Deprecated: The each() function is deprecated. This message will be suppressed on further calls in /home/zhenxiangba/zhenxiangba.com/public_html/phproxy-improved-master/index.php on line 456
JPS6324960B2 - - Google Patents
[go: Go Back, main page]

JPS6324960B2 - - Google Patents

Info

Publication number
JPS6324960B2
JPS6324960B2 JP54151586A JP15158679A JPS6324960B2 JP S6324960 B2 JPS6324960 B2 JP S6324960B2 JP 54151586 A JP54151586 A JP 54151586A JP 15158679 A JP15158679 A JP 15158679A JP S6324960 B2 JPS6324960 B2 JP S6324960B2
Authority
JP
Japan
Prior art keywords
fatty acid
acid ester
sucrose fatty
urea
water
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
JP54151586A
Other languages
Japanese (ja)
Other versions
JPS5678485A (en
Inventor
Masabumi Ishii
Shinshichi Fujita
Hajime Takiguchi
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Mitsubishi Chemical Corp
Original Assignee
Mitsubishi Chemical Industries Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Mitsubishi Chemical Industries Ltd filed Critical Mitsubishi Chemical Industries Ltd
Priority to JP15158679A priority Critical patent/JPS5678485A/en
Publication of JPS5678485A publication Critical patent/JPS5678485A/en
Publication of JPS6324960B2 publication Critical patent/JPS6324960B2/ja
Granted legal-status Critical Current

Links

Landscapes

  • Fertilizers (AREA)

Description

【発明の詳細な説明】[Detailed description of the invention]

本発明は葉面散布用肥料、特に尿素と蔗糖脂肪
酸エステルとを含む安定性の良い液状ないしクリ
ーム状肥料の製造法に関するものである。 生育中の茶葉に尿素と蔗糖脂肪酸エステルとを
散布すると、茶葉とくに二番茶や三番茶等の低品
位茶葉の品質が向上することが知られている。し
かし蔗糖脂肪酸エステルは水に極めて難溶であ
り、また市販の蔗糖脂肪酸エステル粉末は水に分
散し難いので、均一な散布液を調製するのが困難
である。 本発明者らは尿素と蔗糖脂肪酸エステルとを含
む濃厚で保存安定性のよい液状ないしクリーム状
肥料の製造法について検討した結果、尿素と蔗糖
脂肪酸エステルとを該蔗糖脂肪酸エステルの融点
以上の温度で水に溶解することにより所期の目的
を達成し得ることを知得し、本発明を完成した。 本発明について更に詳しく説明すると、本発明
では尿素と蔗糖脂肪酸エステルとを加熱下に水に
溶解する。生成物中の尿素および蔗糖脂肪酸エス
テルの濃度は出来るだけ高い方が望ましいので、
通常、尿素および蔗糖脂肪酸エステルの合計量が
全体の20%以上、好ましくは30%以上を占めるよ
うにする。 尿素および蔗糖脂肪酸エステルの割合が多くな
ると、生成物は一般に溶液状から常温で流動性の
あるクリーム状、さらには流動状のないクリーム
状になる。この傾向は蔗糖脂肪酸エステルの多い
ほど著しい。例えば生成物中に占める尿素と蔗糖
脂肪酸エステルの合計量が全体の約33%である場
合、尿素と蔗糖脂肪酸エステルとの比率が94:6
のときは溶液状であるが、この比率が84:16のと
きには常温で流動性のあるクリーム状となる。ま
た尿素と蔗糖脂肪酸エステルとの比率が94:6で
あつても、両者の合計量が全体の50%に達すると
常温で流動性のないクリーム状となる。従つて尿
素と蔗糖脂肪酸エステルとの合計量は全体の30〜
50%が好ましい。 蔗糖脂肪酸エステルは尿素に対し通常、2%以
上となるように用いる。好ましくは3〜25%、特
に3〜10%となるように用いる。蔗糖脂肪酸エス
テルとしては市販の任意のものを用いることがで
きる。 尿素および蔗糖脂肪酸エステルの水への溶解
は、該蔗糖脂肪酸エステルの融点以上の温度で行
なう。蔗糖脂肪酸エステルは混合物であつて明確
な融点を示さず、一般に数度Cの範囲で軟化しつ
つ融解するが、本発明においては蔗糖脂肪酸エス
テルが完全に融解する温度、すなわち軟化点の上
限を融点とする。蔗糖脂肪酸エステルは常温では
一般に水に極めて難溶性であるが、加熱すると溶
解性が増し、融点以上では水と均一な溶液をつく
る。この溶液を冷却すると蔗糖脂肪酸エステル―
水の二成分系では蔗糖脂肪酸エステルが析出す
る。しかし尿素が存在すると、蔗糖脂肪酸エステ
ルは析出せず、全体が均一な液状ないしクリーム
状となる。このものは水に容易に溶解するので、
使用時に水で所定の濃度に稀釈すればよい。 なお、尿素および蔗糖脂肪酸エステルを加熱下
に水に溶解するに際し、所望ならば塩化カリや燐
酸アンモニウムなどの肥料成分や硼素、マンガン
その他の微量成分等を添加してもよい。 本発明によれば、保存安定性がよく且つ濃厚な
液状ないしクリーム状の葉面散布用肥料を容易に
製造することができる。 以下に実施例により本発明をさらに具体的に説
明するが、本発明はその要旨をこえない限り以下
の実施例に限定されるものではない。 実施例 500mlの三角フラスコに尿素および蔗糖脂肪酸
エステル(リヨートーシユガーエステル)を合せ
て100g入れ、これに所定量の水を加えた。70℃
で5分間撹拌して溶解させたのち放冷した。これ
を5℃で1週間保存したのち放置して室温に戻
し、水で1%尿素溶液となるように稀釈した。結
果を第1表に示す。 なお、使用した蔗糖脂肪酸エステルのHLB値
は、S1570がHLB=15、S570がHLB=5、S970
がHLB=9である。
The present invention relates to a method for producing a fertilizer for foliar spraying, particularly a highly stable liquid or cream fertilizer containing urea and sucrose fatty acid ester. It is known that spraying urea and sucrose fatty acid ester on growing tea leaves improves the quality of tea leaves, especially low-grade tea leaves such as second-grade tea and third-grade tea. However, sucrose fatty acid ester is extremely poorly soluble in water, and commercially available sucrose fatty acid ester powder is difficult to disperse in water, making it difficult to prepare a uniform spray solution. The present inventors investigated a method for producing a concentrated, storage-stable liquid or cream fertilizer containing urea and sucrose fatty acid ester, and found that urea and sucrose fatty acid ester were heated at a temperature higher than the melting point of the sucrose fatty acid ester. The present invention was completed based on the knowledge that the desired purpose could be achieved by dissolving the product in water. To explain the present invention in more detail, in the present invention, urea and sucrose fatty acid ester are dissolved in water while heating. It is desirable that the concentration of urea and sucrose fatty acid ester in the product be as high as possible.
Usually, the total amount of urea and sucrose fatty acid ester is 20% or more, preferably 30% or more of the total amount. When the proportion of urea and sucrose fatty acid ester increases, the product generally changes from a solution-like state to a cream-like state that is fluid at room temperature, or even a non-flowing cream-like state. This tendency becomes more pronounced as the amount of sucrose fatty acid ester increases. For example, if the total amount of urea and sucrose fatty acid ester in the product is about 33% of the total, the ratio of urea to sucrose fatty acid ester is 94:6.
When the ratio is 84:16, it is in the form of a liquid liquid at room temperature. Even if the ratio of urea and sucrose fatty acid ester is 94:6, if the total amount of both reaches 50% of the total, the product will become creamy with no fluidity at room temperature. Therefore, the total amount of urea and sucrose fatty acid ester is 30~
50% is preferred. Sucrose fatty acid ester is usually used in an amount of 2% or more based on urea. It is preferably used in an amount of 3 to 25%, particularly 3 to 10%. Any commercially available sucrose fatty acid ester can be used. Urea and sucrose fatty acid ester are dissolved in water at a temperature higher than the melting point of the sucrose fatty acid ester. Sucrose fatty acid ester is a mixture and does not have a clear melting point, and generally melts while softening within a range of several degrees Celsius, but in the present invention, the temperature at which sucrose fatty acid ester completely melts, that is, the upper limit of the softening point, is defined as the melting point. shall be. Sucrose fatty acid esters are generally extremely poorly soluble in water at room temperature, but their solubility increases when heated, and above their melting point they form a homogeneous solution with water. When this solution is cooled, sucrose fatty acid ester-
In a two-component system of water, sucrose fatty acid ester precipitates. However, in the presence of urea, the sucrose fatty acid ester does not precipitate, and the whole becomes uniformly liquid or creamy. This substance dissolves easily in water, so
Before use, it may be diluted with water to a predetermined concentration. In addition, when dissolving urea and sucrose fatty acid ester in water while heating, fertilizer components such as potassium chloride and ammonium phosphate, and trace components such as boron and manganese may be added, if desired. According to the present invention, it is possible to easily produce a fertilizer for foliar spraying that has good storage stability and is in the form of a thick liquid or cream. The present invention will be explained in more detail with reference to Examples below, but the present invention is not limited to the following Examples unless it exceeds the gist thereof. Example A total of 100 g of urea and sucrose fatty acid ester (lyotosugar ester) was placed in a 500 ml Erlenmeyer flask, and a predetermined amount of water was added thereto. 70℃
After stirring for 5 minutes to dissolve the mixture, the mixture was allowed to cool. This was stored at 5°C for one week, then allowed to return to room temperature, and diluted with water to form a 1% urea solution. The results are shown in Table 1. The HLB values of the sucrose fatty acid esters used were: HLB = 15 for S1570, HLB = 5 for S570, and HLB = 5 for S970.
is HLB=9.

【表】【table】

【表】【table】

Claims (1)

【特許請求の範囲】 1 尿素および蔗糖脂肪酸エステルを蔗糖脂肪酸
エステルの融点以上の温度で水に溶解することを
特徴とする液状ないしクリーム状の葉面散布用肥
料の製造方法。 2 尿素および蔗糖脂肪酸エステルの重量が生成
する液状肥料の全重量の20%以上を占めることを
特徴とする特許請求の範囲第1項記載の葉面散布
用肥料の製造方法。 3 尿素に対して3〜25%の蔗糖脂肪酸エステル
を含むことを特徴とする特許請求の範囲第1項ま
たは第2項記載の葉面散布用肥料の製造方法。
[Scope of Claims] 1. A method for producing a liquid or cream fertilizer for foliar spraying, which comprises dissolving urea and sucrose fatty acid ester in water at a temperature higher than the melting point of the sucrose fatty acid ester. 2. The method for producing a fertilizer for foliar spraying according to claim 1, wherein the weight of urea and sucrose fatty acid ester accounts for 20% or more of the total weight of the liquid fertilizer produced. 3. The method for producing a fertilizer for foliar spraying according to claim 1 or 2, characterized in that it contains 3 to 25% of sucrose fatty acid ester based on urea.
JP15158679A 1979-11-22 1979-11-22 Manufacture of foliar fertilizer Granted JPS5678485A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP15158679A JPS5678485A (en) 1979-11-22 1979-11-22 Manufacture of foliar fertilizer

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP15158679A JPS5678485A (en) 1979-11-22 1979-11-22 Manufacture of foliar fertilizer

Publications (2)

Publication Number Publication Date
JPS5678485A JPS5678485A (en) 1981-06-27
JPS6324960B2 true JPS6324960B2 (en) 1988-05-23

Family

ID=15521746

Family Applications (1)

Application Number Title Priority Date Filing Date
JP15158679A Granted JPS5678485A (en) 1979-11-22 1979-11-22 Manufacture of foliar fertilizer

Country Status (1)

Country Link
JP (1) JPS5678485A (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR2675014B1 (en) * 1991-04-09 1993-06-25 Rhone Poulenc Chimie AQUEOUS COMPOSITIONS OF PHYTOSANITARY ACTIVE MATERIALS COMPRISING SUCROGLYCERIDES.

Also Published As

Publication number Publication date
JPS5678485A (en) 1981-06-27

Similar Documents

Publication Publication Date Title
WO2010096265A1 (en) Buffered amino alcohol solutions of n-(n-butyl)thiophosphoric triamide (nbpt) and urea fertilizers using such solutions as urease inhibitors
CN110392675A (en) Mixtures containing 3,4-dimethylpyrazole and uses thereof
US3022153A (en) Method of preparing a stable liquid fertilizer from wet-process phosphoric acid
JPS6324960B2 (en)
JPH01318034A (en) Promoter for epoxide curing agent containing cyanamide
US1988991A (en) Manufacture of solid products containing alkali hypochlorite
US3245798A (en) Soluble fumaric acid and adipic acid compositions
US1939165A (en) Fertilizers stable for storage and capable of being scattered
KR860001541A (en) Gelatin Dessert Mix Soluble in Cold Water and Manufacturing Method
CN105641848A (en) Compound cocrystallization preparation method for water-soluble condensed fire extinguishing aerosol fire extinguishing agent ingredients
JP3667791B2 (en) L-menthol-containing powder
US597454A (en) Walter beacall bishop and alfred bishop
JPS5942843A (en) Preparation of fat and oil in fluid state
JPS63107880A (en) Granular fertilizer composition and manufacture
JPS63301759A (en) Production of instant powder food
JPH0476729B2 (en)
US2134672A (en) Pyridine derivatives of barbituric
CN107827594A (en) A kind of humic acid Water soluble fertilizer of long-acting stabilization and preparation method thereof
JPS5824098B2 (en) Process for producing water-soluble cocoa
US4084995A (en) Preparation of a cap sensitive particulate explosive composition comprising calcium nitrate
JPH0475017B2 (en)
US2901472A (en) Method of converting difficultly soluble organic compounds to readily soluble complex compounds, and said complex compounds
JP4117045B2 (en) Emulsifier granulation method
US2867504A (en) Preparation of potassium polyphosphate
US2947741A (en) Isobebeerine nicotinate