CN102493277A - Alkenyl succinic anhydride sizing agent emulsion and preparation method thereof - Google Patents

Alkenyl succinic anhydride sizing agent emulsion and preparation method thereof Download PDF

Info

Publication number
CN102493277A
CN102493277A CN2011104045703A CN201110404570A CN102493277A CN 102493277 A CN102493277 A CN 102493277A CN 2011104045703 A CN2011104045703 A CN 2011104045703A CN 201110404570 A CN201110404570 A CN 201110404570A CN 102493277 A CN102493277 A CN 102493277A
Authority
CN
China
Prior art keywords
succinic anhydride
alkenyl succinic
waste residue
water
sizing agent
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.)
Granted
Application number
CN2011104045703A
Other languages
Chinese (zh)
Other versions
CN102493277B (en
Inventor
王哲
魏明志
刘温霞
薛菁雯
王慧丽
王兴琪
王晓卫
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.)
Shandong Institute of Light Industry
Original Assignee
Shandong Institute of Light Industry
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 Shandong Institute of Light Industry filed Critical Shandong Institute of Light Industry
Priority to CN201110404570.3A priority Critical patent/CN102493277B/en
Publication of CN102493277A publication Critical patent/CN102493277A/en
Application granted granted Critical
Publication of CN102493277B publication Critical patent/CN102493277B/en
Expired - Fee Related legal-status Critical Current
Anticipated expiration legal-status Critical

Links

Landscapes

  • Paper (AREA)

Abstract

The invention relates to the field of sizing agents in the papermaking industry, in particular to alkenyl succinic anhydride sizing agent emulsion, which comprises white mud waste residue, alkenyl succinic anhydride and water, wherein a mass ratio of the alkenyl succinic anhydride to the water is 1:(1-4), and a mass ratio of the white mud waste residue to the alkenyl succinic anhydride is 1:(20-1,000). The preparation method comprises the following steps of: dispersing the white mud waste residue into the alkenyl succinic anhydride, adding the water, and mixing uniformly; or dispersing the white mud waste residue into the water, and uniformly mixing with the alkenyl succinic anhydride to prepare the stable oil-in-water (O/W) alkenyl succinic anhydride (ASA) emulsion. The industrial waste residue is recycled, and virtuous economic cycle is realized; the white mud serving as an emulsifier is lower in consumption compared with an inorganic nano-material serving as an emulsifier; under the condition of low consumption of the emulsifier, a good sizing effect can be achieved, so that the emulsification cost is lower; the alkenyl succinic anhydride sizing agent emulsion has the advantages of simple emulsification process and high concentration of the prepared emulsion; and after the alkenyl succinic anhydride sizing agent emulsion is diluted with water and added into a paper stock for sizing in pulp, and the sizing efficiency is high.

Description

A kind of alkenyl succinic anhydride sizing agent emulsion and preparation method thereof
 
Technical field
The present invention relates to paper industry sizing agent field, particularly a kind of alkenyl succinic anhydride sizing agent emulsion also relates to the preparation method of said alkenyl succinic anhydride sizing agent emulsion.
Background technology
Report 2008 according to Chinese industrial, world's soda ash production capacity mainly is distributed in China, North America and Europe, accounts for 85 % of global aggregated capacity.To the year ends 2006, Chinese soda ash production capacity reaches 1,720 ten thousand t, accounts for 34 % of global aggregated capacity, occupies the first in the world, and Europe and North America then account for 29% and 23% respectively.Every production 1t soda ash discharges 0.3 ~ 0.6t alkaline residue approximately, is commonly called as " white alkali-making mud ".Calculate that in view of the above China reaches 6,800,000 t by " white clay " that system alkali industry is produced every year.Pulping and paper-making factory similarly can produce a large amount of causticization white claies (also claiming paper white sludge) in the black liquor alkali recovery process, character and white alkali-making mud are close.The thick slurry of every production 1 t will produce nearly 0.5 t white clay, and the annual white clay that produces in national paper mill surpasses 3,000,000 t.Therefore the annual white clay that produces of China is nearly about 1 000 ten thousand t; Have only few part to obtain utilizing at present in these white claies; Major part all is outdoor stacking, not only takies a large amount of soils, contaminated environment; Consume great amount of manpower and material resources, financial resources manage, and have wasted resources a large amount of in the white clay.If can rationally utilize this type white clay, not only solve white clay outlet and problem of environmental pollution, and can reduce entreprise cost significantly, improve enterprise competitiveness.The paper white sludge main component is CaO, SiO 2Deng, also contain magnesium salts and molysite partly.White alkali-making mud mainly is with CaCO 3, CaSO 4, CaCl 2Form Deng calcium salt, also have a spot of SiO 2The amount of the annual white clay that produces is huge, up to the present, and the real industrial applications of white clay few; Just few part is utilized; Need the scientific worker to actively develop scientific research, explore new white clay comprehensive utilization technique, many-sided effort could progressively solve China's white clay problem of outlet.
Alkenyl succinic anhydride is called for short ASA, for the water-fast material of oily, is used for paper sizing as reactive sizing agent, has that applying glue efficient is high, slaking is fast, the characteristics of pH value wide accommodation, is widely used in the plasm-glue-blending of fine paper and cardboard.ASA must process water-based when being used as internal sizing agent emulsion joins in the slurry, yet the ASA facile hydrolysis need be in the on-the-spot emulsification of machine room.ASA emulsifying agent commonly used has cationic starch 、 Yang ∕ PAMA or surfactant, and compound.Because starch needs first gelatinization, re-use after the cooling, emulsifying process is complicated, and is wayward, thereby and low-molecular-weight surfactant can reduce the sizing efficiency of ASA to the paper migration, also can produce bubble-related issues.Therefore, the emulsification method of more easy, the ASA that is prone to row of development and to improve emulsification system be the important channel that paper industry improves ASA applying glue efficient to the emulsifiability of ASA.
In recent years, developed some inorganic particles, used these emulsifying agents can not only prepare stable ASA emulsion, and applying glue efficient is high as the ASA emulsifying agent.It like application number 200910020447.4 Chinese invention patent application; A kind of preparation method of ASA papermaking sizing agent emulsion of high stability is disclosed; This method is fine to the emulsifying effectiveness of ASA, but has inevitably used a small amount of weak base, can quicken the hydrolysis of ASA; Identical applicant has applied for that again application number is 200810017130.0 and is called that " a kind of preparation method of ASA paper-making sizing agent emulsion " and application number are 201110061783.0 and are called the application for a patent for invention of " a kind of self-emulsifying type alkenyl succinic anhydride sizing agent and preparation method thereof "; The thinking of two patent schemes all is to use the stabilizing agent of inorganic particles as the ASA sizing agent emulsion substantially; These two kinds of method emulsifying process are simple but because the emulsifying agent that uses is inorganic nano material bentonite, hydrotalcite and titanium dioxide, have the relative problem of higher of cost.
Summary of the invention
For pollution and the resource problem that solves the white clay waste residue; Be directed against the deficiency and the relative problem of higher of inorganic nano material cost of the emulsifying technology of existing ASA simultaneously, the invention provides a kind of alkenyl succinic anhydride sizing agent emulsion that utilizes the white clay waste residue as emulsifying agent.
Another object of the present invention provides the preparation method of said alkenyl succinic anhydride sizing agent emulsion.
The present invention realizes through following measure:
A kind of alkenyl succinic anhydride sizing agent emulsion; Contain white clay waste residue, alkenyl succinic anhydride (ASA) and water; ASA is the various ASA industrial products that are used for paper-making sizing without emulsification that exist with liquid form under the normal temperature, and wherein the mass ratio of alkenyl succinic anhydride and water is 1:1 ~ 4; The mass ratio of white clay waste residue and alkenyl succinic anhydride is 1:19 ~ 2000.
Said white clay waste residue is the white alkali-making mud of system alkali industry or the causticization white clay (also claiming paper white sludge) that pulping and paper-making factory produces in the black liquor alkali recovery process.
Described alkenyl succinic anhydride sizing agent emulsion, the mass ratio of preferred alkenyl succinic anhydride and water is 1:1 ~ 3.
Described alkenyl succinic anhydride sizing agent emulsion, the mass ratio of preferred white clay waste residue and alkenyl succinic anhydride is 1:98 ~ 625.
Described alkenyl succinic anhydride sizing agent emulsion, the mass ratio of preferred alkenyl succinic anhydride and water is 1:1, the mass ratio of white clay waste residue and alkenyl succinic anhydride is 1:250.
A kind of preparation method of alkenyl succinic anhydride sizing agent emulsion can be that the white clay waste residue is distributed in the alkenyl succinic anhydride, adds entry again and mixes; Or the white clay waste residue is distributed in the water, mix with alkenyl succinic anhydride again, prepare stable O/W type ASA emulsion.
Among the preparation method of the present invention; Mechanical shearing effect in the related mixed process can be provided by any stirring or mechanical shearing equipment, and emulsifying device commonly used in the industry has venturi emulsifying device, turbine emulsifying device and Cavitron system and centrifugal multistage pump multiple centrifugal pump.If common mixing plant requires 2000 ~ 11000 rev/mins of mixing speeds, preferred rotating speed is 5000 ~ 11000 rev/mins; Mixing time is 1 ~ 15 minute, and the preferred time is 3 ~ 5 minutes.
The present invention has following outstanding advantage and effect:
1. utilize the white alkali-making mud of system alkali industry and the paper white sludge waste residue of paper industry generation to be applied to paper industry sizing agent field; Realized the recycling of industrial residue; Realized optimum economic circulation; Not only solve white clay outlet and problem of environmental pollution, and can reduce entreprise cost significantly, improved enterprise competitiveness;
2. the alkenyl succinic anhydride sizing agent emulsion of the present invention preparation need not add any surfactant and complex polyelectrolyte particle and just can be emulsified into stable emulsion to ASA; The emulsifying agent consumption that white clay uses when making emulsifying agent as emulsifying agent than inorganic nano material is lower; And under lower emulsifying agent consumption, can reach good sizing efficiency; Therefore the emulsification cost is lower, also has simple, the prepared emulsion of emulsifying process simultaneously and has the high advantage of concentration, adds after the dilute with water emulsification in the paper stock; Carry out plasm-glue-blending, applying glue efficient is high.
The specific embodiment
Below in conjunction with specific embodiment the present invention is described further, does not constitute any restriction of the present invention.Remove other and indicate, all umbers among the embodiment all in mass.
Embodiment 1
0.05 part of paper white sludge waste residue powder is distributed in 100 parts the deionized water; Under 10000 rev/mins mixing speed, be distributed among 100 parts of commodity ASA then; Continue to stir 6 minutes, prepare stable O/W type ASA emulsion, this emulsion homogeneous, stable, not stratified in 24 hours.
Get the poplar BCTMP slurry that 100 parts of beating degrees are about 42 ° of SR and add in 9900 parts of water, after defiberizing machine is discongested, add 1 part of above-mentioned sizing agent and 1 part of Al 2(SO 4) 3, mix the back and form paper stock, and copy to quantitatively being 60g/m through quick kayser method sheet forming apparatus 2Handsheet, and through drying cylinder in 105 ℃ down behind the dry 10min, the degree of sizing that utilizes liquid osmosis (GB/T5405-2002) to record handsheet is 98s.
The emulsion of preparing was placed after 1 hour, carried out identical operations by above-mentioned steps, and the degree of sizing of measuring handsheet is 95s.This emulsion is not obvious to the influence of sizing efficiency, shows that this emulsion has stability and water repelling property preferably.
Embodiment 2
0.1 part of paper white sludge waste residue powder is distributed in 100 parts the deionized water, under 7000 rev/mins mixing speed, is distributed to then among 100 parts of commodity ASA, continue to stir 3 minutes, prepare stable O/W type ASA emulsion.
Get the poplar BCTMP slurry that 100 parts of beating degrees are about 42 ° of SR and add in 9900 parts of water, after defiberizing machine is discongested, add 1 part of above-mentioned sizing agent and 1 part of Al 2(SO 4) 3, mix the back and form paper stock, and copy to quantitatively being 60g/m through quick kayser method sheet forming apparatus 2Handsheet, and through drying cylinder in 105 ℃ down behind the dry 10min, the degree of sizing that utilizes liquid osmosis (GB/T5405-2002) to record handsheet is 116s.
Embodiment 3
0.16 part of paper white sludge waste residue powder is distributed to 100 parts deionized water, under 6000 rev/mins mixing speed, is distributed to then among 100 parts of commodity ASA, continue to stir 4 minutes, prepare stable O/W type ASA emulsion.
Get the poplar BCTMP slurry that 100 parts of beating degrees are about 42 ° of SR and add in 9900 parts of water, after defiberizing machine is discongested, add 1 part of above-mentioned sizing agent and 1 part of Al 2(SO 4) 3, mix the back and form paper stock, and copy to quantitatively being 60g/m through quick kayser method sheet forming apparatus 2Handsheet, and through drying cylinder in 105 ℃ down behind the dry 10min, the degree of sizing that utilizes liquid osmosis (GB/T5405-2002) to record handsheet is 135s.
Embodiment 4
0.4 part of paper white sludge waste residue powder is distributed under 8000 rev/mins mixing speed among 100 parts of commodity ASA, and the deionized water that adds 100 parts then continues to stir 2 minutes, prepares stable O/W type ASA emulsion.
Get the poplar BCTMP slurry that 100 parts of beating degrees are about 42 ° of SR and add in 9900 parts of water, after defiberizing machine is discongested, add 1 part of above-mentioned sizing agent and 1 part of Al 2(SO 4) 3, mix the back and form paper stock, and copy to quantitatively being 60g/m through quick kayser method sheet forming apparatus 2Handsheet, and through drying cylinder in 105 ℃ down behind the dry 10min, the degree of sizing that utilizes liquid osmosis (GB/T5405-2002) to record handsheet is 143s.
Embodiment 5
1 part of paper white sludge waste residue powder is distributed under 11000 rev/mins mixing speed among 99 parts of commodity ASA, and the deionized water that adds 200 parts then continues to stir 1 minute, prepares stable O/W type ASA emulsion.
Get the poplar BCTMP slurry that 100 parts of beating degrees are about 42 ° of SR and add in 9900 parts of water, after defiberizing machine is discongested, add 1.5 parts of above-mentioned sizing agents and 1 part of Al 2(SO 4) 3, mix the back and form paper stock, and copy to quantitatively being 60g/m through quick kayser method sheet forming apparatus 2Handsheet, and through drying cylinder in 105 ℃ down behind the dry 10min, the degree of sizing that utilizes liquid osmosis (GB/T5405-2002) to record handsheet is 136s.
Embodiment 6
2 parts of paper white sludge waste residue powder are distributed under 2000 rev/mins mixing speed among 98 parts of commodity ASA, and the deionized water that adds 300 parts then continues to stir 10 minutes, prepares stable O/W type ASA emulsion.
Get the poplar BCTMP slurry that 100 parts of beating degrees are about 42 ° of SR and add in 9900 parts of water,, after defiberizing machine is discongested, add 2 parts of above-mentioned sizing agents and 1 part of Al 2(SO 4) 3, mix the back and form paper stock, and copy to quantitatively being 60g/m through quick kayser method sheet forming apparatus 2Handsheet, and through drying cylinder in 105 ℃ down behind the dry 10min, the degree of sizing that utilizes liquid osmosis (GB/T5405-2002) to record handsheet is 124s.
Embodiment 7
5 parts of paper white sludge waste residue powder are distributed under 8000 rev/mins mixing speed among 95 parts of commodity ASA; The deionized water that adds 400 parts then continues to stir 5 minutes; Prepare stable O/W type ASA emulsion, this emulsion homogeneous, stable, not stratified in 24 hours.
Get the poplar BCTMP slurry that 100 parts of beating degrees are about 42 ° of SR and add in 9900 parts of water, after defiberizing machine is discongested, add 2.6 parts of above-mentioned sizing agents and 1 part of Al 2(SO 4) 3, mix the back and form paper stock, and copy to quantitatively being 60g/m through quick kayser method sheet forming apparatus 2Handsheet, and through drying cylinder in 105 ℃ down behind the dry 10min, the degree of sizing that utilizes liquid osmosis (GB/T5405-2002) to record handsheet is 118s.
The emulsion of preparing was placed after 1 hour, carried out identical operations by above-mentioned steps, and the degree of sizing of measuring handsheet is 116s.This emulsion is not obvious to the influence of sizing efficiency, shows that this emulsion has stability and water repelling property preferably.
Embodiment 8
0.16 part of white alkali-making mud waste residue powder is distributed to 100 parts deionized water, under 6000 rev/mins mixing speed, is distributed to then among 100 parts of commodity ASA, continue to stir 4 minutes, prepare stable O/W type ASA emulsion.
Get the poplar BCTMP slurry that 100 parts of beating degrees are about 42 ° of SR and add in 9900 parts of water, after defiberizing machine is discongested, add 1 part of above-mentioned sizing agent and 1 part of Al 2(SO 4) 3, mix the back and form paper stock, and copy to quantitatively being 60g/m through quick kayser method sheet forming apparatus 2Handsheet, and through drying cylinder in 105 ℃ down behind the dry 10min, the degree of sizing that utilizes liquid osmosis (GB/T5405-2002) to record handsheet is 116s.
Embodiment 9
0.4 part of white alkali-making mud waste residue powder is distributed under 8000 rev/mins mixing speed among 100 parts of commodity ASA, and the deionized water that adds 100 parts then continues to stir 2 minutes, prepares stable O/W type ASA emulsion.
Get the poplar BCTMP slurry that 100 parts of beating degrees are about 42 ° of SR and add in 9900 parts of water, after defiberizing machine is discongested, add 3 parts of above-mentioned sizing agents and 1 part of Al 2(SO 4) 3, mix the back and form paper stock, and copy to quantitatively being 60g/m through quick kayser method sheet forming apparatus 2Handsheet, and through drying cylinder in 105 ℃ down behind the dry 10min, the degree of sizing that utilizes liquid osmosis (GB/T5405-2002) to record handsheet is 125s.

Claims (8)

1. an alkenyl succinic anhydride sizing agent emulsion is characterized in that containing white clay waste residue, alkenyl succinic anhydride and water, wherein
The mass ratio of alkenyl succinic anhydride and water is 1:1 ~ 4; The mass ratio of white clay waste residue and alkenyl succinic anhydride is 1:19 ~ 2000.
2. alkenyl succinic anhydride sizing agent emulsion according to claim 1 is characterized in that said white clay waste residue is the white alkali-making mud of system alkali industry or the causticization white clay that pulping and paper-making factory produces in the black liquor alkali recovery process.
3. alkenyl succinic anhydride sizing agent emulsion according to claim 1 and 2, the mass ratio that it is characterized in that alkenyl succinic anhydride and water is 1:1 ~ 3.
4. alkenyl succinic anhydride sizing agent emulsion according to claim 1 and 2, the mass ratio that it is characterized in that white clay waste residue and alkenyl succinic anhydride is 1:98 ~ 625.
5. alkenyl succinic anhydride sizing agent emulsion according to claim 1 and 2, the mass ratio that it is characterized in that alkenyl succinic anhydride and water is 1:1, the mass ratio of white clay waste residue and alkenyl succinic anhydride is 1:250.
6. the preparation method of an alkenyl succinic anhydride sizing agent emulsion is characterized in that the white clay waste residue is distributed in the alkenyl succinic anhydride, adds entry again and mixes; Perhaps the white clay waste residue is distributed in the water, mixes with alkenyl succinic anhydride again.
7. preparation method according to claim 4, the mixing speed that it is characterized in that described mixed process is 2000 ~ 11000 rev/mins; Mixing time is 1 ~ 15 minute.
8. preparation method according to claim 4, the mixing speed that it is characterized in that described mixed process is 5000 ~ 11000 rev/mins; Mixing time is 3 ~ 5 minutes.
CN201110404570.3A 2011-12-08 2011-12-08 Alkenyl succinic anhydride sizing agent emulsion and preparation method thereof Expired - Fee Related CN102493277B (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201110404570.3A CN102493277B (en) 2011-12-08 2011-12-08 Alkenyl succinic anhydride sizing agent emulsion and preparation method thereof

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201110404570.3A CN102493277B (en) 2011-12-08 2011-12-08 Alkenyl succinic anhydride sizing agent emulsion and preparation method thereof

Publications (2)

Publication Number Publication Date
CN102493277A true CN102493277A (en) 2012-06-13
CN102493277B CN102493277B (en) 2014-08-13

Family

ID=46185133

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201110404570.3A Expired - Fee Related CN102493277B (en) 2011-12-08 2011-12-08 Alkenyl succinic anhydride sizing agent emulsion and preparation method thereof

Country Status (1)

Country Link
CN (1) CN102493277B (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103015262A (en) * 2012-12-27 2013-04-03 山东轻工业学院 Method for preparing nanometer TiO2 styrene-acrylic latex surface sizing agent

Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1240009A (en) * 1996-12-06 1999-12-29 埃卡化学公司 Process for production of paper
CN1291249A (en) * 1998-02-17 2001-04-11 赫尔克里士公司 Paper sizing
CN1432088A (en) * 2000-05-30 2003-07-23 赫尔克里士公司 Use of alkenyl succinic anhydride compsns., and its uses
CN1546789A (en) * 2003-12-12 2004-11-17 山东博汇纸业股份有限公司 Improved lime mud recovering process and its application for producing neutral glue blending paper
CN101333789A (en) * 2008-06-26 2008-12-31 山东轻工业学院 Method for preparing ASA paper-making sizing agent emulsion

Patent Citations (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN1240009A (en) * 1996-12-06 1999-12-29 埃卡化学公司 Process for production of paper
CN1291249A (en) * 1998-02-17 2001-04-11 赫尔克里士公司 Paper sizing
CN1432088A (en) * 2000-05-30 2003-07-23 赫尔克里士公司 Use of alkenyl succinic anhydride compsns., and its uses
CN1546789A (en) * 2003-12-12 2004-11-17 山东博汇纸业股份有限公司 Improved lime mud recovering process and its application for producing neutral glue blending paper
CN101333789A (en) * 2008-06-26 2008-12-31 山东轻工业学院 Method for preparing ASA paper-making sizing agent emulsion

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN103015262A (en) * 2012-12-27 2013-04-03 山东轻工业学院 Method for preparing nanometer TiO2 styrene-acrylic latex surface sizing agent
CN103015262B (en) * 2012-12-27 2015-03-04 山东轻工业学院 Method for preparing nanometer TiO2 styrene-acrylic latex surface sizing agent

Also Published As

Publication number Publication date
CN102493277B (en) 2014-08-13

Similar Documents

Publication Publication Date Title
CN102080341B (en) Cationic organic particles and preparation and application thereof
CN102080342B (en) Anionic organic particles and preparation and application thereof
CN102852031B (en) Modified calcium sulfate crystal whisker papermaking filler, preparation method and applications thereof
CN108505372A (en) A method of producing the low special craft paper of gram weight and high strength degree electric business using domestic waste paper
CN104284945A (en) Treatment of calcium carbonate containing materials for increased filler load in paper
CN100446847C (en) Water soluble compound organosilicon emulsion highly effective defoaming agent and its synthetic method
CN102268839A (en) Method for preparing Pickering emulsion type alkenyl succinic anhydrides (ASA) papermaking sizing agent
CN101228315A (en) Reduced shear cellulose reactive sizing agent for wet end applications
NO328752B1 (en) Aqueous dispersion of a cellulose-reactive adhesive and process for its preparation and use
CN107881842A (en) A kind of method that high-strength corrugated base paper is prepared using stalk and secondary stock
CN103435082B (en) A kind of method utilizing lignin from pulping black liquor to regulate and control calcium carbonate crystal particle growth
CN109837799A (en) A kind of preparation method improving low grammes per square metre T cardboard ring crush intensity
CN110004766A (en) A kind of alginate coated caco3 particle stablizes the preparation method of paper-making sizing agent emulsion
JP2004332193A (en) Method for improving yield and dewatering of papermaking raw material in production of paper, cardboard, pasteboard, or the like
CN102493277B (en) Alkenyl succinic anhydride sizing agent emulsion and preparation method thereof
AU2020102641A4 (en) Alkenyl succinic anhydride paper sizing agent emulsion and preparation method and application thereof
CN104120621A (en) Application of calcium silicate as retention aiding intensifier in papermaking
CN104744995A (en) Multifunctional wastepaper deinking agent
CN102493272B (en) ASA emulsion sizing agent and preparation method thereof
CN103881468A (en) Raw materials and method for preparing environment-friendly mixed waste paper deinking agent
CN106917320A (en) A kind of new papermaking filler and preparation method thereof
CN102505548B (en) Synchronous remover for mixed impurities of ink and adhesive in waste paper, and preparation method thereof
CN103343479A (en) Method for improving AKD (Alkyl Ketene Dimer) sizing efficiency for white mud filled paper material
US20070131372A1 (en) Phyllosilicate Slurry For Papermaking
CN102691232A (en) Multifunctional papermaking auxiliary agent with high retention

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: 20140813

Termination date: 20151208

EXPY Termination of patent right or utility model