CF-Matter and the
Cold Fusion Phenomenon*
Hideo Kozima†
Physics
Department, Portland State University
Portland,
OR97207‑0751, USA
Email
address: cf‑lab.kozima@nifty.ne.jp
The
working concept of “cf-matter,” defined as “neutron drops in a thin neutron
liquid” as described in previous papers, is used to explain complex events, especially
nuclear transmutations, in cold fusion phenomenon (CFP). In samples used in CF
experiments, the cf‑matter contains high‑density neutron drops in surface/boundary
regions while in the volume it contains only a few of them, in accordance with
experimental data. Generation of various nuclear transmutations, the most interesting
features in CFP, are explained naturally if we use the concept of the cf-matter.
Qualitative correspondence between the relative isotopic abundance of elements
in the universe and the number of observations of elements in CFP is shown
using more than 40 experimental data, sets. This facts is an evidence showing
statistically that CFP in transition‑metal hydrides/deuterides is a low energy version
of nuclear processes occurring in the stars catalyzed by, specific neutrons in the
cf‑matter formed in surface/boundary regions of CF materials.
A characteristic of stability of nuclides is
relative isotopic abundance in the universe. A data is given in Tables 1 and 2
picked up from Table III of' Suess et al.1) The relative abundance
of the observed stable species depends oil the process of creation, which may
have singled out particular nuclear types for preferential formation and also
depends on the nuclear stability limits.2)
These
characteristics of nuclides in the stars (and the primordial universe) given in
Tables 1 and 2 should be closely related to appearance of new nuclides in
experimental observations of CFP if the processes in CF materials have some common
nature to those, in the stars. It is probable that the more stable a nuclide
is, the more often observed the nuclide produced in complex processes occurring
in CF materials.
Table
1: Relative isotopic abundance in the universe (I). Light even-even nuclei (A
< 60) at around abundance peaks from Table III of Suess et al.1)
The “Log10H” in the second row stands for “Log10 relative
abundance.”
Nuclides |
115B |
126C |
147N |
168O |
2010Ne |
2412Mg |
2713Al |
2814Si |
3115P |
Log10H |
1.3 |
6.6 |
6.8 |
7.3 |
6.9 |
5.9 |
5.0 |
6.0 |
4.0 |
Nuclides |
3216S |
3617Cl |
18A |
19K |
4020Ca |
4521Sc |
22Ti |
23V |
24Cr |
Log10H |
5.6 |
4.0 |
5.2 |
3.5 |
4.7 |
0.4 |
3.4 |
2.3 |
3.9 |
Nuclides |
5525Mn |
5626Fe |
5927Co |
5828Ni |
29Cu |
6430Zn |
|
|
|
Log10H |
3.8 |
5.8 |
3.3 |
4.4 |
2.3 |
2.7 |
|
|
|
Table 2: Relative isotopic abundance in the universe
(II). Heavy nuclei (element) (A > 88) from Table III of Suess et al.1)
The "Log10H" in the second row stands for "Log10
relative abundance."
Nuclides |
8838Sr |
9040Zr |
42Mo |
44Ru |
46Pd |
47Ag |
50Sn |
52Te |
54Xe |
56Ba |
Log10H |
1.2 |
1.5 |
0.4 |
0.2 |
0.08 |
0.04 |
0.12 |
0.67 |
0.60 |
0.56 |
Nuclides |
13957La |
58Ce |
59Pr |
13977Ir |
78Pt |
79Au |
80Hg |
82Pb |
83Bi |
|
Log10H |
0.30 |
0.35 |
0.06 |
0.09 |
0.21 |
0.02 |
0.05 |
0.07 |
0.02 |
|
2. Formation of the cf‑matter
By
the mechanism shown in previous papers,4-6) the cf‑matter
(interacting particle feature) is formed in boundary/surface regions when there
are the neutron valence bands (independent-particle feature) mediated by
hydrogen isotopes in fcc/hcp transition‑metal
hydrides/deuterides and proton conductors where hydrogen isotopes are in states
with extended wave functions
In a homogeneous neutron star matter, i.e. a neutral
medium composed of high density (nG) neutrons, protons and
electrons, as the simulation by Negele et al.7) had shown, there
appears the Coulomb lattice of neutron drops AZ in a thin neutron liquid (with a density of nb)
by the self‑organization. In the case of the cf-matter in CF materials, there
is a crystal lattice, which seems to make appearance of the Coulomb lattice of
neutron drops easier as experimental facts in CFP suggest than in the neutron
star matter.
3. Coulomb lattice in the cf‑matter
Several features of the characteristics of the
Coulomb lattices of neutron drops (clusters of neutron, proton and electron) in
neutron star matter are tabulated in Table 3.7) In this table, we
added the proton‑to‑neutron ratios x
of palladium, iron, and carbon nuclei averaged over isotopes by natural abundance,
which are 0.77, 0.87, and 1, respectively.
In
the work by Negele et al.,7) it was shown that a neutron star
appears as a stable state when the density nG of the neutron
star matter increased from 3×1035
to about 1038cm-3. If we change the parameter nG
to the opposite direction, we will reach a situation where appear various
atoms, principally the situation where elements are created in the stars; the
more stable a nuclide is, the higher its production rate becomes. Comparing
isotopic abundances in the universe (Tables 2 and 3) to experimental data of
nuclear transmutation in CFP, we can show that CFP in CF materials is a similar
process to those producing elements in the stars.
Table
3: The theoretical 7) and extrapolated to nG = 1×1030 cm-3
values of the lattice constant a of Coulomb lattice, the proton‑to-neutron
ratio x in
the neutron drops AZ (n-p clusters) and
background neutron density nb as functions of nG, the
density of the original neutron gas, where nb is the density
of the neutron liquid surrounding the neutron drops. The density of nucleons
init neutron drop n is approximately constant and equal to 1038 cm-3 in the range where simulation is performed;
n ≈1038 cm-3.
For reference, a and x for the lattice of Pd metal and x,
of Fe and C nuclei (all averaged over isotopes with natural abundances) are
added along with extrapolated values of nb corresponding to
their x.
nG cm−3 |
5×1037 |
5.7×1036 |
6×1035 |
1×1030 |
Pd |
Fe |
C |
nb a (A) x |
4×1037 4×10−4
0.28 |
5×1036 7×10−4
0.45 |
2×1035 9×10−4
0.53 |
1×1029 2×10−3 0.75 |
1027 2.5 0.77 |
1022 0.87 |
1016 1 |
nb /nΔ |
4×10−1 |
5×10−2 |
3×10−3 |
1×10−9 |
5×10−11 |
10−16 |
10−22 |
4. Interaction of the cf‑matter with
extraneous nuclides in terms of experimental data
We assume
that the cf‑matter is formed in surface/boundary regions of CF materials when
there are formed neutron valence bands.4,5) We concentrate at nuclear
transmutations in CFP in this paper, while other events are naturally
accompanied with them. It should be pointed out here about emission of light
particles and photons from CF materials sometimes measured in experiments. The
cf‑matter is formed principally in boundary/surface regions of CF materials and
dissipation of liberated energy in the unclear reactions is confined in the cf‑matter.
When the place where the nuclear reaction occurs is on the border of the cf‑matter
very close to a surface of the sample, however, it is possible light particles
and/or photons are emitted outward to be measured outside. Especially, emission
of neutrons with up to more than 10 MeV is observed often as an example of this
mechanism.8)
5. Production of New Nuclides in CFP
There
are very many data of the nuclear transmutations (NTs) in CFP.
In Table 4, we give a summary of
experimental data sets obtained mainly after 1996 showing broad production of
new elements (Elements) with a number of papers reporting them (No. of papers).
In this table, about 40 data sets*) are counted including such
productions of Ag (from Pd) and Fe (from C and others), which is not
necessarily obvious but frequently occurring. A relation of frequency Nob
of the observations of elements in CFP and “Log10H relative
abundance” in Tables 1 and 2 will be discussed later.
The nuclear transmutations are
phenomenologically classified into four groups; NTA, NTD,
NTF, and NTT, i.e. nuclear transmutations (NT) by
absorption, by decay, by fission and by transformation,
respectively. The first three types of NTs are
induced by a transfer of a nucleon cluster azδ between the cf‑matter (or a neutron drop AZ) and a nuclides A’Z’X followed by various nuclear
processes in the systems to produce the final stable nuclide A”Z”X". Then the isotopic ratio of
the produced elements will differ from the natural abundance ratio. In the case
of NTT, we can expect the same isotopic ratio as the natural one as
explained below.
Table 4: Elements observed more than once in Cf
experiments (Z > 3). Number of papers reporting the observation, Nob,
is calculated from 40 papers mainly after 1996.
Elements Nob |
3Li 3 |
5B 1 |
6C 5 |
8O 1 |
9F 4 |
11Na 1 |
12Mg 6 |
13Al 9 |
14Si 12 |
15P 1 |
Elements Nob |
16S 6 |
17Cl 6 |
19K 6 |
20Ca 9 |
21Sc 1 |
22Ti 6 |
23V 2 |
24Cr 13 |
25Mn 6 |
26Fe 19 |
Elements Nob |
27Co 4 |
28Ni 10 |
29Cu 11 |
30Zn 13 |
31Ga 1 |
32Ge 3 |
33As 1 |
34Se 1 |
35Br 2 |
37Rb 2 |
Elements Nob |
38Sr 5 |
39Y 1 |
40Zr 1 |
41Nb 1 |
42Mo 5 |
46Pd 3 |
47Ag 7 |
48Cd 3 |
49In 2 |
50Sn 3 |
Elements Nob |
51Sb 1 |
52Te 2 |
54Xe 2 |
55Cs 1 |
56Ba 4 |
59Pr 1 |
62Sm 1 |
63Eu 1 |
64Gd 1 |
66Dy 1 |
Elements Nob |
67Ho 1 |
70Yb 1 |
72Hf 1 |
75Re 1 |
76Os 2 |
77Ir 2 |
78Pt 2 |
79Au 2 |
80Hg 2 |
82Pb 6 |
The
isotopic ratios observed in experiments differ sometimes from those calculated
from natural abundances while does not differ in others. The cause of the
discrepancy due to the processes of NTs will give a key to investigate nuclear
reactions in CFP.
In
these processes, no emission of photons and/or light nuclides to outside is
expected to occur different from reactions in free space except the processes that
occur on the border of the cf‑matter at surfaces of the sample.
5-1) Nuclear
Transmutation by Absorption (NTA)
The nuclear transmutation by
absorption, NTA, is a result of a process where a nuclide AZX
simply absorbs a cluster azδ of ν (= a −z:) neutrons and ν’= z protons from the cf‑matter: AZX + azδ= A+aZ+zX. In this process, the more stable the final
nuclide A+aZ+zX,
the more frequent it will be produced.
There
are many experimental data, showing production of new nuclides explicable only
by NTA if we do not use concepts outside the realm of modern
physics. Production of following nuclides are explained by NTA:
24Cr from 22Ti,
26Fe from 22Ti, 30Zn from 28Ni, 4019K
from 3919K, 4119K from 3919K,
4319K from 3919K, 8937Rb
from 85,8737Rb, 13455Cs from 13355Cs,
42Mo from 38Sr, 48Cd from 46Pd, 50Sn
from 46Pd, 52Cd from 46Pd, 56Ba from
46Pd, 59Pr from 53Cs, 82Pb from 74W,
82Pb from 46Pd.
Some
reactions producing nuclides with large decreases of Z and A occur and are
explained as a result of NTF (cf. Section c) below). However. it is
probable to assume reactions where occur transfer of a cluster of nuclides azδ from a nuclide AZX to a
neutron drop A+aZ+zΔ as inverse
processes of the normal NTA. Some examples of these reactions are
productions of following nuclides:
26Fe from 28Ni,
27Co from 28Ni, 25Mn from 28Ni, 24Cr
from 28Ni, 42Mo from 46Pd, 77Ir from
78Pt, 76Os from 78Pt, 78Pt from 79Au,
76Os from 79Au, 30Zn from 46Pd.
We
include these reactions in NTA hereafter.
5-2) Nuclear Transmutation by Decay (NTD)
One of the most frequently detected NTs in CFP
from early days of research is the nuclear transmutation by decay (NTD).
The
nuclear transmutation by decay, NTD is a result of a process where
the nuclides A+aZ+zX
(a=1, z=0) thus formed decays by emission of light nuclides, n, p,
or α, to form a new nuclide A’Z’X’.8)
Many data showing production of
nuclides with increase of proton number by one are explained successfully by this mechanism with ν= 1 and ν’ = 0 as shown in the analyses by the TNCF model.8,9) In this
process, the probability of the nuclide production will be governed by
stability of A+1ZX and also by that of the final nuclide A+1Z+1X’
(β decay) or A-3Z-2X’
(α decay).
Several
examples of this mechanism are production of following nuclides:
42He from 63Li, 83Li
from 115B, 14Si from 13Al, 20Ca
from 19K, 23V from 22Ti, 29Cu from 28Ni,
38Sr from 37Rb, 47Ag from 46Pd, 13554Xe
from 13455Cs, 79Au from 78Pt, 80Hg
from 79Ag.
5-3) Nuclear Transmutation
by Fission (NTF)
The
nuclear transmutation by fission, NTF, is a result of a process
where the nuclides A+aZ+zX (a≫1) suffers
fission producing several nuclides with nucleon and proton numbers largely shifted
from the value A + a and Z + z, respectively.8,13) The mass spectra
of nuclear products in the nuclear transmutation by fission, NTF,
observed in CFP can be explained as fission products of unstable nuclides A’+aZ’+zX’
formed by the above process similar to fission of 235U induced by a
fast neutron. In this process, the mass spectrum is determined by stabilities
of product nuclides.
There are many
experimental data showing production of various medieval mass-number nuclides
simultaneously. It is possible to explain dispersion of mass spectrum by the
liquid‑drop model of nucleus popular in nuclear physics assuming formation of
extra‑neutron rich nuclides from pre‑existing nuclides in the systems absorbing
several neutrons from the cf‑matter.13)
There
occur simultaneous productions of such many elements as follows: Mg, Al, Si, S,
Cl, K, Ca, Cr, Mn, Fe, Co, Ni, Cu, Zn, Os, Ir.
In
experiments where observed many new elements simultaneously, explanation of the
results by NTF seems most appropriate even if there remains a
possibility to explain them by successive transmutations by NTA, NTD
and/or NTT.
5-4) Nuclear Transmutation by Transformation (NTT)
The
nuclear transmutation by transformation, NTT, is a result of a
process where a neutron drop AZΔ in the cf‑matter transforms itself into a stable nuclide AZX
in the material. Naturally, the more stable a neutron drop AZΔ is, the more frequent a nuclide AZX will be
produced.
When products of nuclear transmutation are
observed alone, it seems to be explained by NTT if the new elements
have mass number A less 50 and that shifts from pre‑existing nuclides by more
than 10. The nuclear transmutation by transformation, e.g. AZΔ
into AZX seems probable only if there
are neutron drops with stability that is sensitive to environment.
Products
possibly explained by NTT (cf. Tables 1 and 2) are as follows:
126C, 2412Mg, 2814Si,
3216S, 35,3717Cl, 4020Ca,
5626Fe, 5828Ni, 20882Pb.
The
production of Fe is observed very often in electrolytic experiments, in arcing
between carbon rods and in others and is possibly explained as a result of NTT.
6. Relation of CFP Data
with Abundances of the Elements
We
can see correspondence of nuclear products of NTs in CFP with the abundances of
the elements given in Section 1.
The most remarkable
statistical data is seen in overall correspondence between the frequency Nob
observing elements in CFP (Table 4) and the relative abundances log10H of elements in the universe (Tables 1 and 2) as shown in Figs. 1
and 2. This qualitative correspondence between two data (Nob
and log10H) may be
explained as follows.
Here,
we point out only several of the most remarkable characteristics of them.
i).
Accordance of log10H
and Nob: There are several peaks with coincidence of Nob
and log10H at Z = 14
(Si), 20 (Ca), 26 (Fe), 38 (Sr), and 82 (Pb). In these peaks, the one at Z = 26
(Fe) is the most remarkable despite the isotopic abundance of elements in the
universe is in a logarithmic scale. Quantitative explanation of these data will
need to use concrete experimental conditions.
ii).
Discrepancy between log10H
and Nob: Missing data in CFP at Z = 7 (N), 8 (O), 10 (Ne), 18
(Ar), and 40 (Zr) are noticeable. The first four of them may be explained as a
result of difficulty in their observation. About the last one (Zr), we have
no idea to explain the discrepancy, at present. The remarkable peak at Z = 47 (Ag)
is a characteristic of CFP explained by NTD, from Pd that does not
exist in the stars.
Figs. 1 and 2. Correspondence between the frequency Nob observing elements in CFP and the relative abundances log10H of elements in the universe for elements with atomic numbers Z = 3 −38 (Fig. 1) and Z = 39 −84 (Fig. 2).
Therefore,
it is possible to conclude that the good coincidence of Nob
and log10H discussed
above is an evidence showing similarity of mechanisms working in CF materials
and in the stars to produce new nuclides. This mechanism to produce nuclides
from chaotic states of nucleons according to their stability is called
“mechanism by stability." The coincidence of data in astrophysics and in
CFP is called “stability effect": The more stable a nuclide is, the more
frequent it is produced.
Discussion
As shown in this paper, there is the stability effect, a good coincidence of the isotopic abundance of elements in the universe log10H and frequency of observations of elements in CFP Nob. This effect shows that the mechanism to produce new nuclides in CFP is a low energy, localized version of the mechanism working in the stars catalyzed by the cf‑matter and nuclides in CF materials. Participation of neutrons as a catalyst makes nuclear reactions in CFP as effective to produce new nuclides as high‑energy processes in the stars.
Isotopic
ratios of new isotopes produced in CFP reflect characteristics of nuclear
processes participating to the production processes. It is most probable that
products by NTT have similar isotopic ratios to natural ratios of
the same element. Detailed investigation of these features will help to explore
dynamics of nuclear interactions in the cf‑matter.
Thus,
variety of nuclear transmutations observed in CFP are qualitatively and
consistently explained by the existence of the cf‑matter worked out
semi-quantitatively in previous papers.4,5)
Acknowledgement
The author
would like to express his heart‑felt thanks to John Dash of Portland Stale
University, USA, who made his stay at PSU from September 2000 possible, for
valuable discussions on physics of CFP. Dash read a part of tile manuscript of
this paper and improved the English. He is also thankful to Hiroshi Yamada of Iwate
University, Japan for information about the nuclear transmutation and for
valuable discussions throughout this work.
References
(*) Papers
used to calculate Nob in Table 4 are listed on the end of
this paper.
(1) H.E.
Suess and H.C. Urey, ‑Abundances of the Elements" Rev. Mod. Phys. 28, 53 ‑ 74 (1956).
(2) W.E.
Burcham, Nuclear Physics, 2nd
Edition, Longman, London 1973. Chapter 10. The mass and isotopic abundance of
nuclei.
(3) D.
Pines and D. Bohm. "A Collective Description of Electron Interactions: II.
Collective vs. Individual Particle Aspects of the Interactions" Phys.
Rev. 85. 338 353
(1952).
(4) H. Kozima,
"Excited States of Nucleons in a Nucleus and Cold Fusion Phenomenon in
Metal Hydrides and Deuterides” Proc. ICCF9, pp. 186 ‑ 191 (2003).
(5) H. Kozima, “New Neutron State in Transition‑Metal
Hydrides and Cold Fusion Phenomenon" Trans. Nucl. Society 88, 615 ‑ 617
(2003). And also H. Kozima, “Cold Fusion Phenomenon in Transition‑Metal
Hydrides/Deuterides and Its Application to Nuclear Technology" Fusion
Science and Technol. (submitted).
(6) H. Kozima. “Neutron Drop: Condensation of
Neutrons in Metal Hydrides and Deuterides", Fusion, Technol. 37, 253 ‑ 258 (2000).
(7) J.W. Negele and D. Vautherin, Nuclear Physics, A207, 298 ‑ 320 (1973).
(8) H. Kozima.
Discovery of the Cold Fusion Phenomenon – Evolution of the Solid State-Nuclear Physics and the Energy Crisis in 21st Century. Ohtake
Shuppan KK.. Tokyo, Japan. 1998.
(9) H. Kozima,
K. Kaki and M. Ohta, "Anomalous Phenomenon in Solids Described by the TNCF
Model”. Fusion Technol. 33,52 ‑
62 (1998).
(10) H.
Kozima, "Trapped Neutron Catalyzed Fusion of Deuterons and Protons in
Inhomogeneous Solids,” Trans. Fusion
Technol. 26, 508 ‑ 515 (1994).
(11) H. Kozima, K. Hiroe, M. Nomura, M. Ohta
and K. Kaki, “Analysis of Cold Fusion Experiments Generating Excess Heat,
Tritium and Helium", J. Electroanal.
Chem.. 425, 173 ‑ 178
(1997) and 445, 223 (1998).
(12) H. Kozima, J. Warner, C. Salas Cano and J.
Dash. "TNCF Model Explanation of Cold Fusion Phenomenon in Surface Layers
of Cathodes in Electrolytic Experiments" .J. New Energy, 7‑1. 64 ‑ 78 (2003). And also H. Kozima, .J. Warner, C. Salas Cano and
.J. Dash, "Consistent Explanation of Topography Change and Nuclear
Transmutation in Surface Layers of Cathodes in Electrolytic Cold Fusion Experiments”
Proc. ICCF9, pp. 178 ‑ 181 (2003).
(13) J.C.
Fisher, ‑Liquid‑Drop Model for Extremely Neutron Rich Nuclei” Fusion Technol. 34. 66‑75 (1998).
Papers used to count Nob
in Table 4
(1*) A. Arapi, B. Ito, N. Sato, M. Itagaki. S. Narita and H. Yamada,
"Experimental Observation of the New Elements Production in the Deuterated
and/or Hydride Palladium Electrodes, Exposed to the Low Energy DC Glow
Discharge", Condensed Matter Nuclear
Surface (Proc. ICCF9) (2002.
Peking, China), pp. 1‑4 (2003). And also A. Arapi et al. J. Appl. Phys. 41, L1181‑L1183
(2002). [Pd‑Au/D2,H2: Li. Mo. Ba].
(2*) J.O'M. Bockris and Z. Minevski, "Two
Zones of “Impurities” Observed after Prolonged Electrolysis of Deuterium on
Palladium'. Infinite Energy Nos. 5 & 6. 67-69 (1996). [Pd‑Pt/LiOD (?); Mg, Ag,
Si, Cl, K, Ca, Ti, Fe, Cu, Zn]
(3*) R.T. Bush, “A Light Water Excess Heat
Reaction suggests that ‘Cold Fusion' may be 'Alkali‑Hydrogen Fusion' " Fusion
Technol. 22, 301 (1992). [Ni-Pt/H2O/K2CO3; Ca]
(4*) R.T. Bush and D.R. Eagleton, "Evidence
for Electrolytically Induced Transmutation and Radioactivity Correlated with
Excess Heat in Electrolytic Cells with Light Water Rubidium Salt Electrolytes",
Trans. Fusion Technol. 26. 344 ‑ 354 (1994). [Ni‑Pt/H2O/RbCO3; Sr]
(5*)
KG. Campari, S. Focardi, V.
Gabbani, V. Montalbano., F. Piantelli. E. Porcu, E. Tosti and S. Veronesi.
"Ni‑H System” Proc. ICCF8 pp. 69
‑ 71 (2000). [Ni/H2; F, Na, Mg, Al, Si, P, S, Cl, K, Ca, Cr, Mn, Fe,
Cu, Zn]
(6*)
D. Chicea, "On New Elements on Cathode Surface after Hydrogen Isotopes Absorption”‑Condensed Matter Nuclear Science (Proc.
ICCF9) (2002, Peking. China), pp.53‑56 (2003). [Ti, Pd//H2O/Li2SO4;
C, Si, Cu & Pd; C].
(7*)
J. Dash. G. Noble and D. Diman, "Changes in Surface Topography and
Microcomposition of a Palladium Cathode caused by Electrolysis in Acidific
Light Water,” Cold, Fusion Source Book (Proceedings
of International Conference on Cold Fusion and. Advanced Energy Sources, Minsk,
Belarus) pp. 172 ‑ 180 (1994). [Pg-Pt/H2O/H2SO4,
Cl, Ag]
(8*) J. Dash. G. Noble and D. Diman.
"Surface Morphology and Microcomposition of Palladium Cathodes after
Electrolysis in Acidified Light and Heavy Water; Correlation with Excess Heat, Trans. Fusion. Technol. 26. 299 ‑ 306 (1994) [Pd-Pt/H2SO4: Au, Ag]
(9*) J. Dufour, D. Murat, X. Dufour and J.
Foos, "Hydrix Catalysed Transmutation of Uranium and Palladium:
Experimental Part,” Proc. ICCF8 pp. 153 ‑ 158 (2000). [Pd; Mg, Al, Cr, Fe, Zn]
(10*) T. Hanawa, “X‑ray Spectrometric Analysis
of Carbon Arc Products in Water” Proc.
ICCF8, pp. 147 ‑ 152 (2000). [C‑C/H2O; Fe, Si, Ni,
Al, Cl, Mn]
(11*) Y. lwamura, T. Itoh, N. Gotoh, M. Sakano,
I. Toyoda and H. Sakata, "Detection of Anomalous Elements, X‑Ray and
Excess Heat induced by Continuous Diffusion of Deuterium through Multi‑Layer
Cathode (Pd/CaO/Pd)" Proc. ICCF7, pp.167 ‑ 171 (1998).[Pd//LiOD; Ni,
Fe]
(12*) Y. lwamura, T. Itoh and M. Sakano, "Nuclear
Products and Their Time Dependence induced by Continuous Diffusion of Deuterium
through Multi‑Layer Palladium Containing Low Work Function Material” Proc.
ICCF8, pp.141 ‑ 146 (2000).[Pd/D2: Mg, Si, S, F, Al]
(13*)
Y‑ lwamura, M. Sakano and T. Itch, "Elemental Analysis of Pd Complexes: Effects
of D2 Gas Penetration” Jpn. J. Appl. Phys., 41, 4642 ‑
4650 (2002). [Pd/D2; Mg, Si, S, F, Al, Fe]
(14*) Y. Iwamura, T. Itoh, M. Sakano and S. Sakai. "Observation of
low Energy Nuclear Reactions induced by D2 Gas Permeation through Pd
Complexes” Condensed Matter Nuclear Science, (Proc. ICCF9) (2002, Poking, China), pp.141-146
(2003). And also Y. lwamura et al. Jpn. J, Appl. Phys. 41, 4642‑4650
(2002). [Pd (Cs, Sr)/D2; Pr, Mo]
(15*) A.B. Karabut, YM, Kucherov and I.B. Savvatimova,
“Possible Nuclear Reactions Mechanisms at Glow Discharge in Deuterium" Proc.
ICCF3, pp.165 ‑ 168 (1993). [Pd/D2;
Mg, Al, Si, S, Ca, Ti, Cr, Fe, Ni, Zn, Ge, Br, Sr, Mo in 1 μm surface layer]
(16*)
R. Kopecek arid J. Dash, “Excess Heat and Unexpected Elements from Electrolysis
of Heavy Water with Titanium Cathodes” Proc. 2nd Low Energy Nuclear Conference,
College Station, Texas, pp. 46 ‑ 53 (1996).[Ti-Pt//H2SO4;
V, Cr]
(17*) X.Z. Li. S.X. Zheng, G.S. Huang, WZ. Yu,
"New Measurements of Excess Heat in a Gas‑Loaded D/Pd System” Proc.
ICCF7, pp. 197 ‑ 201 (1998). [Pd/D2: Zn, Pb, Fe, Cu, Sr]
(18*) X.Z. Li, Y.J. Yan, J. Tian, M.Y. Mei, Y.
Deng, W.Z. Yu, G.Y. Tang, and D.X. Cao, “Nuclear Transmutation in Pd Deuteride”
Proc. ICCF8, pp. 123 ‑ 128 (1998). [Pd‑Pt/D2O/?; Cr, Fe, Ni, Zn]
(19*) G.H. Miley, G. Narne, M.J. Williams. J.A.
Patterson, J. Nix, D. Cravens and H. Hora. "Quantitative Observation of
Transmutation Products. Occurring in Thin-Film Coated Microspheres during
Electrolysis” Proc. ICCF6. pp.
629 ‑ 644 (1996) [Ni,Pd/H2O//LiSO4; Al, Cu, Ni, Fe, Zn,
Ag]
(20*) G.H. Miley, “Product Characteristics and
Energetics in Thin‑Film Electrolysis Experiments", Proc. ICCF7, pp. 241 ‑ 246 (.1998). And
also G.H. Miley and J.A. Patterson. J. New Energy, 1-3, 5 ‑ 30
(1996). [Ni,Pd,Ti‑Pt/H2O/LiSO4: A=22‑23. 50-80, 103-120,
200-210]
(21*) T. Mizuno, T. Akimoto, K. Azumi. M.
Kitaichi anti K. Kurokawa, “Excess Heat Evolution and Analysis of Elements for
Solid State Electrolyte in Deuterium Atmosphere during Applied Electric Field” J.
New Energy 1‑1. 79 ‑ 86 (1995). [Sr,Ce,Y,Nb,O/D2: Pt, Cu,
Cr, Pd, Zn, Br, Xe, Cd, Hf, Re, Ir, Pb]
(22*) T. Mizuno, T, Ohmori and M. Enyo,
"Isotopic Changes of the Reaction Products induced by Cathodic
Electrolysis in Pd” J. New Energy 1‑3. 31 ‑15 (1996). [Pd-Pt/D2O/LiOH;
C, O, S, Cl, Si, Ca, Ti, Cr, Mn, Fe, Co, Ni, Cu, Zn, Mo, Sn, Pt, Hg, Pb]
(23*)
T. Mizuno, T. Ohmori and T. Akimoto, "Detection of Radiation Emission,
Heat Generation and Elements from a Pt Electrode Induced by Electrolytic Discharge in Alkaline Solutions” Proc. ICCF7, pp.
253 ‑ 258 (1998). [Pt‑Pt/D2O.H2O/Na2CO3;
Fe, Ni, Cu, Mn, Ca, K, Cl]
(24*) T. Mizuno, T. Ohmori, K. Azumi, T. Akimoto
arid A. Takahashi, "Confirmation of Heat Generation and Anomalous Element
caused by Plasma Electrolysis in the Liquid" Proc. ICCFS pp.75 ~ 80 (2000). [W‑Pt/H2O/K2CO3:
Al, Cl, Si, Ca, Ti, Cr, Fe, Ni, Zn, Ge, Pd, Ag, In]
(25*) R. Notoya, "Cold Fusion by
Electrolysis in a Light Water‑Potassium Carbonate Solution with a, Nickel
Electrode” J, Fusion Technol. 24, 202 ‑ 204 (1993). [Ni-Pt/H2O/K2CO3;
Ca]
(26*)
R. Notoya, T. Ohnishi and Y. Noya, “Reaction Caused by Electrolysis in Light
and Heavy Water Solutions" Proc. ICCF6, pp. 675 ‑ 679
(1996). [Ni-Pt/H2O, D2O/Na2 (K2:Rb2:Cs2)CO3;
22,2411Na(4119K: 8737Rb,
9238Sr: 13455Cs, 13554Xe)
5627Co, 6429Cu, 6530Zn
in all electrolytes.]
(27*) R. Notoya. T. Ohnishi and Y. Noya. “Products
of Nuclear Processes caused by Electrolysis on Nickel and Platinum Electrodes
in Solutions of Alkali‑Metallic Ions" Proc. ICCF7, pp. 269 - 273 (1995). [Ni‑Pt/H2O/K2CO3;
Os, Ir, Au, 40K, 43K]
(28*) T. Ohmori, T. Mizuno and M. Enyo,
"Production of Heavy Metal Element and the Anomalous Surface Structure of
the Electrode Produced during the Light Water Electrolysis on an Electrode” Proc. ICCF6, pp. 670 ‑ 674 (1996)‑ And
also T. Ohmori et al. J. New Energy
1‑3, 90 ‑ 99 (1996). [An‑Pt/H2O/‑Na2SO4,
Na2CO3; Hg, Os, Fe, Si, F. Anomalous isotopic abundances
of Hg, Fe, Si but F]
(29*) T. Ohmori and M. Enyo, "Iron
Formation in Gold and Palladium Cathodes" J. New Energy 1‑1, 15 ‑ 19 (1996). [Au,Pd/H2O/Na2SO4;
K2CO3; KOH; Fe]
(30*) T. Ohmori and T. Mizuno, "Strong
Excess Energy Evolution, New Element Production and Electromagnetic Wave and/or
Neutron Emission in the Light Water Electrolysis with a Tungsten Cathode",
Proc‑ ICCF7. pp. 279 ‑ 284 (1998). [W-Pt/
H2O/Na2SO4: Pb, Fe, Ni, Cr, C. Isotopic
abundances are similar to natural ones for Fe and Cr but deviate a little for
Pb.]
(31*) T. Ohmori, H. Yamada, S. Narita and T.
Mizuno, “Excess Energy and Anomalous Concentration of 41K Isotopes
in Potassium formed on/in a Re Electrode during the Plasma Electrolysis in K2CO3/H2O
and K2CO3/D2O Solutions” Condensed Matter Nuclear Science, (Proc.
ICCF9) (2002. Peking. China), pp. 284‑294 (2003). [Re‑Pt/H2O, D2O/K2CO3;
41K]
(32*) M. Okamoto. H. Ogawa, Y. Yoshinaga, T.
Kusunoki and 0. Odawara‑ "Behavior of Key Elements in Pd for the Solid
State Nuclear Phenomena Occurred in Heavy Water Electrolysis", Proc. ICCF4,
3,14‑1
‑ 14‑8 (1994). [Pd(Al)‑Pt//LiOD; Si]
(33*) T.O. Passell, "Search for Nuclear
Reaction Products in Heat‑Producing Palladium” Proc. ICCF6, pp. 282 ‑ 290 (1996). [Pd‑Pt/LiOD; Decrease
of 115B]
(34*) T.O. Passell. "Evidence for Li‑6
Depletion In Pd Exposed To Gaseous Deuterium" Condensed Matter Nuclear Science (Proc. ICCT9) (2002. Peking. China), pp.299~304 (2003). [Pd/D2;
Decrease of 63Li]
(35*) I. Savvatimova, "Transmutation
Effects in the Cathode Exposed Glow Discharge. Nuclear Phenomena or Ion Irradiation
Results” Proc. ICCF7, pp. 342-350
(1998). [Pd/D2: Cd, Sn, Ag, Te, Bal
(36*) R. Sundaresan and J. O’M. Bockris,
"Anomalous Reactions during Arcing between Carbon Rods in Water," Fusion
Technol. 26, 261 ‑ 265 (1994). [C‑C/H2O; Fe]
(37*)
J. Warner and J. Dash. “Heat Production during the Electrolysis of D2O
with Titanium Cathodes” Conference Proceedings 70 (Proceedings of 8th
Conference on Cold Fusion, Lerici, Italy). pp. 161 ‑ 167 (2000). [Ti‑Pt//H2SO4:
Cr, Fe]
(38*) H. Yamada. H. Nonaka, A. Dohi, H. Hirahara,
T. Fujihara, X. Li and A. Chiba, “Carbon Production on Palladium Point
Electrode with Neutron Burst under DC Glow Discharge in Pressurized Deuterium
Gas” Proc. ICCF6, pp. 610 ‑
614 (1996). [Pd/D2; C]
(39*) H. Yamada, S. Narita, Y. Fujii, T. Sato.
S. Sasaki and T. Ohmori, “Production of Ba and Several Anomalous Elements in Pd
under Light Water Electrolysis," Condensed
Matter Nuclear Science (Proc. ICCF9) (2002, Peking, China), pp.420-423
(2003). [Pd‑Pt/H2O/Na2SO4; Li, B, Mg, Al, K,
Ca, Ti, Cr. Mn, Fe, Co, Ni, Cu, Zn, Ba, Pb].
* This work
is supported by a grant from the New York Community Trust and by the
Professional Development Fund for part‑time faculty of Portland State University.
† On leave
from Cold Fusion Research Laboratory, Yatsu 597‑16,
Shizuoka. Shizuoka 421‑1202, Japan.
E mail: cf-lab.kozima@nifty.ne.jp,
Website: http://www.geocities.jp/hjrfq930/