Nano-Photonic
Purification & Sterilization
CLEAN – EFFICIENT – COMPACT -
QUICK
What
is Nano-Photonic Purification & Sterilization?
A unique, non-filtration
process that -
Purifies water and juices,
Decontaminates air, and Sterilizes medical supplies
and implants
without introducing chemicals
or altering the originality of the water, juice, air or medical implement.
What
is Nano-Photonics?
Photonics is the science of
producing energy photons from light waves measured along a nanometer scale.
Examples of photonics are fiber optics, lasers and solar panels.
What
is the unique process?
The process is nano-photonic Synergistic Isogenous Active Decontamination
.
What
is
?
The
process
simultaneously combines a set number of specific light waves from the same
origin to eradicate harmful micro-organisms.
How
does
eradicate micro-organisms?
The
photonic energy
from the specific light waves causes the micro-organism to produce enzyme “free-radicals”.
“Free-radicals” cause a dysfunctional micro-organism life process which quickly
results in eradication. The public has become increasingly aware of
“free-radical” science from sun block and sun screen advertising.
Why
is
unique?
research
isolated and combined a set number (more than two) of specific light waves from
trillions of light wave combinations to produce the desired effects.
Is
different from UV?
is different. UV uses a single light wave
(253.7 nm) to possibly break the DNA chain within the nucleus of the
micro-organism.
Is
safe?
Over two decades of research
studies and tests by national hospitals, institutions, and universities
document
use of
“free-radical” science in a useful and safe format. Samplings of the studies
are at http://www.synergena.com/Research.htm
.
What
is Synergena?
Synergena is the small,
private research and development corporation that has conducted the
research and
controls the
technology,
prototypes and patents.
Is
FDA and EPA approved?
Being a small R&D
company, Synergena has focused resources on the studies and testing of
technology and
devices. Although
devices were
successfully tested in accordance with FDA and EPA criteria, additional legal
and capital resources are necessary for regulatory agency approvals.
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