• 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:
    Laminates of glazing material and polyvinyl butyral plasticized with propylene oxide oligomers.
    公开号:SU1090259A3
    申请号:SU813289502
    申请日:1981-05-29
    公开日:1984-04-30
    发明作者:Боуэн Гриффит；Алан Фауэл Питер
    申请人:Е.И.Дюпон Де Немур Энд Компани (Фирма)；
    IPC主号:
    专利说明:

    so fi The invention relates to plastic masses, namely to laminated plasticizers containing plasticized polyvinyl butyral. A laminate is known that contains a layer of polyvinyl butyral plated with the triethyl glycol glycetate diheptanoate. The disadvantage of this material is the low compatibility of plasticized polyvinyl butyral with polycarbonate layers. The closest to the proposed Technical essence and the achieved result is a triplex material containing layers of mineral glass, polymethyl methacrylate or polycarbonate, and layers based on half-vinyl butyral plasticized with triethylene glycol di-2-ethyl butyrate. The content of hydroxyl groups in polyvinyl butyral is 19-27.2 wt.% (In terms of sex vinyl alcohol) C 21.. The disadvantages of the known material are strong turbidity and the ability to form (microcracks and cracking. The purpose of the invention is to prevent the laminate from tarnishing. This goal is achieved by the layered material containing layers of mineral glass, polymethyl methacrylate or polycarbonate and polyvinyl butyral layers since 1927 , 2 May.% In terms of polyvinyl alcohol of hydroxyl groups with a plasticizer, as a plasticizer contains 19-65 parts by weight per 100 parts by weight of polyvinyl butyry propyl oxide oligomer by the formulas Rfo-CCHj —CH — 0) pN m where R is C ,, —C ,,, is alkyl, cyclohexyl, benzyl, phenyl, butoxyethyl or tetrahydrofuryl; p 4.7-9.2; m 1-3. . The invention provides for the preparation of layered structures having at least one layer of glazing material and a layer of plasticized polyvinyl butyral with a content of hydroxyl groups of 19-27.2 wt.% (In terms of polyvinyl alcohol) in a mixture of 19-65 parts by weight. per 100 weight parts Resins based on at least one propylene oxide oligomer of the formula (CH2-CH-0) nl m CHj The invention is based on the interaction of propylene oxide oligomers and 2-ethyl-1-hexanol with layered polyvinyl butyral plates. The compositions have the general formula СНгСНз СНз (СН2) з-СН-СН2-0- (СН2 СН-о) пН. Such compositions can be obtained by first forming the potassium salt of 2-ethylhexanol by reacting the alcohol with metallic potassium in an appropriate solvent, for example, in tetrahydrofuran, in an inert atmosphere, for example, in a nitrogen atmosphere. The reaction is expediently carried out at elevated temperature, preferably at the boiling point of the solvent. Initially, metallic potassium is supplied to the solvent with vigorous stirring, then the alcohol is added in an additional amount of zirvtel after the metal has melted and is in a fine state. The resulting mixture is heated to reflux, until the potassium reacts to stop, and then cooled to room temperature. The solvent is removed under reduced pressure to give the desired potassium salt as a waxy residue. The potassium salt of 2-ethylhexanol can be directly introduced in with propylene oxide at a moderate high temperature of 50-100 ° C with the floor of the oligomer. The resulting product can be purified by washing with dilute hydrochloric acid with a complete solution of sodium bicarbonate and brine. The final product, at room temperature, is a liquid, colorless to lightly-colored. The known oligomers of propylene oxide can be used as plasticizers for polyvinyl butyral. used for the manufacture of laminated plastics with glazing material. The average molecular weight of the propylene oxide oligomers is in the range of about 300-2500. Oligomers with a molecular weight below 300 show excessive volatility, while an increase in the molecular weight of oligomers of 2500 is their incompatibility. Propylene oxide oligomers are introduced as plasticizers in polyvinyl butyral, using the usual technique of adding a plasticizer. Poly vinyl butyral and plasticizer are used in amounts that make the mixture compatible, and the amount of plasticizer that can be added to polyvinyl butyral varies according to the final hydroxyl content of the polyvinyl butyral, as well as the specific character of the oligomer used. As a rule, less than 10 hours of storage per 10 hours polyvinyl butyral does not provide an adequate plasticizing effect, while a concentration of 70 hours per 100 hours leads to insufficient structural homogeneity of the material. Within this range, the plasticizer concentration is determined by the concentration at which this compound is incompatible with polyvinyl butyral. Incompatibility of the plasticizer may occur in the clouding of the sheet polyvinyl butyral, especially in the case of high molecular weight plasticizers, which leads to a reduced adhesiveness of the film. Incompatibility may also occur in the form of a sweating plasticizer on the surface of the finished film. Maximum plasticizer compatibility ratio at .100 weight.h. Yolivinyl butyral can be determined on the basis of guidelines that are applicable to oligomers with a narrow distribution over a modular one. weight, i.e. oligomers, in which the ratio of the weight average molecular weight to the numerical average molecular weight is less than approximately 1.2. If the plasticizer is based on a triol, i.e. m 3, the maximum concentration at 594 room temperature and a relative humidity of less than 90% can be determined as follows. When the hydroxyl content in polyvinyl butyral is less than or equal to 22, the maximum concentration is 275-10X - -; when the content of hydroxyls in polyvinyl butyral is greater than or equal to 22, the maximum concentration is - 243 - 4X Chv-I where X is the content of hydroxyls in wt.% in polyvinyl butyral (in terms of alcohol) in which the plasticizer is introduced; Y is the average molecular weight of the oligomer. In the case when the plasticizer is based on diol, i.e. m 2 and R are the propylene glycol radical, the maximum compatibility concentration is 420-10X - (- y), where X and Y have the indicated values. The maximum concentration of compatibility for oligomers of propylene oxide derived from monostables, i.e. when m 1, varies depending on the configuration and the number of C-atoms in the R-radical of the oligomer. Dp calculating the maximum concentration of plasticizer compatibility is typical of the following: R Maximum concentration, compatibility 485-1 OX - (- I-) 44 0-1 OX - (- | -) 430-10X- (|) Ethylhexyl about 420-10X- (| | ) Tridecyl o I The indicated concentrations correspond to t) t maximal concentrations of consistency within 5 hours per 10Q. Propylene oxide oligomers on isobetics exhibit exceptional plastifying ability with respect to polyvinyl butyral. The offered residues are compatible with polyvinylbutyl with a wide range of iroxyl content and provide scrolling with good spatial stability, high - tensile strength and rigidity. Moreover, such plasticizers are compatible with other plasticizers used for plasticization of polyvinyl butyral, including triethylene glycol di-2-ethyl butyrate and tetraethylene glycol di-heptanoate. Plasticized poly sheet. Vinyl butyral (PVB) can be interlaced with one or more layers of glazing material in accordance with commonly used methods. An advantage of the invention is that the obtained sheet plasticized PVB can be used not only
    in combination with glass, but also with polymethylene methacrylate or polycarbonate sheet, while the known PVB plasticizers tend not to: 20 interact with plastics.
    Thus, dihexyl adipate, triethylene glycol di-2-ethylbutyrate and triethylene glycol di-n-heptanoate used as plasticizers cause turbidity and microcrack formation in plastic sheet materials such as polycarbonate.
    In the examples given, the following test methods and procedures are used.
    fools.
    The residual content of hydroxyls in PVB (wt.% On the sun) - ASTMP 1396.
    The tensile strength of ASTIiP 1708 when testing a sample at 35–20.6 ± 0.6 ° C and 23.5t2% relative humidity (instead of relative humidity).
    5% secant modulus - ASTMP 882 when testing a sample at 20.6 + 0.6 C AND 23.5 + 2% relative humidity (instead of 50 ± 5% relative humidity). Pammel-SAE 1208 gap. Medium level gap (ANSIZ 26.1). determined by the ladder method, while by a known method (U.S. Pat. No. 3,718,516) tests are conducted at the same level (Z 26.1). Edge stability - AHSIZ26.1 (% stretch). Test specimens with a nominal thickness of 0.76 m are conditioned for 4 hours at 20.0 ± 1 ,. The specimen is then cut with a die-cutter into slices of 1.9x10.2 cm, marked and fixed, in a test furnace at 65i for 1 hour. For each specimen
    The mixture was heated to reflux until the potassium reacted, then cooled to room temperature and the solvent was removed under reduced pressure, and 2-ethylhexanol in the potassium salt was removed as a waxy mass.
    The solid potassium salt is dissolved in propylene oxide (58 g, 70 ml, IjO mol) and the solution is transferred under nitrogen to a stainless steel autoclave. The autoclave is heated to 70 ° C for 1 hour and then for another 6 hours at 90 ° C. The contents of the autoclave are recovered (250 m ether), the ether solution is washed successively with 2-100 ml of dilute hydrochloric acid, 2-100 ml of saturated sodium bicarbonate and 2-100 ml of brine. The ether layer is dried over magnesium sulfate. The mixture is filtered, the solvent is evaporated under reduced pressure to give 69.9 g (92%) of a pale yellow liquid. The load applied is 69 kPa and after 30 minutes the stretch is measured. The result is calculated by dividing the measured length after testing for the initial length and multiplying by 100. Example 1. Metallic potassium (5.58 g, 0.143 mol) is placed in 100 ml of dry tetrahydrofuran in a nitrogen atmosphere. The mixture was heated to reflux with vigorous stirring. After the potassium melts and becomes finely dispersed, 2-ethylhexanol (18.5 g, 22.3 ml. O, 143 mol) in 50 mp of dry tetrahydrofuran is slowly added. average molecular weight (hydroxyl number) is 400. Propylene oxide oligomer is obtained, with 2-ethylhexanol of the formula CHqiCHj CHjCCHgljCH-CH, j -0- {CH CH-0) where n 4.7; ffl 1. Example 2. 4.0 g of PVB in the form of flakes with a hydroxyl content of 22.8 wt.% (in terms of polyvinyl alcohol) are mixed in a glass with 2 g (50 parts per 100) of propylene oxide diol, in which R - a propylene glycol derivative, with an average molecular weight of 1025. After a few minutes, the softened flakes are compressed in a laboratory hydraulic press at 140 ° C for 4 minutes, ending pressing at 20700 kPa. The resulting film is cut into small pieces, and the pressing is repeated several times for better mixing. The result is a transparent plasticized film with no visible signs of plasticizer on the surface. The film is left in a closed 100 ml bottle. After more than 10 days, there was no sweating at a temperature of about 10% and a relative humidity of 90%. PRI me R A (comparative). The process is carried out analogously to example 2 with the exception that take 3 g of propylene diol. The mixture to prevent bonding is pressed between the sheets of fluoroplastic at a final pressure of 20,700 kPa. The process is repeated three times. When storing, plasticizer balls, i.e. The amount of the plasticator exceeds the compatibility limit. Example 3. 4 g of PVB with a hydroxyl content of about 19% is mixed in a dry form with 1.8 g (45 h per 100) of the propylene triol with co. an average molecular weight of 1500, in which R is a derivative of trioxymethylpropane. The mixture is pressed at 160 ° C between the sheets of fluoroplastic to prevent adhesion and a final pressure of 20,700 kPa. The sheets are cut and the pressing is repeated three times. When storing, no plasticizing agent is noted. Example 4. The process is carried out similarly to Example 2 using a combination of plasticizers: 4 g of PVB is mixed with 0.75 g of propylene oxide diol with an average molecular weight of about 450, in which R is a propylene glycol derivative, and 0.75 g of propylene triol, in which V. is a derivative of trioxymethylpropane. In this case, a transparent film is obtained, on the surface of which the storage of the plasticizer is not observed during storage. PRI me R In (comparative). The process is carried out analogously to example 4 using 4 g of PVB containing 22.8% of hydroxyls, and as a plasticizer 1.6 g (40 parts per 100) of propylene triol, in which R is a derivative of trioxymethylpropane opane. The sweating of plasticizer balls, i.e. The amount of plasticizer exceeds the compatibility limit. Example 5. The process is carried out analogously to example 2, except that monospyles with a terminal methoxy group and an average molecular weight of approximately 700 are used as a plasticizer. 45 h. To 100. Plasticization and compatibility are noted. Example 6. The process is carried out analogously to example 2 using PVB containing hydroxyls of 22.8%, and 50 parts per 100 mono-alcohol with a terminal butoxy group. Compatibility is achieved at this level. Example 7. A propylene diol with an average molecular weight of about 425 and PVB is fed to a 83 ml Werner-Pfl twin screw extruder with a tap and a L / D ratio of 20: 1. Applied PVB contains approximately 23% hydroxyls. The ratio of diol to PVB 31:69 (45 h, per 100). The extrusion is carried out at a screw rotation speed of 90 rpm, a melt temperature at the extruder outlet of 200 ° C and a residual pressure of 508 mm Hg. outlet to remove any moisture. 80 ppm of magnesium are added to the melt, magnesium is in the form of the magnesium salt of 2-ethylbutyric acid as a means for controlling the agglutination. A gear pump (at 200 ° C) is used to transfer the melt from the extruder to the sheet die. Total holding time min. Sheets with a thickness of 762-813 µm and a width of 76.2 cm are extruded from the head into a tank of water at 20 s for curing. Then the sheets are air dried, dusted with NaHCO and rolled up. These sheets are made of laminated plastic, first with a NaHCO shake, by conditioning at a relative humidity of 22% (22 s) for 8 hours, by layering on glass, npoN & r in water containing 350 ppm of CaC1j. Lamination is carried out at 135 ° C for 9 minutes and a pressure of 8–28 kPa. Plastic is obtained with the following mechanical properties: stiffness (5% secant modulus) 3174 kPa; -the average level of rupture is 91.4 cm / Bhb; (ball level of discharge (ball weighing 2268 g) 91, L CM / -18 C; 457.2 cm / 22 C; 304.8 cm / 38 s, clouding of the rib (VSAS 2.26) 14, weeks, 19/64 (4 weeks. Example 8. The process is carried out similarly to Example 7, except that the oligomer of the formula according to the invention is used as a plasticizer, where R is butyl, m 1, the average pH of molecules is 400. Oligomer and PVB are used in a ratio of 32 : 68 or 47 parts per 100. In addition, 2-ethyl-butyric acid magnesium salt is added in an amount of only 40 parts per million. Laminated plastic is prepared and tested as in Example 7, with the characteristics of plasticthe following: tensile strength at stretching 27324 kPa, stiffness (5% secant modulus) 3036 kPa, deformation 26%, rupture according to Pammel 8, average level of rupture (ball weighing 2268 g) 243.8 cm / -18 С; 594 cm / 22 C; 329.18 cm / 38 s. Example 9. The process is carried out analogously to example 7 except that the oligomer according to the formula of the invention is used as a plasticizer, where R is ethylhexyl, th 1, average molecular weight - 425. Oligomer and PVB are used in a ratio of 33:67 or 49 parts per 100. Potassium formate is used as a means for controlling adhesion. Laminates are obtained and tested as in Example 7. The resulting plastic is characterized by the following mechanical properties: tensile strength i 27943 kPa, stiffness 6776 kPa, rupture according to Pummel 7, average level of rupture (ball weighing 2268 g) 359.7 cm / -18 С; 554.7 cm / 22 C; 320.0 cm / 38 ° C. Examples 10-20. The process will be carried out analogously to example 2 with the use of oligomers, the values of w, R, lo lo coolant and the concentrations of which, as well as the content of hydroxyls in PVB are given in Table. 1. At the indicated concentrations, compatibility and good plasticizing properties are noted. EXAMPLE 21 The process is carried out in analogy to Example 2, except that a mono alcohol with ethyl hexoxy group of molecular weight at a concentration of 48 ppm 100 is used. Good compatibility and plasticization results are obtained. Laminated plastic is obtained from plasticized sheet of PVB with a thickness of 6.4-7.6 microns by layering between two ducts with two layers of polycarbonate by pressing at 3450 kPa. The resulting plastic is transparent, after manufacture, and will remain transparent after storage for 5 days at KoiAaT and tepere Example ((comparative). The process is carried out analogously to example 21, except that di- (2-ethyl butyrate) tetraethylene glycol at a concentration of 49 parts per 100 is used as a plasticizer in the interlayer. Turbidity is observed in the manufacture of plastic. Examples 22-25. , To test the possibility of microcracking, the propylene oxide oligomer of the invention is brought into contact with a molded polycarbate. To do this, several drops of oligomer are deposited on ribbons of sheet polycarbonate with dimensions of 2.54 X 10.16 cm and thickness of 3.2 microns. In these examples, the following oligomers are used: ethylhexyl mono-alcohol with an average molecular weight of 425, a triol derived from a tri- (metric-1-propane) derivative with a molecular weight of 400, a diol derived from a derived glycol with a molecular weight. 1025, and mono-alcohol, (R-butyl) with an average molecular weight of 400. 1 hour after application of the oligomer, each ribbon is manually bent into an arc of 80. Then, a scratch is made on the surface of the sheet and after 30 minutes the ribbon is again bent. In all cases, the occurrence of microcracks is not noted. . Examples 26 and 27. The process is carried out analogously to example 2 using oligomers, values of t, R, molecular weight and concentration of KoTL1RX, and also the content of hydroxyls in PVB are given in Table. 2. Example 28. The process is carried out analogously to example 21, except that the sheet material is placed between two layers of polymethyl methacrylate lucite. The resulting layered plastics are light after production and remain. light under ambient conditions after five days. PRI me R s Di E, F (comparative-5). The process is carried out analogously to examples 22-25 using plasticizers containing mainly di ihexyl adipate, di- (2-ethyl butyrate) triethylene glycol and diheptanoate tetra-10 ethylene glycol. In all cases, coating with a plasticizer leads to clouding, microcracking and cracking. Thus, plasticized PVB is not only suitable for laminated fiberglass, but can also be used without microcracking with plastic materials such as polycarbonate. Results of using validators (examples 1, 22-25, C, D, E, F) with polycarbonate sheet material are given in table. 3 T a b i c a 1
    .13
    Plasticizer
    Example
    1090259
    14
    /
    - T a b l and c a 3
    results
    21
    Propylene oxide oligomer Di- (2-ethylbutIrate) tetraethyl
    WITH
    lenglikol
    2-25
    Propylene oxide oligomer
    Digeksiladipinat D
    Di- (2-ethylbutyrate) trimethyl glycol
    Di-n-heptayl6 tetramethylene glyc. Ol
    Light
    MyTHbifi
    Light, without microcracks
    Strong turbidity, the formation of microcracks, cracking
    Strong opacification, formation of microcracks j cracking
    Strong clouding, micro-cracking, cracking
    权利要求:
    Claims (1)
    [1]
    LAYERED MATERIAL containing a layer of mineral glass, polymethyl methacrylate or polycarbonate and layers of polyvinyl butyral with 19 27.3 wt.%, Calculated on the basis of polyvinyl alcohol of hydroxyl groups with a plasticizer, and so on. that, in order to prevent tarnishing, it contains 19-65 parts by weight as a plasticizer. per 100 parts by weight polyvinyl butyral of the propylene oxide oligomer of the formula g-fo- (CH2CH-o) n H] m cr 3 where R is C 2 -C ^ alkyl, cyclohexyl, benzyl, phenyl, butoxyethyl or tetrahydrofuryl; η - 4.7-9.2;
    W - 1-3.
    . 1
    类似技术:
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    EP0513470A2|1992-11-19|Adipate compositions
    US5013780A|1991-05-07|Plasticized polyvinyl butyral and interlayer thereof
    EP0432124B1|1996-02-28|Plasticizer composition, plasticized polyvinyl butyral and interlayer thereof
    US5212014A|1993-05-18|Polycarbonate sheet laminated to plasticized polyvinyl butyral sheet
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    同族专利:
    公开号 | 公开日
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    US4293615A|1981-10-06|
    CA1153681A|1983-09-13|
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    法律状态:
    优先权:
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