会员体验
专利管家(专利管理)
工作空间(专利管理)
风险监控(情报监控)
数据分析(专利分析)
侵权分析(诉讼无效)
联系我们
交流群
官方交流:
QQ群: 891211   
微信请扫码    >>>
现在联系顾问~
热词
    • 2. 发明公开
    • 터치 패널
    • 触控面板及其驱动方法
    • KR1020130083303A
    • 2013-07-22
    • KR1020120004007
    • 2012-01-12
    • 동진홀딩스 주식회사
    • 이준혁
    • G06F3/041
    • G06F3/041B32B33/00B32B2457/208G06F3/045G06F2203/04103
    • PURPOSE: A touch panel is provided to reduce the production cost without requiring a scan driver. CONSTITUTION: A first electrode (60) is located on a first substrate (10) and is mutually detached. A second electrode (50) is located on the first substrate and is mutually detached with the first electrode. The second electrode has a shape which enables contacting the surface, and receives the voltage. A third electrode (40) is mutually detached with the second electrode, located on the second electrode. A second substrate (12) is located on the third electrode. The first and the third electrodes have a linear shape which crosses three-dimensionally, are mutually electrified by the pressure directly applied to the second substrate, and sense the current.
    • 目的:提供触摸屏以降低生产成本,而不需要扫描驱动程序。 构成:第一电极(60)位于第一基板(10)上并相互分开。 第二电极(50)位于第一基板上并与第一电极相互分离。 第二电极具有能够接触表面并接收电压的形状。 第三电极(40)与位于第二电极上的第二电极相互分离。 第二基板(12)位于第三电极上。 第一和第三电极具有三维交叉的直线形状,通过直接施加到第二基板的压力相互通电,并感测电流。
    • 3. 发明公开
    • 뷰렛을 이용한 하이드라조디카본아미드의 제조 방법
    • 使用微生物制备氢化二苯甲酰胺的方法
    • KR1020030096792A
    • 2003-12-31
    • KR1020020033814
    • 2002-06-17
    • 동진홀딩스 주식회사
    • 이준혁한상진
    • C07C231/12
    • C07C281/06
    • PURPOSE: An environment-friendly and economical method for preparing hydrazodicarbonamide is provided to improve the reaction yield and to reduce the reaction time and the consumption of reaction materials and catalyst. CONSTITUTION: The method for preparing a hydrazodicarbonamide comprises the steps of: reacting biuret of the formula 1 with a metal hypohalogen compound or with a halogenating agent to obtain a monohalobiuret of the formula 4 or formula 5 and reacting the monohalobiuret with a base to obtain a monohalobiuret metal salt of the formula 2 or formula 3, in the presence of the catalyst which contains bromine or iodine and generates an bromide or iodide ion during the reaction; and then reacting the monohalobiuret metal salt obtained from the preceding step with ammonia: wherein M is a metal and X is a halogen, in the formula 2-5.
    • 目的:提供制备肼基二酰胺的环保经济方法,以提高反应产率,减少反应时间和反应材料和催化剂的消耗。 构成:制备肼基二酰胺的方法包括以下步骤:使式1的缩二脲与金属低卤化合物或与卤化剂反应以获得式4或式5的单卤代双酚A,并使单卤代硼烷与碱反应,得到 在含有溴或碘的催化剂存在下,在反应过程中产生溴化物或碘离子,式2或式3的单卤代二价金属盐; 然后使由前述步骤获得的单卤代羰基金属盐与氨反应:其中M为金属,X为卤素。
    • 4. 发明公开
    • 터치 패널 및 그 제조 방법
    • 触控面板及其制造方法
    • KR1020140128880A
    • 2014-11-06
    • KR1020140050724
    • 2014-04-28
    • 동진홀딩스 주식회사
    • 이준혁신민승노기봉
    • G06F3/041
    • G06F3/041G06F2203/04103
    • 터치 패널 및 그 제조 방법을 제공한다. 터치 패널은 제1 터치패널부 및 제1 터치패널부 위에 위치하는 제2 터치패널부를 포함한다. 제1 터치패널부 및 제2 터치패널부로 이루어진 군에서 선택된 하나 이상의 터치패널부는, i) 터치용 표시영역과 터치용 표시영역의 한 가장자리와 인접하는 비표시 영역을 포함하는 광투과성 기판, ii) 터치용 표시영역 내에 위치하는 감지전극, iii) 감지전극과 전기적으로 연결되고, 비표시 영역내에 위치하는 인출전극, 및 iv) 인출전극 위에 위치하는 감광층을 포함한다.
    • 提供一种触摸面板及其制造方法。 触摸面板包括布置在第一触摸面板单元上的第一触摸面板单元和第二触摸面板单元。 从包括第一触摸面板单元和第二触摸面板单元的组中选择的至少一个触摸面板单元包括:i)透光衬底,其包括触摸显示区域和与所述第二触摸面板单元的边缘相邻的非显示区域 触摸显示区域; ii)布置在触摸显示区域上的感测电极; iii)引出电极,其电连接到感测电极并且布置在非显示区域上; 和iv)布置在提取电极上的感光层。
    • 5. 发明公开
    • 요소를 출발물질로 사용하는 하이드라조디카본아미드의제조방법 및 제조장치
    • 通过使用UREA作为起始材料生产氢化二苯甲酰胺的方法和装置
    • KR1020030033629A
    • 2003-05-01
    • KR1020010065704
    • 2001-10-24
    • 동진홀딩스 주식회사
    • 이준혁한상진
    • C07C231/22
    • PURPOSE: Provided are a process and an apparatus for producing hydrazodicarbonamide(HDCA) by using urea as a starting material, which are economical and friendly to environment. CONSTITUTION: The process for producing the hydrazodicarbonamide(HDCA) comprises the steps of: heat-decomposing the urea to obtain biuret(formula 1) and ammonia in a heat decomposition furnace; refining the obtained biuret in a recrystallization reactor; reacting the recrystallized biuret with a metal hypohalogen compound, or a halogen and a base to obtain a monohalobiuret metal salt(formula 2 or 3) in a first reactor; reacting the monohalobiuret metal salt with ammonia to synthesize the hydrazodicarbonamide(HDCA) in a second reactor; separating the obtained hydrazodicarbonamide(HDCA) from surplus ammonia in an ammonia evaporator and transferring the separated ammonia to a concentrator, wherein the concentrator concentrates the surplus ammonia and the ammonia obtained from the heat decomposition furnace and supplies to the second reactor. In the formula, M is metal and X is halogen.
    • 目的:提供以尿素为起始原料生产肼基二酰胺(HDCA)的方法和装置,对环境是经济和友好的。 构成:生产肼基二酰胺(HDCA)的方法包括以下步骤:在热分解炉中热分解尿素以获得缩二脲(式1)和氨; 在再结晶反应器中精制得到的缩二脲; 使重结晶的缩二脲与金属低卤化合物或卤素和碱反应,以在第一反应器中获得单卤代硼烷金属盐(式2或3); 使单卤代羰基金属盐与氨反应,以在第二反应器中合成肼基二酰胺(HDCA); 在氨蒸发器中将得到的肼二酰胺(HDCA)与多余的氨分离,并将分离的氨转移到浓缩器中,其中浓缩器将剩余的氨和从热分解炉获得的氨浓缩并供给至第二反应器。 在该式中,M是金属,X是卤素。
    • 8. 发明授权
    • 뷰렛 및 시아누르산의 제조 방법 및 그 제조 장치
    • 生物素和氰尿酸的制备方法及其制备方法
    • KR100798109B1
    • 2008-01-28
    • KR1020060076212
    • 2006-08-11
    • 동진홀딩스 주식회사
    • 이준혁신민승이훈
    • C07C275/62C07C275/04
    • C07D251/32B01D9/0013B01D9/004B01D9/0059B01J2219/00006B01J2219/0004C07C275/64
    • A method for preparing biuret, a method for preparing cyanuric acid by using the prepared biuret, an apparatus for preparing biuret, and an apparatus for preparing cyanuric acid are provided to improve purity, to lower cost and to simplify the process. Biuret is prepared by melting urea; heating the molten urea for pyrolysis; adding water the product obtained by the pyrolysis to cool it, precipitating crystal, and filtering the crystal to obtain crude biuret crystal; dissolving the crude biuret crystal with an alkali aqueous solution; cooling the obtained solution to precipitate biuret crystal; and filtering and washing the obtained biuret crystal. Preferably the melting temperature is 130-160 deg.C, the heating temperature is 130-200 deg.C, and the cooling temperature is 5-40 deg.C.
    • 制备缩二脲的方法,使用制备的缩二脲制备氰尿酸的方法,制备缩二脲的装置和制备氰尿酸的装置,以提高纯度,降低成本和简化方法。 缩二脲通过溶解尿素制备; 加热熔融的尿素进行热解; 加水通过热解获得的产物冷却,沉淀晶体,过滤晶体得到粗缩二脲晶体; 用碱性水溶液溶解粗制缩二脲晶体; 冷却所得溶液沉淀缩二脲晶体; 并过滤并洗涤所获得的缩二脲晶体。 熔点温度优选为130-160℃,加热温度为130-200℃,冷却温度为5-40℃。