Method of vulcanizing rubber mixture

专利摘要:
Copolymers of vinylidene fluoride with at least one other fluorinated- ethylenically unsaturated monomer are press-cured at about 163 DEG -204 DEG C. by crosslinking with an aromatic polyhydroxy compound in the presence of an accelerator in a weakly basic system, at least a portion of the polyhydroxy compound being blocked by conversion to acetal or thioacetal groups. At the press-cure temperature some of the acetal or thioacetal groups are decomposed and the free hydroxyl groups are reformed, thus providing crosslinking capability. The remainder of acetal or thioacetal groups are decomposed during post-cure oven heating at a higher temperature, and under those conditions copolymer vulcanization is completed. Press-cured compositions of this invention have excellent hot tensile elongation, which permits easy demoldability; and very good recyclability, which eliminates or reduces fluoropolymer waste. The compositions of this invention also have excellent mold flow properties at press-cure temperature.
公开号:SU818490A3
申请号:SU782700557
申请日:1978-12-26
公开日:1981-03-30
发明作者:Джеймс Архарт Ричард；Нерсейсиан Артур
申请人:Е.И.Дюпон Де Немур Энд Компани(Фирма)；
IPC主号:

专利说明:

(54) METHOD FOR VOLKANIZATION OF RUBBER MIX
And evaporated to dryness under reduced pressure. After drying overnight in a vacuum dryer at 80 ° C, a light brown solid is obtained. Yield 98.1%, m.p. 60-100 C.
After purification by recrystallization from acetone-petroleum ether, two types of crystals are obtained: the first is a white solid with mp. 136-139 C (yield 21.8%), the second - whitish solid with so pl. 130-137 ° C, yield 22.0% (total yield 43.8%, based on the starting materials).
The elemental composition of the crystals of the first type.
Found,%: C 59.5, H 5.1. Calculated,%: C 59.7, H 5.2. The results of NMR analysis confirm the proposed structure.
Other acid catalysts have been successfully used, for example, concentrated sulfuric and p-toluenesulfonic acid, but hydrochloric acid is preferred. The use of concentrated sulfuric acid leads to excessively exothermic reactions.
Variants of the cleaning method. A suitable method for treating the crude reaction product is the neutralization of the acid catalyst with a slight excess of base, for example, hydroxide. However, the product is a sticky semi-solid. It can be dissolved in a solvent and touched on some solid carriers as described above. Calcium hydrosilicate is preferred because of its excellent absorption capacity (only 30 wt.% Required) and inertness (does not affect the properties of the vulcanizate). Moreover, its basicity is sufficient, so that it does not require preliminary addition of base to neutralize the acidic catashist.
Example 2. Bis (tetrahydropnranyl) new ester of hydroquinone.
To 73.0 ml (0.8 mol) of dihydropyran, heated to 45 ° C, 2 drops of concentrated (37.3%) hydrochloric acid are added under a nitrogen atmosphere and then 22.0 g (0.2 mol) of hydruhinone in for 3.0 minutes while stirring. The reaction temperature rises to a maximum of 90 ° C in 5 minutes, to which the external supply of TenhA is stopped. After cooling, a pale pink color is formed. After 1 hour and 50 minutes from the start of the addition, 0.2 g of calcium hydroxide was added to the reaction suspension, the reaction mixture was stirred for 5 minutes and then evaporated under reduced pressure. After drying for 1-1 / 2 days. in a vacuum dryer, a free-flowing reddish-brown solid is obtained with mp. 119-129 5c (pre-softened), yield 95.5%. The crude product was also recovered by vacuum filtration of a suspension containing calcium hydroxide. In this case, get a whitish, free flowing solid product with so pl. 97-120s (pre-softened), yield 86.0%.
As a result of purification by recrystallization from a mixture of acetone-petrol ether, a white solid is obtained with a mp. 128-132 s (slightly softened beforehand). Although recrystallization It is carried out quickly and easily as compared to the recrystallization of the bis5 derivative of phenol AF, however, the losses and yield reduction are significant.
Due to the fact that the raw product is a free flowing, easily processed solid substance, it is not required to be applied to a solid carrier. However, it is practical to apply the raw product to a carrier, for example, calcium hydrosilicate, in order to reduce odor, which is sometimes used with raw material prepared from crude dihydropyran.
Example 3. Blocked n-butylvinyl ether hydroquinone.
Under a nitrogen atmosphere, 2 drops of concentrated hydrochloric acid and then 22.0 g (0.2 mol) of hydroquinone are added to 140 ml (0.8 mol) of n-butyl vinyl ether over 4 minutes with stirring. When heated, hydrochi5 non dissolves and reacts, which shows a self-induced increase in temperature, when the temperature reaches 105 ° C, the external heat supply is stopped. After stirring 0 for 2 hours from the start of the addition, the reaction mixture is cooled to. Calcium hydroxide (0.1 g) is added to the clear solution, then 100 ml of acetone and 26.7 g of calcium hydrosilicate. The resulting suspension is evaporated
5 under reduced pressure and dried in vacuum dryers at 80-100 C for 1 day. in each of the dryers. The resulting product, consisting of 70% by weight of active ingredient per 30% by weight of Ridro0 calcium silicate (micro-village E), is a whitish, free flowing solid, yield 92.4%.
PRI me R 4. Curing under
5 pressure fluoroelastomer.
Vulcanizable elastomeric compositions (Table 1) were prepared as follows.
A crosslinking agent and an accelerator (benzyltriphenyl phosphonium chloride) are added to a copolymer with a wide molecular weight range consisting of 60% by weight of vinylidene fluoride and 40% by weight of hexafluoropropene on a two-roll mill. For this add5
Next is the addition of the remaining ingredients. This is the recommended order of addition. In case of its violation (the last addition of a cross-linking agent), lower CPD values are obtained. The crosslinking agent is based on bisphenol AF, either completely blocked by dihydropyran, or a mixture of free and blocked crosslinking agent. Blocked bisphenol AF is applied to calcium hydrogen hydrate (micro-village E) as carrier (30% carrier, 70% active material),
Rubber compounds are tested according to the rheometer method with a swing disk. The experiment was carried out in 30 missions at 177 ° C.
Torque values (Nm) are given in Table. 2
The data presented shows that in all cases a satisfactory degree of cure is achieved in 5 min.
Example 5. This example shows that the blocked bisphenol AF has the same good properties / as the adsorbed product.
In several parallel experiments, bisphenol AF is converted to a tetrahydropyranyl ether derivative using a catalyzed reaction with dihydropyran, as in Example 1, except that the relative molar ratio of the reagent is changed. Unreacted bisphenol is extracted with a 10% aqueous solution of sodium hydroxide, sometimes chloroform is added to the mixture before extraction. The volatiles are removed under reduced pressure, and the residue is dried in a vacuum dryer at. The yield of raw blocked derivatives is approximately 71-100%, but these products are heavily polluted, as shown by their generally low melting point, although the elemental composition of some batches is close to the calculated values. Then these raw products are used either individually or in mixed form. x with the corresponding unblocked bisphenol as a hardening agent for the orioan range of the molecular weight of the copolymer finilidefluoride / hexafluoropropene. Benzyltriphenylphosphonium chloride was used as an accelerator.
The results are shown in table 3 and 4
Mixtures A – E were cured under pressure for 10 minutes at, then, then additionally cured in an oven for 24 hours at 232 seconds. The physical properties of the cured elastomers are determined according to ASTM procedures:
Module I D-412
Tensile strength
when stretched D-412
Extension D-412
Hardness D-2240
Residual compression D-395
Example 6. p, p-Isopropylidenediphenol (bisphenol A) is converted to tetrahydropyranyl diester according to the procedure described in Example 1 and processed in the same manner. Raw product with so pl. 28-32 s, used without further purification. The properties of this blocked bisphenol as a curing agent are compared in parallel experiments with the properties of the also blocked SOPHOGO bisphenol AFc, mp. 37-38 C. A copolymer with a wide M4 molecular weight, consisting of 60 parts by weight, is used as a fluoroelastomer. vinylidene fluoride and 40 "her.ch. hexaftopropene. In all cases, the compositions also contain 30 parts by weight. (per 100 wt. of elastomer) carbon orazhiTmaraks and 3-3 / 5 weight.h. Magnesium oxide meglight.
The composition of the mixture and the test results in raschege on 100 th.e. elastomer are given in table. 5. Benzyltriphenylphosphonium chloride is used as an accelerator.
Dare the A – D holes under pressure for 10 minutes at 177 s, then additionally cured in an oven for 24 hours, after which the physical properties of the cured elastomers are determined.
The results are shown in Table. 6
The results show that cure with bisphenol A is slower than with bisphenol AF, and the opening with blocked bnsphenol A occurs very slowly, but at 204s it reaches acceptable values in approximately 10 minutes. The maximum degree of cure / achieved with blocked bisphenol A at 204% / is approximately half the cure achieved with blocked with bisphenol AG. The physical properties of the fluoroelastomer (subjected to subsequent vulcanization) are satisfactory in all four experiments for most applications of fluoroelastomers. The desired properties can be obtained by using blocked disintegrating agents, either individually or in mixture with each other or with free bisphenols.
Example 7. The properties of tetrahydropyranyl diester of bisphenol AH without carrier are compared with the properties of the preparation with microcellular carrier E prepared (as described in Example 1) and with the properties of hydroquinone tetrahydropyranyl diester obtained / as described in Example 2. Equimolar amounts are used in all experiments vulcanizing agents. As elastomer is used
a copolymer of vinylidene fluoride and hexafluoropropene 60f40.
In tab. 7 shows the composition and properties of mixtures and rubbers of them.
A-D mixtures are cured for 10 minutes at i 7, followed by curing for 24 hours at
The physical properties of rubber are given in table. eight.
From the above data, it can be seen that the blocked hydroquinone provides a sufficient degree of cure at 177 ° C and gives vulcanized products with good physical properties upon subsequent curing at 2320 s.
Example 8. The blocked n-butyl vinyl ether hydroquinone obtained as in Example 3 was evaluated in the same manner as for the other vulcanizing agents in Example 7.
The composition and results of the experiments are presented in table. 9.
It can be seen from the above data that the hydroquinone blocked by n-butylvinyl ether is a good curing agent for fluoroelastomers,
Example 9. The fluidity during the molding of vinylidenefluoride / hexafluoropropene compositions containing tetrahydropyranyl diester of bisphenol AF, is compared with the flowability during molding of compositions based on the same elathomer containing free bisphenyl AF. For the 60MO copolymer with a wide range of molecular weights, the experiments were carried out by injection molding in a cross-shaped form at a pressure of 3.49; 6.90 / 13.79 and 20.69 MPa through the head 0.32 cm for 10 minutes at 177 ° C. For the highly viscous copolymer 60. 40. The experiment was carried out at a pressure of 20.69 MPa.
In experiments with a copolymer with a wide range of molecular weights, approximately the same degree of filling of the mold was obtained for trace pairs of samples at a pressure, MPa:
Visphenol AF Blocked
bisphenol AF 20,713,8
13,07,0
6.93.4
Consequently, the blocked bisphenol AF ensures a better fluidity of the composition, since the same degree of filling of the form is achieved at a LL less pressure.
In the case of a highly viscous polymer, ezycium containing blocked bisphenol AF more completely fills the form than a composite containing free bisphenol AF.
Example 10. Reuse of pressure-cured fluoroelastomer. 20% by weight of a vinylidenefluoride / hexafluoropropene copolymer mixture with a wide molecular weight range, which is solidified under pressure for 10 minutes, is mixed using the bisphenol AF tetrahydropyranyl diester as an accelerator with an uncured mixture on double rolls. The cured mixture, taken in the form of 0.19 cm plates, is cut into pieces of approximately 0.19x1.9 to 0.32 cm to facilitate mixing with the uncured material. After 5–10 minutes of treatment on a narrow-gap roller mill and water-cooled, the press-approved mixture under pressure forms a smooth sheet, completely dispersed in the uncured mixture. This material (first cycle) is then cured under pressure. Curing under pressure The plates are dispersed and dispersed, as before, in the same proportion in the fresh mixture (second cycle), which again undergoes curing under pressure. The procedure is repeated a third time. In the third cycle, the machining conditions on the rollers are the same as in the first, the surface of all three mixtures is the same and almost the same as the original mixture.
The composition of the mixture and the test results are presented in table. 10 and 11.
Example 11. Evaluation of the dispersion of a blocked curing agent in a fluoroelastomer.
Bis (tetrahydropyranyl) hydroquinone ester is applied to calcium hydrosilicate to form a curing agent on a carrier containing 30% of a carrier and 70% of the active material. A part of this carrier composition is dispersed in a copolymer consisting of 60 parts of vinylidene fluoride and 40 parts of hexafluoropropene, with a Mooney viscosity of 45. A copolymer of vinylidene fluoride / hexa-fluoropropene 60:40 with a Mooney viscosity of 60 is mixed, as shown in Table. 11, and subjected to tests according to the RKD method, or is first cured under pressure and then tested. In experiments A and B, equimolar amounts of curing agents were used.
The results of the experiments are presented in table. 12.
Curing under pressure for 10 minutes at, then further curing for 24 hours at 232 C.
The results show
5 that the dispersion of a blocked aromatic polyoxy compound in a fluoroelastomer is as effective as a curing agent as one material.
Example 12. The use of fluoroelastomer, which. is a terpolymer and not a dipolymer.
In this example, a terpolymer consisting of 45 parts by weight serves as a fluoroelastomer. vinylidene fluoride, 30 weight.h. hexafluoroprene and 25 weight.h. ethylene tetrafto, with Mooney viscosity 80, Blocked opening of an agent bis (tetrahydropyranyl) new ester of bisphenol AF, Composition and properties of mixtures and rubbers of which are listed in Table. 13. Curing under pressure for 10 minutes at 177 ° C, then further curing for 24 hours at. These results show that significantly lower torques are obtained with a blocked curing agent than with bisphenol AF, but the final cure is the same. Example 13. Effect of molar ratio of reagents in preparing a blocked curing agent. Bis (tetrahydropyranyl) ov bisphenol AF ester was obtained at three different ratios of reagents. A product with quenen as a curing agent for a vinylidene fluoride / g copolymer / 60:40 safluoropropene. The results are shown in Table. 14. Due to the content of a certain amount of unblocked or incompletely blocked bisphenol in formulations prepared with lower ratios of dihydropropane bisphenol AF, a high degree of cure was obtained, as indicated by a higher torque. Example 14. This example shows the results obtained with the blocked hydroquinone n-butylvinyl ether prepared with three different ratios of reagents. Used the same Fluoroastomer as in example 13. The results are shown in table. 15. . From the table it can be seen that at lower ratios of reagents less complete substitution is achieved and a higher degree of cure is achieved. Example 15. Processing blocked curing agent, received with a low ratio of reagents.
The composition of rubber compounds
Table Even with a dihydropyran: bisphenol AF ratio of 1.05: 1, some amount of fully blocked bisphenol AF is formed. Together with some monosubstituted bisphenol AF and free unchanged bisphenol AF. Due to the high content of free bisphenol in the raw product, it is advisable to carry out the purification by extraction with a base, and neutralization alone is not enough. In tab. 16 shows the composition and properties of mixtures and rubbers of them. Curing under pressure for 10 minutes at 177s and subsequent curing for 24 hours at 232. Better manufacturability was achieved in experiment C, as shown by the RKD test. “The fully cured product is equivalent to the products obtained in experiments A and B. The product in experience C is characterized by extremely good residual compression . Example 16. The resistance to rupture when heated. This example shows that the fluoroelastomers, hardened under pressure with the proposed method, have very good elongation at break at the temperature of solidification under pressure. This good heating elongation makes it easy to remove articles from the fory without damage. The composition and properties of mixtures and rubbers of them are given in table. 17. Bis {tetrahydropyranyl) bisphenol AF ether in equimolar amounts was used in each pair of experiments (A-B and C-D); From the analysis of the presented examples, it follows that the proposed method, in comparison with the known method, provides for obtaining mixtures based on copolymers of halo-olefins with improved technological properties. Rubber products offer mixtures with high physical and mechanical properties.
Elastomer
Soot
Oxide Md (Meglight)
Ca (OH) 2
Accelerator
100
thirty
3
3.67 0.37 Blocked bisphenol AF 0.86 1.50 Free bisphenol AF, mol.% 1008065 Free bisphenol AF, mmol 64.83.9
Includes weight.h. carrier Composition of rubber mixtures, properties of mixtures Raw blocked bisphenol AF, so pl. 40-47 C Blocked O 50 bisphenol AF, mol.% Sub-vulcanization 36 36 Minimum Before lifting by 5 days 33 18 minutes, min
Continued tabl, 1
4.29
Table 2 1.5 2,141,793,43 503520 3.02, 11.2 - T a b l and c a and rubber, of which 3 3 3 100 100 100 y, Mc / 12lc (original) 36 36 34 5 17 32
Continued table. 3 After aging during Stress at 100% elongation, NPa3.9 3.9 Tensile strength at break, MPa10.6 9.9 Elongation at break,% 230 240 Hardness, Hardness Tester A 70 69
Residual compression (V) cm x 0,353 cm O-rings
70 hours at
18 35 70 h at 2320s
Ca {OH) 2i
Accelerator
Bisphenol AF (6 mmol)
Blocked bisphenol AF. (6 mmol}
Bisphenol A (9 mmol)
Blocked bisphenol A-35 (9 mmol)
Mooney podvulkanizatsiya, ms / 121 s, initial
Minimum
Up to 5 divisions, min
DL lifting 10 divisions, min
Rise in 45 minutes, dividing
. Mooney podvulcanization, ms / 121 s, after 3 days at and 100% rel, humidity
Minimum
The rise of 5 divisions, min
The rise of 10 divisions, min
Continuation of table 4
18 46
24 49
24 46
24 47
Table 5
3 0.3
6 0.6
6 "0.6
3.6
27
32
30 15 18 70 h at 276 C 3.4 3.3 2.6 8.6 9.5 9.6 245 260 280; 69 69 69
5,, 2
13,012,512,5
250190170
727276
After aging for 70 hours at 216 ° C
Voltage at 100%
elongation, MPa
Strength at
gap, MPa
Elongation at break,%
Hardness, Hardness Tester A
Residual compression (B), 2.54 cmxO, 353 cm O-rings
70 hours at 393 ° F 70 hours at 450 ° F
Continuation of table.5
Table 6
4.9
11.5
200
77
5.6
4.6
9.4
9.0 175 210 75 77
46 65
30 49
18 38
24 33
Blocked Hydroquinone - Mooney Chew {121s)
38.9
rise
0.3 0.3 Method RKD (30 MIN / 1770C) Shore hardness, A74 Residual compress Granules44 Rings 2.54 cmxO, 353 cm Stress / strain Stress at 100% elongation, MPa7,1 Stress at 200% elongation, MPaPreparation at break, MPa11.9 Elongation at break,% 150
Table 7
1.17
33.4
Table 3 7071 БЗ В (70 ч / 232с) 4642 47 -43 54 4.34.1 3.3 - 8.5 10.810.1 11.0 190200 250
21
RKD method
(30 min / 177 "s)
Minimum torque
Maximum torque
Hardness
, BUT
Residual compression
AT
Granules
O-KOL'TSA,
2.54 cmxO, 353 cm
Stress at 100% elongation, MPa
Voltage at 200% Component
Elastomer
Soot (Thermax MT)
MDO (Meglayt D,
Ca {OHi2
Accelerator
Vulcanizer
81849022
table 9:
1.6
3.7
69
59
72
2.8
Table 10
Content, weight.h.
100
thirty
3
3
0.3 3
Table 11
RKD method with, torque, NM
15
20, 30
Strain / strain, initial mixture
Stress at 100% elongation, MPa
Tensile strength at break, MPa
Elongation at break, Hardness, Hardness Tester A
After aging for 70 hours at
%
53 cm
Components
Blocked Curing Agent
Continued table 12
3.05 3.05 3.16
h, h
10.8
235
73
2.2
2.5
7.7
8.2 330 290
45 62
44 63
Table 13
Content, parts
27
Components
and properties of rubbers
RCD method at 177 C, torque, Nm
2.5 min 5 min
7.5 min 10 min
15 20 30
min
min
min
Strain / strain, initial mixture
Stress at 100% elongation, MPa
Tensile strength at break, MPa
Elongation at break,% Hardness, Hardness Tester A
After aging for 70 hours at
Stress at 100% elongation, MPa
Strength at
Blocked Bisphenyl AF
30% microssel
Molar ratio 2.2: 1
81849028
Continuation of table 13
Content, h
I A IB
4.0
15.6
260
70
2.7
3.2
Table 14
4.29
RCD method at, cool moment,, min
Blocked hydroquinone at 30% microcell
Molar ratio (ether: hydroquinone)
Method RKD at t ° s torque, Nm, per, min
2.5
five
7.5
ten
15
20
thirty
Continuation of table 14
T a b l and c a 15
2.64
2.64
2.64
1.58
1.24 2.26 3.84 3.05 5.08 3.39 5.31 3.73 5.54 3.84 5.65 3.95 5.76
RCD at 177, torque, n m, for, min
2.5
five
7.5
ten
15
20
thirty
Residual compression, B (70
Granules
Stress / Deformation
Fluoroelastomer A, Fluoroelastomer and Soot (Thermax MT) KgО (Meglayt D) Ca (aH) rj
Table 16
0.68
0.79 1.47 1, 24 1.81 4.97 5.20 5.20 2.26 5.31 2.37 5.31 2.49
51
28
Table 17
100
100
30 30 3 3
3
6
Stress / strain at lljOc (10 min / 177 ° C), only curing under pressure
Stress at 100% elongation, MPa
Tensile strength of a vinylophenol fluoride copolymer: 60:40 hexafluoropropene with Mooney viscosity 155.
Vinyl-denfluorod copolymer: 60:40 hexafluoropro ene with Mooney viscosity 60.

权利要求:
Claims (1)
[1]
1. US patent 3876654, cl. 260-30.4, publ. 1976 (prototype).

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同族专利:

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法律状态:

优先权:

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申请号 | 申请日 | 专利标题

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US05/864,606|US4177223A|1977-12-27|1977-12-27|Press-curable fluoropolymer compositions and process|

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