GB2115829A - Cationic polymer compositions - Google Patents

Cationic polymer compositions Download PDF

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GB2115829A
GB2115829A GB08302375A GB8302375A GB2115829A GB 2115829 A GB2115829 A GB 2115829A GB 08302375 A GB08302375 A GB 08302375A GB 8302375 A GB8302375 A GB 8302375A GB 2115829 A GB2115829 A GB 2115829A
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water
composition
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GB8302375D0 (en
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Bernard Danner
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Sandoz KK
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Sandoz KK
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    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/52Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
    • C02F1/54Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using organic material
    • C02F1/547Tensides
    • CCHEMISTRY; METALLURGY
    • C02TREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02FTREATMENT OF WATER, WASTE WATER, SEWAGE, OR SLUDGE
    • C02F1/00Treatment of water, waste water, or sewage
    • C02F1/52Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities
    • C02F1/54Treatment of water, waste water, or sewage by flocculation or precipitation of suspended impurities using organic material
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2/00Processes of polymerisation
    • C08F2/12Polymerisation in non-solvents
    • C08F2/16Aqueous medium
    • C08F2/22Emulsion polymerisation
    • C08F2/24Emulsion polymerisation with the aid of emulsifying agents
    • C08F2/28Emulsion polymerisation with the aid of emulsifying agents cationic
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08FMACROMOLECULAR COMPOUNDS OBTAINED BY REACTIONS ONLY INVOLVING CARBON-TO-CARBON UNSATURATED BONDS
    • C08F2/00Processes of polymerisation
    • C08F2/32Polymerisation in water-in-oil emulsions
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08JWORKING-UP; GENERAL PROCESSES OF COMPOUNDING; AFTER-TREATMENT NOT COVERED BY SUBCLASSES C08B, C08C, C08F, C08G
    • C08J3/00Processes of treating or compounding macromolecular substances
    • C08J3/02Making solutions, dispersions or lattices by other methods than by solution, emulsion or suspension polymerisation techniques
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/03Non-macromolecular organic compounds
    • D21H17/05Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
    • D21H17/07Nitrogen-containing compounds
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/03Non-macromolecular organic compounds
    • D21H17/05Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
    • D21H17/09Sulfur-containing compounds
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/03Non-macromolecular organic compounds
    • D21H17/05Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
    • D21H17/14Carboxylic acids; Derivatives thereof
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20Macromolecular organic compounds
    • D21H17/33Synthetic macromolecular compounds
    • D21H17/34Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H17/41Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups
    • D21H17/44Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds containing ionic groups cationic
    • D21H17/45Nitrogen-containing groups
    • D21H17/455Nitrogen-containing groups comprising tertiary amine or being at least partially quaternised
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W10/00Technologies for wastewater treatment
    • Y02W10/30Wastewater or sewage treatment systems with climate change mitigation effect characterised by the origin of the energy
    • Y02W10/37Wastewater or sewage treatment systems with climate change mitigation effect characterised by the origin of the energy using solar energy

Abstract

A cationic polymer composition suitable for use as a flocculating agent and as a retention aid in paper making consists of a mixture of a) a hydrophilic cationic polymer, b) an anionic surfactant, optionally c) a water-immiscible oil in which the polymer a) is insoluble, and, if c) is present, optionally d) a lipophilic non-ionic surfactant, optionally e) water and optionally f) an oil-miscible polar solvent. The compositions may be prepared by water-in-oil emulsion polymerisation and are readily diluted with water. Examples of vinyl monomers used to produce such cationic polymers are:- <IMAGE>

Description

SPECIFICATION Improvements in or relating to organic compounds This invention relates to hydrophilic cationic polymers useful for example as flocculating agents.

For such uses, it is important that compositions containing the polymer can be rapidly dispersed or dissolved in water.

It has now been found that compositions containing an excess of a hydrophilic cationic polymer together with an anionic surfactant, which optionally forms a salt with the cationic polymer, can easily be dispersed or dissolved in water.

Accordingly, the present invention provides a water-miscible composition comprising a) a hydrophilic cationic polymer and b) an anionic surfactant, the molar quantity of b) being not greater than the molar quantity of the cationic monomer units of a).

The polymer a) is free of anionic monomer components, and is composed either entirely of cationic monomer units or of both cationic and non-ionic monomer units. By the term cationic is meant that the monomer unit includes a group which either carries a positive charge or which has basic properties and can be protonated under mild acid conditions. Preferably such groups are amino or quaternary ammonium groups. Suitable polymers a) include cationic addition and condensation polymers such as polyamideamines, polyethyleneimines and polyetheramines, as described for example in US Patents 3 210308, 3 275 588, 3 329 657, 3 632 559,3 753 931 and 4056 510.

Preferably however polymer a) is at least partly composed of vinyl addition polymers of cationic and optionally non-ionic vinyl monomers. Preferably polymer a) comprises at least 70% by weight of such vinyl addition polymers, more preferably at least 90%; especially preferred polymers a) consist entirely of such vinyl addition polymers.

Preferred vinylic monomers are water-soluble monomers based upon esters and amides of acrylic and methacrylic acid, vinylpyridines, diallylamines, N-vinylpyrrolidones and vinyl ethers. Of the cationic monomers, preferred types include the dialkylaminoalkyl and dialkylaminohydroxyalkyl esters of acrylic and methacrylic acid, and the corresponding trialkylammonium compounds; dialkylaminoalkyl amides of acrylic and methacrylic acid and the corresponding trialkylammonium compounds; dialkylsulphoniumalkyl esters of acrylic and methacrylic acid; 2- and 4-vinyipyridine and the corresponding N-alkylpyridinium derivatives; and N-alkyl diallylamines and the corresponding N,Ndialkyldiallylammonium derivatives.In these compounds, the alkylene group forming the bridge between the N and 0, 0 and S or N and N atoms preferably contains 2 to 4, more preferably 2 to 3 carbon atoms, and the alkyl groups on nitrogen or sulphur contain preferably 1 to 4, more preferably 1 or 2 carbon atoms and may be unsubstituted or substituted by phenyl. Phenyl-substituted alkyl is preferably benzyl; more preferably, however, the alkyl groups are unsubstituted.

More preferred cationic monomers are those of formula 1-VIll <img class="EMIRef" id="027381113-00010001" />

<img class="EMIRef" id="027381113-00020001" />

In the above formulae, R1 is H or methyl R2 is methyl or ethyl R3 is methyl or ethyl R4 is hydrogen, methyl or ethyl X is -0- or-NH- Y is H or-OH when X is -0- and H when X is -NH n is O or 1, provided that when Y is -OH, n=1.

and As is an anion.

Preferably, R2, R3 and R4 are all methyl. As may be any conventional anion, preferably a halide ion (particularly Clue, Bre or le) or an R4SO4# anion. In a preferred form of the invention, however, A# is A,f3 where Ale is the anion of the anionic surfactant b).

Particularly preferred cationic monomers are those of formulae I and 11, especially those in which Y is hydrogen and particularly those in which Y is hydrogen and X is --OO-.

Preferred non-ionic monomers are acrylamide, methacrylamide, N-vinylpyrroiidone, methyl vinyl ether, ethyl vinyl ether and compounds of formula IX <img class="EMIRef" id="027381113-00020002" />

where R, is as defined above.

Of these acrylamide and methacrylamide, particularly acrylamide, are preferred.

Preferred cationic polymers a) are copolymers of cationic monomers of formula I or II (Y=H, X=+) with methacrylamide anchor acrylamide. In the cationic polymers a), the molar quantity of cationic monomer units is preferably at least 5% of the total, more preferably 10-80 mol%, particularly 1040 mol%. It may be advantageous, however, to employ a mixture of two cationic polymers of differing cationic content, for example a weakly cationic polymer of e.g. 5~20 mol% cationic units and a strongly cationic polymer of e.g. 20-80 mol%, preferably 30~60 mol% cationic units. Any desired cationic content within a defined range may then be obtained by mixing the two polymers in various proportions.

The molecular weight (weight average MW) of the polymer is preferably > 100,000, more preferably > 500,000, particularly > 1,000,000. The MW may be as high as desired, for example up to 20,000,000.

The preferred polymers may be structurally defined as random copolymers containing units of the following three types. <img class="EMIRef" id="027381113-00020003" />

in which R, is as defined above, Ks is a cationic residue preferably derived from a monomer of formula II, IV, VII or VIII, Ale is the anion of the surfactant b), A2# is a non-surfactant anion such as halide or R4OSO3e and Z is a non-ionic residue, preferably of formula -CONH2,-OCH3, -0C2H5 or -CONHC(CH3)2CH2COCH3.

If a, p and y represent the molar proportions of units (1) (2) and (3) respectively, so that a+#+y=l 00, la+p) is preferably > 5, more preferably 10-80, particularly 10 40 and a is preferably < 1 5, more preferably A10.

The anionic surfactant b) may be any conventional surfactant having at least one lipophilic hydrocarbon residue and at least one hydrophilic anionic group. Suitable surfactants are described for example in "Surfactant Science Series" (M. Dekker Inc., New York and Basle), vol. 7; and "Anionic Surfactants" (ed. W. M. Linfield, 1 976), parts 1 and 2. The lipophilic residue is preferably araliphatic or aliphatic and contains at least 9 carbon atoms, preferably 12~36 carbon atoms. The anionic group may be any conventional acid group, optionally in salt form, for example carboxylate, phosphate, phosphonate, sulphate and sulphonate, of which sulphonate is most preferred and phosphonate least preferred. The molecule may contain polyalkylene glycol ether groups, but these are preferably absent.

Preferred classes of anionic surfactants are: sulphated fatty acid mono- di- and triglycerides, particularly sulphated natural fats or oils and suiphated monoglycerides; sulphated fatty alcohols; sulphated fatty acid alkanolamides; sulphonated hydrocarbons, particularly alkylsulphonates, olefin sulphonates and alkarylsulphonates, especially petroleum sulphonates; sulphonated aliphatic carboxylic acids and esters, particularly a-sulphomonocarboxylic acids and esters and alkyl sulphosuccinates; partial alkyl esters of phosphoric acid; aliphatic carboxylic acids (soaps); and carboxymethylation products of fatty alcohols, monoglycerides and fatty acid alkanolamides. Of the above, the sulphonates, particularly petroleum sulphonates, are preferred.

It is preferred that the anionic surfactant is originally present at least partially in the form of a salt with a conventional cation, for example that of an alkali metal, alkaline earth metal, ammonium or substituted ammonium, Zn2+, Al3+ and Zr4+; Preferably it is in the form of a salt of a polyvalent inorganic cation, of which Ca2+ is particularly preferred. In the compositions of the inventions, however, after polymer a) is mixed with surfactant b), the cation of the anionic surfactant may be wholly or partially replaced by cationic units of the polymer. Salts of the surfactant with a polyvalent metal may be prepared in situ by treating the sodium salt of the surfactant with a water-soluble salt of the metal, for example the formate or chloride. In the case of calcium, calcium chloride is preferred.

The anionic surfactant may have a greater or lesser degree of water solubility or dispersability.

Preferred anionic surfactants are lipophilic, and preferably are such that their sodium salts are oilsoluble. Especially preferred are those which in salt form (particularly the calcium salts) give no true solution in water, but act as W/O (water-in-oil) emulsifiers, particularly with the oils defined below under c).

The compositions of the invention preferably contain, in addition to a) and b), c) a water-immiscible oil in which the polymer a) is insoluble.

When component c) is present, polymer a) is finely dispersed in the oil c).

Component c) may be a single oil or a mixture of oils, and may be either natural or synthetic.

Suitable oils include oils from refining crude petroleum, vegetable and animal oils, synthetic hydrocarbons, modified paraffins and fatty acid esters. Examples of these types include the following: 1. Hydrocarbons 1.1. Hydrocarbons from petroleum refining, particularly 1.1.1. petroleum spirit, b.p. 65-1 400C (de-aromatised or aromatic-containing) 1.1.2. white spirits, paint thinners etc., b.p. 100-31 00C, preferably 1 40-3000C especially those in Table I Table I % aromatic content h.p. 0C aromatic-free 100~270 12~19 160~210 24~45 140~310 80~90 160~260 fully aromatic 160~310 1.1.3. Isoparaffins, 110-2600C 1.1.4. Paraffin oils (=mineral oils, e.g. diesel oil, spindle oil, machine oil, cylinder oil, lubricating oil, medicinal paraffin oil) 1.1.5. petrolatum (preferably mixed with an oil liquid at 200C) 1.2. Synthetic hydrocarbons, particularly from Fischer-Tropsch synthesis or high pressure hydrogenation of carbon, e.g.

synthetic petrol (gasoline) b.p. 65-1 700C Kogasin I b.p. 1 90-2300C Kogasin II b.p. 230-3300C synthetic paraffin oil b.p. 300--4500C 1.3. Benzenes and alkylbenzenes, e.g. toluene, xylene, and methyl-ethyl-, trimethyl-, dimethylethyl-, tetramethyl- and higher (C6~,2) alkyl benzenes.

2. Natural vegetable or animal triglycerides, particularly olive oil, peanut oil, cottonseed oil, coconut fat, rape oil, sunflower oil, corn oil, castor oil and neats foot oil.

3. Fatty acid monoesters, primarily C,~4alkyl esters of C,2~24, preferably C,4~24 fatty acids, particularly methyl, butyl and isopropyl esters of stearic, oleic, palmitic and myristic acids and mixtures thereof.

Preferred oils are low-aromatic hydrocarbons and aliphatic fatty acid esters, particularly hydrocarbons listed under 1.1.2., 1.1.3. and 1.1.4. above, especially aromatic-free and low-aromatic white spirits, isoparaffin and paraffin oils.

In one particular embodiment of the invention component c) comprises a mixture of at least two oils, particularly of a mixture of an oil c,) and an oil c2) chosen such that the oil/water required hydrophile/lipophile balance (O/W-RHLB) value of C1) is greater than that of the mixture of c1) and c2).

The O/W-RHLB value of an oil is the optimum HLB-value of a hypothetical surfactant which is sufficient to produce stable O/W emulsion of that oil and water; see for example "Cosmetics, Science and Technology" Wiley, 2nd edition, volume 3, 1974, pp 602~7, or "Emulsion Science" P. Sherman, Academic Press, 1968 pp 146-7 or "Emulsion, Theory and Practice" P. Becher, Amer. Chem. Soc.

Monograph series No. 162, 2nd edition, 1965.

Preferably the O/W-RHLB value of c2) is less than that of C1). Preferred oils C1) have O/W-RHLB values in the range 10~15; such oils include hydrocarbon oils listed under 1.1.1., 1.1.2., 1.1.3. and 1.3. above. Preferred oils C2) have 0/W-RHLB values in the range 7~10; such oils include those listed under 1.1.4., 1.1.5. 2. and 3. above.

Preferably the compositions according to the invention contain, in addition to a), b) and c), d) a lipophilic non-ionic surfactant.

Component d) is preferably oil-soluble and may be a single surfactant or a mixture. Component d) must function as a W/O (water-in-oil) emulsifier, that is, it must be capable of forming a W/O emulsion with at least part of the oil c) in the presence of water. The surfactant d) is preferably insoluble in water, and has an HLB value < 8, more preferably in the range 3-8, particularly in the range 4-7. If d) is a mixture, these values apply to the average HLB value of the mixture.

Component d) generally is one or more compounds having at least one lipophilic hydrocarbon residue of at least 9, preferably 9~24 carbon atoms and at least one non-ionic hydrophilic residue, which is preferably a mono- or polyethylene glycol group, optionally containing propylene glycol units, or the residue of a polyol e.g. glycerol, mannitol and sorbitol. Other suitable types include hydrophobic.

Pluronics and Tetronics in which the high propylene oxide content can be regarded as the lipophilic residue.

Specific types of non-ionic surfactants include: Products obtainable by addition of ethylene oxide (EO) and/or propylene oxide (PO) (preferably EO alone) to aliphatic alcohols, alkyl phenols, fatty acids, fatty acid alkanolamides, partial fatty acid esters of polyols, and vegetable or animal fats or oils; partial fatty acid esters of polyols; EO/PO copolymers with high PO content (Plumnic type); EO/PO addition products to ethylene diamine, having a high PO content (Tetronic type); diethers of mono- or polyethylene glycols with aliphatic alcohols and alkyl phenols; and diesters of mono- or polyethylene glycols with aliphatic fatty acids.

The preferred number of ethylene oxide units in addition products of EO to fatty alcohols and alkyl phenols is 1-6 and in addition products to fatty acids and in di-esters of polyalkylene glycol, the number of EO units is preferably 1~10. These numbers are average values and need not be integral.

Fatty acid residues may be saturated or unsaturated (if unsaturated, preferably monoethylenically unsaturated) and are preferably acyl groups having 9~24, preferably 12~20, carbon atoms, particularly residues of lauric, myristic, stearic and oleic acids. If an alkyl group is the sole lipophilic group, it has preferably 9~24, more preferably 9-1 8, carbon atoms, and may be straight chain or branched. In alkylaryl groups the alkyl group preferably has 4~12 carbon atoms and may also be straight or branched.

Particularly preferred surfactants are those of formula X-Xlll <img class="EMIRef" id="027381113-00040001" />

in which R8 is C4-,2 alkyl Rg is C9~18alkyl or alkenyl R1oCO is the acyl residue of an aliphatic C12#18 fatty acid o is the monovalent residue of sorbitol, glycerol, or di- to tetra-ethylene glycol tis2~3 ris 1 or2 k is 3~5 and m is 4-9.

The HBL values of non-ionic surfactants may be calculated by use of a standard formula. In order to function as a W/O emulsifier in this system, the calculated HLB value must be greater than 2.5.

When the oil c) is a mixture of oils c,) and c2) then the oil mixture and the surfactant d) are preferably so chosen that the O/W-RHLB value of the oil mixture is as close as possible to the HLB value of d), or at least is not less than this value.

Preferably the compositions according to the invention contain, in addition to components a), b), c) and preferably d), e) water.

The polymer a) and salts of the polymer with surfactant b) are hydrophilic and will take up water or form with water a gel or sol and in sufficient water will form a true or a colloidal solution. The quantity of water e) is chosen so that the polymer together with the water becomes finely dispersed in the oil. The dispersion may be in the form of a suspension of wet or water-swollen polymer or of an aqueous polymer gel in the oil, or an emulsion of an aqueous polymer sol or polymer solution in the oil.

In one particular aspect of the invention, the composition contains, in addition to components a)-c) preferably d) and optionally e).

f) an oii-miscible polar solvent which is only slightly soluble in water, not self-dispersing in water, and which has no emulsifying properties of its own, but which reduces the water/oil interfacial surface tension.

Suitable solvents f) are compounds which have extremely low HLB values but whose molecules are polar enough to orientate themselves at the oil/water interface. Preferred solvents are C5#10 aliphatic alcohols, phosphoric acid triesters or Pluronics. Examples of suitable solvents include methyl isobutyl carbinol, 2-ethylhexanol, isononanol, isodecanol, 2,4,7,9-tetramethyl-5-decyn-4,7-diol, tributyl phosphate, tri-isobutyl phosphate, tri(butoxyethyl)phosphate and Pluronic L101. The presence off) is desirable when little or no water e) is present.

Compositions according to the invention may be prepared by mixing surfactant b) before, during or after the polymerisation, with the polymer a) or the corresponding monomers, the polymer or monomers being present in finely divided form. When a) is other than a vinyl addition polymer it is preferred to add the surfactant to the already formed polymer. The polymer should be in finely-divided form for example as an aqueous solution, a dispersion in oil, or, preferably, as a W10 emulsion of an aqueous solution of the polymer in oil. When polymer a) is a vinyl addition polymer, it is advantageous to carry out the polymerisation in a W/O emulsion system and to have at least part of the anionic surfactant b) present before polymerisation, or at least before addition of the cationic monomer.After polymerisation water and/or oil can if desired be removed by distillation, and optionally further additions of any of components a)-f) may be made.

Preferably the vinyl monomers are emulsified in the form of their aqueous solution in at least part of the oil c) in the presence of the anionic surfactant b) and preferably also in the presence of the lipophilic non-ionic surfactant d). This W/O emulsion may be formed by adding the vinyl monomers to an already-formed W/O emulsion, or the monomers may be added to an aqueous solution or dispersion of the anionic surfactant b), to which is then added the oil and optionally the non-ionic surfactant d), and polymerisation is initiated by addition of a suitable catalyst.

The presence of the anionic surfactant in the monomer-containing W/O emulsion before polymerisation enables part of the cationic monomers, particularly in neutral to acid conditions, to form salts with the surfactants, which salts are less water-soluble and more lipophilic than the monomers themselves. These monomer-surfactant salts are novel and form part of the present invention.

Preferred salts have the formula XIV <img class="EMIRef" id="027381113-00050001" />

where B1, Ke and As are as defined above.

Preferably Ks is of formula XV <img class="EMIRef" id="027381113-00050002" />

where X, n, Y, R2, R3 and R4 are defined above, and Y is preferably H, and Ale is the anion of a hydrocarbon sulphonate, particularly petroleum sulphonate.

An alternative method of preparing compositions according to the present invention consists in forming a dispersion containing polymer a), water e) and lipophilic non-ionic surfactant d) in oil c) in the absence of anionic surfactant b), and then adding the anionic surfactant b) to this dispersion. For this process variant, it is preferred that the anionic surfactant is an oil-soluble, practically water-insoluble sulphonated hydrocarbon, and that the oil is a hydrocarbon oil of the type listed under 1.1. above, particularly white spirit. Preferably the dispersion is obtained by emulsion polymerisation of the monomer solution in oil in the presence of surfactant d) as emulsifier, and optionally partial removal of water by distillation.

The emulsion polymerisation, preferably in the presence of anionic surfactant b) may be carried out in conventional manner (see for example "High Polymers" vol. 9, 1 955-"Emulsion Polymerisation, Interscience Publishers, N.Y.). Conventional free radical initiators are used to catalyse the polymerisation. Suitable initiator systems include peroxide compounds, e.g. t-butyl hydroperoxide, in combination with redox systems, e.g. ferric salts plus sodium thiosulphate. To sequester impurities, it is preferred to add a complexing agent such as salts of ethylenediaminetetraacetic acid (EDTA). The aqueous phase may contain further additives; e.g. acids, bases or buffer systems to regulate pH and salts e.g. sodium sulphate and calcium chloride.

The air above the emulsion is normally replaced by an inert gas and polymerisation is started by the addition of initiator. The polymerisation takes place for example at pH values between 2 and 8, preferably under acid conditions (pH 2.5~5, preferably 3~4). The water content of the W/O emulsion during polymerisation is preferably 15~80 wt.%, more preferably 30~65 wt.% based on the total weight of the emulsion.

The polymerisation is normally exothermic, and may be carried out under adiabatic or isothermal conditions, but preferably is carried out partially adiabatically, i.e. the temperature is allowed to increase within certain limits, e.g. up to 1 200C, under pressure if necessary. Preferred reaction temperatures are from 30-11 00C. If the reaction mixture contains hydrolysable monomers, e.g. esters or primary amides, it is necessary to avoid reaction conditions under which significant amounts of hydrolysis would occur.

For the W/O emulsion polymerisation it is advantageous to use an oil c) comprising at least 50%, preferably at least 80% by wt. hydrocarbons, which should preferably be as completely aliphatic as possible. The concentration of monomers in the emulsion is not critical, but for economic reasons it is advantageous to work with as high concentrations as is practicable. The concentration of surfactant used is adjusted to be sufficient to give a stable W/O emulsion under the polymerisation conditions.

After polymerisation is complete the polymer-containing W/O emulsion can be treated by addition of further quantities of components a)-f) or, if desired, the amount of components c) and/or e) can be reduced by distillation. By such adjustments properties of the emulsion such as stability and ease of dilution with water can be influenced and improved. If in addition to vinyl addition polymer other cationic polymers a) are to be present, these are preferably added after the emulsion polymerisation is complete.

If component f) is to be present, this is preferably added after the emulsion polymerisation, more preferably after all other components have been added. It may be advantageous to mix f) with a little oil c) before addition.

If a mixture of oils c1) and c2) is to be used, the polymerisation is preferably carried out either in the mixture or in c1) alone or in a mixture of c,) with less than all of the c2). The oil c2), or that part of it not already present, may be added after the emulsion polymerisation, optionally after some or all of the water has been distilled off.

The relative weights of the various components in the compositions according to the invention may be represented as follows: for every 100 parts by weight of the polymer a), the composition contains x parts by weight of b, y of c), z of d) u of e) and v off). The figures 100 for a) and x for b) do not take into account the salt formation between a) and b); that is, the weight of surfactant which forms a salt with the polymer is not counted as part of the polymer weight, but remains part of weight x.

The preferred ranges of x-v are set out in Table II below, the values for each component being independent of each other except where otherwise stated. For certain applications, the value of x may be as low as 0.5.

Table II (component a=lOO) component value of preferred more preferred most preferred b x 1~30 1~15 1.5~10 c y 30~400 40~200 40~200 d z 0~80 1~80 2-30 e u O~300 1~300 2~200 f v < y O~30 0~15 ( < y/3) ( < y/5) The water content (u) can vary within wide limits and in theory it is possible to remove the water completely by distillation giving u=0.In practice, it is difficult to remove the last traces of water from the polymer; also it is possible to add water in the form of a further amount of W/O emulsion or aqueous polymer solution; so that the water content of the consumption can be high. As it is not economically feasible to remove all the water, u can preferably be 5~300, more preferably 1 0-200.

Preferred compositions contain, for 100 parts by weight of a), 1-30 parts b), 30-400 parts c), 1~80 parts d), 0-300 parts e) and 0~30 parts f) where the weight off) is less than 3 that of c).

Particularly preferred compositions are those in which the weight of each component present is within the range given in the "most preferred" column of Table II.

The oil-containing compositions according to the invention are dispersions which may show a wide range of viscosities. The Brookfield rotation viscosity (measured in an LV-viscometer) may vary between 5 cp (spindle no. 2) and 10,000 cp (spindle no. 4), preferably between 50 cp (spindle no. 2) and 5000 cp (spindle no. 4). The dispersions are stable and can be stored for long periods of time without change or, if separation into two layers occurs, can be restored to the original form by simple stirring. The compositions of the invention, particularly those containing the oil c) have particularly good dispersability in water and can rapidly be diluted with water by stirring or by the use of conventional dilution apparatus.

In a preferred method of dilution, the dispersion is pumped through a nozzle into a stream of water which surrounds the nozzle. The water stream has a higher velocity than that of the stream of dispersion, and this velocity is sufficient to overcome at least partially the internal adhesive and cohesive forces in the dispersion, but not sufficient to reduce the size of the polymer molecules. The mixture of product and water is then alternatively accelerated in narrow tubes and decelerated in wider mixing zones until the desired degree of mixing is obtained. No sieves or filters are used in this process from the time the streams of water and of dispersion contact each other.

A mixing apparatus suitable for carrying out the above process comprises at least two cylindrical mixing chambers connected by rigid or flexible tubing of diameter not greater than half that of each mixing chamber. The first chamber is furnished with a coaxially mounted tube for the inflow of a stream of water and a second tube, substantially at right angles to the first, ending in a jet situated between the axis and circumference of the first tube and just beyond the end of the first tube. Means are provided for pumping the dispersion through this second tube. Near the other end of the mixing chamber is an exit tube leading to the second mixing chamber. The second and any subsequent mixing chambers are each provided with an inlet and an exit tube, preferably set into the side walls one near each end of the chamber.Finally an exit tube from the last mixing chamber leads to the apparatus in which the dilute aqueous dispersion of the composition according to the invention is to be used.

A particularly preferred apparatus is illustrated by way of example in Figures 1 and 2. Figure 1 is a vertical elevation of a six-chamber mixing apparatus, the upper chamber 1 being shown in cross section. Figure 2 is a horizontal cross-section along XX' of Figure 1.

The chambers 1-6 are mounted alternately on opposite sides of a frame 7 and secured with clips 8. The chambers are constructed of cylindrical tubing 9 closed with screw caps 10 which can be removed for cleaning. In chamber 1 the tubing 9 is of transparent material to allow direct observation of the mixing process, in the other chambers it is of metal.

Chamber 1 is fitted with a coaxial water inlet tube 11, at right angles to which is mounted a dispersion inlet tube 12 which ends in a six-holed jet 13 positioned so as to be completely within the stream of water delivered by tube 11. In the cylindrical tubing 9, near the end remote from tube 11 is an opening 14 leading to a flexible hose 15 which connects to a similar opening in the side wall of chamber 2. From a second opening in chamber 2 a further hose 16 leads to chamber 3. Chambers 2-6 are all identical in construction and are connected, each to the next, by hoses 1 6-1 9. Finally, chamber 6 is provided with a flexible delivery hose 20.

In operation, a stream of water is led through tube 11 into chamber 1, and is allowed to run until all chambers are filled and the water is delivered from hose 20. The Reynolds number of the water flow at the exit of tube 11 is preferably between 25,000 and 75,000, and the pressure drop across the apparatus will for a medium size apparatus of total volume 1-100 litre preferably be from 0.5 to 2.5 bar, more preferably from 0.6 to 1.5 bar.

The dispersion is then pumped through tube 12 at a rate sufficient to give the desired concentration of product. The dispersion passes through the jet 13, the size and number of whose holes may be varied according to the viscosity of the dispersion and is rapidly mixed in the stream of water from tube 11. The mixture passes from chamber 1 through the narrow hose 1 5 in which its flow is accelerated, and then into the wide chamber 2 in which its flow is again slowed down. The alternating acceleration and slowing of the flow in the successive connecting hoses and mixing chambers provides a complete mixing of the dispersion in the water, and the water containing the product is delivered through hose 20 to the apparatus in which it is to be be used.

The compositions according to the invention can be very rapidly diluted with water and thus are suitable for use in many large-scale continuous processes, in which cationic polymers are used. By the use of the mixer described above, fully diluted solutions or dispersions can be obtained without the use of any dwell tanks; the mixer may simply be connected up to the equipment in which the diluted product will be used.

The compositions may contain very high concentrations of cationic polymer, enabling the minimum handling of bulk liquids.

Not only the concentrated compositions described above, but also partially diluted compositions containing at least 0.001% by weight of polymer a), more preferably at least 0.1% by weight of a) are included within the scope of the present invention. The partially diluted compositions may be further diluted as required before use.

The compositions of the invention are useful as flocculating agents, particularly as retention and dewatering agents in paper-making and as flocculating agents for aqueous sludge, particularly crude and treated sludge from sewage purification works. They may also be used in other processes where cationic polymers are employed, for example flotation of minerals or recovery of oil waste.

In paper making, the use of the compositions according to the invention can give a particularly homogeneous sheet formation. The compositions also show good biodegradability.

The following Examples illustrate the invention: all parts and percentages are by weight unless otherwise stated.

Examples Emulsifiers used: Br sodium salt of petroleum monosulphonate, MW 440~470 (62% solution in mineral oil) B2 sodium salt of petroleum monosulphonate, MW 480 (60% solution in mineral oil) B3 sodium salt of secondary n-alkane sulphonate, obtained from sulphoxidation of paraffin.The alkyl group has the following average composition: C13-15 58%, C1,-17 39%, > C17 < 3%, < C13 < 1% D, C,2H25(OCH2CH2)2OH, HLB 6.5 D2 C18H35(OCH2CH2)3OH, HLB 6.5 D3 sorbitol monooleate, HLB 4.0 D4 1:1 molar mixture of mono- and di-oleates of H(OCH2CH2)8.50H, HLB 7.0 (average value) Oils used: C, white spirit: aromatic-free, b.p 1 93--247 OC, mean MW 173 C2 white spirit: low-aromatic, b.p. 1 9o-25a0C mean MW 180, aromatic content 0.5% C3 mineral oil: partially unsaturated mineral oil with following properties: specific gravity (SG) 0.85--0.95 aniline point 70#800 C, iodine number 20-30 C4 petrolatum: solidification point 50--85 Od cone penetration 160~180 at 25 OC C8 olive oil: Cs isoparaffin: b.p. 21 0-2600C, aniline point 880C isoparaffin content 80%, SG 0.78 C7 mixture of methyl esters of C12-2o fatty acids SG 0.87--0.90, acid number 1.12, saponification number 190~200, iodine number 100-110, hydroxy number 40~60 C8 mineral oil:SG 0.85-0.95, aniline point 950C, viscosity (200C) 30 cp Solvent used: F1 triisobutyl phosphate (50% in isobutanol) F2 2 ethylhexanol F3 tri(butoxyethyl)phosphate F4 2,4,7 ,9-tetramethyl-6-decyn-4,7-diol F5 Pluronic L101 10:90 EO/PO copolymer, MW 3610 Example 1 43.5 Parts emulsifier Bt are mixed with 800 parts water, giving a fine opalescent emulsion. On addition of 8.2 parts calcium chloride, a precipitate of the water-insoluble calcium salt of B, is formed.

Finally 440 parts white spirit C, is added with stirring, giving a water-in-oil emulsion which is stabilised by addition of 99.5 parts emulsifier D,. To this emulsion is added in the following order 353 parts of 75% aqueous methacryloyloxyethyltrimethylammonium chloride, 454 parts acrylamide, 1.4 parts EDTA sodium salt, 0.7 parts ferric sulphate and 0.7 parts t-butylhydroperoxide, after which the pH of the aqueous phase is 3.0. The emulsion is heated to 350C under nitrogen, and an air-free solution of 2.7 parts sodium thiosulphate in 50 parts water is added dropwise over 8 hours, the temperature being kept at 35-400C by cooling.

Polymerisation is complete when all the thiosulphate solution has been added. A stable, fine dispersion of polymer is obtained, of Brookfield viscosity 1000 cp (spindle 3 60 rpm). The product is very easily diluted with water, the maximum viscosity of a 0.5% aqueous dilution with cold water being reached after only 30~40 seconds. The viscosity of a freshly-prepared 1% aqueous dilution is approx.

500 cp (Brookfield 3 60 rpm).

Example 2 454 Parts acrylamide, 353 parts of 75% aqueous methacryloyloxyethyltrimethylammonium chloride 1.4 parts disodium EDTA, 0.7 parts ferric sulphate and 9.8 parts calcium chloride are added in the stated order to 600 parts water. The solution so obtained is then mixed with a solution of 52 parts emulsifier B, and 80 parts emulsifier D1 in 600 parts white spirit C1, giving a water-in-oil emulsion whose aqueous phase has a pH of 3.0. Under a nitrogen atmosphere is added first 0.7 parts tbutylhydroperoxide and then an air-free solution of 1.1 parts sodium thiosulphate in 12 parts water. A strongly exothermic reaction sets in, giving a temperature rise of up to 900C even under light cooling.

On cooling, a fine dispersion of polymer is obtained, which is easily diluted with water.

Example 3 24 Parts emulsifier B, is mixed with 480 parts of water, giving a fine opalescent emulsion. To this is added 564 parts of 75% aqueous methacryloyloxyethyltrimethylammonium chloride, whereby the surfactant salt of the cationic monomer is formed. The following components are then added in the stated order, with stirring: 408.3 parts acrylamide, 1.43 parts disodium EDTA, 0.77 parts ferric sulphate, 480 parts white spirit C1, 30 parts emulsifier D1, 30 parts emulsifier D2, 4.8 parts calcium chloride and 0.6 parts t-butylhydroperoxide.

The resulting dispersing is purged with nitrogen and warmed to 300C, then an air-free solution of 2.97 parts sodium thiosulphate in 42 parts water is added over 8 hours, the temperature rising to 500 C. A fine dispersion of polymer is obtained, which is easily diluted with water.

Example 4 500 parts of the product of Example 1 is stirred with 10 parts white spirit C, and 10 parts emulsifier B2 and then distilled with a Dean-Starke apparatus at 26 mbar, 400C until approx. 200 parts water has been removed. A fine, stable polymer dispersion is obtained, which in spite of its low water content is readily diluted with water.

Example 5 The procedure of Example 1 is repeated and to the product is added 10% of the total weight of the product of Example 3.1 of USP 3 632 559, containin#g 20% wt. cationic polymer and 80% water. A stable W/O emulsion is obtained.

Example 6 i) Preparation of polymer dispersion without surfactant b) 454 Parts acrylamide and 353 parts 75% aqueous methacryloyloxyethyltrimethylammonium chloride are dissolved in 800 parts water, and 1.43 parts disodium EDTA and 0.72 parts ferric sulphate are added. The pH is adjusted to 3.0 with approx.0.1 part 30% caustic soda, then a solution of 143 parts emulsifier D, in 440 parts white spirit C2 is added with vigorous stirring. A milky W/O emulsion is formed, which is thoroughly de-aerated and stirred while bubbling a stream of nitrogen through the mixture.

After addition of 0.67 parts t-butyl hydroperoxide, the mixture is heated to 350C, and a solution of 2.7 parts sodium thiosulphate in 50 parts water is added dropwise over 5 hours, the temperature being held at 36-380C by cooling. After addition is complete, reaction is continued for 2 hours at 350C, and the product is then cooled to room temperature.

ii) Addition of surfactant b) A 20% aqueous emulsion of B, (sodium petroleum sulphonate) is treated with excess Cacti2, and the precipitated calcium salt collected by filtration, dried under vacuum at 60-700C and taken up in mineral oil to give a 30% solution. 20 Parts of this solution and 20 parts white spirit C2 are added to 200 parts of the suspension prepared in i) above. A viscous product is obtained which in spite of its high viscosity may be rapidly diluted with water.

Example 7 The calcium salt of emulsifier B3 is prepared as described above for B,, and 10 parts of this salt are dissolved in a mixture of 80 parts white spirit C2 and 30 parts mineral oil C3. 25 Parts of this solution are added to 200 parts of the suspension prepared in Example 6 i). The resulting mixture is readily diluted with water.

Example 8 To 200 parts of the suspension prepared in Example 6 i) are added 30 parts of a solution containing 14.3% sodium petroleum sulphonate B2, 57.0% mineral oil C3 and 28.6% of a 50% solution of triisobutyl phosphate in isobutanol (F,). A viscous product is obtained, which is readily diluted on addition to water.

Example 9 To 2210 parts of the polymer emulsion prepared in Example 1 are added 330 parts mineral oil C3 and 330 parts petrolatum C4, and the mixture is evacuated to 26 mbar under stirring and heated to 400C over ca. 6 hours, collecting 860 parts water in a Dean-Stark trap, any oil which distilled being returned to the distillation mixture. A very fine, stable, slightly viscous dispersion is obtained, which may be diluted with water approximately as readily as the product of Example 1.

Example 10 A dispersion containing 960 parts water, 81 6.6 parts acrylamide, 11 28 parts 75% aqueous methacryloyloxyethyltrimethylammonium chloride, 2.9 parts disodium EDTA, 1.5 parts ferric sulphate, 9.1 parts calcium chloride, 48 parts emulsifier B,, 60 parts emulsifier D1, 60 parts emulsifier D2 and 960 parts white spirit C, is adjusted to pH 3.0 and 1.2 parts t-butylhydroperoxide are added.

Polymerisation is carried out under nitrogen by adding 6.5 parts sodium thiosulphate in 20 parts water over 8 hours, the temperature rising to approx. 480C in spite of cooling.

To the product are added 165.7 parts mineral oil C3, and 27.7 parts emulsifier D3, and 1186 parts water is distilled off at 20~26 mbar, 500C. The resulting fine mobile dispersion is mixed with 157.5 parts olive oil C5 and 157.5 parts 2-ethylhexanol (F2). The product is practically instantaneously diluted in water.

Examples 11~13 Example 10 is repeated, with F2 replaced by equal quantities of F1, F3 and F4, respectively.

Example 14 43.5 Parts emulsifier B, are mixed with 834 parts water to give a very fine opalescent emulsion.

In order to form the calcium salt of B,, 8.2 parts calcium chloride are added. The following components are then added with stirring: 557 parts acrylamide, 216 parts 75% aqueous methacryloyloxyethyltrimethylammonium chloride, 1.4 parts disodium EDTA, and 0.7 parts ferric sulphate, giving a cloudy solution, to which are added 400 parts isoparaffin C6, 40 parts mineral oil C3, 100 parts emulsifier D, and 13 parts emulsifier B2, to give a W/O emulsion which is polymerised under nitrogen by the addition of 0.7 parts t-butyl hydroperoxide then 6 parts of a solution of 2.7 parts sodium thiosulphate in 50 parts water. The temperature rises to 850C, even with cooling. The resulting dispersion may be rapidly diluted with water.

Example 15 Example 14 is repeated with the following changes: 709 Parts water, 183.3 parts acrylamide and 714 parts of the aqueous cationic monomer are used; the temperature rises to approx. 430C under adiabatic conditions; and after the polymerisation 33 parts Pluronic L101 (F5) and 165 parts fatty acid esters C7 are added.

Example 16 Example 14 is repeated with the following changes: 160 Parts mineral oil C8 are used in place of 40 parts C3; and the temperature is kept between 35 and 400C.

Example 17 43.5 Parts emulsifier B, are mixed with 800 parts water, and to the resulting emulsion are added 8.8 parts calcium chloride, 363 parts acrylamide, 124 parts diallylamine, 353 parts 75% aqueous methacryloyloxyethyltrimethylammonium chloride, 1 31 parts 34% hydrochloric acid to adjust the pH to 3.0, 1.4 parts disodium EDTA and 0.7 parts ferric sulphate. A homogeneous monomer solution is formed, to which is added 400 parts white spirit C1, 40 parts mineral oil C3 and 100 parts emulsifier D,.

A fine emulsion is formed, which is polymerised under nitrogen by the addition of 0.7 parts tbutylhydroperoxide followed by 16 parts of a solution of 2.7 parts sodium thiosulphate in 50 parts water. The temperature during polymerisation rises under adiabatic conditions to 650C.

Example 18 Example 2 is repeated with the following changes: 29 Parts emulsifier B, are used; and the 80 parts emulsifier D, are replaced by a mixture of 49 parts D3 and 65 parts D4.

Example 19 Example 17 is repeated with the following changes: 454 Parts acrylamide replace 363 parts acrylamide+ 124 parts diallylamine; no HCL is used; 54 parts B2 replace 100 parts D1; 45 parts thiosulphate solution replaces 16 parts; and the temperature rises within 90 minutes to 900C.

Example 20 43.5 Parts emulsifier B, is mixed with 600 parts water. To this is added 8.2 parts calcium chloride, 454 parts acrylamide, 1.4 parts disodium EDTA, 0.7 parts ferric sulphate, 400 parts white spirit C1, 40 parts mineral oil C3, 100 parts emulsifier D1 and 13 parts emulsifier B2. A water-in-oil emulsion is formed which is polymerised under nitrogen by adding 0.7 parts t-butyl hydroperoxide and 1 part of a solution of 2.7 parts sodium thiosulphate in 50 parts water. The polymerisation reaction is held at a temperature of 600C. When the temperature begins to fall off, a solution of 265 parts methacryloyloxyethyltrimethylammonium chloride in 288 parts water is added dropwise, giving a further rise of temperature, which is held at 55-600C by cooling.After the addition is complete, the product is stirred 1 hour at 550C then cooled to room temperature.

Example 21 Example 15 is repeated with the following changes: 11 parts B1 are used in place of 43.5 parts; 25 parts D, are used in place of 100 parts; 3.25 parts B2 are used in place of 13 parts; and no F8 and C7 are added after polymerisation.

Example 22 Example 16 is repeated with the following changes: 21.75 parts B, are used in place of 43.5 parts 50.00 parts D, are used in place of 100 parts 6.50 parts B2 are used in place of 13 parts.

Dilution Example A mixing apparatus as shown in Figure 1 is used, having 6 chambers each of inner diameter 11 cm and volume 2.5 1. The connecting hoses have an inner diameter of 15 mm and are each 40 cm long.

Into the first chamber of the mixture is fed through a 1 5 mm diam. jet a stream of water of 2000 I/hour, giving a speed of 3.2 m/sec. at the jet (Reynolds number 47000). Into the water stream is fed, by means of a pump operating at a frequency of 50 Hz, 5 l/hr of the product of Example 1. The polymer jet has six holes of 1 mm diameter, and is equipped with a non-return valve.

The diluted product delivered from the mixer is a ready-to-use aqueous solution of the product suitable for use in paper making.

Application Example A A 2% aqueous paper slurry of the following composition is prepared; 100 parts bleached sulphite pulp, 20 parts kaolin, 3 parts resin size, 2 parts aluminium sulphate.

Four samples (250 ml) of this slurry are mixed with 5, 10, 15 and 20 ml respectively of a 0.0125% aqueous stock dilution of the product of Example 1 and 750 ml water. After stirring 5 sec. at 250 rpm, each mixture is poured into 3 1 of water in the filling chamber of a Rapid-Köthen sheet former, and after a 20 sec. pause the suction valve is operated to form the sheet. After drying and conditioning the paper sheet is incinerated and the ash content measured and calculated as a percentage of the weight of filler which was used, giving the % retention. The results are given in Table A.

Table A <img class="EMIRef" id="027381113-00110001" />

<tb> <SEP> concentration <SEP> of <tb> <SEP> polymer <SEP> emulsion <tb> amount <SEP> of <SEP> stock <SEP> based <SEP> on <SEP> dry <SEP> paper <SEP> % <SEP> ash <SEP> % <SEP> retention <tb> dilution <SEP> added <SEP> weight <SEP> (%) <SEP> <SEP> (average <SEP> of <SEP> 2 <SEP> <SEP> measurements) <tb> <SEP> 0 <SEP> - <SEP> <SEP> 8.51 <SEP> 51.1 <tb> <SEP> 5 <SEP> 0.0125 <SEP> 13.31 <SEP> 79.9 <tb> <SEP> 10 <SEP> 0.025 <SEP> 14.34 <SEP> 86.0 <tb> <SEP> 15 <SEP> ; <SEP> <SEP> 0.0375 <SEP> 14.66 <SEP> 88.0 <tb> <SEP> 20 <SEP> , <SEP> <SEP> 0.05 <SEP> 14.73 <SEP> 88.4 <tb> Application Example B 200 Parts of a sewage suspension of 5% dry solids content are treated with W parts of a 0.23% aqueous stock dilution of the product of~ Example 1, stirred 1 0 sec. in a 'Triton' stirrer at 1000 rpm, then immediately filtered through a cloth filter. For each sample, the volume of filtrate after 30, 60, 99, 120 and 180 seconds is measured, and the mean value of these is calculated. The results are shown in Table B.

Table B <img class="EMIRef" id="027381113-00120001" />

<tb> <SEP> mean <SEP> filtrate <SEP> volume <tb> Parts <SEP> <SEP> by <SEP> weight) <SEP> parts <SEP> <SEP> by <SEP> volume) <tb> <SEP> 0 <SEP> 1.5 <tb> <SEP> 13 <SEP> 15.3 <tb> <SEP> 15 <SEP> 40.4 <tb> <SEP> 17 <SEP> 49.1 <tb> <SEP> 19 <SEP> 81.9 <tb> The products of Examples 2~22 may be used in analogous manner to Application Examples A and B.

Claims (36)

Claims
1. A water-miscible composition comprising a) a hydrophilic cationic polymer and b) an anionic surfactant, the molar quantity of b) being not greater than the molar quantity of the cationic monomer units of a).
2. A composition as claimed in Claim 1 in which component a) comprises at least 70% by weight of vinyl addition polymers of cationic and optionally non-ionic vinyl monomers.
3. A composition as claimed in Claim 2 in which the cationic vinyl monomer is selected from compounds of formula 1-VIll <img class="EMIRef" id="027381114-00120002" />
in which R, is H or methyl R2 is methyl or ethyl R3 is methyl or ethyl R4 is hydrogen, methyl or ethyl Xis -0- or -NH- YisHor-OHwhenXis-0-and HwhenXis-NH- n is 0 or 1, provided that when Y is -OH, n=1 and 1 or 2 when X is -NH and As is an anion.
4. A composition as claimed in Claim 2 or Claim 3 in which the non-ionic vinyl monomer is selected from acrylamide, methacrylamide, N-vinylpyrrolidone, methyl vinyl ether, ethyl vinyl ether and compounds of formula IX <img class="EMIRef" id="027381114-00130001" />
where R, is as defined in Claim 3.
5. A composition as claimed in any one of Claims 2 to 4 in which component a) is a copolymer of a methacryloyloxyethyltrimethylammonium salt and acrylamide.
6. A composition as claimed in any one of the preceding claims in which component b) is selected from sulphated fatty acid mono- di- and triglycerides; sulphated fatty alcohols; sulphated fatty alkanolamides; sulphonated hydrocarbons; sulphonated aliphatic carboxylic acids and esters; partial alkyl esters of phosphoric acid; aliphatic carboxylic acids; and carboxymethylation products of fatty alcohols, monoglycerides and fatty acid alkanolamides.
7. A composition as claimed in Claim 6 in which component b) is a petroleum sulphonate.
8. A composition as claimed in Claim 7 in which the petroleum sulphonate is initially present in calcium salt form.
9. A composition as claimed in any one of the preceding claims containing, in addition to a) and b) c) a water-immiscible oil in which the polymer a) is insoluble.
10. A composition as claimed in Claim 9 in which the oil c) is selected from low-aromatic hydrocarbons and aliphatic fatty acid esters.
11. A composition as claimed in Claim 9 or Claim 10 in which component c) comprises a mixture of at least two oils, c,) and c2) chosen such that the oil/water required hydrophile/lipophile balance (O/W-RHLB) value of c) is greater than that of the mixture of c,) and c2).
12. A composition as claimed in any one of the preceding claims comprising, in addition to a), b) and c) d) a lipophilic non-ionic surfactant.
13. A composition as claimed in Claim 12 in which d) is either i) one or more compounds having at least one lipophilic hydrocarbon residue of at least 9 carbon atoms and at least one non-ionic hydrophilic residue, which is either a mono- or polyethylene glycol group, optionally containing propylene glycol units, or the residue of a polyol or ii) one or more hydrophobic Pluronics and Tetronics having a high propylene oxide content.
14. A composition according to any one of the preceding claims containing, in addition to components a), b) and c), e) water.
15. A composition according to any one of the preceding claims containing, in addition to components a), b) and c), f) an oil-miscible polar solvent which is only slightly soluble in water, not self-dispersing in water, and which has no emulsifying properties of its own, but which reduces the water/oil interfacial surface tension.
16. A composition according to Claim 15 in which component f) is selected from C5#10aliphatic alcohols, phosphoric acid triesters and Pluronics.
1 7. A composition according to any one of Claims 12 to 16 having the composition, for every 100 parts by wt. of component a); 1 to 30 parts b), 30 to 400 parts c), 1 to 80 parts d), 0 to 300 parts e) and 0 to 30 parts f), where the weight off) is less than + that of c).
18. A composition according to 17 having the composition; for every 100 parts by wt. of component a), 1.5--10 parts b), 40-200 parts c), 2-30 parts d), 2-200 parts e) and 0-1 5 parts f) where the weight off) is less than 1/5 that of c).
19. A composition as claimed in Claim 1 as described in any one of the Examples.
20. A partially diluted composition according to any one of the preceding claims, containing at least 0.001% by weight of component a).
21. A salt of a cationic vinyl monomer and an anionic surfactant.
22. A salt of a cationic vinyl monomer as defined in Claim 3 and an anionic surfactant as defined in Claim 7.
23. A salt of formula <img class="EMIRef" id="027381114-00130002" />
where R X, n, Y,R2, R3 andR and R4 are defined in Claim 3 and Ale is the anion of a hydrocarbon sulphonate.
24. A salt of a cationic polymer in which at least part of the cationic groups are associated with the anions of an anionic surfactant.
25. A water-in-oil emulsion containing a salt as claimed in any one of Claims 21~24.
26. A process for the preparation of a composition as claimed in Claim 1, comprising the steps of mixing component b) before, during or after the polymerisation with polymer a) or the corresponding monomers.
27. A process as claimed in Claim 26 in which a water-in-oil emulsion containing water-soluble vinyl monomers in the aqueous phase is polymerised in the presence of component b).
28. A process as claimed in Claim 27 in which water is subsequently removed by distillation.
29. A process as claimed in Claim 27 or 28 in which the cationic monomers are at least in part in the form of surfactant salts as claimed in any one of Claims 21 to 23.
30. A process for the preparation of a composition as claimed in Claim 1, as described in any one of the examples.
31. A method of dilution of a composition as claimed in any one of Claims 1 to 19 in which the composition is pumped through a nozzle into a stream of water which surrounds the nozzle, the water stream having a higher velocity than that of the stream of composition, and this velocity being sufficient to overcome at least partially the internal adhesive and cohesive forces in the composition, but not sufficient to reduce the size of the polymer molecules; and the mixture of product and water is then alternately accelerated in narrow tubes and decelerated in wider mixing zones until the desired degree of mixing is obtained.
32. A mixing apparatus suitable for carrying out the process of Claim 31 comprising at least two cylindrical mixing chambers connected by rigid or flexible tubing of diameter not greater than half that of each mixing chamber; the first chamber being furnished with a) a coaxially mounted tube for the inflow of a stream of water; b) a second tube, substantially at right angles to the first, ending in a jet situated between the axis and circumference of the first tube and just beyond the end of the first tube; and c), near the other end of the mixing chamber, an exit tube leading to the second mixing chamber; the second and any subsequent mixing chambers being each provided with an inlet and an exit tube.
33. A process for flocculation of an aqueous sludge comprising the step of adding to the sludge an effective amount of a composition as claimed in any one of Claims 1 to 19.
34. A process for flocculation of an aqueous sludge as described in Application Example B.
35. A process for the manufacture of paper comprising the addition of a composition as claimed in any one of Claims 1 to 19 to the paper-making slurry.
36. A process for the manufacture of paper as described in Application Example A.
GB8302375A 1982-02-01 1983-01-28 Cationic polymer compositions Expired GB2115829B (en)

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EP0156646A1 (en) * 1984-03-28 1985-10-02 HI-TEK POLYMERS, INC. (a Georgia corporation) High charge density, cationic methacrylamide based monomers and their polymers
FR2585712A1 (en) * 1985-07-31 1987-02-06 Sandoz Sa Mixtures of vinyl addition polymers for use as flocculation and dehydration agents
US4824894A (en) * 1985-07-12 1989-04-25 Rohm Gmbh Chemische Fabrik Biodegradable organosol flocculants
GB2205591B (en) * 1987-05-01 1990-03-07 Grace W R & Co Pitch control aid
GB2327049A (en) * 1997-07-10 1999-01-13 Atotech Deutschland Gmbh Pretreatment and coating of electrically non-conductive surfaces
US6723207B2 (en) * 2002-08-05 2004-04-20 Johnsondiversey, Inc. Method of treating paper making rolls
EP1508363A1 (en) * 2003-08-21 2005-02-23 Rohm And Haas Company Process for treating aqueous systems
WO2006071175A3 (en) * 2004-12-30 2007-01-11 Akzo Nobel Nv Composition and its use in papermaking
US7658819B2 (en) 2004-12-30 2010-02-09 Akzo Nobel N.V. Composition
US8052704B2 (en) 2000-12-20 2011-11-08 Foxhollow Technologies, Inc. High capacity debulking catheter with distal driven cutting wheel
US8192452B2 (en) 2009-05-14 2012-06-05 Tyco Healthcare Group Lp Easily cleaned atherectomy catheters and methods of use
US8226674B2 (en) 2000-12-20 2012-07-24 Tyco Healthcare Group Lp Debulking catheters and methods
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US8328829B2 (en) 1999-08-19 2012-12-11 Covidien Lp High capacity debulking catheter with razor edge cutting window
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US9028512B2 (en) 2009-12-11 2015-05-12 Covidien Lp Material removal device having improved material capture efficiency and methods of use
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US9687266B2 (en) 2009-04-29 2017-06-27 Covidien Lp Methods and devices for cutting and abrading tissue
US9801647B2 (en) 2006-05-26 2017-10-31 Covidien Lp Catheter including cutting element and energy emitting element
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US10213224B2 (en) 2014-06-27 2019-02-26 Covidien Lp Cleaning device for catheter and catheter including the same
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US4824894A (en) * 1985-07-12 1989-04-25 Rohm Gmbh Chemische Fabrik Biodegradable organosol flocculants
FR2585712A1 (en) * 1985-07-31 1987-02-06 Sandoz Sa Mixtures of vinyl addition polymers for use as flocculation and dehydration agents
GB2205591B (en) * 1987-05-01 1990-03-07 Grace W R & Co Pitch control aid
GB2327049A (en) * 1997-07-10 1999-01-13 Atotech Deutschland Gmbh Pretreatment and coating of electrically non-conductive surfaces
GB2327049B (en) * 1997-07-10 2000-01-19 Atotech Deutschland Gmbh Solution for pretreatment of electrically non-conductive surfaces,and method of coating the surfaces with solid material particles
US6235182B1 (en) 1997-07-10 2001-05-22 Atotech Deutschland Gmbh Solution for pretreatment of electrically non-conductive surfaces, and method of coating the surfaces with solid material particles
US8328829B2 (en) 1999-08-19 2012-12-11 Covidien Lp High capacity debulking catheter with razor edge cutting window
US8597315B2 (en) 1999-08-19 2013-12-03 Covidien Lp Atherectomy catheter with first and second imaging devices
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DE3302069C3 (en) 1996-11-21
ATA30483A (en) 1993-07-15
IT1219777B (en) 1990-05-24
DE3302069C2 (en) 1990-03-29
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FR2530239A1 (en) 1984-01-20
CA1219699A1 (en)
ES519408D0 (en)
SE8300453D0 (en) 1983-01-28
ES8403327A1 (en) 1984-03-16
IT8319365D0 (en) 1983-01-31
ES519408A0 (en) 1984-03-16
HK10786A (en) 1986-02-21
FR2530239B1 (en) 1987-10-02
SE458526B (en) 1989-04-10
GB8302375D0 (en) 1983-03-02
AT397215B (en) 1994-02-25
NL8300326A (en) 1983-09-01
CH660015A5 (en) 1987-03-13
CA1219699A (en) 1987-03-24
DE3302069A1 (en) 1983-08-04
SE8300453L (en) 1983-08-02

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