CN104903355B - The improved method of rubber is reclaimed from the clear natural rubber latex of glue - Google Patents

The improved method of rubber is reclaimed from the clear natural rubber latex of glue Download PDF

Info

Publication number
CN104903355B
CN104903355B CN201380056669.6A CN201380056669A CN104903355B CN 104903355 B CN104903355 B CN 104903355B CN 201380056669 A CN201380056669 A CN 201380056669A CN 104903355 B CN104903355 B CN 104903355B
Authority
CN
China
Prior art keywords
potassium hydroxide
latex
membrane module
gel resin
retentate
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 - Fee Related
Application number
CN201380056669.6A
Other languages
Chinese (zh)
Other versions
CN104903355A (en
Inventor
贾亚·库马尔·韦卢
扎南·阿卜杜拉
艾哈迈德·亚里·阿西斯
迈扎图·普特里·艾哈迈德·萨布里
海尔·穆伊斯·穆罕默德·尤索夫
尼克·梅里亚姆·宾节·尼克·苏莱曼
穆罕默德·海尔丁·本·塔伊布·阿鲁瓦
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Sime Darby Malaysia Bhd
Original Assignee
Sime Darby Malaysia Bhd
Priority date (The priority date 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 date listed.)
Filing date
Publication date
Application filed by Sime Darby Malaysia Bhd filed Critical Sime Darby Malaysia Bhd
Publication of CN104903355A publication Critical patent/CN104903355A/en
Application granted granted Critical
Publication of CN104903355B publication Critical patent/CN104903355B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08CTREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
    • C08C1/00Treatment of rubber latex
    • C08C1/02Chemical or physical treatment of rubber latex before or during concentration
    • C08C1/075Concentrating
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08CTREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
    • C08C1/00Treatment of rubber latex
    • C08C1/02Chemical or physical treatment of rubber latex before or during concentration
    • C08C1/075Concentrating
    • C08C1/08Concentrating with the aid of creaming agents
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08CTREATMENT OR CHEMICAL MODIFICATION OF RUBBERS
    • C08C1/00Treatment of rubber latex
    • C08C1/02Chemical or physical treatment of rubber latex before or during concentration
    • C08C1/075Concentrating
    • C08C1/10Concentrating by centrifugation
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L17/00Compositions of reclaimed rubber

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Medicinal Chemistry (AREA)
  • Polymers & Plastics (AREA)
  • Organic Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Separation Using Semi-Permeable Membranes (AREA)

Abstract

The present invention relates to a kind of improved method reclaiming rubber from the clear natural rubber latex of glue.Described method includes glue gel resin breast described in pretreatment, a membrane module or two membrane modules of continuous print are used to concentrate described glue gel resin breast and add potassium hydroxide or containing ammonium laurate and the solution of potassium hydroxide, the glue gel resin breast concentrated is processed alternatively by tetramethylthiuram disulfide (TMTD) and zinc oxide (ZnO) dispersion, the latex of this concentration is blended with fresh field latex, by centrifugal for this blend to obtain latex concentration thing.Described latex concentration thing is blended with fresh latex concentration thing and uses ammonia treatment further, to obtain final latex concentration thing.

Description

The improved method of rubber is reclaimed from the clear natural rubber latex of glue
Technical field
The present invention relates to a kind of improved method reclaiming rubber from the clear natural rubber latex of glue.In particular it relates to A kind of reclaim rubber from the clear natural rubber latex of glue and use membrane filtration and centrifugal separation technology to combine described rubber to turn The improved method of chemical conversion latex concentration thing.
Background technology
The clear natural rubber latex of glue or glue gel resin breast as relate to by centrifugal described rubber latex is separated into concentrate and Side-product in the technique of the concentrated natural rubber latex of glue gel resin breast produces.Glue gel resin breast generally only comprises about 5% Dry rubber substance, and it is recovered usually used as the clear crepe rubber of glue (crepe rubber).
It is well known in the art that and sulphuric acid can be used to pass through to solidify from glue gel resin breast recovery rubber.Then rubber is being made Before selling for the clear rubber of glue, the rubber of dried recovered out of doors.But, this freezing method the glue clear rubber tool obtained There is inferior quality, because it comprises a high proportion of nonrubber composition carried secretly and acid content.The clear rubber of glue also has not Good physical characteristic, including producing foul odour, this causes the economic worth of the clear rubber of glue low.Additionally, the method is also Producing the sewage of highly acidic, if processing this sewage before being discharged into environment the most by rights, then it can Cause the pollution to environment.
Also by the solidification using proteolytic enzyme to carry out glue gel resin breast, the enzyme catalysis wherein achieving glue gel resin breast takes off Albumen.But this process is uneconomic, because it needs to use substantial amounts of enzyme, and relate in process deammoniation and Acid coagulation step.
Therefore, there is a need in the art for a kind of method for reclaiming rubber from the clear natural rubber latex of glue to solve State at least one in problem, or provide at a kind of replacement.
Summary of the invention
By according to the present invention from the clear natural rubber latex of glue reclaim rubber improved method solve the problems referred to above and its Its problem, and achieve progress in the art.One advantage of the method according to the invention is by using membrane filtration Combine with centrifugal separation technology and implement to reclaim rubber from the clear natural rubber latex of glue, and described rubber is changed into latex Concentrate, thus decrease the needs that the acid cure for reclaiming rubber from the clear natural rubber latex of glue is solid.The of the present invention Two advantages are the sewage that described method produces the quality with improvement, thus environment causes less pollution.
According to an embodiment of the invention, implement described method in the following manner.The first pretreatment of described method Glue gel resin breast.Then pretreated glue gel resin breast is made to pass through membrane module repeatedly and add hydroxide at set intervals Potassium or containing ammonium laurate and the solution of potassium hydroxide, to obtain retentate and penetrant.By described retentate with fresh Field latex is blended and is centrifuged, to obtain latex concentration thing.Described latex concentration thing is entered with fresh latex concentration thing One step is blended and uses ammonia treatment, to obtain final latex concentration thing.
According to certain embodiments of the present invention, described method further includes at retentate and fresh field latex Process described by tetramethylthiuram disulfide (TMTD) and zinc oxide (ZnO) dispersion before the step being blended Retentate.
According to another implementation of the invention, described method further includes at retentate and fresh field glue Breast carries out second level concentration to described retentate before being blended.By making described retentate repeatedly by the second membrane module And add other potassium hydroxide or the solution enforcement second level concentration containing ammonium laurate and potassium hydroxide, to obtain second Retentate and the second penetrant.Alternatively the second retentate is carried out chemical treatment and controllably with fresh field latex It is blended.The second blended retentate is centrifuged, to obtain latex concentration thing.Then by described latex concentration thing with fresh Latex concentration thing further control to be blended, to obtain final latex concentration thing.
According to certain embodiments of the present invention, described method further includes at and makes described retentate by the second film group With retentate described in potassium hydroxide or the solution pretreatment containing ammonium laurate and potassium hydroxide before part.
According to an embodiment of the invention, every 10 minutes to 30 minutes by described potassium hydroxide or containing lauric acid The solution of ammonium and potassium hydroxide joins pretreated glue gel resin breast, until obtaining about 80 weight % to 90 weight % Penetrant.
According to certain embodiments of the present invention, every 10 minutes to 30 minutes by described potassium hydroxide or containing lauric acid The solution of ammonium and potassium hydroxide joins pretreated glue gel resin breast, until obtaining about 60 weight % to 70 weight % Penetrant.Every 10 minutes to 30 minutes by other potassium hydroxide or containing ammonium laurate and the solution of potassium hydroxide Join described retentate, until obtaining the second penetrant of about 40 weight % to 50 weight %.
According to certain embodiments of the present invention, the described solution containing ammonium laurate and potassium hydroxide comprises and has 1:1 ratio The ammonium laurate of example and potassium hydroxide.
According to an embodiment of the invention, described method farther includes by membrane module is immersed in 2% to 5% Hydrogen peroxide in carry out rinsing membrane module;Sodium hydroxide backwash with 1% to 2% or just rinsing membrane module;And with 1% Nitric acid backwash to 2% or just rinsing membrane module.
Accompanying drawing explanation
Describe above and other advantage and the feature of the present invention in the following detailed description, and be shown in the following drawings:
Fig. 1 is the flow chart illustrating the single-stage method for concentration according to the present invention.
Fig. 2 is the flow chart illustrating the secondary concentration method according to the present invention.
Detailed description of the invention
According to the present invention, it is provided that by natural rubber latex being separated into the butterfat part rich in rubber and the clear part of glue And concentrated natural rubber latex or glue gel resin breast, thus reclaim the side of rubber from the clear natural rubber latex of glue or glue gel resin breast Method.Glue gel resin breast usually contains the dry rubber substance of about 5%.
Method according to an embodiment of the invention includes the step of pre-treating adhesive gel resin breast.
In an embodiment of the invention, with ammonia and potassium hydroxide pre-treating adhesive gel resin breast.Another embodiment party In formula, with ammonia and the solution pre-treating adhesive gel resin breast containing ammonium laurate and potassium hydroxide.At one preferred embodiment In, the ammonia with about 0.35% to 0.65% and the potassium hydroxide pre-treating adhesive gel resin breast of about 0.025% to 0.10%.? Another preferred embodiment in, with about 0.35% to 0.65% ammonia and about 0.025% to 0.10% containing Laurel The solution pre-treating adhesive gel resin breast of acid ammonium and potassium hydroxide.Preferably, described solution comprises the Laurel with 1:1 ratio Acid ammonium and potassium hydroxide.
By simply ammonia and potassium hydroxide or ammonia and the solution containing ammonium laurate and potassium hydroxide being joined glue gel resin Breast carrys out pre-treating adhesive gel resin breast.Then mixture is homogenized by such as stirring.Then to pretreated glue gel resin Breast carries out first order concentration technology.
In first order concentration technology, glue gel resin breast is concentrated into the dry rubber content of about 11% to 13%.By making glue Gel resin breast implements first order concentration technology by multitube membrane module repeatedly.Glue gel resin breast is made to pass through multitube by pump Formula membrane module.The example of the pump that can use in the present invention includes but not limited to diaphragm type pump or centrifugal pump.For For large-scale film device, preferably centrifugal pump.Multitube membrane module can be made up of any suitable material.? One preferred embodiment in, it is made up of pottery, and preferably has the aperture of about 0.05 μ.
When glue gel resin breast is repeatedly by multitube membrane module, at set intervals by potassium hydroxide or containing ammonium laurate Described glue gel resin breast is joined with the solution of potassium hydroxide.Preferably, every 10 minutes to 30 minutes by potassium hydroxide Or the solution containing ammonium laurate and potassium hydroxide joins glue gel resin breast.In one preferred embodiment, each Time interval by about 0.025% to 0.10% potassium hydroxide or about 0.025% to 0.10% containing ammonium laurate and hydroxide The solution of potassium joins glue gel resin breast.The inlet pressure of multitube membrane module is set in about 2.5 bars to 4.5 bars (2.5×105Pa to 4.5 × 105Pa).Preferably, transmembrane pressure is set in about 1.5 bars to 3.0 bars (1.5 × 105Pa To 3.0 × 105Pa).The solution used in this step can be potassium hydroxide or molten containing ammonium laurate and potassium hydroxide Liquid, and do not limit it for the solution identical with the solution used in the step of pre-treating adhesive gel resin breast.
Continue first order concentration technology, until acquisition about 60 weight % are to the milk surum of the clarification of 70 weight %.Will clarification Milk surum as penetrant remove, leave retentate, described retentate be concentrate glue gel resin breast.
Before the glue gel resin breast concentrated carries out second level concentration technology, can use other potassium hydroxide or containing ammonium laurate With the glue gel resin breast that the solution of potassium hydroxide processes retentate or concentration.The solution used in this step can be hydrogen-oxygen Change potassium or containing ammonium laurate and the solution of potassium hydroxide, and do not limit it for in the step of pre-treating adhesive gel resin breast The identical solution of solution used.Preferably, by about 0.025% to 0.10% potassium hydroxide or about 0.025% to 0.10% The solution containing ammonium laurate and potassium hydroxide join concentration glue gel resin breast with process glue gel resin breast.
In the concentration technology of the second level, the glue gel resin breast of concentration is concentrated into further the dry rubber content of approximately more than 20%. By making the glue gel resin breast of concentration implement second level concentration technology by the second multitube membrane module repeatedly.More than second Tubular membrane component can be and the film of the same type of use in first order concentration technology, or it can be adapted at this Any type used in technique.Make the glue gel resin breast of concentration by the second multitube membrane module by pump.Can be described The example of the pump used in method includes but not limited to diaphragm type pump or centrifugal pump.For large-scale film device, Preferably centrifugal pump.Multitube membrane module can be made up of any suitable material.It is preferable to carry out of the present invention In mode, multitube membrane module is made up of pottery, and has the aperture of about 0.05 μ.It has about 3.0mm to 4.0mm Channel internal diameter and the total length of about 1.0m to 1.2m.
Preferably, make concentration glue gel resin breast at about 2.5 bars to 4.5 bars (2.5 × 105Pa to 4.5 × 105Pa) entrance By the second multitube membrane module under pressure.At set intervals by other potassium hydroxide or containing ammonium laurate and hydrogen-oxygen The solution changing potassium joins the glue gel resin breast of concentration, to enter when glue gel resin breast is repeatedly by the second multitube membrane module One step concentrates glue gel resin breast.In one preferred embodiment, every 10 minutes to 30 minutes by potassium hydroxide or Solution containing ammonium laurate and potassium hydroxide joins the glue gel resin breast of concentration.Preferably, will about in each time interval The potassium hydroxide of 0.025% to 0.10% or the solution containing ammonium laurate and potassium hydroxide of about 0.025% to 0.10% add To described glue gel resin breast.Potassium hydroxide can be used in this step or containing ammonium laurate and the solution of potassium hydroxide, and Do not limit it for the solution identical with the solution used in the step of pre-treating adhesive gel resin breast.
Continue second level concentration technology, until obtaining the second milk surum of the clarification of about 40 weight % to 50 weight %.Will Second milk surum of clarification removes as the second penetrant, leaves the second retentate, and described retentate is to concentrate further Glue gel resin breast.
Before the field latex that the glue gel resin that will concentrate further is newborn Yu fresh is blended, can be alternatively with having 30% Concentration, the tetramethylthiuram disulfide (TMTD) with 1:1 ratio and zinc oxide (ZnO) dispersion process The glue gel resin breast concentrated further.Preferably, with the TMTD/ZnO dispersion of about 0.05 weight % to 0.10 weight % Body processes the glue gel resin breast concentrated further.Matter according to the glue gel resin concentrated the further breast obtained after concentration technology Amount (such as, volatile fatty acid is at the content in the glue gel resin Ruzhong concentrated further) implements this step.Preferably, This step is implemented when the volatile fatty acid number in the glue gel resin Ruzhong concentrated further is more than 0.10.Preferably, at inciting somebody to action The field latex that the glue gel resin of the concentration managed is newborn Yu fresh is blended in the ratio of 1 part: 9 parts.
Then the glue gel resin breast of the concentration being blended containing fresh field latex is centrifuged, to obtain latex concentration thing. Latex concentration thing is blended in the ratio of 1 part: 9 parts with fresh latex concentration thing.Then ammonia is joined blended glue Breast concentrate is to more than 0.60%m/m, to obtain final latex concentration thing.Thus obtained final latex concentration Thing contains the dry rubber substance more than 60%.
In yet another embodiment of the present invention, according to the feedstock quality used in the method, the first order concentrates work Skill and second level stage concentration technology can be implemented in a single step.
In single stage process, with ammonia and potassium hydroxide or with ammonia and the solution containing ammonium laurate and potassium hydroxide to glue gel resin Breast carries out the pretreatment being similar to.In one preferred embodiment, the ammonia and about 0.025% of about 0.35% to 0.65% is used To the potassium hydroxide pre-treating adhesive gel resin breast of 0.10%.Another preferred embodiment in, with about 0.35% to The ammonia of 0.65% and the breast of the solution pre-treating adhesive gel resin containing ammonium laurate and potassium hydroxide of about 0.025% to 0.10%.Excellent Selection of land, the solution containing ammonium laurate and potassium hydroxide has the ratio of 1:1.
By simply ammonia and potassium hydroxide or ammonia and the solution containing ammonium laurate and potassium hydroxide being joined glue gel resin breast Carry out pre-treating adhesive gel resin breast.Then mixture is homogenized by such as stirring.Then to pretreated glue gel resin breast Implement single-stage concentration technology.
According to this embodiment of the present invention, by making glue gel resin breast implement single-stage by multitube membrane module repeatedly Concentration technology.Make glue gel resin breast by multitube membrane module by pump.The example bag of the pump that can use in the process Include but be not limited to diaphragm type pump or centrifugal pump.For large-scale film device, preferably centrifugal pump.Multitube Membrane module can be made up of any suitable material.One of the present invention preferred embodiment in, multitube film group Part is made up of pottery, and has the aperture of about 0.05 μ.It has about 3.0mm to 4.0mm channel internal diameter and The total length of about 1.0m to 1.2m.
When glue gel resin breast is repeatedly by multitube membrane module, by potassium hydroxide or containing ammonium laurate and potassium hydroxide Solution joins described glue gel resin breast.At set intervals by potassium hydroxide or containing ammonium laurate and the solution of potassium hydroxide Join glue gel resin breast.Preferably, every 10 minutes to 30 minutes by potassium hydroxide or containing ammonium laurate and hydroxide The solution of potassium joins glue gel resin breast.In one preferred embodiment, each time interval will about 0.025% to The potassium hydroxide of 0.10% or the solution containing ammonium laurate and potassium hydroxide of about 0.025% to 0.10% add glue gel resin breast In.The inlet pressure of film is set in about 2.5 bars to 4.5 bars (2.5 × 105Pa to 4.5 × 105Pa).At one preferably Embodiment in, for optimum penetrant flux, transmembrane pressure is set in about 1.5 to 3.0 bars (1.5 × 105 Pa to 3.0 × 105Pa)。
Continue single-stage concentration technology, until acquisition about 80 weight % are to the milk surum of the clarification of 90 weight %.By clarification Milk surum removes as penetrant, leaves retentate, and described retentate is the glue gel resin breast concentrated.
Can be alternatively with there is the concentration of 30%, there is the glue that the TMTD/ZnO dispersion process of 1:1 ratio concentrates Gel resin breast.Preferably, the glue concentrated is processed by the TMTD/ZnO dispersion of about 0.05 weight % to 0.10 weight % Gel resin breast.(such as, volatile fatty acid is dense for the quality of the glue gel resin breast according to the concentration obtained after concentration technology The content in the glue gel resin Ruzhong of contracting) implement this step.Preferably, when the volatile fatty acid in the glue gel resin Ruzhong concentrated This step is implemented when value is more than 0.10.Then by field latex newborn Yu fresh for the glue gel resin of the concentration processed preferably It is blended in the ratios of 1 part: 9 parts.
The glue gel resin breast of the concentration being blended containing fresh field latex is centrifuged, to obtain latex concentration thing.Then Latex concentration thing is blended in the ratio of 1 part: 9 parts with fresh latex concentration thing.It is subsequently adding ammonia to more than 0.60% M/m, to obtain final latex concentration thing.Thus obtained final latex concentration thing contains the dry rubber more than 60% Glue.
The solution of ammonium laurate mentioned above and potassium hydroxide can contain any proper amount of ammonium laurate and hydroxide Potassium.In one preferred embodiment, described solution comprises ammonium laurate and the potassium hydroxide with 1:1 ratio.
In the present invention, the milk surum of the clarification produced in glue gel resin breast concentration technology may be used in known in the art Appropriate method reclaims the valuable biochemical being included in.Film becomes contaminated after a procedure.Can Contaminated film is cleaned by being immersed in the hydrogen peroxide of about 2% to 5%, and by the hydroxide of about 1% to 2% Sodium backwash or just rinsing.Can also be with nitric acid backwash or just rinsing contaminated film, to remove mineral contaminants regeneration membrane For further using.Preferably, use the nitric acid backwash of about 1% to 2% or just rinsing contaminated film.
In method according to the embodiment of the present invention, field latex newborn Yu fresh for glue gel resin is being blended and weight Newly it is centrifuged back before being latex concentration thing, concentrates glue gel resin breast by membranous system.As concentrating the newborn means of glue gel resin The use of film eliminates the needs that the acid cure for reclaiming rubber from glue gel resin breast is solid.This also contributes to improve by described side The quality of the sewage that method produces.The combination of chemical substance can be used to clean contaminated film so that its regeneration is for follow-up Concentration.The recovery of rubber and to convert it into latex concentration thing be value-added technique for rubber industry.
It is favourable for using potassium hydroxide in the present invention, because potassium hydroxide serves latex stabilizer and latex anticorrosion The effect of agent.This also stirring to being caused by any suitable mechanical means provide more preferable shear resistant.
Provide following example to further illustrate and to describe the specific detailed description of the invention of the present invention and real below Execute example to be interpreted never in any form to limit the invention to concrete steps described herein, condition or composition.
Embodiment
Embodiment 1: secondary concentration technique
Sieved by the glue gel resin breast of the 60 mesh metal gauzes dry rubber content to having 5%, and with 0.65% Ammonia and the potassium hydroxide pretreatment of 0.1%.Then make the glue gel resin breast processed repeatedly by multitube membrane module.? The multitube membrane module used in the present embodiment has the aperture of about 0.05 μ, the channel internal diameter of about 3.0mm to 4.0mm Total length with 1.0m to 1.2m.The inlet pressure of membrane module is set in about 3 bars (3 × 105Pa).Every 30 Minute the potassium hydroxide of about 0.05% is joined glue gel resin breast, thus concentrates glue gel resin breast.
Continue this concentration step, until acquisition about 60 weight % are to the milk surum of the clarification of 70 weight %, and as First penetrant removes, and leaves the first retentate of the dry rubber substance containing about 11%.
Then with other 0.1% potassium hydroxide treatment the first retentate.Then make the first retentate processed about 3 bars (3 × 105Pa) repeatedly by the second multitube membrane module under inlet pressure.Every 30 minutes by about 0.05% Potassium hydroxide join the first retentate, thus concentrate glue gel resin breast further.Carry out further concentration step, Until obtaining the second milk surum of the clarification of about 40 weight % to 50 weight % and removing as the second penetrant.? The second retentate containing the dry rubber substance more than 20% is also obtain after second concentration step.
Then before the second retentate is blended in the ratio of 1 part: 9 parts with fresh field latex, with about 0.05% TMTD/ZnO (in the ratio of 1:1) dispersion (concentration of 30%) process the second retentate.Then, use The skimming screw element (skim screw) (No. 12 or 12.5mm length) selected is to being blended containing fresh field latex Retentate be centrifuged, to obtain latex concentration thing.Then by dense with fresh latex for the latex concentration thing that processed Contracting thing is blended further in the ratio of 1 part: 9 parts, and by ammonification to more than 0.60%m/m ammonia, to obtain final glue Breast concentrate.
The final latex concentration thing obtained by this technique has the quality suitable with common fresh latex concentrate. This is a birth process in rubber industry, because compared with being recovered and converted to the clear crepe rubber of glue with by glue gel resin breast, from Glue gel resin breast reclaims rubber and converts it into latex concentration thing and fetch better price.
Embodiment 2: secondary concentration technique
Sieved by the glue gel resin breast of the 60 mesh metal gauzes dry rubber content to having 5%, and with 0.65% Ammonia and 0.1% the solution containing the ammonium laurate and potassium hydroxide with 1:1 ratio carry out pretreatment.Then make to process Glue gel resin breast repeatedly by multitube membrane module.The multitube membrane module used in the present embodiment has about 0.05 μ Aperture, the channel internal diameter of about 3.0mm to 4.0mm and the total length of 1.0m to 1.2m.By the entrance of membrane module Pressure is set in about 3 bars (3 × 105Pa).Every 30 minutes, ammonium laurate and the potassium hydroxide of about 0.05% are joined Glue gel resin breast, thus concentrate glue gel resin breast.
Continue this concentration step, until acquisition about 60 weight % are to the milk surum of the clarification of 70 weight %.Breast by clarification Remove as the first penetrant clearly, leave the first retentate of the dry rubber substance containing about 11%.
Then the first retentate is processed with the solution containing ammonium laurate and potassium hydroxide of other 0.1%.Then process is made The first retentate crossed is at about 3 bars (3 × 105Pa) repeatedly by the second multitube membrane module under inlet pressure.Often Every 30 minutes, ammonium laurate and the potassium hydroxide of about 0.05% are joined the first retentate, thus it is clear to concentrate glue further Latex.Carry out further concentration step, until obtaining the second milk surum of the clarification of about 40 weight % to 50 weight %. Second milk surum of clarification is removed as the second penetrant.Also obtain after the second concentration step containing more than 20% Second retentate of dry rubber substance.
Then before the second retentate is blended in the ratio of 1 part: 9 parts with fresh field latex, with about 0.05% TMTD/ZnO (in the ratio of 1:1) dispersion (concentration of 30%) process the second retentate.Then, use The skimming screw element (skim screw) (No. 12 or 12.5mm length) selected is to being blended containing fresh field latex Retentate be centrifuged, to obtain latex concentration thing.Then by dense with fresh latex for the latex concentration thing that processed Contracting thing is blended further in the ratio of 1 part: 9 parts, and by ammonification to more than 0.60%m/m ammonia, to obtain final glue Breast concentrate.
The final latex concentration thing obtained by this technique has the quality suitable with common fresh latex concentrate.
Embodiment 3: single-stage concentration technology
In this single stage process, glue gel resin breast is implemented only one concentration step.Except continuing the list in this single stage process Concentration step, until obtaining about 80 weight % to the milk surum of the clarification of 90 weight % and to remove it as penetrant Outward, the Secondary process class described in pre-treatment step in the process and operating condition and embodiment 1 and embodiment 2 Seemingly.The retentate obtained in this single stage process contains the dry rubber substance more than 20%.
After concentration step, before retentate is blended in the ratio of 1 part: 9 parts with fresh field latex, use TMTD/ZnO (in the ratio of the 1:1) dispersion (concentration of 30%) of about 0.05% processes and obtains from concentration step Retentate.Then, use the skimming screw element (skim screw) (No. 12 or 12.5mm length) selected to containing The retentate being blended of fresh field latex is centrifuged, to obtain latex concentration thing.Then the latex that will process Concentrate and fresh latex concentration thing are blended further in the ratio of 1 part: 9 parts, and by ammonification to more than 0.60%m/m Ammonia, to obtain final latex concentration thing.
The final latex concentration thing obtained by this single stage process have with common fresh latex concentrate and with by such as The quality that latex concentration thing that above-mentioned secondary process obtains is suitable.
It is above the description of the subject of the present invention that inventor is thought, and it is believed that based on disclosure above, Other people can and will the design packet system of replacement containing the present invention.

Claims (20)

1. by natural rubber latex is separated into rubber latex and glue gel resin breast and a concentrated natural rubber latex, from And the method reclaiming rubber from glue gel resin breast, described method includes:
With glue gel resin breast described in ammonia and potassium hydroxide or ammonia and the solution pretreatment containing ammonium laurate and potassium hydroxide;
Make described pretreated glue gel resin breast repeatedly by membrane module and every 10 minutes to 30 minutes addition hydrogen-oxygens Change potassium or containing ammonium laurate and the solution of potassium hydroxide, to obtain retentate and penetrant;
Described retentate is blended with fresh field latex;
Described blended retentate is centrifuged, to obtain latex concentration thing;
Described latex concentration thing is blended with fresh latex concentration thing;With
With described in ammonia treatment be blended after latex concentration thing, to obtain final latex concentration thing.
Method the most according to claim 1, farther includes:
Before the step described retentate and fresh field latex being blended, use tetramethylthiuram disulfide (TMTD) and zinc oxide (ZnO) dispersion process described retentate.
Method the most according to claim 1, farther includes:
Before the step described retentate and fresh field latex being blended, make described retentate repeatedly by the Two membrane modules also added other potassium hydroxide or molten containing ammonium laurate and potassium hydroxide every 10 minutes to 30 minutes Liquid, to obtain the second retentate and the second penetrant.
Method the most according to claim 3, farther includes:
Described second retentate is processed by tetramethylthiuram disulfide (TMTD) and zinc oxide (ZnO) dispersion.
Method the most according to claim 3, farther includes:
Before by described retentate by described second membrane module, with potassium hydroxide or containing ammonium laurate and potassium hydroxide Solution pretreatment described in retentate.
Method the most according to claim 1, wherein, every 10 minutes to 30 minutes by described potassium hydroxide or Solution containing ammonium laurate and potassium hydroxide joins described pretreated glue gel resin breast, until obtaining 80 weight % extremely The described penetrant of 90 weight %.
Method the most according to claim 3, wherein, every 10 minutes to 30 minutes by described potassium hydroxide or Solution containing ammonium laurate and potassium hydroxide joins described pretreated glue gel resin breast, until obtaining 60 weight % extremely The described penetrant of 70 weight %.
Method the most according to claim 7, wherein, every 10 minutes to 30 minutes by described other hydrogen-oxygen Change potassium or the solution containing ammonium laurate and potassium hydroxide joins described retentate, until obtaining 40 weight % to 50 weights Described second penetrant of amount %.
Method the most according to claim 1, wherein, with the ammonia and 0.025 of 0.35 weight % to 0.65 weight % Weight % to 0.1 weight % potassium hydroxide pretreatment described in glue gel resin breast.
Method the most according to claim 1, wherein, with the ammonia and 0.025 of 0.35 weight % to 0.65 weight % Weight % is to glue gel resin breast described in solution pretreatment containing ammonium laurate and potassium hydroxide described in 0.1 weight %.
11. according to the method for claim 1,3,5 or 10, wherein said containing ammonium laurate with the solution of potassium hydroxide Comprise ammonium laurate and the potassium hydroxide with 1:1 ratio.
12. methods according to claim 1, wherein said membrane module is multitube film.
13. methods according to claim 12, wherein said membrane module has 2.5 × 105Pa to 4.5 × 105Pa In the range of inlet pressure.
14. methods according to claim 3, wherein said second membrane module is multitube film.
15. methods according to claim 14, wherein said second membrane module has 2.5 × 105Pa to 4.5 × 105 Inlet pressure in the range of Pa.
16. methods according to claim 3, wherein said second retentate and the measurer of described fresh field latex There is the ratio of 1:9.
17. methods according to claim 12, wherein said multitube membrane module includes diaphragm type pump or centrifugal type Pump.
18. methods according to claim 14, wherein said second multitube membrane module include diaphragm type pump or from Cardioid pump.
19. methods according to claim 1, farther include:
By the described membrane module of following cleaning:
Described membrane module is immersed in the hydrogen peroxide of 2% to 5%;
Sodium hydroxide backwash with 1% to 2% or just rinsing described membrane module;With
Nitric acid backwash with 1% to 2% or just rinsing described membrane module, to regenerate described membrane module for further Use.
20. methods according to claim 3, farther include:
By described second membrane module of following cleaning:
Described second membrane module is immersed in the hydrogen peroxide of 2% to 5%;
Sodium hydroxide backwash with 1% to 2% or just rinsing described membrane module;With
Nitric acid backwash with 1% to 2% or just rinsing described membrane module, to regenerate described membrane module for further Use.
CN201380056669.6A 2012-10-29 2013-04-01 The improved method of rubber is reclaimed from the clear natural rubber latex of glue Expired - Fee Related CN104903355B (en)

Applications Claiming Priority (3)

Application Number Priority Date Filing Date Title
MYPI2012700834 2012-10-29
MYPI2012700834A MY183968A (en) 2012-10-29 2012-10-29 An improved method of recovering rubber from skim natural rubber latex
PCT/MY2013/000070 WO2014069979A1 (en) 2012-10-29 2013-04-01 An improved method of recovering rubber from skim natural rubber latex

Publications (2)

Publication Number Publication Date
CN104903355A CN104903355A (en) 2015-09-09
CN104903355B true CN104903355B (en) 2016-11-23

Family

ID=48446577

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201380056669.6A Expired - Fee Related CN104903355B (en) 2012-10-29 2013-04-01 The improved method of rubber is reclaimed from the clear natural rubber latex of glue

Country Status (5)

Country Link
CN (1) CN104903355B (en)
HK (1) HK1210485A1 (en)
MY (1) MY183968A (en)
PH (1) PH12015500908A1 (en)
WO (1) WO2014069979A1 (en)

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
MY173398A (en) * 2015-06-18 2020-01-22 Sime Darby Plantation Berhad A process and system for concentrating epoxidized natural rubber latex into epoxidized natural rubber latex concentrate
CN109369826B (en) * 2018-09-21 2020-08-21 昌江金达乳胶制品有限公司 Production method of ammonia-free natural concentrated latex
CN113385035A (en) * 2021-06-09 2021-09-14 海南天然橡胶产业集团股份有限公司 Automatic colloidal-clear concentration system and concentration method thereof

Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB739750A (en) * 1953-10-02 1955-11-02 Firestone Tire & Rubber Co Improvements in or relating to high grade rubber and method of making same
GB1464462A (en) * 1974-04-22 1977-02-16 Firestone Tire & Rubber Co Process for producing concentrated latex
WO2005007703A1 (en) * 2003-07-21 2005-01-27 B.C. Sekhar Sdn Bhd Method of producing deproteinised natural rubber in solid and latex form
CN101842421A (en) * 2007-08-30 2010-09-22 卡伯特公司 An elastomer composite and method for producing it

Patent Citations (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB739750A (en) * 1953-10-02 1955-11-02 Firestone Tire & Rubber Co Improvements in or relating to high grade rubber and method of making same
GB1464462A (en) * 1974-04-22 1977-02-16 Firestone Tire & Rubber Co Process for producing concentrated latex
WO2005007703A1 (en) * 2003-07-21 2005-01-27 B.C. Sekhar Sdn Bhd Method of producing deproteinised natural rubber in solid and latex form
CN101842421A (en) * 2007-08-30 2010-09-22 卡伯特公司 An elastomer composite and method for producing it

Non-Patent Citations (2)

* Cited by examiner, † Cited by third party
Title
Effect of field natural rubber latex with different ammonia contents and storage period on physical properties of latex concentrate, stability of skim latex and dipped film;Sirinapa Santipanusopona, et al.;《Physics Procedia》;20090701;第2卷(第1期);第127-134页 *
Evaluating the use of in-situ ultrasonication to reduce fouling during natural rubber skim latex (waste latex) recovery by ultrafiltration;D. Veerasamy,et al.;《Desalination》;20090131;第236卷;第202-207页 *

Also Published As

Publication number Publication date
CN104903355A (en) 2015-09-09
WO2014069979A8 (en) 2015-07-30
PH12015500908A1 (en) 2015-07-13
HK1210485A1 (en) 2016-04-22
WO2014069979A1 (en) 2014-05-08
MY183968A (en) 2021-03-17

Similar Documents

Publication Publication Date Title
CN101857320B (en) Method for treatment of silk degumming wastewater and recovery of silk gum
CN101041486B (en) Method for treatment and comprehensive utilization of silk production waste water
CN104903355B (en) The improved method of rubber is reclaimed from the clear natural rubber latex of glue
CN103551055B (en) Modifying method of cellulose acetate filtration membrane
CN101945826B (en) Method of purifying water containing metallic ingredient and apparatus for purification
CN102160969B (en) Method for preparing fluorocarbon polymer microporous film with interpenetrating network bicontinuous pore structure
JP2017537692A (en) Method for producing high-concentration collagen for use as a medical material
CN108187511A (en) High flux and high retention ratio polyamide composite reverse osmosis membrane and preparation method thereof
CN103917564B (en) From the method for the clear natural rubber latex regenerated rubber of glue
CN105771700A (en) Mixed diamine monomer adopted chlorine-resistant nanofiltration membrane and preparation method therefor
CN103724459B (en) The method of the clear utilization of wastewater resource of a kind of glue
JPH05103958A (en) Cleaning method of membrane module
KR101724118B1 (en) Method for preparing high purity protein concentrate from rice bran
CN104291501A (en) Method of treating ammonium nitrate wastewater by adoption of integrated membrane technology
CN110787512A (en) Pickling process for metal filter element
CN103420520B (en) Processing method of vanadium-containing aluminum-containing wastewater
CN213085756U (en) Recycling device of protein wastewater
CN106693722B (en) A kind of HA-DA/PVDF composite micro porous film with good biocompatibility
CN106422798A (en) Preparation method of antibacterial and pollution-resistant renewable ultra-filtration membrane
CN109467263A (en) The basic copper carbonate preparation process that board wastewater efficiently utilizes
CN110330151A (en) A kind of water purifier based on electrodialytic technique
CN210620490U (en) Leachate concentrated solution processing apparatus and recoverable zero discharge system
CN115873442B (en) Method for preparing synthetic paint by using spraying residual material, spraying residual material treatment method and system
CN103130322A (en) Unit assembling type membrane biological reactor element
CN106007081A (en) Ink wastewater efficient treatment process

Legal Events

Date Code Title Description
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
REG Reference to a national code

Ref country code: HK

Ref legal event code: DE

Ref document number: 1210485

Country of ref document: HK

C14 Grant of patent or utility model
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20161123

Termination date: 20180401

REG Reference to a national code

Ref country code: HK

Ref legal event code: WD

Ref document number: 1210485

Country of ref document: HK