CN106087564A - The preparation method of a kind of wet strength agent and wet strength agent - Google Patents

The preparation method of a kind of wet strength agent and wet strength agent Download PDF

Info

Publication number
CN106087564A
CN106087564A CN201610452057.4A CN201610452057A CN106087564A CN 106087564 A CN106087564 A CN 106087564A CN 201610452057 A CN201610452057 A CN 201610452057A CN 106087564 A CN106087564 A CN 106087564A
Authority
CN
China
Prior art keywords
weight portion
wet strength
strength agent
water
weight
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.)
Pending
Application number
CN201610452057.4A
Other languages
Chinese (zh)
Inventor
不公告发明人
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.)
Guangzhou Juzhu Patent Research And Development Co Ltd
Original Assignee
Guangzhou Juzhu Patent Research And Development 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 Guangzhou Juzhu Patent Research And Development Co Ltd filed Critical Guangzhou Juzhu Patent Research And Development Co Ltd
Priority to CN201610452057.4A priority Critical patent/CN106087564A/en
Publication of CN106087564A publication Critical patent/CN106087564A/en
Pending legal-status Critical Current

Links

Classifications

    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H21/00Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties
    • D21H21/14Non-fibrous material added to the pulp, characterised by its function, form or properties; Paper-impregnating or coating material, characterised by its function, form or properties characterised by function or properties in or on the paper
    • D21H21/18Reinforcing agents
    • D21H21/20Wet strength agents
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/03Non-macromolecular organic compounds
    • D21H17/05Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
    • D21H17/06Alcohols; Phenols; Ethers; Aldehydes; Ketones; Acetals; Ketals
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/03Non-macromolecular organic compounds
    • D21H17/05Non-macromolecular organic compounds containing elements other than carbon and hydrogen only
    • D21H17/14Carboxylic acids; Derivatives thereof
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20Macromolecular organic compounds
    • D21H17/21Macromolecular organic compounds of natural origin; Derivatives thereof
    • D21H17/24Polysaccharides
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20Macromolecular organic compounds
    • D21H17/21Macromolecular organic compounds of natural origin; Derivatives thereof
    • D21H17/24Polysaccharides
    • D21H17/25Cellulose
    • D21H17/26Ethers thereof
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20Macromolecular organic compounds
    • D21H17/33Synthetic macromolecular compounds
    • D21H17/34Synthetic macromolecular compounds obtained by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H17/36Polyalkenyalcohols; Polyalkenylethers; Polyalkenylesters
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/20Macromolecular organic compounds
    • D21H17/33Synthetic macromolecular compounds
    • D21H17/46Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D21H17/54Synthetic macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds obtained by reactions forming in the main chain of the macromolecule a linkage containing nitrogen
    • D21H17/55Polyamides; Polyaminoamides; Polyester-amides
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/63Inorganic compounds
    • D21H17/67Water-insoluble compounds, e.g. fillers, pigments
    • DTEXTILES; PAPER
    • D21PAPER-MAKING; PRODUCTION OF CELLULOSE
    • D21HPULP COMPOSITIONS; PREPARATION THEREOF NOT COVERED BY SUBCLASSES D21C OR D21D; IMPREGNATING OR COATING OF PAPER; TREATMENT OF FINISHED PAPER NOT COVERED BY CLASS B31 OR SUBCLASS D21G; PAPER NOT OTHERWISE PROVIDED FOR
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/71Mixtures of material ; Pulp or paper comprising several different materials not incorporated by special processes
    • D21H17/74Mixtures of material ; Pulp or paper comprising several different materials not incorporated by special processes of organic and inorganic material

Landscapes

  • Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Inorganic Chemistry (AREA)
  • Paper (AREA)

Abstract

The invention discloses the present invention and preparation method and the wet strength agent of a kind of wet strength agent are provided, the method includes: carries out homogenizing in homogenizer 15 hours at 50 80 DEG C after being mixed by the water of the Polyamide-Polyamsne-Epichlorohydrin solution of 30 100 weight portions, the polyvinyl alcohol of 40 80 weight portions, the Nipagin ester of 55 120 weight portions, the potassium titanate crystal whisker of 5 35 weight portions, the linolenic acid of 10 30 weight portions, the propylene glycol of 10 20 weight portions, the water-soluble cellulose of 2 15 weight portions and 150 1000 weight portions, obtains wet strength agent.The wet strength agent of the present invention ensures the intensity of paper while ensure that paper pliability.

Description

The preparation method of a kind of wet strength agent and wet strength agent
Technical field
The present invention relates to pulp technology for making paper, be specifically related to preparation method and the wet strength agent of a kind of wet strength agent.
Background technology
Wet strength agent is mainly applied in paper industry.Different its consumptions of paper kind differs widely, as (toilet paper, fruit paper bag, Paperboard, wettable water surface paper etc.).Wet strength agent is primarily now based on PAE wet strength agent.Factory is also a lot, mostly on a small scale Change, but its production product quality is pretty good.
Chinese patent CN103981759A discloses a kind of emulsion-type wet strength agent and preparation method thereof, and wet strength agent includes following Raw material: dimethyl diallyl ammonium chloride, Polyamide-Polyamsne-Epichlorohydrin resin, dicyandiamide, polyoxyethylene stearic acid ester, meat Myristate stearic acid, hyaluronate sodium, sodium formate, polyoxyethylene ether, aluminium sesquioxide, azodiisobutyronitrile, formic acid, carbonic acid Sodium, sulfamic acid sodium water solution, catalyst.Its preparation method is by dimethyl diallyl ammonium chloride, polyamide polyamines epoxy Chloropropane resin, dicyandiamide, polyoxyethylene stearic acid ester, myristinate stearic acid, hyaluronate sodium mix homogeneously, then add Enter sodium formate, polyoxyethylene ether, aluminium sesquioxide, azodiisobutyronitrile, be warming up to 40~60 DEG C reaction 1~2h, add formic acid, Sodium carbonate, sulfamic acid sodium water solution, catalyst, mix homogeneously, stand.
Chinese patent CN 101704947A discloses a kind of wet strength agent for papermaking and preparation method thereof, preparation method include as Lower step: (1) is by polyamine, polynary acyl chlorides and acid binding agent hybrid reaction, it is thus achieved that condensation substance;(2) condensation substance of step (1) is added Enter epichlorohydrin reaction, it is thus achieved that wet strength agent for papermaking.
Existing paper, such as toilet paper, it is desirable to have certain pliability, but simultaneously need to ensure the intensity of paper.
Summary of the invention
It is an object of the invention to provide preparation method and the wet strength agent of a kind of wet strength agent, this wet strength agent ensure that paper The intensity of paper is ensured while pliability.
For achieving the above object, the present invention provides the preparation method of a kind of wet strength agent, and the method includes: by 30-100 weight The Polyamide-Polyamsne-Epichlorohydrin solution of part, the polyvinyl alcohol of 40-80 weight portion, the Nipagin ester of 55-120 weight portion, 5- The potassium titanate crystal whisker of 35 weight portions, the linolenic acid of 10-30 weight portion, the propylene glycol of 10-20 weight portion, 2-15 weight portion water-soluble Property cellulose and 150-1000 weight portion water mixing after at 50-80 DEG C, in homogenizer, carry out homogenizing 1-5 hour, obtain wet Strong agent.
Preferably, by the Polyamide-Polyamsne-Epichlorohydrin solution of 50-70 weight portion, the polyvinyl alcohol of 60-80 weight portion, The Nipagin ester of 70-100 weight portion, 10-30 measure the potassium titanate crystal whisker of part, the linolenic acid of 20-30 weight portion, 15-20 weight portion Propylene glycol, the water-soluble cellulose of 6-10 weight portion and 300-800 weight portion water mixing after carry out described homogenizing.
Preferably, the viscosity of described Polyamide-Polyamsne-Epichlorohydrin is 15-50mPa s-1, pH is 3-5, and solid content is 10-30 weight %, density is 1.01-1.1g cm3
Preferably, the diameter 100-500 nanometer of described potassium titanate crystal whisker, length 10-15 micron, tensile strength is 6.5- 7.5GPa, elastic modelling quantity is 200-500GPa.
Preferably, described water-soluble cellulose is chitosan or hydroxypropyl methyl cellulose.
Preferably, the condition of described homogenizing is: temperature is 60-70 DEG C, and homogenizing time is 2-3 hour.
The present invention also provides for a kind of wet strength agent, and described wet strength agent includes the polyamide polyamines epoxy chloropropionate of 30-100 weight portion Alkane solution, the polyvinyl alcohol of 40-80 weight portion, the Nipagin ester of 55-120 weight portion, the potassium titanate crystal whisker of 5-35 weight portion, The linolenic acid of 10-30 weight portion, the propylene glycol of 10-20 weight portion, the water-soluble cellulose of 2-15 weight portion and 150-1000 weight The water of amount part.
Preferably, the viscosity of described Polyamide-Polyamsne-Epichlorohydrin is 15-50mPa s-1, pH is 3-5, and solid content is 10-30 weight %, density is 1.01-1.1g cm3
Preferably, the diameter 100-500 nanometer of described potassium titanate crystal whisker, length 10-15 micron, tensile strength is 6.5- 7.5GPa, elastic modelling quantity is 200-500GPa.
Preferably, described water-soluble cellulose is chitosan or hydroxypropyl methyl cellulose.
The inventive method has the advantage that
The wet strength agent that the present invention provides on the premise of ensureing pliability, can maintain the degree of sizing of paper, improves paper Surface strength, bursting strength and ring crush intensity and wet strength.
Detailed description of the invention
Detailed description below is merely to illustrate the present invention, but the present invention is not therefore subject to any restriction.
The present invention provides the preparation method of a kind of wet strength agent, and the method includes: by the polyamide polyamines of 30-100 weight portion Epoxychloropropane solution, the polyvinyl alcohol of 40-80 weight portion, the Nipagin ester of 55-120 weight portion, the metatitanic acid of 5-35 weight portion Potassium whisker, the linolenic acid of 10-30 weight portion, the propylene glycol of 10-20 weight portion, the water-soluble cellulose of 2-15 weight portion and 150- At 50-80 DEG C, in homogenizer, carry out homogenizing 1-5 hour after the water mixing of 1000 weight portions, obtain wet strength agent;Preferably, will The Polyamide-Polyamsne-Epichlorohydrin solution of 50-70 weight portion, the polyvinyl alcohol of 60-80 weight portion, the Buddhist nun of 70-100 weight portion Pool gold ester, 10-30 measure the potassium titanate crystal whisker of part, the linolenic acid of 20-30 weight portion, the propylene glycol of 15-20 weight portion, 6-10 weight Described homogenizing is carried out after the water-soluble cellulose of part and the water mixing of 300-800 weight portion.
Polyamide-Polyamsne-Epichlorohydrin (PAE) resin be current in, the wet strength agent of alkaline bleach liquor sizing, it is by divinyl three Amine (DE TA) and adipic acid react and prepare intermediate, then react the most available with epoxychloropropane (EPI).Such as, described polyamides The viscosity of amine epoxy polyamine chloropropane can be 15-50mPa s-1, pH is 3-5, and solid content can be 10-30 weight %, and density can Think 1.01-1.1g cm3
Potassium titanate crystal whisker is the chopped fiber complex of a kind of novel needle-like, has the most excellent mechanical property and physical property Can, it is referred to as the novel enhanced composite of 21st century, can use as heat-barrier material, reinforcing material, friction material, coating Raw material etc..The diameter of potassium titanate crystal whisker of the present invention can be 100-500 nanometer, and length can be 10-15 micron, tension Intensity can be 6.5-7.5GPa, and elastic modelling quantity can be 200-500GPa.
Water-soluble fibre is that one can be dissolved or meet water in water and slowly hydrolysed to water soluble molecules (or compound) Fiber, such as, described water-soluble cellulose can be chitosan or hydroxypropyl methyl cellulose.
Homogenizing also referred to as homogenate, is to make dispersion micronized in suspension (or emulsion) system, the process of homogenization Journey, this process plays simultaneously and reduces dispersion yardstick and improve the effect of dispersion distributing homogeneity.The condition of described homogenizing can Thinking: temperature is 60-70 DEG C, homogenizing time is 2-3 hour.
The present invention also provides for a kind of wet strength agent, and described wet strength agent includes the polyamide polyamines epoxy chloropropionate of 30-100 weight portion Alkane solution, the polyvinyl alcohol of 40-80 weight portion, the Nipagin ester of 55-120 weight portion, the potassium titanate crystal whisker of 5-35 weight portion, The linolenic acid of 10-30 weight portion, the propylene glycol of 10-20 weight portion, the water-soluble cellulose of 2-15 weight portion and 150-1000 weight The water of amount part.
Polyamide-Polyamsne-Epichlorohydrin (PAE) resin be current in, the wet strength agent of alkaline bleach liquor sizing, it is by divinyl three Amine (DE TA) and adipic acid react and prepare intermediate, then react the most available with epoxychloropropane (E PI).Such as, described poly- The viscosity of polyamide-polyamino epoxychloropropane can be 15-50mPa s-1, pH is 3-5, and solid content can be 10-30 weight %, density Can be 1.01-1.1g cm3
Potassium titanate crystal whisker is the chopped fiber complex of a kind of novel needle-like, has the most excellent mechanical property and physical property Can, it is referred to as the novel enhanced composite of 21st century, can use as heat-barrier material, reinforcing material, friction material, coating Raw material etc..The diameter of potassium titanate crystal whisker of the present invention can be 100-500 nanometer, and length can be 10-15 micron, tension Intensity can be 6.5-7.5GPa, and elastic modelling quantity can be 200-500GPa.
Water-soluble fibre is that one can be dissolved or meet water in water and slowly hydrolysed to water soluble molecules (or compound) Fiber, such as, described water-soluble cellulose can be chitosan or hydroxypropyl methyl cellulose.
Following example are used for illustrating the present invention, but are not limited to the scope of the present invention.
The method of testing of the embodiment of the present invention and comparative example is as follows:
Degree of sizing: use Cobb water absorbent surface gravimetric method, the quality absorbed water in paper unit are after comparing immersion, use g/ m2Represent.Measure according to GB GB/T461.3-2005.
Surface strength of paper: the surface of the speed printing paper to increase continuously, until plucking occurs in surface, uses cm s-1Table Show.Measure according to GB GB/T2679.15-1997.
Bursting strength: refer to the maximum pressure uniformly increased that Paper or cardboard can bear in unit are, carry out table with kPa Show.Burst index=bursting strength/quantitatively.Measure according to GB GB/T454-1989.
Dry tensile strength detects according to GB/T453-2002 method, and wet tensile (strength) is carried out according to GB/T652 method Detection, wet strength=wet tensile (strength)/dry tensile strength × 100%.
Ring crush intensity uses standard GB/T/T 2679.8-1995 to measure, and unit is N m/g.
Pliability uses DCRR Y 1000 type computer observing and controlling pliability instrument to be measured, and the numerical value of pliability is the least, represents Paper is the most soft, and unit is mN.
Manufacturing paper with pulp of page: under slow stirring, adds wet strength agent (or being added without) 100g/Kg in wood pulp and starches (wet feed Amount), carry out handsheet after stirring 5min, the quantitative 60g/m of handsheet2, pattern, in 110 DEG C of ripening 15min, is cooled in exsiccator Room temperature, places 24h standby.
Embodiment 1
By the Polyamide-Polyamsne-Epichlorohydrin solution of 30 grams, (viscosity is 35mPa s-1, pH is 3.3, and solid content is 21.3 Weight %, density is 1.05g cm3), the polyvinyl alcohol of 50 grams, the Nipagin ester of 55 grams, the potassium titanate crystal whisker (diameter 200 of 5 grams Nanometer, length 13 microns, tensile strength is 7.5GPa, and elastic modelling quantity is 300GPa), the linolenic acid of 10 weight portions, 15 weight portions Propylene glycol, the hydroxypropyl methyl cellulose of 2 weight portions and 800 weight portions water mixing after carry out in homogenizer at 50 DEG C Homogenizing 1 hour, obtains wet strength agent S1.Wet strength agent S1 is used for manufacturing paper with pulp of page, and specific experiment the results are shown in Table 1.
Embodiment 2
By the Polyamide-Polyamsne-Epichlorohydrin solution of 60 grams, (viscosity is 35mPa s-1, pH is 3.3, and solid content is 21.3 Weight %, density is 1.05g cm3), the polyvinyl alcohol of 40 grams, the Nipagin ester of 70 grams, the potassium titanate crystal whisker (diameter 200 of 20 grams Nanometer, length 13 microns, tensile strength is 7.5GPa, and elastic modelling quantity is 300GPa), the linolenic acid of 20 weight portions, 10 weight portions Propylene glycol, the hydroxypropyl methyl cellulose of 8 weight portions and 1000 weight portions water mixing after enter in homogenizer at 80 DEG C Row homogenizing 5 hours, obtains wet strength agent S2.Wet strength agent S2 is used for manufacturing paper with pulp of page, and specific experiment the results are shown in Table 1.
Embodiment 3
By the Polyamide-Polyamsne-Epichlorohydrin solution of 100 grams, (viscosity is 35mPa s-1, pH is 3.3, and solid content is 21.3 weight %, density is 1.05g cm3), the polyvinyl alcohol of 80 grams, the Nipagin ester of 120 grams, the potassium titanate crystal whisker of 35 grams (straight Footpath 200 nanometer, length 13 microns, tensile strength is 7.5GPa, and elastic modelling quantity is 300GPa), the linolenic acid of 30 weight portions, 20 weights At 70 DEG C, in homogenizer, homogenizing 5 is carried out after the water mixing of the amount propylene glycol of part, the chitosan of 12 weight portions and 300 weight portions Hour, obtain wet strength agent S3.Wet strength agent S3 is used for manufacturing paper with pulp of page, and specific experiment the results are shown in Table 1.
Comparative example 1
Carrying out manufacturing paper with pulp of page, be added without wet strength agent, specific experiment the results are shown in Table 1.
Comparative example 2
Comparative example 2 is substantially the same manner as Example 1, and difference is, is added without polyvinyl alcohol, obtains wet strength agent D1.By wet by force Agent D1 manufactures paper with pulp for page, and specific experiment the results are shown in Table 1.
Comparative example 3
Comparative example 3 is substantially the same manner as Example 1, and difference is, is added without potassium titanate crystal whisker, obtains wet strength agent D2.By wet Strong agent D2 manufacturing paper with pulp for page, specific experiment the results are shown in Table 1.
Comparative example 4
Comparative example 4 is substantially the same manner as Example 1, and difference is, is added without linolenic acid, obtains wet strength agent D3.By wet strength agent D3 manufactures paper with pulp for page, and specific experiment the results are shown in Table 1.
From the results shown in Table 1, the wet strength agent that the present invention provides can maintain paper on the premise of ensureing pliability The degree of sizing opened, improves surface strength of paper, bursting strength and ring crush intensity and wet strength.
Table 1

Claims (10)

1. the preparation method of a wet strength agent, it is characterised in that the method includes: by the polyamide polyamines ring of 30-100 weight portion Oxygen chloropropane solution, the polyvinyl alcohol of 40-80 weight portion, the Nipagin ester of 55-120 weight portion, the potassium titanate of 5-35 weight portion Whisker, the linolenic acid of 10-30 weight portion, the propylene glycol of 10-20 weight portion, the water-soluble cellulose of 2-15 weight portion and 150- At 50-80 DEG C, in homogenizer, carry out homogenizing 1-5 hour after the water mixing of 1000 weight portions, obtain wet strength agent.
Preparation method the most according to claim 1, it is characterised in that by the polyamide polyamines epoxy chlorine of 50-70 weight portion Propane solution, the polyvinyl alcohol of 60-80 weight portion, the Nipagin ester of 70-100 weight portion, 10-30 measure part potassium titanate crystal whisker, The linolenic acid of 20-30 weight portion, the propylene glycol of 15-20 weight portion, the water-soluble cellulose of 6-10 weight portion and 300-800 weight Described homogenizing is carried out after the water mixing of part.
Preparation method the most according to claim 1, it is characterised in that the viscosity of described Polyamide-Polyamsne-Epichlorohydrin is 15-50mPa·s-1, pH is 3-5, and solid content is 10-30 weight %, and density is 1.01-1.1g cm3
Preparation method the most according to claim 1, it is characterised in that the diameter 100-500 nanometer of described potassium titanate crystal whisker, Length 10-15 micron, tensile strength is 6.5-7.5GPa, and elastic modelling quantity is 200-500GPa.
Preparation method the most according to claim 1, it is characterised in that described water-soluble cellulose is chitosan or hydroxypropyl Methylcellulose.
Preparation method the most according to claim 1, it is characterised in that the condition of described homogenizing is: temperature is 60-70 DEG C, Homogenizing time is 2-3 hour.
7. a wet strength agent, it is characterised in that described wet strength agent includes the Polyamide-Polyamsne-Epichlorohydrin of 30-100 weight portion Solution, the polyvinyl alcohol of 40-80 weight portion, the Nipagin ester of 55-120 weight portion, the potassium titanate crystal whisker of 5-35 weight portion, 10- The linolenic acid of 30 weight portions, the propylene glycol of 10-20 weight portion, the water-soluble cellulose of 2-15 weight portion and 150-1000 weight portion Water.
Wet strength agent the most according to claim 7, it is characterised in that the viscosity of described Polyamide-Polyamsne-Epichlorohydrin is 15-50mPa·s-1, pH is 3-5, and solid content is 10-30 weight %, and density is 1.01-1.1g cm3
Wet strength agent the most according to claim 7, it is characterised in that the diameter 100-500 nanometer of described potassium titanate crystal whisker, long Degree 10-15 micron, tensile strength is 6.5-7.5GPa, and elastic modelling quantity is 200-500GPa.
Wet strength agent the most according to claim 7, it is characterised in that described water-soluble cellulose is chitosan or hydroxypropyl Methylcellulose.
CN201610452057.4A 2016-06-20 2016-06-20 The preparation method of a kind of wet strength agent and wet strength agent Pending CN106087564A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
CN201610452057.4A CN106087564A (en) 2016-06-20 2016-06-20 The preparation method of a kind of wet strength agent and wet strength agent

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
CN201610452057.4A CN106087564A (en) 2016-06-20 2016-06-20 The preparation method of a kind of wet strength agent and wet strength agent

Publications (1)

Publication Number Publication Date
CN106087564A true CN106087564A (en) 2016-11-09

Family

ID=57238322

Family Applications (1)

Application Number Title Priority Date Filing Date
CN201610452057.4A Pending CN106087564A (en) 2016-06-20 2016-06-20 The preparation method of a kind of wet strength agent and wet strength agent

Country Status (1)

Country Link
CN (1) CN106087564A (en)

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107044071A (en) * 2017-04-12 2017-08-15 镇江市天亿化工研究设计院有限公司 A kind of production method of wet strength agent
CN109610227A (en) * 2018-11-22 2019-04-12 山东同创精细化工股份有限公司 A kind of low chlorine ion wet strength agent and preparation method thereof

Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120160437A1 (en) * 2010-12-22 2012-06-28 Bayer Materialscience Ag Process for the production of sized and/or wet-strength papers, paperboards and cardboards
CN103806330A (en) * 2012-11-09 2014-05-21 王慧 Papermaking enhancing method
CN103866638A (en) * 2014-02-28 2014-06-18 苏州恒康新材料有限公司 Environment-friendly wet strength agent and preparation method thereof
CN103866631A (en) * 2014-02-25 2014-06-18 苏州恒康新材料有限公司 Wet strength agent rich in fumaric acid and preparation method thereof
CN103981758A (en) * 2014-04-21 2014-08-13 苏州恒康新材料有限公司 Kraft paper wet strength agent and preparation method thereof
CN104179074A (en) * 2013-05-28 2014-12-03 陈银凤 Method for producing polyamide resin wet strength agent
CN105568761A (en) * 2014-10-17 2016-05-11 东升新材料(山东)有限公司 Tearing strength reinforcing agent for papermaking and preparation method of tearing strength reinforcing agent

Patent Citations (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US20120160437A1 (en) * 2010-12-22 2012-06-28 Bayer Materialscience Ag Process for the production of sized and/or wet-strength papers, paperboards and cardboards
CN103806330A (en) * 2012-11-09 2014-05-21 王慧 Papermaking enhancing method
CN104179074A (en) * 2013-05-28 2014-12-03 陈银凤 Method for producing polyamide resin wet strength agent
CN103866631A (en) * 2014-02-25 2014-06-18 苏州恒康新材料有限公司 Wet strength agent rich in fumaric acid and preparation method thereof
CN103866638A (en) * 2014-02-28 2014-06-18 苏州恒康新材料有限公司 Environment-friendly wet strength agent and preparation method thereof
CN103981758A (en) * 2014-04-21 2014-08-13 苏州恒康新材料有限公司 Kraft paper wet strength agent and preparation method thereof
CN105568761A (en) * 2014-10-17 2016-05-11 东升新材料(山东)有限公司 Tearing strength reinforcing agent for papermaking and preparation method of tearing strength reinforcing agent

Cited By (2)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CN107044071A (en) * 2017-04-12 2017-08-15 镇江市天亿化工研究设计院有限公司 A kind of production method of wet strength agent
CN109610227A (en) * 2018-11-22 2019-04-12 山东同创精细化工股份有限公司 A kind of low chlorine ion wet strength agent and preparation method thereof

Similar Documents

Publication Publication Date Title
Balea et al. Industrial application of nanocelluloses in papermaking: a review of challenges, technical solutions, and market perspectives
EP2616585B1 (en) Modified cellulose fibres
EP3049568B1 (en) Method for preparing furnish and paper product
Kajanto et al. The potential use of micro-and nanofibrillated cellulose as a reinforcing element in paper
JP6132020B2 (en) Method for producing fine fiber-containing sheet
BRPI0608971B1 (en) process for producing a paper and paper produced according to the process
CN106087564A (en) The preparation method of a kind of wet strength agent and wet strength agent
CN104213469B (en) Micro-retractility printed form decorating base paper and preparation method thereof
Sabazoodkhiz et al. Interaction of chitosan biopolymer with silica nanoparticles as a novel retention/drainage and reinforcement aid in recycled cellulosic fibers
CN112761027A (en) Environment-friendly medical gummed paper
Milanovic et al. The effect of nanofibrillated tempo-oxidized cotton linters on the strength and optical properties of paper
US3445330A (en) Method of sizing paper with carboxylic acid anhydride particles and polyamines
CN105940157B (en) A kind of stabilisation sizing preparation
CN106917324A (en) A kind of paper-making sizing method and its paper of preparation
WO2008143580A1 (en) Process for the production of a cellulosic product
CN104364442B (en) Method, gained emulsion for producing a kind of emulsion of the alkenyl succinic anhydride (ASA) in the aqueous solution of cationic starch metallic substance and application thereof
CN114960290B (en) Cover paper special for license, and preparation method and application thereof
JP2015522725A (en) Aqueous suspensions of titanium dioxide and cationic starch-like substances for making paper and cardboard
JP5242365B2 (en) Method for producing pharmaceutical composition for papermaking
JP6525896B2 (en) Paper strength agent and method of producing paper
US3250665A (en) Process of modifying a paper web with epoxy resins by addition of polyalkyl-acrylamide degradation product in formation of the paper
JP2018165418A (en) Method of producing paper towel
Ghofran et al. Application of cellulosic nanofibers to replace with imported long-fiber pulps in paper made from bagasse
CN112982018B (en) Method for improving physical strength performance of paper by using cellulose nanofibril-hyaluronic acid-chitosan mixed emulsion
Yurtayeva et al. Industrial Hemp Hurd Processing for Microcrystalline Cellulose Production and its Usage as a Filler in Paper

Legal Events

Date Code Title Description
C06 Publication
PB01 Publication
C10 Entry into substantive examination
SE01 Entry into force of request for substantive examination
CB02 Change of applicant information
CB02 Change of applicant information

Address after: Nansha District Fengze road Guangzhou city Guangdong province 511458 No. 106 X1301-B437

Applicant after: Guangzhou poly injection General Technology Research Institute Co Ltd

Address before: Nansha District Fengze road Guangzhou city Guangdong province 511458 No. 106 X1301-B437

Applicant before: GUANGZHOU JUZHU PATENT RESEARCH AND DEVELOPMENT CO., LTD.

RJ01 Rejection of invention patent application after publication
RJ01 Rejection of invention patent application after publication

Application publication date: 20161109