GB1565185A - Creation of Inventions and Patents with Artificial Intelligence

GB1565185A – Process for preparing pvp-iodine complex
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GB1565185A – Process for preparing pvp-iodine complex
– Google Patents
Process for preparing pvp-iodine complex

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Publication number
GB1565185A

GB1565185A
GB15472/78A
GB1547278A
GB1565185A
GB 1565185 A
GB1565185 A
GB 1565185A
GB 15472/78 A
GB15472/78 A
GB 15472/78A
GB 1547278 A
GB1547278 A
GB 1547278A
GB 1565185 A
GB1565185 A
GB 1565185A
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Prior art keywords
pvp
iodine
suspension
process according
complex
Prior art date
1977-04-27
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GB15472/78A
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GAF Corp

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GAF Corp
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1977-04-27
Filing date
1978-04-19
Publication date
1980-04-16

1978-04-19
Application filed by GAF Corp
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GAF Corp

1980-04-16
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patent/GB1565185A/en

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Classifications

A—HUMAN NECESSITIES

A01—AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING

A01N—PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS

A01N59/00—Biocides, pest repellants or attractants, or plant growth regulators containing elements or inorganic compounds

A01N59/12—Iodine, e.g. iodophors; Compounds thereof

Description

PATENT SPECIFICATION ( 11) 1 565 185
hn ( 21) Application No 15472/78 ( 22) Filed 19 Apr 1978 ( 19) ( 31) Covention Application No 791520 ( 32) Filed 27 Apr 1977 in ( 33) United States of America (US)
3 ( 44) Complete Specification Published 16 Apr 1980
U’ ( 51) INT CL 3 A 61 K 31/79 33/18 CO 8 F 8/00 ( 52) Index at Acceptance C 3 J AT ( 54) PROCESS FOR PREPARING PVP-IODINE COMPLEX ( 71) We, GAF CORPORATION, a corporation organized and existing under the laws of the State of Delaware, United States of America, having its main office at 140 West 51st Street, New York, New York 10020, United States of America, do hereby declare the invention, for which we pray that a patent may be granted to us, and the method by which it is to be performed, to be particularly described in and by the following statement: 5
This invention relates to a process for preparing a polyvinylpyrrolidoneiodine complex, generally called PVP-iodine, and, more particularly, it is concerned with an improved process which provides a stable complex for use as a germicidal and bactericidal composition The invention also embraces PVP-iodine complex made by the process.
PVP-iodine has been used extensively in hospitals and elsewhere for some time because 10 of its germicidal, bactericidal, fungicidal and generally disinfecting properties Usually it is sold as a brown powder, which contains about 10 % available, or active iodine, and about % inactive iodine, in the form of the iodide ion.
The known processes for making commercial PVP-iodine are represented by such patents as U S 2,706,701; U S 2,739,922; U S 2 826,532; U S 2,900,305; U S 3,028, 300; 15 German Patent 1,037,075 and German Offenlegungsschrift 2,439197 These prior art processes are characterized by being deficient in one or more respects, particularly in that they are time-consuming and expensive, or require a large amount of iodine to produce a stable complex having an acceptable available iodine level.
In accordance with the present invention, there is provided herein a process for making 20 stable PVP-iodine complex having a high level of iodine power The process of this invention is carried out by adding a pre-determined amount of free water to a PVP suspension in a non-aqueous solvent, or providing a PVP suspension in a non-aqueous solvent and having a predetermined content of free water, and admixing iodine therewith to form the desired solid complex The amount of free water is 1-10 % by weight of PVP The 25 PVP suspension may be obtained by suspension polymerization of N-vinylpyrrolidone (VP) in a suitable non-aqueous solvent, and used directly for succeeding steps of the process Accordingly a preferred form of the invention comprises (a) suspension polymerizing vinylpyrrolidone in a non-aqueous solvent to form polyvinyl pyrrolidone, 30 (b) adding water to the suspension in an amount of 1-10 % by weight of said polyvinylpyrrolidone, and (c) reacting iodine therewith at a temperature of 650-850 C to form said desired complex.
Suspension Polymerization of VP 35 In the first step of the preferred embodiment of the invention, vinylpyrrolidone is polymerized by a suspension polymerization technique to provide the PVP moiety of the desired PVP-iodine complex The suspension polymerization is carried out by dissolving VP in a suitable solvent.
The solvents in the present suspension polymerization of vinylpyrrolidone are those in 40 which vinylpyrrolidone is miscible and in which the vinylpyrrolidone polymeric product is substantially insoluble Saturated aliphatic hydrocarbons are suitable solvents Illustrative of those solvents suitable for the present process are the saturated aliphatic hydrocarbons containing from 5 to 20 carbon atoms which include mixtures of such compounds as may be prepared for such purpose or as may be found in commercially available mixtures such as 45 -I 1 565 185 L for example, a petroleum cut of C 6-C 16 alkanes or other sources of hydrocarbon mixtures such as a kerosene or petroleum fraction boiling at about 1750 C, e g Varsol; (Registered Trade Mark) but above the temperature at which the polymerization is effected The preferred solvents for the present process are those alkanes having boiling points between 50 C and 100 C which are more easily separated from the polymeric product by boiling or 5 evaporation Most preferred of this group are normal and branched chain hexane, heptane, octane, and cycloalkanes, such as, cyclopentane and cyclohexane Solvent mixtures including even minor amounts of reactive oxygen-containing compounds are best avoided in the present process since they tend to prematurely terminate polymer chains formed in the system and, in the case of certain azo initiators or catalysts, cause apparent deactivation 10 which also materially limits the length of the polymer chains formed in the process by halting the reaction.
The amount of solvent needed for any suspension depends on several factors; namely, on the efficiency of agitation, the choice of catalyst, the temperature and pressure of operation and the optional use and amount of suspending agent present in the suspension medium 15 However, generally, the solvent is employed in an amount equal to monomer up to a slight excess or as much as about 3 5 parts by weight per part by weight of monomer The preferred amount of solvent employed in the present polymerization is between 1 5 and 2 parts by weight per part of monomer Such a mixture provides an adequate dissipation of heat built up in the reaction zone by the formation of polymer in the beads or globules of 20 the suspension while still maintaining the reaction volume at a reasonable level so as to avoid the need for oversized equipment and other inefficiencies and difficulties in product recovery Generally, the amount of solvent employed is that necessary to maintain the suspension and avoid agglomeration of suspended particles.
As stated above, the dispersion in the present process is maintained primarily by 25 mechanical agitation in a standard type mixing zone such as in a stirred reactor However, maintenance of the suspension is enhanced and prolonged during polymerization by the addition of small amounts of suspension stabilizers of the type used to prevent agglomeration of the suspended droplets or globules which become more viscous and sticky as polymerization progresses In effect, the stabilizer adheres to the surface of the globule 30 and protects it from direct contact with another during the period when the polymeric globules are forming The function of the stablizer is particularly important in the present process where a high solids concentration is achieved.
Such stabilizers or suspension aids which are found to be useful in the suspension polymerization step are the poly-N-vinylpyrrolidone alkyl-modified polymers (e g N-vinyl 35 methylpyrrolidone polymers and copolymers with methyl substituted monomer) and the N-vinylpyrrolidone C 10 to C 20 olefin copolymers commercially available through GAF Corporation and marketed under the commercial names of ANTARON(Trademark of GAF Corporation) P-904, ANTARON(Trademark of GAF Corporation) P-804, ANTARON (Trademark of GAF Corporation) V-816, GANEX(Trademark of GAF Corporation) 40 V-516, (preferred) GANEX(Trademark of GAF Corporation) P-904, GANEX(Trademark of GAF Corporation) V-220, GANEX(Trademark of GAF Corporation) V-516, etc, which are substantially insoluble in the solvents of the present process Generally, for the present purposes, the stabilizer is employed in an amount between 0 5 % and 5 % preferably between 1 % and 3 % by weight based on the weight of monomer Conveniently, the above 45 stabilizers are polymers having a number average molecular weight between about 8,000 and about 20,500.
The catalyst or polymerization initiators found to be most effective in the suspension polymerization step are those of the free radical type which are soluble in the monomer.
Accordingly, suitable initiators for the present process include azobisisobutyronitrile 50 (commercially available as VAZO(Trademark of du Pont Corporation)-64), azobisisovaleronitrile (commercially available as VAZO(Trademark of du Pont Corporation) -52), dimethyl azodiisobutyrate, benzoyl peroxide, t-butyl hydroperoxide, tbutyl peracetate, acetyl peroxide, di-t-butyl peroxide, di-cumyl peroxide, cumyl hydroperoxide and generally any of the oil-soluble free radical initiators conventionally employed for polymerization 55 The particular initiator may be selected in accordance with the temperature of polymerization so that the catalyst remains in the liquid phase during reaction In an oxygen free system, the proportion of initiator employed is between about 0 02 % and 2 % by weight, preferably between about 0 05 % and about 1 0 % by weight based on total weight of monomer However, when oxygen contaminant is present, an additional amount of 60 initiator is employed e g the above amount plus an equimolar amount for every mol of oxygen in a free state or reducible to a free state Instead of, or in addition to, the initiators listed above, actinic light with or without the aid of a photosensitizer, e g benzophenone, fluorescein, eosin, etc, may be used but is less desirable.
In general, the present suspension polymerization can be carried out by forming a 65 3 1 565 185 3 mixture of the solvent, monomer, catalyst and suspension stabilizer This mixture can be formed initially in the same zone or the mixture of monomer and solvent can be performed with or without the stabilizer and at least the initiator can be separately added thereto.
Instead of this, a separate initiator mixture can be prepared and added to the monomeric suspension 5 The molecular weights of the resultant PVP polymer produced thereby usually are about K-15 to about K-90 ( 10,000 to 360,000), which may be varied by kind and amount of catalyst used, and the temperature of the reaction Higher molecular weights are obtained with a minimum amount of a given catalyst and lower temperatures, while lower molecular weights are obtained with increased amounts of catalyst and a higher temperature 10 Alternatively, but less desirably, commercially available PVP powder of a given molecular weight may be used directly as a reactant for succeeding steps in the process.
Accordingly, PVP K-30 powder may be suspended in a liquid, using a suitable suspending aid, and made available for the steps of addition of water and complexation with iodine, as described below However, PVP prepared via suspension polymerization of VP generally 15 requires less iodine to form the complex than with commercial material, probably due to particle size differences.
Addition of Water to PVP Suspension Addition of water to the PVP suspension prior to complexation with iodine is necessary 20 to form stable PVP iodine powders 1-10 % by weight of water is added to the PVP suspension, based on the PVP content, and preferably 5-8 % by weight The water may be added during the preceding polymerization step, but it is preferred to include it after polymerization has taken place, particularly if a lower molecular weight PVP polymer is desired 25 Some water already may be present in the PVP itself, bound or otherwise, particularly in commercial material; however, this water usually is insufficient to provide the amount of water desired to form a stable complex.
Complexation of PVP and Iodine 30 Iodine is reacted with the suspension of PVP containing the added water Usually an elevated temperature is employed for this complexation step in order to reduce the time required for complete reaction For rapid complex formation, a temperature above 650 C is preferred; however, if the reaction temperature is too high, the complex will exhibit a loss of available iodine Preferably a temperature of 650 C to 850 C is used, more preferably 35 70-750 C A product having excellent stability properties may be prepared by heating at 750 C for as short a time as 1-1 k hours.
Generally, the amount of iodine used is 5-25 %, preferably 10-20 %, based on the weight of the PVP-iodine complex However, the present process requires considerably less iodine (approximately 19 % less) than commercial processes which employ dry milling of both 40 reactants to prepare complex powder having an available iodine level of about 9 5-10 % Of course, if higher levels of available iodine are desired, then an increased iodine charge is employed Similarly, if only a lower level of available iodine in the product is necessary, then a reduced charge of iodine is used For any given available iodine level, however, the process of this invention requires less iodine than the commercial process mentioned 45 Recovery of PVP Iodine-Complex The solid PVP-iodine produced in the complexation step is recovered by filtration and dried The solid product is a pale yellow powder which is stable to washing with heptane even after prolonged storage Later it may be made into a commercial solution by addition 50 of a solvent therefor.
Example 1
A 1 liter 4-necked cylindrical resin flask equipped with a stirrer, thermometer, dropping funnel and gas inlet tube is purged with nitrogen for about 15 minutes prior to charging 55 Then the following charge is added to the flask:
335 ml ( 225 g) of heptane 1.4 g of Ganex V-516 55.5 g of vinylpyrrolidone 0 6 g Vazo; and, 60 55.5 g vinylpyrrolidone is charged into the dropping funnel.
The funnel and flask are stoppered and a slight positive nitrogen pressure is maintained.
The flask then is heated in a constant temperature bath to 750 C whereupon a slight exotherm results, requiring cooling to 71 ‘C thereafter, addition of vinylpyrrolidone is begun dropwise from the dropping funnel, and continued for three hours while maintaining 65 A 1 565 185 the reaction temperature at about 71-75 C, and thereafter for an additional 18 hours at C.
To the polyvinylpyrrolidone suspension thus prepared is added 1 0 g Arlacel 85 (Atlas Chem) sorbitan trioleate a surfactant dissolved in 5 0 ml of heptane, and 8 8 g of water ( 7 9 % water based upon PVP content) is added dropwise over a period of 15 minutes 5 (“Arlacel” is a Registered Trade Mark).
The water-containing slurry then is stirred for 1/2 hour at 70-72 C and 18 g of finely divided iodine is added incrementally over a period of 1/2 hour at 70 75 C The contents of the flask then are heated for an additional two hours at 75 C, cooled, filtered and rinsed with heptane 10 The product is dried in air overnight to give a yellow powder weighing 137 g ( 99 7 % yield), which is analyzed as follows:
Available iodine (thiosulfate titration) = 9 93 % 15 Water in powder = 5 3 % Available iodine (excluding water) = 10 48 % 20 Loss in stability test ( 6 hours at 75 C) = 2 28 % Example 2
The procedure of Example 1 is followed except that the polymerization is carried out by raising the temperature to 90 -95 C after final addition of vinylpyrrolidone, followed by 25 heating at this temperature for only three hours The resultant solid complex product is otherwise the same as in Example 1.
Example 3
The procedure of Example 1 is followed except that 5 5 g to 8 8 g of water ( 5 5 to 8 8 % 30 by weight water based on PVP) is added to the PVP suspension to provide a similar product.
Example 4
The procedure of Example 1 is followed using hexane at 65 C in place of heptane to 35 provide a similar product.
Example S
To the apparatus of Example 1 is charged 100 g of heptane and agitation is started while 0 5 g Ganex V-516 is added followed by 50 0 g polyvinylpyrrolidone K-30 The resultant 40 slurry is stirred for 1/2 hour at ambient temperature, and then 2 5 g of water is added dropwise with stirring for 1/2 hour Then 10 0 g of iodine is added as a fine powder over a period of 3/4 hour After the addition is complete, the mixture is heated to 70 C within 1 hour, and held at 70 C for 3 hours The contents then are cooled, filtered, rinsed, dried.
The solid complex product has properties similar to that prepared in Example 1 45

Claims (1)

WHAT WE CLAIM IS:
1 An improved process of forming a stable PVP-iodine complex which comprises:
(a) providing a suspension of PVP in a non-aqueous solvent, b) adding water to the suspension in an amount of 1-10 % by weight of said PVP, and (c) reacting iodine therewith to form said desired complex 50 2 A process according to claim 1 wherein said water is added in an amount of 5-8 % by weight.
3 An improved process of forming a stable PVP-iodine complex which comprises:
providing a suspension of PVP in a non-aqueous solvent and having a water content of 1-10 % by weight of said PVP, and 55 reacting iodine therewith to form said desired complex.
4 A process according to claim 3 wherein said water is present in the suspension in an amount of 5-8 % by weight.
A process according to claim 1 wherein said iodine is reacted at a temperature of 65 -85 C 60 6 A process according to any one of the preceding claims wherein said suspension is in a saturated aliphatic hydrocarbon.
7 A process according to claim 6 wherein said saturated aliphatic hydrocarbon is selected from the group consisting of hexane and heptane.
8 An improved process of forming a stable PVP-iodine complex which comprises: 65 A 1 565 185 (a) suspension polymerizing vinylpyrrolidone in a non-aqueous solvent to form polyvinyl pyrrolidone, (b) adding water to the suspension in an amount of 1-10 % by weight of said polyvinylpyrrolidone, and (c) reacting iodine therewith at a temperature of 65 -85 C to form said desired complex 5 9 A process according to claim 7 wherein said water is added in an amount of 5-8 % by weight.
A process according to claim 8 or claim 9 wherein said suspension polymerization is carried out in saturated aliphatic hydrocarbon.
11 A process according to claim 10 wherein said saturated aliphatic hydrocarbon is 10 selected from the group consisting of hexane and heptane.
12 A process according to claim 5 or any one of claims 8 to 11 wherein said iodine is reacted at a temperature of 70-75 C.
13 A process for forming a PVP-iodine complex substantially as described with reference to any of the Examples herein 15 14 A PVP-iodine complex made by the process of any one of the preceding claims.
MEWBURN ELLIS & CO Chartered Patent Agents, 70/72 Chancery Lane 20 London WC 2 A l AD, Agents for the Applicants.
Printed for Her Majesty’s Stationer) Office by Croydon Printing Company Limited Croydon, Surrey, 1980.
Published by The Patent Office 25 Southampton Buildings, London, WC 2 A l AY,from which copies may be obtained.

GB15472/78A
1977-04-27
1978-04-19
Process for preparing pvp-iodine complex

Expired

GB1565185A
(en)

Applications Claiming Priority (1)

Application Number
Priority Date
Filing Date
Title

US05/791,520

US4128633A
(en)

1977-04-27
1977-04-27
Process for preparing PVP-iodine complex

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GB1565185A
true

GB1565185A
(en)

1980-04-16

Family
ID=25154001
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Title
Priority Date
Filing Date

GB15472/78A
Expired

GB1565185A
(en)

1977-04-27
1978-04-19
Process for preparing pvp-iodine complex

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US4128633A
(en)

JP
(1)

JPS53134894A
(en)

CA
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CA1102492A
(en)

DE
(1)

DE2814203A1
(en)

FR
(1)

FR2388832A1
(en)

GB
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GB1565185A
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Title

US4310509A
(en)

1979-07-31
1982-01-12
Minnesota Mining And Manufacturing Company
Pressure-sensitive adhesive having a broad spectrum antimicrobial therein

DE2942179A1
(en)

1979-10-18
1981-05-07
Basf Ag, 6700 Ludwigshafen

METHOD FOR PRODUCING PVP IOD

US4810489A
(en)

1986-12-04
1989-03-07
Bristol-Myers Company
High oil phase pharmaceutical vehicles and sunscreen compositions having waterproof sun protection factors

US4897259A
(en)

1986-12-04
1990-01-30
Bristol-Myers Company
High oil phase pharmaceutical vehicles and sunscreen compositions having waterproof sun protection factors

US5071648A
(en)

1989-04-06
1991-12-10
Merocel Corporation
Polymeric broad-spectrum antimicrobial materials

AU5135293A
(en)

1992-09-22
1994-04-12
Arda Technologies, Co.
Antimicrobial composition and method of preparation

US6365169B1
(en)

1999-09-30
2002-04-02
Solomon Rosenblatt
Polymeric broad spectrum antimicrobial coatings

US6797743B2
(en)

2000-09-27
2004-09-28
Michigan Biotechnology Institute
Antimicrobial polymer

US6939554B2
(en)

2002-02-05
2005-09-06
Michigan Biotechnology Institute
Antimicrobial polymer

WO2003080730A1
(en)

2002-03-20
2003-10-02
Michigan Biotechnology Institute
Conductive polymer-based material

US6951902B2
(en)

2002-08-16
2005-10-04
Michigan Biotechnology Institute
Two dimensional polymer that generates nitric oxide

CN101161688B
(en)

2006-10-13
2010-12-08
北京北大明德化学制药有限公司
Novel process for synthesizing povidone iodine by gas phase/ solid phase reaction

WO2011055388A2
(en)

2009-11-05
2011-05-12
Indian Institute Of Technology
Wound dressing polymer matrix

CN102093279B
(en)

2011-01-07
2012-05-23
上海宇昂化工科技发展有限公司
High-stability nonionic N-vinyl butyrate lactam iodine and preparation method thereof

US20130171203A1
(en)

2011-12-16
2013-07-04
Solomon Rosenblatt
Composition And Methods For Antimicrobial Articles

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Priority date
Publication date
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Title

US2739922A
(en)

1952-03-13
1956-03-27
Herman A Shelanski
Mixtures of polymeric n-vinyl pyrrolidone and halogens

US2900305A
(en)

1952-04-15
1959-08-18
Gen Aniline & Film Corp
Preparation of iodine polyvinylpyrrolidone adducts

US3898326A
(en)

1973-05-14
1975-08-05
West Laboratories Inc
Polyvinylpyrrolidone-iodide compositions and polyvinylpyrrolidone-iodide-iodine complexes prepared therefrom

US4017407A
(en)

1973-05-14
1977-04-12
West Laboratories, Inc.
Methods for preparing solid iodine carrier mixtures and solid formulations of iodine with iodine carriers

YU193875A
(en)

1974-08-16
1982-02-28
Basf Ag
Process for producing polyvinyl pyrrolidone-iodine

1977

1977-04-27
US
US05/791,520
patent/US4128633A/en
not_active
Expired – Lifetime

1978

1978-02-23
CA
CA297,625A
patent/CA1102492A/en
not_active
Expired

1978-04-03
DE
DE19782814203
patent/DE2814203A1/en
not_active
Withdrawn

1978-04-18
FR
FR7811329A
patent/FR2388832A1/en
not_active
Withdrawn

1978-04-19
GB
GB15472/78A
patent/GB1565185A/en
not_active
Expired

1978-04-20
JP
JP4601678A
patent/JPS53134894A/en
active
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CA1102492A
(en)

1981-06-02

FR2388832A1
(en)

1978-11-24

JPS53134894A
(en)

1978-11-24

DE2814203A1
(en)

1978-11-02

US4128633A
(en)

1978-12-05

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