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Slice food as thin as possible ( First, let`s collect empty pop cans for solar panel assembly. Try to wash them thoroughly, otherwise they will begin to spread odors very quickly. Cans are generally produced out of aluminum, but there are some made of iron. You can test different cans easily with magnet. Please pay attention and try to precisely cut and form small fins at the top of each can. Idea is to encourage turbulent airflow inside pop cans so that air passing through the tube can collect more heat from the warm wall of pop cans. Carefully cut the top of the can in the form of a star, and then distort free parts using pliers (Image no. It is important to do all this before gluing the cans together. We have marked three holes on each can with a nail, then drilled the bottom using tools shown on images 2 and 3. More details can be found on diy solar panels video tutorial page. Image 1 ! This procedure is extremely dangerous because pop can walls are very thin. Sharp parts may cause hand injury. After drilling is completed, small parts of the metal could remain in the can. Use pliers to remove these parts. Do not remove pieces of sheet metal and debris with bare hands! Remove grease and dirt from the surface of cans. Any synthetic degrease agent will do the job. Do this outdoors or in a well- ventilated room. WARNING! This procedure is flammable! It is dangerous to do this near open flame or cigarette!!! Glue all cans together using adhesive silicone resistant to high temperatures, at least up to 2. There are products for bonding that can withstand temperature up to 3. Top and bottom of all pop cans are compatible and fit perfectly one onto another. Put some glue or silicone on the edge of one can and press it against another one. In this way the glue/silicone will not run away from the edge. Picture 4 shows inside view of two pop cans glued together, while series of stacked and finished cans is shown in Picture 5. Picture 4. You can use two ordinary flat wooden planks and nail them together. Template will provide necessary support for solar pipe during the drying process. In addition, secure the cans onto a template using ordinary jar rubber. Pictures 7, 8 and 9 show the gluing process. Series of glued cans form a solar pipe. Picture 1. 0 shows the pipe fixed in motionless position until the glue gets completely dry. Image 1. 1. Gaps around the edges are filled with adhesive tape or heat- resistant silicone. Drilled parts can be seen on images 1. This is where the first row of cans will be glued to the air intake/exhaust boxes. Check out how it looks when all parts are assembled and prepared for painting (Image 1. The adhesive dries very slowly. Leave it to dry for at least 2. Solar absorber fits in the casing made of wood (Fig. Back side of diy solar panels box is made out of plywood. Insulation of solar panel is achieved by applying rock wool or styrodur. Installed insulation can be seen in Figure 1. Pay special attention onto insulation around the openings for the solar collector air inlet/outlet. Next step is preparation, protection and painting of timber box (solar panel housing). Special hooks have to be attached to all four corners of the solar collector, so that it can be easily mounted on the wall (Fig. Fig. Empty box is placed on the wall in order to precisely mark the spot for drilling the air inlet/exhaust. Picture 1. 4. The casing of diy solar panels is covered with plexiglass attached to the frame and thoroughly corked with silicone. Polycarbonate / plexiglass is slightly convex in order to gain additional strength. You can see installed solar absorber without plexiglass in picture 1. Complete solar collector is shown on Picture 1. Picture 2. 0. Check out our diy solar panels on You. Tube. Video shows how solar panel operates on a bright day. After first 2. 0 minutes, panel raised the air temperature inside living room to 5. If the sun does not shine, it is necessary to interrupt the air supply to the solar collector, otherwise the room will begin to slowly cool off. This can be solved by installing shut- off valve, which will reduce unnecessary heat loss. Differential thermostat (snap disc) controls the fan. This thermostat can be bought in better- equipped electronic component stores. Thermostat has two sensors. One placed inside the top opening for warm air, the other inside the lower opening for the supply of cold air in the solar collector. If on/off temperatures are set carefully, diy solar panels are able to produce an average 2 k. W of energy for home heating. This generally depends on how much sun do we have during the day. Final Chapter: Pop Cans Solar Panel Test Drive. Solar collector dress rehearsal was carried out in the backyard before installing the system on the house. It was a sunny winter day, without clouds. Our air blower fan is actually a big PC cooler extracted from a faulty power supply of PC. After 1. 0 minutes in the sun from the solar collector is out hot air temperatures of 7. The test results have encouraged us to install solar heater on the house as soon as possible. After completing installation of collector, the outside temperature was - 3. For the home version we have used more powerful fan than the one for testing. Heated air temperature went up to +7. Temperature was measured by digital thermometer. To calculate total heating power of the collector, we took into calculation the air flow and average air temperature on output. Calculated power which DIY solar panels produced, was approximately 1. W (watts) which is almost 3 HP (3 horsepowers)!!! Considering that the results are quite satisfactory, conclusion is that DIY solar panels are definitely worth making. The collector, at the very least, can be used for additional heating of your home, and it is up to you to calculate and figure out how much money you can save. Type in a share code or part of a company’s name in the Company Lookup box. Go to view its. tearsheet with share data, news and more. Applications are presented that link RDF technologies to methods from statistics and cheminformatics. Calculated molecular descriptors can also.
Python for molecular modeling. Python Molecular Viewer (PMV) http://mgltools.scripps.edu. Chemistry toolkits and utilities. Molecular Descriptors: LINK. Modular Chemical Descriptor Language (MCDL): Stereochemical modules . In the majority of cases it is a four- coordinated atom (such as a carbon atom), but there is a substantial number of stereoisomers having chiral centers with three substituents. Notable examples include chiral sulfoxides. The priorities of the substituents attached to a chiral center are the MCDL priorities (based on ASCII codes) of the attached fragments and terminal atoms, if any (see below). Once these are known, a Fischer projection of the configuration at the chiral atom is drawn. A Fischer projection is a planar representation of a molecule that preserves information about chirality. With the chiral atom at its center, a horizontal line represents two bonds bending forward toward the viewer, and a vertical line represents two bonds bending back away from the viewer. In the projection, the highest MCDL priority substituent on the chiral atom is placed at the top and the second highest at the bottom. The other two substituents appear at the left and right and are positioned to preserve the configuration of the chiral atom. Once oriented in this way, the atom stereochemistry is specified in the MCDL linear descriptor as . The MCDL composition and connectivity modules for both of these are C; CHH; 2. CHHH; CO; 2. OH. The chiral atom is fragment 1 in the descriptor. Its substituents and their priorities are CHH (2), CHHH (3), CO (5), and OH (6). Three- dimensional representations of this compound's enantiomers are shown in Figure 2 with the priorities of the substituents indicated. Figure 1. Structural formula of 2- hydroxy- 2- methylbutanoic acid. Figure 2. Three- dimensional representations of 2- hydroxy- 2- methylbutanoic acid's enantiomers with the MCDL priorities of the substituents on the chiral atom indicated. The two structures are redrawn as Fischer projection formulas in Figure 3. The four substituents have been placed on the projection so the fragment having the highest priority is at the top and the next highest at the bottom. Thus, the stereochemistry for the left structure is specified in the MCDL as . The MCDL composition module of lactic acid is CH; CHHH; CO; 2. OH, and the chiral carbon is part of the first fragment. The attached fragments and their MCDL priorities are CHHH (2), CO (3), and OH (4). The fourth substituent on the chiral carbon, H, is actually part of fragment 1, but it must be considered on its own in order to specify the stereochemistry in the linear descriptor. To handle this situation, a new rule is added to the MCDL: Structural fragments have higher priorities than terminal atoms (numbers have lower ASCII codes than letters). Thus, of the four substituents attached to the chiral atom in lactic acid, the terminal atom H has the lowest priority. Orienting the R configuration as the Fischer projection in Figure 4 gives the MCDL descriptor . While treatment of structures with multiple chiral centers in the MCDL is straightforward in many cases, the presence of multiple chiral centers in certain quasi- symmetrical structures may lead to complications due to the fact that the unique part of the MCDL linear descriptor is generated without consideration of stereochemistry. As a result, constitutionally, but not stereochemically, equivalent chiral centers may receive arbitrarily selected fragment numbers. Figure 5 shows the 3- dimensional structure of meso- tartaric acid having two constitutionally identical, but stereochemically different, chiral centers (opposite configurations). Because of the topological symmetry of the molecule, two MCDL numbering schemes are possible. The MCDL stereochemistry descriptor for this numbering scheme is . Since 5 is a higher priority than H, this difference allows us to choose . As a general rule, for quasi- symmetrical structures where multiple equivalent numbering schemes are possible, all must be explored for selection of the canonical (the lowest ASCII code sequence) stereochemistry descriptor. An alternative approach entails the use of hash variables for constitutionally equivalent stereogenic fragments (see Generation of atomic MCDL stereodescriptors from structure diagrams section below). Three- substituent chiral centers. The MCDL can also specify chirality of atomic centers with only three substituents in those cases where the fourth substituent position is occupied by an electron pair. In this case, the electron pair is treated as a . The priority of the electron pair is defined in the MCDL as 0 (zero), giving it, maybe surprisingly, higher priority than structural fragments and terminal atoms. For example, the chirality descriptors of ethyl(fluoromethyl)sulfoxide (CFHH; CHH; CHHH; SO. Vls. 3d - Chemistry toolkits and utilities. Chemistry toolkits & utilities. Future Developments Studies on fauna diversity in the inselbergs of the Brazilian Semi-arid are rare. Rare to see it like this.
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