Personal care products comprising microfibrous cellulose and methods of making the same

Information

  • Patent Grant
  • 10030214
  • Patent Number
    10,030,214
  • Date Filed
    Monday, May 11, 2015
    9 years ago
  • Date Issued
    Tuesday, July 24, 2018
    5 years ago
Abstract
Surfactant systems are provided using microfibrous cellulose to suspend particulates. In one embodiment the surfactant system includes a microfibrous cellulose at a concentration from about 0.05% to about 1.0% (w/w), a surfactant at a concentration of about 5% to about 50% (w/w active surfactant), and a particulate. Also provided herein are methods for preparing surfactant systems including microfibrous cellulose.
Description
BACKGROUND

Surfactant-based products such as body washes, shampoos, dishwashing detergents, laundry detergents, and automotive detergents, among others, are often thickened by utilizing high concentration of surfactants, by combining viscosity synergistic surfactants, or by combining the surfactants with small amounts of salts, such as sodium salts. These formulations result in high viscosity products that appear rich and smooth but they are limited in that they do not provide sufficient low shear viscosity to allow for suspension of particles. Such particulates might include aesthetic agents (decorative beads, pearlescents, air bubbles, fragrance beads, etc.) or active ingredients (insoluble enzymes, encapsulated actives such as moisturizers, zeolites, exfoliating agents (e.g. alpha hydroxyl and/or glycolic acids or polyethylene beads), vitamins (e.g. vitamin E)) etc. or both.


Conventional thickeners and suspension aids such as xanthan gum, carboxymethyl cellulose (CMC), hydroxyethylcellulose (HEC), hydroxypropylmethylcellulose (HPMC), and many types of polyacrylates do not function well in surfactant-thickened systems and often lead to a loss of transparency due to clouding, gelling, and/or phase separation or lack sufficient suspension properties. For example, xanthan gum imparts excellent suspension properties in certain body wash formulations with low surfactant-thickening but the gum often loses its suspension ability in systems with high surfactant thickening, usually resulting in a hazy, irregular appearance, and a grainy or lumpy texture. Cellulosic products (CMC, HEC, HPMC, etc.), as another example of conventional thickeners, provide unreliable suspension and have significant limitations with respect to surfactant compatibilities. Acrylates systems are common, however, these systems do not always achieve a sufficient clarity level, require high concentrations of polymer, and are not considered natural. Salts are often capable of increasing high shear viscosity in surfactant-thickened systems but do not impart long-term suspension ability.


There is presently a desire in the consumer products industry to provide for transparent surfactant-thickened systems with particulates suspended therein, as well as a suspension aid for high surfactant systems where many alternative thickeners will not function.


It has been discovered that microfibrous cellulose (MFC), bacterially derived or otherwise, can be used to provide suspension of particulates in surfactant-thickened systems as well as in formulations with high surfactant concentrations. It was also discovered that the MFC may be used for this purpose with or without co-agents. When bacterially-derived microfibrous cellulose is utilized, cellular debris can be eliminated which results in transparent solutions at typical use levels.


The microfibrous cellulose appears unaffected by the surfactant micelle development and maintains good suspension in these systems. Microfibrous cellulose is unique in its ability to function in these systems in large part because it is dispersed rather than solubilized, thereby achieving the desired suspension properties in formulations that would otherwise display the hazing and/or precipitation often seen using alternative solubilized polymers.


SUMMARY OF THE INVENTION

Surfactant systems comprising microfibrous cellulose are described. “Surfactant systems” is intended to include but is not limited to surfactant-thickened and high surfactant systems. Microfibrous cellulose (MFC) includes MFC prepared by microbial fermentation or MFC prepared by mechanically disrupting/altering cereal, wood, or cotton-based cellulose fibers. When bacterially-derived microfibrous cellulose is utilized, cellular debris can be eliminated which results in transparent solutions at typical use levels. The present invention utilizes surfactants to achieve a very thick (highly viscous) system at high shear rates with particulates suspended therein by using microfibrous cellulose.


The surfactant concentration of these systems ranges from about 5% to about 50% (w/w active surfactant) wherein the specific concentration is product dependent. Body washes typically contain about 5% to about 15% (w/w) surfactant, dishwashing liquids typically contain about 20% to about 40% (w/w) surfactant (with 40% being an “ultra” concentrated product), and laundry detergents typically contain about 15% to about 50% (w/w) surfactant.


The MFC is present at concentrations from about 0.05% to about 1.0%, but the concentration will depend on the desired product. For example, while about 0.06% (w/w) MFC is preferred for suspending small alginate beads in a body wash, about 0.075% is preferred for suspending air bubbles in a body wash, and about 0.150% (w/w) is preferred for suspending either air bubbles or beads in a system containing about 40% (w/w) surfactant. Furthermore, the concentration of MFC will be adjusted accordingly if a highly transparent system is desired. Specifically, a very transparent body wash at about 5% to about 15% (w/w active surfactant) can be achieved with a MFC level of from about 0.055 to about 0.25% (w/w active surfactant).


Particulates to be suspended could include aesthetic agents (decorative beads, pearlescents, air bubbles, fragrance beads, etc.) or active ingredients (insoluble enzymes, encapsulated actives such as moisturizers, zeolites, exfoliating agents (e.g. alpha hydroxyl and/or glycolic acids or polyethylene beads), vitamins (e.g. vitamin E) etc. or both. Other suitable particulates would be apparent to one of skill in the art.


The invention is also directed to the use of co-agents and/or co-processing agents such as CMC, xanthan, and/or guar gum with the microfibrous cellulose in the surfactant systems described herein. Microfibrous cellulose blends are microfibrous cellulose products which contain co-agents. Two blends are described MFC, xanthan gum, and CMC in a ratio of 6:3:1, and MFC, guar gum, and CMC in a ratio of 3:1:1. These blends allow MFC to be prepared as a dry product which can be “activated” with high shear or high extensional mixing into water or other water-based solutions. “Activation” occurs when the MFC blends are added to water and the co-agents/co-processing agents are hydrated. After the hydration of the co-agents/co-processing agents, high shear is generally then needed to effectively disperse the microfibrous cellulose fibers to produce a three-dimensional functional network that exhibits a true yield point. Unexpectedly, the co-agent and/or co-processing agents CMC, xanthan, and/or guar gum present in these microfibrous cellulose blends appear to remain solubilized (after activation in water) in many high surfactant formulations despite their general lack of compatibility in the high surfactant systems, most likely due to the low use level of these polymers in these formulations with MFC.


The invention is further directed to methods of making the surfactant systems described, with or without co-agents and/or co-processing agents.





BRIEF DESCRIPTION OF THE DRAWINGS


FIG. 1 provides an illustration of a microfibrous cellulose blend in a surfactant thickened body wash with bubbles suspended therein.



FIG. 2 provides an illustration of a microfibrous cellulose blend in a surfactant thickened body wash with alginate beads suspended therein.



FIG. 3 provides two illustrations of microfibrous cellulose blends in ultra concentrated dish soaps.



FIG. 4 provides an illustration of a microfibrous cellulose blend in an ultra concentrated liquid laundry detergent.



FIG. 5 provides an illustration of a microfibrious cellulose in an ultra concentrated liquid laundry detergent with air bubbles suspended therein.





DETAILED DESCRIPTION

Body wash formulations demonstrating both the surfactant-thickening and suspension properties using a 0.125% MFC/xanthan/CMC (6:3:1) blend are described in Examples 1 and 2. The body washes exhibit very good clarity and the ability to suspend air bubbles and beads.


Manual dishwashing liquid and liquid laundry detergents, which have a higher surfactant level than found in body washes, are also described. Manual dishwashing liquids with alginate suspended therein are described in Example 3.


A liquid laundry detergent with fragrance beads suspended therein is described in Example 4.


A wet-cake form of microfibrous cellulose was used in Example 5 for preparing a high surfactant system comprising a concentrated liquid laundry soap with air bubbles suspended therein.


EXAMPLE 1

A liquid body wash with air bubbles was prepared. FIG. 1 displays the clarity and suspensive qualities of this system. The resulting body wash exhibited very thick surfactant rheology based on visual inspection, possessed the ability to suspend air bubbles, and a yield value of about 3.4 Pa (as measured with a Brookfield® Yield Rheometer).


Step A: Deionizied water, 10% NaCl solution, and Kathon® CG were added to a small Oster® mixing jar. Microfibrous cellulose (MFC/xanthan/CMC 6:3:1 blend) was added to the top of the water and then the Oster® mixer blade was assembled and the combination was mixed at top speed for 5 minutes (“Liquify” speed).


Step B: The contents were transferred to a 400 mL tall-form beaker with a paint mixing blade. Sodium laureth sulfate (JEELATE® ES-3) was added to the solution described in Step A and mixed at about 1000 rpm for 5 minutes. Sodium cocamidopropyl betaine (JEETERIC® CAB-LC) was then added to the mix and mixed an additional 5 minutes at 1000 rpm. Fragrance was then added.


Step C: Cocamide DEA was added to the solution described in Step B. Thickening occurred as more DEA was added. Citric Acid was then added as a 50% solution to reduce the pH to the desired level (pH 5.5 in this case). The contents were removed form the mixer. Air entrained during mixing was stabilized by the presence of the MFC/xanthan/CMC 6:3:1 blend.









TABLE 1







Body Wash Shower Gel










Process Step
Ingredient
% (w/w)
Grams













A
Deionized Water
54.775
219.10



Microfibrous Cellulose blend
0.125
.50



(MFC/xanthan/CMC 6:3:1 blend)


A
10% NaCl Solution
5.00
20.00


A
Kathon CG
0.10
0.40


B
Jeeteric ® CAB-LC sodium
7.00
28.00



cocamidopropyl betain


B
Jeelate ® ES-3 Sodium Laureth
25.00
100.00



Sulfate


B
Fragrance
1.00
4.00


C
Cocamide DEA
7.00
28.00


C
Citric Acid (50% solution)
To Suit
To Suit


Totals

100.00
400.00









EXAMPLE 2

A body wash was prepared as described in Example 1 but incorporated the suspension of beads instead of air bubbles. Alginate beads were added as the conclusion of step C. A visual representation of this embodiment can be seen in FIG. 2.


EXAMPLE 3

High surfactant systems were prepared using manual dishwashing liquid and laundry detergent. Alginate beads or air was suspended in the solutions. Palmolive Ultra® dish soap was diluted in half to make a “normal” concentration dish soap. A concentrate was first prepared containing 0.25% microfibrous cellulose blend (MFC/xanthan/CMC 6:3:1 blend) in deionized water. The concentrate was made by mixing the solution in an Oster® blender at “liquefy” (top speed) for 5 minutes. The microfibrous cellulose mixture was then diluted 1:1 with Palmolive Ultra ® detergent or Dawn Ultra® detergent (the Palmolive® contained 0.1% triclosan) using a paint mixing or propeller blade. The dish soap was added to the microfibrous cellulose solution while mixing. Excellent clarity and suspension of air and/or alginate beads were achieved for both the Palmolive Ultra® detergent and Dawn Ultra® detergent samples. The microfibrous cellulose diluted well notwithstanding the relative low shear of the paint or propeller mixing blade. The yield point for these solutions was about 2.5 Pa. A visual representation can be found in FIG. 3.


EXAMPLE 4

A high surfactant system using a concentrated liquid laundry soap was prepared. “All Small and Mighty® three times concentrated” detergent was used. A 0.25% microfibrous cellulose blend (MFC/xanthan/CMC 6:3:1 blend) concentrate was activated in distilled water with an Oster® blender set at top speed (liquefy). Mix time was 5 minutes. The microfibrous cellulose solution was diluted 1:1 with All Small and Mighty® three times concentrated detergent. Very good clarity and suspension was achieved for the dilution resulting in a yield point of 0.62 Pa. The detergents were put in a 45° C. oven to assess heat stability and showed excellent stability with no loss in clarity or suspension over 4 weeks of aging. A visual representation can be seen in FIG. 4.


EXAMPLE 5

A high surfactant system using a concentrated liquid laundry soap was prepared using the wet-cake version of microfibrous cellulose. “All Small and Mighty® three times concentrated” detergent was used. A 1.56% wet-cake microfibrous cellulose concentrate was activated in distilled water with an Oster® blender set at top speed (liquefy). Mix time was 5 minutes. The activity (% solids) of this wet-cake form of MFC was about 16% so the active MFC level was about 0.25% in the concentrate. The microfibrous cellulose solution was diluted 1:1 with All Small and Mighty® three times concentrated detergent. Very good suspension was achieved for the dilution resulting in a yield point of 13 Pa. A visual representation can be seen in FIG. 5.

Claims
  • 1. A personal care product comprising: an aqueous personal care composition comprising a surfactant system that comprises,a microfibrous cellulose present in the aqueous personal care composition at a concentration from about 0.05% to about 1.0% (w/w),an anionic surfactant present in the aqueous personal care composition at a concentration from about 5% to about 20% (w/w active surfactant),a suspended particulate, anda salt.
  • 2. The personal care product of claim 1, wherein the microfibrous cellulose is present in the aqueous personal care composition at a concentration from about 0.05% to about 0.15% (w/w).
  • 3. The personal care product of claim 1, wherein the microfibrous cellulose is present in the aqueous personal care composition at a concentration from about 0.06% to about 0.09% (w/w).
  • 4. The personal care product of claim 1, wherein the anionic surfactant is present in the aqueous personal care composition at a concentration from about 5% to about 15% (w/w active surfactant).
  • 5. The personal care product of claim 1, wherein the surfactant system further comprises one or more co-agents.
  • 6. The personal care product of claim 5, wherein the microfibrous cellulose and the one or more co-agents is a blend of microfibrous cellulose, guar gum, and carboxymethyl-cellulose.
  • 7. The personal care product of claim 5, wherein the microfibrous cellulose and one or more co-agents is a blend of microfibrous cellulose, xanthan gum, and carboxymethyl-cellulose.
  • 8. The personal care product of claim 1, wherein the aqueous personal care composition is clear.
  • 9. A method for preparing an aqueous personal care composition comprising a microfibrous cellulose, an anionic surfactant, a suspended particulate, and a salt, said method comprising: combining a powdered microfibrous cellulose with water and mixing with high shear;adding the anionic surfactant and then mixing; adding the salt and then mixing; andadding particulates followed by mixing,wherein the microfibrous cellulose is present in the aqueous personal care composition at a concentration from about 0.05% to about 1.0% (w/w), the anionic surfactant is present in the aqueous personal care composition at a concentration from about 5% to about 50% (w/w active surfactant).
  • 10. The method of claim 9, further comprising adding one or more co-agents and then mixing, wherein the aqueous personal care composition further comprises the one or more co-agents.
  • 11. A personal care product comprising: an aqueous personal care composition comprising a surfactant system that comprises,a microfibrous cellulose present in the aqueous personal care composition at a concentration from about 0.05% to about 1.0% (w/w),an anionic surfactant present in the aqueous personal care composition at a concentration from about 20% to about 50% (w/w active surfactant), anda suspended particulate.
  • 12. The personal care product of claim 11, wherein the microfibrous cellulose is present in the aqueous personal care composition at a concentration from about 0.05% to about 0.15% (w/w).
  • 13. The personal care product of claim 11, wherein the microfibrous cellulose is present in the aqueous personal care composition at a concentration from about 0.06% to about 0.09% (w/w).
  • 14. The personal care product of claim 11, wherein the surfactant is present in the aqueous personal care composition at a concentration from about 20% to about 40% (w/w active surfactant).
  • 15. The personal care product of claim 11, wherein the surfactant system further comprises one or more co-agents.
  • 16. The personal care product of claim 15, wherein the microfibrous cellulose and co-agent is a blend of microfibrous cellulose, guar gum, and carboxymethyl-cellulose.
  • 17. The personal care product of claim 15, wherein the microfibrous cellulose and co-agent is a blend of microfibrous cellulose, xanthan gum, and carboxymethyl-cellulose.
  • 18. The personal care product of claim 11, wherein the aqueous personal care composition is clear.
  • 19. A method for preparing an aqueous personal care composition comprising a microfibrous cellulose, an anionic surfactant, and a suspended particulate, said method comprising: combining a powdered microfibrous cellulose with water and mixing with high shear;adding the anionic surfactant and then mixing; andadding particulates followed by mixing,wherein the microfibrous cellulose is present in the aqueous personal care composition at a concentration from about 0.05% to about 1.0% (w/w), the anionic surfactant is present in the aqueous personal care composition at a concentration from about 20% to about 50% (w/w active surfactant).
  • 20. The method of claim 19, further comprising adding one or more co-gents and then mixing, wherein the aqueous personal care composition further comprises the one or more co-agents.
CROSS-REFERENCE TO RELATED APPLICATIONS

The present application is a continuation of U.S. patent application Ser. No. 11/557,622, filed on Nov. 8, 2006, which is incorporated herein by reference in its entirety.

US Referenced Citations (59)
Number Name Date Kind
3858854 Win et al. Jan 1975 A
3975536 Stevenson et al. Aug 1976 A
4378381 Turbak et al. Mar 1983 A
4379059 Hockey et al. Apr 1983 A
4452722 Turbak et al. Jun 1984 A
4483743 Turbak et al. Nov 1984 A
4500546 Turbak et al. Feb 1985 A
5087471 Combes et al. Feb 1992 A
5441753 McGinley et al. Aug 1995 A
5951910 Skaggs Sep 1999 A
5998349 Guillou Dec 1999 A
6224663 Cantiani et al. May 2001 B1
6231651 Schultz et al. May 2001 B1
6241812 Smith et al. Jun 2001 B1
6302209 Thompson et al. Oct 2001 B1
6306207 Cantiani et al. Oct 2001 B2
6846785 Patel et al. Jan 2005 B2
6967027 Heux et al. Nov 2005 B1
7776807 Canto Aug 2010 B2
7888308 Swazey Feb 2011 B2
7981855 Palla-Venkata et al. Jul 2011 B1
7994111 Caggioni et al. Aug 2011 B2
8097574 Heath et al. Jan 2012 B2
8361239 Bettiol et al. Jan 2013 B2
8470755 Tajmamet et al. Jun 2013 B1
8541355 Fleckenstein et al. Sep 2013 B2
8546318 D'Ambrogio et al. Oct 2013 B2
8642529 Palla-Venkata Feb 2014 B2
8772359 Swazey Jul 2014 B2
9045716 Swazey Jun 2015 B2
9506018 D'Ambrogio Nov 2016 B2
9534191 Fernandez-Prieto Jan 2017 B2
9862916 Van Engelen Jan 2018 B2
20030109391 Midha et al. Jun 2003 A1
20030162689 Schymitzele Aug 2003 A1
20040267006 Yamane Dec 2004 A1
20050119151 Mayer et al. Jun 2005 A1
20060029625 Niebauer Feb 2006 A1
20060083761 Yoshimi et al. Apr 2006 A1
20060110416 Ryles et al. May 2006 A1
20060127345 Hilvert et al. Jun 2006 A1
20060281859 Suzuki et al. Dec 2006 A1
20070027108 Yang et al. Feb 2007 A1
20070197779 Yang et al. Aug 2007 A1
20080108541 Swazey May 2008 A1
20080108714 Swazey et al. May 2008 A1
20090306254 van der Wielen et al. Dec 2009 A1
20100009891 Canto et al. Jan 2010 A1
20100016575 Yang et al. Jan 2010 A1
20110039744 Heath et al. Feb 2011 A1
20110059883 Swazey et al. Mar 2011 A1
20110104096 Swazey May 2011 A1
20120122998 Palla-Venkata et al. May 2012 A1
20120309662 D'Ambrogio et al. Dec 2012 A1
20130025500 Jones Jan 2013 A1
20130274149 Lafitte et al. Oct 2013 A1
20140128480 Swazey et al. May 2014 A1
20150240191 Swazey Aug 2015 A1
20150240193 Swazey Aug 2015 A1
Foreign Referenced Citations (17)
Number Date Country
0859011 Aug 1998 EP
2379223 May 2003 GB
62172099 Jul 1987 JP
6043600 Jun 1994 JP
09165402 Jun 1997 JP
11255806 Sep 1999 JP
2000026229 Jan 2000 JP
2003095904 Apr 2003 JP
0047626 Aug 2000 WO
0105837 Jan 2001 WO
0105838 Jan 2001 WO
0218486 Mar 2002 WO
03062361 Jul 2003 WO
03085074 Oct 2003 WO
9940153 Oct 2003 WO
2004074420 Sep 2004 WO
2005048986 Jun 2005 WO
Non-Patent Literature Citations (13)
Entry
Machine Translation of Publ. No. JP 11-255806 A, published Sep. 1999, Japan Patent Office, Tokyo, Japan, online at https://dossier1.j-platpat.inpit.go.jp/tri/all/odse/ODSE_GM101_Top.action (Downloaded Jun. 26, 2017), pp. 1-13.
Machine Translation of Publ. No. JP 09-165402 A, published Jun. 1997, Japan Patent Office, Tokyo, Japan, online at https://dossier1.j-platpat.inpit.go.jp/tri/all/odse/ODSE_GM101_Top.action (Downloaded Jun. 26, 2017), pp. 1-24.
Ash, Michael Ash, Irene (2005:2008). Handbook of Industrial Surfactants (4th Edition), pp. 1596 & 5487, Synapse Information Resources, Inc., Online version available at: http://app.knovel.com/hotlink/toc/id:kpHISE000G/handbook-industrial-surfactants, (downloaded Oct. 17, 2013).
Gangolli, S. (2005). Dictionary of Substances and Their Effects (DOSE, 3rd Electronic Edition). Royal Society of Chemistry, p. C381. Online version available at http://app.knovel.com/hotlink/toc/toc/id:kpDSTEDOS3/dictionary-substances (downloaded Oct. 17, 2013).
Jeen International Corp., Jeeteric CAB-LC Coco-amido-N-propyl-Betaine, Technical data sheet, (revision date Mar. 1, 2001), p. 1 of 1, online @ http://www.jeen.com/technical/SPEC%20JEETERIC%20CAB-LC.pdf (downloaded Oct. 17, 2013).
Australian Examination Report of Singapore 200903483-6, dated Jan. 25, 2011, Australian Patent Office, pp. 1-7.
Extended European Search Report/Opinion of EP07863824.4, dated Mar. 9, 2011, EPO, The Hague, pp. 1-13.
Chinese Office Action Application No. 200780041617.6 dated Dec. 21, 2010.
PCT Search Report for PCT/US07/83422 dated Mar. 19, 2008.
PCT Search Report for PCT/US07/87229 dated Apr. 9, 2008.
Milton, Rosen J., “Surfactants and Interfacial Phenomena”, Third Edition, (Published Online: Aug. 31, 2004), John Wiley & Sons, Inc., Hoboken, New Jersey, USA, pp. 105-106, 120-121, 127-130, 138-139.
European Search Report/Opinion of EP07865575, dated Dec. 1, 2011, EPO, The Hague, pp. 1-9.
PCT/US2007/087216, Written Opinion of the International Searching Authority, dated May 6, 2008, 4 pages.
Related Publications (1)
Number Date Country
20150240191 A1 Aug 2015 US
Continuations (1)
Number Date Country
Parent 11557622 Nov 2006 US
Child 14709115 US