• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
  • 同族专利
  • 引用文献
  • 法律状态
  • 优先权
    • 专利摘要:
    The present invention relates to vinyl, wherein the initiator comprises at least one compound selected from dialkyl peroxydicarbonates, peroxy-tert-alkanoates and diacyl peroxides, wherein the vinyl consists of using stable nitroxyl radicals as polymerization short stoppers. A method of polymerizing chloride in an aqueous suspension, alone or in admixture with other vinyl monomers. The resulting resin has good whiteness.
    公开号:KR20030090709A
    申请号:KR10-2003-7012975
    申请日:2002-03-28
    公开日:2003-11-28
    发明作者:크리스티앙 보나디；장-뤼 쿠뛰리에；상드라 그리말디；올리비에 구에레；자크 케브날；피에르 허브라드；브쉬라 타하
    申请人:아토피나；
    IPC主号:
    专利说明:

    Polymerization in Aqueous Suspension of Vinyl Chloride
    [6] Commonly used oil soluble initiator systems consist of one or more compounds that generate free radicals that cause polymerization of monomer components. These free radicals are generally derived from the thermal decomposition of diacyl peroxides, dialkyl peroxydicarbonates or peroxy-tert-alkanoates. A common industrial method of indicating the amount of initiator (s) introduced into the reaction mixture is to use the total amount of active oxygen that can be released by the initiator system. The total amount of active oxygen generally used is 0.0005 to 0.01 parts by weight, preferably 0.0015 to 0.005 parts by weight per 100 parts by weight of the monomer component. When using a mixture of initiators having different half-lives for a given temperature, the ratio of one initiator to the other initiator may range from 1 to 99% by weight, preferably from 10 to 90% by weight. At the same temperature, the more initiator is introduced into the reaction medium, the faster the reaction. For the same polymerization time, the higher the polymerization temperature, the less initiator remains in the reaction medium.
    [7] In an aqueous suspension polymerization process carried out industrially in a batch form, once the desired conversion is obtained, it is preferable to terminate the polymerization in order to obtain a stable and uniform polymer. Also in some cases, i.e. when the conversion rate reaches a value greater than 60% by weight, to avoid any final exothermic phenomenon that is difficult to control by simple heat exchange in the wall (jacket or condenser), or If not, it may be necessary to terminate or slow the reaction during the final stage of the polymerization in order to terminate the polymerization in a hurry. The formulations used for this purpose are called short-stoppers.
    [8] The most commonly used short-stoppers (or killers) for aqueous suspension polymerization of vinyl chloride are ATSC (acetone thiosemicarbazone), bisphenol A (4,4'-isopropylidenediphenol), butylhydroxyanisole ( BHA) and Irganox® 245 (2,4-dimethyl-6-sec-hexadecylphenol) alone or Irganox® 1076 (octadecyl [3- (3,5-di) -tert-butyl-4-hydroxyphenyl)] propionate). Irganox® 1141 (hereinafter referred to as IGX 1141) is a commercial mixture of 80 parts by weight of Irganox® 245 and 2076 parts by weight of Irganox® 1076. However, these formulations are not entirely satisfactory, and there has now been a search for compounds that can replace them, are easier to use (solubility in aqueous media), and at least efficient.
    [1] The present invention relates to the preparation of vinyl chloride based polymers and copolymers by aqueous suspension polymerization of vinyl chloride alone or in mixtures with other vinyl monomers, using nitroxide-based stable radicals as short-stoppers. It is about.
    [2] The expression “aqueous suspension polymerization” is carried out by dispersing the monomer component (vinyl chloride alone or in admixture with other vinyl monomers) by mechanical means in an aqueous medium comprising at least one suspending agent in the presence of at least one oil soluble initiator. Means polymerization.
    [3] The proportion of vinyl chloride in the monomer component is at least 50% by weight, preferably at least 80% by weight. Vinyl monomers that can be copolymerized in vinyl chloride and aqueous suspensions are known and non-limiting examples which may be mentioned include vinyl esters such as vinyl acetate, vinylidene halides such as vinylidene chloride and vinylidene fluoride, acrylics. Esters such as butyl acrylate and methacrylic acid esters such as methyl methacrylate.
    [4] Suspending agents commonly used in suspension polymerization are known protective colloids, for example water-soluble polymers such as polyvinyl alcohol, polyethylene oxide, water-soluble cellulose derivatives such as methylcellulose, polyvinylpyrrolidone , Gelatin and vinyl acetate-maleic anhydride copolymers. These suspending agents can be used in amounts of 0.01 to 0.5 parts by weight, preferably 0.04 to 0.2 parts by weight, alone or in the form of a mixture, per 100 parts by weight of the monomer component.
    [5] Systems that buffer the pH of an aqueous medium are generally used. For example, the amount of the system which is citric acid for acidic pH or sodium hydrogen carbonate for basic pH is 0.01 to 0.2 parts by weight, preferably 0.02 to 0.1 parts by weight per 100 parts by weight of the monomer component.
    [9] One or more shorts selected from stable free radicals of the initiator system comprising at least one compound now selected from dialkyl peroxydicarbonates, peroxy-tert-alkanoates and diacyl peroxides, and nitroxides It has been found that the combination of stoppers can provide PVC resins or copolymer resins that not only terminate the polymerization efficiently, but at the same time provide materials with good whiteness. In addition, compared to conventional short-stoppers, the reason for selecting nitroxide is that it has the advantage that it can be diluted immediately in water to a useful concentration without the addition of stabilizers or solvents.
    [10] Accordingly, the gist of the present invention includes that the polymerization initiator system comprises at least one compound selected from dialkyl peroxydicarbonate, peroxy-tert-alkanoate and diacyl peroxide, A process for the aqueous suspension polymerization of vinyl chloride alone or a mixture of vinyl chloride with less than 50% of other vinyl monomers and vinyl chloride, characterized by the use of at least one short-stop selected.
    [11] In general, the aqueous suspension polymerization of vinyl chloride or vinyl chloride based monomer components is carried out at 45-80 ° C., preferably 50-70 ° C., which allows extensive use of initiators of the dialkyl peroxydicarbonate family.
    [12] In the dialkyl peroxydicarbonates, each alkyl radical may contain 2 to 16 carbon atoms and may be linear, branched or cyclic. Non-limiting examples of such dialkyl peroxydicarbonates that may be mentioned include diethyl, diisopropyl, di-n-propyl, dibutyl, dicetyl, dimyristyl, di (4-tert-butylcyclohexyl) Or di (2-ethylhexyl) peroxydicarbonate. Preference is given to peroxydicarbonates, more particularly di (2-ethylhexyl) peroxydicarbonate, wherein each alkyl radical comprises 6 to 16 carbon atoms.
    [13] Dialkyl peroxydicarbonates used according to the invention are classified as fast initiators. They generally have a half life of 1 hour in the region of 56 to 67 ° C. and thus can be used for vinyl chloride polymerization temperatures of 50 to 70 ° C.
    [14] However, if the selected polymerization temperature is not so high (50-57 ° C.), combinations of initiators having different half-lives at selected temperatures, for example dialkyl peroxydicarbonates and very fast peroxy-tert-alkanoate initiators, It may prove useful to use combinations that include, or combinations of peroxy-tert-alkanoate initiators, including fast initiators and very fast initiators.
    [15] Very fast peroxy-tert-alkanoates generally have a half-life of 1 hour in the region of 53 to 61 ° C. Non-limiting examples of very fast peroxy-tert-alkanoate initiators that may be mentioned include 1,1-dimethyl-3-hydroxybutyl peroxynedecanoate, cumyl peroxyne decanoate, 1,1, 3,3-tetramethylbutyl peroxyneodecanoate and 1,3-di (2-neodecanoylperoxyisopropyl) benzene.
    [16] If the selected polymerization temperature is slightly high (56-63 ° C.), a combination of initiators having different half-lives at the selected temperature, for example a combination comprising a dialkyl peroxydicarbonate and a fast peroxy-tert-alkanoate initiator, Or using a combination of fast peroxy-tert-alkanoates may prove useful.
    [17] Fast peroxy-tert-alkanoates generally have a half-life of 1 hour at 61-71 ° C. and thus can be used at vinyl chloride polymerization temperatures of 50-70 ° C. Non-limiting examples of fast peroxy-tert-alkanoates that may be mentioned are tert-butyl peroxyneodecanoate and tert-amyl peroxyneodecanoate.
    [18] For very high polymerization temperatures (62 to 70 ° C.), combinations of initiators having different half-lives at selected temperatures, for example dialkyl peroxydicarbonates or fast peroxy-tert-alkanoates and relatively slow diacyl perlocks It may prove useful to use a combination comprising a seed initiator such as dilauroyl peroxide, or peroxy-tert-alkanoate such as tert-butyl peroxypivalate.
    [19] The short-stopper (or killer) according to the invention is preferably selected from stable free radicals of the nitroxide system of the general formula (I).
    [20]
    [21] In the above formula, the Y 1 to Y 6 groups may be the same or different, hydrogen atom, linear or branched alkyl radical having 1 to 10 carbon atoms, cycloalkyl radical having 3 to 20 carbon atoms, halogen atom, cyano A radical, a phenyl radical, a hydroxyalkyl radical having 1 to 4 carbon atoms, a dialkoxyphosphonyl radical, a diphenoxyphosphonyl radical, an alkoxycarbonyl radical or an alkoxycarbonylalkyl radical, or Y 1 to Y 6 Two or more of the groups are linked to the carbon atoms they contain, such as HO-, CH 3 C (O)-, CH 3 O-, H 2 N-CH 3 C (O) NH-, (CH 3 ) 2 N- and R May comprise one or more externalcyclic functional groups selected from 1 C (O) O—, wherein R 1 represents a hydrocarbon-based radical containing 1 to 20 carbon atoms, or is external or internal, such as O or N May contain cyclic heteroatoms It may form a cyclic structure.
    [22] As an example of nitroxide (I) which can be used according to the invention,
    [23] 2,2,5,5-tetramethyl-1-pyrrolidinyloxy (commercially available under the trade name PROXYL);
    [24] 3-carboxy-2,2,5,5-tetramethylpyrrolidinyloxy (commonly referred to as 3-carboxy PROXYL);
    [25] 2,2,6,6-tetramethyl-1-piperidinyloxy (commonly referred to as TEMPO);
    [26] 4-hydroxy-2,2,6,6-tetramethyl-1-piperidinyloxy (commonly referred to as 4-hydroxy-TEMPO);
    [27] 4-methoxy-2,2,6,6-tetramethyl-1-piperidinyloxy (commonly referred to as 4-methoxy-TEMPO);
    [28] 4-oxo-2,2,6,6-tetramethyl-1-piperidinyloxy (commonly referred to as 4-oxo-TEMPO);
    [29] 4-amino-2,2,6,6-tetramethyl-1-piperidinyloxy (commonly referred to as 4-amino-TEMPO);
    [30] 4-acetamido-2,2,6,6-tetramethyl-1-piperidinyloxy (commonly referred to as 4-acetamido-TEMPO);
    [31] N-tert-butyl-1-phenyl-2-methylpropyl nitroxide,
    [32] N- (2-hydroxymethylpropyl) -1-phenyl-2-methylpropyl nitroxide,
    [33] N-tert-butyl-1-diethylphosphono-2,2-dimethylpropyl nitroxide,
    [34] N-tert-butyl-1-dibenzylphosphono-2,2-dimethylpropyl nitroxide,
    [35] N-tert-butyl-1-di (2,2,2-trifluoroethyl) phosphono-2,2-dimethylpropyl nitroxide,
    [36] N-tert-butyl-[(1-diethylphosphono) -2-methylpropyl] nitroxide,
    [37] N- (1-methylethyl) -1-cyclohexyl-1- (diethylphosphono) nitroxide,
    [38] N- (1-phenylbenzyl)-[(1-diethylphosphono) -1-methylethyl] nitroxide,
    [39] N-phenyl-1-diethylphosphono-2,2-dimethylpropyl nitroxide,
    [40] N-phenyl-1-diethylphosphono-1-methylethyl nitroxide,
    [41] N- (1-phenyl-2-methylpropyl) -1-diethylphosphonomethylethyl nitroxide,
    [42] Bis (1-oxyl-2,2,6,6-tetramethylpiperidin-4-yl) sebacate (commercially available under the trade name “CXA 5415” by CIBA SPEC. CHEM.) May be mentioned. .
    [43] These nitroxides can be used on their own or in the form of formulations.
    [44] In the present invention, the term "compound" means an aqueous, organic or aqueous / organic composition comprising at least one nitroxide and optionally organic and / or inorganic additives (NaCl, NaOH, KOH). Examples of organic solvents that can be used in organic or aqueous / organic compositions include alcohols such as methanol or ethanol.
    [45] Most particularly 4-hydroxy-TEMPO and N-tert-butyl-1-diethylphosphono-2,2-dimethylpropyl nitroxide will be used.
    [46] 4-hydroxy-TEMPO is preferably used in the form of a formulation comprising a 4-hydroxy-TEMPO content in the range of 0.01 to 90% by weight.
    [47] The process according to the invention is a process known per se, for example, protective colloids are dissolved in an aqueous medium or monomer component, an oil soluble polymerization initiator is dispersed in an aqueous medium or dissolved in a monomer component, and the pH of the aqueous medium is It can be used in a method consisting of dissolving the system for buffering. Trace amounts of oxygen are removed so that the residual content of oxygen dissolved in water is 0.0005 to 0.05 parts by weight, preferably 0.001 to 0.02 parts by weight, relative to 100 parts by weight of water. The monomer component is then introduced into the reactor and the reaction mixture is stirred to bring the temperature to 45 to 80 ° C, preferably 50 to 70 ° C.
    [48] During the polymerization, it is not necessary to keep the pressure and temperature of the reaction mixture at constant values. Increasing the programmed temperature at the beginning or end of the polymerization cycle can increase the rate of polymerization and the rate of degradation of the initiator. If this temperature and pressure are kept constant, the polydispersity of the molecular mass of the polymer chain will be between 1.8 and 2.5. For polymerisations with planned temperature gradients throughout the polymerisation period, polydispersities of 1.8 to 3.5 will be observed.
    [49] As a result of the polymerization, the concentration of the liquid monomer is reduced and the result is a change in the monomer vapor / liquid equilibrium, and a pressure drop is observed. The weight conversion of the monomer when the pressure drop begins is in the 65 to 75% region.
    [50] In its role as a short-stopper, the nitroxide used according to the invention is introduced at a weight conversion of 60 to 90%, preferably 70 to 80% when the pressure drop has already begun. The amount of nitroxide used per 100 parts by weight of the monomer component may range from 0.0001 to 0.1 parts by weight, preferably 0.00015 to 0.01 parts by weight.
    [51] The nitroxides used according to the invention can be used in combination with other short-stoppers, for example dialkylhydroxylamines, for example diethylhydroxylamine (DEHA).
    [52] Once the polymerization is complete, the formed polymer is separated from the aqueous medium and then dehydrated and dried. It is generally in the form of particles of approximately 80-250 μm size.
    [53] The following examples illustrate the invention without limitation, and the parts and percentages shown are expressed on a weight basis unless otherwise indicated.
    [54] Example 1 (Control)
    [55] 14 kg of deionized water, 2.52 g citric acid, 3.73 g of polyvinyl alcohol having 78 mol% hydrolysis degree, 3.73 g of polyvinyl alcohol having 72 mol% hydrolysis degree, 8.08 g of aqueous solution of polyvinyl alcohol having 55 mol% hydrolysis degree ( 13.63 g of an emulsion of di (2-ethylhexyl) peroxydicarbonate having 40% active substance) and 40% active substance (Luperox® 223 EN40), It was introduced into a 30 L volume jacketed reactor equipped with stirring (250 rpm) at ambient temperature. The active oxygen content relative to the weight of vinyl chloride monomer (VCM) introduced was then 28 ppm.
    [56] After the reactor was closed, it was partially discharged (6.66 absolute kPa) and this pressure was maintained for 15 minutes. Then it was stirred at 330 rpm and then 9 kg of VCM were introduced.
    [57] Heating was controlled by circulating cooling water in the jacket to reach a polymerization temperature of 56.5 ° C. after 30 minutes. It considers the moment of the polymerization medium reaches 56.5 ℃ to the start (time t = 0) of the polymerization, which was based on the pressure (P 0) of the period.
    [58] After 30 minutes of polymerization (ie at t 0 +30 minutes), 4 kg of water was continuously introduced into the reactor at a constant flow rate of 1.2 kg / h to improve heat exchange while keeping the surface area of the heat exchangeable jacket constant , After 60% conversion of VCM to PVC, the viscosity of the aqueous suspension was reduced (wherein the conversion was calculated via a calorimeter measured at the limit of the reactor).
    [59] The concentration drop of the VCM gas phase in the reactor caused a pressure drop at 65-70% conversion. Once the pressure had dropped by 1 bar relative to P 0 , the polymerization was terminated by rapidly cooling the medium with the cooling water injected into the jacket.
    [60] The residual content of di (2-ethylhexyl) peroxydicarbonate was approximately 90 ppm relative to the initial weight of the monomers.
    [61] Residual VCM was then removed from the reaction medium by conventional techniques of restoring atmospheric pressure (degassing) and then trace amounts of VCM were removed by stripping under vacuum at 13.33 kPa at 50 ° C.
    [62] The PVC resin thus obtained (K value = 67) was then dehydrated, dried for 6 hours in a fluidized bed by a flow of dry air heated to 50 ° C. and sieved through a 500 μm mesh.
    [63] The evaluation method of the color index of the resin on the compression plate or WIPP (white index compression plate) is as follows.
    [64] 150 g of resin is mixed with 12 g of a solution of 1 part of dioctyl phthalate in 17 parts of MOK (tin-based heat stabilizer in liquid form sold by CIBA), and mixed for 5 minutes at 96 ° C. at 50 rpm in a 600 ml Brabender mixer. . The mixture was discharged in the next 15 minutes using a WEBER compressor and 20 g of the mixture was compressed for 2 minutes at 184 ° C. and 300 bar in a 70 mm diameter and 3 mm thick mold between two 0.05 mm thick aluminum sheets. The plate obtained is then cooled in water for 45 seconds and then for a period of 30 to 90 minutes after compression, this color is measured using a Hunterlab D 25 M DP 9000 apparatus and WIPP Expressed in terms of ASTM standard E 313.
    [65] WIPP = L / 100 (L-5.71b)
    [66] L and b values are given by the device.
    [67] Examples 2-4
    [68] As soon as the pressure drop reached 0.3 bar (that is, P 0 - at 0.3 bar), 4- hydroxy -TEMPO (4- hydroxy-2,2,6,6-tetramethyl-piperidinyloxy, below OH-TEMPO 0.04% aqueous solution of the solution was injected into the reaction medium over 2 minutes (the ratio of OH-TEMPO to the initial weight of VCM is 1.5, 3 and 6 ppm by weight, respectively), and the reaction medium was 56.5 minutes for 15 minutes before cooling. The process was the same as in Example 1 except for maintaining at 占 폚. Degassing, stripping, dehydration, drying and sieving were then carried out in the same manner as in Example 1, and the PVC resin thus obtained was evaluated in WIPP terms according to the same test.
    [69] Example 5
    [70] As soon as the pressure drop reaches a 0.3 bar - 5.35% (i.e., P 0 eseo 0.3 bar), SG1 in methanol (N-tert- butyl-1-diethyl phosphono-2,2-dimethylpropyl nitroxide) was added Was injected into the reaction medium (the ratio of SG1 to the initial weight of VCM was 115 ppm by weight) and the process was the same as in Example 1 except the reaction medium was kept at 56.5 ° C. for 15 minutes before cooling. Degassing, stripping, dehydration, drying and sieving were then carried out in the same manner as in Example 1.
    [71] Example 6
    [72] As soon as the pressure drop reached 0.3 bar (that is, P 0 - at 0.3 bar), and injected into a 3 ppm by weight and 130 ppm by weight content of a mixture of OH-TEMPO and DEHA respectively to the reaction mixture for the initial weight of VCM, reaction The process was the same as in Example 1 except the mixture was kept at 56.5 ° C. for 15 minutes before cooling. Degassing, stripping, dehydration, drying and sieving were then carried out in the same manner as in Example 1, and the PVC resin thus obtained was evaluated in WIPP terms according to the same test.
    [73] Examples 7 and 8 (comparative)
    [74] Bisphenol A (BPA) using an aqueous solution of OH-TEMPO in the form of a 35% methanolic solution (the ratio of BPA to the initial weight of VCM is 370 ppm by weight) (Example 7), or 8 in epoxidized soybean oil. Example except for replacing with Irganox® 1141 (IGX 1141) in the form of% solution (the ratio of IGX 1141 to the initial weight of VCM is 620 ppm by weight) (Example 8) 2 was repeated.
    [75] Examples 1-8 and the results are summarized in Table 1 below.
    [76] ExampleShort StopperΔP / Δt (mbar / min)WIPP KindsWeight / monomermole Onenone004035 2OH-TEMPO1.5 ppm0.00007825nd 3OH-TEMPO3 ppm0.00015715nd 4OH-TEMPO6 ppm0.000314042 5SG1115 ppm0.00350nd 6OH-TEMPO / DEHA3 ppm / 130 ppm0.000157 / 0.0131040 7BPA370 ppm0.0151046 8IGX 1141620 ppm0.0152347
    [77] nd = not measured
    [78] OH-TEMPO functions as a short-stopper because the slope of the pressure drop decreases under the conditions of Examples 2-4. The polymerization termination effect was obtained for 6 ppm of OH-TEMPO. The resin had a high whiteness quality. In the case of SG1, the effect of terminating polymerization was achieved at a content of less than 115 ppm.
    [79] Example 9
    [80] 13.63 g of an emulsion of di (2-ethylhexyl) peroxydicarbonate with 40% active substance (Luperox® 223 EN40) was added to tert-butyl peroxyneodecanoate (lupe) with 40% active substance. Replace with 12.98 g of emulsion of Rox 10M75, and when the pressure drop reaches 0.3 bar, 50 g of 0.22% aqueous solution of 4-hydroxy-TEMPO (the ratio of OH-TEMPO to the initial weight of VCM is 12.5 ppm by weight). Process was the same as in Example 1 except that the reaction medium was injected over 2 minutes and the reaction medium was kept at 56.5 ° C. for 15 minutes before cooling. Degassing, stripping, dehydration, drying and sieving were then carried out in the same manner as in Example 1, and the PVC resin thus obtained was evaluated in WIPP terms according to the same test.
    [81] Example 10
    [82] The process was the same as in Example 9, except that 100 g of 0.03% aqueous solution of 4-hydroxy-TEMPO (the ratio of OH-TEMPO to the initial weight of VCM was 3 ppm by weight).
    [83] The results of Examples 9 and 10 are shown in Table 2 below.
    [84] ExampleShort StopperΔP / Δt (mbar / min)WIPP KindsWeight / monomermole 9OH-TEMPO12.5 ppm0.00065052.7 10OH-TEMPO3 ppm0.0001573053.5
    [85] Example 11
    [86] 14 kg of deionized water, 2.52 g citric acid, 7.2 g polyvinyl alcohol with 78 mol% hydrolysis degree, 5.4 g polyvinyl alcohol with 72 mol% hydrolysis degree, and 3.06 g aqueous solution of polyvinyl alcohol with 55 mol% hydrolysis degree (39% active material) was introduced into a 30 L volume jacketed reactor equipped with a 3-arm vane stirrer at ambient temperature with stirring (250 rpm).
    [87] Once the reactor was sealed, it was partially vented (6.66 absolute kPa) and this pressure was maintained for 30 minutes. Then it was stirred at 330 rpm and then 9 kg of VCM were introduced.
    [88] The heating was adjusted to reach a polymerization temperature of 70 ° C. (time = t 0 ) after 45 minutes. At this temperature, 20 g of a solution comprising 3.75 g of tert-butyl peroxypivalate (luperox 11M75) and 16.25 g of isododecane were added.
    [89] After 30 minutes of polymerization (ie at t 0 +30 minutes), 3.4 kg of water were continuously introduced into the reactor at a constant flow rate of 1.2 kg / h to improve heat exchange by keeping the surface area of the heat exchangeable jacket constant. , After 60% conversion of VCM to PVC, the viscosity of the aqueous suspension was reduced (wherein the conversion was calculated via a calorimeter measured at the limit of the reactor).
    [90] As soon as the pressure drop reached 0.3 bar, 50 g of 0.09% aqueous solution of OH-TEMPO (i.e., 5 ppm by weight of OH-TEMPO relative to the initial weight of VCM) were injected into the reaction medium, and the reaction medium was charged at Hold for a minute.
    [91] Degassing, stripping, dehydration, drying and sieving were then carried out in the same manner as in Example 1.
    [92] WIPP and ΔP / Δt measured according to the test described in Example 1 were measured.
    [93] The result is as follows.
    [94] ΔP / Δt (mbar / min) = 0
    [95] WIPP = 63.4
    [96] Examples 12 and 13 (Emergency Termination of Polymerization)
    [97] Example 12
    [98] Aqueous solution of polyvinyl alcohol with 500 kg deionized water, 90 g citric acid, 132.5 g polyvinyl alcohol with 78 mol% hydrolysis degree, 132.5 g polyvinyl alcohol with 72 mol% hydrolysis degree, 55 mol% hydrolysis degree 166 g of di (2-ethylhexyl) peroxydicarbonate having 75% of active material (39%), and 75% of active material (Luperox® 223M 75) with a 3-arm winged stirrer and a killer A 1200 L volume jacketed reactor equipped with a pressure vessel was introduced with stirring (125 rpm) at ambient temperature. The active oxygen content relative to the weight of the VCM introduced subsequently was 18 ppm.
    [99] Once the reactor was sealed, it was partially vented (6.66 absolute kPa) and this pressure was maintained for 30 minutes. It was then stirred at 250 rpm and then 320 kg of VCM were introduced.
    [100] Heating was controlled by circulating cooling water in the jacket to reach a polymerization temperature of 56.5 ° C. after 30 minutes. It considers the moment when the polymerization medium reaches 56.5 ℃ to the start (time t = 0) of the polymerization, which was based on the pressure (P 0) of the period.
    [101] After 40 minutes of polymerization (ie at t 0 +40 minutes) the circulation of cooling water in the jacket was stopped. Pressure and temperature increases were measured and defined as ΔP / Δt and ΔT / Δt.
    [102] 170 g of OH-TEMPO aqueous solution with 5.88 wt% OH-TEMPO contained in the nitrogen pressurized vessel (i.e. 31 ppm by weight of OH-TEMPO relative to the VCM weight introduced into the reactor) were introduced at t 0 + 45 min.
    [103] Changes in temperature and pressure were recorded and presented in Table 3 below.
    [104] Example 13 (Comparative Example)
    [105] The process is the same as in Example 12, except that 1.5 l of methanol-based solution with 25 weight percent bisphenol A (BPA) (i.e., 1313 weight ppm BPA based on the weight of VCM introduced into the reactor) was introduced at t 0 +45. It was.
    [106] As in Example 12, changes in temperature and pressure were recorded and presented in Table 3 below.
    [107] ExamplekillerΔP / Δt (mbar / min)ΔT / Δt (° C / min) KindsWeight / monomerI'mafterI'mafter Killer additionKiller addition 12OH-TEMPO31 ppm6000.20 13BPA1313 ppm9430.30.03
    [108] At very low contents, OH-TEMPO action as an urgent short-stopper (killer) was noted.
    权利要求:
    Claims (20)
    [1" claim-type="Currently amended] The polymerization initiator system comprises at least one compound selected from dialkyl peroxydicarbonates, peroxy-tert-alkanoates and diacyl peroxides and at least one short-stopper selected from stable free radicals of nitroxides ( short-stopper), characterized in that an aqueous suspension polymerization process of vinyl chloride alone or a mixture of vinyl chloride with less than 50% of other vinyl monomers.
    [2" claim-type="Currently amended] The process of claim 1 wherein the short-stopper is selected from nitroxides of formula
    <Formula I>

    (Wherein the Y 1 to Y 6 groups may be the same or different, hydrogen atoms, linear or branched alkyl radicals having 1 to 10 carbon atoms, cycloalkyl radicals having 3 to 20 carbon atoms, halogen atoms, cyan No radical, phenyl radical, hydroxyalkyl radical having 1 to 4 carbon atoms, dialkoxyphosphonyl radical, diphenoxyphosphonyl radical, alkoxycarbonyl radical or alkoxycarbonylalkyl radical, or Y 1 to Y Two or more of the six groups are linked to the carbon atoms included therein to form H 2 N—CH 3 C (O) NH—, (CH 3 ) 2 N—, and R 1 C (O) O—, wherein R 1 is 1; Cyclic structure which may include one or more external cyclic functional groups selected from hydrocarbon radicals containing from 20 to 20 carbon atoms, or may include external or internal cyclic heteroatoms such as O or N. It can be configured).
    [3" claim-type="Currently amended] The method of claim 2 wherein the nitroxide is used as such or in the form of a formulation.
    [4" claim-type="Currently amended] The method of claim 2, wherein the short-stopper is 4-hydroxy-2,2,6,6-tetramethyl-1-piperidinyloxy (4-hydroxy-TEMPO).
    [5" claim-type="Currently amended] 5. Process according to claim 3 or 4, characterized in that 4-hydroxy-TEMPO is used in the form of a combination comprising a 4-hydroxy-TEMPO content in the range of 0.01 to 90% by weight.
    [6" claim-type="Currently amended] The method according to claim 2, wherein the short-stopper is N-tert-butyl-1-diethylphosphono-2,2-dimethylpropyl nitroxide (SG1).
    [7" claim-type="Currently amended] The process according to claim 2, wherein the nitroxide is combined with other short-stoppers such as dialkylhydroxylamines.
    [8" claim-type="Currently amended] 8. The method of claim 7, wherein the dialkylhydroxylamine is diethylhydroxylamine.
    [9" claim-type="Currently amended] The process according to claim 1, wherein the alkyl radicals of the dialkyl peroxydicarbonates each comprise 2 to 16 carbon atoms, preferably 6 to 16 carbon atoms.
    [10" claim-type="Currently amended] 10. The process of claim 9, wherein the dialkyl peroxydicarbonate is di (2-ethylhexyl) peroxydicarbonate.
    [11" claim-type="Currently amended] The process of claim 1, wherein the polymerization initiator system comprises dialkyl peroxydicarbonate and very fast peroxy-tert-alkanoate.
    [12" claim-type="Currently amended] The method of claim 11, wherein the very fast peroxy-tert-alkanoate is 1,1-dimethyl-3-hydroxybutyl peroxynedecanoate.
    [13" claim-type="Currently amended] The method of claim 1, wherein the polymerization initiator system comprises dialkyl peroxydicarbonate and fast peroxy-tert-alkanoate.
    [14" claim-type="Currently amended] The process of claim 1 wherein the polymerization initiator system is a dialkyl peroxydicarbonate or a mixture of fast peroxy-tert-alkanoate and diacyl peroxide.
    [15" claim-type="Currently amended] The method of claim 14, wherein the fast peroxy-tert-alkanoate is tert-butyl peroxyneodecanoate and the diacyl peroxide is dilauroyl peroxide.
    [16" claim-type="Currently amended] The method of claim 1 wherein the polymerization initiator system is a mixture of two fast peroxy-tert-alkanoates or a mixture of very fast peroxy-tert-alkanoates and fast peroxy-tert-alkanoates.
    [17" claim-type="Currently amended] The method of claim 16, wherein the very fast peroxy-tert-alkanoate is 1,1-dimethyl-3-hydroxybutyl peroxyneodecanoate.
    [18" claim-type="Currently amended] The process of claim 1 wherein the polymerization initiator system is a slow peroxy-tert-alkanoate such as tert-butyl peroxypivalate.
    [19" claim-type="Currently amended] 19. The method according to any one of claims 1 to 18, wherein the short-stopper is 0.0001 to 0.1 parts by weight, preferably 0.00015 to 0.01 parts by weight per 100 parts by weight of vinyl chloride alone or a mixture with less than 50% of other vinyl monomers. Characterized in that it is used in proportions.
    [20" claim-type="Currently amended] Polymers and copolymers based on vinyl chloride obtained using the method of any one of claims 1 to 19.
    类似技术:
    公开号 | 公开日 | 专利标题
    KR100460826B1|2004-12-09|Method for the production of a controlled-rheology polypropylene resin
    US6806305B2|2004-10-19|Dispersion stabilizer for suspension polymerization of vinyl compound
    JP4094433B2|2008-06-04|Organic peroxide heat stabilizer
    JP2012067324A|2012-04-05|Low-crystallinity vinylidene fluoride hexafluoropropylene copolymer
    JP5506392B2|2014-05-28|Aqueous process for producing fluoropolymers
    US7763690B2|2010-07-27|Method for producing peroxydicarbonates and their use in the radical polymerization of monomers
    EP0813550B1|1999-11-24|Cyclic ketone peroxides as polymer initiators
    EP0662096B1|1996-11-20|Iodine containing chain transfer agents for fluoromonomer polymerizations
    EP2274377B1|2012-02-01|Composition containing a halogenated vinyl polymer and a copolymer bearing associative groups
    TWI236482B|2005-07-21|Process for the |polymerization of vinyl chloride in the presence of a stable free nitroxyl radical
    TWI616458B|2018-03-01|Dispersion stabilizer for suspension polymerization and method for producing vinyl resin
    EP1824892B1|2008-08-13|Polymerisation of vinyl chloride monomer
    US6617408B2|2003-09-09|Process for polymerization of vinyl chloride
    US8367784B2|2013-02-05|Continuous dosing of extremely fast initiators during polymerization reactions
    EP1618137B1|2008-06-11|Increased polymerization reactor output by using a specific initiator system
    RU2327705C2|2008-06-27|Polymerisation degree regulator
    JP6704350B2|2020-06-03|Dispersion stabilizer for suspension polymerization and method for producing vinyl resin
    RU2128667C1|1999-04-10|Method of |polymerization of fluorinated olefin monomers
    US20030060664A1|2003-03-27|Method for producing a fluoropolymer
    KR101198530B1|2012-11-06|Manufacturing Method of Bulk Polymerization of PVC Polymer and PVC Copolymer Using Organic Base Material As pH Control Agent
    US2746944A|1956-05-22|Process for preparing vinyl halide copolymers and copolymers produced thereby
    TW201512227A|2015-04-01|Dispersion stabilizer for suspension polymerization, and manufacturing method for vinyl resin
    KR101595240B1|2016-02-18|Polyvinyl chloride resin composition and manufacturing method thereof
    FR2542319A1|1984-09-14|Process for the polymerization in an aqueous medium of suspending vinylidene fluoride
    ES2761563T3|2020-05-20|Synthesis of block copolymers based on chlorotrifluoroethylene by transfer polymerization with iodine
    同族专利:
    公开号 | 公开日
    MXPA03008986A|2004-03-18|
    DE60204957D1|2005-08-11|
    IL157798A|2007-05-15|
    CZ20032607A3|2004-02-18|
    HU0304089A3|2007-11-28|
    BR0207637B1|2011-09-20|
    JP3831807B2|2006-10-11|
    WO2002079279A1|2002-10-10|
    CN1501945A|2004-06-02|
    PT1383809E|2005-10-31|
    CZ299022B6|2008-04-02|
    PL363692A1|2004-11-29|
    IL157798D0|2004-03-28|
    FR2822832A1|2002-10-04|
    CA2441807A1|2002-10-10|
    JP2004534867A|2004-11-18|
    NO20034354D0|2003-09-29|
    BR0207637A|2004-03-02|
    AT299155T|2005-07-15|
    EP1383809B1|2005-07-06|
    ES2243723T3|2005-12-01|
    CN1219801C|2005-09-21|
    MA26111A1|2004-04-01|
    TWI242017B|2005-10-21|
    US20040132930A1|2004-07-08|
    EP1383809A1|2004-01-28|
    KR100567300B1|2006-04-04|
    CA2441807C|2009-05-12|
    HU226900B1|2010-01-28|
    DE60204957T2|2006-04-20|
    AU2002257855B2|2004-10-28|
    NO20034354L|2003-09-29|
    NO331828B1|2012-04-16|
    HU0304089A2|2004-04-28|
    FR2822832B1|2005-01-14|
    引用文献:
    公开号 | 申请日 | 公开日 | 申请人 | 专利标题
    法律状态:
    2001-04-02|Priority to FR01/04425
    2001-04-02|Priority to FR0104425A
    2002-03-28|Application filed by 아토피나
    2002-03-28|Priority to PCT/FR2002/001094
    2003-11-28|Publication of KR20030090709A
    2006-04-04|Application granted
    2006-04-04|Publication of KR100567300B1
    优先权:
    申请号 | 申请日 | 专利标题
    FR01/04425|2001-04-02|
    FR0104425A|FR2822832B1|2001-04-02|2001-04-02|Acqueous suspension polymerization of vinyl chloride alone or in mixture with another vinyl monomer with the use of a nitroxide type stable radical as a polymerization stop agent|
    PCT/FR2002/001094|WO2002079279A1|2001-04-02|2002-03-28|Polymerisation in aqueous suspension of vinyl chloride|
    [返回顶部]