US3598677A - Method of securing stacked packages against slipping - Google Patents

Method of securing stacked packages against slipping Download PDF

Info

Publication number
US3598677A
US3598677A US3598677DA US3598677A US 3598677 A US3598677 A US 3598677A US 3598677D A US3598677D A US 3598677DA US 3598677 A US3598677 A US 3598677A
Authority
US
United States
Prior art keywords
dispersion
film forming
dispersions
aqueous
parts
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
Inventor
Eduard Bergmeister
Joseph Heckmaier
Heinz Winkler
Hubert Wiest
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.)
Wacker Chemie AG
Original Assignee
Wacker Chemie AG
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 Wacker Chemie AG filed Critical Wacker Chemie AG
Application granted granted Critical
Publication of US3598677A publication Critical patent/US3598677A/en
Anticipated expiration legal-status Critical
Expired - Lifetime legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09JADHESIVES; NON-MECHANICAL ASPECTS OF ADHESIVE PROCESSES IN GENERAL; ADHESIVE PROCESSES NOT PROVIDED FOR ELSEWHERE; USE OF MATERIALS AS ADHESIVES
    • C09J131/00Adhesives based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by an acyloxy radical of a saturated carboxylic acid, of carbonic acid, or of a haloformic acid; Adhesives based on derivatives of such polymers
    • C09J131/02Homopolymers or copolymers of esters of monocarboxylic acids
    • C09J131/04Homopolymers or copolymers of vinyl acetate
    • CCHEMISTRY; METALLURGY
    • C09DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
    • C09KMATERIALS FOR MISCELLANEOUS APPLICATIONS, NOT PROVIDED FOR ELSEWHERE
    • C09K3/00Materials not provided for elsewhere
    • C09K3/14Anti-slip materials; Abrasives
    • C09K3/149Antislip compositions
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
    • C08L2666/28Non-macromolecular organic substances
    • CCHEMISTRY; METALLURGY
    • C08ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
    • C08LCOMPOSITIONS OF MACROMOLECULAR COMPOUNDS
    • C08L2666/00Composition of polymers characterized by a further compound in the blend, being organic macromolecular compounds, natural resins, waxes or and bituminous materials, non-macromolecular organic substances, inorganic substances or characterized by their function in the composition
    • C08L2666/54Inorganic substances
    • 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
    • Y10TECHNICAL SUBJECTS COVERED BY FORMER USPC
    • Y10STECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y10S206/00Special receptacle or package
    • Y10S206/813Adhesive

Definitions

  • the slippage-preventing agents which have been used heretofore in an attempt to solve the above problem are aqueous alkali silicate solutions, starch solutions, rubber or natural resin dispersions.
  • the alkali silicate solutions have the drawback that they have the effect of sticking so tenaciously that when the stacks are taken down the packings are damaged by tearing of the paper fibers, or after removal from the stacks films remain on the packing which crumbles easily and thus can easily contaminate the merchandise when the packages are emptied.
  • Natural resin dispersions have the same drawback.
  • the other anti-slipping adhesives that have been used heretofore could not be adjusted in their adhesive power to such an extent as to achieve a sufficient adhesive effect for reducing slippage in the stacks and at the same time to prevent damage to the packing due to tearing of the paper fibers or tearing of the packages when the stacks were removed.
  • Our invention provides a method of securing stacked packages against slipping while at the same time permitting such packages to be readily separated without tearing or otherwise damaging the packages, such as the fibers of paper bags when the latter are separated, and without crumbling or shredding in such a way as to contaminate the contents of the packages when the latter are opened and in use.
  • the adhesives which we use as anti-slipping agents are characterized by the fact that they comprise an aqueous dispersion of an olefinic unsaturated compound which forms a film at a temperature of not more than +10 C., in admixture with inorganic and/or organic pigments.
  • the film forming temperature also called white point or lowest temperature for film forming (for the definition see R. Houwink and A. I. Stavermann, Chemistry and Technology of Plastics, 4th ed., vol. II/2, p. 653) can be obtained from advertising pamphlets of the com 3,598,677 Patented Aug.
  • aqueous dispersions from polymerizates of olefinic unsaturated compounds with a film-forming temperature of not exceeding +10 C those preferred are aqueous dispersions of polymerizates and/or copolymerizates of vinyl acetate with a film forming temperature of +10 C.
  • aqueous dispersions of polyvinyl acetate which contain plasticizers for polyvinyl acetate like dibutyl phthalate or tricresyl phosphate, and/or soft resins like low-molecular polyesters or polyvinyl ethers in quantities of 5 to 50 weight percent, preferably 20 to 30 weight percent, always referred to the weight of the polyvinyl acetate, i.e. which are externally softened dispersions of polymerizates of vinyl acetate. At times these aqueous dispersions could also be dispersions of copolymerizates of vinyl acetate.
  • plasticizers for polyvinyl acetate are esters of phosphoric acid like tributyl phosphate and diphenyl cresylphosphate, esters of phthalic acid like di-2-ethylhexyl phthalate and di-nbutylglycol phthalate, esters of adipic acid like dibutyl adipate, dihexyl adipate and dioctyl adipate, esters of sebacic acid like diethylhexyl sebacate, dibutyl and dihexyl sebacate.
  • aqueous externally softened dispersions of polymerizates or copolymerizates of vinyl acetate are those aqueous dispersions of copolymerizates of vinyl acetate with a film forming temperature not exceeding +10 C. which can be called aqueous, internally softened polyvinyl acetate dispersions.
  • the polymers in the last-mentioned kind of dispersions are preferably copolymers of 30 to 90 weight percent vinyl acetate and 70 to 10 weight percent vinyl esters of saturated aliphatic monocarboxylic acids with 3 to 18 carbon atoms, like vinyl propionate, vinyl laurate or vinyl stearate, esters of saturated aliphatic alcohols with 3 to 18 carbon atoms, aliphatic unsaturated dicarboxylic acids with 4 carbon atoms like maleic acid dibutyl ester, maleic acid di-2 ethylhexyl ester, fumaric acid dibutyl ester or fumaric acid di-2-ethylhexyl ester, esters of saturated aliphatic alcohols with 1 to 18 carbon atoms, of acrylic acid or methacrylic acid, like acrylic acid butyl ester and/or ethylene.
  • aqueous internally softened polyvinyl acetate dispersions with a film forming temperature of not exceeding +10 C. is well known.
  • copolymerizates of vinyl acetate which are principally contained in an aqueous internally softened polyvinyl acetate dispersion with a film forming temperature of not more than +10 C. are copolymerizates of 60% vinyl acetate and 40% maleic acid dibutyl ester 60% vinyl acetate and 40% vinyl laurate vinyl acetate and 25% vinyl laurate (Each of the above percentages refers to the total weight of the polymerizate.)
  • fillers which are not soluble in water or which are hard to dissolve in water, i.e. which dissolve not more than 1 weight part in 100 to 1000 weight parts of water at 20 C., which are inert towards the polymerizate dispersion, in the form of more or less dry powders.
  • the following examples may be mentioned for such fillers: chalk, light spar, i.e. unburned ground gypsum, kaolin, silicon dioxide produced or precipitated pyrogenically in the gaseous phase, wood flour or products similar to wood flour like peanut shell flour and cork powder.
  • pigments aqueous dispersions of plastics, particularly of polymerizates of olefinic unsaturated compounds with a film forming temperature of at least +40 C.--because of the decreased danger of the finished mixtures separating.
  • pigments of this kind as finely dispersed particles used in the form of aqueous dispersions which do not form any film below +40 C., consisting of polymerizates of olefinic unsaturated compounds.
  • the upper limit of dispersions with film forming temperatures of at least +40 C. is not decisive.
  • the film forming temperature of these dispersions may be 150 C. or more.
  • polymerizates in aqueous dispersions of polymerizates of olefinic unsaturated compounds with a film forming temperature of at least +40 C. may be named: Polyvinyl chloride, polystyrol, copolymerizates of 2 to 70 weight parts vinyl acetate and 98 to 30 weight percent vinyl chloride, copolymerizates of 70 to 95 weight percent styrol and 30 to 5 weight percent butadiene as well as copolymerizates of 70 to 95 weight percent acrylic nitrile and 30 to 5 weight percent butadiene.
  • aqueous dispersions of polymerizates of olefinic unsaturated compounds with a film forming temperature of at least +40 C. is likewise well known.
  • copolymerizates which are contained in such dispersions are those of:
  • aqueous dispersions of polymerizates of olefinic unsaturated compounds with a film forming temperature of at least +40 C. are available commercially, for instance from Wacker-Chemie G.m.b.H., Kunststoff, Germany, under the name Vinnol-Dispersion 45 and from the Chemical Works Hills A.G., Marl-Hiils, Germany, under the name Litex SB 15. (The name Vinnol as well as the name Litex are registered trademarks.)
  • the aqueous dispersions with a film forming .4 temperature of at least +40 C. are used in such quanti ties that 20 to 500, especially from 60 to 200, weight percent (each time referred to the polymerizate in the aqueous polymerizate dispersion with a film forming temperature of not more than 10 C.) of the polymerizate of the aqueous polymerizate dispersion with a film forming temperature of at least +40 C. are available.
  • aqueous dispersions with a film forming temperature of at least +10 C. it is particularly helpful to use as aqueous dispersions with a film forming temperature of not more than +10 C. no dispersions containing any softeners, but to use internally softened polyvinyl acetate dispersions in order to avoid having the film forming temperature of the dispersion used as a pigment reduced by the softener content of the dispersions with a low film forming temperature.
  • the aqueous polymerizate dispersions with a film forming temperature of not more than +10 C. as well as the aqueous polymerizate dispersions with film forming temperatures of at least +40 C. should have in each case to weight percent of the dispersed polymer particles with a diameter of a maximum of 2 microns.
  • Such polymerizate dispersions are usually manufactured in accordance with known methods of the so-called dispersion polymerization or by emulsion polymerization.
  • the manufacture of the adhesives used as anti-slipping agents pursuant to our invention consists of mixing the compounds with each other until a homogeneous mixture is obtained.
  • the temperature and pressure are of no consequence during mixing and during use of the antislipping agents.
  • the water content of the anti-slipping agents can be adjusted to the viscosity required for each other.
  • the application of the anti-slipping agents is done by applying said anti-slipping agents during stacking to the sides of the packages that get in contact with the sides of other packages, and perhaps also to the side of the pallet which gets in contact with the first layer of packages, in each case immediately before the packages are placed upon it.
  • the anti-slipping agents can be applied by spraying on or brushing on, e.g. with a brush or with a roller over the entire surface where slippage is to be prevented, or only on certain spots on these surfaces, e.g. by point or Wave patterns.
  • the anti-slipping agents are particularly useful for paper bags, but they can also be used effectively on cartons made of full or corrugated cardboard and folding boxes and other packaging materials made of paper or cardboard.
  • the anti-slipping agents disclosed herein will bind Within one-half to one whole hour after application, and even if application is made only in certain spots the result is safe stacks which will not slip during loading or transportation.
  • the packages can be separated again easily and without damage.
  • the film remaining on the packages adheres firmly to the package surfaces, it is pliable and will not crumble even when the surfaces are bent.
  • EXAMPLE 1 67 parts of a 50% aqueous dispersion of a copolymerizate of 60 parts vinyl acetate and 40 parts vinyl laurate, with a film forming temperature of 0 0., containing as a dispersion agent about 3 percent polyvinyl alcohol with the saponification number (milligrams KOH, required for splitting off and neutralizing the remaining acetyl groups in 1 g. polyvinyl alcohol) of and wherein at least 80% of the dispersed polymer particles have diameters within the range from 1 to 2 microns, are stirred with 133 parts light spar which were first mixed with 75 parts wat un il a homogeneous mix is obtained.
  • the anti-slipping agent obtained in this manner is properly diluted before use with three parts of water per one part of anti-slipping agent.
  • EXAMPLE 2 70 parts of an aqueous dispersion with a film forming temperature of below C. containing 43% polyvinyl acetate, as a softener 11% dibutyl phthalate and as a dispersion agent about 3% polyvinyl alcohol with a saponification number of 140, and wherein at least 80% of the dispersed polymer particles have diameters in the range from 1 to 2 microns, are stirred with 140 parts chalk which were first mixed with 100 parts water until a homogeneous mix is obtained.
  • the anti-slipping agent obtained in this manner can be diluted before use with up to 4 parts water per part of anti-slipping-agent.
  • EXAMPLE 3 100 parts of an aqueous dispersion of a copolymerizate with a film forming temperature of 0 C., of 75 parts vinyl acetate and 25 parts vinyl laurate, containing as a dispersion agent about 3% of a phenolpolyoxethylene glycol ether available commercially as an emulsifier and 0.3% sec.
  • sodium C -alkyl-sulfonate and wherein at least 80% of the dispersed polymer particles have a diameter of about 0.1 micron, are stirred with 80 parts of an aqueous dispersion with a film forming temperature of over 100 C., containing 45% polyvinyl chloride and as a dispersion agent 2% sodium lauryl sulfate, and wherein at least 80% of the polymer particles have a diameter of less than 0.5 micron; and with 550 parts of water, to form a homogeneous mixture.
  • EXAMPLE 4 100 parts of the dispersion described in Example 3 as a dispersion with a film forming temperature of 0 C. are stirred with 80 parts of a 45% aqueous dispersion of a mixed polymerizate with a film forming temperature of 60 C. containing 60 parts vinyl chloride and 40 parts vinyl acetate, and containing as a dispersion agent 2% sodium lauryl sulfate, and wherein at least 80% of the polymer particles have a diameter of less than 0.5 micron; and with 500 parts of water, until a homogeneous mixture is formed.
  • EXAMPLE 5 100 parts of an aqueous dispersion with a film forming temperature of +6 C. containing 50% of a copolymerizate of 60 parts vinyl acetate and 40 parts maleic acid dibutyl ester and as a dispersion agent 0.5% polyvinyl alcohol with a saponification number of 140, 0.33% of a mixture of 1 part sodium cetyl sulfate and 1 part sodium stearyl sulfate and 0.75% of a cetyl polyoxy ethylene glycol ether with an average of about 10 oxyethylene units per molecule, and wherein at least 80% of the dispersed polymer particles have a diameter in the range from 0.5 to 2 microns, are stirred with 100 parts of an aqueous dispersion with a film forming temperature of over 100 C.
  • the mixtures produced in accordance with Examples 1 through 6 are used in such a manner that 4 squirts (each about 3 ml.) of each mixture are applied from a polyethylene spray bottle by hand pressure to a paper bag and the next bag is laid on the treated side of the first bag. After 40 hours the bags are separated. No damage to the paper occurs, and the films of the adhesive will not crumble off even if the paper is creased.
  • said first aqueous dispersion comprises polyvinyl acetate and a plasticizer for said polyvinyl acetate in a quantity of 10 to 50 weight percent referred to the weight of the polyvinyl acetate.

Abstract

METHOD OF SECURING OBJECTS SUCH AS STACKED PACKAGES OF PAPER, CARDBOARD AND THE LIKE AGAINST SLIPPING, IN WHICH ADJACENT CONTACTING PORTIONS OF SUCH PACKAGES ARE UNITED BY AN ADHESIVE COMPRISING AN AQUEOUS DISPERSION OF A POLYERIZATE OF AN OLEFINIC UNSATURATED COMPOUND WHICH FORMS A FILM AT A TEMPERATURE OF NOT MORE THAN +10*C., IN A HOMOGENEOUS MIXTURE WITH A SUBSTANCE SELECTED FROM THE GROUP CONSISTING OF INORGANIC AND ORGANIC PIGMENTS.

Description

United States Patent 3,598,677 METHOD OF SECURING STACKED PACKAGES AGAINST SLIPPING Eduard Bergmeister, Hubert Wiest, Joseph Heckmaier,
and Heinz Winkler, Burghausen, Upper Bavaria, Germany, assignors to Wacker-Chemie G.m.b.H., Munich, Bavaria, Germany No Drawing. Original application Dec. 5, 1966, Ser. No. 598,897. Divided and this application Feb. 24, 1969, Ser. No. 801,814 Claims priority, application Germany, Dec. 24, 1965, W 40,595 Int. Cl. B32b 31/00 11.8. C]. 156-276 7 Claims ABSTRACT OF THE DISCLOSURE Method of securing objects such as stacked packages of paper, cardboard and the like against slipping, in which adjacent contacting portions of such packages are united by an adhesive comprising an aqueous dispersion of a polymerizate of an olefinic unsaturated compound which forms a film at a temperature of not more than +10 C., in a homogeneous mixture with a substance selected from the group consisting of inorganic and organic pigments.
This application is a division of our pending application Ser. No. 598,897, filed Dec. 5, 1966, now abandoned.
It is quite a task to prevent stacked goods, which are packed in paper or cardboard, from slipping, i.e. shifting, during loading and shipping aboard vehicles running on or without rails, particularly railroads and trucks. This problem exists in an increasing degree in the case of goods packed on fiat pallets, i.e. grid-like supports, on top of each other, in paper bags.
The slippage-preventing agents which have been used heretofore in an attempt to solve the above problem are aqueous alkali silicate solutions, starch solutions, rubber or natural resin dispersions. The alkali silicate solutions have the drawback that they have the effect of sticking so tenaciously that when the stacks are taken down the packings are damaged by tearing of the paper fibers, or after removal from the stacks films remain on the packing which crumbles easily and thus can easily contaminate the merchandise when the packages are emptied. Natural resin dispersions have the same drawback. The other anti-slipping adhesives that have been used heretofore could not be adjusted in their adhesive power to such an extent as to achieve a sufficient adhesive effect for reducing slippage in the stacks and at the same time to prevent damage to the packing due to tearing of the paper fibers or tearing of the packages when the stacks were removed.
Our invention provides a method of securing stacked packages against slipping while at the same time permitting such packages to be readily separated without tearing or otherwise damaging the packages, such as the fibers of paper bags when the latter are separated, and without crumbling or shredding in such a way as to contaminate the contents of the packages when the latter are opened and in use.
The adhesives which we use as anti-slipping agents are characterized by the fact that they comprise an aqueous dispersion of an olefinic unsaturated compound which forms a film at a temperature of not more than +10 C., in admixture with inorganic and/or organic pigments. The film forming temperature, also called white point or lowest temperature for film forming (for the definition see R. Houwink and A. I. Stavermann, Chemistry and Technology of Plastics, 4th ed., vol. II/2, p. 653) can be obtained from advertising pamphlets of the com 3,598,677 Patented Aug. 10, 1971 Ice mercially available polymerizate dispersions, or from the manufacturers of such dispersions, or it can be determined by applying the dispersion whose film-forming temperature is to be found in a thickness of 0.3 mm. (measured on the moist, newly applied dispersion) on a glass plate by means of a film-forming apparatus and drying in a closed space (thermal chamber without air circulation).
Of aqueous dispersions from polymerizates of olefinic unsaturated compounds with a film-forming temperature of not exceeding +10 C., those preferred are aqueous dispersions of polymerizates and/or copolymerizates of vinyl acetate with a film forming temperature of +10 C.
at the most.
For the adhesives for use as anti-slippage agents according to our method, very suitable are aqueous dispersions of polyvinyl acetate which contain plasticizers for polyvinyl acetate like dibutyl phthalate or tricresyl phosphate, and/or soft resins like low-molecular polyesters or polyvinyl ethers in quantities of 5 to 50 weight percent, preferably 20 to 30 weight percent, always referred to the weight of the polyvinyl acetate, i.e. which are externally softened dispersions of polymerizates of vinyl acetate. At times these aqueous dispersions could also be dispersions of copolymerizates of vinyl acetate. Examples of plasticizers for polyvinyl acetate, besides those named above, are esters of phosphoric acid like tributyl phosphate and diphenyl cresylphosphate, esters of phthalic acid like di-2-ethylhexyl phthalate and di-nbutylglycol phthalate, esters of adipic acid like dibutyl adipate, dihexyl adipate and dioctyl adipate, esters of sebacic acid like diethylhexyl sebacate, dibutyl and dihexyl sebacate.
The manufacture of aqueous externally softened dispersions of polymerizates and/ or copolymerizates of vinyl acetate with a film forming temperature not exceeding +10 C. is well known.
Many externally softened polyvinyl acetate dispersions which are well suited for use according to our method are commercially available, for instance from Wacker- Chemie G.m.b.H., Munich, Germany, under the names Vinnapas-Dispersion M 54/25 C, Vinnapas-Disper'sion M 54/25 TC and Vinnapas-Dispersion Z 54/20 C. (The word Vinnapas is a registered trademark.)
Even more preferred than aqueous externally softened dispersions of polymerizates or copolymerizates of vinyl acetate are those aqueous dispersions of copolymerizates of vinyl acetate with a film forming temperature not exceeding +10 C. which can be called aqueous, internally softened polyvinyl acetate dispersions. The polymers in the last-mentioned kind of dispersions are preferably copolymers of 30 to 90 weight percent vinyl acetate and 70 to 10 weight percent vinyl esters of saturated aliphatic monocarboxylic acids with 3 to 18 carbon atoms, like vinyl propionate, vinyl laurate or vinyl stearate, esters of saturated aliphatic alcohols with 3 to 18 carbon atoms, aliphatic unsaturated dicarboxylic acids with 4 carbon atoms like maleic acid dibutyl ester, maleic acid di-2 ethylhexyl ester, fumaric acid dibutyl ester or fumaric acid di-2-ethylhexyl ester, esters of saturated aliphatic alcohols with 1 to 18 carbon atoms, of acrylic acid or methacrylic acid, like acrylic acid butyl ester and/or ethylene.
The manufacture of aqueous internally softened polyvinyl acetate dispersions with a film forming temperature of not exceeding +10 C. is well known. Some examples for copolymerizates of vinyl acetate which are principally contained in an aqueous internally softened polyvinyl acetate dispersion with a film forming temperature of not more than +10 C. are copolymerizates of 60% vinyl acetate and 40% maleic acid dibutyl ester 60% vinyl acetate and 40% vinyl laurate vinyl acetate and 25% vinyl laurate (Each of the above percentages refers to the total weight of the polymerizate.)
Many internally softened polyvinyl acetate dispersions which are even more suitable for application within the limits of the present invention than the externally softened polyvinyl acetate dispersions are available commercially, for instance from Wacker-Chemie G.m.b.H., Munich, Germany, under the names Vinnapas-Dispersion 50/ 66 H, Vinnapas-Dispersion 50/40 VL, Vinnapas-Dispersion A 50/25 VL, Vinnapas-Dispersion Z 53/43 M and Vinnapas Dispersion Z 50/25 VL.
One can use mixtures of various externally softened or of various internally softened or of externally softened and internally softened dispersions.
As inorganic or organic pigments one can use all fillers which are not soluble in water or which are hard to dissolve in water, i.e. which dissolve not more than 1 weight part in 100 to 1000 weight parts of water at 20 C., which are inert towards the polymerizate dispersion, in the form of more or less dry powders. The following examples may be mentioned for such fillers: chalk, light spar, i.e. unburned ground gypsum, kaolin, silicon dioxide produced or precipitated pyrogenically in the gaseous phase, wood flour or products similar to wood flour like peanut shell flour and cork powder. Preferably one uses 200 to 500, especially about 400 weight percent, always referred to the weight of the polymerizate, of fillers in the aqueous polymerizate dispersion which has a film forming temperature of not more than +10 C. One can also use mixtures of various fillers.
.Against the above fillers in powder form, however, there are to be preferred as pigments aqueous dispersions of plastics, particularly of polymerizates of olefinic unsaturated compounds with a film forming temperature of at least +40 C.--because of the decreased danger of the finished mixtures separating. One can also designate pigments of this kind as finely dispersed particles used in the form of aqueous dispersions which do not form any film below +40 C., consisting of polymerizates of olefinic unsaturated compounds. The upper limit of dispersions with film forming temperatures of at least +40 C. is not decisive. For instance, the film forming temperature of these dispersions may be 150 C. or more.
Among the preferred examples for polymerizates in aqueous dispersions of polymerizates of olefinic unsaturated compounds with a film forming temperature of at least +40 C. may be named: Polyvinyl chloride, polystyrol, copolymerizates of 2 to 70 weight parts vinyl acetate and 98 to 30 weight percent vinyl chloride, copolymerizates of 70 to 95 weight percent styrol and 30 to 5 weight percent butadiene as well as copolymerizates of 70 to 95 weight percent acrylic nitrile and 30 to 5 weight percent butadiene.
The manufacture of aqueous dispersions of polymerizates of olefinic unsaturated compounds with a film forming temperature of at least +40 C. is likewise well known. Some examples of copolymerizates which are contained in such dispersions, in particular are those of:
60% vinyl chloride and 40% vinyl acetate 85% styrol and 15% butadiene 80% acrylic nitrile and 20% butadiene (Each of the above percentages refers to the total weight of the polymerizates.)
Many aqueous dispersions of polymerizates of olefinic unsaturated compounds with a film forming temperature of at least +40 C. are available commercially, for instance from Wacker-Chemie G.m.b.H., Munich, Germany, under the name Vinnol-Dispersion 45 and from the Chemical Works Hills A.G., Marl-Hiils, Germany, under the name Litex SB 15. (The name Vinnol as well as the name Litex are registered trademarks.)
One can use various aqueous dispersions with a film forming temperature of at least +40 C.
Preferably the aqueous dispersions with a film forming .4 temperature of at least +40 C. are used in such quanti ties that 20 to 500, especially from 60 to 200, weight percent (each time referred to the polymerizate in the aqueous polymerizate dispersion with a film forming temperature of not more than 10 C.) of the polymerizate of the aqueous polymerizate dispersion with a film forming temperature of at least +40 C. are available.
If one uses for pigments aqueous dispersions with a film forming temperature of at least +10 C., it is particularly helpful to use as aqueous dispersions with a film forming temperature of not more than +10 C. no dispersions containing any softeners, but to use internally softened polyvinyl acetate dispersions in order to avoid having the film forming temperature of the dispersion used as a pigment reduced by the softener content of the dispersions with a low film forming temperature.
It is preferred that the aqueous polymerizate dispersions with a film forming temperature of not more than +10 C. as well as the aqueous polymerizate dispersions with film forming temperatures of at least +40 C. should have in each case to weight percent of the dispersed polymer particles with a diameter of a maximum of 2 microns. Such polymerizate dispersions are usually manufactured in accordance with known methods of the so-called dispersion polymerization or by emulsion polymerization.
The manufacture of the adhesives used as anti-slipping agents pursuant to our invention consists of mixing the compounds with each other until a homogeneous mixture is obtained. The temperature and pressure are of no consequence during mixing and during use of the antislipping agents. The water content of the anti-slipping agents can be adjusted to the viscosity required for each other.
The application of the anti-slipping agents is done by applying said anti-slipping agents during stacking to the sides of the packages that get in contact with the sides of other packages, and perhaps also to the side of the pallet which gets in contact with the first layer of packages, in each case immediately before the packages are placed upon it. The anti-slipping agents can be applied by spraying on or brushing on, e.g. with a brush or with a roller over the entire surface where slippage is to be prevented, or only on certain spots on these surfaces, e.g. by point or Wave patterns. The anti-slipping agents are particularly useful for paper bags, but they can also be used effectively on cartons made of full or corrugated cardboard and folding boxes and other packaging materials made of paper or cardboard.
The anti-slipping agents disclosed herein will bind Within one-half to one whole hour after application, and even if application is made only in certain spots the result is safe stacks which will not slip during loading or transportation. The packages can be separated again easily and without damage. The film remaining on the packages adheres firmly to the package surfaces, it is pliable and will not crumble even when the surfaces are bent.
The parts and percentages shown in the examples below refer in each case to the Weight. The percentages are calculated in each case for the total weight of the dispersions, provided nothing to the contrary is stated.
EXAMPLE 1 67 parts of a 50% aqueous dispersion of a copolymerizate of 60 parts vinyl acetate and 40 parts vinyl laurate, with a film forming temperature of 0 0., containing as a dispersion agent about 3 percent polyvinyl alcohol with the saponification number (milligrams KOH, required for splitting off and neutralizing the remaining acetyl groups in 1 g. polyvinyl alcohol) of and wherein at least 80% of the dispersed polymer particles have diameters within the range from 1 to 2 microns, are stirred with 133 parts light spar which were first mixed with 75 parts wat un il a homogeneous mix is obtained.
The anti-slipping agent obtained in this manner is properly diluted before use with three parts of water per one part of anti-slipping agent.
EXAMPLE 2 70 parts of an aqueous dispersion with a film forming temperature of below C. containing 43% polyvinyl acetate, as a softener 11% dibutyl phthalate and as a dispersion agent about 3% polyvinyl alcohol with a saponification number of 140, and wherein at least 80% of the dispersed polymer particles have diameters in the range from 1 to 2 microns, are stirred with 140 parts chalk which were first mixed with 100 parts water until a homogeneous mix is obtained.
The anti-slipping agent obtained in this manner can be diluted before use with up to 4 parts water per part of anti-slipping-agent.
EXAMPLE 3 100 parts of an aqueous dispersion of a copolymerizate with a film forming temperature of 0 C., of 75 parts vinyl acetate and 25 parts vinyl laurate, containing as a dispersion agent about 3% of a phenolpolyoxethylene glycol ether available commercially as an emulsifier and 0.3% sec. sodium C -alkyl-sulfonate, and wherein at least 80% of the dispersed polymer particles have a diameter of about 0.1 micron, are stirred with 80 parts of an aqueous dispersion with a film forming temperature of over 100 C., containing 45% polyvinyl chloride and as a dispersion agent 2% sodium lauryl sulfate, and wherein at least 80% of the polymer particles have a diameter of less than 0.5 micron; and with 550 parts of water, to form a homogeneous mixture.
EXAMPLE 4 100 parts of the dispersion described in Example 3 as a dispersion with a film forming temperature of 0 C. are stirred with 80 parts of a 45% aqueous dispersion of a mixed polymerizate with a film forming temperature of 60 C. containing 60 parts vinyl chloride and 40 parts vinyl acetate, and containing as a dispersion agent 2% sodium lauryl sulfate, and wherein at least 80% of the polymer particles have a diameter of less than 0.5 micron; and with 500 parts of water, until a homogeneous mixture is formed.
EXAMPLE 5 100 parts of an aqueous dispersion with a film forming temperature of +6 C. containing 50% of a copolymerizate of 60 parts vinyl acetate and 40 parts maleic acid dibutyl ester and as a dispersion agent 0.5% polyvinyl alcohol with a saponification number of 140, 0.33% of a mixture of 1 part sodium cetyl sulfate and 1 part sodium stearyl sulfate and 0.75% of a cetyl polyoxy ethylene glycol ether with an average of about 10 oxyethylene units per molecule, and wherein at least 80% of the dispersed polymer particles have a diameter in the range from 0.5 to 2 microns, are stirred with 100 parts of an aqueous dispersion with a film forming temperature of over 100 C. which contains 50% of a copolymerizate of 85 parts styrol and parts butadiene and as a dispersion agent 4% sec. sodium C '=alkyl sulfonate, and wherein at least 80% of the dispersed polymer particles have a diameter of below 0.5 micron; and with 800 parts of water, until a homogeneous mixture is formed.
EXAMPLE 6 100 parts of the dispersion described in Example 3 as a dispersion with a film forming temperature of 0 C. are stirred with 100 parts of an aqueous dispersion with a film forming temperature of over 100 C. containing 50% of a copolymerizate of 80 parts acrylonitrile and parts butadiene and as a dispersion agent 4% sec. sodium C =alkyl sulfonate, and wherein at least of the dispersed polymer particles have a diameter of less than 0.5 micron: and 1000 parts of water, until a homogeneous mixture is formed.
The mixtures produced in accordance with Examples 1 through 6 are used in such a manner that 4 squirts (each about 3 ml.) of each mixture are applied from a polyethylene spray bottle by hand pressure to a paper bag and the next bag is laid on the treated side of the first bag. After 40 hours the bags are separated. No damage to the paper occurs, and the films of the adhesive will not crumble off even if the paper is creased.
All temperatures shown above and in the appended claims, in front of which there is no plus sign represent temperatures above 0 C. if there is no minus sign in front of them and if the temperature shown is not 0 C.
The invention claimed is:
1. Method of securing stacked packages of paper, cardboard and the like against slipping, wherein adjacent contacting portions of said packages are united by an adhesive comprising a first aqueous dispersion of a polymerizate or copolymerizate of vinyl acetate, said first dispersion having a film forming temperature of not more than 10 C., in being a homogeneous mixture with a second aqueous dispersion of an organic pigment consisting essentially of a polymerizate of an olefinic unsaturated compound, said second dispersion having a film forming temperature of at least +40 C. I
2. Method according to claim 1, in which said first aqueous dispersion comprises polyvinyl acetate and a plasticizer for said polyvinyl acetate in a quantity of 10 to 50 weight percent referred to the weight of the polyvinyl acetate.
3. Method according to claim 1, in which said first aqueous dispersion is an aqueous internally softened polyvinyl acetate dispersion.
4. Method according to claim 1, in which the organic pigment is present in a quantity of 20 to 500 weight percent calculated as polymerizate and referred to the weight of the polymerizate in the first aqueous polymerizate dispersion.
5. Method according to claim 1, wherein 80 to weight percent of each of the dispersed polymerizate consists of polymer particles which have a diameter of not more than 2 microns.
6. Method according to claim 1, in which said pigment is in the form of a powder in a quantity of 200 to 500 weight percent referred to the weight of the polymerizate in the aqueous dispersion.
7. Method according to claim 1, in which an internally softened polyvinyl acetate dispersion with a film forming temperature of not more than -+10 C. is homogeneously mixed with a polymerizate of an olefinic unsaturated compound having a film forming temperature of at least +40 C.
References Cited UNITED STATES PATENTS 3,036,977 5/1962 Koch et a1. 156-327 3,268,496 8/1966 Germain 156-327 3,301,809 1/1967 Goldberg et al. 26029.6 3,365,409 1/1968 Lanthier 156327 3,419,641 12/1968 Peterkin et al. 156327 3,444,037 5/ 1969 Armour 15 6-327 CARL D. QUARFORTH, Primary Examiner S. J. LECHERT, JR., Assistant Examiner US. Cl. X.R.
US3598677D 1965-12-24 1969-02-24 Method of securing stacked packages against slipping Expired - Lifetime US3598677A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
DEW40595A DE1262897B (en) 1965-12-24 1965-12-24 Adhesive

Publications (1)

Publication Number Publication Date
US3598677A true US3598677A (en) 1971-08-10

Family

ID=7602526

Family Applications (1)

Application Number Title Priority Date Filing Date
US3598677D Expired - Lifetime US3598677A (en) 1965-12-24 1969-02-24 Method of securing stacked packages against slipping

Country Status (5)

Country Link
US (1) US3598677A (en)
BE (1) BE691733A (en)
DE (1) DE1262897B (en)
ES (1) ES334864A1 (en)
FR (1) FR1506736A (en)

Cited By (21)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3734801A (en) * 1970-08-25 1973-05-22 Henkel & Cie Gmbh Method for preventing the sliding or riding up of packaged articles by coating with adhesive compositions
US3755044A (en) * 1970-06-27 1973-08-28 H Sebel Adhesive compositions and method of application
US3869309A (en) * 1972-03-21 1975-03-04 Norsk Hydro As Antiskid agent for bags
US3891595A (en) * 1972-08-30 1975-06-24 Ici Ltd Friction material
US4421805A (en) * 1982-04-29 1983-12-20 Mobil Oil Corporation Slip-resistant shipping sacks
US4771862A (en) * 1988-01-22 1988-09-20 Tufco Industries Inc. Ladder guards
US4832189A (en) * 1983-04-13 1989-05-23 Csa Inc. Point-of-purchase stationery system
US4905824A (en) * 1983-04-13 1990-03-06 Csa Inc. Point-of-purchase stationary system
US4982839A (en) * 1983-04-13 1991-01-08 Csa Inc. Point-of-purchase stationery
US5074411A (en) * 1983-04-13 1991-12-24 Csa Inc. Point-of-purchase stationary system
US5110657A (en) * 1990-05-22 1992-05-05 Reichhold Chemicals, Inc. Anti-skid coating composition
US5273227A (en) * 1992-02-13 1993-12-28 Smith Jr Jonathan R Rotation-retarded product roll
US5331038A (en) * 1992-09-28 1994-07-19 Shell Oil Company Adhesive for multipacks
US5339957A (en) * 1993-03-08 1994-08-23 Key Tech Corporation High friction package retainer
US5356466A (en) * 1993-03-18 1994-10-18 Lawson Michael B Anti-slip agents
US5415357A (en) * 1992-02-13 1995-05-16 Smith, Jr.; Jonathan R. Product roll with rotation impedance
US5648031A (en) * 1994-07-28 1997-07-15 Custom Plastics Molding, Inc. Method of forming antislip surfaces on thermoformed products
US5672199A (en) * 1993-11-20 1997-09-30 Henkel Kommanditgesellschaft Auf Aktien Water-containing antislip composition
US5907011A (en) * 1994-09-02 1999-05-25 Clariant Gmbh Heterogeneous polyvinyl ester dispersions and powders
AU752050B2 (en) * 1998-10-19 2002-09-05 Ecolab Inc. Tackifying treatment for floor mats
US6509084B2 (en) 1994-07-28 2003-01-21 Custom Plastics Molding, Inc. Thermoplastic products having antislip surfaces

Families Citing this family (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE4230472A1 (en) * 1992-09-14 1994-03-17 Henkel Kgaa Anti-slip agent
DE4230473A1 (en) * 1992-09-14 1994-03-17 Henkel Kgaa Anti-slip agent
DE10357530B4 (en) * 2003-12-08 2006-12-21 Meneghini, Thomas, Dr. Liquid dispenser and liquid dispenser

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US2580230A (en) * 1950-03-24 1951-12-25 Le Page S Inc Improved polyvinyl acetate emulsion capable of depositing water-resistant films and bonds

Cited By (24)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3755044A (en) * 1970-06-27 1973-08-28 H Sebel Adhesive compositions and method of application
US3734801A (en) * 1970-08-25 1973-05-22 Henkel & Cie Gmbh Method for preventing the sliding or riding up of packaged articles by coating with adhesive compositions
US3869309A (en) * 1972-03-21 1975-03-04 Norsk Hydro As Antiskid agent for bags
US3891595A (en) * 1972-08-30 1975-06-24 Ici Ltd Friction material
US4421805A (en) * 1982-04-29 1983-12-20 Mobil Oil Corporation Slip-resistant shipping sacks
US4832189A (en) * 1983-04-13 1989-05-23 Csa Inc. Point-of-purchase stationery system
US4905824A (en) * 1983-04-13 1990-03-06 Csa Inc. Point-of-purchase stationary system
US4982839A (en) * 1983-04-13 1991-01-08 Csa Inc. Point-of-purchase stationery
US5074411A (en) * 1983-04-13 1991-12-24 Csa Inc. Point-of-purchase stationary system
US4771862A (en) * 1988-01-22 1988-09-20 Tufco Industries Inc. Ladder guards
US5110657A (en) * 1990-05-22 1992-05-05 Reichhold Chemicals, Inc. Anti-skid coating composition
US5415357A (en) * 1992-02-13 1995-05-16 Smith, Jr.; Jonathan R. Product roll with rotation impedance
US5273227A (en) * 1992-02-13 1993-12-28 Smith Jr Jonathan R Rotation-retarded product roll
US5331038A (en) * 1992-09-28 1994-07-19 Shell Oil Company Adhesive for multipacks
US5339957A (en) * 1993-03-08 1994-08-23 Key Tech Corporation High friction package retainer
US5356466A (en) * 1993-03-18 1994-10-18 Lawson Michael B Anti-slip agents
US5672199A (en) * 1993-11-20 1997-09-30 Henkel Kommanditgesellschaft Auf Aktien Water-containing antislip composition
US5648031A (en) * 1994-07-28 1997-07-15 Custom Plastics Molding, Inc. Method of forming antislip surfaces on thermoformed products
US5858508A (en) * 1994-07-28 1999-01-12 Custom Plastics Molding, Inc. Method of forming antislip surfaces on thermoformed products
US6509084B2 (en) 1994-07-28 2003-01-21 Custom Plastics Molding, Inc. Thermoplastic products having antislip surfaces
US5907011A (en) * 1994-09-02 1999-05-25 Clariant Gmbh Heterogeneous polyvinyl ester dispersions and powders
AU752050B2 (en) * 1998-10-19 2002-09-05 Ecolab Inc. Tackifying treatment for floor mats
US6630042B2 (en) * 1998-10-19 2003-10-07 Ecolab Inc. Tackifying treatment for floor mats
DE19950141B4 (en) * 1998-10-19 2007-04-12 Ecolab Inc., St. Paul Anti-slip floor mats treatment

Also Published As

Publication number Publication date
FR1506736A (en) 1967-12-22
BE691733A (en) 1967-06-23
DE1262897B (en) 1968-03-07
ES334864A1 (en) 1967-11-16

Similar Documents

Publication Publication Date Title
US3598677A (en) Method of securing stacked packages against slipping
US3784391A (en) Finely divided hollow microcapsules of polymeric resins
GB707549A (en) Improvements in or relating to the surface treatment of films, sheets and coatings comprising organic thermoplastic materials
US5389425A (en) Packaging materials
ES508631A0 (en) "PROCEDURE FOR THE PREPARATION OF A POLYMER COMPOSITION CONTAINING SILICON ACID IN THE FORM OF POWDER".
US3264136A (en) Polyethylene terephthalate film with finely divided polymethyl methacrylate coating
US4753831A (en) Cardboard container with anti-slip property
US3902596A (en) Additive package for compounding resins
US5500470A (en) Composition for utilizing synthetic polymer packages
US3375215A (en) Cellophane coating compositions comprising vinylidene chloride copolymer, candelillawax and stearate salt
US3018195A (en) Method of treating polyethylene structures
US3246831A (en) Slip-resistant thermoplastic resin sheets and process for producing same
US3778399A (en) Novel emulsion adhesive compositions of vinyl acetate polymers
US2804205A (en) Container for packaging tacky materials
US5288780A (en) Water based adhesion promoting compositions
US3297477A (en) Heat-sealable composite sheet
US3804933A (en) Chemical embossing
US4246319A (en) Coating for polyolefinic products and products covered by said coatings
US3835086A (en) Polymeric dispersions of pressure-sensitive adhesives and process
US2163228A (en) Soap package
JP4154866B2 (en) Aqueous anti-slip composition and molded article
US3695923A (en) Composite sheet
US3382128A (en) Heat sealable polystyrene pellicles
JPH1053742A (en) Antislip agent for paper article
JPH07150055A (en) Slip resistant composition and its production