Anionic polymerization initiators based on alkali metal amides in combination with alkali metal salts and anionic polymerization process using these initiators

The present invention relates to new initiator systems for anionic polymerisation, to an anionic polymerisation process using these initiators and to the polymers obtained by this process.
The first anionic polymerisations were carried out by Wurz with ethylene oxide. However, it is especially Ziegler who deserves the credit for the explanation of the anionic polymerisation mechanism.
In this connection, it is necessary to distinguish clearly between pure anionic polymerisation, which is involved throughout the text which follows, and coordinated anionic polymerisation, which employs initiators such as salts of aluminium, of antimony and of the transition metals (for example the so-called Ziegler-Natta two-metal catalysts) and which has no bearing on the field in which the invention applies.
It has been known for a number of years that it is possible to polymerise lactones and lactams using sodium amide as the polymerisation initiator (German Pat. No. 1,960,385 and German Pat. No. 2,111,545).
Equally, Sigwalt et al. (C.R. Acad. Sci., Volume 252, pages 882-884, Session of Feb. 6, 1961) have shown that sodium amide initiates the polymerisation of propylene sulphide.
Unfortunately, the efficiency of the amide as an initiator is confined to particular monomers, especially to very easily polymerisable heterocyclic compounds such as propylene sulphide, the lactones or the lactams.
Furthermore, it has been shown by Sanderson and Hauser (JACS 71, 1595 (1949)) that it is possible to polymerise styrene using an alkali metal amide in liquid ammonia as the anionic polymerisation initiator.
Unfortunately, apart from the fact that this process suffers from the major disadvantage that it is carried out under conditions which are not industrially viable (a reaction temperature of between -30.degree. and -70.degree. C.), the presence of ammonia causes the premature and random termination of the polymerisation.
Other authors (German Pat. No. 2,365,439) have found that it is possible to upgrade the alkali metal amide by means of sulphoxides such as:
.phi.--SO--(CH.sub.2).sub.6 --SO--.phi.
in which .phi. represents a phenyl nucleus.
However, once again the complexes of the latter only give good results with easily polymerisable monomers such as propylene sulphide.
Furthermore, these complexes are prepared under conditions which are not industrially viable (at -70.degree. C., in liquid ammonia, followed by reaction for 10 hours at -45.degree. C.).
Applicants has now discovered anionic polymerisation initiators which make it possible to overcome the abovementioned disadvantages and which result from the combination, in the presence of a solvent, of an alkali metal amide selected from the group comprising sodium amide, potassium amide or lithium amide and an alkali metal salt of which the cation is selected from the group comprising potassium, lithium or sodium and the anion is selected from the group comprising the thiocyanate, nitrite, cyanide or cyanate anions, the molar ratio of alkali metal amide to salt associated therewith being at least 1.
The Applicant Company has in fact found that the alkali metal salts cited above have a surprisingly pronounced upgrading effect on alkali metal amides as polymerisation initiators.
It is true that BIEHL et al. have already indicated, in Journal of Organic Chemistry, Volume 35, No. 7, 1970, page 2,454, that the combination of an alkali metal amide with a certain number of salts, including nitrites and thiocyanates, makes it possible to activate the amide in aryne condensation reactions, using dimethylamine as the solvent.
However, if the activity of a combination such as sodium amide/sodium nitrite is tested using the combination as a basic catalyst for the formation reaction of the triphenylmethyl anion from triphenylmethane in THF, which is known to be a good anionic polymerisation solvent, it is found that this combination is hardly more active than sodium amide used by itself.
It should furthermore be noted that in the organic chemistry reactions which have just been considered, a large amount of basic catalyst relative to the reactants themselves is used.
According to a preferred variant of the invention, from 1.5 to 3 mols of alkali metal amide are used per mol of alkali metal salt associated therewith. However, it is equally possible to use a large excess of amide over the salt associated therewith; for example, it is possible to use up to ten mols of amide per mol of salt associated therewith.
The solvents which can be used to prepare the initiators according to the invention must be aprotic and can be polar, slightly polar or even non-polar. It is possible to use polar solvents to the extent that their structure does not make them susceptible to the action of the complex bases used according to the invention. Thus, hexamethyl-phosphotriamide (HMPT) can be used up to about 25.degree. C. but, for example, dimethylsulphoxide (DMSO), dimethylformamide (DMF) and N-methylpyrrolidone are degraded by the complex bases and should preferably be avoided. The polar solvents are from every point of view of little economic and industrial value in the field concerned by the invention. Other aprotic solvents of markedly lower polarity can be used, for example pyridine (.epsilon.=12.3 at 25.degree. C.), though they can suffer degradation after a certain time, especially if the temperature is somewhat elevated.
The aprotic solvents of low polarity (of dielectric constant <10 at 25.degree. C.) are particularly suitable for the preparation of the initiators according to the invention. Thus, linear or cyclic ethers and polyethers, such as tetrahydrofurane (THF) and dimethoxyethane (DME), give good results, generally within a very short time. The glymes are also suitable.
However, and this is a considerable advantage, the initiators according to the invention, can also be prepared easily in a non-polar solvent which can be the same solvent as that wherein, advantageously, the subsequent polymerisation is carried out. Thus it is possible to use alkanes or cycloalkanes such as hexane, heptane or cyclohexane, or arenes such as benzene or toluene.
If solvents containing ether bridges are used, it is important carefully to remove the oxygen and peroxides present, by means of known methods.
According to a second variant of the invention, the initiators are prepared using the monomer to be polymerised as the solvent. In this case, the polymerisation is carried out in bulk.
It has in fact been discovered, and this is another surprising aspect of the present invention, that the initiators according to the invention can be prepared in the absence of any solvent other than the monomer itself and that it is possible to do so without significant change in the activity of the initiator.
The initiators according to the invention can be prepared with the aid of several substantially equivalent methods because what is involved is bringing together the alkali metal amide and the associated salt in a solvent.
For example, it is possible first to introduce the solvent into the reactor, whilst stirring, then to introduce the alkali metal amide and finally to introduce the associated salt.
It is also possible to add a suspension of the alkali metal amide in a solvent to a solution-suspension of the associated salt in the same solvent or in a solvent miscible therewith.
Alternatively, the associated salt and the amide can be introduced into the reactor and the solvent can then be poured on top.
The alkali metal amide is preferably employed ground, in the form of particles whose mean size depends on the size of the polymerisation reactor, the size of the particles being preferably larger when the size of the reactor is itself large. Grinding can be effected in the presence of a small amount of an aprotic solvent of low polarity.
The alkali metal amide used can be of analytical grade or of commercial purity. It can contain a certain amount of sodium hydroxide, provided this proportion is sufficiently well known so that the initiator can be prepared with the proportions of reactants proposed above.
As regards moisture, the latter should be removed from the reactants, solvents and apparatuses used. However, it should be noted that the cost of sodium amide makes it possible to employ less thorough drying than in the preparation of the known initiators. In fact, the use of a slight excess of alkali metal amide makes it possible to remove traces of moisture quite sufficiently by reaction of the said amide with the said traces of moisture, thereby forming products which do not interfere with the initiator formation reaction or subsequently with the polymerisation reaction.
The initiator formation reaction is advantageously carried out, in certain cases, in the reactor which subsequently serves for the polymerisation, because this makes it possible to reduce the introduction of water into the apparatus. This reaction is preferably carried out at a temperature of 20.degree. to 60.degree. C. It is possible to use a lower temperature but the formation reaction becomes correspondingly longer and ultimately in general ceases below 0.degree. C. It is also possible to work at a higher temperature, but in that case the danger of degradation of the alkali metal amide or of the solvent increases. It is advisable to stir the mixture.
In the majority of cases, the duration of the initiator formation reaction is at least one hour but does not exceed 4 hours. However, much longer heating may prove necessary in difficult cases.
Finally, it should be noted that the initiators according to the invention exhibit an adaptability in use which is rarely found with the previously known initiators. In fact, if, for reasons of convenience or necessity the initiator must be prepared in a solvent which is not the same as that wherein the polymerisation is subsequently carried out, difficulties are subsequently generally encountered. In fact, the polarity of the medium is affected and, for example, the micro-structure of the polymer obtained does not conform to what is expected. In contrast, the initiators according to the invention can be prepared in a first solvent, for example a solvent of low polarity, after which the said solvent is evaporated under an almost complete vacuum, and finally a second solvent, for example a non-polar solvent, in which it is desired to carry out the polymerisation, is introduced over the initiator, the properties of which have remained preserved. The invention thus makes it possible to achieve predetermined ideal conditions for carrying out the polymerisation.
Furthermore, it must be clearly recognised that the formation of the initiators according to the invention is not accompanied by any evolution of gas which could create an unnecessary or even objectionable excess pressure in the reactor. Furthermore, the initiators according to the invention are easy to prepare because the starting materials from which they are produced are in the solid state. Finally, no organic peroxide, the presence of which is extremely undesirable in activated anionic polymerisation, can result from the introduction of the associated salts, which would not normally contain a peroxide.
As with all anionic polymerisations, it is desirable to use dry reactants, dry solvents and dry apparatuses. However, this limitation, which determines the outcome of the polymerisation, applies less strictly when using the process according to the invention in view of the property of the alkali metal amide, a low cost product, of reacting with traces of moisture to give products which do not interfere with the course of the reaction.
The reaction can be terminated in a known manner, for example by introducing a protonising agent such as an alcohol (methanol or hexanol). The reaction medium is subsequently precipitated in methanol or hexane.
Purification of the solvents and of the reactants is obviously desirable. The solvents, which are the same as those wherein the complex base can be formed, and which in particular comprises the solvents of dielectric constant less than or equal to 10 at 25.degree. C., are purified in a manner known to polymerisation specialists. Thus, for example, a distillation over solid sodium hydroxide or potassium hydroxide, followed by a distillation over sodium, can be carried out, finally finishing by drying the solvent over sodium wires. The monomers, for their part, are purified in a known and usual manner, which depends on the nature of the monomers and which can range from simple distillation to double distillation over molecular sieves, calcium hydride, an alkali metal or even a living polymer (polyisopropenyl-lithium).
The invention also relates to a polymerisation process characterised in that an initiator such as has just been described is used.
The polymerisation process according to the invention thus consists in using as the initiator the combination of an alkali metal amide with a salt selected from the group comprising the alkali metal nitrites, cyanates, thiocyanates and cyanides, in the absence or presence of a solvent.
The process according to the invention is particularly, but not uniquely, of value when an alkali metal nitrite or thiocyanate is used as the associated salt. It has in fact been discovered that for a given alkali metal amide and a given alkali metal of the associated salt, the effectiveness of the initiator increases in the sequence
CN.sup.- <OCN.sup.- <SCN.sup.- .perspectiveto.NO.sub.2.sup.-
This is a particularly surprising result if account is taken of the fact that, on the one hand, Biehl et al. (op. cit.) have only shown the ability of certain salts to boost alkali metal amides in the case of a particular reaction of organic chemistry, and only in the presence of solvents (dimethylamine) unsuitable for anionic polymerisation, and that, on the other hand, one of the preferred salts in the process according to the invention proves virtually ineffective in another reaction (triphenylmethane test) which is carried out in THF, which is one of the preferred solvents for anionic polymerisation. Anyone skilled in anionic polymerisation thus had to doubt the possibility of applying the combinations according to the invention in his field and was in no case able to foresee their good efficiency. This is all the more so since the low activity of the combinations according to the invention in the media required for the polymerisation could only be aggravated by the fact that in anionic polymerisation it is necessary to use amounts of basic initiators which are at least 1,000 times lower than in the reactions of synthetic organic chemistry.
It is also possible to combine the alkali metal amide with a mixture of activators, the respective proportions of which can vary substantially without affecting the result of the polymerisation reaction.
Furthermore, it has also been found advantageous, in particular as regards the yield, to combine an alkali metal amide with a salt of a different alkali metal. This is all the more the case if the difference between the ionic radii of the cations is large.
However, in general the selection of different cations has less influence than the selection of the associated anion.
On the other hand, the advantageous effects resulting from the selection of different cations and of preferred anions (nitrite or thiocyanate) are generally cumulative.
In fact, the preferred variants of the process according to the invention consist in using one of the following initiators:
NaHN.sub.2, NaNO.sub.2
NaNH.sub.2, NaSCN
KNH.sub.2, KNO.sub.2
KNH.sub.2, KSCN
NaNH.sub.2, KNO.sub.2
NaNH.sub.2, KSCN
KNH.sub.2, NaNO.sub.2
KNH.sub.2, NaSCN
LiNH.sub.2, KSCN
LiNH.sub.2, KNO.sub.2
The monomers to which the invention is applicable are, as has already been stated, those of which it is known that they undergo polymerisation by a purely anionic mechanism or, to put it another way, which are capable of polymerising anionically by the opening of an ethylenic double bond or of a heterocyclic ring. Bearing in mind that the first anionic polymerisations date back more than a century, it will be seen that the list of these monomers is very long and that this mechanism is very well known. However, it must be clearly appreciated that this mechanism is the same regardless of whether the monomer is a heterocyclic compound or whether it exhibits ethylenic unsaturation or aldehyde unsaturation (which can be considered as a two-atom heterocyclic structure), because the initiation gives rise, by scission of a bond, to the formation of an active centre which, regardless of the nature of the atom which carries the negative charge, attacks a fresh molecule of monomer which in turn carries the negative charge and so on, until the monomer is exhausted or the reaction is terminated. On this subject, reference may be made, for example, to the work by Professor Georges Champetier "Chimie Macromoleculaire" ("Macromolecular Chemistry"), Volume I, Editions Hermann, Paris (1969).
However, the following monomers may be mentioned as relevant monomers, without pretending that this list is exhaustive:
In the case of vinyl monomers, those of the general formula ##STR1## R.sub.1 =R.sub.2 =R.sub.3 =H and R.sub.4 =alkyl ##STR2## where X=H, Cl, --OCH.sub.3 or --C(CH.sub.3).sub.3 ##STR3## (where R'=alkyl or cycloalkyl), or ##STR4## (where R"=alkyl) ##STR5## (where
R=alkyl, especially methyl, or aryl, especially phenyl), or
R.sub.1 =R.sub.2 =H,
R.sub.3 =--CH.sub.3 and
R.sub.4 =phenyl, cyano or ##STR6## (R'=alkyl or cycloalkyl).
In the case of the heterocyclic monomers, the alkylene oxides, the alkylene sulphides, the lactones, the lactams, the thiethanes and the cyclic carbonates, such as ethylene oxide, propylene oxide, propylene sulphide, .beta.-propiolactone, .epsilon.-caprolactone, pivalolactone, .epsilon.-caprolactam, propylene glycol carbonate, neopentylglycol carbonate and the like.
In the case of the conjugated diene monomers, those of the general formula: ##STR7## where:
R.sub.1 =R.sub.2 =R.sub.3 =R.sub.4 =R.sub.5 =R.sub.6 =H (1,3-butadiene)
R.sub.1 =R.sub.2 =R.sub.4 =R.sub.5 =R.sub.6 =H and R.sub.3 =alkyl or aryl
R.sub.1 =R.sub.2 =R.sub.3 =R.sub.4 =R.sub.5 =H and R.sub.6 =alkyl, aryl, nitrile or nitro
R.sub.1 =R.sub.2 =R.sub.5 =R.sub.6 =H and R.sub.3 =R.sub.4 =--CH.sub.3
R.sub.1 =CH.sub.3 and R.sub.2 =R.sub.3 =R.sub.4 =R.sub.5 =R.sub.6 =H or alkyl
R.sub.1 =R.sub.3 =R.sub.4 =R.sub.5 =H and R.sub.1 =R.sub.6 =phenyl
In the case of the dienes with ethylenic double bonds which are not directly conjugated: divinylbenzene, substituted cyclohexadienes such as 3,3,6,6-tetramethyl-1,2,4,5-hexadiene and vinyl or allyl carbonates of polyols or of polyether-polyols, such as allyl-diglycol carbonate.
The process according to the invention is applicable to homopolymerisation reactions and to copolymerisation reactions, either of monomers of the same family or of monomers of different families.
The polymerisation process according to the invention is carried out under conventional conditions as regards the atmosphere which must be present in the reactor; thus, the reaction is carried out in vacuo or under an atmosphere of an inert gas such as nitrogen or argon.
The temperature at which the polymerisation is carried out is not necessarily the same as that at which the initiator has been prepared, and can be between -80.degree. C. and +70.degree. C.
Furthermore, the temperature can be varied during the polymerisation, and this is of particular value in copolymerisations which are carried out to give a certain distribution of copolymerised species or a particular microstructure or more rapid reaction kinetics.
The amount of initiator required by the process obviously depends generally on the mean molecular weight which it is desired to achieve. For example a molar ratio of amide/monomer of the order of 0.1 to 1% can be used, but it should be emphasised that a higher ratio can be used, all the more so since the amide is relatively inexpensive.
The duration of the polymerisation reaction depends on a very large number of factors and varies from a few seconds to 24 and even 48 hours.

In the examples which follow, and which are given by way of illustration of the invention and must not be considered as limiting the scope of the latter, particular emphasis has been given to the variety of possibilities offered by the initiators according to the invention, as well as to the numerous variants of the process which are mentioned in the preceding description. Other aspects which integrally form part of the invention are also described in the said examples below.
EXAMPLE OF PREPARATION OF THE INITIATORS
A reaction flask which has been dried beforehand is swept with argon, and 25.times.10.sup.-3 mol of NaNH.sub.2 and 16.6.times.10.sup.-3 mol of an alkali metal salt (NaNO.sub.2, NaSCN, NaCN or KSCN) in 20 ml of solvent such as THF or toluene are then introduced. The whole is heated for 2 hours at 50.degree. C. The solvent is either retained, if it is desired to carry out the anionic polymerisation in the same solvent, or is removed if it is desired to carry out the anionic polymerisation in bulk or in a different solvent.
All the initiators are prepared in accordance with the same process.
EXAMPLES 1 TO 20: ANIONIC POLYMERISATION OF STYRENE
10.sup.-1 mol of styrene is introduced into the reaction flask in which the initiator has been prepared. The solution is then heated for a given time, after which the reaction is stopped by precipitating the polymer by means of methanol. The results obtained are summarised in the tables which follow:
Table 1
The experiments were carried out in 20 ml of toluene, using sodium amide as the alkali metal amide, and an activator. R is the molar ratio of amide/activator.
__________________________________________________________________________ No. ACTIVATOR T 0.degree. C. Yield ##STR8## ##STR9## ##STR10##__________________________________________________________________________1 KNO.sub.2 3mM (R = 6) 18 h 50.degree. C. 33% 3,000 20,000 6.72 NaCN 3mM (R = 6) 18 h 50.degree. C. 11% 4,000 50,000 123 NaSCN 8mM (R = 6) 24 h 60.degree. C. 5% 13,000 75,000 64 NaNO.sub.2 3mM (R = 6) 18 h 50.degree. C. 45% 5,500 12,000 2.25 NaSCN 3mM (R = 6) 18 h 50.degree. C. 49% 3,000 10,000 3.3__________________________________________________________________________
Table 2
The experiments were carried out in 20 ml of toluene, using potassium amide as the alkali metal amide, and an activator, at a temperature of 50.degree. C. for 18 hours. R is the molar ratio of amide/activator.
______________________________________ No. ACTIVATOR Yield ##STR11## ##STR12## ##STR13##______________________________________6 KCN 3mM (R = 2) 27% 2,650 5,500 27 KOCN 3mM (R= 2) 15% 4,000 45,000 118 KSCN 3mM (R = 2) 30% 4,500 45,000 109 NaNO.sub.2 3mM (R = 6) 45% 5,600 11,950 2.110 NaSCN 3mM (R = 6) 49% 3,000 9,600 3.211 KNO.sub.2 3mM (R = 6) 33% 3,140 18,900 6.012 NaCN 3mM (R = 6) 11% 4,040 53,150 3.1______________________________________
Table 3
The experiments were carried out in 40 ml of THF, using 16.times.10.sup.-3 mol of sodium amide and 8.times.10.sup.-3 mol of activator, at a temperature of 50.degree. C.
______________________________________ No. VATORACTI- T Yield ##STR14## ##STR15## ##STR16##______________________________________13 KSCN 6 h 100% 28,000 400,000 1414 NaNO.sub.2 22 h 100% 12,000 80,000 6.715 KNO.sub.2 5 h 100% 60,000 650,000 1116 KCN 24 h 90% 10,000 20,000 217 NaCN 24 h 11% 45,000 450,000 1018 KOCN 20 h 3% 14,500 100,000 719 NaSCN 7 h 30 56% 6,500 50,000 820 KSCN 24 h 4% 20,000 73,000 3.7 (alone)______________________________________
EXAMPLES 21 TO 47: ANIONIC POLYMERISATION OF 2-VINYLPYRIDINE
Table 4
The experiments were carried out with 10 .sup.-1 mol of 2-vinylpyridine in 20 ml of toluene, using 25.times.10.sup.-3 mol of sodium amide and 12.5.times.10.sup.-3 mol of activator, at a temperature of 40.degree. C.
______________________________________ No. ACTIVATOR T Yield ##STR17##______________________________________21 NaNO.sub.2 4 h 50% 4,10022 KNO.sub.2 5 h 58% 5,60023 NaSCN 18 h 60% 4,80024 KCNO 18 h 53% 3,90025 NaCNO 18 h 50% 3,00026 NaCN 18 h 39% 2,200______________________________________
Table 5
The experiments were carried out with 10.sup.-1 mol of 2-vinylpyridine in 20 ml of THF, using 25.times.10.sup.-3 mol of sodium amide and 12.5.times.10.sup.-3 mol of activator, at a temperature of 40.degree. C.
______________________________________ No. ACTIVATOR t Yield ##STR18##______________________________________27 NaNO.sub.2 4 h 60% 4,90028 KNO.sub.2 4 h 70% 7,30029 NaSCN 18 h 65% 4,30030 KCNO 18 h 62% 4,00031 NaCNO 18 h 60% 3,70032 NaCN 18 h 57% 3,000______________________________________
Table 6
The experiments were carried out with 10.sup.-1 mol of 2-vinylpyridine, without a solvent, using 25.times.10.sup.-3 mol of sodium amide and 12.5.times.10.sup.-3 mol of activator, at a temperature of 40.degree. C.
______________________________________ No. ACTIVATOR t Yield ##STR19##______________________________________33 NaNO.sub.2 1 h 60% 4,60034 KNO.sub.2 1 h 57% 6,30035 NaSCN 3 h 48% 5,00036 KCNO 3 h 52% 4,80037 NaCNO 3 h 39% 4,00038 NaCN 5 h 28% 3,700______________________________________
Table 7
The experiments were carried out with 10.sup.-1 mol of 2-vinylpyridine, using 25.times.10.sup.-3 mol of alkali metal amide and 12.5.times.10.sup.-3 mol of activator in 30 ml of different solvents, at a temperature of 40.degree. C. for 18 hours.
______________________________________ No. ACTIVATOR SOLVENT Yield ##STR20##______________________________________39 NaNO.sub.2 Hexane 47% 4,00040 NaCNO Hexane 40% 3,80041 NaCN Hexane 33% 2,90042 NaNO.sub.2 Pyridine 25% 1,70043 NaCN Pyridine 20% 1,50044 NaCN DME 68% 7,00045 NaNO.sub.2 DME 70% 6,70046 NaCNO DME 63% 5,300______________________________________
EXAMPLES 47 TO 66: ANIONIC POLYMERISATION OF .alpha.-METHYLSTYRENE
The procedure is the same as for styrene. The results obtained are summarised in the tables which follow:
Table 8
The polymerisation experiments were carried out with 10.sup.-1 mol of .alpha.-methylstyrene in 20 ml of toluene, using 25.times.10.sup.-3 mol of sodium amide and 12.5.times.10.sup.-3 mol of activator, at a temperature of 40.degree. C. for 4 hours.
______________________________________ No. ACTIVATOR Yield ##STR21##______________________________________47 NaNO.sub.2 45% 45048 KNO.sub.2 50% 70049 NaSCN 30% 52050 KCNO 30% 42051 NaCN 10% 30052 NaCNO 25% 36053 NaCN 9% 310______________________________________
Table 9
The experiments were carried out with 10.sup.-1 mol of .alpha.-methylstyrene in 20 ml of THF, using 25.times.10.sup.-3 mol of sodium amide and 12.times.10.sup.-3 mol of activator, at a temperature of 40.degree. C. for 4 hours.
______________________________________ No. ACTIVATOR Yield ##STR22##______________________________________54 NaNO.sub.2 40% 60055 KNO.sub.2 55% 83056 NaSCN 37% 50057 KCNO 35% 38058 NaCN 17% 34059 NaCNO 30% 40060 NaCN 23% 335______________________________________
Table 10
The polymerisation experiments were carried out with 10.sup.-1 mol of .alpha.-methylstyrene, without a solvent, using 25.times.10.sup.-3 mol of sodium amide and 12.5.times.10.sup.-3 mol of activator, at a temperature of 40.degree. C.
______________________________________ No. ACTIVATOR t Yield ##STR23##______________________________________61 NaNO.sub.2 4 h 60% 80062 KNO.sub.2 4 h 47% 1,20063 NaSCN 18 h 35% 68064 KCNO 18 h 38% 59065 NaCNO 18 h 35% 61066 NaCN 18 h 30% 420______________________________________
EXAMPLES 67 TO 102: ANIONIC POLYMERISATION OF ACRYLONITRILE
The procedure is the same as for styrene. The results obtained are summarised in the tables which follow.
Table 11
The polymerisation experiments were carried out with 5.times.10.sup.-2 mol of acrylonitrile, without a solvent, using 25.times.10.sup.-3 mol of sodium amide and 12.5.times.10.sup.-3 mol of activator, at a temperature of 35.degree. C.
______________________________________ No. ACTIVATOR t Yield ##STR24##______________________________________67 NaNO.sub.2 10 mins 80% 5,00068 KNO.sub.2 15 mins 88% 5,50069 NaSCN 20 mins 75% 4,60070 KCNO 15 mins 80% 3,90071 NaCNO 15 mins 80% 4,20072 NaCN 20 mins 70% 3,800______________________________________
Table 12
The experiments were carried out with 5.times.10.sup.-2 mol of acrylonitrile in 20 ml of THF, using 25.times.10.sup.-3 mol of sodium amide and 12.5.times.10.sup.-3 mol of activator, at a temperature of 40.degree. C.
______________________________________ No. ACTIVATOR T Yield ##STR25##______________________________________73 NaNO.sub.2 20 mins 100% 6,30074 KNO.sub.2 20 mins 100% 7,00075 NaSCN 20 mins 100% 4,20076 KCNO 1 h 90% 5,40077 NaCNO 1 h 90% 4,90078 NaCN 1 h 90% 4,700______________________________________
Table 13
The experiments were carried out with 5.times.10.sup.-2 mol of acrylonitrile in 20 ml of toluene, using 25.times.10.sup.-3 mol of sodium amide and 12.5.times.10.sup.-3 mol of activator, at a temperature of 40.degree. C.
______________________________________ No. ACTIVATOR T Yield ##STR26##______________________________________79 NaNO.sub.2 30 mins 90% 4,00080 KNO.sub.2 30 mins 88% 4,70081 NaSCN 40 mins 80% 3,80082 KCNO 1 h 87% 2,90083 NaCNO 1 h 79% 3,30084 NaCN 2 h 63% 2,400______________________________________
Table 14
The experiments were carried out with 5.times.10.sup.-2 mol of acrylonitrile in 20 ml of THF, using 25.times.10.sup.-3 mol of LiNH.sub.2 and 12.5.times.10.sup.-3 mol of activator, at a temperature of 40.degree. C. for 18 hours.
______________________________________ No. ACTIVATOR Yield ##STR27##______________________________________85 NaSCN 20% 2,70086 NaNO.sub.2 25% 5,20087 KCNO 17% 4,30088 KNO.sub.2 35% 6,20089 NaCNO 15% 4,00090 NaCN 10% 2,500______________________________________
Table 15
The experiments were carried out with 5.times.10.sup.-2 mol of acrylonitrile, without a solvent, using 25.times.10.sup.-3 mol of lithium amide and 12.5.times.10.sup.-3 mol of activator, at a temperature of 40.degree. C. for 18 hours.
______________________________________ No. ACTIVATOR Yield ##STR28##______________________________________91 NaSCN 38% 5,80092 NaNO.sub.2 40% 6,40093 KCNO 45% 7,00094 KNO.sub.2 68% 9,30095 NaCNO 40% 6,00096 NaCN 22% 2,900______________________________________
Table 16
The experiments were carried out with 5.times.10.sup.-2 mol of acrylonitrile in 20 ml of toluene, using 25.times.10.sup.-3 mol of lithium amide and 12.5.times.10.sup.-3 mol of activator, at a temperature of 40.degree. C. for 18 hours.
______________________________________ No. ACTIVATOR Yield ##STR29##______________________________________ 97 NaSCN 20% 4,000 98 NaNO.sub.2 15% 2,900 99 KCNO 12% 3,600100 KNO.sub.2 28% 4,200101 NaCNO 10% 3,200102 NaCN 7% 1,850______________________________________
EXAMPLES 103 TO 114: POLYMERISATION OF METHYL METHACRYLATE
The procedure is the same as for styrene. The results obtained are summarised in the table which follow.
Table 17
The experiments were carried out with 10.sup.-1 mol of methyl methacrylate in 30 ml of THF, using 25.times.10.sup.-3 mol of sodium amide and 12.5.times.10.sup.-3 mol of activator, at a temperature of 35.degree. C.
______________________________________ No. VATORACTI- Time %Yield ##STR30## ##STR31## ##STR32##______________________________________103 NaNO.sub.2 18 h 100 14,000 22,000 1.56 12.5 .times. 10.sup.-3 mol104 KNO.sub.2 2 h 100 12,400 25,700 2.1 12.5 .times. 10.sup.-3 mol105 NaSCN 3 h 100 10,000 25,000 2.5 12.5 .times. 10.sup.-3106 KCNO 11/2 h 100 41,100 109,300 2.66 12.5 .times. 10.sup.-3 mol______________________________________
Table 18
The experiments were carried out with 10.sup.-1 mol of methyl methacrylate in 30 ml of toluene, using 25.times.10.sup.-3 mol of sodium amide and 12.5.times.10.sup.-3 mol of activator, at a temperature of 35.degree. C.
______________________________________ No. VATORACTI- Time %Yield ##STR33## ##STR34## ##STR35##______________________________________107 NaNO.sub.2 2 h 100 41,000 195,600 4.77 12.5 .times. 10.sup.-3 mol108 KNO.sub.2 2 h 100 27,700 82,600 2.98 12.5 .times. 10.sup.-3 mol109 NaSCN 2 h 100 19,000 87,000 1.95 12.5 .times. 10.sup.-3 mol110 KCNO 11/2 h 100 61,600 254,400 4.13 12.5 .times. 10.sup.-3 mol______________________________________
Table 19
The experiments were carried out with 10.sup.-1 mol of methyl methacrylate, without a solvent, using 25.times.10.sup.-3 mol of sodium amide and 12.5.times.10.sup.-3 mol of activator.
__________________________________________________________________________ No. ACTIVATOR .degree.C. Time %Yield ##STR36## ##STR37## ##STR38##__________________________________________________________________________111 NaNO.sub.2 35 45 mins 100 33,600 113,000 3.36 12.5 .times. 10.sup.-3 mol112 KNO.sub.2 40 30 mins 100 24,600 45,600 1.86 12.5 .times. 10.sup.-3 mol113 NaSCN 40 55 mins 100 13,700 24,500 1.79 12.5 .times. 10.sup.-3 mol114 KCNO 35 15 mins 100 47,000 138,400 2.95 12.5 .times. 10.sup.-3 mol__________________________________________________________________________
Microstructure determinations were carried out on the product which results from the polymerisation of methyl methacrylate using sodium amide and an associated salt as the initiator.
The results are shown in the table below.
Table 20
______________________________________ NMRACTIVATOR SOLVENT T H S______________________________________NaNO.sub.2 THF 11.8 56.6 31.5NaSCN THF 21.1 53.9 25.0NaNO.sub.2 Toluene 36.5 44 19.5KNO.sub.2 Toluene 26.5 52.1 21.4KCNO Toluene 22.4 51.7 25.9______________________________________
EXAMPLES 115 TO 140: POLYMERISATION OF METHACRYLONITRILE
The procedure is the same as for styrene. The results obtained are summarised in the tables which follow.
Table 21
The experiments were carried out with 10.sup.-1 mol of methacrylonitrile in 30 ml of THF, using 25.times.10.sup.-3 mol of sodium amide and 12.5.times.10.sup.-3 mol of activator, at a temperature of 35.degree. C.
______________________________________ No. ACTIVATOR .degree.C. Time Yield % ##STR39##______________________________________115 NaNO.sub.2 35 10 mins 100 20,000 12.5 .times. 10.sup.-3 mol116 KNO.sub.2 35 15 mins 90 16,000 12.5 .times. 10.sup.-3 mol117 NaSCN 35 30 mins 80 12,000 12.5 .times. 10.sup.-3 mol118 KCNO 35 10 mins 90 17,000 12.5 .times. 10.sup.-3 mol______________________________________
Table 22
The polymerisation experiments were carried out with 10.sup.-1 mol of methacrylonitrile in 30 ml of toluene, using 25.times.10.sup.-3 mol of sodium amide and 12.5.times.10.sup.-3 mol of activator, at a temperature of 35.degree. C.
______________________________________ No. ACTIVATOR Time Yield % ##STR40##______________________________________119 NaNO.sub.2 12.5 .times. 10.sup.-3 mol 20 mins 85 18,000120 KNO.sub.2 12.5 .times. 10.sup.-3 mol 35 mins 98 14,000121 NaSCN 12.5 .times. 10.sup.-3 mol 30 mins 95 10,000122 KCNO 12.5 .times. 10.sup.-3 mol 30 mins 90 12,500______________________________________
Table 23
The experiments were carried out with 10.sup.-1 mol of methacrylonitrile, without a solvent, using 25.times.10.sup.-3 mol of sodium amide and 12.5.times.10.sup.-3 mol of activator, at a temperature of 35.degree. C.
______________________________________ No. ACTIVATOR Time Yield % ##STR41##______________________________________123 KNO.sub.2 12.5 .times. 10.sup.-3 mol 5 mins 100 38,000124 KCNO 12.5 .times. 10.sup.-3 mol 15 mins 100 32,000125 NaNO.sub.2 12.5 .times. 10.sup.-3 mol 10 mins 100 29,000126 NaSCN 12.5 .times. 10.sup.-3 mol 20 mins 100 35,000______________________________________
Table 24
The experiments were carried out with 5.times.10.sup.-2 mol of methacrylonitrile, without a solvent, using 25.times.10.sup.-3 mol of lithium amide and 12.5.times.10.sup.-3 mol of activator, at a temperature of 40.degree. C. for 8 hours.
______________________________________ No. ACTIVATOR Yield % ##STR42##______________________________________127 NaSCN 40 6,000128 NaNO.sub.2 48 7,200129 KNO.sub.2 75 10,500130 NaCNO 45 6,300131 NaCN 30 3,200132 KCNO 50 8,100______________________________________
Table 25
The experiments were carried out with 5.times.10.sup.-2 mol of methacrylonitrile in 20 ml of solvent, using 25.times.10.sup.-3 mol of lithium amide and 12.5.times.10.sup.-3 mol of activator, at a temperature of 40.degree. C. for 18 hours.
______________________________________ No. ACTIVATOR SOLVENT Yield % ##STR43##______________________________________133 NaSCN THF 25 3,000134 NaNO.sub.2 THF 28 6,200135 KCNO THF 19 5,100136 KNO.sub.2 THF 40 73,000137 NaSCN Toluene 23 4,300138 NaNO.sub.2 Toluene 16 3,700139 KCNO Toluene 14 4,000140 KNO.sub.2 Toluene 30 5,000______________________________________
EXAMPLES 141 TO 152: POLYMERISATION OF ISOPRENE
The procedure is the same as for styrene. The results are summarised in the tables below.
Table 26
The experiments were carried out with 10.sup.-1 mol of isoprene in 20 ml of THF, using 25.times.10.sup.-3 mol of sodium amide and 12.5.times.10.sup.-3 of activator, at a temperature of 40.degree. C. for 18 hours.
______________________________________ No. ACTIVATOR Yield ##STR44##______________________________________141 KNO.sub.2 12% 1,500142 NaNO.sub.2 10% 800143 KCNO 10% 1,000144 NaCNO 9% 1,300145 NaSCN 10% 1,200146 NaCN 5% 1,100______________________________________
Table 27
The experiments were carried out with 10.sup.-1 mol of isoprene, without a solvent, using 25.times.10.sup.-3 mol of sodium amide and 12.5.times.10.sup.-3 mol of activator, at a temperature of 40.degree. C. for 18 hours.
______________________________________ No. ACTIVATOR Yield ##STR45##______________________________________147 KNO.sub.2 10% 2,500148 NaNO.sub.2 10% 2,000149 KCNO 10% 1,500150 NaCNO 10% 1,300151 NaSCN 10% 1,400152 NaCN 10% 900______________________________________
EXAMPLES 153 to 158: POLYMERISATION OF HETEROCYCLIC COMPOUNDS
Table 28
The experiments were carried out using 25.times.10.sup.-3 mol of sodium amide and 12.5.times.10.sup.-3 mol of activator.
__________________________________________________________________________ No. Monomer vatorActi- Solvent t 0.degree. C. Yield ##STR46##__________________________________________________________________________153 ethylene oxide NaNO.sub.2 toluene 18 h 40.degree. C. 100% 6,000 0.19 mol 30 ml154 ethylene oxide NaNO.sub.2 -- 18 h 25.degree. C. 100% 4,500 0.20 mol155 cyclic carbonate NaSCN -- 2 h 25.degree. C. 100% 10,000 of 2-ethyl-2- butyl-propane- 1,3-diol 5.4 .times. 10.sup.-2 mol156 cyclic carbonate NaSCN toluene 24 h 25.degree. C. 100% 6,800 of 2-methyl-2- propyl-propane- 1,3-diol 6.3 .times. 10.sup.-2 mol__________________________________________________________________________
The experiments carried out with propylene oxide, using 25.times.10.sup.-3 mol of sodium amide and 12.5.times.10.sup.-3 mol of sodium cyanide for 48 hours at 25.degree. C. show a substantial increase in the molecular weight. The results are summarised in Examples 161 and 162.
______________________________________ SOLVENT ##STR47##______________________________________Example 157 THF 20 ml 7,500Example 158 without solvent 12,500______________________________________
EXAMPLES 159 to 163: ANIONIC POLYMERISATION CARRIED OUT USING, AS THE INITIATOR, AN ALKALI METAL AMIDE AND A MIXTURE OF ASSOCIATED SALTS
Table 29
The procedure is the same as for styrene. The results are summarised in the table below.
The experiments were carried out with 10.sup.-1 mol of methyl methacrylate, in a solvent or without a solvent, using 25.times.10.sup.-2 mol of lithium amide and a mixture of associated salts as the activator, at a temperature of 40.degree. C.
______________________________________ No. ACTIVATOR SOLVENT T Yield ##STR48##______________________________________159 NaSCN + NaNO.sub.2 THF 18 h 25% 4,500 6 .times. 10.sup.-3 6 .times. 10.sup.-3160 NaSCN + NaCNO THF 18 h 23% 5,000 2 .times. 10.sup.-3 10.sup.-3161 KNO.sub.2 + KCNO Toluene 18 h 22% 4,500 5 .times. 10.sup.-3 7 .times. 10.sup.-3162 KNO.sub.2 + NaCN Toluene 18 h 25% 3,900 9 .times. 10.sup.-3 3 .times. 10.sup.-3163 KNO.sub.2 + NaCNO -- 8 h 30% 4,500 5 .times. 10.sup.-3 7 .times. 10.sup.-3______________________________________
EXAMPLES 164 to 175: ANIONIC POLYMERISATION IN THE ABSENCE OF AN ALKALI METAL AMIDE
The procedure is the same as for styrene. The results obtained are summarised in the table below.
Table 30
The experiments were carried out with 10.sup.-1 mol of methyl methacrylate in 20 ml of solvent or without a solvent, using exclusively 12.5.times.10.sup.-3 mol of activator. All the experiments proved negative.
______________________________________ ACTIVATOR SOLVENT______________________________________164 NaNO.sub.2 toluene165 KCNO toluene166 KNO.sub.2 toluene167 NaSCN toluene168 KNO.sub.2 THF169 NaNO.sub.2 THF170 KCNO THF171 NaSCN THF172 KNO.sub.2 --173 NaNO.sub.2 --174 NaSCN --175 KCNO --______________________________________
EXAMPLES 176 TO 181: POLYMERISATION OF STYRENE IN TOLUENE
88 mM of styrene were polymerised, in 8 hours, in 40 ml of toluene at 40.degree. C. in the presence of 25 mM of NaNO.sub.2 and of an amount of NaNH.sub.2 corresponding to the molar ratio indicated in column 2 of Table 31, which table also shows the results obtained:
Table 31
______________________________________ Example ##STR49## Yield (%) ##STR50## ##STR51## I *______________________________________176 1 80 101,000 292,900 2.9177 2 100 95,600 210,300 2.2178 4 77 64,200 173,300 2.7179 6 58 41,430 128,430 3.1180 10 40 13,300 59,850 4.5181 12 40 10,000 48,000 4.8______________________________________ *measured by GPC at 30.degree. C. in THF.
It is found that the best yields are obtained with a ratio of about 2 but variation of the proportion of amide provides a means of achieving an Mn of between 100,000 and 10,000.
EXAMPLES 182 TO 186: BULK POLYMERISATION OF STYRENE
88 mM of styrene were polymerised at 40.degree. C. for one hour in the presence of 25 mM of NaNO.sub.2 and of an amount of NaNH.sub.2 corresponding to the molar ratio indicated in column 2 of Table 32, which table shows the results obtained.
Table 32
______________________________________ Example ##STR52## Yield (%) ##STR53## ##STR54## I (*)______________________________________182 1 85 45,500 409,500 9183 2 100 53,400 341,750 6.4184 4 87 42,600 404,700 9.5185 6 85 37,500 412,500 11186 10 80 23,600 283,200 12______________________________________ (*)measured by GPC at 30.degree. C. in THF.
It is found that in bulk polymerisation, as in solution polymerisation, the highest results are obtained for a ratio of about 2 and that it is possible to vary Mn by varying the proportion of NaNH.sub.2.
EXAMPLES 187 TO 193: POLYMERISATION OF STYRENE IN THF
88 mM of styrene were polymerised for 4 hours in 40 ml of THF in the presence of 8.3 mM of NaNO.sub.2 and 16.7 mM of NaNH.sub.2. The polymerisation was carried out at various temperatures between -80.degree. C. and +40.degree. C. The results obtained are shown in Table 33.
Table 33
______________________________________ Example .degree.C. (%)Yield ##STR55## ##STR56## (*)I______________________________________187 40 100 35,700 151,500 2188 20 100 85,000 161,500 1.9189 0 100 87,000 165,300 1.9190 -20 100 110,000 187,000 1.7191 -40 100 120,000 180,000 1.5192 -60 100 137,000 205,500 1.5193 -80 100 175,000 262,500 1.5______________________________________
It is found that the yields are excellent at all temperatures and that when the polymerisation temperature decreases, the polydispersity index decreases whilst the molecular weights increase.
EXAMPLES 194 TO 200: POLYMERISATION OF STYRENE IN SOLUTION
88 mM of styrene were polymerised for 4 hours in the presence of 16.7 mM of NaNH.sub.2 and 8.3 mM of NaNO.sub.2 in various solvents. The polymerisation temperature was 40.degree. C. (except for HMPT, where it was 20.degree. C.). The results obtained are given in Table 34.
Table 34
______________________________________ Example Solvent (%)Yield ##STR57## ##STR58## (c) (*)I______________________________________194 HMPT (d) 100 42,000 50,400 1.2195 THF 100 75,700 151,500 1.3196 DME 100 85,000 110,500 1.3197 diglyme 100 123,000 221,400 1.8198 toluene 45 55,600 122,300 2.2199 benzene 40 41,300 95,000 2.3200 cyclohexane 8 10,000 51,000 5.1______________________________________ (*) measured by GPC in THF at 30.degree. C.
It is found that the polymerisation medium is another possible means of selection of the molecular weights.
EXAMPLES 201 TO 208: BULK POLYMERISATION OF STYRENE
88 mM of styrene were polymerised for 4 hours at 40.degree. C. (20.degree. C. only in Example 202) in the presence of 8.3 mM of NaNO.sub.2 and 16.7 mM of NaNH.sub.2 and in the absence of solvent.
The initiator was prepared in various solvents which were then evaporated to dryness (Examples 202 to 208), or the monomer was simply run onto the salts which had been ground together (Example 201).
The results obtained are shown in Table 35.
Table 35
______________________________________ Yield Mn MpExample Solvent (%) (*) (*) I______________________________________201 -- 100 173,100 917,450 5.3202 HMPT 100 74,400 290,150 3.9203 THF 100 133,600 587,850 4.4204 DME 100 128,750 527,900 4.1205 diglyme 100 141,200 663,650 4.7206 toluene 95 103,600 507,650 4.9207 benzene 98 101,900 509,500 5.0208 cyclohexane 90 99,900 479,500 4.8______________________________________ (*) measured by GPC in THF at 30.degree. C.
EXAMPLES 209 TO 232: POLYMERISATION OF METHYL METHACRYLATE IN THF
All the polymerisations shown below were carried out at 35.degree. C. for 2 hours in 30 ml of THF with 100 mM of methyl methacrylate in the presence of 16.7 mM of amide and 8.3 mM of associated salt.
Tables 36, 37 and 38 show the results obtained respectively with LiNH.sub.2, NaNH.sub.2 and KNH.sub.2.
Table 36
______________________________________ Example Activator %Yield ##STR59## ##STR60## I*______________________________________209 NaNO.sub.2 57 34,400 72,240 2.1210 NaSCN 50 29,500 67,850 2.3211 NaCNO 38 19,550 52,800 2.7-212 NaCN 35 17,500 43,750 2.5 8213 KNO.sub.2 64 28,800 54,700 1.9214 KSCN 59 24,800 52,100 2.1215 KCNO 45 15,100 37,750 2.5216 KCN 40 12,000 27,600 2.3______________________________________ *measured by GPC at 30.degree. C. in THF.
Table 37
______________________________________ Example Activator %Yield ##STR61## ##STR62## I*______________________________________217 NaNO.sub.2 100 43,500 56,550 1.3218 NaSCN 100 22,000 46,200 2.1219 NaCNO 96 19,200 48,000 2.5220 NaCN 90 16,200 38,900 2.4221 KNO.sub.2 100 18,000 23,400 1.3222 KSCN 100 15,000 28,500 1.9223 KCNO 100 13,000 29,900 2.3224 KCN 100 10,000 22,000 2.2______________________________________ *measured by GPC at 30.degree. C. in THF.
Table 38
______________________________________ Example Activator %Yield ##STR63## ##STR64## I*______________________________________225 NaNO.sub.2 100 23,700 28,450 1.2226 NaSCN 100 23,000 34,500 1.5227 NaCNO 100 21,000 44,100 2.1228 NaCN 100 19,000 34,200 1.8229 KNO.sub.2 100 12,700 19,050 1.5230 KSCN 100 11,000 20,900 1.9231 KCNO 100 8,200 18,850 2.3232 KCN 100 7,500 18,000 2.4______________________________________ *measured by GPC at 30.degree. C. in THF.
As far as is known, polymethyl methacrylate having a polydispersity index of between 1.2 and 1.6 and a number-average molecular weight of between 12,000 and 45,000 was not previously known.
EXAMPLES 233 TO 256: BULK POLYMERISATION OF STYRENE
All the polymerisations shown below were carried out at 45.degree. C. for 2 hours, without a solvent, with 88 mM of styrene poured onto 16.7 mM of amide and 8.3 mM of associated salt which had been ground together.
Tables 39, 40 and 41 show the results respectively obtained with LiNH.sub.2, NaNH.sub.2 and KNH.sub.2.
Table 39
______________________________________ Example Activator Yield % ##STR65## ##STR66## I*______________________________________233 NaNO.sub.2 15 36,000 140,400 3.9234 NaSCN 10 21,000 90,300 4.3235 NaCNO 10 16,000 81,600 5.1236 NaCN 7 9,300 454,500 4.9237 KNO.sub.2 20 15,600 60,850 3.9238 KSCN 15 9,300 38,150 4.1239 KCNO 15 7,800 41,350 5.3240 KCN 20 1,600 7,500 4.7______________________________________ *measured by GPC at 30.degree. C. in THF.
Table 40
______________________________________ Example Activator Yield % ##STR67## ##STR68## I*______________________________________241 NaNO.sub.2 55 104,500 376,200 3.6242 NaSCN 60 102,000 357,000 3.5243 NaCNO 45 54,000 226,800 4.2244 NaCN 40 42,000 222,600 5.3245 KNO.sub.2 60 33,600 110,900 3.3246 KSCN 55 21,450 87,950 4.1247 KCNO 50 10,000 38,000 3.8248 KCN 45 2,700 14,850 5.5______________________________________ *measured by GPC at 30.degree. C. in THF.
Table 41
______________________________________ Example Activator Yield % ##STR69## ##STR70## I*______________________________________249 NaNO.sub.2 70 98,000 294,000 3.0250 NaSCN 55 56,400 236,800 4.2251 NaCNO 65 52,000 192,400 3.7252 NaCN 50 31,000 99,200 3.2253 KNO.sub.2 75 22,500 92,250 4.1254 KSCN 60 9,600 30,700 3.2255 KCNO 60 6,000 18,600 3.1256 KCN 55 2,750 10,450 3.8______________________________________ *measured by GPC at 30.degree. C. in THF.
Particularly high values of Mn were obtained.
EXAMPLE 257: COPOLYMERIZATION OF STYRENE AND METHYL METHACRYLATE IN SOLUTION
The initiator was prepared by reacting 17 mM of NaNH.sub.2 with 8,5 mM of NaNO.sub.2 in 100 ml of THF, during 2 hours at 40.degree. C.
The reactor containing the initiator was cooled at -20.degree. C. and 88 mM of styrene were then introduced on the initiator. After one hour one half of the formed polystyrene was taken. This polymer which was "killed" when a small amount of methanol, had a Mn equal to 42,500, i.e., to the theoritical Mn value.
On the second half which remained in the reactor, 20 mM of methyl methacrylate (MAM) were introduced and let polymerize during one hour, the temperature of -20.degree. C. being still maintained. The obtained copolymer has a Mn of 58800: the poly MAM had therefore a Mn of 16300 (whereas the theoritical value was 20,000) (yield: 80%).
The Mn were measured by Gel Permeation Chromatograhy (GPC) at 30.degree. C., in THF.
EXAMPLE 258: MASS COPOLYMERIZATION OF STYRENE AND METHYL METHACRYLATE
The initiator was prepared in the same way as in example 257 in about 50 ml of THF. The THF was then evaporated and 88 mM of styrene were introduced upon the initiator at -30.degree. C., during one hour. One half of the formed polystyrene was taken and showed a Mn equal to 13,400 (yield 100%). On the remaining half, 100 mM of MAM were then introduced and the mixture was allowed to stand at -30.degree. C. for one hour. The copolymer thus obtained had a Mn equal to 30 900 (theory: 46 000). The yield of the copolymerization of the MAM was 54%. The Mn were measured by Gel Permeation Chromatography at 30.degree. C., in THF.

Number	Name	Date	Kind
3006894	Evans et al.	Oct 1961
3642734	Cheng et al.	Feb 1972

Anionic polymerization initiators based on alkali metal amides in combination with alkali metal salts and anionic polymerization process using these initiators

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