The vector stencils library "Chemical elements" contains 118 icon symbols of chemical elements.
Use these shapes for drawing atoms, structural formulas of inorganic and organic molecules and ions, and schemes of chemical reaction mechanisms in the ConceptDraw PRO diagramming and vector drawing software extended with the Chemistry solution from the Science and Education area of ConceptDraw Solution Park.
www.conceptdraw.com/ solution-park/ science-education-chemistry
Use these shapes for drawing atoms, structural formulas of inorganic and organic molecules and ions, and schemes of chemical reaction mechanisms in the ConceptDraw PRO diagramming and vector drawing software extended with the Chemistry solution from the Science and Education area of ConceptDraw Solution Park.
www.conceptdraw.com/ solution-park/ science-education-chemistry
The vector stencils library "Application" contains 40 icons of software applications.
Use it to design your computer and telecom illustrations and infographics with ConceptDraw PRO diagramming and vector drawing software.
The vector stencils library "Application" is included in the Computers and Communications solution from the Illustration area of ConceptDraw Solution Park.
Use it to design your computer and telecom illustrations and infographics with ConceptDraw PRO diagramming and vector drawing software.
The vector stencils library "Application" is included in the Computers and Communications solution from the Illustration area of ConceptDraw Solution Park.
The vector stencils library "Aromatics" contains 23 symbols of aromatic rings for chemical drawing of molecular structural formulas and reaction mechanism schemes in organic chemistry.
"In organic chemistry, aromaticity is a chemical property describing the way in which a conjugated ring of unsaturated bonds, lone pairs, or empty orbitals exhibits a stabilization stronger than would be expected by the stabilization of conjugation alone. ... Aromaticity can also be considered a manifestation of cyclic delocalization and of resonance. This is usually considered to be because electrons are free to cycle around circular arrangements of atoms that are alternately single- and double-bonded to one another. These bonds may be seen as a hybrid of a single bond and a double bond, each bond in the ring identical to every other. This commonly seen model of aromatic rings, namely the idea that benzene was formed from a six-membered carbon ring with alternating single and double bonds (cyclohexatriene), was developed by Kekulé (see History section below). The model for benzene consists of two resonance forms, which corresponds to the double and single bonds superimposing to give rise to six one-and-a-half bonds. Benzene is a more stable molecule than would be expected without accounting for charge delocalization. ... Types of aromatic compounds. The overwhelming majority of aromatic compounds are compounds of carbon, but they need not be hydrocarbons. 1. Neutral homocyclics. Benzene, as well as most other annulenes (cyclodecapentaene excepted) with the formula CnHn where n is an even number, such as cyclotetradecaheptaene. 2. Heterocyclics. In heterocyclic aromatics (heteroaromats), one or more of the atoms in the aromatic ring is of an element other than carbon. This can lessen the ring's aromaticity, and thus (as in the case of furan) increase its reactivity. Other examples include pyridine, pyrazine, imidazole, pyrazole, oxazole, thiophene, and their benzannulated analogs (benzimidazole, for example). 3. Polycyclics. Polycyclic aromatic hydrocarbons are molecules containing two or more simple aromatic rings fused together by sharing two neighboring carbon atoms (see also simple aromatic rings). Examples are naphthalene, anthracene, and phenanthrene. 4. Substituted aromatics. Many chemical compounds are aromatic rings with other functional groups attached. Examples include trinitrotoluene (TNT), acetylsalicylic acid (aspirin), paracetamol, and the nucleotides of DNA. 5. Atypical aromatic compounds. Aromaticity is found in ions as well: the cyclopropenyl cation (2e system), the cyclopentadienyl anion (6e system), the tropylium ion (6e), and the cyclooctatetraene dianion (10e). Aromatic properties have been attributed to non-benzenoid compounds such as tropone. Aromatic properties are tested to the limit in a class of compounds called cyclophanes. A special case of aromaticity is found in homoaromaticity where conjugation is interrupted by a single sp³ hybridized carbon atom. When carbon in benzene is replaced by other elements in borabenzene, silabenzene, germanabenzene, stannabenzene, phosphorine or pyrylium salts the aromaticity is still retained. Aromaticity also occurs in compounds that are not carbon-based at all. Inorganic 6-membered-ring compounds analogous to benzene have been synthesized. Hexasilabenzene (Si6H6) and borazine (B3N3H6) are structurally analogous to benzene, with the carbon atoms replaced by another element or elements. In borazine, the boron and nitrogen atoms alternate around the ring." [Aromaticity. Wikipedia]
The organic compound structural formulas example "Aromatics - Vector stencils library" was created using the ConceptDraw PRO software extended with the Chemistry solution from the Science and Education area of ConceptDraw Solution Park.
"In organic chemistry, aromaticity is a chemical property describing the way in which a conjugated ring of unsaturated bonds, lone pairs, or empty orbitals exhibits a stabilization stronger than would be expected by the stabilization of conjugation alone. ... Aromaticity can also be considered a manifestation of cyclic delocalization and of resonance. This is usually considered to be because electrons are free to cycle around circular arrangements of atoms that are alternately single- and double-bonded to one another. These bonds may be seen as a hybrid of a single bond and a double bond, each bond in the ring identical to every other. This commonly seen model of aromatic rings, namely the idea that benzene was formed from a six-membered carbon ring with alternating single and double bonds (cyclohexatriene), was developed by Kekulé (see History section below). The model for benzene consists of two resonance forms, which corresponds to the double and single bonds superimposing to give rise to six one-and-a-half bonds. Benzene is a more stable molecule than would be expected without accounting for charge delocalization. ... Types of aromatic compounds. The overwhelming majority of aromatic compounds are compounds of carbon, but they need not be hydrocarbons. 1. Neutral homocyclics. Benzene, as well as most other annulenes (cyclodecapentaene excepted) with the formula CnHn where n is an even number, such as cyclotetradecaheptaene. 2. Heterocyclics. In heterocyclic aromatics (heteroaromats), one or more of the atoms in the aromatic ring is of an element other than carbon. This can lessen the ring's aromaticity, and thus (as in the case of furan) increase its reactivity. Other examples include pyridine, pyrazine, imidazole, pyrazole, oxazole, thiophene, and their benzannulated analogs (benzimidazole, for example). 3. Polycyclics. Polycyclic aromatic hydrocarbons are molecules containing two or more simple aromatic rings fused together by sharing two neighboring carbon atoms (see also simple aromatic rings). Examples are naphthalene, anthracene, and phenanthrene. 4. Substituted aromatics. Many chemical compounds are aromatic rings with other functional groups attached. Examples include trinitrotoluene (TNT), acetylsalicylic acid (aspirin), paracetamol, and the nucleotides of DNA. 5. Atypical aromatic compounds. Aromaticity is found in ions as well: the cyclopropenyl cation (2e system), the cyclopentadienyl anion (6e system), the tropylium ion (6e), and the cyclooctatetraene dianion (10e). Aromatic properties have been attributed to non-benzenoid compounds such as tropone. Aromatic properties are tested to the limit in a class of compounds called cyclophanes. A special case of aromaticity is found in homoaromaticity where conjugation is interrupted by a single sp³ hybridized carbon atom. When carbon in benzene is replaced by other elements in borabenzene, silabenzene, germanabenzene, stannabenzene, phosphorine or pyrylium salts the aromaticity is still retained. Aromaticity also occurs in compounds that are not carbon-based at all. Inorganic 6-membered-ring compounds analogous to benzene have been synthesized. Hexasilabenzene (Si6H6) and borazine (B3N3H6) are structurally analogous to benzene, with the carbon atoms replaced by another element or elements. In borazine, the boron and nitrogen atoms alternate around the ring." [Aromaticity. Wikipedia]
The organic compound structural formulas example "Aromatics - Vector stencils library" was created using the ConceptDraw PRO software extended with the Chemistry solution from the Science and Education area of ConceptDraw Solution Park.
Organic Chemistry Symbols
ConceptDraw DIAGRAM diagramming and vector drawing software extended with Chemistry solution from the Science and Education area of ConceptDraw Solution Park is effective for drawing various organic chemistry schemes, diagrams, illustrations thanks to the included collection of predesigned organic chemistry symbols.The vector stencils library "Laboratory equipment" contains 31 clipart icons of chemical laboratory equipment and labware.
Use these shapes for drawing part assembly and mounting schemes of glassware apparatus in chemical experiment diagrams and illustrations in the ConceptDraw PRO diagramming and vector drawing software extended with the Chemistry solution from the Science and Education area of ConceptDraw Solution Park.
Use these shapes for drawing part assembly and mounting schemes of glassware apparatus in chemical experiment diagrams and illustrations in the ConceptDraw PRO diagramming and vector drawing software extended with the Chemistry solution from the Science and Education area of ConceptDraw Solution Park.
The vector stencils library "Conformations" contains 32 symbols of ring conformations, Newman and Fisher projections for chemical and biochemical drawing the molecular models and structural formulas of organic molecules and biochemical metabolites, the conformers spatial structures of organic molecules, the schemes of stereospecific chemical reactions in organic synthesis.
Use these shapes to draw your stereochemistry drawings in the ConceptDraw PRO diagramming and vector drawing software extended with the Chemistry solution from the Science and Education area of ConceptDraw Solution Park.
www.conceptdraw.com/ solution-park/ science-education-chemistry
Use these shapes to draw your stereochemistry drawings in the ConceptDraw PRO diagramming and vector drawing software extended with the Chemistry solution from the Science and Education area of ConceptDraw Solution Park.
www.conceptdraw.com/ solution-park/ science-education-chemistry
Chemical Engineering
ConceptDraw DIAGRAM is a powerful diagramming and vector drawing software. Extended with Chemical and Process Engineering Solution from the Industrial Engineering Area of ConceptDraw Solution Park, it became the best Chemical Engineering software.Chemistry Symbols and Meanings
Chemistry solution offers 5 libraries with large collection of vector chemistry symbols and meanings, chemistry equation symbols, organic chemistry symbols, and chemical clipart: Chemical Elements Library, Chemical Drawings Library, Conformations Library, Laboratory Equipment Library, Periodic Table of Chemical Elements Library.The vector stencils library "Application" contains 40 icons of software applications.
Use it to design your computer and telecom illustrations and infographics with ConceptDraw PRO diagramming and vector drawing software.
The vector stencils library "Application" is included in the Computers and Communications solution from the Illustration area of ConceptDraw Solution Park.
Use it to design your computer and telecom illustrations and infographics with ConceptDraw PRO diagramming and vector drawing software.
The vector stencils library "Application" is included in the Computers and Communications solution from the Illustration area of ConceptDraw Solution Park.
HelpDesk
How to Draw a Chemical Process Flow Diagram
Process Flow Diagram widely used in modeling of processes in the chemical industry. A Chemical Process Flow diagram (PFD) is a specialized type of flowchart. With the help of Chemical Process Flow Diagram engineers can easily specify the general scheme of the processes and chemical plant equipment. Chemical Process Flow Diagram displays the real scheme of the chemical process, the relationship between the equipment and the technical characteristics of the process. Chemical Process Flow Diagram illustrates the connections between the basic equipment as well as the overall structure of pipelines and other supporting equipment. The purpose of the PFD is to build the image of the basic idea of the chemical process. ConceptDraw DIAGRAM together with its Chemical and Process Engineering solution delivers the possibility to design Chemical Process Flow diagrams. It is designed for chemical industry engineers and designers.- Visio Chemistry Stencils
- Chemistry Stencils For Laboratory Drawings
- Laboratory equipment - Vector stencils library | Chemistry Adapter ...
- Laboratory equipment - Vector stencils library | Laboratory ...
- Chemical and Process Engineering | Process Flow Diagram ...
- Laboratory equipment - Vector stencils library | Pictures Of Glass ...
- Laboratory equipment - Vector stencils library | Water Or Steam Bath ...
- Laboratory equipment - Vector stencils library | 100 Apparatus Used ...
- Laboratory equipment - Vector stencils library | Pictures Of ...
- Design elements - Laboratory equipment | Laboratory equipment ...