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    • 11. 发明授权
    • 수동조작장치
    • 手动操作装置
    • KR101431515B1
    • 2014-08-21
    • KR1020130023013
    • 2013-03-04
    • 노경부장지은
    • 노경부장지은
    • B66B1/46A61L2/00
    • A61L2/10A61L2202/11A61L2202/14B66B1/46
    • The present invention relates to a manual manipulator for generating electric signal for controlling the operation of various controllable devices by being manipulated by button manipulations of a user operating switches and, more specifically, to a manual manipulator for resolving hygienic problem due to the button manipulations done by many and unspecified users by efficiently sterilizing the contact surfaces between the manipulated buttons and fingers. According to the present invention, an electric signal for controlling the operation of various controllable devices is generated by driving switches in accordance with the manual manipulation of the buttons by a user, while preventing the irradiation of an ultraviolet sterilizing ray onto the user during the sterilization of the contact surfaces when the user is performing a manual manipulation. Thereby, a safe sterilization can be conducted, at the same time, maintaining a hygienic status of the button contact surfaces by efficiently sterilizing the contact surfaces immediately after the manual manipulation ends, regardless of the existence or the use of a user.
    • 本发明涉及一种用于产生电信号的手动操纵器,用于通过用户操作开关的按钮操作来操纵各种可控制装置的操作,更具体地说,涉及用于解决由于按钮操作所完成的卫生问题的手动操纵器 通过有效地消毒操作的按钮和手指之间的接触表面,由许多和未指定的使用者。 根据本发明,通过根据用户的按钮的手动操作来驱动开关来产生用于控制各种可控装置的操作的电信号,同时防止在灭菌期间向用户照射紫外线杀菌射线 当用户正在执行手动操作时,接触表面。 由此,可以进行安全灭菌,同时通过在手动操作结束后立即对接触面进行有效的消毒来保持按钮接触面的卫生状态,而与使用者的存在或使用无关。
    • 14. 发明公开
    • 종교용품 디스플레이용 상자
    • 宗教物品陈列箱
    • KR1020170066051A
    • 2017-06-14
    • KR1020150172596
    • 2015-12-04
    • 장지은
    • 장지은
    • A47G33/02F21V33/00
    • 전면에개방된외부상자와, 외부상자내부에수용된상태로외부상자의전방으로출몰가능하게설치되며내부에종교용품이거치되어수용되는내부상자와, 외부상자의전방을개폐하도록양측에회동가능하게연결되는한 쌍의도어와, 도어와내부상자를연결하며도어의개폐동작에연동하여내부상자가외부상자외부로출몰가능하도록하는연동부재와, 내부상자의내측에설치되는제1조명부와, 내부상자의위치를감지하는스위칭센서및 스위칭센서의감지신호를근거로하여제1조명부의온/오프동작을제어하는제어부를포함하는것을특징으로하는종교용품디스플레이용상자가개시된다.
    • 和外箱在前面打开,在被安装到在两侧可旋转地缩回所述外部盒的前进,以便打开和关闭所述内箱以及容纳在宗教用品的外箱的前部安装在所述内部容纳在外箱内部的状态下 以及第一照明部,其安装在内部,并与一对门和门和内盒连接的连接,并且在与所述门互锁构件的所述内箱的打开和关闭操作关联,以允许缩回内箱外侧的外箱,所述内 以及控制器,用于基于开关传感器的感测信号和用于感测盒的位置的开关传感器来控制第一照明单元的开/关操作。
    • 19. 发明公开
    • 발효 초콜릿 조성물과 이를 이용하여 제조된 발효 초콜릿 및 그 제조방법
    • 发酵的巧克力组合物及其制备的产生的巧克力产品及其制备方法
    • KR1020130035293A
    • 2013-04-09
    • KR1020110099463
    • 2011-09-30
    • 장지은
    • 장지은
    • A23G1/42
    • A23G1/423A23G2200/02
    • PURPOSE: A manufacturing method of fermented chocolate is provided to offer the good taste, flavor, eating texture, and useful effects of polyphenol and microorganisms in the chocolate using a fermented product fermented by yeast, a rice-wine starter, and/or acetic acid bacteria. CONSTITUTION: A fermented chocolate composition comprises fermented grains and cocoa. The fermented grains are fermented by using yeast, a rice-wine starter, and acetic acid bacteria. The cocoa comprises 5-10 parts by weight of one or more cocoa mass or cocoa powder corresponded to the fermented grains. A manufacturing method of the fermented grains comprises the following step: producing a first microorganism by adding 3-9 weight% of Saccharomyces cerevisiae into water with 0.1-1 weight% of table salt, and culturing at 40-36 deg. C for 60 hours; preparing a second microorganism by adding 0.1-0.5 weight% of rice wine starter to the first microorganism, and culturing at 35-38 deg. C for 48-80 hours; adding 5-20 weight% of grain powder to the second microorganism, and culturing at 35-38 deg. C for 36-60 hours; and adding 0.1-0.3 weight% of acetic acid bacteria to the cultured medium having the grains, and culturing at 20-30 deg. C for 36-80 hours.
    • 目的:提供发酵巧克力的制造方法,以使用由酵母发酵的发酵产品,米酒发酵剂和/或乙酸提供巧克力中多酚和微生物的良好的味道,风味,进食质地和有用效果 菌。 构成:发酵巧克力组合物包含发酵谷物和可可粉。 发酵谷物通过使用酵母,米酒起始物和乙酸菌发酵。 可可包含5-10重量份的一种或多种对应于发酵谷物的可可粉或可可粉。 发酵谷物的制造方法包括以下步骤:通过将3-9重量%的酿酒酵母加入0.1-1重量%的餐盐的水中制备第一微生物,并在40-36℃培养。 C 60小时; 通过向第一微生物中加入0.1-0.5重量%的米酒起始剂并在35-38℃培养来制备第二微生物。 C为48-80小时; 向第二微生物中加入5-20重量%的谷物粉末,并在35-38度培养。 C为36-60小时; 并向具有颗粒的培养基中加入0.1-0.3重量%的乙酸细菌,并在20-30℃培养。 C为36-80小时。