of sulfuric acid. Stir to a
smooth paste, and cautiously add water in portions of 20 mL or less, with stirring, until the salt is dissolved. Dilute, if
Po
necessary, to approximately 500 mL, and mix thoroughly by stirring. Allow to stand for at least 8 h. If a residue has formed
© 2017 American Chemical Society C ACS Reagent Chemicals, Part 3

.
es
or the solution is turbid, filter through a fine-porosity sintered-glass filter (do not filter through paper or similar material).
ng
Transfer the filtrate to a 1 L volumetric flask, dilute to volume, and mix thoroughly. Standardize as follows: Titrate against
ha
freshly standardized 0.1 N ferrous sulfate solution described in [Part 3: Volumetric Solutions; Solutions; Ferrous Sulfate]
using a Ferroin indicator, 0.025 M.
c
of
ry
ma
s um
Cupric Sulfate, 0.1 M
nd
na
Weigh accurately 24.97 g of cupric sulfate pentahydrate. Dissolve in 500 mL of water and quantitatively transfer to a 1 L
volumetric flask. Dilute to volume with water, and mix thoroughly. Standardize as follows: Using a 50 mL burette, measure
o
40.0 mL of the cupric sulfate solution into a 250 mL beaker. From a burette, add 45.0 mL of freshly standardized 0.1 M EDTA
rsi
and 50 mL of methanol. Stir magnetically, and using a pH meter, adjust the pH of the solution to 5 with saturated aqueous
ve
ammonium acetate. Maintain the pH between 5.1 and 5.3 throughout the titration. Add 0.1 mL of PAN indicator solution,
and continue to titrate with the 0.1 M copper sulfate volumetric solution to a permanent blue end point.
nt
rre
cu
to
nk
li
EDTA, 0.1 M
or
rf
Dissolve 37.22 g of Na2EDTA · 2H2O in 500 mL of water. Transfer quantitatively to a 1 L volumetric flask, dilute to volume
de
with water, and mix thoroughly. Standardize as follows: Weigh accurately 0.40 g of calcium carbonate, chelometric
ea
standard (NIST SRM 915), previously dried at 210 °C for 4 h. Transfer to a 400 mL beaker, and add water. Cover the beaker
with a watch glass, and introduce 4 mL of hydrochloric acid (1:1) from a pipette inserted between the lip of the beaker and
eh
the edge of the watch glass. Swirl the contents of the beaker to dissolve the calcium carbonate. Wash down the sides of the
beaker and the watch glass with water, and dilute to 200 mL. While stirring, add from a 50 mL burette about 30 mL of the
Se
EDTA standard solution. Adjust the solution to pH 12–13 with 10% sodium hydroxide, and add 300 mg of hydroxy naphthol
blue indicator mixture. Continue the titration with the EDTA volumetric standard solution to a blue end point.
.
ed
ng
ha
ec
av
hh
Ferrous Ammonium Sulfate, 0.1 N

ap
Dissolve 39.21 g of ferrous ammonium sulfate hexahydrate in 200 mL of 25% sulfuric acid. Transfer quantitatively to a 1 L
volumetric flask, dilute to volume with water, and mix thoroughly. On each day of use, standardize as follows: Measure
gr
accurately 40 mL of the solution into a 250 mL conical flask, add 0.1 mL of 1,10-phenanthroline reagent solution, and titrate
no
with a freshly standardized 0.1 N ceric ammonium sulfate volumetric solution to the change from pink to pale blue.
mo
s
thi
of
ns
rtio
Po
© 2017 American Chemical Society D ACS Reagent Chemicals, Part 3

.
es
Ferrous Sulfate, 0.1 N
ng
ha
Dissolve 27.80 g of clear ferrous sulfate heptahydrate crystals in about 500 mL of water containing 50 mL of sulfuric acid.
Transfer quantitatively to a 1 L volumetric flask, dilute to volume with water, and mix thoroughly. On each day of use,
c
standardize as follows: Measure accurately 40 mL of the solution into a 250 mL conical flask, add 60 mL of water, and titrate
of
with freshly standardized 0.1 N potassium permanganate to a pink end point. Perform a blank titration using only water.
ry
ma
s um
nd
na
Hydrochloric Acid, 1 N
sio
Add 85 mL of hydrochloric acid to 50 mL of water in a 1 L volumetric flask. Cool to room temperature, dilute to volume with
water, and mix thoroughly. Standardize as follows: Weigh accurately about 2.2 g of sodium carbonate, alkalimetric standard
er
(NIST SRM 351), that previously has been heated at 285 °C for 2 h. Dissolve in 100 mL of water, and add 0.1 mL of methyl red
tv
indicator solution. Add the acid slowly from a burette, with stirring, until the solution becomes faintly pink. Heat the
n
solution to boiling, cool, and again titrate until the solution becomes faintly pink. Repeat this procedure until the faint
re
color is no longer discharged on further boiling.
ur
oc
kt
lin
or
rf
Iodine, 0.1 N
e
ad
Place approximately 40 g of potassium iodide and 10 mL of water in a large glass-stoppered weighing bottle. Mix the
he
contents by swirling, allow to come to room temperature, and then weigh accurately. Add approximately 12.7 g of assayed
iodine [Part 4: Iodine], previously weighed on a rough balance, and reweigh the stoppered bottle and contents to obtain the
ee
exact weight of the iodine added. Mix and transfer quantitatively to a 1 L amber volumetric flask. Dilute to volume with
water, and mix thoroughly. Standardize as follows: Weigh accurately 0.21 g of arsenic trioxide reductometric standard (NIST
S
SRM 83), previously dried for 12 h at 110 °C and cooled in a desiccator for 2 h, into a 250 mL iodine flask. Add 10 mL of 1.0 N
d.
sodium hydroxide, warm gently, and swirl to hasten dissolution, being certain that no particles of arsenic trioxide remain on
ge
the sides of the flask, and add 0.15 mL of phenolphthalein indicator solution. Neutralize with 6 M hydrochloric acid, and add
n
1 mL in excess of the acid. Add 75 mL of water and 2 g of sodium bicarbonate dissolved in 20 mL of water. Titrate with the
ha
iodine solution until within about 2 mL of the anticipated equivalence point. Then add 3 mL of starch indicator solution, and
ec
continue the titration to the first permanent blue color of the starch–iodine complex. Store in an opaque or amber glass
bottle.
av
hh
ap
gr
no
mo
Lead Nitrate, 0.1 M

s
Dissolve 33.12 g of lead nitrate in 300 mL of water. Transfer quantitatively to a 1 L volumetric flask, dilute to the mark with
thi
water, and mix thoroughly. Standardize as follows: Measure accurately 40 mL of the solution into a 400 mL beaker. Add 0.15
mL of acetic acid and 15 mL of a saturated aqueous solution of hexamethylenetetramine. Add a few milligrams of xylenol
of
orange indicator mixture and titrate with freshly standardized 0.1 M EDTA volumetric solution to a yellow color.
ns
rtio
Po
© 2017 American Chemical Society E ACS Reagent Chemicals, Part 3

.
es
Oxalic Acid, 0.1 N
ng
ha
Dissolve 6.30 g of oxalic acid dihydrate in 200 mL of water in a 1 L volumetric flask, dilute to volume with water, and mix
thoroughly. Standardize as follows: Measure accurately 40 mL of the solution in a 250 mL conical flask and add 50 mL of
c
water and 7 mL of sulfuric acid. Add slowly, with stirring, 30 mL of freshly standardized 0.1 N potassium permanganate
of
volumetric solution. Heat the solution to 70 °C, and continue the titration until the pink color persists for 30 s.
ry
ma
s um
nd
Perchloric Acid in Glacial Acetic Acid, 0.1 N
na
o
rsi
ve
C a u t i o n : Perchloric acid in contact with some organic materials can form explosive mixtures. Use safety goggles and
rubber gloves when preparing the solution. Rinse any glassware that has been in contact with perchloric acid before
nt
setting it aside.
rre
cu
Add slowly, with stirring, 8.5 mL of 70% perchloric acid to a mixture of 500 mL of glacial acetic acid and 21 mL of acetic
anhydride. Cool, dilute to volume in a 1 L volumetric flask with glacial acetic acid, and mix thoroughly. Wait 30 min and
to
determine the water content of the solution by titrating 30 g with Karl Fischer reagent [Part 3: Reagents, Buffers, and
nk
Indicators; Solutions and Mixtures; Karl Fischer Volumetric Reagent]. If the water content is greater than 0.05%, add a small
li
amount of acetic anhydride, mix thoroughly, and again determine the water. Repeat until the water content is between
or
0.02% and 0.05%. In a similar manner, if the original water content is below 0.02%, add water to bring the water content into
rf
the 0.02–0.05% range. Allow the solution to stand for 24 h, and check the water content to be certain that it remains in this
range. Standardize as follows: Weigh accurately about 0.7 g of potassium hydrogen phthalate, acidimetric standard (NIST
de
SRM 84), previously lightly crushed and dried for 2 h at 120 °C. Dissolve in 50 mL of glacial acetic acid, add 0.1 mL of crystal
ea
violet indicator solution, and titrate with the perchloric acid solution until the violet color changes to blue-green. Perform a
eh
blank titration on 50 mL of glacial acetic acid in the same manner, and subtract the volume of perchloric acid solution
consumed in the blank titration from that consumed in the first titration.
. Se
ed
ng
ha
ec
Potassium Bromate, 0.1 N

av
Weigh accurately 2.78 g of potassium bromate, transfer to a 1 L volumetric flask, dilute to volume with water, and mix
hh
thoroughly. Standardize as follows: Measure accurately 40 mL of the solution into a 250 mL iodine flask, add 3 g of potassium
ap
iodide and 3 mL of hydrochloric acid, stopper the flask, and allow to stand in the dark for 5 min. Titrate the liberated iodine
with a freshly standardized 0.1 N sodium thiosulfate volumetric solution. Add 3 mL of starch indicator solution near the end
gr
of the titration and continue to the absence of the blue starch–iodine complex.
no
smo
thi
of
ns
Potassium Dichromate, 0.1 N

rtio
Weigh accurately 4.90 g of potassium dichromate, previously dried for 2 h at 110 °C. Transfer to a 1 L volumetric flask,
Po
dilute to volume with water, and mix thoroughly. Standardize as follows: Measure accurately 40 mL of the solution into a
© 2017 American Chemical Society F ACS Reagent Chemicals, Part 3

.
es
250 mL iodine flask, and add 100 mL of water, 3 g of potassium iodide, and 3 mL of hydrochloric acid. Stopper immediately,
ng
and allow to stand in the dark for 5 min. Titrate the liberated iodine with a freshly standardized 0.1 N sodium thiosulfate
ha
solution. Add 3 mL of a starch indicator solution near the end of the titration, and continue to the absence of the blue
starch–iodine complex.
c
of
ry
ma
s um
Potassium Hydroxide, Methanolic, 0.1 N
nd
na
Dissolve 6.8 g of potassium hydroxide in a minimum amount of water (about 5 mL) in a 1 L volumetric flask. Dilute to volume
with methanol, and mix thoroughly. Allow to stand in a container protected from carbon dioxide for 24 h. Carefully decant
o
the clear solution, leaving any residue behind, into a suitable container, mix well, and store protected from carbon dioxide.
rsi
Standardize as follows: Weigh accurately about 0.85 g of potassium hydrogen phthalate, acidimetric standard (NIST SRM
ve
84), previously lightly crushed and dried for 2 h at 120 °C. Dissolve in 100 mL of carbon dioxide-free water, add 0.15 mL of
phenolphthalein indicator solution, and titrate with the methanolic potassium hydroxide solution to a permanent faint pink
nt
color.
rre
cu
to
nk
li
or
Potassium Iodate, 0.05 M (0.3 N)

rf
de
Weigh exactly 10.70 g of potassium iodate, previously dried at 110 °C to constant weight, transfer to a 1 L volumetric flask,
dilute to volume with water, and mix thoroughly. Standardize as follows: To 15.0 mL of solution in a 250 mL iodine flask, add
ea
3 g of potassium iodide and 3 mL hydrochloric acid previously diluted with 10 mL of water. Stopper immediately, and allow
eh
to stand in the dark for 5 min. Then add 50 mL of cold water, and titrate the liberated iodine with freshly standardized 0.1 N
sodium thiosulfate. Add 3 mL of starch indicator solution near the end of the titration, and continue to the absence of the
Se
blue starch–iodine complex.

.
ed
ng
ha
ec
av
hh
ap
Potassium Permanganate, 0.1 N

gr
no
Dissolve 3.3 g of potassium permanganate in 1 L of water in a 1500 mL conical flask, heat to boiling, and boil gently for 15
mo
min. Allow to cool, stopper, and keep in the dark for 48 h. Then filter through a fine-porosity sintered-glass filter, and place
in a glass-stoppered amber bottle. Standardize as follows: Weigh accurately about 0.26 g of sodium oxalate (NIST SRM
s
8040), previously dried for 2 h at 105 °C, transfer to a 500 mL conical flask containing 250 mL of water and 7 mL of sulfuric
thi
acid, and heat to 70 °C. Titrate immediately with the permanganate solution to a pink color that persists for 15 s. The
temperature at the end of the titration should not be less than 60 °C. Perform a blank titration containing 250 mL of water
of
and 7 mL of sulfuric acid in the same manner, and subtract the volume of the potassium permanganate consumed in the
ns
blank from the first titration. Store in an opaque or amber glass container.
rtio
Po
© 2017 American Chemical Society G ACS Reagent Chemicals, Part 3

.
es
ng
c ha
of
ry
Potassium Thiocyanate, 0.1 N
ma
Weigh exactly 9.72 g of potassium thiocyanate, previously dried for 2 h at 110 °C, transfer to a 1 L volumetric flask, dilute
um
to volume, and mix thoroughly. Standardize as follows: Measure accurately 40 mL of freshly standardized 0.1 N silver nitrate
s
volumetric solution into a 250 mL conical flask, and add 100 mL of water, 1 mL of nitric acid, and 2 mL of ferric ammonium
nd
sulfate indicator solution. Titrate with the thiocyanate solution, with agitation, to a permanent light pink-brown color of
the supernatant solution.
na
o
rsi
ve
nt
rre
Silver Nitrate, 0.1 N
cu
Weigh exactly 16.99 g of silver nitrate, previously dried for 1 h at 100 °C, transfer to a 1 L amber volumetric flask, dilute to
to
volume, and mix thoroughly. Standardize as follows: Weigh accurately about 0.33 g of potassium chloride (NIST SRM 999)
nk
ignited at 500 °C. Place in a 250 mL beaker, and dissolve in 100 mL of water. Add 2 mL of dichlorofluorescein indicator
solution. With stirring, titrate with silver nitrate solution until the silver chloride flocculates and the mixture acquires a
li
or
faint pink color. Store in an opaque container.

rf
de
ea
eh
Se
Sodium Acetate in Glacial Acetic Acid, 0.1 N

.
ed
Place 8.20 g of sodium acetate, anhydrous, previously dried to constant weight at 120 °C, in a 1 L volumetric flask. Add 500
ng
mL of glacial acetic acid and 10 mL of acetic anhydride, and dissolve. Dilute to volume with glacial acetic acid, and mix
thoroughly. Standardize as follows: Measure accurately 40 mL of freshly standardized perchloric acid in glacial acetic acid
ha
volumetric solution, and add 0.1 mL of crystal violet indicator solution. While stirring, titrate with the sodium acetate until
ec
the solution changes from an emerald green to a violet color.

av
hh
ap
gr
no
Sodium Hydroxide, 1 N
mo
Dissolve 162 g of sodium hydroxide in 150 mL of carbon dioxide-free water, and cool the solution to room temperature.
s
Prepare a 1 N solution by diluting 54.5 mL of the concentrated solution to 1 L with carbon dioxide-free water. Mix
thi
thoroughly, and store in a tight polyolefin container. Standardize as follows: Weigh accurately about 8.5 g of potassium
of
hydrogen phthalate, acidimetric standard (NIST SRM 84), previously lightly crushed and dried for 2 h at 120 °C. Dissolve in
100 mL of carbon dioxide-free water, add 0.15 mL of phenolphthalein indicator solution, and titrate with the sodium
ns
hydroxide solution to a permanent faint pink color.

rtio
Po
© 2017 American Chemical Society H ACS Reagent Chemicals, Part 3

.
es
ng
c ha
of
ry
Sodium Methoxide in Methanol, 0.01 N
ma
Dilute 20.0 mL of sodium methoxide in methanol, 0.5 M methanolic solution, with methanol to 1 L and mix thoroughly.
um
Standardize as follows: Measure accurately 40 mL of 0.01 N sulfuric acid volumetric solution into a suitable container, add
0.10 mL of thymol blue indicator solution, and titrate with the sodium methoxide in methanol solution to a blue end point.
s
nd
na
o
rsi
ve
Sodium Nitrite, 0.1 N
nt
rre
Weigh accurately 6.90 g of sodium nitrite. Dissolve in 100 mL of water in a 1 L volumetric flask, dilute to volume, and mix
cu
thoroughly. Standardize as follows: Add 5 mL of sulfuric acid to 200 ml of water, and while the solution is still warm, add 0.1
N potassium permanganate until a faint pink color persists for 2 min. Measure accurately 50 mL of freshly standardized 0.1
to
N potassium permanganate, transfer to the solution, and mix gently. Pipette, slowly and with constant agitation, 40 mL of
nk
the sodium nitrite solution, holding the tip of the pipette well below the surface of the liquid. Add 3 g of potassium iodide,
and titrate the liberated iodine from the excess of potassium permanganate with 0.1 N sodium thiosulfate. Add 3 mL of
li
starch indicator near the end point, and titrate to the absence of the blue starch–iodine complex. Perform a complete blank
or
using all reagents except the 0.1 N sodium nitrite solution.

rf
de
ea
eh
. Se
Sodium Thiosulfate, 0.1 N

ed
ng
Dissolve 24.82 g of sodium thiosulfate pentahydrate and 200 mg of sodium carbonate, anhydrous, in 1 L of recently boiled
and cooled water, and mix thoroughly. Allow to stand for 24 h, and standardize as follows: Weigh accurately about 0.21 g of
ha
NIST potassium dichromate, oxidimetric standard (NIST SRM 136), previously crushed and dried at 110 °C for 2 h. Dissolve in
ec
100 mL of water in a glass-stoppered iodine flask. Swirl to dissolve the sample, remove the stopper, and quickly add 3 g of
potassium iodide, 2 g of sodium bicarbonate, and 5 mL of hydrochloric acid. Insert the stopper, swirl slightly to release
av
excess carbon dioxide, cover the stopper with water, and allow to stand in the dark for 10 min. Rinse the stopper and the
hh
inner walls of the flask with water and titrate the liberated iodine with the sodium thiosulfate until the solution becomes
faintly yellow. Add 3 mL of starch indicator solution, and continue the titration to the disappearance of the blue
ap
starch–iodine complex. Restandardize the solution frequently.

gr
no
smo
thi
of
Sulfuric Acid, 1 N
ns
Add slowly (use caution), with stirring, 30 mL of sulfuric acid to about 500 mL of water. Allow the mixture to cool to room
rtio
temperature, dilute to 1 L, and mix thoroughly. Standardize against sodium carbonate, alkalimetric standard, as directed
for hydrochloric acid, 1 N.
Po
© 2017 American Chemical Society I ACS Reagent Chemicals, Part 3

.
es
Zinc Chloride, 0.1 M
ng
ha
Weigh accurately 6.54 g of zinc (13.63 g of ZnCl2), and dissolve in 80 mL of 10% hydrochloric acid. Warm if necessary to
complete dissolution, cool, dilute with water to volume in a 1 L volumetric flask, and mix thoroughly. Standardize as
c
follows: Pipette and transfer 40.0 ml of zinc chloride solution to a 400 mL beaker with sufficient hexamethylene tetramine
of
to produce a purple-red color. Titrate with freshly standardized 0.1 M EDTA to a color change of purple-red to lemon yellow.
ry
ma
s um
nd
na
Zinc Sulfate, 0.1 M
o
Weigh accurately 28.76 g of zinc sulfate heptahydrate, and dissolve in 500 mL of water in a 1 L volumetric flask. Dilute to
rsi
the mark with water, and mix thoroughly. Standardize as follows: To 40.0 mL of freshly standardized 0.1 M EDTA volumetric
ve
solution, in a suitable beaker, add 10 mL of ammonium acetate–acetic acid buffer solution, 50 mL of ethyl alcohol, and 2 mL
of dithizone indicator solution. Titrate with the zinc sulfate solution to a pink end point.
nt
rre
cu
to
nk
li
or
rf
de
ea
eh
. Se
ed
ng
ha
ec
av
hh
ap
gr
no
smo
thi
of
ns
rtio
Po
© 2017 American Chemical Society J ACS Reagent Chemicals, Part 3


Volumetric Solutions 2

Încărcat de

Informații document

Drepturi de autor

Formate disponibile

Partajați acest document

Partajați sau inserați document

Opțiuni de partajare

Vi se pare util acest document?

Este necorespunzător acest conținut?

Drepturi de autor:

Formate disponibile

Volumetric Solutions 2

Încărcat de

Drepturi de autor:

Formate disponibile

Preparation

SUPPLEMENTS & UPDATES

Published Authoritative Expired Type Summary Other Versions

appropriate volumetric solution of known strength.

oxidation–reduction potential) anticipated during subsequent use.

ACS Reagent Chemicals

repeated until the criteria are met.

ACS Reagent Chemicals

Bromine, 0.1 N, Solution II

Ceric Ammonium Sulfate, 0.1 N

ACS Reagent Chemicals

Ferrous Ammonium Sulfate, 0.1 N

ACS Reagent Chemicals

Lead Nitrate, 0.1 M

ACS Reagent Chemicals

Potassium Bromate, 0.1 N

Potassium Dichromate, 0.1 N

ACS Reagent Chemicals

Potassium Iodate, 0.05 M (0.3 N)

blue starch–iodine complex.

Potassium Permanganate, 0.1 N

ACS Reagent Chemicals

faint pink color. Store in an opaque container.

Sodium Acetate in Glacial Acetic Acid, 0.1 N

the solution changes from an emerald green to a violet color.

hydroxide solution to a permanent faint pink color.

ACS Reagent Chemicals

using all reagents except the 0.1 N sodium nitrite solution.

Sodium Thiosulfate, 0.1 N

starch–iodine complex. Restandardize the solution frequently.

ACS Reagent Chemicals

ACS Reagent Chemicals

S-ar putea să vă placă și