Remoistenable adhesive composition for prepasted wall coverings
    11.
    发明授权
    Remoistenable adhesive composition for prepasted wall coverings 失效
    用于预处理的墙壁覆盖物的可脱除粘合剂组合物

    公开(公告)号:US3690938A

    公开(公告)日:1972-09-12

    申请号:US3690938D

    申请日:1970-11-18

    Inventor: SWIFT THOMAS G

    CPC classification number: C09J105/00

    Abstract: A REMOISTENABLE ADHESIVE COMPOSITION PARTICULARLY USEFUL FOR PREPASTED WALL COVERINGS WHICH INCLUDES A DRY BLEND OF A WATER SOLUBLE LOW VISCOSITY STARCH, A LOW VISCOSITY CELLULOSE MATERIAL SUCH AS HYDROXYETHYL CELLULOSE, CARBOXYMETHYL CELLULOSE OR METHYL CELLULOSE ETHER, AND A PLASTICIZER SUCH AS SODIUM NITRATE, UREA, CALCIUM CHLORIDE, GLYCERIN OR SODIUM METHACRYLATE. THE ABOVE BLEND MAY ALSO INCLUDE AN EXTENDER MATERIAL SUCH AS SODIUM METHACRYLATE OR A CLAY, OR BOTH IN COMBINATION. THE ADHESIVE IS NOT DISTURBED BY FURTHER HANDLING AND CAN BE APPLIED TO THE WALL COVERING EITHER BEFORE OR AFTER PRINTING THE DECORATIVE SURFACE. THE WALL COVERINGS TREATED WITH THIS ADHESIVE ARE EASILY APPLIED WHEN REMOISTENED, BECAUSE THEY HAVE GOOD "SLIP" PROPERTIES. THEY ARE ALSO EASILY REMOVED AFTER INSTALLATION WITHOUT THE USE OF STEAM OR OTHER STRIPPING AGENTS, SIMPLY BY PULLING THE COVERING AWAY FROM THE UNDERSURFACE.

    Predetermined chemical reactions in photographic imagewise configuration
    12.
    发明授权
    Predetermined chemical reactions in photographic imagewise configuration 失效
    摄影图像配置中预测的化学反应

    公开(公告)号:US3676145A

    公开(公告)日:1972-07-11

    申请号:US3676145D

    申请日:1970-09-21

    CPC classification number: B41M5/398 G03F7/28

    Abstract: PROCESS FOR CARRYING OUT A PREDETERMINED CHEMICAL REACTION IN IMAGWISE CONFIGURATION WHICH COMPRISES EXPOSING AN ELEMENT COMPRISING (A) A FIRST SOLID LAYER COMPRISING A COMPOSITION CAPABLE OF UNDERGOING A PREDETERMINED CHEMICAL REACTION BEARING (B) A SECOND LAYER COMPRISING A COMPOSITION CAPABLE OF RECEIVING A POWDER IN IMAGE-WISE CONFIGURATION TO ACTINIC RADIATION TO FORM A LATENT POWDER-RECEPTICE IMAGE WITHOUT INITIALTING SAID PREDETERMINED CHEMICAL REACTION; DEVELOPING SAID LATENT IMAGE WITH POWDER PARTICELS COMPRISING A COMPLEMENTARY REAGENT WHICH, IN MINOR PROPORTION, EXERTS A MAJOR INFLUENCE ON THE COURSE OF SAID PREDETERMINED CHEMICAL REACTION TO FORM A LAYER OF POWDER PARTICLES IN IMAGE-WISE CONFIGURATION; BRINGING SAID COMPLEMENTARY REGENT INTO REACTIVE CONTACT WITH SAID COMPOSITION CAPABLE OF UNDERGOING SAID PREDETERMINED CHEMICAL REACTION; AND CARRYING OUT SAID PREDETERMINED CHEMICAL REACTION IN A PREDETERMINED CONFIGURATION CONFORMING TO THE IMAGE-WISE CONFIGURATION OF THE POWDER PARTICLES OF SAID SECOND LAYER.

    Method of producing amylo-1 6-glucosidase
    14.
    发明授权
    Method of producing amylo-1 6-glucosidase 失效
    生产AMYLO-1 6 -GLUCOSIDASE的方法

    公开(公告)号:US3654088A

    公开(公告)日:1972-04-04

    申请号:US3654088D

    申请日:1969-10-22

    CPC classification number: C12Y302/01041 C12N9/2457

    Abstract: METHOD OF UTILIZING ANYLOPECTIN AS THE PRINCIPAL CARBOHYDRATE SOURCE FOR THE PRODUCTION OF AMYLO-1,6-GLUCOSIDASE. WHICH COMPRISES (1) CONDITIONING CELLS OF A CULTURE CAPABLE OF PRODUCING AMYLO-1,6-GLUCOSIDASE IN AN AQUEOUS MEDIUM COMPRISING A CARBOHYDRATE INDUCER SELECTED FROM THE GROUP CONSISTNG OF MALTOSE, MALTOTRIOSE, PULLULAN AND MIXTURES THEREOF, (2) BRINGING TOGETHER IN AN AQUEOUS MEDIUM THE INDUCED CELLS AND PASTED AMYLOPECTIN AND (3) INCUBATING AT PH 6.0 TO 8.1 TO PRODUCE AMYLO-1,6GLUCOSIDASE, WHEREIN THE AMYLOPECTIN CONSTITUTES THE PRINCIPAL CARBOHYDRATES SOURCE IN STEP (3).

    Method for preparing low d.e. starch hydrolyzates
    15.
    发明授权
    Method for preparing low d.e. starch hydrolyzates 失效
    制备低密度脂蛋白的方法 STARCH水解产物

    公开(公告)号:US3616220A

    公开(公告)日:1971-10-26

    申请号:US3616220D

    申请日:1968-10-30

    CPC classification number: C12P19/14 A23L29/35

    Abstract: Aqueous starch paste is acid converted to a hydrolyzate having a dextrose equivalent constant (D.E.) in the range of from about 8 to about 16 percent, then after removal of any insoluble fatty material present, the acid hydrolyzate is cooled for at least 1 hour at a temperature below about 60* F., e.g., in the range of from about 32* F. to about 50* F., and precipitated material formed then is separated from the chilled hydrolyzate liquor. The resultant hydrolyzates, as well as hydrolyzates formed by slight alpha-amylase conversion of the resultant liquor, form aqueous syrups having excellent stability against haze formation. The lower D.E. hydrolyzates produced also are essentially nonsweet and nonhygroscopic.

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