JPS6366072B2 - - Google Patents
Info
- Publication number
- JPS6366072B2 JPS6366072B2 JP58109415A JP10941583A JPS6366072B2 JP S6366072 B2 JPS6366072 B2 JP S6366072B2 JP 58109415 A JP58109415 A JP 58109415A JP 10941583 A JP10941583 A JP 10941583A JP S6366072 B2 JPS6366072 B2 JP S6366072B2
- Authority
- JP
- Japan
- Prior art keywords
- solar cell
- eva
- cells
- filler
- temperature
- 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.)
- Expired
Links
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
- B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
- B32B17/10—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
- B32B17/10005—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
- B32B17/1055—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer
- B32B17/10788—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the resin layer, i.e. interlayer containing ethylene vinylacetate
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B15/00—Layered products comprising a layer of metal
- B32B15/20—Layered products comprising a layer of metal comprising aluminium or copper
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B17/00—Layered products essentially comprising sheet glass, or glass, slag, or like fibres
- B32B17/06—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material
- B32B17/10—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin
- B32B17/10005—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing
- B32B17/10009—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the number, the constitution or treatment of glass sheets
- B32B17/10018—Layered products essentially comprising sheet glass, or glass, slag, or like fibres comprising glass as the main or only constituent of a layer, next to another layer of a specific material of synthetic resin laminated safety glass or glazing characterized by the number, the constitution or treatment of glass sheets comprising only one glass sheet
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F19/00—Integrated devices, or assemblies of multiple devices, comprising at least one photovoltaic cell covered by group H10F10/00, e.g. photovoltaic modules
- H10F19/80—Encapsulations or containers for integrated devices, or assemblies of multiple devices, having photovoltaic cells
-
- H—ELECTRICITY
- H10—SEMICONDUCTOR DEVICES; ELECTRIC SOLID-STATE DEVICES NOT OTHERWISE PROVIDED FOR
- H10F—INORGANIC SEMICONDUCTOR DEVICES SENSITIVE TO INFRARED RADIATION, LIGHT, ELECTROMAGNETIC RADIATION OF SHORTER WAVELENGTH OR CORPUSCULAR RADIATION
- H10F19/00—Integrated devices, or assemblies of multiple devices, comprising at least one photovoltaic cell covered by group H10F10/00, e.g. photovoltaic modules
- H10F19/80—Encapsulations or containers for integrated devices, or assemblies of multiple devices, having photovoltaic cells
- H10F19/85—Protective back sheets
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B32—LAYERED PRODUCTS
- B32B—LAYERED PRODUCTS, i.e. PRODUCTS BUILT-UP OF STRATA OF FLAT OR NON-FLAT, e.g. CELLULAR OR HONEYCOMB, FORM
- B32B2327/00—Polyvinylhalogenides
- B32B2327/12—Polyvinylhalogenides containing fluorine
-
- 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
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02E—REDUCTION OF GREENHOUSE GAS [GHG] EMISSIONS, RELATED TO ENERGY GENERATION, TRANSMISSION OR DISTRIBUTION
- Y02E10/00—Energy generation through renewable energy sources
- Y02E10/50—Photovoltaic [PV] energy
Landscapes
- Photovoltaic Devices (AREA)
Description
〔発明の技術分野〕
本発明は太陽電池パネルに関するものである。
〔発明の技術的背景〕
太陽電池パネルの一例として低コスト、高信頼
性を目標としたスーパーストレート型太陽電池パ
ネルの一例を第1図及び第2図により説明する。
即ち、透明カバー・ガラス1がパネル全体の構
造的支持体となつており、このカバー・ガラス1
の片面には、内部に直列に接続された太陽電池セ
ル3より成るストリングが埋め込まれた充填材2
が接着されている。この充填材2としては、通常
ポリ・ビニル・プチラール(以下PVBと云う)
が多く用いられて来た。充填材2の裏面には、裏
面材料4が接着されている。この裏面材料4とし
ては第2図に示すように中間にサンドイツチされ
た金属箔例えばアルミニウム箔6及び両側のポ
リ・ビニル・フロライド(以下PVFと云う)の
三層構造より成る。このアルミニウム箔6は外部
からの水蒸気の透過を防ぐためのものである。こ
の太陽電池パネルの周辺部は第1図に示すように
絶縁材7を介してアルマイト処理を施したアルミ
ニウム枠8に固定されている。この絶縁材7とし
ては、長期の信頼性を保持し、しかも低コストな
材料としてブチルゴムが用いられる。
然るに、近年、太陽電池パネルの低コスト化及
び高信頼性を促進させるために充填材2として
PVBに代つてエチレン・ビニル・アセテート
(以下EVAと云う)が開発されている。
即ち、EVAはPVBと比較すると次のような利
点があるからである。
(1) 材料費がEVAの方が安く現在PVBの約2/3
の値段である。
(2) 材料のプロセツシングの場合にもEVAの方
が簡単である。
即ちPVBはPVB自身の接着を防止するため
通常表面に重そうを塗布してロール状に巻いて
ある。そのため太陽電池パネルの組立て工程に
用いる場合には水洗処理後、約1日の調湿処理
を施さなければならない。これに対し、EVA
は水洗工程を省略でき、調湿処理もPVBほど
厳しくない。
(3) EVAによる貼合せは、架橋反応を経て形成
されるため、耐熱性、信頼性に優れている。一
方PVBは架橋反応を用いない原理により貼合
されるため温度に対する軟化性は可逆的であ
り、高温で軟化する。
また、太陽電池パネルの信頼性試験項目につい
ては、JPL(Jet Propulsion Laboratory)等か
ら提案されており、日本でも標準化されつつある
が、その試験項目は、例えば−40℃〜80℃、RH
(相対湿度)90%以上の雰囲気下での温湿度サイ
クル試験;80℃、RH90%以上での高温高湿試
験;−40℃での低温試験;−40℃〜80℃での温度
衝撃試験;5%塩水下での塩水霧試験などであ
り、その目的は約20年間と言われる太陽電池パネ
ルの寿命を保証することである。このような試験
項目を合格する高信頼性の太陽電池パネルを得る
ためにEVAを用いて貼合せを行なうには通常行
なわれている、ゴム袋を用いた一重の真空排気方
式とは異なり、第3図に示す如く二重真空方式を
用いる必要がある。
即ち、第1の室11及び第2の室12の周囲は
例えば剛体により囲まれ、ダイヤフラム(隔膜)
13により分離されており、それぞれバルブV
1,V2を経て図示しない真空ポンプへと通じて
いる。
この第2の室12に入れられる太陽電池セルを
含む斜線で示す積層体14は通常、第4図に示す
ように構成されている。
即ち、強化処理を施した白板ガラスなどからな
る透明カバー・ガラス1,EVA21、太陽電池
セル3から成るストリング、EVA22裏面材料
4がこの順または逆の順に積層されている。
そして太陽電池パネルを製造する場合の貼合せ
工程は例えば次の如くである。即ち第1の室1
1、第2の室12を真空に排気し、積層体14を
EVA21及び22が溶融状態で、しかも架橋反
応を起さない温度領域例えば約120℃で加熱する。
次いで第2の室12を真空に保つたまま、第1の
室11を大気圧に戻す。するとダイヤフラム13
を介して積層体14は真中で大気圧により圧着さ
れる。次にEVAが架橋反応を起こす温度領域迄
加熱する。この温度は約150℃である。この温度
で架橋反応が終了する迄保持し、次いで冷却後、
積層体14を取り出す。以上の工程により第1図
の一部に示すようなEVAの充填材2を用いた太
陽電池パネルが形成され、貼合せ工程が終了す
る。
〔背景技術の問題点〕
しかし、上述の材料の構成の積層体を用いる
と、EVAが溶融状態の真空下で加圧されるため、
太陽電池セルの移動が発生する。即ち、所望の位
置にセル3を半田付により固定セツトしても貼合
せ後は例えば第5図の如く中央の2列のセル3が
接触し両側の列セル3は外側へ移動する現象が生
じる。そして甚しい場合にはガラス板1の外側へ
出てしまうセル3もある。この外側への移動を防
止するには、積層体14の周辺をテーピングする
ことが考えられるがこの場合には第6図に示すよ
うに各列のセル3が中央へ移動し、セル3同志が
接触するという現象が生じる。そしてセル3同志
で接触すると、外観的な問題ばかりでなく、太陽
電池として所望の起電力が得られない短絡現象が
生じる。
更に、移動によるセル3間の接触を防ぐため、
第7図に示す如くセル3の裏面側において、セル
3間を電気的に接続するリボンリード25の他に
横方向の隣接セル間の距離を一定に保つため剛体
よりなる絶縁体のブリツジ26を接着剤を介して
セル3に固定することが考えられる。しかしブリ
ツジ26の数が多いこと、接着作業があることに
より、工程が煩雑になり更にセル3間の接触は防
止出来ても貼合せ工程後ストリング全体が移動す
るという問題点がある。即ち、カバー・ガラス端
面付近迄セル3が移動するとか、ガラス板の外側
へ出てしまうという現象である。
〔発明の目的〕
本発明は上述の問題点に鑑みなされたものであ
り充填材としてEVAを用いた場合にもセルの移
動が起らない低コスト、高信頼性の太陽電池パネ
ルを提供することを目的としている。
〔発明の概要〕
本発明は透明カバーガラスと、この透明カバー
ガラスの一面に接着され、内部に直列しまたは並
列に接続される複数個の太陽電池セルよりなるス
トリングを含有する充填材と、この充填材の裏面
に設けられる裏面材料とを有する太陽電池パネル
に於てガラス繊維群を少くとも充填材中のストリ
ングの直下または直下に設けたことを特徴とする
太陽電池パネルであり、ガラス繊維群が主に長さ
100mm以上のガラス繊維からなること、ガラス繊
維群がマツト状に形成されていること、充填材が
エチレン・ビニルアセテートであることを実施態
様としている。
〔発明の実施例〕
次に第8図により本発明の太陽電池パネルの実
施例を説明する。図中従来例と同一符号は同一部
分を示す。
即ち、全体の構造的支持体となる肉厚3mmの強
化ガラスからなる透明カバーガラス1の片面には
肉厚0.8mmのEVAシートからなる充填材21太陽
電池セル3を直列または並列に接続したストリン
グ、例えば日本板硝子(株)製商品名マイクログラス
CFG―24(肉厚0.20mm)長ガラス繊維のマツトを
2枚重ねたガラス繊維群31、肉厚0.8mmのEVA
シートからなる充填材22肉厚20μmのアルミニ
ウム箔が中間にサンドイツチされ両側に肉厚
25μmのPVFを有するシートからなる裏面材料4
を積層体14とする。この場合実際の製造工程で
は透明カバー・ガラス1上に順に乗せる。即ち第
8図とは上下反対となる。
ところで従来ガラス繊維を太陽電池パネルに使
用した例としては本発明のセルの移動を防止する
というものとは別の観点により、U.S.
Department of EnergyのAnnual Report,
“Investigation of Test Methods,Materials
Properties and Process for Solar Cell
Encapsulations”(June 1979)のpage10―1,
および“Final Report on the Investigation of
Proposed Process Sequence for the Array
Automated Assembly Task(Aug・1980)の
page233によつて知られている。そしてこれらの
主要な目的は
a 太陽電池セルとカバーガラスとの距離を固定
し応力を緩和する。
b セルと裏面材料間の絶縁抵抗を維持する。
c 真空排気の際の空気の通路となる。
である。そしてこれら文献での結論として
“Craneglass230”が最も良く、Crane and
Companyにより製造されているとしている。
このCraneglass230は長さ数10mm以下の短ガラ
ス繊維を主成分としてバインダを10%以上用いて
固めたガラス不織布であつて、本発明に使用され
るバインダの成分が数%程度以下であり、長さが
例えば2mの連続繊維からなる長ガラス繊維のも
のとは明確に区別される。
特にマイクログラスCFG―24では、長さ約2m、
太さ10μmの長ガラス繊維群が約120度の角度で交
差しているのに対し、Craneglass230は、長さ数
10mm以下の短ガラス繊維がランダムに和紙のよう
に固められているものである。
本実施例ではマイクログラスCFG―24と共に
Craneglass230(肉厚0.005インチ)も第8図の3
1として用いた同様の実験を行なつた。
第8図に示すようにセツトした積層体14は従
来と同様に第3図に示す二重真空方式の貼合せ装
置によつて貼合せる。
貼合せ工程での典型的なスケジユールを第9図
に示す。即ち先ず予備的な真空排気を例えば10分
間行なう。これにより加熱前での真空度は例えば
0.05Torr程度になる。次に加熱を開始する。昇
温勾配は例えば4℃/minである。EVAが溶融
する温度は約85℃であり、架橋反応が開始するの
は130℃である。積層体14の温度が120℃に到達
した時、第1の室11を大気圧に戻し積層体14
を真空中で圧着する。次いで150℃に到達するま
で温度上昇し、150℃に到達した後、架橋反応を
充分に行なわせるために例えば20分間保持する。
次いで冷却し積層体14の温度が例えば50℃以下
に冷却された後、第2の室12を大気圧に戻す。
この場合マイクログラスCFG―24及び
Crameglass230は、太陽電池セル3の移動を抑え
ると共にEVAとも良くなじみ気泡の欠陥も生ぜ
ずにストリングが貼合される。
以上により貼合め工程が終了するが、さらに太
陽電池パネルとして完成させるためには第1図に
示すようにアルミニウム枠8と絶縁材7として例
えばブチル・ゴムを介して枠組みを行ない終了す
る。
マイクログラスCFG―24及びCraneglass230を
用いた太陽電池パネルの信頼性試験として高温高
湿試験を行ない比較した結果を第1表に示す。
条件は80℃、RH90%であり、時間は500時間
迄行なつた。
[Technical Field of the Invention] The present invention relates to solar cell panels. [Technical Background of the Invention] As an example of a solar cell panel, an example of a superstrate type solar cell panel aiming at low cost and high reliability will be explained with reference to FIGS. 1 and 2. That is, the transparent cover glass 1 serves as a structural support for the entire panel;
One side of the filling material 2 has a string of solar cells 3 connected in series embedded therein.
is glued. This filler 2 is usually polyvinyl petitral (hereinafter referred to as PVB).
has been used a lot. A back material 4 is adhered to the back surface of the filler 2. As shown in FIG. 2, the back surface material 4 has a three-layer structure consisting of a sandwiched metal foil, such as an aluminum foil 6, in the middle and polyvinyl fluoride (hereinafter referred to as PVF) on both sides. This aluminum foil 6 is for preventing water vapor from permeating from the outside. As shown in FIG. 1, the periphery of this solar cell panel is fixed to an alumite-treated aluminum frame 8 via an insulating material 7. As the insulating material 7, butyl rubber is used as a material that maintains long-term reliability and is low in cost. However, in recent years, in order to promote cost reduction and high reliability of solar cell panels, it has been used as filler 2.
Ethylene vinyl acetate (hereinafter referred to as EVA) has been developed to replace PVB. That is, EVA has the following advantages when compared to PVB. (1) The material cost of EVA is lower and is currently about two-thirds the price of PVB. (2) EVA is also easier when processing materials. That is, PVB is usually rolled into a roll with a heavy coating applied to its surface to prevent the PVB from adhering itself. Therefore, when used in the process of assembling solar cell panels, it is necessary to perform humidity conditioning treatment for about one day after washing with water. In contrast, EVA
The washing process can be omitted, and the humidity control process is not as strict as with PVB. (3) Since EVA lamination is formed through a crosslinking reaction, it has excellent heat resistance and reliability. On the other hand, PVB is laminated using a principle that does not involve cross-linking reactions, so its softening properties with respect to temperature are reversible, and it softens at high temperatures. In addition, reliability test items for solar cell panels have been proposed by JPL (Jet Propulsion Laboratory) and others, and are being standardized in Japan.
(Relative humidity) Temperature/humidity cycle test in an atmosphere of 90% or higher; High temperature/humidity test at 80°C, RH90% or higher; Low temperature test at -40°C; Temperature shock test at -40°C to 80°C; These include salt fog tests under 5% salt water, and the purpose is to guarantee the lifespan of solar panels, which is said to be approximately 20 years. In order to obtain highly reliable solar panels that pass these test items, lamination using EVA requires a first vacuum pumping method, unlike the usual single vacuum pumping method using a rubber bag. It is necessary to use a double vacuum system as shown in Figure 3. That is, the first chamber 11 and the second chamber 12 are surrounded by, for example, a rigid body, and a diaphragm (diaphragm)
13, each with a valve V
1, and connects to a vacuum pump (not shown) via V2. A stacked body 14 shown by diagonal lines and containing solar cells placed in this second chamber 12 is normally constructed as shown in FIG. 4. That is, a transparent cover glass 1 made of tempered white glass or the like, an EVA 21, a string made of solar cells 3, and a back material 4 of the EVA 22 are laminated in this order or in the reverse order. The bonding process for manufacturing a solar cell panel is, for example, as follows. That is, the first chamber 1
1. Evacuate the second chamber 12 and remove the laminate 14.
EVA 21 and 22 are heated in a molten state at a temperature range at which no crosslinking reaction occurs, for example, at about 120°C.
Next, the first chamber 11 is returned to atmospheric pressure while the second chamber 12 is kept in vacuum. Then diaphragm 13
The laminate 14 is compressed at the center by atmospheric pressure. Next, the EVA is heated to a temperature range where a crosslinking reaction occurs. This temperature is approximately 150°C. Maintain at this temperature until the crosslinking reaction is completed, then cool,
The laminate 14 is taken out. Through the above steps, a solar cell panel using the EVA filler 2 as shown in a part of FIG. 1 is formed, and the bonding step is completed. [Problems with the background art] However, when using a laminate with the above-mentioned material structure, EVA is pressurized in a vacuum while it is in a molten state.
Movement of solar cells occurs. That is, even if the cells 3 are fixedly set in a desired position by soldering, after bonding, for example, as shown in FIG. 5, the two rows of cells 3 in the center come into contact with each other, and the cells 3 on both sides move outward. . In severe cases, some cells 3 may even come out to the outside of the glass plate 1. To prevent this outward movement, it is possible to tape the periphery of the laminate 14, but in this case, as shown in FIG. 6, the cells 3 in each column will move to the center and the cells 3 will A phenomenon of contact occurs. If the cells 3 come into contact with each other, not only will there be problems in appearance, but also a short circuit phenomenon will occur in which the desired electromotive force cannot be obtained as a solar cell. Furthermore, in order to prevent contact between the cells 3 due to movement,
As shown in FIG. 7, on the back side of the cells 3, in addition to the ribbon leads 25 that electrically connect the cells 3, insulating bridges 26 made of a rigid body are installed to maintain a constant distance between adjacent cells in the horizontal direction. It is conceivable to fix it to the cell 3 via an adhesive. However, the large number of bridges 26 and the adhesion work make the process complicated, and even if contact between the cells 3 can be prevented, there is a problem that the entire string moves after the bonding process. That is, this is a phenomenon in which the cells 3 move to the vicinity of the end face of the cover glass or come out to the outside of the glass plate. [Object of the Invention] The present invention was made in view of the above-mentioned problems, and it is an object of the present invention to provide a low-cost, highly reliable solar cell panel in which cell movement does not occur even when EVA is used as a filler. It is an object. [Summary of the Invention] The present invention comprises a transparent cover glass, a filler containing a string consisting of a plurality of solar cells bonded to one side of the transparent cover glass and connected in series or parallel therein; A solar cell panel having a back surface material provided on the back surface of the filler, in which a group of glass fibers is provided at least directly below or immediately below the strings in the filler, the group of glass fibers is mainly the length
In an embodiment, it is made of glass fibers of 100 mm or more, the glass fiber group is formed into a mat shape, and the filler is ethylene vinyl acetate. [Embodiment of the Invention] Next, an embodiment of the solar cell panel of the present invention will be described with reference to FIG. In the figure, the same reference numerals as in the conventional example indicate the same parts. That is, on one side of a transparent cover glass 1 made of tempered glass with a thickness of 3 mm, which serves as the overall structural support, a string in which a filler 21 made of an EVA sheet with a thickness of 0.8 mm and solar cells 3 are connected in series or in parallel is attached. For example, the product name Microglass manufactured by Nippon Sheet Glass Co., Ltd.
CFG-24 (wall thickness 0.20mm) Glass fiber group 31 made by stacking two long glass fiber mats, EVA with wall thickness 0.8mm
Filler material 22 consisting of a sheet Aluminum foil with a wall thickness of 20 μm is sandwiched in the middle and thick walls are placed on both sides.
Back material 4 consisting of a sheet with 25 μm PVF
is the laminate 14. In this case, in the actual manufacturing process, they are placed on the transparent cover glass 1 in order. In other words, it is upside down from FIG. By the way, as an example of conventional use of glass fiber in solar cell panels, the US
Department of Energy Annual Report,
“Investigation of Test Methods, Materials
Properties and Process for Solar Cell
Encapsulations” (June 1979) page 10-1,
and “Final Report on the Investigation of
Proposed Process Sequence for the Array
Automated Assembly Task (Aug・1980)
Known by page233. The main purpose of these is a. To fix the distance between the solar cell and the cover glass and relieve stress. b Maintain insulation resistance between the cell and backside material. c Serves as an air passage during evacuation. It is. The conclusion from these documents is that “Craneglass 230” is the best, and Crane and
It is said to be manufactured by Company. This Craneglass 230 is a glass nonwoven fabric made of short glass fibers with a length of several tens of mm or less as a main component and hardened with a binder of 10% or more. It is clearly distinguished from, for example, long glass fibers consisting of 2m continuous fibers. Especially for micro glass CFG-24, the length is about 2m,
Whereas groups of long glass fibers with a thickness of 10 μm intersect at an angle of approximately 120 degrees, Craneglass 230 has a
It is made of short glass fibers of 10mm or less that are randomly packed together like Japanese paper. In this example, together with Microglass CFG-24
Craneglass230 (wall thickness 0.005 inch) is also 3 in Figure 8.
A similar experiment was conducted using the same method as No. 1. The laminate 14 set as shown in FIG. 8 is pasted together using a double vacuum type pasting apparatus shown in FIG. 3 in the same manner as in the prior art. A typical schedule in the bonding process is shown in FIG. That is, first, preliminary evacuation is performed for 10 minutes, for example. This allows the degree of vacuum before heating to be, for example,
It will be about 0.05Torr. Next, start heating. The temperature increase gradient is, for example, 4° C./min. The temperature at which EVA melts is approximately 85°C, and the crosslinking reaction begins at 130°C. When the temperature of the laminate 14 reaches 120°C, the first chamber 11 is returned to atmospheric pressure and the laminate 14
Crimp in vacuum. Next, the temperature is increased until it reaches 150°C, and after reaching 150°C, it is held for 20 minutes, for example, to allow the crosslinking reaction to occur sufficiently.
Next, after cooling the laminate 14 to a temperature of, for example, 50° C. or lower, the second chamber 12 is returned to atmospheric pressure.
In this case, microglass CFG-24 and
Crameglass 230 suppresses the movement of the solar cell 3 and is also compatible with EVA, allowing the string to be bonded without causing bubble defects. The bonding process is completed as described above, but in order to complete the solar cell panel, as shown in FIG. 1, a frame is formed using an aluminum frame 8 and an insulating material 7, for example, butyl rubber. Table 1 shows the results of a high temperature and high humidity test conducted as a reliability test for solar cell panels using Microglass CFG-24 and Craneglass 230. The conditions were 80°C and RH90%, and the test was carried out for up to 500 hours.
【表】
即ちマイクログラスを用いた場合には高温高湿
試験において良好であるのに対し、
Craneglass230を用いた場合にはCraneglassの変
色現象が168hr経過後に起きた。
次にマイクログラスCFG―24及び
Craneglass230を用いた場合の信頼性試験にかけ
る前の初期外観試験として貼合せ時の最高温度と
外観との関係を第2表に示す。なお最高温度の保
持時間は20分とした。[Table] In other words, when microglass is used, it performs well in high temperature and high humidity tests, whereas
When Craneglass 230 was used, discoloration of Craneglass occurred after 168 hours. Next, microglass CFG-24 and
Table 2 shows the relationship between the maximum temperature during lamination and the appearance as an initial appearance test before conducting the reliability test when Craneglass 230 is used. The maximum temperature was maintained for 20 minutes.
【表】
即ち、マイクログラスを用いた場合には、145
℃〜160℃の温度範囲にわたつて外観良好である
のに対し、Craneglassを用いた場合には約155℃
でCraneglassの変色が開始する。
次にマイクログラスCFG―24及び
Craneglass230自身の大気中での焼成実験、即
ち、焼成温度と外観との関係を第3表に示す。但
し保持時間は30分である。[Table] In other words, when using microglass, 145
Appearance is good over a temperature range of ℃ to 160℃, whereas when Craneglass is used, the temperature is about 155℃
Craneglass begins to discolor. Next, microglass CFG-24 and
Table 3 shows the firing experiment of Craneglass 230 itself in the atmosphere, that is, the relationship between firing temperature and appearance. However, the holding time is 30 minutes.
上述のように本発明によれば充填材として安価
なEVAを用いた場合にもセルの移動が起らない
低コスト、高品位、高信頼性の太陽電池パネルが
提供できる。
As described above, according to the present invention, it is possible to provide a low-cost, high-quality, highly reliable solar cell panel in which cell movement does not occur even when inexpensive EVA is used as a filler.
第1図は太陽電池パネルの断面図、第2図は裏
面材料の概略断面図、第3図は二重真空方式の貼
合せ装置の概略説明図、第4図は従来の太陽電池
パネルの積層体を示す断面図、第5図及び第6図
は太陽電池パネルの製造工程中に発生するそれぞ
れ異なるセルの配列の不具合を示す説明図、第7
図はセルの配列の不具合をなくす構造の一例を示
す裏面図、第8図は本発明の太陽電池パネルの一
実施例の積層体を示す断面図、第9図は貼合せ工
程の典型的なスケジユール図、第10図は
Craneglassを使用した時のセルの配列を示す説
明図、第11図はマイクログラスを使用した時の
セルの配列を示す説明図である。
1…カバーガラス、2,21,22…充填材、
3…太陽電池セル、4…裏面材料、11…第1の
室、12…第2の室、13…ダイヤフラム、14
…積層体、26…ブリツジ、31…長ガラス繊維
群。
Figure 1 is a cross-sectional view of the solar panel, Figure 2 is a schematic cross-sectional view of the back material, Figure 3 is a schematic illustration of a double vacuum laminating device, and Figure 4 is a conventional lamination of solar panels. 5 and 6 are explanatory diagrams illustrating defects in the arrangement of different cells that occur during the manufacturing process of solar cell panels, and Figure 7 is a cross-sectional view showing the body.
The figure is a back view showing an example of a structure that eliminates defects in cell arrangement, Figure 8 is a sectional view showing a laminate of an embodiment of the solar cell panel of the present invention, and Figure 9 is a typical lamination process. Schedule diagram, Figure 10 is
FIG. 11 is an explanatory diagram showing the cell arrangement when using Craneglass, and FIG. 11 is an explanatory diagram showing the cell arrangement when using microglass. 1... Cover glass, 2, 21, 22... Filler,
3... Solar cell, 4... Back material, 11... First chamber, 12... Second chamber, 13... Diaphragm, 14
... Laminate, 26... Bridge, 31... Long glass fiber group.
Claims (1)
配置され、内部に直列または並列に接続された複
数個の太陽電池セルよりなるストリングを含み、
エチレン・ビニル・アセテートよりなる充填材と
を有する太陽電池パネルにおいて、少なくとも前
記充填材料中の前記ストリングの直下あるいは直
上に、主に長さ100mm以上の長ガラス繊維からな
るガラス繊維群を設けたことを特徴とする太陽電
池パネル。1. A cover glass, a backing material, and a string consisting of a plurality of solar cells arranged in between and connected in series or in parallel,
In a solar cell panel having a filler made of ethylene vinyl acetate, a group of glass fibers mainly made of long glass fibers with a length of 100 mm or more is provided at least immediately below or directly above the string in the filler material. A solar panel featuring:
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58109415A JPS601875A (en) | 1983-06-20 | 1983-06-20 | Solar battery panel |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| JP58109415A JPS601875A (en) | 1983-06-20 | 1983-06-20 | Solar battery panel |
Publications (2)
| Publication Number | Publication Date |
|---|---|
| JPS601875A JPS601875A (en) | 1985-01-08 |
| JPS6366072B2 true JPS6366072B2 (en) | 1988-12-19 |
Family
ID=14509664
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| JP58109415A Granted JPS601875A (en) | 1983-06-20 | 1983-06-20 | Solar battery panel |
Country Status (1)
| Country | Link |
|---|---|
| JP (1) | JPS601875A (en) |
Cited By (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104380482A (en) * | 2012-06-22 | 2015-02-25 | 松下知识产权经营株式会社 | Solar cell module |
Families Citing this family (13)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6095959A (en) * | 1983-10-31 | 1985-05-29 | Nippon Sheet Glass Co Ltd | Solar panel and its manufacturing method |
| JPS61251176A (en) * | 1985-04-30 | 1986-11-08 | Toppan Printing Co Ltd | Protective sheet for reverse side surface of solar cel |
| JPS63143879A (en) * | 1986-12-08 | 1988-06-16 | Hitachi Ltd | solar cell device |
| JPH04124237U (en) * | 1991-04-22 | 1992-11-12 | 株式会社ニコン | Camera capable of long exposure photography |
| DE4301404C1 (en) * | 1993-01-20 | 1994-07-28 | Michael C Lenz | Process for the production of solar generators |
| US5480494A (en) * | 1993-05-18 | 1996-01-02 | Canon Kabushiki Kaisha | Solar cell module and installation method thereof |
| JP3170105B2 (en) * | 1993-07-01 | 2001-05-28 | キヤノン株式会社 | Solar cell module |
| JP2719114B2 (en) * | 1994-04-25 | 1998-02-25 | キヤノン株式会社 | Solar cell module |
| US5474620A (en) * | 1994-05-16 | 1995-12-12 | United Solar Systems Corporation | Cut resistant laminate for the light incident surface of a photovoltaic module |
| EP0769818A3 (en) | 1995-10-17 | 1998-10-28 | Canon Kabushiki Kaisha | Solar cell module having a surface side covering material with a specific nonwoven glass fiber member |
| JP4086713B2 (en) * | 2002-05-27 | 2008-05-14 | 日東電工株式会社 | Liquid crystal cell substrate |
| WO2003099912A1 (en) | 2002-05-27 | 2003-12-04 | Nitto Denko Corporation | Resin sheet and liquid-crystal cell substrate comprising the same |
| JP4597150B2 (en) * | 2007-02-01 | 2010-12-15 | 三洋電機株式会社 | Solar cell module and manufacturing method thereof |
Family Cites Families (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| JPS6112694Y2 (en) * | 1980-05-23 | 1986-04-19 |
-
1983
- 1983-06-20 JP JP58109415A patent/JPS601875A/en active Granted
Cited By (2)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| CN104380482A (en) * | 2012-06-22 | 2015-02-25 | 松下知识产权经营株式会社 | Solar cell module |
| CN104380482B (en) * | 2012-06-22 | 2017-04-12 | 松下知识产权经营株式会社 | Solar cell module |
Also Published As
| Publication number | Publication date |
|---|---|
| JPS601875A (en) | 1985-01-08 |
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