JPH02229101A - Method and agent for controlling algae - Google Patents
Method and agent for controlling algaeInfo
- Publication number
- JPH02229101A JPH02229101A JP4969789A JP4969789A JPH02229101A JP H02229101 A JPH02229101 A JP H02229101A JP 4969789 A JP4969789 A JP 4969789A JP 4969789 A JP4969789 A JP 4969789A JP H02229101 A JPH02229101 A JP H02229101A
- Authority
- JP
- Japan
- Prior art keywords
- algae
- compound
- genus
- controlling
- dione
- 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.)
- Granted
Links
- 241000195493 Cryptophyta Species 0.000 title claims abstract description 62
- 238000000034 method Methods 0.000 title claims description 9
- SXRSQZLOMIGNAQ-UHFFFAOYSA-N Glutaraldehyde Chemical compound O=CCCCC=O SXRSQZLOMIGNAQ-UHFFFAOYSA-N 0.000 claims abstract description 14
- CAWXEEYDBZRFPE-UHFFFAOYSA-N Hexazinone Chemical compound O=C1N(C)C(N(C)C)=NC(=O)N1C1CCCCC1 CAWXEEYDBZRFPE-UHFFFAOYSA-N 0.000 claims abstract description 8
- 241000243190 Microsporidia Species 0.000 claims abstract description 6
- 239000004480 active ingredient Substances 0.000 claims abstract description 6
- 150000001875 compounds Chemical class 0.000 claims description 23
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims description 16
- 229940126062 Compound A Drugs 0.000 claims description 11
- NLDMNSXOCDLTTB-UHFFFAOYSA-N Heterophylliin A Natural products O1C2COC(=O)C3=CC(O)=C(O)C(O)=C3C3=C(O)C(O)=C(O)C=C3C(=O)OC2C(OC(=O)C=2C=C(O)C(O)=C(O)C=2)C(O)C1OC(=O)C1=CC(O)=C(O)C(O)=C1 NLDMNSXOCDLTTB-UHFFFAOYSA-N 0.000 claims description 11
- 239000003795 chemical substances by application Substances 0.000 claims description 7
- 241000192608 Phormidium Species 0.000 claims description 5
- 241000159614 Ulothrix Species 0.000 abstract description 4
- 238000005187 foaming Methods 0.000 abstract description 4
- 239000000126 substance Substances 0.000 abstract description 4
- 229960000587 glutaral Drugs 0.000 abstract 2
- 230000000694 effects Effects 0.000 description 7
- 230000002195 synergetic effect Effects 0.000 description 7
- 239000003619 algicide Substances 0.000 description 6
- 238000002835 absorbance Methods 0.000 description 5
- 238000001816 cooling Methods 0.000 description 5
- 241000192542 Anabaena Species 0.000 description 3
- 241000195649 Chlorella <Chlorellales> Species 0.000 description 3
- 241000195628 Chlorophyta Species 0.000 description 3
- 230000002353 algacidal effect Effects 0.000 description 3
- XMTQQYYKAHVGBJ-UHFFFAOYSA-N 3-(3,4-DICHLOROPHENYL)-1,1-DIMETHYLUREA Chemical compound CN(C)C(=O)NC1=CC=C(Cl)C(Cl)=C1 XMTQQYYKAHVGBJ-UHFFFAOYSA-N 0.000 description 2
- 241000192700 Cyanobacteria Species 0.000 description 2
- 238000007792 addition Methods 0.000 description 2
- 239000007864 aqueous solution Substances 0.000 description 2
- 238000005260 corrosion Methods 0.000 description 2
- 230000006866 deterioration Effects 0.000 description 2
- 239000003814 drug Substances 0.000 description 2
- 229940079593 drug Drugs 0.000 description 2
- 238000011156 evaluation Methods 0.000 description 2
- 239000008235 industrial water Substances 0.000 description 2
- 231100000053 low toxicity Toxicity 0.000 description 2
- 239000000203 mixture Substances 0.000 description 2
- IZUPBVBPLAPZRR-UHFFFAOYSA-N pentachlorophenol Chemical compound OC1=C(Cl)C(Cl)=C(Cl)C(Cl)=C1Cl IZUPBVBPLAPZRR-UHFFFAOYSA-N 0.000 description 2
- UUIVKBHZENILKB-UHFFFAOYSA-N 2,2-dibromo-2-cyanoacetamide Chemical compound NC(=O)C(Br)(Br)C#N UUIVKBHZENILKB-UHFFFAOYSA-N 0.000 description 1
- HSQFVBWFPBKHEB-UHFFFAOYSA-N 2,3,4-trichlorophenol Chemical compound OC1=CC=C(Cl)C(Cl)=C1Cl HSQFVBWFPBKHEB-UHFFFAOYSA-N 0.000 description 1
- 241000894006 Bacteria Species 0.000 description 1
- LVDKZNITIUWNER-UHFFFAOYSA-N Bronopol Chemical compound OCC(Br)(CO)[N+]([O-])=O LVDKZNITIUWNER-UHFFFAOYSA-N 0.000 description 1
- ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 description 1
- 229910019142 PO4 Inorganic materials 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 230000005791 algae growth Effects 0.000 description 1
- 230000000844 anti-bacterial effect Effects 0.000 description 1
- 239000003899 bactericide agent Substances 0.000 description 1
- 125000004432 carbon atom Chemical group C* 0.000 description 1
- 150000001735 carboxylic acids Chemical class 0.000 description 1
- 229910052801 chlorine Inorganic materials 0.000 description 1
- 239000000460 chlorine Substances 0.000 description 1
- 238000004140 cleaning Methods 0.000 description 1
- 230000000052 comparative effect Effects 0.000 description 1
- 230000001276 controlling effect Effects 0.000 description 1
- 239000000498 cooling water Substances 0.000 description 1
- 230000007797 corrosion Effects 0.000 description 1
- 230000006378 damage Effects 0.000 description 1
- 230000003247 decreasing effect Effects 0.000 description 1
- 238000010586 diagram Methods 0.000 description 1
- SXUYADQBBAAFOO-UHFFFAOYSA-N dithiol-3-one Chemical compound O=C1C=CSS1 SXUYADQBBAAFOO-UHFFFAOYSA-N 0.000 description 1
- 230000005611 electricity Effects 0.000 description 1
- 238000005516 engineering process Methods 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- ZHCJUZJGMJDUKJ-UHFFFAOYSA-M ethyl(phosphonatooxy)mercury;hydron Chemical compound CC[Hg+].OP(O)([O-])=O ZHCJUZJGMJDUKJ-UHFFFAOYSA-M 0.000 description 1
- LYCAIKOWRPUZTN-UHFFFAOYSA-N ethylene glycol Natural products OCCO LYCAIKOWRPUZTN-UHFFFAOYSA-N 0.000 description 1
- 230000003203 everyday effect Effects 0.000 description 1
- 239000000835 fiber Substances 0.000 description 1
- -1 glycol ethers Chemical class 0.000 description 1
- 150000002334 glycols Chemical class 0.000 description 1
- WGCNASOHLSPBMP-UHFFFAOYSA-N hydroxyacetaldehyde Natural products OCC=O WGCNASOHLSPBMP-UHFFFAOYSA-N 0.000 description 1
- 230000007794 irritation Effects 0.000 description 1
- 150000002731 mercury compounds Chemical class 0.000 description 1
- 150000002736 metal compounds Chemical class 0.000 description 1
- 239000007769 metal material Substances 0.000 description 1
- VLAPMBHFAWRUQP-UHFFFAOYSA-L molybdic acid Chemical compound O[Mo](O)(=O)=O VLAPMBHFAWRUQP-UHFFFAOYSA-L 0.000 description 1
- 231100000252 nontoxic Toxicity 0.000 description 1
- 230000003000 nontoxic effect Effects 0.000 description 1
- 235000019645 odor Nutrition 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 239000000546 pharmaceutical excipient Substances 0.000 description 1
- XEBWQGVWTUSTLN-UHFFFAOYSA-M phenylmercury acetate Chemical compound CC(=O)O[Hg]C1=CC=CC=C1 XEBWQGVWTUSTLN-UHFFFAOYSA-M 0.000 description 1
- 235000021317 phosphate Nutrition 0.000 description 1
- 150000003009 phosphonic acids Chemical class 0.000 description 1
- 150000003013 phosphoric acid derivatives Chemical class 0.000 description 1
- 239000000843 powder Substances 0.000 description 1
- 230000035755 proliferation Effects 0.000 description 1
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 1
- 230000001105 regulatory effect Effects 0.000 description 1
- 230000000717 retained effect Effects 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 239000004094 surface-active agent Substances 0.000 description 1
- 231100000331 toxic Toxicity 0.000 description 1
- 230000002588 toxic effect Effects 0.000 description 1
- 231100000419 toxicity Toxicity 0.000 description 1
- 230000001988 toxicity Effects 0.000 description 1
- 238000011179 visual inspection Methods 0.000 description 1
- 229920003169 water-soluble polymer Polymers 0.000 description 1
Landscapes
- Agricultural Chemicals And Associated Chemicals (AREA)
Abstract
Description
【発明の詳細な説明】
(イ)産業上の利用分野
この発明は、藻類防除剤及び藻類防除方法に関する。さ
らに詳しくは、各種工業用水・排水系や各種貯水系にお
ける藻類の繁殖によって生じる障害の防止に著効を発揮
する藻類防除剤及び藻類防除方法に関する。DETAILED DESCRIPTION OF THE INVENTION (a) Field of Industrial Application This invention relates to an algae control agent and an algae control method. More specifically, the present invention relates to algae control agents and algae control methods that are highly effective in preventing problems caused by algae growth in various industrial water/drainage systems and various water storage systems.
(ロ)従来の技術
各種工業用水・排水系や各種貯水系、より具体的には、
冷却水系におけるクーリングタワーや貯水ピット及びプ
ールや開放貯水槽などの日光が照射する各種水系におい
て、クロレラ属やアナベナ属等で代表されろ緑藻類や藍
藻類が繁殖し、水質の悪化、悪臭の発生及び美感を損う
等の障害をもたらし、特にクーリングタワーにおいては
冷却効率が低下したり、金属材料の腐食を誘起したり、
剥離したこれら藻類が冷却系を閉塞する等の種々の障害
をもたらすことは従来から知られている。(b) Conventional technology Various industrial water/drainage systems and various water storage systems, more specifically,
In various water systems that are exposed to sunlight, such as cooling towers, water storage pits, pools, and open water tanks in cooling water systems, green algae and blue-green algae, such as those of the genus Chlorella and Anabaena, proliferate, resulting in deterioration of water quality, generation of bad odors, and aesthetic appearance. In particular, in cooling towers, cooling efficiency may be reduced, corrosion of metal materials may be induced, and
It has been known that these exfoliated algae cause various problems such as clogging the cooling system.
そのため従来からの種々の殺藻剤が提案されており、古
くは、エチルりん酸水銀や酢酸フェニル水銀等の有機水
銀化合物、ペンタクロロフェノールやトリクロロフェノ
ール等の塩素系化合物が使用されていた。しかし、かか
る薬剤は毒性が強いため好ましいものではなく公害上の
点から使用の規制もなされている。Therefore, various algaecides have been proposed in the past, and in the past, organic mercury compounds such as ethylmercury phosphate and phenylmercury acetate, and chlorine-based compounds such as pentachlorophenol and trichlorophenol were used. However, such drugs are not desirable because they are highly toxic, and their use is regulated from the viewpoint of pollution.
この点に関し、比較的毒性の低い化合物を殺藻剤として
用いる提案も従来から種々なされている。In this regard, various proposals have been made to use relatively low toxicity compounds as algaecides.
この発明に用いるグルタルジアルデヒドは単独で藻類防
除剤として公知であり、また第4級アンモニウム塩と併
用することにより相乗効果が発揮されることも知られて
いる(特開昭62−96401号公報)。一方、この発
明に用いる3−シクロへキシル−6−(ツメチルアミノ
)−1−メチル−1,35−トリアジン−2,4(LH
,3H)ジオン(一般名へキサジノン)も藻類防除剤と
して公知である(特公昭60−3361号公報)。The glutardialdehyde used in this invention is known alone as an algae control agent, and it is also known that a synergistic effect is exhibited when used in combination with a quaternary ammonium salt (JP-A-62-96401). ). On the other hand, 3-cyclohexyl-6-(tumethylamino)-1-methyl-1,35-triazine-2,4(LH
, 3H) dione (common name: hexazinone) is also known as an algae control agent (Japanese Patent Publication No. 3361/1983).
(ハ)発明が解決しようとする課題
しかしながら、上記低毒性の化合物を使用しても、現場
における藻類の防除効果が実用濃度使用下で不充分な場
合が多々あった。そして、この発明の発明者らがこの原
因を調査した結果、防除効果の低減が著しい対象藻類は
、緑藻網であるヒビミドロ亜目(旧otrichine
ae)を含む藻類であることを確認した。かかるヒビミ
ドロ亜目の藻類は、すべて無分技の糸状体を形成して繊
維状に繁殖するため各種スケール成分やスライム構成菌
を巻き込んで成長し、これらスケール等で部分的に保護
された形態である。このため同じ緑藻網に属するクロレ
ラ属(Chlorella)や藍藻綱に属するアナベナ
属(Anabaena)に属する藻類等と比較して化合
物による防除作用に耐性を示しその結果、防除効果が不
充分になるものと考えられる。そしてこの亜目中、特に
障害となる藻類はホルミディウム属(Hormidiu
m)、ヒビミドロ属(Ulothrix)又はミクロス
ポラ属(Microspora)に属し、これらの藻類
に対しては、前述したグルタルジアルデヒドやヘキサジ
ノンを通常の添加濃度(クロレラ属やアナベナ属を防除
出来る濃度)で使用しても有効ではなかった。(c) Problems to be Solved by the Invention However, even when the above-mentioned low toxicity compounds are used, the algae control effect in the field is often insufficient at practical concentrations. As a result of investigating the cause of this, the inventors of the present invention found that the target algae with a markedly reduced control effect were members of the green algae, the suborder Hibimidorinae (formerly otrichine).
It was confirmed that the algae contained Ae). All of these algae of the suborder Hibimida form undivided filaments and reproduce in the form of fibers, so they grow by involving various scale components and slime-forming bacteria, and are partially protected by these scales. be. For this reason, compared to algae belonging to the genus Chlorella, which belongs to the same green algae network, and algae, which belong to the genus Anabaena, which belongs to the cyanobacteria, they are resistant to the control action of compounds, and as a result, the control effect is insufficient. Conceivable. Within this suborder, the algae that cause particular problems are of the genus Hormidium.
m) belongs to the genus Ulothrix or Microspora, and for these algae, use the aforementioned glutardialdehyde or hexazinone at the usual concentration (concentration that can control Chlorella and Anabaena). However, it was not effective.
この発明はかかる問題点を解決すべくなされたものであ
る。This invention has been made to solve these problems.
この発明の発明者らは、実用上の殺藻性を示す多数の化
合物について種々研究を行った結果、上記したグルタル
ジアルデヒドとへキサジノンとを併用した際に、単独使
用時では得られない相乗的に優れた防除効果が得られる
こと、特にホルミディウム属、ヒビミドロ属又はミクロ
スポラ属に属するヒビミドリ亜目の藻類に対して顕著な
相乗効果が発揮されるため、他の藻類の防除濃度と同程
度の低濃度でこれら藻類を効率良く防除出来る事実を見
い出した。そしてかかる組合せにおいては毒性のみなら
ず腐食性、刺激性、発泡性等の点でも工業上有利である
ことに着目しこの発明に到達した。The inventors of this invention have conducted various studies on a large number of compounds that exhibit practical algicidal properties, and have found that when the above-mentioned glutardialdehyde and hexazinone are used in combination, a synergistic effect that cannot be obtained when used alone. In particular, it has a remarkable synergistic effect against algae belonging to the suborder Phormidium, Hibimidoro, or Microspora, so it can be used at a concentration comparable to that of other algae. We have discovered that these algae can be effectively controlled at low concentrations. The present invention was achieved based on the fact that such a combination is industrially advantageous not only in terms of toxicity but also in terms of corrosiveness, irritation, and foaming properties.
(ニ)課題を解決するための手段
かくしてこの発明によれば有効成分としてグルタルジア
ルデヒド(化合物A)と3−シクロヘキシル−6−(ジ
メチルアミノ)−1−メチル−1,35−トリアジン−
2,4−(LH,3H)ジオン(化合物B)とを99・
1〜50・50の重量比で含有してなる藻類防除剤が提
供される。(d) Means for Solving the Problems Thus, according to the present invention, glutardialdehyde (compound A) and 3-cyclohexyl-6-(dimethylamino)-1-methyl-1,35-triazine-
2,4-(LH,3H)dione (compound B) at 99.
An algae control agent containing the algae in a weight ratio of 1 to 50.50 is provided.
この発明に用いるグルタルジアルデヒドは、任意の市販
級のものでもよく、一般にグルタルジアルデヒドを約5
0W/Y%まで含有する水溶液として人手出来る。The glutardialdehyde used in this invention may be of any commercially available grade, and generally contains about 50% glutardialdehyde.
It can be prepared manually as an aqueous solution containing up to 0 W/Y%.
一方、3−シクロへキシル−6−(ジメチルアミノ)−
1−メチル−1,3,5−トリアジン−2,4−C11
(3H)ジオンは、特開昭53−56323号公報記載
に従って合成することも出来るが、一般にはへキサジノ
ン[化合物(B)100%の粉末]として入手出来る。On the other hand, 3-cyclohexyl-6-(dimethylamino)-
1-methyl-1,3,5-triazine-2,4-C11
Although (3H)dione can be synthesized according to the description in JP-A-53-56323, it is generally available as hexazinone [100% powder of compound (B)].
上記化合物(A)と化合物(B)の併合比率は99:1
〜50:50とされ、この範囲から逸脱すると相乗効果
の発揮される程度か低下し適さない。The combination ratio of the above compound (A) and compound (B) is 99:1
~50:50, and if it deviates from this range, the degree of synergistic effect will decrease and is not suitable.
化合物(A)と化合物(B)の比率として98・2〜6
0:40とずろのか顕著な相乗効果が発揮されるためよ
り好ましく、95.5〜70:30とするのが特に好ま
しい。The ratio of compound (A) and compound (B) is 98.2 to 6
A ratio of 0:40 is more preferable because a remarkable synergistic effect is exhibited, and a ratio of 95.5 to 70:30 is particularly preferred.
上記化合物は通常これらを直接混合した形態で種々の対
象系に用いられる。この際両者とも水に易溶であるため
、有効成分として3〜60重量%含有する水溶液の形態
で用いるのか適している。この際、池の有機溶媒(グリ
コール類、グリコールエーテル類、炭素数8までのアル
コール類、エステル類など)や界面活性剤、防食・スケ
ール防止剤(重合リン酸塩、ポスホン酸類、モリブデン
酸又はその塩、二価金属化合物、各種カルボン酸類、水
溶性ポリマーなど)又は殺菌剤(5−クロル−2メヂル
ーイソチアゾロン−3−オン、メヂレンビスチオシアナ
ート、4,5−ジクロル−12−ジチオール−3−オン
、2,2−ジブロモ−3−ニトリロプロピオンアミド及
び2−ブロモ−2−二トロプロパン−1,3−ジオール
等の脂肪族ニトロアルコール類など)などを併用しても
よい。The above compounds are usually used in the form of direct mixtures for various target systems. In this case, since both are easily soluble in water, it is suitable to use them in the form of an aqueous solution containing 3 to 60% by weight as an active ingredient. At this time, organic solvents (glycols, glycol ethers, alcohols with up to 8 carbon atoms, esters, etc.), surfactants, anti-corrosion/scaling agents (polymerized phosphates, phosphonic acids, molybdic acid or their salts, divalent metal compounds, various carboxylic acids, water-soluble polymers, etc.) or bactericides (5-chloro-2-medylyisothiazolone-3-one, medilene bisthiocyanate, 4,5-dichloro-12- Aliphatic nitro alcohols such as dithiol-3-one, 2,2-dibromo-3-nitrilopropionamide, and 2-bromo-2-nitropropane-1,3-diol, etc.) may be used in combination.
たたし、訂記各化合物は、場合によっては別々に添加し
てもよい。従って池の観点から、この発明によれば、藻
類防除対象水系に化合物Aと化合物Bとを99.1〜5
0・50(重量比)の比率て微量添加することを特徴と
する藻類防除方法か提供される。この場合の併用比率も
前記のように982〜6040とするのが好ましく、9
55〜70:30とするのがより好ましい。However, each compound may be added separately depending on the case. Therefore, from the viewpoint of ponds, according to the present invention, compound A and compound B are added to the water system for algae control at 99.1 to 5
A method for controlling algae is provided, which is characterized in that a trace amount of the algae is added at a ratio of 0.50 (weight ratio). In this case, the combination ratio is preferably 982 to 6040 as described above, and 9
More preferably, the ratio is 55 to 70:30.
特に防除対象藻類としてホルミディウム属、ヒビミトロ
属又はミクロスポラ属で代表されるヒヒミドロ亜目に属
する藻類が存在する場合には、化合物A又は化合物B単
独では、多量電力0しても、良好な防藻効果が発揮され
ないのに比較して、この発明においては、顕著な相乗効
果が発揮され低添加量でこれら障害となる藻類を防除出
来る。In particular, when the algae to be controlled are algae belonging to the suborder Hihimidorinae represented by the genus Phormidium, genus Hibimitoro, or Microspora, compound A or compound B alone has a good algae control effect even when the amount of electricity is 0. In contrast, in the present invention, a remarkable synergistic effect is exhibited and these harmful algae can be controlled with a low addition amount.
この発明において有効成分(化合物Aと化合物B)の添
加量は、藻類防除対象水に対して0.5〜50x’i/
Q、好ましくは、1〜30屑g/Qである。添加量が0
.5mg/Q未満であると藻類防除効果が低下するため
好ましくない。また、5Qtttgi1以上添加しても
良いが経済的な理由で好ましくない。In this invention, the amount of the active ingredients (compound A and compound B) added is 0.5 to 50x'i/ to the water targeted for algae control.
Q, preferably 1 to 30 scraps/Q. Added amount is 0
.. If it is less than 5 mg/Q, the algae control effect will decrease, which is not preferable. Further, 5Qtttgi1 or more may be added, but this is not preferred for economical reasons.
一
この発明を以下の代表的な実施例及び試験例を用いて説
明する。- This invention will be explained using the following representative examples and test examples.
(ポ)実施例
実施例
某石油化学系会社の小型クリーニングタワーの散水板に
大量の藻類が付着し著しい機能低下が認められた。そこ
でグルタルジアルデヒドを有効成分として保有水量に対
し、30rttg/Qとなるように1週間に1度バッチ
添加を行った。1ケ月後、藻類はわずかに減少したかに
見えたが、なお障害は解決出来なかった(比較例)。こ
れらの藻類を採取し同定したところ、ヒビミドロ亜目の
ホルミディウム属(I(ormidium)、ヒビミド
ロ属(Ulothrix)及びミクロスポラ属(Mic
rospora)に属する藻類がその主体をなしていた
。(Po) Example Example A large amount of algae adhered to the water sprinkling plate of a small cleaning tower of a certain petrochemical company, and a significant deterioration in functionality was observed. Therefore, glutardialdehyde was added as an active ingredient in batches once a week so that the amount of water retained was 30 rttg/Q. After one month, the algae seemed to have decreased slightly, but the problem still remained unresolved (comparative example). When these algae were collected and identified, it was found that the genus Phormidium (ormidium I), the genus Ulothrix, and the genus Microspora (Mic) belong to the suborder Hybimyridae.
The main body was algae belonging to the genus rospora.
そこでグルタルンアルデヒド9重量部、3−シクロへキ
シル−6−(ジメチルアミノ)−1−メチル−1,3,
5−トリアジノ−2,4(IH,,3)t)ジオン1重
量部、水90重量部からなる組成物を有効成分として保
有水量に対して5mg/lバツチ添加したところ、1週
間後には藻類の付着は認められなかった。その後の1週
間に1度上記濃度でバッチ添加を行った。2力月経過後
においても藻類の付着は認められず良好であった。Therefore, 9 parts by weight of glutaraldehyde, 3-cyclohexyl-6-(dimethylamino)-1-methyl-1,3,
When a composition consisting of 1 part by weight of 5-triazino-2,4(IH,,3)t)dione and 90 parts by weight of water was added as an active ingredient in batches of 5 mg/l to the amount of water held, algae appeared after one week. No adhesion was observed. Batch additions were made once a week thereafter at the above concentrations. Even after 2 months, no algae adhesion was observed and the condition was good.
試験例
某冷却塔の散水板より採取したホルミディウム属(Ho
rmidium)及びヒヒミドロ属(Ulothrix
)の藻類をそれぞれMIN培地の入った培養フラスコに
入れ温度25℃において照度1500ルクスの光を与え
ながら10日間振盪し十分培養繁殖させた。培養した藻
類を10ccづつL型試験管に分注し、次に薬剤を添加
し、光電比色系にて初期吸光度を測定した。その後一定
温度(25°C)で光1LL500ルクスの光を与えて
7日間連続振盪し、−日一度定時に吸光度を測定し、濁
度の経口変化を確認すると共に7日間の吸光度の増減に
より次式によって殺藻率を算出した。Test example Phormidium (Ho) collected from the water sprinkler plate of a certain cooling tower
rmidium) and Ulothrix
) were placed in culture flasks containing MIN medium and shaken for 10 days at a temperature of 25° C. while providing light with an illuminance of 1500 lux to allow sufficient culture and propagation. 10 cc of the cultured algae was dispensed into L-shaped test tubes, then the drug was added, and the initial absorbance was measured using a photoelectric colorimetric system. After that, the light of 1 LL 500 lux was applied at a constant temperature (25°C) and the light was continuously shaken for 7 days, and the absorbance was measured at a fixed time once every - day to confirm the oral change in turbidity and the increase or decrease in absorbance over the 7 days. The algaecide rate was calculated using the formula.
(以下余白) Ax A。(Margin below) Ax A.
Bx B。Bx B.
BX: 78目のブランク吸光度 Bo=初期の 〃 AX+7日目の薬剤添加物吸光度 Ao:初期の 〃 試験結果を第1表に示す。BX: 78th blank absorbance Bo = early Drug additive absorbance on AX+7th day Ao: Early The test results are shown in Table 1.
(以下余白)
第1表、試験結果
*1.殺藻率評価・・・・・・第1表中殺藻率の評価は
、次の基準に従って評価し
評価1・
2・・・
3・・・・・・
4・・・・・
5・・・
6・・・・・・
7・・・・
*2.化合物A
*3.化合物B・・・
100%
80〜100%
60〜80%
40〜60%
20〜40%
0〜20%
0%
・・グルタルジアルデヒド
・3−シクロへキシル−6−(ジ
メチルアミノ)−1−メチル
1.3.5− )リアジン−2,4
(1H,3H)ジオン
*4.DCMU・・・・・3− (3,4−ジクロロフ
ェニル)1.1−ジメチル尿素(公知の
除藻剤)
但し、評価Iについては、目視により藻類の緑色が脱色
し、試験後の藻類を新しいMIN培地の入った培養フラ
スコに入れ、温度25°Cにおいて照度1500ルクス
の光を与えながら10日間振盪培養を行ったが藻類は増
殖せず、この結果から上記試験後の藻類は死滅している
ことを確認した。(Left below) Table 1, Test results *1. Evaluation of algaecide rate...The algaecide rate in Table 1 was evaluated according to the following criteria and evaluated as 1, 2... 3... 4... 5...・ 6... 7... *2. Compound A *3. Compound B... 100% 80-100% 60-80% 40-60% 20-40% 0-20% 0% Glutardialdehyde 3-cyclohexyl-6-(dimethylamino)-1- Methyl 1.3.5-) riazine-2,4 (1H,3H)dione*4. DCMU...3-(3,4-dichlorophenyl)1,1-dimethylurea (known algaecide) However, for evaluation I, the green color of the algae is bleached by visual inspection, and the algae after the test is The algae were placed in a culture flask containing MIN medium and cultured with shaking for 10 days at a temperature of 25°C while providing light with an illuminance of 1500 lux, but the algae did not proliferate, and from this result, the algae after the above test were dead. It was confirmed.
なお、グルタルジアルデヒド(化合物A)とへキサジノ
ン(化合物B)の使用比率と、殺藻効果との関係を、第
1図に示した。このように、化合物Aと化合物Bを約9
9:l〜50:50の使用比率の範囲内で各単独使用時
では得られない優れた相乗的殺藻効果が得られているこ
とが判る。Incidentally, the relationship between the usage ratio of glutardialdehyde (compound A) and hexazinone (compound B) and the algicidal effect is shown in FIG. In this way, compound A and compound B can be combined at about 9
It can be seen that an excellent synergistic algicidal effect, which cannot be obtained when each of these is used alone, is obtained within the range of usage ratios of 9:1 to 50:50.
(へ)発明の効果
この発明によれば、藻類ことにヒビミドロ亜目系の藻類
の繁殖による各種の障害を、より低濃度の薬剤の使用に
より解消することができ、ことに他の藻類と同様な使用
濃度で障害防除が可能となる。(f) Effects of the invention According to this invention, various problems caused by the proliferation of algae, especially algae of the suborder Hibimyridae, can be eliminated by using a lower concentration of chemicals, and in particular, the same as that of other algae. It is possible to prevent damage at a concentration that is suitable for use.
そして、用いる薬剤自体も毒性、腐食性、刺激性、発泡
性がないか又は低いものである。The chemicals used themselves are also non-toxic, corrosive, irritating, and foaming, or have low foaming properties.
従って、この発明の工業上の有用性は極めて大きなもの
である。Therefore, the industrial utility of this invention is extremely large.
第1図は、この発明におけるグルタルジアルデヒトとヘ
キサノノンとの使用比率と投原効果との関係を例示する
グラフ図である。FIG. 1 is a graph diagram illustrating the relationship between the usage ratio of glutardialdehyde and hexanonone and the cast effect in the present invention.
Claims (1)
と3−シクロヘキシル−6−(ジメチルアミノ)−1−
メチル−1,3,5−トリアジン−2,4−(1H,3
H)ジオン(化合物B)とを99:1〜50:50の重
量比で含有してなる藻類防除剤。 2、化合物Aと化合物Bとを重量比で98:2〜60:
40で含有してなる請求項1記載の藻類防除剤。 3、藻類防除対象水系に化合物Aと化合物Bとを99:
1〜50:50(重量比)の比率で微量添加することを
特徴とする藻類防除方法。 4、化合物Aと化合物Bの添加比率が98:2〜60:
40である請求項3記載の藻類防除方法。 5、添加量が、藻類防除対象水に対して0.5〜50m
g/lである請求項3及び請求項4記載の藻類防除方法
。 6、防除すべき藻類がヒビミドロ亜目に属する藻類であ
る請求項3〜5のいずれかに記載の藻類防除方法。 7、防除すべき藻類が、ホルミディウム属、ヒビミドロ
属又はミクロスポラ属の藻類である請求項6記載の藻類
防除方法。[Claims] 1. Glutardialdehyde (compound A) as an active ingredient
and 3-cyclohexyl-6-(dimethylamino)-1-
Methyl-1,3,5-triazine-2,4-(1H,3
H) dione (compound B) in a weight ratio of 99:1 to 50:50. 2. Compound A and compound B in a weight ratio of 98:2 to 60:
40. The algae control agent according to claim 1, comprising: 3. Add 99% of compound A and compound B to the water system for algae control.
A method for controlling algae, characterized by adding a small amount at a ratio of 1 to 50:50 (weight ratio). 4. Addition ratio of compound A and compound B is 98:2 to 60:
40. The method for controlling algae according to claim 3. 5. The amount added is 0.5 to 50 m to the water targeted for algae control.
The method for controlling algae according to claims 3 and 4, wherein the amount is g/l. 6. The method for controlling algae according to any one of claims 3 to 5, wherein the algae to be controlled are algae belonging to the suborder Hibimida. 7. The algae control method according to claim 6, wherein the algae to be controlled are algae of the genus Phormidium, genus Hibimidoro, or genus Microspora.
Priority Applications (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4969789A JP2502731B2 (en) | 1989-02-28 | 1989-02-28 | Algae controlling agent and algae controlling method |
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
JP4969789A JP2502731B2 (en) | 1989-02-28 | 1989-02-28 | Algae controlling agent and algae controlling method |
Publications (2)
Publication Number | Publication Date |
---|---|
JPH02229101A true JPH02229101A (en) | 1990-09-11 |
JP2502731B2 JP2502731B2 (en) | 1996-05-29 |
Family
ID=12838372
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
JP4969789A Expired - Lifetime JP2502731B2 (en) | 1989-02-28 | 1989-02-28 | Algae controlling agent and algae controlling method |
Country Status (1)
Country | Link |
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JP (1) | JP2502731B2 (en) |
Cited By (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114621874A (en) * | 2021-12-28 | 2022-06-14 | 宁波浮田生物技术有限公司 | Microalgae culture medium and application |
-
1989
- 1989-02-28 JP JP4969789A patent/JP2502731B2/en not_active Expired - Lifetime
Cited By (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
CN114621874A (en) * | 2021-12-28 | 2022-06-14 | 宁波浮田生物技术有限公司 | Microalgae culture medium and application |
CN114621874B (en) * | 2021-12-28 | 2023-09-29 | 宁波浮田生物技术有限公司 | Microalgae culture medium and application thereof |
Also Published As
Publication number | Publication date |
---|---|
JP2502731B2 (en) | 1996-05-29 |
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