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    专

    Battery system for vehicle, comprises control device, that is configured to perform first control and second control, first control includes placing all-solid-state battery in over-discharge state, second control including pressurizing all-solid-state battery in over-discharge state.

    PL59095859A
    发明人
    大瀧 光俊, 中西 真二, 早稲田 哲也, 吉田 淳, 右田 翼, 内田 義宏
    受让人
    TOYOTA JIDOSHA KK (TOYT-C), TOYOTA MOTOR CORP (TOYT-C)
    申请人
    SPATER CHRISTOPHER B
    申请号
    2427990
    申请日
    2002-10-31
    公开(公告)号
    PL59095859A
    公开(公告)日
    1993-07-22
    IPC分类号
    H04M003/54H04Q003/58
    CPC分类号
    -
    优先权号
    138737
    057539
    优先权日
    2006-12-28
    2007-06-11
    摘要

    Substrate materials, coated on at least one side with a pressure-sensitive adhesive comprising a hot-melt adhesive material that has a dynamic complex Tg < -3 (-9 to -25) C at a frequency of 0.1 rad/s.

    Preferably the adhesive contains a block copolymer, preferably of the A-B or A-B-A type, or a mixture of these, in which A is polystyrene or a derivative thereof and B is propylene, butadiene or isoprene, or mixtures of these, preferably ethylene and/or butylene. Styrene content in the polymer is less than 35 (5-30) wt.%. The adhesive comprises 10-90 wt.% block copolymer, 5-80 wt.% tackifier (eg. oil, wax or resin, or a mixture of these, preferably a resin/oil mixture), less than 60 wt.% emulsifier, less than 15 wt.% additives and less than 5 wt.% stabiliser.

    USE -Used for medical products, especially plasters, medicinal fixing patches, wound dressings or orthopaedic or phlebologic bandages or slings, as well as for technical adhesive mounting products that can be removed without damaging the underlay (claimed).

    ADVANTAGE -The adhesive products are easily removed from the underlay yet maintain a sufficient adhesive strength without any detrimental reduction in air or water vapour permeability.

    权利要求
    1.시멘트 47~56 중량%;슬래그 15~23 중량%;무수석고 2.5~4.5 중량%;실리카퓸 4~20 중량%;벤토나이트 2.5~4.5 중량%;분말형 유동화제 0.1~0.3중량%;물 8~10중량%;알코올 3~5중량%;를 포함하는 조성물(A)로 제조된 콘크리트 표면 균열 보수용 스틱.
    2.제1항에 있어서,상기 슬래그는 동제련슬래그와 고로슬래그가 혼합된 것을 특징으로 하는 표면균열 보수용 스틱.
    3.제1항에 있어서,상기 실리카퓸은 고순도 규소철(Fe-si)의 생산과정에서 발생하는 부산물을 집진하여 반압축 상태로 압축한 것으로서, 부피비중이 500~650kg/㎥인 것을 특징으로 하는 콘크리트 표면 균열 보수용 스틱.
    4.제3항에 있어서,상기 실리카퓸은 비표면적이 13,000~17,000㎡/kg인 것을 특징으로 하는 콘크리트 표면 균열 보수용 스틱.
    5.제1항에 있어서,상기 벤토나이트는 Al2O3계 또는 SiO2계 중 어느 하나인 것을 특징으로 하는콘크리트 표면 균열 보수용 스틱.
    6.제1항 내지 제5항 중 어느 한 항의 콘크리트 표면 균열 보수용 스틱(10) 제조방법으로서,상기 실리카퓸과 상기 물을 혼합하여 상기 실리카퓸을 슬러리화하는 실리카퓸슬러리화단계;상기 시멘트, 상기 슬래그, 상기 무수석고, 상기 벤토나이트, 상기 분말형 유동화제, 상기 알코올, 상기 물을 슬러리화되어 있는 상기 실리카퓸과 혼합하여 상기 조성물(A)을 혼합하는 혼합단계;상기 조성물(A)을 상기 콘크리트 표면 균열 보수용 스틱(10)의 제작용 몰드(1)에 투입하는 몰드투입단계;초기 수화반응을 촉진함과 아울러, 상기 스틱(10) 내부의 수분을 증발시켜 완전 수화반응을 억제하도록 고온으로 상기 조성물(A)을 건조하는 고온경화단계;상기 스틱(10) 내부의 잔여 수분을 완전히 경화시키기 위해 전자파를 이용하여 건조하는 전자파경화단계;를 포함하는 것을 특징으로 하는 균열 보수용 스틱 제조방법.
    7.제6항에 있어서,상기 고온경화단계는상기 몰드(1)에 투입된 상기 조성물(A)을 100~110℃의 온도에서 2~3시간 동안 건조하는 것을 특징으로 하는 균열 보수용 스틱 제조방법.
    8.제6항에 있어서,상기 전자파경화단계는주파수가 2250~2650Mhz인 건조장치(2)에서 상기 고온경화단계 이후의 상기 조성물(A)을 건조하는 것을 특징으로 하는 균열 보수용 스틱 제조방법.
    9.제8항에 있어서,상기 전자파경화단계는 0.5~5분간 건조하는 것을 특징으로 하는 균열 보수용 스틱 제조방법.
    10.제6항에 있어서,상기 실리카퓸슬러리화단계는상기 실리카퓸 중량의 2~3배인 상기 물을 먼저 혼합하는 것을 특징으로 하는 균열 보수용 스틱 제조방법.
    11.제6항의 제조방법으로 제작된 균열 보수용 스틱(10)을 이용한 콘크리트 표면 보수방법으로서,균열(101)이 발생한 콘크리트 구조물(100)의 표면 균열부(111)를 정리하는 표면정리단계;상기 균열부(111)의 표면에 물을 분사하여 상기 균열(101)에 물을 침투시키는 물분사단계;상기 균열 보수용 스틱(10)을 상기 균열부(111)에 문질러 상기 균열 보수용 스틱(10) 가루가 상기 균열(101)의 내부로 침투시키는 스틱처리단계;표면처리장치(20)를 이용하여 상기 스틱(10) 가루가 침투된 상기 균열(101)의 표면을 정리하는 표면처리단계;상기 균열(101) 내부에 침투된 상기 물과 상기 스틱(10) 가루가 상호 접촉하여 경화되는 경화단계;를 포함하는 것을 특징으로 하는 콘크리트 표면 보수방법.
    12.제11항에 있어서,상기 표면처리장치(20)는 손가락에 끼워지는 골무 타입으로 형성된 것을 특징으로 하는 콘크리트 표면 보수방법.
    说明书
    [0001]FIELD OF THE INVENTION [0001] The present invention relates to an optical sensor as well as a method for producing the same, and its use. BACKGROUND INFORMATION [0002] Optical sensors for determining the carbon monoxide content in the air are used, among other things, in fire alarms. Their function is based on the fact that a layer sensitive to carbon monoxide changes color reversibly upon contact with the gas to be ascertained. This change of color is recorded by a detector, and when a predetermined minimum concentration is exceeded, an alarm is triggered. [0003] In U.S. Pat. No. 5,618,493 such a carbon monoxide sensor is described. It includes two substrates to which sensitive layers are applied. One of the layers is provided especially for low humidity and low air temperature, the other for a higher temperature and humidity. In order to be able to detect the color change of the sensitive layers at contact with carbon monoxide, a light-emitting diode is provided as radiation source in the fire alarm described, whose light passes through the sensitive layers. The absorption appearing during this process is ascertained, using a photodiode. However, such a sensor does not have the sensitivity suited to strict standards, and has a long response time. [0004] The present invention is based on the object of making available a carbon monoxide sensor having great sensitivity and a short response time. SUMMARY OF THE INVENTION [0005] The optical sensor according to the present invention has the advantage that it has a very short response time and very high sensitivity to carbon monoxide. This is achieved by adding a transition metal compound to the sensitive layer of the sensor, which reversibly undergoes chemical bonding with CO, and thus actively brings carbon monoxide in the air to the sensitive layer. This makes possible the rapid reaction of the sensor to changing carbon monoxide concentrations, but also a lowering of the response threshold of the sensitive layer. The sensitive layer is preferably deposited as a thin film on a translucent substrate. [0006] As a transition metal compound, copper(I) chloride is suitable above all, since it rapidly and effectively forms complexes with carbon dioxide at room temperature. [0007] In a particularly advantageous embodiment, the sensitive layer includes a matrix of hydrogel, since carbon monoxide has a substantially higher diffusion constant and solubility in aqueous media than in the usual polymer layers. This further raises the sensitivity and lowers the response time.
    [0002]BRIEF DESCRIPTION OF THE DRAWING [0008] The FIGURE shows a schematic representation of an exemplary embodiment of the optical sensor according to the present invention.
    [0003]DETAILED DESCRIPTION [0009] The optical sensor 10 illustrated in the FIGURE contains a radiation source 12 which may be such as a light-emitting diode, and a detector 14 which is developed, for example, as a photodiode. Between the radiation source 12 and the detector 14 a translucent substrate 16 is positioned. For the material of the translucent substrate 16, other optically transparent substances such as polymethacrylates can be used. [0010] On the substrate 16 there is a sensitive layer 18, which reversibly changes its color when a minimum concentration of carbon monoxide is exceeded. The sensitive layer 18 includes a matrix in which there are the compounds responsible for the sensitivity of the sensor. In a preferred embodiment of the sensitive layer 18, this matrix is made of a hydrogel, but other polymers are also suitable, such as PVC and ethylcellulose. The use of hydrogel as matrix simplifies the production of the sensitive layer, since the substances further provided in the sensitive layer are predominantly water soluble metal salts, and, because of the water content of the hydrogel, they distribute themselves in it very homogeneously in dissolved form. [0011] Beyond that, the sensitive layer 18 demonstrates a very good response to carbon monoxide when a hydrogel is used as matrix, since the diffusion constant and the solubility of CO in water are substantially higher than in the usual polymers. [0012] In order to deliver the carbon monoxide present in the air as rapidly as possible, and in sufficient quantity to the sensitive layer 18, the latter preferably contains a transition metal compound which reversibly forms so-called carbonyl complexes with carbon monoxide, rapidly and with high yield. Suitable for this are compounds of the transition metals manganese, rhenium or iron (II), as well as the halides of rhodium, iridium and copper (I). The use of copper(I) chloride is especially preferred. [0013] Besides a transition metal compound for the improved take-up of carbon monoxide into the sensitive layer 18, the latter contains further substances used for detecting the carbon monoxide content of the air. These may be divided into three groups. Specifically, these are palladium salts as redox catalysts, molybdenum compounds as redox indicators, whose color change indicates the presence of carbon monoxide, and copper(II) compounds to guarantee the reversibility of the color change. [0014] In general, as the palladium salts, all water soluble salts of bivalent palladium can be used which are able to catalyze the reaction from CO to CO2 This applies above all to palladium halides. During the oxidation of carbon monoxide to carbon dioxide the bivalent palladium goes over into an oxidation state of 0. [0015] Palladium in oxidation state 0 is in a position to reduce a molybdenum(VI) compound which is also contained in the sensitive layer. As molybdenum compound, for example, molybdoorthosilicic acid, H4[Si(Mo3O10)4]*xH2O is used. In this process, the molybdenum goes over into oxidation state +III, and the compound shows a color change from yellow to blue. This is detected by an absorption or transmission measurement in the wavelength range from 500 to 1100 nm. [0016] To guarantee the reversibility of the color change, the sensitive layer 18 also contains a copper(II) compound, such as copper sulfate or a copper(II) halide. The molybdenum(III) compounds formed during the color reaction are returned to the hexavalent state by the Cu2+. [0017] The Cu+ thus formed is reoxidized to Cu2+ by such as the oxygen in the air. The backward reaction of the color change as well as the regeneration of the copper(II) compound take longer than the reactions leading to the color change. That is why the color change of the molybdenum compound is detectable at all. [0018] In order to make the gas permeability of the sensitive layer 18 as great as possible, a softening agent is also added to the layer. As softening agent, bis-(2-ethylhexyl)sebacate is preferably used. [0019] During the production of the optical sensor, a solution of the metal salts, the hydrogel or polymers, and the softening agent in water or tetrahydrofuran are applied and dried. Films are produced thereby, which advantageously have a thickness of 10 to 20 &mgr;m. [0020] The present invention is not limited to the exemplary embodiment described, but rather, in addition to the optical sensor for determining carbon monoxide, further applications can be imagined, in which a transition metal compound is used to form complexes for the improvement of the sensitivity of a gas sensor. This would apply, for instance, to the detection of hydrogen cyanide gas.
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