Patent Application
20180044853
Anthraquinone (AQ) is a solid that is insoluble in water. There is a need to provide a stable and homogeneous suspension of anthraquinone to be used in pulping processes to provide pulp having good papermaking quality. “Pulping” generally refers to the reduction or break-down of a bulk fiber source material into its component fibers. Wood and other plant materials used to make pulp generally contain three main components (apart from water): cellulose fibers (desired for papermaking), lignin (a three-dimensional polymer that binds the cellulose fibers together) and hemicelluloses (shorter branched carbohydrate polymers). Fiber sources include wood fibers, e.g., soft woods and hard woods and mixtures thereof, and non-wood fibers obtained from agricultural productions, such as without limitation, bagasse, wheat straw, rice straw, corn stover (stalks, leaves and husks), soy residuals, coconut tissues, cotton stalks, palm baskets, kenaf, industrial hemp, seed flax straw, textile flax straw, sisal, hesperaloe, rye grass, and mixtures thereof.
A more detailed description of the present disclosure will be rendered by reference to specific embodiments thereof. Other features and advantages of the present disclosure will become apparent from the following detailed description. It should be understood, however, that the detailed description and the specific examples, while indicating the preferred embodiments of the present disclosure, are given by way of illustration only, since various changes and modifications within the spirit and scope of the present disclosure will become apparent to those skilled in the art from this detailed description.
One aspect of the present disclosure relates to an AQ composition comprising AQ, one or more metal ions, a dispersant, a polyglycol, and water, wherein the AQ composition is a substantially homogeneous and stable suspension. One embodiment is a composition comprising anthraquinone, one or more calcium salts, one or more magnesium salts, a salt of diisopropylnaphthalene sulfonate, polyethylene glycol, and water, wherein the composition is a substantially homogeneous and stable suspension.
As used herein, the term “substantially homogeneous and stable” means the AQ in the “substantially homogeneous and stable” suspension is dispersed evenly and the AQ does not settle during extended storage for at least 24 hours. The settling of AQ in the suspension is determined by measuring a % Transparency, as described in the Examples section. A % Transparency of about 25% or less, about 20% or less, about 15% or less, or about 10% or less, indicative of a substantially homogeneous and stable suspension.
As used herein, the term “about” means a range of ±10%, ±5% or ±1%.
The mean particle size of AQ in the AQ composition is about 150 μm or less, about 135 μm or less, about 125 μm or less, about 100 μm or less, about 75 μm or less, about 50 μm or less, about 25 μm or less, about 20 μm or less, about 15 μm or less, about 10 μm or less, about 8 μm or less, about 5 μm or less, about 3 μm or less, about 1 μm or less, 100 μm to about 1 μm, about 75 μm to about 1 μm, about 50 μm to about 1 μm, about 25 μm to about 1 μm, about 20 μm to about 1 μm, about 15 μm to about 1 μm, about 10 μm to about 1 μm, about 8 μm to about 1 μm, about 5 μm to about 1 μm, about 3 μm to about 1 μm, about 100 μm to about 3 μm, about 75 μm to about 3 μm, about 50 μm to about 3 μm, about 25 μm to about 3 μm, about 20 μm to about 3 μm, about 15 μm to about 3 μm, about 10 μm to about 3 μm, about 8 μm to about 3 μm, about 5 μm to about 3 μm, about 100 μm to about 5 μm, about 75 μm to about 5 μm, about 50 μm to about 5 μm, about 25 μm to about 5 μm, about 20 μm to about 5 μm, about 15 μm to about 5 μm, 10 μm to about 5 μm, about 8 μm to about 5 μm, about 100 μm to about 8 μm, about 75 μm to about 8 μm, about 50 μm to about 8 μm, about 25 μm to about 8 μm, about 20 μm to about 8 μm, about 15 μm to about 8 μm, about 10 μm to about 8 μm, about 100 μm to about 10 μm, about 75 μm to about 10 μm, about 50 μm to about 10 μm, about 25 μm to about 10 μm, about 20 μm to about 10 μm, about 15 μm to about 10 μm, about 100 μm to about 15 μm, about 75 μm to about 15 μm, about 50 μm to about 15 μm, about 25 μm to about 15 μm, about 20 μm to about 15 μm, about 100 μm to about 20 μm, about 75 μm to about 20 μm, about 50 μm to about 20 μm, about 25 μm to about 20 μm, about 100 μm to about 25 μm, 75 μm to about 25 μm, about 50 μm to about 25 μm, about 100 μm to about 50 μm, about 75 μm to about 50 μm, or about 100 μm to about 75 μm.
The AQ composition can include a concentration of AQ by weight (wt %) of about 50% or higher, about 30% to about 70%, about 40% to about 60%, about 45% to about 55%, about 50% to about 70%, about 50% to about 55%, or about 50%.
The metal ions, the dispersant, and the polyglycol are water soluble. The one or more metal ions may be monovalent, divalent, trivalent, tetravalent, their salts thereof, and mixtures thereof. The divalent metal ion salts include, without limitation, calcium salt(s) and magnesium salt(s), and they may be any water soluble salt, e.g. chlorides, bromides, nitrates.
In one embodiment, molar ratio of calcium to magnesium in the AQ composition is about 1:1, about 1.1:0.9, or about 0.9:1.1.
The dispersant may be a cationic dispersant, an anionic dispersant, or a nonionic dispersant. In one embodiment, the anionic dispersant is, for example and without limitation, an aromatic sulfonate, such as a naphathalene sulfonate, and preferably a dialkylnaphthalene sulfonate dispersant. Examples of dialkylnaphthalene sulfonate include, without limitation, sodium salts of dialkylnaphthalene sulfonic acid. In one embodiment, the dispersant is sodium diisopropylnaphthalene sulfonate, for example Naxan® DIL dispersant, purchased from the Nease Corporation.
The concentration of the dispersant in the AQ composition is from about 0.1% to about 5%, from about 0.2% to about 3% or from about 0.5 to about 2%.
The polyglycol is a polymer or copolymer of alkylene oxides. In preferred embodiments, the alkylene oxides are ethylene oxide, propylene oxide and butylene oxide. The polyglycols are polyethylene glycol, polypropylene glycol, polybutylene glycol, and mixtures thereof.
The polyglycol comprises a polyglycol having an average molecular weight of from about 200 to about 5,000, from about 500 to about 3,000, from about 750 to about 2,000, or about 1,000. The concentration of a polyglycol in the AQ composition is from about 1% to about 10%, from about 2% to about 8%, from about 3% to about 6%, or about 5%. In one embodiment of the present disclosure, the poiyglycol is polyethylene glycol.
In one embodiment, the molar ratio of AQ to the total calcium in the AQ composition is about 50:1, about 51:1 to about 49:1, or about 55:1 to about 45:1.
The AQ composition comprising 50% AQ (w/w) as disclosed herein has a viscosity of about 500 to about 10,000 cP at 25° C., about 1,000 to about 7,000 cP at 25° C., or less than about 2,000 to about 5,000 cP at 25° C.
The AQ composition as disclosed herein remains stable at room temperature in a closed container for about 24 hours or longer, about 1 week or longer, about 1 month or longer, about 3 months or longer, or about 6 months or longer. In some embodiments, the AQ composition is stable up to about a year. The AQ composition is generally more stable than a composition comprising the same components without the metal ion salts.
Another aspect of the present disclosure relates to an AQ composition comprising AQ having a mean particle size of about 150 μm or less, one or ore metal ions, a dispersion, a polyglycol, and water. One embodiment is a composition comprising AQ having a mean particle size of about 150 μm or less, one or more calcium salts, one or more magnesium salts, a salt of diisopropylnaphthalene sulfonate, polyethylene glycol, and water. In certain embodiments, the mean particle size of AQ in the AQ composition is about 150 μm or less, about 135 μm or less, about 125 μm or less, about 100 μm or less, about 75 μm or less, about 50 μm or less, about 25 μm or less, about 20 μm or less, about 15 μm or less, about 10 μm or less, about 8 μm or less, about 5 μm or less, about 3 μm or less, about 1 μm or less, 100 μm to about 1 μm, about 75 μm to about 1 μm, about 50 μm to about 1 μm, about 25 μm to about 1 μm, about 20 μm to about 1 μm, about 15 μm to about 1 μm, about 10 μm to about 1 μm, about 8 μm to about 1 μm, about 5 μm to about 1 μm, about 3 μm to about 1 μm, about 100 μm to about 3 μm, about 75 μm to about 3 μm, about 50 μm to about 3 μm, about 25 μm to about 3 μm, about 20 μm to about 3 μm, about 15 μm to about 3 μm, about 10 μm to about 3 μm, about 8 μm to about 3 μm, about 5 μm to about 3 μm, about 100 μm to about 5 μm, about 75 μm to about 5 μm, about 50 μm to about 5 μm, about 25 μm to about 5 μm, about 20 μm to about 5 μm, about 15 μm to about 5 μm, 10 μm to about 5 μm, about 8 μm to about 5 μm, about 100 μm to about 8 μm, about 75 μm to about 8 μm, about 50 μm to about 8 μm, about 25 μm to about 8 μm, about 20 μm to about 8 μm, about 15 μm to about 8 μm, about 10 μm to about 8 μm, about 100 μm to about 10 μm, about 75 μm to about 10 μm, about 50 μm to about 10 μm, about 25 μm to about 10 μm, about 20 μm to about 10 μm, about 15 μm to about 10 μm, about 100 μm to about 15 μm, about 75 μm to about 15 μm, about 50 μm to about 15 μm, about 25 μm to about 15 μm, about 20 μm to about 15 μm, about 100 μm to about 20 μm, about 75 μm to about 20 μm, about 50 μm to about 20 μm, about 25 μm to about 20 μm, about 100 μm to about 25 μm, 75 μm to about 25 μm, about 50 μm to about 25 μm, about 100 μm to about 50 μm, about 75 μm to about 50 μm, or about 100 μm to about 75 μm.
Yet another aspect of the invention relates to a method for preparing the AQ composition as disclosed herein, comprising:
a. providing a first solution comprising one or more metal ion, a dispersant, and a polyglycol; and
b. adding AQ with agitation to the first solution at a speed such that the composition remains a substantially homogeneous and stable suspension, and the mean particle size of AQ remains about 150 μm or less.
The AQ composition is stable after being left at room temperature in a closed container for at least about 24 hours, greater than about 1 week, greater than about 1 month, greater than about 3 months, or about a year.
The metal ion salts (e.g., calcium and magnesium salts), the dispersant (e.g., a salt of diisopropylnaphthalene sulfonate), and the polyglycol (e.g., polyethylene glycol), may be added separately or together into water to provide the first solution. Alternatively, the metal ion salts, the dispersant, and the polyglycol may be provided as individual solutions and then mixed together to provide the first solution.
AQ may be added as a powder having a mean particle size of about 150 μm or less, about 135 μm or less, about 125 μm or less, about 100 μm or less, about 75 μm or less, about 50 μm or less, about 25 μm or less, about 20 μm or less, about 15 μm or less, about 10 μm or less, about 8 μm or less, about 5 μm or less, about 3 μm or less, about 1 μm or less, 100 μm to about 1 μm, about 75 μm to about 1 μm, about 50 μm to about 1 μm, about 25 μm to about 1 μm, about 20 μm to about 1 μm, about 15 μm to about 1 μm, about 10 μm to about 1 μm, about 8 μm to about 1 μm, about 5 μm to about 1 μm, about 3 μm to about 1 μm, about 100 μm to about 3 μm, about 75 μm to about 3 μm, about 50 μm to about 3 μm, about 25 μm to about 3 μm, about 20 μm to about 3 μm, about 15 μm to about 3 μm, about 10 μm to about 3 μm, about 8 μm to about 3 μm, about 5 μm to about 3 μm, about 100 μm to about 5 μm, about 75 μm to about 5 μm, about 50 μm to about 5 μm, about 25 μm to about 5 μm, about 20 μm to about 5 μm, about 15 μm to about 5 μm, 10 μm to about 5 μm, about 8 μm to about 5 μm, about 100 μm to about 8 μm, about 75 μm to about 8 μm, about 50 μm to about 8 μm, about 25 μm to about 8 μm, about 20 μm to about 8 μm, about 15 μm to about 8 μm, about 10 μm to about 8 μm, about 100 μm to about 10 μm, about 75 μm to about 10 μm, about 50 μm to about 10 μm, about 25 μm to about 10 μm, about 20 μm to about 10 μm, about 15 μm to about 10 μm, about 100 μm to about 15 μm, about 75 μm to about 15 μm, about 50 μm to about 15 μm, about 25 μm to about 15 μm, about 20 μm to about 15 μm, about 100 μm to about 20 μm, about 75 μm to about 20 μm, about 50 μm to about 20 μm, about 25 μm to about 20 μm, about 100 μm to about 25 μm, 75 μm to about 25 μm, about 50 μm to about 25 μm, about 100 μm to about 50 μm, about 75 μm to about 50 μm, or about 100 μm to about 75 μm. In certain embodiments, AQ is added slowly in small portions with agitation to enable rapid dispersion of AQ in the first solution.
In one embodiment, the AQ composition is prepared according to the flow chart shown in
a. adding water of a pre-determined amount into a tank equipped with an agitator;
b. adding the dispersant (e.g., a dialkylnaphthalene sulfonate, such as sodium diisopropylnaphthalene sultanate) of a pre-determined amount into the water, and stirring until the dispersant dissolves;
c. adding metal ion salt(s) of a pre-determined amount into the dispersant solution prepared in step b., and stirring until all salt(s) dissolve, wherein the metal ion salt(s) may be added together or separately;
d. adding a polyglycol (e.g., polyethylene glycol) of a pre-determined amount into the solution prepared in step c., and stirring until the polyglycol dissolves;
e. adding AQ of a pre-determined amount into the solution prepared in step (d) slowly and in small portions with agitation to provide a substantially homogeneous AQ composition; and
f. optionally, adding a dye of a pre-determined amount into the substantially homogeneous AQ composition of step e. to provide a substantially homogeneous AQ composition with dye.
The above steps b., c., d., and f., can be added to the water in any order, and preferably AQ is added in the final step to avoid the formation of clumps. Other compounds that can be used in a pulping process can be added to the substantially homogeneous AQ composition.
AQ, PEG 1000, NAXAN-DIL dispersant, Zetasperse® 179 and 3600 dispersant, DOWFAX 2A1 and 8390 dispersant, and C6L Petro ULF dispersant, Aerosol® OS dispersant, and CaCl2 and MgCl2.6H20 were purchased from commercially available sources.
After mixing, samples of suspensions of the different AQ compositions were slowly poured into scintillation vials (27.5 mm outer diameter, 72.7 mm height without cap). The headspace above the surface of the sample remained clear. The vial was capped tightly. A measurement was taken on Day 0, as well as periodically over weeks and months, after letting the samples sit at room temperature.
A % Transparency was calculated. The % Transparency is the fraction of the sample in the vial that is transparent or clear (i.e., the supernatant). Measuring the total height of the AQ composition and the height of the supernatant will yield % Transparency.
% Transparency=100×(supernatant height/total height of the AQ composition)
The present application claims priority to U.S. Provisional Application No. 61/474,035, filed Apr. 11, 2011, the disclosure of which is incorporated by reference herein in its entirety. AQ compositions having a formulation listed in Table 1 were prepared according to the block flow diagram in
1. Naxan DIL dispersant (34-36% actives in aqueous solution from Neese Co. Ohio, USA) was added into water of the desired amount. The mixture was stirred for about 10 to 15 minutes until the Naxan DIL dissolved completely;
2. Magnesium chloride hexahydrate was added to the mixture of step 1 with agitation, and stirred for about 5 to about 10 minutes until the magnesium chloride dissolved completely.
3. Anhydrous calcium chloride was added to the mixture of step 2 with agitation, and stirred for about 5 to about 10 minutes until the calcium chloride dissolved completely.
4. PEG 1000 (50% aqueous solution, ˜1,000 average molecular weight) was added to the mixture of step 3 with agitation, and stirred for about 10 to about 15 minutes until the PEG 1000 dissolved completely.
5. AQ powder was added slowly in small portions with agitation to provide a well-dispersed suspension, and stirred for about 15 to about 20 minutes to ensure the AQ was well-dispersed. The dispersion obtained was visually homogeneous.
The calcium chloride and magnesium chloride used in the formulation can be anhydrous or hydrates. The amount of water used in the formulation is adjusted accordingly.
An AQ composition was prepared according to the method described in Example 1.
Several AQ compositions were prepared according to the method described in Example 1, except that the NAXAN DIL dispersant was replaced with other dispersants listed in Table 2. The % of each dispersant is shown in Table 2 and was kept the same in the AQ compositions.
Table 2 shows that dispersants affected the homogeneity and viscosity of the resulting AQ compositions, AQ dispersed quickly into solution without clumping or foaming with the desired viscosity using the anionic dispersant, e.g., sodium diisopropylnaphthalene sulfonate (NAXAN DIL dispersant). Another anionic dispersant, Petro ULF Liquid dispersant, had similar effect as the NAXAN DIL dispersant. Aerosol OS dispersant, a powder, is also an anionic dispersant and, while no specific observations were made, it should have similar effect as the NAXAN DIL dispersant. Compared to the AQ composition with NAXAN DIL dispersant, the AQ composition with the non-ionic dispersant, ZetaSperse® 179 dispersant, was similar except it was more viscous.
Two samples (Samples A and B) were prepared according to the method described in Example 1, except that in one sample (Sample B) the calcium and magnesium salts were left out. The difference was made up with water (i.e., 37.14 g H2O instead of 35.61 g H2O). The majority of AQ particles that settled happened in the first 7 days after preparation. The AQ composition showed insignificant changes (less than 5% change of the % Transparency) at various months (e.g., 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, or 12 months) from the eighth day after preparation.
In
AQ compositions were prepared according to Example 1, except that the PEG 1000 was left out, and the level of dispersant was increased. In Example 1, the AQ composition formulation contained 1% of the active ingredient contained in NAXAN DIL dispersant (i.e., the AQ composition formulation contains 2.86% NAXAN DIL dispersant and at a 35% aqueous solution, the final concentration of the active ingredient is 1%). The amount of active ingredient in the AQ compositions was increased to 2% (DIL-2) and 5% (DIL-5), respectively, in order to determine if the dispersants could compensate for the absence of PEG1000. The two samples (DIL-2-A and DIL-2-B) on the left in
AQ compositions were prepared according to Example 1 using AQ of different particle sizes. The AQ used had mean particle sizes of 3 μm, 5 μm, and 135 μm, respectively.
The present application claims priority to U.S. Provisional Application No. 62/130,950, filed Mar. 10, 2015, the disclosure of which is incorporated by reference herein in its entirety.
| Filing Document | Filing Date | Country | Kind |
|---|---|---|---|
| PCT/US16/20957 | 3/4/2016 | WO | 00 |
| Number | Date | Country | |
|---|---|---|---|
| 62130950 | Mar 2015 | US |
