Potential Reduced Exposure Products
United States Patent 4,257,430 Tobacco Composition Including Palladium
Fields
- Author
- Bryant, H.G., J.R.
- Collins, P.F.
- Pullman, J.O.
- Collins, P.F.
- Named Organization
- Lig, Liggett
- 164 195 100 11 Netacgi Nph Parser Sect1
- Subject
- scor
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United States Patent: 4,257,430
Page 11 of 16
A series of experiments was undertaken to evaluate the effect of temperature on the
rate of formation of insoluble palladium in a casing formulation containing:
Component Weight Percent
Invert Sugar 15.4
Flavor 4.4
Propylene glycol 2,2-
Glycerine 6.5
Corn Syrup 4.9
Lactic Acid 0.5
(NH.sub.4).sub.2 PdCi.sub.6
1.2
Mg(NO.sub.3).sub.2 . 6H.sub.2 0
Water 33 2
100.0
Three separate mixtures were prepared, held at 23.degree. C., 60.degree. C. or
70.degree. C., and periodically analyzed to determine soluble palladium. The
insoluble palladium formed after one hour was determined, and is used as a measure
of the rate of the first stage reaction. In addition, the first order rate constant, k was
calculated from a plot of the logarithm of soluble palladium against time. The data are
summarized as follows:
Insoluble Palladium
Formed in 1 Hr., as %
Rate Constant,
Temperature, .degree.C.
of Total Palladium
k, hr..sup.-1
23 0 0.00
60 36 0.03
70 41 0.19 0
0
w
co -
~-
a
rn
EXAMPLE 3
Employing procedures and materials similar to those described in Example 2, except
0
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United States Patent: 4,257,430
EXAMPLE 1
Page 10 of 16
A casing formulation was prepared in accordance with the following table:
Component
Invert Sugar
Glycerine
Corn Syrup
Flavor
Gum Tragacanth
Mg(NO.sub.3).sub.2
5% Aq*(NH.sub.4 2
(pH = 1.5)
Water
*Aqueous
Weight Percent
23.56
3.84
6.12
3.87
0.25
6H.sub.2 0
34.30
Pd(Cl.sub.4)
10.30
17.76
100.00
The resulting solution was heated at 77.degree. C. and the solution was periodically
analyzed for soluble palladium and total palladium. The results of these analyses are
summarized as follows:
Time, hr. Palladium Present in Casing
as % of Total Palladium
Soluble Insoluble
1 27.5 72.5
2 15 85
3 10 90
4 7 93
5 3 97
20 1 99
The formation of insoluble palladium was found to occur in two stages: the first, by a
rapid reaction which is essentially complete in about 1 hour, and the second by a
slower reaction which appears to obey first order kinetics.
EXAMPLE 2
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United States Patent: 4,257,430 Page 16 of 16
*Added as Mg(NO.sub.3).sub.2 . 6H.sub.2 O
**Extrapolated from data curve from 74 week results to 80 weeks
As is evident from the foregoing, the yield of polycyclic aromatic hydrocarbons and
the incidence of tumors in mice both decrease as the amount of non-extractable
palladium increases. In general, substantial reductions in the incidence of tumors are
achieved when the amount of total nitrate is in excess of about 0.4 weight percent and
the amount of non-extractable palladium is greater than about 100 ppm. It is preferred,
however, that there be employed at least about 0.7 weight percent total nitrate nitrogen
and at least about 250 ppm of non-extractable palladium. Most preferably, there
should be employed at least about 0.7 weight percent total nitrogen and at least about
450 ppm of non-extractable palladium.
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United States Patent: 4,257,430
Page 15 of 16
purposes of evaluating the effect of changes in nitrate and palladium content, and the
amount of non-extractable palladium on biological activity, the individual values for
percent tumor incidence and yield of PCAH were averaged.
% of
Sample Yield of PCAH Tumor Incidence
A-1 2.258 42.0
B-1 2.329 47.9
C-1 2.245 41.9
D-1 2.148 55.3
Average 2.245 46.8
For each experimental run, the ratios of the observed yield of PCAH and tumor
incidence to the average of the control values were calculated. The results are
summarized in Table III.
TABLE III
PCAH Yields and Tumor Incidence
of Test Samples Compared With Controls
Biological
Response
Total Nit.
Added Nit.
ppm Pd PCAH Yield
as % of
Sample
Nitrogen %
Nitrogen %*
Total
Non-Ext
As % of Ave. Con.
Avg Control
A-2 0.22 -- 470 300 92.3 84.6
C-2 0.55 -- 0 -- 88.4 88.2
B-2 0.47 -- 580 80 69.1 69.7
B-3 0.59 -- 580 140 68.5 (56)**
D-4 0.80 -- 820 210 56.0 53.4
D-3*
0.69 -- 660 180 63.2 46.4
C-3 0.75 0.47 0 -- 84.4 57.9
D-2 0.77 0.46 550 160 56.7 36.3
C-4 0.73 0.44 440 260 68.5 17.7
A-3 0.74 0.44 550 360 62.9 4.9
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llnited States Patent: 4,257,430
Page 1 of 16
US PATENT & TRADEMARK OFFICE
PA"1"I~N`?' FULL `7]~X"[" AND llh+AGIE4 ~`1..Fi"'E"AMASZ
1Te+,vSl-iapPirig U'art
(_1,of1)
United States Patent 4,257,430
Collins, et at. March 24, 1981
Tobacco composition including palladium
Abstract
Improved palladium-containing smoking tobacco compositions wherein the palladium
in a highly active form is obtained by depositing on the tobacco palladium which has
been insolubilized by admixing in an aqueous medium a water-soluble palladium
compound and a reducing agent capable of reducing dissolved palladium cations to
insoluble palladium. Methods for determining the amount of insoluble or active
palladium are described.
Inventors: Collins; Peter F. (Durham, NC); Bryant, Jr.; Herman G. (Durham, NC);
Pullman; James O. (Chapel Hill, NC)
Assignee: Liggett Group Inc. (Montvale, NJ)
Appl. No.: 013575
Filed: February 21, 1979
Current U.S. Class: 131f300; 131/309; 131/352
Intern'l Class: A24B 015/28; A24B 015/42
Field of Search: . 131/t40 B,17 R,2,15 R,140 R
Referenc,es Cited.Referenged Byj N
°
-
Patent Documents
U
S o
o
~ _ .
.
.
4055191 Oct., 1977 Norman et al. 131/9. rn
cc
~
Primary Examiner: Millin; Vincent
Attorney, Agent or Firm: Ross, Jr.; J. Bowen cn~
W_
Claims
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United States Patent: 4,257,430 Page 14 of 16
Series
Sample
Native
Total
Total Non-Extractable
A 1* 0.22 0.22 0 --
2* 0.22 0.22 470 300
3* 0.30 0.74 550 360
B 1 0.22 0.22 0 --
2 0.47 0.47 580 80
3 0.59 0.59 580 140
C 1 0.17 0.17 0 --
2 0.55 0.55 0 --
3 0.28 0.75 0 --
4 0.29 0.73 440 260
D 1 0.23 0.23 0 --
2 0.31 0.77 550 160
3** 0.69 0.69 660 180
4 0.80 0.80 820 210
*These samples are the controls and Samples A and B employed in
"Biological Test" of U.S. Pat. No. 4,055,191.
**0.42 weight % Mg.sup.++ added as a 1/1 mixture of magnesium ma
magnesium acetate to the tobacco
TABLE II
eummary of Evaluation of Tobacco Smoke and Condensate
Active PCAH Yield,
f A
i
l
%
Series Sam o
n
ma
s
ple mg per gram of dry smoke
with Tumors
A 1 2.258 42.0
2 2.073 39.6
3 1.412 2.3
B 1 2.329 47.9
2 1.551 32.6
3 1.538 43.8(22.5)*
C 1 2.245 41.9
2 1.948 41.3
3 1.895 27.1
4 1.537 8.3
D 1 2
148 55
3 PJ
. . 0
2 1
272 17
0 00
. . -1 .
3 1.419 21.7 CF)
4 1
258 25
0 to:
. . da
A
*In this experiment, there was a sudden anomolous increase in th O) ''
CO ^
of tumor bearing mice following the 74th week. The value in pare
estimated from the tumor incidence observed through the 74th wee
In the four series of tests, Samples A-1, B-1, C-1 and D-1 served as controls. For
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United States Patent: 4,257,430 Page 3 of 16
This invention relates to smoking compositions comprising tobacco having associated
therewith palladium as a catalytic agent. More particularly, the present invention is
concerned with tobacco compositions including palladium as a catalytic agent wherein
the palladium is in a highly active form. This invention is also concerned with a
method for admixing smoking tobacco and palladium whereby the palladium is
deposited in a highly active catalytic form.
RELATED APPLICATIONS AND PATENTS
The subject matter of this invention is related to the subject matter of U.S. Pat. No.
4,055,191, granted Oct. 25, 1977 to V. Norman and H. G. Bryant, Jr. for "Tobacco
Composition", and (Ser. No. 344,589 filed Mar. 26, 1973 by H. G. Bryant, Jr., T. B.
Williams and V. Norman for "Smoking Composition").
BACKGROUND
As is summarized in U.S. Pat. No. 4,055,191, the proportion of polycyclic aromatic
hydrocarbons (PCAH) in the smoke from tobacco can be materially reduced by
incorporating palladium into the tobacco. It is further disclosed that palladium in
combination with a nitrate salt, preferably magnesium nitrate, is even more efficient in
reducing PCAH. Moreover, the combination of palladium and nitrate was shown in
tests on mice to materially reduce the biological activity of tobacco smoke condensate
obtained by smoking cigarettes on a wheel-type smoker as described in
DESCRIPTION OF THE INVENTION
In work undertaken to evaluate the effect of palladium and nitrate on the biological
activity of tobacco smoke, certain anomalous results were observed. Subsequent
evaluation of the data obtained in the course of this work indicated that the activity of
the palladium depended on the form of the palladium which was deposited on the
tobacco, which in turn was highly dependent upon the procedure employed. More
particularly, it has been found in accordance with this invention that the effectiveness
of palladium in reducing the biological activity of tobacco smoke is dependent on the
amount of "non-extractable palladium", as hereinafter defined, which is deposited on
the tobacco. The amount of "non-extractable palladium", in turn, is dependent on the
deposition of the palladium from an aqueous composition including "insoluble
palladium", as hereinafter defined.
Accordingly, it is an object of this invention to provide a smoking tobacco including
palladium in a highly active form.
It is another object of this invention to provide palladium-treated smoking articles
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United States Patent: 4,257,430
What is claimed is:
Page 2 of 16
1. A method for the deposition of catalytically active metallic palladium on smoking
tobacco comprising:
(a) Forming an aqueous solution containing a soluble palladium compound, and a
compound capable of reducing ionic palladium cations to palladium metal, said
solution having a pH of no more than 3;
(b) Heating said solution at an elevated temperature for a period of time sufficient to
convert at least about 50 percent of the palladium to insoluble palladium; and
(c) Admixing the casing solution with tobacco to deposit thereon said insoluble
palladium.
2. A method according to claim 1 wherein said reducing agent is a hydroxyl
containing aldehyde.
3. A method according to claim 2 wherein said reducing agent is a sugar.
4. A method according to claim 1 wherein said aqueous solution containing palladium
is a casing solution including at least one sugar and at least one polyhydroxy
compound.
5. A method according to claim 4 wherein said soluble palladium compound is
selected from the group consisting of palladium nitrate, palladium chloride, palladous
dichlorodiamine, ammonium tetrachloropalladate and ammonium
hexachloropalladate.
6. A method according to claim 5 wherein said palladium salt is ammonium
tetrachloropalladate.
7. A method according to claim 1 wherein said heating is at a temperature of from
about 50.degree. C. to about 90.degree. C.
8. A method according to claim 4 wherein said heating is at a temperature of from
about 50.degree. C. to about 90.degree. C. for a period of time sufficient to convert at
least 95 percent of soluble palladium to insoluble palladium.
_ _ .......... ._........... - --- - --
--------
Description_
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United States Patent: 4,257,430 Page 13 of 16
EXAMPLE 5
Several casing solutions containing various amounts of soluble palladium were
prepared and employed to treat tobacco samples which then were analyzed for
extractable palladium. The data for these runs is summarized as follows:
% of Total Palladium
Sample Soluble Pd
in Casing Extractable Pd
in Tobacco
1 74.7 87.1
2 67.0 80.4
3 61.4 68.3
4 46.9 63.3
5 32.8 49.7
6 25.8 42.7
As is evident from the foregoing, the proportion of extractable palladium in the
tobacco is proportional to, but greater than, the proportion of soluble palladium in the
casing solution. Consequently, even if the amount of soluble palladium in the casing
is reduced to zero, the resulting tobacco will nonetheless contain extractable
palladium, perhaps amounting to 10 percent or less of the total palladium.
EXAMPLE 6
Employing procedures similar to those described in the Biological Test described in
U.S. Pat. No. 4,055,191, cigarette tobacco was treated with casings including
palladium. The tobaccos employed had varying natural nitrate contents, and in some
instances the casings also contained added magnesium nitrate. The tobacco samples
were then employed to prepare sample cigarettes which then were smoked on the
wheel-type smoker to collect smoke condensate used for mouse-painting tests. For
each tobacco sample, the incidence of tumor-bearing mice, as a percentage of the total
mice at risk, was determined after 80 weeks. In addition, the nitrate content (native
nitrate and added nitrate) and the palladium content (total and non-extractable) was
determined. Finally, the yield of polycyclic aromatic hydrocarbons in the dry smoke
was determined. The data are summarized in Tables I and II.
~ ~.
TABLE I
O)
Summary of Content of Tobacco Samples V
Nitrate Content, %
Palladium Content, ppm
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United States Patent: 4,257,430 Page 9 of 16
hydrochloric acid is added, the cover is replaced and the mixture is heated to boiling.
Then 10 ml of water are added to the residue and the mixture is digested by heating
near boiling (80.degree.-100.degree. C.) for 10 minutes. The solution is then cooled to
room temperature and diluted to 25 ml with water to form a sample to be subjected to
analysis for palladium.
II. Analysis for Insoluble Palladium in Casing
The insoluble palladium in the casing is that palladium in casing which is not soluble
in water, and is determined by subtracting soluble palladium from total palladium.
Total and soluble palladium are determined by the following procedures:
Determination of "Total Palladium" In Casing
An accurately weighed sample of about 0.3 gm of well mixed casing is placed in a
100-m1 beaker, and 5 to 10 ml of 1:1 nitric acid and perchloric acid is added. The
resulting mixture is then worked up following the procedures described for
determining total palladium in tobacco.
Determination of "Soluble Palladium" In Casing
A 0.3 to 3.0 ml portion of casing is accurately weighed in a 10 ml volumetric flask,
and is diluted to 10 ml with water. The resulting solution is thoroughly mixed and is
immediately filtered through a membrane filter having a pore size of not greater than
0.45 microns. A 2 to 5 aliquot of filtrate is mixed with 5 to 10 ml of 1:1 nitric acid and
perchloric acid, and the resulting solution is treated as described above to achieve a
sample for analysis for "soluble palladium". In carrying out this procedure, it is
desirable to select sample and aliquot sizes so that there will be at least 15
micrograms, and preferably 50 to 200 micrograms, of palladium in the sample for
analysis.
III. Palladium Analysis
Any procedure capable of accurately determining the quantity of palladium in the
thus-obtained samples of "Total", "Extractable" and "Soluble" palladium may be
employed. When analyzing for total palladium, atomic absorption spectroscopy has
been found sufficient. When analyzing for "Extractable" or "Soluble" palladium,
however, a more sensitive procedure is desirable. It has been found that the procedure
of O. Menis and T. C. Rains, "Colorimetric Determination of Palladium With Alpha-
Furildioxime," Anal. Chem., 27, 1932-34 (1955), is suitable for this purpose. In the
examples which follow, "Extractable" or "Soluble" palladium was determined by
adapting the Menis et al. procedure to automatic analysis with a Technicon Auto-
Analyzer I.
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United States Patent: 4,257,430 Page 8 of 16
composition of the extraction medium is maintained constant, reliable results
permitting accurate control of the process are obtained.
The following examples are illustrative of the present invention, including the
preparation of casings containing insoluble palladium, the formation of tobacco
compositions containing non-extractable palladium, and the testing of such tobacco
compositions. In the examples, the tobacco samples and the casing samples were
analyzed for non-extractable and insoluble palladium, respectively, by the following
procedures:
I. Analysis for Non-Extractable Palladium in Tobacco
The "non-extractable" palladium is the palladium in tobacco which is not extracted
with ammoniacal ethylenediamine tetra-acetic acid, and is determined by subtracting
the extractable palladium from total palladium. The total palladium and extractable
palladium are determined by the following procedure:
Determination of "Total Palladium" In Tobacco
An accurately weighed sample of about 1 gram of tobacco is placed in a 100-ml
beaker, 5 to 10 ml of 1:1 reagent grade nitric acid and reagent grade perchloric acid is
added, the beaker is covered with a cover glass and heated on an electrical hot plate at
a moderate rate for at least 2 hours. The cover is then removed, and heating is
continued to evaporate the sample to dryness. The beaker is then cooled to ambient
temperature, 1 ml of reagent grade concentrated hydrochloric acid is added, and the
cover is replaced. The mixture is heated to boiling momentarily, 10 ml of 0.1 N nitric
acid is added, and the solution is digested by heating near boiling (80.degree.-
100.degree. C.) for 10 minutes. The solution is cooled to ambient temperature, and
diluted with 0.1 N nitric acid to 25 ml to form an analytical sample.
Determination of "Extractable Palladium" From Tobacco
An accurately weighted sample of tobacco weighing from about 1 to about 2 grams is
mixed with 50 ml of an ammoniacal solution of ethylenediamine tetra-acetic acid
(EDTA) (0.1 M in EDTA and 1 M in NH.sub.4 OH) having a pH of about 10. The
resulting mixture is continuously agitated for 30 minutes, and is immediately filtered
through a membrane filter having pore size of not greater than 0.45 microns. A 10.0
ml portion of the filtrate is evaporated to dryness in a 100-ml beaker and 5 to 10 ml of
1:1 reagent grade nitric acid and reagent grade perchloric acid is added to the residue.
The beaker is covered with a cover glass and heated on an electrical hot plate at a
moderate rate for at least 2 hours after the appearance of HC1O.sub.4 fumes, the cover
is then removed and heating is continued to evaporate the sample to dryness. The
beaker is cooled to ambient temperature, 1 ml of concentrated reagent grade
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United States Patent: 4,257,430
about 70.degree. C. to about 80.degree. C. being preferred.
Page 7 of 16
The heating is carried out for a period of time sufficient to effect the desired degree of
conversion of soluble palladium to insoluble palladium. It is preferred that there be
substantially total conversion of soluble palladium to insoluble palladium, thereby
achieving the maximum catalytic activity possible. Complete conversion is not
essential, however, and useful results are achieved when the proportion of soluble
palladium is reduced to less than about 50 percent of the total palladium in the
solution. It is preferred, however, that the soluble palladium in the solution be reduced
to not more than 5 percent of total palladium. In general, this will require heating for
at least about 4 hours at 75.degree.-80.de ree. C., and a correspondingly longer time
at lower temperatures. Heating for still longer times can be employed if desired, but
ordinarily is unnecessary. Extended heating periods, i.e., for 24 hours or more,
especially at temperatures of about 80.degree. C., or above, are not desired because of
the increased risk of agglomeration or the formation of undesirable degradation
products.
After formation of insoluble palladium, the resulting aqueous mixture is then applied
to the tobacco by any suitable technique, such as those commonly employed to apply
casing solutions to tobacco. For example, the mixture may be sprayed onto the
tobacco. The thus-treated tobacco is then formed into smoking articles such as cigars
or cigarettes, or packaged as pipe tobacco.
The resulting tobacco product will contain non-extractable palladium in an amount
proportional to the amount of insoluble palladium in the solution used to treat the
tobacco. However, the relative proportion of non-extractable to total palladium in the
tobacco will be somewhat less than the proportion of insoluble to total palladium in
the treating solution. When the preferred levels of soluble palladium (5 percent or less
of the total palladium) are achieved in the aqueous medium, the extractable palladium
ordinarily comprises no more than about 10 percent of the total palladium in the
tobacco.
This difference may be due to the use of alkaline EDTA as the extracting medium. It
also has been observed that the specific base employed in preparing the alkaline
EDTA extraction medium will affect the absolute value of extractable palladium
found. Consequently, in analyzing for extractable palladium it is important that the
same extraction medium be employed. The alkali metal hydroxides, e.g., sodium
hydroxide and potassium hydroxide, and ammonium hydroxide are the preferred
alkaline materials used to form the extraction medium. Ammonium hydroxide is
especially preferred. The pH of the extraction medium is not narrowly critical, nor is
the concentration of EDTA. It is preferred, however, that the pH be approximately 10
(i.e., from about 9.5 to about 10.5), and that the concentration of EDTA be
approximately 0.1 molar (i.e., from about 0.09 to about 0.11 molar). So long as the
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United States Patent: 4,257,430 Page 4 of 16
wherein the palladium is in a form which minimizes the biological activity of the
smoke therefrom.
Still another object of this invention is to provide a method for depositing palladium
on tobacco in a more active form.
More specifically, an object of this invention is the provision of a method for
depositing palladium on smoking tobacco which maximizes the proportion of non-
extractable palladium on the tobacco.
A still further object of this invention is the provision of an analytical method for
determining the proportion of palladium which is in a form capable of reducing the
biological activity of tobacco smoke.
According to U.S. Pat. No. 4,055,191, palladium is incorporated into a tobacco
composition either in finely-divided metallic form and/or in the form of a palladium
salt which is decomposable, in situ, preferably by heat, into metallic palladium. A
preferred procedure which is disclosed is the deposition of palladium, initially in the
form of an ammonium chloropalladate salt, in combination with a nitrate com ound,
from a solution of these additives in a conventional casing so ution comprising
glycerine, propylene glycol and sugars.
It has been discovered in accordance with this invention that the catalytic activity of
the palladium is highly dependent upont the proportion of palladium which is in the
form of "non-extractable palladium", which in turn is highly dependent upon the
conditions under which the palladium is applied to the tobacco.
As employed herein, the term "extractable palladium" is that palladium deposited on
the tobacco which can be extracted from treated tobacco by aqueous, alkaline
ethylenediamine tetraacetic acid (EDTA). The chemical form of this "extractable
palladium" is not known; it may be a form of metallic palladium in view of available
evidence that the extracting medium can dissolve small particles of palladium metal,
or it may be ioNc palladium or a mixture of metallic anc ionic palladium. The term
"non-extractable palladium" as employed herein is that palladium deposited on the
tobacco which is not extracted from treated tobacco by aqueous, alkaline EDTA. The
form of this "non-extractable" palladium is thought to be metallic palladium on the
basis of available evidence. The specific value of extractable palladium which is
obtained will be dependent, inter alia, on the composition of the EDTA reagent, and
the conditions of the treatment of the casing or tobacco. However, for each set of
conditions, consistent results are obtained, and it is estimated that a single
determination of extractable palladium has a standard deviation of 0.001 percent
palladium, which corresponds to about 1 to about 10 percent of the total palladium
preferably employed in accordance with U.S. Pat. No. 4,055,191.
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United States Patent: 4,257,430 Page 12 of 16
that the casing solution contained 1.5 percent (NH.sub.4).sub.2 PdCl.sub.4 rather than
1.2 percent (NH.sub.4).sub.2 PdCl.sub.6, and the amounts of Mg
(NO.sub.3).sub.2.6H.sub.2 0, glycerine and water were each reduced by 0.1 percent,
there was prepared a casing solution having a pH of 2.5, in contrast to a pH of 0.8 for
the solutions of Example 2. The solution was heated at 70.degree. C. and periodically ,
analyzed for soluble palladium. The insoluble palladium formed in the first hour was
59 percent of the total palladium, and the first order rate constant, k was 0.25 hr..sup.-
1.
EXAMPLE 4
The experiments described in Example 3 suggested that pH affected the rate of
formation of insoluble palladium; however, the level of total palladium in that
experiment was greater than in the experiments described in Example 2.
Consequently, two new experiments were performed at constant total palladium
content to evaluate the effect of pH alone. The compositions of the casing solution
and the analytical results after heating at 70.degree. are as follows:
Solution
Component, weight %
A B
Invert Sugar 10.2 10.1
Flavor 2.9 2.8
Propylene glycol 1.4 1.4
Glycerine 4.3 4.3
Corn Syrup 3.2 3.2
Lactic acid 0.3 0.3
(NH.sub.4).sub.2 PdCl.sub 6
0.80
(NH.sub.4).sub.2 PdCl.sub.4
0
6
.
(Total Pd) (0.22) (0.22)
Mg(NO.sub.3).sub.2 .sub.2
~18_7 18.6
Water 58.2 58-'T
Total 100.00 100.00
pH 0.8 2.5
Insoluble Pd as %
Total Palladium, 1 of
hr.
56
3
C `
00
Reaction Constant,
k, hr..sup.-1
0.25
0.61 i -..
to ,
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United States Patent: 4,257,430 Page 5 of 16
In the practice of this invention, there is formed an aqueous solution containing a
dissolved palladium compound and a compound which acts as a reducing agent for
ionic palladium. The solution is heated at a temperature of up to about 80.degree. C.
for a period of time sufficient to form "insoluble palladium", and the resulting mixture
is blended with tobacco to deposit the palladium on the tobacco.
As employed herein, "soluble palladium" is that palladium in an aqueous mixture,
which when the mixture is diluted with water and filtered through a membrane filter
with 0.45.mu. pores, appears in the filtrate. The palladium which is retained on the
filter is defined as "insoluble palladium". The chemical form of this "insoluble
palladium" has been found to be predominantly, if not completely, metallic palladium.
The chemical form of the "soluble palladium" is considered to be essentially all ionic,
based on available evidence. Though the precise forms of soluble and insoluble
palladium have not been conclusively established, the present invention is intended to
extend to "insoluble palladium" formed in the manner described, regardless of the
precise chemical and physical form of the palladium.
The palladium compound which is employed can be any water-soluble compound
containing palladium which is capable of yielding ionic palladium, such as the salts
disclosed in U.S. Pat. No. 4,055,191. Such compounds include simple salts such as
palladium nitrate, palladium halides such as palladium chloride, diammine complexes
such as palladous dichlorodiammine (Pd(NH.sub.3).sub.2 Cl.sub.2), and palladate
salts, especially ammonium salts such as anunonium tetrachloropalladate and
ammonium hexachloropalladate.
The amount of palladium compound in solution is not critical, provided the
concentration is adequate to deposit sufficient palladium on the tobacco to provide the
desired catalytic effect. As is taught by U.S. Pat. No. 4,055,191, the palladium can be
present in the tobacco in amounts of from about 0.001 to about 1 wei ht ercent and
preferably from a out 0.01 to about 0.1 wei~h~ercent. It has been found that the rate
~~~n ~~~
o t"I 1i "~e re uc on o~~~f b~e pallac~iumto insoluble palladium increases with decreasing
palladium concentration. On the other hand, if the solution is too dilute, excessive
amounts of solution may be required to deposit a catalytically effective amount of
palladium. In general, palladium concentrations of from about 0.1 to about 2 weight
percent palladium are useful, with concentrations of from about 0.2 to about 0.5
weight percent palladium being preferred.
A second required component of the solution (other than water) is a reducing agent
capable of reducing dissolved palladium ionic to metallic palladium. Since palladium
salts are well known as oxidizing agents any mild reducing agent may be used.
Although any compound capable of reducing ionic palladium can be employed, as a
practical matter the reducing agent should be non-toxic and should not form toxic by-
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United States Patent: 4,257,430
Page 6 of 16
products when pyrolyzed during smoking. In addition, the reducing agent should be
water soluble. Preferred reducing a ents are organic aldeh des, m~Cl~in4 hydroxyl
containing aldehydes such as the ugars e.g. ucose t~tnannos (galactos~,~xylose~
tribos abinose. Other sugars containing hemiacetal or~kefo groupings may be
employed, e.g. maltose, sucrose, lactose, fructose and sorbose. Pure sugars may be
employed, but crude sugars and syrups such as honey, corn syrup, invert syrup and the
like may also be employed. Other, albeit less effective reducing agents include
alcohols, preferably polyhydric alcohols, such as Ig ycer~l, sorb~itol, the ls
especially ethylene glyco and propylene glycol, and polyglycols such as ol eth~lene
a dn polyprop~ ylerie gTycols Meit '~MT"1VMdfft?'gtMe re uc~" ng agnts may be used
suc as car on monox~. e, hydrogen, ethylene, and titanous salts.
The solution may contain still other additives which do not interfere with the
interaction of the palladium compound and the reducing agent. Thus, the solution may
contain a nitrate salt of the type disclosed in U.S. Pat. No. 4,055,191.
It will be appreciated by those skilled in the art that the reducing agents referred to
above are commonly employed components of casing solutions heretofore employed
in the manufacture of smoking tobacco, and indeed the addition of a water-soluble
palladium salt to a conventional casing solution is a convenient, and preferred, method
of practicing the present invention. Although the use of such casing solutions has been
described in U.S. Pat. No. 4,055,191, there is no recognition in that patent that a
heating step, as hereinafter described, is required as a practical matter to form
insoluble palladium.
The insolubilization of~alladium will occur very slowly at ambient temperature, and
. .~.,.a;a~n .e...s.° .w,av:cx~.ua.m,vwww.u.....c .< ~nt~s,zcaa,a. :.,..nw~s..~ r^a
exce vel lon ~enods of time are re~uirec to ac~iieve practica conversions of the
ua3ru ap. e TFCa.A`Yd~e~ ~vf isul^'..3.a.1.mLrcw.:-.(:tir. 2cRa+ ~~ .T~kNl1nY'~' VS".4Yu4-4Y.Csolu e
p adium to msolubpe palla~ium. Conse uen~C ~o achieve practica~ rates o~
~
~ ~
~
~.~ ~ : . ~ .~ ~ ' ~
conversi
_on_the so~uhon is heaiec~at eEl'evated temperatures, with the rate of ormarion
~ ,~.~~ ~~.~..d.~.,- of insoluble palladium increasmg wil7i increasmg temperature. However, as the
temperature increases, the insoluble palladium tends to form agglomerates of
insoluble palladium which presents difficulties in obtaining uniform distribution of
the metal. The formation of such agglomerates can be inhibited through the inclusion
of pro elatin ums such as gum tragacanth, and the like, in
1 weight percent, and pre era y rom a out . o a ou 6Z" "
amounts of up to 7
weight percent ac ~. "~ica ion, er~o Ou Re~Cas 2e 89),~ fi on
d
.. .:..n ...w= ec. -...+
.
""'
44-^%m+.*»r++4
'^'
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N
o
°° -
ve.. W
.
.
Mai%+haYa:u:xlYr
.J sc oF3:
T'
even date herewitclosure of wluc~ is mcorporated ~ierem by reference
7h
~
. ~~
However, at tempn excess of about~g ilegree. C the formation of the
palladium agglomerates becomes excessive. Fu~ftYreitYio~ xtended heating at fk- ;:
elevated temperatures can cause breakdown of sugars or other compounds present in
the aqueous solution, forming decomposition products which have an adverse effect
on the taste of tobacco smoke. In general, then, temperatures in the range of from
about 50.degree. C. to about 90.degree. C. are employed, with temperatures of from
0
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