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WO1997032003A1 - Procede de production de granules detergents de haute densite - Google Patents

Procede de production de granules detergents de haute densite Download PDF

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Publication number
WO1997032003A1
WO1997032003A1 PCT/US1996/002848 US9602848W WO9732003A1 WO 1997032003 A1 WO1997032003 A1 WO 1997032003A1 US 9602848 W US9602848 W US 9602848W WO 9732003 A1 WO9732003 A1 WO 9732003A1
Authority
WO
WIPO (PCT)
Prior art keywords
amount
component
microns
carbonate
particle size
Prior art date
Application number
PCT/US1996/002848
Other languages
English (en)
Inventor
Donald Scott Adams
Burce Albert Yeazell
Eric Fitzgerald Riddick
Junan Kao
Original Assignee
The Procter & Gamble Company
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Family has litigation
First worldwide family litigation filed litigation Critical https://patents.darts-ip.com/?family=22254790&utm_source=google_patent&utm_medium=platform_link&utm_campaign=public_patent_search&patent=WO1997032003(A1) "Global patent litigation dataset” by Darts-ip is licensed under a Creative Commons Attribution 4.0 International License.
Priority to US09/125,550 priority Critical patent/US6207635B1/en
Application filed by The Procter & Gamble Company filed Critical The Procter & Gamble Company
Priority to HU9901066A priority patent/HUP9901066A3/hu
Priority to PCT/US1996/002848 priority patent/WO1997032003A1/fr
Priority to AT96908611T priority patent/ATE267240T1/de
Priority to EP96908611A priority patent/EP0883678B1/fr
Priority to JP9516573A priority patent/JP2898102B2/ja
Priority to CZ982730A priority patent/CZ273098A3/cs
Priority to BR9612535A priority patent/BR9612535A/pt
Priority to DE69632549T priority patent/DE69632549T2/de
Priority to AU51794/96A priority patent/AU5179496A/en
Priority to ZA9701381A priority patent/ZA971381B/xx
Priority to EG14697A priority patent/EG21214A/xx
Priority to ARP970100799A priority patent/AR006032A1/es
Publication of WO1997032003A1 publication Critical patent/WO1997032003A1/fr

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D11/00—Special methods for preparing compositions containing mixtures of detergents
    • C11D11/0082—Special methods for preparing compositions containing mixtures of detergents one or more of the detergent ingredients being in a liquefied state, e.g. slurry, paste or melt, and the process resulting in solid detergent particles such as granules, powders or beads
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D17/00—Detergent materials or soaps characterised by their shape or physical properties
    • C11D17/06—Powder; Flakes; Free-flowing mixtures; Sheets
    • C11D17/065—High-density particulate detergent compositions
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02—Inorganic compounds ; Elemental compounds
    • C11D3/04—Water-soluble compounds
    • C11D3/06—Phosphates, including polyphosphates
    • C—CHEMISTRY; METALLURGY
    • C11—ANIMAL OR VEGETABLE OILS, FATS, FATTY SUBSTANCES OR WAXES; FATTY ACIDS THEREFROM; DETERGENTS; CANDLES
    • C11D—DETERGENT COMPOSITIONS; USE OF SINGLE SUBSTANCES AS DETERGENTS; SOAP OR SOAP-MAKING; RESIN SOAPS; RECOVERY OF GLYCEROL
    • C11D3/00—Other compounding ingredients of detergent compositions covered in group C11D1/00
    • C11D3/02—Inorganic compounds ; Elemental compounds
    • C11D3/04—Water-soluble compounds
    • C11D3/10—Carbonates ; Bicarbonates

Definitions

  • the invention involves a process for making built high active detergent agglomerates having improved free flow properties.
  • Laundry detergent granules comprise one or more surfactants (usually of the anionic type) and one or more detergency builders ( typically phosphates, carbonates, zeolites, etc.)
  • Detergent granules are typically made by preparing a paste of the detergent ingredients, and spray drying the paste to form granules. Such products also can be made by agglomerating a mixture of the surfactant and builder in a mixer. In an agglomeration process, the anionic surfactant in its neutralized form can be used or it can be introduced into the agglomeration process in its acid form and be neutralized in situ by alkaline materials (e.g. sodium carbonate).
  • alkaline materials e.g. sodium carbonate
  • Optional detergent materials such as brighteners, soil release agents, etc. can be agglomerated along with the surfactant and builder or can be mixed with the agglomerates after they are formed. Generally, agglomeration provides the ability to produce higher density detergent products than those which are produced by spray drying.
  • flow aids such as clay, talc, zeolites or silica are typically used.
  • Representative examples of prior patents relating to agglomeration processes for the production of detergent granules are: U.S. Pat. 5,133,924 (Appel); U.S. Pat 5,164,108 (Appel); U.S Pat. 5,160,657 ( Bartolloti); Brit. Pat. 1,517,713 (Unilever); Euro. Appln.
  • the object of the present invention is to provide a process for producing detergent agglomerates having high surfactant levels and improved free flow characteristics.
  • the present invention is directed to a process comprising the steps of:
  • paniculate phosphate builder selected from the group consisting of polyphosphate, pyro- phosphate, and mixtures thereof;
  • a paniculate carbonate selected from the group consisting of sodium carbonate, potassium carbonate, and mixtures thereof; wherein when an acid precursor of an anionic surfactant is used in (a)(1), the amount of carbonate is at least 2 times that which is sufficient to neutralize the said acid precursor;, wherein at least about 20% of the total amount of Components (2) and (3) meets a particle size specification of 97% particles less than 50 microns and a median particle size of 5 to 20 microns, and
  • Step (b) agglomerating the mixture from Step (a) in a second mixer to produce detergent agglomerates.
  • Anionic surfactant is an essential component of compositions prepared by the present process.
  • Such surfactants are well known in the art.
  • the anionic surfactants useful in the subject invention are preferably the alkali metal (i.e., sodium and potassium) salts of alkylbenzene sulfonates or alkyl sulfates or mixtures thereof.
  • Examples of other anionic surfactants which are also useful are the alkali metal salts of paraffin sulfonates, alkyl glyceryl ether sulfonates and alkyl ether sulfates, all having about 8 to about 18 carbon atoms in their alkyl chains.
  • the anionic surfactant raw materials preferably have a moisture content of less than about 1.0%, more preferably less than about 0.5%. Based on the total weight of raw materials added during the process of the subject invention, the amount of anionic surfactant is from about 20% to about 35%, preferably from about 20% to about 30%.
  • Preferred alkylbenzene sulfonates useful in the subject process include those with an alkyl portion which is straight chain or branched chain, preferably having from about 8 to about 18 carbon atoms, more preferably from about 10 to about 16 carbon atoms.
  • the alkyl chains of the alkylbenzene sulfonate preferably have an average chain length of from about 1 1 to about 14 carbon atoms.
  • Alkylbenzene sulfonate which includes branched chain alkyl is termed ABS.
  • Alkylbenzene sulfonate which is all straight chain is preferred because it is more easily biodegraded; it is termed LAS.
  • Preferred alkyl sulfates useful in the subject process include those with an alkyl portion which is straight chain or branched chain, preferably having from about 8 to about 24 carbon atoms, more preferably from about 10 to about 20 carbon atoms, more preferably still from about 12 to about 18 carbon atoms.
  • the alkyl chains of the alkyl sulfates preferably have an average chain length of from about 14 to about 16 carbon atoms.
  • the alkyl chains are preferably linear.
  • Alkyl sulfates are typically obtained by sulfating fatty alcohols produced by reducing the glycerides of fats and/or oils from natural sources, especially from tallow or coconut oil.
  • Preferred anionic surfactants useful in the subject invention process may also be combinations of alkylbenzene sulfonates and alkyl sulfates, whether mixed together or added during the process separately. Combinations having a ratio of alkylbenzene sulfonate to alkyl sulfate of from about 20:80 to about 80:20 are preferred; those having a ratio of from about 40:60 to about 60:40 are more preferred. Additional disclosure of anionic synthetic surfactants can be found in U.S. Pat. 3,664,961, Norris, issued May 23, 1972, incorporated by reference herein.
  • the anionic surfactant can be introduced in its neutralized (i.e., alkali metal) form or it can be introduced in its unneutralized acid precursor form, in which case it is neutralized by excess alkali metal carbonate, as discussed later herein.
  • phosphates are used as builders in compositions made according to the process herein.
  • the phosphate builder raw materials useful in the subject invention process are in paniculate form and consist essentially of the water-soluble salts (e.g., the sodium and potassium salts) of polyphosphates (e.g., tripolyphosphate, hexametaphosphate, etc.) or pyrophosphates or mixtures thereof.
  • the phosphate builder raw materials preferably have a moisture content of less than about 2%, more preferably less than about 1%. Based on the total weight of raw materials added during the process of the subject invention, the amount of phosphate builder is typically from about 5% to about 65%, preferably from about 15% to about 55%, more preferably from about 25% to about 45%.
  • Phosphate builder raw materials are typically supplied from their manufacturers in powder form, usually having a median particle size of from about 25 microns to about 50 microns.
  • Carbonate raw materials are typically supplied from their manufacturers in granular form, usually having a particle size of from about 25 microns to about 150 microns.
  • As is median particle size for polyphosphate and carbonate varies for supplies obtained in different geographies as well as by supplier.
  • the polyphosphate builder and/or carbonate are ground to a particle size such that at least about 20% preferably at least about 40% of the total amount of particles of phosphate/carbonate used in the process meet a particle size specification of 97% of panicles less than 50 microns (preferably less than 40 microns) and median particle size of 5 to 20 microns, preferably 10 to 20 microns.
  • the carbonate, phosphate or both can be ground to achieve the specified amount of total phosphate/carbonate particles within the required size requirements.
  • all of the particles of phosphate and carbonate used in the process will be within an overall size range of 5 to 300 microns. Grinding can be accomplished in conventional powder grinding equipment such as an ACM Classifier Mill (Hosokawa Micron Powder Systems). During grinding, or after grinding, if necessary, the panicles are classifed to assure that the ground panicles to be used are within the required specification. For classification, a Micron Pulsaire Classifier (Hosokawa Powder Systems) can be used.
  • a preferred phosphate builder useful in the subject process is sodium tripolyphosphate (STPP); STPP can be obtained commercially from, for example, FMC Corp.
  • STPP sodium tripolyphosphate
  • TSPP tetrasodium pyrophosphate
  • TSPP can be obtained commercially from, for example, FMC Corp.
  • the subject invention process utilizes paniculate alkali metal carbonate preferably consisting essentially of sodium carbonate or potassium carbonate or a mixture thereof as builders. If an acid precursor of anionic surfactant is used in the process the carbonate also functions as a neutralizing agent to convert the acid precursor to the alkali metal salt.
  • the alkali metal carbonate raw materials preferably have a moisture content of less than about 2%, more preferably less than about 1%. Based on the total weight of raw materials added to the process of the subject invention, the amount of alkali metal carbonate is from about 6% to about 60%, preferably from about 10% to about 50%, more preferably from about 30% to about 40%.
  • the amount of carbonate fed to the process is at least about 2 times that theoretically needed to neutralize the acid.
  • the amount of carbonate will be from about 4 times to about 12 times, more preferably still from about 6 times to about 12 times, the amount needed to neutralize the acid precursor.
  • substantially the only water present in the materials as they go through the process is the minor amounts of moisture present in the raw materials and the water generated by neutralization of acid precursor of anionic surfactant.
  • the maximum amount of water in the materials being processed is preferably about 10%, more preferably about 7%, more preferably still about 5%, still more preferably about 3%.
  • the detergent agglomerates produced by the process may be somewhat hygroscopic and pick up moisture from the atmosphere.
  • the detergent agglomerates from the process of the subject invention typically have an average particle size of from about 200 microns to about 800 microns, more preferably from about 300 microns to about 700 microns, more preferably still from about 400 microns to about 600 microns.
  • An advantage of the process of the invention is that the use of flow aids such as silicas, clays, diatomaceous earth, aluminosilicates (e.g., zeolites), perlite, and calcite can be substantially reduced or eliminated.
  • flow aids such as silicas, clays, diatomaceous earth, aluminosilicates (e.g., zeolites), perlite, and calcite can be substantially reduced or eliminated.
  • Process Steps The subject invention can be carried out in a continuous or batch manner.
  • the first step of the process is preferably carried out in a high-speed, high- shear mixer.
  • Suitable mixers for this step include, for example, the Loedige CB®, the Shugi Granulator®, and the Drais K-TTP®.
  • the preferred mixer for the first step is the Loedige CB®.
  • the high-speed mixer has a substantially cylindrical mixing chamber which is from about 0.3m to about lm in diameter and from about 1m to about 3.5m in length.
  • Preferred mixers for the first step have a central shaft, with mixer blades attached, which preferably rotates at a speed of from about 300 rpm to about 1800 rpm, more preferably from about 350 rpm to about 1250 rpm, more preferably still from about 400 rpm to about 1000 rpm, the speed generally being lower for larger mixers.
  • the high-speed mixer preferably is water- jacketed to permit cooling water to flow through the mixer jacket, in order to remove heat generated by the neutralization reaction.
  • the essential raw materials i.e., surfactant or surfactant acid precursor; carbonate; and phosphate, if used
  • the essential raw materials are typically fed to the high-speed mixer near one end of the cylindrical chamber and intimately mixed as they proceed through the chamber; the mixture is discharged near the other end of the cylindrical chamber.
  • the typical average throughput rate is from about 0.2 kg/sec to about 17 kg/sec, especially from about 2kg/sec to about 13 kg/sec, the higher throughput rates generally being achieved using larger mixers.
  • the average residence time of materials in the first-step mixer is preferably from about 2 seconds to about 30 seconds, more preferably from about 5 seconds to about 20 seconds, more preferably still from about 10 seconds to about 15 seconds.
  • the neutralization reaction may be completed after the mixture discharges from the first- step mixer.
  • the acid is substantially completely neutralized during the process. Cooling water at a temperature of from about 5°C to about 25°C is preferably fed to the water jacket of the high-speed mixer.
  • the temperature of the mixture at the discharge from the high-speed mixer is typically from about 35°C to about 70°C, preferably from about 45°C to about 55°C.
  • the materials discharged from the first-step mixer are typically fed substantially immediately into the second-step mixer.
  • the average residence time for materials between the mixers is preferably less than about 5 minutes, more preferably less than about 1 minute.
  • the second step of the process of the subject invention is preferably carried out in a moderate-speed mixer.
  • Suitable mixers for this step include plowshare mixers, for example, the Loedige KM® and the Drais K-T®.
  • the Loedige KM® is the preferred mixer for the second step of the subject invention process.
  • the moderate-speed mixer has a substantially cylindrical mixing chamber which is from about 0.6m to about 2m in diameter and from about 2m to about 5m in length.
  • the preferred mixers have a central shaft, with mixer blades attached, which preferably rotates at a speed of from about 40 rpm to about 160 rpm, more preferably from about 45 rpm to about 140 rpm, more preferably still from about 50 rpm to about 100 rpm, the speed generally being lower for larger mixers.
  • the moderate-speed mixer preferably is water-jacketed to permit water to flow through the mixer jacket, in order to maintain the temperature of product in the moderate- speed mixer at about its incoming temperature.
  • the mixture of materials discharged from the first-step mixer is typically fed to the moderate-speed mixer near one end of the cylindrical chamber, mixed as it proceeds through the chamber, and discharged near the other end of the cylindrical chamber.
  • the throughput rate for the second step is the same as for the first step.
  • the average residence time of the materials in the second-step mixer is preferably from about 0.5 minutes to about 10 minutes, more preferably from about 0.5 minutes to about 5 minutes, more preferably still from about 1 minute to about 4 minutes.
  • the temperature of the mixture at the discharge of the moderate-speed mixer is typically from about 35°C to about 70°C, preferably from about 45°C to about 55°C.
  • agglomerates produced by the process herein can be used "as is" for detergent purposes.
  • materials normally included in detergent compositions can be included in the agglomerates ger se or combined with the agglomerates in one or more subsequent mixing steps.
  • Such materials include organic polymeric builders such as polycarboxylates (see U.S.Patent 4, 144,226 Diehl), phosphonic acid builders such as disclosed in U.S. Patents 3, 159,581; 3,213,030; 3,422,021; 3,442,137; 3,400,176; and 3,400,148, alkali metal silicates, zeolite builders as disclosed in U.S.
  • Patent 4,605,509 bleaches, bleach activators, soil suspending agents, enzymes, perfumes, chelating agents, and additional surfactants such as alkyl polyethoxylates, ethoxoylated fatty amines, etc.
  • Compostion A was made according to the process of the present invention, utilizing acid precursor of the alkylbenzene sulfonate surfactant.
  • a Loedige CB mixer was used in Step 1 and a Loedige KM mixer in Step 2. All materials were added in Step 1, except that 20% of the zeolite (i.e., 1.44 parts) was added in Step 2. All of the sodium carbonate which, "as received” had a particle size of 97% less than approximately 200 microns and a median particle size of 50 microns was ground and classified to meet a specification of 97% less than 40 microns and a median particle size of 10 microns.
  • the tripolyphosphate had an "as received" particle size of 97% less than 200 microns and a median particle size of 50 microns.
  • the tripolyphosphate was not ground and classified prior to use.
  • 44 parts carbonate which is 67% of the total amount phosphate and carbonate used to prepare the composition was pretreated to meet the particle size specification required by the invention.
  • Composition B was made in the same manner as Composition A, except that both the carbonate and phosphate were used with their "as received" particle size. Also, in Composition B, 90% of the zeolite was added in Step 1 and 10% (i.e., 1.52 parts) was added in Step 2.
  • Composition A had excellent free flow characteristics, whereas Composition B had poor free flow characteristics.
  • compositions were subjected to an "arch test".
  • an agglomerate product to form an arch under pressure can be used to determine potential flowability problems in conveying equipment and storage silos.
  • the agglomerate product is pressed into the form of an arch in a cylindrical vessel, and the stickiness of the product is assessed by measuring the force required to break the arch. The stickier the product, the greater the force required. 1.5 kg force was required for Composition A and 3-5 kg was required for Composition B.

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  • Chemical & Material Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Engineering & Computer Science (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Wood Science & Technology (AREA)
  • Organic Chemistry (AREA)
  • Inorganic Chemistry (AREA)
  • Detergent Compositions (AREA)

Abstract

On a préparé des agglomérats détergents à écoulement libre contenant des niveaux élevés de tensioactif anionique dans un procédé utilisant des adjuvants de détergence particulaires ultrafins.
PCT/US1996/002848 1995-05-31 1996-02-29 Procede de production de granules detergents de haute densite WO1997032003A1 (fr)

Priority Applications (13)

Application Number Priority Date Filing Date Title
CZ982730A CZ273098A3 (cs) 1996-02-29 1996-02-29 Způsob výroby detergentních aglomerátů
JP9516573A JP2898102B2 (ja) 1996-02-29 1996-02-29 高密度洗剤粒の製造方法
HU9901066A HUP9901066A3 (en) 1996-02-29 1996-02-29 Process for manufacture of high density detergent granules
PCT/US1996/002848 WO1997032003A1 (fr) 1996-02-29 1996-02-29 Procede de production de granules detergents de haute densite
AT96908611T ATE267240T1 (de) 1996-02-29 1996-02-29 Verfahren zur herstellung kompakter waschmittelgranulate
EP96908611A EP0883678B1 (fr) 1996-02-29 1996-02-29 Procede de production de granules detergents de haute densite
BR9612535A BR9612535A (pt) 1996-02-29 1996-02-29 Processo para a produção de grânulos de detergentes de alta densidade
US09/125,550 US6207635B1 (en) 1995-05-31 1996-02-29 Process for manufacture of high density detergent granules
AU51794/96A AU5179496A (en) 1996-02-29 1996-02-29 Process for manufacture of high density detergent granules
DE69632549T DE69632549T2 (de) 1996-02-29 1996-02-29 Verfahren zur herstellung kompakter waschmittelgranulate
ZA9701381A ZA971381B (en) 1996-02-29 1997-02-18 Process for manufacture of high density detergent granules.
EG14697A EG21214A (en) 1996-02-29 1997-02-27 Process for manufacture of high desity detergent granules
ARP970100799A AR006032A1 (es) 1996-02-29 1997-02-28 Proceso para la fabricacion de granulos de detergente de alta densidad

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
PCT/US1996/002848 WO1997032003A1 (fr) 1996-02-29 1996-02-29 Procede de production de granules detergents de haute densite

Publications (1)

Publication Number Publication Date
WO1997032003A1 true WO1997032003A1 (fr) 1997-09-04

Family

ID=22254790

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1996/002848 WO1997032003A1 (fr) 1995-05-31 1996-02-29 Procede de production de granules detergents de haute densite

Country Status (10)

Country Link
EP (1) EP0883678B1 (fr)
JP (1) JP2898102B2 (fr)
AR (1) AR006032A1 (fr)
AT (1) ATE267240T1 (fr)
AU (1) AU5179496A (fr)
CZ (1) CZ273098A3 (fr)
DE (1) DE69632549T2 (fr)
EG (1) EG21214A (fr)
WO (1) WO1997032003A1 (fr)
ZA (1) ZA971381B (fr)

Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998020104A1 (fr) * 1996-11-06 1998-05-14 The Procter & Gamble Company Procede de neutralisation destine a la fabrication de granules agglomerees de detergent
WO1998016618A3 (fr) * 1996-10-15 1998-08-20 Procter & Gamble Procede de fabrication d'une composition detergente de densite elevee par malaxage/densification apres sechage
WO2001014511A1 (fr) * 1999-08-20 2001-03-01 Kao Corporation Procede de preparation de compositions detersives a poids specifique apparent eleve
DE10258011A1 (de) * 2002-12-12 2004-07-08 Henkel Kgaa Trockenneutralisationsverfahren
DE102005005499A1 (de) * 2005-02-04 2006-08-17 Henkel Kgaa Verfahren zur Herstellung von Wasch- oder Reinigungsmitteln

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0351937A1 (fr) * 1988-07-21 1990-01-24 Unilever Plc Compositions détergentes et procédé pour leur préparation
EP0420317A1 (fr) * 1989-09-29 1991-04-03 Unilever N.V. Procédé de préparation de compositions détergentes à haute densité apparente
EP0555622A1 (fr) * 1992-02-14 1993-08-18 The Procter & Gamble Company Procédé pour la production de granules de détergent par neutralisation des acides sulfoniques
WO1994002573A1 (fr) * 1992-07-15 1994-02-03 The Procter & Gamble Company Procede et compositions pour detergents compacts
WO1995006109A1 (fr) * 1993-08-27 1995-03-02 The Procter & Gamble Company Procede de fabrication d'agglomerats detersifs de masse volumique elevee

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
EP0351937A1 (fr) * 1988-07-21 1990-01-24 Unilever Plc Compositions détergentes et procédé pour leur préparation
EP0420317A1 (fr) * 1989-09-29 1991-04-03 Unilever N.V. Procédé de préparation de compositions détergentes à haute densité apparente
EP0555622A1 (fr) * 1992-02-14 1993-08-18 The Procter & Gamble Company Procédé pour la production de granules de détergent par neutralisation des acides sulfoniques
WO1994002573A1 (fr) * 1992-07-15 1994-02-03 The Procter & Gamble Company Procede et compositions pour detergents compacts
WO1995006109A1 (fr) * 1993-08-27 1995-03-02 The Procter & Gamble Company Procede de fabrication d'agglomerats detersifs de masse volumique elevee

Cited By (6)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO1998016618A3 (fr) * 1996-10-15 1998-08-20 Procter & Gamble Procede de fabrication d'une composition detergente de densite elevee par malaxage/densification apres sechage
WO1998020104A1 (fr) * 1996-11-06 1998-05-14 The Procter & Gamble Company Procede de neutralisation destine a la fabrication de granules agglomerees de detergent
WO2001014511A1 (fr) * 1999-08-20 2001-03-01 Kao Corporation Procede de preparation de compositions detersives a poids specifique apparent eleve
CN100419056C (zh) * 1999-08-20 2008-09-17 花王株式会社 制备高堆积密度洗涤剂组合物的方法
DE10258011A1 (de) * 2002-12-12 2004-07-08 Henkel Kgaa Trockenneutralisationsverfahren
DE102005005499A1 (de) * 2005-02-04 2006-08-17 Henkel Kgaa Verfahren zur Herstellung von Wasch- oder Reinigungsmitteln

Also Published As

Publication number Publication date
EP0883678B1 (fr) 2004-05-19
DE69632549D1 (de) 2004-06-24
JPH10505631A (ja) 1998-06-02
EP0883678A1 (fr) 1998-12-16
AR006032A1 (es) 1999-07-21
CZ273098A3 (cs) 1998-12-16
DE69632549T2 (de) 2005-05-12
ZA971381B (en) 1997-08-28
EG21214A (en) 2001-02-28
AU5179496A (en) 1997-09-16
JP2898102B2 (ja) 1999-05-31
ATE267240T1 (de) 2004-06-15

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