Patent number: WO 00177340
(where
Inventor: B.J. Miller
membrane,
Publication date: 21 December
Me = CH,,
development
2000
composite
of efficient
of energy water
Elektronik,
addition
Universitit
The invention which
and ceramic
of organic
phyllosilicates
and
water
concentration
(I-100
hydroxyl)
particles
allows of
membrane
that is necessary
up to an operating composite heterogeneous
are
formed
powder.
transport
of of
polymer/ceramic modified have
different
polymer equilibrium proton can
be used,
mixtures
if
Composite polyamide A composite
polyamide
surface
to which
than
If
groups
preferably
is that
at
the
establishment
example
of
strength
for
of the
This effect
the MeOH
passage
it are
improved
of anionic membrane
was studied
for drinking-water
This hybrid
process
exchange
transport
nitrogen.
combines
continuous dialysis)
bio-reduction
A non-porous
in
(IEMB)
to gaseous
mono-anion
perm-
selective
membrane
between
the polluted
culture,
and prevents
secondary
treated
water
dissolved
nutrients
Complete
denitrification
metabolic
with
products.
may be achieved and NO,study
water
without
direct
contact
and the denitrifying pollution
accumulation
of the
focused
of NO,The
on the effect of the concentration counter-ions
IEMB
performance.
transfer
coefficient
The
and
ethanol
nitrate
in this hybrid
this
patent.
may
or
and
both.
The
and the
contain
pendant
acid groups. D.A. Ylitalo
Publication date: 28 December
2000
Gas-diffusion electrode
and
It
Applicant: Johnson
Matthey Plc, UK
An
conducting
electrically
substrate,
which
between
oxidisable
impurities
gas-diffusion
capable
structure
polyalkylene
component,
oxide provides
supported
offering
support.
while
performance. use
of
The
of
which
an electrically
comprises
The patent
scale-up,
each
conducting
of
an electrode, and
comprises
gas-difision
catalyst
non-conducting
assembly
which
a catalytic a
also describes
membrane-electrode
gas stream,
and
on an electrically
chemical
removing
from an impure It comprises
the
Inventors: SC.
00176641
G. Hoogers,
the
a
a fuel cell, electrically
substrate.
denitrification.
the ratio
the bio-compartment compartment,
the
of each individual
regulated,
allowing
and control.
containing
135-350
rate of 33 g NOs-/m2 obtained
N03-/m3.day, efficiency
the optimisation
anion
flux can be
A surface
denitrification of 360
in a nitrate
Rodrigues,
g
M.A.
Reis, J.G. 71(4)
(2000).
L.
Cat;lyst paper
models
-
membranes electrolytes
concerned
prepared of cationic on a porous
resulting
with on and
composite
solved separating
layer-by-layer anionic
substructure.
A.
Symposia
Toutianoush:
163( 1)
97-l
12
layer models for PEM fuel
poly-
The use of
membranes
for
presents
two simple
model
@‘EM)
polymer
fuel
gas as the feedstock. analytically,
whereas
numerically.
The emphasis factors affecting
the fuel cell using
a simple
going into detailed
catalyst
Chan,
W.A. Tun:
Technology 24( 1) 5 l-57
layer
model,
and
for the proton-exchange
parameterise
S.H.
catalyst
the macro-homogeneous
the agglomerate membrane
Tailor-made membranes for alcohol/water pervaporation is
Krasemann,
2001).
hydrogen
work
with excellent
removal
Biotechnology & Bioengineering
245-254
to be produced
and
conditions
per day was
rate
This
C.M.
of monovalent
It is demonstrated
capability.
Tieke,
(January
of 85%.
S. Velizarov, Crespo:
B.
pervaporation
of the preparation
Macromolecular
was treated
under
choice of the poly-electrolytes
allows membranes separation
groundwater
of membrane
resulting
process
2000
ions is described.
that a suitable
for flexible
loading
separation
and divalent
and
G.A. Hards,
and for the separation
and the polluted
Synthetic
at a nitrate
conditions,
of co-ions
28 December
alcohol/water
magnitude
mg N03-/litre
system.
Ball, S.J. Cooper,
D. Thompsett
Publication he:
2000
than that in a pure
by adjusting
operation
the
is
here.
dialysis process without
Furthermore,
The
substrate
porous
to commercial
to be 2.8 times higher
Donnan
adsorption
was
one
is described
Publication hte: 21 December
mass-
process
polymer
Patent number: WO 00179628
on the
overall
polymer
the
polymer,
conducting
membrane
require
used to
and
ions in the bio-compartment.
of co-ions,
w
precludes
ion-
of nitrate
an ionomeric
and a cross-linked
to fouling
Patent number: WO
in the IEMB
denitrification.
(Donnan
and its simultaneous
removal
bio-reactor
not
USA
initiators.
direction
pollutant
of
The
is easily adapted
does
easily an ion-exchange
of making
is also described.
film-forming
cross-linking
of
Patent number: WO 00179629
2000
flux and salt passage
method
water
denitrification
coalescing
been film-
used may be fluoro-polymers,
sulfonic
with modified
subject
resistance
excellent and
the
are grafted.
found
ResearchTrends
optionally ionomeric
Inventor: W.E. Mickols
alcohol/water
A method membrane
polymers
and processing
and the method
and at
is influenced.
The mechanism
membrane
at low pressure
layer
polymer. electrolyte
involves
has
mixture
a structural
forming
Znventorr: S. Hamrock,
membrane surface
support
groups
and
polymer
a structural
further
membrane of an ‘intimate’
polymer
and
in a water-
and
Inventors: J. Kerres, N. Nicoloso
a porous
boundary
electrolyte composed
This
membrane.
make
the
polymer
developed,
catalysed from
membranes
Applicant: 3M Innovative Properties Co, USA A
increased
WO OOl77080
comprises
as a fuel, to reduce
Drinking-water
invention
of producing
(high
the local
for
The
atmosphere.
in
working
out
allow
of boundary
carriers
elevated
to
are carried
Polymer electrolyte then- production
an ionomeric
which
ranges
Applicant: Dow Cheniical Company,
interfaces,
and thus the binding
charge
pressure
quantity
polarities,
skeleton,
the
micro-
100°C.
in
at
which
relates to a method Patent number
out
at a pressure or that
vapour
required or
chemically
carried
particles),
particle
by means
atmospheric
in which
or
current
Publication date: 21 December
the polymer
These high
more
the
temperatures,
fuel
The
by
in
nano-scale
of the protons
temperatures
of 300°C.
between
in a sufficiently share
in the
for the conductivity
formed
mixture
the ceramic
and
concentration
produced or
are
methanol
to its use in fuel
technology,
electric
such a composite
mechanical
is characterised
which
(for
material
temperature
material
interfaces
high
is
to
pressures,
surface
groups
composite
of the proton
with
high
The use of such
sufficiently
stabilisation
phase
a
and water.
the
except
tectosilicates,
and/or
in acidic/alkaline
example
and
nm),
process
vapour
reactions
polymers
direct
for the
can also be used in the field
electrochemically
membrane
functional
nano-particles
intercalating
stability
Germany
relates to a composite
consists
for
Stuttgart,
and
across the
important
In addition
cells, the membrane
Applicant: Institut &r Physikalische
or C,H,7)
is especially
cells (DMFCs).
Ceramic/polymer membrane
C,H5
which
cell
The
the latter
using
former
is
is solved
of this research
is to
the performance approach,
of
without
layer modelling.
Chemical
Engineering
(January
2001).
&
Membrane Technology No. 133