The present application claims priority to Japanese Priority Patent Application JP 2013-051430 filed in the Japan Patent Office on Mar. 14, 2013, the entire content of which is hereby incorporated by reference.
The present disclosure relates to a substrate detection device and a biofuel cell with a substrate detection function. More specifically, the present disclosure relates to a preferred substrate detection device that is applied in determining the concentration of various kinds of substrate in liquids, and a biofuel cell with a substrate detection function in which a substrate detection device is integrated in a biofuel cell that uses a glucose solution as a fuel.
Compact urine sugar measurement devices and blood sugar self-monitoring devices have been commercially available in the past (e.g., refer to JP 2007-532266T). The power consumption of most of these urine sugar measurement devices or blood sugar self-monitoring devices is about 18 mW (including a 6 mA/3V/LCD) to 100 mW. These urine sugar measurement devices or blood sugar self-monitoring devices, which use a compact button battery, such as the coin type lithium battery CR2032, are capable of performing measurement about 1,000 times.
However, previous urine sugar measurement and blood sugar self-monitoring commercial products have had a high cost.
Accordingly, it is desirable to provide a substrate detection device that is capable of determining the concentration of sugars, including glucose, or various kinds of substrate, and that also has a circuit configuration that can be produced simply and inexpensively.
Further, it is also desirable to provide a biofuel cell with a substrate detection function that has a function of determining the concentration of a substrate included in the fuel of the biofuel cell.
These and other points will become clear based on the following descriptions in the present specification with reference to the attached drawings.
According to an embodiment of the present disclosure, there is provided a substrate detection device which includes
a sensor unit configured to extract electrons by oxidizing a substrate, which is a test target,
a capacitor connected in series to the sensor unit, and a circuit for measuring a voltage across terminals of the capacitor,
wherein the substrate detection device determines a concentration of the substrate based on the voltage across the terminals of the capacitor.
This substrate detection device further has, for example, a power supply, a constant voltage generation circuit that is supplied with a voltage from the power supply, and a sensor unit constant voltage application circuit for applying the constant voltage generated by the constant voltage generation circuit to the sensor unit. Typically, this substrate detection device also has at least one comparison circuit into which a voltage across the capacitor terminals is input. The resolution performance of the determination of the substrate concentration can be adjusted by selecting the number of comparison circuits. This substrate detection device preferably further has an operational amplifier into which a voltage across the capacitor terminals is input. The output voltage of this operational amplifier is input into the comparison circuit and compared with a reference voltage. This reference voltage is selected based on a desired substrate concentration. The constant voltage generation circuit has, for example, a first DC/DC converter that reduces the voltage of the power supply. Further, the sensor unit constant voltage application circuit has, for example, a second DC/DC converter, which has a feedback terminal, that reduces the voltage that was reduced by the first DC/DC converter. The sensor unit is connected to the feedback terminal of this second DC/DC converter, and preferably the sensor unit is connected via a fixed resistor. The voltage applied to the sensor unit can be adjusted to an arbitrary value by adjusting the resistance value of this fixed resistor. This substrate detection device also typically has a display unit that is supplied with an output voltage of the comparison circuit. The configuration of the display unit and the content and the like that is displayed may be selected as appropriate. For example, content indicating the detected substrate concentration may be displayed. The sensor unit includes an enzyme or a microorganism that oxidizes the substrate. The enzyme or microorganism may be selected as appropriate based on the substrate from among known enzymes or microorganisms. In addition to the enzyme or microorganism that oxidizes the substrate, the sensor unit may optionally include an electron mediator for transferring the electrons produced by the oxidation of the substrate to the sensor unit. Examples of microorganisms that can be used include, but are not especially limited to, various types of microorganisms known in the related art, such as bacteria belonging to the genera Saccharomyces, Hansenula, Candida, Micrococcus, Staphylococcus and the like, filamentous bacteria, and yeasts, as well as microorganisms produced by genetic engineering and the like. The substrate detected by this substrate detection device is typically included in a liquid. Although the substrate may basically be anything, examples include at least one kind selected from the group consisting of glucose, bile acid, pyruvic acid, dissolved oxygen, formaldehyde, and carbon monoxide.
According to an embodiment of the present disclosure, there is provided a biofuel cell with a substrate detection function, including
a biofuel cell configured to generate electricity by extracting electrons by oxidizing a substrate included in a fuel solution, and
a substrate detection device integrally provided with the biofuel cell,
wherein the substrate detection device includes
wherein the substrate detection device determines a concentration of the substrate based on the voltage across the terminals of the capacitor.
The biofuel cell with a substrate detection function according to an embodiment of the present disclosure may include the above-described substrate detection device, as long as this device does not run counter to the nature of the biofuel cell. Although the details of the biofuel cell are described in, for example, JP 2000-133297A, JP 2003-282124, JP 2004-71559A, JP 2005-13210A, JP 2005-310613A, JP 2006-24555A, JP 2006-49215A, JP 2006-93090A, JP 2006-127957A, JP 2006-156354A, JP 2007-12281A, and JP 2007-35437A, an outline will be described below.
The biofuel cell has a positive electrode, a negative electrode, and a proton conductor arranged between the positive electrode and the negative electrode. An enzyme is immobilized on the positive electrode and the negative electrode. The overall configuration of the biofuel cell is typically in a thin sheet-like form by configuring each of the positive electrode, the negative electrode, and the proton conductor in a thin sheet shape. The enzyme immobilized on the negative electrode typically includes an oxidase that decomposes a fuel, such as glucose, by promoting oxidation of the fuel. Further, this enzyme also typically includes a coenzyme oxidase that returns a coenzyme reduced during oxidation of the fuel back into an oxidant, and transfers electrons to the negative electrode via the electron mediator. Specifically, the enzyme immobilized on the negative electrode preferably includes an oxidase that decomposes the fuel, such as glucose, by promoting oxidation of the fuel and a coenzyme oxidase that returns the coenzyme that is reduced by this oxidase back into an oxidant. Due to the action of this coenzyme oxidase, electrons are produced when the coenzyme is turned back into an oxidant, and the electrons are transferred from the coenzyme oxidase to the negative electrode via the electron mediator. For example, if glucose is used as the fuel, glucose dehydrogenase (GDH) (in particular, NAD-dependent glucose dehydrogenase), for example, is used as the oxidase, NAD+, or NADP+, for example, is used as the coenzyme, and diaphorase (DI), for example, is used as the coenzyme oxidase.
Although basically anything can be used as the electron mediator, preferably, a compound having a quinone skeleton is used. Specifically, for example, 2,3-dimethoxy-5-methyl-1,4-benzoquinone (Q0), or a compound having a naphthoquinone skeleton, for example, various kinds of naphthoquinone derivative, such as 2-amino-1,4-naphthoquinone (ANQ), 2-amino-3-methyl-1,4-naphthoquinone (AMNQ), 2-methyl-1,4-naphthoquinone (VK3), 2-amino-3-carboxy-1,4-naphthoquinone (ACNQ), and vitamin K1, is used. As the compound having a quinone skeleton, for example, anthraquinone or a derivative thereof can be used. In addition to the compound having a quinone skeleton, the electron mediator may optionally also include one kind or two or more kinds of other compound that act as an electron mediator. This electron mediator may be immobilized on the negative electrode along with a ribosome that includes an enzyme and a coenzyme, or may be included in this ribosome, or may be immobilized on this ribosome, or may be included in a fuel solution.
The enzyme immobilized on the positive electrode typically includes an enzyme that reduces oxygen. Examples of this oxygen-reducing enzyme include bilirubin oxidase, laccase, ascorbic acid oxidase and the like. In this case, preferably, in addition to the enzyme, an electron mediator is also immobilized on the positive electrode. As the electron mediator, for example, potassium hexacyanoferrate, potassium ferricyanide, potassium octacyanotungstate and the like is used. Preferably, the electron mediator is immobilized at a sufficiently high concentration, for example, 0.64×10−6 mol/mm2 or more on average.
As for the proton conductor, various substances can be used and selected as appropriate. Specific examples thereof include substances formed from cellophane, perfluorocarbon sulfonic acid (PFS)-based resin films, copolymer films of trifluorostyrene derivatives, phosphoric acid-impregnated polybenzimidazole films, aromatic polyether ketone sulfonic acid films, PSSA-PVA (polystyrene sulfonic acid-polyvinyl alcohol copolymers), PSSA-EVOH (polystyrene sulfonic acid-ethylene vinyl alcohol copolymers), and ion exchange resins having a fluorine-containing carbon sulfonic acid group (Nafion (trade name, DuPont, USA)) and the like.
When using an electrolyte including a buffer solution (buffering substance) as the proton conductor, it is desirable to design the buffer so that a sufficient buffering performance can be obtained during a high output operation, and so that the enzyme can sufficiently exhibit its inherent capabilities. Consequently, it is effective if the concentration of the buffering substance included in the electrolyte is 0.2 M or more to 2.5 M or less, and preferably 0.2 M or more to 2 M or less, more preferably 0.4 M or more to 2 M or less, and even more preferably 0.8 M or more to 1.2 M or less. Generally, although any buffering substance having a pKa of 6 or more to 9 or less can be used, specific examples of the buffering substance include dihydrogen phosphate ions (H2PO4−), 2-amino-2-hydroxymethyl-1,3-propanediol (abbreviated as Tris), 2-(N-morpholino)ethanesulfonic acid (MES), cacodylic acid, carbonic acid (H2CO3), hydrogen citrate ions, N-(2-acetamido)iminodiacetic acid (ADA), piperazine-N,N′-bis(2-ethanesulfonic acid) (PIPES), N-(2-acetamido)-2-aminoethanesulfonic acid (ACES), 3-(N-morpholino)propanesulfonic acid (MOPS), N-2-hydroxyethylpiperazine-N′-2-ethanesulfonic acid (HEPES), N-2-hydroxyethylpiperazine-N′-3-propanesulfonic acid (HEPPS), N-[tris(hydroxymethyl)methyl]glycine (abbreviated as Tricine), glycylglycine, and N,N-bis(2-hydroxyethyl)glycine (abbreviated as Bicine). The dihydrogen phosphate ions (H2PO4−) may be produced from, for example, substances such as sodium dihydrogen phosphate (NaH2PO4) and potassium dihydrogen phosphate (KH2PO4). A compound including an imidazole ring is preferred as the buffering substance. Specific examples of compounds including an imidazole ring include imidazole, triazole, pyridine derivatives, bipyridine derivatives, and imidazole derivatives (histidine, 1-methylimidazole, 2-methylimidazole, 4-methylimidazole, 2-ethylimidazole, ethyl imidazole-2-carboxylate, imidazole-2-carboxaldehyde, imidazole-4-carboxylic acid, imidazole-4,5-dicarboxylic acid, imidazol-1-yl-acetic acid, 2-acetylbenzimidazole, 1-acetylimidazole, N-acetylimidazole, 2-aminobenzimidazole, N-(3-aminopropyl)imidazole, 5-amino-2-(trifluoromethyl)benzimidazole, 4-azabenzimidazole, 4-aza-2-mercaptobenzimidazole, benzimidazole, 1-benzylimidazole, and 1-butylimidazole etc.). In addition to these buffering substances, at least one kind of substance selected from the group consisting of, for example, hydrochloric acid (HCl), acetic acid (CH3COOH), phosphoric acid (H3PO4), and sulfuric acid (H2SO4) may optionally be added as a neutralizing agent. By adding such a neutralizing agent, the activity of the enzyme can be maintained at a higher level. Although the pH of the electrolyte including the buffering substance is preferably around 7, the pH may be anywhere between 1 and 14.
Although various electrode materials can be used for the positive electrode and the negative electrode, examples thereof include carbonaceous materials, such as porous carbon, carbon pellets, carbon felt, and carbon paper. As the electrode material, a porous conductive material that includes as its main components a skeleton formed from a porous material and a carbonaceous material that covers at least a part of this skeleton may be used (refer to JP 2007-35437A).
As the fuel, various substances may be selected and used as appropriate. Examples of fuels other than glucose include various organic acids that are involved in the citric acid cycle, and sugars and organic acids that are involved in the pentose phosphate cycle. Examples of various organic acids involved in the citric acid cycle include lactic acid, pyruvic acid, acetyl-CoA, citric acid, isocitric acid, α-ketoglutarate, succinyl-CoA, succinic acid, fumaric acid, malic acid, oxaloacetic and the like. Examples of sugars and organic acids that are involved in the pentose phosphate cycle include glucose-6-phosphate, 6-phosphogluconolactone, 6-phosphogluconic acid, ribulose-5-phosphate, glyceryl aldehyde 3-phosphate, fructose 6-phosphate, xylilose 5-phosphate, sedoheptulose 7-phosphate, erythrose 4-phosphate, phosphoenolpyruvic acid, 1,3-bisphosphoglyceric acid, ribose 5-phosphate, and the like. As the fuel, an alcohol, such as methanol and ethanol, may be used. These fuels are typically used in the form of a fuel solution in which the fuel is dissolved in a buffer solution known in the related art, such as a phosphate buffer, a tris buffer solution and the like.
Thus, in the present disclosure, a substrate detection device can be configured with a simple circuit configuration. Consequently, production of the substrate detection device is simple, so that production costs can be reduced. Further, by connecting a second DC/DC converter feedback terminal to the sensor unit, the voltage applied to the sensor unit can be set at a fixed level. In addition, during use the concentration of a substrate in the fuel solution can be determined by a biofuel cell with a substrate detection function in which this substrate detection device is integrated in the biofuel cell.
According to one or more of embodiments of the present disclosure, a substrate detection device can be obtained that is capable of determining the concentration of a sugar, including glucose, or of various kinds of substrate, and yet whose circuit configuration can be produced simply and inexpensively. Further, the concentration of a substrate included in the fuel solution of a biofuel cell can be determined with a biofuel cell with a substrate detection function in which this excellent substrate detection device is integrated in the biofuel cell.
Additional features and advantages are described herein, and will be apparent from the following Detailed Description and the figures.
Hereinafter, preferred embodiments of the present disclosure will be described in detail with reference to the appended drawings. Note that, in this specification and the appended drawings, structural elements that have substantially the same function and structure are denoted with the same reference numerals, and repeated explanation of these structural elements is omitted. It is noted that description will be made in the following order.
1. First embodiment of the present disclosure (substrate detection device)
2. Second embodiment of the present disclosure (biofuel cell with a substrate detection function)
As illustrated in
As illustrated in
The step-down value VDD output from an output terminal 23b of the DC/DC converter 23 is supplied to two input terminals of a multiplexer 24. The multiplexer 24 has switches 25 and 26 connected to the two input terminals. The output terminal of the switches 25 and 26 are connected to power supply lines 27 and 28 that supply the VDD. The selection of power supply line 27 or 28 is made by switching the switches 25 and 26. The power supply line 27 is connected to a display unit 29. The power supply line 27 is also grounded via resistors R1 and R2 connected in series. The power supply line 28 is connected to an input terminal 30a of a DC/DC converter 30. An output terminal 30b of the DC/DC converter 30 is connected to an input terminal of a multiplexer 31. The multiplexer 31 has two switches 32 and 33 connected in series. The DC/DC converter 30 has a feedback (FB) terminal 30c. This feedback terminal 30c is connected to one terminal of a sensor strip Rsens via a fixed resistor R3, and is grounded via a fixed resistor R4. Further, the other terminal of the sensor strip Rsens is grounded. Vsens represents the applied voltage to the sensor strip Rsens. The voltage Vsens can be adjusted to an arbitrary value by adjusting the value of the resistor R3. The DC/DC converter 30 includes a feedback mechanism for maintaining a voltage VFB of the feedback terminal 30c at a fixed level, which enables the voltage Vsens to be maintained at a fixed value. The DC/DC converter 30 and the fixed resistors R3 and R4 configure the sensor strip constant voltage application circuit 13.
A line 34 connecting switches 32 and 33 of the multiplexer 31 is connected to one terminal of a capacitor C1. The other terminal of the capacitor C1 is connected to switches 36 and 37 of a multiplexer 35. The switch 36 is connected to both the fixed resistor R3 and to the sensor strip Rsens. One terminal of the switch 37 is grounded.
The switch 33 of the multiplexer 31 is connected to a non-inverting input terminal of an operational amplifier 38. The voltage Vin across the terminals of the capacitor C1 is input to this non-inverting input terminal. The electrons flowing due to the application of the voltage Vsens to the sensor strip Rsens accumulate in the capacitor C1. Vin increases based on the current value and the time to an upper limit of VDD−Vsens. An inverting input terminal of the operational amplifier 38 is connected to an output terminal of the operational amplifier 38, and configures a voltage follower. The voltage VDD supplied by the power supply line 27 is divided by fixed resistors R1 and R2 connected in series to a line 39 that branches from the power supply line 27, so that a voltage R2/(R1+R2)/VDD is input to a non-inverting input terminal of a comparator 40. This voltage R2/(R1+R2)/VDD serves as the reference voltage Vref of the comparator 40. An arbitrary reference voltage Vref that is based on the concentration of the substrate to be determined can be adjusted based on the resistance value of the fixed resistors R1 and R2. An inverting input terminal of the comparator 40 is connected to an output terminal of the operational amplifier 38. Based on the voltage value Vin of a signal input to an inverting input terminal of the comparator 40, if Vin exceeds Vref, the output of the comparator 40 changes to a negative direction. If Vref is an inverting input and Vin is a non-inverting input, when Vin exceeds Vref, the output of the comparator 40 changes to a positive direction. Although the selection about which voltage to input for the inverting input and the non-inverting input of the comparator 40 is determined based on how the comparison result output from the comparator 40 is processed as an electronic circuit, in the circuit illustrated in
Here, a supplementary description will be made regarding the DC/DC converter 30. The DC/DC converter 30 is a unit that converts an input voltage into an arbitrary voltage, and outputs the converted voltage. To enable this to occur, as illustrated in
This relationship is represented by the following formula.
V
FB
=V
out
′×R11/(R10+R11)
In this formula, R10 and R11 represent the resistance values of the fixed resistor R10 and the fixed resistor R11, respectively.
The DC/DC converter 30 performs the action reducing the conversion voltage when, for example, Vout′ has increased for some reason, namely, when VFB<Vout′×R11/(R10+R11). In other words, it can be said that when a voltage greater than VFB is applied to the feedback terminal 30c, the DC/DC converter 30 performs an operation for reducing the output voltage.
The operation of the DC/DC converter 30 illustrated in
As illustrated in
Next, the relationship between the sensor current flowing from the sensor strip Rsens and the voltage across the terminals of the capacitor C will be described. The sensor strip Rsens oxidizes the substrate, which is the test target. By applying a constant voltage across the terminals of the sensor strip Rsens, a flow of a current is (sensor current) is generated by the electrons produced by oxidation. Further, the electrons produced by oxidation are stored in the capacitor C1. A charge amount Q that is stored in the capacitor C1 can be expressed as in formula (1) by integrating the current is over time.
Q=∫
0
ti
s
dt (1)
Further, the voltage Vc across the terminals of the capacitor C1 and the accumulated charge amount Q have the relationship shown in formula (2).
V
c
=Q/C (wherein C represents the electrostatic capacitance of the capacitor C1) (2)
Consequently, a voltage Vc is generated across the terminals of the capacitor C1.
Although a direct current does flow through the capacitor C1, a transient current can flow through. Consequently, after the constant current is applied to the sensor strip Rsens, the relationship after to between the voltage Vc across the terminals of the capacitor C1 and the terminal voltage Vs of the sensor strip Rsens is as illustrated in
In
Formula (2) illustrates the fact that the voltage Vc across the terminals of the capacitor C1 can be expressed by the stored charge amount Q and the electrostatic capacitance C of the capacitor C1. Based on the magnitude of the electrostatic capacitance C of the capacitor C1, the rate of increase in the voltage Vc across the terminals of the capacitor C1 can be changed. An example of this is illustrated in
The voltage value applied to the sensor strip Rsens can be easily changed using a fixed resistor.
When the fixed resistor R3 is added, since the value obtained by dividing with the fixed resistor R3 and the fixed resistor R4 is input to the feedback terminal of the 305, the voltage value applied to the sensor strip Rsens has a greater value than the reference voltage Vref′. Namely:
V
s=(R3+R4)÷R4×Vref′
Here, R3 and R4 represent the resistance value of the fixed resistor R3 and the fixed resistor R4. When R3=R4=1, from the above formula, Vs=2×Vref′.
Next, the principles behind the improvement in the determination accuracy of the substrate concentration by employing a constant voltage using the DC/DC converter 30 will be described.
As illustrated in
On the other hand, by employing a configuration like that illustrated in
In the substrate detection device illustrated in
The input voltage to the non-inverting input terminal of each of the comparators P1 to Pn illustrated in
V1=VDD×{(R2+R3+ . . . +Rn)/(R1+R2+R3+ . . . +Rn)}
V2=VDD×{(R3+ . . . +Rn)/(R1+R2+R3+ . . . +Rn)}
Vn=V
DD×{(Rn)/(R1+R2+R3+ . . . +Rn)}
From the above, it can be seen that the input voltage value to the comparators P1 to Pn can be changed by setting the resistance value of the fixed resistors R1, R2, R3 . . . Rn for division at an arbitrary value. For example, if R1=R2= . . . Rn, the input voltage to the comparators P1 to Pn can be set at a value in which VDD is divided equally. In addition, if the value of the divided-voltage resistance is selected so that R1 >>R2=R3= . . . Rn, the input voltage value to the comparators P1 to Pn can be set at a lower value than VDD. Further, if R1=Rn>>R2=R3= . . . Rn-1, a voltage value centered around ½ VDD can be set as the input voltage value to the comparators P1 to Pn.
Therefore, a more precise resolution performance can be obtained by arbitrarily selecting the division resistance value while also increasing the number n of comparators P1 to Pn.
Examples of this substrate detection device will now be described.
The substrate detection device illustrated in
To confirm operation of this substrate detection device as a glucose sensor, an experiment to measure the glucose concentration was carried out using glucose solutions having a known glucose concentration. Glucose solutions were prepared having a glucose concentration (expressed as “Glc”) of 0 mg/dL, 100 mg/dL, 200 mg/dL, and 300 mg/dL. The change over time from when the power supply voltage (VDD) was applied in the voltage Vin across the terminals of the capacitor C1, the applied voltage Vsens of the sensor strip Rsens, the input voltage of the comparator 40, the applied voltage of the light-emitting diode 42, and the 10× circuit current of the substrate detection device when the glucose concentration of these four kinds of glucose solution was measured is illustrated in
To confirm operation of the substrate detection device illustrated in
Glucose solutions were prepared having a glucose concentration (expressed as “Glc”) of 0 mg/dL, 100 mg/dL, 200 mg/dL, and 300 mg/dL. The change over time from when the power supply voltage was applied in the voltage across the terminals of the capacitor C1 of the substrate detection device when the glucose concentration of these glucose solutions was measured is illustrated in
This substrate detection device can be used to detect various kinds of substrate. Examples of the substrate may include, but are not limited to, glucose, bile acid, pyruvic acid, dissolved oxygen, formaldehyde, carbon monoxide and the like.
For example, a substrate detection device that detects glucose is a glucose sensor. A glucose sensor can be used as a urine sugar measurement device or a blood sugar self-monitoring device to diagnose diabetes, for example. The diagnostic criteria for diabetes is blood sugar level (any of a blood sugar level ≧126 mg/dL on an empty stomach, ≧200 mg/dL 2 hours after an OGTT, or ≧200 mg/dL normally). Here, OGTT is a test for determining diabetes based on the fluctuation in blood sugar level after drinking water in which 75 g of glucose is dissolved after fasting for not less than 10 hours.
A substrate detection device that detects bile acid is a bile acid sensor. A bile acid sensor can be used to diagnose disease of the hepatobiliary system. When enterohepatic circulation breaks down due to bile acid malabsorption or impaired excretion in the liver, bile acid leaks into the greater circulatory system, so that the bile acid concentration in the blood and the urine increases.
A substrate detection device that detects pyruvic acid is a pyruvic acid sensor. Management of the concentration of pyruvic acid in Japanese sake mash is important in terms of determining the point to add alcohol. To prevent a costus-like odor, it is desirable to perform alcohol addition and lees separation after the pyruvic acid concentration has reached 1.14 mM (100 ppm) or less. Further, since the concentration of pyruvic acid during aging influences the odor of the sake, the pyruvic acid concentration in the mash is 0.23 to 11.36 mM (20 to 1,000 ppm), and the pyruvic acid concentration in the sake is 0.06 to 0.91 mM (5 to 80 ppm).
A substrate detection device that detects dissolved oxygen is a dissolved oxygen acid sensor. A BOD sensor rapidly measures BOD (biochemical oxygen demand), which is a representative index of water pollution. The greater the amount of organisms in the water, the lower the level of dissolved oxygen. In addition, in food industry processes and fermentation processes, various concentration measurements can be carried out with a Clark oxygen electrode that uses microorganisms which utilize organic matter, such as acetic acid, alcohol, formic acid, glutamic acid, methane and the like.
A substrate detection device that detects formaldehyde is a formaldehyde sensor. Formaldehyde heads the list of substances that cause sickhouse syndrome. In the amended enforcement orders of the Japanese Building Health and Management Act that came into force in April, 2003, a standard is set at 0.08 ppm per cubic meter of air (100 μg/m3). In July 2003, the amended Building Standards Law came into effect, which limits the used surface area of building materials that give off large amounts of formaldehyde, and stipulates the installation of mechanical ventilator equipment.
Work electrode: HCHO+H20→CO2+4H+4e−
Counter electrode: O2+4H++4e−→2H2O
A substrate detection device that detects carbon monoxide is a carbon monoxide sensor. A carbon monoxide sensor is effective in preventing accidents caused by poor air circulation, accidents caused by inflow of exhaust gases, accidents caused by a weapons equipment malfunction, and accidents caused by the failure to put out embers. The measurement principles are as follows.
Work electrode: CO+H20→CO2+2H+2e−
Counter electrode: ½CO2+2H++2e−→H2O
According to the first embodiment of the present disclosure, various advantageous effects such as the following can be obtained. Namely, since the voltage Vcc of the battery 21 is reduced by the DC/DC converters 23 and 30, which are Chopper-type voltage lowering circuits, and a sensor unit, namely, the sensor strip Rsens, is connected to the feedback terminal 30c of the DC/DC converter 30, the voltage applied to the sensor strip Rsens during measurement of the substrate concentration can be made constant. Further, the voltage applied to this sensor strip Rsens can be arbitrarily set. In addition, the reference voltage Vref that is based on a predetermined substrate concentration and the voltage across the terminals of the capacitor C1 can be compared by the comparator 40, and this result reflected on the display unit 29. Still further, the resolution performance of the target substrate concentration can be freely adjusted by selecting the number of comparators to be used. Moreover, the resolution performance can also be adjusted by changing the output voltage of the DC/DC converter 30 and the voltage application time to the sensor strip Rsens or the electrostatic capacitance C of the capacitor C1. Further, leak current from the capacitor C1 can be suppressed, and consequently the input voltage to the comparator 40 can be maintained, by the operational amplifier 38 voltage follower and the multiplexers 24, 31, and 35. In addition, as illustrated in
As illustrated in
During use of this biofuel cell 70 with a substrate detection function, as illustrated in
The method for supplying the fuel solution to the battery unit 80 is not especially limited, and may be selected as appropriate. For example, the method disclosed in JP 2011-22204A may be employed. An outline of this method will be described below. Since a biofuel cell starts to generate electricity as soon as fuel is supplied, it is desirable to separate the power generation unit and the fuel before use, and supply the fuel when the biofuel cell is to be used. Accordingly, JP 2011-22204A discloses a biofuel cell in which the power generation unit and the fuel tank are integrated, in which a separator is arranged between these two parts, and fuel is supplied by removing (folding or splitting) this separator when supplying fuel.
As illustrated in
As illustrated in
As illustrated in
A fuel capsule may be used as the method for supplying fuel to the battery unit 80 of the biofuel cell 70 with a substrate detection function illustrated in
The principles of a liquid fuel capsule will be described with reference to
It is noted that, for example, in the container 505 illustrated in
A method using such a capsule 504 of a liquid is applied in the supply of a fuel solution to the battery unit 80 of the biofuel cell 70 with a substrate detection function. Namely, a fuel capsule 604 that encapsulates a fuel solution 602 with a film 603 is placed on a negative electrode 601 of the battery unit 80. Thus, by forming the fuel capsule 604 in which the fuel solution 602 is encapsulated by the film 603, the fuel solution 602 can be stably stored for a long period. Next, a container 605 is placed so as to cover the fuel capsule 604. During usage of the fuel capsule 604, the film 603 is broken by applying an external stimulus, such as physical pressure, light, temperature change, pH change and the like, whereby fuel solution 602 inside the fuel capsule 604 flows out, and immerses the negative electrode 601. Here, since the fuel capsule 604 is covered with the container 605, the fuel solution 602 can be prevented from scattering when the film 603 is broken.
As illustrated in
It should be understood by those skilled in the art that various modifications, combinations, sub-combinations and alterations may occur depending on design requirements and other factors insofar as they are within the scope of the appended claims or the equivalents thereof.
For example, the numerical values, structures, configurations, shapes, materials and the like mentioned in the above embodiments of the present disclosure and the working examples are merely examples which may be changed as appropriate to different numerical values, structures, configurations, shapes, materials and the like.
Additionally, the present application may also be configured as below.
(1) A substrate detection device including:
a sensor unit configured to extract electrons by oxidizing a substrate, the substrate being a test target;
a capacitor connected in series to the sensor unit; and
a circuit configured to measure a voltage across terminals of the capacitor,
wherein the substrate detection device determines a concentration of the substrate based on the voltage across the terminals of the capacitor.
(2) The substrate detection device according to (1), further including:
a power supply;
a constant voltage generation circuit supplied with a voltage from the power supply; and
a sensor unit constant voltage application circuit configured to apply a constant voltage generated by the constant voltage generation circuit to the sensor unit.
(3) The substrate detection device according to (1) or (2), further including at least one comparison circuit into which the voltage across the terminals of the capacitor is input.
(4) The substrate detection device according to any one of (1) to (3), further including:
an operational amplifier into which the voltage across the terminals of the capacitor is input,
wherein an output voltage of the operational amplifier is input to the comparison circuit and compared with a reference voltage.
(5) The substrate detection device according to any one of (2) to (4), wherein the constant voltage generation circuit has a first DC/DC converter configured to reduce the voltage of the power supply.
(6) The substrate detection device according to any one of (2) to (5),
wherein the sensor unit constant voltage application circuit has a second DC/DC converter that has a feedback terminal which reduces the voltage that was reduced by the first DC/DC converter, and
wherein the sensor unit is connected to the feedback terminal of the second DC/DC converter.
(7) The substrate detection device according to (6), wherein the sensor unit is connected to the feedback terminal of the second DC/DC converter via a fixed resistor.
(8) The substrate detection device according to any one of (3) to (7), further including a display unit supplied with an output voltage from the comparison circuit.
(9) The substrate detection device according to any one of (1) to (8), wherein the sensor unit includes an enzyme or a microorganism that oxidizes the substrate.
(10) The substrate detection device according to any one of (1) to (9), wherein the substrate is included in a liquid.
(11) The substrate detection device according to any one of (1) to (10), wherein the substrate is at least one kind selected from the group consisting of glucose, bile acid, pyruvic acid, dissolved oxygen, formaldehyde, and carbon monoxide.
It should be understood that various changes and modifications to the presently preferred embodiments described herein will be apparent to those skilled in the art. Such changes and modifications can be made without departing from the spirit and scope of the present subject matter and without diminishing its intended advantages. It is therefore intended that such changes and modifications be covered by the appended claims.
Number | Date | Country | Kind |
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2013-051430 | Mar 2013 | JP | national |