WO2007119229A1 - Sensor comprising conducting polymer materials - Google Patents
Sensor comprising conducting polymer materials Download PDFInfo
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- WO2007119229A1 WO2007119229A1 PCT/IE2007/000047 IE2007000047W WO2007119229A1 WO 2007119229 A1 WO2007119229 A1 WO 2007119229A1 IE 2007000047 W IE2007000047 W IE 2007000047W WO 2007119229 A1 WO2007119229 A1 WO 2007119229A1
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- polyaniline
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/53—Immunoassay; Biospecific binding assay; Materials therefor
- G01N33/543—Immunoassay; Biospecific binding assay; Materials therefor with an insoluble carrier for immobilising immunochemicals
- G01N33/54366—Apparatus specially adapted for solid-phase testing
- G01N33/54373—Apparatus specially adapted for solid-phase testing involving physiochemical end-point determination, e.g. wave-guides, FETS, gratings
- G01N33/5438—Electrodes
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/001—Enzyme electrodes
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- C—CHEMISTRY; METALLURGY
- C12—BIOCHEMISTRY; BEER; SPIRITS; WINE; VINEGAR; MICROBIOLOGY; ENZYMOLOGY; MUTATION OR GENETIC ENGINEERING
- C12Q—MEASURING OR TESTING PROCESSES INVOLVING ENZYMES, NUCLEIC ACIDS OR MICROORGANISMS; COMPOSITIONS OR TEST PAPERS THEREFOR; PROCESSES OF PREPARING SUCH COMPOSITIONS; CONDITION-RESPONSIVE CONTROL IN MICROBIOLOGICAL OR ENZYMOLOGICAL PROCESSES
- C12Q1/00—Measuring or testing processes involving enzymes, nucleic acids or microorganisms; Compositions therefor; Processes of preparing such compositions
- C12Q1/001—Enzyme electrodes
- C12Q1/005—Enzyme electrodes involving specific analytes or enzymes
- C12Q1/006—Enzyme electrodes involving specific analytes or enzymes for glucose
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- G—PHYSICS
- G01—MEASURING; TESTING
- G01N—INVESTIGATING OR ANALYSING MATERIALS BY DETERMINING THEIR CHEMICAL OR PHYSICAL PROPERTIES
- G01N33/00—Investigating or analysing materials by specific methods not covered by groups G01N1/00 - G01N31/00
- G01N33/48—Biological material, e.g. blood, urine; Haemocytometers
- G01N33/50—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing
- G01N33/84—Chemical analysis of biological material, e.g. blood, urine; Testing involving biospecific ligand binding methods; Immunological testing involving inorganic compounds or pH
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- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10T—TECHNICAL SUBJECTS COVERED BY FORMER US CLASSIFICATION
- Y10T428/00—Stock material or miscellaneous articles
- Y10T428/24—Structurally defined web or sheet [e.g., overall dimension, etc.]
- Y10T428/24802—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.]
- Y10T428/24893—Discontinuous or differential coating, impregnation or bond [e.g., artwork, printing, retouched photograph, etc.] including particulate material
Definitions
- Conducting polymer materials are a unique class of organic materials that exhibit electrical and optical properties of metals and semiconductors (Saxena & Malhotra, 2003). They offer prospects for practical applications due to their levels of conductivity, inexpensiveness, and ease of synthesis.
- polyaniline is probably the most widely studied because it has a broad range of tunable properties derived from its structural flexibility. It has potential in numerous applications including sensors, rechargeable batteries, light-emitting diodes, corrosion protection of metals and gas separation membranes.
- polyaniline has proved difficult to exploit for a number of reasons. It is insoluble in common solvents which seriously hinders its processability.
- the monomer, aniline is a carcinogen.
- PANI polyaniline
- Conducting polymers are attractive for electronic applications and using inkjet printing, ultra-thin films can be patterned with resolution up to 20-30 ⁇ m (Calvert, 2001).
- Chen et al., 2003 describes inkjet printing an all-polymer RC filter circuit using soluble conducting polyaniline and poly(3,4-ethylenedioxythiophene).
- US Patent No. 6,576,975 to Yang et al. discloses an organic semiconductor device that employed inkjet printing for patterning high quality 'buffer' layers of conducting polymer between upper and lower electrodes to regulate current flow between the electrodes.
- US Patent No. 6,762,050 to Fukushima et al. discloses the manufacture of a microsensor device where soluble conducting polymers such as polypyrrole, polythiophene and polyaniline were inkjet printed between two microelectrodes, and used for the detection of biomolecular or other organic species.
- InkJet printing of conducting polymers described to date relies on soluble conducting polymer which has inherent disadvantages.
- the polymer When the polymer is soluble in water, nonaqueous solvents must be used for the sensor application (Ballarin et al., 2004), or alternatively, a membrane must be applied on top in order to prevent dissolution of the films in the aqueous buffer solutions that are employed (Setti et al., 2005).
- a polymer is soluble in organic media, incorporation of protein is not favourable.
- inkjet printing is very vulnerable to blockage due to solvent drying and hence a printing method that relies on rapid evaporation of solvent can be intrinsically difficult to maintain (Calvert, 2001).
- US Patent No. 6,762,050 discloses that if the polymer is insoluble in both common organic and water-based solvents, the polymer needs to be synthesised directly on the substrate, wherein monomer is printed onto oxidant-containing films.
- Prior art publications are limited to water- or organic-soluble conducting polymers such as doped polyaniline derivatives or Poly(3,4-ethylenedioxythiophene) poly(styrenesulphonate) (PEDOT/PSS). Films cast from water-soluble materials are generally unstable in aqueous media, and hence often require the use of additional materials, such as polycations, in order to render the polymer insoluble (Ngamna et al., 2005).
- the invention provides a sensor comprising a substrate having nanoparticles of a conducting polymer printed thereon.
- the nanoparticles may be formed ofpolyaniline.
- the nanoparticles may be substantially spherical in shape.
- the size distribution of the nanoparticles may be in the range of from lnm to lOOnm, such as in the range of from lOnm to 50nm.
- the size distribution of the nanoparticles may be in the range of from 20 to 80nm, typically 30nm to 80nm.
- the nanoparticles may be inkjet printed onto the substrate.
- the nanoparticles may be inkjet printed onto the substrate using piezoelectric technology.
- the substrate may be an electrode.
- the sensor may be electrochemical in nature.
- the sensor may be used for chemical sensing.
- the senor may be used for direct sensing of an entity.
- the sensor may be used for indirect sensing of an entity.
- the sensor may be a biosensor.
- the sensor may comprise a protein such as an enzyme.
- the enzyme may be immobilized on the substrate.
- the enzyme may be horse radish peroxidase.
- the enzyme may be glucose oxidase. - A -
- the senor may be an immunosensor.
- the entity detected by the sensor may comprise an amine such as ammonia.
- the entity may comprise hydrogen peroxide or glucose
- the sensor may be used for the direct sensing of hydrogen peroxide.
- the sensor may have a detection range from about 8xlO '3 to about 1.12XlO "1 M.
- the substrate may be a thermostable material for example a thermostable material that may undergo dynamic recovery upon the application of heat.
- the invention also provides for a printing composition for printing onto a substrate, the composition comprising nanoparticles of a conducting polymer.
- the composition may be an inkjet composition for inkjet printing onto a substrate.
- the nanoparticles of the composition may be formed of polyaniline.
- the nanoparticles of the composition may be substantially spherical in shape.
- the size distribution of the nanoparticles of the composition may be in the range of from lnm to lOOnm. For example, in the range of from lOnm to 50 nm. Alternatively, the size distribution of the nanoparticles may be in the range of from 20nm to 80nm, typically 30nm to 80nm
- the invention also provides a method for obtaining a pattern on a substrate comprising printing nanoparticles of a conducting polymer onto the substrate.
- An ink containing nanoparticles of a conducting polymer may be printed onto a substrate, the nanoparticles may be formed of polyaniline.
- the printing may be inkjet printing.
- the nanoparticles may be substantially spherical in shape.
- the size distribution of the nanoparticles may be in the range of from lnm to lOOnm, such as in the range of from lOnm to 50 nm. For example, in the range of from 20nm to 80nm, typically 30nm to 80nm
- the invention also provides nanoparticles of a conducting polymer, the nanoparticles being substantially spherical in shape.
- the diameter distribution of the nanoparticles may be in the range of from lnm to lOOnm, such as from lOnm to 50nm for example, 20 to 80 nm, typically 30nm to 80nm.
- the nanoparticles may be formed of polyaniline.
- the invention provide a method of regenerating a sensor comprising a substrate having nanoparticles of a conducting polymer printed thereon, the method comprising applying heat to the sensor.
- the heat source may be a stream of heated air.
- the heat source may be applied directly to the sensor.
- the invention also provides a method of sensing hydrogen peroxide comprising the steps of:
- the auxiliary electrode may be platinum.
- the reference electrode may be Ag/AgCl.
- the nanoparticles may be formed of polyaniline.
- the electrolyte solution may be phosphate buffered saline pH6.8.
- Fig. A is a schematic representation of a polyaniline nanoparticle synthesised according to Example 1 by the dodecylbenzenesulphonic acid (DBSA) micellar system, where after dialysis, there should be substantially no monomer remaining;
- Fig IA is a line graph depicting the % volume vs. diameter of a dispersion of polyaniline nanoparticles, synthesized according to Example 1, with an average size of approximately 40nm;
- Fig IB is a line graph depicting the % volume vs. diameter of a dispersion of polyaniline nanoparticles, synthesized according to Example 1, with an average size of approximately 70nm;
- Fig 2 is a transmission electron microscopy (TEM) image of polyaniline nanoparticles synthesised according to Example 1, the image was obtained at 100 keV and at a magnification of x 200k;
- TEM transmission electron microscopy
- Fig. 3A is a 3-D profilometry of an inkjet printed film (Example 3) of the polyaniline nanoparticles (Example 1) on Polyethylene Terephthalate (PET) (Example 2D) comprising 24 bi-directional prints;
- Fig 3B is a 3-D profilometry of a 5 ⁇ l drop-coated film of polyaniline nanoparticles (Example 1) on PET (Example 2D);
- Fig. 4A is a scan of Atomic Force Microscopy (AFM) analysis of a bare gold mylar substrate (scan size l ⁇ m);
- AFM Atomic Force Microscopy
- Fig. 4B is a scan of Atomic Force Microscopy (AFM) analysis of inkjet printed (Example 3) polyaniline nanoparticles (Example 1) (1 print) on gold mylar (scan size l ⁇ m) (Example 2E);
- AFM Atomic Force Microscopy
- Fig. 4C is a scan of Atomic force microscopy (AFM) analysis of inkjet printed (Example 3) polyaniline nanoparticles (Example 1) (10 prints) on gold mylar (scan size l ⁇ m) (Example 2E);
- Fig. 5 A is a graph showing a scan rate study in IM HCl of an inkjet printed polyaniline nanoparticle film, comprising 24 bi-directional prints, on a screen-printed carbon paste electrode (Example 3 a);
- Fig. 5B is a line graph showing the dependency of the peak current of peaks I and II of Fig 5 A on scan rate;
- Fig. 5 C is a line graph showing the dependency of the peak current of peaks I and II of Fig 5A on (scan rate) 172 ;
- Fig 6B is a bar chart of the % RDS for peak I of Fig. 6A for inkjet printed polyaniline films in both the mono (black) and bi directional modes (grey);
- Fig. 7 is a cyclic voltammogram comparison of the electrochemistry of an inkjet printed film (50 prints) and a 5 ⁇ l drop-coated film on screen printed electrodes (cyclic voltammetry was carried out in 1 M HCl at 500 mV s "1 );
- Fig. 8 is a graph showing a rheological study of the polyaniline nanoparticle dispersions and a commercial Epson ink (T038);
- Fig. 9A is a graph showing amperometric response of ammonium ions at a concentration of 51, 17, 9 and 4 ppm respectively in 0.1 M phosphate buffer pH 6.6, -0.4 V vs. Ag/AgCl;
- Fig. 9B is a graph showing amperometric response of ammonium ions at a concentration of 2, 1 and 0.25 ppm respectively in 0.1 M phosphate buffer pH 6.6, -0.4V vs. Ag/AgCl;
- Fig. 1OA, B and C are line graphs showing amperometric data for inkjet printed films of polyaniline nanoparticles (50 prints) on screen-printed carbon paste electrodes in 0.1 M Phosphate buffer pH 6.6 and a potential of -0.4V vs. Ag/AgCl;
- Fig. 11 is a photographic representation of a 25 layered inkjet printed polyaniline nanoparticle film on a screen-printed silver interdigitated array (IDA) electrode.
- the numbers at the base (200 x 1500) refer to the digit width (200 ⁇ m) and digit space (1500 ⁇ m);
- Fig. 12 is a current-potential plot obtained when a varying potential is applied to a PANI- IDA;
- Fig. 13A is a plot showing the raw current-potential response (as recorded) of a PANI- IDA exposed to ammonia gas;
- Fig. 13B is a plot of current-potential response of PANI-IDA exposed to ammonia gas where the current was sampled at +0.5V vs. time (cycle is 20 s);
- Fig 14A is a graph showing the effect of ambient heat on electrode response (in an atmosphere free of ammonia) of a PANI-IDA electrode exposed to temperatures of between 20 to 120°C;
- Fig 14B is a graph showing the effect of ambient heat on electrode response (in an atmosphere free of ammonia) of a PANI-IDA electrode exposed to temperatures of between 20 to 160°C;
- Fig. 15 is a graph showing the effect on the response of a PANI-IDA electrode following long term exposure to a temperature of 75 0 C (the electrode was removed from the oven for 10 minutes prior to each measurement);
- Fig. 16A and B are graphs showing the response (A) and recovery (B) of a 25 layer PANI-IDA sensor when exposed to vapour from a 0.25% ammonia solution with a concentration of approximately 60ppm;
- Fig. 17 is a graph showing headspace analysis of ammonia gas using a PANI-IDA sensor with 25 inkjet prints at a digit width of 200 ⁇ m and a digit space of 1500 ⁇ m.
- the main graph shows the plot of I 0 - I (wherein I 0 is the initial current and I is the measured current) vs. log of the ammonia concentration (measured with an Impulse XP ammonia probe).
- the insert graph shows the measured current vs. ammonia concentration;
- Fig. 18A is a plot showing real-time amperometric responses for inkjet printed polyaniline nanoparticle films (20 prints) on screen-printed carbon paste electrodes to a plurality of additions of 8mM hydrogen peroxide, the potential was held at -10OmV vs. Ag/AgCl;
- Fig. 18B is a plot showing real-time amperometric responses for electropolymerised polyaniline film (10 cycles) on screen printed carbon paste electrodes to a plurality of additions of 8mM hydrogen peroxide, the potential was held at -10OmV vs. Ag/ AgCl;
- Fig. 20 is an amperogram illustrating the binding of HRP to the inkjet printed polyaniline nanoparticle films. Binding begins at 800 s and becomes saturated at 1250 s. Buffer is then passed over resulting in a return to background steady state signal. At approximately 1400 s, hydrogen peroxide only was passed over resulting in a catalytic signal confirmed by the binding of horse radish peroxidase (HRP) to the electrode surface;
- HRP horse radish peroxidase
- Fig. 21 is a schematic representation of an electrically wired immunosensor using polyaniline.
- the right hand schematic illustrates a system that provides mediated electron transfer between the electrode and any surface-bound species present in the polymer, the system also acts as a point of electrostatic protein deposition. Fig.
- Example 22 is a plot showing multi-calibrant analysis of HRP on a single polyaniline (Example 1) nanoparticle film inkjet printed (Example 3) onto a carbon paste, screen- printed electrode (Example 2A) surface.
- HRP standards (5 - 0.001 mg ml '1 ) were passed over the electrode surface for 30 s with 1 M hydrogen peroxide. HRP bound to the electrode surface in real-time with the resulting changes in slope of the catalytic signal corresponding to changes in binding concentrations.
- Nanoparticles of conducting polymers offer a route to overcome issues of solubility post- deposition. Once printed on a suitable substrate, nanoparticles adhere to the surface, and are rendered insoluble in mild media, hi contrast, incorporation of water-soluble protein into the conducting polymer films (by printing, or otherwise), will, in the case of doped polyaniline, attach to the polymer and not be vunerable to detachment or dissolution in buffer. Not only do nanoparticles overcome vital processibilty issues, they possess numerous other advantages over their soluble counterparts, as described above, including higher conductivity and more rapid, electrochemical switching processes.
- the printhead is assembled in the ink cartridge.
- the printing head consists of a nozzle plate with several ink ejection orifices connected to resistive heater elements and placed in contact with an ink reservoir.
- each individual heater element is actuated, rapid transfer of heat to a small portion of the ink located in the nozzles causes evaporation, creating a solvent bubble that leads to droplet formation.
- piezoelectric actuators the ink cartridge is detachable from the printhead. Crystalline materials in the printhead undergo mechanical stress upon application of an electric field. A very small contraction or expansion of these crystals, confined into the nozzles, allows for a reduction of space available for the ink, thus increasing pressure and causing ejection of the drop. Droplet sizes in both piezo and thermal technologies vary according to the temperature gradient applied, frequency, and ink viscosity.
- Aniline was purchased from Aldrich (13,293-4), vacuum distilled and stored frozen under nitrogen. Ammonium persulphate (APS), distilled aniline, dodecylbenzene sulphonic acid (DBSA) and sodium dodecylsulphonate (SDS).
- APS Ammonium persulphate
- DBSA dodecylbenzene sulphonic acid
- SDS sodium dodecylsulphonate
- Dialysis is the separation of small solute particles from colloid particles by means of a semi-permeable membrane. Using a dialysis membrane with a cutoff point of 12,000 molecular weight (as in this instance), all species with molecular weights lower than this can be removed over time. Therefore, after dialysis for 42 hours, unreacted aniline monomer (93.13 molecular weight) would be completely removed
- the initiator molecules Ammonium Persulphate (APS)
- APS Ammonium Persulphate
- the initiator molecules are evenly distributed (by a rapid mixing in this instance), they should be consumed very quickly. Therefore secondary growth of polyaniline is very limited due to lack of available reagents. Carrying out the technique of. Huang & Kaner (2006) results in nanofibrillar formation.
- DBSA dodecylbenzenesulphonic acid
- Figure A is a schematic representation of a polyaniline nanoparticle synthesised in the DBSA micellar system as described in Example 1.
- HRP horseradish peroxidase
- PVS Polyvinylsulphonate
- the silver/silver chloride (Ag/ AgCl) reference electrode was purchased from Bioanalytical Systems Ltd. (Cheshire, UK).
- the platinum mesh auxiliary electrode (29,809-3) was purchased from Aldrich.
- Gwent (C10903D14) carbon paste ink was purchased from Gwent Electronic Materials Ltd. (Gwent, UK).
- Electrodag ® PF-410S silver ink and Electrodag ® 452 SS BLUE insulation ink were purchased from Acheson Poly(ethylene) terephthalate (PET) substrates were purchased from HiFi Industrial Film Ltd (Dublin, Ireland). Indium Tin Oxide sputtered PET was purchased from CPfilms.
- the ink-jet printing system was an Epson Stylus C45 printer.
- the chip resetter was purchased from www.9to6.ie. All electrochemical protocols were performed on a CHlOOO potentiostat with CHlOOO software, using either cyclic voltammetry or time- based amperometric modes.
- a DEK 248 screen-printer was used for fabrication of the carbon-paste and inter-digitated array electrodes.
- Example 2 Substrates employed for inkjet printing, to include electrode substrates
- Example 2A Screen-printed electrodes were fabricated in-house using a DEK 248 according to Grennan et al. (2001). Briefly, electrodes were screen-printed onto pre- shrunk polyethylene terephthalate (PET) substrate. For the carbon paste electrodes: initially a layer of silver was deposited as the conducting path. A layer of Gwent carbon paste ink (C10903D14) was deposited as the working electrode. Finally, an insulation layer was deposited to eliminate cross-talk and to define the working electrode area (9 mm 2 ).
- PET polyethylene terephthalate
- Example 2B Screen-printed electrodes were fabricated in-house using a DEK 248 according to Grennan et al. (2001).
- IDA interdigitated array
- a layer of silver was screen-printed as the electrode layer onto pre-shrunk PET substrate.
- the resulting electrodes measured 30 mm from top to base and 24 mm across the base.
- a variety of pitch sizes were utilised, though the most commonly employed were IDAs with a digit width of 200 ⁇ m and a spacing of 1000 or 1500 ⁇ m. These dimensions were printed along the base of the electrode (i.e. 200 x 1500 for an IDA with 200 ⁇ m digits and 1500 ⁇ m spacing).
- the 200 x 1000 and 200 x 1500 IDAs had a total digit number of 17 and 12 respectively in an active area measuring approximately 20 x 20 mm.
- Example 2C Indium Tin Oxide sputtered PET
- Example 2E Gold sputtered PET
- Epson print cartridges (T036 and T037), compatible with the Epson C45 were cut open and emptied of ink and the sponge inside was removed. All colour tanks of the cartridges (black, cyan, magenta and yellow) were cleaned thoroughly with deionized water. The chip on the cartridge was then reset using the chip resetter so that the printer would read the cartridge as full. Polyaniline nanoparticle dispersions (Example 1) were then poured into a tank in the cartridge, e.g., yellow. All other tanks were filled with deionized water.
- Powerpoint® was used to draw coloured circles (3 mm diam.). The design was printed in colour, e.g., yellow, on plain printing paper (210 mm x 210 mm). Screen-printed electrodes were then affixed to the printed page where the Powerpoint® circles were aligned with the electrode area. The colour cartridge was then removed from the printer and replaced with the polyaniline-filled cartridge. Polyaniline was then printed as many times as required, on the screen-printed electrodes using 'Best Photo' mode as the printer setting.
- Example 4 A -Ammonia sensing (aqueous phase)
- Electrodes modified with polyaniline nanoparticles were incorporated into a flow-cell set-up as described by Killard et al., 2001. A potential of -400 mV vs. Ag/AgCl was applied. Following the reaching of a steady state, ammonium chloride at varying concentrations was passed over the sensor at a flow rate of 400 ⁇ l mm "1 for 20 s and the amperometric outputs monitored.
- Example 4B Ammonia sensing (gas phase) Interdigitated electrodes with polyaniline nanoparticles (synthesised according to Example 1) were incorporated into a gas jar for headspace analysis.
- An Impulse XP (Honeywell Analytics) ammonia sensor was employed as the reference method. Ammonia solution was introduced into the chamber dropwise.
- the polyaniline interdigitated electrode was connected in a 2 electrode configuration and cyclic voltammetry was applied (+0.1 V to -0.1 V at 0.2 V s "1 , cycled for duration of analysis). The current was sampled at +0.1 V and -0.1 V and plotted against time, yielding an i-t plot.
- Electrodes modified with polyaniline nanoparticles were incorporated into a batch-cell set-up as described by Killard et al., 2001. A potential of -100 mV vs. Ag/AgCl was applied. Following the reaching of a steady state, a number of additions of H 2 O 2 (8 mM) were added to the cell, and the amperometric outputs monitored.
- Electrodes modified with polyaniline nanoparticles were incorporated into a flow-cell set-up as described by Killard et al., 2001. A potential of -100 mV vs. Ag/ AgCl was applied. Following the reaching of a steady state, horseradish peroxidase (HRP) at varying concentrations from 5 to 0.01 ⁇ g ml "1 , were passed over with H 2 O 2 (1 mM) at a flow rate of 400 ⁇ l min "1 for 20 s and the amperometric outputs monitored.
- HRP horseradish peroxidase
- a critical property of the polyaniline nanoparticle dispersions is the particle size in concentrated solution. Dynamic light scattering was used to determine the particle sizes with the size distribution shown in Figure Ia & b. This indicates that the particle sizes in the dispersions are in the range of 10-50 nm or 20 - 80 nm. There may have been conditions such as changes in physical conditions such as temperature or slight experimental differences to result in two distinctly different size ranges. Beyond these ⁇ ,
- the typical pigment particle size is 100-400 nm (Magdassi & Ben Mo She, 2003) which can be printed using ink-jet printer with the nozzle diameter ca. 30-60 ⁇ m (Le, 1998). Therefore, the particle size of polyaniline nanoparticles should be at least in the same order of magnitude to the typical pigment particle size or even smaller. Due to effects of polymer aggregation, particle sizes bigger than 1000 nm was deemed unsuitable due to the possibility of clogging the print head.
- a Transmission Electron Microscope (TEM) image of the polyaniline nanoparticles shows that the emulsion polymerisation approach used results in spherical particle formation.
- the polyaniline nanoparticles were imaged on a carbon sheet where the particles were measured to be between 30 — 80 nm ( Figure 2).
- a desktop Epson printer that uses piezoelectric technology was used for printing the polyaniline nanoparticles (synthesised as per Example 1). Unlike thermal printers such as Hewlett Packard printers, heat is not required for droplet formation. Thermal printing uses 'shots' of heat at temperatures around 300 0 C. Although the flashtime of these shots are only just 2 ⁇ s, such high temperatures could induce thermal degradation of the printing material. Piezoelectric technology does not use heat, and does not degrade the material in any way. Another important advantage is more flexible ink formulations and substrates can be used in piezo technology over thermal printing.
- Example 3 Printing of polyaniline nanoparticles (2.3 % w/v) was carried out as described herein (Example 3) using an Epson Desktop C45 printer.
- particle size within the dispersion must be several orders of magnitude smaller than the nozzle of the inkjet printhead in order to prevent clogging and blockages of the nozzle.
- the diameter of the nozzle in Epson piezo printheads is reported to be of the order of 30 ⁇ m.
- the polyaniline nanoparticles used in this research have been demonstrated to have a diameters ranging betweenlnm and lOOnm, such as 10 and 50 nm, 20 and 80 nm, and 30 and 80nm according to Particle Size Distribution Analysis (PSD) and hence could easily be printed on an Epson printer.
- the nanoparticle dispersions contained the surfactants SDS and DBSA that helped prevent clogging of the nozzles if any aggregation of the nanoparticles did occur in the printhead.
- Both DBSA and SDS are present in the aqueous dispersion which, as surfactants will serve to decrease the surface energy of the dispersion. Whilst not wishing to be bound by theory, it is thought that this decrease in surface energy of the dispersion assists with the piezoelectric printing and the spreading of the ink on a substrate as it is deposited to form a homogenous film.
- a major advantage of the nanoparticle dispersions that was exploited was their insolubility in aqueous media despite being deposited from an aqueous dispersion. This results in an environmentally friendly, facile method to deposit films that can be exploited for solvent sensitive applications such as bio- or immunosensing. However, it was demonstrated that although the deposited films were insoluble, the films were not stable on all substrates.
- Two conductive flexible substrates were employed for the printing of the nanoparticles - Indium Tin Oxide (ITO) (Example 2C) and screen-printed electrodes (Example 2A).
- ITO-sputtered plastic had a smooth morphology and although the nanoparticles adhered well to the substrate, the films peeled off in aqueous media.
- nanoparticles themselves maybe deposited in a number of ways - for example, but not limited to, electrochemical deposition, dip-coating, drop- coating, spin-coating, inkjet and screen-printing and roll-to-roll printing.
- Atomic Force Microscopy was used to investigate the resulting nanostructure of the inkjet printed polyaniline nanoparticulate films.
- Gold mylar was used as substrate (Example 2E) as the carbon-paste surfaces (Example 2A) proved to have too rough a morphology to visualise the nanoparticles.
- Figure 4a shows the morphology of the bare gold and the gold substrate modified with a single print of nanoparticles (Figure 4b) for a scan size area of 1 micron. It can be observed that the nanoparticles cover the background of the gold film.
- Figure 4c shows a film printed using 10 prints. The nodule size is much larger in this instance, probably due to increased aggregation upon drying in thicker films. Section analysis was also carried out.
- the individual nanoparticle sizes were measured in the different films.
- the maximum width of these nanoparticles is about 66 nm for 5 prints and 133 nm for 10 prints. These particle sizes are larger than what was measured by the PSD analysis, attributed to aggregation and increased agglomeration of the nanoparticles upon drying (i.e., removal of solvent). AFM tip distortion may also contribute.
- All desktop printers use mono-directional printing, where the printhead and the cartridge traverse across and back in the x-direction on a metal rod in a line recording operation, ejecting ink from nozzles according to the computer program it is in communication with.
- the substrate feeds out at a defined rate beneath the moving printhead, and takes the ink that is being printed.
- a bi-directional printing method was employed, where the substrate was rotated 90° for every alternate print. This resulted in much higher coverage in the x and y direction of the surface of the electrode.
- Cyclic voltammograms were generated for multilayer films printed in the mono- and bidirectional direction ( Figure 6a). Five films of each type were fabricated and the data shows that there are is no overall difference in the CVs between mono- and bi-directional printing. % RSD values were obtained for Peak I for a number of prints ( Figure 6b). It was shown that when films composed of 20 or more prints, the % RSD for each of the prints was significantly lower for bi-directional than mono-directional printing, possibly due to enhanced homogenity. As a result, all further printing was carried out in the bidirectional mode.
- Electrochemistry was carried out on both types of films, and was shown to be comparable in terms of peak potentials.
- the inkjet printed film has however a CV that is much more defined at potentials lower than 400 mV.
- the inkjet printed films were estimated to be 10 times thinner than the bulk area of the drop-coated film, the peak currents of both films were approximately of equal magnitude. This allows us to estimate the volume of - 2 -
- Nanoparticle dispersions synthesised using different ratios of aniline:APS:DBSA have all been demonstrated to be inkjet printable, however the size of the resulting nanoparticles may vary, but are all within the 'inkjet printable' range i.e. less than lOOOnm.
- Epson black ink (T038) 30 ⁇ 0.1
- the viscosity of all of the polyaniline nanoparticle dispersions are in the suitable range for inkjet printing (0.5-40 mPa s) although it was considerably lower than the viscosity of the Epson T038 ink when shear rates lower than 500 s "1 were applied.
- Conducting polymers in particular, polyaniline, are beginning to emerge as excellent sensing materials for ammonia.
- the polymer is believed to be deprotonated by ammonia, which results in a measurable change in conduction.
- InkJet printed films were examined as a potential sensing platform for detecting ammonium ions.
- Ammonia in equilibrium with ammonium ions, which comes from rain and snow. It is used frequently in refridgeration systems and needs to be monitored for effective cooling and for personal safety.
- Chemical fertilizers containing ammonia can stimulate the growth of plankton and be toxic for fishes. To prevent the water pollution, it is very important to monitor the level of ammonium ions.
- ammonium ions are a metabolic product in many enzymatic reactions.
- ammonium and bicarbonate ions can be produced by the metabolism of urea with enzymatic action of urease. Therefore, urea can be detected by sensing its metabolic product, i.e., ammonium ions.
- Other applications for ammonia sensing are given in Table 3.
- the polyaniline backbone On exposure to ammonia, the polyaniline backbone is deprotonated.
- certain amines such as dimethylamine, trimethylamine and triethylamine interact with the polyaniline, though the interactions will be influenced in part by the substituents on the nitrogen of the amine.
- Inkjet printed films of polyaniline (Example 3) on a disposable screen-printed carbon- paste electrode platforms (Example 2A) provides a facile route to fabricating ammonia sensors. They can be mass-produced at extremely low cost and can provide comparable detection limits and linear ranges as commercial sensors based on metal oxides.
- Figure 9a & b are the amperometric responses of the inkjet printed polyaniline films (deposited on the carbon paste screen-printed electrode platform, Example 2A) to ammonium ions in solution using a flow injection setup (Example 4A). Using a flow rate of 400 ⁇ l min "1 , the response time is approximately 350 s at high concentrations of ammonia (50 ppm).
- the response time decreases to about 150 s. With further optimisation, these response times could be further reduced.
- the flow rate determines the rate at which steady state conditions are established in the flow cell. Relative humidity may also effect the response time, and this was not investigated for these experiments.
- Figure 10a shows the amperometric responses for the inkjet printed polyaniline nanoparticle films on carbon-paste screen-printed electrodes to the ammonium ion from 0 to 85 ppm.
- the potential was held at -0.4 V vs. Ag/AgCl.
- the buffer used was a phosphate buffer (0.1 M, pH 6.6).
- Figures 10b & c show the two linear ranges for NH 4 + (0-5.3 ppm and 10 - 85 ppm) within that range.
- InkJet printed polyaniline films can also be used to detect ammonia in the gas phase (Example 4B).
- the substrate/electrode is of the form of an Interdigitated Array (IDA); screen printed using silver ink (see Example 2B).
- the polyaniline nanoparticle film is inkjet printed as described in Example 3. Once printed, these polyaniline nanoparticle-modified IDAs were heat cured at 75°C for 30 minutes.
- Various configurations and dimensions of IDA can be employed and Figure 11 shows an example of the silver IDA electrode with a 25 layer polyaniline nanoparticle film inkjet printed over it (25 x 14 mm dimension, in this example). This configuration will be referred to as a PANI-IDA electrode from here on.
- the PANI-IDA electrodes are used in a 2-electrode cell configuration (i.e. anode and cathode). At a particular potential, the current passed between the electrodes is dependent on the conductivity of the film.
- Figure 13 shows the response of the PANI-IDA electrode when exposed to ammonia vapour.
- Figure 13a shows the current-potential raw data plot while figure 13b shows the current-time response obtained when the current is sampled at the indicated potentials.
- the stable Ohmic plot is obtained.
- the conductivity of the polyaniline rapidly decreases - as evidenced by the decreasing slope in Figure 13a and the drop in sampled current in Figure 13b. Once the ammonia is removed, the electrode slowly recovers.
- the effect of ambient temperature on the electrode response is given in Figure 14.
- the current measured for the PANI-IDA is seen to display a positive coefficient with temperature for the range 20 to 120°C - implying that the inherent conductivity of the polyaniline nanoparticles is increasing with temperature.
- the electrode displays good thermal stability over short time scales for temperatures up to approximately 120°C. This effect is reversible with the measured current returning to base as the temperature drops. At temperatures over 140 0 C 3 an irreversible drop in measured current is observed as the polyaniline undergoes thermal degradation. This drop in conductivity accelerates with increasing temperature.
- FIG 16a displays the response obtained for a 25 layer inkjet-printed PANI-IDA electrode when exposed to the vapour of 0.25 % ammonia solution (-60 ppm). From 4 replicates, it can be seen that the T50 (the time required to come to 50% of the final volume) and T90 (the time required to come to 90% of the final volume) of the sensor fall well within the 90s response required by the Instrument Society of America. In Figure 13 it can be noted that the sensor does not recover as rapidly. To this end a number of different methods of enhancing the sensor recovery were investigated. In Figure 16b, the results of the different techniques are present along with normal recovery in atmosphere.
- Figure 17 shows the results of headspace analysis performed on a 25 inkjet layered PANI- IDA.
- the PANI-IDA was placed within the gas jar with a commercially available ammonia sensor (Impulse XP, Honeywell Analytics). As the ammonia concentration within the gas jar was built up, the response of the PANI-IDA and Impulse XP were noted.
- the inset of Figure 17 shows the current drop recorded for the PANI- IDA as the concentration of ammonia increases.
- the main plot shows the results obtained when the difference of measured and initial current (9.23 ⁇ A, in this case) is plotted against the log of ammonia concentration.
- the initial current, I 0 is the value measured with no ammonia present.
- etching baths based on sulphuric acid for various production processes, such as the manufacture of through-hole plating for multiplayer PCBs (black-hole method). In most cases, the etching baths consist of a hydrogen peroxide component of about 25 g/1. The concentration of hydrogen peroxide, in particular, is decisive for the quality of the product, and should be kept as nearly constant as possible.
- the Jumo Corrotrode is a potentiometric sensor that is marketed for this niche market and functions as a hydrogen peroxide detector.
- H 2 O 2 analysis Another market that demands H 2 O 2 analysis is the clinical field, where exhaled breath is often monitored for H 2 O 2 . Hydrogen peroxide in the breath is indicative of lung diseases such as asthma and chronic obstructive pulmonary diseases.
- a common method to collect the exhaled breath condensate is to use a special cooling collector including a freezing cooling tube (usually cooled using ice or liquid nitrogen) and cooling machine, which has a refrigerator's circuit. Once collected, the condensate is analyzed off-line by techniques, such as spectroscopy, with assistance of peroxidase.
- H 2 O 2 is also the most valuable marker for oxidative stress, recognized as one of the major risk factors in progression of disease-related pathophysiological complications in diabetes, atherosclerosis, renal disease, cancer, aging and other condition.
- Hydrogen peroxide sensors are also needed for the development of biosensors based on enzyme oxidases. Universal Sensors market an amperometric peroxide electrode based on a platinum electrode for these types of applications at a cost of approximately $630 USD.
- Corrosion control destroys residual chlorine and reduced sulphur compounds thiosulphates, sulphites, and sulphides) which form corrosive acids when condensed onto processing equipment and oxidised by air.
- BOD Biological Oxygen Demand
- COD Chemical Oxygen Demand
- Oxidizes both organic and inorganic pollutants which contribute to BOD and COD - H 2 O 2 may be needed to oxidize the more resistant substances. H 2 O 2 may also affect BOD/COD removal by enhancing the performance of other processes.
- Disinfection/Bio-control - Checks excess biogrowth in water supplies and cooling circuits, and (with catalysis) disinfects process waters and biological effluents.
- polyaniline nanoparticle films were prepared using 20 prints. These modified electrodes were studied for their sensing properties towards H 2 O 2 . Amperograms were recorded for the reduction Of H 2 O 2 at -100 mV vs Ag/AgCl in phosphate buffer, pH 6.8 (Example 4C). This was compared to the same process at an electropolymerised bulk polyaniline film (fabricated according to Grennan et al., 2001). These amperograms on the different polyaniline materials was compared in Figure 18. The current observed for H 2 O 2 reduction was significantly higher for the inkjet printed nanoparticulate thin film than that observed on bulk polymer (approx. 100 fold). This significant increase in the current observed for H 2 O 2 reduction at the nanoparticulate films was attributed to the higher surface area to volume ratio of these materials along with their good electrical properties compared with bulk polymer.
- Figure 19 shows the amperometric responses for the inkjet printed films towards H 2 O 2 , where the sensitivity was found to be 0.5419 ⁇ A mM '1 and the detection limit was found to be 1.146 x 10 "3 M based on a signal-to-noise ratio of 3.
- Figure 20 demonstrates that the inkjet printed films are capable of charge transfer mediation between bound, catalyzed HRP and the electrode surface.
- the figure shows the binding curve of HRP to the electrode surface in the presence of H 2 O 2 .
- the binding if HRP is confirmed as a permanent one by the replacement of buffer with H 2 O 2 , subsequent to the HRP binding event.
- Enzymatic catalytic signal is restored showing that the catalytic signal was purely due to bound, rather than free HRP.
- enzymes such as urease or creatinine iminohydrolase, that catalyse their respective substrates, urea and creatinine, to produce ammonia.
- enzymes such as urease or creatinine iminohydrolase
- Immunoassays use the specific antigen-antibody complexation for analytical purposes. Enzyme immunoassays are well established in clinical diagnostics. For the development of hand-held devices which can be used for point of care measurements, electrochemical immunoassays are promising alternatives to existing immunochemical tests. Moreover, for opaque or optically dense matrices electrochemical methods are superior. Competitive and non-competitive electrochemical immunoassays have been developed often with enzymes as labels using conducting polymer as the diffusionless mediator. - -
- the patterned polyaniline films may be used as an enzyme-based immunosensor in the following theoretical situation:
- a detection antibody is immobilized to the polyaniline surface in the first instance. This surface is then exposed to an unknown concentration of antigen of interest and an enzyme- (e.g., HRP) labeled antigen. Both of these species are allowed to bind to the antibody immobilized to the surface of PANI. AU excess (unbound) material is then removed and the surface of PANI is exposed to substrate (e.g., H 2 O 2 ) which is catalysed at the surface by the bound enzyme-labeled antigen (HRP).
- substrate e.g., H 2 O 2
- the polyaniline nanoparticle inkjet printed film would be used as a direct electron transfer mediator in tins instance (rather than using a soluble mediator). The amount of electrochemical signal generated would be inversely proportional to the amount of 'free' unknown antigen ( Figure 21).
- a method to pattern high quality conducting polymer films on conducting substrates by exploiting the nanoparticulate form of the polymer for inkjet printing is illustrated.
- Aqueous dispersions of polyaniline nanoparticles were inkjet printed onto PET-based screen-printed carbon electrodes (Example 2A).
- the resulting films adhered well to the electrode surface, and electrochemistry was performed in aqueous media with no effect on the film stability.
- the polyaniline films had well-defined, reversible electrochemistry in acidic media and their use is described in two applications: direct ammonia sensing and a biosensing application using HRP.
- the results indicate that the conducting polymer nanoparticles have a wide range of applications in areas such as chemical and biosensing. . 3 .
- any suitable conducting polymer material may be used.
- suitable conducting polymers are polyacetylenes, polydiacetylenes, polyparaphenylenes, polypyrroles, polythiophenes, polybithiophenes, polyisothiophenes, polyphenylenesulphides and polyanilines.
- a more comprehensive list is given in Handbook of organic conductive molecules and polymers / edited by Hari Singh Nalwa (1997).
- Grennan K., Hansen, C, Cafolla, A., Killard, A.J., Smyth, M.R. (2005). Optimisation and characterisation of biosensors based on polyaniline. Talanta, In Press.
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AU2007237821A AU2007237821A1 (en) | 2006-04-13 | 2007-04-13 | Sensor comprising conducting polymer materials |
JP2009504893A JP2009533674A (en) | 2006-04-13 | 2007-04-13 | Sensors containing conductive polymer material |
EP07736103.8A EP2004840B1 (en) | 2006-04-13 | 2007-04-13 | Sensor comprising conducting polymer materials |
US12/226,223 US20100000883A1 (en) | 2006-04-13 | 2007-04-13 | Sensor Comprising Conducting Polymer Materials |
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EP (1) | EP2004840B1 (en) |
JP (1) | JP2009533674A (en) |
CN (1) | CN101466845A (en) |
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WO2009153777A1 (en) * | 2008-06-16 | 2009-12-23 | Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd | Electrode, method and system for determining an analyte in a liquid medium |
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GB2506863A (en) * | 2012-10-09 | 2014-04-16 | Univ Dublin City | System and method for analysing and measuring ammonia levels in a sample |
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WO2009153777A1 (en) * | 2008-06-16 | 2009-12-23 | Yissum Research Development Company Of The Hebrew University Of Jerusalem Ltd | Electrode, method and system for determining an analyte in a liquid medium |
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WO2012104870A1 (en) | 2011-02-04 | 2012-08-09 | Council Of Scientific & Industrial Research | Molecularly imprinted conducting polymer film based aqueous amino acid sensors |
EP2674759A1 (en) | 2011-02-04 | 2013-12-18 | Council of Scientific & Industrial Research | Molecularly imprinted conducting polymer film based aqueous amino acid sensors |
US9239311B2 (en) | 2011-02-04 | 2016-01-19 | Council of Industrial & Scientific Research | Molecularly imprinted conducting polymer film based aqueous amino acid sensors |
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CN101466845A (en) | 2009-06-24 |
AU2007237821A1 (en) | 2007-10-25 |
JP2009533674A (en) | 2009-09-17 |
EP2004840A1 (en) | 2008-12-24 |
US20100000883A1 (en) | 2010-01-07 |
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IE20070269A1 (en) | 2008-12-10 |
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