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Moisturizing Agents

Abstract: A concentrated aqueous composition may be prepared by from a formulation including: a. from 10 to 30 % by weight (% wt) of a depolymerized carboxymethyl cellulose having a weight average molecular weight of from about 10 000 to about 80 000 dalton (Da); b. from 15 to 50% of a compatibilizer selected from the group consisting of glycerol and sodium xylene sulfonate; and c. from about 0.5 to about 20 % by weight of a surfactant. The concentrated aqueous solution may be employed to prepare an aqueous solution which is useful for moisturizing soil.

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Patent Information

Application #
Filing Date
17 October 2016
Publication Number
45/2016
Publication Type
INA
Invention Field
POLYMER TECHNOLOGY
Status
Email
Parent Application
Patent Number
Legal Status
Grant Date
2021-02-02
Renewal Date

Applicants

LAMBERTI SPA
Ufficio Brevetti via Piave 18 I 21041 Albizzate (VA)

Inventors

1. DI MODUGNO Rocco
18 Mystic Glade Spring Texas 77382
2. SPIER Don
106 West Dells Road Silver Lake Wisconsin 53170
3. CHIAVACCI Dario
Via Brughiera 25/B I 21040 Castronno (VA)
4. CIPRIANI Chiara
Via Chiesa 35/G I 21045 Gazzada Schianno (VA)
5. VECCHI Stefania
via XX Settembre 21 I 22020 Cavallasca (CO)
6. FLORIDI Giovanni
Via Regaldi 2c I 28100 Novara
7. LI BASSI Giuseppe
Via Stretti 4 I 21026 Gavirate (VA)

Specification

MOISTURIZING AGENTS
[0001] The present invention relates to aqueous, concentrated compositions for
preparing moisturizing agents for soils comprising a depolymerized carboxymethyl
cellulose, a compatibilizer and at least one surfactant.
[0002] This invention also pertains to aqueous solutions prepared from the compositions
and to a method for moisturizing soils.
[0003] Plants require specific amounts of moisture to germinate, grow and remain
viable. In conditions of water scarcity and/or high evaporation/transpiration, soil loses
water rapidly due to high temperatures, low humidity, high winds and plant transpiration.
Moisture in the soil is drawn to exposed soil surfaces by capillary action and lost by
evaporation into the air. At the same time, moisture drawn from the soil into plant root
fibers by osmosis is transpired through the plant stems and leaf systems, and that
fraction not converted by photosynthesis is then lost by evaporation from pores of leaf
surfaces. Under such conditions, soil volumetric water content can decrease
significantly.
[0004] Moreover, irrigation water applied to coarse, sandy soils, can move past the plant
root zone due to channeling, defined as the rapid movement of water downward through
large pore spaces, and lack of retention, caused by lack of organic matter available to
absorb available water.
[0005] Also water repellent soils present significant hydrologic and agronomic
challenges. Since they are characterized by changes in the surface chemistry that
impede or completely inhibit hydration, they show retarded water infiltration into the soil
(leading to runoff, erosion, and leaching) and strong effects on the regular growth and
maintenance of turf grass and a variety of agricultural crops.
[0006] Where there is a marked change in ground temperatures between day and night,
there is a significant air inhalation into porous soils during the night-time cooling
(contraction) cycle and exhalation of air and moisture in the heat of the day. This further
aggravates the overall evaporative moisture loss.
[0007] Moisture is typically added to the soil by watering using manual or automatic
means, such as sprinkler and drip irrigation systems. Such systems must nevertheless
be connected to expensive and elaborate irrigation conduits and controls, which
severely limit usage and have high energy consumption.
[0008] A further method for maintaining the ground moisture, utilizes the sponge like
materials which are previously mixed with the soil surrounding the plant roots and then
imbued with water during the sprinkling watering either natural or artificial. These
materials usually are not biodegradable and contaminate the soils in which are inserted.
[0009] Many methods use moisturizing agents as soil additives to increase volumetric
water content. The moisturizing agents are usually compositions of (co)polymers of
natural, semi-synthetic or synthetic origin.
[0010] These polymer compositions are mixed into an aqueous solution or suspension
and applied to the soil surface. The application can be accomplished in variety of ways,
including but not limited to, spraying, casting, mulching, tilling or otherwise incorporating
into the top layers of soils.
[001 1] One of the polymers suitable as moisturizing agents is carboxymethyl cellulose
(CMC). Carboxymethyl cellulose is able to absorb and hold water, when irrigation water
is applied, and release it during irrigation intervals or dry periods.
[0012] For example, WO 2007/146055 describes a substrate, which releases
impregnated water, gas and nutrients when interacting with biological organisms,
comprising a mixture of a salt of carboxymethyl cellulose compound, having an average
molecular weight ranging between 90,000 and 700,000, a hydrated metallic salt, water,
a micro-nutrient selected from the group consisting of zinc and zinc salts, at least one
plant growth additive selected from the group consisting of plant growth hormones and
plant growth regulators, at least one preservative, a surfactant, and an acetic acid
component selected from the group consisting of acetic acid or acetic acid salts.
[0013] US 4,865,640 claims a substrate which gradually releases impregnated water
and gas when interacting with a biological organism essentially comprising a mixture of:
a) cellulosic compound ranging from 13% by weight having an average molecular
weight ranging between 90,000 and 700,000 represented by the formula: R--O--COOM,
in which "M" is a metal substituted for hydrogen on the carboxyl group of the cellulosic
compound and "R" is cellulosic chain; b) a hydrated metallic salt ranging from 0.1 -0.3%
by weight; and c) water ranging from 97-99% by weight.
[001 4] Sometimes, when watering process is supposed to be optimized for the growing
conditions, localized dry spots ("LDS") may take place also in the presence of a
moisturizing agent. It can be caused by excessive thatch, compacted soil, poor irrigation
coverage, steep sloping grade (water runoff), high soil salinity, improper chemical
usage, insects, diseases and water-repellent soil. LDS is characterized by irregular,
isolated, hydrophobic areas problematic in the crop or turf stand.
[001 5] The number of localized dry spots caused by inhomogeneous water distribution
can be minimized by adding surfactants to the moisturizing agents. In fact the
surfactants acting as wetting agent allow water to spread horizontally and to penetrate
to a useful depth through the small channels and capillaries of the soil without being
repelled or retained mainly on the surface or in defined area.
[001 6] This solution is described in WO 02/1 5687, which relates to soil treatment
compositions comprising:
an active ingredient selected from the group consisting of a water soluble or dispersible
polymer, a surfactant, and a combination of ingredients I and II; and B) the balance
carriers and other adjunct ingredients.
[001 7] The water soluble or dispersible polymer can be a polysaccharide and
carboxymethyl cellulose is mentioned among the polysaccharides. In the Examples,
three CMC with molecular weight ranging from 90,000 to 700,000 dalton are utilized. No
particular effect of the molecular weight on the performances is described.
[0018] Usually the moisturizing agents, such as CMC, are directly applied on soil as
aqueous solutions which are prepared at the application site. It is important that all the
components of the moisturizing agents are correctly dosed and well dissolved to ensure
that no under dosing or overdosing on the soil is obtained.
[0019] However, carboxymethyl cellulose can be difficult to be used in field situations
and in solid form it takes a long time to dissolve, also under high shear stirring.
[0020] A good solution to this problem would be preparing a concentrated aqueous
composition of carboxymethyl cellulose and surfactants which can be easily dosed and
homogenized.
[0021] Unfortunately, it is difficult to combine adequate quantities of carboxymethyl
cellulose and surfactants in concentrates and/or to obtain stable compositions in all
cases. Furthermore, the types of surfactants will be limited to those compatible with the
carboxymethyl cellulose.
[0022] Accordingly, there is still a need for a concentrated aqueous composition of
carboxymethyl cellulose and a surfactant which can be easily diluted and applied, has
increased efficacy on any kind of soil and can improve water usage efficiency by plants
and grasses.
[0023]We have discovered that a concentrated aqueous composition of a
depolymerized carboxymethyl cellulose (depolymerized CMC) and surfactants can be
prepared with the help of a compatibilizer.These concentrates may contain high
amounts of carboxymethyl cellulose and surfactants, are stable, pourable and can be
easily diluted at the application or mixing site to prepare ready-to-use moisturizing
agents.
[0024] The moisturizing agent can be applied to the soil and will reduce the losses of
moisture from direct evaporation or from channelling and run-through, improves the
proportion of soil moisture accessible to plants, and in certain conditions prevents or
even reverses the evaporative loss from day/night movement in and out of porous soils.
At the same time the presence of the surfactant allows water to properly hydrate the
soil.
[0025] As far as the Applicant knows, no one has described the specific combination of
depolymerized CMC, surfactant and compatibilizer of the present disclosure.
[0026] According to the invention, the expression "depolymerized CMC" defines a
carboxymethyl cellulose whose weight average molecular weight has been reduced
between 10,000 and 80,000 dalton through a chemical, enzymatic or physical treatment
or a combination of these treatments.
[0027] According to the invention, the weight average molecular weight of CMC is
determined by gel permeation chromatography (GPC) calibrated with pullulane
standards.
[0028] The expression "degree of substitution" (DS) means the average number of
carboxymethyl groups for each hydroglycosidic unit of the cellulose.
SUMMARY OF THE INVENTION
[0029] It is therefore an object of the present invention concentrated aqueous
composition for the preparation of moisturizing agents comprising:
a. from 10 to 30 % by weight (wt.%) of a depolymerized carboxymethyl cellulose
(depolymerized CMC) having a weight average molecular weight comprised
between 10,000 and 80,000 dalton (Da);
b. from 15 to 50 % by weight of a compatibilizer chosen among glycerol and sodium
xylene sulfonate;
c . from 0.5 to 20 % by weight of at least a surfactant.
[0030] In an another aspect, the present invention relates to a method for moisturizing
soils comprising i) preparing an aqueous solution ready to be applied comprising from
0.1 to 3.5 % by weight, more preferably from 0.5 to 2 % by weight, of the concentrated
aqueous composition, and ii) applying the aqueous solution on soil.
DETAILED DESCRIPTION OF THE INVENTION
[0031] According to a preferred aspect of the invention, the aqueous concentrated
composition comprises:
a. from 12 to 25 wt. % of the depolymerized CMC;
b. from 25 to 45 wt.% of the compatibilizer;
c . from 0.5 to 10 wt.% of at least a surfactant.
[0032] In a particularly preferred embodiment of the invention, the aqueous
concentrated composition comprises:
a. from 12 to 25 wt.% of the depolymerized CMC;
b. from 32 to 45 wt.% of the compatibilizer;
c . from 0.5 to 5 wt.% of at least a surfactant.
[0033] According to the invention, a preferred depolymerized CMC has a weight
average molecular weight comprised between 15,000 and 50,000 Da, more preferably
from 20,000 to 40,000 Da.
[0034] Advantageously, the depolymerized CMC has a degree of substitution (DS)
ranging from 0.4 to 1.6, more preferably from 0.6 to 1.2.
[0035] The Brookfield viscosity of the depolymerized CMC measured at 20 rpm and 20
°C in water solution at 25 wt.% concentration is usually below 6500 mPa*s, preferably
below 4000 mPa*s.
[0036] Usually, the depolymerized CMC of the invention is salified with alkali metal ions,
such as sodium or potassium, or ammonium or quaternary ammonium ions. Preferably,
the depolymerized carboxymethyl cellulose of the invention is salified with potassium or
sodium ions, more preferably with potassium ions.
Many methods useful for the depolymerisation of carboxymethyl cellulose are known;
we cite, by way of example, those reported in: EP 382577, where enzymatic hydrolysed
from cellulose derivative are described; GB 2,281 ,073, where the procedure for
obtaining solutions of low viscosity carboxymethyl cellulose from the dissolution of solid
mixtures of carboxymethyl cellulose and enzymes is described; EP 465992, where a
procedure for the depolymerisation of cellulose ethers with hydrogen peroxide in water
is described; EP 7081 13, where the obtainment of low molecular weight cellulose ethers
by irradiation is described;
WO/2005/01 2540, which describes a procedure for theenzymatic depolymerization of
medium viscosity carboxymethyl cellulose in the form of dispersed powder in a hydroalcoholic
heterogeneous medium;
[0037] Practically all these methods are utilizable for the preparation of a depolymerized
CMC suitable for the composition of the invention. Depolymerized CMC obtained from
an enzymatic depolymerization process is the preferred choice.
[0038] The depolymerization methods can be applied both on purified and technical
grade carboxymethyl cellulose.
[0039] Advantageously, the depolymerized CMC is obtained from a technical grade
carboxymethyl cellulose having a content of active substance of from 55 to 75 wt.% as
dry matter. Technical grade CMC are not washed after the etherification reaction and
usually contain from 25 to 45 wt.% as dry matter of the carboxymethylation by-products.
These by-products are mainly, depending on the salification of the CMC, salts of
chloride and glycolate, such as sodium chloride and sodium glycolate.
[0040] Preferably, in the concentrated aqueous composition for the preparation of
moisturizing agents of the present disclosure the compatibilizer is glycerol.
[0041] Anionic, cationic, non-ionic and ampholytic surfactants and mixtures thereof can
be used as the surfactant c). Preferably the surfactants are anionic surfactants.
[0042] Suitable surfactants are, for example, nonionic emulsifiers and dispersants, such
as: polyalkoxylated, preferably polyethoxylated, saturated and unsaturated aliphatic
alcohols, having 8 to 24 carbon atoms in the alkyl radical, which is derived from the
corresponding fatty acids or from petrochemical products, and having 1 to 100,
preferably 4 to 40, ethylene oxide units (EO); polyalkoxylated, preferably
polyethoxylated, arylalkylphenols, such as, for example, tristyrylphenol having an
average degree of ethoxylation of between 8 and 80, preferably from 16 to 40;
polyalkoxylated, preferably polyethoxylated, alkylphenols having one or more alkyl
radicals, such as, for example, nonylphenol or tri-sec-butylphenol, and a degree of
ethoxylation of between 2 and 40, preferably from 4 to 20; polyalkoxylated, preferably
polyethoxylated, hydroxy-fatty acids or glycerides of hydroxy-fatty acids, such as, for
example, castor oil, having a degree of ethoxylation of between 10 and 80; sorbitan or
sorbitol esters with fatty acids or polyalkoxylated, preferably polyethoxylated, sorbitan or
sorbitol esters; polyalkoxylated, preferably polyethoxylated, amines; di- and tri-block
copolymers, for example from alkylene oxides, for example from ethylene oxide and
propylene oxide, having average molar masses between 200 and 8000 g/mol,
preferably from 1000 to 4000 g/mol; alkylpolyglycosides or polyalkoxylated, preferably
polyethoxylated, alkylpolyglycosides.
[0043] Preferred nonionic surfactants are polyethoxylated alcohols, preferably from
renewable resources, such as ethoxylated (4-8 EO) C 2-C natural alcohol;
polyethoxylated triglycerides of hydroxy-fatty acids and polyethylene
oxide/polypropylene oxide block copolymers.
[0044] Also suitable are anionic surfactants, for example:
polyalkoxylated, preferably polyethoxylated, surfactants which are ionically modified, for
example by conversion of the terminal free hydroxyl function of the alkylene oxide block
into a sulfate or phosphate ester;
alkali metal and alkaline earth metal salts of alkylarylsulfonic acids having a straightchain
or branched alkyl chain;
alkali metal and alkaline earth metal salts of paraffin-sulfonic acids and chlorinated
paraffin-sulfonic acids;
polyelectrolytes, such as lignosulfonates, condensates of naphthalenesulfonate and
formaldehyde, polystyrenesulfonate or sulfonated unsaturated or aromatic polymers;
anionic esters of alkylpolyglycosides, such as alkylpolyglucosidesulfosuccinate or
citrate; sulfosuccinates which are esterified once or twice with linear, or branched
aliphatic, cycloaliphatic and/or aromatic alcohols, or sulfosuccinates which are esterified
once or twice with (poly)alkylene oxide adducts of alcohols.
[0045] Preferred anionic surfactants are, for example, salts of alkyl sulfosuccinic acids,
such as sodium dioctyl sulfosuccinate, and anionic esters of alkylpolyglycosides, in
particular alkylpolyglucoside citrate.
[0046] Examples of cationic and ampholytic surfactants are quaternary ammonium salts,
alkyl amino acids, and betaine or imidazoline amphotensides.
[0047] Optionally, the concentrated aqueous composition also includes drift retardants,
humectants, corrosion inhibitors, microbial inhibitors, pH adjusters, anti-foam agents or
mixture thereof.
[0048] The concentrated aqueous composition of the invention can be prepared by
simply mixing the various components and the other optional additives with water. Since
the depolymerized CMC is typically provided as a concentrated liquid solution or
dispersion (20-45% by weight), usually the compatibilizer, the at least one surfactant
and the other additives are added, possibly with water, to the solution or dispersion of
depolymerized CMC.
[0049] The concentrated compositions of the invention have a Brookfield® viscosity
comprised between 100 and 800 mPa*s, preferably between 200 and 500 mPa*s.
[0050] These concentrated aqueous compositions can be diluted just before use with
water to provide the aqueous solutions, which can be directly applied on the soil.
[0051] Preferably, the aqueous solutions of the present invention comprise from 1 to 2%
by weight of the above described concentrated aqueous composition.
[0052] The here disclosed aqueous solutions may consists of depolymerized CMC, a
compatibilizer and at least one surfactant; conveniently they may also contain
agrochemical active ingredients such as insecticides, herbicides, stabilizers, adjuvants,
pH adjusters, anti-foam agents, plant nutrients including fertilizers and heavy metals,
and the like. Preferred agrochemical active ingredients are plant nutrients.
[0053] The aqueous solutions of the present invention can comprise from about 0.01 to
about 8 wt.%, preferably from about 1 to about 4 wt.%, of agrochemical active
ingredients.
[0054] Examples of suitable fertilizers include sources of nitrogen, of phosphorous, of
potassium and mixture thereof. Non-limiting examples of sources of available nitrogen
include, urea, ammonium nitrate, potassium nitrate, and mixtures thereof. Examples of
available phosphorous include ammonium phosphate, diammonium hydrogen
phosphate, ammonium dihydrogen monophosphate, sodium phosphate, sodium
hydrogen phosphate, and mixtures thereof. Available sources of potassium include any
suitable water soluble potassium salt.
[0055] Non-limiting examples of sources of heavy metals include chelated iron (chelated
with EDTA), manganese, and zinc.
[0056] The disclosed aqueous solutions of the invention can be applied by, e. g.,
spraying between 60 to 500 l/ha, preferably 150 to 300 l/ha, or by sprinkling or dripping
between 0.4 and 120 l/hour per emitter.
[0057] They can be applied to any kind of soil but they are particularly suited to: sandy
soil, loamy soil, sandy clay loam, sandy clay, sandy as defined in "Soil Survey Manual"
United States Dept. of Agric. U. S. Government Printing Office, Washington, D. C.
20402. (CHAPTER 3).
[0058] Since the preferred components of the aqueous solution are biodegradable, it
may be periodically reapplied. The following experimental data show the stability and
efficacy of the concentrated aqueous compositions of the invention.
EXAMPLES
Characterization Methods
[0059] The Brookfield® (BRK) viscosity of the CMC solutions was measured with a DVE
Brookfield® viscometer at 20 °C andat 20 rpm.
[0060] The degree of substitution (DS) of the carboxymethyl cellulose was measured
following the ASTM Standard Test Method D 1439-03 (Degree of Etherification).
[0061] The active matter content of the carboxymethyl cellulose was determined
following the ASTM Standard Test Method D 1439-03 (Purity).
[0062] The reaction by-products content of the carboxymethyl cellulose was calculated
by difference between the dry weight and the active matter content.
[0063] Gel permeation chromatography (GPC) was used to determine the weight
average molecular weight (Mw), by using the following method.
[0064] Depolymerized CMC samples were prepared by dissolving at a concentration of
0.3 % w/vol of sample in 0.1 0 M ammonium acetate ("mobile phase solution").
[0065] Pullulanes with molecular weights ranging from 5900 to 788000 Da were used as
molecular weight standards.
[0066] Two hundred microliters of each solution, filtered on a 0.45 micron membrane
filter were injected into a HPLC equipped with an evaporative light scattering detector.
[0067] The following columns were used at a temperature of 60 °C: SupelcoProgel -
TSK G3000 PWXL, G5000 PWXL, G6000 PWXL, and Progel-TSK PWXL guard
columns. The HPLC was set at a flow rate of 0.8 ml/min for 50 minutes.
Preparation of Depolymerized CMC
[0068] Four different CMC were depolymerized (see their characteristics in Table 1)
according to the following method.
[0069] In a 130 I reactor 20 Kg of carboxymethyl cellulose were dispersed under
in 80 Kg of a water/isopropanol mixture (containing 4 1 wt.% of isopropanol).
Table 1
[0070] The pH was adjusted to 6.4 with 0.1 6 Kg of 50 wt.% NaOH and 9.1 Kg of 80
wt.% acetic acid, and the mixture was heated to 40 °C. Then from 100 to 300 g of
Indiage® Super L (a preparation of cellulose commercialized by Genencor International,
having enzymatic activity of 2850 GTU/g) were added.
[0071] The dispersion was stirred for an appropriate time (between 30 and 180
minutes); the alcohol was then removed by distillation under vacuum at 40-45 °C until
its residual concentration was about 0.5 wt.% (determined by Gas Chromatography);
NaOH was added to raise the pH to 11.5 and the mixture was stirred at 67 °C for 60
minutes.
[0072] The mixture was cooled to 50 °C, 0.6 Kg of a 30 wt.% aqueous solution of
hydrogen peroxide were added, then heated to 65 °C and stirred for 30 minutes.
300 g of Terminox 50 Ultra (a catalase from Novozymes, DK) were added and the
mixture was stirred for 10 minutes. The solution was cooled to 30 °C and 75 g of
Carbosan CD40 (biocide from Lamberti SpA) were added.
[0073] Aqueous solutions of depolymerized carboxymethyl cellulose (see Table 2) were
obtained.
Table 2
from technical grade potassium CMC
from purified grade potassium CMC
3 from purified grade sodium CMC
4 from technical grade sodium CMC
Examples 1-20
[0074] Concentrated aqueous compositions according to the invention were prepared by
mixing different amounts of CMC1 -CMC5, the compatibilizers and coco-alkyl
polyglucoside citrate (APG-Citrate, commercialized by Lamberti SpA as Eucarol AGE
EC) or sodium dioctyl sulfosuccinate as described in Table 3, Table 4 and Table 5.
[0075] Table 3, Table 4 and Table 5 report also the appearance of the compositions,
their Brookfield viscosity and their stability to a treatment at 54 °C for two weeks.
Table 3
"Comparative; OK = No phase separation; PS = Phase separation
Table 4
Comparative; OK = No phase separation ; ND = Not Determined ; PS = Phase separation
Table 5
'Comparative
OK = No phase separation
ND = Not Determined
PS = Phase separation
[0076] The concentrated aqueous compositions prepared according to the invention are
more stable and/or have a much lower viscosity then the comparative compositions.
Application Tests
[0077] Aqueous solutions were prepared diluting the concentrated compositions of
Example 2-3, 5-8, 12-1 5, 17-1 9 and 2 1-22 with CIPAC D standard water. Soil columns
(with diameter 5 cm) filled with 400 grams of sandy soil were prepared by carefully
packing the soil to provide a bulk density of about 1.7 kg/dm3 or greater. The
composition of sandy soil used in the test was, by weight, 90.75 % sand, 3.75% silt, and
5.5% clay.
[0078] A Waterscout Moisture Sensor by Spectrum Technologies was placed in the
center of the column and buried at a depth of 6 cm, where the entire sensor was
covered with soil. The volumetric water content (VWC%) was recorded using a
Watchdog 1400 Microstation Drip irrigation was achieved dosing 36 mL of aqueous
solution over a six hours period using a 798 MPT Titrino by Metrohm. The water sensor
recorded the VWC% every thirty minutes for a 48 hours period in order to monitor soil
wetting and water retention. Table 6 reports the concentration of the concentrated
compositions and the VWC% after 24 and 48 hours.
Table 6
Comparative
[0079] The reported data demonstrate that the application of the aqueous solutions
prepared diluting the concentrated aqueous composition of the invention increases the
soil water retention to a marked extent. Particularly efficient are the aqueous solutions
prepared from concentrated aqueous compositions comprising depolymerized technical
CMC.
CLAIMS
1) A concentrated aqueous composition comprising:
a. from 10 to 30 % by weight (wt.%) of a depolymerized carboxymethyl cellulose
having a weight average molecular weight of from 10,000 to 80,000 dalton
(Da);
b. from 15 to 50% of a compatibilizer selected from the group consisting of
glycerol and sodium xylene sulfonate; and
c . from 0.5 to 20 % by weight of at least surfactant.
2) The concentrated aqueous composition of Claim 1) comprising:
a. from 12 to 25 wt.% of the depolymerized carboxymethyl cellulose;
b. from 25 to 45 wt.% of the com patibilizer;
c . from 0.5 to 10 wt.%. of at least a surfactant.
3) The concentrated aqueous composition of Claim 1) , wherein the depolymerized
carboxymethyl cellulose has a weight average molecular weight of from 15,000 to
50,000 Da.
4) The concentrated aqueous composition of Claim 1) , wherein the depolymerized
carboxymethyl cellulose is a potassium salt.
5) The concentrated aqueous composition of Claim 1) , wherein the depolymerized
carboxymethyl cellulose is prepared using a technical carboxymethyl cellulose with,
as dry matter, an active substance content of from 55 to 75 wt% and from 25 to
45% of carboxymethylation by-products.
6) The concentrated aqueous composition of Claim 1) , wherein the compatibilizer is
glycerol.
7) The concentrated aqueous composition of Claim 1) , wherein the surfactant is
selected from the group consisting of salts of alkyl sulfosuccinic acids and anionic
esters of alkylpolyglycosides.
8) A method for moisturizing soil comprising:
i) preparing an aqueous solution comprising from 0.1 to 3.5 % by weight of a
concentrated aqueous composition comprising:
a. from 10 to 30 wt.% of a depolymerized carboxymethyl cellulose having a
weight average molecular weight of from 10,000 to 80,000 Da;
b. from 15 to 50 wt.% of a compatibilizer selected from the group consisting
of glycerol and sodium xylene sulfonate; and
c . from 0.5 to 20 wt.% of at least surfactant;
ii) and applying the aqueous solution on the soil.
9) The method for moisturizing soils of Claim 8, wherein the aqueous solution
comprises from 0.5 to 2 wt.% of the concentrated aqueous composition.
10) The method for moisturizing soils of Claim 8, wherein the aqueous solution further
comprises from about 0.01 to about 8 wt.% of agrochemical active ingredients.
11) The method for moisturizing soils of Claim 8, wherein the compatibilizer is glycerol.
12) The method for moisturizing soils of Claim 8, wherein the surfactant is selected
from the group consisting of salts of alkyl sulfosuccinic acids and anionic esters of
alkylpolyglycosides.

Documents

Application Documents

# Name Date
1 201627035444-RELEVANT DOCUMENTS [02-08-2023(online)].pdf 2023-08-02
1 PROOF OF RIGHT [17-10-2016(online)].pdf 2016-10-17
2 Priority Document [17-10-2016(online)].pdf 2016-10-17
2 201627035444-RELEVANT DOCUMENTS [06-08-2022(online)].pdf 2022-08-06
3 Power of Attorney [17-10-2016(online)].pdf 2016-10-17
3 201627035444-IntimationOfGrant02-02-2021.pdf 2021-02-02
4 Form 5 [17-10-2016(online)].pdf 2016-10-17
4 201627035444-PatentCertificate02-02-2021.pdf 2021-02-02
5 Form 3 [17-10-2016(online)].pdf 2016-10-17
5 201627035444-CLAIMS [05-06-2020(online)].pdf 2020-06-05
6 Description(Complete) [17-10-2016(online)].pdf 2016-10-17
6 201627035444-COMPLETE SPECIFICATION [05-06-2020(online)].pdf 2020-06-05
7 Form 8 [26-10-2016(online)].pdf 2016-10-26
7 201627035444-FER_SER_REPLY [05-06-2020(online)].pdf 2020-06-05
8 201627035444-POWER OF ATTORNEY-27-10-2016.pdf 2016-10-27
8 201627035444-FER.pdf 2019-12-06
9 201627035444.pdf 2018-08-11
9 201627035444-FORM 1-27-10-2016.pdf 2016-10-27
10 201627035444-CORRESPONDENCE-27-10-2016.pdf 2016-10-27
10 201627035444-FORM 18 [20-03-2018(online)].pdf 2018-03-20
11 Form 3 [13-04-2017(online)].pdf 2017-04-13
11 Form 3 [22-02-2017(online)].pdf 2017-02-22
12 Form 3 [13-04-2017(online)].pdf 2017-04-13
12 Form 3 [22-02-2017(online)].pdf 2017-02-22
13 201627035444-CORRESPONDENCE-27-10-2016.pdf 2016-10-27
13 201627035444-FORM 18 [20-03-2018(online)].pdf 2018-03-20
14 201627035444-FORM 1-27-10-2016.pdf 2016-10-27
14 201627035444.pdf 2018-08-11
15 201627035444-FER.pdf 2019-12-06
15 201627035444-POWER OF ATTORNEY-27-10-2016.pdf 2016-10-27
16 201627035444-FER_SER_REPLY [05-06-2020(online)].pdf 2020-06-05
16 Form 8 [26-10-2016(online)].pdf 2016-10-26
17 201627035444-COMPLETE SPECIFICATION [05-06-2020(online)].pdf 2020-06-05
17 Description(Complete) [17-10-2016(online)].pdf 2016-10-17
18 201627035444-CLAIMS [05-06-2020(online)].pdf 2020-06-05
18 Form 3 [17-10-2016(online)].pdf 2016-10-17
19 Form 5 [17-10-2016(online)].pdf 2016-10-17
19 201627035444-PatentCertificate02-02-2021.pdf 2021-02-02
20 Power of Attorney [17-10-2016(online)].pdf 2016-10-17
20 201627035444-IntimationOfGrant02-02-2021.pdf 2021-02-02
21 Priority Document [17-10-2016(online)].pdf 2016-10-17
21 201627035444-RELEVANT DOCUMENTS [06-08-2022(online)].pdf 2022-08-06
22 PROOF OF RIGHT [17-10-2016(online)].pdf 2016-10-17
22 201627035444-RELEVANT DOCUMENTS [02-08-2023(online)].pdf 2023-08-02

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