NZ734615B2 - Solutions for enhancing the effectiveness of insecticides and fungicides on living plants and related methods - Google Patents
Solutions for enhancing the effectiveness of insecticides and fungicides on living plants and related methods Download PDFInfo
- Publication number
- NZ734615B2 NZ734615B2 NZ734615A NZ73461515A NZ734615B2 NZ 734615 B2 NZ734615 B2 NZ 734615B2 NZ 734615 A NZ734615 A NZ 734615A NZ 73461515 A NZ73461515 A NZ 73461515A NZ 734615 B2 NZ734615 B2 NZ 734615B2
- Authority
- NZ
- New Zealand
- Prior art keywords
- amine oxide
- solution
- amount
- carbon length
- buffered
- Prior art date
Links
- 230000000749 insecticidal Effects 0.000 title abstract description 31
- 239000002917 insecticide Substances 0.000 title abstract description 31
- 239000000417 fungicide Substances 0.000 title abstract description 19
- 230000000855 fungicidal Effects 0.000 title abstract description 18
- 230000002708 enhancing Effects 0.000 title description 7
- 150000001412 amines Chemical class 0.000 claims abstract description 86
- OKTJSMMVPCPJKN-UHFFFAOYSA-N carbon Chemical compound [C] OKTJSMMVPCPJKN-UHFFFAOYSA-N 0.000 claims abstract description 23
- 229910052799 carbon Inorganic materials 0.000 claims abstract description 23
- 239000007853 buffer solution Substances 0.000 claims abstract description 14
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 claims abstract description 11
- TYJJADVDDVDEDZ-UHFFFAOYSA-M Potassium bicarbonate Chemical compound [K+].OC([O-])=O TYJJADVDDVDEDZ-UHFFFAOYSA-M 0.000 claims abstract description 7
- 239000011736 potassium bicarbonate Substances 0.000 claims abstract description 7
- 229910000028 potassium bicarbonate Inorganic materials 0.000 claims abstract description 7
- 229940094025 potassium bicarbonate Drugs 0.000 claims abstract description 7
- 235000015497 potassium bicarbonate Nutrition 0.000 claims abstract description 7
- 239000000463 material Substances 0.000 claims abstract description 4
- 239000000243 solution Substances 0.000 claims abstract 20
- RLLPVAHGXHCWKJ-HKUYNNGSSA-N (3-phenoxyphenyl)methyl (1R,3R)-3-(2,2-dichloroethenyl)-2,2-dimethylcyclopropane-1-carboxylate Chemical compound CC1(C)[C@@H](C=C(Cl)Cl)[C@H]1C(=O)OCC1=CC=CC(OC=2C=CC=CC=2)=C1 RLLPVAHGXHCWKJ-HKUYNNGSSA-N 0.000 claims abstract 7
- 229960000490 Permethrin Drugs 0.000 claims abstract 7
- STJLVHWMYQXCPB-UHFFFAOYSA-N Propiconazole Chemical compound O1C(CCC)COC1(C=1C(=CC(Cl)=CC=1)Cl)CN1N=CN=C1 STJLVHWMYQXCPB-UHFFFAOYSA-N 0.000 claims abstract 6
- 239000005822 Propiconazole Substances 0.000 claims abstract 6
- 229910000396 dipotassium phosphate Inorganic materials 0.000 claims abstract 6
- 235000019797 dipotassium phosphate Nutrition 0.000 claims abstract 6
- 229910000402 monopotassium phosphate Inorganic materials 0.000 claims abstract 6
- 235000019796 monopotassium phosphate Nutrition 0.000 claims abstract 6
- BWHMMNNQKKPAPP-UHFFFAOYSA-L potassium carbonate Chemical compound [K+].[K+].[O-]C([O-])=O BWHMMNNQKKPAPP-UHFFFAOYSA-L 0.000 claims abstract 5
- 241000233866 Fungi Species 0.000 claims description 18
- 239000000203 mixture Substances 0.000 claims description 11
- 241000238631 Hexapoda Species 0.000 claims description 9
- ZLMJMSJWJFRBEC-UHFFFAOYSA-N potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 claims description 2
- 229910052700 potassium Inorganic materials 0.000 claims description 2
- 239000011591 potassium Substances 0.000 claims description 2
- 229940035295 Ting Drugs 0.000 claims 3
- 229940048866 LAURAMINE OXIDE Drugs 0.000 abstract 2
- SYELZBGXAIXKHU-UHFFFAOYSA-N Lauryldimethylamine oxide Chemical compound CCCCCCCCCCCC[N+](C)(C)[O-] SYELZBGXAIXKHU-UHFFFAOYSA-N 0.000 abstract 2
- 241000196324 Embryophyta Species 0.000 description 13
- UIIMBOGNXHQVGW-UHFFFAOYSA-M buffer Substances [Na+].OC([O-])=O UIIMBOGNXHQVGW-UHFFFAOYSA-M 0.000 description 13
- 235000021170 buffet Nutrition 0.000 description 9
- 238000010186 staining Methods 0.000 description 7
- NBIIXXVUZAFLBC-UHFFFAOYSA-K [O-]P([O-])([O-])=O Chemical compound [O-]P([O-])([O-])=O NBIIXXVUZAFLBC-UHFFFAOYSA-K 0.000 description 6
- 239000002253 acid Substances 0.000 description 6
- 239000010452 phosphate Substances 0.000 description 6
- 241000721703 Lymantria dispar Species 0.000 description 5
- 235000014121 butter Nutrition 0.000 description 5
- 229950008597 drug INN Drugs 0.000 description 5
- 230000002195 synergetic Effects 0.000 description 5
- 241001275954 Cortinarius caperatus Species 0.000 description 4
- LWIHDJKSTIGBAC-UHFFFAOYSA-K Tripotassium phosphate Chemical compound [K+].[K+].[K+].[O-]P([O-])([O-])=O LWIHDJKSTIGBAC-UHFFFAOYSA-K 0.000 description 4
- 230000002401 inhibitory effect Effects 0.000 description 4
- 230000002378 acidificating Effects 0.000 description 3
- 239000003153 chemical reaction reagent Substances 0.000 description 3
- 239000003063 flame retardant Substances 0.000 description 3
- 230000002335 preservative Effects 0.000 description 3
- 239000003755 preservative agent Substances 0.000 description 3
- 239000002023 wood Substances 0.000 description 3
- 200000000019 wound Diseases 0.000 description 3
- 241000272517 Anseriformes Species 0.000 description 2
- 240000007216 Quercus alba Species 0.000 description 2
- 235000009137 Quercus alba Nutrition 0.000 description 2
- 241000607479 Yersinia pestis Species 0.000 description 2
- RTZKZFJDLAIYFH-UHFFFAOYSA-N diethyl ether Chemical compound CCOCC RTZKZFJDLAIYFH-UHFFFAOYSA-N 0.000 description 2
- 238000002474 experimental method Methods 0.000 description 2
- 239000008363 phosphate buffer Substances 0.000 description 2
- 229910000160 potassium phosphate Inorganic materials 0.000 description 2
- 239000007921 spray Substances 0.000 description 2
- 235000019798 tripotassium phosphate Nutrition 0.000 description 2
- UHIWBQIWXWWDKT-MRVPVSSYSA-N (4S)-4-hydroxy-2-(3-methoxypropyl)-1,1-dioxo-3,4-dihydrothieno[3,2-e]thiazine-6-sulfonamide Chemical compound O=S1(=O)N(CCCOC)C[C@@H](O)C2=C1SC(S(N)(=O)=O)=C2 UHIWBQIWXWWDKT-MRVPVSSYSA-N 0.000 description 1
- 210000003165 Abomasum Anatomy 0.000 description 1
- 241000486679 Antitype Species 0.000 description 1
- BVKZGUZCCUSVTD-UHFFFAOYSA-L Carbonate dianion Chemical compound [O-]C([O-])=O BVKZGUZCCUSVTD-UHFFFAOYSA-L 0.000 description 1
- 241000221866 Ceratocystis Species 0.000 description 1
- 240000007582 Corylus avellana Species 0.000 description 1
- 235000007466 Corylus avellana Nutrition 0.000 description 1
- ZPWVASYFFYYZEW-UHFFFAOYSA-L Dipotassium phosphate Chemical compound [K+].[K+].OP([O-])([O-])=O ZPWVASYFFYYZEW-UHFFFAOYSA-L 0.000 description 1
- 101700001948 F2R Proteins 0.000 description 1
- 101700019629 HMGA1 Proteins 0.000 description 1
- 240000005979 Hordeum vulgare Species 0.000 description 1
- 235000007340 Hordeum vulgare Nutrition 0.000 description 1
- 241000257303 Hymenoptera Species 0.000 description 1
- 241000256602 Isoptera Species 0.000 description 1
- 241001139947 Mida Species 0.000 description 1
- 101700067608 NPNT Proteins 0.000 description 1
- 210000003739 Neck Anatomy 0.000 description 1
- 206010039897 Sedation Diseases 0.000 description 1
- 210000000582 Semen Anatomy 0.000 description 1
- 240000003670 Sesamum indicum Species 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- QGZKDVFQNNGYKY-UHFFFAOYSA-O ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 description 1
- BWKOZPVPARTQIV-UHFFFAOYSA-N azanium;hydron;2-hydroxypropane-1,2,3-tricarboxylate Chemical compound [NH4+].OC(=O)CC(O)(C(O)=O)CC([O-])=O BWKOZPVPARTQIV-UHFFFAOYSA-N 0.000 description 1
- 239000011230 binding agent Substances 0.000 description 1
- ZOXJGFHDIHLPTG-UHFFFAOYSA-N boron Chemical compound [B] ZOXJGFHDIHLPTG-UHFFFAOYSA-N 0.000 description 1
- 229910052796 boron Inorganic materials 0.000 description 1
- 239000012267 brine Substances 0.000 description 1
- 239000006172 buffering agent Substances 0.000 description 1
- 239000003795 chemical substances by application Substances 0.000 description 1
- 239000002131 composite material Substances 0.000 description 1
- 230000001066 destructive Effects 0.000 description 1
- 235000013399 edible fruits Nutrition 0.000 description 1
- 230000000694 effects Effects 0.000 description 1
- 235000013305 food Nutrition 0.000 description 1
- 230000002538 fungal Effects 0.000 description 1
- 150000003278 haem Chemical class 0.000 description 1
- 230000002363 herbicidal Effects 0.000 description 1
- 239000004009 herbicide Substances 0.000 description 1
- 150000002500 ions Chemical class 0.000 description 1
- 101700035385 lili Proteins 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- CAZIRXWITRWNJE-UHFFFAOYSA-N oxido(phenyl)azanium Chemical compound O=[NH2]C1=CC=CC=C1 CAZIRXWITRWNJE-UHFFFAOYSA-N 0.000 description 1
- RZVAJINKPMORJF-UHFFFAOYSA-N p-acetaminophenol Chemical compound CC(=O)NC1=CC=C(O)C=C1 RZVAJINKPMORJF-UHFFFAOYSA-N 0.000 description 1
- 230000035515 penetration Effects 0.000 description 1
- 229920000136 polysorbate Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 230000036280 sedation Effects 0.000 description 1
- 239000011780 sodium chloride Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 241000894007 species Species 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 235000013311 vegetables Nutrition 0.000 description 1
Abstract
The present invention relates to a solution for resisting destruction of living plants and a related method. Specifically the invention provides a solution for resisting destruction of living plants comprising: a buffered amine oxide administered admixed with at least one material selected from the group consisting of permethrin and propiconazole in water, the buffered amine oxide has a pH of 6.5 to 10.5 and is present in a concentration of 0.06% to 0.12% weight % and includes at least a 12 carbon length amine oxide (e.g. lauramine oxide), and said buffer system being selected from (a) potassium phosphate monobasic/potassium phosphate dibasic and (b) potassium bicarbonate/potassium carbonate. The solution provides a synergistically effective greater resistance to living plant deterioration than any of the individual buffered amine oxide, insecticides and fungicide achieve considered individually. group consisting of permethrin and propiconazole in water, the buffered amine oxide has a pH of 6.5 to 10.5 and is present in a concentration of 0.06% to 0.12% weight % and includes at least a 12 carbon length amine oxide (e.g. lauramine oxide), and said buffer system being selected from (a) potassium phosphate monobasic/potassium phosphate dibasic and (b) potassium bicarbonate/potassium carbonate. The solution provides a synergistically effective greater resistance to living plant deterioration than any of the individual buffered amine oxide, insecticides and fungicide achieve considered individually.
Description
SQLUTIQNS FOR ENHANCING THE £FE££11\E\£“S 0F
INSECT!CIDES AND FUNGICIDES ON IVJI'VING PLANTS
AND RELATEI} METHQE‘S
BACKGRCKJND ()1: iii-iii. i‘iON
Fieii‘i of'the invention
{sea}; The present invention witness to an. imprm'eti soiutien for enhancing pmtectien of
iii-ring talents through synergistic effects between buffered amine exides and
insecticides and fungicides and related methods.
2. Desoi'iptrimi of the Prior Art
{@0021 Fungi, insects and other pests cause- significant ic ‘iosses in fond crop
production as weii as iosses in forestry; tree animations, pastures flowers and
ether agrieuitntai products. in sdditinn, flingieide and insecticides have been
emnloyeti in a wide variety of locations anti types nfnses to inhibit piant
desttfnetion due to i’nngns anti insect pests. Prohienis created by insects and fungi,
have long existed in many environments incinding, but not iimiied to agrienitnre,
parks, geifeonrses, residentiai ments, highways, vegetable s,
ad necks, recreational faciiities, flomi gardens, ferests, pastures, waterways
and in many other emirrnnnents. ‘i‘his can interfere with desired funetionaiity, the
iieaith of piants, as weii as the aesthetics nf an area sustaining tion.
{sane} it has been known to use a wine variety (2F i'nateriais to t ii'K-"i¥3g piants from
insects and fungi, A wide vari ety of insecticides anti ides inn-e been
employed in order to enhance the lieaith of iiving piants and resist attack thereon
by insects, fungi and other destructive organisms.
geese} it has been known to introduce ’woed atixes inn) inmost in. order to resist
deterioration ofthe same.
genes; Ward, US Patent 7,896,960 diseioses a method. and on for providing
ei'nianeed penetration of wood preservatives into wood to a greater depth. through.
synergism between a buffering agent and an amine oxide. it. piates the use
oi‘vetiens types efwooti preservatives on wand which has been severed from a
fitting tree. Green finnibe'r is also said tn be n‘estahie by the 3353118311.
recast This patent, which reistes to weed as guished from iiving plants does
ineinde within the definition of woes preservatives, a number of eliemieai
cempennds including specific reference to fimgicidai, ieidai, water resistant,
termite teeistant material‘s.
{ann7i US. Patent 6,8i 3,733 is ed toward a fire—retardant weed—based cenrnnsite
created by treating a green wand furnish with a phasphatex’hnrnte fire—retardant
ni. The fireuretardant treated green weed h is hiended with a. binder
and then. bound by nppiying re to form. a nen—ieaehing fire retardant weed
based composite.
{finest Waiker, US. Patent 655732,?88 dinnieees the use nf amine exides as wood
prenervntiven. it states that the amine oxides inhibit. mim‘nbiai gmwth in. wan-(i.
This patent relates to weed which has been severed from granting trees and
diseinsen the use ni‘ wen-d premix-retires which are said in inhibit destruetive
nrganisms such as fungi and sapstaim for exampie. it is ed toward
preserving structural integrity ei‘ weed after the tree has been ltilied and reeinting
destruction ni‘tiie resuitant inmher as the grime tiire.
{it-{mil 13 Tseng, US Patent {5,503,869 discinses the tree et‘nmine nxidee to enhance the
perfennanee at” heron eempnnnds an weed preseri-etiven. There is mentinn of the
amine Oxides improx-Iing the effectiveness of boron emnpounds as insecticides or
iiincvides and piant growth regniatihg agents. They are nine said tn prm-ide better
dispersi 0,1} Ofb-Oi‘Ofl epmpounds when appiied to piants and fungi. it 3130 makes
reference to the seeds; of’piants and the area. on which the pients or Fungi grow.
{fiflldi 'ii‘here remains., therefore. a very real and substantial need for an imprnved system
fer radiating attacks nn and dentruetinn ni‘ fining plants: by insects and fungi.
Sijs'i‘tii‘viAIR‘i’ OF THE INVENYEQN
infill} The t inventinn tn‘m-‘iden a. en and inethnd et‘nhtnining synergistic
aetien betttteen a iimgieide and a buffered amine nxide andfnr an insecticide and a
ed amine oxide in girder to provide enhanced resistance of a iiving piant to
undesired deterioration due tn fungi and inseets.
{3012i "the snlntion and reinted methnd prey-ides fer greater ’piant pretender} than would
he. nineined titrntigh use ni’the iiuigieide alone in the insecticide ainne.
{ants} it: is an nhj eet (if the present in t-"tfitliimi to. pint-tide effective ecnnnmieni means for
enhancing the peribmianee of insecticides and ides en iiving plants.
{8014}; It is mettle: object of the present invention to preside at seintiee and reieted
method which wiii enhance the performance offitngieides and insecticides on
ng plants.
{001-3}; it is; engines object of the present: invention which through synergiso'i with a.
buffei‘efii amine exidef, es the pei‘iin‘manee of COB‘K-‘Bi‘i'iifli'lili insecticides and
t‘imgieides.
{@816}? it is yet. somber obj eat at tire present iiweiitiee te empioy a. synergistic
cambinatitm (if insecticides er fimgieidee with e buffeted émlillc eside s3stem tn
pmduee imprtwed insect and fitngi resistance while einnieying a smaller quantity
ofthe insecticide 0r timgieide.
{ii-{H 7]; ‘i‘iiese and other objects oi‘the ins ention wiii be more i‘t’iii'y understood from the
feiiowmg deseriptieii nf the invention.
PTEON 0F PREFERRED EM BOQEMENTS
{ems} As ed herein? the term flg giant“ is used in its ordinary sense? and is to
be dieiingniehed from both {it} plants whieh haste died and {b} products or items
which once were, but are no ionger iiving or part ofe living piant such as for
exampie, lumber. This defiititien wiil ineiude iiving piant food precincts such as
fruits or \='egetebies which have been returned frem a piant.
{3019i AS employed, herein: a “buffer system” is so aqueous soiution consisting et‘ a
mixture ef‘a weeds acid and its conjugate base car a. weak base with its conjugate
acid. A {miter system may aisle he ed by adding a week acidr‘conjugate base
at e t reek baseieenjugate eeid or by adding the weak acidfweak base and it sitting
fsn‘eng base in sufficient amount t0 form the eenjngate acidiemijngate base.
iii-e291 The preemt inven‘iii'n‘i invokes creating a synergistic. effect by appiying m the
eiani a snitttien which inciudee Ofeither an insecticide or a fungicide er bath
which will achieve a swergistieaiiy created improvement in the resnit through
combining the same with a. buffered amine oxide.
{3031i The amine oxides may be mixed with imft‘ers in a solvent to create a ed
amine oxide sniuiien and, then mixed with a herbicide seitition. The preferred
amine oxides are sefieo-ted fifnin the group censistiog of {e} the i2 carbon iength
amine oxides; even as that soid under the trade designetinn Ratios: 1.2 and {b} a
mixture oftiie 1‘3 and 3.8 Gerber} iengths soid under the trade desigiiatien ;
1318. The buffer system has the preteen}? that the pH (if the on changes very
iittie when a email amount at a strong acid or strong base is added in it. Buffet
enintinns are enrpinyed as; a means of keeping phi at a nearby censtant value within
a wide range ef ni itting. in the present int-entieh, the butter system
heipe tn maintain a. su‘tistantiniiy mnetant pit-i when in contact with hittingicel
syetems, such as iii-ting pianist
[fifllfii The buh‘hr system enneepte‘ can be extended to pniyprotitt species in which em: or
mere preteens may he removed to fenn different buffet s: iei; phosphate
systems. Ameng the preihrred buffets ate ammonium sein’emntonia._
Deprottmetetl ineiih‘miiif; iilienmmnated Itsine, Pfilnstihate iliihtieie, htiiaesinm
Biearhnnat “-fT’Oi’dSSiUYi} Carbonate.
rates} Brine nrax, iuni Phosphate Dihtteici’Pnteesium Fheenhnte ’i'rihneie,
Ammonium Citrate Tribasie: and Pntassium Phennhete Monchesieit’etassium
ate Dihasie.
{8024} it wifil he appreciated that the hnffered amine oxides do not signii‘icentiy hitter the
pH of the insecticide or fungicide pmdncte but, rather, make the pH inneh iese
iiiireiy to change based on the buffer capacity efthe buffer vee
{9325i A series 0f tests were performed in the United States in order tn determine the
effectiveness 0ft"! snlution of the present int-“entinh emnhiniiig an insecticide with
a ed amine oxide and the etTfeetii-eness Ofa seiutien of the present. invention
eettthining a fungicide with ti buffeted amine oxide
{nezei XBLES i«3 describe respectively describe the buffer syeteme employed in the
North American. experiments repetted in TABIES it and 5 with TABLE 2
referring to the expetinientai method and ’I‘ABLE 4 showing a group of buffer
Systems phi and tettii inn strengthn
{$6271 TABLE i recites the emnpneitinn ei‘htti‘ier syetettis 3~-‘i'tht~1txwete used in the
studies. Buf "’et systems 3—4 were prepared. by dissniving the appropriate teztgents
intn tine iiter ot‘deinnixed water until a, hmnngennns seiution was obtained.
"i‘ABLE ti shews, in the ieft hand cohimn; the number assigned tr) a ular
buffer with minim} 3 wntaining the abhteviated name tn“ iiiii name {if the heifers.
‘fi‘he amount ofaeidic ni per titer and hasie ehemieai per liter appear in the
next two pairs nf shinning.
Table 1: Buffet System15 3, 4 Ctmiposition
Acidic Chemicai (per Basic Chemiee} (pet
Buffet Metem am;
Iii-€33 may}
i"Abbreviated Nettie) ‘
' Amount Nettie Amount Nettie
Potaesi um Phosphate
Potassium Potassium
Monobasic
Phosphate ate
Potassium Phosphate iDi'hasie
hiioi'iehasic Biliaeie
(Phosphate Buffer '1.)
Potassium Bicarbonate
ium_ ium_
Potassium Cai‘hmtete 0.5 moi .
, {3.5 n10}
Bieethohate_ (emanate.t _ .
{Latitunate }_ \
{0038}? 'i'fiiifilfii 2 is teti tween? the experimental method in preparation {if the pee
hiended aniline oxide and butter s. The. mitipttsitimns ofbttiii‘et System
identifies the buffer system name in the first coitunii with the next two coitu'inis
providing identification ofthe acidic ehemicai and weight percent amenm
foiioweti b}. the amount ofbaeie enemieai and the name. The iesi: two eoiumne
provide the water weight percent. and Ratio}; 13 {3.0% by weight amine oxide
donor}
{ii-829]? Tile-\BLE '3 dieeioeee the composition 0? p,t'e~i‘)ie}}de~d Amine Qxide and Butter
System 3 that was used in. the studiesi Butter eyetem 3 wee pregame by
dissoivihg the appreeriate reagent se’its in water and then adding the amine exide
donor in sufficient. amount to make me iitei‘ of seiutien.
Table 2: Pre—hienticd Buffet" eitt 3 Coimjoeitimi
Acidic Chemical Basic Chemietii Bet-ism 13
' {30% by
weight
*a [W
Better byetem NettieM ., . WE
Amount. «‘Anitfmi in???time.
i Ameugiii‘
{s—Xbbifiviqiiefi. N ) Ntime Nmm) . .
(wt $3.52)} (wt ‘i-ti) {M 6;} Ami)“:
oxide
Done}:
in! it}
POUISSi-Ufli PhQSphén‘C i‘v’iOI‘iniriSiC ,3! nun Paigggiunl
Petassiimi Fixesphate fiibasic _, .2 I Phosphate to ., Fixesphate
(Phosphate Buiiht 3} ,M'enohasic Dihesic
{(3039}; TABLE; 3 shim-'3 the pH and buffer l inn Strengths {Molar} fer buffer System 3.
Table 3: Buffer System pH and Toi’ai inn Strengths
Buffer Buffer System Name pfi (Butter Butte-r Tami {cm Strength
N0. (Abbreviated Name} SJSiCifl} (Meier)
Potassium Phosphate Monetmsie
{4-} "
Potassnim Phosphate Dtbasm. _ , 0"‘i l .435 it1
{Phosphate Buffer i}
'Pijtaesium Biearbenate r“
4 'Pnttiesium Carbnnete 10,2 {33395 M
{Carbonate Buffet}
{$03113 Refettittg to "EMBLiES 4 and 5, the eeiumne under the heading Buttered Amine
Oxide System eertespetid te the identitieetien provided in TABLES i tlirttiugh '3.
{(3832}; it}, genertti, it}, the present irwentiei}, amine tixides were mixed with buffets and
then added to insecticide 01‘ fungicide fermniations. Ameng the red amine
exities were these et‘ 12 carbon iength truth as that said under the trade
designatien Barley: 1‘3 and a mixture of the i2 and 18 C-al'bflfl s said under
the trade designatinn Bttriox 3218.. The buffer on serves to ize the pH
at e neariy eenstent value iii a wide variety efelieiniea} aperations‘
£6033]? iii the t it‘flr‘entimlg the buffer system maintains a siibetaiitieily eiit pH
when in t with binlegieai syeiams. The buii‘et eystem is an tiqnetms system
centieting eta mixture. ofe weak acid it} its eotiiugate (it a week ease in its.
eenjugete acid. One may ebtain the desired buffer system by directiy adding the
week acidifiediiigate base er weak iieseico-njiigate acid salts or by adding the weak
acidifweait heme and 21 strong acidt‘eirnng base in suit]eieiit amenni in {mm the.
conjugate eenjugate base.
{(1034}; The amine Oxide additives may be mixed as tank biends with the insecticides or
fungicides or may be ineerprirateti into the insecticides or fungicide fortniiiae.
? TIABLE t shows ‘3 different buffers, white "i‘ABLE 3 shows an amine exide biend.
313581333 4 diseieses systems- wherein the aptiri‘ipriate reagents were dieseived in
deienized water until it immegenens sedation was obtained. ‘i‘fi‘xiifiLiiEi 3 deais with
the entiing of the amine wide and buffer ewtems with the apprepriete
reagents saits disseix-red in water and subsequenti}; adding the amine exide deem:
American Field Tests 331‘ Buffered Amine {)xide ves w Fungicide and
Insecticide (fables 4 and 5}
'I‘aMe 4 Maw ‘10 June 21113
Fungicific 2133333 1 ‘
;. . .517 "’13 Amine ()23311: 2331313313 Pfimcmi {31533631133135 with Smining
113331133311 Commzxmiim 131111333 Number 5: amine (Md-el Fungi in Siam 1130131331 of
13PM Dunn: {311.311333'17-1 While 0:31: ‘3 4 S. 8.91
P1333\33m2.0165 {,1
3m! 1.) 1d 2)" wet.) ,A 33.: w. (Z)
m C;a”;
. w w
3011 PPM
1 110 PPM
!} 1311131
51.3 PPM h}C: w
51} P131321 .LA:3C' V
I ll
3;} 333.33.1
- In) n- “d 5"?"
- .32.2». :3. w
53:; PPM
:3 PPM
51} 1’?1\-‘1
50 PPM
3 :1 ‘L‘Vawr 13133123331
2) 21} seediingzs
3} 3:13 33111111313513gsfii'scedhng; 11.33:? 3333mm: 13333311 $3.3m}!
=3?) (1336133315 31133} m{33-‘13itc 333k}
:3) 131333- '
. June. Pennsyhrania, USA
(’33 17612131331331 131111131331 regislssmi} 13y Uni’wd Swiss 1313A (1333313131331. 1?: 113‘3'13})1‘1)p:§1£flij 54131311 and ; (hatiikxi water
1’: Scc 13131335 1. ’3 am} 1‘3 1133133311235; and 15313133: (3.3231 use
8) "3 (1333.3: 1311333: 33333311‘1‘3313013 51355316. razor: 131231.133 wound (317,2 “‘3 1133333115 133 13313113 33331333313 53351111353’ 513333
9,! 14 d . 1111:; 33131333333331. wounds was 111331 1131mm. 3353: L. .
. 3.1333333 11m3:
’} Buffers: and amine oxides wen: 3311313331 1011113333: 513131313313offixngicfidc
6}; Referring ta TA B1413; £1 where-311 a mmnmniy used fungicide. PEGPECONAZOLE
was empioyed in tests in the 313301.333: of 50:200 PPM {parts per 33111113311} empioyed
with 33131133311103“ buffered amine . 5333163338 3 and 61 with 301333: {313.1323 333.9353
employing the 12 carbon 11213911 and others. the 1218. carbon mixture. In a
pukned unbudxmunm 1218 1313 a weight 1351513 113121. 313 1315111133311 be
131888111 in an 3133mm 013130331 1.33H}3’ 1) times the 3133011131 @1718 333113023 16139113 and
inthat{33121131331132113541233333.3331 1.5510 1. 8 times {11323111310111}fo 18 carbon 1e13g1h. The
tests were performed en white oak seediings which were provided with a stem
wound in which wee introduced staining fungi which was ofthe ceratocystis
variety. Staining indicates that the fungicide or other treatment. did not resist
growth oi’the Fungi witl'i the number 1th.} representing 100% with no inhibitions oi"
hihgi growth and the i'nnnher {3 indicating t} % or 0 indicating no fungi growth.
{flfl37} Referring in. TABLE 4 to the heading under No Buffing it is seen that the amine
oxides of both the 13 and iEtS iength in trations of 200:1 and 489:1 did
not in an}; we}; t growth of the staining fungi. Considering the
Pt‘onieonenole entph'iyed alone, it i3 eeen that. with. :30 ppm, Kit} ppm and fifth
point the. inhibition at 50 ppm did not exist as. there was ?» growth and that at
1th} ppm, Shit-ti growth was experieneed. whiie at 308 ppm Eti‘ifi growth existed.
teaser With continued reference to "E'ABLE. it. the combination of the ide with the
hoii’etied amine oxide system No. 3 oying 50 ppm in the 1'3 {lather} iength
ed with 530 npnt propiconazoiefi at Etitjri ooneent‘ratiom there was. t} thngai
growth, and at. 400:1, there was 20% growth. The same 50 ppm oi’the fungicide
employed with 200:1 and 400: i til 18 buffered amine oxide system \o. 3
produced 0 fungal ,
{0039}? 'i'fiti:3ii..i31 4 shows. that both the i2, and 1218 iength ot’imft‘ered amine oxide System
\to 3 used atone at trations (1520011 and, 460:} tttodtieed no fungai growth
inhibition as both showed 1th ‘i-‘Ei staining hmgi.
{fifleht Ct‘iitsidering hnffered amine oxide system \o 4 when the 332‘ iength is used in
combination with St} ppm of the fungicide in weeetttrtttinn oi‘ittit'}: L 20% fringe}
growth was experienced and, in 2509:1310 fttttgat growth was experienced. With
regard to the ti'ingieide being in St? print and the ”38 carbon iengthy a buffered
amine oxide system No. it, as to both 230:3 and 4001i eoiteentrtttiom there was 0
fungai growth.
teoeit Considering both the 12 length and 1233 iength empioyed without: the flingieide in
both concentrations; 300:1 and 4th}: 2 there was a itth‘fi‘tt fringe} growth.
tam]; The test reenhs in TABIE 45 therethre, support the cottehision that, in the absence
rife heifer, there was 1,3130% freight . in the use of 12 length amine exide or
12} 8 iength amine oxide alone with. both buffered amine systems No. '3: and 4:
there was 1802-?) i growth. When? however) the combination offirngieide
and the battered amine Oxide systems were E‘mtjifiyfid, whether length 12 or 1318
was considered? when the mncenu‘atien was 21111:},1’he1e was 110 1111131111 gmwth
and when 11113 concentration was 4013113, there w as 20‘3111 fungai gmwih.
{1111-43}? '3‘he method oftestihg me 1113112111113 was 10 spray the 11111111 111? the seediing with the
1321111611131 5031111011 being tested 111111 '7 days; after such 2113131111311111'1) creating 21
1110111111 0f appmximateiy 2 11111Ii111e'1e1's’by 18 111111111'113181‘3 1111 each seedhhg 1
1301111111211 days 1113:1311er wannding, the 111111111113 were examined 133111111 presence 01‘
staining fungi.
Table 5 M311 1111311118 2313
3115'L116Idc'3'ypfi No Bufibr BUIIUCCI111111111: Oxide $511,111 P13158111 13},- "V'E\-'§-'..1‘1I1 iim‘
Ii'mdmi Concentration 1311111121 \1111112131 & A111111e1‘111111. Dahmgci' 5‘ '
Wk '
P13?“ i3G1“?! ()1 I'T‘rj‘i‘1 I, Mnu‘h :11th.4131lx2»11E-§1:I"3}
I’L111111111111“
H30 PPM
50 RPM
1 1‘! PPM
if: I’FIVI
111 11:11
1} th'et 13111111111.
2) 21'} :1 flags
3} 21} miIéiliiem per seafiiing: 111w Wham hand away
"1111;111:115 1111121,
>3 }"~3131}{2, Pennsylvania, USA
13111111118131 an‘eutmie Luntaénmg 3114 percent {14111131111111
1.1 SL1; 'I‘ahlcs 1‘ 2:11:11 3 {111' buffets 3 111135113 Mides
13) 1'11th than $09.1 11111111511:sz $351331
‘31 1%1111‘L’1x 1311111 11L Midas \S‘LEC 2111111111 1111; 511111111111 111'11~xLL11L1111
111111-14]; Refeming 111 TABLE 5 {here is SI‘31'1W‘11: the 11331115115 11111331111}; 1'31? 31111151301111.1111:
which, 111113111 case: was p-em'lethtihf, which was presented in 113110113 tests 111
quantities of If) ppm 10 51‘} ppm and 100 ppm mneeutratimts 11113131331134 against a
I with no buffer as weII 3.5 buffer 1111111113 oxide systems- e111ph1ying 123 $811th
semen.
{8045}; The cuiai‘ ons tested were applied, to a stem eftiie white oak seediing
using a tow veinme hand. spray and sprayii'ig 2i} miililitei‘s pet seediing. A total of
:20 seediings were tested. The use ethtih alcne in concentration of 10 ppm
resuiteci in 80% gypsy moth catetpiiiai‘ damage. At pernlethi'in etn'icenttation nt‘
50 ppm) the damage afiet tine month was 309-2: and with 100 ppm used alone the
damage was 04 When buffeted amine oxide system No. '3 nan empinyeti in.
concentrations at 489:1 with it} pent ofthe insecticide, the gypsy ninth catetpiiiai'
damage was iG‘il-ii anti when a concentration at Eiiflri nas yeti with it} ppm
insecticide the damage was 0- This shows that a much eif amount {if
insecticide was needed :0 achieve 0 damage when was used in combination with
the buffeted amine oxide system which. created. a desired. synergistic eiiect. if less
than 50 percent at the ’iea‘f mass was eaten. this shows successful inhibition of
gfiisy moth damage.
i904fii Using buffeted amine oxide system Na. 3 aione in concentrations 0.1940833, and
Etifiri tesnhed in 100% gypsy moth catetniilat dai‘nage after one month.
{ti-c4713 ’tising bnffeteti amine aside system No. it in enmhinaticn with 3.8 ppm of the
insecticide, reduce the gypsy moth cateiipiiiat damage to 10% when using a
concentration 0f 480:1 anti t0 0 when using a concentration efEQGfl.
{3043i Using buffered amine oxide system Ne. at withent the insecticide tesuited in 200%
gypsy i'nnth catet‘piiiat daii‘iage.
{ti-c4913 'Ti‘he fnregeing tests Show that neither buffeted amine oxide system 3 not ii in
ccnccntraticns {if 209: 2 and 400;? pmtinced any measurable tiiii‘etence in gypsy
ninth caterpiiiat damage over the } which had. neither icide net
imitated amine naide systems. Wl'ien, however, the buffeted amine oxide systems
3 and ti were yeti with insecticide cnncenti‘ations oi‘ i0 ppm, at 4%:'1.
ccncentration ofthe 13 length carbon buffeted amine oxide systems, there was
only ii iii: gypsy ninth catetniilat damage and. with 200:} concentratinn, there was
0 damage.
ififi5fil ii‘desit‘ech a singie snintion may cnniain both an insecticide anti 3 fungicide.
was: i it: wiil he annreciatect {hie that both in connection with fungicide tests and
insecticide tests? neither the insecticide net fungicide employed aione achieved!
any meaningful reduction in staining thngi or gypsy moth caterpiilat in the iicwet
concentrations oftiie niatei‘iai. iiy, the buffeted amine osicle system, when
used inane, produced tie sigi’iifieem reduetien in staining fungi er gypsy moth
catet'piiiar damage When? r? the fungicic’ie was; used at: inwet‘ parts per
miiiiei} in eei'nbinatinn with the buffered amine oxide e there was, due to:
synergism, a substantini reduetit'nzt t‘n‘ eiii‘ninntit‘nt nfstniiztittg fungi. Similarly
when the insecticide was; used in lower concenttat'iens in cmnbinatim: with
buffered, amine wide systems, there nae Substantial inn 01‘ eliminatinn 0’?
.31m moth eaterpiiier .
geese}; While pettittniar embodiments of‘tnie inventinn have been described herein for
p‘turpesee efiliuetrati 01% it will be evident. to. titeee skilled in. the art that rnttrtei‘nue
variatiens 0f the details of‘the present imtentien may be made without departing
fine} the inventinn as defined in the appended eia’ime.
Claims (11)
1. A solution for resisting destruction of living plants comprising: a buffered amine oxide administered admixed with at least one material selected from the group consisting of permethrin and propiconazole in water, when used on living , wherein said buffered amine oxide having a pH of 6.5 to 10.5; wherein said buffered amine oxide being present in a concentration of 0.06% to 0.12% weight %; wherein said buffered amine oxide being a 12 carbon length amine oxide and said buffer system being selected from the group ting of (a) Potassium Phosphate Monobasic/Potassium Phosphate Dibasic and (b) Potassium Bicarbonate/Potassium ate; or said buffered amine oxide comprising a e of 12 carbon length amine oxide and 18 carbon length amine oxide and said buffer system being selected from the group consisting of (a) Potassium Phosphate Monobasic/Potassium Phosphate Dibasic and (b) Potassium Bicarbonate/Potassium Carbonate, wherein said 12 carbon length amine oxide being present on a weight basis in an amount of 1.3 to 2.0 times the amount of 18 carbon length amine oxide.
2. The solution of claim 1 including said solution having said propiconazole present in an amount of at least 50 ppm on a total solution weight basis.
3. The solution of claim 1 including said solution having said permethrin t in an amount of at least 10 ppm on a total solution weight basis.
4. The solution of claim 3 including said solution having said permethrin t in an amount of 10 to 100 ppm.
5. The solution of claim 1 including said 12 carbon length amine oxide being present on a weight basis in an amount of 1.5 to 1.8 times the amount of 18 carbon length amine oxide.
6. The solution of claim 1 including said buffered amine oxide having a pH of 7 to 9.
7. A method of resisting destruction of living plants comprising: providing a solution having a buffered amine oxide d with at least one material selected from the group ting of permethrin and propiconazole in water, and applying said solution to said living plants against insects and/or fungi wherein said buffered amine oxide having a pH of 6.5 to 10.5; wherein said buffered amine oxide being resent in a concentration of 0.06% to 0.12% weight %; and wherein said ed amine oxide being a 12 carbon length amine oxide and said buffer system being selected from the group ting of (a) Potassium Phosphate Monobasic/Potassium Phosphate Dibasic and (b) Potassium Bicarbonate/Potassium Carbonate; or said buffered amine oxide comprising a mixture of 12 carbon length amine oxide and 18 carbon length amine oxide and said buffer system being selected from the group consisting of (a) Potassium Phosphate Monobasic/Potassium Phosphate Dibasic and (b) Potassium Bicarbonate/Potassium Carbonate, n said 12 carbon length amine oxide being present on a weight basis in an amount of 1.3 to 2.0 times the amount of 18 carbon length amine oxide.
8. The method of claim 7 including said on having said propiconazole present in an amount of at least 50 ppm on a total solution weight basis.
9. The method of claim 7 including said permethrin in an amount of 10 to 100 ppm on a solution total weight basis.
10. The method of claim 7 including said 12 carbon length amine oxide on a weight basis being present in an amount of 1.5 to 1.8 times the amount of 18 carbon length amine oxide.
11. The method of claim 7 including said solution containing a buffered amine oxide having a pH of 7 to 9.
Applications Claiming Priority (3)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US14/674,465 | 2015-03-31 | ||
US14/674,465 US20160286798A1 (en) | 2015-03-31 | 2015-03-31 | Solutions for enhancing the effectiveness of insecticides and fungicides on living plants and related methods |
PCT/US2015/052562 WO2016160055A1 (en) | 2015-03-31 | 2015-09-28 | Solutions for enhancing the effectiveness of insecticides and fungicides on living plants and related methods |
Publications (2)
Publication Number | Publication Date |
---|---|
NZ734615A NZ734615A (en) | 2020-12-18 |
NZ734615B2 true NZ734615B2 (en) | 2021-03-19 |
Family
ID=
Similar Documents
Publication | Publication Date | Title |
---|---|---|
AU2020294285B2 (en) | Solutions for enhancing the effectiveness of insecticides and fungicides on living plants and related methods | |
US20240057594A1 (en) | Solutions for enhancing the effectiveness of insecticides and fungicides on living plants and related methods | |
AU2023229807A1 (en) | Solutions employing herbicides and buffered amine oxides to kill weeds and related methods | |
ES2326717B1 (en) | UNTILIZATION OF ANTIMICROBIAL AGENTS DERIVED FROM ALIACEAS FOR THE PREVENTION AND CONTROL OF CULTURE DISEASES, POST-DUTY POWERS AND AS ENVIRONMENTAL DISINFECTION PRODUCTS. | |
US11779016B2 (en) | Solutions for enhancing the effectiveness of insecticides and fungicides on living plants and related methods | |
NZ734615B2 (en) | Solutions for enhancing the effectiveness of insecticides and fungicides on living plants and related methods | |
CN114451415A (en) | Preventive preparation for preventing and controlling pine wilt disease | |
WO2020117315A1 (en) | Solutions for enhancing the effectiveness of insecticides and fungicides on living plants and related methods | |
CN111713502A (en) | Preparation for preventing and treating longicorn and preparation method thereof | |
CN111869672A (en) | Bactericidal composition and application thereof | |
CN106857616A (en) | A kind of Herbicidal combinations containing orthosulfamuron Yu bispyribac-sodium | |
Tanigoshi et al. | Overview of Our First Season’s Experiences to Chemically Manage the Spotted Wing Drosophila through Lab and Field Research on Red Raspberry in Western Washington | |
Jayanthi et al. | Studies on the possibility of managing fruit sucking moth, Eudocima (Othreis) materna (L.)(Lepidoptera: Noctuidae) using feeding repellents | |
Blintsov et al. | Assessment of biological efficiency of existent insecticides against forest pests | |
BR112019018460B1 (en) | PREPARATION CONTAINING AT LEAST ONE CHEMICAL FUNGICIDE OF FLUODIOXONYL AND CYPRODINYL, AS WELL AS STRAINS OF AUREOBASIDIUM PULLULANS, ITS USE AND METHOD FOR PROPHYLAXIS OR FOR REDUCING THE SPREAD OF AT LEAST ONE PLANT DISEASE CAUSED BY A FUNGAL PATHOGEN | |
CN106818863A (en) | A kind of insecticide for being applied to agricultural crops | |
Phillips | Fungicides in forestry in Great Britain | |
Hoebeke | Invasive insects as major pests in the United States |