CN102811975A - Functionally effective urea composition - Google Patents
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Abstract
本发明提供了用于植物生长和产量提高的功能上有效的尿素组合物,其用于与或不与其它肥料一起使用,其中使尿素与碱金属之硅酸盐或盐或其混合物反应,和/或使尿素与过渡金属之盐或硅酸盐或氧化物或其混合物反应,和/或使尿素与褐煤之有机提取物反应。The present invention provides a functionally effective urea composition for plant growth and yield improvement, for use with or without other fertilizers, wherein urea is reacted with an alkali metal silicate or salt or mixture thereof, and/or urea is reacted with a transition metal salt or silicate or oxide or mixture thereof, and/or urea is reacted with an organic extract of lignite.
Description
技术领域 technical field
本发明涉及用于植物营养和生长的功能上有效的尿素组合物,特别地,本发明涉及制备性能有效之尿素肥料的方法。这些尿素肥料具有用作植物营养物的显著潜力。The present invention relates to functionally effective urea compositions for plant nutrition and growth, and in particular, the present invention relates to a process for preparing urea fertilizers with effective properties. These urea fertilizers have significant potential for use as plant nutrients.
背景技术 Background technique
已知尿素(即,酰胺)迅速地消耗和转化,挥发损失使得难于向植物长时间应用尿素。已进行了很多尝试以向植物系统有效地应用尿素,例如添加尿素酶抑制剂。然而,结果并不令人满意。因此,本发明开发了用于植物营养的功能上有效的尿素,其在开发性能有效的尿素肥料中具有其应用。Urea (ie, amide) is known to be consumed and converted rapidly, and volatilization losses make prolonged application of urea to plants difficult. Many attempts have been made to efficiently apply urea to plant systems, such as the addition of urease inhibitors. However, the results were not satisfactory. Accordingly, the present invention develops a functionally effective urea for plant nutrition, which has its application in developing performance-effective urea fertilizers.
发明目的purpose of invention
本发明的主要目的是提供用于植物生长的功能上有效的尿素组合物,其用于与或不与其它肥料一起使用。The main object of the present invention is to provide a functionally effective urea composition for plant growth, for use with or without other fertilizers.
本发明的另一目的是通过使尿素与碱金属之硅酸盐或盐或其混合物反应而提供功能上有效的尿素组合物。Another object of the present invention is to provide functionally effective urea compositions by reacting urea with alkali metal silicates or salts or mixtures thereof.
本发明的另一目的是通过使尿素与过渡金属之盐或硅酸盐或氧化物或其混合物反应而提供功能上有效的尿素组合物。Another object of the present invention is to provide functionally effective urea compositions by reacting urea with salts or silicates or oxides of transition metals or mixtures thereof.
本发明的另一目的是通过使尿素与褐煤之有机提取物反应而提供功能上有效的尿素组合物。Another object of the present invention is to provide a functionally effective urea composition by reacting urea with an organic extract of lignite.
本发明的另一目的是通过以期望的比例混合上述所产生的有效尿素而提供功能上有效的尿素组合物。Another object of the present invention is to provide a functionally effective urea composition by mixing the above produced effective urea in a desired ratio.
发明概述Summary of the invention
为了实现上述目的,本发明提供了用于植物生长的功能上有效的尿素组合物,其用于与或不与其它肥料一起使用,其中使尿素与碱金属之硅酸盐或盐或其混合物反应,和/或使尿素与过渡金属之盐或硅酸盐或氧化物或其混合物反应,和/或使尿素与褐煤之有机提取物反应。To achieve the above objects, the present invention provides a functionally effective urea composition for plant growth, for use with or without other fertilizers, wherein urea is reacted with a silicate or salt of an alkali metal or a mixture thereof , and/or react urea with transition metal salts or silicates or oxides or mixtures thereof, and/or react urea with organic extracts of lignite.
附图简述Brief description of the drawings
图1涉及本发明实施例6的对比XRD分析。Figure 1 relates to the comparative XRD analysis of Example 6 of the present invention.
图2涉及本发明实施例6的对比FTIR分析。Figure 2 relates to the comparative FTIR analysis of Example 6 of the present invention.
图3涉及本发明实施例7的对比XRD分析。Figure 3 relates to the comparative XRD analysis of Example 7 of the present invention.
图4涉及本发明实施例7的对比FTIR分析。Figure 4 relates to the comparative FTIR analysis of Example 7 of the present invention.
图5涉及本发明实施例8的对比XRD分析。Figure 5 relates to the comparative XRD analysis of Example 8 of the present invention.
图6涉及本发明实施例8的对比FTIR分析。Figure 6 relates to the comparative FTIR analysis of Example 8 of the present invention.
图7涉及本发明实施例9的对比XRD分析。Fig. 7 relates to the comparative XRD analysis of Example 9 of the present invention.
图8涉及本发明实施例9的对比FTIR分析。Figure 8 relates to a comparative FTIR analysis of Example 9 of the present invention.
图9涉及本发明实施例10的对比XRD分析。Fig. 9 relates to the comparative XRD analysis of Example 10 of the present invention.
图10涉及本发明实施例10的对比FTIR分析。Figure 10 relates to a comparative FTIR analysis of Example 10 of the present invention.
图11涉及本发明实施例11的对比XRD分析。Figure 11 relates to the comparative XRD analysis of Example 11 of the present invention.
图12涉及本发明实施例11的对比FTIR分析。Figure 12 relates to a comparative FTIR analysis of Example 11 of the present invention.
图13涉及本发明实施例12的对比XRD分析。Figure 13 relates to the comparative XRD analysis of Example 12 of the present invention.
图14涉及本发明实施例12的对比FTIR分析。Figure 14 relates to a comparative FTIR analysis of Example 12 of the present invention.
图15涉及本发明实施例13的对比XRD分析。Figure 15 relates to the comparative XRD analysis of Example 13 of the present invention.
图16涉及本发明实施例13的对比FTIR分析。Figure 16 relates to a comparative FTIR analysis of Example 13 of the present invention.
图17涉及本发明实施例14的对比XRD分析。Figure 17 relates to the comparative XRD analysis of Example 14 of the present invention.
图18涉及本发明实施例14的对比FTIR分析。Figure 18 relates to a comparative FTIR analysis of Example 14 of the present invention.
图19涉及本发明实施例15的对比XRD分析。Figure 19 relates to the comparative XRD analysis of Example 15 of the present invention.
图20涉及本发明实施例15的对比FTIR分析。Figure 20 relates to the comparative FTIR analysis of Example 15 of the present invention.
图21涉及本发明实施例16的对比XRD分析。Figure 21 relates to the comparative XRD analysis of Example 16 of the present invention.
图22涉及本发明实施例16的对比FTIR分析。Figure 22 relates to a comparative FTIR analysis of Example 16 of the present invention.
图23涉及本发明实施例17的对比XRD分析。Figure 23 relates to the comparative XRD analysis of Example 17 of the present invention.
图24涉及本发明实施例17的对比FTIR分析。Figure 24 relates to a comparative FTIR analysis of Example 17 of the present invention.
图25涉及本发明实施例18的对比XRD分析。Figure 25 relates to the comparative XRD analysis of Example 18 of the present invention.
图26涉及本发明实施例18的对比FTIR分析。Figure 26 relates to a comparative FTIR analysis of Example 18 of the present invention.
图27涉及本发明实施例20的对比XRD分析。Figure 27 relates to the comparative XRD analysis of Example 20 of the present invention.
图28涉及本发明实施例20的对比FTIR分析。Figure 28 relates to a comparative FTIR analysis of Example 20 of the present invention.
发明详述Detailed description of the invention
尽管本发明可以有多种改动和替代形式,其一些具体方面已通过示例性实施例中的实例来显示,并在下文中详细描述。然而,应当理解,其不旨在将本发明限于所公开的具体形式,相反地,本发明将涵盖落入由所附权利要求所限定之本发明宗旨和范围之内的所有改动、等同形式和替代形式。While the invention is susceptible to various modifications and alternative forms, specific aspects thereof have been shown by way of example in exemplary embodiments and described in detail hereinafter. It should be understood, however, that there is no intent to limit the invention to the particular forms disclosed, but on the contrary, the invention is to cover all modifications, equivalents and modifications falling within the spirit and scope of the invention as defined by the appended claims. alternative form.
在详细描述实施方案之前,可以看出本发明的新颖性和创造性在于功能上有效的尿素组合物,包括以多种比例使尿素与碱金属之硅酸盐或盐或其混合物反应、和/或使尿素与过渡金属之盐或硅酸盐或氧化物或其混合物反应、和/或使尿素与褐煤之有机提取物反应以获得功能上有效的尿素组合物。应当注意,本领域技术人员可从本发明获得技术启示,并对上述组合物的不同组成部分进行改动,其可以在作物之间有所不同。然而,这样的改动应当解释为在本发明的范围和宗旨之内。因此,所述实施例仅显示与理解本发明之各方面相关的那些具体细节,以使本公开内容不与对从本文描述获益之本领域技术人员来说很显而易见的细节相混淆。Before describing the embodiments in detail, it can be seen that the novelty and inventive step of the present invention resides in a functionally effective urea composition comprising reacting urea with an alkali metal silicate or salt or mixture thereof in various ratios, and/or Reacting urea with salts or silicates or oxides of transition metals or mixtures thereof, and/or reacting urea with organic extracts of lignite to obtain functionally effective urea compositions. It should be noted that a person skilled in the art can take the technical light of the present invention and make modifications to the different components of the composition described above, which may vary from crop to crop. However, such modifications should be construed as being within the scope and spirit of the invention. Therefore, the examples show only those specific details that are relevant to understanding aspects of the invention so as not to obscure the disclosure with details that would be apparent to those skilled in the art having the benefit of the description herein.
术语“包含”、“包括”或其任何其它变化形式旨在涵盖非排他性的内容,从而使包含一系列组成部分的组合物、设置、装置不仅包括那些组成部分,还可包括未明确列出的或这些组合物、涉及和装置所固有的其它组成部分。换句话说,在没有更多限制的情形下,由“包含......”所限定的组合物或方法中的一个或更多个要素不排除在所述组合物或方法中存在其它要素或额外的要素。以下段落针对功能上有效的尿素组合物来阐释本发明。The terms "comprising", "comprising" or any other variation thereof are intended to cover a non-exclusive content such that a composition, arrangement, device comprising a series of elements includes not only those elements but also elements not expressly listed. Or other components inherent in these compositions, devices and devices. In other words, without more limitations, one or more elements in a composition or method defined by "comprising..." does not exclude the presence of other elements in said composition or method. elements or additional elements. The following paragraphs illustrate the invention with respect to a functionally effective urea composition.
因此,本发明涉及通过使尿素与以下物质反应而获得的功能上有效的尿素组合物:Accordingly, the present invention relates to functionally effective urea compositions obtained by reacting urea with:
碱金属的硅酸盐或盐,和/或Silicates or salts of alkali metals, and/or
过渡金属的盐或硅酸盐或氧化物或其混合物,和/或Salts or silicates or oxides of transition metals or mixtures thereof, and/or
褐煤的有机提取物,或者Organic extracts of lignite, or
将a)、b)和c)所产生的产物混合以获得期望的功能上有效的尿素,其用于与或不与其它肥料一起使用。The products resulting from a), b) and c) are mixed to obtain the desired functionally effective urea for use with or without other fertilizers.
本发明的一个方面,其中所述碱金属的硅酸盐或盐由钠或钾制成。In one aspect of the present invention, wherein the alkali metal silicate or salt is made of sodium or potassium.
本发明的另一方面,其中碱金属的硅酸盐是硅酸钾,其中金属与硅酸盐的比例为1∶2~2∶1。In another aspect of the present invention, wherein the alkali metal silicate is potassium silicate, wherein the ratio of metal to silicate is 1:2 to 2:1.
本发明的另一方面,其中所述硅酸钾具有20~24%的二氧化硅(silica)和10~12%的钾。Another aspect of the present invention, wherein the potassium silicate has 20-24% silica and 10-12% potassium.
本发明的另一方面,其中所述过渡金属选自包含以下的组:锌、铜、锰、锆、二价铜(Cupric)和银及其混合物。Another aspect of the present invention, wherein the transition metal is selected from the group comprising zinc, copper, manganese, zirconium, cupric and silver and mixtures thereof.
本发明的另一方面,其中所述过渡金属的盐是比例为10∶3∶1(体积/体积)的硫酸锌、硫酸铜和硫酸锰的混合物。Another aspect of the present invention, wherein the transition metal salt is a mixture of zinc sulfate, copper sulfate and manganese sulfate in a ratio of 10:3:1 (volume/volume).
本发明的另一方面,其中过渡金属的盐是比例为100∶68∶14(体积/体积)的硫酸锌、硫酸铜和硫酸锰的混合物。Another aspect of the present invention, wherein the transition metal salt is a mixture of zinc sulfate, copper sulfate and manganese sulfate in a ratio of 100:68:14 (vol/vol).
本发明的另一个方面,其中所述硫酸锌具有至少2%的Zn,硫酸铜具有至少0.75的Cu,硫酸锰具有至少0.25%的Mn。Another aspect of the invention wherein the zinc sulfate has at least 2% Zn, copper sulfate has at least 0.75 Cu, and manganese sulfate has at least 0.25% Mn.
本发明的另一方面,其中过渡金属的硅酸盐是比例为5∶3∶1的氯化锌、硫酸铜和硫酸锰的混合物,并且其随后与碱金属的硅酸盐溶液反应。Another aspect of the invention wherein the transition metal silicate is a mixture of zinc chloride, copper sulfate and manganese sulfate in a ratio of 5:3:1 and which is subsequently reacted with an alkali metal silicate solution.
本发明的另一方面,其中所述过渡金属的氧化物是比例为10∶3∶1∶1∶1的氧化锌、氧化铜、氧化锰和二氧化镁的混合物,其中在混合之前用H2O2处理氧化锌。Another aspect of the present invention, wherein the transition metal oxide is a mixture of zinc oxide, copper oxide, manganese oxide and magnesium dioxide in a ratio of 10:3:1:1:1, wherein it is treated with H2O2 before mixing Zinc oxide.
本发明的另一方面,其中所述过渡金属的氧化物是比例为9∶1∶1(重量/体积)的经H2O2处理之氧化锌、氧化锆和氧化铜的混合物。In another aspect of the present invention, wherein the transition metal oxide is a mixture of H2O2-treated zinc oxide, zirconium oxide and copper oxide in a ratio of 9:1:1 (weight/volume).
本发明的另一方面,其中通过用10~50%的H2O2处理褐煤(lignite)而获得褐煤的有机提取物。Another aspect of the present invention, wherein an organic extract of lignite is obtained by treating lignite with 10-50% H2O2.
本发明的另一方面,其中尿素是熔化的或固体的尿素。Another aspect of the invention wherein the urea is molten or solid urea.
本发明的另一方面,其中熔化的尿素维持在130℃~139℃的温度下。Another aspect of the invention wherein the molten urea is maintained at a temperature of 130°C to 139°C.
本发明的另一方面,其中尿素与碱金属硅酸盐(alkali silicate)的比例为0.1∶10~10∶0.1。Another aspect of the present invention, wherein the ratio of urea to alkali metal silicate (alkali silicate) is 0.1:10-10:0.1.
本发明的另一方面,其中尿素与碱金属盐(alkali salt)的比例为0.1∶10~10∶0.1。Another aspect of the present invention, wherein the ratio of urea to alkali metal salt (alkali salt) is 0.1:10-10:0.1.
本发明的另一方面,其中尿素与过渡金属或其混合物的比例为0.1∶10~10∶0.1。Another aspect of the present invention, wherein the ratio of urea to transition metal or a mixture thereof is 0.1:10 to 10:0.1.
本发明的另一方面,其中尿素与褐煤有机溶液的比例为0.1∶10~10∶0.1。Another aspect of the present invention, wherein the ratio of urea to lignite organic solution is 0.1:10-10:0.1.
本发明的另一方面,其中尿素、碱金属硅酸盐和过渡金属的比例为10∶0.1∶0.1~1∶0.5∶0.5。Another aspect of the present invention, wherein the ratio of urea, alkali metal silicate and transition metal is 10:0.1:0.1˜1:0.5:0.5.
本发明的另一方面,其中尿素、碱金属硅酸盐、过渡金属和褐煤有机溶液的比例为10∶0.1∶0.1∶0.1~1∶0.5∶0.5∶0.5。Another aspect of the present invention, wherein the ratio of urea, alkali metal silicate, transition metal and lignite organic solution is 10:0.1:0.1:0.1˜1:0.5:0.5:0.5.
本发明的另一方面,其中如此产生的尿素具有20~50倍提高的迁移(translocation)效率。Another aspect of the present invention, wherein the urea thus produced has a 20-50 times higher translocation efficiency.
本发明的另一方面,其中如此产生之尿素的降解任选地通过酶调节或者通过氨或亚硝酸盐转化来控制。Another aspect of the invention wherein the degradation of the urea thus produced is optionally controlled by enzymatic regulation or by ammonia or nitrite conversion.
本发明的另一方面,其中如此产生的尿素组合物使作物产量提高10~90%。Another aspect of the present invention wherein the urea composition thus produced increases crop yield by 10-90%.
以下将详细描述本发明,以举例说明和阐释本发明的多个显著特征。下文中,通过制备多种类型之尿素肥料组合物的如下实施例来描述本发明的显著特征。The present invention will be described in detail below in order to illustrate and explain several salient features of the invention. Hereinafter, salient features of the present invention are described through the following examples of preparing various types of urea fertilizer compositions.
制备过渡金属盐溶液Preparation of Transition Metal Salt Solutions
在水中制备硫酸锌(0.7g/ml)和硫酸铜(0.3g/ml)、硫酸锰(0.5g/ml)。Prepare zinc sulfate (0.7g/ml) and copper sulfate (0.3g/ml), manganese sulfate (0.5g/ml) in water.
以10∶3∶1的比例添加上述这些过渡金属盐溶液以制备多过渡金属盐溶液(poly transition metal salt solution)。These transition metal salt solutions were added at a ratio of 10:3:1 to prepare a poly transition metal salt solution.
制备硅酸钾溶液(钾与硅酸盐之比例的变化范围是1∶2~2∶1)。Potassium silicate solutions were prepared (ratio of potassium to silicate varied from 1:2 to 2:1).
制备钾盐溶液0.3g/ml(氯化物或硫酸盐)。Prepare potassium salt solution 0.3 g/ml (chloride or sulfate).
实施例1Example 1
向5.0Kg熔化的尿素中添加硅酸钾(2.5ml~10ml)和多过渡金属盐溶液(5ml~10ml)并搅拌均匀。在固化过程中获得所需的形式(例如,粉末或颗粒或小球(prill))。用不同量的反应物制备不同的尿素肥料组合物。Potassium silicate (2.5ml-10ml) and multi-transition metal salt solution (5ml-10ml) were added to 5.0Kg of molten urea and stirred evenly. The desired form (eg powder or granules or prills) is obtained during curing. Different urea fertilizer compositions were prepared with different amounts of reactants.
实施例1(a)Example 1(a)
向5Kg熔化的尿素中添加多过渡金属盐溶液(5ml~10ml)并搅拌均匀。在尿素固化的过程中获得所需的形式(例如,粉末或颗粒或小球)。Add multi-transition metal salt solution (5ml-10ml) to 5Kg of molten urea and stir evenly. The desired form (eg powder or granules or pellets) is obtained during the solidification of the urea.
用不同量的过渡金属盐制备不同的尿素肥料组合物。Different urea fertilizer compositions were prepared with different amounts of transition metal salts.
实施例2Example 2
向5kg熔化的尿素中添加硅酸钾(2.5ml~10ml)和硫酸锌(5ml~10ml),在固化的过程中获得所需的形式(例如,粉末或颗粒或小球)。用不同量的反应物制备不同的尿素肥料组合物。Potassium silicate (2.5ml-10ml) and zinc sulphate (5ml-10ml) are added to 5kg of molten urea to obtain the desired form (eg powder or granules or pellets) during solidification. Different urea fertilizer compositions were prepared with different amounts of reactants.
实施例3Example 3
将5Kg熔化的尿素与硅酸钾[20~24%二氧化硅,10~12%钾](2.5ml~10ml)和硫酸锌(5ml~10ml)以及200ml~300ml的褐煤之碱性提取物混合在一起。用不同量的反应物制备不同的尿素肥料组合物。Mix 5Kg of molten urea with potassium silicate [20-24% silicon dioxide, 10-12% potassium] (2.5ml-10ml) and zinc sulfate (5ml-10ml) and 200ml-300ml of lignite alkaline extract together. Different urea fertilizer compositions were prepared with different amounts of reactants.
实施例4Example 4
向5kg熔化的尿素中添加硅酸钾(10ml~20ml)。用不同量的反应物制备不同的尿素肥料组合物。Potassium silicate (10ml-20ml) was added to 5kg of molten urea. Different urea fertilizer compositions were prepared with different amounts of reactants.
实施例5Example 5
将5Kg熔化的尿素与硅酸钾[20~24%二氧化硅,10~12%钾](1ml~50ml)和褐煤之碱性提取物混合在一起。制备不同的组合物,例如在终产物中具有2~5%的有机成分。用不同量的反应物制备不同的尿素肥料组合物。5Kg of molten urea was mixed together with potassium silicate [20-24% silica, 10-12% potassium] (1ml-50ml) and alkaline extract of lignite. Different compositions are prepared, for example with 2-5% organic content in the final product. Different urea fertilizer compositions were prepared with different amounts of reactants.
实施例6Example 6
在持续混合下,向1160gm熔化的尿素[132~139℃]中添加133ml(20gm)量的有机提取物[用10~25%碱提取褐煤]并混匀。在持续混合下逐渐冷却以避免发生大块固化(bulky solidification),随后使产物干燥和/或制成小球。Under continuous mixing, to 1160 gm of molten urea [132-139° C.] was added an amount of 133 ml (20 gm) of organic extract [lignite extracted with 10-25% alkali] and mixed well. Cool gradually with continuous mixing to avoid bulky solidification, then dry and/or pelletize the product.
实施例7Example 7
在持续的混合下,向1160gm熔化的尿素[132~139℃]中添加10ml量的硅酸钾[20~24%二氧化硅,10~12%钾]并混匀。在持续混合下逐渐冷却以避免发生大块固化,随后使产物干燥和/或制成小球。With continuous mixing, to 1160 gm of molten urea [132-139° C.] was added potassium silicate [20-24% silica, 10-12% potassium] in an amount of 10 ml and mixed well. Cool gradually with constant mixing to avoid bulk solidification, and the product is then dried and/or pelletized.
实施例8Example 8
在持续的混合下,向1160gm熔化的尿素[132~139℃]中添加33ml(50gm)量的有机提取物[用10~25%碱提取褐煤]并混匀。在持续混合下逐渐冷却以避免发生大块固化,随后使产物干燥和/或制成小球。Under continuous mixing, to 1160 gm of molten urea [132-139° C.] was added an amount of 33 ml (50 gm) of organic extract [lignite extracted with 10-25% alkali] and mixed well. Cool gradually with constant mixing to avoid bulk solidification, and the product is then dried and/or pelletized.
实施例9Example 9
在持续的混合下,向1160gm熔化的尿素[132~139℃]中添加200ml(30gm)量的有机提取物[用10~25%碱提取褐煤]并混匀。在持续混合下逐渐冷却以避免发生大块固化,随后使产物干燥和/或制成小球。Under continuous mixing, to 1160 gm of molten urea [132-139° C.] was added an amount of 200 ml (30 gm) of organic extract [lignite extracted with 10-25% alkali] and mixed well. Cool gradually with constant mixing to avoid bulk solidification, and the product is then dried and/or pelletized.
实施例10Example 10
在持续的混合下,向1160gm熔化的尿素[132~139℃]中添加2.5ml量的硅酸钾[20~24%二氧化硅,10~12%钾]、5ml的MSM[比例为10∶3∶1(体积/体积)的硫酸锌[0.5g/ml]、硫酸铜(0.3g/ml)和硫酸锰(0.5g/ml)]并混匀。在持续混合下逐渐冷却以避免发生大块固化,随后使产物干燥和/或使其形成小球。Under continuous mixing, to 1160 gm of molten urea [132-139° C], add 2.5 ml of potassium silicate [20-24% silica, 10-12% potassium], 5 ml of MSM [ratio of 10: 3:1 (v/v) zinc sulfate [0.5 g/ml], copper sulfate (0.3 g/ml) and manganese sulfate (0.5 g/ml)] and mix well. Cool gradually with constant mixing to avoid bulk solidification, then dry and/or pelletize the product.
实施例11Example 11
在持续的混合下,向1160gm熔化的尿素[132~139℃]中添加2.5ml量的硅酸钾[20~24%二氧化硅,10~12%钾]、5ml的硫酸锌[0.5克/ml]并混匀。在持续混合下逐渐冷却以避免发生大块固化,随后使产物干燥和/或制成小球。Add 2.5 ml of potassium silicate [20-24% silicon dioxide, 10-12% potassium], 5 ml of zinc sulfate [0.5 g/ ml] and mix well. Cool gradually with constant mixing to avoid bulk solidification, and the product is then dried and/or pelletized.
实施例12Example 12
在持续的混合下,向1160gm熔化的尿素[132~139℃]中添加2.5ml量的硅酸钾[20~24%二氧化硅,10~12%钾]以及5ml的硫酸锌和200ml的有机提取物[用10~25%碱提取褐煤]并混匀。在持续混合下逐渐冷却以避免发生大块固化,随后使产物干燥和/或使其形成小球。Under continuous mixing, to 1160 gm of molten urea [132-139°C] was added 2.5 ml of potassium silicate [20-24% silica, 10-12% potassium], 5 ml of zinc sulfate and 200 ml of organic Extract [brown coal extracted with 10-25% alkali] and mix well. Cool gradually with constant mixing to avoid bulk solidification, then dry and/or pelletize the product.
实施例13Example 13
在持续的混合下,向1160gm熔化的尿素[132~139℃]中添加20ml量的硅酸钾[20~24%二氧化硅,10~12%钾]并混匀。在持续混合下逐渐冷却以避免发生大块固化,随后使产物干燥和/或制成小球。Under continuous mixing, to 1160 gm of molten urea [132-139° C.] was added potassium silicate [20-24% silica, 10-12% potassium] in an amount of 20 ml and mixed well. Cool gradually with constant mixing to avoid bulk solidification, and the product is then dried and/or pelletized.
实施例14Example 14
在持续的混合下,向1160gm熔化的尿素[132~139℃]中添加5.0ml量的硅酸钾[20~24%二氧化硅,10~12%钾]和10ml的MSM并混匀。在持续混合下逐渐冷却以避免发生大块固化,随后使产物干燥和/或使其形成小球。Under constant mixing, to 1160 gm of molten urea [132-139° C.] was added potassium silicate [20-24% silica, 10-12% potassium] and 10 ml of MSM in an amount of 5.0 ml and mixed well. Cool gradually with constant mixing to avoid bulk solidification, then dry and/or pelletize the product.
实施例15Example 15
在持续的混合下,向1160gm熔化的尿素[132~139℃]中添加2.5ml量的硅酸钾[20~24%二氧化硅,10~12%钾]、5.0ml的MSM和200ml的有机溶液[用10~25%碱提取褐煤]并混匀。在持续混合下逐渐冷却以避免发生大块固化,随后使产物干燥和/或使其形成小球。Under constant mixing, to 1160 gm of molten urea [132-139°C] was added 2.5 ml of potassium silicate [20-24% silica, 10-12% potassium], 5.0 ml of MSM and 200 ml of organic Solution [with 10-25% alkali to extract lignite] and mix well. Cool gradually with constant mixing to avoid bulk solidification, then dry and/or pelletize the product.
其中,MSM溶液制备物:比例为10∶3∶1(体积/体积)的硫酸锌(0.5g/ml)、硫酸铜(0.3g/ml)和硫酸锰(0.5g/ml)。Wherein, MSM solution preparation: zinc sulfate (0.5g/ml), copper sulfate (0.3g/ml) and manganese sulfate (0.5g/ml) in a ratio of 10:3:1 (volume/volume).
实施例16Example 16
在持续的混合下,向1160gm熔化的尿素[132~139℃]中添加100ml量的硅酸钾[20~24%二氧化硅,10~12%钾]、182ml的MSM并混匀。在持续混合下逐渐冷却以避免发生大块固化,随后使产物干燥和/或使其形成小球。With continuous mixing, to 1160 gm of molten urea [132-139° C.] was added potassium silicate [20-24% silica, 10-12% potassium], 182 ml of MSM in an amount of 100 ml and mixed well. Cool gradually with constant mixing to avoid bulk solidification, then dry and/or pelletize the product.
其中,MSM[比例为100∶68∶14(体积/体积)的硫酸锌(0.5g/ml)、硫酸铜(0.3g/ml)和硫酸锰(0.5g/ml)。这将等同于2%的Zn、0.75%的Cu和0.25%的Mn。]Among them, MSM [zinc sulfate (0.5g/ml), copper sulfate (0.3g/ml) and manganese sulfate (0.5g/ml) in a ratio of 100:68:14 (volume/volume). This would equate to 2% Zn, 0.75% Cu and 0.25% Mn. ]
实施例17Example 17
在持续的混合下,向1160gm熔化的尿素[132~139℃]中添加66ml量的硅酸钾[20~24%二氧化硅,10~12%钾]、120.0ml的MSM[比例为100∶68∶14(体积/体积)的硫酸锌[0.5g/ml]、硫酸铜(0.3g/ml)和硫酸锰(0.5g/ml)。这将等同于2%的Zn、0.75%的Cu和0.25%的Mn]并混匀。在持续混合下逐渐冷却以避免发生大块固化,随后使产物干燥和/或制成小球。Under continuous mixing, to 1160 gm of molten urea [132-139° C], add 66 ml of potassium silicate [20-24% silicon dioxide, 10-12% potassium], 120.0 ml of MSM [ratio of 100: 68:14 (v/v) of zinc sulfate [0.5 g/ml], copper sulfate (0.3 g/ml) and manganese sulfate (0.5 g/ml). This would equate to 2% Zn, 0.75% Cu and 0.25% Mn] and mix well. Cool gradually with constant mixing to avoid bulk solidification, and the product is then dried and/or pelletized.
实施例18Example 18
在持续的混合下,向1160gm熔化的尿素[132~139℃]中添加2.5ml量的硅酸钾[20~24%二氧化硅,10~12%钾]以及5ml硫酸锌和200ml的有机提取物[用10~25%碱提取褐煤]并混匀。在持续混合下逐渐冷却以避免发生大块固化,随后使产物干燥和/或使其形成小球。Under constant mixing, to 1160 gm of molten urea [132-139°C] was added potassium silicate [20-24% silicon dioxide, 10-12% potassium] in an amount of 2.5 ml along with 5 ml of zinc sulfate and 200 ml of organic extract [Use 10-25% alkali to extract lignite] and mix well. Cool gradually with constant mixing to avoid bulk solidification, then dry and/or pelletize the product.
实施例19Example 19
向80ml饱和尿素溶液中添加20%硅酸钾[20~24%二氧化硅/10~12%钾]并混匀。该10ml溶液含有硅酸钾,并且尿素混于100ml熔化的尿素中,随后在持续混合下逐渐冷却以避免发生大块固化,随后使产物干燥和/或制成小球。Add 20% potassium silicate [20-24% silicon dioxide/10-12% potassium] to 80ml saturated urea solution and mix well. The 10ml solution contained potassium silicate and urea was mixed in 100ml of molten urea, then cooled gradually with continuous mixing to avoid solidification of large pieces, and the product was then dried and/or pelletized.
实施例20Example 20
将MSM[比例为100∶68∶14(体积/体积)的硫酸锌(0.5g/ml)、硫酸铜(0.36g/ml)和硫酸锰(0.5g/ml),等同于2%的Zn、0.75%的Cu和0.25%的Mn]溶液添加至硅酸钾[20~24%二氧化硅/10~12%钾]中,混合并随后均匀地添加到100ml熔化的尿素中,并在持续混合下逐渐冷却以避免发生大块固化,随后使产物干燥和/或制成小球。MSM [Zinc sulfate (0.5 g/ml), copper sulfate (0.36 g/ml) and manganese sulfate (0.5 g/ml) in a ratio of 100:68:14 (v/v), equivalent to 2% Zn, 0.75% Cu and 0.25% Mn] solution was added to potassium silicate [20-24% silica/10-12% potassium], mixed and then added uniformly to 100ml of molten urea with continuous mixing The product is then allowed to dry and/or pelletized with gradual cooling to avoid bulk solidification.
实施例21:制备多过渡金属氧化物组合物Example 21: Preparation of multi-transition metal oxide compositions
使氧化锌与(5~20%)过氧化氢(1∶5(重量/体积))反应,并向干燥之后所产生的物质中以9∶1∶1(重量/重量)的比例添加氧化锆和氧化铜。使用必要的填充剂和凝胶配制消毒和防腐乳霜。Zinc oxide was reacted with (5-20%) hydrogen peroxide (1:5 (w/v)) and zirconia was added to the resulting mass after drying in a ratio of 9:1:1 (w/w) and copper oxide. Antiseptic and antiseptic creams are formulated with the necessary fillers and gels.
实施例22:制备多过渡金属盐组合物Example 22: Preparation of multi-transition metal salt compositions
制备硫酸锌(0.45g/ml)、硫酸铜(0.3g/ml)、硫酸锰(0.45g/ml)。以10∶3∶1的比例混合这三种溶液,并根据反应物的浓度和最终产物作为具有植物保护活性之植物营养物的要求,以1∶1~1∶50的比例将所产生的溶液添加至从褐煤提取的有机分子(通过一步或顺次多步的与可变浓度之过氧化氢反应而裂解褐煤来获得)。Prepare zinc sulfate (0.45g/ml), copper sulfate (0.3g/ml), manganese sulfate (0.45g/ml). Mix these three solutions in a ratio of 10:3:1, and according to the concentration of the reactants and the requirements of the final product as a plant nutrient with plant protection activity, mix the resulting solution in a ratio of 1:1 to 1:50 Added to organic molecules extracted from lignite (obtained by cleavage of lignite in one or sequential multi-step reactions with variable concentrations of hydrogen peroxide).
实施例23:制备多过渡金属硅酸盐组合物Example 23: Preparation of multi-transition metal silicate compositions
制备氯化锌(0.3g/ml)、硫酸铜(0.1g/ml)、硫酸锰(0.05g/ml)。以5∶3∶1的比例将这三种溶液混合,将50ml所产生的溶液添加至100ml碱金属硅酸盐溶液(0.3g/ml硅酸钾或硅酸钠,1∶2=金属∶二氧化硅)以获得所定义的多过渡金属硅酸盐结构形式。Prepare zinc chloride (0.3g/ml), copper sulfate (0.1g/ml), manganese sulfate (0.05g/ml). These three solutions were mixed in a ratio of 5:3:1, and 50 ml of the resulting solution was added to 100 ml of an alkali metal silicate solution (0.3 g/ml potassium or sodium silicate, 1:2 = metal:di silica) to obtain the defined polytransition metal silicate structural forms.
实施例24:(迁移研究)Example 24: (Migration Study)
将25日龄的稻幼苗移植到100gm土壤、50ml水、0.5gm本发明尿素样品(即,实施例16:含MSM的尿素)的混合物中。48小时后,取50mg根样品,通过添加500milliQ水进行匀浆,并将样品在14000rpm下离心15~20分钟,获得上清液用于通过分光光度计在635nm下利用硝普盐法(nitro prusside method)以及用离子色谱法(METROHM,761COMPACT IC,使用METROSEP C2 150(6.1010.220))评估可获得的氨。对照样品(不含MSM的尿素)采用同样的操作。25-day-old rice seedlings were transplanted into a mixture of 100 gm soil, 50 ml water, 0.5 gm urea sample of the present invention (ie, Example 16: urea containing MSM). After 48 hours, a 50 mg root sample was taken, homogenized by adding 500 milliQ water, and the sample was centrifuged at 14000 rpm for 15-20 minutes to obtain a supernatant for use by the nitroprusside method at 635 nm by a spectrophotometer. method) and evaluation of available ammonia by ion chromatography (METROHM, 761 COMPACT IC, using METROSEP C2 150 (6.1010.220)). The control sample (urea without MSM) adopts the same operation.
对照样品中得到的结果为0.6毫摩尔/L(mili molar)可获得的氨,样品中为1.0毫摩尔/L可获得的氨。The results obtained were 0.6 mmol/L (mili molar) available ammonia in the control sample and 1.0 mmol/L available ammonia in the sample.
类似地,含有2%硅酸锌的尿素和含有3%有机物质的尿素导致稻根中氨的累积增加,因为与对照(仅尿素)中的0.6毫摩尔/L相比,其氨含量为0.9毫摩尔/L(含2%硅酸锌的尿素)和1.0毫摩尔/L(有机尿素)。Similarly, urea containing 2% zinc silicate and urea containing 3% organic matter resulted in increased accumulation of ammonia in rice roots as it contained 0.9 mmol/L compared to 0.6 mmol/L in the control (urea only). mmol/L (urea containing 2% zinc silicate) and 1.0 mmol/L (organic urea).
已利用多种作物(例如,稻、玉米、花生和辣椒)对上述实施例中获得的产物进行试验,并且已观察到同样的作物产量显著提高,这从对多种作物进行的为期5年的试验中明显看出。The products obtained in the above examples have been tested on various crops (e.g. rice, corn, peanuts and peppers) and a significant increase in the yield of the same crops has been observed, starting from a 5-year experiment on various crops. It is evident in the test.
在本发明中,氮有效地迁移至植物是通过调节尿素(即,酰胺)降解循环(包括和不包括调节尿素转化、氨转化和/或亚硝酸盐转化中的酶或相关因子)而实现的,并且还通过在不同量之反应物和实验条件下添加碱性硅酸盐之前或之后添加单或多过渡金属或其盐或其硅酸盐(以获得衍生物)对酰胺进行结构修饰来抑制挥发,使具有多重作用(抗微生物性质)的选择性地功能上有效的酰胺用于选择性的作物或土壤和/或定制植物营养和/或用于一般施用和/或与或不与其它肥料一起施用。In the present invention, efficient transfer of nitrogen to plants is achieved by modulation of the urea (i.e., amide) degradation cycle (including and excluding modulation of enzymes or related factors in urea conversion, ammonia conversion, and/or nitrite conversion) , and also by structural modification of amides by addition of mono- or multi-transition metals or their salts or their silicates (to obtain derivatives) before or after the addition of alkali silicate in different amounts of reactants and experimental conditions Volatilization, enabling selectively functionally effective amides with multiple actions (antimicrobial properties) for selective crop or soil and/or tailored plant nutrition and/or for general application and/or with or without other fertilizers Administer together.
还应注意,将氧化物或盐(例如,氯化物或硝酸盐或硫酸盐或硅酸盐)的多过渡金属(例如,银、铜、锌、锆和锰)组合物与选择含有一个至另一个多重变量的不同比例的多比例可变组合物混合,以获得功能上有效的多过渡金属氧化物或盐或硅酸盐(通过添加碱(例如,硅酸钠或硅酸钾)而获得),It should also be noted that combining oxides or salts (e.g. chlorides or nitrates or sulfates or silicates) with poly-transition metal (e.g. silver, copper, zinc, zirconium and manganese) compositions A multi-variable multi-ratio variable composition mixed in different proportions to obtain a functionally effective multi-transition metal oxide or salt or silicate (obtained by adding a base (e.g., sodium or potassium silicate)) ,
具有或不具有有机杂化(organic hybridization),with or without organic hybridization,
具有或不具有可变反应条件(例如,pH、温度、硅酸盐与金属的比例、压力以及可变的气体环境),With or without variable reaction conditions (e.g., pH, temperature, ratio of silicate to metal, pressure, and variable gas atmosphere),
是否固定在材料(例如,活化氧化铝、氧化铝、农业聚合物(agropolymer)、纤维素、石英砂和硅胶、树脂等材料)上进行制备,是否纳米结构化,Whether it is fixed on the material (such as activated alumina, aluminum oxide, agropolymer, cellulose, quartz sand and silica gel, resin, etc.) for preparation, whether it is nanostructured,
是否与制备化妆品中的净化剂(decontaminant)、消毒剂、解毒剂、吸收剂、酶抑制剂、抗微生物剂、治疗剂、填充剂和配制化合物以及去污剂中碱性物质、香烟过滤器(cigarette filer)、催化剂,多重作用分子(例如,营养物和杀微生物剂)和防腐乳霜的生物活性分子和/或与其它金属反应。Whether it is compatible with decontaminants, disinfectants, antidotes, absorbents, enzyme inhibitors, antimicrobials, therapeutic agents, fillers and formulation compounds in the preparation of cosmetics and alkaline substances in detergents, cigarette filters ( cigarette filer), catalysts, multi-action molecules (e.g., nutrients and microbicides) and bioactive molecules for antiseptic creams and/or react with other metals.
一般地,将本发明的组合物与农业上可接受的载体一起施加于植物或其部分。术语“农业上可接受的载体”意为可用于溶解、分散或扩散组合物中活性化合物而不损害所述化合物之有效性的物质,并且其本身对土壤、设备、作物或农艺环境无不利影响。In general, the compositions of the present invention are applied to plants or parts thereof together with an agriculturally acceptable carrier. The term "agriculturally acceptable carrier" means a material which can be used to dissolve, disperse or diffuse an active compound in a composition without impairing the effectiveness of said compound and which does not itself adversely affect the soil, equipment, crop or agronomic environment .
本发明的组合物可以是固体或液体制剂或者溶液。例如,所述化合物可配制为可润湿粉末或可乳化之浓缩物。根据常规的农业实践,常常需要包括辅料,例如润湿剂、铺展剂(spreading agent)、分散剂、粘着剂(sticker)和粘合剂(adhesive)。The compositions of the invention may be solid or liquid formulations or solutions. For example, the compounds may be formulated as wettable powders or emulsifiable concentrates. According to conventional agricultural practice, it is often necessary to include adjuvants such as wetting agents, spreading agents, dispersing agents, stickers and adhesives.
对于可乳化浓缩物的制备来说,可将一种或更多种活性成分与允许在水中分散的乳化剂一起溶于一种或更多种有机溶剂(例如,苯、甲苯、二甲苯、甲基化的萘、玉米油、松油、邻-二氯苯、异佛尔酮(isophorone)、环己烷以及油酸甲酯或其混合物)中。For the preparation of emulsifiable concentrates, one or more active ingredients can be dissolved in one or more organic solvents (for example, benzene, toluene, xylene, toluene, naphthalene, corn oil, pine oil, o-dichlorobenzene, isophorone (isophorone), cyclohexane, and methyl oleate or mixtures thereof).
可通过将一种或更多种活性成分与细碎的固体(例如,粘土、无机硅酸盐和碳酸盐以及硅石)混合并且通过在这样的混合物中掺入润湿剂、粘着剂和/或分散剂来制备适于喷洒的可润湿粉末。can be obtained by mixing one or more active ingredients with finely divided solids (for example, clays, inorganic silicates and carbonates and silicas) and by incorporating wetting agents, binders and/or Dispersant to prepare a wettable powder suitable for spraying.
本发明的优势Advantages of the invention
本发明的主要优势是开发出功能上有效的尿素组合物,其使多种作物(稻、玉米等)的生长和产量提高10~90%。The main advantage of the present invention is the development of a functionally effective urea composition that increases the growth and yield of various crops (rice, corn, etc.) by 10-90%.
本发明的另一有利目的是生产生态友好型组合物。Another advantageous object of the invention is to produce eco-friendly compositions.
本发明人已开发了本发明,从而可以以经济、实用和容易的方式实现优势。尽管已显示和描述了优选的方面和示例配置,应当理解,对于本领域技术人员来说,多种其它改动和额外配置是显而易见的。本文中公开的具体实施方案和配置旨在举例说明本发明的优选特性,而不应解释为对本发明范围的限制。The present inventors have developed the present invention so that the advantages can be realized in an economical, practical and easy manner. While preferred aspects and example configurations have been shown and described, it is to be understood that various other modifications and additional configurations will be apparent to those skilled in the art. The specific embodiments and configurations disclosed herein are intended to illustrate the preferred characteristics of the invention and should not be construed as limitations on the scope of the invention.
Claims (24)
Applications Claiming Priority (9)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| IN195/CHE/2010 | 2010-01-27 | ||
| IN191CH2010 | 2010-01-27 | ||
| IN195CH2010 | 2010-01-27 | ||
| IN191/CHE/2010 | 2010-01-27 | ||
| IN194/CHE/2010 | 2010-01-27 | ||
| IN194CH2010 | 2010-01-27 | ||
| IN2841CH2010 | 2010-09-27 | ||
| IN2841/CHE/2010 | 2010-09-27 | ||
| PCT/IB2011/000124 WO2011092577A1 (en) | 2010-01-27 | 2011-01-27 | A functionally effective urea composition |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CN102811975A true CN102811975A (en) | 2012-12-05 |
Family
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Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CN2011800121585A Pending CN102811975A (en) | 2010-01-27 | 2011-01-27 | Functionally effective urea composition |
Country Status (3)
| Country | Link |
|---|---|
| CN (1) | CN102811975A (en) |
| BR (1) | BR112012018832A2 (en) |
| WO (1) | WO2011092577A1 (en) |
Families Citing this family (1)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US20150274606A1 (en) * | 2012-10-24 | 2015-10-01 | Jan Helskens | Plant growth enhancer |
Family Cites Families (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| DE1022243B (en) * | 1956-07-30 | 1958-01-09 | Kalk Chemische Fabrik Gmbh | Reaction products of metal salts with urea as micronutrient fertilizers |
| US3446612A (en) * | 1965-06-21 | 1969-05-27 | Frank W Taylor | Basic fertilizers containing derivatives of an olivine mineral |
| DK531278A (en) * | 1977-12-22 | 1979-06-23 | Fisons Ltd | MEASURE TO REDUCE AMMONIA ACT BY USING URINE SUBSTANCE AS FERTILIZER |
| GB2010797B (en) * | 1977-12-22 | 1982-07-21 | Fisons Ltd | Fertilizer composition |
| WO1996013169A1 (en) * | 1994-10-27 | 1996-05-09 | Stoller Enterprises, Inc. | Method for inhibiting plant disease |
| ES2156746B1 (en) * | 1999-07-20 | 2002-05-01 | Inabonos Sa | NITROGEN FERTILIZER, CONTAINING UREIC NITROGEN, AMMONIC AND ORGANIC NITRIC, GRADUAL SOLUBILITY AND PROGRESSIVE NITRIFICATION, AND METHOD OF OBTAINING. |
| US20070119221A1 (en) * | 2005-11-30 | 2007-05-31 | John Wolford | Addition of Gelling Grade Clays to Direct Applied Nitrogen Solutions to Reduce Nitrogen Loss |
| EA200970481A1 (en) * | 2006-11-15 | 2009-12-30 | Биджам Байосайенсиз Прайвет Лимитед | STRUCTURALLY MODIFIED LIGNITIS WITH EXTRACTION OF FUNCTIONALLY ACTIVATED ORGANIC MOLECULES OR WITHOUT IT |
-
2011
- 2011-01-27 BR BR112012018832A patent/BR112012018832A2/en not_active Application Discontinuation
- 2011-01-27 WO PCT/IB2011/000124 patent/WO2011092577A1/en not_active Ceased
- 2011-01-27 CN CN2011800121585A patent/CN102811975A/en active Pending
Also Published As
| Publication number | Publication date |
|---|---|
| BR112012018832A2 (en) | 2016-04-12 |
| WO2011092577A1 (en) | 2011-08-04 |
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