JP2691466B2 - Water pollution prevention resin composition - Google Patents

Water pollution prevention resin composition

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Publication number
JP2691466B2
JP2691466B2 JP2064148A JP6414890A JP2691466B2 JP 2691466 B2 JP2691466 B2 JP 2691466B2 JP 2064148 A JP2064148 A JP 2064148A JP 6414890 A JP6414890 A JP 6414890A JP 2691466 B2 JP2691466 B2 JP 2691466B2
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JP
Japan
Prior art keywords
acid
zinc
parts
weight
resin composition
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 - Fee Related
Application number
JP2064148A
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Japanese (ja)
Other versions
JPH03267147A (en
Inventor
明 星野
廣彦 川崎
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.)
Dainichiseika Color and Chemicals Mfg Co Ltd
Original Assignee
Dainichiseika Color and Chemicals Mfg Co Ltd
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Application filed by Dainichiseika Color and Chemicals Mfg Co Ltd filed Critical Dainichiseika Color and Chemicals Mfg Co Ltd
Priority to JP2064148A priority Critical patent/JP2691466B2/en
Publication of JPH03267147A publication Critical patent/JPH03267147A/en
Application granted granted Critical
Publication of JP2691466B2 publication Critical patent/JP2691466B2/en
Anticipated expiration legal-status Critical
Expired - Fee Related legal-status Critical Current

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    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02CCAPTURE, STORAGE, SEQUESTRATION OR DISPOSAL OF GREENHOUSE GASES [GHG]
    • Y02C20/00Capture or disposal of greenhouse gases
    • Y02C20/40Capture or disposal of greenhouse gases of CO2

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  • Water Treatment By Sorption (AREA)
  • Solid-Sorbent Or Filter-Aiding Compositions (AREA)

Description

【発明の詳細な説明】 (産業上の利用分野) 本発明は、水質汚濁防止樹脂組成物に関し、更に詳し
くは水槽等の各種水の汚濁防止に有用な水質汚濁防止樹
脂組成物に関する。
TECHNICAL FIELD The present invention relates to a water pollution preventing resin composition, and more particularly to a water pollution preventing resin composition useful for preventing pollution of various water such as an aquarium.

(従来の技術及びその問題点) 近年、食生活の向上により味覚の趣向も一段とレベル
アップし高級化されつつある。特に活魚料理はグルメブ
ームに乗り活況を呈している。これら活魚は、漁場より
水揚げされた後、市場より卸業者に生きたまま貯蔵され
るが、消費者の口に入るまでには、割烹料理店等の水槽
で更に養魚され、水揚げから料理までには1〜3ケ月も
要する。従来はこの養魚期間中に魚が死亡したり、病気
にかかったりして使用不能となったり、又、新鮮な味覚
を失うと云う問題がある。
(Prior Art and Problems Thereof) In recent years, the taste of taste has been further upgraded and upgraded due to improvement in eating habits. In particular, live fish dishes are booming due to the gourmet boom. These live fish are landed from the fishing grounds and then stored as alive by wholesalers from the market, but by the time they reach the consumers' mouth, they are further cultivated in aquariums such as cooking restaurants, and from landing to cooking. Takes 1-3 months. Conventionally, there are problems that the fish die during the period of fish farming, become sick and become unusable, or lose their fresh taste.

この様な問題は、水槽内の炭酸ガス濃度、アンモニア
態窒素濃度、硝酸態窒素濃度、硫化水素濃度等の上昇に
より水質が汚濁することが原因であり、これらの汚濁物
質を除去する為に種々の提案が為されているが、個々の
小規模料理店等で容易に利用できる簡便な装置や薬剤は
未だ開発されていない。
Such problems are caused by pollution of water quality due to increase of carbon dioxide gas concentration, ammonia nitrogen concentration, nitrate nitrogen concentration, hydrogen sulfide concentration, etc. in the water tank. However, simple devices and medicines that can be easily used in individual small-scale restaurants have not yet been developed.

従って、本発明の目的は、上記従来の問題を解決し、
水の汚濁を容易に防止できる水質汚濁防止樹脂組成物を
提供することである。
Therefore, an object of the present invention is to solve the above conventional problems,
A water pollution preventing resin composition capable of easily preventing water pollution.

(問題点を解決するための手段) 上記目的は以下の本発明によって達成される。(Means for Solving the Problems) The above object is achieved by the present invention described below.

即ち、本発明は、熱可塑性樹脂99.9〜50重量部及び有
効成分0.1〜50重量部(但し、両者の合計量は100重量
部)からなる水質汚濁防止樹脂組成物において、有効成
分が(a)酸化亜鉛、塩化亜鉛、リン酸亜鉛、硝酸亜鉛
及び炭酸亜鉛並びに有機亜鉛塩から選ばれる少なくとも
1種の亜鉛化合物10〜90重量部と(b)有機酸90〜10重
量部(但し、両者の合計量は100重量部)との混合物で
あることを特徴とする水質汚濁防止樹脂組成物である。
That is, the present invention provides a water pollution prevention resin composition comprising 99.9 to 50 parts by weight of a thermoplastic resin and 0.1 to 50 parts by weight of the active ingredient (however, the total amount of both is 100 parts by weight), wherein the active ingredient is (a). 10 to 90 parts by weight of at least one zinc compound selected from zinc oxide, zinc chloride, zinc phosphate, zinc nitrate and zinc carbonate, and organic zinc salts, and (b) 90 to 10 parts by weight of organic acid (however, the total of both The amount is 100 parts by weight) and the mixture is a water pollution control resin composition.

(作用) 亜鉛化合物及び有機酸を熱可塑性樹脂と混合して、例
えば、ペレット状に造粒して水槽に入れ水と接触させる
と、水槽内で魚から発生した種々の汚濁物質、特にアン
モニア態窒素、硝酸態窒素、及び硫化水素等の硫黄分が
吸着され、水槽内の水が浄化される。
(Function) When a zinc compound and an organic acid are mixed with a thermoplastic resin, for example, when granulated into pellets and put in a water tank and brought into contact with water, various pollutants generated from fish in the water tank, particularly ammonia Nitrogen, nitrate nitrogen, and sulfur components such as hydrogen sulfide are adsorbed, and the water in the water tank is purified.

(好ましい実施態様) 次に好ましい実施態様を挙げて本発明を更に詳細に説
明する。
Preferred Embodiment Next, the present invention will be described in more detail with reference to preferred embodiments.

本発明において使用する熱可塑性樹脂とは、従来各種
の成形物、例えば、プラスチックフイルム、プラスチッ
クシート、プラスチック容器、繊維等の成形に使用され
ているポリエチレン、ポリプロピレン等のポリオレフィ
ン樹脂、ポリ塩化ビニル、ビニロン、ポリスチレン、ポ
リアミド、ポリエステル、セルロースアセテート等の合
成又は変性の熱可塑性樹脂であり、これらの熱可塑性樹
脂はいずれも市場から容易に入手して使用し得るもので
あり、これらの熱可塑性樹脂は固体状でもペースト状等
の液状でもよいものである。本発明において特に好適な
熱可塑性樹脂はポリエチレンである。
The thermoplastic resin used in the present invention refers to various molded products conventionally used, for example, plastic film, plastic sheet, plastic container, polyethylene resin used for molding fibers, polyolefin resin such as polypropylene, polyvinyl chloride, vinylon. , A synthetic or modified thermoplastic resin such as polystyrene, polyamide, polyester, cellulose acetate, etc., all of these thermoplastic resins can be easily obtained and used from the market, and these thermoplastic resins are solid. It may be a liquid such as a paste or a paste. A particularly suitable thermoplastic resin in the present invention is polyethylene.

本発明で使用する個々の有効成分はそれ自体はいずれ
も公知の化合物であり、(a)亜鉛化合物としては、酸
化亜鉛、塩化亜鉛、リン酸亜鉛、硝酸亜鉛及び炭酸亜
鉛、並びに酢酸亜鉛、シュウ酸亜鉛、クエン酸亜鉛、フ
マル酸亜鉛、ギ酸亜鉛等の有機亜鉛塩から選ばれる少な
くとも1種が使用される。特に好ましいものは亜鉛華
(酸化亜鉛)及び炭酸亜鉛である。
The individual active ingredients used in the present invention are all known compounds per se, and (a) zinc compounds include zinc oxide, zinc chloride, zinc phosphate, zinc nitrate and zinc carbonate, as well as zinc acetate and shu At least one selected from organic zinc salts such as zinc acid salt, zinc citrate, zinc fumarate and zinc formate is used. Particularly preferred are zinc white (zinc oxide) and zinc carbonate.

本発明で使用する(b)有機酸とは、脂肪酸、芳香族
酸及びポリマー酸が挙げられる。
Examples of the (b) organic acid used in the present invention include fatty acids, aromatic acids and polymeric acids.

脂肪族酸として好ましいのは脂肪族ポリカルボン酸で
あり、例えば、シュウ酸、マロン酸、コハク酸、グルタ
ル酸、アジピン酸、ピメリン酸、フマル酸、マレイン
酸、メチルマレイン酸、メチルフマル酸、イタコン酸、
シトラコン酸、メサコン酸、アセチレン酸、リンゴ酸、
メチルリンゴ酸、クエン酸、イソクエン酸、酒石酸等の
ジ又はトリカルボン酸又はそれらの塩であり、本発明に
おいて特に好ましいものはクエン酸及びフマル酸であ
る。
Preferred aliphatic acids are aliphatic polycarboxylic acids, for example, oxalic acid, malonic acid, succinic acid, glutaric acid, adipic acid, pimelic acid, fumaric acid, maleic acid, methylmaleic acid, methylfumaric acid, itaconic acid. ,
Citraconic acid, mesaconic acid, acetylenic acid, malic acid,
Di- or tricarboxylic acids such as methylmalic acid, citric acid, isocitric acid and tartaric acid, or salts thereof, and particularly preferred in the present invention are citric acid and fumaric acid.

芳香族酸として好ましいのは芳香族ポリカルボン酸で
あり、例えばフタル酸、テレフタル酸、イソフタル酸、
トリメリット酸、1,2,3−ベンゼントリカルボン酸、1,
3,5−ベンゼントリカルボン酸、ピロメリット酸、ベン
ゼンヘキサカルボン酸、ナフタレンジカルボン酸、ナフ
タレントリカルボン酸、ナフタレンテトラカルボン酸、
ジフェニルテトラカルボン酸、ジフェニルエーテルテト
ラカルボン酸、アゾベンゼンテトラカルボン酸等の芳香
族ポリカルボン酸或いはそれらの無水物であり、本発明
において特に好ましい芳香族ポリカルボン酸は、ベンゼ
ントリカルボン酸、特にトリメリット酸である。
Preferred aromatic acids are aromatic polycarboxylic acids such as phthalic acid, terephthalic acid, isophthalic acid,
Trimellitic acid, 1,2,3-benzenetricarboxylic acid, 1,
3,5-benzenetricarboxylic acid, pyromellitic acid, benzenehexacarboxylic acid, naphthalenedicarboxylic acid, naphthalenetricarboxylic acid, naphthalenetetracarboxylic acid,
Aromatic polycarboxylic acids such as diphenyl tetracarboxylic acid, diphenyl ether tetracarboxylic acid, azobenzene tetracarboxylic acid and the like, and particularly preferable aromatic polycarboxylic acid in the present invention is benzene tricarboxylic acid, particularly trimellitic acid. is there.

ポリマー酸としてはその分子中にスルホン酸基、カル
ボン酸基、硫酸エステル基、燐酸エステル基、フェノー
ル性水酸基を有するものであり、例えば下記のものを包
含する。
The polymer acid has a sulfonic acid group, a carboxylic acid group, a sulfuric acid ester group, a phosphoric acid ester group, and a phenolic hydroxyl group in the molecule, and includes, for example, the followings.

イ.カルボン酸基を有するポリマークエン酸、酒石酸、
フタル酸等の多価カルボン酸と、エチレングリコール、
1,4ブタンジオール、ジエチレングリコール等の多価ア
ルコールとを酸過剰で反応させて得られる末端カルボキ
シル基ポリエステル;各種多価カルボン酸で変性した酸
性セルロース誘導体;多価カルボン酸のビニルエーテル
エステルモノマー等の単独重合体又は一般的なモノマー
とのランダム共重合体、ブロック共重合体、グラフト共
重合体等;アクリル酸又はメタクリル酸等の6モノマー
の単独重合体又は他の一般的なモノマーとのランダム共
重合体、ブロック共重合体、グラフト共重合体等;無水
マレイン酸、イタコン酸等のα,β−不飽和ビニルモノ
マー等の単独重合体又は他の一般的なモノマーとのラン
ダム共重合体、ブロック共重合体、グラフト共重合体
等; ロ.スルホン酸基を有するポリマー エチルセルロース酢酸水素硫酸水素フタル酸エステ
ル、セルロース酢酸水素硫酸水素フタル酸、エチルセル
ロース水素スルホ安息香酸エステル、スルホンベンジル
セルロース酢酸エステル、エチルスルホエチルセルロー
ス酢酸エステル等の如きセルロース誘導体;ポリビニル
アルコール又はビニルアルコール共重合体のスルホン酸
化合物(例えば、o−スルホ安息香酸、スルホプロピオ
ン酸、スルホバレリック酸、スルホベンズアルデヒド、
スルホフタル酸等)によるスルホン酸変性ポリマー等; ハ.水酸基を有するポリマー その他スルホン酸やフェノール基を含有するモノマー
の単独重合体又は他の一般的なモノマーとのランダム共
重合体、ブロック共重合体、グラフト共重合体等; その他カルボキシル基又はスルホン酸基又はフェノー
ル基含有化合物による各種重合体の酸性変性物等が挙げ
られる。
I. Polymers having carboxylic acid groups citric acid, tartaric acid,
Polycarboxylic acid such as phthalic acid, ethylene glycol,
Terminal carboxyl group polyesters obtained by reacting polyhydric alcohols such as 1,4 butanediol and diethylene glycol in excess acid; acidic cellulose derivatives modified with various polycarboxylic acids; vinyl ether ester monomers of polycarboxylic acids alone Polymers or random copolymers with general monomers, block copolymers, graft copolymers, etc .; homopolymers of 6 monomers such as acrylic acid or methacrylic acid, or random copolymers with other general monomers. Copolymers, block copolymers, graft copolymers, etc .; homopolymers of α, β-unsaturated vinyl monomers such as maleic anhydride, itaconic acid, etc., or random copolymers with other general monomers, block copolymers Polymers, graft copolymers, etc .; b. Polymers having sulfonic acid groups Cellulose derivatives such as ethyl cellulose hydrogen acetate hydrogensulfate phthalate, cellulose acetate hydrogen hydrogen sulfate phthalate, ethyl cellulose hydrogen sulfobenzoate, sulfone benzyl cellulose acetate, ethyl sulfoethyl cellulose acetate, etc .; polyvinyl alcohol or Sulfonic acid compounds of vinyl alcohol copolymers (for example, o-sulfobenzoic acid, sulfopropionic acid, sulfovaleric acid, sulfobenzaldehyde,
Sulfonic acid-modified polymers with sulfophthalic acid, etc.); Polymers having hydroxyl groups Homopolymers of other monomers containing sulfonic acid or phenol groups or random copolymers, block copolymers, graft copolymers with other general monomers; other carboxyl groups or sulfonic acid groups Alternatively, acidic modified products of various polymers with a phenol group-containing compound may be mentioned.

特に好ましいものは、食品添加剤として安全性が確認
されている脂肪族酸である。
Particularly preferred are aliphatic acids whose safety has been confirmed as a food additive.

以上の如き亜鉛化合物と有機酸からなる有効成分は、
それらの使用比率も重要であって、合計量を100重量部
とすれば、亜鉛化合物が10〜90重量部に対し、有機酸が
90〜10重量部の割合であり、このような組み合わせ及び
配合比において、本発明の目的が最良に達成される。使
用比率が上記範囲から外れると、汚濁防止効果は有るも
のの最適とは云えない。
The active ingredient consisting of a zinc compound and an organic acid as described above,
The ratio of their use is also important, and if the total amount is 100 parts by weight, the zinc compound is 10 to 90 parts by weight, and the organic acid is
The ratio is 90 to 10 parts by weight, and the object of the present invention is best achieved in such a combination and a compounding ratio. If the usage ratio is out of the above range, the effect of preventing pollution is obtained but it cannot be said to be optimum.

又、上記有効成分は熱可塑性樹脂との合計を100重量
部とすると、熱可塑性樹脂99.9〜50重量部及び有効成分
0.1〜50重量部の割合が好適で、熱可塑性樹脂の量が少
なすぎると造粒や成形が困難になり、一方、熱可塑性樹
脂の量が多すぎると汚濁防止効果が不充分になる。
Further, the above-mentioned active ingredient, when the total amount with the thermoplastic resin is 100 parts by weight, the thermoplastic resin is 99.9 to 50 parts by weight and the active ingredient.
A proportion of 0.1 to 50 parts by weight is preferable, and if the amount of the thermoplastic resin is too small, granulation or molding becomes difficult, while if the amount of the thermoplastic resin is too large, the pollution preventing effect becomes insufficient.

本発明の水質汚濁防止樹脂組成物は上記の3成分を必
須成分とするが、その他従来公知の樹脂用の各種添加
剤、例えば、着色剤、充填剤、体質顔料、可塑剤、安定
剤、紫外線吸収剤等は必要に応じて任意に配合し得る。
The water pollution control resin composition of the present invention comprises the above-mentioned three components as essential components, and other various conventionally known additives for resins such as colorants, fillers, extender pigments, plasticizers, stabilizers, and ultraviolet rays. Absorbents and the like may be optionally mixed as needed.

本発明の水質汚濁防止樹脂組成物は粉末状でもよい
が、成形品であることが好ましく、成形品は上記成分を
単に混合し圧縮成形によっても得ることができるが、コ
スト的には混合物を溶融混練押出してペレット状等に造
粒する方法がよい。得られるペレットの粒径は約1〜5m
m程度が好適であるが、用途によっては更に細かくても
粗くてもよい。更に表面積が大きい各種成形物としても
勿論有用である。
Although the water pollution control resin composition of the present invention may be in powder form, it is preferably a molded product, and the molded product can be obtained by simply mixing the above components and compression molding, but in terms of cost, the mixture is melted. A method of kneading and extruding and granulating into pellets or the like is preferable. The particle size of the obtained pellets is about 1-5 m
About m is preferable, but it may be finer or coarser depending on the application. Of course, it is also useful as various molded products having a large surface area.

(実施例) 次に実施例を挙げて本発明を更に具体的に説明する。
尚、文中、部又は%とあるのは特に断りの無い限り重量
基準である。
(Examples) Next, the present invention will be described more specifically with reference to examples.
In the text, parts and% are based on weight unless otherwise specified.

実施例1 低密度ポリエチレン80部に、重量比が8:2のフマル酸
及び酸化亜鉛からなる混合物20部を配合し、ミキサーで
混合し、40mm押出機(L/D=28、C.R.=3.1、ダルメージ
付スクリュー、シリンダー温度130℃、スクリュー回転
速度70rpm)にて混練し、粒径約3mm程度のペレット状の
本発明の水質汚濁防止樹脂組成物を得た。
Example 1 80 parts of low-density polyethylene was mixed with 20 parts of a mixture of fumaric acid and zinc oxide in a weight ratio of 8: 2, mixed with a mixer, and a 40 mm extruder (L / D = 28, CR = 3.1, The mixture was kneaded with a screw equipped with Dullage, a cylinder temperature of 130 ° C., and a screw rotation speed of 70 rpm) to obtain a pellet-like water pollution control resin composition of the present invention having a particle size of about 3 mm.

次いで上記樹脂ペレット1Kgを30メッシュのナイロン
編み袋に入れ、10m3の活魚水槽内に設置し、試験区とし
て鯛50、ヒラメ50尾、ハマチ30尾の養魚を行い、2ケ月
間試験した。その間、水槽中の海水は上記樹脂ペレット
1Kgを含む30メッシュのナイロン編み袋を循環通過する
ようにした。対照区として別の同容量の水槽で鯛50尾、
ヒラメ50尾及びハマチ30尾を、前記ペレットを入れるこ
となく養魚した。これらの2種の水槽中の水質汚濁物質
を比較して下記第1表の結果を得た。
Next, 1 kg of the above resin pellets was placed in a 30-mesh nylon knitting bag, placed in a 10 m 3 tank of live fish, and 50 sea breams, 50 flounders, and 30 yellowtails were cultivated as test areas, and tests were carried out for 2 months. Meanwhile, the seawater in the aquarium is the above resin pellets.
It was circulated through a 30 mesh nylon woven bag containing 1 kg. As a control, another fish tank of the same capacity has 50 sea breams,
50 flounders and 30 yellowtails were cultivated without the pellets. The results of Table 1 below were obtained by comparing the water pollutants in these two types of water tanks.

尚、生存率は対照区が77%で、試験区は98%であっ
た。
The survival rate was 77% in the control group and 98% in the test group.

実施例2〜5 下記の成分を使用し、他は実施例1と同様にして本発
明の水質汚濁防止樹脂組成物を得、実施例1と同様にし
てその性能を測定したところ同様の結果が得られた。
Examples 2 to 5 The following components were used, and the other components were obtained in the same manner as in Example 1 to obtain the water pollution control resin composition of the present invention, and the performance was measured in the same manner as in Example 1. The same results were obtained. Was obtained.

実施例2 高密度ポリエチレン 60部 酸化亜鉛及びクエン酸の8:2混合物 40部 実施例3 ポリプロピレン 70部 炭酸亜鉛及びリンゴ酸の5:5混合物 30部 実施例4 ポリスチレン 75部 塩化亜鉛及びポリアクリル酸の3:7混合物 実施例5 ポリプロピレン 70部 酸化亜鉛及びトリメリット酸の5:5混合物 30部 実施例6 実施例1の樹脂ペレット1Kgを用いてハニカム構造の
成形品を作成し、10m3の活魚水槽内に設置し、試験区と
して鯛40尾、ヒラメ50尾、ハマチ30尾の養魚を行い、2
ケ月間試験した。その間、水槽中の海水は上記成形物の
ハニカム層を循環通過するようにした。一方、対照区と
して別の同容量の水槽中で鯛40尾、ヒラメ50尾及びハマ
チ30尾を、上記成形体を設置することなく養魚した。こ
れらの2種の水槽中の水質汚濁物質を比較して下記第2
表の結果を得た。
Example 2 60 parts of high density polyethylene 40 parts of an 8: 2 mixture of zinc oxide and citric acid Example 3 70 parts of polypropylene 30 parts of a 5: 5 mixture of zinc carbonate and malic acid Example 4 75 parts of polystyrene Zinc chloride and polyacrylic acid 3: 7 mixture of Example 5 Polypropylene 70 parts 5: 5 mixture of zinc oxide and trimellitic acid 30 parts Example 6 A molded product having a honeycomb structure was prepared using 1 kg of the resin pellet of Example 1, and 10 m 3 of live fish was prepared. Installed in the aquarium, 40 sea breams, 50 flounders, and 30 yellowtails were cultivated as test areas.
I tested for a month. Meanwhile, seawater in the water tank was allowed to circulate through the honeycomb layer of the above-mentioned molded product. On the other hand, in another aquarium having the same capacity as a control group, 40 sea breams, 50 flounders and 30 yellowtails were cultivated without installing the above-mentioned molded body. Comparing the water pollutants in these two types of aquariums, the following second
The results in the table were obtained.

尚、生存率は対照区が70%で、試験区は95%であっ
た。
The survival rate was 70% in the control group and 95% in the test group.

又、前記実施例1〜5において試験区と対照区とを比
較した場合、対照区の海水は濁っていること、及び試験
区は海水が透明であることが肉眼ではっきりと認められ
た。
Further, when the test plot and the control plot were compared in Examples 1 to 5, it was clearly visible that the seawater in the control plot was cloudy and that the test plot was transparent.

(効果) 以上の如き本発明によれば、亜鉛化合物及び有機酸を
熱可塑性樹脂と混合して、例えば、ペレット状に造粒し
て水槽に入れ水と接触させると、水槽内で魚から発生し
た種々の汚濁物質、特にアンモニア態窒素、硝酸態窒
素、及び硫化水素等の硫黄分が吸着され、水槽内の水が
浄化される。
(Effect) According to the present invention as described above, when a zinc compound and an organic acid are mixed with a thermoplastic resin, for example, when granulated into pellets and put in a water tank and brought into contact with water, the fish are generated in the water tank. The various pollutants, particularly ammonia nitrogen, nitrate nitrogen, and sulfur components such as hydrogen sulfide are adsorbed, and the water in the water tank is purified.

Claims (3)

(57)【特許請求の範囲】(57) [Claims] 【請求項1】熱可塑性樹脂99.9〜50重量部及び有効成分
0.1〜50重量部(但し、両者の合計量は100重量部)から
なる水質汚濁防止樹脂組成物において、有効成分が
(a)酸化亜鉛、塩化亜鉛、リン酸亜鉛、硝酸亜鉛及び
炭酸亜鉛並びに有機亜鉛塩から選ばれる少なくとも1種
の亜鉛化合物10〜90重量部と(b)有機酸90〜10重量部
(但し、両者の合計量は100重量部)との混合物である
ことを特徴とする水質汚濁防止樹脂組成物。
1. A thermoplastic resin 99.9 to 50 parts by weight and an active ingredient.
In a water pollution control resin composition consisting of 0.1 to 50 parts by weight (however, the total amount of both is 100 parts by weight), the active ingredient is (a) zinc oxide, zinc chloride, zinc phosphate, zinc nitrate and zinc carbonate and organic compounds. Water quality characterized by being a mixture of 10 to 90 parts by weight of at least one zinc compound selected from zinc salts and (b) 90 to 10 parts by weight of organic acid (however, the total amount of both is 100 parts by weight). Pollution control resin composition.
【請求項2】有機酸が脂肪酸である請求項1に記載の水
質汚濁防止樹脂組成物。
2. The water pollution control resin composition according to claim 1, wherein the organic acid is a fatty acid.
【請求項3】ペレット状である請求項1に記載の水質汚
濁防止樹脂組成物。
3. The water pollution control resin composition according to claim 1, which is in the form of pellets.
JP2064148A 1990-03-16 1990-03-16 Water pollution prevention resin composition Expired - Fee Related JP2691466B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP2064148A JP2691466B2 (en) 1990-03-16 1990-03-16 Water pollution prevention resin composition

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP2064148A JP2691466B2 (en) 1990-03-16 1990-03-16 Water pollution prevention resin composition

Publications (2)

Publication Number Publication Date
JPH03267147A JPH03267147A (en) 1991-11-28
JP2691466B2 true JP2691466B2 (en) 1997-12-17

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Country Status (1)

Country Link
JP (1) JP2691466B2 (en)

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* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP6093533B2 (en) * 2012-09-28 2017-03-08 雅広 大塚 Denitrification methods for water treatment and biological wastewater

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JPS5299218A (en) * 1976-02-17 1977-08-19 Toshio Tooyama Deodrant for excrementitious matter
JPS5316459A (en) * 1976-07-28 1978-02-15 Mitsubishi Rayon Co Ltd Fibrous waste water-treating material
JPS5433289A (en) * 1977-08-18 1979-03-10 Mitsubishi Rayon Co Ltd Adsorbent
JPS58180283A (en) * 1982-04-14 1983-10-21 Eitaro Hattori Method for decreasing concentration of nitrous acid in fishpond

Also Published As

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