US3565669A - Process for improving the permanent shrinkage properties of regenerated cellulose film - Google Patents
Process for improving the permanent shrinkage properties of regenerated cellulose film Download PDFInfo
- Publication number
- US3565669A US3565669A US705158A US3565669DA US3565669A US 3565669 A US3565669 A US 3565669A US 705158 A US705158 A US 705158A US 3565669D A US3565669D A US 3565669DA US 3565669 A US3565669 A US 3565669A
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- United States
- Prior art keywords
- film
- web
- regenerated cellulose
- coated
- shrinkage
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- 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
Links
- 239000004627 regenerated cellulose Substances 0.000 title abstract description 31
- 238000000034 method Methods 0.000 title abstract description 30
- 230000008569 process Effects 0.000 title abstract description 30
- 238000000576 coating method Methods 0.000 abstract description 40
- 239000011248 coating agent Substances 0.000 abstract description 39
- 230000006872 improvement Effects 0.000 description 16
- 230000003750 conditioning effect Effects 0.000 description 13
- 239000003570 air Substances 0.000 description 10
- 239000000758 substrate Substances 0.000 description 10
- 239000000463 material Substances 0.000 description 9
- 239000000243 solution Substances 0.000 description 9
- 230000008859 change Effects 0.000 description 8
- 239000002904 solvent Substances 0.000 description 8
- 238000012360 testing method Methods 0.000 description 8
- 230000000694 effects Effects 0.000 description 7
- 229920000298 Cellophane Polymers 0.000 description 6
- 238000001035 drying Methods 0.000 description 6
- 239000000020 Nitrocellulose Substances 0.000 description 5
- 229920001220 nitrocellulos Polymers 0.000 description 5
- 238000004806 packaging method and process Methods 0.000 description 5
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 5
- 229920002678 cellulose Polymers 0.000 description 4
- 239000001913 cellulose Substances 0.000 description 4
- 125000004122 cyclic group Chemical group 0.000 description 4
- 238000010981 drying operation Methods 0.000 description 4
- 230000002093 peripheral effect Effects 0.000 description 4
- ZWEHNKRNPOVVGH-UHFFFAOYSA-N 2-Butanone Chemical compound CCC(C)=O ZWEHNKRNPOVVGH-UHFFFAOYSA-N 0.000 description 3
- CSCPPACGZOOCGX-UHFFFAOYSA-N Acetone Chemical compound CC(C)=O CSCPPACGZOOCGX-UHFFFAOYSA-N 0.000 description 3
- XEKOWRVHYACXOJ-UHFFFAOYSA-N Ethyl acetate Chemical compound CCOC(C)=O XEKOWRVHYACXOJ-UHFFFAOYSA-N 0.000 description 3
- YXFVVABEGXRONW-UHFFFAOYSA-N Toluene Chemical compound CC1=CC=CC=C1 YXFVVABEGXRONW-UHFFFAOYSA-N 0.000 description 3
- 230000001143 conditioned effect Effects 0.000 description 3
- WYURNTSHIVDZCO-UHFFFAOYSA-N Tetrahydrofuran Chemical compound C1CCOC1 WYURNTSHIVDZCO-UHFFFAOYSA-N 0.000 description 2
- 230000015572 biosynthetic process Effects 0.000 description 2
- 230000001351 cycling effect Effects 0.000 description 2
- 230000001419 dependent effect Effects 0.000 description 2
- 238000009499 grossing Methods 0.000 description 2
- 238000007654 immersion Methods 0.000 description 2
- 229920006280 packaging film Polymers 0.000 description 2
- 239000012785 packaging film Substances 0.000 description 2
- 229920000642 polymer Polymers 0.000 description 2
- 230000002040 relaxant effect Effects 0.000 description 2
- 230000002441 reversible effect Effects 0.000 description 2
- 238000007789 sealing Methods 0.000 description 2
- CLXPYTBRAZHUFD-UHFFFAOYSA-N 2-(4-fluorophenyl)-3-methylmorpholine Chemical compound CC1NCCOC1C1=CC=C(F)C=C1 CLXPYTBRAZHUFD-UHFFFAOYSA-N 0.000 description 1
- 101100165177 Caenorhabditis elegans bath-15 gene Proteins 0.000 description 1
- DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 description 1
- 229920000297 Rayon Polymers 0.000 description 1
- 239000000654 additive Substances 0.000 description 1
- 230000002411 adverse Effects 0.000 description 1
- 239000012080 ambient air Substances 0.000 description 1
- 239000007864 aqueous solution Substances 0.000 description 1
- 235000019504 cigarettes Nutrition 0.000 description 1
- 230000001112 coagulating effect Effects 0.000 description 1
- 239000008199 coating composition Substances 0.000 description 1
- 230000001427 coherent effect Effects 0.000 description 1
- 238000010276 construction Methods 0.000 description 1
- 229920001577 copolymer Polymers 0.000 description 1
- 230000007423 decrease Effects 0.000 description 1
- 238000007791 dehumidification Methods 0.000 description 1
- 230000001627 detrimental effect Effects 0.000 description 1
- ZOOODBUHSVUZEM-UHFFFAOYSA-N ethoxymethanedithioic acid Chemical compound CCOC(S)=S ZOOODBUHSVUZEM-UHFFFAOYSA-N 0.000 description 1
- 238000002474 experimental method Methods 0.000 description 1
- 238000010438 heat treatment Methods 0.000 description 1
- 230000002427 irreversible effect Effects 0.000 description 1
- 239000003960 organic solvent Substances 0.000 description 1
- 238000012856 packing Methods 0.000 description 1
- 230000035699 permeability Effects 0.000 description 1
- 229920000728 polyester Polymers 0.000 description 1
- 238000002360 preparation method Methods 0.000 description 1
- 238000012545 processing Methods 0.000 description 1
- 230000001681 protective effect Effects 0.000 description 1
- 229920006395 saturated elastomer Polymers 0.000 description 1
- 230000003678 scratch resistant effect Effects 0.000 description 1
- 229910052708 sodium Inorganic materials 0.000 description 1
- 239000011734 sodium Substances 0.000 description 1
- 239000007921 spray Substances 0.000 description 1
- 238000012956 testing procedure Methods 0.000 description 1
- YLQBMQCUIZJEEH-UHFFFAOYSA-N tetrahydrofuran Natural products C=1C=COC=1 YLQBMQCUIZJEEH-UHFFFAOYSA-N 0.000 description 1
- 238000012546 transfer Methods 0.000 description 1
- 238000004804 winding Methods 0.000 description 1
- 239000012991 xanthate Substances 0.000 description 1
Images
Classifications
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D7/00—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials
- B05D7/02—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials to macromolecular substances, e.g. rubber
- B05D7/04—Processes, other than flocking, specially adapted for applying liquids or other fluent materials to particular surfaces or for applying particular liquids or other fluent materials to macromolecular substances, e.g. rubber to surfaces of films or sheets
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29D—PRODUCING PARTICULAR ARTICLES FROM PLASTICS OR FROM SUBSTANCES IN A PLASTIC STATE
- B29D7/00—Producing flat articles, e.g. films or sheets
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D1/00—Processes for applying liquids or other fluent materials
- B05D1/18—Processes for applying liquids or other fluent materials performed by dipping
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D2252/00—Sheets
- B05D2252/02—Sheets of indefinite length
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B05—SPRAYING OR ATOMISING IN GENERAL; APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D—PROCESSES FOR APPLYING FLUENT MATERIALS TO SURFACES, IN GENERAL
- B05D3/00—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials
- B05D3/04—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by exposure to gases
- B05D3/0406—Pretreatment of surfaces to which liquids or other fluent materials are to be applied; After-treatment of applied coatings, e.g. intermediate treating of an applied coating preparatory to subsequent applications of liquids or other fluent materials by exposure to gases the gas being air
- B05D3/0413—Heating with air
-
- B—PERFORMING OPERATIONS; TRANSPORTING
- B29—WORKING OF PLASTICS; WORKING OF SUBSTANCES IN A PLASTIC STATE IN GENERAL
- B29C—SHAPING OR JOINING OF PLASTICS; SHAPING OF MATERIAL IN A PLASTIC STATE, NOT OTHERWISE PROVIDED FOR; AFTER-TREATMENT OF THE SHAPED PRODUCTS, e.g. REPAIRING
- B29C71/00—After-treatment of articles without altering their shape; Apparatus therefor
Definitions
- the substrate regenerated cellulose film employed is generally manufactured by the viscose process which is described in United States Pats. 1,548,864 and 1,601,289 to Brandenberger. ⁇ In this process an alkaline, aqueous solution of sodium celluolse xanthate is forced through an elongate orifice in the form of a continuous sheet into a coagulating bath where a coherent web is formed and subsequently regenerated, washed, desulfured, bleached, and softened. The web in this softened state is then dried by a drying method such as taught by Alles et al., U.S.P. 2,115,132; Britton et al., U.S.P.
- the dried web of regenerated cellulose generally contains from 3.0% to 7.0% moisture based on the dry cellulose content of the web.
- the web of regenerated cellulose in this state is not generally useful as a packaging film because of its hydrophilic nature and absence of heat sealing qualities. In this state it is designated as plain transparent film in order to differentiate it from other regenerated cellulosic film which is subsequently coated with one or more types of moisture-proofing and heat scalable materials.
- Regenerated cellulosic sheet material as it leaves the drying operation possesses properties which limit its utility to ornamental and sanitary protective packing applications.
- One of the main deterrents in using plain regenerated cellulose as an overwrap film for packaging rigid nondeformable items is the tendency of such film to shrink in one or more directions when it is exposed to cyclic humidity conditions. This often results in undesirable shrinkage of the overwrapped article causing poor package appearance and, in extreme cases, causing the film either to split or to crush the package contents.
- Shrinkage in cellulosic film consists of both permanent and reversible shrinkage.
- Permanent shrinkage is an irreversible shrinkage which dried regenerated cellulosic films often manifest due to age and certain ambient air conditions. It should be distinguished from reversible shrinkage which normally results from gains or losses in sheet moisture. Permanent shrinkage is accentuated by ambient moisture increases and decreases and by tensile forces that are applied to the web or developed within the web during moisture removal or addition processes. Permanent film shrinkage or net film shrinkage can cause physical damage to a package. Most commercially available types of cellophane will have 3.5% or more permanent shrinkage capability and will exhibit a net machine-direction shrinkage when brought to a 60% moisture equilibrium condition.
- Plain regenerated cellulose film is normally coated with a transparent, organic, polymeric material in order to irnprove such specific performance characteristics of the web as moisture-proofness, heat-scalability, dimensional stability, and gas permeability.
- Coating materials containing nitrocellulose and vinylidene chloride copolymers are commonly employed to broaden the end use applications of cellophane in the packaging industry. These materials are first put into solution by use of volatile organic solvents such as acetone, methyl ethyl ketone, ethyl acetate, tetrahydrofuran, and toluene.
- the solutions of the organic polymeric coatings are applied to the regenerated cellulose web by passing the continuous web through the coating solution, metering a. given amount of the solution onto the webs surface, smoothing the solution uniformly across the web and drying the web to remove the solvent and solidify the coating material while the web is subjected to tensile forces. Moisture is lost from the substrate during this solvent removal operation and such moisture is replaced by conditioning the coated web in a post-coating, humidifying atmosphere as taught by Charch et al., U .S.P. 1,826,- 698.
- This humidication process improves the durability properties of the regenerated cellulose web but the gained improvement is limited by the softener additives in the web, by the degree of exposure of the web to the humidified atmosphere and by the magnitude of the tensile forces being exerted on the web during the humidification process.
- the salient feature of the process of this invention is the controlled shrinking of the coated cellulose film structure achieved by operating the rolls at the exit of the postcoating conditioning section at a lower peripheral speed than the peripheral speed of the roll at the entrance to the post-coating conditioning section. Strains that are built into the substrate regenerated cellulose web during its wet processing and drying operations are relieved during this film conditioning operation in which it is humidied and simultaneously shrunken preferably at least 0.5% in its machine direction.
- the conditioner relaxation attainable in any specic web substrate is dependent on the shrinkage capabilities of the substrate web entering the coating operation.
- the process of this invention greatly improves the permanent shrinkage and durability properties of regenerated cellulose film.
- Film so produced is advantageously used as the overwrap for packages that are subjected to cyclic humidity conditions during warehousing, shipping, and merchandising.
- FIG. 1 is a diagrammatic side elevation of a coating and humidifying apparatus that is suitable for carrying out the critical relaxation step of this invention
- FIG. 2 shows typical transverse and machine direction dimensional changes for coated regenerated cellulose webs that have been subjected to cyclic humidification changes after having been subjected to a post-coating drawing operation of 0.4%;
- FIG. 3 shows typical transverse and machine direction dimensional changes for coated regenerated cellulose webs that have been subjected to cyclic humidification changes after having been subjected to a post-coating relaxation operation of 1.5%.
- FIG. 1 is an elevation view of one form of apparatus Which is suitable for carrying out the process of this invention.
- the uncoated regenerated cellulose film A is unwound from the mill roll 11 and enters the coating tower 12 through opening 13.
- the film 10 enters the coating compartment 14 and passes through the coating solution bath 15, under the dip tank roll 16, through the doctor rolls 17 and 18 and the coating solution smoothing rolls ⁇ 19 and 20, and ⁇ then into the coating solution drying section 21.
- Hot, dry air is circulated through the drying section 21 by air blower 22, air heater 23 and exhaust duct 24. This hot circulating air vaporizes the solvent from the substrate 10 and conveys the solvent vapors through the exhaust duct 24.
- the coated film after being dried in the drying section 21 passes into the head roll compartment 25, over the head roll 26 and into the conditioning section 27. Moisture lost in the substrate 10 during the coating and drying operations is replaced in the conditioning section 27 by passing humidified air through the conditioning section as the coated film passes through the same secton. This is accomplished by passing air through the blower 23, humidifying means 29, conditioning section 27 and exhaust duct 30. After being humidified the coated web is passed out of the conditioning section 27, under roll 31, around portions of the chill roll or rolls ⁇ 32 and onto the mill roll windup 33.
- the peripheral speed of the chill rolls 32 are operated 0.5 to 1.5% less than the peripheral speed of the head roll 26 while the coated ⁇ web is passed around the surfaces of the head roll and the chill roll, or chill rolls, while the web span between the head roll and the chill roll is simultaneously humidified to effect a controlled relaxation of the web and a controlled shrinkage thereof.
- Typical roll speeds that have been used are 1200 f.p.m. for the chill rolls and 1208.4 fpm. for the head roll to achieve a 0.7% relaxation. Higher and lower speeds may of course, be feasible for commercial uses. As speeds vary, residence times must remain constant, however, to the extent that suliicient heat transfer may be effected to relieve internal strains in the web.
- the humidification atmosphere for this process is conveniently attained by using saturated steam or slightly superheated steam in the humidifying means 29.
- Steam having a saturation temperature of about 103 C. or steam at atmospheric pressure having a superheat temperature of about 103 C. to 110 C. can be employed successfully in the process of this invention.
- Humidifying atmospheres formed by use of hot water sprays and live steam so that the atmosphere has an 80 C. to 90 C. dry-bulb temperature and a 75 C. to 85 C. wet-bulb temperature work equally well.
- the relaxation range that provides the improvement in film properties without an adverse effect upon roll formation is from just above 0% to 1.5%.
- the limits of the range are a function of the characteristics of the base web.
- Experimental data indicates that the practical limits of the relaxation range are from 0.5% to 1.5% in order to attain the maximum improvement in the web due to the controlled shrinkage without loss of other desirable web characteristics.
- the salient feature of the process of the present invention is the controlled shrinking of the cellulose film structure in its longitudinal or length direction preferably between about 0.5% and 1.5% based upon its initial length, by relaxing the film structure and relieving the stresses therein while contained within a humidifying atmosphere.
- the time of exposure of the film to this atmosphere to effect the 0.5 to 1.5 shrinkage is dependent upon the thickness of' and ⁇ the type of coating material on the substrate comprising a cellulose web structure. Experience had indicated that this exposure time varies from approximately 4 seconds to 5 seconds for most commercial film types.
- the advantages of the process of this invention are graphically shown by comparing the machine-direction curves of FIGS. 2 and 3.
- the curves shown in FIG. 2 are typical transverse-direction and machine-direction dimensional changes versus moisture changes for coated film which had been humidified while being subjected to 0.4% draw, or stretching, to insure sheet flatness. It is common practice to employ approximately 0.4% draw in the post coating humidification process in order to assure consistently good subsequent roll formation.
- the dimensional changes of the film shown in FIG. 2 are determined by recording the dimensional changes which test samples of the film evidence when the samples are slowly humidified in a variable humidity atmosphere up to 60% moisture content state at room temperature and slowly dehumidified back to its original moisture level by reversing the humidity cycle of its atmosphere. It is seen from the TD graph of FIG. 2 that a large transversedirection dimensional change takes place in the web during the humiditication portion of the cycle and that this change is essentially nullified during the dehumidification portion of the cycle.
- MD machinedirection
- FIG. 3 The improvement in the dimensional change properties resulting from the use of the process of this invention is shown in FIG. 3. It is seen that there is no significant change in the transverse-direction properties as compared with those shown in FIG. 2 but the original curve for this direction shown in FIG. 2 is such that it would never cause package crushing but merely a loose wrap. There is a significant change to be noted in the dimensional change properties in the machine-direction. It is seen :in FIG. 3 that the dimensional change in the machinedirection upon being humidified is always in the form of an expansion and that the change upon being dehumidified does effect a shrinkage of the web but at a significantly lower lever. The importance of the effect on the machine-direction is that the machinedirection of the film is around the package-the weakest direction-and consequently has the greatest effect upon package crushing.
- EXAMPLE I A regenerated cellulose film of 0.0009-inch gage thickness with a 5% moisture content and a 26% softener content was solvent coated with a nitrocellulose coating such as disclosed in Example I of U.S.P. 2,307,057 in a coating apparatus as shown in FIG. 1.
- the coated web had 3.4gm./m.2 of coating and had a final moisture content of 7.5%.
- the coated web was exposed for a period of 4 to 5 seconds in the conditioning section to a conditioning atmosphere of live steam having a superheat temperature of 105 C., then withdrawn from the conditioning atmosphere at a rate of 0.7% less than the feed rate into the section, and wound onto a core.
- Film samples measuring 6 x 6 were taken from the wound roll and immersed in water for 24 hours. The samples were then measured and showed a machinedirection ⁇ wet shrinkage of 1.04%. The same samples were then dried for 72 hours under ambient room conditions of 75 F. dry bulb temperature at 35% relative humidity and remeasured in the machine-direction. The dry shrinkage amounted to 4.43% in the machine-direction.
- This exposure of the film to extended immersion in water followed by redrying of the film demonstrated a 30% improvement in the wet-state machine-direction shrinkage properties and an 11% improvement in the redried state machine-direction shrinkage properties when the web was relaxed 0.7% in the post coating operation over such a sample submitted to the same testing but having had a 0.5% draw in the conditioning section.
- EXAMPLE III A mill roll of cellophane was coated in a manner similar to that described in the previous two examples. The first half of this mill roll 'was conditioned as previously described while the web was subjected to a sub-normal 0.2% draw and the second half of the roll was conditioned while the web was relaxed 0.7%.
- Film samples measuring 4" x 6 were taken from the first and second halves of the mill roll and were placed in an oven and cycled through the following ambient conditions:
- EXAMPLE IV A third roll was processed and tested as described in Example III with the first portion of the roll subjected to 0.2% draw and the second half of the roll was conditioned while the web was relaxed 1.0%.
- the machine-direction shrinkage of the film subjected to 0.2% draw was 3.4% while the machine-direction shrinkage of the film which was relaxed 1.0% during the post-coating operation was 2.6%.
- This exposure of the film to cycling humidified air conditions demonstrated a 24% improvement in the machine-direction shrinkage properties for film relaxed 1.0% as compared with film processed with a subnormal degree of tension imposed during the post-coating operation.
- EXAMPLE V Softened and dried regenerated cellulose film was taken from a cellophane dryer as in Example I and was coated and subjected to normal conditioner drawing of 0.5%. Samples of this film were tested for machine-direction elongation. It was determined that the film produced under these operating conditions had a 15% machinedirection elongation.
- Example II Additional film produced under the same operating conditions was coated and subjected to a post-coating treatment of 0.7% relaxation as in Example I. Samples of this film were tested for machine-direction elongation. It was determined that the film produced under these operating conditions had a 15% machine-direction elongation.
- Example II Additional film produced under the same operating conditions was coated and subjected to a post-coating treatment of 0.7% relaxation as in Example I. Samples of this film were tested for machine-direction elongation and it was determined that the film produced in this manner had a 20% machine-directional elongation which demonstrated a 33% improvement in this property. Improvement in the machine-direction elongation property of regenerated cellulose film also affects an improvement in the durability properties of the film.
- EXAMPLE VI The regenerated cellulose film used in the preparation of Example I was coated to the same coating thickness as the film in Example I using a saran polyester coating such as described in U.S. Pat. 2,570,478 and processed in the post-coating operation under the same conditions as was the lm in Example I.
- test results demonstrate that the web improvements resulting for the use of the process of this invention is independent of the type of coating on the substrate and that the post-coating relaxation process is, therefore, a regenerated cellulose film substrate improvement process. It has been noted, however, that saran polymer coated film produced by the process of this invention yields superior performance characteristics in packaging applications than does similarly produced nitrocellulose coated regenerated cellulose film. This performance superiority is attributable to the greater sealing and scratch-resistant characteristics of Saran polymer coated film.
- a process for coating a lweb of regenerated cellulose film including applying a coating composition of at least a film forming coating material and a solvent onto the web, heating the coated web while in a circulating air stream to remove the solvent and solidify the coating material, passing the coated web around a driven head roll at a constant rate of speed after the solvent is removed by heat and circulating air and into a humidification chamber, humidifying the coated web, passing the humidied and coated web around a driven chill roll and winding the coated web onto a core, the improvement comprising:
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- Life Sciences & Earth Sciences (AREA)
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- Application Of Or Painting With Fluid Materials (AREA)
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- Wrappers (AREA)
Abstract
Description
Applications Claiming Priority (1)
Application Number | Priority Date | Filing Date | Title |
---|---|---|---|
US70515868A | 1968-02-13 | 1968-02-13 |
Publications (1)
Publication Number | Publication Date |
---|---|
US3565669A true US3565669A (en) | 1971-02-23 |
Family
ID=24832279
Family Applications (1)
Application Number | Title | Priority Date | Filing Date |
---|---|---|---|
US705158A Expired - Lifetime US3565669A (en) | 1968-02-13 | 1968-02-13 | Process for improving the permanent shrinkage properties of regenerated cellulose film |
Country Status (3)
Country | Link |
---|---|
US (1) | US3565669A (en) |
FR (1) | FR2001818A1 (en) |
GB (1) | GB1251418A (en) |
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3656993A (en) * | 1970-06-04 | 1972-04-18 | Du Pont | Preparation of coated regenerated cellulose film |
US3939000A (en) * | 1973-11-21 | 1976-02-17 | E. I. Du Pont De Nemours And Company | Flat photographic film produced by heating above the second order transition temperature of the base |
US3959526A (en) * | 1974-12-20 | 1976-05-25 | E. I. Du Pont De Nemours And Company | Process for preparing high barrier, heat-sealable packaging film |
US20030125683A1 (en) * | 2001-12-31 | 2003-07-03 | Reeves William G. | Durably hydrophilic, non-leaching coating for hydrophobic substances |
US20030143388A1 (en) * | 2001-12-31 | 2003-07-31 | Reeves William G. | Regenerated carbohydrate foam composition |
US20030155679A1 (en) * | 2001-12-31 | 2003-08-21 | Reeves William G. | Method of making regenerated carbohydrate foam compositions |
US20050148922A1 (en) * | 2003-12-31 | 2005-07-07 | Reeves William G. | Thermoplastic composition and products made therefrom |
Families Citing this family (2)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
FR2962666B1 (en) * | 2010-07-16 | 2014-10-10 | Univ Paris Curie | METHOD FOR DEPOSITING A LAYER ON THE SURFACE OF A SUBSTRATE |
CN109701826B (en) * | 2018-12-21 | 2020-05-19 | 东莞兆发五金玻璃制品有限公司 | Glass door and window's glass glues fast curing equipment |
-
1968
- 1968-02-13 US US705158A patent/US3565669A/en not_active Expired - Lifetime
-
1969
- 1969-02-12 GB GB1251418D patent/GB1251418A/en not_active Expired
- 1969-02-13 FR FR6903431A patent/FR2001818A1/fr not_active Withdrawn
Cited By (7)
Publication number | Priority date | Publication date | Assignee | Title |
---|---|---|---|---|
US3656993A (en) * | 1970-06-04 | 1972-04-18 | Du Pont | Preparation of coated regenerated cellulose film |
US3939000A (en) * | 1973-11-21 | 1976-02-17 | E. I. Du Pont De Nemours And Company | Flat photographic film produced by heating above the second order transition temperature of the base |
US3959526A (en) * | 1974-12-20 | 1976-05-25 | E. I. Du Pont De Nemours And Company | Process for preparing high barrier, heat-sealable packaging film |
US20030125683A1 (en) * | 2001-12-31 | 2003-07-03 | Reeves William G. | Durably hydrophilic, non-leaching coating for hydrophobic substances |
US20030143388A1 (en) * | 2001-12-31 | 2003-07-31 | Reeves William G. | Regenerated carbohydrate foam composition |
US20030155679A1 (en) * | 2001-12-31 | 2003-08-21 | Reeves William G. | Method of making regenerated carbohydrate foam compositions |
US20050148922A1 (en) * | 2003-12-31 | 2005-07-07 | Reeves William G. | Thermoplastic composition and products made therefrom |
Also Published As
Publication number | Publication date |
---|---|
DE1907258A1 (en) | 1970-07-30 |
GB1251418A (en) | 1971-10-27 |
FR2001818A1 (en) | 1969-10-03 |
DE1907258B2 (en) | 1977-06-16 |
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