US1607518A - Process of treating paper pulp - Google Patents

Process of treating paper pulp Download PDF

Info

Publication number
US1607518A
US1607518A US101581A US10158126A US1607518A US 1607518 A US1607518 A US 1607518A US 101581 A US101581 A US 101581A US 10158126 A US10158126 A US 10158126A US 1607518 A US1607518 A US 1607518A
Authority
US
United States
Prior art keywords
pulp
wax
emulsion
paper
hydrocellulose
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired - Lifetime
Application number
US101581A
Inventor
Ellis Carleton
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.)
Ellis Foster Co
Original Assignee
Ellis Foster Co
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 Ellis Foster Co filed Critical Ellis Foster Co
Priority to US101581A priority Critical patent/US1607518A/en
Application granted granted Critical
Publication of US1607518A publication Critical patent/US1607518A/en
Anticipated expiration legal-status Critical
Expired - Lifetime 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
    • D21H17/00Non-fibrous material added to the pulp, characterised by its constitution; Paper-impregnating material characterised by its constitution
    • D21H17/60Waxes
    • 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
    • D21H23/00Processes or apparatus for adding material to the pulp or to the paper
    • D21H23/02Processes or apparatus for adding material to the pulp or to the paper characterised by the manner in which substances are added
    • D21H23/04Addition to the pulp; After-treatment of added substances in the pulp
    • D21H23/06Controlling the addition
    • D21H23/08Controlling the addition by measuring pulp properties, e.g. zeta potential, pH

Definitions

  • lhis invention relates to a process of treating paper pulp for use in paper mak ing and involves a new and novel method for increasing the absorptive capacity of the a pulp for wax emulsions or dispersions and other sizes.
  • the treatment is of particular value in the preparation of waterproof and transparent or translucent paper.
  • an emulsion oi the wax, or mixtures thereof with oils, resins, starches, and the like employing water as a vehicle, and preferably usin a colloid mill to convert the waterproo ng agent into a state of extreme fineness or dispersion.
  • a small amount of a soluble soap such as sodium, potassium or ammonium stearate, palmitate, resinate, and the like.
  • an alkaline salt such as sodium phosphate, soda ash, or of an alkali, such as caustic soda or potash, may be employed instead of the soap.
  • the use of such salts is particularly desirable when tree rosin or fatty acids have been added to the mixture.
  • the sheet is formed in the usual manner.
  • Such waxes as paraiiin, Montan, ceresin, carnauba, japan, beeswax, etc., are suitable for the purpose of my invention, although, I in most cases, I employ paraffin, particularly as on accountof its low cost.
  • hydrocellulose may to be formed by a very prolonged action of pulp in the beater engine, I find it more economical, in most cases, to accelerate the "formation of hydrocellulose by means of acid hydrolysis.
  • acid hydrolysis it is desirable 7 to conduct this acid hydrolysis separately and previous to the introduction of the wax dispersion, although, in some cases, the acid hydrolysis may be employed in the beater simultaneously with the incorporation of the so wax emulsion. Since the various acids and salts which may be employed for this treatment are rather corrosive, it is, however, more preferable to treat the pulp previous to the treatment in the beater. In order to a accelerate the formation of hydrocellulose,
  • I may add to the pulp such substances as sulphuric, hydrochloric, phosphoric and oxalic acids, or acid salts such as sodium or pota:sium bisulphates, zinc chloride, and such other salts as potassium iodide, calcium thiocyanide and various other salts which are found to accelerate the formation or production of hydrocellulose.
  • sulphuric, hydrochloric, phosphoric and oxalic acids, or acid salts such as sodium or pota:sium bisulphates, zinc chloride, and such other salts as potassium iodide, calcium thiocyanide and various other salts which are found to accelerate the formation or production of hydrocellulose.
  • 'lhese substances generally exert the most pronounced 95 effect when used at an elevated temperature, i. e., over 80 C. and it is usually necessary to heat the pulp with'the concentrated salt solutions above 80 C. for proper. modification or the fibres with formation of hydrocellulose. Stronger chemicals such as sulhuric acid, when used,
  • a pulp which has been brought substantially on the acid side that is, having a p value of less than 7, but not substantially less than 1.5, since too great an acidity is harmful since it is apt to break down the emulsion and cause coagulation of the colloidally dispersed wax particles, whereby the proper absorption .will not occur.
  • soaps tend to make the emulsion too alkaline and are apt to cause foaming in the beater engine when the emulsion and pulp are blended.
  • a suitable emulsion may be made in a colloid mill, employing, say, paraflin wax of 135 F. melting point. This was melted in a steam jacketed container and introduced into the mill with an aqueous solution of potassium oleate in equal volumes, the water containing one per cent of potassium oleate. This calculated to give a concentration of per cent of potassium oleate in the finished emulsion.
  • Emulsions prepared by the use of a colloid mill are stable with the presence of a very materially less quantity of stabilizing agent (as the potassium oleate lose is formed in substantial amount.
  • emulsions prepared by other means ous other acids or salts may be used in lieu in this case) than emulsions prepared by other means.
  • the dispersion of the wax is in a state of much finer division than emulsions prepared by other methods.
  • This particular emulsion exhibits Brownian movement, which is common in emulsions prepared by the use of a colloid mill. This is not characteristic of the usual emulsions pre ared by other means.
  • the novel feature of my invention consists in the use of a ulp, either with or without, the presence of the adjustment of the hydrogen ion concentration, in order to promote sizing efficiency.
  • I may treat the aper or paper pulp to accelerate the forma tion of hydrocellulose, but in the preferred form I use sulphuric acid of specific gravity of approximately 1.52 and treat the pulp with this acid for several hours at room temperature, then wash and adjust hydrogen ion concentration. Hydrocellu- Variof this treatment, as previously described.
  • What I claim is 1.
  • the step which comprises the adjustment of the hydrogen ion concentration of the pulp so as to increase the absorption of a wax emulsion.
  • a process for treating paper pulp a wax in an aqueous medium. which contains hydrocellulose comprising 3.
  • the adjustment of thehydrogen ion concen- 10 step which consists in bringing the pulp to a tration of said pulp so as to increase the 5 p value of between 1.5 and 7, and incorabsorption of a wax emulsion.

Description

Patented Nov. 16, 1926.
GARLETON ELLIS, OE
MONTCLAIR, NEW JERSEY, ASSIGNQR '10 ELLIS-FOSTER; COM- FANY, A. CORPORATION @E NEW JERSEY.
rnocnss or ranarnra nnrnn rear.
Ito Drawing. Application filed April is,
lhis invention relates to a process of treating paper pulp for use in paper mak ing and involves a new and novel method for increasing the absorptive capacity of the a pulp for wax emulsions or dispersions and other sizes. The treatment is of particular value in the preparation of waterproof and transparent or translucent paper.
Various sizes and methods of sizing for paper and paper products have been suggested, and in many cases, used. The most generally used method for Waterproofing paper consists in preparing a sheet of paper, immersing it in a bath of molten wax, oil or resin. In same cases, the emulsions containing waxes have been incorporated with the pulp prior to paper manufacture. In general considerable dificulty has been experienced in securing proper absorption and dispersion.
In carrying out my invention ll prepare an emulsion oi the wax, or mixtures thereof with oils, resins, starches, and the like, employing water as a vehicle, and preferably usin a colloid mill to convert the waterproo ng agent into a state of extreme fineness or dispersion. It is advantageous, but not essentially necessary to previously dissolve in the water a small amount of a soluble soap, such as sodium, potassium or ammonium stearate, palmitate, resinate, and the like. In other cases, a small amount of an alkaline salt such as sodium phosphate, soda ash, or of an alkali, such as caustic soda or potash, may be employed instead of the soap. The use of such salts is particularly desirable when tree rosin or fatty acids have been added to the mixture.
Having prepared the emulsion by means of a powerful emulsifying means such as the aforesaid colloid mill, 1 introduce'said emulsion into the beater with the pulp. I find it highly desirable to add the emulsion to the pulp substantially at the beginning of the beating operation, as this accom lishes a very much better dispersion and a sorption than by adding the emulsion at a later stage. The dis ersion is rapidly absorbed by the fibres (t e speed and extent of absorption depending to a large extent on the propor- 1926. 1 serial l lo. 103L593.
tion of hydrocellulose present) and after suficient time has elapsed, the sheet is formed in the usual manner.
In order to obtain the maximum amount of absorption, 1 find it occasionally desirable 55 to add the wax dispersion to the pulp in the beater at a temperature substantially above the melting point of the wax employed. In most cases the temperature of boiling water is about right, although temperatures as low so as 90 C. are in some cases suitable.
Such waxes as paraiiin, Montan, ceresin, carnauba, japan, beeswax, etc., are suitable for the purpose of my invention, although, I in most cases, I employ paraffin, particularly as on accountof its low cost.
In order to obtain the maximum absorption I have found that it is necessary to use a pulp containing. a substantial amount of hydrocellulose. While hydrocellulose may to be formed by a very prolonged action of pulp in the beater engine, I find it more economical, in most cases, to accelerate the "formation of hydrocellulose by means of acid hydrolysis. In general, it is desirable 7 to conduct this acid hydrolysis separately and previous to the introduction of the wax dispersion, although, in some cases, the acid hydrolysis may be employed in the beater simultaneously with the incorporation of the so wax emulsion. Since the various acids and salts which may be employed for this treatment are rather corrosive, it is, however, more preferable to treat the pulp previous to the treatment in the beater. In order to a accelerate the formation of hydrocellulose,
I may add to the pulp such substances as sulphuric, hydrochloric, phosphoric and oxalic acids, or acid salts such as sodium or pota:sium bisulphates, zinc chloride, and such other salts as potassium iodide, calcium thiocyanide and various other salts which are found to accelerate the formation or production of hydrocellulose. 'lhese substances generally exert the most pronounced 95 effect when used at an elevated temperature, i. e., over 80 C. and it is usually necessary to heat the pulp with'the concentrated salt solutions above 80 C. for proper. modification or the fibres with formation of hydrocellulose. Stronger chemicals such as sulhuric acid, when used, usually require no heating.
In order to obtain maximum absorption of wax sizes or emulsions by the pulp I have found not only that the PIGZGHCG of hydro-' Gellulose is of particular value, but that in 'drder'to obtain maximum absorptlon of the wax, it is highly desirable to bring the pulp to a definite hydrogen ion concentratlon prior to the incorporation with the wax emulsion. It would seem that the pulp should be maintained sli htly on the acid side in order to bring=a out the greater, more uniform and rapid absorption of the wax emulsion or size employed.
The hydrogen ion concentration which is an exact measure of acidity, particularly when in low concentrations, is usually stated on what is known as a p scale. 7.0 is the neutral point. Higher values of p above 7, indicate increase in alkalinity. The lower values below 7 indicate increase in acidity.
Accordingly, I prefer to employ a pulp which has been brought substantially on the acid side, that is, having a p value of less than 7, but not substantially less than 1.5, since too great an acidity is harmful since it is apt to break down the emulsion and cause coagulation of the colloidally dispersed wax particles, whereby the proper absorption .will not occur.
Ordinary sulphite pulp was found to have a p value of approximately 6.8, and it was found that when this pulp was subjected to a beating treatment over a period of twentyfour h0u1s, or so, or merely heated in boiling water for several hours, that the acidity increased. My invention includes the treatment of pulp in such manner to bring about a change of the hydrogen ion concentration, or, in case the p value of any given pulp needs adjustment, I may readily do so by the addition of a proper amount of acid or alkali, as the case may require.
I prefer to employ wax dispersions or emulsions containing a minimum of soap since soaps tend to make the emulsion too alkaline and are apt to cause foaming in the beater engine when the emulsion and pulp are blended.
A suitable emulsion may be made in a colloid mill, employing, say, paraflin wax of 135 F. melting point. This was melted in a steam jacketed container and introduced into the mill with an aqueous solution of potassium oleate in equal volumes, the water containing one per cent of potassium oleate. This calculated to give a concentration of per cent of potassium oleate in the finished emulsion. Emulsions prepared by the use of a colloid mill are stable with the presence of a very materially less quantity of stabilizing agent (as the potassium oleate lose is formed in substantial amount.
ous other acids or salts may be used in lieu in this case) than emulsions prepared by other means. The dispersion of the wax is in a state of much finer division than emulsions prepared by other methods. This particular emulsion exhibits Brownian movement, which is common in emulsions prepared by the use of a colloid mill. This is not characteristic of the usual emulsions pre ared by other means. A
1i parts by weight of glassine or other ulp, may be lncorporated with 10 parts y weight of paraffin wax emulsion containing 5.75 parts by weight of water, 4% parts by weight of paraflin and E; part by weight of potassium oleate. Many other emulsions and various preportions may be used for the production of various papers, and I do not wish to limit myself to any specific proportion, the exact proportion for any given paper being readily determined by anyone skilled in the art.
The novel feature of my invention consists in the use of a ulp, either with or without, the presence of the adjustment of the hydrogen ion concentration, in order to promote sizing efficiency.
There are several ways in which I may treat the aper or paper pulp to accelerate the forma tion of hydrocellulose, but in the preferred form I use sulphuric acid of specific gravity of approximately 1.52 and treat the pulp with this acid for several hours at room temperature, then wash and adjust hydrogen ion concentration. Hydrocellu- Variof this treatment, as previously described.
In order to produce a more flexible waterproof paper suitable for the manufacture of milk bottle caps and waterproof papers suitable for use on food containers, I prefer to use a wax dispersion containing a substantial amount of a colorless paraflin oil, such as is known to the trade as marcol and whose boiling point is substantially over 200 C. and specific gravity .850 at 17 C. The use of this oil confers added flexibility upon thewaterproof product and is therefore highly advantageous especially where product is to be drawn through dies. In certain cases various other petroleum oils may be used, although the pure, almost medicinal grade of oil, known to the trade as marcol is to be preferred for the production of waterproof papers which are to be used on food containers.
What I claim is 1. In the process of making paper, the step which comprises the adjustment of the hydrogen ion concentration of the pulp so as to increase the absorption of a wax emulsion.
2. In the process of making paper, the step which consists in bringing the pulp to a p value of between 1.5 and 7, and incorhvdrocellulose, with porating therewith a colloidal dispersion of 4. A process for treating paper pulp a wax in an aqueous medium. which contains hydrocellulose comprising 3. In the process of making paper, the the adjustment of thehydrogen ion concen- 10 step which consists in bringing the pulp to a tration of said pulp so as to increase the 5 p value of between 1.5 and 7, and incorabsorption of a wax emulsion.
porating therewith a colloidal dispersion of a wax and a size. Y CARLETQN ELLIS.
US101581A 1926-04-12 1926-04-12 Process of treating paper pulp Expired - Lifetime US1607518A (en)

Priority Applications (1)

Application Number Priority Date Filing Date Title
US101581A US1607518A (en) 1926-04-12 1926-04-12 Process of treating paper pulp

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US101581A US1607518A (en) 1926-04-12 1926-04-12 Process of treating paper pulp

Publications (1)

Publication Number Publication Date
US1607518A true US1607518A (en) 1926-11-16

Family

ID=22285399

Family Applications (1)

Application Number Title Priority Date Filing Date
US101581A Expired - Lifetime US1607518A (en) 1926-04-12 1926-04-12 Process of treating paper pulp

Country Status (1)

Country Link
US (1) US1607518A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3000383A (en) * 1955-09-01 1961-09-19 American Mach & Foundry Method of forming tobacco composition

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3000383A (en) * 1955-09-01 1961-09-19 American Mach & Foundry Method of forming tobacco composition

Similar Documents

Publication Publication Date Title
US2113034A (en) Starch sizing of paper
US2430674A (en) Method of bleaching
US2228976A (en) Molding material and method of producing the same
US1607518A (en) Process of treating paper pulp
US2225100A (en) Manufacture of sheets or boards containing mineral wool
US1958202A (en) Method of making sizing material
US2192488A (en) Method of making paper
US2096129A (en) Manufacture of sized papers
US1607517A (en) Process of paper making
US2197383A (en) Sizing of paper
US2178606A (en) Paper manufacture
US3817768A (en) Method of preparing aqueous dispersions of fortified rosin.
US2099880A (en) Composition of matter adapted for increasing the water-resistance of fibrous substances specifically paper products and process of making same
US2015796A (en) Waterproofing composition and method of making and applying the same
US1897694A (en) Paper composition and process of making same
US2116768A (en) Sizing paper
US1882680A (en) Sizing fibrous materials
US2132607A (en) Bituminous emulsions and method of producing same
US1993750A (en) Composition of matter and process of making the same
US1808068A (en) Manufacture of paper
US1953085A (en) Paper waxing composition
US2067853A (en) Method for the preparation of aralkyl ethers of cellulose
US2693424A (en) Sized paper product, size and method of making the same
US1899086A (en) Paper product sized with petroleum hydrocarbons and process of making the same
US1886120A (en) Paper manufacture