JPH08191632A - Container for cultivating plant - Google Patents

Container for cultivating plant

Info

Publication number
JPH08191632A
JPH08191632A JP1991495A JP1991495A JPH08191632A JP H08191632 A JPH08191632 A JP H08191632A JP 1991495 A JP1991495 A JP 1991495A JP 1991495 A JP1991495 A JP 1991495A JP H08191632 A JPH08191632 A JP H08191632A
Authority
JP
Japan
Prior art keywords
composite material
zeolite
resin
weight
container
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
JP1991495A
Other languages
Japanese (ja)
Inventor
Susumu Kusakaishi
進 日下石
Noriko Umetsu
典子 梅津
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.)
Tohoku Munekata Co Ltd
Original Assignee
Tohoku Munekata 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 Tohoku Munekata Co Ltd filed Critical Tohoku Munekata Co Ltd
Priority to JP1991495A priority Critical patent/JPH08191632A/en
Publication of JPH08191632A publication Critical patent/JPH08191632A/en
Pending legal-status Critical Current

Links

Landscapes

  • Cultivation Receptacles Or Flower-Pots, Or Pots For Seedlings (AREA)

Abstract

PURPOSE: To provide a lightweight container for cultivating a plant, molded from a composite material comprising a rock powder and a thermoplastic resin and excellent in flow properties of water or air, sustained releasability of a fertilizer or an agrochemical and designability. CONSTITUTION: This container for cultivating a plant is molded from a composite material comprising (A) preferably 32-77wt.%, more preferably 35-64wt.% rock powder consisting essentially of a porous rock such as zeolite and (B) a thermoplastic resin such as PP, PE or PS resin. Furthermore a heat stabilizer, an antioxidant or an ultraviolet light absorber is preferably blended in the composite material.

Description

【発明の詳細な説明】Detailed Description of the Invention

【0001】[0001]

【産業上の利用分野】本発明は、水分の吸収性及び放出
性並びに肥料、農薬等の徐放性を有する複合材からなる
植物栽培用容器に関する。
BACKGROUND OF THE INVENTION 1. Field of the Invention The present invention relates to a container for plant cultivation, which is made of a composite material having absorbability and release of water and sustained release of fertilizer, pesticide and the like.

【0002】[0002]

【発明の目的】従来、植物栽培用容器としては、主に素
焼き鉢、あるいは融薬を素焼き鉢にかけたいわゆる化粧
鉢、あるいはポリプロピレン樹脂やポリスチレン樹脂で
作られたいわゆるプラ鉢、あるいはポリ塩化ビニル樹脂
やポリエチレン樹脂で作られた、植物苗栽培用のいわゆ
るビニルポツト等が市販されている。素焼き鉢は、植物
の成長に好ましい水分や空気の流通性に優れるといわれ
ているが、破損し易く且つ重く意匠性も悪くまた運搬に
も不便である。融薬を使用した化粧鉢は、意匠性に優れ
且つ破損しにくいが、植物の成長に必要な水分や空気の
流通性はわずかである。さらに、いわゆるプラ鉢は破損
し難く軽量で、運搬に便利でありまた意匠性に優れるこ
とから多く用いられているが、水分や空気の透過性がほ
とんどないことから、栽培された植物が根腐れを起こす
等の問題点が指摘されている。更にビニルポツトは廉価
であることから、育苗、種苗用に用いられるが、空気流
通性はない。
A container for plant cultivation has heretofore been used mainly as a clay pot, a so-called make-up pot in which a melting agent is placed in a clay pot, a so-called plastic pot made of polypropylene resin or polystyrene resin, or polyvinyl chloride resin. So-called vinyl pots and the like made of polyethylene resin for plant seedling cultivation are commercially available. The unglazed pot is said to have excellent water and air circulation properties that are favorable for plant growth, but it is easily damaged and heavy, has poor design, and is inconvenient to carry. A vanity containing a flux has excellent design and is not easily damaged, but has a small flowability of water and air necessary for plant growth. In addition, so-called plastic pots are often used because they are not easily damaged, are lightweight, are convenient to transport, and have excellent designability, but because they have almost no moisture or air permeability, cultivated plants are root-rotted. It has been pointed out that problems such as Furthermore, vinyl pots are inexpensive and therefore used for raising seedlings and seedlings, but have no air circulation.

【0003】本発明は、これらの問題を解決し、水分や
空気の流通を素焼き鉢同等かまたはそれ以上とし、また
プラ鉢の軽量化と意匠性を併せもたした植物栽培用容器
を提供することを目的とする。
The present invention solves these problems and provides a container for plant cultivation in which the distribution of water and air is equal to or more than that in a unglazed pot, and the weight of a plastic pot and the design are combined. The purpose is to

【0004】さらに本発明は、肥料、農薬等を吸着しこ
れを時間経過と共に徐々に放出することができる植物栽
培用容器を提供することを目的とする。
A further object of the present invention is to provide a container for plant cultivation which can adsorb fertilizers, agricultural chemicals and the like and gradually release them over time.

【0005】[0005]

【発明の構成、作用】本発明者らは、鋭意複合材の研究
を重ねてきた結果、多孔質岩石の粉末あるいは細粒を混
合した樹脂複合材を作り、この複合材を使用して植物栽
培用容器を完成した。すなわち本発明は、多孔質岩石を
主たる成分とする岩石粉末と熱可塑性樹脂とより成る複
合材から成形され植物栽培用容器を提供する。
[Structure and Action of the Invention] As a result of repeated studies on the composite material, the present inventors have made a resin composite material in which powder or fine particles of porous rock are mixed, and plant cultivation using this composite material. Completed the container for use. That is, the present invention provides a container for plant cultivation, which is formed from a composite material composed of rock powder containing porous rock as a main component and a thermoplastic resin.

【0006】本発明に用いられる多孔質岩石としては、
東北地方や関東地方の北部が主として産出するゼオライ
トが好ましい。熱可塑性樹脂の中においても好ましくは
ポリプロピレン樹脂、ポリエチレン樹脂、ポリスチレン
樹脂等が用いられるが、これ以外の樹脂であつても良
く、更に室温で粉末状である塩化ビニル樹脂や共重合樹
脂であるABS樹脂等であつても良い。
As the porous rock used in the present invention,
Zeolites mainly produced in the northern part of the Tohoku region and Kanto region are preferred. Among the thermoplastic resins, polypropylene resin, polyethylene resin, polystyrene resin and the like are preferably used, but other resins may be used, and vinyl chloride resin or copolymer resin ABS which is powdery at room temperature. It may be made of resin or the like.

【0007】多孔質岩石の粉末と樹脂との混練物から所
望の形状の植物栽培用容器を成形する。成形法として
は、射出成形、圧縮成形、ロール成形後に真空成形や圧
空成形等が好ましく用いられるが、もちろんこれ以外の
方法であつてもよい。
A container for plant cultivation having a desired shape is formed from a kneaded product of porous rock powder and resin. As the molding method, injection molding, compression molding, vacuum molding and pressure molding after roll molding are preferably used, but other methods may of course be used.

【0008】本発明の植物栽培用容器の材料たる複合材
は、好ましくは32〜77重量%、特に好ましくは35
〜64重量%の多孔質岩石を含有し残りが樹脂である。
多孔質岩石の含量が77重量%を越えると、成形に必要
な複合材料の流通性が得られなかつたり、また十分な強
度を有する成形物が得られ難い。また多孔質岩石が31
重量%未満の場合は水分の吸放出特性や徐放性が低下す
る。これは樹脂の中に多孔質岩石が埋め込まれた状態と
なり、多孔質岩石がもつ水分の吸放出特性が失われてし
まう為と考えられる。多孔質岩石、好ましくはゼオライ
トの含有量が適切に調合された複合材によつて構成され
た植物栽培用容器は、水分吸収性、放出性ならびに徐放
性に優れるばかりではなく、空気の導通にも優れかつ軽
量であり運搬性にも優れ破損しにくい。
The composite material as a material for the container for plant cultivation of the present invention is preferably 32 to 77% by weight, and particularly preferably 35.
It contains up to 64% by weight of porous rock and the rest is resin.
When the content of porous rock exceeds 77% by weight, the flowability of the composite material required for molding cannot be obtained, and a molded product having sufficient strength is difficult to obtain. 31 porous rocks
If it is less than weight%, the water absorption / release characteristics and the sustained release property deteriorate. It is considered that this is because the porous rock is embedded in the resin and the water absorption / release characteristics of the porous rock are lost. Porous rocks, preferably a container for plant cultivation constituted by a composite material having an appropriate content of zeolite is not only excellent in water absorption, releasability and sustained release, but also for air conduction. It is also excellent in light weight, has excellent transportability, and is not easily damaged.

【0009】複合材には、一般的に樹脂に添加される熱
安定剤、酸化防止剤、紫外線吸収剤等は当然含まれて良
いし、また、補強の為、各種の有機・無機の強化繊維や
ウイスカーなどが含まれてもかまわない。
The composite material may naturally contain a heat stabilizer, an antioxidant, an ultraviolet absorber, etc., which are generally added to the resin, and for the purpose of reinforcement, various organic / inorganic reinforcing fibers. It doesn't matter if it contains whiskers or the like.

【0010】[0010]

【実施例】以下の実施例により、本発明を更に詳しく説
明する。
The present invention will be described in more detail by the following examples.

【0011】実施例1 モルデナイト系ゼオライト(新東北化学工業(株)製ゼ
オライト No.1424宮城県仙台市愛子産)を約4k
g程度をステンレス製バツトに入れ、乾燥機にて160
℃48時間乾燥を行い、80℃まで自然冷却後、速やか
にポリプロピレン製広口ビンに保管した。これから7
7.0gをポリプロピレン製ビーカーに採取し、ポリプ
ロピレン樹脂(昭和電工(株)製 PP;MK−85
2)を23.0g加え軽く撹拌後、210℃に調節した
ミキシングロール(西村工機(株)製NS−200型)
上に投入し、ステンレス製へらにて撹拌しながら7分間
十分に混合した。これを取り出し内のり15cm×15
cm×深さ0.2cm穴のあいたステンレス板にはさみ
込み、あらかじめ210℃に調整した圧縮機((株)山
口機械製210型)で120kg/cm2で圧縮後、取
り出し冷却後固化したゼオライト/ポリプロピレン樹脂
複合材料を取り出した。この時のゼオライト含有量は7
7重量%である。外観状態を、○は充分な強度を保持、
△は充分な強度を保持するが流通性が少なく成形しずら
い、×は成形不可、の凡例で示し結果を表1に記載し
た。さらにゼオライトが樹脂によつて完全に覆われてし
まうと吸放湿性が失われてしまう恐れがあるので、樹脂
状態を観察した結果、A:樹脂の光沢はない、B:樹脂
の光沢があつてゼオライト粒子間に隙間がある、C:完
全に樹脂の中にゼオライト粒子が埋め込まれている状
態、の状態を観察し、同じく表1に記載した。この複合
材をPP−A−77と呼ぶ。
Example 1 About 4 k of mordenite type zeolite (Zeohto Chemical Co., Ltd. zeolite No. 1424 produced by Aiko, Sendai City, Miyagi Prefecture)
Approximately g is put in a stainless steel butter and 160
It was dried at 48 ° C for 48 hours, naturally cooled to 80 ° C, and immediately stored in a polypropylene wide-mouth bottle. From now on 7
7.0 g was collected in a polypropylene beaker, and polypropylene resin (Showa Denko KK PP; MK-85) was used.
2) 23.0 g was added, and the mixture was lightly stirred, and then mixed at 210 ° C. (Nishimura Koki Co., Ltd. NS-200 type).
The mixture was put on the above and thoroughly mixed for 7 minutes while stirring with a stainless spatula. Take this out and paste inside 15 cm x 15
cm × Depth 0.2 cm Sandwiched in a stainless plate with holes, compressed at 120 kg / cm 2 with a compressor (210 type manufactured by Yamaguchi Kikai Co., Ltd.) adjusted to 210 ° C. in advance, taken out, cooled and solidified Zeolite / The polypropylene resin composite material was taken out. The zeolite content at this time is 7
It is 7% by weight. Appearance state, ○ keeps sufficient strength,
The results are shown in Table 1 with a legend that Δ indicates that sufficient strength is maintained but flowability is low and molding is difficult, and × indicates that molding is not possible. Furthermore, if the zeolite is completely covered with the resin, the moisture absorption and desorption properties may be lost, so the results of observing the resin state show that A: the resin has no luster, B: the resin has luster. The state in which there is a gap between the zeolite particles and C: the state in which the zeolite particles are completely embedded in the resin was observed, and the results are also shown in Table 1. This composite material is called PP-A-77.

【0012】実施例2 ゼオライトの重量%を76重量%から32重量%まで、
2重量%ごとに変化させ、実施例1と全く同様にして複
合材を作製した。結果を表1に併せて記載する。
Example 2 The weight% of zeolite is from 76% to 32% by weight,
A composite material was produced in the same manner as in Example 1 except that the content was changed every 2% by weight. The results are also shown in Table 1.

【0013】比較例1 実施例1と全く同様にして、78及び80重量%のゼオ
ライトを含有する複合材を作製し、結果を表1に併せて
記載した。ゼオライト含有量78重量%以上においては
ゼオライトの粉末が樹脂とよく混練が出来ず、得られた
複合材料は脆く、かつゼオライトの粉末も表面から剥離
した。
Comparative Example 1 A composite material containing 78 and 80% by weight of zeolite was prepared in exactly the same manner as in Example 1, and the results are also shown in Table 1. When the zeolite content was 78% by weight or more, the zeolite powder could not be kneaded well with the resin, the obtained composite material was brittle, and the zeolite powder was also exfoliated from the surface.

【0014】比較例2 実施例1と全く同様にして、31及び30重量%のゼオ
ライトを含有する複合材を作製した。結果を表1に併せ
て記載する。ゼオライト含有量が低く、樹脂分が多くな
ると、ゼオライトが樹脂に覆われ、好ましくない。
Comparative Example 2 In exactly the same manner as in Example 1, a composite material containing 31 and 30% by weight of zeolite was prepared. The results are also shown in Table 1. When the zeolite content is low and the resin content is high, the zeolite is covered with the resin, which is not preferable.

【0015】[0015]

【表1】 [Table 1]

【0016】実施例3 前述の実施例1〜2及び比較例1〜2の中でモルデナイ
ト系ゼオライトをクリノプチロライト系ゼオライト(ジ
ークライト工業(株)製ゼオライトZ−12、山形県板
谷産)に変えた以外は全く同様にして複合材を作製し
た。結果を表−1に併せて記載する。この複合材料をP
P−1−77と呼ぶ。
Example 3 In the above-mentioned Examples 1 and 2 and Comparative Examples 1 and 2, the mordenite-based zeolite was replaced by a clinoptilolite-based zeolite (Zelite Co., Ltd. Zeolite Z-12, Itaya, Yamagata Prefecture). A composite material was produced in exactly the same manner except that the above was changed. The results are also shown in Table 1. This composite material is
It is called P-1-77.

【0017】表1の結果は、ゼオライト含量は32〜7
7重量%の範囲が好ましいこと、及び、ゼオライトの産
出地によつて複合材の特性が影響されないことを示して
いる。
The results of Table 1 show that the zeolite content is 32 to 7
A range of 7% by weight is preferred and indicates that the origin of the zeolite does not affect the properties of the composite.

【0018】実施例4 実施例1で作つたモルデナイト系ゼオライト77重量%
含有品と実施例3で作つたクリノプチロライト系ゼオラ
イト77重量%含有品を60℃48時間乾燥し、重量を
求めた後、温度23℃湿度90%RHに設定してある恒
温恒湿機(ベツセル(株)製CHF−S型)内に投入
し、一定時間ごとに電子天秤(日本シイベルヘグナー
(株)製METTLER BD 1201)にて重量測定
することにより温度23℃湿度90%RH内での水分吸
着性を測定した。乾燥したゼオライト/ポリプロピレン
複合材を基準にして増加量を百分率で求めた。また、時
間を分単位で計算し、これを対数として図1に結果を記
載する。図1は、本発明による複合材は充分な吸湿性を
もつ植物栽培用容器材料となることを示している。
Example 4 77% by weight of the mordenite zeolite prepared in Example 1
The contained product and the product containing 77% by weight of the clinoptilolite-based zeolite prepared in Example 3 were dried at 60 ° C. for 48 hours, the weight was determined, and then the temperature and humidity were set to 23 ° C. and 90% RH. (CHF-S type manufactured by Betsucell Co., Ltd.), and the weight is measured with an electronic balance (METTLER BD 1201 manufactured by Japan Siber Hegner Co., Ltd.) at regular intervals to obtain a temperature of 23 ° C. and humidity of 90% RH. The water adsorption was measured. The increase was determined as a percentage based on the dried zeolite / polypropylene composite. In addition, the time is calculated in minutes, and the result is shown as a logarithm in FIG. FIG. 1 shows that the composite material according to the present invention becomes a container material for plant cultivation having sufficient hygroscopicity.

【0019】比較例3 市販されている、いわゆる素焼き鉢(4号鉢)をハンマ
ーで割おおむね5cm×7cm程度の大きさにした。こ
れを実施例1のゼオライト複合材に変えて、水分を吸収
する量を測定したところ、ほとんど水分を吸収しなかつ
た。結果を図1に併せて記載する。
Comparative Example 3 A commercially available so-called unglazed pot (No. 4 bowl) was cut with a hammer into a size of about 5 cm × 7 cm. When this was changed to the zeolite composite material of Example 1 and the amount of water absorbed was measured, almost no water was absorbed. The results are also shown in FIG.

【0020】市販されている、いわゆるプラ鉢(ポリプ
ロピレン製4号鉢)を、おおむね5cm×7cmの大き
さにのこぎりで切り取り、比較例3と全く同様にして水
分の吸収を測定した。結果を図1に併せて記載する。図
1から分るように、ポリプロピレン樹脂製プラ鉢の場合
には全く吸湿することはなかつた。
Commercially available so-called plastic bowls (polypropylene No. 4 bowls) were cut with a saw to a size of approximately 5 cm × 7 cm, and moisture absorption was measured in exactly the same manner as in Comparative Example 3. The results are also shown in FIG. As can be seen from FIG. 1, the polypropylene resin plastic bowl did not absorb moisture at all.

【0021】実施例5 実施例1及び3で作つた77重量%のゼオライト/ポリ
プロピレン樹脂複合材(クリノプチロライト及びモルデ
ナイト系ゼオライト使用)を、重量測定後、300ml
の純水を入れたガラス製ビーカー内に浸漬した。この時
の水温は19℃だつた。試験片を取り出し、ろ紙で水分
を拭い、そのまま30分間、23℃内の室温に放置し
た。重量測定後、温度23℃、湿度50%RHに調整さ
れた恒温恒湿機(ベツセル(株)製CHF−S型)内に
放置し、各時間ごとに重量測定した。さらに、乾燥した
試験片を基準に水分が放出されていく量を放湿量として
重量%で求めた。結果を図2に記載する。図2から分か
るように、ゼオライト複合材料は水分を28〜35%を
吸収し、さらに、吸収した水分を少しずつ放出していく
機能をもつている。なお、図2は、図1と同様に時間を
分とし、常用対数の数値とした。
Example 5 77 wt% of the zeolite / polypropylene resin composite material (using clinoptilolite and mordenite type zeolite) prepared in Examples 1 and 3 was weighed to obtain 300 ml.
It was immersed in a glass beaker containing pure water. The water temperature at this time was 19 ° C. The test piece was taken out, the water was wiped off with a filter paper, and the sample was left at room temperature within 23 ° C. for 30 minutes. After the weight measurement, the sample was left in a thermo-hygrostat (CHF-S type manufactured by Beth Cell Co., Ltd.) adjusted to a temperature of 23 ° C. and a humidity of 50% RH, and the weight was measured every time. Further, the amount of released moisture based on the dried test piece was determined as a moisture release amount in% by weight. The results are shown in Figure 2. As can be seen from FIG. 2, the zeolite composite material has a function of absorbing 28 to 35% of water and further releasing the absorbed water little by little. It should be noted that in FIG. 2, as in FIG. 1, time is defined as minutes and common logarithmic values are set.

【0022】比較例5〜6 比較例3及び4で使用した素焼き鉢片及びプラ鉢試験片
を実施例5と全く同様にして、水分の吸水量と放出量を
求めた結果、素焼き鉢の水分放出量は、ゼオライト複合
材の4分の1〜6分の1程度、プラ鉢に関してはほとん
ど吸水性も放出性もなかつた。結果を図2に併せて記載
する。
Comparative Examples 5 to 6 The unglazed pot pieces and the plastic pot test pieces used in Comparative Examples 3 and 4 were processed in exactly the same manner as in Example 5 to determine the water absorption and release amounts. The released amount was about 1/4 to 1/6 of the zeolite composite material, and the plastic pot had almost no water absorption or release property. The results are also shown in FIG.

【0023】実施例6 室温23℃において1リツトルガラスビーカーに500
mlの純水を採取し、100gの食塩(新日本化学工業
(株)製 日本たばこ産業(株)販売 食塩塩化ナトリ
ウム99%以上)を投入し、ガラス棒で10分間撹拌後
24時間放置し、更にそこに残つていた食塩を撹拌溶解
させた。1時間後、更にビーカーの底にまだ溶けていな
い食塩を確認した後、新たな1リツトルガラス製ビーカ
ーに400mlの上澄み液を移し換え、これを飽和食塩
水とした。実施例1及び2で作つた各ゼオライト/ポリ
プロピレン樹脂複合材の中からゼオライト含有量77重
量%、70重量%、60重量%、50重量%、40重量
%のもの5種をそれぞれ選び、この飽和食塩水に浸漬し
24時間放置後引き上げ、表面をろ紙で拭つた後30分
間室内に放置した。清浄なビーカーに純水(共栄製薬
(株)製 蒸留水日本薬局方精製水)を300ml採取
し、飽和食塩水浸漬後の複合材料の一片を浸漬し、ガラ
ス棒で純水を5分間撹拌後純水より試験片を取り出し
た。この純水を清浄な20ml試験管に3〜5ml採取
し、5%硝酸銀銀水溶液を数滴加え、塩素イオンと銀イ
オンによつて塩化銀が生成する際に白濁することをもつ
て、複合材が吸収した塩化ナトリウムを純水の中で放出
していくことを検証した。新たな純水の中に、更に純水
から引き上げた複合材を浸漬し、同じ操作を行つて塩化
ナトリウム中の塩素イオンが硝酸銀によつて検出されな
くなるまで繰り返し続けた。結果を表2に記す。なお硝
酸銀は、関東化学工業(株)製 試薬特級を用いた。表
2の凡例としては、◎は強く白濁、○は牛乳以下米の研
ぎ汁程度、△は米の研ぎ汁以下、×は何も白濁しないと
いう基準である。
Example 6 500 in 1 liter glass beaker at room temperature 23 ° C
After collecting ml of pure water, 100 g of salt (manufactured by Shin-Nippon Kagaku Kogyo Co., Ltd. sold by Japan Tobacco Inc., sodium chloride 99% or more) was added, and the mixture was stirred with a glass rod for 10 minutes and left for 24 hours, Further, the salt remaining therein was dissolved by stirring. After 1 hour, the undissolved salt was further confirmed at the bottom of the beaker, and 400 ml of the supernatant was transferred to a new 1-liter glass beaker, which was used as a saturated saline solution. From each of the zeolite / polypropylene resin composite materials prepared in Examples 1 and 2, five kinds having zeolite contents of 77% by weight, 70% by weight, 60% by weight, 50% by weight, and 40% by weight were respectively selected and saturated. It was immersed in a saline solution, left standing for 24 hours, then pulled up, wiped the surface with a filter paper, and left for 30 minutes in a room. Collect 300 ml of pure water (Kyoei Pharmaceutical Co., Ltd. distilled water Japanese Pharmacopoeia purified water) in a clean beaker, immerse one piece of the composite material after soaking in saturated saline solution, and stir the pure water with a glass rod for 5 minutes. A test piece was taken out from pure water. 3 to 5 ml of this pure water was sampled in a clean 20 ml test tube, and several drops of 5% silver silver nitrate aqueous solution were added, and the mixture was clouded when silver chloride was formed by chlorine ions and silver ions. It was verified that the absorbed sodium chloride was released in pure water. The composite material further pulled from pure water was immersed in fresh pure water, and the same operation was repeated until the chloride ions in sodium chloride were not detected by silver nitrate. The results are shown in Table 2. The silver nitrate used was a reagent special grade manufactured by Kanto Chemical Co., Inc. The legend of Table 2 is that ⊚ is strongly cloudy, ○ is milk or less rice polishing liquid, Δ is rice polishing liquid or less, and × is nothing.

【0024】表2からわかる様に、22回まで純水を交
換しても塩化ナトリウムが放出していることがわかる。
従つて、優れた徐放性を有することが判明した。
As can be seen from Table 2, sodium chloride is released even if the pure water is replaced up to 22 times.
Therefore, it was found to have excellent sustained release properties.

【0025】比較例7〜8 市販の素焼き鉢(5号素焼き鉢:福島市鳥谷野「PRE
AU」より購入品)をおおよそ5〜7cm角に切り出し
て試料に変えた以外は、実施計6と全く同様に行つた。
(比較例7) また、同店にて入手したプラ鉢といわれるポリプロピレ
ン製植木鉢(5号鉢)を同様に切り出し、実施例2と全
く同様に行つた。(比較例8) 結果を表2にあわせて記載する。素焼き鉢はわずかな徐
放性が見られるが充分ではなく、プラ鉢には全く徐放性
は見られなかつた。
Comparative Examples 7 to 8 Commercial unglazed pot (No. 5 unglazed pot: Toriyano, Fukushima-shi "PRE
The procedure was exactly the same as that of Example 6 except that a sample purchased from "AU") was cut into a piece of about 5 to 7 cm and replaced with a sample.
(Comparative Example 7) Further, a polypropylene plant pot (No. 5 pot) called a plastic pot, which was obtained at the same store, was cut out in the same manner and carried out in exactly the same manner as in Example 2. Comparative Example 8 The results are also shown in Table 2. The unglazed pot showed a slight sustained release, but it was not sufficient, and the plastic pot did not show any sustained release.

【0026】比較例9 比較例2で作つたゼオライト31重量%、30重量%の
2つの複合材について、実施例6と全く同様に徐放性実
験を行つた。結果を表2に併せて記載する。表2から分
るように樹脂分が多くなりゼオライトが少なくなると、
理由は定かでないが徐放性はほとんどなくなる。
Comparative Example 9 With respect to the two composite materials of 31% by weight and 30% by weight of the zeolite prepared in Comparative Example 2, the sustained release test was carried out in exactly the same manner as in Example 6. The results are also shown in Table 2. As can be seen from Table 2, when the resin content increases and the zeolite decreases,
Although the reason is not clear, the sustained release is almost lost.

【0027】[0027]

【表2】 [Table 2]

【0028】実施例7 実施例6で使用したと同じゼオライト含有量を有する5
種の複合材について新しい試験片を作製した。
Example 7 5 with the same zeolite content as used in Example 6
New specimens were prepared for some composites.

【0029】一方、清浄な1リツトルビーカーに450
gの純水を採取し、更に硫酸アンモニウム(関東化学
(株)製 試薬1級)を50gを加え、ガラス棒で撹拌
溶解し、10%硫安肥料溶液とした。更に、硫安検出用
指示薬として塩化バリウム(関東化学(株)製 試薬特
級)5%水溶液を20mlを作製した。実施例6の中で
飽和食塩水に変えて、硫安水溶液を用い、硝酸銀水溶液
の変わりに塩化バリウム水溶液を用いた以外は全く同様
にして硫安の徐放性実験を行つた。なお、硫安検出は (NH4)2SO4 →2NH+ 4+SO2- 4 …(1)式 BaCl2 →Ba2++2Cl- …(2)式 Ba2++SO4 2-→BaSO4↓ …(3)式 の反応式で(3)式を利用し、硫酸バリウムの生成が水
中で水に溶けず、白濁沈殿することを利用したものであ
る。結果を表3に各試験片ごとに併せて記載した。
On the other hand, 450 in a clean 1-liter beaker
g of pure water was sampled, 50 g of ammonium sulfate (Kanto Kagaku Co., Ltd. reagent grade 1) was further added, and dissolved by stirring with a glass rod to obtain a 10% ammonium sulfate fertilizer solution. Furthermore, 20 ml of a 5% aqueous solution of barium chloride (special grade reagent manufactured by Kanto Chemical Co., Inc.) was prepared as an indicator for detecting ammonium sulfate. A controlled release experiment of ammonium sulfate was carried out in the same manner as in Example 6, except that the aqueous solution of ammonium sulfate was used instead of the saturated saline solution, and the aqueous solution of barium chloride was used instead of the aqueous solution of silver nitrate. Incidentally, ammonium sulfate Detection (NH 4) 2 SO 4 → 2NH + 4 + SO 2- 4 ... (1) Equation BaCl 2 → Ba 2+ + 2Cl - ... (2) Equation Ba 2+ + SO 4 2- → BaSO 4 ↓ ... (3) is used in the reaction formula of (3), and the fact that the production of barium sulfate does not dissolve in water in water and cloudy precipitation occurs. The results are shown in Table 3 for each test piece.

【0030】表3から分る様に、複合材は極めて優れた
肥料の徐放性を示す。
As can be seen from Table 3, the composite material exhibits extremely excellent fertilizer sustained release property.

【0031】比較例10〜11 比較例7〜8で用いた素焼き鉢及びプラ鉢から同様に試
験片を切り出し、実施例7と全く同様に試験を行つた。
結果を表3に併せて記載する。
Comparative Examples 10 to 11 Test pieces were similarly cut out from the unglazed pots and plastic bowls used in Comparative Examples 7 to 8 and tested in exactly the same manner as in Example 7.
The results are also shown in Table 3.

【0032】この表3からわかる様に、素焼き鉢は肥料
の徐放性はなく、プラ鉢にいたつては全く徐放性は見ら
れなかつた。
As can be seen from Table 3, the unglazed pot has no sustained release of fertilizer, and the plastic pot has no sustained release.

【0033】比較例12 比較例2と全く同様に試験片を作製し、実施例7と同じ
操作を行つた。結果を表3に併せて記載する。ここで
は、樹脂分が多く好ましい徐放性を得ることができなか
つた。
Comparative Example 12 A test piece was prepared in the same manner as in Comparative Example 2, and the same operation as in Example 7 was performed. The results are also shown in Table 3. In this case, it was impossible to obtain a preferable sustained-release property because the resin content was large.

【0034】[0034]

【表3】 [Table 3]

【0035】実施例8 ポリプロピレン樹脂をポリスチレン樹脂(昭和電工
(株)製GPポリスチレン2V−62F)に変えた以外
は、全く実施例1と同様に行つた。ポリプロピレン樹脂
とポリスチレン樹脂では比重がわずかに異なり、ポリプ
ロピレン樹脂は0.98g/cm3、ポリスチレン樹脂は
1.05g/cm3のそれぞれの比重差があり、ここで
は、この比重差を用いてゼオライトと樹脂量をそれぞれ
所定量計量し、ゼオライト含有量77重量%、ポリスチ
レン樹脂23重量%で行つた。
Example 8 The procedure of Example 1 was repeated except that the polypropylene resin was changed to polystyrene resin (GP polystyrene 2V-62F manufactured by Showa Denko KK). The specific gravity is slightly different between polypropylene resin and polystyrene resin, polypropylene resin has a specific gravity difference of 0.98 g / cm 3 and polystyrene resin has a specific gravity difference of 1.05 g / cm 3 , respectively. A predetermined amount of each resin was weighed and the zeolite content was 77% by weight and the polystyrene resin was 23% by weight.

【0036】この複合材料は十分な通気性を持ち、かつ
強度もあり、圧縮成形によつて成形することも十分可能
であつた。
This composite material had sufficient air permeability and strength, and could be sufficiently molded by compression molding.

【0037】[0037]

【発明の効果】本発明の植物栽培用容器は、水分や空気
の流通性に優れており、根腐れの発生が防止され、植物
の成長に対して良好な環境を提供することができる。ま
た徐放性にすぐれており、施用した肥料や農薬を吸着し
た後これを少量づつ徐々に放出することができ、肥料や
農薬の効果を長期間維持することができる。更にまた、
成形が容易であり、意匠性も優れており、また比較的軽
量であつて、取り扱いや運搬にも便利である。
INDUSTRIAL APPLICABILITY The plant cultivation container of the present invention has excellent water and air circulation properties, prevents root rot from occurring, and can provide a favorable environment for plant growth. Moreover, it is excellent in sustained-release property, and it can adsorb applied fertilizers and pesticides and then gradually release them little by little, so that the effects of fertilizers and pesticides can be maintained for a long period of time. Furthermore,
It is easy to mold, has good design, and is relatively lightweight, which is convenient for handling and transportation.

【図面の簡単な説明】[Brief description of drawings]

【図1】本発明の実施例4及び比較例3〜4の試料の水
分吸着性を示す図である。
FIG. 1 is a diagram showing the water adsorption properties of samples of Example 4 of the present invention and Comparative Examples 3-4.

【図2】本発明の実施例5及び比較例5〜6の試料の水
分吸着性を示す図である。
FIG. 2 is a diagram showing the water adsorption properties of the samples of Example 5 of the present invention and Comparative Examples 5-6.

Claims (3)

【特許請求の範囲】[Claims] 【請求項1】 多孔質岩石を主たる成分とする岩石粉末
と熱可塑性樹脂とより成る複合材から成形された植物栽
培用容器。
1. A container for plant cultivation, which is molded from a composite material composed of a rock powder containing porous rock as a main component and a thermoplastic resin.
【請求項2】 多孔質岩石がゼオライトである請求項1
に記載の植物栽培用容器。
2. The porous rock is a zeolite.
The container for cultivating a plant according to.
【請求項3】 複合材中の岩石粉末含量が32〜77重
量%である請求項1に記載の植物栽培用容器。
3. The container for plant cultivation according to claim 1, wherein the content of rock powder in the composite material is 32 to 77% by weight.
JP1991495A 1995-01-13 1995-01-13 Container for cultivating plant Pending JPH08191632A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP1991495A JPH08191632A (en) 1995-01-13 1995-01-13 Container for cultivating plant

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP1991495A JPH08191632A (en) 1995-01-13 1995-01-13 Container for cultivating plant

Publications (1)

Publication Number Publication Date
JPH08191632A true JPH08191632A (en) 1996-07-30

Family

ID=12012490

Family Applications (1)

Application Number Title Priority Date Filing Date
JP1991495A Pending JPH08191632A (en) 1995-01-13 1995-01-13 Container for cultivating plant

Country Status (1)

Country Link
JP (1) JPH08191632A (en)

Similar Documents

Publication Publication Date Title
Roldán et al. An incubation experiment to determine factors involving aggregation changes in an arid soil receiving urban refuse
US9730393B2 (en) Microenvironment for efficient uptake of fertilizers and other agrochemicals in soil
EP2064942B1 (en) Plant cultivation system and method
JPS61254132A (en) Support for soil free culture
CN106665566A (en) Multi-effect slow/controlled-release pesticide-added fertilizer as well as preparation method and application thereof
EP2868187A1 (en) Artificial soils and process for producing same
EP3397054A1 (en) Controlled release agrochemical delivery units, their manufacture and use
JPH08509485A (en) Concentrated composition containing agricultural active ingredients
AU2016245416A1 (en) Water absorbent composition
CZ15996A3 (en) High concentrated, solid mepiquat-chloride and chloromequat-chloride articles
CN101605451A (en) Irrigation system and irrigation or fertilizing method
JPH08191632A (en) Container for cultivating plant
US5867937A (en) Method for decreasing hydrophobicity of peat, bark and rockwool in soilless mixes used for plant growth, promoting easier, faster and more even watering of such mixes without plant injury and providing activity for future watering
JPH08107721A (en) Vessel for plant cultivation
JP2018117549A (en) Coated seed, production method of coated seed, and dissemination method of coated seed
Rakhmad et al. Release pattern of ammonium, nitrate, and potassium from Slow-Release Fertilizer (SRF) in the Soil
MX2010010894A (en) Process for the manufacture of pelleted granules based on endomycorrhyzal fungi coated with mineral clays and the composition thereof.
JP2021177735A (en) Method for producing seedling culture soil, seedling culture soil, and method for culturing plants
JPH08217563A (en) Building material
JP2020100524A (en) Fertilizer and method for growing cultivated plant
JP4562839B2 (en) Deodorant composition
WO2002083740A1 (en) A urea-based nitrogenous fertilizer coated with zeolite
WO2024084938A1 (en) Binder for seed coating, composition for seed coating, coated seed, and method for producing and cultivating coated seed
JPH08217562A (en) Building material
AU781919B2 (en) A soil conditioner and slow release bio-pesticidal and fertilizer composition