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Publication numberUS3821021 A
Publication typeGrant
Publication dateJun 28, 1974
Filing dateFeb 29, 1972
Priority dateFeb 29, 1972
Also published asCA969816A, CA969816A1
Publication numberUS 3821021 A, US 3821021A, US-A-3821021, US3821021 A, US3821021A
InventorsMc Millin C
Original AssigneeDu Pont
Export CitationBiBTeX, EndNote, RefMan
External Links: USPTO, USPTO Assignment, Espacenet
Antistatically protected nonwoven polyolefin sheet
US 3821021 A
Abstract  available in
Images(5)
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Claims  available in
Description  (OCR text may contain errors)

United States Paten n91 McMillin fl 1 1111 3,821,021 1 51 June 28, 1974 ANTISTATICALLY PROTECTED NONWOVEN POLYOLEFIN SHEET [75] Inventor: Carl Kenneth McMillin,

Wilmington, Del.

[22] Filed: Feb. 29, 1972 [2]] App]. No.: 230,448

[52] U.S.Cl..' 117/1355, 117/1388 E,

} 117/139.5CQ [51] Int. Cl C09d 3/00 [58] Field of Search ..117/138.8 E, 135.5,

[56] References Cited UNITED STATES PATENTS 2,413,428 12/1946 Billings 117/1395 X 2/1965 Steuber l56/62.2X

3,442,740 5/1969 David 156/181 3,478,141 11/1969 Dempsey et a1. 156/166X 3,658,573 4/1972 Guestaux etal. 117/1388 X 3,703,588 11/1972 Saito et al ll7/l38.8 X

Primary Examiner-Michael Sofocleous Assistant Examiner-Bernard D. Pianalto [57] ABSTRACT 4 Claims, No Drawings ANTISTATICALLY PROTECTED NONWOVEN POLYOLEFIN SHEET BACKGROUND OF THEINVENTION Methods are available for preparing nonwoven polyolefin sheets which exhibit the ability to function as a barrier to liquid water while still permitting passage of water vapor, by fibrillating an oriented polymeric film to form a network and then laminating together several layers with fibrilsoriented in different directions in the various layers. In one method, a solution of polymer is flash-spun at a temperature above the boiling point of the solvent and at a high pressure intoa low pressure area, whereupon a three-dimensional network of filmfibrils forms at the spinneret. The network is spread by means of a baffle and is then collected in multidirectional, overlapping, and intersecting arrangement on a moving belt. The sheet may be consolidated by passing it through the nip of .a pair of cold rolls. A hot embossing process for improving the delamination and abrasion resistance of such sheets while retaining the softenability of the sheet is also known. Such nonwoven products exhibit desirable combinations of softness, drape, breatheability, etc., which has led to their acceptance for use in disposable or limited-use garments, as protective wrapping materials, drapes and curtains, etc.

The ability to function as a barrier to liquid water while still permitting passage of water vapor results from the film-fibril structure of the nonwoven sheet which permits passage of water (and other gaseous) vapor through the tortuous paths from one surface of the sheet to the opposite surface provided by the microscopic channels between the relatively close packed film-fibril elements, while liquid water is precluded from penetrating these same channels due to their small size and the hydrophobic character of the polyoletinpolymer surface. The relative freedom for passage of vapor through the nonwoven sheets can be varied over a substantial range, depending on how tightly compacted (how highly'calendered or embossed) the sheets may be, whether subsequent to bonding or embossing the sheet has been mechanically worked to loosen up the film-fibril structure between bond points, and: on the total basis weight of the sheet etc. In any event, the water barrier property continues to be exhibited, provided the nonwoven sheet remains free from gross holes as might be deliberately introduced.

Such nonwoven fibrous sheets having vapor transmission and liquid: water barrier properties have obvious potential utility in a multitude of applications, e.g., disposable, protective garments such as surgeons gowns; protective wrap for various commodities such as carpets, fiber bales, lumber, grain, etc.'; sterile packaging permeable tosterilizing gases but impermeable to bacteriaor liquids; consumer products suchas wind breakers, rainwear, sleeping bag liners, etc. However, the wellknownlpropensity ofpolyolefin articles to accumulate static chargesisadisadvantage. Unfortunately, the conventionaltechnique of simply applying antistat finishes to the nonwoven sheets does not ordinarily lead to a satisfactory. solution, since eventhough certain of such finishes will: adequately suppress static charge generation, they simultaneously confer a hydrophilic, rewettable character: to the polyolefin nonwovensheet,

and thus completely destroy its liquid water barrier property.

SUMMARY OF THE INVENTION According to the present invention, we have discovered a limited class of agents having a balance of high antistat activity and moderate aqueous surfactant power such that they may be applied as a finish onto nonwoven sheets composed of polyolefin film-fibril elements to confer antistatprotection without destruction of the sheets inherent liquid water barrier (hydrophobic) properties. i i

The present invention concerns a nonwoven sheet comprised of film-fibril elements of an olefin polymer which sheet bears at least 0.1 percent by weight, preferably at least 0.3 percent by weight of a non-rewettable finish agent defined by the formula: M,,R;,-,,PO where M is selected from the group consisting of lithium, sodium, potassium, and ammonium ions, R represents an alkyl group containing 3 to 5 carbon atoms, and n is selected from the integers l and 2. The preferred agents are those where M represents the potassium ion, and the most highly preferred finish is a mixture of approximately equimolar quantities of the two agents potassium dibutyl phosphate and dipotassium butyl phosphate. The preferred polyolefin is linear polyethylene. It is preferred that at least 0.3 percent but no more than about 2 percent by weight of agent be present on the sheet. Excessive amounts of agent are not only unwarranted for economic reasons but are also undesirable because the water barrier properties of the sheet are adversely affected. 1 i

The antistat finish of this invention may be applied to the polyolefin nonwoven sheets by immersing the sheet in an aqueous solution of the agent; by kiss-roll, gravure roll, or similar application of a coating of an aqueous solution of the agent; or by spraying an aqueous solution of the agent onto the surface of the sheet. For those agents whose water solutions have surface tensions appreciably in excess of thecritical surface tension of the polyolefin substrate, it is advantageous to lower the surface tension of the applied solution by addition of a third component such as a non-rewettable surfactant or a volatile alcohol.

DESCRIPTION OF THE PREFERRED EMBODIMENTS The nonwoven fibrous sheets useful for this invention may be prepared from any crystalline olefin polymer but linear (high density) polyethylene is the preferred polyolefin; They are composed of film-fibril elements having a: surface area greater than 2 meter lgm. and may be produced by a flashextrusion method as dis closed in US. Pat. No. 3,169,899. The nonwoven sheets may be cold consolidated as described in said US. Pat. No. 3,169,899, or point embossed as disclosed in US. Pat. No. 3,478,141, or surface bonded type as disclosed inIlS. Pat. No. 3,442,740.

The operable agents for the finish/coatings of the present invention possess a critical balance of high antistat activity and moderate aqueous surfactant power. The mono and dialkyl phosphates wherein the alkyl group contains 3 to 5 carbon'ato'ms (i.e., n-propyl, isopropyl, n-butyl, isobutyl, secondary butyl, tertiary butyl, n-amyl, andthe various C alkyl isomers) have been found to possess the requiredlevelof aqueous surfactant power to be useful in the present invention.

Although we do not wish to be bound by any theory, a working hypothesis consistent with the present invention is that the antistat agent must exhibit a certain level of aqueous surfactant power. If the antistat is too good a surfactant, then when the coated nonwoven sheet subsequently comes adventitiously in contact with water, a quantity of antistat will dissolve into the water to form a solution whose surface tension would be lower than the critical surface tension of the polyolefin substrate, and this solution will therefore wet the nonwoven sheet, penetrate the microscopic capillary channels between the individual film-fibril elements, and thereby destroy theliquid water barrier property of the sheet. This critical surfactant activity limit appears to be exceeded when the alkyl group of the alkyl phosphate antistat contains six or more carbon atoms. On the other hand, some minimum level of surfactant power is required of the antistat simply in order that it may be applied onto the nonwoven sheet (either by immersion, surface coating, spraying, etc.) from aqueous solution. The requirement is believed to be that the surface tension of the antistat solution should be such that the solution almost wets the nonwoven sheet. For example, in application of the antistat finish to linear polyethylene, the antistat solution should have a surface tension of about 37 i 3 dynes/cm. A 0.2 1 percent aqueous solution of potassium amyl phosphate or a l-2 percent solution of potassium butyl phosphate will satisfy this requirement directly. Potassium propyl phosphate, however, is not powerful enough a surfactant to meet this surface tension requirement at reasonable concentrations (less than 2 percent) in pure water, but it may successfully be applied to linear polyethylene from a 1 percent solution in a l7-volume percent isopropanol aqueous solvent (surface tension equal 35 dynes/cm.). In like fashion, sodium butyl phosphate and ammonium butyl phosphate are both somewhat poorer surfactants than potassium butyl phosphate so that their water solutions at less than 2 percent concentration fail to meet the surface tension requirement; but they too may successfully be applied to linear polyethylene from an alcohol/water solvent. Similarly, potassium butyl phosphate aqueous solutions at concentrations less than 1 percent have surface tensions which are too high (greater than 40 dynes/cm.), but such solutions can be made operable for coating linear polyethylene nonwoven sheets by adding a small quantity (e.g., 0.05 to 0.] percent) of a non-rewettable surface active agent, such as Igepal CO-880 or CO-890 (registered trademark of GAF Corporation's nonionic nonylphenoxy polyoxyethylene ethanol surfactants). These materials are termed non-rewettable here in the sense that a linear polyethylene nonwoven sheet coated with these surfactants is not penetrated by a drop of water subsequently placed on the surface of the treated sheet.

The antistat finishes of the present invention may comprise a single agent of the formula: M,,R ,,PO (as previously defined) or it may be a mixture of such agents, e.g., potassium butyl phosphate plus potassium isoamyl phosphate. Frequently mixtures are obtained directly in commercial operations. M may be chosen to be lithium, sodium, potassium, or ammonium ion but the potassium salts are preferred. The agent must contain at least one R group and at least one M group. It is to be noted that the finishes employed in this invention are not hydrophobic materials like the water repellent coatings conventionally applied to various woven and nonwoven fabrics in order to render them waterproof," but are rather a very restricted group of antistat materials which may be applied to polyolefin film-fibril nonwoven sheets without destroying their inherent hydrophobic liquid water barrier property.

In the Examples which follow, all samples are prepared on a laboratory scale by immersing a portion of the nonwoven sheet material in an aqueous bath of the specified composition. The sheet is removed from the bath and passed through the nip of a pair of elastomcric squeeze rolls 2% inch (5.4 cm.) in diameter of t 5 Shore A Durometer hardness operated at a nip pressure of 4-8 pli to remove excess solution from the surface of the sheet. The wet sheet is then air dried followed by an additional two minutes drying period at l 10C. The antistat protection provided by the finish is determined by submitting the sample previously conditioned at least 24-hours at the indicated temperature and relative humidity to test NFPA (National Fire Protection Association) Code 56A, Section 25433; paragraph A, part 3. The result is reported as Log R" with values of 11 (75F. and 50 percent'RH.) being passing and lower values preferred. The water barrier performance of the sample is measured by two tests the hydrostatic head test ASTM D-583, paragraph 53A, Method II, results reported in inches" (cms.) with high values preferred; and the rain penetration test ASTM D-583, paragraph 32-37, results reported in grams with lower values preferred.

EXAMPLE I This example illustrates the effect of varying the size of the alkyl groups of the phosphate antistat agents. Samples of nonwoven sheet comprising film-fibril elements of linear polyethylene are prepared by the pro cess of U.S. Pat. No. 3,169,899 at a basis weight of approximately 2.2 oz./yd. (75 gms./m. and subsequently bonded by the process of U.S. Pat. No. 3,442,740. These samples are treated with 0.5 weight percent aqueous solutions of various antistats as indicated in Table I. These antistats are all mixtures (approximately equimolar) of monopotassium dialkyl and dipotassium monoalkyl phosphate salts with the alkyl group indicated. At the 0.5 percent concentrations employed, potassium butyl phosphate, having the lowest surfactant power, can be successfully applied to the linear polyethylene substrate only by adding a small quantityof a surface tension depressant, in this case Igepal CO-890. This latter material by itself provides essentially no antistat protection for the linear polyethylene substrate.

TABLE I Rain Penetration Log R Run Antistut Hydrostatic Head 2 .12 min. (ol cm/Z min) 75F./55Z RH l-A None 60 in. 152 cm.) 0 g. Y l4 l-B Potassium butyl phosphate 50 in. I27 cm.) 0 g. 8.0 l-C Potassium amyl phosphate 47in. H9 cm.) 0.2 g. 8.l

TABLE 199901115 1 Rain Penetration Log R 75F./557z RH Run Antistat Hydrostatic Head 2 0.12 min. (61 cm/2 min) l-D Potassium hexyl phosphate 31 in. 79 cm.) 3.6 g. 8.0 l'E Potassium octyl phosphate 4 in. 10 cm.) 4.0 g. 7.5

Plus 0.11% lgepal" (-1190 Note that although all treated samples exhibit excellent antistat protection (values of Log R less than 1 l the good liquid water barrier properties of the samples are lost when the size of the alkyl group is increased beyond the C (amyl) limit of the present invention.

EXAMPLE II This example illustrates the effect of changing the quantity of antistat agent applied as a finish to the nonwoven sheet. Samples of nonwoven sheet comprising film-fibril elements of linear polyethylene prepared by the process of U.S. Pat. No. 3,169,899 at a basis weight of approximately 1.3 oz./yd. (44.2 gms./m. and subsequently embossed on one side with rows of pointbonds (rib pattern) and surface-embossed on the opposite side with a linen pattern" (as in Examples VI and VII of U.S. Pat. No. 3,427,376) are treated with alkali metal or ammonium alkyl phosphate salts represent an approximately equimolar mixture of a salt con taining one alkyl group with twoalkali metal or ammonium ions and a salt containing two alkyl groups with one alkali metal or ammoniumion.

EXAMPLE 1111 This example illustrates the effect of various candidate antistat finishes, both within and outside the limitation of the present invention. All candidates are appliedfrorn a solution at the specified concentration, as indicated in Table 111, in a solvent comprising 17 volume percent isopropanol in water such that in each case the surface tension of the solution is low enough to insure good wetting during application to the same linear polyethylene nonwoven substrate employed in Example 11. Note that only the alkali metal and ammonium alkyl phosphates furnish good antistat protection (Runs 3A through 31 versus 3.1 and 3K), that presence of an alkyl group is essential (Run 3L), and that common quaternary alkyl. ammonium halides are ineffective (Runs 3M through 3R V .TABLE 111 Antistat Concentration Linen Side/Rib side 3-A Potassium propyl phosphate 0.5 wt. 7: 13/1 1.9 3-B do. 1.0 l0/9.5 3-C do. 2.0 9.0/8.5 3-D do. 3.0 7.6/7.3 3-E Potassium butyl phosphate 0.5 9.9l0 0/9.0-9 5 3 F do. 1.0 8.99.0/8.4-8 7 13-6 do. 1.7 7.8/7.3 3-H Sodium butyl phosphate 1.0 9.0/9.0 3-1 Ammonium butyl phosphate ,1 .0' 9.0/9.0 3-.l Diethanolamine butyl phosphate 1.0 12-13/12-13 3-K Guanidine butyl phosphate 1.0 13-14/13-14 3-L Tri-potassium phosphate 3.0 l4l l4 3-M Tetramethyl ammonium chloride 7 .1.10 13/ 13 "3-N Tetramethyl ammonium bromide 1,54 13/ 13 3-0 Tetraethyl ammonium chloride 1.66 13/ 13 34" Tetraethyl ammonium bromide 2.10 13/ 13 3-Q Tetrabutyl ammonium bromide 3.22 12/ 1 1 3-R Tetrabutyl ammonium iodide (sat. solution) 12/ 12 ings achieved with the more concentrated solutions do EXAMPLE 1V lead to small incremental improvements in antistat protection (lower values of Log R), the excellent water Products of the present invention are prepared as inbarrier property of the sheets is not destroyed.

dicated at Table IV, employing the same linear polyeth- ABL Cone. of Log R Potassium Hydrostatic Rain Pene. 70F (21C.)/ Run Butyl Phosphate Head 2 ft/2 min. 55% RH 2-A 1.0 wt. 41 in. (104 cm.) 0 g. 8.8 2-B 1.5 41 in. (104 cm.) 0 8.1 2-C 2.0 39 in; 99 cm.) 0 7.7 2-D 3.0 41 in. (104 cm.) 0 7.0 2-E 4.0 in. (102 cm.) 0 6.8 ZF None 0 l4.0

40-50 in. (102-127 cm.)

In this example and inExamples 111 and IV which folylene nonwoven substrate employed in Example 11. The

low, it should be understood that each of the indicated quantity of antistat finish on the treated sheet may be determined either by standard analytical techniques (e.g., phosphorous or potassium analysis, using either chemical or spectroscopic techniques) or simply by calculating the amount of antistat contained in the quantity of treating solution picked up by the nonwoven sheet prior to drying, since the volatility of the antistat salts is very low.

The antistats are dissolved in water to the indicated weight percent, the sheet samples immersed in the solution and subsequently run through squeeze rolls at the indicated pressures, at which point the percent solution pickup is immediately determined by measuring weight gain, and the sample is then dried. The pickup of anti stat, based on the dried sheet, is computed from the sowhile permitting passage of water vapor, comprised of film-fibril elements having a surface area greater than 2 meter /gm, said sheet bearing from 0.1 percent to 2 percent by weight of a finish defined by the formula: M,,R ,,PO where M is selected from the group consisting of lithium, sodium, potassium, and ammonium ions, R represents an alkyl group containing 3 to 5 carbon atoms, and n is selected from the integers l and 2.

2. The sheet of claim 1 bearing from 0.3 percent to 2 percent by weight of said finish.

3. The product of claim 1 wherein the finish is a mixture of approximately equimolar quantities of potassium dibutyl phosphate and dipotassium butyl phoslution pickup and antistat concentration. W P I TABLE IV Run Antistat Conc. Squeeze Roll Pressure Solution Pickup Antistat on Sheet Log R 4A Potassium Propyl Phosphate 2.5% 4.3 p11 20.5% 0.51% 8.8 43 o. 5.0 do. 262 1.31 8.0 4C Potassium Butyl Phosphate 1.5 8.5 26. 0.39 7.9 4D do. do. do. 21. 0.32 7.9 4E do. .0 do. 30.5 0.61 77 4E do. do. do. 27.6 0.55 7.8 46 do. do. do. 25.3 0.51 7.8 4H do. 3.0 do. 30.5 0.91 7.35 41 do. do. 4.3 31.5 0.94 7.3 4] do. do. do. 34.3 1.03 6.7 4K Potassium Butyl Phosphate 0.5 do. 31. 0.16 7.8

lgepal CO-890 0.1 4L do. do. 8.5 25. 0.12 7.8

4. The product of claim 3 wherein the polyolefin is linear polyethylene.

Referenced by
Citing PatentFiling datePublication dateApplicantTitle
US3900631 *Oct 24, 1973Aug 19, 1975Du PontFlexible nonwoven sheets for use against splashing liquids
US4082887 *May 14, 1976Apr 4, 1978E. I. Du Pont De Nemours And CompanyCoating composition for a fibrous nonwoven sheet of polyolefin
US5403426 *Sep 2, 1993Apr 4, 1995Hercules IncorporatedProcess of making cardable hydrophobic polypropylene fiber
US5540953 *Jun 1, 1995Jul 30, 1996Hercules IncorporatedProcess of preparing fabric comprising hydrophobic polyolefin fibers
US5545481 *Feb 11, 1993Aug 13, 1996Hercules IncorporatedPolyolefin fiber
US5614306 *May 17, 1995Mar 25, 1997Kimberly-Clark CorporationConductive fabric and method of producing same
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US5807366 *Jun 18, 1997Sep 15, 1998Milani; JohnAbsorbent article having a particle size gradient
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US5877099 *Jan 27, 1997Mar 2, 1999Kimberly Clark CoFilter matrix
US5916204 *Jan 26, 1998Jun 29, 1999Kimberly-Clark Worldwide, Inc.Method of forming a particle size gradient in an absorbent article
US5998308 *May 22, 1996Dec 7, 1999Kimberly-Clark Worldwide, Inc.Nonwoven barrier and method of making the same
US6365088Jun 24, 1999Apr 2, 2002Kimberly-Clark Worldwide, Inc.Electret treatment of high loft and low density nonwoven webs
US6537932 *Oct 8, 1998Mar 25, 2003Kimberly-Clark Worldwide, Inc.Sterilization wrap, applications therefor, and method of sterilizing
USRE35621 *Jun 7, 1995Oct 7, 1997Hercules IncorporatedCardable hydrophobic polypropylene fiber, material and method for preparation thereof
EP0557024A1 *Feb 12, 1993Aug 25, 1993Hercules IncorporatedPolyolefin fiber
EP0640329A1 *Aug 17, 1994Mar 1, 1995Hercules IncorporatedBarrier element fabrics, barrier elements, and protective articles incorporating such elements
WO1999022635A2 *Oct 30, 1998May 14, 1999Kimberly-Clark Worldwide, Inc.Sterilization wrap, applications therefor, and method of sterilizing
WO1999022635A3 *Oct 30, 1998Jul 8, 1999Kimberly Clark CoSterilization wrap, applications therefor, and method of sterilizing
Classifications
U.S. Classification442/76, 442/114, 442/170, 428/523
International ClassificationD06M13/02, D06M13/244, D06M11/00, D06M13/282, D04H13/00, D04H13/02, D06M11/71, D06M13/00, D06M13/292
Cooperative ClassificationD06M13/292, D06M11/71
European ClassificationD06M11/71, D06M13/292