WO2023220779A1 - Composition d'engrais et/ou d'amélioration du sol, procédé de préparation et procédé d'utilisation - Google Patents
Composition d'engrais et/ou d'amélioration du sol, procédé de préparation et procédé d'utilisation Download PDFInfo
- Publication number
- WO2023220779A1 WO2023220779A1 PCT/AU2023/050414 AU2023050414W WO2023220779A1 WO 2023220779 A1 WO2023220779 A1 WO 2023220779A1 AU 2023050414 W AU2023050414 W AU 2023050414W WO 2023220779 A1 WO2023220779 A1 WO 2023220779A1
- Authority
- WO
- WIPO (PCT)
- Prior art keywords
- fertiliser
- soil improver
- improver composition
- urea
- eutectic melt
- Prior art date
Links
- 239000002689 soil Substances 0.000 title claims abstract description 112
- 239000000203 mixture Substances 0.000 title claims abstract description 107
- 239000003337 fertilizer Substances 0.000 title claims abstract description 96
- 238000000034 method Methods 0.000 title claims abstract description 53
- 238000002360 preparation method Methods 0.000 title description 13
- 230000005496 eutectics Effects 0.000 claims abstract description 115
- 239000012620 biological material Substances 0.000 claims abstract description 56
- 235000015097 nutrients Nutrition 0.000 claims abstract description 45
- 230000008635 plant growth Effects 0.000 claims abstract description 22
- 230000002708 enhancing effect Effects 0.000 claims abstract description 14
- XSQUKJJJFZCRTK-UHFFFAOYSA-N Urea Chemical compound NC(N)=O XSQUKJJJFZCRTK-UHFFFAOYSA-N 0.000 claims description 111
- IJGRMHOSHXDMSA-UHFFFAOYSA-N Atomic nitrogen Chemical compound N#N IJGRMHOSHXDMSA-UHFFFAOYSA-N 0.000 claims description 62
- 210000002268 wool Anatomy 0.000 claims description 62
- 239000004202 carbamide Substances 0.000 claims description 59
- 102000011782 Keratins Human genes 0.000 claims description 46
- 108010076876 Keratins Proteins 0.000 claims description 46
- 229910052757 nitrogen Inorganic materials 0.000 claims description 42
- 102000004169 proteins and genes Human genes 0.000 claims description 41
- 108090000623 proteins and genes Proteins 0.000 claims description 41
- 239000001763 2-hydroxyethyl(trimethyl)azanium Substances 0.000 claims description 40
- 235000019743 Choline chloride Nutrition 0.000 claims description 40
- SGMZJAMFUVOLNK-UHFFFAOYSA-M choline chloride Chemical compound [Cl-].C[N+](C)(C)CCO SGMZJAMFUVOLNK-UHFFFAOYSA-M 0.000 claims description 40
- 229960003178 choline chloride Drugs 0.000 claims description 40
- 150000001413 amino acids Chemical class 0.000 claims description 30
- 108090000765 processed proteins & peptides Proteins 0.000 claims description 26
- 102000004196 processed proteins & peptides Human genes 0.000 claims description 20
- 102000007079 Peptide Fragments Human genes 0.000 claims description 13
- 108010033276 Peptide Fragments Proteins 0.000 claims description 13
- 210000003746 feather Anatomy 0.000 claims description 11
- 210000004209 hair Anatomy 0.000 claims description 11
- 210000003323 beak Anatomy 0.000 claims description 8
- 210000000003 hoof Anatomy 0.000 claims description 8
- 239000007788 liquid Substances 0.000 claims description 8
- 239000002028 Biomass Substances 0.000 claims description 7
- 210000000078 claw Anatomy 0.000 claims description 7
- 239000000284 extract Substances 0.000 claims description 7
- 210000003284 horn Anatomy 0.000 claims description 7
- 210000000282 nail Anatomy 0.000 claims description 7
- 210000003491 skin Anatomy 0.000 claims description 7
- 241001494479 Pecora Species 0.000 claims description 5
- 239000000654 additive Substances 0.000 claims description 4
- 230000000996 additive effect Effects 0.000 claims description 4
- 235000002198 Annona diversifolia Nutrition 0.000 claims description 3
- 241000283707 Capra Species 0.000 claims description 3
- 241000282842 Lama glama Species 0.000 claims description 3
- 241000283973 Oryctolagus cuniculus Species 0.000 claims description 3
- 241001416177 Vicugna pacos Species 0.000 claims description 3
- 241000196324 Embryophyta Species 0.000 description 56
- 239000012634 fragment Substances 0.000 description 17
- 238000011282 treatment Methods 0.000 description 15
- 125000001477 organic nitrogen group Chemical group 0.000 description 14
- UMGDCJDMYOKAJW-UHFFFAOYSA-N thiourea Chemical compound NC(N)=S UMGDCJDMYOKAJW-UHFFFAOYSA-N 0.000 description 14
- 239000002904 solvent Substances 0.000 description 13
- 238000010438 heat treatment Methods 0.000 description 12
- 239000000243 solution Substances 0.000 description 10
- 239000004381 Choline salt Substances 0.000 description 9
- 241000209140 Triticum Species 0.000 description 9
- 235000021307 Triticum Nutrition 0.000 description 9
- 235000019417 choline salt Nutrition 0.000 description 9
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 9
- 239000000463 material Substances 0.000 description 8
- 239000002699 waste material Substances 0.000 description 8
- 239000000374 eutectic mixture Substances 0.000 description 7
- 150000003248 quinolines Chemical class 0.000 description 7
- 238000002415 sodium dodecyl sulfate polyacrylamide gel electrophoresis Methods 0.000 description 7
- 238000009331 sowing Methods 0.000 description 7
- 239000000126 substance Substances 0.000 description 7
- 125000003275 alpha amino acid group Chemical group 0.000 description 6
- 230000008901 benefit Effects 0.000 description 6
- 229960001231 choline Drugs 0.000 description 6
- 238000007865 diluting Methods 0.000 description 6
- 230000000694 effects Effects 0.000 description 6
- 238000004519 manufacturing process Methods 0.000 description 6
- 229910052698 phosphorus Inorganic materials 0.000 description 6
- 239000002244 precipitate Substances 0.000 description 6
- QGZKDVFQNNGYKY-UHFFFAOYSA-N Ammonia Chemical compound N QGZKDVFQNNGYKY-UHFFFAOYSA-N 0.000 description 5
- 241001465754 Metazoa Species 0.000 description 5
- 238000010899 nucleation Methods 0.000 description 5
- 238000010979 pH adjustment Methods 0.000 description 5
- 239000011492 sheep wool Substances 0.000 description 5
- OFOBLEOULBTSOW-UHFFFAOYSA-N Malonic acid Chemical compound OC(=O)CC(O)=O OFOBLEOULBTSOW-UHFFFAOYSA-N 0.000 description 4
- OEYIOHPDSNJKLS-UHFFFAOYSA-N choline Chemical class C[N+](C)(C)CCO OEYIOHPDSNJKLS-UHFFFAOYSA-N 0.000 description 4
- 150000003672 ureas Chemical class 0.000 description 4
- 241001474374 Blennius Species 0.000 description 3
- PEDCQBHIVMGVHV-UHFFFAOYSA-N Glycerine Chemical compound OCC(O)CO PEDCQBHIVMGVHV-UHFFFAOYSA-N 0.000 description 3
- 101710172711 Structural protein Proteins 0.000 description 3
- 239000003905 agrochemical Substances 0.000 description 3
- 230000004071 biological effect Effects 0.000 description 3
- 230000015572 biosynthetic process Effects 0.000 description 3
- 238000005119 centrifugation Methods 0.000 description 3
- -1 choline halide Chemical class 0.000 description 3
- KRKNYBCHXYNGOX-UHFFFAOYSA-N citric acid Chemical compound OC(=O)CC(O)(C(O)=O)CC(O)=O KRKNYBCHXYNGOX-UHFFFAOYSA-N 0.000 description 3
- 239000012141 concentrate Substances 0.000 description 3
- 238000000354 decomposition reaction Methods 0.000 description 3
- 239000012895 dilution Substances 0.000 description 3
- 238000010790 dilution Methods 0.000 description 3
- 230000007613 environmental effect Effects 0.000 description 3
- 238000013467 fragmentation Methods 0.000 description 3
- 238000006062 fragmentation reaction Methods 0.000 description 3
- 239000000499 gel Substances 0.000 description 3
- 239000001257 hydrogen Substances 0.000 description 3
- 229910052739 hydrogen Inorganic materials 0.000 description 3
- 229910052700 potassium Inorganic materials 0.000 description 3
- 230000008569 process Effects 0.000 description 3
- 239000007787 solid Substances 0.000 description 3
- JJCWKVUUIFLXNZ-UHFFFAOYSA-M 2-hydroxyethyl(trimethyl)azanium;bromide Chemical compound [Br-].C[N+](C)(C)CCO JJCWKVUUIFLXNZ-UHFFFAOYSA-M 0.000 description 2
- 229920002101 Chitin Polymers 0.000 description 2
- NZNMSOFKMUBTKW-UHFFFAOYSA-N Cyclohexanecarboxylic acid Natural products OC(=O)C1CCCCC1 NZNMSOFKMUBTKW-UHFFFAOYSA-N 0.000 description 2
- 238000005481 NMR spectroscopy Methods 0.000 description 2
- MUBZPKHOEPUJKR-UHFFFAOYSA-N Oxalic acid Natural products OC(=O)C(O)=O MUBZPKHOEPUJKR-UHFFFAOYSA-N 0.000 description 2
- OAICVXFJPJFONN-UHFFFAOYSA-N Phosphorus Chemical compound [P] OAICVXFJPJFONN-UHFFFAOYSA-N 0.000 description 2
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 description 2
- FEWJPZIEWOKRBE-UHFFFAOYSA-N Tartaric acid Natural products [H+].[H+].[O-]C(=O)C(O)C(O)C([O-])=O FEWJPZIEWOKRBE-UHFFFAOYSA-N 0.000 description 2
- VYWQTJWGWLKBQA-UHFFFAOYSA-N [amino(hydroxy)methylidene]azanium;chloride Chemical compound Cl.NC(N)=O VYWQTJWGWLKBQA-UHFFFAOYSA-N 0.000 description 2
- 239000002253 acid Substances 0.000 description 2
- AFVLVVWMAFSXCK-VMPITWQZSA-N alpha-cyano-4-hydroxycinnamic acid Chemical compound OC(=O)C(\C#N)=C\C1=CC=C(O)C=C1 AFVLVVWMAFSXCK-VMPITWQZSA-N 0.000 description 2
- 229910021529 ammonia Inorganic materials 0.000 description 2
- 238000004458 analytical method Methods 0.000 description 2
- 235000013339 cereals Nutrition 0.000 description 2
- 238000004090 dissolution Methods 0.000 description 2
- 230000012202 endocytosis Effects 0.000 description 2
- 230000006862 enzymatic digestion Effects 0.000 description 2
- 230000007717 exclusion Effects 0.000 description 2
- 230000012010 growth Effects 0.000 description 2
- 230000001965 increasing effect Effects 0.000 description 2
- 239000012803 melt mixture Substances 0.000 description 2
- 238000002844 melting Methods 0.000 description 2
- 230000008018 melting Effects 0.000 description 2
- 238000002156 mixing Methods 0.000 description 2
- 150000007523 nucleic acids Chemical class 0.000 description 2
- 102000039446 nucleic acids Human genes 0.000 description 2
- 108020004707 nucleic acids Proteins 0.000 description 2
- 239000011368 organic material Substances 0.000 description 2
- 239000011574 phosphorus Substances 0.000 description 2
- 239000011591 potassium Substances 0.000 description 2
- 238000001556 precipitation Methods 0.000 description 2
- 239000000047 product Substances 0.000 description 2
- 150000003242 quaternary ammonium salts Chemical class 0.000 description 2
- 238000003756 stirring Methods 0.000 description 2
- 239000010414 supernatant solution Substances 0.000 description 2
- 230000002277 temperature effect Effects 0.000 description 2
- 238000012360 testing method Methods 0.000 description 2
- 150000003585 thioureas Chemical class 0.000 description 2
- QDGIAPPCJRFVEK-UHFFFAOYSA-N (1-methylpiperidin-4-yl) 2,2-bis(4-chlorophenoxy)acetate Chemical compound C1CN(C)CCC1OC(=O)C(OC=1C=CC(Cl)=CC=1)OC1=CC=C(Cl)C=C1 QDGIAPPCJRFVEK-UHFFFAOYSA-N 0.000 description 1
- HFVMEOPYDLEHBR-UHFFFAOYSA-N (2-fluorophenyl)-phenylmethanol Chemical compound C=1C=CC=C(F)C=1C(O)C1=CC=CC=C1 HFVMEOPYDLEHBR-UHFFFAOYSA-N 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- 239000005874 Bifenthrin Substances 0.000 description 1
- 239000005947 Dimethoate Substances 0.000 description 1
- KCXVZYZYPLLWCC-UHFFFAOYSA-N EDTA Chemical compound OC(=O)CN(CC(O)=O)CCN(CC(O)=O)CC(O)=O KCXVZYZYPLLWCC-UHFFFAOYSA-N 0.000 description 1
- 241000287828 Gallus gallus Species 0.000 description 1
- 108010084680 Heterogeneous-Nuclear Ribonucleoprotein K Proteins 0.000 description 1
- 239000004166 Lanolin Substances 0.000 description 1
- 235000007688 Lycopersicon esculentum Nutrition 0.000 description 1
- 102100023482 Mitogen-activated protein kinase 14 Human genes 0.000 description 1
- 229910002651 NO3 Inorganic materials 0.000 description 1
- NHNBFGGVMKEFGY-UHFFFAOYSA-N Nitrate Chemical compound [O-][N+]([O-])=O NHNBFGGVMKEFGY-UHFFFAOYSA-N 0.000 description 1
- 101100420928 Oryza sativa subsp. japonica SE14 gene Proteins 0.000 description 1
- 102000035195 Peptidases Human genes 0.000 description 1
- 108091005804 Peptidases Proteins 0.000 description 1
- 108010009736 Protein Hydrolysates Proteins 0.000 description 1
- 240000003768 Solanum lycopersicum Species 0.000 description 1
- KDYFGRWQOYBRFD-UHFFFAOYSA-N Succinic acid Natural products OC(=O)CCC(O)=O KDYFGRWQOYBRFD-UHFFFAOYSA-N 0.000 description 1
- PNNCWTXUWKENPE-UHFFFAOYSA-N [N].NC(N)=O Chemical compound [N].NC(N)=O PNNCWTXUWKENPE-UHFFFAOYSA-N 0.000 description 1
- OIPILFWXSMYKGL-UHFFFAOYSA-N acetylcholine Chemical compound CC(=O)OCC[N+](C)(C)C OIPILFWXSMYKGL-UHFFFAOYSA-N 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 239000002671 adjuvant Substances 0.000 description 1
- 239000012670 alkaline solution Substances 0.000 description 1
- YSKUZVBSHIWEFK-UHFFFAOYSA-N ammelide Chemical compound NC1=NC(O)=NC(O)=N1 YSKUZVBSHIWEFK-UHFFFAOYSA-N 0.000 description 1
- 238000000540 analysis of variance Methods 0.000 description 1
- VJBCNMFKFZIXHC-UHFFFAOYSA-N azanium;2-(4-methyl-5-oxo-4-propan-2-yl-1h-imidazol-2-yl)quinoline-3-carboxylate Chemical compound N.N1C(=O)C(C(C)C)(C)N=C1C1=NC2=CC=CC=C2C=C1C(O)=O VJBCNMFKFZIXHC-UHFFFAOYSA-N 0.000 description 1
- 230000009286 beneficial effect Effects 0.000 description 1
- OMFRMAHOUUJSGP-IRHGGOMRSA-N bifenthrin Chemical compound C1=CC=C(C=2C=CC=CC=2)C(C)=C1COC(=O)[C@@H]1[C@H](\C=C(/Cl)C(F)(F)F)C1(C)C OMFRMAHOUUJSGP-IRHGGOMRSA-N 0.000 description 1
- OWMVSZAMULFTJU-UHFFFAOYSA-N bis-tris Chemical compound OCCN(CCO)C(CO)(CO)CO OWMVSZAMULFTJU-UHFFFAOYSA-N 0.000 description 1
- OHJMTUPIZMNBFR-UHFFFAOYSA-N biuret Chemical compound NC(=O)NC(N)=O OHJMTUPIZMNBFR-UHFFFAOYSA-N 0.000 description 1
- 238000006664 bond formation reaction Methods 0.000 description 1
- 239000000872 buffer Substances 0.000 description 1
- 230000015556 catabolic process Effects 0.000 description 1
- 230000032823 cell division Effects 0.000 description 1
- 230000008859 change Effects 0.000 description 1
- 238000012512 characterization method Methods 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000007796 conventional method Methods 0.000 description 1
- NKLPQNGYXWVELD-UHFFFAOYSA-M coomassie brilliant blue Chemical compound [Na+].C1=CC(OCC)=CC=C1NC1=CC=C(C(=C2C=CC(C=C2)=[N+](CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=2C=CC(=CC=2)N(CC)CC=2C=C(C=CC=2)S([O-])(=O)=O)C=C1 NKLPQNGYXWVELD-UHFFFAOYSA-M 0.000 description 1
- 238000011033 desalting Methods 0.000 description 1
- 238000011026 diafiltration Methods 0.000 description 1
- MCWXGJITAZMZEV-UHFFFAOYSA-N dimethoate Chemical compound CNC(=O)CSP(=S)(OC)OC MCWXGJITAZMZEV-UHFFFAOYSA-N 0.000 description 1
- 238000009826 distribution Methods 0.000 description 1
- 231100000673 dose–response relationship Toxicity 0.000 description 1
- 210000002919 epithelial cell Anatomy 0.000 description 1
- 150000002148 esters Chemical class 0.000 description 1
- 239000000417 fungicide Substances 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 239000000413 hydrolysate Substances 0.000 description 1
- 230000003301 hydrolyzing effect Effects 0.000 description 1
- 239000002917 insecticide Substances 0.000 description 1
- ZFSLODLOARCGLH-UHFFFAOYSA-N isocyanuric acid Chemical compound OC1=NC(O)=NC(O)=N1 ZFSLODLOARCGLH-UHFFFAOYSA-N 0.000 description 1
- 229940039717 lanolin Drugs 0.000 description 1
- 235000019388 lanolin Nutrition 0.000 description 1
- 239000012160 loading buffer Substances 0.000 description 1
- 230000007774 longterm Effects 0.000 description 1
- 235000021073 macronutrients Nutrition 0.000 description 1
- 239000003550 marker Substances 0.000 description 1
- 238000001819 mass spectrum Methods 0.000 description 1
- 239000011159 matrix material Substances 0.000 description 1
- 238000000816 matrix-assisted laser desorption--ionisation Methods 0.000 description 1
- 238000012986 modification Methods 0.000 description 1
- 230000004048 modification Effects 0.000 description 1
- OMNKZBIFPJNNIO-UHFFFAOYSA-N n-(2-methyl-4-oxopentan-2-yl)prop-2-enamide Chemical compound CC(=O)CC(C)(C)NC(=O)C=C OMNKZBIFPJNNIO-UHFFFAOYSA-N 0.000 description 1
- ALIFPGGMJDWMJH-UHFFFAOYSA-N n-phenyldiazenylaniline Chemical compound C=1C=CC=CC=1NN=NC1=CC=CC=C1 ALIFPGGMJDWMJH-UHFFFAOYSA-N 0.000 description 1
- 235000016709 nutrition Nutrition 0.000 description 1
- 150000007524 organic acids Chemical class 0.000 description 1
- 150000002894 organic compounds Chemical class 0.000 description 1
- 230000037361 pathway Effects 0.000 description 1
- 230000001863 plant nutrition Effects 0.000 description 1
- 229920005862 polyol Polymers 0.000 description 1
- 230000002797 proteolythic effect Effects 0.000 description 1
- 229940024999 proteolytic enzymes for treatment of wounds and ulcers Drugs 0.000 description 1
- 238000012216 screening Methods 0.000 description 1
- 230000019491 signal transduction Effects 0.000 description 1
- PCMORTLOPMLEFB-ONEGZZNKSA-N sinapic acid Chemical compound COC1=CC(\C=C\C(O)=O)=CC(OC)=C1O PCMORTLOPMLEFB-ONEGZZNKSA-N 0.000 description 1
- PCMORTLOPMLEFB-UHFFFAOYSA-N sinapinic acid Natural products COC1=CC(C=CC(O)=O)=CC(OC)=C1O PCMORTLOPMLEFB-UHFFFAOYSA-N 0.000 description 1
- 239000011877 solvent mixture Substances 0.000 description 1
- 238000001228 spectrum Methods 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000003860 storage Methods 0.000 description 1
- 239000001384 succinic acid Substances 0.000 description 1
- 239000011975 tartaric acid Substances 0.000 description 1
- 235000002906 tartaric acid Nutrition 0.000 description 1
- WNVQBUHCOYRLPA-UHFFFAOYSA-N triuret Chemical compound NC(=O)NC(=O)NC(N)=O WNVQBUHCOYRLPA-UHFFFAOYSA-N 0.000 description 1
- 238000009736 wetting Methods 0.000 description 1
Classifications
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05F—ORGANIC FERTILISERS NOT COVERED BY SUBCLASSES C05B, C05C, e.g. FERTILISERS FROM WASTE OR REFUSE
- C05F1/00—Fertilisers made from animal corpses, or parts thereof
- C05F1/005—Fertilisers made from animal corpses, or parts thereof from meat-wastes or from other wastes of animal origin, e.g. skins, hair, hoofs, feathers, blood
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05C—NITROGENOUS FERTILISERS
- C05C9/00—Fertilisers containing urea or urea compounds
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05C—NITROGENOUS FERTILISERS
- C05C3/00—Fertilisers containing other salts of ammonia or ammonia itself, e.g. gas liquor
-
- C—CHEMISTRY; METALLURGY
- C05—FERTILISERS; MANUFACTURE THEREOF
- C05F—ORGANIC FERTILISERS NOT COVERED BY SUBCLASSES C05B, C05C, e.g. FERTILISERS FROM WASTE OR REFUSE
- C05F1/00—Fertilisers made from animal corpses, or parts thereof
- C05F1/007—Fertilisers made from animal corpses, or parts thereof from derived products of animal origin or their wastes, e.g. leather, dairy products
-
- C—CHEMISTRY; METALLURGY
- C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
- C09K—MATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
- C09K17/00—Soil-conditioning materials or soil-stabilising materials
- C09K17/14—Soil-conditioning materials or soil-stabilising materials containing organic compounds only
- C09K17/18—Prepolymers; Macromolecular compounds
- C09K17/32—Prepolymers; Macromolecular compounds of natural origin, e.g. cellulosic materials
Definitions
- the present invention relates to a fertiliser and/or soil improver composition. More specifically, the present invention relates to one or more organic sources of plant nutrient(s), contained in a fertiliser and/or soil improver composition. The present invention also relates to a method of preparation and method of use of the fertiliser and/or soil improver composition.
- Fertilisers and soil improvers are commonly used in the agricultural industry and even by home gardeners, and indeed fertilisers and soil improvers have many applications and uses between the two.
- the growth of plants can be enhanced with the use of fertilisers by providing nutrients for uptake by the plant and/or with the use of soil improvers by enhancing the effectiveness of the soil in which the plant grows.
- the nutritional aspect of fertilisers and soil improvers can involve the provision of one or more of the three main macronutrients, nitrogen (N), phosphorus (P) and potassium (K), for various growth enhancement activity.
- a fertiliser and/or soil improver composition for use in enhancing the growth of plants, the composition comprising one or more organic sources of plant nutrient(s), obtained through deconstruction of one or more biological materials by a eutectic melt.
- a method of preparing a fertiliser and/or soil improver composition comprising one or more organic sources of plant nutrient(s), the method comprising the steps of: a) forming a eutectic melt; and b) deconstructing one or more biological materials using the eutectic melt, to obtain the one or more organic sources of plant nutrient(s).
- the eutectic melt in the first or second aspect of the present invention comprises at least one hydrogen bond donor (HBD) and at least one hydrogen bond acceptor (HBA).
- the at least one HBA is a quaternary ammonium salt, such as a choline salt (including a choline halide), and the at least one HBD is a urea, thiourea or a derivative thereof.
- the eutectic melt comprises a HBA in the form of a choline salt and a HBD in the form of a urea, thiourea, or a derivative of these.
- the eutectic melt comprises a choline salt and a urea, or urea derivative.
- the deconstruction of one or more biological materials by a eutectic melt in the first or second aspect of the present invention is at a temperature in a range of approximately: 135 - 170 °C, more preferably 140 - 165°C, or most preferably 145 - 160°C, or even 145 - 155 °C.
- the temperatures/temperature ranges in the present invention are measured at ambient pressure, or atmospheric pressure, conditions.
- the molar ratio of the eutectic melt (between the at least one HBD and the at least one HBA) in the first or second aspect of the present invention may be from about 20:1 to about 1:20.
- the eutectic solvent comprises a choline salt (as a HBA) and a urea, thiourea or a derivative these (as a HBD)
- the molar ratio of HBD: HBA is in a range of from 10:1 to 1:10; more preferably, from about 8:1 to about 3:1, or most preferably from about 7.5 to about 4:1 (e.g.
- the HBD being a urea, thiourea or a derivative of these
- the HBA the choline salt
- the one or more organic sources of plant nutrient(s) includes, or is in the form of, one or more biomolecules, preferably selected from the group consisting of proteins, peptides, chitins, amino acids, nucleic acids, and combinations thereof.
- the one or more biomolecules is selected from the group consisting of proteins, peptides, protein or peptide fragments/fractions, amino acids, and combinations thereof, as the, or the predominant, organic source(s) of nitrogen.
- the one or more biomolecules are in a molecular weight range of from 0 to 40 kDa, from 1 to 30 kDa, or from 1 to 20 kDa.
- the one or more biomolecules in the first or second aspect of the present invention is obtained through deconstruction of one or more biological materials selected from the group consisting of wool, hair, feathers, horns, hooves, nails, skins, claws, beaks, and combinations thereof.
- the one or more biological materials may originate from a human, or an animal, source (e.g. the biological materials may be human hair, sheep wool and/or chicken feather).
- the one or more biomolecules obtained preferably comprises at least a protein and/or fragments/fractions thereof, in particular a keratin protein and/or fragments/fractions thereof.
- the keratin protein and/or fragments/fractions thereof is obtained from wool, through the deconstruction of wool using a eutectic melt.
- the one or more biomolecules may be fragments/fractions of one or more proteins, obtained from one or more biological materials, through deconstruction of the biological material(s) using a eutectic melt according to the present invention.
- the one or more biomolecules may be fragment(s)/fraction(s) of a protein (e.g. keratin protein), obtained from wool, through deconstruction of wool (and the protein) using a eutectic melt according to the present invention.
- step b) provides a eutectic mixture comprising the one or more organic sources of plant nutrient(s), or the one or more biomolecules.
- the method according to the second aspect of the present invention may comprise one or more further steps of diluting and/or adjusting the pH of the eutectic melt mixture comprising the one or more organic sources of plant nutrient(s) from the deconstructed one or more biological materials.
- the method may comprise a further step of: c) diluting the eutectic mixture comprising the deconstructed one or more biological materials, or comprising the one or more organic sources of plant nutrient(s).
- the method comprises a further step of: d) adjusting the pH of the eutectic mixture comprising the deconstructed one or more biological materials, or comprising the one or more organic sources of plant nutrient(s).
- the order of the steps c) and d) may be alternated, thus step c) may become step d) and step d) may become step c).
- a method according to the second aspect of the present invention may also comprise a plurality of diluting steps only, a plurality of pH adjusting steps only, or a plurality of diluting and pH adjusting steps (in various orders).
- a fertiliser and/or soil improver composition prepared according to the method of the second aspect of the present invention, or obtained from the preparation method of the second aspect of the present invention.
- a method of enhancing the growth of plants comprising a step of applying a fertiliser and/or soil improver composition according to the first, or third, aspect of the present invention to plants and/or soil supporting the plants.
- a use of a eutectic melt in the preparation of a fertiliser and/or soil improver composition comprising the deconstruction of one or more biological materials using the eutectic melt.
- the eutectic melt, or the deconstruction of the one or more biological materials is according to that defined in the first or second aspect of the present invention.
- one or more of the following plant growth parameters may be enhanced: plant height, biomass, normalised difference vegetation index (ND VI), root weight, foliage weight and total plant weight.
- ND VI normalised difference vegetation index
- the deconstruction of the biological material(s) using the eutectic melt as in any of the aspects of the present invention may involve a weight to volume ratio of the biological material(s) to the eutectic melt of from about 1 g:l ml to about 1 g:100 ml, to about lg:70ml, lg:50ml, to about lg:25ml, or to about lg:15ml (e.g. a weight to volume ratio of the biological material(s) to the eutectic melt of about 1g: 13.6ml, lg:10ml, lg:8ml, lg:6.1ml, lg:4.5ml, or lg:3ml).
- a method of enhancing the growth of plants using a fertiliser and/or soil improver composition comprising keratin, keratin fragments/fractions and/or amino acids thereof, which may be obtained through deconstruction of one or more biological materials selected from the group consisting of wool, hair, feathers, horns, hooves, nails, skins, claws, beaks, and combinations thereof.
- the method of enhancing the growth of plants according to the fourth aspect of the present invention may comprise the use of the fertiliser and/or soil improver composition according to the first or third aspect of the present invention as an additive to a known fertiliser and/or soil improver.
- the method of enhancing the growth of plants may comprise multiple, separate applications of the fertiliser and/or soil improver composition according to the first or third aspect of the present invention to the soil and/or plants.
- An application of the fertiliser and/or soil improver composition according to the first or third aspect of the present invention may be as a liquid to a surface of soil, proximal to a location of the plant within that soil.
- the method of enhancing the growth of plants according to the fourth aspect of the present invention may comprise an application of the fertiliser and/or soil improver according to the first or third aspect of the present invention as a concentrate, or in a diluted form, to provide a desired % (w/v) or concentration of one or more nutrient(s), e.g.
- N, P and/or K 5 - 50% (w/v) of N, P and/or K, or 10 - 40% (w/v) of N, P and/or K, or 5% (w/v), 12% (w/v), 15% (w/v), 20% (w/v), 27% (w/v), 35%, (w/v), 40% (w/v), or 44% (w/v) of N, P and/or K, for example.
- Figure 1 is a graph displaying the plant height results according to Example I;
- Figure 2 is a graph displaying the plant biomass results according to Example I;
- Figure 3 is a graph displaying the ND VI results according to Example I;
- Figure 4 is a graph displaying the foliage weight results according to Example I.
- Figure 5 is a graph displaying the root weight results according to Example I.
- Figure 6 is a graph displaying the total plant weight results according to Example I.
- a fertiliser and/or soil improver composition comprises one or more organic sources of plant nutrient(s) in a eutectic melt, obtained through deconstruction of one or more biological materials by the eutectic melt.
- the fertiliser and/or soil improver composition according to the present invention is in a liquid form, which renders the nutrient(s) more accessible/available to plants.
- the one or more organic sources of plant nutrient(s) are dissolved in a eutectic melt according to the present invention, with the one or more organic sources of plant nutrient(s) being obtained through deconstruction of one or more biological materials by the eutectic melt.
- the liquid/solvated form enables the fertiliser and/or soil improver composition according to the present invention to be provided as a concentrate, or be diluted to provide a desired level/concentration of the nutrient(s) present, and/or a desired level/concentration of the eutectic solvent components present.
- additional nutrient element(s), if required, may be conveniently added to a fertiliser and/or soil improver composition according to the present invention.
- the fertiliser and/or soil improver composition according to the present invention may be applied alone, or together with or subsequent to another composition beneficial or relevant to plant growth.
- a fertiliser and/or soil improver composition according to the present invention may be applied to soil only to improve or condition the soil before planting, and/or applied at a frequency required after planting.
- a eutectic melt according to the present invention comprises deep eutectic solvents, with the melting point of the solvent mixture at a temperature significantly lower than the melting point of the individual eutectic solvent components, due to charge delocalisation through hydrogen bond formation.
- a fertiliser and/or soil improver composition comprising one or more organic sources of plant nutrient(s) (which may be one or more organic sources of nitrogen, or one or more organic nitrogen sources) prepared through deconstruction of one or more biological materials by a eutectic melt, as in any of the aspects of the present invention.
- a eutectic melt in any of the aspects of the present invention may comprise a quaternary ammonium salt (such as a choline salt) and a urea, thiourea, or a derivative thereof.
- a quaternary ammonium salt such as a choline salt
- Other deep eutectic solvents particularly those involving a choline salt, may also be used, for example, a choline salt-polyol eutectic system (such as choline chloride and glycerol), or a choline salt-organic acid eutectic system (such as choline chloride and malonic acid).
- a choline halide such as choline chloride or choline bromide
- a urea/urea derivative or thiourea/thiourea derivative based eutectic system is used in the present invention.
- a choline chloride-urea eutectic melt or system is used in the present invention.
- a eutectic melt according to the present invention may be used to deconstruct one or more biological materials to provide one or more organic sources of plant nutrient(s).
- organic source refers to an organic compound or molecule capable of providing/supplying one or more plant nutrients (as opposed to an inorganic nutrient source), or at least providing/supplying one or more of the major plant nutrients N, P and K.
- the organic source of plant nutrient(s) may be an organic source of nitrogen/organic nitrogen source, including one which provides/supplies predominantly nitrogen but may also provide/supply one or more of other plant nutrients.
- the one or more organic sources is in the form of one or more biomolecules.
- biomolecule refers to a molecule present in an organism and capable of contributing to a biological structure or process (e.g. signal transduction, cell division or formation etc.) in the organism.
- the one or more biomolecules may be selected from the group consisting of proteins, peptides, chitins, amino acids, nucleic acids, and combinations thereof.
- the one or more biomolecules is selected from the group consisting of proteins, peptides, protein or peptide fragments/fractions, amino acids, and combinations thereof, as the, or the predominant, organic source(s) of nitrogen.
- a eutectic melt is preferably used to deconstruct one or more biological materials to provide one or more organic sources of plant nutrient(s) in the form of one or more biomolecules.
- the one or more biological materials is selected from the group consisting of wool, hair, feathers, horns, hooves, nails, skins, claws, beaks, and combinations thereof.
- the one or more organic sources of plant nutrients is one or more organic nitrogen sources (but may also include other plant nutrient sources, e.g. organic phosphorus or potassium sources).
- the one or more biomolecules is selected from the group consisting of proteins, peptides, protein/peptide fragments/fractions, amino acids, and/or combinations thereof.
- the one or more biomolecules may be selected from the group consisting of at least one protein, fragments/fractions of the protein(s) including peptide and/or amino acid fragments/fractions of the protein(s), and combinations thereof.
- a eutectic melt according to the present invention is able to break down such materials, to provide one or more organic plant nutrient sources, such as one or more biomolecules selected from the group consisting of proteins, peptides, amino acids, and/or combinations thereof, which are at least capable of acting as one or more organic nitrogen sources.
- the one or more biomolecules may comprise (in addition to or in the absence of one or more proteins) peptides and/or amino acids, which may, or may not, be the peptide and/or amino acid fragments of the one or more proteins.
- the one or more biomolecules may have a molecular weight of less than 50 kilodaltons (kDa), preferably in the range of from 0 to 40 kDa, more preferably from 1 to 30 kDa, most preferably from 1 to 20 kDa.
- the one or more biomolecules may be or may comprise peptide and/or amino acid fragments of one or more proteins, with the peptide and/or amino acid fragments being in a molecular weight range of from 1 to 20, 1 to 10, 1 to 7, or more preferably from 1 to 5 kDa, e.g. 1, 2, 2.4, 3.5, 4, 5, 5.7, 7, 9.6 kDa.
- a fertiliser and/or soil improver composition for use in enhancing the growth of plants, the composition comprising one or more biomolecules in a molecular weight range of from 1 to 20 kDa in a eutectic melt, obtained through deconstruction of one or more biological materials by the eutectic melt, wherein the eutectic melt is urea and choline chloride.
- the one or more biological materials is/are selected from those described herein above, e.g. wool, hair and/or feather.
- the molecular weight of the one or more biomolecules is/are in a range of from 1 to 10, more preferably from 1 to 5 kDa.
- the eutectic melt is at a molar ratio in a range as described hereinabove, e.g. at a ratio of urea:choline chloride of 7.5:1.
- the deconstruction is at a temperature in a range as described hereinabove.
- a preferred form of protein present in the one or more biological materials according to the present invention is keratin. Keratin is a fibrous structural protein naturally occurring in epithelial cells. There are two varieties of keratin fibres, being a-keratins found in hair and wool etc. and P-keratins, which are harder and are found in such material as nails and beaks. Being a protein, keratin comprises nitrogen from the amino acids which form its structure. The activity of nitrogen on plant growth is well known.
- compositions comprising the keratin protein and/or its fragments/fractions, including that obtained from wool extracts, possess marked biological stimulant activity and have consequently proved effective as an organic nitrogen source and hence a fertiliser and/or soil improver, or an additive to a fertiliser and/or soil improver, for enhanced plant growth.
- a eutectic melt as in any of the aspects of the present invention is able to deconstruct one or more biological materials comprising keratin, or a significant portion of keratin, as a structural protein.
- the one or more biological materials may be selected from the group consisting of wool, hair, feathers, horns, hooves, nails, skins, claws, beaks, and combinations thereof. These biological materials may originate from a human and/or non-human animal source. It is known that these biological materials comprise keratin only, or a significant portion of keratin, in the structural makeup of the material.
- a fertiliser and/or soil improver composition comprising a protein, and/or one or more peptide and/or amino acid fragments thereof, in a eutectic melt.
- a fertiliser and/or soil improver composition according to the first or third aspect of the present invention comprises protein fragments, e.g.
- the eutectic melt comprises a HBD:HBA molar ratio in a range of from about 7.5 to about 4:1, e.g. with a HBD:HBA molar ratio of 7.5:1, 6.0:1, 5.2:1, or 4.1:1.
- the HBD is preferably a urea, thiourea or a derivative of these, more preferably the HBD is urea.
- the HBA is preferably a choline salt, e.g. choline chloride.
- the deconstruction of the one or more biological materials using the eutectic melt according to the present invention is in a temperature range of about: 135 - 170°C, preferably 140 - 165°C, more preferably 145 - 160°C, most preferably 145 - 155 °C.
- wool from sheep is deconstructed to obtain the keratin protein, keratin peptide fragments, and/or amino acids of keratin protein and/or keratin peptides, available for uptake by plants, thereby providing one or more organic nitrogen source to plants.
- This wool extract has demonstrated fertiliser and/or soil improver activity itself or as an additive to fertiliser and/or soil improver.
- wool from other animals e.g. Alpaca, Llama, goats or rabbits
- wool from other animals e.g. Alpaca, Llama, goats or rabbits
- a method of preparing a fertiliser and/or soil improver composition comprising one or more organic sources of nitrogen, the method comprising the steps of: a) forming a eutectic melt of urea and choline chloride; and b) deconstructing one or more biological materials using the eutectic melt, to provide a eutectic melt or mixture comprising the one or more organic sources of nitrogen.
- step a) comprises forming a eutectic melt of urea and choline chloride at a molar ratio (of urea:choline chloride) in a range of from about 7.5:1 to 4:1 (e.g. 7:1, 6.5:1, 5.4:1 or 4:1).
- step b) comprises deconstructing the one more biological materials at a temperature in a range of about: 135 - 170°C, preferably 140 - 165°C, more preferably about 145 - 160°C, most preferably 145 - 155 °C.
- the one or more biological materials in step b) is wool.
- step b) provides a eutectic mixture comprising keratin peptides and/or amino acids in the molecular weight range of from 1 to 20 kDa, preferably 1 to 15 kDa, more preferably 1 to 10 kDa, most preferably 1 to 5 kDa.
- the embodiment of the method according to the second step of the present invention may further comprise one or more steps selected from diluting the eutectic mixture with water, adjusting the pH of the eutectic mixture with an acid or base, and combinations thereof.
- the eutectic mixture in step b) of the method according to the second aspect of the present invention is a wool extract comprising keratin peptides and/or amino acids in a eutectic melt (or solvent mix) comprising or formed of urea and choline chloride.
- the wool extract is obtained by the deconstruction of wool using the eutectic melt, and is preferably prepared from the solvent and deconstruction conditions described hereinabove.
- the keratin peptides and/or amino acids are preferably in a molecular weight range of from 1 to 10 kDa, or from 1 to 5 kDa, e.g. 1, 1.5, 2, 2.4, 3, 4, 4.7 and/or 5 kDa).
- the wool extract prepared according to the second aspect of the present invention may be stored as a concentrate, or diluted (with or without pH adjustment) and used directly as a fertiliser and/or soil improver composition.
- a fertiliser and/or soil improver composition in the form of a wool extract comprising one or more organic sources of nitrogen dissolved in a eutectic melt, the one or more organic sources of nitrogen obtained through deconstruction of one or more biological materials by the eutectic melt.
- the one or more biological materials is preferably wool from one or more animals selected from the group consisting of sheep, Alpaca, Llama, goats, rabbits and combinations thereof.
- the wool is sheep wool.
- the eutectic melt is preferably urea and choline chloride.
- the one or more organic sources of nitrogen, or the one or more biomolecules is/are preferably keratin peptides and/or amino acids in a molecular weight range of from 1 to 10 kDA (e.g. 1, 3, 4.5, 6, 7.8 or 9 kDa), more preferably from 1 to 5 kDA (e.g. 1, 1.5, 2, 2.4, 3,
- the eutectic melt is preferably at a molar ratio (of urea:choline chloride) in the range of from about 7.5:1 (e.g. 7:1, 6.5:1, 5.4:1 or 4:1).
- the deconstruction of the one or more biological materials is preferably at a temperature in a range of about: 135 - 170°C, preferably 140 - 165°C, more preferably about 145 - 160°C, most preferably 145 - 155 °C, e.g. 137, 145, 147.2, 150, 152, 155,
- wool in deconstructing wool, the present inventors found that, with the eutectic melt (or eutectic melt deconstruction) of the present invention, wool may be used as is, i.e. uncleaned and/or with wool fat present.
- the preparation of an eutectic melt comprises fabrication of keratin through deconstruction of sheep’s wool using a benign choline chloride-urea deep eutectic solvent melt.
- the eutectic melt may be formulated by mixing choline chloride and urea at a molar ratio of between about 20:1 and 1:20, preferably at a molar ratio of choline chloride to urea of about 4: 1 to about 7.5:1, while heating for a number of minutes, or for hours (depending on the scale of production).
- Wool is then dissolved in the eutectic melt at a weight to volume ratio of between about 1 g:l ml and about 1 g:100 ml (preferably between about lg:lml and about lg:25ml, more preferably between about lg:lml and about lg:15ml, or even between about lg:lm and about lg:10ml, e.g. about lg:9ml, lg:8ml or lg:6.5ml) using heat.
- the heating step of the above process would be understood by the skilled person to cause conversion of at least some of the urea content to ammonia.
- the resultant ammonia gas escapes to the atmosphere, thereby reducing the nitrogen content of the mixture.
- a pungent smell is also observable, due to the presence of this ammonia.
- the following examples utilise the ‘urea + choline chloride’ solvent mix and sheep’s wool to illustrate a eutectic melt according to the present invention, its preparation, the deconstruction of a biological material through a eutectic melt and effectiveness of the resultant fertiliser/soil improver composition according to the present invention.
- Example I Temperature effect on the eutectic melt and/or deconstruction of wool
- a eutectic melt is prepared by heating urea (20 g, 0.33 mol) and choline chloride (23.2 g, 0.17 mol) at 70 °C until a clear solution was formed. For each temperature study, the eutectic melt is then further heated until 110 °C, 140 °C, 170 °C and 200 °C. When the desired temperature is reached, unwashed/uncleaned wool (1g) was added portion-wise to the eutectic melt over a 2-minute period. The resulting mixture was then continued to be heated at the desired temperature (110 °C, 140 °C, 170 °C, or 200 °C) with stirring, preferably until the wool is fully dissolved.
- the mixture was then cooled to room temperature, diluted with water (15 ml), stirred for 5 to 30 minutes, then filtered or centrifuged to afford a clear solution comprising the deconstructed/solubilized wool, in the form of keratin protein and fragments/fractions thereof (with the clear solution being a fertiliser and/or soil improver composition in accordance with the first or third aspect of the present invention). Any undissolved wool present is dried and weighted.
- the filtered solution, or supernatant solution was kept at room temperature for several weeks to observe for storage stability of the solution (e.g. whether there was precipitate formation).
- the NMR analysis indicates the formation of multiple decomposition products of urea at 200 °C, including biuret, triuret, ammelide and cyanuric acid, some of which may have formed within the temperature range of 170 °C - 200 °C.
- a temperature range of 140 °C - 170 °C may be used for the eutectic deconstruction of the wool.
- eutectic deconstruction at 140 °C of 1 g of wool still required a timeframe of approximately 2 hours, which would not be commercially appropriate or economically viable for scaled-up productions.
- the wool appeared to be fully dissolved after heating at this temperature for 15 minutes; however, the energy input for heating the eutectic melt up to 170 °C would not be economical/viable for commercial scale productions.
- a temperature for the eutectic deconstruction of a biological material containing keratin protein is preferably in the range of approximately 145 - 165 °C, more preferably approximately 145 - 160 °C, e.g. 145 - 155 °C.
- a eutectic melt can also be achieved at a HBD:HBA molar ratio higher than 2:1.
- the present inventors surprisingly found that even at a HBD:HBA molar ratio in a range of from about 7.5:1 to about 4:1, a eutectic melt is still achievable. This was unexpected and would be commercially advantageous, as a significantly less amount of choline chloride, which is considerably more expensive than urea, may be used for the eutectic deconstruction.
- a significant proportion, or even the bulk of the eutectic solvents remains in a solid form even when heated at approximately 100 °C for 30 minutes, thus a molar ratio range of urea:choline chloride which presents a significant commercial advantage and yet is able to achieve a eutectic melt to ensure proper mixing, wetting and dissolution of the biological material(s) is from about 7.5:1 to about 4:1.
- Example III Preparation of a preferred embodiment of a fertiliser and/or soil improver composition according to the present invention
- a fertiliser and/or soil composition according to the present invention is prepared by a method including at least the steps of: a) forming a eutectic melt; and b) deconstructing one or more biological materials selected from the group consisting of wool, hair, feathers, horns, hooves, nails, skins, claws, beaks, and combinations thereof using the eutectic melt, to obtain one or more organic nitrogen sources.
- Step a) may include heating deep eutectic solvents until a eutectic melt is formed.
- the eutectic solvents preferably comprise a HBA selected from a choline salt (e.g. choline chloride, choline bromide or choline acetate) and a HBD selected urea, a urea derivative, thiourea, a thiourea derivative, and combinations thereof.
- a HBA selected from a choline salt (e.g. choline chloride, choline bromide or choline acetate) and a HBD selected urea, a urea derivative, thiourea, a thiourea derivative, and combinations thereof.
- the HBD:HBA molar ratio of the eutectic solvents may be in a ratio of about 10:1 to about 1:10, but preferably in a ratio of from about 8:1 to about 3:1, or from about 7.5:1 to about 4:1.
- the deconstruction is preferably at a temperature in a range of approximately 145 - 165 °C, or in a range of approximately 145 - 160 °C (e.g. 147 °C, 150 °C, 156°C or 160 °C).
- the organic nitrogen sources is preferably a keratin protein, or fragments thereof (such as peptide fragments, but there may also be amino acid fragments).
- the preparation method may comprise a step of diluting a eutectic melt mixture comprising the one or more organic nitrogen sources, e.g. with water, or a liquid comprising one or more plant nutrients (such as a nutrient solution or an existing fertiliser solution in absence of nitrogen, or needing additional nitrogen).
- a eutectic melt mixture comprising the one or more organic nitrogen sources, e.g. with water, or a liquid comprising one or more plant nutrients (such as a nutrient solution or an existing fertiliser solution in absence of nitrogen, or needing additional nitrogen).
- the preparation method may also comprise a step of adjusting the pH of the fertiliser and/or soil improver composition prepared to a desired pH range, for example, pH 5.4 - 7.5, or more preferably pH 5.5 - 7 (e.g. pH 5.8, 6.2, 6.5 or 7).
- a natural organic acid is used for the pH adjustment.
- Exemplary acids include oxalic, malonic, succinic, tartaric and citric acid.
- the dilution and pH adjustment steps can either be steps c) and d), or d) and c), i.e. the order of the steps may change, and there may also be additional, or alternating, dilution and/or pH adjustment steps.
- the present inventors found that, with the fertiliser and/or soil improver composition preparation method of the present invention, a biological material such as wool can be used as is in an uncleaned state, without the need to remove the wool fat (or a fat layer) first. This was both unexpected and has a clear commercial advantage of reducing the preparation of the one or more biological materials before the eutectic deconstruction.
- Example IV Molecular weight/fragmentation characterization of the one or more biological molecules in a fertiliser and/or soil improver composition according to the present invention
- Molecular weight/fragmentation analysis is performed on a fertiliser and/or soil improver composition (nV-1) prepared using a method exemplified in Example III, with a sheep wool material being deconstructed using a eutectic melt comprising urea:choline chloride at a ratio in the range of from about 7.5:1 to about 4:1, and with the temperature for the deconstruction of wool being in a range of approximately 145 - 165 °C (or more specifically approximately 145 - 160 °C).
- nV-1 Sodium dodecyl-sulfate polyacrylamide gel electrophoresis
- 1 mF of composition nV-1 was desalted by diafiltration using an Amicon Ultra-0.5 mL 3-kDa Centrifugal Filter (Merck- Millipore) following the manufacturer’s instruction.
- the desalted sample was mixed either with an equal volume of non-reducing SDS-PAGE loading buffer or with an equal volume of reducing buffer (containing 30 mM DTT and 3 mM EDTA).
- composition nV- 1 contains far less than expected keratin proteins in the ⁇ 10 to 150 kDa range from the deconstruction of wool. This is completely unexpected, given that the temperature of deconstruction was lower than 160 °C.
- nV-1 a small sample of nV-1 was desalted and analysed by a MALDI mass spectrometer.
- a fertiliser and/or soil improver composition according to the invention was tested on potted Grosse Lisse tomatoes to evaluate plant growth.
- Treatments applied were Verigrow-1: choline chloride (2 moles) + urea (1 mole), without heating; Verigrow-2: choline chloride (2 moles) + urea (1 mole), with heating; and Verigrow- 3: choline chloride (2 moles) + urea (1 mole) + wool, with heating (to fully dissolve the wool at a temperature that may be in the range of 170 - 200 °C); each prepared as 1:10 dilutions with water and at 5.4, 10.8 and 21.6 mL/plant (pot); as well as a commercially available seaweed plant treatment (Seasol®) at 141.3 mL/plant.
- Veasol® seaweed plant treatment
- Verigrow refers to the 3 test samples (Verigrow -1, Verigrow -2 and Verigrow-3) for this study. Also for this study, Verigrow-3 was at a weight to volume ratio of the wool to eutectic melt in the range of about lg: l ml to about lg:50ml.
- Table 2 Treatments (Verigrow compositions: 150 mL/1.5 L of water; seaweed treatments: 6.67 mL/2 L of water).
- Plant height, biomass, normalised difference vegetation index (NDVI) and weights (root and foliage) were measured and all factors were significantly increased by all three Verigrow compositions, with a significant dose response to increasing rates of all Verigrow compositions.
- Double applications of Verigrow compositions provided greater increases in plant height, biomass, NDVI and weights (root and foliage) than single applications.
- Single and double applications of the seaweed plant treatment were not significantly different to the untreated control in plant height, biomass, NDVI or weights (root and foliage).
- a fertiliser and/or soil improver composition (nV-2) is prepared using a method exemplified in Example III, with a sheep wool material (uncleaned and/or containing the fat layer) being deconstructed using a eutectic melt comprising urea:choline chloride at a ratio in the range of from about 7.5:1 to about 4:1 as described herein above, and with the temperature for the deconstruction of wool being in a range of approximately 145 - 165 °C (or more specifically approximately 145 - 160 °C).
- the composition (nV-2) was also prepared at a weight to volume ratio of the wool to eutectic melt in the range of from about lg:lml to about lg:25 ml.
- the resultant fertiliser and/or soil improver composition (nV-2) comprises 35% (w/v) of total N (nitrogen) and has pH in the range of pH 5.5 - 6.5.
- the composition nV-2 was mixed with water (as a carrier) in a ratio of approximately 52 L water to approximately 48 L of nV-2.
- the field wheat trial was established as a randomised complete block of 5 treatments and 4 replicates in a single bank with each plot 12 meter long by 2 meter wide.
- the effectiveness of the fertiliser and/or soil improver composition nV-2 according to the present invention on plant growth (wheat in this instance) and/or as an organic nitrogen nutrient source, is compared with a commercial inorganic fertiliser (Flexi-N, which is a commercially available fertiliser distributed by the Australian Company CSBP and contains three forms of N - urea, ammonium and nitrate, with a total N concentration of 42%), and with Urea alone (at 46% total N).
- Flexi-N which is a commercially available fertiliser distributed by the Australian Company CSBP and contains three forms of N - urea, ammonium and nitrate, with a total N concentration of 42%), and with Urea alone (at 46% total N).
- Treatments containing 17 units of N were applied either as nV-2 at 35% (w/v) N, Flexi-N at 42% (w/v) N or Urea at 46% (w/v) N.
- the nV-2 and Flexi-N treatments were liquid banded in-furrow at seeding whilst Urea treatment was top-dressed and incorporated by sowing. All plots were sown to Sceptre wheat at a rate of 91 kg/ha to a depth of 2.5 cm.
- At 43 days after sowing there was a second application of the Flexi-N and Urea treatments providing a further 42 units of N each, to the plots of these treatments.
- nV-2 fertiliser and/or soil improver composition is superior in performance compared to the commercial inorganic nitrogen fertiliser Flexi-N and to Urea.
- 17 units of N applied as nV -2 (35% N) infurrow at seeding was equal to or even better than 59 units of N supplied by Flexi- N (42% N) or Urea (46% N) on the growth, yield and grain quality of Scepter wheat.
- the results show that per unit of N, the nV-2 fertiliser and/or soil improver composition according to the present invention had a net crop yield that was ⁇ 4.5 times higher than that of Flexi-N and Urea.
- the composition according to the present invention may still be more effective than, or at least similarly effective to, a commercial, inorganic and/or urea nitrogen fertiliser.
- a further wheat field trial is conducted using a fertiliser and/or soil improver composition nV-3 in accordance with the present invention, which is prepared in a same or similar manner, and has same/similar chemical properties to nV-1 and nV-2, except with the nv-3 fertiliser being diluted to provide nV-3 (27% N).
- nv-3 (27% N) fertiliser in accordance with the present invention was administered via liquid banding in furrow at seeding, and spray application via hand boom at 6 weeks after sowing.
- Example VI comparisons were made with trial plots applied with the commonly used nitrogen fertilisers Flexi-N and Urea.
- nv-3 (27% N) fertiliser has shown similar or better results to Flexi-N and Urea.
- nv-3 (27% N) applied at 13 units of N at seeding and 32 units of N 6 weeks after sowing is an optimal product equivalent to urea at 17 units of N at seeding and 42 units of N 6 weeks after sowing.
- a fertiliser and/or soil improver composition according to the present invention is compatible with chemicals commonly used in agricultural industry, including the herbicides (e.g. Velocity, MPCA 750, Ester 680, Tenet 500 SC etcetera), fungicides (e.g. Uplift, Prosaro, Impact, Oritus 430 and Soprano 500 etcetera), insecticides (e.g. Lemat, Bifenthrin 240, Dimethoate etcetera) and Adjuvants (e.g. SE14 and Adigor etcetera).
- herbicides e.g. Velocity, MPCA 750, Ester 680, Tenet 500 SC etcetera
- fungicides e.g. Uplift, Prosaro, Impact, Oritus 430 and Soprano 500 etcetera
- insecticides e.g. Lemat, Bifenthrin 240, Dimethoate etcetera
- Adjuvants e.g
- a fertiliser and/or soil improver composition according to the present invention may be applied simultaneously with, or subsequently to, one or more commonly used agricultural chemicals without the concern of chemical instability or incompatibility leading to precipitation occurring and/or loss of effectiveness of the composition of the present invention and/or the one or more agricultural chemical(s).
- organic nitrogen is available to plants in the form of protein or as amino acids.
- the effect of treating wool, as exemplified in the present invention using a eutectic melt according to the present invention means that the resulting keratin protein, and fragments/fractions thereof (such as peptides and amino acids), are bioavailable, or even surprisingly highly bioavailable, as an organic nitrogen source.
- the nitrogen can be accessed by plants through root uptake in the form of the protein itself via endocytosis, or as simpler amino acids resulting from enzymatic digestion (either by the proteolytic activity of the roots or from microbes present in the soil).
- the present invention has been found to possess a myriad of advantages over inorganic nitrogen sources, including a longer durability. Further, protein, or fragments/fractions thereof (such as peptides and/or amino acids), as one or more nitrogen sources results in an increase in a plant’s ability to develop a more extensive root network. It is understood that the keratin protein, or fragments/fractions thereof, available from the present composition through the deconstruction of wool, is bioavailable, or even highly bioavailable, as an organic nitrogen source available to plants. The present invention additionally provides the advantages of being an avenue for reducing or eliminating wool waste and also serving as an additional income stream for wool producers. Since other biomaterials such as those mentioned earlier (e.g.
- feathers, hair, hooves etc. all comprise keratin or predominantly keratin as a structural protein
- an eutectic melt according to the present invention is at least able to be used to deconstruct such biomaterials, thus turning further waste materials into income streams and environmentally friendly and effective organic sources of plant nutrients.
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- Engineering & Computer Science (AREA)
- Environmental & Geological Engineering (AREA)
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- General Life Sciences & Earth Sciences (AREA)
- Soil Sciences (AREA)
- Materials Engineering (AREA)
- Fertilizers (AREA)
Abstract
La présente invention concerne une composition d'engrais et/ou d'amélioration du sol destinée à être utilisée pour améliorer la croissance de plantes, la composition comprenant une ou plusieurs sources organiques d'un ou de plusieurs nutriments végétaux, obtenues par la déconstruction d'un ou de plusieurs matériaux biologiques par une masse fondue eutectique. La présente invention concerne également un procédé de préparation d'une composition d'engrais et/ou d'amélioration du sol selon la présente invention, et un procédé d'amélioration de la croissance de plantes à l'aide d'une composition d'engrais et/ou d'amélioration du sol selon la présente invention.
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NZ788293A NZ788293A (en) | 2022-05-16 | Fertiliser and/or soil improver composition, method of preparation and method of use |
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WO2013078517A1 (fr) * | 2011-12-02 | 2013-06-06 | The University Of Western Australia | Procédés d'isolement de constituants d'une coquille ou d'une perle recouverte de nacre |
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WO2021180996A1 (fr) * | 2020-03-12 | 2021-09-16 | Consejo Superior De Investigaciones Científicas (Csic) | Procédé d'obtention d'un extrait phénolique provenant de grignons d'olives humides ("alpeorujo") |
WO2022036010A1 (fr) * | 2020-08-11 | 2022-02-17 | Cellacure Llc | Procédé de raffinage de déchets biologiques en boucle fermée écologique pour la production d'extraits actifs intelligents et systèmes de distribution pour leur application |
US20220281779A1 (en) * | 2016-09-01 | 2022-09-08 | Veratin Pty Ltd | Fertiliser and/or Soil Improver Composition, Method of Preparation and Method of Use |
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