CN104262676B - A kind of method recycling polyacrylamide superfines - Google Patents

A kind of method recycling polyacrylamide superfines Download PDF

Info

Publication number
CN104262676B
CN104262676B CN201410522713.4A CN201410522713A CN104262676B CN 104262676 B CN104262676 B CN 104262676B CN 201410522713 A CN201410522713 A CN 201410522713A CN 104262676 B CN104262676 B CN 104262676B
Authority
CN
China
Prior art keywords
polyacrylamide
superfines
fine powder
add
dispersant
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
CN201410522713.4A
Other languages
Chinese (zh)
Other versions
CN104262676A (en
Inventor
李元军
王欢
刘洁
刘存辉
李雷振
张胜
郑胜
李远方
崔萌
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.)
TIANJIN BO HONG CHEMICAL Co Ltd
Original Assignee
TIANJIN BO HONG CHEMICAL Co Ltd
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 TIANJIN BO HONG CHEMICAL Co Ltd filed Critical TIANJIN BO HONG CHEMICAL Co Ltd
Priority to CN201410522713.4A priority Critical patent/CN104262676B/en
Publication of CN104262676A publication Critical patent/CN104262676A/en
Application granted granted Critical
Publication of CN104262676B publication Critical patent/CN104262676B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Classifications

    • YGENERAL 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
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/62Plastics recycling; Rubber recycling

Abstract

The present invention relates to a kind of method recycling polyacrylamide superfines, comprise the following steps: the polyacrylamide superfines less than 100 mesh reclaimed is added hydrolyzer, add the sodium carbonate hydrolytic reagent of 2%, hydrolyze 3 hours under the conditions of being placed in 80 DEG C, take out material;Above-mentioned material is added comminutor, adds pelletize dispersant, obtain granular material;Granular material obtained above is inputted drying machine, through being dried to obtain wanted product.The beneficial effects of the present invention is: originally can only undersell less than the polyacrylamide superfines of 100 mesh, the invention provides the method that thin powder recovery utilizes, add the added value of fine powder, the net profit 0.4 ten thousand that realizes per ton, polyacrylamide superfines success backing up hydrolyzer in batches, fine powder conversion ratio is 99.16%, high conversion and do not affect product quality, need not additionally increase pelletize dispersant, will not additionally produce more fine powder, the method is suitable for commercial introduction.

Description

A kind of method recycling polyacrylamide superfines
Technical field
The invention belongs to chemical technology field, particularly relate to a kind of method recycling polyacrylamide superfines.
Background technology
Polyacrylamide (PAM) is high molecular weight water soluble polymer, has good fall resistive, is widely used in stone Oil exploitation.Polyacrylamide can produce substantial amounts of fine particle due to the shearing of comminutor in process of production, and these are tiny Granule is dried the air inducing of system owing to the loss of moisture can become superfine dust in dry run, dust pelletizing system separates Out, after using in this course, hydrolysis carries out the technique of twice pelletize and is particularly acute.It addition, dried polypropylene Amide also can produce substantial amounts of fine powder due to the rolloff of mill and the pipe friction of induced draught system in crushing process.
Particle diameter when polyacrylamide is used by oil field has strict control, it is necessary to control at the 18 above particle size content≤4-5% of mesh, The 100 following particle size content≤4-5% of mesh.Main cause one is that fine powder exceeds standard and can affect the mobility of product, causes oilfield injection The ratio of product injection rate and injected water volume of standing is inharmonious, has a strong impact on the mother liquid concentration at the poly-station of note, and causes noting poly-viscosity Unstable;Two is that in particle diameter, fine powder exceeds standard and can affect the course of dissolution of product.This is because fine powder exceeds standard in note collecting process Can affect product dispersion in water, cause fine powder to coalesce, agglomerate periphery is surrounded by water, and the inside is honeycomb texture impact The infiltration of water, thus affect the water-soluble speed of product, it is simply that " flake " that we are usually said.Life of the prior art Produce producer be usually in crushing process by being provided with 20 mesh, the riddle of 100 mesh sorts out packing and undersells, this Hui Shi producer profit is affected.
Summary of the invention
It is an object of the invention to provide a kind of method recycling polyacrylamide superfines, improve finished product Output capacity, makes the fine powder produced in production process obtain effectively recycling.
For realizing above-mentioned goal of the invention, technical scheme is as follows:
A kind of method recycling polyacrylamide superfines, comprises the steps:
1, the polyacrylamide superfines of recovery is proportionally added in the hydrolyzer containing polyacrylamide colloid granule, Add sodium carbonate hydrolytic reagent, hydrolyze 3 hours under the conditions of 80 DEG C, take out material;
2, above-mentioned material is added comminutor, and add pelletize dispersant, obtain granular material;
3, granular material obtained above is inputted drying machine, through being dried to obtain desired product.
Further, in described step 1, the particle diameter of polyacrylamide superfines is less than 100 mesh.
Further, in described step 1, the additional proportion of polyacrylamide superfines is polyacrylamide colloid granule gross weight The 2-6% of amount ratio.
Further, in described step 1, the additional proportion of sodium carbonate hydrolytic reagent is polyacrylamide colloid granule gross weight ratio 2%.
The consumption not adding the material granulation dispersant after the hydrolysis of polyacrylamide superfines is 0.6%-0.75%, adds poly- The usage amount of the material granulation dispersant after acrylamide superfines is 0.65-0.72%;Do not add polyacrylamide ultra-fine Material after powder hydrolysis is through dried, and drying system fine powder quantum of output is 40kg-55kg/T, adds polyacrylamide and surpasses Material after fine powder is through dried, and drying system fine powder quantum of output is 40kg-60kg/T;Do not add polyacrylamide to surpass The fine powder dried material of hydrolysis is after pulverizing, and crushing system fine powder quantum of output is 20kg-30kg/T, adds polypropylene Material after amide superfines is after pulverizing, and crushing system fine powder quantum of output is 23kg-32kg/T;Do not add polypropylene Amide superfines hydrolysis sampling Detection viscosity is 71.0Cp-72.5Cp, and degree of hydrolysis is 26.9%-28.1%, adds polypropylene Amide superfines hydrolysis sampling Detection viscosity is 70.5Cp-73.0Cp, and degree of hydrolysis is 27.2%-28.3%.Illustrate to add and gather After acrylamide superfines, it is not required to additionally increase the consumption of pelletize dispersant, also will not additionally increase the product of fine powder Output, the hydrolysis on polyacrylamide colloid granule also will not produce impact.
The present invention has the advantage that with good effect: originally can only be at a low price less than the polyacrylamide superfines of 100 mesh Sell, the invention provides the method that thin powder recovery utilizes, add the added value of fine powder, per ton realize net profit 0.4 Ten thousand, polyacrylamide superfines success backing up hydrolyzer in batches, fine powder conversion ratio is 99.16%, high conversion and not Affect product quality, it is not necessary to extra increase pelletize dispersant, will not additionally produce more fine powder, be suitable for commercial introduction.
Detailed description of the invention
Below in conjunction with specific embodiment, the invention will be further described, but does not limit protection scope of the present invention.
Embodiment 1
Adding 100g acrylamide content in hydrolyzer is the colloidal solid of 23%, adds polyacrylamide superfines Content is 2%, adds the sodium carbonate of 2% as hydrolytic reagent, hydrolyzes 3 hours at 80 DEG C, takes out material and adds and makes Grain machine, and add pelletize dispersant, obtain granular material, be dried, after drying in this granular material is placed in baking oven Weigh, weight 29.595g, solid content: 88.5%, yield is: 97.01%, viscosity: 71.8Cp, degree of hydrolysis: 27.5%, Water-insoluble: 0.13%.
Embodiment 2
Adding 100g acrylamide content in hydrolyzer is the colloidal solid of 23%, adds polyacrylamide superfines Content is 3%, adds the sodium carbonate of 2% as hydrolytic reagent, hydrolyzes 3 hours at 80 DEG C, takes out material and adds and makes Grain machine, and add pelletize dispersant, obtain granular material, be dried, after drying in this granular material is placed in baking oven Weigh, weight 30.509g, solid content: 89.0%, yield is: 96.98%, viscosity: 72.0Cp, degree of hydrolysis: 27.2%, Water-insoluble: 0.15%.
Embodiment 3
Adding 100g acrylamide content in hydrolyzer is the colloidal solid of 23%, adds polyacrylamide superfines Content is 4%, adds the sodium carbonate of 2% as hydrolytic reagent, hydrolyzes 3 hours at 80 DEG C, takes out material and adds and makes Grain machine, and add pelletize dispersant, obtain granular material, be dried, after drying in this granular material is placed in baking oven Weigh, weight 31.18g, solid content: 90.2%, yield is: 96.98%, viscosity: 70.5Cp, degree of hydrolysis: 26.9%, Water-insoluble: 0.16%.
Embodiment 4
Adding 100g acrylamide content in hydrolyzer is the colloidal solid of 23%, adds polyacrylamide superfines Content is 5%, adds the sodium carbonate of 2% as hydrolytic reagent, hydrolyzes 3 hours at 80 DEG C, takes out material and adds and makes Grain machine, and add pelletize dispersant, obtain granular material, be dried, after drying in this granular material is placed in baking oven Weigh, weight 32.8136g, solid content: 88.7%, yield is: 97.02%, viscosity: 69.0Cp, degree of hydrolysis: 28.1%, Water-insoluble: 0.10%.
Embodiment 5
Adding 100g acrylamide content in hydrolyzer is the colloidal solid of 23%, adds polyacrylamide superfines Content is 6%, adds the sodium carbonate of 2% as hydrolytic reagent, hydrolyzes 3 hours at 80 DEG C, takes out material and adds and makes Grain machine, and add pelletize dispersant, obtain granular material, be dried, after drying in this granular material is placed in baking oven Weigh, weight 33.636g, solid content: 89.5%, yield is: 97.11%, viscosity: 70.0Cp, degree of hydrolysis: 27.7%, Water-insoluble: 0.13%.
Above embodiments of the invention are described in detail, but described content has been only presently preferred embodiments of the present invention, no The practical range for limiting the present invention can be considered.All impartial changes made according to the present patent application scope and improvement etc., Within all should still belonging to the patent covering scope of the present invention.

Claims (2)

1. the method recycling polyacrylamide superfines, comprises the steps:
(1) the polyacrylamide superfines of recovery is proportionally added into containing polyacrylamide gel In the hydrolyzer of body granule, add sodium carbonate hydrolytic reagent, under the conditions of 80 DEG C, hydrolyze 3 little Time, take out material;
(2) above-mentioned material is added comminutor, and add pelletize dispersant, obtain granular substance Material;
(3) granular material obtained above is inputted drying machine, desired through being dried to obtain Product;
In described step (1), the particle diameter of polyacrylamide superfines is less than 100 mesh;
In described step (1), the additional proportion of polyacrylamide superfines is polyacrylamide gel The 2-6% of body granule gross weight ratio.
A kind of polyacrylamide superfines of recycling the most according to claim 1 Method, it is characterised in that: in described step (1), the additional proportion of sodium carbonate hydrolytic reagent is poly-third The 2% of acrylamide colloidal solid gross weight ratio.
CN201410522713.4A 2014-09-30 2014-09-30 A kind of method recycling polyacrylamide superfines Expired - Fee Related CN104262676B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201410522713.4A CN104262676B (en) 2014-09-30 2014-09-30 A kind of method recycling polyacrylamide superfines

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201410522713.4A CN104262676B (en) 2014-09-30 2014-09-30 A kind of method recycling polyacrylamide superfines

Publications (2)

Publication Number Publication Date
CN104262676A CN104262676A (en) 2015-01-07
CN104262676B true CN104262676B (en) 2016-10-26

Family

ID=52154277

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201410522713.4A Expired - Fee Related CN104262676B (en) 2014-09-30 2014-09-30 A kind of method recycling polyacrylamide superfines

Country Status (1)

Country Link
CN (1) CN104262676B (en)

Families Citing this family (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN111976057A (en) * 2020-07-27 2020-11-24 甘肃中科聚合石油科技有限公司 Polyacrylamide suspending agent granulation recovery unit

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1022758C (en) * 1990-06-04 1993-11-17 中国科学院长春应用化学研究所 Preparation of high molecular anion type polycrylamide
JP3392266B2 (en) * 1995-08-11 2003-03-31 日本マイヤー株式会社 Track plate for spindle guide in torsion race machine
CN1084339C (en) * 1996-06-06 2002-05-08 山东工业大学 Method for preparing high molecular wt. anionic polyacrylamide
CN1240799A (en) * 1998-07-06 2000-01-12 中国石油天然气总公司石油勘探开发科学研究院 Process for preparing powder-type partially hydrolytic polyacrylamide
CN101649022B (en) * 2009-07-01 2011-08-17 山东宝莫生物化工股份有限公司 Preparing method of lowering residual monomer content of ultra high molecular weight anion-type polyacrylamide

Also Published As

Publication number Publication date
CN104262676A (en) 2015-01-07

Similar Documents

Publication Publication Date Title
CN102205972B (en) Modification method of attapulgite
CN103694055B (en) Organic-inorganic compound mixed fertilizer granulation compound binding agent and preparation method and application
CN105368442B (en) A kind of low-density ultrahigh-strength corrosion-resistant oil proppant and preparation method thereof
CN102296177A (en) Method for reinforcing sintering of iron ores difficult to pelletize by biomass fuel
CN110314763A (en) A method of pellet feed is prepared using fine ore
CN106498156A (en) A kind of lead cadmia balling technique
CN104262676B (en) A kind of method recycling polyacrylamide superfines
CN104261866A (en) Production method for coal gangue ceramsite
CN103497757A (en) Petroleum fracturing propping agent containing fly ash in raw materials and preparation method thereof
EP3218526B1 (en) Binder compositions and processes of preparing iron ore pellets
CN111807878A (en) Method for rapidly preparing dealuminized silicon fertilizer from fly ash
CN104998624A (en) Dephosphorization absorbent granulation method
CN109824309A (en) A method of acidproof ore aggregate is prepared using geopolymeric reaction
CN104151598A (en) Method for preparing porous microspheres from waste rubber
CN113683094A (en) Dry preparation method of modified bentonite
CN103395784B (en) Crushing process reducing crystal material excessive crushing and increasing outputs of products of specified grades
CN105399143A (en) Iron oxide red for lithium iron phosphate and preparation method and application thereof
CN103387264B (en) Comprehensive utilization method of molybdenum in waste molybdenum
CN106755985A (en) The composite dry powder binding agent and iron powder forming method of iron powder shaping
CN105733594A (en) Preparation method of micro powder soil conditioner
CN106831002A (en) A kind of granular double superhosphate energy-saving production method
CN102021322A (en) Method for preparing novel binder for metallurgic pellets
CN110845279A (en) Application of serpentine magnesium extraction tailings in field of compound fertilizer, sandy soil compound fertilizer and preparation method thereof
CN105039692A (en) Aspergillus niger granulating and leaching method of copper tailings
CN110510997A (en) The dry preparation process of gold fired slags production sintering road surface landscape brick

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
C14 Grant of patent or utility model
GR01 Patent grant
CF01 Termination of patent right due to non-payment of annual fee

Granted publication date: 20161026

Termination date: 20170930

CF01 Termination of patent right due to non-payment of annual fee