DE4018395A1 - Inhibition of nitrification of ammonium nitrogen in soils - Google Patents
Inhibition of nitrification of ammonium nitrogen in soilsInfo
- Publication number
- DE4018395A1 DE4018395A1 DE4018395A DE4018395A DE4018395A1 DE 4018395 A1 DE4018395 A1 DE 4018395A1 DE 4018395 A DE4018395 A DE 4018395A DE 4018395 A DE4018395 A DE 4018395A DE 4018395 A1 DE4018395 A1 DE 4018395A1
- Authority
- DE
- Germany
- Prior art keywords
- nitrogen
- nitrification
- soil
- active ingredient
- inhibition
- 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.)
- Withdrawn
Links
- XKMRRTOUMJRJIA-UHFFFAOYSA-N ammonia nh3 Chemical compound N.N XKMRRTOUMJRJIA-UHFFFAOYSA-N 0.000 title claims description 7
- 239000002689 soil Substances 0.000 title description 22
- 230000005764 inhibitory process Effects 0.000 title description 4
- 239000003795 chemical substances by application Substances 0.000 claims abstract description 10
- 230000002401 inhibitory effect Effects 0.000 claims abstract description 5
- GWLRCPBBLXQXRZ-UHFFFAOYSA-N 3-methylpyrazole-1-carboximidamide Chemical compound CC=1C=CN(C(N)=N)N=1 GWLRCPBBLXQXRZ-UHFFFAOYSA-N 0.000 claims abstract description 4
- 230000001105 regulatory effect Effects 0.000 claims abstract description 4
- 239000002253 acid Substances 0.000 claims abstract description 3
- 239000000969 carrier Substances 0.000 claims abstract description 3
- 150000001875 compounds Chemical class 0.000 claims description 3
- 239000004480 active ingredient Substances 0.000 abstract description 13
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 description 20
- 229910052757 nitrogen Inorganic materials 0.000 description 10
- 239000003337 fertilizer Substances 0.000 description 9
- 229910002651 NO3 Inorganic materials 0.000 description 6
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 6
- MMDJDBSEMBIJBB-UHFFFAOYSA-N [O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[NH6+3] Chemical compound [O-][N+]([O-])=O.[O-][N+]([O-])=O.[O-][N+]([O-])=O.[NH6+3] MMDJDBSEMBIJBB-UHFFFAOYSA-N 0.000 description 6
- QAOWNCQODCNURD-UHFFFAOYSA-N Sulfuric acid Chemical compound OS(O)(=O)=O QAOWNCQODCNURD-UHFFFAOYSA-N 0.000 description 5
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 description 5
- 239000004202 carbamide Substances 0.000 description 5
- 239000007787 solid Substances 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 230000007062 hydrolysis Effects 0.000 description 4
- 238000006460 hydrolysis reaction Methods 0.000 description 4
- 238000000034 method Methods 0.000 description 4
- IOVCWXUNBOPUCH-UHFFFAOYSA-M Nitrite anion Chemical compound [O-]N=O IOVCWXUNBOPUCH-UHFFFAOYSA-M 0.000 description 3
- 239000013543 active substance Substances 0.000 description 3
- 230000008901 benefit Effects 0.000 description 3
- 229910052500 inorganic mineral Inorganic materials 0.000 description 3
- 239000011707 mineral Substances 0.000 description 3
- 239000000203 mixture Substances 0.000 description 3
- 235000011149 sulphuric acid Nutrition 0.000 description 3
- XKVUYEYANWFIJX-UHFFFAOYSA-N 5-methyl-1h-pyrazole Chemical compound CC1=CC=NN1 XKVUYEYANWFIJX-UHFFFAOYSA-N 0.000 description 2
- JVMRPSJZNHXORP-UHFFFAOYSA-N ON=O.ON=O.ON=O.N Chemical compound ON=O.ON=O.ON=O.N JVMRPSJZNHXORP-UHFFFAOYSA-N 0.000 description 2
- BFNBIHQBYMNNAN-UHFFFAOYSA-N ammonium sulfate Chemical compound N.N.OS(O)(=O)=O BFNBIHQBYMNNAN-UHFFFAOYSA-N 0.000 description 2
- 229910052921 ammonium sulfate Inorganic materials 0.000 description 2
- 235000011130 ammonium sulphate Nutrition 0.000 description 2
- 230000000694 effects Effects 0.000 description 2
- JEIPFZHSYJVQDO-UHFFFAOYSA-N iron(III) oxide Inorganic materials O=[Fe]O[Fe]=O JEIPFZHSYJVQDO-UHFFFAOYSA-N 0.000 description 2
- 239000007788 liquid Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 239000004576 sand Substances 0.000 description 2
- 238000001179 sorption measurement Methods 0.000 description 2
- 239000000126 substance Substances 0.000 description 2
- 238000000870 ultraviolet spectroscopy Methods 0.000 description 2
- 238000009736 wetting Methods 0.000 description 2
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- KAESVJOAVNADME-UHFFFAOYSA-N Pyrrole Chemical class C=1C=CNC=1 KAESVJOAVNADME-UHFFFAOYSA-N 0.000 description 1
- 230000004071 biological effect Effects 0.000 description 1
- 230000033228 biological regulation Effects 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 239000004927 clay Substances 0.000 description 1
- 238000005056 compaction Methods 0.000 description 1
- QGBSISYHAICWAH-UHFFFAOYSA-N dicyandiamide Chemical compound NC(N)=NC#N QGBSISYHAICWAH-UHFFFAOYSA-N 0.000 description 1
- 239000003651 drinking water Substances 0.000 description 1
- 235000020188 drinking water Nutrition 0.000 description 1
- 239000003814 drug Substances 0.000 description 1
- 229940079593 drug Drugs 0.000 description 1
- 230000004720 fertilization Effects 0.000 description 1
- 239000011521 glass Substances 0.000 description 1
- 239000005337 ground glass Substances 0.000 description 1
- 239000003673 groundwater Substances 0.000 description 1
- 231100000086 high toxicity Toxicity 0.000 description 1
- 239000003864 humus Substances 0.000 description 1
- 238000010348 incorporation Methods 0.000 description 1
- 238000011534 incubation Methods 0.000 description 1
- 230000002262 irrigation Effects 0.000 description 1
- 238000003973 irrigation Methods 0.000 description 1
- 238000002386 leaching Methods 0.000 description 1
- 235000014666 liquid concentrate Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 239000000155 melt Substances 0.000 description 1
- 230000000813 microbial effect Effects 0.000 description 1
- 238000002156 mixing Methods 0.000 description 1
- DCUJJWWUNKIJPH-UHFFFAOYSA-N nitrapyrin Chemical compound ClC1=CC=CC(C(Cl)(Cl)Cl)=N1 DCUJJWWUNKIJPH-UHFFFAOYSA-N 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 230000035764 nutrition Effects 0.000 description 1
- 238000001556 precipitation Methods 0.000 description 1
- 230000002265 prevention Effects 0.000 description 1
- 150000003217 pyrazoles Chemical class 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 238000005070 sampling Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05G—MIXTURES OF FERTILISERS COVERED INDIVIDUALLY BY DIFFERENT SUBCLASSES OF CLASS C05; MIXTURES OF ONE OR MORE FERTILISERS WITH MATERIALS NOT HAVING A SPECIFIC FERTILISING ACTIVITY, e.g. PESTICIDES, SOIL-CONDITIONERS, WETTING AGENTS; FERTILISERS CHARACTERISED BY THEIR FORM
- C05G3/00—Mixtures of one or more fertilisers with additives not having a specially fertilising activity
- C05G3/90—Mixtures of one or more fertilisers with additives not having a specially fertilising activity for affecting the nitrification of ammonium compounds or urea in the soil
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y02—TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
- Y02P—CLIMATE CHANGE MITIGATION TECHNOLOGIES IN THE PRODUCTION OR PROCESSING OF GOODS
- Y02P60/00—Technologies relating to agriculture, livestock or agroalimentary industries
- Y02P60/20—Reduction of greenhouse gas [GHG] emissions in agriculture, e.g. CO2
- Y02P60/21—Dinitrogen oxide [N2O], e.g. using aquaponics, hydroponics or efficiency measures
Landscapes
- Life Sciences & Earth Sciences (AREA)
- Soil Sciences (AREA)
- Pest Control & Pesticides (AREA)
- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Fertilizers (AREA)
Abstract
Description
Die Erfindung betrifft die Verhinderung bzw. Regelung der Nitrifikation von Ammoniumstickstoff, insbesondere aus mineralischen und organischen Düngemitteln, in Kulturböden.The invention relates to the prevention or regulation of nitrification of ammonium nitrogen, in particular from mineral and organic Fertilizers, in cultivated soils.
Ammoniumstickstoff unterliegt im Boden in relativ kurzer Zeit der mikrobiellen Umwandlung über die Zwischenstufe des Nitratstickstoffs. Dieser Prozeß wird maßgeblich von der Temperatur, der Bodenfeuchtigkeit, dem pH-Wert und der biologischen Aktivität des Bodens beeinflußt.Ammonium nitrogen is subject to the microbial in the soil in a relatively short time Conversion via the intermediate stage of nitrate nitrogen. This The process is largely determined by the temperature, the soil moisture, the pH and the biological activity of the soil affected.
Nitratstickstoff wird im Gegensatz zum Ammoniumstickstoff nicht von den Sorptionsträgern des Bodens, Tons und Humus sorbiert. Die Folge davon ist, daß Nitratstickstoff während des Winterhalbjahres und bei starken Niederschlägen bzw. intensiver Beregnung auch während des Sommerhalbjahres, vor allem auf leichten Böden, der Auswaschung unterliegt. Die Auswaschungsverluste können im jährlichen Durchschnitt bis zu 20% des Düngemittelstickstoffs betragen.In contrast to ammonium nitrogen, nitrate nitrogen is not Sorption carriers of the soil, clay and humus sorbed. The consequence of this is that nitrate nitrogen during the winter half year and in strong Precipitation or intensive irrigation even during the summer half-year, especially on light soils that are subject to leaching. The washout losses can average up to 20% of fertilizer nitrogen annually be.
Der ausgewaschene Stickstoff geht nicht nur für die Ernährung der Kulturpflanzen verloren, sondern führt darüber hinaus zur Anreicherung von Nitratstickstoff im Grundwasser. Dies kann im Zusammenhang mit der Trinkwasserversorgung zu gesundheitlichen Schäden bei Mensch und Tier führen. The washed out nitrogen is not only for the nutrition of crops lost, but also leads to the enrichment of nitrate nitrogen in the groundwater. This can be related to the drinking water supply lead to damage to human and animal health.
Neben den Auswaschverlusten können unter bestimmten Bedingungen, insbesondere bei hoher Feuchtigkeit bzw. Bodenverdichtung, jährlich erhebliche gasförmige Stickstoffverluste durch Denitrifikation des Nitratstickstoffs auftreten. Durch eine Hemmung bzw. Regelung der Nitrifikation kann die Ausnutzung des Düngemittelstickstoffs entscheidend verbessert und somit der ökonomische Nutzen der Stickstoffdüngung erhöht werden.In addition to the washout losses, under certain conditions, in particular with high humidity or soil compaction, annually considerable gaseous nitrogen losses due to denitrification of the nitrate nitrogen occur. By inhibiting or regulating nitrification can significantly improve the use of fertilizer nitrogen and thus increases the economic benefits of nitrogen fertilization will.
Es ist bereits bekannt, daß für diese Zwecke, neben substituierten Pyrazolen (US-PS 34 94 757, JP-PS 7 24 718, DD-PS 1 31 063, DD-PS 1 33 088) und deren Azoliumsalzen (US-PS 36 35 690, JP-PS 72 47 182, JP-PS 72-47 183), Substanzen wie Dicyandiamid (DOS 27 02 284, DOS 27 14 601, DOS 3 54 482), Nitrapyrin (US-PS 34 24 754, SU-PS 10 85 966) und Guanylthioharnstoffe sowie deren Salze (JP-PS 5 852/59, JP-PS 5-60 02 958) verwendet werden können. Diese Verbindungen weisen jedoch Nachteile auf, wie geringe Wirksamkeit, zu geringe Thermo- und Hydrolysestabilität, zu hohe Toxizität, zu hohe Flüchtigkeit und aufwendige Herstellungsverfahren, die einer ökonomischen Anwendung entgegenstehen. Eine zu hohe Flüchtigkeit sowie eine geringe thermische und Hydrolysestabilität der Wirkstoffe schränken die Anwendungsverfahren sehr stark ein und lassen nur eine Einbringung in den Boden zu.It is already known that for these purposes, in addition to substituted Pyrazoles (US-PS 34 94 757, JP-PS 7 24 718, DD-PS 1 31 063, DD-PS 1 33 088) and their azolium salts (US-PS 36 35 690, JP-PS 72 47 182, JP-PS 72-47 183), Substances such as dicyandiamide (DOS 27 02 284, DOS 27 14 601, DOS 3 54 482), Nitrapyrin (US-PS 34 24 754, SU-PS 10 85 966) and guanylthioureas as well whose salts (JP-PS 5 852/59, JP-PS 5-60 02 958) can be used. However, these compounds have disadvantages such as low activity, too low thermal and hydrolysis stability, too high toxicity, too high Volatility and complex manufacturing processes that are economical Oppose application. Too high a volatility and a low one thermal and hydrolysis stability of the active ingredients limit the Application methods very strongly and only allow an introduction in the floor too.
Ziel der Erfindung ist es, Wirkstoffe zur Hemmung bzw. Regelung der Nitrifikation von Ammoniumstickstoff im Boden zur Verfügung zu stellen, die eine ausreichende Residualwirkung aufweisen und die auf Grund ihrer geringen Flüchtigkeit alle Applikationsverfahren, insbesondere die Oberflächenapplikation, zulassen. The aim of the invention is to provide active substances for inhibiting or regulating nitrification of ammonium nitrogen in the soil, which have a sufficient residual effect and which are based on their low volatility all application methods, especially surface application, allow.
Es wurde überraschend gefunden, daß 1-Guanyl-3-methylpyrazol (GMP) entsprechend Formel I,It has surprisingly been found that 1-guanyl-3-methylpyrazole (GMP) corresponds Formula I,
dessen Säureadditionsprodukte bzw. Koordinationsverbindungen die Nitrifikation von Ammoniumstickstoff hemmen bzw. regulieren.whose acid addition products or coordination compounds nitrification inhibit or regulate ammonium nitrogen.
Tabelle 1 vermittelt einen Überblick über einige Substanzen.Table 1 gives an overview of some substances.
Die erfindungsgemäßen Mittel besitzen den Vorteil einer sehr geringen Flüchtigkeit, wodurch geringere Wirkstoffverluste bei Oberflächenapplikation auftreten. Darüber hinaus zeichnen sich die erfindungsgemäßen Mittel durch eine hohe thermische und Hydrolysestabilität aus, die eine Inkorporation in das Düngemittel erlaubt und vorherige Mischprozesse bzw. eine getrennte Ausbringung von Wirkstoff und Düngemittel umgeht. The agents according to the invention have the advantage of being very low Volatility, which means less loss of active ingredient in surface application occur. In addition, the invention Medium characterized by a high thermal and hydrolysis stability, which a Incorporation into the fertilizer allowed and previous mixing processes or bypassing the separate application of active ingredient and fertilizer.
Die erfindungsgemäßen Mittel können im Gemisch mit oder gemeinsam mit festen oder flüssigen mineralischen oder organischen Düngemitteln, die den Stickstoff in reduzierter Form enthalten, angewendet werden. Sie können außerdem in festen mineralischen Ammoniumdüngemitteln eingeschmolzen werden sowie in Form eines festen oder flüssigen Konzentrates, z. B. in Wasser oder im Gemisch mit einem festen, vermahlenen oder granulierten Trägerstoff, zur Anwendung kommen.The agents according to the invention can be mixed with or together with solid or liquid mineral or organic fertilizers that contain the nitrogen in a reduced form. they can also be melted in solid mineral ammonium fertilizers are as well as in the form of a solid or liquid concentrate, for. B. in water or in a mixture with a solid, ground or granulated Carrier to be used.
Verwendet man die neuen Mittel zusammen mit festen oder flüssigen Düngemitteln, so können sie mit 0,1-50 Gew.-% des Düngemittelstickstoffs angewendet werden, vorzugsweise mit 0,2-15 Gew.-%.If the new agents are used together with solid or liquid fertilizers, so you can apply with 0.1-50 wt .-% of the fertilizer nitrogen be, preferably with 0.2-15 wt .-%.
Die nachfolgenden Beispiele dienen der Erläuterung der Erfindung.The following examples serve to explain the invention.
Die erfindungsgemäßen Mittel wurden als Ammoniumsulfat-Wirkstoffgemische einem schwarzerdeähnlichen sandigen Lehmboden zugesetzt und gleichmäßig vermischt.The agents according to the invention were used as ammonium sulfate active ingredient mixtures added to a black earth-like sandy loam soil and evenly mixed.
Die Konzentration betrug 16 ppm (auf Bodenmasse bezogen) bei einer Stickstoffgabe von 20 mg N/100 g Boden.The concentration was 16 ppm (based on soil mass) when nitrogen was added of 20 mg N / 100 g soil.
Nach Befeuchten des Bodens auf 50% der maximalen Wasserkapazität wurde bei 20°C 28 Tage inkubiert und danach der gebildete Nitrat- bzw. Nitratstickstoff bestimmt. Als Kontrolle diente die gleiche Ammoniumsulfatzugabe zum Boden wie in den Prüfvarianten.After wetting the soil to 50% of the maximum water capacity was incubated at 20 ° C for 28 days and then the nitrate or nitrate nitrogen formed certainly. The same ammonium sulfate addition served as a control to the floor as in the test variants.
Die Berechnung der Hemmwirkung in Prozent erfolgt nach:The inhibitory effect in percent is calculated according to:
a = Nitrit- und Nitratgehalt der Kontrolle
b = Nitrit- und Nitratgehalt der Proben mit Wirkstoff
c = Nitrit- und Nitratgehalt des verwendeten Bodensa = nitrite and nitrate content of the control
b = nitrite and nitrate content of the samples with active ingredient
c = nitrite and nitrate content of the soil used
Die Ergebnisse gehen aus Tabelle 2 hervor.The results are shown in Table 2.
Die erfindungsgemäßen Mittel wurden als Harnstoff-Wirkstoffgemisch einem schwarzerdeähnlichen sandigen Lehmboden zugesetzt und gleichmäßig vermischt.The agents according to the invention were one as a urea-active ingredient mixture black clay-like sandy loam soil added and mixed evenly.
Die Konzentrationen betrugen 4,2 und 1 ppm (auf Bodenmasse bezogen) bei einer Stickstoffgabe von 20 mg N/100 g Boden. Nach Befeuchten des Bodens auf 50% der maximalen Wasserkapazität wurde bei 20°C inkubiert und in Abständen von 14 Tagen Nitrat- und Nitritstickstoff bestimmt. Als Kontrolle diente die gleiche Harnstoffzugabe zum Boden wie in den Prüfvarianten.The concentrations were 4.2 and 1 ppm (based on soil mass) a nitrogen dose of 20 mg N / 100 g soil. After moistening the floor to 50% of the maximum water capacity was incubated at 20 ° C and in Nitrate and nitrite nitrogen intervals determined every 14 days. As a control served the same urea addition to the floor as in the test variants.
Die Berechnung der Hemmung erfolgte analog Beispiel 1.The inhibition was calculated analogously to Example 1.
Die Ergebnisse gehen aus Tabelle 3 hervor.The results are shown in Table 3.
3 mg der erfindungsgemäßen Mittel wurden oberflächig auf 10 g einer Sand-Rosterde, die auf 10% der maximalen Wasserkapazität eingestellt war, aufgegeben. Ein Vorlageschälchen mit 4 mg 0,1 n H₂SO₄ diente als Adsorptionsgefäß, in dem die flüchtigen Wirkstoffverluste adsorbiert wurden. Das Ganze wurde in einem Glasgefäß mit Schliffdeckel bei 20°C inkubiert und der Wirkstoffgehalt an den entsprechenden Probenahmetagen UV-spektroskopisch ermittelt. Als Vergleich dienten 3 mg oberflächig appliziertes 3-Methyl-pyrazol.3 mg of the agents according to the invention were superficially on 10 g of a sand rust, which was set to 10% of the maximum water capacity. A serving dish with 4 mg 0.1 n H₂SO₄ served as an adsorption vessel, in which the volatile loss of active ingredient was adsorbed. The whole was incubated in a glass vessel with a ground glass cap at 20 ° C and the Active substance content on the corresponding sampling days by UV spectroscopy determined. 3 mg of 3-methyl-pyrazole applied on the surface served as a comparison.
Die Vorteilswirkung gegenüber 3-Methylpyrazol geht aus Tabelle 4 hervor.The advantage over 3-methylpyrazole is shown in Table 4.
1,25 mg des erfindungsgemäßen Mittels wurde in 100 ml 0,1 n H₂SO₄ gelöst und der Wirkstoffgehalt zeitabhängig UV-spektroskopisch bestimmt. Die Ergebnisse der Wirkstoffstabilität in verdünnter Schwefelsäure sind aus Tabelle 5 ersichtlich.1.25 mg of the agent according to the invention was dissolved in 100 ml 0.1 n H₂SO₄ and the active substance content was determined by UV spectroscopy as a function of time. The results the drug stability in dilute sulfuric acid are from table 5 can be seen.
Die erfindungsgemäßen Mittel wurden als Harnstoff-Wirkstoffeinschmelzung (2% und 4% Wirkstoff in der Einschmelzung) einem schwarzerdeähnlichen sandigen Lehmboden zugesetzt und gleichmäßig vermischt. Die Konzentrationen betrugen 4,2 und 1 ppm Wirkstoff (auf Bodenmasse bezogen) bei einer ergänzenden Stickstoffzugabe von 20 mg N/100 g Boden.The agents according to the invention were melted as a urea active ingredient (2% and 4% active ingredient in the melt) a black earth-like sandy loam soil added and mixed evenly. The concentrations were 4.2 and 1 ppm active ingredient (based on soil mass) in one additional nitrogen addition of 20 mg N / 100 g soil.
Nach Befeuchten des Bodens auf 50% der maximalen Wasserkapazität wurde bei 20°C inkubiert und in Abständen von 14 Tagen Nitrat- und Nitritstickstoff bestimmt. Als Kontrolle diente die gleiche Harnstoffzugabe zum Boden wie in den Prüfvarianten. Die Berechnung der Hemmung erfolgte analog Beispiel 1.After wetting the soil to 50% of the maximum water capacity was Incubated at 20 ° C and every 14 days nitrate and nitrite nitrogen certainly. The same urea addition served as a control to the floor as in the test variants. The inhibition was calculated analogous to example 1.
Claims (1)
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4018395A DE4018395A1 (en) | 1990-06-08 | 1990-06-08 | Inhibition of nitrification of ammonium nitrogen in soils |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| DE4018395A DE4018395A1 (en) | 1990-06-08 | 1990-06-08 | Inhibition of nitrification of ammonium nitrogen in soils |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| DE4018395A1 true DE4018395A1 (en) | 1992-02-20 |
Family
ID=6408051
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| DE4018395A Withdrawn DE4018395A1 (en) | 1990-06-08 | 1990-06-08 | Inhibition of nitrification of ammonium nitrogen in soils |
Country Status (1)
| Country | Link |
|---|---|
| DE (1) | DE4018395A1 (en) |
Cited By (5)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1993021134A1 (en) * | 1992-04-08 | 1993-10-28 | Stickstoffwerke Ag Wittenberg-Piesteritz | Combinations of active substances for preventing or regulating the nitrification of ammonium nitrogen in arable grounds and substrates |
| WO2005035509A1 (en) | 2003-09-18 | 2005-04-21 | Skw Stickstoffwerke Piesteritz Gmbh | 1h-azolyl-methyl-amides, method for the production thereof and use thereof as nitrification inhibitors |
| DE102008020785A1 (en) | 2008-04-25 | 2009-10-29 | Skw Stickstoffwerke Piesteritz Gmbh | Use of 5-amino-1,2,4-thiadiazole for inhibiting or controlling the nitrification |
| DE102011120098A1 (en) | 2011-12-02 | 2013-06-06 | Skw Stickstoffwerke Piesteritz Gmbh | N- (1H-pyrazolylmethyl) formamides, process for their preparation and their use as nitrification inhibitors |
| DE102006015705B4 (en) | 2006-04-04 | 2018-07-19 | Skw Stickstoffwerke Piesteritz Gmbh | 1,2-bis (azol-1-yl) ethane-1,2-diol derivatives, processes for their preparation and their use as nitrification inhibitors |
-
1990
- 1990-06-08 DE DE4018395A patent/DE4018395A1/en not_active Withdrawn
Cited By (8)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| WO1993021134A1 (en) * | 1992-04-08 | 1993-10-28 | Stickstoffwerke Ag Wittenberg-Piesteritz | Combinations of active substances for preventing or regulating the nitrification of ammonium nitrogen in arable grounds and substrates |
| US5637131A (en) * | 1992-04-08 | 1997-06-10 | Skw Stickstoffwerke Piesteritz Gmbh | Agent combinations to inhibit or control nitrification of ammonia nitrogen in cultivated soils and substrates |
| WO2005035509A1 (en) | 2003-09-18 | 2005-04-21 | Skw Stickstoffwerke Piesteritz Gmbh | 1h-azolyl-methyl-amides, method for the production thereof and use thereof as nitrification inhibitors |
| DE102006015705B4 (en) | 2006-04-04 | 2018-07-19 | Skw Stickstoffwerke Piesteritz Gmbh | 1,2-bis (azol-1-yl) ethane-1,2-diol derivatives, processes for their preparation and their use as nitrification inhibitors |
| DE102008020785A1 (en) | 2008-04-25 | 2009-10-29 | Skw Stickstoffwerke Piesteritz Gmbh | Use of 5-amino-1,2,4-thiadiazole for inhibiting or controlling the nitrification |
| DE102008020785B4 (en) | 2008-04-25 | 2021-11-04 | Skw Stickstoffwerke Piesteritz Gmbh | Use of simple derivatives of 5-amino-1,2,4-thiadiazole to inhibit or control nitrification |
| DE102011120098A1 (en) | 2011-12-02 | 2013-06-06 | Skw Stickstoffwerke Piesteritz Gmbh | N- (1H-pyrazolylmethyl) formamides, process for their preparation and their use as nitrification inhibitors |
| WO2013079197A1 (en) | 2011-12-02 | 2013-06-06 | Skw Stickstoffwerke Piesteritz Gmbh | N-(1h-pyrazolylmethyl)formamides, process for the preparation thereof and use thereof as nitrification inhibitors |
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