JPH0523331Y2 - - Google Patents
Info
- Publication number
- JPH0523331Y2 JPH0523331Y2 JP1987144076U JP14407687U JPH0523331Y2 JP H0523331 Y2 JPH0523331 Y2 JP H0523331Y2 JP 1987144076 U JP1987144076 U JP 1987144076U JP 14407687 U JP14407687 U JP 14407687U JP H0523331 Y2 JPH0523331 Y2 JP H0523331Y2
- Authority
- JP
- Japan
- Prior art keywords
- net
- thermoplastic resin
- light
- reflective metal
- metal layer
- 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 - Lifetime
Links
- 239000000835 fiber Substances 0.000 claims description 20
- 229910052751 metal Inorganic materials 0.000 claims description 15
- 239000002184 metal Substances 0.000 claims description 15
- 229920005992 thermoplastic resin Polymers 0.000 claims description 15
- -1 polyethylene Polymers 0.000 claims description 10
- XAGFODPZIPBFFR-UHFFFAOYSA-N aluminium Chemical group [Al] XAGFODPZIPBFFR-UHFFFAOYSA-N 0.000 claims description 5
- 238000010030 laminating Methods 0.000 claims description 5
- 239000004743 Polypropylene Substances 0.000 claims description 4
- 229910052782 aluminium Inorganic materials 0.000 claims description 4
- 229920001155 polypropylene Polymers 0.000 claims description 4
- 239000004698 Polyethylene Substances 0.000 claims description 3
- 229920000573 polyethylene Polymers 0.000 claims description 3
- 239000010410 layer Substances 0.000 description 18
- 239000000463 material Substances 0.000 description 9
- 238000000034 method Methods 0.000 description 7
- 229920003002 synthetic resin Polymers 0.000 description 6
- 239000000057 synthetic resin Substances 0.000 description 6
- 241000196324 Embryophyta Species 0.000 description 4
- 238000000151 deposition Methods 0.000 description 3
- 230000008021 deposition Effects 0.000 description 3
- 230000000694 effects Effects 0.000 description 3
- 229920000098 polyolefin Polymers 0.000 description 3
- 238000009423 ventilation Methods 0.000 description 3
- CURLTUGMZLYLDI-UHFFFAOYSA-N Carbon dioxide Chemical compound O=C=O CURLTUGMZLYLDI-UHFFFAOYSA-N 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N Diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- ATUOYWHBWRKTHZ-UHFFFAOYSA-N Propane Chemical compound CCC ATUOYWHBWRKTHZ-UHFFFAOYSA-N 0.000 description 2
- 239000006096 absorbing agent Substances 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 206010061592 cardiac fibrillation Diseases 0.000 description 2
- 230000002600 fibrillogenic effect Effects 0.000 description 2
- 229920001903 high density polyethylene Polymers 0.000 description 2
- 239000004700 high-density polyethylene Substances 0.000 description 2
- QUAMTGJKVDWJEQ-UHFFFAOYSA-N octabenzone Chemical compound OC1=CC(OCCCCCCCC)=CC=C1C(=O)C1=CC=CC=C1 QUAMTGJKVDWJEQ-UHFFFAOYSA-N 0.000 description 2
- 238000004544 sputter deposition Methods 0.000 description 2
- 229910001220 stainless steel Inorganic materials 0.000 description 2
- 239000010935 stainless steel Substances 0.000 description 2
- 239000006097 ultraviolet radiation absorber Substances 0.000 description 2
- USVVENVKYJZFMW-ONEGZZNKSA-N (e)-carboxyiminocarbamic acid Chemical class OC(=O)\N=N\C(O)=O USVVENVKYJZFMW-ONEGZZNKSA-N 0.000 description 1
- VYZAMTAEIAYCRO-UHFFFAOYSA-N Chromium Chemical compound [Cr] VYZAMTAEIAYCRO-UHFFFAOYSA-N 0.000 description 1
- RYGMFSIKBFXOCR-UHFFFAOYSA-N Copper Chemical compound [Cu] RYGMFSIKBFXOCR-UHFFFAOYSA-N 0.000 description 1
- 240000000599 Lentinula edodes Species 0.000 description 1
- 239000004952 Polyamide Substances 0.000 description 1
- 244000269722 Thea sinensis Species 0.000 description 1
- ATJFFYVFTNAWJD-UHFFFAOYSA-N Tin Chemical compound [Sn] ATJFFYVFTNAWJD-UHFFFAOYSA-N 0.000 description 1
- HCHKCACWOHOZIP-UHFFFAOYSA-N Zinc Chemical compound [Zn] HCHKCACWOHOZIP-UHFFFAOYSA-N 0.000 description 1
- 238000010521 absorption reaction Methods 0.000 description 1
- 239000000853 adhesive Substances 0.000 description 1
- 230000001070 adhesive effect Effects 0.000 description 1
- 150000008064 anhydrides Chemical class 0.000 description 1
- 238000010009 beating Methods 0.000 description 1
- 239000012965 benzophenone Substances 0.000 description 1
- 150000008366 benzophenones Chemical class 0.000 description 1
- 230000000903 blocking effect Effects 0.000 description 1
- 229910002092 carbon dioxide Inorganic materials 0.000 description 1
- 239000001569 carbon dioxide Substances 0.000 description 1
- 229910052804 chromium Inorganic materials 0.000 description 1
- 239000011651 chromium Substances 0.000 description 1
- 239000011248 coating agent Substances 0.000 description 1
- 238000000576 coating method Methods 0.000 description 1
- 238000004040 coloring Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- 229910052802 copper Inorganic materials 0.000 description 1
- 239000010949 copper Substances 0.000 description 1
- 238000005336 cracking Methods 0.000 description 1
- 238000005520 cutting process Methods 0.000 description 1
- MCPKSFINULVDNX-UHFFFAOYSA-N drometrizole Chemical compound CC1=CC=C(O)C(N2N=C3C=CC=CC3=N2)=C1 MCPKSFINULVDNX-UHFFFAOYSA-N 0.000 description 1
- 238000000313 electron-beam-induced deposition Methods 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 238000001125 extrusion Methods 0.000 description 1
- 239000000945 filler Substances 0.000 description 1
- 239000004088 foaming agent Substances 0.000 description 1
- 230000004927 fusion Effects 0.000 description 1
- 238000010413 gardening Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000003949 imides Chemical class 0.000 description 1
- 238000001659 ion-beam spectroscopy Methods 0.000 description 1
- 238000001755 magnetron sputter deposition Methods 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 150000002739 metals Chemical class 0.000 description 1
- 238000000465 moulding Methods 0.000 description 1
- 239000002362 mulch Substances 0.000 description 1
- MZYHMUONCNKCHE-UHFFFAOYSA-N naphthalene-1,2,3,4-tetracarboxylic acid Chemical compound C1=CC=CC2=C(C(O)=O)C(C(=O)O)=C(C(O)=O)C(C(O)=O)=C21 MZYHMUONCNKCHE-UHFFFAOYSA-N 0.000 description 1
- 150000002815 nickel Chemical class 0.000 description 1
- 239000002420 orchard Substances 0.000 description 1
- 229920000620 organic polymer Polymers 0.000 description 1
- DXGLGDHPHMLXJC-UHFFFAOYSA-N oxybenzone Chemical compound OC1=CC(OC)=CC=C1C(=O)C1=CC=CC=C1 DXGLGDHPHMLXJC-UHFFFAOYSA-N 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 239000003208 petroleum Substances 0.000 description 1
- 229920002647 polyamide Polymers 0.000 description 1
- 229920000515 polycarbonate Polymers 0.000 description 1
- 239000004417 polycarbonate Substances 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 239000002861 polymer material Substances 0.000 description 1
- 239000004800 polyvinyl chloride Substances 0.000 description 1
- 229920000915 polyvinyl chloride Polymers 0.000 description 1
- 239000001294 propane Substances 0.000 description 1
- 239000011241 protective layer Substances 0.000 description 1
- 230000000630 rising effect Effects 0.000 description 1
- 229960001860 salicylate Drugs 0.000 description 1
- 229940058287 salicylic acid derivative anticestodals Drugs 0.000 description 1
- 150000003872 salicylic acid derivatives Chemical class 0.000 description 1
- 229910052709 silver Inorganic materials 0.000 description 1
- 239000004332 silver Substances 0.000 description 1
- 239000002689 soil Substances 0.000 description 1
- 229910052718 tin Inorganic materials 0.000 description 1
- 239000011135 tin Substances 0.000 description 1
- 238000001771 vacuum deposition Methods 0.000 description 1
- 238000007740 vapor deposition Methods 0.000 description 1
- 229910052725 zinc Inorganic materials 0.000 description 1
- 239000011701 zinc Substances 0.000 description 1
Classifications
-
- 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
- Y02A—TECHNOLOGIES FOR ADAPTATION TO CLIMATE CHANGE
- Y02A40/00—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production
- Y02A40/10—Adaptation technologies in agriculture, forestry, livestock or agroalimentary production in agriculture
- Y02A40/25—Greenhouse technology, e.g. cooling systems therefor
Description
【考案の詳細な説明】
〔産業上の利用分野〕
本考案は遮光ネツトに関し、特には各種農業、
園芸に用いられる優れた遮光ネツトに関する。[Detailed description of the invention] [Field of industrial application] The present invention relates to a shading net, and is particularly applicable to various types of agriculture,
This article relates to excellent shading nets used in gardening.
各種農産物や園芸作物の育成時に、植物の遮光
のために種々の植物に対して多数の場所でシー
ト、ネツト形状の遮光資材が用いられている。
2. Description of the Related Art When growing various agricultural products and horticultural crops, sheet and net-shaped shading materials are used in many places for shading the plants.
遮光資材としては、黒色等に着色された合成樹
脂糸を通気間隙を有するように比較的ラフな織物
組織に構成したもの、黒色等に着色された合成樹
脂テープを通気間隙を有するよう織成又は編成し
たものが一般的に用いられてきた。 Examples of light-shielding materials include synthetic resin threads colored black, etc., constructed into a relatively rough woven structure with ventilation gaps, and synthetic resin tapes colored black, etc., woven or woven with ventilation gaps. The organized version has been commonly used.
しかしながら、上記の様な遮光資材は着色によ
つて熱エネルギーを吸収するため、遮光と同時に
吸熱による昇温が生じ、遮光資材によつて被われ
た内部は異常な高温となつて植物の生育には不向
きな環境となりがちであつた。この問題を解決す
るために、アルミニウム粉を練り込んだ合成樹脂
テープを用いることによつて太陽光線の反射率を
高めたネツト、及びシートも提案されているが、
反射効率は十分ではなく、更に優れた遮光資材が
求められていた。
However, since the above-mentioned shading materials absorb heat energy through coloring, the temperature rises due to heat absorption at the same time as shading, and the interior covered by the shading material becomes abnormally high temperature, making it difficult for plants to grow. tended to be an unsuitable environment. To solve this problem, nets and sheets have been proposed that use synthetic resin tape mixed with aluminum powder to increase the reflectance of sunlight.
Reflection efficiency was not sufficient, and there was a need for even better light-shielding materials.
本考案者らは、上記遮光資材における問題点を
解決するために種々検討した結果、特定のネツト
上に反射金属層と更にその上に保護層を設けるこ
とによつて、太陽光線を十分に反射し、高強度を
有すると共に製造上も工程が少ない等の優れた効
果を有する遮光ネツトが得られることを知得して
本考案に到達した。
As a result of various studies to solve the problems with the above-mentioned light-shielding materials, the inventors of the present invention found that by providing a reflective metal layer on a specific net and a protective layer on top of it, the sun's rays could be reflected sufficiently. However, the present invention was developed based on the knowledge that a light-shielding net having high strength and excellent effects such as fewer manufacturing steps can be obtained.
即ち、本考案の要旨は、熱可塑性樹脂のスプリ
ツトフアイバーを積層し、繊維方向を交差させた
ネツト上に反射金属層及び熱可塑性樹脂層を順次
積層してなる遮光ネツトに存する。 That is, the gist of the present invention resides in a light-shielding net formed by laminating thermoplastic resin split fibers and sequentially laminating a reflective metal layer and a thermoplastic resin layer on the net with the fiber directions crossing each other.
以下、本考案を詳細に説明する。 The present invention will be explained in detail below.
本考案で使用するスプリツトフアイバー(割繊
維)は、合成樹脂のフイルムに、延伸方向に多数
の不連続の裂け目を設け網状としたものである。 The split fiber used in the present invention is a synthetic resin film with a large number of discontinuous fissures in the stretching direction to form a net shape.
熱可塑性樹脂としては、フイルム成形が可能な
ものであればよく例えば、ポリエチレン、ポリプ
ロピレン等のポリオレフイン、ポリエステル、ポ
リアミド、ポリカーボネート、ポリ塩化ビニル等
が挙げられる。好ましくは、ポリオレフイン、更
に好ましくは高密度ポリエチレンがよい。 The thermoplastic resin may be one that can be formed into a film, and examples thereof include polyolefins such as polyethylene and polypropylene, polyester, polyamide, polycarbonate, and polyvinyl chloride. Preferably, polyolefin is used, more preferably high-density polyethylene.
この合成樹脂は、成膜した後、一軸延伸を行い
通常、3〜100μm、好ましくは、5〜50μmの厚
さのフイルムとされる。該フイルムは、成膜及
び/又は、一軸延伸の工程においてスプリツトフ
アイバーとするため、ひび割れが生じ易い状態と
される。この状態は、フイブリル化(小繊維化)
し易い高密度ポリエチレン、ポリプロピレン等を
用いる場合は、例えば円形ダイによるインフレー
シヨン成形、Tダイ押出成形等により成膜した
後、ロール延伸等の延伸方法で一軸高倍率延伸、
例えば5〜10倍に延伸を施すことにより形成され
る。また、フイブリル化し難い合成樹脂の場合
は、成膜に際して、プロパン、石油エーテル、炭
酸ガス、ジアゾアミノ誘導体、アゾニトリル、ア
ゾジカルボン酸誘導体等の発泡剤を添加して成膜
し、得られたフイルムを一軸延伸することにより
形成される。スプリツトフアイバーは、上記フイ
ルムに叩打、捻転、切削、摩擦、空気流等周知の
方法によりひび割れを発生させ、不連続の裂け目
を形成することにより得られる。該、スプリツト
フアイバーの単繊維の大きさは、通常3〜100デ
ニール、好ましくは、5〜50デニールとされる。 After this synthetic resin is formed into a film, it is uniaxially stretched to form a film having a thickness of usually 3 to 100 μm, preferably 5 to 50 μm. Since the film is made into a split fiber during the film formation and/or uniaxial stretching process, it is in a state where cracks are likely to occur. This state is called fibrillation (fibrillation)
When using high-density polyethylene, polypropylene, etc., which are easy to process, the film is formed by, for example, inflation molding using a circular die, T-die extrusion molding, etc., and then uniaxial high-magnification stretching using a stretching method such as roll stretching.
For example, it is formed by stretching 5 to 10 times. In addition, in the case of synthetic resins that are difficult to fibrillate, foaming agents such as propane, petroleum ether, carbon dioxide, diazoamino derivatives, azonitrile, and azodicarboxylic acid derivatives are added during film formation, and the resulting film is uniaxially formed. It is formed by stretching. Split fibers can be obtained by cracking the above-mentioned film by a well-known method such as beating, twisting, cutting, friction, air flow, etc. to form discontinuous fissures. The size of the single fiber of the split fiber is usually 3 to 100 deniers, preferably 5 to 50 deniers.
次に図面を参照して本考案を説明する。第1図
は、遮光ネツトの縦断面図であり、第2図は、基
材であるスプリツトフアイバーからなるネツトの
平面図の一例である。 Next, the present invention will be explained with reference to the drawings. FIG. 1 is a longitudinal sectional view of a light-shielding net, and FIG. 2 is an example of a plan view of the net made of split fiber as a base material.
スプリツトフアイバー1と1′とは、夫々の繊
維方向が異なるように、即ち交差させた状態で積
層する。交差角5は通常、45〜135度、好ましく
は、70〜110度とされる。積層するスプリツトフ
アイバーの積層数は限定されないが、通常2〜5
層とされる。積層したスプリツトフアイバー1と
1′とは、熱融着または接着剤を用いてネツト状
に固定される。 The split fibers 1 and 1' are stacked so that their fiber directions are different, that is, in a crossed state. The intersection angle 5 is usually 45 to 135 degrees, preferably 70 to 110 degrees. The number of layers of split fibers to be laminated is not limited, but is usually 2 to 5.
It is considered to be a layer. The stacked split fibers 1 and 1' are fixed in a net shape using heat fusion or adhesive.
このようなネツトとしては、「ワリフ」(商品
名、日本石油化学(株)製)、「タフベル」(商品名、
鐘紡(株)製)等の市販品を使用することもできる。 Examples of such nets include "Warif" (product name, manufactured by Nippon Petrochemical Co., Ltd.) and "Tuffbel" (product name,
Commercially available products such as those manufactured by Kanebo Co., Ltd.) can also be used.
スプリツトフアイバーを積層してなるネツト上
に設ける反射金属層2の金属としては、アルミニ
ウム、錫、亜鉛、銅、クロム、ステンレス鋼、銀
等各種の金属が使用できる。中でも太陽光の反射
率が高く、比較的安価である、アルミニウム、ス
テンレス鋼が好ましく用いられる。 Various metals such as aluminum, tin, zinc, copper, chromium, stainless steel, and silver can be used as the metal for the reflective metal layer 2 provided on the net formed by stacking split fibers. Among them, aluminum and stainless steel are preferably used because they have a high reflectance of sunlight and are relatively inexpensive.
上記金属をネツト上に積層する方法は、公知の
蒸着法であれば特に限定されない。例えば抵抗加
熱、フラツシユ蒸着、アーク蒸着、電子ビーム蒸
着、レーザー蒸着等の真空蒸着、イオンビームス
パツタリング、マグネトロンスパツタリング等の
スパツタリング法等が挙げられる。スパツタリン
グ法は、基材であるネツトが比較的低温の状態で
蒸着されるので好ましい。 The method for laminating the metal on the net is not particularly limited as long as it is a known vapor deposition method. Examples include resistance heating, vacuum deposition such as flash deposition, arc deposition, electron beam deposition, and laser deposition, and sputtering methods such as ion beam sputtering and magnetron sputtering. The sputtering method is preferred because the base material net is deposited at a relatively low temperature.
反射金属層2の厚さは、金属の種類によつても
異なるが、アルミニウムの場合、通常100〜800
Å、好ましくは、400〜600Åとされる。 The thickness of the reflective metal layer 2 varies depending on the type of metal, but in the case of aluminum, it is usually 100 to 800 mm.
Å, preferably 400 to 600 Å.
反射金属層2の上に積層される熱可塑性樹脂層
3に用いられる熱可塑性樹脂としては耐候性を有
する樹脂であればよく、特に限定はされない。好
ましくは、ポリオレフイン、特に好ましくはポリ
エチレン、ポリプロピレンが用いられる。 The thermoplastic resin used for the thermoplastic resin layer 3 laminated on the reflective metal layer 2 is not particularly limited as long as it has weather resistance. Preferably, polyolefins are used, particularly preferably polyethylene and polypropylene.
なお、熱可塑性樹脂層3、及び前述のスプリツ
トフアイバー1,1′に用いる熱可塑性樹脂には、
常法に従い、紫外線吸収剤、充填剤等を添加する
ことができる。特に、熱可塑性樹脂層に耐候性向
上のために紫外線吸収剤を使用することが好まし
い。紫外線吸収剤は通常の有機高分子材料に使用
できるものはいずれでも良く、例えば、2−ヒド
ロキシ−4−メトキシベンゾフエノン、2−ヒド
ロキシ−4−n−オクトキシベンゾフエノン等の
ベンゾフエノン類、p−t−ブチルフエニルサリ
シレート等のサリチル酸誘導体、2−(2′−ヒド
ロキシ−5′−メチルフエニル)ベンゾトリアゾー
ル、2−(2′−ヒドロキシ−3′−t−ブチル−5′−
メチルフエニル)−5−クロロベンゾトリアゾー
ル等のベンゾトリアゾール類、〔ビス(3,5−
ジ−t−ブチル−4−ヒドロキシベンジル)フオ
スフオン酸モノエチルエステル〕ニツケル塩等の
ニツケル錯体、ナフタリンテトラカルボン酸、そ
の無水物、イミドもしくはエステル等が例として
挙げられる。これらの紫外線吸収剤は、合成樹脂
または熱可塑性樹脂に対して通常、100〜
10000ppm使用される。 The thermoplastic resin used for the thermoplastic resin layer 3 and the aforementioned split fibers 1 and 1' includes:
Ultraviolet absorbers, fillers, etc. can be added according to conventional methods. In particular, it is preferable to use an ultraviolet absorber in the thermoplastic resin layer to improve weather resistance. The ultraviolet absorber may be any one that can be used in ordinary organic polymer materials, such as benzophenones such as 2-hydroxy-4-methoxybenzophenone and 2-hydroxy-4-n-octoxybenzophenone; Salicylic acid derivatives such as pt-butylphenyl salicylate, 2-(2'-hydroxy-5'-methylphenyl)benzotriazole, 2-(2'-hydroxy-3'-t-butyl-5'-
Benzotriazoles such as methylphenyl)-5-chlorobenzotriazole, [bis(3,5-
Examples include nickel complexes such as di-t-butyl-4-hydroxybenzyl)phosphonic acid monoethyl ester nickel salt, naphthalene tetracarboxylic acid, its anhydride, imide, or ester. These UV absorbers are typically 100~
10000ppm used.
熱可塑性樹脂層3の積層方法は、ネツトの通気
性を損なわないように開孔部4を閉塞せず、薄く
塗布できる方法で実施され、例えばエアーナイ
フ、コーター等が用いられる。この熱可塑性樹脂
層3は通常、5〜50μm、好ましくは、10〜20μm
の厚さとされる。 The thermoplastic resin layer 3 is laminated by a method that allows thin coating without blocking the openings 4 so as not to impair the air permeability of the net, for example, using an air knife, a coater, or the like. This thermoplastic resin layer 3 is usually 5 to 50 μm, preferably 10 to 20 μm
The thickness is said to be .
本考案の遮光ネツトの遮光率は、通常2〜60
%、好ましくは5〜40%とされる。遮光ネツトを
使用する対象植物、使用場所、通気性等を考慮し
て、ネツトの開孔率、反射金属層2の金属等を選
択することにより適宜の遮光率を有する遮光ネツ
トとすることができる。 The shading rate of the shading net of this invention is usually 2 to 60.
%, preferably 5 to 40%. By selecting the porosity of the net, the metal of the reflective metal layer 2, etc. in consideration of the target plants for which the shade net will be used, the place of use, ventilation, etc., it is possible to obtain a shade net with an appropriate shade rate. .
本考案の遮光ネツトは、高い反射率を有するの
で
(1) 農業ハウスにおいて、ハウスの骨格に沿つて
当該ネツトを掛け種々の植物の遮光に用いるこ
とができる。
Since the light-shielding net of the present invention has a high reflectance, (1) it can be used in agricultural greenhouses to shade various plants by hanging the net along the frame of the greenhouse;
(2) ハウスを使わずに地面と水平に張ることによ
つて、茶の防霜・遮光、椎茸の遮光に用いるこ
とができる。(2) By placing it horizontally to the ground without using a greenhouse, it can be used to protect tea from frost and shade, and to shade shiitake mushrooms.
(3) 作物の根元に敷くマルチングとして使用し
て、地温上昇防止と共に作物に太陽光線の反射
光を当てることができる。(3) It can be used as mulch to spread around the roots of crops, preventing soil temperature from rising and allowing reflected sunlight to shine on the crops.
(4) 果樹園等に張つておくことにより防鳥効果を
奏する。(4) It has a bird-preventing effect when placed in orchards, etc.
また、スプリツトフアイバーが一軸延伸処理を
受けているので強度が縦、横共に高い。更に、従
来の遮光ネツトに比べ平面性が高いので、嵩張ら
ず、市販のスプリツトフアイバーからなるネツト
を用いた場合、該ネツト上に反射金属層及び熱可
塑性樹脂層を設けるのみでよく、少ない工程で製
造できる。 In addition, since the split fiber has undergone uniaxial stretching, its strength is high both vertically and horizontally. Furthermore, since it has higher flatness than conventional light-shielding nets, it is less bulky, and when using a commercially available net made of split fiber, it is only necessary to provide a reflective metal layer and a thermoplastic resin layer on the net, which requires fewer steps. It can be manufactured by
第1図は本考案の遮光ネツトの縦断面図であ
り、第2図は基材であるスプリツトフアイバーか
らなるネツトの平面図である。
1,1′……スプリツトフアイバー、2……反
射金属層、3……熱可塑性樹脂層、4……開孔
部、5……交差角。
FIG. 1 is a longitudinal sectional view of the light-shielding net of the present invention, and FIG. 2 is a plan view of the net made of split fiber as a base material. 1, 1'... Split fiber, 2... Reflective metal layer, 3... Thermoplastic resin layer, 4... Opening portion, 5... Intersection angle.
Claims (1)
し、繊維方向を交差させたネツト上に反射金属
層及び熱可塑性樹脂層を順次積層してなる遮光
ネツト。 (2) 熱可塑性樹脂がポリエチレン又はポリプロピ
レンであることを特徴とする実用新案登録請求
の範囲第1項記載の遮光ネツト。 (3) 反射金属層がアルミニウム層であることを特
徴とする実用新案登録請求の範囲第1項記載の
遮光ネツト。[Claims for Utility Model Registration] (1) A light-shielding net made by laminating thermoplastic resin split fibers and sequentially laminating a reflective metal layer and a thermoplastic resin layer on the net with the fiber directions crossed. (2) The light-shielding net according to claim 1, wherein the thermoplastic resin is polyethylene or polypropylene. (3) The light-shielding net according to claim 1, wherein the reflective metal layer is an aluminum layer.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1987144076U JPH0523331Y2 (en) | 1987-09-21 | 1987-09-21 |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP1987144076U JPH0523331Y2 (en) | 1987-09-21 | 1987-09-21 |
Publications (2)
Publication Number | Publication Date |
---|---|
JPS6448232U JPS6448232U (en) | 1989-03-24 |
JPH0523331Y2 true JPH0523331Y2 (en) | 1993-06-15 |
Family
ID=31411462
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP1987144076U Expired - Lifetime JPH0523331Y2 (en) | 1987-09-21 | 1987-09-21 |
Country Status (1)
Country | Link |
---|---|
JP (1) | JPH0523331Y2 (en) |
Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5138978U (en) * | 1974-09-14 | 1976-03-23 | ||
JPS56126155A (en) * | 1980-03-10 | 1981-10-02 | Oji Yuka Goseishi Kk | Multilayer resin film having excellent light resistance |
JPS5988364A (en) * | 1982-11-09 | 1984-05-22 | 日本石油化学株式会社 | Hydraulic blend |
JPS6255435B2 (en) * | 1982-10-15 | 1987-11-19 | Nippon Musical Instruments Mfg |
Family Cites Families (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS51106751U (en) * | 1975-02-24 | 1976-08-26 | ||
JPS6255435U (en) * | 1985-09-26 | 1987-04-06 |
-
1987
- 1987-09-21 JP JP1987144076U patent/JPH0523331Y2/ja not_active Expired - Lifetime
Patent Citations (4)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
JPS5138978U (en) * | 1974-09-14 | 1976-03-23 | ||
JPS56126155A (en) * | 1980-03-10 | 1981-10-02 | Oji Yuka Goseishi Kk | Multilayer resin film having excellent light resistance |
JPS6255435B2 (en) * | 1982-10-15 | 1987-11-19 | Nippon Musical Instruments Mfg | |
JPS5988364A (en) * | 1982-11-09 | 1984-05-22 | 日本石油化学株式会社 | Hydraulic blend |
Also Published As
Publication number | Publication date |
---|---|
JPS6448232U (en) | 1989-03-24 |
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