Counterfeit prevention paper and manufacturing method thereof
    1.
    发明授权
    Counterfeit prevention paper and manufacturing method thereof 有权
    防伪纸及其制造方法

    公开(公告)号:US08105977B2

    公开(公告)日:2012-01-31

    申请号:US12189074

    申请日:2008-08-08

    IPC分类号: B41M5/26

    摘要: The present invention relates to a counterfeit prevention paper and manufacturing method thereof, and more particularly to currency, securities, official document and several certificates, etc.The counterfeit prevention paper according to the present invention comprises a paper and a thermopaint layer which is formed on a paper and is discolored according to a temperature.The counterfeit prevention paper according to the present invention can detect easily a counterfeit by an unaided eye. Also, a function for preventing a counterfeit is not copied by a counterfeit device, thus the counterfeit prevent paper according to the present invention can improve a reliability of various official documents and several certificates, etc.

    摘要翻译: 本发明涉及防伪纸及其制造方法,更具体地涉及货币,证券,官方文件和若干证书等。根据本发明的防伪纸包括纸和热电影层,其形成在 一张纸,根据温度变色。 根据本发明的防伪纸可以通过肉眼容易地检测伪造的伪造品。 此外,防伪品的功能不被仿冒装置复制,因此根据本发明的防伪纸可以提高各种官方文件和几种证书等的可靠性。

    COUNTERFEIT PREVENTION PAPER AND MANUFACTURING METHOD THEREOF
    2.
    发明申请
    COUNTERFEIT PREVENTION PAPER AND MANUFACTURING METHOD THEREOF 有权
    防伪纸及其制造方法

    公开(公告)号:US20090047488A1

    公开(公告)日:2009-02-19

    申请号:US12189074

    申请日:2008-08-08

    IPC分类号: B32B3/10 B05D1/36

    摘要: The present invention relates to a counterfeit prevention paper and manufacturing method thereof, and more particularly to currency, securities, official document and several certificates, etc.The counterfeit prevention paper according to the present invention comprises a paper and a thermopaint layer which is formed on a paper and is discolored according to a temperature.The counterfeit prevention paper according to the present invention can detect easily a counterfeit by an unaided eye. Also, a function for preventing a counterfeit is not copied by a counterfeit device, thus the counterfeit prevent paper according to the present invention can improve a reliability of various official documents and several certificates, etc.

    摘要翻译: 本发明涉及防伪纸及其制造方法,更具体地涉及货币,证券,官方文件和若干证书等。根据本发明的防伪纸包括纸和热电影层,其形成在 一张纸,根据温度变色。 根据本发明的防伪纸可以通过肉眼容易地检测伪造的伪造品。 此外,防伪品的功能不被仿冒装置复制,因此根据本发明的防伪纸可以提高各种官方文件和几种证书等的可靠性。

    Alginate gel based adsorbents for heavy metal removal
    5.
    发明授权
    Alginate gel based adsorbents for heavy metal removal 失效
    用于重金属去除的藻酸盐凝胶基吸附剂

    公开(公告)号:US06989102B1

    公开(公告)日:2006-01-24

    申请号:US09469818

    申请日:1999-12-22

    IPC分类号: C02F1/28

    摘要: An alginate gel adsorbent to remove heavy metal ions according to the present invention is prepared by adding dropwisely 0.1-5 wt % alginate solution to a polyvalent cationic solution thereby cross-linking alginic acid with polyvalent cations. An alginate gel adsorbent containing activated carbon capable of simultaneously removing heavy metal ions and organotoxic materials, that is, activated carbon/alginate gel adsorbent, is prepared by adding dropwisely a mixed solution of 0.17-10 wt % of alginate and 0.1-10 wt % of activated carbon powder to a polyvalent cationic solution thereby cross-linking alginic acid with polyvalent cations in order to immobilize polyvalent cation to alginic acid containing activated carbon. The polyvalent cationic solution is selected from the group consisting of calcium chloride (CaCl2), strontium chloride (SrCl2), barium chloride (BaCl2) and aluminium chloride (AlCl3). A flat board or a thin membrane coated alginate gel adsorbent can be prepared by coating alginate gels onto a supporter such as paper, wood plate and textile fabrics. The alginate gel adsorbent for water purification can be applied to a water purifier as well as a process of wastewater treatment. The alginate gel coated onto a supporter is prepared by immersing a supporter in 0.05-5 wt % alginate solution so that the supporter may uniformly adsorb the alginate solution, immersing the supporter in a polyvalent cationic solution thereby forming alginate gel on the surface of the supporter, and drying the supporter formed with alginate gel thereon.

    摘要翻译: 通过将0.1-5重量%的藻酸盐溶液滴加到多价阳离子溶液中,由此将藻酸与多价阳离子交联,制备了根据本发明的用于去除重金属离子的藻酸盐凝胶吸附剂。 通过滴加0.17-10重量%的藻酸盐和0.1-10重量%的藻酸盐的混合溶液,制备含有能够同时除去重金属离子和有机毒物质的活性炭的藻酸盐凝胶吸附剂,即活性炭/藻酸盐凝胶吸附剂, 的活性炭粉末与多价阳离子溶液反应,从而将藻酸与多价阳离子交联,以便将多价阳离子固定在含藻酸的活性炭中。 多价阳离子溶液选自氯化钙(CaCl 2 Cl 2),氯化锶(SrCl 2 Cl 2),氯化钡(BaCl 2 N 2) >)和氯化铝(AlCl 3 3)。 可以通过将藻酸盐凝胶涂布在诸如纸,木板和纺织品的支撑物上来制备平板或薄膜包衣藻酸盐凝胶吸附剂。 用于水净化的藻酸盐凝胶吸附剂可以应用于净水器以及废水处理过程。 通过将支持体浸渍在0.05-5重量%的藻酸盐溶液中来制备涂覆在支持体上的藻酸盐凝胶,使得载体可以均匀地吸附藻酸盐溶液,将载体浸入多价阳离子溶液中,从而在支持物的表面上形成藻酸盐凝胶 ,并将其上形成有藻酸盐凝胶的载体干燥。

    Gene analysis method using SDL-PCR
    6.
    发明授权
    Gene analysis method using SDL-PCR 有权
    基因分析方法采用SDL-PCR

    公开(公告)号:US09523117B2

    公开(公告)日:2016-12-20

    申请号:US14002662

    申请日:2012-01-30

    IPC分类号: C12Q1/68

    摘要: The present invention relates to a method for analyzing genes using SDL-PCR (separation of displaced ligation probe-based PCR), and more particularly to a method for analyzing genes using SDL-PCR, in which probes comprising a nucleotide sequence complementary to the gene of interest are ligated with each other by ligase, and another probe capable of hybridizing to the probes is hybridized and extended, thereby preparing a template probe, and the template probe for the gene of interest is amplified using universal primers.According to the SDL-PCR method of the present invention, non-specific amplification can be minimized by removing non-ligated probes or genomic DNA using a tag, and separation can be achieved within a shorter time compared to a separation method that is performed using exonuclease. In addition, ligation, separation and polymerase chain reaction processes can be performed in a single solution in a single tube, and thus a plurality of genes can be amplified at the same time in an accurate and rapid manner.

    摘要翻译: 根据本发明的SDL-PCR方法,通过使用标签除去未连接的探针或基因组DNA,可以使非特异性扩增最小化,并且与使用 核酸外切酶 此外,连接,分离和聚合酶链反应方法可以在单个管中的单个溶液中进行,因此可以以准确和快速的方式同时扩增多个基因。

    Method, apparatus, and recording medium for playing game with server transferring in online game environment
    8.
    发明授权
    Method, apparatus, and recording medium for playing game with server transferring in online game environment 有权
    用于在网络游戏环境中进行服务器转移的玩游戏的方法,装置和记录介质

    公开(公告)号:US08992328B2

    公开(公告)日:2015-03-31

    申请号:US13698482

    申请日:2011-05-17

    IPC分类号: A63F13/00 A63F13/30 H04L29/06

    摘要: Disclosed are a method, an apparatus, and a recording medium for playing a game with server transferring in an online game environment. The method includes: receiving identification information for login from a first client; transmitting online game environment information to the first client; performing an advance operation of the server transferring for a server transferring of a second client with an outside server; receiving data for playing the game transmitted from the outside server or the second client; transmitting a resulting data of game play, in which the received data is applied to the online game environment, to the outside server or the second client, which has transmitted the data for playing the game; and storing a result of an interaction generated between the first client and the second client in a game history of the first client.

    摘要翻译: 公开了一种用于在在线游戏环境中玩服务器传送的游戏的方法,装置和记录介质。 该方法包括:从第一客户端接收用于登录的识别信息; 将网络游戏环境信息传送给第一客户端; 执行所述服务器的传送的前进操作,用于服务器与外部服务器传送第二客户端; 从外部服务器或第二客户端接收用于播放游戏的数据; 将接收到的数据应用于在线游戏环境的游戏结果数据发送到已经发送用于玩游戏的数据的外部服务器或第二客户端; 以及将在所述第一客户端和所述第二客户端之间生成的交互的结果存储在所述第一客户端的游戏历史中。

    GENE ANALYSIS METHOD USING SDL-PCR
    10.
    发明申请
    GENE ANALYSIS METHOD USING SDL-PCR 有权
    使用SDL-PCR的基因分析方法

    公开(公告)号:US20140171334A1

    公开(公告)日:2014-06-19

    申请号:US14002662

    申请日:2012-01-30

    IPC分类号: C12Q1/68

    摘要: The present invention relates to a method for analyzing genes using SDL-PCR (separation of displaced ligation probe-based PCR), and more particularly to a method for analyzing genes using SDL-PCR, in which probes comprising a nucleotide sequence complementary to the gene of interest are ligated with each other by ligase, and another probe capable of hybridizing to the probes is hybridized and extended, thereby preparing a template probe, and the template probe for the gene of interest is amplified using universal primers.According to the SDL-PCR method of the present invention, non-specific amplification can be minimized by removing non-ligated probes or genomic DNA using a tag, and separation can be achieved within a shorter time compared to a separation method that is performed using exonuclease. In addition, ligation, separation and polymerase chain reaction processes can be performed in a single solution in a single tube, and thus a plurality of genes can be amplified at the same time in an accurate and rapid manner.

    摘要翻译: 本发明涉及使用SDL-PCR(基于取代的基于连接探针的PCR的分离)分析基因的方法,更具体地涉及使用SDL-PCR分析基因的方法,其中探针包含与该基因互补的核苷酸序列 通过连接酶连接相互连接,并且能够与探针杂交的另一个探针杂交并扩展,从而制备模板探针,并使用通用引物扩增目的基因的模板探针。 根据本发明的SDL-PCR方法,通过使用标签除去未连接的探针或基因组DNA,可以使非特异性扩增最小化,并且与使用 核酸外切酶 此外,连接,分离和聚合酶链反应方法可以在单个管中的单个溶液中进行,因此可以以准确和快速的方式同时扩增多个基因。