• 专利附录
  • 专利说明
  • 权利要求
  • 类似技术
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  • 引用文献
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    • 专利摘要:

    公开号:SU1053758A3
    申请号:SU803302904D
    申请日:1980-11-11
    公开日:1983-11-07
    发明作者:Кюстер Эрих；Дамен Курт；Бартелль Эдуард
    申请人:Хемише Фабрик Штокхаузен Унд Ко (Фирма)；
    IPC主号:
    专利说明:

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    This invention relates to a process for the preparation of polymers based on urea derivatives, which are used as coagulants or sedimentation agents.
    A known method for producing a copolymer based on a nitrogen-containing acrylic monomer (2-dimethylaminoethyl methacrylate) copolymerizing this monomer with other monomers capable of copolymerizing C1 J.,
    However, the known method does not allow to obtain copolymers with sufficiently good coagulating sedimentation, dewatering and retention properties.
    The aim of the invention is to obtain copolymers with improved performance and technical properties when used as a coagulating, sedimenting, dehydrating and retaining agent.
    This goal is achieved by the fact that according to the method of obtaining sopo. nitrogen-based acrylic monomer based copolymerization of a nitrogen-containing acrylic monomer with a second monomer, a compound of the general formula used as a nitrogen-containing acrylic monomer
     JC O o eH2- i- -30i-C-2ilH - ((ll2) fr3f "f Z®
    where X is H or SND; n - 2-3; R - CHg; 2 — CS or J, as the second monomer — acrylate, and copolymerization — is carried out at a mass ratio of nitrogen-containing monomer and acrylamide 1: 9 to 3: 7.
    The polymerization is carried out according to known methods. It can be initiated thermally, photochemically, by irradiation, or by conventional radical initiators. In this case, the polymerization can be carried out in solution, suspension or emulsion. Suitable initiators are, for example, inorganic peroxides, for example hydrogen peroxide, or organic hydroperoxides, for example tert-butyl hydroperoxide, cumene hydroperoxide or dibenzoyl peroxide, which are split into aliphatic azo compounds, for example, 2,2-azo-bis-iso-pro-α-pro-isoproteron. - reconstitution of innovative initiators, as systems of persulfate or chlorate with disulfite or iron salts (and) known as sources of radicals, chelates of transition metals. The initiators are used in an amount of 0.001-1 wt D based on the amount of monomers. The optimal amount and optimally active initiator can be easily determined experimentally.
    The polymerization is preferably carried out with a radical initiator, as well as in the presence of a solvent or diluent. For the proposed polymerizations, suspension, emulsion polymerization and solvent polymerization methods customary for other monomers are also suitable. Under known conditions, adjuvants can be used as buffers, dispersants, protective colloids, and the like.
    The products offered can be used as coagulants, sedimentary means, dehydrating agents and retaining agents (retention means. They are water soluble. Further, these aqueous solutions have only low viscosity, which is very advantageous for use. Due to the very stable the urea groups in the polymers are also resistant to hydrolysis.
    Acrylamide can be used as a comonomer.
    D .. Getting urea.
    Example K M-Acryl-N- {2-chloroethyl) -urea
    A mixture of 71.1 g (1.0 mol) of acrylamide, 0.5 g of triethylamine, 0.5 g of 2,6-di-tert-butyl-4-methyl-phenol and 250 ml of benzene is mixed with 110.8 g ( 1.05 mol) of 2-chloroethyl isocyanate and heated for 10 m in an autoclave at 110 ° C. The crystalline precipitate which is precipitated upon cooling is filtered off. This gives a g of substance which is recrystallized from 700 ml of acetonitrile, and 115 g (O, 65 mol 65 per theory) of white crystalline needles with mp. 156-158 С,
    Calculated: CE 20.07; N 15.86
    SLNoSR NjOo
    Found: From 19.80 15.90
    Molecular weight 176.00
    NMR n-center (in SDS): 3.5-3.8 (multiplet, k), 5,, 8 (multiplet, G), 9.05 (multiplet, 1), 10.4 (multiplet, 1) . Example 2. M-Acryl-N - (2bromoethyl) -urea. Analogously to Example 1, from 165 g (1.1 mol) of 2-bromoethyl isocyanate after 10 hours at 110 ° C., 184 g of crude product, which, after recrystallization from 600 ml of nitrile acetic acid, gives 10 g (0.7 mol, 70% from theory) white crystalline needles with so pl. 157-159 ° C. Calculated D: Br 36.15; N 12, B7 C HgBrN O Found,%: Br 35.90; 12.90 molecular weight 221.06. NMR-H-spectrum (c): 3-4, 0 (multiplet, 4), 5.7-6.8 (multiplet, 3), 9.0 (multiplet, 1), 10.2 (multiplet, ). Example 3. M-Acryl-H- (3-chloropropyl) -urea. In Example 1, from 131.6 (1.1 mol) 3 chloropropylisocyanate is obtained, after 16 h at PO ° C, 130 g of a crude product, which, after recrystallization from 400 ml, gives acetonitre 86 g (0.45 mol 45 from the theory of white crystalline needles with a melting point of 107 ° C. Calculated: CI 18.60; N 14.70 C H CeN202 Found: CE 18.33; N 14.49 Molecular weight 190.63. NMR-H spectrum (in SDS): cG 1, 2.3 (multiplet, 2), 3.25-3.8 (mule tiplet, 4), 5.7-6.8 (multiplet, 3 8.8 (multiplet, 1) , 10.55 (multiplet, 1).
    Example 4. M- (2-Chloroethyl) -N-methacrylylurea. . In example 1, 85.1 g (1.0 mol) of methacrylamide and 110.8 g (1.05 mol) of 2-chloroethyl isocyanate are obtained, after recrystallization from 600 ml of acetonitrile, 104 g (Q, 7 mol, 701 from ) white crystal needles with so pl. 157-159 ° C.
    Calculated,%: Vg Zb, 15; N 12,6
    CgHgBrN202
    Found,%: Br 35.90; N 12.90
    Molecular weight 221.06.
    NMR-H spectrum (in SDSe): c 3.34, 0 (multiplet, 4), 5.7-6.8 (multiplet, 3), 9.0 (multiplet, 1), 10.2 (multiplet, one).
    125.5 g (1.05 mol) of 2-chloroacetyl isocyanate at 25-30 ° C are added dropwise to a solution of 71.1 g (1.0 mol) of acrylamide in 150 ml of 1,2-dimethoxyethane.
    and then stirred for 24 hours. Filtration gives 140 g of crude product, which is recrystallized from 540 ml of acetonitrile. The result is 106 g (0.5b mol, 5b% of
    theory) of white crystals with t, pl. 144145 ° C.
    Calculated,%: About 18.60; N 24.70 СЛН СгК20з
    Found: CE 18,70; N 14.90 Molecular weight 190.59 NMR-H-spectrum (in de-DMSO): (D 4.65 (singlet, 2), 5.8-6.7 (multi. Example 5. N-Acyl .- N - (3-chloropropyl) -urea. In Example 1, from 131.6 g (1.1. Mol) of 3-chloropropylisocyanate, after 16 hours at 110 ° C, 130 g of crude product, which after recrystallization from 400 ml of acetonitrile, gives 86 g (0.45 mol, 45% of theory) of white crystalline needles with mp, 105–107 ° C. Calculated,%: ce 18.60; N 14.70 sem, Naydo, 18.33; N 14.49 Molecular weight 190.63 NMR-H spectrum (in SDS): cG 1.752, 3 (multiplet, 2), 3.25-3.8 (multiplet, 4), 5.7-6.8 ( multiplet, 3), 8.8 (multiplet, 1, 10.55 M multiplet, 1). Example 6. N- (2-Chloroethyl) -N-methacrylylurea. In Example 1, 85.1 f (1.0 mol) of methacrylamide and 110.8 g (1.05 mol) of 2-chloro ethyl isocyanate are obtained, after 10 hours at 110 ° C , 140 g of the crude product, which, after recrystallization from 350 ml of acetonitrile, gives 105 g (0.55 mol, 55% of theory) of white crystalline needles with a mp of 122-123 C. Calculated,%: Wed. 18.60; N 14.70 StN SRNzO Found:% Ce 18.73; Nl4.78. Molecular weight 100.63. NMR-H-spectrum (in SDSvz): cG 2.05 (doublet, 3), 3.7 (doublet, 4), 5.56, 2 (multiplet, 2), 9.0 (multiplet, 95), ( multiplet, 1). Example 7. N-Acryle-M- (2-chloroethyl) -urea.
    tiplet, 3), 11.0, 11.35 (multiplet,).
    B. Preparation of ureas of formula (I)
    Example 8. Acrylyl-ureylene-ethylene-trimethylammonium chloride.
    35.3 g (0.2 mol) of M-acrylyl-H- {2-chloroethyl) -urea with 0.2 g of 2,6-di-tert-butyl - "- methylphenol in 400 ml of acetone is cooled to 0 C and 23.6 g (0.4 mol) of liquid trimethylamine are added. The mixture is heated in an autoclave for 20 hours, cooled, and the precipitate formed is filtered off. After washing with acetone and ether, 33 g (0.14 mol, 70% of theory) of a white crystalline powder are obtained.
    Calculated I: C2 15.04; N 17.83
    s n vsosen
    Not found: SS 14.30; 17,12
    Nuclear weight 235.71NMR-H-spectrum (in DGO): cG 3.25. (singlet, 9), 3.5-4.0 (multiplet, 4) 5.8-6.5 (multiplet, 3).
    Example 9. Methacrylyl-ureilen, ethylene-trimethyl-ammonium chloride.
    In Example 6, 38.1 g (.0.2 mol) of N- (2-chloroethyl) -N-methacrylyl-urea, 34 g (0.14 mol, 68 from theory) of a white crystalline powder is obtained.
    Calculated: CE 14,20; N 16.83
    with ONE comMesso
    Found: CE 14.56; N 16.76
    Molecular weight 249.74.
    NMR spectrum (H) (in D20): c-1.95 (doublet, 3), 3.2 (singlet, 9), 3.54, 0 (multiplet, 4), 5.6-5.9 (multiplet, 2).
    Example 10. Acrylyl-ureylene-propylene trimethylammonium chloride.
    According to the method of example 6, out of 38.1 g (0.2 mol) of N-acyl-N-N - (3-chloropropyl) -murene, get 47 g (0.19 mol, 94 from theory) of a white crystalline powder, which contains more crystallization acetone.
    Calculated: C 14.20; N 16.83
    C HgoCPNjOg
    Found: Cf 12.87; N 14,59
    Molecular weight 249.74. NMR-H-spectrum (in cG 1.72, 4 (multiplet, 2), 3.15 (singlet, 9), 3.1-3.8 (multiplet, 4), 5.8-6.7 (multiplet , 3).
    Example P. Acrylyl-ureylene-ethylene-trimethylammonium iodide.
    26.8 g (0.1 mol) of N-Acryl-N- (2-iodoethyl) urea with 0.2 g of 2,6-di-tert-butyl-4-methyl-phenol in 300 ml of acetone is cooled to and 11.8 g (0.2 mol) of liquid trimethylamine are added. The mixture is stirred for 24 hours and the precipitate formed is filtered off. After washing with acetone and ether, 30 g (0.092 mol, 92% of theory) of a white crystalline powder are obtained.
    Calculated: se 38.79; N 12.84
    SdN vSRMz02
    Found: From € 39,24; N 12.55.
    . NMR-n-spectrum (c): cG 3.3 (s 1nglet, 9), 3.6-4 (multiplet, 4), 5.9-6.7 (multiplet, 3).
    B. Preparation and use of polymers of the formula (V).
    PRI mery 12-16. Acrylamide copolymerizates and monomers according to the invention (general procedure).
    Acrylamide, as well as cationic monomers, is dissolved in water and the temperature of the solution is adjusted to pH at 3.0. Solution by purging,
    nitrogen is released from oxygen (1 h), Initiated using the amounts indicated in Table 2, 1, 2, 2-azobisisobutyronitrile, (AJBN), potassium persulfate, and sodium dithionite and
    ferrous sulfate (M) -, after which the polymerization immediately proceeds (Table 1).
    Table 1
    The maximum temperature is reached after about 30-60 minutes. Cool, crush the resulting colorless gel and dehydrate it with 2-3 liters of methanol. After the distillation baths, the residual methanol is removed in vacuo. The output is about quantitative.
    12920
    13720
    Product based
    DMAEMA, СН Се9000
    li 2000
    1510 0
    Product Based
    DMAEMA, CHjCe 9000
    DMAEMA-2-dimethylamino-ethyl methacrylate.
    Example 17. The applicability of the polymers according to the invention as dewatering agents, for example for municipal sludge, is illustrated by the following studies. The dewatering times are established according to the C T S method (capillary absorption in time) given in Table. 2
    Table 2
    five
    21
    II
    thirty
    63
    22
    200 9 In spite of the low viscosity of aqueous solutions, the products always give better values than hitherto used DMAEMA-based copolymers,. Example 18. The applicability of the products as dewatering and delaying agents in the manufacture of paper is elucidated by the studies described below, which were carried out on standardized cellulose suspensions. Paper Weight: 60 Spruce Sulphite; 0 pulp from hardwood. Filler 30 SPS - SOAU. Grinding rate: 38 sr. The dosage of the auxiliary agent is 0.02 with respect to the paper stock. , To estimate the activity of the products, the dewatering times and the retention effect of a SchopperRiegler apparatus for measuring the degree of grinding of the mass are determined. The results are presented in table. 3. Table 3
    Single trial
    Example 12
    Example 13
    Copolymerisate
    based
    DMAEMA, SNOS
    DMAEMA-2-dimethylamino-ethylmathacrylate. It was shown that the obtained products under test conditions that correspond to research methods in paper production technology are active. Since the products in aqueous solution are also easily volatile and therefore easy to handle, i.e. they are easily metered and easily dissolved, then they can preferably be used in the manufacture of paper.
    Example 19- The products obtained according to the invention are tested as sedimentation agents.
    From example 15 it can be seen that the polymers corresponding to the proposed method (examples 10-13J have a significantly lower viscosity than the known products corresponding to the prior art and obtained from dimethylaminoethyl methacrylate. In addition, Table 2, shown in Example 15, shows the superiority of the corresponding The proposed method of polymers, when used as a dehydrating agent, due to the significantly shorter duration of capillary flow, which was studied using the method of determining the time of capillary suction. indicates that the application corresponding to the proposed method obezEYuZhivaets polymers Appliance slurry faster than productive you based on dimethylaminoethyl methacrylate.
    From Example 16 (Table 3), the data confirms faster dehydration during paper production (21 or 18 seconds, compared with 29 seconds, in the case of a product according to the state of the art).
    Finally, Example 17 shows the effectiveness of the corresponding prerequisites in coagulation tests. By determining the sedimentation time, the coagulating properties in aqueous solution are investigated after adding to clay slurries in water, which are prepared by suspending kaolin in water and in which aluminum sulfate solution pH is set to about 4.8. The results are presented in table. k. Table A
    11105375812
    when polymers are used to coagulate with improved compared to lucia aqueous suspensions containing (I) operational and technical clay. properties when used in this way, copolymers of the resulting, dehydrating and retentate ones according to the proposed method, facilities.
    coagulating, sedimentary
    权利要求:
    Claims (1)
    [1]
    METHOD FOR PRODUCING A COPOLYMER BASED ON A NITROGEN-CONTAINING MONOMER OF ACRYLIC RANGE 'by copolymerization of a nitrogen-containing acrylic series monomer with a second monomer, which consists in that, in order to obtain copolymers with improved operational and technical properties, they are used as co-additives , dehydrating and retaining means, as a nitrogen-containing monomer of an acrylic series, a compound of the general formula
    X 0. 2 O · C = C- C-3JH- C-invariant (CH 2 Ζ Θ where X - H or CH 3; η - 2-3; R - CH ^; S Ζ - C or E in as the second monomer, acrylamide and copolymerization are carried out at a mass ratio of nitrogen-containing monomer and acrylamide 1: 9 3: 7.
    SU <w 1053758> · ι
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    同族专利:
    公开号 | 公开日
    DE2856384B2|1980-10-23|
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    EP0037590B1|1985-06-19|
    EP0014767B1|1982-05-05|
    DE2962753D1|1982-06-24|
    引用文献:
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    RU2471773C2|2007-03-23|2013-01-10|Родиа Инк.|Method of producing acrylic monomer having one or more quaternary ammonium groups and polymers thereof|DE888316C|1943-12-25|1953-08-31|Cassella Farbwerke Mainkur Ag|Process for the production of arylacrylureas and polymers derived therefrom|
    US3551159A|1966-05-25|1970-12-29|Ciba Ltd|Process for hardening gelatine|
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    JP3911973B2|1999-07-26|2007-05-09|三菱化学株式会社|Azo dye, recording liquid using the same, and ink jet recording liquid|JPS6052421U|1983-09-20|1985-04-12|
    DE3585763D1|1984-07-03|1992-05-07|Nippon Paint Co Ltd|ACRYLAMIDE DERIVATIVES.|
    JP2553034B2|1985-05-27|1996-11-13|日本ペイント株式会社|Photosensitive monomer|
    ES8800696A1|1985-05-27|1987-11-16|Nippon Paint Co Ltd|Functional polymers and their production.|
    JP2721566B2|1989-12-20|1998-03-04|花王株式会社|Water disintegration paper, method for producing the same, and water disintegratable cleaning articles using the same|
    法律状态:
    优先权:
    申请号 | 申请日 | 专利标题
    DE2856384A|DE2856384C3|1978-12-27|1978-12-27|Acrylyl or methacrylyl ureas containing quaternary ammonium groups and process for their preparation|
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