Method and Apparatus for Surface Treatment of Materials
Utilizing Multiple Combined Energy s
CROSS-REFERENCE TO RELATED APPLICATION(S)
This application claims filing date benefit from US 61/501 ,874 filed 6/28/2011.
TECHNICAL FIELD
The invention relates to surface treatment of als and various ates, more particularly
such as textiles, and more particularly to treatment of the materials with combined multiple
diverse energy sources, typically one of which may be an atmospheric plasma (AP).
BACKGROUND
Development of “smart textiles” has been an active area of st to improve various properties
such as stain resistance, waterproofing, colorfastness and other characteristics achievable through
advanced treatment using plasma technologies, microwave energy sources and in some cases,
chemical treatments.
Atmospheric Plasma Treatment (APT) improves fiber surface properties such as hydrophilicity
without affecting the bulk properties of these fibers, and can be used by textile manufacturers
and converters to improve the surface properties of natural and tic fibers to improve
adhesion, wettability, printability, dyeability, as well as to reduce material shrinkage.
Atmospheric-pressure plasma (or AP plasma or normal pressure ) is the name given to the
special case of a plasma in which the re approximately matches that of the surrounding
here. AP plasmas have prominent technical significance because in contrast with low-
pressure plasma or high-pressure plasma no cost-intensive reaction vessel is needed to ensure the
nance of a pressure level differing from atmospheric pressure. Also, in many cases these
AP plasmas can be easily orated into the production line. Various forms of plasma
excitation are possible, including AC nating t) excitation, DC (direct current) and
low-frequency excitation, excitation by means of radio waves and microwave excitation. Only
AP plasmas with AC excitation, however, have attained any noteworthy industrial significance.
Generally, AP plasmas are generated by AC excitation (corona discharge) and plasma jets. In
the plasma jet, a pulsed electric arc is generated by means of high-voltage discharge (5–15 kV,
–100 kHz) in the plasma jet. A process gas, such as oil-free compressed air flowing past this
discharge section, is excited and ted to the plasma state. This plasma then passes through a
jet head to arrive on the surface of the material to be treated. The jet head is at earth potential and
in this way largely holds back potential-carrying parts of the plasma stream. In addition, the jet
head determines the geometry of the emergent beam. A plurality of jet heads may be used to
interact with a corresponding area of a substrate being treated. For e, sheet als
having treatment widths of several meters can be treated by a row of jets.
AP and vacuum plasma methods have been utilized to clean and activate surfaces of materials in
preparation for bonding, printing, painting, polymerizing or other functional or decorative
coatings. AP processing may be preferred over vacuum plasma for continuous processing of
material. Another e treatment method utilizes microwave energy to polymerize precursor
coatings.
It is an object of the invention to at least provide the public with a useful choice.
SUMMARY
The invention is generally directed to providing improved techniques for treatment (such as
surface treatment and modification) of materials, such as substrates, more particularly such as
textiles ding woven or d textiles and ven fabrics), and broadly involves the
combining of various additional energy sources (such as laser irradiation) with high voltage
generated plasma(s) (such as atmospheric pressure (AP) plasmas) for performing the ents,
which may alter the core of the al being treated, as well as the surface, and which may use
introduced gases or precursor materials in a dry nment. Combinations of various energy
sources are disclosed.
An embodiment of the invention y comprises method and apparatus to treat and produce
technical textiles and other materials utilizing at least two combined mutually interacting energy
sources such as laser and high voltage generated atmospheric (AP) plasma.
The techniques disclosed herein may y be incorporated into a system for the automated
processing of textile materials. Functionality may be achieved through non-aqueous cleaning like
etching or ng, activating by way of radical formation on the surface(s) and aneously
and selectively increasing or decreasing desired fianctional properties. Properties such as
hydrophobicity, hydrophilicity fire retardency, anti-microbial properties, shrink reduction, fiber
ng, water repelling, low temperature dyeing, increased dye take up and colorfastness, may
be enabled or enhanced, increased or decreased, by the process(es) which produces chemical
and/or morphological changes, such as radical formation on the surface ofthe material. Coatings
of material, such as nano-scale coatings of advanced materials composition may be applied and
processed.
Combining (or hybridizing) AP plasma energy with one or more additional (or secondary)
energy sources such as a laser, X-ray, electron beam, ave or other diverse energy sources
may create a more effective (and cially viable) energy milieu for substrate treatment. The
secondary energy source(s) may be applied in combination (concert, simultaneously) with and/or
in sequence (tandem, selectively) with the AP plasma energy to achieve desired ties.
Secondary energy sources may act upon the separately generated plasma plume and produce a
more effective, tic plasma milieu, while also having the ability to act directly on the
surface and in some cases, the core of the material ted to this hybrid treatment.
The techniques disclosed herein may be applicable, but not d to the treatment of textiles
(both organic and nic), paper, synthetic paper, plastic and other similar materials which are
typically in flat sheet form (“yard goods”). The techniques disclosed herein may also be d
to the sing of plastic or metal extrusion, rolling mills, injection molding, spinning, g,
weaving, glass making, substrate etching and cleaning and coating of any material as well as
applicability to practically any material sing technique. Rigid materials such as flat sheets
of glass (such as for touch screens) may be treated by the techniques disclosed herein.
According to one aspect of the t invention, there is ed a method for treatment of a
substrate (102, 402, 404) comprising:
creating a plasma in a treatment region (124) comprising two spaced-apart electrodes (e1 /e2 ;
212/214; 412/414; 452/454) wherein the electrodes are provided as rollers with one roller being
disposed substantially parallel to the other , with a gap therebetween, to allow the ate
material to be fed between the rollers;
directing at least one second energy source which is different than the first energy source
into the plasma to ct with the plasma, resulting in a hybrid plasma; and
causing the hybrid plasma to interact with the ate in a ent region (124).
In another aspect, the present invention encompasses an apparatus (100, 400A, 400B, 400C,
400D, 400E, 400F, 400G) for treating materials comprising:
two spaced-apart electrodes (e1 /e2 ; 4; 412/414) for generating a plasma in a
treatment region (124);
wherein the two electrodes are first and second rollers disposed substantially parallel to each
other with a gap therebetween, to allow the substrate al to be fed between the rollers; and
one or more lasers (130) directing corresponding one or more beams (132) into the treatment
area to ct with at least one of the plasma and the material being treated.
In a further aspect, the present invention comprehends a use of the apparatus described herein for
treating a textile substrate.
In a different aspect, the present invention ges a textile material obtained by the method
described herein.
In yet a further aspect, the present invention contemplates a method of creating a plasma for
material treatment comprising providing two electrodes in the form of a rod, or a tube or other
rotatable cylindrical electrode material, spaced apart from one another a distance sufficient to
allow for clearance of the thickness of a material being processed; energizing the electrodes in
any suitable manner to create an atmospheric plasma along their length in a treatment region
(followed by page 4a)
between and immediately nding the electrodes; directing a laser beam into the treatment
region, approximately parallel to and between the electrodes so as to interact with the plasma
generated by the two electrodes.
Some advantages of the present ion may include, without limitation, a method of creating a
more energetic and ive plasma to clean and activate surfaces for subsequent processing or
finishing. For example, ultra-violet (UV) laser radiation, either continuous wave (CW) or
pulsed, may be combined with electromagnetically generated AP plasma to create a more highly
(followed by page 5)
ionized and energetic reaction milieu for treating surfaces. The resulting hybridized energy may
have effects that are greater than the sum of its individual parts. Pulsed laser energy may be used
to drive the plasma, creating waves, and the laser energy accelerates the resultant plasma waves
which act upon the ate like waves crashing on the beach.
The accelerated and more energetic plasma may initiate radicals in the fiber or surface of the
treated substrate and attach ionized groups to the ted radicals. Attachment of such
functional groups as carboxyl, hydroxyl or others attach to the surface increasing polar
characteristics may result in greater hydrophilicity and other desirable functional properties.
The invention advantageously combines energy sources in a controlled atmospheric environment
in the presence of a material substrate. The net result may be conversion and material sis
in the surface of the substrate - the ate may be physically changed, in st with simply
being coated.
In an exemplary embodiment, a high frequency RF plasma is created in an pe (or cavity,
or chamber) formed between rotating and driven rollers which extend across the width of the
processing window. The plasma field generated is consistent across the width of a treatment
area, and may operate at atmospheric pressure. A high power Ultra Violet UV) laser is provided
for interacting with the plasma and/or the al being treated. The beam from the laser may
be shaped to have a rectangular cross-section exhibiting a consistent power density over the
entire treatment area. A gas delivery system may be used to combine any combination of a
plurality (such as 4) of nmental gases and precursors into a single feed which populates the
hybrid plasma chamber. Additionally, a spray or misting ry system may be provided,
e of applying a thin, consistent layer of sol-gel or process accelerants to the material being
treated, either pre- or post- processing.
The process of ing plasma and photonics (such as UV laser) is dry, is carried out at
atmospheric pressures and uses safe and inert gases (such as Nitrogen, Oxygen, Argon & Carbon
Dioxide). Changing the power intensity of the laser and the plasma, and then varying the
environmental gases or the addition of sol-gels and/or other organic or nic precursors -
i.e., changing the “recipe” - allows the system to generate a wide variety of process applications.
There are at several applications for the process, including: cleaning, preparation and
performance enhancement of materials.
- For cleaning, the laser may ify the effective power of the plasma as well as acting
on the substrate material in its own right.
- For preparing the substrate material for secondary processing, such as dyeing, the surface
of the fibers may be ablated in a controlled manner, thereby increasing the hydrophilicity
of the material (such as a e material). Additionally, be introducing environmental
gases into the process zone of the system, chemistries may be created at the surface of the
material (e.g., fabric) which may result in chemistries that react with a dyeing media to
effect a more ent dye penetration or a more intense coloring process or reduction of
dye temperature. For example, preparing the fibers of the textile to give a better
controlled uptake of chrome oxide dyes to improve the intensity of black ed. There
is, therefore, potential for this process to reduce the chemical content of dyes which could
reduce both negative environmental impact and sing costs.
- For mance Enhancement, the s may achieve material synthesis in the surface
of the substrate. By altering the laser and plasma frequencies and the power intensities,
and introducing other materials into the process environment, the system s the
surface of the substrate and a series of chemical reactions between the substrate and the
environmental gases synthesize new materials in the surface of the fibers in the textile
web.
Unless the context clearly requires otherwise, hout the description and claims the terms
“comprise”, “comprising” and the like are to be construed in an inclusive sense, as opposed to an
exclusive or exhaustive sense. That is, in the sense of “including, but not limited to”.
BRIEF DESCRIPTION OF THE DRAWINGS
Reference may be made in detail to embodiments of the disclosure, some non-limiting es
of which may be illustrated in the accompanying drawing figures (FIGs). The figures are
lly ms. Some elements in the figures may be exaggerated, others may be omitted,
for illustrative clarity. The relationship(s) between different ts in the figures may be
ed to by how they appear and are placed in the drawings, such as "top", "bottom", "left",
"right", "above", "below", and the like. It should be understood that the phraseology and
terminology employed herein is not to be construed as limiting, and is for descriptive purposes
only.
is a diagram of a treatment system, according to an embodiment ofthe invention.
is a partial perspective View of a plasma region of the treatment system of
is a partial perspective View of a plasma region ofthe treatment system of
is a partial ctive View of a pre-treatment region, plasma region and post-treatment
region ofthe treatment system of according to some embodiments of the invention.
FIGs. 4A - 4G are diagrams of elements in a treatment region of the treatment system of
according to some embodiments ofthe invention.
DETAILED DESCRIPTION
The ion s generally to treatment (such as surface treatment) of materials (such as
textiles) to modify their properties.
Various embodiments will be described to illustrate teachings of the invention(s), and should be
construed as rative rather than limiting. Although the invention is generally described in the
context of various exemplary embodiments, it should be understood that it is not intended to
limit the invention to these particular embodiments. An embodiment may be an example or
implementation of one or more aspects of the invention(s). gh various features of the
invention(s) may be bed in the context of a single embodiment, the features may also be
provided separately or in any suitable ation with one r. Conversely, although the
invention(s) may be described in the context of separate embodiments, the invention(s) may also
be implemented in a single embodiment.
In the main hereinafter, surface treatment of substrates which may be textiles supplied in roll
form (long sheets of material rolled on a cylindrical core) will be discussed. One or more
treatments, including but not d to material sis, may be applied to one or both
es of the textile ate, and additional als may be introduced. As used herein, a
“substrate” may be a thin “sheet” of al haVing two surfaces, which may be termed “front”
and “back” surfaces, or “top” and “bottom” surfaces.
Some Embodiments of the Invention
The following embodiments and aspects thereof may be described and illustrated in ction
with systems, tools and methods which are meant to be exemplary and rative, not limiting in
scope. Specific configurations and details may be set forth in order to provide an understanding
of the invention(s). However, it should be apparent to one skilled in the art that the invention(s)
may be practiced without some of the specific details being presented herein. Furthermore, well-
known features may be omitted or simplified in order not to obscure the descriptions of the
ion(s).
shows an overall surface treatment system 100 and method of performing ent, such
as a surface treatment of a substrate 102. In the figures presented herein, the substrate 102 will
be shown advancing from right-to-left through the system 100.
The substrate 102 may for example be a textile material and may be supplied as “yard goods” as
a long sheet on a roll. For example, the substrate to be treated may be fibrous textile material
such as cotton/polyester, approximately 1 meter wide, approximately 1mm thick, and
approximately 100 meters long.
A section 102A, such as a 1m x 1m section of the substrate 102 which is not yet d is
illustrated paying out from a supply reel R1 at an input section 100A of the system 100. From
the input section 100A, the substrate 102 passes through a treatment section 120 of the apparatus
100. After being treated, the substrate 102 exits the treatment apparatus 120, and may be
collected in any suitable manner, such as wound up on a take-up reel R2. A section 102B, such
as a 1m x 1m section of the substrate 102 which has been treated is illustrated being wound onto
an takeup reel R1 at an output section 100A of the system 100. Various rollers “R” may be
provided between (as shown) and within (not shown) the various ns of the system 100 to
guide the material through the system.
The treatment section 120 may generally comprise three regions (or areas, or zones):
- ally, a pre-treatment (or precursor) region 122,
- a treatment (or plasma) region 124, and
- optionally, a post-treatment (or ing) region 126.
The treatment region 124 may comprise components for generating a high voltage (HV)
alternating t (AC) atmospheric plasma (AP), the elements of which are generally well
known, some ofwhich will be described in some detail hereinbelow.
A laser 130 may be provided, as the secondary energy source, for providing a beam 132 which
interacts with the AP in the main treatment region 124, and which may also e on a e
of the substrate 102.
A controller 140 may be provided for controlling the operation of the various components and
elements bed hereinabove, and may be ed with the usual human interfaces (input,
y, etc.).
shows a portion of and some operative elements within the main treatment region 124.
Three orthogonal axes x, y and z are illustrated. (In the corresponding x and y axes are
illustrated.)
Two elongate electrodes 212 (el) and 214 (e2) are shown, one of which may be considered to be
a cathode, the other of which may be considered to be an anode. These two electrodes el and e2
may be disposed generally parallel with one another, extending parallel to the y axis, and spaced
apart from one another in the x direction. For example, the electrodes el and e2 may be formed
in any suitable , such as in the form of a rod, or a tube or other rotatable cylindrical
electrode material, and spaced apart from one another nominally, a distance sufficient to allow
for clearance of the thickness of the material processed. The electrodes el and e2 may be
disposed approximately 1 mm above the top surface 102a of the substrate 102 being treated.
The electrodes el and e2 may be energized in any suitable manner to create an atmospheric
plasma (AP) along the length of the resulting cathode/anode pair in a space between and
immediately surrounding the electrodes el and e2, which may be referred to as a “plasma
reaction zone”.
As mentioned above, a laser beam 132 may be ed into the main treatment region 124, and
may also impinge on a surface of the substrate 102. Here, the laser beam 132 is shown being
directed approximately along the y axis, approximately el to and between the electrodes el
and e2, and slightly above the top surface 102a of the ate 102, so as to interact with the
plasma (plume) generated by the two electrodes el and e2. In an exemplary ation, the
beam footprint may be a rectangle approximately 30mm x 15mm. The beam may be oriented
vertically or horizontally to best achieve the d interaction of plasma and/or direct substrate
irradiation
The laser beam 132 may be directed minutely but ently “off angle” to directly irradiate the
ate 102 to be treated as it coincidently reacts with the plasma being generated by the two
electrodes el and e2. More particularly, the laser beam 132 may make an angle of “a” which is
approximately 0 degrees with the top e 102a of the substrate 102 so as not to impinge on
its surface 102a. Alternatively, the laser beam 132 may make an angle of “a” which is
approximately less than 1 - 10 degrees with the top surface 102a of the substrate 102 so as to
impinge on its surface 102a. Other orientations of the beam 132 are possible, such as
perpendicular (“a” = 90 degrees) with the surface 102a of the ate 102. The laser beam
132 may be scanned, using conventional galvanometers and the like, to ct with any selected
portion of the plasma generated by the two electrodes el and e2 or the substrate 102, or both.
The plasma may be created using a first energy source such as high voltage (HV) alternating
current (AC). A second, different energy source (such as laser) may be caused to interact with
the plasma, resulting in a “hybrid plasma”, and the hybrid plasma may be caused to interact (in a
treatment region) with the substrate (material) being d. In addition to interacting with the
first energy source, the second energy source can be caused to also ct directly with the
material being treated. The direct interaction with the substrate or other gas dary or
precursor) may produce its’ own laser sustained plasma which in turn may further interact with
the high voltage ted plasma to more highly energize the reaction milieu.
The substrate 102 (material being treated) may be guided by rollers as it passes through the main
ent region (area) 124. illustrates that one of these rollers 214 may serve as the
anode, and the other roller 212 may serve as the cathode (or vice-versa) of a cathode/anode pair
for generating the plasma. It may be noted that in the substrate 102 is disposed to one
side of (below, as viewed) both of the two electrodes el and e2, and in the substrate 102
is disposed between the two odes el and e2. In both cases, the plasma created by the
electrodes el and e2 acts on at least one surface of the substrate 102. The anodes and cathodes
may be coated with an ting material, such as ceramic.
It should be understood that the invention is not limited to any particular arrangement or
configuration of electrodes el and e2, and that the examples set forth in FIGs. 2, 2A are intended
to be merely illustrative of some of the possibilities. Furthermore, for example, as an alternative
to using two electrodes el and e2, a row of plasma jets (not shown) delivering a plasma may be
provided to create the desired plasma above the surface 102a ofthe substrate 102.
shows that in the pre-treatment region (area) 122, a row of spray heads (nozzles) 322
covering the filll width of the material to be treated, or other suitable means, may be used to
dispense precursor materials 323 in solid, liquid or s phase onto the ate 102 to
enable the processing of/for specific properties such as crobial, fire retardant or super-
hydrophobic/hydrophilic characteristics.
There may be an intermediate “buffer” zone between the eatment region (area) 122 and the
main treatment region (area) 124, to allow time for the materials d in pre-treatment to soak
into (be absorbed by) the substrate. The s still runs a single length of material, but the
buffer may hold, for example, up to 200m of . For example, when al being treated
(such as yard goods) is feeding through the system at 20 meters/min, this would allow for several
minutes “drying time” between eatment (122) and hybrid plasma treatment (124), without
stopping the flow of material through the system.
Similarly, in the post-treatment region (area) 126, a row of spray heads (nozzles) 326 covering
the full width of the material which was treated (124), or other suitable means, may be used to
dispense finishing materials 327 in solid, liquid or gaseous phase onto the substrate 102 to imbue
it with desired characteristics.
Some embodiments of the treatment region ( 124)
FIGS. 4A - 4G illustrate various embodiments of elements in the treatment region 124.
illustrates an embodiment 400A wherein:
- A first (“top”) roller 412 is operative to fiJnction as an electrode el, and may have a
diameter of approximately 10cm, and a length (into the page) of 2 . The roller 412
may have a metallic core and a ceramic (electrically insulating) outer e.
- A second (“bottom”) roller 414 is operative to fiJnction as an electrode e2, and may have
a er of approximately 15cm, and a length (into the page) of 2 meters. The roller
414 may have a metallic core and a ceramic (electrically insulating) outer surface.
- The second roller 414 is disposed parallel to and directly underneath (as viewed) the first
roller 412, with a gap therebetween corresponding to (such as slightly less than) the
thickness of the substrate material 402 (compare 102) being fed between the rollers 412
and 414. The direction of material travel may be right-to-left, as indicated by the arrow.
The substrate 402 has a top surface 402a (compare 102a) and a bottom e 402b
(compare 102b).
- The first roller 412 may serve as the “anode” of an anode/cathode pair, having high
voltage (HV) supplied thereto. The second roller 414 may serve as the “cathode” of the
anode/cathode pair, and may be grounded.
- A first (“right”) nip or feed roller 416 (n1) is disposed adjacent a bottom-right (as
viewed) quadrant of the first roller 412, and against a top-right (as viewed) quadrant of
the second roller 414. The roller 416 may have a er of approximately 12cm, and a
length (into the page) of 2 meters. The outer surface of the roller 416 may engage the
outer surface of the roller 412. A gap between the outer surface of the roller 416 and the
outer surface of the roller 414 corresponds to (such as slightly less than) the thickness of
the substrate al 402 (compare 102) being fed between the s 416 and 414.
- A second (“left”) nip or feed roller 418 (n2) is disposed adjacent a bottom-left (as
viewed) quadrant ofthe first roller 412, and against a ft (as ) nt of the
second roller 414. The roller 418 may have a diameter of approximately 12cm, and a
length (into the page) of 2 meters. The outer surface of the roller 418 may engage the
outer surface of the roller 412. A gap between the outer surface of the roller 418 and the
outer surface of the roller 414 corresponds to (such as slightly less than) the thickness of
the substrate al 402 (compare 102) being fed between the rollers 418 and 414.
- Generally, the nip or feed rollers 416, 418 should have an ting outer surface so as to
avoid shorting the anode and cathode 412, 414.
With such an arrangement of rollers 412, 414, 416, 418, a semi-airtight cavity (“440”) may be
formed between the outer surfaces of the four rollers 412, 414, 416, 418 for defining the
treatment region 124 and containing the plasma. The overall cavity 440 may comprise a first
(“right”) portion 440a in the space n the top, right and bottom rollers 412, 416, 414 and a
second (“left”) portion 440b in the space between the top, left and bottom rollers 412, 418, 414.
The filled circle at the end of the lead line for the right portion 440a of the cavity 440 represents
gas flow into the cavity. The filled rectangle at the end of the lead line for the left portion 440b
of the cavity 440 represents the laser beam (132).
The plasma generated in the cavity 440 may be an atmospheric pressure (AP) .
Therefore, sealing of the cavity 440 is not necessary. However, end caps or plates (not shown)
may be disposed at the ends of the rollers 412, 414, 416, 418 to contain (semi-enclose) and
control the gas flow in and out of the cavity 440.
illustrates an embodiment 400B wherein the left and right rollers 416 and 418 are
moved slightly outward from the s 412 and 414, thereby opening up the caVity 440 to allow
for thicker and /or stiffer substrates to be processed . This would however require independent or
direct drive of each electrode, anode and cathode. The material would be driven through the
reaction zone by outside feeding and take up rollers.
illustrates an embodiment 400C wherein a generally inverted U-shaped shield 420 is
used instead of the left and right s (416 and 418) to define the caVity 440 haVing right and
left portions 440a and 440b. The shield 420 is disposed substantially completely around one
roller 412 (except for where the material feeds through), and at least partially around the other
roller 414. An additional shield (not shown) could be disposed under the bottom roller 414.
illustrates an embodiment 400D adapted to treat rigid substrates. The substrate 402
described above was e, such as textile. Rigid substrates such as glass for touchscreen
displays may also be treated with a hybrid plasma and precursor materials. A rigid substrate 404
haVing a top surface 404a and bottom surface 404b passes through the top roller (e1) 412 and the
bottom roller (e2) 414. A row of nozzles 422 (compare 322) may be arranged to provide
precursor material, such as in , solid or atomized form. A shield (not shown) such as 420
(refer to ) may be incorporated to contain the hybrid plasma.
shows an arrangement 400E incorporating a row of HV plasma nozzles (jets) 430,
rather than the cylindrical electrodes el and e2. For example, ten jets 430 spaced at 20cm
intervals in the treatment region 124. A rigid ate 404 is shown. A row of nozzles 422
re 322) may be arranged to e sor material, such as in atomized form, onto the
substrate 404, in a pre-treatment region 122, before it is exposed to the hybrid . For
example, ten nozzles 422 spaced at 20cm intervals in the pre-treatment region 122. A shield
(not shown) such as 420 (refer to ) may be incorporated to contain the hybrid plasma.
This arrangement enables treatment of ic or other conductive substrates.
illustrates an ment 400F a first (“top”) roller 412 operative to fianction as an
electrode e1 (or anode), a second (“bottom”) roller 414 operative to fianction as an electrode e2
(or cathode), and two nip rollers 436 and 438 (compare 416 and 418).
In contrast with the embodiment 400A (), in this embodiment the rollers 436 and 438)
are spaced outward slightly (such as 1 cm) from the top and bottom rollers 412 and 414.
ore, although they will still help n the plasma, they may not fianction as feed s,
and separate feed rollers (not shown) may need to be provided .
The right roller 436 (compare 416) is shown having a layer or coating 437 on its surface. The
left roller 438 (compare 418) is shown having a layer or coating 439 on its surface. For e,
the rollers 436 and 438 in the hybrid plasma treatment region 124 may be wrapped with metallic
foil (or otherwise have a metallic outer layer) which may be etched away, in process, by the
highly energetic hybrid plasma and/or by the laser (second energy source) creating a plume
containing reactive ic plasma which may y couple with the substrate surface radicals
to create nano-layer coatings with metallic composition on the substrate material. The metallic
material (foil, layer) may be controllably etched or ablated by the plasma, and the effluent
metallic constituents may react with the plasma and be deposited on the substrate, such as in
nano-scale .
The metallic material coating the rollers 436 and 438 may comprise any one or combination of
titanium, copper, aluminum, gold or silver, for example. One of the rollers may be coated with
one material, the other of the rollers may be coated with another material. Different portions of
the rollers 436 and 438 may be coated with different materials. Generally, when these materials
are ablated, they form vapor precursor al, in the treatment region 124 (and may therefore
be contrasted with the nozzles 322 and 422 providing precursor material in the pre-treatment
region 124.)
illustrates an embodiment 400G using two flat sheet, plate electrodes 452 and 454,
rather than rollers (412, 414), spaced apart from one another to form a treatment region
(reaction/synthesis zone) 124 through which a sheet of material 404 may be fed. Gas feed to the
treatment region is indicated by the circle 440a, the laser beam is indicated by the rectangle
440b. Nozzles 422 may be provided to deliver precursor material(s) in the pre-treatment zone
122. Nozzles 426 may be provided to deliver finishing material(s) in the post-treatment zone
126.
onal Features
Although not specifically shown, finishing materials dispensed onto the substrate 102 after
hybrid energy treatment (124) may be subjected to an immediate secondary plasma or hybrid
plasma exposure to dry, seal or react finishing materials which have been dispensed following
activation ofthe e by the hybrid plasma.
Although not specifically shown, it should be understood that s gases, such as 02, N2, H,
CO2, Argon, He, or compounds such as silane or siloxane based materials may be introduced
into the plasma, such as in the treatment region 124, to impart various desired characteristics and
properties to the treated substrate.
To impart anti-microbial ties to the material being treated, precursor materials may be
introduced such as non-silver based silanes/siloxanes and the aluminum chloride family such as
3 (trihydroxylsilyl) propyldimethyl cyl, ammonium chloride. Other Silane/Siloxane
groups may be used to affect hydrophobicity as well as siloxones and ethoxy silanes (to increase
hydrophilicity). thylidisiloxane d in the gaseous phase in the plasma may smooth
the surface of textile fibers and increase the contact angle which is an indication of the level of
hobicity.
Negative draft or atmospheric partial vacuum may be ed to draw plasma constituents into
and filrther penetrate the thickness of porous substrates. shows that suction means, such
as platen (bed) 324 over which the substrate 102 passes, in the treatment area 124, may be
provided with a ity of holes and connected in a suitable manner to n means (not
shown) to create the d effect. The platen 324 may function as one of the electrodes for
generating the plasma. Alternatively, a roller or the like could readily be modified (with holes
and connected with suction means) to perform this fianction.
It should be understood that the process is dry and has a low environmental impact, and that
leftover or byproduct gases or constituents are inherently safe and may be ted from the
system and recycled or disposed of in an appropriate manner.
There is thus provided a method of treating materials with at least two energy sources, wherein
the two energy sources comprise (i) an AP plasma produced by various gases passing through a
high energy electromagnetic field and (ii) at least one laser interacting with said plasma to create
a “hybrid plasma”. The laser may operate in the ultra-violet wave length range, at 308nm or
less. The laser may comprise an excimer laser ing with at least 25 watts of output power,
including more than 100 watts, more than 150 watts, more than 200 watts. The laser may be
pulsed, such as at a frequency of 25Hz or higher such as 350-400 Hz, including picosecond and
femtosecond lasers. Although only one laser has been described cting with the plasma (and
the substrate), it is within the scope of the invention that two or more lasers may be used.
Some exemplary parameters for generating the plasma in the treatment region are l - 2 Kw
atts) for the HV generated plasma and ules, 350Hz for the 308nm UV laser, in an
80% argon, 20% Oxygen or CO2 gas mix.
As an ative to or in addition to using a laser, an ultraviolet (UV) source such as a UV lamp
or an array of high powered UV LEDs (light-emitting diodes) disposed along the length of the
treatment area may be used to direct energy into the AP plasma to create the hybrid plasma, as
well as to interact with (such as to etch, react and synthesize upon) the material being treated..
In the main, hereinabove, treating one surface 102a of a substrate al 102 was illustrated,
and some exemplary treatments were described. It is within the scope of the invention that the
opposite bottom surface 102b of the material 102 may also be treated, such as by looping the
material 102 back h the treatment region 124. Different energy sources and milieus,
precursor and finishing materials may be used to treat the second surface of the material. In this
manner, both surfaces of the material may be treated. It should also be understood that the
treatments may extend to within the e of the material being d to alter or enhance
properties of the inner (core) material. In some cases, both top and bottom surfaces as well as
the core ofthe material may be effectively treated from one side.
The system can be used to treat materials which are in other than sheet form. For e, the
system may be used for improving optical and morphological properties of organic light-emitting
diodes (OLEDs) by hybrid energy annealing. These discrete items may be transported
(conveyed) through the system in any suitable manner.
Other types of energy may be applied in combination or in sequence with each other to create
enhanced processing lities. For example, a method of treating materials may utilize the
combination of at least two energy sources such as ave and laser, or microwave and
omagnetically generated plasma, or plasma and microwave, or various combinations of
plasma, laser and pulsable microwave electron cyclotron resonance (ECR).
The two energy sources may se (i) an atmospheric plasma, ing various ionized gases
passed through high energy electromagnetic fields, and (ii) an ultra violet (UV) source
generating and directing radiation into the highly ionized plasma and directly at the surface to be
treated. The UV source may se an array of high powered UV LEDs (light-emitting
diodes) disposed along the extent of the treatment area. The high powered ultra-violet LEDs
may interact with the plasma to more highly energize the plasma, as well as acting directly on the
substrate to etch or react said substrate.
An automated material ng system may controllably feed material through the energy fields
produced by combination energy sources.
A series ofprocess steps may be performed, such as:
step 1 - (optional) precursor application,
step 2 - exposure to hybrid energy,
step 3 - (optional) precursor or finishing material application and,
step 4 - exposure to hybrid energy.
in which all steps are accomplished in serial n immediately within the system.
It is within the scope of the invention to introduce into the process a delivery system capable of
adding gas/vapor phase precursor materials ly in to the plasma reaction zone.
Some Exemplary Treatment Process Parameters
Treatment 1 - Hydrophilicity
Precursor material
polydimethylsiloxane hydroxycut (PMDSO Hydroxycut)
alt: copolymer (Dimethylesiloxane and/or with blend of dimethylesilane)
Laser
ncy 250Hz
Power 380 mJ
Plasma
Carrier Gas Argon 80%
Reactive Gas 02 20%
Flow rate 15 liter/min Pressure: slightly above 1 bar
Power 2 KW
Treatment 2 - lity
Precursor
Either no precursor or other precusor sts
Laser
Frequency 250Hz
Power 380 mJ
Plasma
Carrier Gas Argon 80%
WO 01306
Reactive Gas 02 or N2 20%
Flow rate 15 liter/min re: slightly above 1 bar
Power 2 KW
Treatment 3 - Hydrophobicity
Precursor octamethylcyclotetrasiloxane/polydimethylsilane blend (water soluable,
hydrogen methyl polysiloxane mixed withpolydimethylsiloxane with polyglycolether (water
soluable) or ation ofthe above with polydimethylsiloxane. Using water soluble blends
allows for ng the materials with ised water to the ed concentrations based on
the application, cost effectiveness and output performance results. Water soluble blends may be
produced with relevant additives - these are essentially methods for mixing oil with water to
produce emulsions, generally described by the size of the emulsion dispersant, i.e. macro or
micro (macro is >100 microns, micro<30 microns).
alt: copolymer hylesiloxane and/or with blend of dimethylesilane)
Laser
Frequency at least 350Hz
Power at least 450 mJ
Plasma
Carrier Gas Nitrogen, Argon, Helium 80%
Reactive Gas CO2 or N2 2-20%
Flow rate 10-40 min Pressure: slightly above 1 bar
Power 0.5 — 1 KW
Treatment 4 - Fire retardancy
Precursor
Copolymers and Terpolymers based on siloxane/silane and polyborosiloxane with key
inorganic compounds, essentially transition oxides of titanium, silicon and zirconium and
boron. Also included, Boron containing siloxane Copolymers and Terpolymers, such as
organosilicon/oxyethyl modified polyborosiloxane. Some limited material composition
based recent new phosphorous blends may be used, based on the substrate material types
and output requirements. octamethylcyclotetrasiloxane/polydimethylsilane blend (water
W0 2013/001306
soluable) mixed with polydimethylsiloxane with polyglycolether (water soluble) or
comination of the above with polydimethylsiloxaneWith additives of:
- calcium metaborbate additive to silane/siloxane -
- Silicon oxide additive to silane /siloxane -
- Titanium isopropoxide additive '
- Titanium dioxide le)'
- Ammonium phosphate
- um oxide-
- Zinc borate'
- Boron phosphate containing preceramic oligomores'
- Aerogels and hydrogels, low or high density cross linked rylates.-
- nano/micro encapsulated compositions.
Example: dimethylsiloxane and/or with dimethylsilane with polyborosiloxane, with
added tion oxides, range 5 to 10% volume of oxides such as Tio2, sio2 (filmed, gel
or amorphous), A1203, etc. The precursor materials set forth herein may enhance fire
retardency of materials in the system bed herein utilizing a hybrid plasma (e.g.,
with laser). It is Within the scope of the invention that the precursor materials set forth
herein may enhance fire ency (or other properties) of materials in a material
treatment system utilizing a non-hybrid plasma (e.g., Without the laser).
Laser
Frequency at least 350Hz
Power at least 450 mJ
Plasma
Carrier Gas Nitrogen, Argon, Helium 80%
Reactive Gas C02 or N2 2-20%
Flow rate 10-20 min Pressure: slightly above 1 bar
Power 0.5 — 1 KW
Treatment 5 - Anti Microbial
Precursor
siloxane/silane blends as per hydrophobicity platform, with the addition of
octadecyldimethyl (3triethoxysilpropyl) ammonium de.
octamethylcyclotetrasiloxane/polydimethylsilane blend (water soluble)mixed
Withpolydimethylsiloxane with polyglycolether (water e) or tion of above With
polydimethylsiloxanewith additives of:
- octadecyldimethyl(3-trimethoxysilylpropyl)ammmonium chloride),
- Chitosan
Laser
Frequency at least 350Hz
Power at least 450 mJ
Plasma
Carrier Gas Nitrogen, Argon, Helium 80%
ve Gas C02 or N2 2-20%
Flow rate 10-20 liter/min Pressure: slightly above 1 bar
Power 0.5 - 1 KW
While the invention(s) has been described with respect to a limited number of embodiments,
these should not be construed as limitations on the scope of the invention(s), but rather as
examples of some of the embodiments. Those skilled in the art may envision other possible
variations, modifications, and implementations that are should also be considered to be Within
the scope of the invention(s), based on the disclosure(s) set forth herein, and as may be claimed.