Xanthan gum slurries.
Abstract
High concentration polymer slurries contain up to 60 weight % to 75 weight % xanthan gum in a solvent base treated with suspending agents, dispersants, and thinning agents. Mineral oil, diesel oil, kerosene, alcohols (six to twelve carbons), vegetable oil, ester-alcohols, polyol ethers, and the like may be used as the solvent. The preferred suspending agent is either an organophilic clay or hydroxypropyl cellulose. The preferred dispersant is either an ethoxylated linear alcohol or a fatty acid ester of vegetable , oil or aminal oil. The preferred thinning agent is lecithin. These slurries greatly improve the dispersibility of xanthan gum or any other hydrophilic colloid, such as guar, hydroxypropyl guar, cellulosics, polyacrylamides, and the like.

Term
Term ended
Projected expiry passed 19 March 2000, 26.5 years ago.
- Priority
- Filed
- Published
- Projected expiry
- Today
6 claims: 3 independent, 3 dependent
- 1A high concentration polymer slurry comprising 20-75 weight % of xanthan gum;20-75 weight % hydrophobic solvent base;0.05-0.25 weight % suspending agent;optionally 0.5-1 weight % thinning agent and optionally 0.1-7.0 weight % dispersant.
- 5A slurry as claimed in any preceding claim in which lecithin is included as the thinning agent.
- 6A slurry as claimed in any preceding claim in which ethoxylated linear alcohols or fatty acid esters or vegetable or animal oils are included as the dispersant.
Independent claims3
19 paragraphs in 1 section, as filed
U.S. Patent 3,394,880 discloses the method of thickening alcohol/water solvent systems with xanthan gum. This system is then used to suspend a slurry of alginates. U.S. Patent 3,894,879 discloses the method of thickening alcohol/ water solvent systems with hydroxypropyl cellulose.
Other art includes mechanical and chemical means of improving the dispersibility of xanthan gum and other hydrophilic colloids. Mechanical mixers are not completely effective. Chemical means consist of either treating the colloid with materials such as dialdehydes that delay hydration or slurrying the polymer. The slurries of prior art have two major disadvantages. First, to remain pourable these slurries are limited to polymer concentrations well below 50%. Secondly, volatile solvents in these slurry formulations evaporate when exposed to the atmosphere leaving a crusty film of dried polymer on the surface of the slurry. This crust resists reconstitution into the slurry and is not dispersible in water.
In accordance with the present invention a high concentration polymer slurry comprises 20-75 weight % of fine mesh xanthan gum; 20-75 weight % hydrophobic solvent base; 0.05-0.25 weight % suspending agent; optionally 0.5-1 weight % thinning agent and optionally 0.1-7.0 weight % dispersant. By incorporating a thinning agent such as lecithin, pourable slurries at polymer concentrations exceeding 50% can be obtained. The solvent base used in accordance with the present invention is considerably less volatile than that of the prior art and crust formation can be substantially avoided.
The polymer to be dispersed is preferably xanthan gum. Other similar hydrophilic colloids can be used in these formulations, such as guar gum, hydroxypropyl guar, cellulosics and polyacrylamides.
The total weight of polymer in the final composition is from 20-75 weight %. A finely divided form of polymer is preferable (200-mesh, Tyler screen or finer) to achieve these levels. The sieve opening is 0.074 mm in this 200-mesh screen.
The term "hydrophobic solvents" herein means anhydrous solvents, i.e. those containing less than 0.1% water, that are insoluble in water and do not solvate or swell hydrophilic colloids and that have a melting point of no more than 30°C and a vapor pressure at 20°C of no more than 1 torr.
The solvent base can be one or more of the following: mineral oil, diesel oil, kerosene, C<sub>6-12</sub> alcohols, vegetable oil, ester-alcohols e.g. 2,2,4-trimethyl-pentanediol-1,5-monoisobutyrate (sold under the trade mark Texanol by Eastman Kodak), polyol ethers, e.g. ethylene glycol, polyethylene glycol, propylene glycol, and ethylene glycol monobutyl ether, silicone oils and halogenated solvents. The amount of solvent used is 20-75 weight %. One preferred solvent base is a mixture of diesel oil or kerosene in about eaaal amounts with a mixture of a C<sub>6-10</sub> alcohol. Another preferred solvent is mineral oil.
The rest of the slurry is made up of minor amounts of suspensing agents, dispersants, and thinning agents.
The preferred suspending agent, the amount of which is preferably 0.05-0.25 weight %, is an organophilic clay or hydroxypropyl cellulose. Hydroxypropyl methylcellulose, hydroxybutyl methylcellulose, aluminum/phosphate soaps, aluminum stearate/fatty acid soaps, dehydrated castor oil, fine-mesh fumed silica, quaternary salts of sodium cellulose (Soloid<sup>R</sup>), and similar viscosifiers or thixotropic agents for the beforementioned solvents can also be used.
The preferred dispersants, which are critical only to the most hydrophobic solvent systems, are ethoxylated linear alcohols. Fatty acid esters of vegetable or animal oils, ethoxylated nonyl phenols, and similar surfactants are also acceptable for dispersion of very hydrophobic solvents of the invention. Ethylene glycol monobutyl ether and other glycol ethers are used as dispersants in less hydrophobic solvent systems. When it is present, the amount of dispersant is 0.1-7.0 weight %.
The preferred thinning agent, when used, is lecithin. Lignosulfonate salts, salts of naphthalene formaldehyde condensate and naphthalene sulfonic acid condensate also can be used. The amount of thinning agent is 0.5-1 weight %, preferably 0.85-0.9 weight %.
The percentages of the above components should add up to 100%, so obviously selection of exact amounts from within these ranges can be made by those practising this invention.
The procedure to make the slurries is generally simple: The solvent base is put in a suitable container and agitated. The selected dispersing/suspending agents are added, and the polymer is then slowly added with agitation until a uniform slurry is obtained. Eductors attached to suitable containers equipped with circulating pumps can also acceptably mix the slurries.
) The high-concentration polymer slurries of this invention can be used in any application requiring aqueous polymers. They are particularly applicable in conditions of minimal mixing agitation given to the aqueous fluids to be viscosified. Dosages or formulation of the slurry are dependent upon the end use of the slurry or polymer. High-concentration polymer slurries are particularly useful in oil field applications. When the high-concentration polymer slurry is used, it is mixed into the water to be viscosified under agitation, in a volume sufficient to deliver the desired weight of the polymer, until the polymer is fully hydrated.
This invention is further illustrated by the following examples.
EXAMPLE 1
Mixing Procedure for High Concentration Polymer Slurry
<ul id="ul0001" list-style="none"><li>1. Place solvent in a suitable container.</li><li>2. Agitate solvent with sufficient shear to allow for incorporation of polymer in Step 4.</li><li>3. Add dispersing agents/suspending agents, as required.</li><li>4. Add polymer slowly. Mix until slurry is uniform.</li></ul>
Typical Slurry Formulations
<tables id="tabl0001" num="0001"><img file="EP0016640A1_D0001.tif" /></tables><tables id="tabl0002" num="0002"><img file="EP0016640A1_D0002.tif" /></tables><tables id="tabl0003" num="0003"><img file="EP0016640A1_D0003.tif" /></tables>
3 sheets
Sheet 1 Sheet 2 Sheet 3
Every citation, both waysCites: the store holds 4 of 5
| Document | Relation | Office | Cited during |
|---|---|---|---|
| EP0839888A3 | Cited by | European Patent Office (EPO) | Search report |
| WO2006078266A1 | Cited by | World Intellectual Property Organization (WIPO) | International search |
| WO2013154435A1 | Cited by | World Intellectual Property Organization (WIPO) | International search |
| GB2318797A | Cited by | United Kingdom | Search report |
| EP0839888A2 | Cited by | European Patent Office (EPO) | Search report |
| GB2250761A | Cited by | United Kingdom | Search report |
| EP0243067A3 | Cited by | European Patent Office (EPO) | Search report |
| WO2011080504A1 | Cited by | World Intellectual Property Organization (WIPO) | International search |
| WO2011065831A2 | Cited by | World Intellectual Property Organization (WIPO) | Applicant |
| US8544546B2 | Cited by | United States of America | Applicant |
| US4393151A | Cited by | United States of America | Search report |
| US4454260A | Cited by | United States of America | Search report |
| JPS62257980A | Cited by | Japan | Search report |
| CN104861951A | Cited by | China | Search report |
| EP0039128A2 | Cited by | European Patent Office (EPO) | Search report |
| EP0243067A2 | Cited by | European Patent Office (EPO) | Search report |
| GB2310861A | Cited by | United Kingdom | Search report |
| FR2243228A1 | Cites | France | Search report |
| FR2362893A1 | Cites | France | Search report |
| CH599275A5 | Cites | Switzerland | Search report |
| CH599276A5 | Cites | Switzerland | Search report |
| None | Non-patent | – | Applicant |
11 members in 6 offices
Priority claims4
| Document | Office | Kind | Date |
|---|---|---|---|
| 23511 | United States of America | – | |
| 2351179 | United States of America | A | |
| 23511 | – | – | – |
| US19790023511 | – | – | – |
Members11
| Document | Office | Kind | |
|---|---|---|---|
| NO800808L | Norway | L | |
| EP0016640A1This record | European Patent Office (EPO) | A1 | |
| JPS55137142A | Japan | A | |
| US4312675A | United States of America | A | |
| CA1136355A | Canada | A | |
| KR830001993A | Republic of Korea | A | |
| KR840000398B1 | Republic of Korea | B1 | |
| EP0016640B1 | European Patent Office (EPO) | B1 | |
| NO156130B | Norway | B | |
| NO156130C | Norway | C | |
| JPH0116847B2 | Japan | B2 |
16 legal events, as the office reported them to INPADOC
Over the term
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| Event | Code | |
|---|---|---|
| Gb: patent revoked under art. 102 of the ep convention designating the uk as contracting stateRevokedGBPR | GBPR | |
| Nl: decision of oppositionOppositionNLR2 | NLR2 | |
| Patent revokedRevoked27W | 27W | |
| Patent revokedRevokedORIGINAL CODE: 0009271RDAG | RDAG | |
| Information on the status of an ep patent application or granted ep patentGrantedSTATUS: PATENT REVOKEDSTAA | STAA | |
| Annual fee paid to national office [announced via postgrant information from national office to epo]GrantedPGFP | PGFP | |
| Nl: opposition has been filed with the epoOppositionNLR1 | NLR1 | |
| Opposition filedOpposition26 | 26 | |
| Opposition filedOppositionORIGINAL CODE: 0009260PLBI | PLBI | |
| Annual fee paid to national office [announced via postgrant information from national office to epo]GrantedPGFP | PGFP | |
| Fr: translation filedET | ET | |
| Designated contracting statesAK | AK | |
| (expected) grantORIGINAL CODE: 0009210GRAA | GRAA | |
| Request for examination filed17P | 17P | |
| Designated contracting statesAK | AK | |
| Public reference made under article 153(3) epc to a published international application that has entered the european phaseORIGINAL CODE: 0009012PUAI | PUAI |
Numbers
- Publication
- 0016640
- Publication, DOCDB
- 0016640
- Publication, EPODOC
- EP0016640
- Application
- 80300849
- Application, DOCDB
- 80300849
- Application, EPODOC
- EP19800300849
Titles6
- German
- Breie von Xanthangummi.
- English
- Xanthan gum slurries.
- French
- Bouillies de gomme de xanthane.
- German
- Breie von Xanthangummi
- English
- Xanthan gum slurries
- French
- Bouillies de gomme de xanthane
Classification
- CPC, 3
- C09K8/02
- C08L5/00
- F02B3/06
- IPC, 7
- C08B37 00
- C08J3 02
- C08L5 00
- C08L7 00
- C08L21 00
- C09K8 02
- F02B3 06
Designated states1
- Contracting states, 1
- Netherlands (Kingdom of the)