초록 ▼

Simulated stone texture products are obtained when specially selected materials are properly admixed and formed via rotational molding. These products are manufactured from suitable molds according to a prescribed process methodology using synthetic polymeric materials instead of stone materials. Pr

Simulated stone texture products are obtained when specially selected materials are properly admixed and formed via rotational molding. These products are manufactured from suitable molds according to a prescribed process methodology using synthetic polymeric materials instead of stone materials. Prerequisite surface textures are produced that effectively simulate the corresponding actual stone products.

대표청구항 ▼

Simulated stone texture products are obtained when specially selected materials are properly admixed and formed via rotational molding. These products are manufactured from suitable molds according to a prescribed process methodology using synthetic polymeric materials instead of stone materials. Pr

Simulated stone texture products are obtained when specially selected materials are properly admixed and formed via rotational molding. These products are manufactured from suitable molds according to a prescribed process methodology using synthetic polymeric materials instead of stone materials. Prerequisite surface textures are produced that effectively simulate the corresponding actual stone products. ize cleaning/rinsing performance within the zone. into a stream of the liquid carrier, the injection being carried out over a limited time so that a distinct test section of the stream contains the test sample,(b) passing the stream of liquid carrier containing the test sample over a solid phase in a test chamber, the solid phase comprising the receptor, and(c) examining the stream of liquid carrier leaving the test chamber to ascertain a variable which reflects the interaction of the modifying agent and the receptor in the presence of the liquid carrier.2. The method according to claim 1 wherein modifying agent comprises a non-biological polymer.3. The method according to claim 1 wherein the library is a library of receptors.4. The method according to claim 1 wherein the library is a library of receptors, each of the members of the library comprising a different natural or artificial mammalian tissue.5. The method according to claim 1 wherein the library is a library of receptors, each of the members of the libraries comprising a same common natural or artificial mammalian tissue that has been pretreated with a different non-biological polymer.6. The method according to claim 1 wherein the library is a library of modifying agents.7. The method according to claim 1 wherein the library is a library of modifying agents, each of the at least four members of the library comprising a therapeutic agent or a diagnostic agent.8. The method according to claim 1 wherein the library is a library of modifying agents, each of the at least four members of the library comprising a different therapeutic agent or a different diagnostic agent.9. A method for evaluating the interaction between a receptor comprising natural or artificial mammalian tissue and a modifying agent comprising a non-biological polymer in the presence of a liquid carrier, the method comprising: providing the receptor comprising natural or artificial mammalian tissue, and providing the modifying agent comprising a non-biological polymer, the modifying agent being provided as a member of a combinatorial library having at least four members, each of the at least four members of the library comprising a different non-biological polymer,conducting at least four test procedures with the receptor and liquid carrier being the same in each of the test procedures, and with a different member of the combinatorial library being used in each of the at least four test procedures, each of the test procedures comprising:(a) injecting a liquid test sample comprising the modifying agent into a stream of the liquid carrier, the injection being carried out over a limited time so that a distinct test section of the stream contains the test sample,(b) passing the stream of liquid carrier containing the test sample over a solid phase in a test chamber, the solid phase comprising the receptor, and(c) examining the stream of liquid carrier leaving the test chamber to ascertain a variable which reflects the interaction of the modifying agent and the receptor in the presence of the liquid carrier.10. The method according to claim 9 wherein each of the at least four members of the library of modifying agents further comprises a therapeutic agent or a diagnostic agent.11. The method according to claim 9 wherein each of the at least four members of the library of modifying agents comprises a different non-biological polymer and either a same common therapeutic agent or a same common diagnostic agent.12. The method according to claim 1 or9 wherein the liquid carrier is water or an aqueous solution.13. The method according to claim 1 or9 wherein the receptor comprises natural mammalian tissue.14. The method according to claim 1 or9 wherein the receptor comprises artificial mammalian tissue.15. The method according to claim 1 or9 further comprising:(d) using the results from the steps (c) of the test procedures to select at least one member of the library for further testing; and(e) subjecti