AU634025B2 - Plant micro-element availability - Google Patents
Plant micro-element availability Download PDFInfo
- Publication number
- AU634025B2 AU634025B2 AU71241/91A AU7124191A AU634025B2 AU 634025 B2 AU634025 B2 AU 634025B2 AU 71241/91 A AU71241/91 A AU 71241/91A AU 7124191 A AU7124191 A AU 7124191A AU 634025 B2 AU634025 B2 AU 634025B2
- Authority
- AU
- Australia
- Prior art keywords
- coal
- composition according
- oxidised
- trace element
- humic acids
- 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.)
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Classifications
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- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05F—ORGANIC FERTILISERS NOT COVERED BY SUBCLASSES C05B, C05C, e.g. FERTILISERS FROM WASTE OR REFUSE
- C05F11/00—Other organic fertilisers
- C05F11/02—Other organic fertilisers from peat, brown coal, and similar vegetable deposits
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05D—INORGANIC FERTILISERS NOT COVERED BY SUBCLASSES C05B, C05C; FERTILISERS PRODUCING CARBON DIOXIDE
- C05D9/00—Other inorganic fertilisers
- C05D9/02—Other inorganic fertilisers containing trace elements
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- Chemical & Material Sciences (AREA)
- Organic Chemistry (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Inorganic Chemistry (AREA)
- Fertilizers (AREA)
- Agricultural Chemicals And Associated Chemicals (AREA)
Description
COMMONWEALTH OF AUSTRALIA 6 3 4 PATENTS ACT 1952 Form SUBSTITUTE COMPLETE SPECIFICATION
(ORIGINAL)
FOR OFFICE USE Short Title: Int Cl: Application Number: Lodged: Complete Specification-Lodged: Accepted: Lapsed: Published: Priority: Related Art: TO BE COMPLETED BY APPLICANT Name of Applicant: Address of Applicant: Actual Inventor: Address for Service: NA-T-I-ONAL-E-NERG-Y-6 UN-I-LE Pet-se-tts-Pa-r-k--P-ri-ory--Ro-ad--Lynnwood Ri±dge--PretoriaT-TRANS-VAAL, SOUTH AFRTCA Hendrik Van Heerden Van Der Watt; Robin Oxley Barnard and Izak SEC.
Johannes Cronje 3 GRIFFITH HACK CO 71 YORK STREET .1 SYDNEY NSW 2000 Complete Specification for the invention entitled: PLANT MICRO-ELEMENT AVAILABILITY The following statement is a full description of this invention, including the best method of performing it known to us:- GH&CO REF: 20697-I:PJW:RK 2111A:rk
M
2 BACKGROUND OF THE INVENTION This invention relates to the supply of micro-elements, or trace elements as they are also known, such as Fe, Zn, Mn and Cu, to plants in soils where problems are experienced with uptake of these elements.
It is well known that the availability of several trace elements, especially Fe and Zn, decreases at high pH, creating nutritional problems under these conditions.
In order to alleviate these problems, use is often made of synthetic organic chelates added to the soil, which are usually both expensive and not very efficient.
Alternatively, foliar applications are made.
SUMMARY OF THE INVENTION According to the present invention, a composition for applying to a soil locus, particularly a basic soil, includes a trace element such as Fe, Zn, Mn or Cu in one or both of the following forms: suspended or complexed with humic acids in an aqueous medium, the humic acids being derived from oxidized low to medium ranked coal; (ii) captured in or by an oxidized coal.
r P20679-1/429 3 Further according to the invention, a method of applying a trace element to a basic soil locus includes the step of applying a composition as described above to that locus.
Still further according to the invention, a method of improving the uptake of a trace element by a plant from a basic soil locus includes the step of applying a composition as described above to the locus in the region of the plant.
DESCRIPTION OF EMBODIMENTS The oxidised coal will preferably be an oxidised low to medium ranked coal. Examples of such coals are sub-bituminous and bituminous coals.
The oxidised coal is preferably produced by the wet oxidation process described in United States patent No. 4,912,256. This process produces an oxidised coal which contains humic acids. The oxidised coal has an acidic pH, for example a pH in the range 2 to 3. The trace elements are captured by this oxidised coal by contacting it with an aqueous solution of the trace element. Typicaiiy, the aqueous solution is a sulphate solution. The trace element is captured by the oxidised coal and is subsequently made available to the plant growing in the alkaline soil.
cc -4 In the production of an oxidised coal using a wet oxidation process, some water-soluble fulvic acids will also be produced. The fulvic acids can be removed from the oxidised coal (by filtration) before treatment with the solution of the trace element. However, it is not necessary to remove the fulvic acids from the oxidised coal.
The humic acids for the practice of the invention are preferably produced from an oxidised coal, particularly an oxidised low to medium ranked coal. The humic acids will be mixed with an aqueous solution of a trace element. The trace element will be either complex with the humic acids or will be suspended with the humic acids, in both cases in the aqueous medium. The trace element will be used in this form for application to a soil locus.
The coal-derived humic acids and the oxidised coal will typically have an elemental analysis (on an air-dried basis) of: Element Range Carbon 45 Hydrogen 2- 6 Oxygen 20 The coal-derived humic acids and oxidised coal will also typically have a functional group analysis of: Functional Group Range (meq/g) Total acidity 3 13 Carboxylic groups 0,5 12 Phenolic groups 0,5 9 Trace elements, particularly iron and zinc, are not easily taken up by a plant from basic soils because the trace element or a proportion thereof, will exist in such soils in insoluble form. The trace elements in the compositions of the invention are in a form which enable them to be taken up by a plant from these basic soils in a way which makes them readily accessible to the metabolic processes of the plant.
The invention will now be illustrated with the following example.
PREPARATION
A bituminous coal (200g) and water (400ml) were slurried in a 2 litre stirred reactor. The reactor was pressurised to 8,0 MPa with oxygen, heated with external bar heaters to 200 0 C. Oxygen was allowed to flow through the slurry at a rate of 4 litres/minute. After one hour the 6 oxygen flow was terminated, the reactor cooled down to room temperature and the pressure released to atmospheric.
The slurry contained oxidised coal (insoluble in water and hereinafter referred to as "oxicoal") and a solution of fulvic acids in water. By filtration, the oxicoal was separated from the solution of fulvic acids in water. The concentration of the fulvic acids in water was determined to be 8,45% (on a mass per volume basis). The oxicoal was found to have the following elemental analysis (on an air-dried basis) and functional group analysis: Elemental Analysis Element Carbon Hydrogen Oxygen Percentage 51,3 2,3 28,7 Functional Group Analysis Functional Group Total acidity Carboxylic groups Phenolic groups Amount (meq/g) 6,25 2,16 4,09 -7 Humic acids were obtained by refluxing the oxicoal slurry with aqueous sodium hydroxide for 5 hours. The insoluble residue was removed by centrifugation and the humic acids (80% yield) were recovered by acidic precipitation of the supernatant. This will be referred to as "oxihumic acids".
The oxihumic acids were found to have the following elemental analysis (on an air-dried basis) and functional group analysis: Elemental Analysis Element Carbon Hydrogen Oxygen Percentage 55,5 2,7 32,1 Function Groun Analysis Functional Group Total acidity Carboxylic groups Phenolic groups Amount (meq/g) 7,45 3,38 4,07
__M
8 Fe AND Zn OXIHUMIC ACIDS FORMULATION The oxihumic acids were mixed with 0,1 M solutions of Fe and Zn sulphate to obtain a concentration of 7,21 and 8,44 meq/ml of Fe and Zn respectively in the formulation.
Fe AND Zn OXICOAL FORMULATION The oxicoal was mixed with 0,1 M solutions of Fe and Zn sulphate.
The thus formulated oxicoals were filtered off and dried.
The formulated oxicoals were analysed and found to contain 10,4% Fe and 0,37% Zn.
APPLICATION PROCEDURE A sand culture experiment, using 4kg quartz sand in Mitscherlich vegetation vessels, was conducted. Hoagland nutrient solution, containing nitrogen as both NH, and NO, but excluding both Fe and Zn, was supplied initially and augmented during the growing season.
Iron, at the rate of 0,5 mg/dm 3 or zinc, at the rate of 0,05 mg/dm 3 were supplied to the vessels in appropriate treatments as different sources control sulphate, EDTA, oxihumic acids, and oxicoal.
9 Two levels of liming were employed the equivalent of 10t and 300mm depth of calcium carbonate which was thoroughly incorporated prior to the commencement of the experiment. Maize (Zea mays cv TX24) was used as test crop, with five plants per pot and three replicates of each treatment. Plant growth was monitored and photographs taken at appropriate growth stages.
Both tops and roots were harvested, at approximately 14 weeks, and dry 0 C) mass determined. Fe and Zn were also determined in both tops and roots according to the method of Barnard, R.O. and Filscher, W 1.
1988, Growth of Legumes at Different Levels of Liming, Trop. Agric.
(Trinidad) 65 113-116.
For standard statistical analysis the two aspects of the experiment, Fe and Zn, were considered separately, which is how the respective data is presented. The Tukey test at the 5% level of significance was carried out according to Steel, R.G.D. and Torrie, 1980, "Principles and t Procedures of Statistics" McGraw-Hill Book Corporation, New York.
RESULTS
The results are given in Tables 1 and 2 for iron anL in Tables 3 and 4 for zinc.
1
RESULTS
TABLE 1 Yield and Fe-content of top growth of maize with different Fe treatments Top growth yield Fe-content of top growth Treatnant (g/pot) (mg x 100/pot) lot 20t T- 10t 20t T- CaCO 3 CaCO 3 me-.ns CaCO 3 CaCO 3 means Control-Fe 58,05 59,24 58,64 357 397 375 Sulphate 57,08 56,89 56,98 227 340 283 EDTA 71,55 64,29 67,92 214 225 219 Oxihumic acids 66,85 68,50 67,68 267 380 324 Oxicoal 64,19 61,41 62,80 369 338 353 Lime level (L) means 64,69 63,83 296 343 LSD, for Treatment 9,62 168 Lime Level 3,69 64 C.V. 8,3 29,0 TABLE 2 Yield and Fe-content of roots of maize with different Fe treatments Root yield Fe-content of roots Treatment (g/pot) (mg x 100/por) 20t T- 10t 20t T- CaCO CaCO means CaCO CaCO- means 3 3 3 Control-Fe 22,70 22,25 22,47 736 990 863 Sulphate 21,50 25,67 23,58 943 659 801 EDTA 28,11 21,58 24,85 1277 661 969 Oxihumic acids 25,28 27,55 26,42 519 1624 1071 Oxicoal 26,58 24,92 25,75 1099 670 885 Lime level means 24,93 25,86 923 1175 LSDT for: Treatment (T) Lime Level (L) C.V. 6,15 2,35 13,0 1208 462 62, S11 TABLE 3 Yield and Zn-content of roots of maize with different Zn treatments Top growth yield Zn-content of top growth Treatment (g/pot) (mg x 100/pot) 20t T- 10t 20t T- CaCO 3 CaCO means CaCO CaCO means Control-Zn 74,94 68,15 71,55 180 82 131 Sulphate 67,95 75,28 71,62 74 84 79 EDTA 82,03 78,40 80,22 (non-est) 78 (non-est) Oxihumic acids 78,89 93,19 86,04 308 323 315 Oxicoal 80,23 88,71 84,47 453 470 461 Lime level means 77,72 82,69 (293) 236 LSDT Treatment 7,72 101 Lime level 2,96 72 C V. 5,0 14,0 TABLE 4 Yield and Zn-content of roots of maize with :fferent Zn treatments Root yield Zn-content of roots Treatment (g/pot) (me x 100/pot) 20t T- 10t 20t T- CaCO 3 C- )3 means CaCO 3 CaCO means Control-Zn 19,62 27,67 23,65 35 33 34 Sulphate 27,99 21,31 24,65 68 24 46 EDTA 29,16 28,21 28,69 40 36 38 Oxihumic acids 23,92 22,97 23,45 229 174 201 Oxicoal 25,61 25,57 26,59 253 2-3 258 Lime level means 25,80 25,70 149 134 LSDT for: Treatment (T) Lime Level (L) c.V. 6,31 2,93 14,0 19 19,0
L
12
CONCLUSION
From he results set out in Tables 1 to 4 it can be seen that in many instances excellent uptake of iron and zinc from soils of high pH levels was achieved with both oxihumic acids and oxicoal. However, it should be noted that the amount of iron and zinc taken up by the plant is not always a true reflection of the quality of the iron and zinc which is made available to the plant. Both the oxicoal and oxihumic acids provided excellent iron and zinc metabolites to the plant which is mirrored in the appearance of tile plant. For example, maize treated with the iron and zinc oxicoal and oxihumic acids exhibited a far better quality than the maize treated with the iron and zinc EDTA or the iron and zinc sulphate. The plants had a more healthy appearance, the leaves were more shiny and had a deeper shade of green, indicating that the iron and zinc taken up from the oxidised coal derived products provided the plant with a more accessible source of iron and zinc for the metabolic processes of the plant. There is also a very major cost advantage, i.e. in excess of 10 times, with the use of an iron and zinc oxicoal in comparison with an iron and zinc EDTA product.
Claims (11)
1. A composition for applying to a soil locus includes a trace element in a form selected from: suspended or complexed with humic acids in an aqueous medium, the humic acids being derived from oxidized low to medium ranked coal; (ii) captured in or by an oxidized coal; (iii) mixtures of and (ii).
2. A composition according to claim 1 wherein the trace element is selected from iron, zinc, copper, manganese and mixtures thereof.
3. A method according to claim 1 wherein the trace element is selected from iron, zinc and mixtures thereof.
4. A composition according to any one of claims 1 to 3 wherein the oxidised coal is an oxidised low to medium ranked coal.
A composition according to any one of the preceding claims wherein the humic acids and oxidised coal have an elemental analysis (on an air-dried basis) of: l 25 Element Range Carbon 45 Hydrogen 2 6 Oxygen 20
6. A composition according to any one of the preceding claims wherein the humic acids and oxidised coal have a functional group analysis of: Functional Group Range (meq/g) Total acidity 3 13 Carboxylic groups 0,5 12 Phenolic groups 0,5 9 P20679-1/429 r: 14
7. A composition according to any one of the preceding claims wherein the oxidised coal has an acidic pH.
8. A composition according to claim 7 wherein the oxidised coal has a pH in the range 2 to 3.
9. A composition according to claim 1 and substantially as hereinbefore described.
A method of applying a trace element to a basic soil locus includes the step of applying a composition according to any one of the preceding claims to that locus.
11. A method of improving the uptake of a trace element by a plant from a basic soil locus includes the steps of applying a composition according to any one of claims 1 to 9 to that locus in the region of a plant. Dated this 9th day of November 1992 NATIONAL ENERGY COUNCIL By its Patent Attorneys GRIFFITH HACK CO. P20679-1/429
Applications Claiming Priority (2)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
ZA901535 | 1990-02-28 | ||
ZA90/1535 | 1990-02-28 |
Publications (2)
Publication Number | Publication Date |
---|---|
AU7124191A AU7124191A (en) | 1991-08-29 |
AU634025B2 true AU634025B2 (en) | 1993-02-11 |
Family
ID=25580028
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
AU71241/91A Ceased AU634025B2 (en) | 1990-02-28 | 1991-02-20 | Plant micro-element availability |
Country Status (6)
Country | Link |
---|---|
JP (1) | JPH04214085A (en) |
AU (1) | AU634025B2 (en) |
DE (1) | DE4105247A1 (en) |
FR (1) | FR2658810B1 (en) |
GB (1) | GB2241498B (en) |
IT (1) | IT1249342B (en) |
Families Citing this family (6)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB2234746B (en) * | 1989-07-12 | 1992-09-30 | Nat Energy Council | Crusting soil water and plant root penetration improvement |
GB9414968D0 (en) * | 1994-07-26 | 1994-09-14 | Lambson Ltd | Fertiliser composition |
NL1008820C2 (en) * | 1998-04-06 | 1999-10-07 | Holland Chemical Internat N V | Mixture suitable as fertilizer. |
CN102531765B (en) * | 2011-08-18 | 2013-07-17 | 杨栓明 | Organic plant nutrient mineral residue removal element and preparation method thereof |
UA116535C2 (en) * | 2012-03-30 | 2018-04-10 | Рдінновейшн Апс | Benzene polycarboxylic acid compounds and their use as drug |
ES2805525T3 (en) * | 2016-02-17 | 2021-02-12 | Fertinagro Biotech Sl | Fertilizer composition that includes ions complexed with humic substances to improve the biological fixation of nitrogen by microorganisms present in the soil |
Family Cites Families (11)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
GB438114A (en) * | 1933-04-01 | 1935-11-04 | Joost Hudig | Improved soil improvers and a process for their manufacture |
GB652000A (en) * | 1946-12-28 | 1951-04-11 | Rumianca Spa | Akaline clay soil improvers |
US3630710A (en) * | 1969-01-31 | 1971-12-28 | Mary Maxine Frederickson | Production of metabolic demand seaweed-type fertilizer |
SU588219A1 (en) * | 1974-06-25 | 1978-01-15 | Chikhladze Gulnara M | Method of obtaining complex organic mineral fertilizer |
CA1056598A (en) * | 1975-07-07 | 1979-06-19 | John W. Willard (Sr.) | Process for treating solid carbonaceous fossil fuels and the products thus prepared |
EP0243400A1 (en) * | 1985-10-21 | 1987-11-04 | THOMPSON, Jennings, B. | Method of making a complexing agent for plant micronutrients |
YU43949B (en) * | 1985-11-06 | 1989-12-31 | Francek Pajenk | Process for producing universal organo-mineral and bio-stimulated manure |
ES2023492B3 (en) * | 1987-03-09 | 1992-01-16 | American Colloid Co | CROP LIQUID STIMULANT. |
EP0290704A3 (en) * | 1987-05-12 | 1988-12-14 | Anlad N.V. | Formulation for agricultural use suitable for improving the nutritional activity and development of plants |
NZ225271A (en) * | 1987-07-08 | 1991-02-26 | Nat Energy Council | Oxidising coal using a gaseous oxidant |
GB2231564B (en) * | 1989-05-15 | 1992-08-12 | Nat Energy Council | Seedling growth stimulation |
-
1991
- 1991-02-20 AU AU71241/91A patent/AU634025B2/en not_active Ceased
- 1991-02-20 DE DE4105247A patent/DE4105247A1/en not_active Ceased
- 1991-02-26 JP JP3053229A patent/JPH04214085A/en active Pending
- 1991-02-27 IT ITMI910504A patent/IT1249342B/en active IP Right Grant
- 1991-02-27 GB GB9104148A patent/GB2241498B/en not_active Expired - Fee Related
- 1991-02-28 FR FR9102399A patent/FR2658810B1/en not_active Expired - Fee Related
Also Published As
Publication number | Publication date |
---|---|
AU7124191A (en) | 1991-08-29 |
DE4105247A1 (en) | 1991-08-29 |
IT1249342B (en) | 1995-02-23 |
FR2658810B1 (en) | 1994-06-03 |
ITMI910504A1 (en) | 1992-08-27 |
GB2241498A (en) | 1991-09-04 |
JPH04214085A (en) | 1992-08-05 |
GB9104148D0 (en) | 1991-04-17 |
FR2658810A1 (en) | 1991-08-30 |
ITMI910504A0 (en) | 1991-02-27 |
GB2241498B (en) | 1993-06-30 |
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Legal Events
Date | Code | Title | Description |
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MK14 | Patent ceased section 143(a) (annual fees not paid) or expired |