US2371722A - Process for washing and drying coagula of rubber and similar materials - Google Patents
Process for washing and drying coagula of rubber and similar materials Download PDFInfo
- Publication number
- US2371722A US2371722A US362557A US36255740A US2371722A US 2371722 A US2371722 A US 2371722A US 362557 A US362557 A US 362557A US 36255740 A US36255740 A US 36255740A US 2371722 A US2371722 A US 2371722A
- Authority
- US
- United States
- Prior art keywords
- coagulum
- rubber
- washing
- drying
- worm
- 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.)
- Expired - Lifetime
Links
- 239000000463 material Substances 0.000 title description 29
- 238000000034 method Methods 0.000 title description 16
- 238000001035 drying Methods 0.000 title description 7
- 238000005406 washing Methods 0.000 title description 7
- 229920001971 elastomer Polymers 0.000 title description 5
- 239000005060 rubber Substances 0.000 title description 5
- 239000006185 dispersion Substances 0.000 description 19
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 12
- YACLQRRMGMJLJV-UHFFFAOYSA-N chloroprene Chemical compound ClC(=C)C=C YACLQRRMGMJLJV-UHFFFAOYSA-N 0.000 description 8
- 239000008346 aqueous phase Substances 0.000 description 7
- 244000043261 Hevea brasiliensis Species 0.000 description 6
- HEMHJVSKTPXQMS-UHFFFAOYSA-M Sodium hydroxide Chemical compound [OH-].[Na+] HEMHJVSKTPXQMS-UHFFFAOYSA-M 0.000 description 6
- 229920003052 natural elastomer Polymers 0.000 description 6
- 229920001194 natural rubber Polymers 0.000 description 6
- 230000003247 decreasing effect Effects 0.000 description 5
- 230000001112 coagulating effect Effects 0.000 description 4
- 238000001125 extrusion Methods 0.000 description 4
- 229920001084 poly(chloroprene) Polymers 0.000 description 4
- 229920000642 polymer Polymers 0.000 description 4
- 239000002195 soluble material Substances 0.000 description 4
- 230000015271 coagulation Effects 0.000 description 3
- 238000005345 coagulation Methods 0.000 description 3
- 239000002270 dispersing agent Substances 0.000 description 3
- 239000012071 phase Substances 0.000 description 3
- RSWGJHLUYNHPMX-UHFFFAOYSA-N Abietic-Saeure Natural products C12CCC(C(C)C)=CC2=CCC2C1(C)CCCC2(C)C(O)=O RSWGJHLUYNHPMX-UHFFFAOYSA-N 0.000 description 2
- KAKZBPTYRLMSJV-UHFFFAOYSA-N Butadiene Chemical compound C=CC=C KAKZBPTYRLMSJV-UHFFFAOYSA-N 0.000 description 2
- CSNNHWWHGAXBCP-UHFFFAOYSA-L Magnesium sulfate Chemical compound [Mg+2].[O-][S+2]([O-])([O-])[O-] CSNNHWWHGAXBCP-UHFFFAOYSA-L 0.000 description 2
- KHPCPRHQVVSZAH-HUOMCSJISA-N Rosin Natural products O(C/C=C/c1ccccc1)[C@H]1[C@H](O)[C@@H](O)[C@@H](O)[C@@H](CO)O1 KHPCPRHQVVSZAH-HUOMCSJISA-N 0.000 description 2
- PPBRXRYQALVLMV-UHFFFAOYSA-N Styrene Chemical compound C=CC1=CC=CC=C1 PPBRXRYQALVLMV-UHFFFAOYSA-N 0.000 description 2
- -1 acrylic nitrile Chemical class 0.000 description 2
- DIZPMCHEQGEION-UHFFFAOYSA-H aluminium sulfate (anhydrous) Chemical compound [Al+3].[Al+3].[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O.[O-]S([O-])(=O)=O DIZPMCHEQGEION-UHFFFAOYSA-H 0.000 description 2
- ROOXNKNUYICQNP-UHFFFAOYSA-N ammonium persulfate Chemical compound [NH4+].[NH4+].[O-]S(=O)(=O)OOS([O-])(=O)=O ROOXNKNUYICQNP-UHFFFAOYSA-N 0.000 description 2
- 239000000701 coagulant Substances 0.000 description 2
- AUZONCFQVSMFAP-UHFFFAOYSA-N disulfiram Chemical compound CCN(CC)C(=S)SSC(=S)N(CC)CC AUZONCFQVSMFAP-UHFFFAOYSA-N 0.000 description 2
- 230000001804 emulsifying effect Effects 0.000 description 2
- 239000004033 plastic Substances 0.000 description 2
- 229920003023 plastic Polymers 0.000 description 2
- 239000007787 solid Substances 0.000 description 2
- 238000003860 storage Methods 0.000 description 2
- 229920003051 synthetic elastomer Polymers 0.000 description 2
- 239000005061 synthetic rubber Substances 0.000 description 2
- KHPCPRHQVVSZAH-UHFFFAOYSA-N trans-cinnamyl beta-D-glucopyranoside Natural products OC1C(O)C(O)C(CO)OC1OCC=CC1=CC=CC=C1 KHPCPRHQVVSZAH-UHFFFAOYSA-N 0.000 description 2
- WSLDOOZREJYCGB-UHFFFAOYSA-N 1,2-Dichloroethane Chemical compound ClCCCl WSLDOOZREJYCGB-UHFFFAOYSA-N 0.000 description 1
- ZMESHQOXZMOOQQ-UHFFFAOYSA-N 1-(naphthalen-1-ylmethyl)naphthalene Chemical compound C1=CC=C2C(CC=3C4=CC=CC=C4C=CC=3)=CC=CC2=C1 ZMESHQOXZMOOQQ-UHFFFAOYSA-N 0.000 description 1
- ZNSMNVMLTJELDZ-UHFFFAOYSA-N Bis(2-chloroethyl)ether Chemical compound ClCCOCCCl ZNSMNVMLTJELDZ-UHFFFAOYSA-N 0.000 description 1
- LFQSCWFLJHTTHZ-UHFFFAOYSA-N Ethanol Chemical compound CCO LFQSCWFLJHTTHZ-UHFFFAOYSA-N 0.000 description 1
- RRHGJUQNOFWUDK-UHFFFAOYSA-N Isoprene Chemical compound CC(=C)C=C RRHGJUQNOFWUDK-UHFFFAOYSA-N 0.000 description 1
- VVQNEPGJFQJSBK-UHFFFAOYSA-N Methyl methacrylate Chemical compound COC(=O)C(C)=C VVQNEPGJFQJSBK-UHFFFAOYSA-N 0.000 description 1
- 241001605695 Pareronia Species 0.000 description 1
- NINIDFKCEFEMDL-UHFFFAOYSA-N Sulfur Chemical compound [S] NINIDFKCEFEMDL-UHFFFAOYSA-N 0.000 description 1
- 239000002253 acid Substances 0.000 description 1
- 150000007513 acids Chemical class 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 238000013019 agitation Methods 0.000 description 1
- 238000007605 air drying Methods 0.000 description 1
- 150000001298 alcohols Chemical class 0.000 description 1
- 229910001870 ammonium persulfate Inorganic materials 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 238000006243 chemical reaction Methods 0.000 description 1
- 238000013329 compounding Methods 0.000 description 1
- 238000010924 continuous production Methods 0.000 description 1
- 239000000110 cooling liquid Substances 0.000 description 1
- 150000001993 dienes Chemical class 0.000 description 1
- 239000003995 emulsifying agent Substances 0.000 description 1
- 238000001704 evaporation Methods 0.000 description 1
- 230000008020 evaporation Effects 0.000 description 1
- 235000012438 extruded product Nutrition 0.000 description 1
- 239000012530 fluid Substances 0.000 description 1
- 238000007710 freezing Methods 0.000 description 1
- 230000008014 freezing Effects 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 150000002576 ketones Chemical class 0.000 description 1
- 238000004898 kneading Methods 0.000 description 1
- 229920000126 latex Polymers 0.000 description 1
- 239000004816 latex Substances 0.000 description 1
- 238000012886 linear function Methods 0.000 description 1
- 229910052943 magnesium sulfate Inorganic materials 0.000 description 1
- 235000019341 magnesium sulphate Nutrition 0.000 description 1
- 238000004519 manufacturing process Methods 0.000 description 1
- 229940098779 methanesulfonic acid Drugs 0.000 description 1
- AFVFQIVMOAPDHO-UHFFFAOYSA-N methanesulfonic acid Substances CS(O)(=O)=O AFVFQIVMOAPDHO-UHFFFAOYSA-N 0.000 description 1
- 238000003801 milling Methods 0.000 description 1
- 229920006173 natural rubber latex Polymers 0.000 description 1
- 238000006116 polymerization reaction Methods 0.000 description 1
- 229920001021 polysulfide Polymers 0.000 description 1
- 239000005077 polysulfide Substances 0.000 description 1
- 150000008117 polysulfides Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 150000003839 salts Chemical class 0.000 description 1
- 159000000000 sodium salts Chemical class 0.000 description 1
- ITCAUAYQCALGGV-XTICBAGASA-M sodium;(1r,4ar,4br,10ar)-1,4a-dimethyl-7-propan-2-yl-2,3,4,4b,5,6,10,10a-octahydrophenanthrene-1-carboxylate Chemical compound [Na+].C([C@@H]12)CC(C(C)C)=CC1=CC[C@@H]1[C@]2(C)CCC[C@@]1(C)C([O-])=O ITCAUAYQCALGGV-XTICBAGASA-M 0.000 description 1
- 239000000243 solution Substances 0.000 description 1
- 239000002904 solvent Substances 0.000 description 1
- 239000000126 substance Substances 0.000 description 1
- 150000003460 sulfonic acids Chemical class 0.000 description 1
- 239000011593 sulfur Substances 0.000 description 1
- 229910052717 sulfur Inorganic materials 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29B—PREPARATION OR PRETREATMENT OF THE MATERIAL TO BE SHAPED; MAKING GRANULES OR PREFORMS; RECOVERY OF PLASTICS OR OTHER CONSTITUENTS OF WASTE MATERIAL CONTAINING PLASTICS
- B29B13/00—Conditioning or physical treatment of the material to be shaped
- B29B13/06—Conditioning or physical treatment of the material to be shaped by drying
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29K—INDEXING SCHEME ASSOCIATED WITH SUBCLASSES B29B, B29C OR B29D, RELATING TO MOULDING MATERIALS OR TO MATERIALS FOR MOULDS, REINFORCEMENTS, FILLERS OR PREFORMED PARTS, e.g. INSERTS
- B29K2021/00—Use of unspecified rubbers as moulding material
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S260/00—Chemistry of carbon compounds
- Y10S260/22—Concentration
-
- Y—GENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10—TECHNICAL SUBJECTS COVERED BY FORMER USPC
- Y10S—TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
- Y10S528/00—Synthetic resins or natural rubbers -- part of the class 520 series
- Y10S528/931—Physical treatment of natural rubber or natural rubber containing material or chemical treatment of non-rubber portion thereof, e.g. extraction of rubber from milk weed
- Y10S528/934—Latex
- Y10S528/936—Coagulating
Definitions
- This invention relates to the treatment of rubber-like materials, and' more particularly, to a process for coagulating, washing, and drying aqueous dispersions of rubber-like materials comprising chloroprene.
- Natural rubber is usually converted into the solid form in which it appears in commerce by coagulating the latex in the form of sheets or slabs, passing'these between rollers, sometimes in the presence of water, to assist in the removal of soluble material, and finally drying the sheets or slabs thus obtained.
- Rubber-like materials synthetically prepared in aqueous dispersion cannot, in general, be obtained in a satisfactory solid form by the methods used for natural rubber, since usually the properties of the rubber-like material are adversely affected if any substantial quantity of the dispersing agent is allowed to remain and since the methods used by working up natural rubber remove only a part of the water-soluble material.
- the invention is accomplished by passing a dispersion of rubberlike material or natural rubber latex into a hopper, simultaneously passing a coagulating agent into the hopper, forcing the coagulum through a truncated cone from the larger end to the smaller and by means of a rotating worm and out of the cone under pressure through a perforated plate, passing the coagulum through a similar operation with a washing fiuid, and then passing the coagulum through one or more similar operations, without additional fluid, to dry the said coagulum.
- Figure 1 is a vertical section through a suitable coagulating, washing, or drying apparatus
- Figures 2 to 5 are suitable perforated plates for such apparatus.
- Figure 6 is an elevation of an apparatus for the preferred continuous process.
- FIG. 1 is a vertical section through a suitable coagulating, washing, or drying apparatus.
- housing I has a hopper 2 and a revolving worm 3 which is driven by a shaft 4 by any suitable means (not shown).
- the coagulum enters hopper 2 and issqueezed and compressed by worm 3 and is extruded, under pressure, through extruding head 5 having therein orifice 6.
- Head 5 is attached to housing I by screws 1, passing through suitable openings 8 and into threaded openings Sin the housing I.
- the water which is thereby removed from the coagulum leaves housing I through openings l0, a small amount also escaping through orifice 6.
- Figure 2 is a planned view of extruding head 5 having extruding opening 6 and holes 8 for screws.
- Figure 3 is another type of extruding head I05 having extruding openings I06 and screw holes
- the invention is not limited thereto as will become more apparent hereinafter.
- Example I Chloroprene (100 parts) containing 0.6 'part of sulfur and 4 parts of rosin, is mulsified by 'mechanical agitation in 233 parts of water, containing 0.5 part of ammonium persulfate, 0.8 part of sodium hydroxide and 0.5 part of the 'Sodium salts of the dinaphthyl methane sulfonic acid prepared according to U. S. Patent 1,336,- 759.
- the rosin is neutralized by the sodium hydroxide forming sodium abietate which, along with the sulfonic acids mentioned above, acts as the emulsifying and dispersing agent.
- the dispersion is kept at 40 C.
- the dispersion so prepared which contains about 30 per cent of neoprene, is processed in an apparatus illustrated in Figure 6.
- This figure shows an apparatus consisting of 4 successive units.
- similar parts in the various units are indicated by numerals which differ from each other by 100, and any part not specifically described hereinafter by number will be understood to be the same as the corresponding part of the first unit of the apparatus.
- the dispersion of neoprene enters housing I through hopper 2 from conduit ll.
- Vs of 7 its weight of a 3 per cent aqueous solution of aluminum sulfate is passed into hopper 2 from conduit l2. Coagulation occurs in the hopper.
- the coagulum descends upon revolving worm 3 which forces it through housing I and out of extruding head 5.
- the size of the opening 6 in extrusion head 5 is of such size that the revolving worm builds up pressure within the housing and'the coagulum is thus subjected to a combined pressure and tearing action which removes much of the aqueous phase and water-soluble materials.
- This aqueous phase escapes through perforations l and also, to a small extent, through opening head I purified and containing less than 20 per cent water.
- Extrusion head I05 has therein several, openings I06 and the coagulum in the form of several strings l6 passes into hopper 202 of housing 20l where it is subjected to the action of a revolving worm as before.
- the coagulum is extruded from this unit through extrusion head 205 having an increased number of openings 206.
- the coagulum, in the form of more numerous and smaller strings l'l, then passes into hopper 302 of housing 30l where it is again subjected to the action of a revolving worm and is extruded through head 305 through still smaller openings 308.
- the strings of coagulum 18 contain less than 5 per cent, water and is very porous in structure. The remaining waterquickly evaporates on air-drying and the 'coagulum is collected in container l9.
- the process has been described in terms of the treatment of a dispersion of polymerized chloroprene in apparatus of specific form, the invention is, in fact, very much broader. Thus, it may be applied to the treatment of rubber or any rubber-like material in the form of a wet coagulum. It is clear from the above disclosure that the invention has to do with unvulcanized rubber and rubber-like materials. These may be generically called vulcanizable plastic materials.
- the coagulum may be introduced into the apparatus in the form of separate pieces or in the form of a continuous sheet or strip such as, for example, that formed by the operation of the preferred form of the above patent. It is often advantageous tocarry out the coagulation within the hopper of the extrusion apparatus as in the above speciific example.
- the apparatus described above may also be varied, for example, as to the size, shape, and pitch of the worm, and the volume and shape of the chamber between it and the plate through which a material is extruded. It is preferred, however, that the chamber in which the worm rotates and the worm itself should be of conical rather than cylindrical form with the outlet at the narrow end.
- the number of holes through which material is extruded andalso their crosssection may be varied. Thus, in the first stage, when the material has only slight plasticity, a large hole is used, whileseveral smaller holes are used as the material becomes more plastic in the later stage.
- the size and number of the openings are small enough to cause the exertion of considerable pressure by the worm upon the material being procdrying apparatus in the form of porous strings having a small amount of moisture, may be passed upon a moving belt through a drying tunnel counter-current to a stream of warm air, and then collected. When so treated, less than 0.37 per cent of moisture remains in the coagulum.
- the conditions under which the apparatus is operated may also be varied, These variables include the rate of rotation of the worm, the rate at which the material is supplied to the machine and the temperature. Because of the work done upon the material, the temperature of the extruded material is higher than that of the material introduced. This is generally advantageous where it is desired to remove part of the water content by evaporation, but, if the material be processed is sensitive to heat, this heating may be reduced by jacketing the apparatus with a cooling liquid or by operating at a slower speed.
- the principle of the present invention is roughly similar to that by which natural latex coagulum is usually processed in that the coagulum is dehydrated by pressure.
Landscapes
- Engineering & Computer Science (AREA)
- Mechanical Engineering (AREA)
- Processing And Handling Of Plastics And Other Materials For Molding In General (AREA)
- Addition Polymer Or Copolymer, Post-Treatments, Or Chemical Modifications (AREA)
Description
March 20, 1945. F. w. WANDERER 2,371,722
PROCESS FOR WASHING AND DRYING COAGULA OF RUBBER AND SIMILAR MATERIALS Filed Oct. 24, 1940 Ml lllllllim INVENTOR WW I ATTORNEY Freda 20% WMzzdz er Ill 5 L A 4 21 III Patented Mar. 20, 1945 raoonss roa WASHING emitomrmo 'AGULA or RUBBER AND snvnma MATE- RIALS Frederick W. Wanderer, Penns Grove, N. J., as-
signor to E. I. du Pont de Nemours & Company, Wilmington, Del., a corporation otDelaware Application October 24, 1940, Serial No. 362,557
3 Claims.
This invention relates to the treatment of rubber-like materials, and' more particularly, to a process for coagulating, washing, and drying aqueous dispersions of rubber-like materials comprising chloroprene.
Natural rubber is usually converted into the solid form in which it appears in commerce by coagulating the latex in the form of sheets or slabs, passing'these between rollers, sometimes in the presence of water, to assist in the removal of soluble material, and finally drying the sheets or slabs thus obtained. Rubber-like materials synthetically prepared in aqueous dispersion cannot, in general, be obtained in a satisfactory solid form by the methods used for natural rubber, since usually the properties of the rubber-like material are adversely affected if any substantial quantity of the dispersing agent is allowed to remain and since the methods used by working up natural rubber remove only a part of the water-soluble material. In the processes now used for obtaining the synthetic rubber-like materials from their aqueous dispersions, they must, accordingly, be thoroughly washed with water, alcohol, or other solventeither by kneading them in apparatus in which fresh surfaces are continuall exposed to the action of the solvent or by converting them into a form such as thin sheets or small crumbs which present a large surface relative to the volume. In either case, the material must finally be dried and converted into a form suitable for storage and shipment. It is obvious that such processes for converting the coagulum into the final dry form require elaborate equipment and considerable attention from the operating force. Both these factors add considerably to the cost of production of the synthetic rubber and form one of the main reasons why none of these synthetic products is yet as cheap as natural rubber. Furthermore, it would be noted that, although the present processes for working up coagulated natural rubber'are considered satisfactory, they, too, are in need of further improvement,
It is an object of this invention to provide a simple and efiicient method of removing the water phase from coagula of rubber-like materials, especially neoprene polymeric chloro-2-butadiene-1,3). Another object is to coagulate such dispersions; wash the coagulum, dry the coagulum, and convert it into a form suitable for further processing, storage, or shipment.
Other objects will appear hereinafter.
It has been discovered that the first of these sure to a coagulum by means of a rotating worm in a suitable housing and forcing it through small openings. The other objects can be accomplished by passing a dispersion and a coagulating agent into a housing containing a worm and forcing the coagulum through an opening or openings under pressure, and subsequently passing the coagulum through one or more similar steps. In its preferred form, the invention is accomplished by passing a dispersion of rubberlike material or natural rubber latex into a hopper, simultaneously passing a coagulating agent into the hopper, forcing the coagulum through a truncated cone from the larger end to the smaller and by means of a rotating worm and out of the cone under pressure through a perforated plate, passing the coagulum through a similar operation with a washing fiuid, and then passing the coagulum through one or more similar operations, without additional fluid, to dry the said coagulum.
In the drawing:
Figure 1 is a vertical section through a suitable coagulating, washing, or drying apparatus;
Figures 2 to 5 are suitable perforated plates for such apparatus; and
Figure 6 is an elevation of an apparatus for the preferred continuous process.
Referring now more particularly to the drawing, Figure 1 is a vertical section through a suitable coagulating, washing, or drying apparatus. In the figure, housing I has a hopper 2 and a revolving worm 3 which is driven by a shaft 4 by any suitable means (not shown). The coagulum enters hopper 2 and issqueezed and compressed by worm 3 and is extruded, under pressure, through extruding head 5 having therein orifice 6. Head 5 is attached to housing I by screws 1, passing through suitable openings 8 and into threaded openings Sin the housing I. The water which is thereby removed from the coagulum leaves housing I through openings l0, a small amount also escaping through orifice 6.
Figure 2 is a planned view of extruding head 5 having extruding opening 6 and holes 8 for screws.
Figure 3 is another type of extruding head I05 having extruding openings I06 and screw holes In order that the invention may be more fully understood, it will be described with reference to a dispersion of neoprene, but it is to be understood that the invention is not limited thereto as will become more apparent hereinafter.
Example I Chloroprene (100 parts) containing 0.6 'part of sulfur and 4 parts of rosin, is mulsified by 'mechanical agitation in 233 parts of water, containing 0.5 part of ammonium persulfate, 0.8 part of sodium hydroxide and 0.5 part of the 'Sodium salts of the dinaphthyl methane sulfonic acid prepared according to U. S. Patent 1,336,- 759. The rosin is neutralized by the sodium hydroxide forming sodium abietate which, along with the sulfonic acids mentioned above, acts as the emulsifying and dispersing agent. The dispersion is kept at 40 C. in a suitable vessel, which can be externally cooled or heated, until the polymerization is substantially complete, as shown by the density of the dispersion which is approximately a linear function of the proportion of chloroprene which is polymerized. The dispersion is then treated with 2.5 parts of tetra ethyl thiuram disulfide dispersed in 10 parts of the'above emulsifying solution, The entire process up to this point may conveniently be carried out in a continuous manner as described in the application of Calcott and Starkweather, Serial No. 308,386, filed December 9, 1939.
The dispersion so prepared, which contains about 30 per cent of neoprene, is processed in an apparatus illustrated in Figure 6. This figure shows an apparatus consisting of 4 successive units. In the figure, similar parts in the various units are indicated by numerals which differ from each other by 100, and any part not specifically described hereinafter by number will be understood to be the same as the corresponding part of the first unit of the apparatus. Referring more particularly to Figure 6, the dispersion of neoprene enters housing I through hopper 2 from conduit ll. Simultaneously, Vs of 7 its weight of a 3 per cent aqueous solution of aluminum sulfate is passed into hopper 2 from conduit l2. Coagulation occurs in the hopper. The coagulum descends upon revolving worm 3 which forces it through housing I and out of extruding head 5. The size of the opening 6 in extrusion head 5 is of such size that the revolving worm builds up pressure within the housing and'the coagulum is thus subjected to a combined pressure and tearing action which removes much of the aqueous phase and water-soluble materials. This aqueous phase escapes through perforations l and also, to a small extent, through opening head I purified and containing less than 20 per cent water. Extrusion head I05 has therein several, openings I06 and the coagulum in the form of several strings l6 passes into hopper 202 of housing 20l where it is subjected to the action of a revolving worm as before. The coagulum is extruded from this unit through extrusion head 205 having an increased number of openings 206. The coagulum, in the form of more numerous and smaller strings l'l, then passes into hopper 302 of housing 30l where it is again subjected to the action of a revolving worm and is extruded through head 305 through still smaller openings 308. The strings of coagulum 18 contain less than 5 per cent, water and is very porous in structure. The remaining waterquickly evaporates on air-drying and the 'coagulum is collected in container l9.
Although the process has been described in terms of the treatment of a dispersion of polymerized chloroprene in apparatus of specific form, the invention is, in fact, very much broader. Thus, it may be applied to the treatment of rubber or any rubber-like material in the form of a wet coagulum. It is clear from the above disclosure that the invention has to do with unvulcanized rubber and rubber-like materials. These may be generically called vulcanizable plastic materials. In addition to natural rubber and rubber-like polymers of chloroprene, it may be applied to other types of so-called synthetic rubbers such as the polymers of butadiene and homologous dienes prepared with or without the use of other polymerizable substances, such as styrene, methyl methacrylate, and acrylic nitrile. It may also be applied to the products obtained from the reaction of organic dichlorides, such as ethylene dichloride, and beta, beta-dichloro-diethyl ether with metallic polysulfides. 'The type of dispersing agent used in the preparation of the dispersions of these rubber-like materials is not critical to the present invention. The coagulum used in the invention may be prepared by any of the appropriate methods known in the art such as the addition of salts, such, for example, as
aluminum sulfate, magnesium sulfate, etc., acids,
alcohols, and ketones, or by freezing as described in U. S. Patent No. 2,187,146. The coagulum may be introduced into the apparatus in the form of separate pieces or in the form of a continuous sheet or strip such as, for example, that formed by the operation of the preferred form of the above patent. It is often advantageous tocarry out the coagulation within the hopper of the extrusion apparatus as in the above speciific example.
The apparatus described above may also be varied, for example, as to the size, shape, and pitch of the worm, and the volume and shape of the chamber between it and the plate through which a material is extruded. It is preferred, however, that the chamber in which the worm rotates and the worm itself should be of conical rather than cylindrical form with the outlet at the narrow end. The number of holes through which material is extruded andalso their crosssection may be varied. Thus, in the first stage, when the material has only slight plasticity, a large hole is used, whileseveral smaller holes are used as the material becomes more plastic in the later stage. It is always preferred, however, that the size and number of the openings are small enough to cause the exertion of considerable pressure by the worm upon the material being procdrying apparatus in the form of porous strings having a small amount of moisture, may be passed upon a moving belt through a drying tunnel counter-current to a stream of warm air, and then collected. When so treated, less than 0.37 per cent of moisture remains in the coagulum.
The conditions under which the apparatus is operated may also be varied, These variables include the rate of rotation of the worm, the rate at which the material is supplied to the machine and the temperature. Because of the work done upon the material, the temperature of the extruded material is higher than that of the material introduced. This is generally advantageous where it is desired to remove part of the water content by evaporation, but, if the material be processed is sensitive to heat, this heating may be reduced by jacketing the apparatus with a cooling liquid or by operating at a slower speed. The principle of the present invention is roughly similar to that by which natural latex coagulum is usually processed in that the coagulum is dehydrated by pressure. The process, however, diflers by compressing the material by a worm rather than by rolls and by keeping it compressed for a much longer time with the result that the removal of the aqueous phase (and, hence, the removal of water-soluble materials) is much more eflicient and complete. Moreover, the action of the worm breaks up the cells of the coagulum more completely, thus aiding in releasing imprisoned water. Another unexpected therefore, it is not intended to be limited except as indicated in the appended claims.
I claim:
1. The process which comprises passing-an aqueous dispersion of a vulcaniz able" material comprised essentially of chloroprene polymerinto a path of decreasing cross-section, simultaneously subjecting the dispersion to coagulationconditions, forcing the mass-'along'saidpath of phase therefrom.
advantage is that the extruded product is porous milling necessary in subsequent compounding operations.
It is apparent that many widely diflerent embodiments of this invention may be made without departing from the spirit and scope thereof, and,
' 2. The process of washing and coagulum, obtained by coagulating-an. aqueous dispersion of a vulcanizable material comprised essentially of chloroprene polymer whichcomprises forcing the coagulum and fresh wash water to traverse a path'of decreasing cross-section whereby the coagulum becomes more andmorecompact while simultaneouslylsubiecting the coagulum to tearing action whereby the aqueous phase is released from the coagulum, simultaneously drawing off the wash w'ater and exuded aqueous phase, and then forcing the coagulum simultaneously through .a plurality of orifices, said orifices having a total cross-section area less than the cross-section areaofthe'pathjust preceding them. I
3. The process which comprises passing an aqueous dispersion of a vulcanizable material comprised essentially of chloroprene' polymer into a path of decreasing cross-section, simultaneously subjecting the dispersion to coagulation conditions, forcing the mass along said pathoi decreasing cross-section, subjecting the mass to,
tearing action, and withdrawing the aqueous phase therefrom, then forcing the coagulum and fresh wash water to traverse-a second path of decreasing cross-section whereby the coagulum becomes more and more compact while simultaneously subjecting the coagulum to tearing action whereby the aqueous. phase is released from the coagulum, simultaneously drawing-oi! the wash water and exuded aqueous phase, and then forcing the coagulum simultaneously through a plurality of orifices, said orifices having a total cross-section area less than the cross-section area of the path just preceding them.
FREDERICK W. WANDmER.
Priority Applications (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US362557A US2371722A (en) | 1940-10-24 | 1940-10-24 | Process for washing and drying coagula of rubber and similar materials |
Applications Claiming Priority (1)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US362557A US2371722A (en) | 1940-10-24 | 1940-10-24 | Process for washing and drying coagula of rubber and similar materials |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| US2371722A true US2371722A (en) | 1945-03-20 |
Family
ID=23426571
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| US362557A Expired - Lifetime US2371722A (en) | 1940-10-24 | 1940-10-24 | Process for washing and drying coagula of rubber and similar materials |
Country Status (1)
| Country | Link |
|---|---|
| US (1) | US2371722A (en) |
Cited By (23)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2418782A (en) * | 1944-04-07 | 1947-04-08 | Dewey And Almy Chem Comp | Method of producing a free-flowing high solids aqueous dispersion of a butadiene-styrene copolymer |
| US2444626A (en) * | 1942-05-09 | 1948-07-06 | Goodrich Co B F | Method and apparatus for continuously transforming a dispersion of a rubbery material into a sheet |
| US2472037A (en) * | 1949-05-31 | Method fob finishing polymers | ||
| US2804651A (en) * | 1953-11-09 | 1957-09-03 | Us Rubber Reclaiming Co | Methods of providing reclaimed rubber |
| US2985912A (en) * | 1954-02-05 | 1961-05-30 | Robertson Co H H | Method of and apparatus for producing a mastic caulking compound |
| US2994105A (en) * | 1959-01-01 | 1961-08-01 | Shell Oil Co | Screw press and method of treating material |
| US3035306A (en) * | 1959-12-01 | 1962-05-22 | Welding Engineers | Dewatering means for plastic materials |
| US3046609A (en) * | 1955-10-26 | 1962-07-31 | Wacker Chemie Gmbh | Process for drying thermoplastic materials |
| US3086243A (en) * | 1959-12-30 | 1963-04-23 | Wacker Chemie Gmbh | Process and apparatus for continuously washing highly viscous masses |
| US3111498A (en) * | 1961-08-30 | 1963-11-19 | Exxon Research Engineering Co | Process for preparing latices of isobutylene polymers |
| US3119146A (en) * | 1958-01-31 | 1964-01-28 | Phillips Petroleum Co | Polymer drying process and apparatus |
| US3239943A (en) * | 1961-12-21 | 1966-03-15 | Phillips Petroleum Co | Cooling rubber crumb for dryer feed |
| US3248455A (en) * | 1963-08-14 | 1966-04-26 | Us Rubber Co | Method of recovering resinous polymer from latex |
| DE1232340B (en) * | 1963-03-16 | 1967-01-12 | Bayer Ag | Device for drying rubber crumbs |
| US3304355A (en) * | 1963-06-06 | 1967-02-14 | Columbian Carbon | Process for forming aggregates of powdered materials |
| DE1273804B (en) * | 1963-10-11 | 1968-07-25 | Bayer Ag | Device for drying rubber crumbs |
| DE1275283B (en) * | 1965-10-08 | 1968-08-14 | French Oil Mill Machinery | Device for the mechanical removal of liquid or gas from rubber or a similar material |
| US4103074A (en) * | 1976-11-15 | 1978-07-25 | International Basic Economy Corporation | Process for coagulating polymer latices using screw-type extruder |
| US4148991A (en) * | 1974-12-13 | 1979-04-10 | W Bar E | Method of coagulating polymer latex emulsions |
| US4408038A (en) * | 1982-03-29 | 1983-10-04 | E. I. Du Pont De Nemours & Co. | In-line coagulation process for fluoroelastomer emulsions |
| US20100305301A1 (en) * | 2009-05-29 | 2010-12-02 | Yeh Richard C | Method And Apparatus For Elastomer Finishing |
| WO2018219631A1 (en) * | 2017-05-30 | 2018-12-06 | Compagnie Generale Des Etablissements Michelin | Kneading an elastomeric composite using continuous liquid mixing |
| WO2018219630A1 (en) * | 2017-05-30 | 2018-12-06 | Compagnie Generale Des Etablissements Michelin | Continuous liquid mixing for producing composites destined for use in elastomeric products |
-
1940
- 1940-10-24 US US362557A patent/US2371722A/en not_active Expired - Lifetime
Cited By (29)
| Publication number | Priority date | Publication date | Assignee | Title |
|---|---|---|---|---|
| US2472037A (en) * | 1949-05-31 | Method fob finishing polymers | ||
| US2444626A (en) * | 1942-05-09 | 1948-07-06 | Goodrich Co B F | Method and apparatus for continuously transforming a dispersion of a rubbery material into a sheet |
| US2418782A (en) * | 1944-04-07 | 1947-04-08 | Dewey And Almy Chem Comp | Method of producing a free-flowing high solids aqueous dispersion of a butadiene-styrene copolymer |
| US2804651A (en) * | 1953-11-09 | 1957-09-03 | Us Rubber Reclaiming Co | Methods of providing reclaimed rubber |
| US2985912A (en) * | 1954-02-05 | 1961-05-30 | Robertson Co H H | Method of and apparatus for producing a mastic caulking compound |
| US3046609A (en) * | 1955-10-26 | 1962-07-31 | Wacker Chemie Gmbh | Process for drying thermoplastic materials |
| US3119146A (en) * | 1958-01-31 | 1964-01-28 | Phillips Petroleum Co | Polymer drying process and apparatus |
| US2994105A (en) * | 1959-01-01 | 1961-08-01 | Shell Oil Co | Screw press and method of treating material |
| US3035306A (en) * | 1959-12-01 | 1962-05-22 | Welding Engineers | Dewatering means for plastic materials |
| US3086243A (en) * | 1959-12-30 | 1963-04-23 | Wacker Chemie Gmbh | Process and apparatus for continuously washing highly viscous masses |
| US3111498A (en) * | 1961-08-30 | 1963-11-19 | Exxon Research Engineering Co | Process for preparing latices of isobutylene polymers |
| US3239943A (en) * | 1961-12-21 | 1966-03-15 | Phillips Petroleum Co | Cooling rubber crumb for dryer feed |
| DE1232340B (en) * | 1963-03-16 | 1967-01-12 | Bayer Ag | Device for drying rubber crumbs |
| US3304355A (en) * | 1963-06-06 | 1967-02-14 | Columbian Carbon | Process for forming aggregates of powdered materials |
| US3248455A (en) * | 1963-08-14 | 1966-04-26 | Us Rubber Co | Method of recovering resinous polymer from latex |
| DE1273804B (en) * | 1963-10-11 | 1968-07-25 | Bayer Ag | Device for drying rubber crumbs |
| DE1275283B (en) * | 1965-10-08 | 1968-08-14 | French Oil Mill Machinery | Device for the mechanical removal of liquid or gas from rubber or a similar material |
| US4148991A (en) * | 1974-12-13 | 1979-04-10 | W Bar E | Method of coagulating polymer latex emulsions |
| US4103074A (en) * | 1976-11-15 | 1978-07-25 | International Basic Economy Corporation | Process for coagulating polymer latices using screw-type extruder |
| US4408038A (en) * | 1982-03-29 | 1983-10-04 | E. I. Du Pont De Nemours & Co. | In-line coagulation process for fluoroelastomer emulsions |
| US20100305301A1 (en) * | 2009-05-29 | 2010-12-02 | Yeh Richard C | Method And Apparatus For Elastomer Finishing |
| WO2010138257A1 (en) * | 2009-05-29 | 2010-12-02 | Exxonmobil Chemical Patents Inc. | Method and apparatus for elastomer finishing |
| US7858735B2 (en) | 2009-05-29 | 2010-12-28 | Exxonmobil Chemical Patents Inc. | Method and apparatus for elastomer finishing |
| CN102448691A (en) * | 2009-05-29 | 2012-05-09 | 埃克森美孚化学专利公司 | Method and apparatus for elastomer finishing |
| CN102448691B (en) * | 2009-05-29 | 2015-02-18 | 埃克森美孚化学专利公司 | Method and apparatus for elastomer finishing |
| WO2018219631A1 (en) * | 2017-05-30 | 2018-12-06 | Compagnie Generale Des Etablissements Michelin | Kneading an elastomeric composite using continuous liquid mixing |
| WO2018219630A1 (en) * | 2017-05-30 | 2018-12-06 | Compagnie Generale Des Etablissements Michelin | Continuous liquid mixing for producing composites destined for use in elastomeric products |
| FR3066947A1 (en) * | 2017-05-30 | 2018-12-07 | Compagnie Generale Des Etablissements Michelin | MIXING OF AN ELASTOMERIC COMPOSITE BY CONTINUOUS LIQUID PHASE MIXING |
| FR3066946A1 (en) * | 2017-05-30 | 2018-12-07 | Compagnie Generale Des Etablissements Michelin | CONTINUOUS LIQUID PHASE MIXTURE FOR THE PRODUCTION OF COMPOSITES FOR USE IN ELASTOMERIC PRODUCTS |
Similar Documents
| Publication | Publication Date | Title |
|---|---|---|
| US2371722A (en) | Process for washing and drying coagula of rubber and similar materials | |
| US3683511A (en) | Method of removing volatiles from an elastomer | |
| US3067462A (en) | Extruder for drying synthetic rubber | |
| DE69017587T2 (en) | Process for the removal of dimers of chloroprene from polychloroprene. | |
| CA1091391A (en) | Process for coagulating polymer latices using screw- type extruder | |
| EP0867463B1 (en) | Method of producing of elastomer modified thermoplastics | |
| US5205972A (en) | Process for incorporating organic fibrous fillers in elastomers | |
| CN105599164B (en) | A kind of natural rubber/white carbon black wet process mixing continuous production line | |
| US4183887A (en) | Method for producing free flowing particles of elastomeric material | |
| DE69033505T2 (en) | Process for the introduction of organic fibrous fillers into rubber | |
| US2545144A (en) | Process and apparatus for the production of high molecular weight polymers | |
| US3119146A (en) | Polymer drying process and apparatus | |
| US3578740A (en) | Dewatering pelletizer apparatus | |
| US4446309A (en) | Method and apparatus for continuously coagulating a rubbery polymer latex | |
| US3225453A (en) | Process and apparatus for drying elastomeric materials | |
| US3160620A (en) | Coagulation of chloroprene polymer latices and isolation of the polymer therefrom | |
| US3108982A (en) | Process of coagulating carbon blacksynthetic rubber latex masterbatches | |
| JPS58183235A (en) | Manufacture of rubber carbon master batch | |
| US3207828A (en) | Process for isolating chloroprene polymers from aqueous dispersions thereof | |
| US3768171A (en) | Drying wet elastomeric material | |
| US2854426A (en) | Process of milling synthetic rubber latex coagulum containing water | |
| US3240746A (en) | Removal of water from solid elastomers | |
| JP2697182B2 (en) | Washing and dewatering apparatus and method for recovering polymer using the same | |
| US3345430A (en) | Process for recovering graft copolymer latex solids | |
| US3499878A (en) | Removal of water from solid polymers |