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
JPH0236559B2 - KANKOSEIKEISANHIRYONOSEIZOHOHO - Google Patents
[go: Go Back, main page]

JPH0236559B2 - KANKOSEIKEISANHIRYONOSEIZOHOHO - Google Patents

KANKOSEIKEISANHIRYONOSEIZOHOHO

Info

Publication number
JPH0236559B2
JPH0236559B2 JP23813188A JP23813188A JPH0236559B2 JP H0236559 B2 JPH0236559 B2 JP H0236559B2 JP 23813188 A JP23813188 A JP 23813188A JP 23813188 A JP23813188 A JP 23813188A JP H0236559 B2 JPH0236559 B2 JP H0236559B2
Authority
JP
Japan
Prior art keywords
silicic acid
rice husk
dolomite
component
iron oxide
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 - Lifetime
Application number
JP23813188A
Other languages
Japanese (ja)
Other versions
JPH0288485A (en
Inventor
Katsutoshi Yamada
Toshio Ogata
Yoshio Noda
Koichi Nakagawa
Kensaku Haraguchi
Kazuji Ishibashi
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.)
National Institute of Advanced Industrial Science and Technology AIST
Original Assignee
Agency of Industrial Science and Technology
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 Agency of Industrial Science and Technology filed Critical Agency of Industrial Science and Technology
Priority to JP23813188A priority Critical patent/JPH0236559B2/en
Publication of JPH0288485A publication Critical patent/JPH0288485A/en
Publication of JPH0236559B2 publication Critical patent/JPH0236559B2/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Landscapes

  • Fertilizers (AREA)

Description

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

(技術分野) 本発明は、籾殻又は籾殻灰、ドロマイト、カリ
ウム化合物、酸化鉄及び必要に応じてその他の補
助原料から、可溶性(塩酸溶解性)及びク溶性
(クエン酸溶解性)のCa2SiO4、Fe2SiO4
K2CaSiO4、K2MgSiO4等を主成分とする緩効性
ケイ酸肥料を製造する方法に関するものである。 (従来技術及びその問題点) ケイ酸肥料は、稲、麦のようにケイ酸を多く含
む作物に対してその効果が顕著であることが実証
されている。また、ケイ酸は直接作物に吸収され
なくても土壌に施すことによつて活性アルミニウ
ムの害を軽減し、陽イオン交換容量を増大して養
分の流出を防ぐ効果があることなどが知られてい
る。 従来、緩効性ケイ酸肥料(通常、緩効性ケイ酸
カリ肥料)の製造方法について種々研究がなされ
てきたが、いずれの方法においてもアルミニウム
を含有する鉱さい類、火力発電所から発生するフ
ライアツシユなどの産業排出物あるいはカリ長石
などの天然鉱物をケイ酸原料としている。これら
のケイ酸原料に含まれるアルミニウム分(第1表
を参照)は、ケイ酸とともに土壌中の主成分を構
成するものであり、植物体中にも多量に取り込ま
れるが、植物体内では根に沈積するものが大部分
で、リンの不活性化やカルシウム、マグネシウム
の吸収抑制を起こす。従つて、茶樹など特定の好
酸性、あるいは耐酸性植物を除いては、その毒性
が重要視され、植物に対する酸性障害の一因とみ
なされており、一般の植生には有害元素の一つで
ある。それ故、アルミニウム含有しない、あるい
はその含有量が極めて微量の肥料を製造するため
にはアルミニウムを含有しない、あるいはその含
有量が極めて微量である原料を使用する必要があ
る。
(Technical field) The present invention produces soluble (hydrochloric acid soluble) and citric acid soluble Ca 2 SiO from rice husk or rice husk ash, dolomite, potassium compounds, iron oxide, and other auxiliary raw materials as necessary. 4 , Fe2SiO4 ,
The present invention relates to a method for producing a slow-release silicate fertilizer containing K 2 CaSiO 4 , K 2 MgSiO 4 , etc. as main components. (Prior Art and its Problems) It has been demonstrated that silicic acid fertilizers have a remarkable effect on crops containing a large amount of silicic acid, such as rice and wheat. In addition, even if silicic acid is not directly absorbed by crops, it is known that by applying it to the soil, it can reduce the harm caused by activated aluminum, increase cation exchange capacity, and prevent nutrient runoff. There is. In the past, various studies have been conducted on manufacturing methods for slow-release silicate fertilizers (usually slow-release potassium silicate fertilizers), but none of these methods use aluminum-containing slag, fly ash generated from thermal power plants, etc. The raw material for silicic acid is industrial waste or natural minerals such as potassium feldspar. Aluminum contained in these silicic acid raw materials (see Table 1) constitutes the main component in soil together with silicic acid, and is also taken up into plants in large quantities, but in plants it is absorbed into roots. Most of it is deposited, causing inactivation of phosphorus and inhibition of absorption of calcium and magnesium. Therefore, with the exception of certain acidophilic or acid-resistant plants such as tea plants, its toxicity is considered important and is considered to be a cause of acid damage to plants, and it is considered a harmful element for general vegetation. be. Therefore, in order to produce a fertilizer that does not contain aluminum or has a very small amount of aluminum, it is necessary to use raw materials that do not contain aluminum or have a very small amount of aluminum.

【表】 (発明の課題) 本発明は、アルミニウムを含有しない緩効性ケ
イ酸肥料の製造方法を提供することをその課題と
する。 (課題を解決するための手段) そこで本発明者らは、前記課題を解決すべく
種々研究を行つた結果、植性に有害なアルミニウ
ムをほとんど含有しない米作地帯から大量に発生
する籾殻や籾殻灰、ドロマイト、カリウム化合物
及び必要に応じての酸化鉄を原料としてその粒状
混合物を調製し、次いでこれを900〜950℃の温度
で焼成して籾殻又は籾殻灰中のケイ酸成分、ドロ
マイト中のカルシウム成分、マグネシウム成分、
カリウム化合物、酸化鉄を反応させることによつ
て、前記課題を解決し得ることを見出し、本発明
を完成した。 即ち、本発明によれば、アルミニウムを含有し
ない籾殻又は籾殻灰をケイ酸原料にして、このケ
イ酸原料に、ドロマイト、カリウム化合物及び必
要に応じて酸化鉄を添加し、さらに液体バインダ
ーを添加して混練し、造粒し、乾燥した後、流動
炉で焼成して籾殻又は籾殻灰中のケイ酸成分と、
ドロマイト中のカルシウム成分及びマグネシウム
成分と、カリウム化合物と、必要に応じて添加さ
れる酸化鉄とを反応させることを特徴とする緩効
性ケイ酸肥料の製造方法が提供される。 本発明の方法においては、ケイ酸原料として、
籾殻又は籾殻灰を用いる。このケイ酸原料は、後
記の第2表からわかるように、シリカ成分を主成
分とするもので、アルミニウム成分は含まない。 本発明を実施するには、先ず、このケイ酸原料
に、ドロマイト、カリウム化合物、必要に応じて
酸化鉄を加え、さらに液体バインダー添加し、混
練し、造粒し、乾燥して、造粒混合を形成する。
この場合、カリウム化合物としては、炭酸カリウ
ムや水酸化カリウム等が用いられる。液体バイン
ダーとしては、廃糖密の他、でん粉、ポリビニル
アルコール、アルギン酸ソーダ等の水溶性高分子
の水溶液が用いられる。 次に、前記のように得られた造粒混合物を高
温、好ましくは900〜950℃の温度で焼成する。こ
の焼成により、籾殻又は籾殻灰中のケイ酸成分、
ドロマイト中のカルシウム成分及びマグネシウム
成分、カリウム化物及び酸化鉄が各反応して、ケ
イ酸塩化合物、例えば、Ca2SiO4、Fe2SiO4
K2CaSiO4、K2MgSIO4を主成分とするケイ酸肥
料が得られる。 (発明の効果) 本発明のケイ酸肥料は、従来のケイ酸肥料とは
異なり、植性に有害なアルミニウム成分を実質的
に含まないもので、アルミニウム害を生じること
のないものである。また、このケイ酸肥料は、緩
効性を有するもので、植物が根から分泌する弱酸
によつて溶解され、植物に吸収される。 (実施例) 次に、本発明の実施例および比較例を挙げて、
具体的に説明する。なお、原料として用いた籾
殻、籾殻灰およびドロマイトの化学組成を第2表
に示した。また、各例で試製された緩効性ケイ酸
肥料の性状を第4表、第5表に、そして比較例で
試製された焼成物の性状を第6表にそれぞれ示し
た。
[Table] (Problem of the Invention) An object of the present invention is to provide a method for producing a slow-release silicic acid fertilizer that does not contain aluminum. (Means for Solving the Problems) Therefore, as a result of conducting various studies in order to solve the above problems, the present inventors discovered that rice husks and rice husks, which are generated in large quantities from rice cultivation areas that contain almost no aluminum, which is harmful to vegetation, have been found. A granular mixture is prepared using ash, dolomite, potassium compounds, and iron oxide as necessary as raw materials, and then calcined at a temperature of 900 to 950°C to remove the silicic acid component in the rice husk or rice husk ash, and the silicic acid component in the dolomite. Calcium component, magnesium component,
The inventors have discovered that the above-mentioned problems can be solved by reacting a potassium compound and iron oxide, and have completed the present invention. That is, according to the present invention, rice husk or rice husk ash that does not contain aluminum is used as a silicic acid raw material, and dolomite, a potassium compound, and if necessary iron oxide are added to this silicic acid raw material, and a liquid binder is further added. After kneading, granulating, and drying, it is fired in a fluidized furnace to remove the silicic acid component in the rice husk or rice husk ash.
A method for producing a slow-release silicate fertilizer is provided, which comprises reacting calcium and magnesium components in dolomite, a potassium compound, and iron oxide added as needed. In the method of the present invention, as the silicic acid raw material,
Use rice husk or rice husk ash. As can be seen from Table 2 below, this silicic acid raw material contains a silica component as a main component and does not contain an aluminum component. To carry out the present invention, first, dolomite, a potassium compound, and iron oxide are added as necessary to this silicic acid raw material, and a liquid binder is further added, kneaded, granulated, dried, and granulated and mixed. form.
In this case, potassium carbonate, potassium hydroxide, etc. are used as the potassium compound. As the liquid binder, in addition to waste molasses, an aqueous solution of a water-soluble polymer such as starch, polyvinyl alcohol, or sodium alginate is used. The granulated mixture obtained as described above is then calcined at a high temperature, preferably at a temperature of 900-950°C. By this firing, the silicic acid component in the rice husk or rice husk ash,
Calcium and magnesium components, potassium oxides, and iron oxides in dolomite react to form silicate compounds such as Ca 2 SiO 4 , Fe 2 SiO 4 ,
A silicic acid fertilizer containing K 2 CaSiO 4 and K 2 MgSIO 4 as main components is obtained. (Effects of the Invention) The silicate fertilizer of the present invention, unlike conventional silicate fertilizers, does not substantially contain aluminum components harmful to vegetation, and does not cause harm to aluminum. Furthermore, this silicate fertilizer has slow-release properties, and is dissolved by weak acids secreted by plants from their roots and absorbed by plants. (Example) Next, examples and comparative examples of the present invention are given,
I will explain in detail. The chemical compositions of rice husk, rice husk ash, and dolomite used as raw materials are shown in Table 2. Further, the properties of the slow-release silicate fertilizers trial-produced in each example are shown in Tables 4 and 5, and the properties of the baked product trial-produced in the comparative example are shown in Table 6.

【表】 実施例 1〜3 200メツシユ全通に粉砕した籾殻とドロマイト
に、炭酸カリウム水溶液及び廃糖蜜50%水溶液を
加えて、混練、造粒、乾燥した後、フルイ分けし
て粒径1〜2mmのものを実験に供した。廃糖蜜は
造粒のバインダーとして用いたものである。造粒
物の成分組成は、SiO2:34.3wt%、CaO:29.2wt
%、MgO:17.0wt%、K2O:19.5wt%、(CaO+
MgO+K2O)/SiOモル比:2である。この造粒
物を回分型流動炉を用いて、焼成温度:930℃附
近、焼成時間:20分(実施例1)、40分(実施例
2)及び60分(実施例3)の条件で焼成して緩効
性ケイ酸肥料を得た。 焼成に用いた流動炉は、第1図に示した回分型
流動炉で、内径:100mm、分散板の開口比:1.4
%、粒径1〜2mmに調製した造粒物の流動静止層
高は約300mmである。流動化ガスには空気を用い、
流量は流量計により調節した。 なお、焼成物の可溶性ケイ酸(0.5N塩酸溶出
量)、ク溶性カリ(2%クエン酸溶出量)等の分
折は全て公定肥料分析法によつたものである。 実施例 4〜6 第2表に示した組成の籾殻灰をケイ酸原料にし
て、造粒物の成分をSiO2:34.1wt%、CaO:
29.2wt%、MgO:17.0wt%、K2O:20.0wt%、
(CaO+MgO+K2O)/SiO2モル比:2となるよ
うに調整した他は、実施例1と同様に実験を行つ
た。 実施例 7〜9 実施例1〜6では、SiO2−CaO−MgO−K2O
の4成分系に調製した混合造粒物の結果を示した
が、この実施例7〜9では上記の4成分に酸化鉄
を加えたSiO2−CaO−MgO−K2O−Fe2O3の5
成分系に原料を調整した。即ち、200メツシユ全
通に粉砕した籾殻、ドロマイト、酸化鉄に、炭酸
カリウム水溶液及び廃糖蜜50%水溶液を加え、混
練、造粒、乾燥した後、フルイ分けして粒径1〜
2mmのものを実験に供した。廃糖蜜は造粒のバイ
ンダーとして用いたものである。造粒物の成分は
SiO2:32.7wt%、CaO:24.8wt%、MgO:
14.5wt%、K2O:19.3wt%、Fe2O3:9.7wt%、
(CaO+MgO+K2O+Fe2O3)/SiO2モル比:2
である。次いでこの造粒物を30分(実施例7)、
40分(実施例8)および60分(実施例9)で焼成
した他は、実施例1と同様に実験を行い、緩効性
ケイ酸肥料を得た。 比較例 1〜3 200メツシユ全通に粉砕した籾殻中のケイ酸と
ドロマイトを第3表に示した配分で混合し、次い
でこの混合物を電気炉用いて、比較例1は900℃
で60分、比較例2は1100℃で60分、比較例3は
1100℃で300分の条件で焼成し、得られた焼成物
について各実施例と同様にして評価した。
[Table] Examples 1 to 3 Potassium carbonate aqueous solution and 50% blackstrap molasses aqueous solution were added to rice husks and dolomite crushed into 200 meshes, kneaded, granulated, dried, and separated through a sieve to obtain particles with a particle size of 1 to 1. A 2 mm one was used in the experiment. Blackstrap molasses was used as a binder for granulation. The composition of the granules is: SiO 2 : 34.3wt%, CaO: 29.2wt%
%, MgO: 17.0wt%, K 2 O: 19.5wt%, (CaO+
MgO+K 2 O)/SiO molar ratio: 2. This granulated material was heated in a batch-type fluidized furnace under the following conditions: firing temperature: around 930°C, firing time: 20 minutes (Example 1), 40 minutes (Example 2), and 60 minutes (Example 3). Slow-release silicic acid fertilizer was obtained by calcination. The fluidized fluidized furnace used for firing was the batch type fluidized furnace shown in Figure 1, with an inner diameter of 100 mm and an aperture ratio of the dispersion plate: 1.4.
%, and the height of the fluidized stationary bed of the granulated product prepared to have a particle size of 1 to 2 mm is approximately 300 mm. Air is used as the fluidizing gas,
The flow rate was controlled by a flow meter. The analysis of soluble silicic acid (amount eluted with 0.5N hydrochloric acid), soluble potash (amount eluted with 2% citric acid), etc. of the fired product was all based on the official fertilizer analysis method. Examples 4 to 6 Rice husk ash having the composition shown in Table 2 was used as a silicic acid raw material, and the components of the granules were SiO 2 :34.1wt%, CaO:
29.2wt%, MgO: 17.0wt%, K2O : 20.0wt%,
The experiment was conducted in the same manner as in Example 1, except that the molar ratio of (CaO+MgO+K 2 O)/SiO 2 was adjusted to 2. Examples 7 to 9 In Examples 1 to 6, SiO2 -CaO-MgO- K2O
However, in Examples 7 to 9, SiO 2 -CaO-MgO-K 2 O-Fe 2 O 3 in which iron oxide was added to the above four components was shown. 5
The raw materials were adjusted to the component system. That is, to rice husk, dolomite, and iron oxide that have been crushed into 200 meshes, an aqueous potassium carbonate solution and a 50% aqueous solution of blackstrap molasses are added, kneaded, granulated, dried, and separated through a sieve to obtain particles with a particle size of 1 to 1.
A 2 mm one was used in the experiment. Blackstrap molasses was used as a binder for granulation. The ingredients of the granules are
SiO2 : 32.7wt%, CaO: 24.8wt%, MgO:
14.5wt% , K2O : 19.3wt%, Fe2O3 : 9.7wt%,
(CaO+MgO+ K2O + Fe2O3 )/ SiO2 molar ratio : 2
It is. Next, this granulated material was heated for 30 minutes (Example 7).
The experiment was conducted in the same manner as in Example 1, except that the firing time was 40 minutes (Example 8) and 60 minutes (Example 9), and slow-release silicate fertilizers were obtained. Comparative Examples 1 to 3 Silicic acid and dolomite in rice husks crushed into 200 meshes were mixed in the proportions shown in Table 3, and then this mixture was heated to 900°C using an electric furnace.
60 minutes at 1100℃ for comparative example 2, and 60 minutes at 1100℃ for comparative example 3.
It was fired at 1100°C for 300 minutes, and the resulting fired product was evaluated in the same manner as in each example.

【表】【table】

【表】【table】

【表】 〓肥料中の可〓
[Table] 〓Possible in fertilizer〓

Claims (1)

【特許請求の範囲】[Claims] 1 アルミニウムを含有しない籾殻又は籾殻灰を
ケイ酸原料にして、このケイ酸原料に、ドロマイ
ト、カリウム化合物、必要に応じて酸化鉄を添加
し、さらに液体バインダーを添加して混練し、造
粒し、乾燥した後、流動炉で焼成して籾殻又は籾
殻灰中のケイ酸成分と、ドロマイト中のカルシウ
ム成分及びマグネシウム成分と、カリウム化合物
と、必要に応じて添加される酸化鉄とを反応させ
ることを特徴とする緩効性ケイ酸肥料の製造方
法。
1 Rice husk or rice husk ash that does not contain aluminum is used as a silicic acid raw material, and dolomite, a potassium compound, and iron oxide as necessary are added to this silicic acid raw material, and a liquid binder is further added, kneaded, and granulated. After drying, it is fired in a fluidized furnace to react the silicic acid component in the rice husk or rice husk ash, the calcium component and magnesium component in the dolomite, the potassium compound, and the iron oxide added as necessary. A method for producing a slow-release silicate fertilizer characterized by:
JP23813188A 1988-09-21 1988-09-21 KANKOSEIKEISANHIRYONOSEIZOHOHO Expired - Lifetime JPH0236559B2 (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
JP23813188A JPH0236559B2 (en) 1988-09-21 1988-09-21 KANKOSEIKEISANHIRYONOSEIZOHOHO

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
JP23813188A JPH0236559B2 (en) 1988-09-21 1988-09-21 KANKOSEIKEISANHIRYONOSEIZOHOHO

Publications (2)

Publication Number Publication Date
JPH0288485A JPH0288485A (en) 1990-03-28
JPH0236559B2 true JPH0236559B2 (en) 1990-08-17

Family

ID=17025646

Family Applications (1)

Application Number Title Priority Date Filing Date
JP23813188A Expired - Lifetime JPH0236559B2 (en) 1988-09-21 1988-09-21 KANKOSEIKEISANHIRYONOSEIZOHOHO

Country Status (1)

Country Link
JP (1) JPH0236559B2 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
JP4985042B2 (en) * 2007-03-30 2012-07-25 独立行政法人産業技術総合研究所 Production system of nutrient composition for silicon supplementation to water area using agricultural and marine product waste and method for modifying nutrient environment of water area
JP5463507B2 (en) * 2008-05-08 2014-04-09 国立大学法人東京農工大学 PK compound fertilizer used as raw fertilizer for wheat cultivation
JP2021146271A (en) * 2020-03-18 2021-09-27 国立大学法人弘前大学 Fertilizer activity substance production method, waste treatment method, fertilizer activity substance production device and waste treatment device

Also Published As

Publication number Publication date
JPH0288485A (en) 1990-03-28

Similar Documents

Publication Publication Date Title
CN107418586B (en) Granular south rice field acid soil conditioner taking rice husks as matrix
CN103436266B (en) Industrial silico-calcium board waste material is utilized to produce the method for moderate-element acidic soil conditioner
US3214261A (en) Granular soil neutralizer and the process of preparing said product
CN114057513A (en) Granular silicon-containing compound fertilizer and preparation method thereof
CN112236405B (en) Silicon-based slow-release potash fertilizer and manufacturing method thereof
JPH0236559B2 (en) KANKOSEIKEISANHIRYONOSEIZOHOHO
CN119020045A (en) A kind of easily disintegrating soil conditioner and its preparation method and application
JPH04243992A (en) Fused compound fertilizer
CN103771911A (en) Method for producing medium element acid soil conditioner by utilizing waste industrial calcium silicate board
JPS6335598B2 (en)
CN102731181A (en) Compound fertilizer containing plant ash
CN104311341A (en) Basic fertilizer granulation method
CN104449747A (en) Silicon-magnesium powder and soil conditioner containing same as well as preparation technology and application of soil conditioner
US4256479A (en) Granulation of fertilizer borate
JPS63270375A (en) Soil improving fertilizer
CN102452858A (en) A kind of fertilizer composition and fertilizer and the preparation method of this fertilizer
JPH03237082A (en) Granular phosphatic fertilizer containing humid acid
JPS5986687A (en) Preparation of zeolite-based soil conditioner from coal ash
JPS581718B2 (en) Method for manufacturing granular soil improvement material
CN1247844A (en) Long-acting granular potash fertilizer
CN101293666B (en) Calcium magnesium phosphor potassium fertilizer particle balling preparation technique
JPS6016399B2 (en) Method for producing slag phosphate fertilizer that also serves as a soil improvement material
JPH0280388A (en) Compound fertilizer
JP3087944B2 (en) Oyster shell mixed fertilizer
JPH0222035B2 (en)

Legal Events

Date Code Title Description
EXPY Cancellation because of completion of term