JP2007326851A - Method of improving volatilization of heat-transpiring preparation and heat-transpiring preparation - Google Patents

Abstract

<P>PROBLEM TO BE SOLVED: To provide a new method which improves the volatilization of chemicals in a heat-transpiring preparation without increasing the amount of the organic foaming agent used and a heat transpiring preparation using the method. <P>SOLUTION: The heat-transpiring preparation in which the chemicals are volatilized by the indirect heating of the mixture of the chemicals and the organic foaming agent contains 5-20 wt.% of an inorganic porous body acting as a volatilization aid to the total amount of the organic foaming agent. <P>COPYRIGHT: (C)2008,JPO&INPIT

Description

  The present invention relates to a method for improving volatilization of a preparation for heating transpiration, which can improve the volatilization of the drug, in the preparation for heating transpiration that volatilizes the drug by the action of the pyrolysis gas by the organic foaming agent, and uses the method for improving volatilization. The present invention relates to a preparation for heat evaporation.

  2. Description of the Related Art Conventionally, a preparation for heat transpiration that can reach every corner of a medicine has been used to control pests present in a space having a certain volume such as a room or a warehouse. In this preparation, an organic foaming agent such as azodicarbonamide is thermally decomposed by indirectly heating, and the agent is efficiently evaporated by the action of the pyrolysis gas (see, for example, Patent Document 1). .

Japanese Patent Laid-Open No. 53-130432 (page 1-6)

In the above-mentioned preparation for heat transpiration agent, since the volatilization of the drug is affected by the amount of the organic foaming agent used, it has been considered that the amount of use should be increased in order to increase the volatilization of the drug. However, since the generation of smoke increases with the increase in the organic foaming agent, it is not necessarily good because it may cause irritation or cause a malfunction of the fire alarm. However, the actual situation is that few effective means for increasing the volatilization of drugs have been studied.
Therefore, the present invention provides a new method capable of improving the volatilization of the medicine without increasing the amount of the organic foaming agent used in the preparation for heat evaporation, and a preparation for heat evaporation using this method. Is.

As a result of intensive studies to solve the above problems, the present inventors indirectly heated a mixture of a drug and an organic foaming agent, and in the preparation for heat evaporation for volatilizing the drug in the mixture, It has been found that the volatilization of the drug can be significantly improved by blending and using a specific amount of a specific inorganic porous material.
That is, the present invention is achieved by the following methods (1) to (5) for improving the volatilization of a heat transpiration preparation and (6) the heat transpiration preparation. (1) Inorganic heating that acts as a volatilization improver for the total amount of the organic foaming agent in a preparation for heat evaporation for indirectly heating a mixture of the chemical and the organic foaming agent to volatilize the chemical The volatilization improvement method of the preparation for heat | fever evaporation characterized by mix | blending a body so that it may become 5 to 20 weight%. (2) The method for improving volatilization of a preparation for heat evaporation according to claim 1, wherein the inorganic porous material is an inorganic fired foam. (3) The method for improving volatilization of a preparation for heat evaporation according to (1) or (2), wherein the preparation is for heat evaporation containing 65 to 80% by weight of an organic foaming agent. (4) The method for improving volatilization of a preparation for heat transpiration according to any one of (1) to (3), which is a preparation for heat transpiration in which azodicarbonamide is blended as an organic foaming agent. (5) It is a preparation for heat transpiration in which one or more of pyrethroid insecticides, carbamate insecticides, oxadiazole insecticides, and sulfonamide insecticides are blended as drugs ( The volatilization improvement method of the preparation for heat transpiration as described in any one of 1)-(4). (6) A preparation for heat transpiration, wherein the volatilization of the drug is improved by the method for improving volatilization of the preparation for heat transpiration described in any one of (1) to (5).

  With the method for improving volatilization of the preparation for heat evaporation of the present invention, the volatilization of the drug can be improved with a smaller amount of the organic foaming agent. Moreover, since generation | occurrence | production of smoke is suppressed, irritation | stimulation is reduced, a usability | use_condition is improved, and the formulation for heat | fever evaporation which can also eliminate problems, such as malfunction of a fire alarm, can be provided.

The method for improving volatilization of the preparation for heat transpiration of the present invention is used for the preparation B for heat transpiration used in the form of the self-heating device 1 as shown in FIG.
The self-heating device 1 includes a cylindrical outer container 2 with a bottom, and a hydrothermal substance A is accommodated from the bottom to the side. The outer container 2 has a plurality of water holes at the bottom, and the water holes are closed by a member having water permeability, for example, a nonwoven fabric sheet 3. Further, the inside of the outer container 2 is partitioned into two spaces by a partition member 4. The partition member 4 is cylindrical and has a bottom that is substantially hollow hemispherical, and its side wall is disposed concentrically with the peripheral wall of the outer container 2.
The hydrothermal exothermic substance A is filled in a space formed by the peripheral wall of the outer container 2, the partition member 4, and the nonwoven fabric sheet 3, and the heat transpiration agent B is accommodated inside the partition member 4. Further, the upper open surface of the outer container 2 is covered with a lid member 6 in which a plurality of openings are formed in a region corresponding to the upper open surface of the partition member 4. It is blocked by a hot-melt resin film 7 having vent holes.
The hydrothermal exothermic substance A is a substance that self-heats by reaction with water. For example, calcium oxide (quick lime) is used. Therefore, in use, when the self-heating device 1 is placed in the container 20 containing the water W, the water W flows into the outer container 2 through the water passage hole, and further penetrates the nonwoven fabric sheet 3 and comes into contact with the hydrothermal substance A. Then, the heat-evaporating preparation B is heated by the reaction heat generated at that time, and the chemical is volatilized together with the pyrolysis gas of the organic foaming agent. Released. Further, since the heat-melting resin film 7 is thermally melted by heat radiation from the preparation B for heat transpiration and contact with the volatilized drug, the volatilized drug becomes smoke from a relatively early stage of transpiration, and the lid member 6 is opened. It is efficiently discharged to the outside through the section.

The preparation for heat evaporation consists of a mixture of a drug and an organic foaming agent, and granulated using a binder or the like. The volatilization improving method of the present invention converts an inorganic porous material into an organic foaming agent at the time of mixing. 5 to 20% by weight, preferably 5 to 15% by weight based on the total amount of the above. Thereby, volatilization of a chemical | medical agent can be improved significantly. That is, the inorganic porous material functions as a chemical volatilization improver in the preparation for heat evaporation.
Furthermore, the volatilization improving method of the present invention can suppress the generation of smoke when the preparation for heat evaporation is indirectly heated. Although details of the mechanism are not clear, it is presumed that the foaming temperature of the organic foaming agent can be suppressed and the generation of smoke can be suppressed by adding a specific amount of the inorganic porous material to the organic foaming agent.
In addition, since a burning odor and a strange odor are reduced during use, the feeling of use is not adversely affected.

  As the inorganic porous material, inorganic fired foams such as pearlite and shirasu balloon are preferable, and pearlite is particularly preferable.

Further, in the preparation for heat evaporation, when the organic foaming agent is blended in an amount of 65 to 80% by weight, preferably 70 to 80% by weight, the improvement of the volatilization of the drug is often exhibited.
The organic foaming agent in the present invention is not particularly limited as long as it thermally decomposes to generate nitrogen gas and the like to volatilize the chemical together, and is preferably one that foams and melts at 300 ° C. or lower to generate gas. For example, azodicarbonamide, benzenesulfonylhydrazide, P-toluenesulfonylhydrazide, P, P′-oxybis (benzenesulfonylhydrazide), dinitrosopentanemethylenetetrazine, N, N′-dinitroso-N, N′-dimethylterephthalamide , Trihydrazinotriazine, azobisisobutyronitrile, 4,4′-azobiscyanovaleric acid, t-butylazoformamide, 2,4-bis- (azosulfonyl) toluene, 2,2′-azobis Examples thereof include one or more of isobutyramide, methyl-2,2′-azobisisobutyrate, 2- (carbamoylazo) isobutyronitrile, 1,1-azobiscyclohexanecarbonitrile and the like.
Among these, blending azodicarbonamide is preferable because it improves the volatilization of the drug and also improves the diffusibility.

As a chemical | medical agent suitable for the volatilization improvement method of this invention, an insecticide, a pest repellent, a disinfectant, a deodorant, a fragrance | flavor, etc. which volatilize with the pyrolysis gas of the said organic foaming agent can be used.
Examples of insecticides include natural pyrethrin, pyrethrin, allethrin, phthalthrin, resmethrin, framethrin, permethrin, phenothrin, ciphenothrin, praretrin, transfluthrin, methfluthrin, profluthrin, imiprothrin, empentrin, ethofenprox, and sylfluofen. Insecticides; Carbamate insecticides such as propoxur and carbaryl; Organophosphorus insecticides such as fenitrothion and DDVP; Oxadiazole insecticides such as metoxadiazone; Phenylpyrazole insecticides such as fipronil; Neonicochi such as imidacloprid and dinotefuran Noid insecticides; sulfonamide insecticides such as amidoflumet; pyrrole compounds such as chlorfenapyr; metoprene, hydroprene Insect juvenile hormone-like compounds; anti-juvenile hormone-like compounds such as plecosene; molting hormone-like compounds such as ecdysone; essential oils such as phytoncide, light-loading oil, orange oil, cinnamon oil, and clove oil; 1 type (s) or 2 or more types, such as ammonium salt and a benzyl salicylate, are mentioned.
Of these, pyrethroid insecticides, carbamate insecticides, oxadiazole insecticides, and sulfonamide insecticides are preferable because of their improved volatility, and in particular, ciphenothrin, permethrin, methoxadiazone, propoxle, amidoflumet, etofenprox. Is preferred.

As a pest repellent, 1 type (s) or 2 or more types, such as a diet, di-n-butyl succinate, hydroxyanisole, rotenone, ethyl-butylacetylamino propionate, are mentioned, for example.
Examples of the bactericidal disinfectant include one or more of isopropylmethylphenol, p-hydroxybenzoate, PCMX, IPBC, chlorhexidine gluconate, chlorhexidine hydrochloride, benzethonium chloride, cetylpyridinium chloride, and the like.
Examples of the deodorant include one or more of lauryl methacrylate, geranyl chlorinate, catechin, polyphenol and the like.
Examples of the fragrance include one or more of pinene, limonene, linalool, menthol, eugenol, lavender and the like.
What is necessary is just to mix | blend these chemical | medical agents so that it may become 0.1 to 30 weight% with respect to the preparation for heat | fever evaporation.

In order to produce the preparation for heat transpiration of the present invention, the above-mentioned agent, organic foaming agent, inorganic porous body and the like are mixed so as to be a predetermined amount, granulated using a binder or a solvent, and dried. Granules, powders, fine granules, etc. may be used.
When granulating these, for example, in the case of granules, the particle size is preferably about 1 to 5 mm.
Examples of binders used for granulation include celluloses such as carboxymethylcellulose, hydroxymethylcellulose, and hydroxypropylmethylcellulose; starches such as starch and starch; natural polymer compounds such as gum arabic; polyvinyl alcohol, polyvinylpyrrolidone, and the like 1 type or 2 types or more, such as these synthetic polymer compounds.
What is necessary is just to mix | blend these binders so that it may become 0.5 to 5 weight% with respect to the preparation for heat | fever evaporation.

Examples of the solvent include alcohols such as water, ethanol, propanol, and benzyl alcohol, paraffins such as liquid paraffin and n-paraffin, ethers such as butyl diglycol, esters such as isopropyl myristate, and glycerin. 1 type, or 2 or more types, such as a monohydric alcohol, N-methylpyrrolidone, a propylene carbonate, is mentioned.
In addition to mixing and kneading at the time of granulation, the drug can be held by spraying and dipping after granulation.

Further, if necessary, disintegrating agents, rust preventives, stabilizers and the like may be blended. For example, organic acid esters such as paraoxybenzoic acid ester, stearic acid ester, ethyl lactate, chlorophenyl salicylate; malic acid, fumaric acid When a disintegrant such as an acid, tartaric acid, adipic acid, or organic acid such as succinic acid is used, disintegration of the preparation by heating is promoted, and the volatilization of the drug can be made smooth.
Examples of the rust inhibitor include 1,2,3-benzotriazole, dicyclohexylammonium nitrite and the like.
Examples of the stabilizer include dibutylhydroxytoluene, butylhydroxyanisole and the like.
In addition, Cd-stearate, Ca-stearate, Zn-stearate, Zn-octate, ZnO, Sn-maleate, ZnCO ₃ , urea, chrome yellow, carbon black, Dyphos and Tribase (manufactured by National Lead), OF-14 and OF-15 (manufactured by Adeka Argus), KV-68A-1 (manufactured by Kyodo Yakuhin Co., Ltd.), Mark-553 (manufactured by Adeka Chemi), Sicostab 60 and Sicostab 61 (manufactured by Sigre), etc. are used in combination. The foaming temperature of the foaming agent can also be lowered.
Furthermore, if necessary, various surfactants, efficacy enhancers, dyes and the like can be used.

  Examples of the hydrothermal exothermic substance A used in the self-heating device 1 include magnesium chloride, aluminum chloride, calcium oxide and the like. In such an exothermic system, it is preferable to use 1 to 10 times the hydropyrogenic substance with respect to the preparation for heat transpiration. Should be used as a guide. Further, water may be added so as to be 0.2 to 2 times by weight with respect to the hydrothermal substance.

The form of use of the preparation for heat evaporation of the present invention is not limited to the self-heating device 1, but instead of an exothermic system based on the reaction between a hydrothermal substance and water, for example, a heating wire such as a nichrome wire, a flat plate, An electric heating system using a ring-shaped, semiconductor-based heater or the like; a mixture of iron powder and an oxidizing agent such as ammonium chlorate, and a metal and a metal oxide or oxidizing agent having a lower ionization tendency than the metal Mix a mixture of iron and potassium sulfate, iron sulfate, metal chloride, iron sulfide, etc. with water or oxygen, and a mixture of a metal that has a higher ionization tendency than iron and a metal halide that has a lower ionization tendency than iron. Contact with water, contact a mixture of metal and bisulfate with water, add water to a mixture of aluminum and alkali metal nitrate, etc. Beam; may be used system and the like generate heat by utilizing an oxidation reaction of the mixture of the metal sulfide is contacted with oxygen in sodium sulfate and iron carbide.
At that time, the heating temperature is about 200 to 500 ° C., preferably about 300 to 400 ° C., as measured by X in FIG. 1 (the bottom of the partition member 4).

  Moreover, as a container (partition member 4) which accommodates the preparation for heating transpiration, a plastic container, a paper container, a metal container, a ceramic container, a glass container etc. can be used, for example.

  EXAMPLES The present invention will be described in more detail with reference to examples below, but the present invention is not limited to these examples.

Test example 1
The self-heating device 1 as shown in FIG. 1 was installed at the center of the floor in an 8 tatami room (32 m ³ ), and the volatilization rate of the insecticide 2 hours after the start of transpiration was measured to determine the volatilization rate. . In this test, 10 g of the preparation for heat evaporation described in Table 1 was used, and 22 g of water was added to 65 g of calcium oxide to volatilize. The volatilized insecticide was collected for 15 minutes using silica gel by a collection device, and the insecticide was extracted from the silica gel using 1 liter of acetone. Thereafter, the extract was suction filtered, and diethylhexyl sebacate was added to the filtrate by permethrin, and dibutyl sebacate was added to methoxadiazone, and quantitative analysis was performed by gas chromatography to obtain the volatilization rate (%) of the drug. The test was repeated twice to obtain an average value.

  The test results are shown in Table 2. Example 1 in which about 11% by weight of pearlite was blended with respect to the organic blowing agent (azodicarbonamide) was compared with Comparative Example 1 in which the same amount of silicic acid was blended, and the volatilization rate was about 33% with permethrin. About 20% higher for methoxadiazone. Further, in Example 1, although the organic foaming agent was 10% less than that in Reference Example 1, the same volatilization rate was obtained for both permethrin and methoxadiazone. Proved to be a significant improvement.

Test example 2
In Example 1, the blending amount of perlite with respect to the organic foaming agent was changed to about 5.3% by weight (Example 2), about 17.6% by weight (Example 3), and about 25% by weight (Comparative Example 2). The same test as in Test Example 1 was performed. The blending amount of azodicarbonamide was adjusted with the increase / decrease amount of pearlite so that the total amount of the preparation was 10 g.
The test results are shown in Table 3. The volatilization rates of permethrin and methoxadiazone in the examples were both improved as compared with Comparative Example 1. In particular, Example 2 was equivalent or better than Reference Example 1.

Test example 3
The insecticidal efficacy was confirmed using the heat transpiration preparation of Example 1. First, on the floor of two diagonals in an 8 tatami room (32 m ³ ), 10 adult male black cockroaches / site are placed in a slit box (a cube with two 10 mm x 100 mm slits and a side of 30 cm). Then, the preparation for heating and transpiration of Example 1 was placed on the floor in the center of the room and volatilized. After 2 hours of exposure, the number of knockdowns was counted over time, and the mortality (%) after 24 hours was calculated. The test was repeated twice to obtain an average value.
The test results are shown in Table 4. Example 1 was demonstrated to exhibit the insecticidal efficacy of Reference Example 1 or more used as a control.

Test example 4
A dust collector (SIBATA DIGITAL DUST INDICATOR MODEL P-5) is installed at a height of 1 m from the center floor of a chamber (32 m ³ ) equivalent to 8 tatami mats, and the drug using the preparation for heat evaporation of Example 1 is used. The amount of smoke was measured for 120 minutes after 120 minutes. Moreover, the amount of smoke in the chamber was measured as a blank before volatilization, and the amount of smoke (cpm) was determined by the following formula. The smoke reduction rate (%) was calculated for Reference Example 1. The test was repeated twice to obtain an average value.
Smoke amount (cpm) = measured smoke amount-blank smoke amount Smoke reduction rate (%) = (control smoke amount-measured smoke amount) / control smoke amount The test results are shown in Table 5. . In Example 1, the amount of azodicarbonamide was 10% less than that of Reference Example 1, whereas the smoke reduction rate exceeded 30%, and it was found that the smoke decreased more than the blending difference of the organic foaming agent.

Test Example 5
A preparation for heating and transpiration was prepared by replacing the pearlite of Example 1 with the same amount of talc and kaolin in Example 1, and using a self-heating device 1 as shown in FIG. It was placed on the floor surface at the center of 32 m ³ ) and volatilized. After 2 hours, ventilation was performed for 10 minutes, and a monitor entered the chamber, and sensory evaluation was performed for burnt odor and odor.
As a result of evaluation with 10 monitors, there was a tendency to feel burnt odor and odor in the order of kaolin and talc, but when using perlite, burn odor and odor are not felt and it is excellent in use feeling I understood.

  From the above results, it was proved that according to the present invention, the volatilization rate of the preparation for heat evaporation is improved and the generation of smoke is also suppressed. Furthermore, it was confirmed that the burning odor and odor reduction effect and insecticidal efficacy were improved.

Test Example 6
Except for the formulation shown in Table 6, the volatilization rate (%) was determined in the same manner as in Test Example 1. The test was repeated twice to obtain an average value. The results are shown in Table 7.

  Even if it was the mixing | blending of a chemical | medical agent as shown in Table 7, the result obtained that the volatilization rate of each chemical | medical agent was fully obtained.

Test Example 7
Except for the formulation shown in Table 8, the volatilization rate (%) was determined in the same manner as in Test Example 1. The test was repeated twice to obtain an average value. The results are shown in Table 9.

  Even if it was a chemical | medical agent mixing | blending as shown in Table 9, the result obtained that the volatilization rate of each chemical | medical agent was fully obtained.

<Formulation example>
Examples of preparations for heat transpiration using the method for improving volatilization of preparations for heat transpiration according to the present invention are shown below, but the present invention is not limited to these as long as the effects of the invention are exhibited.

It is sectional drawing which shows one use form of the preparation for heat transpiration.

Explanation of symbols

DESCRIPTION OF SYMBOLS 1 Self-heating device 2 Outer container 3 Nonwoven fabric sheet 4 Partition member 6 Lid member 7 Heat-melt film 20 Container A Hydrothermal substance B Heating transpiration preparation W Water

Claims (6)

  In the preparation for heat evaporation for heating the mixture of the chemical and the organic foaming agent indirectly to volatilize the chemical, 5 inorganic porous bodies that act as volatilization improvers with respect to the total amount of the organic foaming agent. A method for improving volatilization of a preparation for heat transpiration, which is blended so as to be ˜20% by weight.   2. The method for improving volatilization of a preparation for heat evaporation according to claim 1, wherein the inorganic porous material is an inorganic fired foam.   The method for improving volatilization of a preparation for heat evaporation according to claim 1 or 2, wherein the preparation is for heat evaporation containing 65 to 80% by weight of an organic foaming agent.   The method for improving volatilization of a preparation for heat evaporation according to any one of claims 1 to 3, wherein the preparation is for heat evaporation containing azodicarbonamide as an organic foaming agent.   5. A heat transpiration preparation comprising one or more pyrethroid insecticides, carbamate insecticides, oxadiazole insecticides and sulfonamide insecticides as a drug. The volatilization improvement method of the preparation for heat | fever evaporation of any one of these.   6. A preparation for heat transpiration, wherein the volatilization of the drug is improved by the method for improving volatilization of the preparation for heat transpiration according to any one of claims 1 to 5.

Images