DE1544803A1 - Process for the production of molding compounds based on tactical homo- or copolymers of vinyl chloride - Google Patents
Process for the production of molding compounds based on tactical homo- or copolymers of vinyl chlorideInfo
- Publication number
- DE1544803A1 DE1544803A1 DE19651544803 DE1544803A DE1544803A1 DE 1544803 A1 DE1544803 A1 DE 1544803A1 DE 19651544803 DE19651544803 DE 19651544803 DE 1544803 A DE1544803 A DE 1544803A DE 1544803 A1 DE1544803 A1 DE 1544803A1
- Authority
- DE
- Germany
- Prior art keywords
- tactical
- copolymers
- polyvinyl chloride
- homo
- molding compounds
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Pending
Links
Classifications
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L27/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers
- C08L27/02—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L27/04—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by a halogen; Compositions of derivatives of such polymers not modified by chemical after-treatment containing chlorine atoms
- C08L27/06—Homopolymers or copolymers of vinyl chloride
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L23/00—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers
- C08L23/02—Compositions of homopolymers or copolymers of unsaturated aliphatic hydrocarbons having only one carbon-to-carbon double bond; Compositions of derivatives of such polymers not modified by chemical after-treatment
- C08L23/04—Homopolymers or copolymers of ethene
- C08L23/08—Copolymers of ethene
-
- C—CHEMISTRY; METALLURGY
- C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
- C08L—COMPOSITIONS OF MACROMOLECULAR COMPOUNDS
- C08L31/00—Compositions of homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid or of a haloformic acid; Compositions of derivatives of such polymers
- C08L31/02—Homopolymers or copolymers of esters of monocarboxylic acids
- C08L31/04—Homopolymers or copolymers of vinyl acetate
Landscapes
- Chemical & Material Sciences (AREA)
- Health & Medical Sciences (AREA)
- Chemical Kinetics & Catalysis (AREA)
- Medicinal Chemistry (AREA)
- Polymers & Plastics (AREA)
- Organic Chemistry (AREA)
- Compositions Of Macromolecular Compounds (AREA)
Description
Troisdorf. den 1IjjjTroisdorf. the 1Iyyy
NOBüiL AKTIi]IiGaSEiLLSCHAi1T i'roisdorf Bez. KölnNOBüiL AKTIi] IiGaSEiLLSCHAi 1 T i'roisdorf Bez. Cologne
'Verfahren zur Herstellung von Formmassen auf "der Basis von taktischen Homo- oder Gopolymerisaten.des Vinylchlorids'Process for the production of molding compounds on the basis of tactical homo- or co-polymers of vinyl chloride
t ,Μ ,. _ 1 Il I I I Hl' - t , Μ,. _ 1 Il III H l '-
ils ist bekannt, die mechanischen Eigenschaften von taktischem Polyvinylchlorid durch Zusatz von chloriertem ataktischen Polyvinylchlorid zu verbessern; vergl. belgische Patentschrift 626 843· Produkte aus Formmassen auf dieser Basis zeichnen sich durch eine hohe Formbeständigkeit in der Wärme und. durch verbesserte mechanische Werte gegenüber solchen aus reinem taktischen Polyvinylchlorid aus, indess reichen beispielsweise die U-Kerbzähigkeiten für bestimmte Anwendungszwecke nicht aus«ils is known the mechanical properties of tactical To improve polyvinyl chloride by adding chlorinated atactic polyvinyl chloride; see Belgian patent specification 626 843 · Products made from molding compounds on this basis stand out due to a high dimensional stability in the heat and. through improved mechanical values versus those of purely tactical values Polyvinyl chloride, however, for example, the U-notch toughness is sufficient for certain purposes not off «
Es ist weiter bekannt, ataktischea Polyvinylchlorid mit hochmolekularen Verbindungen, wie chloriertem Polyäthylen zu elastifizieren, welches hier bezüglich der Ü-Kerbzähigkeit optimale Werte ergibt} weiterhin kommen Butadien-Polymerisate, Mischpolymerisate und Pfropfpolymerisate, Polyurethane und Mischpolymerisate aus Äthylen und-Vinylacetat oder Äthylen und Acrylsäureestern als Plastifizierungsmittel zur Anwendung. ' 'It is also known atactic polyvinyl chloride with high molecular weight To elasticize compounds such as chlorinated polyethylene, which results in optimum values here with regard to the Ü-notch toughness} butadiene polymers and copolymers are also used and graft polymers, polyurethanes and copolymers of ethylene and vinyl acetate or ethylene and acrylic acid esters as Plasticizers for use. ''
Wie bereits aus der belgischen Patentschrift 626 843 hervorgeht, versuchteman,auch Formmassen auf der Basis von taktischem Polyvinylchlorid mit Butadienmischpolymerisaten und chloriertem Polyäthylen herzustellen, doch zeigten diese Zusätze nicht die analoge Wirksamkeit wie beim ataktischen Polyvinylchlorid.. As already apparent from the Belgian patent specification 626 843, attempts were made to also use molding compounds based on tactical polyvinyl chloride with butadiene copolymers and chlorinated polyethylene, but these additives did not show the same effectiveness as with atactic polyvinyl chloride ..
Js wurde nun gefunden, daß von den oben genannten iJlastifizie- rune -si£omponenten Llischpolyuere des Vinylacetats rait Äthyl en dem taktischen Polyvinylchlorid zugesetzt, ^Orinmasö&n rait besonders hohen U-iCerbzähigkeiten bezüglich der daraus hergestellten Produkte bei kaum verringerter Vicattemperatur ergeben. Im /erbleich zu entsprechenden jt'ornkürrjern aus ataktschen PolyvinylcLlorid liefen überraschenderweise aie iJ-Kerbzähigkeiten sogar höher, obwohl man diese iiOrnimassen bei x'emperaturen zwischen 19O und ZiO C verarbeiten ::iuß, denn im allgemeinen sinken näralich die U-KerbzLhigiceiten mit steigender Verar >eitungsterrrperatür. ./ie die Beispiele 9 und 10 zeigen, beträgt die U-Kerbzühigkeit einer Prüfplatte aus ataktischein Polyvinylchlorid a it 5 '-'eilen einesJs has now been found that the above-mentioned run of iJlastifizie- e - si £ omponents Llischpolyuere of vinyl acetate Rait ethyl en tactical polyvinyl chloride was added, resulting Orinmasö ^ n & Rait particularly high U-iCerbzähigkeiten with respect to the products produced therefrom with hardly reduced Vicat temperature. In the pale to corresponding grain skins made of atactic polyvinyl chloride, surprisingly, the I-notch toughness ran even higher, although one must process these ordinary materials at temperatures between 190 and 10 ° C, because in general the U-notch strengths decrease with increasing processing > opening body door. As shown in Examples 9 and 10, the U-notch toughness of a test plate made of atactic polyvinyl chloride is 5 'parts
Copolymeren aus Vinylacetat und Äthylen bei 190-210 C Verarbeitungstemperatur 5»9» bei I7O-I8O C Verarbeitun^stemperatur 8,8 cmkp/cm . Ide analog bei 190-210 G hergestellte Prüfplatte aus taktischem Polyvinylchlorid zeigt laut Beispiel 7 eine U-Kerbzähigkeit, die noch weit über der der bis 180 C verarbeiteten Prüfplatte aus ataktischem Polyvinylchlorid liegt.Copolymers of vinyl acetate and ethylene at 190-210 C processing temperature 5 »9» at 170-180 C processing temperature 8.8 cmkp / cm. Ide test plate produced analogously to 190-210 G. made of tactical polyvinyl chloride shows, according to Example 7, a U-notch toughness that is still well above that of that processed up to 180.degree Test plate made of atactic polyvinyl chloride lies.
Die zur Elastifizierung verwendeten Mischpolymerisate aus Vinylacetat und Äthylen sollen einen Gehalt von 30-70 Qevt.fo an Vinylacetat und eine relative Viskosität (1 ^Ag in Chloroform) zwischen 1,8 und 6,5 haben. -Die Mischpolymerisate können auch vernetzt sein, wobei die Vernetzungsgrade zwischen 10 und 40 liegen, bestimmt durch die Chloroformaufnahiae *in g -pro g Polymeres nach 24-stündigeni Lagern bei 20 C in Chloroform. Formmassen aus taktischem Polyvinylchlorid und vernetzten! Mischpolymeren aus Vinylacetat-ii.thylen zeichnen sich auch durch eine erhöhte Chemikalxenbeständigkeit aus. Der Gehalt an Mischpolymeren aus Vinylacetat-Athylen in den Formmassen beträgt zwischen 0,5 und 10The copolymers of vinyl acetate and ethylene used for elasticization should have a vinyl acetate content of 30-70 Qevt.fo and a relative viscosity (1 ^ Ag in chloroform) between 1.8 and 6.5. The copolymers can also be crosslinked, the degrees of crosslinking being between 10 and 40, determined by the chloroform absorption * in g -per g of polymer after storage for 24 hours at 20 ° C. in chloroform. Molding compounds made from tactical polyvinyl chloride and cross-linked! Copolymers made from vinyl acetate-ethylene are also characterized by increased resistance to chemicals. The content of copolymers of vinyl acetate-ethylene in the molding compounds is between 0.5 and 10
y. -v^ r \ t. * iMiii§ y. -v ^ r \ t. * iMiii§
bezogen auf da,s Polyvinylchlorid. r7 * 'based on da, s polyvinyl chloride. r 7 * '
009813/1608 BAD original009813/1608 BAD original
Als taktisches Polyvinylchlorid wird ein Polymer! s-.t bezeichnet, dessen Cnlorätome zu etwa 55-85 >j syndiotaktisch angeordnet sind» Taktisches Polyvinylchlorid ist nach verschiedenen Verfahren herstellbar, vergl. z.B» SAS 1 187 374» die belgische Patentschrift 627 674 und die britischen Patentschriften 895 153 und 93t 629.As a tactical polyvinyl chloride, a polymer! s-.t denotes, whose chloro atoms are arranged syndiotactically to about 55-85> j Tactical polyvinyl chloride can be produced by various processes, see e.g. »SAS 1 187 374» the Belgian patent specification 627 674 and British patents 895 153 and 93t 629.
Zur Charakterisierung von taktisöheö Polyvinylchlorid kanh neben der röntgenoeiraphisehen Untersuchung auch die iiOrmbestänäi jteit in der Wärme nach Vicat (YDE 0302 Paragraph 1Jt) herangezogen werdölii uie Vieatwesitö des taktischen Polyvinylchlorids liegen um Iü-I5°ö ü"ber denen des ataktischen Polyvinylchlorids* Aüiser deri taktischen Hoaopölyiiiereh des Tinylchlorids können auch taktische Gopölyraere Jes '/inylchlörids φΐΐ Cöaonöiaeren ^wischen 0,5 ühd 20 öe#*70, -.vie Beispielsweise Äthylen, Propylen j Vinyl- · acetate Acrylsäureester, i.ichloi"äihyien und ähnliche mit deix Kopolymeren aus Vinylacetat und ethylen fjeiaiis der Jri'itiäu-äg elastifiziert werdena 2üs.tälich %ti diesen ilör.<jonenten üönneh die j'örjaniäöseh weitere HochpGlyaeie, wie chloriertes Polyethylen, tOlypröpyieiij Pölyisoautyleitj Pdlyvinj-laöetatiFor the characterization of tactical polyvinyl chloride, in addition to the X-ray orbital examination, the heat resistance according to Vicat (YDE 0302 Paragraph 1 ) can also be used, and the degree of viability of tactical polyvinyl chloride is around l5 ° above that of atactic polyvinyl chloride Tactical Hoaopölyiiiereh des Tinylchlorids can also tactical Gopölyraere Jes' / inylchlörids φΐΐ Cöaonöiaeren ^ between 0,5 ühd 20öe # * 70, -.vie for example ethylene, propylene, vinyl acetate acrylic acid esters, i.ichloi "Äihyien and similar with deix copolymers made of vinyl acetate and ethylene fjeiaiis der Jri'itiäu-äg are elasticized every day % ti this ilör
j Pdlyvinyldthei* ü» da sowie istähiliaa j Füitstcif-'e usw. eiithälteii*j Pdlyvinyldthei * ü » da as well as istähiliaa j Füitstcif-'e etc. eiithälii *
BADBATH
Ö *; -■:Ö * ; - ■:
15U80315U803
100 Teile taktisches Polyvinylchlorid (rn , 2,8) werden mit 1,5 Teilen Zinnstabilisator (Handelsname 17 M) und 0,5 Teilen gleitmittel (Handelsnamej^-Wachs) bei 190 C gewalzt und bei 210 C zu einer Prüfplatte verpreßt.100 parts of tactical polyvinyl chloride (RN , 2.8) are rolled with 1.5 parts of tin stabilizer (trade name 17 M) and 0.5 part of lubricant (trade name j ^ wax) at 190 ° C. and pressed at 210 ° C. to form a test plate.
Beispiel 2-8; Unter den in Beispiel 1 angegebenen Bedingungen werden in den Ansatz auf der Walze jeweils zusätzlich 5 Teile der Elastifizierungskoniponente eingearbeitet« Example 2-8; Under the conditions given in Example 1, an additional 5 parts of the elasticizing component are incorporated into the batch on the roller.
Anstelle der 100 Jeile taktisches Polyvinylchlorid - wie in Beispiel 7 - werden 100 Teile ataktisches Polyvinylchlorid eingesetzt.Instead of the 100 Jeile tactical polyvinyl chloride - as in Example 7 - 100 parts of atactic polyvinyl chloride used.
."ie Beispiel 9> jedoch enolgt die Verarbeitung auf der i/alze bei 170 und auf der Presse cei 180 C.. "ie Example 9> however, the processing follows on the i / alze at 170 and on the press cei 180c.
.jie nachstehende Tabelle zei.jvt die Ergebnisse.The table below shows the results.
- 5 0098 13/1608- 5 0098 13/1608
iilastifizierungskomponente Zugfestig- Dehnung U-Kerb „ Vicat keit ρ (yo) (cml:p/cm ) ( C) ,- (kp/cm ) .iilastification component Tensile strength-elongation U-notch “Vicat speed ρ (yo) (cml: p / cm) (C) , - (kp / cm).
1. -1. -
2. 5 'i'eile Polyäthylen2.5% polyethylene
(Plaskon 101)*(Plaskon 101) *
3.5 Teile chlor.Polyäthylen. (Plaskon 105)* 6453.5 parts chlorinated polyethylene. (Plaskon 105) * 645
550550
525525
5555
6060
3,13.1
5,45.4
4,9- ' S84.9- 'S8
4«, ο Teile Polyurethan (Estane4 «, ο parts of polyurethane (Estane
645645
2121
2,02.0
5 "'i'eile Gopolyni.iithylen-ii.thylacrylat 5 "i'eile gopolyethylene-II-ethyl acrylate
(DPD 6169)* 53Ö(DPD 6169) * 53Ö
2727
5,25.2
6» 5 Teile Pfropfp.Butadien-Styrol I,'ie thylmethacrylat6 »5 parts of graft butadiene styrene I, 'ie methyl methacrylate
(Paraloid 228)* · 595 (Paraloid 228) * 595
28;28;
5,6.5.6.
7. 5 Teile Copo.lyra*Tinylacetat-ii.thylen7. 5 parts of Copo.lyra * Tinylacetate-II.ethylene
(Levapren 450}* 40(Levapren 450} * 40
.8, 5 Teile iievapren 450* vernetzt 9. 5 'feile LaTäFapren· 450* ' 03* 5 ',teile Befwapren, 450*.8, 5 parts iievapren 450 * networked 9. 5 'file LaTäFapren · 450 *' 03 * 5 ', parts Befwapren, 450 *
5555
5,45.4
a,aa, a
BADBATH
Claims (1)
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
DED0048443 | 1965-10-16 |
Publications (2)
Publication Number | Publication Date |
---|---|
DE1544803A1 true DE1544803A1 (en) | 1970-03-26 |
DE1544803B2 DE1544803B2 (en) | 1974-11-28 |
Family
ID=7051181
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
DE19651544803 Pending DE1544803B2 (en) | 1965-10-16 | 1965-10-16 | Molding compounds based on tactical homo- or copolymers of vinyl chloride |
Country Status (5)
Country | Link |
---|---|
BE (1) | BE688296A (en) |
DE (1) | DE1544803B2 (en) |
FR (1) | FR1500484A (en) |
GB (1) | GB1110427A (en) |
NL (1) | NL6614484A (en) |
Families Citing this family (1)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
DE3204144A1 (en) * | 1982-02-06 | 1983-08-18 | J.H. Benecke Gmbh, 3000 Hannover | Ageing-resistant thermoformable plastic film |
-
1965
- 1965-10-16 DE DE19651544803 patent/DE1544803B2/en active Pending
-
1966
- 1966-10-14 BE BE688296D patent/BE688296A/xx unknown
- 1966-10-14 NL NL6614484A patent/NL6614484A/xx unknown
- 1966-10-14 FR FR80148A patent/FR1500484A/en not_active Expired
- 1966-10-14 GB GB4616066A patent/GB1110427A/en not_active Expired
Also Published As
Publication number | Publication date |
---|---|
GB1110427A (en) | 1968-04-18 |
NL6614484A (en) | 1967-04-17 |
FR1500484A (en) | 1967-11-03 |
BE688296A (en) | 1967-03-16 |
DE1544803B2 (en) | 1974-11-28 |
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