• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    An object of the present invention is bordeaux liquid additives and additives that are excellent in dispersion stability during preparation and long-term storage, excellent electrodeposition stability immediately after dispersion and drying, and satisfies three requirements for easy visual confirmation of adhesion amount immediately after dispersion. It is to provide a Bordeaux liquid containing. The present invention has a molecular weight of 5,000 obtained by copolymerizing an unsaturated monocarboxylic acid alkoxypolyalkylene glycol adduct monomer (a) having an HLB value of 3.0 to 7.0 and a monomer (b) which is an unsaturated carboxylic acid derivative in a molar ratio of 1/1 to 1 / 9.5. It relates to a Bordeaux liquid additive containing a polymer of from 80,000 to 80,000.
    公开号:KR20030010609A
    申请号:KR1020027014325
    申请日:2001-04-27
    公开日:2003-02-05
    发明作者:고바야시도요히사；사카시타마사루
    申请人:닛폰 유시 가부시키가이샤；이노우에셋카이코교가부시키가이샤；
    IPC主号:
    专利说明:

    Bordeaux liquid additive and Bordeaux liquid {Additive for Bordeaux mixtrue and Bordeaux mixture}
    [2] It has long been known that copper ions have bactericidal action, and in 1882, Miylarde of France discovered that a mixture of copper sulfate and lime (Bordeaux) was effective against grape fungal disease. It is widely used as a fungicide of. The active ingredient of the Bordeaux liquid composition is basic copper calcium sulfate, and is generally represented by CuSO 4 .xCu (OH) 2 .yCa (OH) 2 .zH 2 O. Since basic copper sulfate has a large specific gravity (2.24 for hydrated lime and 2.28 for copper sulfate), it segregates and segregates due to specific gravity difference. Therefore, it was necessary to spread as soon as possible after preparation.
    [3] Bordeaux liquid is not only troublesome because it has been self-prepared in the past, but also the quality of the Bordeaux liquid is not constant according to the operator's experience or the quality of copper sulfate or lime. As a result, the effect was uneven and even weakening was caused by the concentration of copper ions or lime in some crops. Instead, the development of Bordeaux liquid as a prescription liquid with uniform quality and easy dispensing of the dispersion liquid has been made.
    [4] In the conventional basic Bordeaux liquid preparation method, first, copper sulfate is pulverized and dissolved in 80 to 90% of the total amount of water, and quicklime is added to the total amount of 10 to 20% of water after adding a small amount of water. The copper sulfate solution is gradually added while stirring and mixing the lime oil, followed by adding an additive such as an electrodeposition agent.
    [5] The types of additives and their preparation methods are described in, for example, Japanese Patent Application Laid-Open No. 51-22573, Japanese Patent Application Laid-Open No. 53-52622, Japanese Patent Application Laid-Open No. 61-63601 Japanese Patent Application Laid-Open No. 62-226905, Japanese Patent Application Laid-Open No. 2-279610, Japanese Patent Application Laid-Open No. 2-279611, Japanese Patent Application Laid-Open No. 198102, etc. It is proposed to use a carboxy-containing vinyl compound homopolymer or a copolymer containing the same as a dispersant. In particular, Japanese Patent Application Laid-Open No. 51-22573 added a water-soluble polymer to an aqueous dispersion to stabilize it as a plant growing agent. Japanese Laid-Open Patent Publication No. 53-52622 is characterized in that lignin sulfonic acid, polyvinyl alcohol, carboxymethyl cellulose, gum arabic or alginate is mixed with calcined lime powder or copper sulfate in advance as a protective colloid.
    [6] In Japanese Unexamined Patent Application Publication No. 61-63601, in formulating a particulate biocidal dispersion, an unsaturated carboxylic acid-based polymer dispersion, a styrene sulfonate polymer, a formalin condensate, and a salt thereof are prescribed. It features. Japanese Laid-Open Patent Publication No. 62-226905 proposes a method for preparing an aqueous solution of a polycarboxylic acid copper amine salt.
    [7] JP-A-60-155403 and JP-A-61-97202 propose stabilization by wet milling particles of agrochemicals as suspensions. Among them, Japanese Patent Application Laid-Open No. 60-155403 proposes to obtain a stable dispersion by obtaining a product of true specific gravity and an average particle diameter of 0.8 µm or less in fine particles of a room temperature solid having a solubility in an aqueous dispersant of 50 ppm or less. It is. Japanese Laid-Open Patent Publication No. 61-97202 is characterized by using a polyoxyalkylene type nonionic surfactant, polyoxyalkylene ether phosphate or alkylaryl polyoxyalkylene ether phosphate as a dispersant.
    [8] However, these additives were excellent in dispersion stability, the amount of adhesion can be easily confirmed on the leaves or fruits, and it was not possible to obtain a Bordeaux liquid with a good balance of the point that it is not easily spilled by alien rain or the like after spray drying.
    [9] In any case, the dispersion stability gradually decreases immediately after preparation of Bordeaux liquid. For example, the Bordeaux dispersion prepared in the evening before the next day precipitates at the bottom of the container when it is to be used the next morning, and thus it is impossible to spread the dispersion. Problems are occurring frequently. In addition, even if the precipitated Bordeaux liquid is forcibly stirred and used for the spreading operation, caking may not be possible to redistribute, or even if it may be redistributed, the nozzle of the chemical dispersing machine may be clogged, or the scattering of leaves, fruits, etc. There was a problem that cannot be evenly distributed on the water surface. Most prior arts have focused on how much these dispersion properties are improved.
    [10] However, as another problem of the Bordeaux liquid, it is necessary to consider that the adhesion amount after the dispersion is easy and to maintain a stable electrodeposition effect against the influence from the outside world. Conventionally, nothing was mentioned about the Bordeaux liquid composition which made the dispersion effect and electrodeposition effect compatible.
    [11] If the electrodeposition stability is poor even with the Bordeaux liquid composition excellent in dispersion stability, depending on the surface state of the product to be produced, the electrodepositing ability such as splashing of the dispersion may be insufficient, resulting in a uniform application of the chemical solution. In addition, the lack of electrodeposition ability causes the drug to be easily peeled off by physico-chemical factors such as rainwater or wind after spray drying, resulting in a long-term stable drug efficacy.
    [12] Therefore, although Bordeaux liquid which satisfy | fills these characteristics simultaneously is calculated | required, it was not discovered that satisfy | fills each required characteristic characteristic.
    [13] It is an object of the present invention to simultaneously satisfy three requirements: excellent dispersion stability during preparation and long-term storage, excellent electrodeposition stability immediately after dispersion and drying, and excellent ease of visual confirmation of adhesion amount immediately after dispersion, and It is to provide a Bordeaux liquid containing this additive.
    [1] The present invention relates to Bordeaux liquid additives and Bordeaux mixture (Bordeaux mixture). More specifically, it can be stored for a long time stably without causing poor dispersion at both concentration and use concentration before spraying, spray concentration can be confirmed from appearance immediately after spraying on leaves or fruits, and even after drying It relates to a Bordeaux liquid additive and Bordeaux liquid, characterized in that not easily peeled out by physical external pressure or rain water.
    [14] As a result of earnestly examining to solve the above problems, the present inventors have come to the conclusion that in order to efficiently disperse Bordeaux particles, the lipophilic property should be maintained at a certain level or more in the balance between the hydrophilic group and the lipophilic group. In addition, it was concluded that, after the Bordeaux solution was distributed, to maintain a constant hydrophilicity in a constant hydrophilicity and lipophilic balance in order to reduce the loss rate due to the influence of the extraterrestrial. Here, focusing on the lipophilic hydrophilic balance (HLB) index that satisfies the opposite characteristics of both, and structural design using this, as a result, the change over time in the Bordeaux liquid particle diameter is small to secure long-term storage stability and electrodeposition rate after dispersion It has been found that an additive having both characteristics, which has not been conventionally used as a Bordeaux liquid, can be exhibited by improving the stability and exhibiting a stable drug.
    [15] That is, the present invention
    [16] (1) Polymer (A) having a molecular weight of 5,000 to 80,000 obtained by copolymerizing monomer (a) of formula (I) having a HLB value of 3.0 to 7.0 and monomer (b) of formula (II) in a molar ratio of 1/1 to 1 / 9.5 Bordeaux liquid additive containing,
    [17] (2) Bordeaux liquid additive as described in (1) whose HLB value of polymer (A) is 6.0-8.0,
    [18] (3) Bordeaux liquid containing Bordeaux liquid additive as described in (1) or (2),
    [19] (4) Bordeaux solution according to (3), wherein the ratio of the sedimentation layer sedimentation rate immediately after the prescription and after 24 hours is 0.6 to 1.5,
    [20] (5) Bordeaux solution as described in (3) whose copper ion loss rate after 48 days immediately after spreading to a to-be-dispersed thing does not exceed 70%,
    [21] (6) Bordeaux solution as described in (4) whose copper ion loss rate after 48 days immediately after spread to a to-be-dispersed thing does not exceed 70%.
    [22]
    [23]
    [24] In the above formulas (I) and (II),
    [25] R 1 and R 2 are a hydrogen atom or a methyl group,
    [26] m is a number from 0 to 2,
    [27] R 3 O is one or a mixture of two or more oxyalkylene groups having 3 to 18 carbon atoms, and in the case of two or more, may be added in a block phase, a random phase, and a combination thereof,
    [28] n and p are the average added moles of oxyethylene group and oxyalkylene group, respectively,
    [29] n is from 1 to 200,
    [30] p is 0 to 200,
    [31] n + p is 1 to 250,
    [32] R 4 is a hydrocarbon group having 1 to 40 carbon atoms,
    [33] R 5 , R 6 and R 7 are hydrogen atoms, methyl groups or (CH 2 ) q COOX groups,
    [34] X is a hydrogen atom, a monovalent metal, a divalent metal, an ammonium group or an organic ammonium group,
    [35] q is a number from 0 to 2,
    [36] When two COOX groups exist, they may form anhydrides.
    [37] Best Mode for Carrying Out the Invention
    [38] Polymer (A) contains monomer (a) and monomer (b) as essential monomers, and can be produced by copolymerizing them.
    [39] In formula (I), R 1 and R 2 are hydrogen atoms or methyl groups and may be the same or different, m is a number from 0 to 2, preferably 0. Especially, (meth) acrylic-acid alkoxy polyalkylene glycol adduct whose R <1> is a hydrogen atom, R <2> is a hydrogen atom or a methyl group, and m is 0 is preferable (henceforth acrylic acid or methacrylic acid is called (meth) acrylic acid). Called).
    [40] R 3 O is an oxyalkylene group having 3 to 18 carbon atoms, specifically, propylene oxide, 1,2-butylene oxide, 2,3-butylene oxide, 1-butene oxide, 2-butene oxide, α-olefin oxide , Trimethylethylene oxide, tetramethylethylene oxide, butadiene monooxide, α-methylstyrene oxide, 1,1-diphenylethylene oxide, cyclohexene oxide, dihydronaphthalin oxide, oxetane and alkyl substituted derivatives thereof and tetrahydro And oxyalkylene groups derived from furan. The oxyalkylene group having 3 to 18 carbon atoms may be one kind or two or more kinds thereof, and in the case of two or more kinds, they may be bonded in a block form, random form or alternately. Preferably, when the carbon number is 3 to 4 and the carbon number exceeds 18, the hydrophilicity is too strong to attenuate the effect of the oxyethylene bonds bonded at the same time, which hinders the dispersion effect of Bordeaux particles.
    [41] The oxyethylene group and the oxyalkylene group having 3 to 18 carbon atoms may be bonded in a block or random phase, but are preferably bonded in a block phase. In the case of bonding in block form, the bonding order thereof may be an oxyethylene group bonded to the ester bond or an oxyalkylene group having 3 to 18 carbon atoms.
    [42] n is the average added mole number of an oxyethylene group, and is 1-200, Preferably it is 1-100. p is the average added mole number of the C3-C18 polyoxyalkylene group, and is 0-200, Preferably it is 1-80.
    [43] n + p is 1 to 250, preferably 1 to 180. If it is larger than 250, the viscosity of the polyoxyethylene compound of general formula (I) becomes high, and manufacture is difficult, and therefore it is not preferable.
    [44] In addition, the higher the ratio of n to the composition ratio of n and p, the higher the affinity for water, which is expected to provide a better dispersion effect as Bordeaux particles in water, but reduces the electrodeposition effect.
    [45] R 4 is a hydrocarbon group having 1 to 40 carbon atoms, specifically, methyl group, ethyl group, allyl group, propyl group, isopropyl group, butyl group, isobutyl group, secondary butyl group, tertiary butyl group, pentyl group, iso Pentyl, neopentyl, hexyl, heptyl, octyl, nonyl, decyl, undecyl, dodecyl, isotridecyl, tetradecyl, hexadecyl, isocetyl, octadecyl, iso Stearyl group, oleyl group, octyl dodecyl group, docosyl group, decyl tetradecyl group, benzyl group, cresyl group, butylphenyl group, dibutylphenyl group, octylphenyl group, nonylphenyl group, dodecylphenyl group, dioctylphenyl group, dinonylphenyl group And saturated hydrocarbon groups such as styrenated phenyl groups, unsaturated hydrocarbon groups, aromatic groups, or substituted aromatic groups, but are preferably saturated hydrocarbon groups having 1 to 18 carbon atoms or unsaturated hydrocarbon groups.
    [46] The HLB value of monomer (a) of formula (I) is between 3.0 and 7.0, preferably between 3.5 and 7.0.
    [47] The HLB value of the polymer (A) is preferably 6.0 to 8.0, more preferably 6.5 to 8.0.
    [48] By carrying out HLB in the said range, the balance of the dispersion effect and electrodeposition effect of Bordeaux particle | grains in water can be maximized.
    [49] HLB was calculated based on the formula of Devies (Proc., 2nd Inter. Congress of Surface Activity, 1426 (1957)).
    [50] That is, it calculates by the following formula.
    [51] HLB = 7 + Σ (Number of HLB groups in hydrophilic group) + Σ (Number of HLB groups in hydrophilic group)
    [52] The number of HLB groups used the following parameters.
    [53] Lipophilic number; CH 3 , CH 2 , CH: each -0.475,
    [54] (CH (CH 3 ) CH 2 O): -0.15
    [55] Hydrophilic number; (CH 2 CH 2 O): +0.33,
    [56] COO: +2.4,
    [57] COOH: +2.1,
    [58] OH: +1.9
    [59] In the polymer (A) and the monomer (a), [-COO] + [X] - if the ion is dissociated to reach easily 20 as HLB, but this does not reflect the actual sex of the dispersibility and settling. HLB is used for the actual calculation because it can reflect the actual characteristic when it calculates as X = H.
    [60] As the monomer (a) of the general formula (I) used in the present invention, ring-opening addition polymerization of ethylene oxide and an alkylene oxide derivative having 3 to 18 carbon atoms to a compound having one functional group of -OH as an active hydrogen in a hydrocarbon having 1 to 40 carbon atoms It can be manufactured as an ester compound by the alkoxy polyalkylene glycol obtained by couple | bonding with and the ester exchange using the dehydration esterification of (meth) acrylic acid or crotonic acid, or the alkyl (meth) acrylic acid or a crotonic acid alkyl group.
    [61] In the monomer (b) of the general formula (II) used in the present invention, R 5 , R 6 and R 7 are hydrogen atoms, methyl groups or (CH 2 ) q COOX groups, each of which may be the same or different and is preferably a hydrogen atom. .
    [62] X represents a hydrogen atom, a monovalent metal, a divalent metal, an ammonium group or an organic ammonium group. For example, lithium, sodium, potassium, cesium, etc. may be mentioned as a monovalent metal, and beryllium, magnesium, Calcium, strontium, barium, etc. are mentioned, Especially, calcium is preferable. Ammonium salts and organic ammonium salts include salts neutralized with ammonia, salts neutralized with alkyl amides, amines having 1 to 30 carbon atoms, N-methylol amides, N, N-dimethyl amides and the like.
    [63] As X, the sodium salt which is a monovalent metal salt is more preferable.
    [64] q is a number of 0-2, and when two or more COOX groups exist, you may form anhydride.
    [65] Specific examples of the monomer (b) include acrylic acid, methacrylic acid, crotonic acid and metal salts thereof, ammonium salts and amine salts. In addition, examples of the unsaturated dicarboxylic acid monomers include maleic acid, itaconic acid, citraconic acid, fumaric acid or metal salts thereof, ammonium salts and organic ammonium salts thereof, and maleic anhydride, itaconic anhydride, Citraconic anhydride etc. are mentioned.
    [66] Among these, unsaturated monocarboxylic acid monomers are preferred, (meth) acrylic acid and salts thereof are more preferred, and acrylic acid and salts thereof are most preferred. These monomers can also be used 1 type or in combination of 2 or more types.
    [67] In order to obtain a polymer (A), the monomer component may be polymerized using a polymerization initiator, and to form a salt, a monomer containing a salt may be used in advance, or a metal hydroxide, a metal anhydride, a carbonate or a bicarbonate may be used after copolymerization. Alternatively, the amidation reaction may be performed by using ammonia gas, ammonia water, or by adding an alkylamine or the like. The polymerization can be carried out by polymerization in a solvent, bulk polymerization or the like. In addition, the copolymer molar ratio of the monomer (a) and the monomer (b) for obtaining the polymer (A) is 1/1 to 1 / 9.5, more preferably 1/2 to 1 / 9.5, the weight average molecular weight is 5,000 To 80,000, more preferably 6,000 to 28,000.
    [68] The polymerization in the solvent may be carried out either batchwise or continuously. In this case, the solvent used may be water or an organic solvent, such as lower alcohols such as methanol, ethanol and propanol, benzene, toluene, xylene, cyclohexane, n Aromatic and alicyclic hydrocarbons, such as -hexane, ester compounds, such as ethyl acetate, ketone compounds, such as acetone and methyl ethyl ketone, are mentioned. Judging from the solubility of the polyalkylene glycol monomer used as a raw material and the form of use obtained by adding the obtained copolymer to Bordeaux liquid, one or two or more lower alcohols such as methanol, ethanol and propanol or water and one or Two or more lower alcohols are preferred, and more preferably water alone is particularly effective.
    [69] When copolymerization is carried out in an aqueous solvent, hydroperoxides such as ammonium persulfate, alkali persulfate metal salts, hydrogen peroxide and tertiary butyl hydroxybenzoxide may be used. At this time, accelerators, such as sodium hydrogen sulfite and a mohr's salt, can also be used together. In the case of copolymerization in an organic solvent, diacyl peroxides such as lauroyl peroxide, benzoyl peroxide, hexanonyl peroxide and stearoyl peroxide, diisopropyl peroxydicarbonate, di-2-ethyl Hexyl peroxydicarbonate, di-n-propylperoxydicarbonate, di-2-ethoxyethylperoxydicarbonate, di-3-methoxybutylperoxydicarbonate and bis (4-t-butylcyclohexyl) peroxydicarbonate Peroxydicarbonate, 1,1,3,3-tetramethylbutylperoxy-2-ethyl hexanonate and t-hexylperoxy-2-ethyl hexanonate, t-butylperoxy-2-ethyl hexano Peroxy esters such as nate and t-butylperoxy isobutylate, aromatic azo compounds such as azobisisobutyronitrile and the like can be used. At this time, accelerators, such as an amine compound, can be used together. Moreover, when superposing | polymerizing in the mixed solvent system of water and a hydrophilic organic solvent, the said polymerization initiator or promoter can be selected suitably and used. The polymerization temperature may be appropriately determined depending on the type of the solvent or the polymerization initiator used, but the polymerization may be generally performed in the range of 0 to 130 ° C, preferably 25 to 115 ° C.
    [70] The bulk polymerization can be carried out in a temperature range of 50 to 200 ° C by appropriately selecting various diacyl peroxides, peroxydicarbonates, peroxy esters and aromatic azo compounds as polymerization initiators.
    [71] A chain transfer agent can be used together for molecular weight adjustment of a polymer. The chain transfer agent used at this time is generally a thiol-based compound, for example, mercaptoethanol, thioglycerol, thioglycolic acid, 2-mercaptopropionic acid, 3-mercaptopropionic acid, and the like can be selected, and one of these Or 2 or more types can be used.
    [72] Preparation of Bordeaux liquid can be performed by the following method. Copper sulfate is pulverized and dissolved in water so as to have a concentration of 20 to 40% by weight to prepare an aqueous solution of copper sulfate. In addition, quicklime (calcium oxide) is similarly dispersed and dissolved in water while stirring to prepare lime oil having a concentration of 20 to 40% by weight. To the lime oil, 0.1 to 6% by weight, preferably 1 to 4% by weight, of the polymer (A) as a Bordeaux liquid additive in terms of solids relative to the total amount of copper sulfate and quicklime is added to disperse and dissolved. If the added amount is less than 0.1% by weight, dispersibility and electrodeposition properties are insufficient, and even if an amount exceeding 6% by weight is added, the effect is not improved further.
    [73] The stock solution of Bordeaux liquid can be prepared by gradually adding the copper sulfate aqueous solution to the lime oil which mix | blended the polymer (A) obtained here, stirring. This stock solution can be used as Bordeaux liquid by further wet grinding in a wet mill and further diluted with water to an applied concentration.
    [74] The wet mill is not particularly limited, but a batch ball mill, a continuous tube mill, a tower mill, or a pearl mill using small beads can be used. Preparation can usually be carried out in a temperature range of 0 to 80 ℃, preferably 5 to 40 ℃.
    [75] The higher the dispersion stability of the Bordeaux particles, the lower the settling rate [% / hour] per unit time of the settling layer as Bordeaux particles. When used in the field, it cannot be used unless the sedimentation rate of the sedimentation layer is obtained, such as immediately after preparation as well as immediately after formulation with Bordeaux liquid. That is, it is necessary to maintain the same stable dispersion state even in the Bordeaux liquid immediately after preparation or in the Bordeaux liquid preserve | saved for a long time.
    [76] Bordeaux liquid in the sedimentation rate of the sedimentation layer, 0.6 ≤ [PS 0h ] / [PS 24h ] ≤ 1.5 (where [PS 0h ]: sedimentation rate of the sedimentation layer immediately after the prescription, [PS 24h ]: sedimentation layer after 24 hours) Sedimentation rate) is more preferable, and 0.8 ≦ [PS 0h ] / [PS 24h ] ≦ 1.3. Even in a long period of 3 years or more, it can be easily preserved and redispersed as a homogeneous Bordeaux liquid.
    [77] However, it is preferable that basic copper calcium sulfate which is an active ingredient of Bordeaux liquid prepares the particle diameter of its Bordeaux particle | grains to 2-4 micrometers. If the particle diameter of Bordeaux particles exceeds 4 μm, the dispersion stability is poor. If the particle diameter is smaller than 2 μm, dispersion stability is not impeded, but the reflection and scattered light of visible light is weakened, and the traces of dispersion remaining on the surface of the product to be scattered become thin. The dispersion amount cannot be confirmed from appearance.
    [78] Bordeaux liquid scattered on fruit or leaf crops, which are to-be-produced, is electrodeposited on the surface of the to-be-spreaded surface, and loses moisture by natural drying. However, it is frequently affected by vibration, wind, rain, friction, etc., which are physical and chemical factors of nature, and are lost in the form of spillage, departure, or peeling together with the active ingredient. The active ingredient of Bordeaux liquid is mainly copper ions, and the loss rate of copper ions after 48 days immediately after dispersion is preferably 70% or less, more preferably 60% or less, thereby sustaining the long-term efficacy and being sensitive to the initial drug concentration. It can be easily applied to the products to be adversely affected.
    [79] The present invention will be described through Examples and Comparative Examples.
    [80] In each example,% represents% by weight unless otherwise specified, and parts represent parts by weight. The weight average molecular weight of the polyalkylene glycol which comprises an essential component for providing to a polymer and superposition | polymerization is computed using the polyethylene glycol conversion method by gel permeation chromatography (GPC).
    [81] Preparation Example 1
    [82] 300 parts of water were put into the glass reaction container equipped with a thermometer, a stirrer, a dropping lot, a nitrogen inlet tube, and a reflux condenser, and it heated up to 80 degreeC under nitrogen atmosphere. Methoxypolyethylene glycol (3 mol), polypropylene glycol (16 mol), monoacrylate (HLB: 6.6) 119.2 parts, acrylic acid 30.8 parts, water 150 parts, 1.2 parts 3-mercaptopropionic acid and 3% ammonium persulfate as chain transfer agents The monomer aqueous solution which mixed 40 parts of aqueous solutions was dripped over 4 hours. Subsequently, 15 parts of 3% aqueous ammonium persulfate solution was added dropwise over 1 hour, and the mixture was kept stirred at 80 ° C for 1 hour and the polymerization reaction was completed to obtain a polymer having a weight average molecular weight of 9000. The average HLB value of the obtained polymer was 7.9. The polymer was further pH-adjusted with a 5% aqueous sodium hydroxide solution to form a sodium salt of pH 5.6, and then water was added to prepare a solids concentration of 40% aqueous solution, obtaining polymer (A). Indicates.
    [83] Preparation Examples 2 to 4
    [84] In the same manner as in Production Example 1, the polymer described in Table 1 and a polymer (A) as a salt thereof were obtained. However, ammonium salt was obtained by pH preparation using ammonia water and potassium salt using 5% aqueous potassium hydroxide solution. Solid content concentration was all 40%.
    [85] Preparation Examples 5 to 8
    [86] In the same manner as in Preparation Example 1, a polymer as described in Table 1 and a polymer as a salt thereof were obtained. However, Production Examples 6 to 8 obtained the respective polymers (A) by using the polymers as they were without adjusting the pH. Solid content concentration was all 40%.
    [87]
    [88] R) palm oil alkyl group (average carbon number: 13.0), AA: acrylic acid, MAA: methacrylic acid
    [89] Example 1
    [90] Copper sulfate (CuSO 4 and 5H 2 O) 150 parts was dissolved in 340 parts of water to prepare a copper sulfate solution. Further, 150 parts of quicklime (calcium oxide) was dissolved and dispersed in 350 parts of water with stirring to prepare a lime oil mother liquor. After adding 13.5 parts of polymer (A) of manufacture example 1 (40% of solid content concentration) to this lime oil mother liquid, the copper sulfate solution was added dropwise little by little, and the Bordeaux solution of which concentration of Bordeaux liquid was about 30% was prepared. This Bordeaux stock solution was pulverized at 30 rpm for 1 hour using a wet mill magnetic ball mill (manufactured by Asada Honko Co., Ltd .: 30 liters having a capacity of 3 L and a magnetic ball diameter of 25 mm) to prepare Bordeaux liquid. This Bordeaux liquid was further diluted 25 times and used as a test Bordeaux liquid. The results are shown in Table 2.
    [91] Examples 2-12 and Comparative Examples 2-9
    [92] Bordeaux liquid was prepared using each polymer (A) of manufacture examples 1-8 by the method similar to the compounding example 1. However, the polymer concentration added the amount of Table 2 according to the total amount of copper sulfate and quicklime. The results are shown in Table 2.
    [93] Comparative Example 1
    [94] Copper sulfate (CuSO 4 and 5H 2 O) 150 parts of a copper sulfate solution was prepared by dissolving in 350 parts of water. Further, 150 parts of quicklime (calcium oxide) was dissolved and dispersed in 350 parts of water with stirring to prepare a lime oil mother liquor. The copper sulfate solution was added dropwise to the lime oil mother liquor little by little to prepare a Bordeaux stock solution having a Bordeaux liquid concentration of about 30%. This Bordeaux stock solution was pulverized at 30 rpm for 1 hour using a wet mill magnetic ball mill (manufactured by Asada Honko Co., Ltd .: 30 liters having a capacity of 3 L and a magnetic ball diameter of 25 mm) to prepare Bordeaux liquid. This Bordeaux liquid was further diluted 25 times and used as a test Bordeaux liquid. The results are shown in Table 2.
    [95] Bordeaux particles were measured immediately after preparation of the test Bordeaux liquid, after 24 hours, after 1 year, after 2 years, and after 3 years, and were stored in a storage room where the room temperature was 0 to 35 ° C., freezing in winter, and free from direct sunlight. The sample was taken out regularly and the sample after aging was stirred for about 5 minutes in a stirrer immediately before measurement, and then measured immediately by a measuring device. At this time, microtrack (manufactured by Nikkiso Co., Ltd.) was used for the measurement of the Bordeaux particle diameter. The results are shown in Table 2.
    [96] The measurement of sedimentation layer concentration was carried out immediately after preparation and after 24 hours of test Bordeaux liquid as it was, just after preparation, the test Bordeaux solution after 24 hours was stirred for about 5 minutes in a stirrer immediately, and then the volume of 100 ml Iv) Fill the measuring cylinder with the graduated cylinder up to 100 ml, shake it vigorously 10 times after installing the idler, and let it stand, and then in the measuring cylinder at intervals of 5 minutes from immediately after to 30 minutes and at intervals of 10 minutes from above to 60 minutes. The scale of sedimentation layer height was visually read and calculated | required as sedimentation rate (%). In both cases immediately after preparation and 24 hours later, the sedimentation rate was calculated as the sedimentation rate of the sedimentation layer per hour. The sedimentation rate of this sedimentation layer is determined by subtracting the sedimentation rate of the sedimentation layer to the time when the rate of change of the sedimentation rate (%) per unit time (minute) is obtained from the sedimentation sedimentation rate time differential curve. The significant digits were rounded off and displayed as two digits.
    [97] That is, in the case immediately after preparation of Table 2 and Example 5,
    [98] Elapsed time (minutes)Sedimentation rate (%) 00 520 1043 1564 2074 2579 3081 4084 5085 6086
    [99] Since the rate of change of the sedimentation rate of the sedimentation layer of the sedimentation layer of 10 minutes or more is small, the slope up to 10 minutes is extrapolated as a linear curve to obtain a value of 260% / hour.
    [100] In addition, about calculation of the sedimentation velocity of the sedimentation layer after 24 hours of Table 2 and the comparative example 1,
    [101] Elapsed time (minutes)Sedimentation rate (%) 00 584 1089 1590 2091 2591 3091 4091 5091 6091
    [102] Since the slope of the straight line of 5 minutes or more is gentle, the linear curve slope up to 5 minutes is extrapolated to obtain a value of 1000% / hour. The results are shown in Table 2.
    [103] The loss rate was determined by dispersing Bordeaux mixture in citrus fruits covered with a vinyl house to avoid rain, and measuring the concentrations of copper and calcium, especially copper ions, before and after aging. The test site was Hoshi-shi, Ehimeken, and spread was carried out for 48 days from March 16, 1997. The spray was sprayed to 500 l per 10 drops with a manual sprayer, and water was not sprayed on the trees immediately before and after the spray. From the 7th day after spreading, natural rain was assumed and the sprayer sprayed water about 30 mm / week. Presumed precipitation was 180 mm. Extraction of calcium ions and copper ions from the leaves was collected in a beaker for 100 leaves extracted indiscriminately from each sphere, and ion-exchanged water was added to the degree that the leaves were sufficiently submerged in water, stirred and left overnight. Using tweezers, each leaf was transferred to another beaker. At this time, until the deposit could not be visually recognized by the surface of the leaf, another tweezers were used to spray and exchange ion exchanged water, and the washing solution was also secured. All aqueous solutions and dispersions used for washing were transferred to a measuring flask, and calcium and copper ion concentrations were measured by ICP (Ion Plasma Emission Analyzer, manufactured by Shimadzu Seisakusho Co., Ltd.). The results are shown in Table 2. In the comprehensive evaluation, it was judged that O or ◎ having excellent balance between the sedimentation rate of the sedimentation layer and the copper loss rate could be used as the Bordeaux liquid.
    [104]
    [105] Note) comprehensive evaluation; Excellent: ◎, Good: O, Possible: △, Impossible: ×
    [106] *:% Of polymer (A) relative to the total amount of copper sulfate and quicklime
    [107] Bordeaux liquid using the Bordeaux liquid additive of the present invention is stable in the particle diameter of Bordeaux particles of 2 to 4㎛, not only excellent stability over time, but also excellent loss rate of copper ions as the active ingredient compared to the comparative example both It turns out that it is this balanced Bordeaux liquid.
    [108] It can be seen that the comparative example is inferior to the Bordeaux liquid using the Bordeaux liquid additive of the present invention as follows.
    [109] Comparative Example 1: The sedimentation rate of the sedimentation layer was 24 hours, 0.08, which is significantly lower than the lower limit of 0.6. From Table 2, the particle diameter exceeds 10 µm, resulting in poor stability of Bordeaux particles. The loss rate of copper ion after 48 days is also 72% exceeding 70%.
    [110] Comparative Examples 2 to 7: The HLB of the monomer (a) contained in the polymer (A) used was 7.5 to 10.7, too large than 7.0 and the HLB of the polymer (A) was also 8.0 to 8.1 to 8.8. Therefore, the 24-hour ratio at the settling velocity of the settling layer is 0.23 to 0.58, which is less than 0.6. The loss rate of copper ion after 48 days is also more than 60%, and is 65 to 80%.
    [111] Comparative Examples 8 and 9: The HLB of the monomer (a) contained in the polymer (A) used was -2.9, below the lower limit 3.0, and the HLB of the polymer (A) was also below 4.2, the lower limit 6.0. Therefore, the ratio of sedimentation layer in the sedimentation layer for 24 hours is 0.10 to 0.11, which is less than 0.6.
    [112] The additive for the Bordeaux liquid composition according to the present invention incorporates a monomer (a) having an HLB value in the range of 3.0 to 7.0 into the polymer (A) so as to have an HLB value in the range of 6.0 to 8.0. By adding and preparing this Bordeaux liquid additive as a Bordeaux liquid, the difference between the sedimentation layer sedimentation rate immediately after the prescription and the sedimentation layer sedimentation rate after 24 hours can be maintained at 0.6 to 1.5, and the storage stability of the Bordeaux liquid can be maintained well even after 3 years or more. have. In addition, since the dispersion stability is excellent, the Bordeaux liquid can be dispersed and electrodeposited onto the blood dispersion at a homogeneous copper ion concentration. Even crops sensitive to the concentration of calcium and copper ions can be scattered at a low concentration of side effects, and furthermore, since the naked eye can be easily identified after scattering, the use can be expanded.
    权利要求:
    Claims (6)
    [1" claim-type="Currently amended] Bordeaux liquid containing polymer (A) having a molecular weight of 5,000 to 80,000 obtained by copolymerizing monomer (a) of formula (I) having a HLB value of 3.0 to 7.0 and monomer (b) of formula (II) in a molar ratio of 1/1 to 1 / 9.5. additive.
    Formula I

    Formula II

    In the above formulas (I) and (II),
    R 1 and R 2 are a hydrogen atom or a methyl group,
    m is a number from 0 to 2,
    R 3 O is one or a mixture of two or more oxyalkylene groups having 3 to 18 carbon atoms, and in the case of two or more, may be added in a block phase, a random phase, and a combination thereof,
    n and p are the average added moles of oxyethylene group, oxyalkylene group having 3 to 18 carbon atoms,
    n is from 1 to 200,
    p is 0 to 200,
    n + p is 1 to 250,
    R 4 is a hydrocarbon group having 1 to 40 carbon atoms,
    R 5 , R 6 and R 7 are hydrogen atoms, methyl groups or (CH 2 ) q COOX groups,
    X is a hydrogen atom, a monovalent metal, a divalent metal, an ammonium group or an organic ammonium group,
    q is a number from 0 to 2,
    When two COOX groups exist, they may form anhydrides.
    [2" claim-type="Currently amended] The Bordeaux liquid additive according to claim 1, wherein the HLB value of the polymer (A) is 6.0 to 8.0.
    [3" claim-type="Currently amended] Bordeaux liquid containing the Bordeaux liquid additive of Claim 1 or 2.
    [4" claim-type="Currently amended] The Bordeaux solution of Claim 3 whose sedimentation rate ratio of the sedimentation layer immediately after prescription and after 24 hours is 0.6-1.5.
    [5" claim-type="Currently amended] The Bordeaux liquid according to claim 3, wherein the copper ion loss rate after 48 days immediately after the scattered product is not more than 70%.
    [6" claim-type="Currently amended] The Bordeaux liquid according to claim 4, wherein the rate of copper ion loss after 48 days immediately after being dispersed in the product to be distributed does not exceed 70%.
    类似技术:
    公开号 | 公开日 | 专利标题
    US5064563A|1991-11-12|Process for producing and use of maleic acid | polymer salt improved in biodegradability
    EP0100947B1|1986-10-15|Grinding aid based on neutralized polymers and/or copolymers for aqueous suspensions of coarse mineral materials in view of pigmenting applications
    EP1767504B1|2013-09-18|Phosphoric ester polymer
    JP3184728B2|2001-07-09|Dispersant for gypsum / water slurry
    US7553903B2|2009-06-30|Swellable hydrogel-forming polymers having a low fraction of fines
    FI104087B|1999-11-15|A process for the preparation of aqueous dispersions of ethylene / a, b-unsaturated carboxylic acid interpolymers
    CN101611112B|2012-04-18|Acrylate adhesives containing silica nanoparticles crosslinked with polyfunctional aziridines
    US5548047A|1996-08-20|Process for the production of highly water absorptive polymers
    DE602004012556T2|2009-04-02|Cement dispersible agents and method for the production and use thereof
    Lowe et al.2000|Well‐defined sulfobetaine‐based statistical copolymers as potential antibioadherent coatings
    JP4112500B2|2008-07-02|C10-alkanol alkoxylates and uses thereof
    CN102014622B|2015-03-11|Composition having biocide activity for aqueous preparations
    EP0751159B1|2000-08-30|Method of preparing water-absorbing resin
    DE69932222T2|2007-07-05|Cement additive, cement composition and polymeric polycarboxylic acid
    KR20030062421A|2003-07-25|Method for the production of water-in-water polymer dispersions
    US7645345B2|2010-01-12|Use of copolymers containing sulfonic acid groups, as an additive in detergents and cleansers
    EP0584771B1|1997-12-29|Easy to disperse polycarboxylic acid thickeners
    CN102404989B|2016-02-17|For the dispersant of agricultural application
    US20080087198A1|2008-04-17|Gypsum composition
    KR100771024B1|2007-10-29|Cement admixture and cement composition
    CA1303452C|1992-06-16|Detergents containing oxyalkylated, carboxyl-containing polymers
    EP1278787B1|2007-03-28|Compositions of pesticides
    TWI308167B|2009-04-01|Curable composition and use thereof
    RU2394841C2|2010-07-20|Method of preparing polymer dispersion and polymer dispersion
    US6395813B1|2002-05-28|Aqueous dispersions
    同族专利:
    公开号 | 公开日
    DE60133456T2|2009-05-07|
    KR100561330B1|2006-03-16|
    ES2302730T3|2008-08-01|
    CN1264402C|2006-07-19|
    EP1277402A4|2006-07-19|
    WO2001082695A1|2001-11-08|
    PT1277402E|2008-05-28|
    EP1277402A1|2003-01-22|
    CN1426274A|2003-06-25|
    EP1277402B1|2008-04-02|
    DE60133456D1|2008-05-15|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    2000-04-28|Priority to JP2000129369
    2000-04-28|Priority to JPJP-P-2000-00129369
    2001-04-27|Application filed by 닛폰 유시 가부시키가이샤, 이노우에셋카이코교가부시키가이샤
    2001-04-27|Priority to PCT/JP2001/003739
    2003-02-05|Publication of KR20030010609A
    2006-03-16|Application granted
    2006-03-16|Publication of KR100561330B1
    优先权:
    申请号 | 申请日 | 专利标题
    JP2000129369|2000-04-28|
    JPJP-P-2000-00129369|2000-04-28|
    PCT/JP2001/003739|WO2001082695A1|2000-04-28|2001-04-27|Additive for bordeaux mixture and bordeaux mixture|
    [返回顶部]