CN101005005A - Electric fluorescent starter and its manufacture method - Google Patents

Electric fluorescent starter and its manufacture method Download PDF

Info

Publication number
CN101005005A
CN101005005A CN 200710002083 CN200710002083A CN101005005A CN 101005005 A CN101005005 A CN 101005005A CN 200710002083 CN200710002083 CN 200710002083 CN 200710002083 A CN200710002083 A CN 200710002083A CN 101005005 A CN101005005 A CN 101005005A
Authority
CN
China
Prior art keywords
mentioned
starter
alkali metal
electron emission
electrode
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Pending
Application number
CN 200710002083
Other languages
Chinese (zh)
Inventor
柳本光章
合田和生
菅沼靖
桥田守雄
明星稔
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Panasonic Holdings Corp
Original Assignee
Matsushita Electric Industrial Co Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Matsushita Electric Industrial Co Ltd filed Critical Matsushita Electric Industrial Co Ltd
Publication of CN101005005A publication Critical patent/CN101005005A/en
Pending legal-status Critical Current

Links

Images

Abstract

The present invention provides a starter which can easily discharge electron and short the start delay time in dark without using radioactive substance and a manufacturing method thereof. In the starter of the present invention, the inner part of a closing container (2) has a pair of electrodes composed of active electrode (3) including thermal element (14) and a partner electrode (4) of the active electrode (3) and discharge gas. It is characterized in that, at least one of the pair of electrodes includes electron emitting part (18, 19) of Fe; the electron emitting part (18, 19) is contacted with alkali metal supply substance (7) including K, and is activated by applying pulse direct voltage to the pair of electrodes.

Description

Starter and manufacture method thereof
Technical field
The present invention relates to make the starter and the manufacture method thereof of fluorescent lamp starting.
Background technology
The general considerations relevant with discharge tubes such as starters is the dark place start delay.So-called dark place start delay is meant, for example to be assembled into device inner and be placed on around the situation that is blocked of light under or for a long time under the situation that the starter of keeping under the packed state starts, the quantity delivered of the initiating electron that is produced by photo ionization and photoelectric effect is less, the phenomenon that needs the suitable time till begin to discharge, that is to say, from turning on the power switch to the phenomenon that produce to postpone till starting.
Therefore, the starter in past portion has within it been enclosed radioactive substance, so that in the dark also can start starter.The enclosed volume of this radioactive substance considers that still society upward to the care of environmental problem, has realized being converted to the starter that does not use radioactive substance in observing the scope of decree.
For example, the starter that does not use radioactive substance is disclosed, comprise following method: the combined photoelectron emissions of utilization and long afterglow coating shortens dark place start delay time method (for example referring to Japanese kokai publication hei 10-255724 communique), perhaps in starter, enclose the low cesium compound of work function, utilize its electronics to launch and shorten dark place start delay time method (for example with reference to TOHKEMY 2002-216703 communique) etc.
But the spy opens the described method existence of flat 10-255724 communique can not fully solve the problem of dark place start delay to the starter that is placed on the dark place for a long time.And, the spy open the described method of 2002-216703 communique exist the dark place start delay time inhomogeneous, if the access times increase inadequate problem of functional reliability such as dark place start delay time growth then.
Summary of the invention
The invention provides a kind of radioactive substance that do not use, can be easy to electron radiation, can shorten the starter of dark place start delay time.
Starter of the present invention is characterized in that, has pair of electrodes and discharge gas that the counter-electrodes by float electrode that comprises temperature-sensitive element and above-mentioned float electrode constitutes in the inside of closed container; At least one electrode in the above-mentioned pair of electrodes comprises the electron emission part that contains iron; Above-mentioned electron emission part is supplied with material with the alkali metal that contains potassium and is contacted, and is activated by the direct voltage that above-mentioned pair of electrodes is applied pulse type.
The manufacture method of starter of the present invention, this starter have pair of electrodes and the discharge gas that the counter-electrodes by float electrode that comprises temperature-sensitive element and above-mentioned float electrode constitutes in the inside of closed container; This manufacture method is characterised in that, at least one electrode during the alkali metal that will contain potassium is supplied with material and is included in above-mentioned pair of electrodes and the electron emission part that contains iron contact and dispose; Above-mentioned pair of electrodes is applied the direct voltage of pulse type, thereby heat above-mentioned electron emission part when making the discharge of above-mentioned discharge gas; Make above-mentioned alkali metal supply with the potassium that is comprised in the material and be adsorbed on above-mentioned electron emission part.
The invention effect
Starter of the present invention carries out the electronics emission easily, even long-time keeping in the dark also can be started the enough very short time.
And starter manufacture method of the present invention can reasonably be made the starter of the invention described above.
Description of drawings
Fig. 1 represents the part sectioned view of an example of starter of the present invention.
Fig. 2 A, 2B are the figure of an example of manufacture method of the stem stem portion of explanation starter of the present invention.
Embodiment
Starter of the present invention has pair of electrodes and discharge gas that the counter-electrodes by float electrode that comprises temperature-sensitive element and above-mentioned float electrode constitutes in the inside of closed container.At least one electrode in the above-mentioned pair of electrodes comprises the electron emission part that contains iron, and above-mentioned electron emission part is supplied with material with the alkali metal that contains potassium and contacted, and activates by the direct voltage that above-mentioned pair of electrodes is applied pulse type.
By adopting such structure, do not use radioactive substance and can shorten the dark place start delay time.This starter is because comprise the electron emission part that is activated that work function is little, so, for example in the dark take care of starter for a long time, also can be easy to emitting electrons.
Preferably, adsorb the potassium of supplying with the material supply from above-mentioned alkali metal by applying above-mentioned voltage on the surface of above-mentioned electron emission part.This is because in the electron emission part of having adsorbed potassium, owing to work function further reduces, so can further shorten the dark place start delay time.
The direct voltage of preferred above-mentioned pulse type has stopping period.This be because, when applying high voltage, the discharging current of starter increases, the temperature of electrode sharply raises, float electrode activity and short circuit.
Preferred above-mentioned electron emission part is containing from iron with the contacted surface of above-mentioned alkali metal supply material and is comprising at least a metal of selecting the alloy of iron.Because at the surface adsorption potassium of the electron emission part that contains iron, so work function further reduces.
It is the glass that contains alkali metal oxide that preferred above-mentioned alkali metal is supplied with material.Especially, the glass that preferably contains potassium oxide.This is because if chemically unsettled alkali metal is included in the glass, then chemically become stable, so handle easily.
It is at least a portion of above-mentioned closed container that preferred above-mentioned alkali metal is supplied with material.This is because can reduce the member of starter.
And the manufacture method of starter of the present invention is the manufacture method that has the starter of the pair of electrodes that constitutes by the float electrode that comprises temperature-sensitive element and with the counter-electrodes of above-mentioned float electrode and discharge gas in the inside of closed container.Promptly, in at least one electrode during the alkali metal that will contain potassium is supplied with material and is included in above-mentioned pair of electrodes and the electronic emission portion of containing iron contact and dispose, by above-mentioned pair of electrodes being applied the direct voltage of pulse type, thereby when being discharged, heats above-mentioned discharge gas above-mentioned electron emission part, make above-mentioned alkali metal supply with the potassium that is comprised in the material and carry out thermal diffusion, be adsorbed on the above-mentioned electron emission part line activating of going forward side by side, thereby can reasonably make the starter of the electrode that comprises k adsorption.
Below utilize accompanying drawing, describe the execution mode of starter of the present invention and manufacture method thereof in detail.And identical position owing to be of identical composition and shape, produces identical effect, so omit its explanation sometimes.
(execution mode 1)
Fig. 1 is the part sectioned view of an example of expression starter of the present invention.
The starter 1 of present embodiment 1 has electrode (float electrode) 3, electrode (counter-electrodes) 4 and the discharge gas paired with above-mentioned float electrode 3 in the inside of airtight container 2 (internal tank 8).
Container 2 is airtight by shell (バ Le Block) 6, tubaeform stem stem (Off レ ア ス テ system) 7 and blast pipe 9.Employed blast pipe 9 when being used for that discharge gas enclosed internal tank 8, being connected with internal tank 8 by steam vent 10 is connected on the tubaeform stem stem 7.An end of blast pipe 9 utilizes steam vent 10 to be connected with tubaeform stem stem 7, and another end is blocked.And, lamp holder 5 is installed so that the end of the packed side of the electrode of covering container 23,4, and is electrically connected with electrode 3,4.
Electrode 3 has as the bimetallic element 14 of temperature-sensitive element and the inner lead 13 that comprises the electron emission part 18 that contains iron.And electrode 4 has the inner lead 15 that comprises the electron emission part 19 that contains iron.
Electronics emission 18,19 contacts and is fixed with the tubaeform stem stem 7 that contains potassium.And by electrode 3,4 being applied the direct voltage of pulse type, electron emission part 18,19 is activated.
The starter 1 of present embodiment is owing to adopting said structure, so can shorten the dark place start delay time.Starter 1 comprises the electron emission part 18,19 that work function is little and be activated, so, for example in the dark take care of starter 1 for a long time and also can be easy to emitting electrons.
The material of tubaeform stem stem 7 is the glass that contains potassium, still, so long as, do not limit especially comprising that with electron emission part 18,19 contacted surfaces the alkali metal that contains potassium supplies with the material of material.
The shape of tubaeform stem stem 7 is the such shapes of umbrella, and is the structure of the end of the shirt rim portion open side that is encapsulated in shell 6, is this shape but be not particularly limited.
The material of shell 6 is if can tolerate the material of above-mentioned discharge and heating, and just not specific qualification generally adopts glass, resin etc. to get final product.
The shape of shell 6 is the general cylindrical shape that the end is blocked, is this shape but be not particularly limited.
Discharge gas is so long as be fit to the gas of discharge and just be not particularly limited.Generally can adopt a kind of gas of from helium, neon, argon and xenon, selecting or their mist etc. to get final product.Especially the suitable mist that adopts argon gas or neon and argon.
As long as can begin and continuous discharge just is not particularly limited the enclosed volume of discharge gas, the air pressure that can make internal tank 8 is in number kPa~number 100kPa, preferably 1~10kPa.
The material of inner lead 13,15 for example can adopt iron and iron-nickel alloy etc. so long as contain the material of iron and just be not particularly limited.
Electron emission part 18,19 both can be in the inner lead 13,15 with 7 contacted of tubaeform stem stems or comprise the periphery of this face, also can be all inner leads 13,15.At this moment, at least a portion of electron emission part 18,19 surface contacts with discharge gas and gets final product.
We can say that tubaeform stem stem 7 is that the alkali metal that contains potassium is supplied with material with 18,19 contacted of electron emission part, the periphery that comprises this face or whole tubaeform stem stem 7.
Applying of the direct voltage of above-mentioned pulse type, if according to the condition of electrode 3,4 not short circuits, promptly bimetallic element 14 inactive conditions apply, so, to the size of voltage (crest voltage and minimum voltage etc.), stopping period and pulse duration etc. is not particularly limited.And, the direct voltage of above-mentioned pulse type is not limited especially, both can be the sinusoidal wave voltage of control, also can be the voltage of control square wave, if but the offset of sinusoidal ripple cuts off the voltage (for example be controlled to during 1 second discharge 2 times voltage) of control, just can control at an easy rate, so preferred.And, if utilize step-up transformer to general alternating voltage (60Hz for example, the voltage that 0.2kV) boosts, then cheap, so preferred.
Applying of the direct voltage of above-mentioned pulse type, for example with each single electrode of electrode 3,4 as negative electrode, direct voltage with crest voltage 0.2kV~1.0kV, minimum voltage 0kV~0.2kV, pulse repetition period 0.1 time/second~10 times/second, pulse duration 0.5ms (millisecond)~10ms, apply 0.1 hour~1.0 hours, can distinguish active electron emission part 18,19 like this.Especially, wish to apply the direct voltage of crest voltage 0.6kV~0.8kV, minimum voltage 0kV~0.1kV, pulse repetition period 1.0 times/second~4.0 times/second, pulse duration 1.0ms~4.0ms.
If above-mentioned crest voltage surpasses 1.0kV, then electric shock waits fail safe that problem is arranged, if less than 0.2kV, does not then begin discharge sometimes.And, if above-mentioned crest voltage is 0.6kV~0.8kV, just too high caused, the peripheral part of the tubaeform stem stem 7 of inner lead 13,15 paradoxical discharge such as discharge only for example of crest voltage can not take place, the active electron emission part 18,19 expeditiously, are more preferably.
If above-mentioned pulse duration surpasses 10ms, then the heat of Chan Shenging is many, and bimetallic element 14 can be movable, if less than 0.5ms, then must shorten the energising cycle, and for example generation sometimes such as has when not discharging at loss.And, if above-mentioned pulse duration is 0.5ms~6.0ms, perhaps be more preferably 1.0ms~4.0ms, do not make bimetallic element 14 activities, the active electron emission part 18,19 expeditiously.
And, if the direct voltage to above-mentioned pulse type is controlled, the formed energising cycle of the discharge that produces between electrode (light period) is become 0.5 time/second~6 times/second, be preferably 1.0 times/second~4.0 times/second, so, because the heat that takes place is little, so, bimetallic element 14 inertias, and can be with active electron emission part 18,19 expeditiously of shorter time.
Here, the method that electron emission part 18,19 is activated is described.
In the internal tank 8 of having enclosed discharge gas,, then between electrode, produce discharge if between electrode 3 and electrode 4, be that negative electrode applies voltage with electrode 4.At this moment, utilize the ion in the discharge gas that the electrode 4 as negative electrode quickens, clash into the impurity on the surface of electron emission part 19, so the surface of electron emission part 19 is cleaned.And if apply above-mentioned voltage, then the tubaeform stem stem 7 as alkali metal supply material is heated, and alkali metal carries out thermal diffusion.Therefore, at the electron emission part 19 that is cleaned and tubaeform stem stem 7 contacted surface adsorption alkali metal, the work function of electron emission part 19 (drawing a needed least energy of electronics from metal) descends.Because easily from the low part emitting electrons of work function, so electron emission part 19 is activated.Equally, as if being that negative electrode applies voltage with electrode 3, then the work function of electron emission part 18 descends, and is activated.
The starter of Huo Deing like this, when the starting starter, the initiating electron quantity delivered of electrode 3,4 increases, so, can start with the short time, also can shorten the dark place start delay time.
Generally, even on starter, apply direct voltage, certain voltage for example continuously, also can be on the electron emission part 18,19 fully before the absorption alkali metal, bimetallic element 14 contact inner leads 15, thereby inter-electrode short-circuit also stops discharge, so electron emission part 18,19 is not activated.And even apply alternating voltage, inter-electrode short-circuit too is not so electron emission part 18,19 is activated.But, by applying the direct voltage of pulse type, electron emission part 18,19 is activated with the short time.
The action of the starter 1 when using starter 1 to light fluorescent lamp (not having diagram) is described here.
If on the electrode 3,4 of starter 1, apply the voltage of regulation, then between electrode, produce glow discharge.Utilize the heat of this glow discharge, bimetallic element 14 distortion, i.e. electrode 3 activities contact with electrode 4.Like this, short circuit current flows through, and the filament electrode of fluorescent lamp (not having diagram) is preheated.And, if electrode 3,4 contacts with each other, short circuit current flow then, glow discharge stops.But if short circuit current flow, then bimetallic element 14 then is cooled, so, be deformed into original shape, that is to say that electrode 4 is left in electrode 3 activities, short circuit current also stops.At this moment, produce pulse voltage, in fluorescent lamp, produce discharge, light fluorescent lamp.
That is to say, relate to electron emission part the 18, the 19th of the present invention, can launch the initiating electron that much is used to make starter 1 beginning glow discharge.
In the starter 1 of present embodiment, the potassium of supplying with from tubaeform stem stem 7 is adsorbed by applying above-mentioned voltage in the surface of preferred above-mentioned electron emission part 18,19.This be because, electrode 3,4 is in the electron emission part 18,19 of having adsorbed potassium, work function further reduces.
In the starter 1 of present embodiment, the direct voltage that preferably is applied to the above-mentioned pulse type on the electrode 3,4 has stopping period.If starter 1 is applied high voltage, then the temperature of float electrode 3 sharply raises immediately, bimetallic element 14 activities and short circuit.
In the starter 1 of present embodiment, wish that electron emission part 18,19 is containing from iron with tubaeform stem stem 7 contacted surfaces and comprising at least a metal of selecting the alloy of iron.This is because the work function of electron emission part 18,19 further reduces on the surface of the electron emission part that contains iron.
In the starter 1 of present embodiment, preferred tubaeform stem stem 7 is the glass that contains alkali metal oxide, especially wishes it is the glass that contains potassium oxide.If being included in the glass, chemically unsettled alkali metal chemically becomes stable, so handle easily.And, because the alkali metal of supplying with from above-mentioned glass exists as ion in this glass, especially potassium is when having applied the direct voltage of pulse type, potassium ion carries out diffusion into the surface, has the character that is adsorbed on the ferrous metal surface and forms the good electron emission part of electron emissivity easily.Above-mentioned glass also have with as the good effect of the electrode compactness of metal.Above-mentioned glass is that the glass that generally is used for discharge tube gets final product, and for example suitably is used in combination K 2O, SiO 2, Na 2O, Li 2O, Al 2O 3, Fe 2O 3Deng getting final product.Especially preferably the glass that contains the potassium of 1 weight %~20 weight %.
In the starter 1 of present embodiment, preferred as alkali is supplied with at least a portion that material constitutes above-mentioned closed container.Because can reduce the member of starter.
In the present embodiment, adopted fixed electrode, but also can be float electrode as counter-electrodes 4.That is to say, in the pair of electrodes can be one and be float electrode, also can be two and be float electrode.
In the present embodiment, electron emission part 18,19 is arranged at least a portion as the inner lead 13,15 of the metal that comprises iron, is electrically connected with electrode and supplies with material with alkali metal and contact and get final product, just do not limit especially at internal tank 8.For example, also the part that can cover with iron in the part on the surface of other metal materials that will be suitable as electrode most and will cover and peel off that it is a part of and expose the part of iron as the surface of the lead-in wire of the metal that comprises iron with other metals is provided with electron emission part.In addition, also can only on an electrode, electron emission part be set.And alkali metal supply material does not contact with electron emission part 18,19 and can be activated.If contact, just absorption is supplied with the potassium that material is supplied with from alkali metal easily.
In the present embodiment, tubaeform stem stem 7 is also used as alkali metal supplies with material, still, contain potassium and contact, then restriction especially such as its shape with electron emission part 18,19 as long as alkali metal is supplied with material.For example, also can be with inner lead on the different member of the contacted tubaeform stem stem of electron emission part of (perhaps on the bimetallic element).
(execution mode 2)
Fig. 2 A, 2B illustrate the figure of an example of manufacture method of the stem stem portion of starter of the present invention.
The manufacture method of the starter of present embodiment at first, shown in Fig. 2 A, is inserted inner lead 13,15 at the little opening 16a of tubaeform glass 16, inserts tubule 17 at the opening 16b of tubaeform glass 16.Shown in Fig. 2 B,, obtain stem stem portion 20 then at the top of tubaeform glass 16 (little opening 16a side) fixing internal lead-in wire 13,15 and tubule 17.
Then, as shown in Figure 1, connect bimetallic element 14 in the end of a side of the tubaeform glass 16 of not being fixed on of inner lead 13.And, stem stem portion 20 and shell 6 are closely bonded airtightly, form the container 2 that constitutes by tubaeform stem stem 7 (being tubaeform glass 16), blast pipe 9 (in Fig. 2 A, 2B, being tubule 17) and shell 6 in Fig. 2 A, 2B.Air from blast pipe 9 amount discharge containers 2 inside is blown into discharge gas, and the end of sealing blast pipe 9 is airtight with container 2.The electrode (float electrode) 3 that will be made of inner lead 13 and bimetallic element 14, the electrode (counter-electrodes) 4 that is made of internal electrode 15 and the lamp holder 5 that is electrically connected respectively are installed in container 2.
At last, on electrode 3,4, apply the direct voltage of pulse type, thereby active electron emission part 18,19 is made starter 1.
Tubaeform glass 16 for example is the such shape of umbrella, and 2 little opening 16a that comprise the opening 16b that is positioned at full skirt and be positioned at umbrella top get final product.
Outside lead 11,12 is connected with inner lead 13,15 conductings.And inner lead 15 is than inner lead 13 long getting final product.
When inner lead 13,15 being inserted above-mentioned little opening 16a, outside lead 11,12 is configured to stretch out to the outside by opening 16b from the inner surface side of tubaeform glass 16 and gets final product.
When being fixed on above-mentioned inner lead 13,15 and tubule 17 on the tubaeform stem stem 7, for example flatten when heating on the top (little opening 16a side) to tubaeform glass 16 from the outside, inner lead 13,15 and tubule 17 is encapsulated in the tubaeform glass 16 get final product.Owing to flatten the top of tubaeform glass 16 from the outside, so can make inner lead 13,15 and manage 17 and closely be connected with tubaeform glass 16.And, when above-mentioned flattening,, be blown into air to the end of the inboard of tubaeform glass 16 from the end of the tubule 17 of the outside that is positioned at tubaeform glass 16, blow brokenly the part of the side of the tubaeform glass 16 that has softened with air, form steam vent 10 and get final product.Utilize steam vent 10, can make tubule 17 not stop up its mouth of pipe and be bonded on the tubaeform glass 16.
Carry out airtightly when bonding at above-mentioned stem stem portion 20 and shell 6, for example, the opening 16b that being roughly of the end columnar edge portion and tubaeform glass 16 are arranged of shell 6 is heated bonding getting final product in addition.At this moment, be the inside of container 2 in the inner surface side of shell 6, the electrode 3 that configuration is made of inner lead 13 and bimetallic element 14 and get final product by the electrode 4 that inner lead 15 constitutes.
Electrode 3,4 by lamp holder 5 is connected with outside lead 11,12, can be connected with the external electric of container 2 and gets final product.
The manufacture method of the starter 1 of present embodiment can be easy to produce and comprises the potassium that absorption is supplied with from tubaeform stem stem 7 and the starter of the electron emission part 18,19 that is activated.
Embodiment
Below be described more specifically the present invention with embodiment, and the present invention is not limited in following examples.
(embodiment 1)
At first, as tubaeform glass, make lead glass (K 2O:4.7 weight %, SiO 2: 57.5 weight %, PbO:29.0 weight %, Al 2O 3: 1.0 weight %, Na 2O:7.8 weight %), form the horn-like of opening arranged on top.50 weight %) and the tubule of glass prepared 2 inner leads that connect Dumet wire (iron: 50 weight %, nickel: as outside lead.Then, shown in Fig. 2 A, 2B, flatten in the time of by heating inner lead and tubule, thereby be fixed in the tubaeform glass.And, as shown in Figure 1, connected bimetallic element (high expansion side: iron 70 weight %-nickel 25 weight %-manganese 5 weight %, low bulk side: iron 64 weight %-nickel 36 weight %) in the end of an inner lead.Fluorescent tube to above-mentioned tubaeform glass and glass carries out airtight closely bonding then.
Like this, formed, comprised the container of the pair of electrodes that constitutes by float electrode and fixed electrode in inside by tubaeform stem stem (above-mentioned tubaeform glass) and blast pipe (above-mentioned tubule) and fluorescent tube formation.Then, utilize the air of blast pipe amount discharge container inside, be blown into discharge gas (neon: 95 volume %, argon: 5 volume %).At this moment, the air pressure of internal tank is made as 5.3kPa.The end that is not connected with tubaeform stem stem of blast pipe is sealed, container is airtight.Make 2 outside leads respectively with after lamp holder is electrically connected, lamp holder is installed on the container.
At last, apply the direct voltage (crest voltage: 0.8kV, minimum voltage 0kV, pulse duration: 3ms, pulse repetition period: 2 times/second) that had the pulse type of stopping period in 0.5 hour to electrode by lamp holder, like this, make electrode with the contacted surface activation of loudspeaker stem stem, make the starter of present embodiment.And, float electrode and fixed electrode have alternately been applied above-mentioned direct voltage as negative electrode.
(comparative example 2)
The starter of this comparative example except utilizing the nickel plating silk as inner lead, does not apply beyond the situation of direct voltage of pulse type, similarly makes with the starter of embodiment 1.
(comparative example 2)
The starter of this comparative example except the direct voltage that does not apply pulse type, is similarly made with the starter of embodiment 1.
(elementary analysis)
(position among Fig. 1 a) utilizes the auger electrons optical spectroscopy to carry out elementary analysis for a part of surface of the fixed electrode in the starter of embodiment 1, comparative example 2.And from the contact-making surface of fixed electrode and tubaeform stem stem, the height of position a is 2mm.
The result who analyzes, about the starter of embodiment 1, a detects potassium from the position.But about the starter of comparative example 2, a does not detect potassium from the position.So, confirmed following situation: applied the electrode of starter of embodiment 1 of the direct voltage of pulse type, the potassium that in tubaeform stem stem has fully been adsorbed on the surface, has been comprised.But do not apply the electrode of starter of comparative example 2 of the direct voltage of pulse type, do not have k adsorption on the surface.
(dark place starting experiment)
The starter of embodiment 1, comparative example 1,2 is respectively prepared 5 respectively, and dark place start delay time of starter is compared.
In this experiment, be the flicker number of times after each starter of 0 time was in the dark placed 15 hours at first, with fluorescent lamp (power: 30W) be connected, measure from be energized to till the glow discharge time (discharge delay time) and from being energized to the time (lighting required time) till the fluorescent lamp lighting.Then, make each starter flicker 6000 times, in the dark placed 15 hours, then,, measure discharge delay time and light required time with identical fluorescent lamp connection.The measurement result of above-mentioned discharge delay time is shown in table 1; The above-mentioned measurement result of lighting required time is shown in table 2.
Table 1
Discharge delay time (second)
Glimmer 0 time Glimmer 6000 times
Embodiment 1-1 0.04 0.06
Embodiment 1-2 0.02 0.04
Embodiment 1-3 0.04 0.08
Embodiment 1-4 0.08 0.02
Embodiment 1-5 0.02 0.06
Comparative example 1-1 10.32 0.02
Comparative example 1-2 7.32 5.28
Comparative example 1-3 0.72 12.28
Comparative example 1-4 0.62 8.72
Comparative example 1-5 18.32 1.40
Comparative example 2-1 0.20 More than 20 seconds
Comparative example 2-2 0.02 0.02
Comparative example 2-3 0.20 0.10
Comparative example 2-4 0.08 0.60
Comparative example 2-5 0.02 12.00
Table 2
Light required time (second)
Glimmer 0 time Glimmer the 6000th time
Embodiment 1-1 3.60 3.28
Embodiment 1-2 2.07 2.33
Embodiment 1-3 3.16 3.56
Embodiment 1-4 3.78 2.48
Embodiment 1-5 2.31 2.75
Comparative example 1-1 12.73 3.04
Comparative example 1-2 10.23 8.22
Comparative example 1-3 3.06 14.55
Comparative example 1-4 3.13 11.40
Comparative example 1-5 20.00 3.96
Comparative example 2-1 2.11 Do not light
Comparative example 2-2 2.42 2.42
Comparative example 2-3 2.75 3.07
Comparative example 2-4 2.27 3.48
Comparative example 2-5 2.79 14.60
As shown in Table 1 and Table 2, each starter of embodiment 1 still is 6000 times the time lighting when number of times is 0 time, and discharge delay time is in 0.1 second, lights in the required time 4 seconds.
On the other hand, the starter of comparative example 1, discharge delay time is that the starter more than 1 second is 3 under 0 time situation of flicker, the starter of lighting the required time and being more than 10 seconds is 3.And under 6000 times situation of flicker, discharge delay time is that the starter more than 1 second is 4, and the starter of lighting the required time and being more than 10 seconds is 2.So as can be seen, compare with the starter that uses in the past of comparative example 1, the starter of embodiment 1 shows good dark place starting characteristic.
And the starter of comparative example 2 is glimmering 6000 times the time, and discharge delay time is that the starter more than 1 second is 2, and the starter of lighting required time and being more than 10 seconds is 1, and the starter of failing to light fluorescent lamp is 1.So, the starter of comparative example 2 that contacts with the tubaeform stem stem that contains potassium with the inner lead that contains iron as can be known and do not apply the direct voltage of pulse type is compared, and the starter of embodiment 1 that has applied the direct voltage of pulse type shows good dark place starting characteristic.
And according to the criterion of the endurance test of the C7603 of Japanese Industrial Standards (JIS) defined, the life-span of starter flicker number of times is set at 6000 times.So, we can say that the starter of present embodiment is not use radioactive substance also can keep the starter of sufficient dark place starting characteristic.
Industrial utilizability
As described above, the present invention can provide starter and the manufacture method thereof of not using radioactive substance and carrying out easily electron emission, dark place start delay time weak point.

Claims (11)

1, a kind of starter is characterized in that, has pair of electrodes and discharge gas that the counter-electrodes by float electrode that comprises temperature-sensitive element and above-mentioned float electrode constitutes in the inside of closed container;
At least one electrode in the above-mentioned pair of electrodes comprises the electron emission part that contains iron;
Above-mentioned electron emission part is supplied with material with the alkali metal that contains potassium and is contacted, and is activated by the direct voltage that above-mentioned pair of electrodes is applied pulse type.
2, starter as claimed in claim 1 is characterized in that, the potassium of supplying with the material supply from above-mentioned alkali metal has been adsorbed by applying above-mentioned voltage in the surface of above-mentioned electron emission part.
3, starter as claimed in claim 1 is characterized in that, the direct voltage of above-mentioned pulse type has stopping period.
4, starter as claimed in claim 1 is characterized in that, above-mentioned electron emission part is containing from iron with the contacted surface of above-mentioned alkali metal supply material and comprising at least a metal of selecting the alloy of iron.
5, starter as claimed in claim 1 is characterized in that, it is the glass that contains alkali metal oxide that above-mentioned alkali metal is supplied with material.
6, starter as claimed in claim 1 is characterized in that, above-mentioned alkali metal is supplied with at least a portion that material constitutes above-mentioned closed container.
7, a kind of manufacture method of starter, this starter have pair of electrodes and the discharge gas that the counter-electrodes by float electrode that comprises temperature-sensitive element and above-mentioned float electrode constitutes in the inside of closed container;
This manufacture method is characterised in that,
In at least one electrode during the alkali metal that will contain potassium is supplied with material and is included in above-mentioned pair of electrodes and the electron emission part that contains iron contact and dispose;
Above-mentioned pair of electrodes is applied the direct voltage of pulse type, thereby heat above-mentioned electron emission part when making the discharge of above-mentioned discharge gas;
Make above-mentioned alkali metal supply with the potassium that is comprised in the material and be adsorbed on above-mentioned electron emission part.
8, the manufacture method of starter as claimed in claim 7 is characterized in that, the direct voltage of above-mentioned pulse type has stopping period.
9, the manufacture method of starter as claimed in claim 7 is characterized in that, above-mentioned electron emission part is containing from iron with the contacted surface of above-mentioned alkali metal supply material and comprising at least a metal of selecting the alloy of iron.
10, the manufacture method of starter as claimed in claim 7 is characterized in that, it is the glass that contains alkali metal oxide that above-mentioned alkali metal is supplied with material.
11, the manufacture method of starter as claimed in claim 7 is characterized in that, above-mentioned alkali metal is supplied with at least a portion that material constitutes above-mentioned closed container.
CN 200710002083 2006-01-18 2007-01-18 Electric fluorescent starter and its manufacture method Pending CN101005005A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
JP010405/2006 2006-01-18
JP2006010405A JP4495678B2 (en) 2006-01-18 2006-01-18 Lighting tube and manufacturing method thereof

Publications (1)

Publication Number Publication Date
CN101005005A true CN101005005A (en) 2007-07-25

Family

ID=38449583

Family Applications (1)

Application Number Title Priority Date Filing Date
CN 200710002083 Pending CN101005005A (en) 2006-01-18 2007-01-18 Electric fluorescent starter and its manufacture method

Country Status (2)

Country Link
JP (1) JP4495678B2 (en)
CN (1) CN101005005A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102573246A (en) * 2012-01-05 2012-07-11 黄山市高立亚照明电器有限责任公司 Non-radioactive material starter
CN102810452A (en) * 2011-06-01 2012-12-05 普罗斯电器(中国)有限公司 Self-trigger

Family Cites Families (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS494383A (en) * 1972-05-01 1974-01-16
JP2004247171A (en) * 2003-02-13 2004-09-02 Matsushita Electric Ind Co Ltd Electron emitting portion, flat panel display, flat light source, cold cathode fluorescent lamp, electrodeless fluorescent lamp and these manufacturing methods

Cited By (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN102810452A (en) * 2011-06-01 2012-12-05 普罗斯电器(中国)有限公司 Self-trigger
CN102573246A (en) * 2012-01-05 2012-07-11 黄山市高立亚照明电器有限责任公司 Non-radioactive material starter
CN102573246B (en) * 2012-01-05 2014-04-23 黄山市高立亚照明电器有限责任公司 Activation circuit of non-radioactive material starter

Also Published As

Publication number Publication date
JP4495678B2 (en) 2010-07-07
JP2007194046A (en) 2007-08-02

Similar Documents

Publication Publication Date Title
JP3599094B2 (en) Discharge lamps and compact fluorescent lamps
US20040046506A1 (en) Gas discharge tube
CN101005005A (en) Electric fluorescent starter and its manufacture method
US4097779A (en) Fluorescent lamp containing a cathode heater circuit disconnect device
JPS6340246A (en) Fluorescent lamp
JP5475948B2 (en) Gas discharge lamp
EP0306257B1 (en) Metal vapour discharge lamp
GB2090464A (en) Starting aid for high pressure lamp
EP2173144B1 (en) Light source device, discharge lamp and its control method
EP0489476A2 (en) Rapid start fluorescent lamp having quick hot restarting
CN1052562C (en) Improved discharge tube
US5932970A (en) Preform for fluorescent lamp, fluorescent lamp prepared by the same, and method for preparing the fluorescent lamp
JP3479657B2 (en) Manufacturing method of electrodeless fluorescent lamp
JP3313869B2 (en) Explosion-proof bulb
TW200307971A (en) Low-pressure discharge lamp with a device for switching it off at the end of its service life
JP3797093B2 (en) lamp
JP3525571B2 (en) High pressure discharge lamp
JP2002505802A (en) Starter circuit
JP2850313B2 (en) High pressure discharge lamp with built-in starter
JPS59180955A (en) High pressure metal vapor discharge lamp
JPS5885266A (en) Glow starter
US1890859A (en) Cathode for electron discharge devices
JPH06111776A (en) Discharge lamp with built-in starter device
CN202565551U (en) Starter with nonradioactive substances
CN101426321A (en) A starter

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
AD01 Patent right deemed abandoned

Effective date of abandoning: 20070725

C20 Patent right or utility model deemed to be abandoned or is abandoned