Abstract seems to belong to this 2007 paper (not freely accessible):
"Catalysis of atomic hydrogen to new hydrides as a new power source"
http://inderscience.metapress.com/index/X832U331J0R38642.pdf 

Google scholar found what seems to be an earlier version (April 2005?):
http://www.blacklightpower.com/papers/CatalysisofAtomicHydrogentoNewHydrides040405.pdf
  
Abstract was a bit longer but said essentially the same things as far as I can 
tell:
<<
ABSTRACT
Plasmas of certain catalysts such as Sr + and Ar+ mixed with hydrogen were
studied for evidence of a novel energetic reaction. These hydrogen plasmas 
called
resonant transfer- or rt-plasmas were observed to form at low temperatures 
(e.g. ˜ 103 K )
and an extraordinary low field strengths of about 1-2 V/cm when argon and 
strontium
were present with atomic hydrogen. Time-dependent line broadening of the H 
Balmer a
line was observed corresponding to extraordinarily fast H (25 eV). An excess 
power of
20 mW ·cm-3 was measured calorimetrically on rt-plasmas formed when Ar+ added to
Sr + as an additional catalyst. Substantial evidence of an energetic catalytic 
reaction was
previously reported [1] involving a resonant energy transfer between hydrogen 
atoms and
K to form very stable novel hydride ions H- (1/ p) called hydrino hydrides 
having a
predicted fractional principal quantum number p = 4 . Characteristic emission 
was
observed from K3+ that confirmed the resonant nonradiative energy transfer of
3· 27.2 eV from atomic hydrogen to K. The product hydride ion H- (1/4) was 
observed
spectroscopically at 110 nm corresponding to its predicted binding energy of 
11.2 eV .
The 1H MAS NMR spectrum of novel compound KH *Cl relative to external
tetramethylsilane (TMS) showed a large distinct upfield resonance at -4.4 ppm
corresponding to an absolute resonance shift of -35.9 ppm that matched the 
theoretical
prediction of p = 4. The predicted catalyst reactions, position of the 
upfield-shifted
NMR peaks for H- (1/4), and spectroscopic data for H- (1/4) were found to be in
agreement with the experimental observations as well as previously reported 
analysis of
KH *Cl containing this hydride ion. Since the comparison of theory and 
experimental
shifts of KH *Cl is direct evidence of lower-energy hydrogen with an implicit 
large
exotherm during its formation, the NMR result were repeated with the further 
analysis by
Infrared (FTIR) spectroscopy which eliminated any known explanation such as U
centered H for the assignment of the extraordinary upfield-shifted NMR peak. The
possibility that a novel catalytic reaction of atomic hydrogen to form more 
stable
hydrides may be a clean new energy source is supported by spectroscopic, 
chemical, and
thermal data.
Key Words: H catalysis, fast H, exothermic, novel hydride ions, upfield NMR 
peaks,
FTIR
>>

33 pages, haven't read it personally (not enough faith in hydrinos I guess), 
maybe Robin has, and is willing to comment  it?

Michel

----- Original Message ----- 
From: "thomas malloy" <[EMAIL PROTECTED]>
To: <vortex-l@eskimo.com>
Sent: Wednesday, April 09, 2008 10:22 AM
Subject: [Vo]:BLP paper on energy production


> Can someone comment on the energy density that is reported in this 
> abstract?
> 
> Abstract: Having the potential for a clean new energy source, rt-plasmas of
> certain catalysts (Sr+, Ar+, K) with H formed at extraordinary low field
> strengths of about 1–2 V/cm. Time-dependent, extraordinarily fast H (25 eV),
> an excess power of 20 mW · cm-3, and characteristic K3+ emission confirmed
> the resonant nonradiative energy transfer of 3 · 27.2 eV from atomic 
> hydrogen
> to K as the rt-plasma catalyst. The predicted very stable novel hydride
> ion H-(1/4) with fractional principal quantum number p = 4 was observed
> spectroscopically at 110 nm corresponding to its predicted binding energy of
> 11.2 eV that further matched the 1H MAS NMR spectrum having an
> extraordinary upfield-shifted peak at –4.4 ppm with the elimination of any
> known assignment by FTIR.
> Keywords: H catalysis; fast H; exothermic; novel hydride ions; upfield NMR
> peaks; FTIR.
> Reference to this
> 
> 
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